A species of protozoa that is the causal agent of falciparum malaria (MALARIA, FALCIPARUM). It is most prevalent in the tropics and subtropics.
Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations.
Proteins found in any species of protozoan.
A genus of protozoa that comprise the malaria parasites of mammals. Four species infect humans (although occasional infections with primate malarias may occur). These are PLASMODIUM FALCIPARUM; PLASMODIUM MALARIAE; PLASMODIUM OVALE, and PLASMODIUM VIVAX. Species causing infection in vertebrates other than man include: PLASMODIUM BERGHEI; PLASMODIUM CHABAUDI; P. vinckei, and PLASMODIUM YOELII in rodents; P. brasilianum, PLASMODIUM CYNOMOLGI; and PLASMODIUM KNOWLESI in monkeys; and PLASMODIUM GALLINACEUM in chickens.
A protozoan parasite that causes vivax malaria (MALARIA, VIVAX). This species is found almost everywhere malaria is endemic and is the only one that has a range extending into the temperate regions.
Agents used in the treatment of malaria. They are usually classified on the basis of their action against plasmodia at different stages in their life cycle in the human. (From AMA, Drug Evaluations Annual, 1992, p1585)
Any part or derivative of any protozoan that elicits immunity; malaria (Plasmodium) and trypanosome antigens are presently the most frequently encountered.
The prototypical antimalarial agent with a mechanism that is not well understood. It has also been used to treat rheumatoid arthritis, systemic lupus erythematosus, and in the systemic therapy of amebic liver abscesses.
A protozoan parasite of rodents transmitted by the mosquito Anopheles dureni.
A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia.
Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN.
Diminished or failed response of an organism, disease or tissue to the intended effectiveness of a chemical or drug. It should be differentiated from DRUG TOLERANCE which is the progressive diminution of the susceptibility of a human or animal to the effects of a drug, as a result of continued administration.
Immunoglobulins produced in a response to PROTOZOAN ANTIGENS.
Deoxyribonucleic acid that makes up the genetic material of protozoa.
Tests that demonstrate the relative effectiveness of chemotherapeutic agents against specific parasites.
A group of SESQUITERPENES and their analogs that contain a peroxide group (PEROXIDES) within an oxepin ring (OXEPINS).
Vaccines made from antigens arising from any of the four strains of Plasmodium which cause malaria in humans, or from P. berghei which causes malaria in rodents.
The functional hereditary units of protozoa.
One of the FOLIC ACID ANTAGONISTS that is used as an antimalarial or with a sulfonamide to treat toxoplasmosis.
The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed)
A species of PLASMODIUM causing malaria in rodents.
A protozoan parasite that occurs primarily in subtropical and temperate areas. It is the causal agent of quartan malaria. As the parasite grows it exhibits little ameboid activity.
A long acting sulfonamide that is used, usually in combination with other drugs, for respiratory, urinary tract, and malarial infections.
Malaria caused by PLASMODIUM VIVAX. This form of malaria is less severe than MALARIA, FALCIPARUM, but there is a higher probability for relapses to occur. Febrile paroxysms often occur every other day.
An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
Multinucleate cells or a stage in the development of sporozoan protozoa. It is exemplified by the life cycle of PLASMODIUM FALCIPARUM in the MALARIA infection cycle.
Single preparations containing two or more active agents, for the purpose of their concurrent administration as a fixed dose mixture.
A republic in west equatorial Africa, south of CAMEROON and west of the CONGO. Its capital is Libreville.
A surface protein found on Plasmodium species which induces a T-cell response. The antigen is polymorphic, sharing amino acid sequence homology among PLASMODIUM FALCIPARUM; PLASMODIUM CHABAUDI; PLASMODIUM VIVAX; and PLASMODIUM YOELII.
A genus of mosquitoes (CULICIDAE) that are known vectors of MALARIA.
The complete genetic complement contained in a set of CHROMOSOMES in a protozoan.
A 4-aminoquinoline compound with anti-inflammatory properties.
A phospholipid-interacting antimalarial drug (ANTIMALARIALS). It is very effective against PLASMODIUM FALCIPARUM with very few side effects.
A country consisting of the eastern half of the island of New Guinea and adjacent islands, including New Britain, New Ireland, the Admiralty Islands, and New Hanover in the Bismarck Archipelago; Bougainville and Buka in the northern Solomon Islands; the D'Entrecasteaux and Trobriand Islands; Woodlark (Murua) Island; and the Louisiade Archipelago. It became independent on September 16, 1975. Formerly, the southern part was the Australian Territory of Papua, and the northern part was the UN Trust Territory of New Guinea, administered by Australia. They were administratively merged in 1949 and named Papua and New Guinea, and renamed Papua New Guinea in 1971.
Uninuclear cells or a stage in the life cycle of sporozoan protozoa. Merozoites, released from ruptured multinucleate SCHIZONTS, enter the blood stream and infect the ERYTHROCYTES.
A protozoan parasite from Southeast Asia that causes monkey malaria. It is naturally acquired by man in Malaysia and can also be transmitted experimentally to humans.
An enzyme that catalyzes the formation of dihydropteroate from p-aminobenzoic acid and dihydropteridine-hydroxymethyl-pyrophosphate. EC 2.5.1.15.
A republic in western Africa, southwest of MAURITANIA and east of MALI. Its capital is Dakar.
Sesquiterpenes are a class of terpenes consisting of three isoprene units, forming a 15-carbon skeleton, which can be found in various plant essential oils and are known for their diverse chemical structures and biological activities, including anti-inflammatory, antimicrobial, and cytotoxic properties.
A species of protozoan parasite causing MALARIA. It is the rarest of the four species of PLASMODIUM infecting humans, but is common in West African countries and neighboring areas.
A biguanide compound which metabolizes in the body to form cycloguanil, an anti-malaria agent.
The co-occurrence of pregnancy and parasitic diseases. The parasitic infection may precede or follow FERTILIZATION.
A protozoan parasite of rodents transmitted by the mosquito Anopheles stephensi.
The product of meiotic division of zygotes in parasitic protozoa comprising haploid cells. These infective cells invade the host and undergo asexual reproduction producing MEROZOITES (or other forms) and ultimately gametocytes.
A condition characterized by somnolence or coma in the presence of an acute infection with PLASMODIUM FALCIPARUM (and rarely other Plasmodium species). Initial clinical manifestations include HEADACHES; SEIZURES; and alterations of mentation followed by a rapid progression to COMA. Pathologic features include cerebral capillaries filled with parasitized erythrocytes and multiple small foci of cortical and subcortical necrosis. (From Adams et al., Principles of Neurology, 6th ed, p136)
The continuous sequence of changes undergone by living organisms during the post-embryonic developmental process, such as metamorphosis in insects and amphibians. This includes the developmental stages of apicomplexans such as the malarial parasite, PLASMODIUM FALCIPARUM.
The relationship between an invertebrate and another organism (the host), one of which lives at the expense of the other. Traditionally excluded from definition of parasites are pathogenic BACTERIA; FUNGI; VIRUSES; and PLANTS; though they may live parasitically.
An enzyme of the oxidoreductase class that catalyzes the reaction 7,8-dihyrofolate and NADPH to yield 5,6,7,8-tetrahydrofolate and NADPH+, producing reduced folate for amino acid metabolism, purine ring synthesis, and the formation of deoxythymidine monophosphate. Methotrexate and other folic acid antagonists used as chemotherapeutic drugs act by inhibiting this enzyme. (Dorland, 27th ed) EC 1.5.1.3.
Cells or feeding stage in the life cycle of sporozoan protozoa. In the malarial parasite, the trophozoite develops from the MEROZOITE and then splits into the SCHIZONT. Trophozoites that are left over from cell division can go on to form gametocytes.
A family of diphenylenemethane derivatives.
The study of parasites and PARASITIC DISEASES.
The constant presence of diseases or infectious agents within a given geographic area or population group. It may also refer to the usual prevalence of a given disease with such area or group. It includes holoendemic and hyperendemic diseases. A holoendemic disease is one for which a high prevalent level of infection begins early in life and affects most of the child population, leading to a state of equilibrium such that the adult population shows evidence of the disease much less commonly than do children (malaria in many communities is a holoendemic disease). A hyperendemic disease is one that is constantly present at a high incidence and/or prevalence rate and affects all groups equally. (Last, A Dictionary of Epidemiology, 3d ed, p53, 78, 80)
A hydroxynaphthoquinone that has antimicrobial activity and is being used in antimalarial protocols.
The concentration of a compound needed to reduce population growth of organisms, including eukaryotic cells, by 50% in vitro. Though often expressed to denote in vitro antibacterial activity, it is also used as a benchmark for cytotoxicity to eukaryotic cells in culture.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A republic in eastern Africa, south of ETHIOPIA, west of SOMALIA with TANZANIA to its south, and coastline on the Indian Ocean. Its capital is Nairobi.
Formerly known as Siam, this is a Southeast Asian nation at the center of the Indochina peninsula. Bangkok is the capital city.
A republic of southeast Asia, northwest of Thailand, long familiar as Burma. Its capital is Yangon, formerly Rangoon. Inhabited by people of Mongolian stock and probably of Tibetan origin, by the 3d century A.D. it was settled by Hindus. The modern Burmese state was founded in the 18th century but was in conflict with the British during the 19th century. Made a crown colony of Great Britain in 1937, it was granted independence in 1947. In 1989 it became Myanmar. The name comes from myanma, meaning the strong, as applied to the Burmese people themselves. (From Webster's New Geographical Dictionary, 1988, p192 & Room, Brewer's Dictionary of Names, 1992, p367)
A republic in central Africa lying east of CHAD and the CENTRAL AFRICAN REPUBLIC and west of NIGERIA. The capital is Yaounde.
AMINO ALCOHOLS containing the ETHANOLAMINE; (-NH2CH2CHOH) group and its derivatives.
A species in the family AOTIDAE, inhabiting the forested regions of Central and South America (from Panama to the Amazon). Vocalizations occur primarily at night when they are active, thus they are also known as Northern night monkeys.
Invertebrate organisms that live on or in another organism (the host), and benefit at the expense of the other. Traditionally excluded from definition of parasites are pathogenic BACTERIA; FUNGI; VIRUSES; and PLANTS; though they may live parasitically.
An aminoquinoline that is given by mouth to produce a radical cure and prevent relapse of vivax and ovale malarias following treatment with a blood schizontocide. It has also been used to prevent transmission of falciparum malaria by those returning to areas where there is a potential for re-introduction of malaria. Adverse effects include anemias and GI disturbances. (From Martindale, The Extra Pharmacopeia, 30th ed, p404)
Ribonucleic acid in protozoa having regulatory and catalytic roles as well as involvement in protein synthesis.
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Aspects of health and disease related to travel.
The use of instrumentation and techniques for visualizing material and details that cannot be seen by the unaided eye. It is usually done by enlarging images, transmitted by light or electron beams, with optical or magnetic lenses that magnify the entire image field. With scanning microscopy, images are generated by collecting output from the specimen in a point-by-point fashion, on a magnified scale, as it is scanned by a narrow beam of light or electrons, a laser, a conductive probe, or a topographical probe.
A family of the New World monkeys inhabiting the forests of South and Central America. There is a single genus and several species occurring in this family, including AOTUS TRIVIRGATUS (Northern night monkeys).
Measure of the number of the PARASITES present in a host organism.
A country in western Africa, east of MAURITANIA and south of ALGERIA. Its capital is Bamako. From 1904-1920 it was known as Upper Senegal-Niger; prior to 1958, as French Sudan; 1958-1960 as the Sudanese Republic and 1959-1960 it joined Senegal in the Mali Federation. It became an independent republic in 1960.
A republic in western Africa, south of BURKINA FASO and west of TOGO. Its capital is Accra.
Insects that transmit infective organisms from one host to another or from an inanimate reservoir to an animate host.
A republic stretching from the Indian Ocean east to New Guinea, comprising six main islands: Java, Sumatra, Bali, Kalimantan (the Indonesian portion of the island of Borneo), Sulawesi (formerly known as the Celebes) and Irian Jaya (the western part of New Guinea). Its capital is Djakarta. The ethnic groups living there are largely Chinese, Arab, Eurasian, Indian, and Pakistani; 85% of the peoples are of the Islamic faith.
A family of the order DIPTERA that comprises the mosquitoes. The larval stages are aquatic, and the adults can be recognized by the characteristic WINGS, ANIMAL venation, the scales along the wing veins, and the long proboscis. Many species are of particular medical importance.
A species of mosquito in the genus Anopheles and the principle vector of MALARIA in Africa.
Membrane proteins whose primary function is to facilitate the transport of molecules across a biological membrane. Included in this broad category are proteins involved in active transport (BIOLOGICAL TRANSPORT, ACTIVE), facilitated transport and ION CHANNELS.
I'm afraid there seems to be a misunderstanding - "Africa" is not a medical term and does not have a medical definition. Africa is the world's second-largest and second-most populous continent, consisting of 54 countries with diverse cultures, peoples, languages, and landscapes. If you have any questions related to medical topics or definitions, I would be happy to help answer those for you!
I'm sorry for any confusion, but "Cambodia" is not a medical term that can be defined in a medical context. It is the name of a country located in Southeast Asia, known officially as the Kingdom of Cambodia. If you have any questions related to health, medicine, or science, I'd be happy to try and help answer those for you.
A republic in eastern Africa, south of UGANDA and north of MOZAMBIQUE. Its capital is Dar es Salaam. It was formed in 1964 by a merger of the countries of TANGANYIKA and ZANZIBAR.
A protozoan parasite that occurs naturally in the macaque. It is similar to PLASMODIUM VIVAX and produces a type of malaria similar to vivax malaria (MALARIA, VIVAX). This species has been found to give rise to both natural and experimental human infections.
The body fluid that circulates in the vascular system (BLOOD VESSELS). Whole blood includes PLASMA and BLOOD CELLS.
A republic in western Africa, constituting an enclave within SENEGAL extending on both sides of the Gambia River. Its capital is Banjul, formerly Bathurst.
A republic in western Africa, south and east of MALI and west of NIGER. Its capital is Ouagadougou. It was formerly called Upper Volta until 1984.
A protozoan parasite that causes avian malaria (MALARIA, AVIAN), primarily in chickens, and is transmitted by the Aedes mosquito.
Zygote-containing cysts of sporozoan protozoa. Further development in an oocyst produces small individual infective organisms called SPOROZOITES. Then, depending on the genus, the entire oocyst is called a sporocyst or the oocyst contains multiple sporocysts encapsulating the sporozoites.
The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B.
Change in the surface ANTIGEN of a microorganism. There are two different types. One is a phenomenon, especially associated with INFLUENZA VIRUSES, where they undergo spontaneous variation both as slow antigenic drift and sudden emergence of new strains (antigenic shift). The second type is when certain PARASITES, especially trypanosomes, PLASMODIUM, and BORRELIA, survive the immune response of the host by changing the surface coat (antigen switching). (From Herbert et al., The Dictionary of Immunology, 4th ed)
The semi-permeable outer structure of a red blood cell. It is known as a red cell 'ghost' after HEMOLYSIS.
Inhibitors of the enzyme, dihydrofolate reductase (TETRAHYDROFOLATE DEHYDROGENASE), which converts dihydrofolate (FH2) to tetrahydrofolate (FH4). They are frequently used in cancer chemotherapy. (From AMA, Drug Evaluations Annual, 1994, p2033)
A phylum of unicellular parasitic EUKARYOTES characterized by the presence of complex apical organelles generally consisting of a conoid that aids in penetrating host cells, rhoptries that possibly secrete a proteolytic enzyme, and subpellicular microtubules that may be related to motility.
The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS.
A sequence-related subfamily of ATP-BINDING CASSETTE TRANSPORTERS that actively transport organic substrates. Although considered organic anion transporters, a subset of proteins in this family have also been shown to convey drug resistance to neutral organic drugs. Their cellular function may have clinical significance for CHEMOTHERAPY in that they transport a variety of ANTINEOPLASTIC AGENTS. Overexpression of proteins in this class by NEOPLASMS is considered a possible mechanism in the development of multidrug resistance (DRUG RESISTANCE, MULTIPLE). Although similar in function to P-GLYCOPROTEINS, the proteins in this class share little sequence homology to the p-glycoprotein family of proteins.
The major sialoglycoprotein of the human erythrocyte membrane. It consists of at least two sialoglycopeptides and is composed of 60% carbohydrate including sialic acid and 40% protein. It is involved in a number of different biological activities including the binding of MN blood groups, influenza viruses, kidney bean phytohemagglutinin, and wheat germ agglutinin.
The process of germ cell development from the primordial GERM CELLS to the mature haploid GAMETES: ova in the female (OOGENESIS) or sperm in the male (SPERMATOGENESIS).
A country in northeastern Africa. The capital is Khartoum.
A republic in central Africa lying between GABON and DEMOCRATIC REPUBLIC OF THE CONGO and south of Cameroon. Its capital is Brazzaville.
I'm sorry for any confusion, but "Colombia" is not a medical term that can be defined in a medical context; rather, it's a country located in South America. If you have any questions related to medical terminology or health-related topics, I would be happy to help with those instead!
A republic in southern Africa, south of TANZANIA, east of ZAMBIA and ZIMBABWE, bordered on the west by the Indian Ocean. Its capital is Maputo. It was formerly called Portuguese East Africa.
An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.
Therapy with two or more separate preparations given for a combined effect.
Bites and stings inflicted by insects.
A genus of the family CEBIDAE consisting of four species: S. boliviensis, S. orstedii (red-backed squirrel monkey), S. sciureus (common squirrel monkey), and S. ustus. They inhabit tropical rain forests in Central and South America. S. sciureus is used extensively in research studies.
Quinolines substituted in any position by one or more amino groups.
Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product.
Proteins which are found in membranes including cellular and intracellular membranes. They consist of two types, peripheral and integral proteins. They include most membrane-associated enzymes, antigenic proteins, transport proteins, and drug, hormone, and lectin receptors.
Genotypic differences observed among individuals in a population.
Proteins prepared by recombinant DNA technology.
Proteins that contain an iron-porphyrin, or heme, prosthetic group resembling that of hemoglobin. (From Lehninger, Principles of Biochemistry, 1982, p480)
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
A French overseas department on the northeast coast of South America. Its capital is Cayenne. It was first settled by the French in 1604. Early development was hindered because of the presence of a penal colony. The name of the country and the capital are variants of Guyana, possibly from the native Indian Guarani guai (born) + ana (kin), implying a united and interrelated race of people. (From Webster's New Geographical Dictionary, 1988, p418 & Room, Brewer's Dictionary of Names, 1992, p195)
Antigens on surfaces of cells, including infectious or foreign cells or viruses. They are usually protein-containing groups on cell membranes or walls and may be isolated.
A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis.
Small synthetic peptides that mimic surface antigens of pathogens and are immunogenic, or vaccines manufactured with the aid of recombinant DNA techniques. The latter vaccines may also be whole viruses whose nucleic acids have been modified.
Pathological processes or abnormal functions of the PLACENTA.
A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN.
One of the Indian Ocean Islands off the southeast coast of Africa. Its capital is Antananarivo. It was formerly called the Malagasy Republic. Discovered by the Portuguese in 1500, its history has been tied predominantly to the French, becoming a French protectorate in 1882, a French colony in 1896, and a territory within the French union in 1946. The Malagasy Republic was established in the French Community in 1958 but it achieved independence in 1960. Its name was changed to Madagascar in 1975. (From Webster's New Geographical Dictionary, 1988, p714)
Cytochromes of the b group that have alpha-band absorption of 563-564 nm. They occur as subunits in MITOCHONDRIAL ELECTRON TRANSPORT COMPLEX III.
Simultaneous resistance to several structurally and functionally distinct drugs.
Phenanthrenes are aromatic hydrocarbons consisting of three benzene rings fused together in a linear arrangement, commonly found in various plants and some animals, and can act as precursors for certain steroid hormones or exhibit pharmacological activities with potential therapeutic uses.
The total number of cases of a given disease in a specified population at a designated time. It is differentiated from INCIDENCE, which refers to the number of new cases in the population at a given time.
A blood group consisting mainly of the antigens Fy(a) and Fy(b), determined by allelic genes, the frequency of which varies profoundly in different human groups; amorphic genes are common.
Compounds based on 4-aminobenzenesulfonamide. The '-anil-' part of the name refers to aniline.
Divisions of the year according to some regularly recurrent phenomena usually astronomical or climatic. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
Any of a group of infections of fowl caused by protozoa of the genera PLASMODIUM, Leucocytozoon, and Haemoproteus. The life cycles of these parasites and the disease produced bears strong resemblance to those observed in human malaria.
The condition of being heterozygous for hemoglobin S.
The degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
Quinolines are heterocyclic aromatic organic compounds consisting of a two-nitrogened benzene ring fused to a pyridine ring, which have been synthesized and used as building blocks for various medicinal drugs, particularly antibiotics and antimalarials.
I'm sorry for any confusion, but "Peru" is not a medical term or concept, it is a country located in South America, known officially as the Republic of Peru. If you have any questions about medical topics that I can help clarify, please let me know!
The oxygen-carrying proteins of ERYTHROCYTES. They are found in all vertebrates and some invertebrates. The number of globin subunits in the hemoglobin quaternary structure differs between species. Structures range from monomeric to a variety of multimeric arrangements.
A purine and a reaction intermediate in the metabolism of adenosine and in the formation of nucleic acids by the salvage pathway.
A republic in western Africa, south of NIGER and between TOGO and NIGERIA. Its capital is Porto-Novo. It was formerly called Dahomey. In the 17th century it was a kingdom in the southern area of Africa. Coastal footholds were established by the French who deposed the ruler by 1892. It was made a French colony in 1894 and gained independence in 1960. Benin comes from the name of the indigenous inhabitants, the Bini, now more closely linked with southern Nigeria (Benin City, a town there). Bini may be related to the Arabic bani, sons. (From Webster's New Geographical Dictionary, 1988, p136, 310 & Room, Brewer's Dictionary of Names, 1992, p60)
A republic in southern Africa, southwest of DEMOCRATIC REPUBLIC OF THE CONGO and west of ZAMBIA. Its capital is Luanda.
A republic in western Africa, south of GUINEA and east of COTE D'IVOIRE. Its capital is Monrovia.
Derivatives of chondroitin which have a sulfate moiety esterified to the galactosamine moiety of chondroitin. Chondroitin sulfate A, or chondroitin 4-sulfate, and chondroitin sulfate C, or chondroitin 6-sulfate, have the sulfate esterified in the 4- and 6-positions, respectively. Chondroitin sulfate B (beta heparin; DERMATAN SULFATE) is a misnomer and this compound is not a true chondroitin sulfate.
The collective name for the islands of the Pacific Ocean northeast of Australia, including NEW CALEDONIA; VANUATU; New Hebrides, Solomon Islands, Admiralty Islands, Bismarck Archipelago, FIJI, etc. Melanesia (from the Greek melas, black + nesos, island) is so called from the black color of the natives who are generally considered to be descended originally from the Negroid Papuans and the Polynesians or Malays. (From Webster's New Geographical Dictionary, 1988, p748 & Room, Brewer's Dictionary of Names, 1992, p344)
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)
A republic in southern Africa east of ZAMBIA and MOZAMBIQUE. Its capital is Lilongwe. It was formerly called Nyasaland.
A group of Indian Ocean Islands, the islands of Great Comoro, Anjouan, Mayotte, and Moheli, lying between northeast Mozambique and northwest Madagascar. The capital is Moroni. In 1914 they became a colony attached to Madagascar administratively and were made a French overseas territory in 1947. Except for Mayotte which remained French, Comoros became an independent republic in 1975. Comoros represents the Arabic qamar, moon, said by some scholars to be linked with the mystical Mountains of the Moon said to be somewhere in equatorial Africa. (From Webster's New Geographical Dictionary, 1988, p283 & Room, Brewer's Dictionary of Names, 1992, p122)
Originally an island of the Malay Archipelago, the second largest island in the world. It divided, West New Guinea becoming part of Indonesia and East New Guinea becoming Papua New Guinea.
A republic in western Africa, south of NIGER between BENIN and CAMEROON. Its capital is Abuja.
A republic in eastern Africa, south of SUDAN and west of KENYA. Its capital is Kampala.
I'm sorry for any confusion, but "Honduras" is a country located in Central America and it doesn't have a medical definition. If you have any questions related to medical topics or definitions, I'd be happy to help with those!
The genetic constitution of individuals with respect to one member of a pair of allelic genes, or sets of genes that are closely linked and tend to be inherited together such as those of the MAJOR HISTOCOMPATIBILITY COMPLEX.
A highly vascularized mammalian fetal-maternal organ and major site of transport of oxygen, nutrients, and fetal waste products. It includes a fetal portion (CHORIONIC VILLI) derived from TROPHOBLASTS and a maternal portion (DECIDUA) derived from the uterine ENDOMETRIUM. The placenta produces an array of steroid, protein and peptide hormones (PLACENTAL HORMONES).
A sulfone active against a wide range of bacteria but mainly employed for its actions against MYCOBACTERIUM LEPRAE. Its mechanism of action is probably similar to that of the SULFONAMIDES which involves inhibition of folic acid synthesis in susceptible organisms. It is also used with PYRIMETHAMINE in the treatment of malaria. (From Martindale, The Extra Pharmacopoeia, 30th ed, p157-8)
Naphthalene rings which contain two ketone moieties in any position. They can be substituted in any position except at the ketone groups.
Any spaces or cavities within a cell. They may function in digestion, storage, secretion, or excretion.
The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH.
Infections that do not exhibit symptoms.
Sites on an antigen that interact with specific antibodies.
A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.
Leukocyte differentiation antigens and major platelet membrane glycoproteins present on MONOCYTES; ENDOTHELIAL CELLS; PLATELETS; and mammary EPITHELIAL CELLS. They play major roles in CELL ADHESION; SIGNAL TRANSDUCTION; and regulation of angiogenesis. CD36 is a receptor for THROMBOSPONDINS and can act as a scavenger receptor that recognizes and transports oxidized LIPOPROTEINS and FATTY ACIDS.
Elements of limited time intervals, contributing to particular results or situations.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
A republic in western Africa, south of MALI and BURKINA FASO, bordered by GHANA on the east. Its administrative capital is Abidjan and Yamoussoukro has been the official capital since 1983. The country was formerly called Ivory Coast.
Long-acting plasma-bound sulfonamide used for respiratory and urinary tract infections and also for malaria.
The level of protein structure in which combinations of secondary protein structures (alpha helices, beta sheets, loop regions, and motifs) pack together to form folded shapes called domains. Disulfide bridges between cysteines in two different parts of the polypeptide chain along with other interactions between the chains play a role in the formation and stabilization of tertiary structure. Small proteins usually consist of only one domain but larger proteins may contain a number of domains connected by segments of polypeptide chain which lack regular secondary structure.
The in vitro formation of clusters consisting of a cell (usually a lymphocyte) surrounded by antigenic cells or antigen-bearing particles (usually erythrocytes, which may or may not be coated with antibody or antibody and complement). The rosette-forming cell may be an antibody-forming cell, a memory cell, a T-cell, a cell bearing surface cytophilic antibodies, or a monocyte possessing Fc receptors. Rosette formation can be used to identify specific populations of these cells.
Variation occurring within a species in the presence or length of DNA fragment generated by a specific endonuclease at a specific site in the genome. Such variations are generated by mutations that create or abolish recognition sites for these enzymes or change the length of the fragment.
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
Diagnostic procedures, such as laboratory tests and x-rays, routinely performed on all individuals or specified categories of individuals in a specified situation, e.g., patients being admitted to the hospital. These include routine tests administered to neonates.
I'm sorry for any confusion, but "India" is not a medical term that can be defined in a medical context. It is a geographical location, referring to the Republic of India, a country in South Asia. If you have any questions related to medical topics or definitions, I would be happy to help with those!
The relationships of groups of organisms as reflected by their genetic makeup.
A variety of simple repeat sequences that are distributed throughout the GENOME. They are characterized by a short repeat unit of 2-8 basepairs that is repeated up to 100 times. They are also known as short tandem repeats (STRs).
Heterocyclic rings containing three nitrogen atoms, commonly in 1,2,4 or 1,3,5 or 2,4,6 formats. Some are used as HERBICIDES.
Reproduction without fusion of two types of cells, mostly found in ALGAE; FUNGI; and PLANTS. Asexual reproduction occurs in several ways, such as budding, fission, or splitting from "parent" cells. Only few groups of ANIMALS reproduce asexually or unisexually (PARTHENOGENESIS).
The number of pregnancies, complete or incomplete, experienced by a female. It is different from PARITY, which is the number of offspring borne. (From Stedman, 26th ed)
I'm sorry for any confusion, but "Laos" is not a medical term; it is the name of a country located in Southeast Asia, officially known as the Lao People's Democratic Republic. If you have any questions related to medical terminology or health-related topics, I would be happy to help with those!
Alkaloids extracted from various species of Cinchona.
Constituent of the 40S subunit of eukaryotic ribosomes. 18S rRNA is involved in the initiation of polypeptide synthesis in eukaryotes.
A tetrameric enzyme that, along with the coenzyme NAD+, catalyzes the interconversion of LACTATE and PYRUVATE. In vertebrates, genes for three different subunits (LDH-A, LDH-B and LDH-C) exist.
Serological reactions in which an antiserum against one antigen reacts with a non-identical but closely related antigen.
An abnormal elevation of body temperature, usually as a result of a pathologic process.
I'm sorry for any confusion, but "Vietnam" is not a medical term that can be defined in a medical context; it is a country located in Southeast Asia. If you have any questions related to medical conditions or terminology, I would be happy to help clarify those topics for you.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
An infant during the first month after birth.
Organisms whose GENOME has been changed by a GENETIC ENGINEERING technique.
The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.
The restriction of a characteristic behavior, anatomical structure or physical system, such as immune response; metabolic response, or gene or gene variant to the members of one species. It refers to that property which differentiates one species from another but it is also used for phylogenetic levels higher or lower than the species.
A measure of the quality of health care by assessment of unsuccessful results of management and procedures used in combating disease, in individual cases or series.
Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series.
A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair.
The science dealing with the earth and its life, especially the description of land, sea, and air and the distribution of plant and animal life, including humanity and human industries with reference to the mutual relations of these elements. (From Webster, 3d ed)
Short sequences (generally about 10 base pairs) of DNA that are complementary to sequences of messenger RNA and allow reverse transcriptases to start copying the adjacent sequences of mRNA. Primers are used extensively in genetic and molecular biology techniques.
The geographical area of Asia comprising BORNEO; BRUNEI; CAMBODIA; INDONESIA; LAOS; MALAYSIA; the MEKONG VALLEY; MYANMAR (formerly Burma), the PHILIPPINES; SINGAPORE; THAILAND; and VIETNAM.
A republic in central Africa, east of the REPUBLIC OF THE CONGO, south of the CENTRAL AFRICAN REPUBLIC and north of ANGOLA and ZAMBIA. The capital is Kinshasa.
A republic in western Africa, southwest of ALGERIA and west of MALI. Its capital is Nouakchott.
An antibiotic produced by Streptomyces fradiae.
Adherence of cells to surfaces or to other cells.
Deliberate stimulation of the host's immune response. ACTIVE IMMUNIZATION involves administration of ANTIGENS or IMMUNOLOGIC ADJUVANTS. PASSIVE IMMUNIZATION involves administration of IMMUNE SERA or LYMPHOCYTES or their extracts (e.g., transfer factor, immune RNA) or transplantation of immunocompetent cell producing tissue (thymus or bone marrow).
I'm sorry for any confusion, but "Brazil" is not a medical term or concept, it is a country located in South America, known officially as the Federative Republic of Brazil. If you have any questions related to health, medicine, or science, I'd be happy to help answer those!
Antigenic determinants recognized and bound by the B-cell receptor. Epitopes recognized by the B-cell receptor are located on the surface of the antigen.
Commercially prepared reagent sets, with accessory devices, containing all of the major components and literature necessary to perform one or more designated diagnostic tests or procedures. They may be for laboratory or personal use.
A genus of protozoa, formerly also considered a fungus. Characteristics include the presence of violet to brown spores.
Compounds containing carbohydrate or glycosyl groups linked to phosphatidylinositols. They anchor GPI-LINKED PROTEINS or polysaccharides to cell membranes.
The reduction or regulation of the population of mosquitoes through chemical, biological, or other means.
Inbred BALB/c mice are a strain of laboratory mice that have been selectively bred to be genetically identical to each other, making them useful for scientific research and experiments due to their consistent genetic background and predictable responses to various stimuli or treatments.
Substances that are destructive to protozoans.

Optical mapping of Plasmodium falciparum chromosome 2. (1/7602)

Detailed restriction maps of microbial genomes are a valuable resource in genome sequencing studies but are toilsome to construct by contig construction of maps derived from cloned DNA. Analysis of genomic DNA enables large stretches of the genome to be mapped and circumvents library construction and associated cloning artifacts. We used pulsed-field gel electrophoresis purified Plasmodium falciparum chromosome 2 DNA as the starting material for optical mapping, a system for making ordered restriction maps from ensembles of individual DNA molecules. DNA molecules were bound to derivatized glass surfaces, cleaved with NheI or BamHI, and imaged by digital fluorescence microscopy. Large pieces of the chromosome containing ordered DNA restriction fragments were mapped. Maps were assembled from 50 molecules producing an average contig depth of 15 molecules and high-resolution restriction maps covering the entire chromosome. Chromosome 2 was found to be 976 kb by optical mapping with NheI, and 946 kb with BamHI, which compares closely to the published size of 947 kb from large-scale sequencing. The maps were used to further verify assemblies from the plasmid library used for sequencing. Maps generated in silico from the sequence data were compared to the optical mapping data, and good correspondence was found. Such high-resolution restriction maps may become an indispensable resource for large-scale genome sequencing projects.  (+info)

8-Aminoquinolines active against blood stage Plasmodium falciparum in vitro inhibit hematin polymerization. (2/7602)

From the Walter Reed Army Institute of Research (WRAIR) inventory, thirteen 8-aminoquinoline analogs of primaquine were selected for screening against a panel of seven Plasmodium falciparum clones and isolates. Six of the 13 8-aminoquinolines had average 50% inhibitory concentrations between 50 and 100 nM against these P. falciparum clones and were thus an order of magnitude more potent than primaquine. However, excluding chloroquine-resistant clones and isolates, these 8-aminoquinolines were all an order of magnitude less potent than chloroquine. None of the 8-aminoquinolines was cross resistant with either chloroquine or mefloquine. In contrast to the inactive primaquine prototype, 8 of the 13 8-aminoquinolines inhibited hematin polymerization more efficiently than did chloroquine. Although alkoxy or aryloxy substituents at position 5 uniquely endowed these 13 8-aminoquinolines with impressive schizontocidal activity, the structural specificity of inhibition of both parasite growth and hematin polymerization was low.  (+info)

Alternative oxidase inhibitors potentiate the activity of atovaquone against Plasmodium falciparum. (3/7602)

Recent evidence suggests that the malaria parasite Plasmodium falciparum utilizes a branched respiratory pathway including both a cytochrome chain and an alternative oxidase. This branched respiratory pathway model has been used as a basis for examining the mechanism of action of two antimalarial agents, atovaquone and proguanil. In polarographic assays, atovaquone immediately reduced the parasite oxygen consumption rate in a concentration-dependent manner. This is consistent with its previously described role as an inhibitor of the cytochrome bc1 complex. Atovaquone maximally inhibited the rate of P. falciparum oxygen consumption by 73% +/- 10%. At all atovaquone concentrations tested, the addition of the alternative oxidase inhibitor, salicylhydroxamic acid, resulted in a further decrease in the rate of parasite oxygen consumption. At the highest concentrations of atovaquone tested, the activities of salicylhydroxamic acid and atovaquone appear to overlap, suggesting that at these concentrations, atovaquone partially inhibits the alternative oxidase as well as the cytochrome chain. Drug interaction studies with atovaquone and salicylhydroxamic acid indicate atovaquone's activity against P. falciparum in vitro is potentiated by this alternative oxidase inhibitor, with a sum fractional inhibitory concentration of 0.6. Propyl gallate, another alternative oxidase inhibitor, also potentiated atovaquone's activity, with a sum fractional inhibitory concentration of 0.7. Proguanil, which potentiates atovaquone activity in vitro and in vivo, had a small effect on parasite oxygen consumption in polarographic assays when used alone or in the presence of atovaquone or salicylhydroxamic acid. This suggests that proguanil does not potentiate atovaquone by direct inhibition of either branch of the parasite respiratory chain.  (+info)

Comparison of in vivo and in vitro tests of resistance in patients treated with chloroquine in Yaounde, Cameroon. (4/7602)

The usefulness of an isotopic in vitro assay in the field was evaluated by comparing its results with the therapeutic response determined by the simplified WHO in vivo test in symptomatic Cameroonian patients treated with chloroquine. Of the 117 enrolled patients, 102 (87%) completed the 14-day follow-up, and 95 isolates obtained from these patients (46 children, 49 adults) yielded an interpretable in vitro test. A total of 57 of 95 patients (60%; 28 children and 29 adults) had an adequate clinical response with negative smears (n = 46) or with an asymptomatic parasitaemia (n = 11) on day 7 and/or day 14. The geometric mean 50% inhibitory concentration of the isolates obtained from these patients was 63.3 nmol/l. Late and early treatment failure was observed in 29 (30.5%) and 9 (9.5%) patients, respectively. The geometric mean 50% inhibitory concentrations of the corresponding isolates were 173 nmol/l and 302 nmol/l. Among the patients responding with late and early treatment failure, five isolates and one isolate, respectively, yielded a discordant result (in vivo resistance and in vitro sensitivity). The sensitivity, specificity, and predictive value of the in vitro test to detect chloroquine-sensitive cases was 67%, 84% and 86%, respectively. There was moderate concordance between the in vitro and in vivo tests (kappa value = 0.48). The in vitro assay agrees relatively well with the therapeutic response and excludes several host factors that influence the results of the in vivo test. However, in view of some discordant results, the in vitro test cannot substitute for in vivo data on therapeutic efficacy. The only reliable definition of "resistance" in malaria parasites is based on clinical and parasitological response in symptomatic patients, and the in vivo test provides the standard method to determine drug sensitivity or resistance as well as to guide national drug policies.  (+info)

Intraerythrocytic Plasmodium falciparum expresses a high affinity facilitative hexose transporter. (5/7602)

Asexual stages of Plasmodium falciparum cause severe malaria and are dependent upon host glucose for energy. We have identified a glucose transporter of P. falciparum (PfHT1) and studied its function and expression during parasite development in vitro. PfHT1 is a saturable, sodium-independent, and stereospecific transporter, which is inhibited by cytochalasin B, and has a relatively high affinity for glucose (Km = 0.48 mM) when expressed in Xenopus laevis oocytes. Competition experiments with glucose analogues show that hydroxyl groups at positions C-3 and C-4 are important for ligand binding. mRNA levels for PfHT1, assessed by the quantitative technique of tandem competitive polymerase chain reaction, are highest during the small ring stages of infection and lowest in gametocytes. Confocal immunofluorescence microscopy localizes PfHT1 to the region of the parasite plasma membrane and not to host structures. These findings have implications for development of new drug targets in malaria as well as for understanding of the pathophysiology of severe infection. When hypoglycemia complicates malaria, modeling studies suggest that the high affinity of PfHT1 is likely to increase the relative proportion of glucose taken up by parasites and thereby worsen the clinical condition.  (+info)

Complexity of Plasmodium falciparum infections is consistent over time and protects against clinical disease in Tanzanian children. (6/7602)

The complexity of Plasmodium falciparum populations in 21 children was studied in repetitive samples over 4 years in an area of Tanzania where the organism is holoendemic. Genotyping was done by a polymerase chain reaction method that targets three highly polymorphic regions of the merozoite surface protein (MSP) 1 block 2, MSP 2, and the glutamine-rich protein. Eight children were repeatedly parasitemic, 5 had scanty parasitemias, and 8 were consistently nonparasitemic. Varying numbers of genotypes were detected in the parasitemic children, but the multiplicity of infection was significantly constant within each child. The children with frequent parasitemias experienced fewer clinical episodes during the study period than those without parasitemias. There was also a tendency for children with more complex infections to experience fewer episodes. The children had consistent parasitologic profiles over the 4 years. Although few subjects were studied and the results will require confirmation, the results suggest that asymptomatic (especially polyclonal) P. falciparum infection protects against clinical disease from new infections.  (+info)

HLA class II factors associated with Plasmodium falciparum merozoite surface antigen allele families. (7/7602)

In Plasmodium falciparum malaria, certain human leukocyte antigens (HLA) and the parasite's merozoite surface antigens 1 and 2 (MSA-1, MSA-2) have been shown to influence the course of the infection. This report is on associations of distinct HLA factors with the occurrence of particular MSA families in a group of patients with either severe or mild P. falciparum malaria in Gabon. Different distributions of HLA-DPB1 alleles were found in the 2 groups. DR *04 alleles were observed more frequently among patients with severe malaria. Several alleles of different loci were associated with distinct MSA allele families. In addition, carriers of the amino acid methionine at position 11 of the DPA1 allele were more often infected by MSA-1 K1 parasites and less frequently by MSA-1 RO33 parasites. Furthermore, associations of HLA factors with polyclonal infections were found.  (+info)

Comparison of a parasite lactate dehydrogenase-based immunochromatographic antigen detection assay (OptiMAL) with microscopy for the detection of malaria parasites in human blood samples. (8/7602)

Microscopic examination of blood smears remains the gold standard for malaria diagnosis, but is labor-intensive and requires skilled operators. Rapid dipstick technology provides a potential alternative. A study was conducted in The Gambia to compare the performance of OptiMAL, an immunochromatographic antigen detection assay for the diagnosis of malaria using parasite lactate dehydrogenase, against standard microscopy in patients with suspected malaria. For initial diagnosis of Plasmodium falciparum, irrespective of stage, this assay had a sensitivity of 91.3%, a specificity of 92%, a positive predictive value of 87.2%, and a negative predictive value of 94.7%. The sensitivity of the test decreased markedly at parasitemias < 0.01%. This assay can be used for the diagnosis of malaria in areas where microscopy is not available and for urgent malaria diagnosis at night and at weekends, when routine laboratories are closed and when relatively inexperienced microscopists may be on duty.  (+info)

'Plasmodium falciparum' is a specific species of protozoan parasite that causes malaria in humans. It is transmitted through the bites of infected female Anopheles mosquitoes and has a complex life cycle involving both human and mosquito hosts.

In the human host, the parasites infect red blood cells, where they multiply and cause damage, leading to symptoms such as fever, chills, anemia, and in severe cases, organ failure and death. 'Plasmodium falciparum' malaria is often more severe and life-threatening than other forms of malaria caused by different Plasmodium species. It is a major public health concern, particularly in tropical and subtropical regions of the world where access to prevention, diagnosis, and treatment remains limited.

Malaria, Falciparum is defined as a severe and often fatal form of malaria caused by the parasite Plasmodium falciparum. It is transmitted to humans through the bites of infected Anopheles mosquitoes. This type of malaria is characterized by high fever, chills, headache, muscle and joint pain, and vomiting. If left untreated, it can cause severe anemia, kidney failure, seizures, coma, and even death. It is a major public health problem in many tropical and subtropical regions of the world, particularly in Africa.

I'm sorry for any confusion, but "Protozoan Proteins" is not a specific medical or scientific term. Protozoa are single-celled eukaryotic organisms, and proteins are large biological molecules consisting of one or more chains of amino acid residues. Therefore, "Protozoan Proteins" generally refers to the various types of proteins found in protozoa.

However, if you're looking for information about proteins specific to certain protozoan parasites with medical relevance (such as Plasmodium falciparum, which causes malaria), I would be happy to help! Please provide more context or specify the particular protozoan of interest.

"Plasmodium" is a genus of protozoan parasites that are the causative agents of malaria in humans and other animals. There are several species within this genus, including Plasmodium falciparum, P. vivax, P. ovale, P. malariae, and P. knowlesi, among others.

These parasites have a complex life cycle that involves two hosts: an Anopheles mosquito and a vertebrate host (such as humans). When a person is bitten by an infected mosquito, the parasites enter the bloodstream and infect red blood cells, where they multiply and cause the symptoms of malaria.

Plasmodium species are transmitted through the bites of infected female Anopheles mosquitoes, which become infected after taking a blood meal from an infected person. The parasites then develop in the mosquito's midgut, eventually making their way to the salivary glands, where they can be transmitted to another human through the mosquito's bite.

Malaria is a serious and sometimes fatal disease that affects millions of people worldwide, particularly in tropical and subtropical regions. It is characterized by fever, chills, headache, muscle and joint pain, and anemia, among other symptoms. Prompt diagnosis and treatment are essential to prevent severe illness and death from malaria.

"Plasmodium vivax" is a species of protozoan parasite that causes malaria in humans. It's one of the five malaria parasites that can infect humans, with P. falciparum being the most deadly.

P. vivax typically enters the human body through the bite of an infected Anopheles mosquito. Once inside the human host, the parasite travels to the liver where it multiplies and matures. After a period of development that can range from weeks to several months, the mature parasites are released into the bloodstream, where they infect red blood cells and continue to multiply.

The symptoms of P. vivax malaria include fever, chills, headache, muscle and joint pain, and fatigue. One distinctive feature of P. vivax is its ability to form dormant stages (hypnozoites) in the liver, which can reactivate and cause relapses of the disease months or even years after the initial infection.

P. vivax malaria is treatable with medications such as chloroquine, but resistance to this drug has been reported in some parts of the world. Prevention measures include using insecticide-treated bed nets and indoor residual spraying to reduce mosquito populations, as well as taking prophylactic medications for travelers visiting areas where malaria is common.

Antimalarials are a class of drugs that are used for the prevention, treatment, and elimination of malaria. They work by targeting the malaria parasite at various stages of its life cycle, particularly the erythrocytic stage when it infects red blood cells. Some commonly prescribed antimalarials include chloroquine, hydroxychloroquine, quinine, mefloquine, and artemisinin-based combinations. These drugs can be used alone or in combination with other antimalarial agents to increase their efficacy and prevent the development of drug resistance. Antimalarials are also being investigated for their potential use in treating other diseases, such as autoimmune disorders and cancer.

Antigens are substances (usually proteins) found on the surface of cells, or viruses, that can be recognized by the immune system and stimulate an immune response. In the context of protozoa, antigens refer to the specific proteins or other molecules found on the surface of these single-celled organisms that can trigger an immune response in a host organism.

Protozoa are a group of microscopic eukaryotic organisms that include a diverse range of species, some of which can cause diseases in humans and animals. When a protozoan infects a host, the host's immune system recognizes the protozoan antigens as foreign and mounts an immune response to eliminate the infection. This response involves the activation of various types of immune cells, such as T-cells and B-cells, which recognize and target the protozoan antigens.

Understanding the nature of protozoan antigens is important for developing vaccines and other immunotherapies to prevent or treat protozoan infections. For example, researchers have identified specific antigens on the surface of the malaria parasite that are recognized by the human immune system and have used this information to develop vaccine candidates. However, many protozoan infections remain difficult to prevent or treat, and further research is needed to identify new targets for vaccines and therapies.

Chloroquine is an antimalarial and autoimmune disease drug. It works by increasing the pH or making the environment less acidic in the digestive vacuoles of malaria parasites, which inhibits the polymerization of heme and the formation of hemozoin. This results in the accumulation of toxic levels of heme that are harmful to the parasite. Chloroquine is also used as an anti-inflammatory agent in the treatment of rheumatoid arthritis, discoid or systemic lupus erythematosus, and photodermatitis.

The chemical name for chloroquine is 7-chloro-4-(4-diethylamino-1-methylbutylamino)quinoline, and it has a molecular formula of C18H26ClN3. It is available in the form of phosphate or sulfate salts for oral administration as tablets or solution.

Chloroquine was first synthesized in 1934 by Bayer scientists, and it has been widely used since the 1940s as a safe and effective antimalarial drug. However, the emergence of chloroquine-resistant strains of malaria parasites has limited its use in some areas. Chloroquine is also being investigated for its potential therapeutic effects on various viral infections, including COVID-19.

"Plasmodium berghei" is a species of protozoan parasites belonging to the genus Plasmodium, which are the causative agents of malaria. This particular species primarily infects rodents and is not known to naturally infect humans. However, it is widely used in laboratory settings as a model organism to study malaria and develop potential interventions, such as drugs and vaccines, due to its similarities with human-infecting Plasmodium species.

The life cycle of P. berghei involves two hosts: an Anopheles mosquito vector and a rodent host. The parasite undergoes asexual reproduction in the red blood cells of the rodent host, leading to the symptoms of malaria, such as fever, anemia, and organ damage. When an infected mosquito bites another rodent, the parasites are transmitted through the saliva and infect the new host, continuing the life cycle.

While P. berghei is not a direct threat to human health, studying this species has contributed significantly to our understanding of malaria biology and the development of potential interventions against this devastating disease.

Malaria is not a medical definition itself, but it is a disease caused by parasites that are transmitted to people through the bites of infected female Anopheles mosquitoes. Here's a simple definition:

Malaria: A mosquito-borne infectious disease caused by Plasmodium parasites, characterized by cycles of fever, chills, and anemia. It can be fatal if not promptly diagnosed and treated. The five Plasmodium species known to cause malaria in humans are P. falciparum, P. vivax, P. ovale, P. malariae, and P. knowlesi.

Erythrocytes, also known as red blood cells (RBCs), are the most common type of blood cell in circulating blood in mammals. They are responsible for transporting oxygen from the lungs to the body's tissues and carbon dioxide from the tissues to the lungs.

Erythrocytes are formed in the bone marrow and have a biconcave shape, which allows them to fold and bend easily as they pass through narrow blood vessels. They do not have a nucleus or mitochondria, which makes them more flexible but also limits their ability to reproduce or repair themselves.

In humans, erythrocytes are typically disc-shaped and measure about 7 micrometers in diameter. They contain the protein hemoglobin, which binds to oxygen and gives blood its red color. The lifespan of an erythrocyte is approximately 120 days, after which it is broken down in the liver and spleen.

Abnormalities in erythrocyte count or function can lead to various medical conditions, such as anemia, polycythemia, and sickle cell disease.

Drug resistance, also known as antimicrobial resistance, is the ability of a microorganism (such as bacteria, viruses, fungi, or parasites) to withstand the effects of a drug that was originally designed to inhibit or kill it. This occurs when the microorganism undergoes genetic changes that allow it to survive in the presence of the drug. As a result, the drug becomes less effective or even completely ineffective at treating infections caused by these resistant organisms.

Drug resistance can develop through various mechanisms, including mutations in the genes responsible for producing the target protein of the drug, alteration of the drug's target site, modification or destruction of the drug by enzymes produced by the microorganism, and active efflux of the drug from the cell.

The emergence and spread of drug-resistant microorganisms pose significant challenges in medical treatment, as they can lead to increased morbidity, mortality, and healthcare costs. The overuse and misuse of antimicrobial agents, as well as poor infection control practices, contribute to the development and dissemination of drug-resistant strains. To address this issue, it is crucial to promote prudent use of antimicrobials, enhance surveillance and monitoring of resistance patterns, invest in research and development of new antimicrobial agents, and strengthen infection prevention and control measures.

Antibodies, protozoan, refer to the immune system's response to an infection caused by a protozoan organism. Protozoa are single-celled microorganisms that can cause various diseases in humans, such as malaria, giardiasis, and toxoplasmosis.

When the body is infected with a protozoan, the immune system responds by producing specific proteins called antibodies. Antibodies are produced by a type of white blood cell called a B-cell, and they recognize and bind to specific antigens on the surface of the protozoan organism.

There are five main types of antibodies: IgA, IgD, IgE, IgG, and IgM. Each type of antibody has a different role in the immune response. For example, IgG is the most common type of antibody and provides long-term immunity to previously encountered pathogens. IgM is the first antibody produced in response to an infection and is important for activating the complement system, which helps to destroy the protozoan organism.

Overall, the production of antibodies against protozoan organisms is a critical part of the immune response and helps to protect the body from further infection.

There doesn't seem to be a specific medical definition for "DNA, protozoan" as it is simply a reference to the DNA found in protozoa. Protozoa are single-celled eukaryotic organisms that can be found in various environments such as soil, water, and the digestive tracts of animals.

Protozoan DNA refers to the genetic material present in these organisms. It is composed of nucleic acids, including deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), which contain the instructions for the development, growth, and reproduction of the protozoan.

The DNA in protozoa, like in other organisms, is made up of two strands of nucleotides that coil together to form a double helix. The four nucleotide bases that make up protozoan DNA are adenine (A), thymine (T), guanine (G), and cytosine (C). These bases pair with each other to form the rungs of the DNA ladder, with A always pairing with T and G always pairing with C.

The genetic information stored in protozoan DNA is encoded in the sequence of these nucleotide bases. This information is used to synthesize proteins, which are essential for the structure and function of the organism's cells. Protozoan DNA also contains other types of genetic material, such as regulatory sequences that control gene expression and repetitive elements with no known function.

Understanding the DNA of protozoa is important for studying their biology, evolution, and pathogenicity. It can help researchers develop new treatments for protozoan diseases and gain insights into the fundamental principles of genetics and cellular function.

Parasitic sensitivity tests, also known as parasite drug susceptibility tests, refer to laboratory methods used to determine the effectiveness of specific antiparasitic medications against a particular parasitic infection. These tests help healthcare providers identify which drugs are most likely to be effective in treating an individual's infection and which ones should be avoided due to resistance or increased risk of side effects.

There are several types of parasitic sensitivity tests, including:

1. In vitro susceptibility testing: This involves culturing the parasite in a laboratory setting and exposing it to different concentrations of antiparasitic drugs. The growth or survival of the parasite is then observed and compared to a control group that was not exposed to the drug. This helps identify the minimum inhibitory concentration (MIC) of the drug, which is the lowest concentration required to prevent the growth of the parasite.
2. Molecular testing: This involves analyzing the genetic material of the parasite to detect specific mutations or gene variations that are associated with resistance to certain antiparasitic drugs. This type of testing can be performed using a variety of methods, including polymerase chain reaction (PCR) and DNA sequencing.
3. Phenotypic testing: This involves observing the effects of antiparasitic drugs on the growth or survival of the parasite in a laboratory setting. For example, a parasite may be grown in a culture medium and then exposed to different concentrations of a drug. The growth of the parasite is then monitored over time to determine the drug's effectiveness.

Parasitic sensitivity tests are important for guiding the treatment of many parasitic infections, including malaria, tuberculosis, and leishmaniasis. These tests can help healthcare providers choose the most effective antiparasitic drugs for their patients, reduce the risk of drug resistance, and improve treatment outcomes.

Artemisinins are a class of antimalarial drugs derived from the sweet wormwood plant (Artemisia annua). They are highly effective against Plasmodium falciparum, the most deadly species of malaria parasite. Artemisinins have become an essential component in the treatment of malaria and are often used in combination therapy regimens to reduce the risk of drug resistance.

The artemisinin compounds contain a unique peroxide bridge that is responsible for their antimalarial activity. They work by generating free radicals that can damage the parasite's membranes, leading to its rapid death. Artemisinins have a fast action and can significantly reduce the parasite biomass in the first few days of treatment.

Some commonly used artemisinin-based combination therapies (ACTs) include:

* Artemether-lumefantrine (Coartem)
* Artesunate-amodiaquine (Coarsucam)
* Artesunate-mefloquine (Artequin)
* Dihydroartemisinin-piperaquine (Eurartesim, Duo-Cotecxin)

Artemisinins have also shown potential in treating other conditions, such as certain types of cancer and viral infections. However, more research is needed to establish their safety and efficacy for these indications.

Malaria vaccines are biological preparations that induce immunity against malaria parasites, thereby preventing or reducing the severity of malaria disease. They typically contain antigens (proteins or other molecules derived from the parasite) that stimulate an immune response in the recipient, enabling their body to recognize and neutralize the pathogen upon exposure.

The most advanced malaria vaccine candidate is RTS,S/AS01 (Mosquirix), which targets the Plasmodium falciparum parasite's circumsporozoite protein (CSP). This vaccine has shown partial protection in clinical trials, reducing the risk of severe malaria and hospitalization in young children by about 30% over four years. However, it does not provide complete immunity, and additional research is ongoing to develop more effective vaccines against malaria.

Genes in protozoa refer to the hereditary units of these single-celled organisms that carry genetic information necessary for their growth, development, and reproduction. These genes are made up of DNA (deoxyribonucleic acid) molecules, which contain sequences of nucleotide bases that code for specific proteins or RNA molecules. Protozoan genes are responsible for various functions, such as metabolism, response to environmental stimuli, and reproduction.

It is important to note that the study of protozoan genes has contributed significantly to our understanding of genetics and evolution, particularly in areas such as molecular biology, cell biology, and genomics. However, there is still much to be learned about the genetic diversity and complexity of these organisms, which continue to be an active area of research.

Pyrimethamine is an antiparasitic medication that is primarily used to treat and prevent protozoan infections, such as toxoplasmosis and malaria. It works by inhibiting the dihydrofolate reductase enzyme, which is essential for the parasite's survival. By doing so, it interferes with the synthesis of folate, a vital component for the growth and reproduction of the parasite.

Pyrimethamine is often used in combination with other medications, such as sulfonamides or sulfones, to increase its effectiveness and prevent the development of drug-resistant strains. Common side effects of pyrimethamine include nausea, vomiting, loss of appetite, and headache. It is important to note that pyrimethamine should only be used under the supervision of a healthcare professional due to its potential for serious side effects and interactions with other medications.

Parasitemia is a medical term that refers to the presence of parasites, particularly malaria-causing Plasmodium species, in the bloodstream. It is the condition where red blood cells are infected by these parasites, which can lead to various symptoms such as fever, chills, anemia, and organ damage in severe cases. The level of parasitemia is often used to assess the severity of malaria infection and to guide treatment decisions.

'Plasmodium yoelii' is a species of protozoan parasite belonging to the genus Plasmodium, which causes malaria in rodents. It is primarily used as a model organism in malaria research due to its similarity to the human malaria parasites, Plasmodium falciparum and Plasmodium vivax. The life cycle of P. yoelii involves two hosts: an Anopheles mosquito vector and a rodent host. The parasite undergoes asexual reproduction in the red blood cells of the rodent host, leading to the symptoms of malaria such as fever, anemia, and organ failure if left untreated. P. yoelii is not known to infect humans.

"Plasmodium malariae" is a species of protozoan parasite that causes malaria in humans. It's one of the five Plasmodium species known to cause malaria in humans, with the other four being P. falciparum, P. vivax, P. ovale, and P. knowlesi.

P. malariae is transmitted through the bites of infected Anopheles mosquitoes. Once inside the human body, the parasites travel to the liver where they multiply and then infect red blood cells. The infection caused by P. malariae can persist for several years, even a lifetime, if not treated properly.

The symptoms of P. malariae infection include fever, chills, headache, muscle and joint pain, and anemia. However, the severity of these symptoms is generally less than that caused by P. falciparum, which is the most deadly form of malaria.

It's worth noting that while P. malariae can be effectively treated with antimalarial drugs such as chloroquine and primaquine, drug resistance has been reported in some areas, making accurate diagnosis and treatment even more critical for controlling the spread of this disease.

Sulfadoxine is an antimicrobial drug, specifically a sulfonamide. It is defined in medical terms as a long-acting synthetic antibacterial that is used to treat and prevent various bacterial infections. Sulfadoxine works by inhibiting the growth of bacteria through interfering with their ability to synthesize folic acid, an essential component for their survival.

It is often combined with pyrimethamine (a dihydrofolate reductase inhibitor) to treat and prevent malaria caused by Plasmodium falciparum, particularly in areas where there is resistance to other antimalarial drugs. The combination of sulfadoxine and pyrimethamine is known as a "sulfonamide-pyrimidine" or "SP" treatment.

Sulfadoxine should be used with caution, as it can cause serious side effects such as severe skin reactions, blood disorders, and allergic reactions. It is also not recommended for use in people who have an allergy to sulfonamides or who are breastfeeding infants younger than two months of age.

Malaria, Vivax:

A type of malaria caused by the parasite Plasmodium vivax. It is transmitted to humans through the bites of infected Anopheles mosquitoes. Malaria, Vivax is characterized by recurring fevers, chills, and flu-like symptoms, which can occur every other day or every third day. This type of malaria can have mild to severe symptoms and can sometimes lead to complications such as anemia and splenomegaly (enlarged spleen). One distinguishing feature of Malaria, Vivax is its ability to form dormant stages in the liver (called hypnozoites), which can reactivate and cause relapses even after years of apparent cure. Effective treatment includes medication to kill both the blood and liver stages of the parasite. Preventive measures include using mosquito nets, insect repellents, and antimalarial drugs for prophylaxis in areas with high transmission rates.

Quinine is defined as a bitter crystalline alkaloid derived from the bark of the Cinchona tree, primarily used in the treatment of malaria and other parasitic diseases. It works by interfering with the reproduction of the malaria parasite within red blood cells. Quinine has also been used historically as a muscle relaxant and analgesic, but its use for these purposes is now limited due to potential serious side effects. In addition, quinine can be found in some beverages like tonic water, where it is present in very small amounts for flavoring purposes.

A schizont is a stage in the life cycle of certain parasites, particularly those that cause malaria. It refers to the stage where the parasite undergoes multiple divisions within the host cell, creating many daughter cells. This typically occurs inside red blood cells in the human body, after the parasite has been transmitted through the bite of an infected mosquito. The term "schizont" is often used in descriptions of the Plasmodium species, which are the malaria-causing protozoans.

A drug combination refers to the use of two or more drugs in combination for the treatment of a single medical condition or disease. The rationale behind using drug combinations is to achieve a therapeutic effect that is superior to that obtained with any single agent alone, through various mechanisms such as:

* Complementary modes of action: When different drugs target different aspects of the disease process, their combined effects may be greater than either drug used alone.
* Synergistic interactions: In some cases, the combination of two or more drugs can result in a greater-than-additive effect, where the total response is greater than the sum of the individual responses to each drug.
* Antagonism of adverse effects: Sometimes, the use of one drug can mitigate the side effects of another, allowing for higher doses or longer durations of therapy.

Examples of drug combinations include:

* Highly active antiretroviral therapy (HAART) for HIV infection, which typically involves a combination of three or more antiretroviral drugs to suppress viral replication and prevent the development of drug resistance.
* Chemotherapy regimens for cancer treatment, where combinations of cytotoxic agents are used to target different stages of the cell cycle and increase the likelihood of tumor cell death.
* Fixed-dose combination products, such as those used in the treatment of hypertension or type 2 diabetes, which combine two or more active ingredients into a single formulation for ease of administration and improved adherence to therapy.

However, it's important to note that drug combinations can also increase the risk of adverse effects, drug-drug interactions, and medication errors. Therefore, careful consideration should be given to the selection of appropriate drugs, dosing regimens, and monitoring parameters when using drug combinations in clinical practice.

I'm sorry for any confusion, but "Gabon" is not a medical term. It is the name of a country located in Central Africa, known officially as the Gabonese Republic. If you have any questions about medical terminology or health-related topics, I would be happy to help with those!

Merozoite Surface Protein 1 (MSP1) is a malarial antigen, which is a protein present on the surface of merozoites, which are the invasive forms of the Plasmodium parasites that cause malaria. MSP1 plays a crucial role in the invasion of red blood cells by the merozoites during the erythrocytic stage of the parasite's life cycle.

The MSP1 protein is synthesized and processed through several stages, resulting in multiple fragments, including the C-terminal 42 kDa fragment (MSP1-42) that is further cleaved into four smaller fragments (MSP1-19, MSP1-33, MSP1-38, and MSP1-42). These fragments are involved in the recognition and attachment of merozoites to the red blood cells, followed by the formation of a tight junction between the parasite and the host cell membranes.

MSP1 is one of the most abundant and immunogenic proteins on the surface of the merozoites, making it an attractive vaccine candidate. However, despite extensive research, a successful MSP1-based malaria vaccine has yet to be developed due to challenges in eliciting a protective immune response against this complex antigen.

'Anopheles' is a genus of mosquitoes that are known for their role in transmitting malaria parasites to humans. These mosquitoes have a distinctive resting posture, with their abdomens raised and heads down, and they typically feed on human hosts at night. Only female Anopheles mosquitoes transmit the malaria parasite, as they require blood meals to lay eggs.

There are over 400 species of Anopheles mosquitoes worldwide, but only about 30-40 of these are considered significant vectors of human malaria. The distribution and behavior of these mosquitoes can vary widely depending on the specific species and geographic location.

Preventing and controlling the spread of malaria involves a variety of strategies, including the use of insecticide-treated bed nets, indoor residual spraying, antimalarial drugs, and vaccines. Public health efforts to reduce the burden of malaria have made significant progress in recent decades, but the disease remains a major global health challenge, particularly in sub-Saharan Africa.

A protozoan genome refers to the complete set of genetic material or DNA present in a protozoan organism. Protozoa are single-celled eukaryotic microorganisms that lack cell walls and have diverse morphology and nutrition modes. The genome of a protozoan includes all the genes that code for proteins, as well as non-coding DNA sequences that regulate gene expression and other cellular processes.

The size and complexity of protozoan genomes can vary widely depending on the species. Some protozoa have small genomes with only a few thousand genes, while others have larger genomes with tens of thousands of genes or more. The genome sequencing of various protozoan species has provided valuable insights into their evolutionary history, biology, and potential as model organisms for studying eukaryotic cellular processes.

It is worth noting that the study of protozoan genomics is still an active area of research, and new discoveries are continually being made about the genetic diversity and complexity of these fascinating microorganisms.

Amodiaquine is an antimalarial medication used to prevent and treat malaria caused by the Plasmodium falciparum parasite. It works by inhibiting the growth of the parasite in red blood cells. Amodiaquine is often used in combination with other antimalarial drugs, such as artesunate or chloroquine.

The chemical name for amodiaquine is 4-[(7-chloro-4-quinolinyl)methyl]-1-(4-amino-1-methylbutyl)piperazine and it has the molecular formula C18H24ClN3O. It is available in the form of tablets for oral administration.

Like all medications, amodiaquine can cause side effects, including nausea, vomiting, loss of appetite, and headache. In rare cases, it can cause more serious side effects such as liver damage, abnormal heart rhythms, and blood disorders. It is important to take amodiaquine exactly as directed by a healthcare provider and to report any unusual symptoms or side effects promptly.

It's important to note that Amodiaquine is not available in all countries and it's use is limited due to the risk of severe side effects, especially when used alone. It should be used only under the supervision of a healthcare provider and with regular monitoring of blood cells, liver function and heart activity.

Mefloquine is an antimalarial medication that is used to prevent and treat malaria caused by the Plasmodium falciparum parasite. It works by interfering with the growth of the parasite in the red blood cells of the body. Mefloquine is a synthetic quinoline compound, and it is available under the brand name Lariam, among others.

Mefloquine is typically taken once a week, starting one to two weeks before traveling to an area where malaria is common, and continuing for four weeks after leaving the area. It may also be used to treat acute malaria infection in conjunction with other antimalarial medications.

It's important to note that mefloquine has been associated with serious neuropsychiatric side effects, including anxiety, depression, hallucinations, and seizures. Therefore, it is usually reserved for use in situations where other antimalarial drugs cannot be used or have failed. Before taking mefloquine, individuals should discuss their medical history and potential risks with their healthcare provider.

I'm sorry for any confusion, but "Papua New Guinea" is not a medical term or concept. It is the name of a country located in the southwest Pacific Ocean, made up of the eastern half of the island of New Guinea and numerous offshore islands. If you have any questions about medical topics or definitions, I would be happy to help with those!

Merozoites are infective forms of certain protozoan parasites, including those that cause malaria. They are produced during the asexual reproduction of these parasites within the red blood cells of their hosts. Merozoites are released from the infected red blood cells when they rupture and can then invade other red blood cells to continue the cycle of infection. These organisms have an outer membrane that allows them to interact with and invade host cells, and they contain proteins on their surface that help them evade the host's immune system. Merozoites are typically small, oval-shaped structures that measure around 1 micrometer in diameter.

"Plasmodium knowlesi" is a species of protozoan parasite that causes malaria in certain primates, particularly macaques. It can also infect humans, and has been identified as a significant cause of malaria in Southeast Asia. The life cycle of P. knowlesi involves two hosts: anopheline mosquitoes and primates. The parasite is transmitted to the host through the bite of an infected mosquito, and then invades and reproduces within the host's red blood cells, leading to symptoms such as fever, chills, headache, and muscle and joint pain. In severe cases, P. knowlesi infections can lead to complications such as respiratory distress, kidney failure, and coma.

It is important to note that "Plasmodium knowlesi" malaria is different from the more common forms of human malaria caused by Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, and Plasmodium malariae. P. knowlesi infections can be effectively treated with antimalarial drugs, but early diagnosis and prompt treatment are crucial to prevent severe disease and complications.

Dihydropteroate synthase is a bacterial enzyme that plays a crucial role in the synthesis of folate, an essential nutrient for many organisms, including bacteria. The enzyme catalyzes the reaction between pteridine and para-aminobenzoic acid (pABA) to form dihydropteroate, which is then converted into folate.

Inhibition of this enzyme by drugs such as sulfonamides has been a successful strategy for developing antibiotics that target bacterial folate synthesis while sparing the host's metabolism. This makes dihydropteroate synthase an important target in the development of antimicrobial therapies.

I'm sorry for any confusion, but "Senegal" is not a medical term. It is the name of a country located in West Africa, known officially as the Republic of Senegal. If you have any questions about medical terms or conditions, I would be happy to help with those.

Sesquiterpenes are a class of terpenes that consist of three isoprene units, hence the name "sesqui-" meaning "one and a half" in Latin. They are composed of 15 carbon atoms and have a wide range of chemical structures and biological activities. Sesquiterpenes can be found in various plants, fungi, and insects, and they play important roles in the defense mechanisms of these organisms. Some sesquiterpenes are also used in traditional medicine and have been studied for their potential therapeutic benefits.

"Plasmodium ovale" is a species of protozoan parasites that are transmitted to humans through the bites of infected female Anopheles mosquitoes. This parasite causes a type of malaria known as "ovale malaria," which is generally milder than other forms of malaria caused by Plasmodium falciparum or Plasmodium vivax.

The life cycle of Plasmodium ovale involves two hosts: the mosquito and humans. When an infected mosquito bites a human, the parasites are injected into the skin along with the mosquito's saliva. The parasites then enter the liver where they multiply and form dormant stages called hypnozoites. After a period of time (usually several weeks to months), the hypnozoites become activated and begin to infect red blood cells, leading to the symptoms of malaria.

The symptoms of ovale malaria are similar to those of other forms of malaria and include fever, chills, headache, muscle and joint pain, and fatigue. However, ovale malaria is less likely to cause severe complications or death than falciparum malaria. Diagnosis of ovale malaria is typically made through microscopic examination of blood smears or by using rapid diagnostic tests (RDTs) that detect parasite antigens in the blood. Treatment usually involves the use of antimalarial drugs such as chloroquine or primaquine.

Proguanil is an antimalarial medication that is primarily used to prevent and treat malaria caused by the Plasmodium falciparum parasite. It works by blocking the development of the parasite in the red blood cells, thereby preventing the disease from progressing. Proguanil is often used in combination with other antimalarial drugs such as chloroquine or atovaquone to increase its effectiveness and reduce the risk of drug resistance.

Proguanil is available under various brand names, including Paludrine and Malarona. It is typically taken daily in tablet form, starting before travel to a malaria-endemic area and continuing for several weeks after leaving the area. Proguanil may also be used off-label for other indications, such as treating certain types of cancer or preventing recurrent urinary tract infections. However, its use for these conditions is not well-established and should be discussed with a healthcare provider.

Like all medications, proguanil can have side effects, including nausea, vomiting, diarrhea, headache, and mouth ulcers. It may also interact with other drugs, such as warfarin and metoclopramide, so it is important to inform a healthcare provider of all medications being taken before starting proguanil. Women who are pregnant or breastfeeding should consult their healthcare provider before taking proguanil, as its safety in these populations has not been well-studied.

Parasitic pregnancy complications refer to a rare condition where a parasitic twin takes over the development of the dominant twin's reproductive system and becomes pregnant. This condition is also known as fetus in fetu or vanishing twin syndrome with a parasitic twin. The parasitic twin may have some organs developed, but it is not fully formed and relies on the dominant twin for survival. The pregnancy can pose risks to the dominant twin, such as abnormal growth patterns, organ damage, and complications during childbirth. This condition is usually detected during prenatal ultrasound examinations.

"Plasmodium chabaudi" is a species of parasitic protozoa belonging to the genus Plasmodium, which includes the causative agents of malaria in various animals and humans. "P. chabaudi" primarily infects rodents, particularly mice, and serves as a model organism for studying the fundamental biology and pathogenesis of malaria.

The life cycle of "P. chabaudi" involves both sexual and asexual reproduction, similar to other Plasmodium species. The parasite is transmitted through the bite of an infected Anopheles mosquito, which injects sporozoites into the host's bloodstream. These sporozoites then infect liver cells, where they undergo schizogony (asexual reproduction) and produce merozoites.

Merozoites released from the liver invade red blood cells, initiating the erythrocytic stage of the life cycle. Within the red blood cells, the parasites multiply by schizogony, forming new merozoites that are eventually released to infect other red blood cells. Some of these parasites differentiate into male and female gametocytes, which can be taken up by a mosquito during a blood meal, completing the life cycle.

"P. chabaudi" infections in mice can lead to various pathological changes, including anemia, splenomegaly (enlarged spleen), and immune responses that contribute to disease progression. Researchers use this model organism to investigate aspects of malaria biology, such as host-parasite interactions, immunity, drug development, and vaccine design.

Sporozoites are a stage in the life cycle of certain parasitic protozoans, including Plasmodium species that cause malaria. They are infective forms that result from the sporulation of oocysts, which are produced in the vector's midgut after the ingestion of gametocytes during a blood meal.

Once mature, sporozoites are released from the oocyst and migrate to the salivary glands of the vector, where they get injected into the host during subsequent feedings. In the host, sporozoites infect liver cells, multiply within them, and eventually rupture the cells, releasing merozoites that invade red blood cells and initiate the erythrocytic stage of the parasite's life cycle.

Sporozoites are typically highly motile and possess a unique gliding motility, which enables them to traverse various host tissues during their invasion process. This invasive ability is facilitated by an actin-myosin motor system and secretory organelles called micronemes and rhoptries, which release adhesive proteins that interact with host cell receptors.

In summary, sporozoites are a crucial stage in the life cycle of Plasmodium parasites, serving as the infective forms responsible for transmitting malaria between hosts via an insect vector.

Cerebral malaria is a severe form of malaria that affects the brain. It is caused by Plasmodium falciparum parasites, which are transmitted to humans through the bites of infected Anopheles mosquitoes. In cerebral malaria, the parasites infect and destroy red blood cells, leading to their accumulation in small blood vessels in the brain. This can cause swelling of the brain, impaired consciousness, seizures, coma, and even death if left untreated.

The medical definition of cerebral malaria is:

A severe form of malaria caused by Plasmodium falciparum parasites that affects the brain and results in altered mental status, seizures, coma, or other neurological symptoms. It is characterized by the sequestration of infected red blood cells in the cerebral microvasculature, leading to inflammation, endothelial activation, and disruption of the blood-brain barrier. Cerebral malaria can cause long-term neurological deficits or death if not promptly diagnosed and treated with appropriate antimalarial therapy.

'Life cycle stages' is a term used in the context of public health and medicine to describe the different stages that an organism goes through during its lifetime. This concept is particularly important in the field of epidemiology, where understanding the life cycle stages of infectious agents (such as bacteria, viruses, parasites) can help inform strategies for disease prevention and control.

The life cycle stages of an infectious agent may include various forms such as spores, cysts, trophozoites, schizonts, or vectors, among others, depending on the specific organism. Each stage may have different characteristics, such as resistance to environmental factors, susceptibility to drugs, and ability to transmit infection.

For example, the life cycle stages of the malaria parasite include sporozoites (the infective form transmitted by mosquitoes), merozoites (the form that infects red blood cells), trophozoites (the feeding stage inside red blood cells), schizonts (the replicating stage inside red blood cells), and gametocytes (the sexual stage that can be taken up by mosquitoes to continue the life cycle).

Understanding the life cycle stages of an infectious agent is critical for developing effective interventions, such as vaccines, drugs, or other control measures. For example, targeting a specific life cycle stage with a drug may prevent transmission or reduce the severity of disease. Similarly, designing a vaccine to elicit immunity against a particular life cycle stage may provide protection against infection or disease.

Host-parasite interactions refer to the relationship between a parasitic organism (the parasite) and its host, which can be an animal, plant, or human body. The parasite lives on or inside the host and derives nutrients from it, often causing harm in the process. This interaction can range from relatively benign to severe, depending on various factors such as the species of the parasite, the immune response of the host, and the duration of infection.

The host-parasite relationship is often categorized based on the degree of harm caused to the host. Parasites that cause little to no harm are called commensals, while those that cause significant damage or disease are called parasitic pathogens. Some parasites can even manipulate their hosts' behavior and physiology to enhance their own survival and reproduction, leading to complex interactions between the two organisms.

Understanding host-parasite interactions is crucial for developing effective strategies to prevent and treat parasitic infections, as well as for understanding the ecological relationships between different species in natural ecosystems.

Tetrahydrofolate dehydrogenase (EC 1.5.1.20) is an enzyme involved in folate metabolism. The enzyme catalyzes the oxidation of tetrahydrofolate (THF) to dihydrofolate (DHF), while simultaneously reducing NADP+ to NADPH.

The reaction can be summarized as follows:

THF + NADP+ -> DHF + NADPH + H+

This enzyme plays a crucial role in the synthesis of purines and thymidylate, which are essential components of DNA and RNA. Therefore, any defects or deficiencies in tetrahydrofolate dehydrogenase can lead to various medical conditions, including megaloblastic anemia and neural tube defects during fetal development.

Trophozoites are the feeding and motile stage in the life cycle of certain protozoa, including those that cause diseases such as amebiasis and malaria. They are typically larger than the cyst stage of these organisms and have a more irregular shape. Trophozoites move by means of pseudopods (false feet) and engulf food particles through a process called phagocytosis. In the case of pathogenic protozoa, this feeding stage is often when they cause damage to host tissues.

In the case of amebiasis, caused by Entamoeba histolytica, trophozoites can invade the intestinal wall and cause ulcers, leading to symptoms such as diarrhea and abdominal pain. In malaria, caused by Plasmodium species, trophozoites infect red blood cells and multiply within them, eventually causing their rupture and release of more parasites into the bloodstream, which can lead to severe complications like cerebral malaria or organ failure.

It's important to note that not all protozoa have a trophozoite stage in their life cycle, and some may refer to this feeding stage with different terminology depending on the specific species.

I believe there may be some confusion in your question. "Fluorenes" is not a medical term, but rather a chemical term referring to organic compounds that contain a fluorene moiety, which is a bicyclic compound made up of two benzene rings fused to a five-membered ring containing two carbon atoms and one double bond.

Fluorenes have various applications in the field of materials science, including organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). They are not typically used in a medical context, although some fluorene derivatives have been explored for potential therapeutic applications.

Therefore, I cannot provide a medical definition of "Fluorenes." However, if you have any questions about the chemical properties or applications of fluorenes, I would be happy to try and answer them.

Parasitology is a branch of biology that deals with the study of parasites, their life cycles, the relationship between parasites and their hosts, the transmission of parasitic diseases, and the development of methods for their control and elimination. It involves understanding various types of parasites including protozoa, helminths, and arthropods that can infect humans, animals, and plants. Parasitologists also study the evolution, genetics, biochemistry, and ecology of parasites to develop effective strategies for their diagnosis, treatment, and prevention.

An endemic disease is a type of disease that is regularly found among particular people or in a certain population, and is spread easily from person to person. The rate of infection is consistently high in these populations, but it is relatively stable and does not change dramatically over time. Endemic diseases are contrasted with epidemic diseases, which suddenly increase in incidence and spread rapidly through a large population.

Endemic diseases are often associated with poverty, poor sanitation, and limited access to healthcare. They can also be influenced by environmental factors such as climate, water quality, and exposure to vectors like mosquitoes or ticks. Examples of endemic diseases include malaria in some tropical countries, tuberculosis (TB) in many parts of the world, and HIV/AIDS in certain populations.

Effective prevention and control measures for endemic diseases typically involve improving access to healthcare, promoting good hygiene and sanitation practices, providing vaccinations when available, and implementing vector control strategies. By addressing the underlying social and environmental factors that contribute to the spread of these diseases, it is possible to reduce their impact on affected populations and improve overall health outcomes.

Atovaquone is an antiprotozoal medication used for the treatment and prevention of certain parasitic infections. It works by inhibiting the mitochondria of the parasites, disrupting their energy production and ultimately leading to their death. Atovaquone is available as a oral suspension or coated tablets and is often prescribed for conditions such as Pneumocystis pneumonia (PCP), Toxoplasma gondii encephalitis, and babesiosis. It is also used for the prevention of PCP in people with weakened immune systems due to HIV/AIDS or other causes.

The medical definition of Atovaquone can be stated as:

"Atovaquone is an antiprotozoal medication (synthetic hydroxynaphthoquinone) that exhibits activity against a variety of protozoa, including Plasmodium falciparum (the parasite responsible for malaria), Pneumocystis jirovecii (the causative agent of PCP), Toxoplasma gondii, and Babesia microti. It is used primarily for the treatment and prevention of PCP in individuals with compromised immune systems, as well as for the treatment of babesiosis and toxoplasmosis."

Inhibitory Concentration 50 (IC50) is a measure used in pharmacology, toxicology, and virology to describe the potency of a drug or chemical compound. It refers to the concentration needed to reduce the biological or biochemical activity of a given substance by half. Specifically, it is most commonly used in reference to the inhibition of an enzyme or receptor.

In the context of infectious diseases, IC50 values are often used to compare the effectiveness of antiviral drugs against a particular virus. A lower IC50 value indicates that less of the drug is needed to achieve the desired effect, suggesting greater potency and potentially fewer side effects. Conversely, a higher IC50 value suggests that more of the drug is required to achieve the same effect, indicating lower potency.

It's important to note that IC50 values can vary depending on the specific assay or experimental conditions used, so they should be interpreted with caution and in conjunction with other measures of drug efficacy.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

I'm sorry for any confusion, but "Kenya" is not a medical term. It is the name of a country located in East Africa, known for its diverse wildlife and geography, including savannas, lakelands, the dramatic Great Rift Valley, and mountain highlands. It is also where you can find the Maasai Mara Reserve, known for its annual wildebeest migrations, and vast Nairobi National Park. The capital city of Kenya is Nairobi. If you have any questions about medical terms or concepts, I would be happy to help with those!

I'm sorry for any confusion, but "Thailand" is not a medical term. It is a country located in Southeast Asia. If you have any questions about medical terms or concepts, I would be happy to help answer those for you!

I'm sorry for any confusion, but "Myanmar" is not a medical term or condition. It is the name of a country in Southeast Asia, also known as Burma. If you have any questions about medical conditions or terminology, I would be happy to help clarify those for you.

I'm not aware of any medical condition or term that is specifically associated with or referred to as "Cameroon." Cameroon is a country located in Central Africa, known for its rich biodiversity and cultural diversity. If you have more context about why you are looking for a medical definition of "Cameroon," I may be able to provide a more helpful response.

Ethanolamines are a class of organic compounds that contain an amino group (-NH2) and a hydroxyl group (-OH) attached to a carbon atom. They are derivatives of ammonia (NH3) in which one or two hydrogen atoms have been replaced by a ethanol group (-CH2CH2OH).

The most common ethanolamines are:

* Monethanolamine (MEA), also called 2-aminoethanol, with the formula HOCH2CH2NH2.
* Diethanolamine (DEA), also called 2,2'-iminobisethanol, with the formula HOCH2CH2NHCH2CH2OH.
* Triethanolamine (TEA), also called 2,2',2''-nitrilotrisethanol, with the formula N(CH2CH2OH)3.

Ethanolamines are used in a wide range of industrial and consumer products, including as solvents, emulsifiers, detergents, pharmaceuticals, and personal care products. They also have applications as intermediates in the synthesis of other chemicals. In the body, ethanolamines play important roles in various biological processes, such as neurotransmission and cell signaling.

'Aotus trivirgatus' is a species of New World monkey, also known as the owl monkey or the white-bellied night monkey. It is native to South America, particularly in countries like Colombia, Ecuador, Peru, and Brazil. This nocturnal primate is notable for being one of the few monogamous species of monkeys, and it has a diet that mainly consists of fruits, flowers, and insects.

The medical community may study 'Aotus trivirgatus' due to its use as a model organism in biomedical research. Its genetic similarity to humans makes it a valuable subject for studies on various diseases and biological processes, including infectious diseases, reproductive biology, and aging. However, the use of this species in research has been controversial due to ethical concerns regarding animal welfare.

A parasite is an organism that lives on or in a host organism and gets its sustenance at the expense of the host. Parasites are typically much smaller than their hosts, and they may be classified as either ectoparasites (which live on the outside of the host's body) or endoparasites (which live inside the host's body).

Parasites can cause a range of health problems in humans, depending on the type of parasite and the extent of the infection. Some parasites may cause only mild symptoms or none at all, while others can lead to serious illness or even death. Common symptoms of parasitic infections include diarrhea, abdominal pain, weight loss, and fatigue.

There are many different types of parasites that can infect humans, including protozoa (single-celled organisms), helminths (worms), and ectoparasites (such as lice and ticks). Parasitic infections are more common in developing countries with poor sanitation and hygiene, but they can also occur in industrialized nations.

Preventing parasitic infections typically involves practicing good hygiene, such as washing hands regularly, cooking food thoroughly, and avoiding contaminated water. Treatment for parasitic infections usually involves medication to kill the parasites and relieve symptoms.

Primaquine is an antimalarial medication used to prevent and treat malaria caused by Plasmodium falciparum and P. vivax parasites. It is the only antimalarial drug effective against the liver stages (hypnozoites) of P. vivax and P. ovale, which can cause relapses if not treated.

Primaquine works by producing free radicals that damage the malaria parasite's DNA, leading to its death. It is a relatively inexpensive drug and is often used in mass drug administration programs for malaria elimination. However, primaquine can cause hemolysis (destruction of red blood cells) in people with glucose-6-phosphate dehydrogenase (G6PD) deficiency, so it is important to screen for this condition before prescribing the drug.

In addition to its antimalarial properties, primaquine has also been used off-label to treat certain types of cutaneous leishmaniasis, a parasitic disease caused by Leishmania species.

I'd be happy to help! However, I believe there might be a slight confusion in your question. RNA stands for Ribonucleic Acid, which is a type of nucleic acid involved in various biological roles in the coding, decoding, regulation, and expression of genes. On the other hand, protozoan refers to a unicellular organism from the kingdom Protista, which includes a wide variety of simple eukaryotic organisms such as amoebas, paramecia, and plasmodium (the malaria-causing parasite).

There isn't a specific medical definition for "RNA, protozoan" since RNA is a molecule present in all living cells, including human cells, and protozoans are a group of organisms. However, I can tell you that RNA plays crucial roles in protozoan biology, such as acting as a messenger between DNA and ribosomes during protein synthesis or regulating gene expression.

If you have any further questions or need more specific information about RNA in protozoans, please let me know!

Polymerase Chain Reaction (PCR) is a laboratory technique used to amplify specific regions of DNA. It enables the production of thousands to millions of copies of a particular DNA sequence in a rapid and efficient manner, making it an essential tool in various fields such as molecular biology, medical diagnostics, forensic science, and research.

The PCR process involves repeated cycles of heating and cooling to separate the DNA strands, allow primers (short sequences of single-stranded DNA) to attach to the target regions, and extend these primers using an enzyme called Taq polymerase, resulting in the exponential amplification of the desired DNA segment.

In a medical context, PCR is often used for detecting and quantifying specific pathogens (viruses, bacteria, fungi, or parasites) in clinical samples, identifying genetic mutations or polymorphisms associated with diseases, monitoring disease progression, and evaluating treatment effectiveness.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

I'm sorry for any confusion, but "travel" is not a term that has a specific medical definition. In general, travel refers to the act of moving or journeying from one place to another, often over long distances. However, in a medical context, it might refer to the recommendation that individuals with certain medical conditions or those who are immunocompromised avoid traveling to areas where they may be at increased risk of exposure to infectious diseases. It's always best to check with a healthcare professional for advice related to specific medical situations and travel.

Microscopy is a technical field in medicine that involves the use of microscopes to observe structures and phenomena that are too small to be seen by the naked eye. It allows for the examination of samples such as tissues, cells, and microorganisms at high magnifications, enabling the detection and analysis of various medical conditions, including infections, diseases, and cellular abnormalities.

There are several types of microscopy used in medicine, including:

1. Light Microscopy: This is the most common type of microscopy, which uses visible light to illuminate and magnify samples. It can be used to examine a wide range of biological specimens, such as tissue sections, blood smears, and bacteria.
2. Electron Microscopy: This type of microscopy uses a beam of electrons instead of light to produce highly detailed images of samples. It is often used in research settings to study the ultrastructure of cells and tissues.
3. Fluorescence Microscopy: This technique involves labeling specific molecules within a sample with fluorescent dyes, allowing for their visualization under a microscope. It can be used to study protein interactions, gene expression, and cell signaling pathways.
4. Confocal Microscopy: This type of microscopy uses a laser beam to scan a sample point by point, producing high-resolution images with reduced background noise. It is often used in medical research to study the structure and function of cells and tissues.
5. Scanning Probe Microscopy: This technique involves scanning a sample with a physical probe, allowing for the measurement of topography, mechanical properties, and other characteristics at the nanoscale. It can be used in medical research to study the structure and function of individual molecules and cells.

Aotidae is a family of nocturnal primates also known as lorises or slow lorises. They are native to Southeast Asia and are characterized by their small size, round head, large eyes, and a wet-nosed face. Slow lorises have a toxic bite, which they use to defend themselves against predators. They are currently listed as vulnerable or endangered due to habitat loss and hunting.

Parasite load, in medical terms, refers to the total number or quantity of parasites (such as worms, protozoa, or other infectious agents) present in a host organism's body. It is often used to describe the severity of a parasitic infection and can be an important factor in determining the prognosis and treatment plan for the infected individual.

Parasite load can vary widely depending on the type of parasite, the route of infection, the immune status of the host, and other factors. In some cases, even a small number of parasites may cause significant harm if they are highly virulent or located in critical areas of the body. In other cases, large numbers of parasites may be necessary to produce noticeable symptoms.

Measuring parasite load can be challenging, as it often requires specialized laboratory techniques and equipment. However, accurate assessment of parasite load is important for both research and clinical purposes, as it can help researchers develop more effective treatments and allow healthcare providers to monitor the progression of an infection and evaluate the effectiveness of treatment.

I'm sorry for any confusion, but "Mali" is not a medical term or condition in English. Mali is the name of a country located in West Africa, and its capital city is Bamako. If you have any questions about Mali or anything else, please let me know!

I'm sorry for any confusion, but "Ghana" is not a medical term. It is the name of a country located in West Africa, known officially as the Republic of Ghana. If you have any questions about medical terms or conditions, I would be happy to help with those!

Insect vectors are insects that transmit disease-causing pathogens (such as viruses, bacteria, parasites) from one host to another. They do this while feeding on the host's blood or tissues. The insects themselves are not infected by the pathogen but act as mechanical carriers that pass it on during their bite. Examples of diseases spread by insect vectors include malaria (transmitted by mosquitoes), Lyme disease (transmitted by ticks), and plague (transmitted by fleas). Proper prevention measures, such as using insect repellent and reducing standing water where mosquitoes breed, can help reduce the risk of contracting these diseases.

I'm sorry for any confusion, but "Indonesia" is not a medical term. It is a country located in Southeast Asia and Oceania, between the Indian and Pacific oceans. It is the world's largest island country, with more than thirteen thousand islands. If you have any questions about medical terms or concepts, I would be happy to help with those!

'Culicidae' is the biological family that includes all species of mosquitoes. It consists of three subfamilies: Anophelinae, Culicinae, and Toxorhynchitinae. Mosquitoes are small, midge-like flies that are known for their ability to transmit various diseases to humans and other animals, such as malaria, yellow fever, dengue fever, and Zika virus. The medical importance of Culicidae comes from the fact that only female mosquitoes require blood meals to lay eggs, and during this process, they can transmit pathogens between hosts.

'Anopheles gambiae' is a species of mosquito that is a major vector for the transmission of malaria. The female Anopheles gambiae mosquito bites primarily during the nighttime hours and preferentially feeds on human blood, which allows it to transmit the Plasmodium parasite that causes malaria. This species is widely distributed throughout much of Africa and is responsible for transmitting a significant proportion of the world's malaria cases.

The Anopheles gambiae complex actually consists of several closely related species or forms, which can be difficult to distinguish based on morphological characteristics alone. However, advances in molecular techniques have allowed for more accurate identification and differentiation of these species. Understanding the biology and behavior of Anopheles gambiae is crucial for developing effective strategies to control malaria transmission.

Membrane transport proteins are specialized biological molecules, specifically integral membrane proteins, that facilitate the movement of various substances across the lipid bilayer of cell membranes. They are responsible for the selective and regulated transport of ions, sugars, amino acids, nucleotides, and other molecules into and out of cells, as well as within different cellular compartments. These proteins can be categorized into two main types: channels and carriers (or pumps). Channels provide a passive transport mechanism, allowing ions or small molecules to move down their electrochemical gradient, while carriers actively transport substances against their concentration gradient, requiring energy usually in the form of ATP. Membrane transport proteins play a crucial role in maintaining cell homeostasis, signaling processes, and many other physiological functions.

I'm sorry for any confusion, but the term "Africa" actually refers to a continent, not a medical condition or concept. Africa is the second-largest continent in the world, consisting of 54 countries and a wide range of diverse ethnic groups, cultures, languages, and landscapes. It is home to a vast array of wildlife, including many species that are not found anywhere else in the world. If you have any questions about Africa's geography, history, or culture, I would be happy to try to help answer them!

I apologize for any confusion, but "Cambodia" is not a medical term or concept. It is the name of a country located in Southeast Asia, bordered by Thailand, Laos, Vietnam, and the Gulf of Thailand. The capital city of Cambodia is Phnom Penh.

If you have any questions related to healthcare, medical conditions, treatments, or other health-related topics, I would be happy to help you with those!

I'm sorry for any confusion, but "Tanzania" is not a medical term. It is the name of a country located in East Africa. If you have any questions about medical terms or conditions, I would be happy to help clarify those for you.

"Plasmodium cynomolgi" is a species of protozoan parasite belonging to the genus Plasmodium, which causes malaria in certain primates. It's primarily found in macaque monkeys in Southeast Asia and is transmitted through the bite of infected mosquitoes.

While it mainly affects non-human primates, it can occasionally infect humans through a process called zoonosis. In rare cases, it can cause mild to severe malaria-like symptoms in humans, similar to those caused by Plasmodium vivax or Plasmodium falciparum, the species that commonly infect humans.

The life cycle of Plasmodium cynomolgi involves two hosts: the mosquito and the primate. The parasite reproduces asexually in the liver cells and red blood cells of the infected host, leading to the characteristic symptoms of malaria such as fever, chills, anemia, and splenomegaly (enlarged spleen).

Research on Plasmodium cynomolgi is important for understanding the biology and epidemiology of malaria parasites, as well as for developing new strategies for preventing and treating this widespread infectious disease.

Blood is the fluid that circulates in the body of living organisms, carrying oxygen and nutrients to the cells and removing carbon dioxide and other waste products. It is composed of red and white blood cells suspended in a liquid called plasma. The main function of blood is to transport oxygen from the lungs to the body's tissues and carbon dioxide from the tissues to the lungs. It also transports nutrients, hormones, and other substances to the cells and removes waste products from them. Additionally, blood plays a crucial role in the body's immune system by helping to fight infection and disease.

I'm sorry for any confusion, but "Gambia" is not a medical term. It is the name of a country located in West Africa, officially known as the Republic of The Gambia. If you have any questions about medical terminology or health-related topics, I would be happy to try and help answer those for you.

I apologize for any confusion, but "Burkina Faso" is not a medical term or concept. It is the name of a country located in West Africa. The name "Burkina Faso" translates to "Land of Incorruptible People" in Mossi and Dioula, two languages spoken in the region. The country was known as Upper Volta when it gained independence from France in 1960. It was renamed Burkina Faso in 1984 by then-President Thomas Sankara, who aimed to promote a sense of national identity and unity among the diverse population.

Burkina Faso is a landlocked country with a population of around 21 million people (as of 2021). It shares borders with six countries: Mali to the northwest, Niger to the northeast, Benin to the southeast, Togo and Ghana to the south, and Côte d'Ivoire to the southwest. The capital city is Ouagadougou.

The primary languages spoken in Burkina Faso are French (the official language), Mooré, Dioula, Fula, and Gourmanchéma. The country has a diverse cultural heritage with numerous ethnic groups, including the Mossi, Fulani, Bobo, Gurunsi, Senufo, and Lobi.

Burkina Faso faces various challenges, such as poverty, food insecurity, limited access to education, and health issues like malaria, HIV/AIDS, and neglected tropical diseases. The country also struggles with political instability and security threats from extremist groups operating in the Sahel region.

"Plasmodium gallinaceum" is not a medical term per se, but it is a scientific name used in the field of parasitology. It refers to a species of protozoan parasites that belong to the genus Plasmodium, which are known to cause malaria in birds, particularly chickens and turkeys.

The life cycle of "Plasmodium gallinaceum" involves two hosts: an Anopheles mosquito vector and a bird host. When an infected mosquito bites a bird, the parasites enter the bloodstream and infect the red blood cells, where they multiply and cause damage, leading to symptoms of malaria in the bird host.

While "Plasmodium gallinaceum" is not a human pathogen, research on this species has contributed significantly to our understanding of the biology and epidemiology of Plasmodium parasites, including those that cause malaria in humans.

An oocyst is a thick-walled, environmentally resistant spore-like structure produced by some protozoan parasites, such as Cryptosporidium and Cyclospora, during their life cycle. These oocysts can survive for long periods in the environment and can infect a host when ingested, leading to infection and disease. The term "oocyst" is specific to certain groups of protozoan parasites and should not be confused with other types of spores produced by fungi or bacteria.

Immunoglobulin G (IgG) is a type of antibody, which is a protective protein produced by the immune system in response to foreign substances like bacteria or viruses. IgG is the most abundant type of antibody in human blood, making up about 75-80% of all antibodies. It is found in all body fluids and plays a crucial role in fighting infections caused by bacteria, viruses, and toxins.

IgG has several important functions:

1. Neutralization: IgG can bind to the surface of bacteria or viruses, preventing them from attaching to and infecting human cells.
2. Opsonization: IgG coats the surface of pathogens, making them more recognizable and easier for immune cells like neutrophils and macrophages to phagocytose (engulf and destroy) them.
3. Complement activation: IgG can activate the complement system, a group of proteins that work together to help eliminate pathogens from the body. Activation of the complement system leads to the formation of the membrane attack complex, which creates holes in the cell membranes of bacteria, leading to their lysis (destruction).
4. Antibody-dependent cellular cytotoxicity (ADCC): IgG can bind to immune cells like natural killer (NK) cells and trigger them to release substances that cause target cells (such as virus-infected or cancerous cells) to undergo apoptosis (programmed cell death).
5. Immune complex formation: IgG can form immune complexes with antigens, which can then be removed from the body through various mechanisms, such as phagocytosis by immune cells or excretion in urine.

IgG is a critical component of adaptive immunity and provides long-lasting protection against reinfection with many pathogens. It has four subclasses (IgG1, IgG2, IgG3, and IgG4) that differ in their structure, function, and distribution in the body.

Antigenic variation is a mechanism used by some microorganisms, such as bacteria and viruses, to evade the immune system and establish persistent infections. This occurs when these pathogens change or modify their surface antigens, which are molecules that can be recognized by the host's immune system and trigger an immune response.

The changes in the surface antigens can occur due to various mechanisms, such as gene mutation, gene rearrangement, or gene transfer. These changes can result in the production of new variants of the microorganism that are different enough from the original strain to avoid recognition by the host's immune system.

Antigenic variation is a significant challenge in developing effective vaccines against certain infectious diseases, such as malaria and influenza, because the constantly changing surface antigens make it difficult for the immune system to mount an effective response. Therefore, researchers are working on developing vaccines that target conserved regions of the microorganism that do not undergo antigenic variation or using a combination of antigens to increase the likelihood of recognition by the immune system.

An erythrocyte, also known as a red blood cell, is a type of cell that circulates in the blood and is responsible for transporting oxygen throughout the body. The erythrocyte membrane refers to the thin, flexible barrier that surrounds the erythrocyte and helps to maintain its shape and stability.

The erythrocyte membrane is composed of a lipid bilayer, which contains various proteins and carbohydrates. These components help to regulate the movement of molecules into and out of the erythrocyte, as well as provide structural support and protection for the cell.

The main lipids found in the erythrocyte membrane are phospholipids and cholesterol, which are arranged in a bilayer structure with the hydrophilic (water-loving) heads facing outward and the hydrophobic (water-fearing) tails facing inward. This arrangement helps to maintain the integrity of the membrane and prevent the leakage of cellular components.

The proteins found in the erythrocyte membrane include integral proteins, which span the entire width of the membrane, and peripheral proteins, which are attached to the inner or outer surface of the membrane. These proteins play a variety of roles, such as transporting molecules across the membrane, maintaining the shape of the erythrocyte, and interacting with other cells and proteins in the body.

The carbohydrates found in the erythrocyte membrane are attached to the outer surface of the membrane and help to identify the cell as part of the body's own immune system. They also play a role in cell-cell recognition and adhesion.

Overall, the erythrocyte membrane is a complex and dynamic structure that plays a critical role in maintaining the function and integrity of red blood cells.

Folic acid antagonists are a class of medications that work by inhibiting the action of folic acid or its metabolic pathways. These drugs are commonly used in the treatment of various types of cancer and certain other conditions, such as rheumatoid arthritis. They include drugs such as methotrexate, pemetrexed, and trimetrexate.

Folic acid is a type of B vitamin that is essential for the production of DNA and RNA, the genetic material found in cells. Folic acid antagonists work by interfering with the enzyme responsible for converting folic acid into its active form, tetrahydrofolate. This interference prevents the formation of new DNA and RNA, which is necessary for cell division and growth. As a result, these drugs can inhibit the proliferation of rapidly dividing cells, such as cancer cells.

It's important to note that folic acid antagonists can also affect normal, non-cancerous cells in the body, particularly those that divide quickly, such as cells in the bone marrow and digestive tract. This can lead to side effects such as anemia, mouth sores, and diarrhea. Therefore, these drugs must be used carefully and under the close supervision of a healthcare provider.

Apicomplexa is a phylum of single-celled, parasitic organisms that includes several medically important genera, such as Plasmodium (which causes malaria), Toxoplasma (which causes toxoplasmosis), and Cryptosporidium (which causes cryptosporidiosis). These organisms are characterized by the presence of a unique apical complex, which is a group of specialized structures at one end of the cell that are used during invasion and infection of host cells. They have a complex life cycle involving multiple stages, including sexual and asexual reproduction, often in different hosts. Many Apicomplexa are intracellular parasites, meaning they live and multiply inside the cells of their hosts.

Genotype, in genetics, refers to the complete heritable genetic makeup of an individual organism, including all of its genes. It is the set of instructions contained in an organism's DNA for the development and function of that organism. The genotype is the basis for an individual's inherited traits, and it can be contrasted with an individual's phenotype, which refers to the observable physical or biochemical characteristics of an organism that result from the expression of its genes in combination with environmental influences.

It is important to note that an individual's genotype is not necessarily identical to their genetic sequence. Some genes have multiple forms called alleles, and an individual may inherit different alleles for a given gene from each parent. The combination of alleles that an individual inherits for a particular gene is known as their genotype for that gene.

Understanding an individual's genotype can provide important information about their susceptibility to certain diseases, their response to drugs and other treatments, and their risk of passing on inherited genetic disorders to their offspring.

Multidrug Resistance-Associated Proteins (MRPs) are a subfamily of ATP-binding cassette (ABC) transporter proteins that play a crucial role in the efflux of various substrates, including drugs and organic anions, out of cells. They are located in the plasma membrane of many cell types, including epithelial cells in the liver, intestine, kidney, and blood-brain barrier.

MRPs are known to transport a wide range of molecules, such as glutathione conjugates, bilirubin, bile acids, and various clinical drugs. One of the most well-known MRPs is MRP1 (ABCC1), which was initially identified in drug-resistant tumor cells. MRP1 can confer resistance to chemotherapeutic agents by actively pumping them out of cancer cells, thereby reducing their intracellular concentration and effectiveness.

The activity of MRPs can have significant implications for the pharmacokinetics and pharmacodynamics of drugs, as they can affect drug absorption, distribution, metabolism, and excretion (ADME). Understanding the function and regulation of MRPs is essential for developing strategies to overcome multidrug resistance in cancer therapy and optimizing drug dosing regimens in various clinical settings.

Glycophorin is a type of protein found on the surface of red blood cells, also known as erythrocytes. These proteins are heavily glycosylated, meaning they have many carbohydrate chains attached to them. Glycophorins play a crucial role in maintaining the structure and flexibility of the red blood cell membrane, and they also help to mediate interactions between the red blood cells and other cells or molecules in the body.

There are several different types of glycophorin proteins, including glycophorin A, B, C, and D. Glycophorin A is the most abundant type and is often used as a marker for identifying the ABO blood group. Mutations in the genes that encode glycophorin proteins can lead to various blood disorders, such as hereditary spherocytosis and hemolytic anemia.

Gametogenesis is the biological process by which haploid gametes, or sex cells (sperm and egg cells), are produced through the meiotic division of diploid germ cells. In females, this process is called oogenesis, where an oogonium (diploid germ cell) undergoes mitosis to form an oocyte (immature egg cell). The oocyte then undergoes meiosis I to form a secondary oocyte and a polar body. After fertilization by a sperm cell, the secondary oocyte completes meiosis II to form a mature ovum or egg cell.

In males, this process is called spermatogenesis, where a spermatogonium (diploid germ cell) undergoes mitosis to form primary spermatocytes. Each primary spermatocyte then undergoes meiosis I to form two secondary spermatocytes, which subsequently undergo meiosis II to form four haploid spermatids. The spermatids then differentiate into spermatozoa or sperm cells through a process called spermiogenesis.

Gametogenesis is essential for sexual reproduction and genetic diversity, as it involves the random segregation of chromosomes during meiosis and the recombination of genetic material between homologous chromosomes.

I'm sorry for any confusion, but "Sudan" is not a medical term. It is a country located in Northeast Africa, known as the Sudan or Sudan proper, and the southern region that seceded to become South Sudan in 2011. If you have any medical terms you would like me to define, please let me know!

I'm not aware of any medical definitions associated with the term "Congo." The term "Congo" is most commonly used to refer to:

1. The Congo River, which is the second longest river in Africa, flowing through the Democratic Republic of the Congo and the Republic of the Congo.
2. The two countries located in Central Africa that share the name "Congo": the Democratic Republic of the Congo (formerly known as Zaire) and the Republic of the Congo (formerly known as French Congo or Middle Congo).
3. In historical contexts, "Congo" may also refer to the Congo Free State (1885-1908), a private colony of King Leopold II of Belgium, which later became the Belgian Congo (1908-1960) and then Zaire (1971-1997).

If you are looking for medical information or definitions related to tropical diseases, healthcare in Africa, or similar topics, I would recommend using more specific terms.

I apologize for any confusion, but "Colombia" is not a medical term. It is the name of a country located in South America, known officially as the Republic of Colombia. If you are looking for medical information related to Colombia or its healthcare system, I would be happy to try to help you with that.

I'm sorry for any confusion, but "Mozambique" is not a medical term or concept. It is the name of a country located in Southeast Africa, known officially as the Republic of Mozambique. If you have any questions related to medicine or healthcare, I would be happy to try and help answer those for you.

An Enzyme-Linked Immunosorbent Assay (ELISA) is a type of analytical biochemistry assay used to detect and quantify the presence of a substance, typically a protein or peptide, in a liquid sample. It takes its name from the enzyme-linked antibodies used in the assay.

In an ELISA, the sample is added to a well containing a surface that has been treated to capture the target substance. If the target substance is present in the sample, it will bind to the surface. Next, an enzyme-linked antibody specific to the target substance is added. This antibody will bind to the captured target substance if it is present. After washing away any unbound material, a substrate for the enzyme is added. If the enzyme is present due to its linkage to the antibody, it will catalyze a reaction that produces a detectable signal, such as a color change or fluorescence. The intensity of this signal is proportional to the amount of target substance present in the sample, allowing for quantification.

ELISAs are widely used in research and clinical settings to detect and measure various substances, including hormones, viruses, and bacteria. They offer high sensitivity, specificity, and reproducibility, making them a reliable choice for many applications.

Genetic polymorphism refers to the occurrence of multiple forms (called alleles) of a particular gene within a population. These variations in the DNA sequence do not generally affect the function or survival of the organism, but they can contribute to differences in traits among individuals. Genetic polymorphisms can be caused by single nucleotide changes (SNPs), insertions or deletions of DNA segments, or other types of genetic rearrangements. They are important for understanding genetic diversity and evolution, as well as for identifying genetic factors that may contribute to disease susceptibility in humans.

Combination drug therapy is a treatment approach that involves the use of multiple medications with different mechanisms of action to achieve better therapeutic outcomes. This approach is often used in the management of complex medical conditions such as cancer, HIV/AIDS, and cardiovascular diseases. The goal of combination drug therapy is to improve efficacy, reduce the risk of drug resistance, decrease the likelihood of adverse effects, and enhance the overall quality of life for patients.

In combining drugs, healthcare providers aim to target various pathways involved in the disease process, which may help to:

1. Increase the effectiveness of treatment by attacking the disease from multiple angles.
2. Decrease the dosage of individual medications, reducing the risk and severity of side effects.
3. Slow down or prevent the development of drug resistance, a common problem in chronic diseases like HIV/AIDS and cancer.
4. Improve patient compliance by simplifying dosing schedules and reducing pill burden.

Examples of combination drug therapy include:

1. Antiretroviral therapy (ART) for HIV treatment, which typically involves three or more drugs from different classes to suppress viral replication and prevent the development of drug resistance.
2. Chemotherapy regimens for cancer treatment, where multiple cytotoxic agents are used to target various stages of the cell cycle and reduce the likelihood of tumor cells developing resistance.
3. Cardiovascular disease management, which may involve combining medications such as angiotensin-converting enzyme (ACE) inhibitors, beta-blockers, diuretics, and statins to control blood pressure, heart rate, fluid balance, and cholesterol levels.
4. Treatment of tuberculosis, which often involves a combination of several antibiotics to target different aspects of the bacterial life cycle and prevent the development of drug-resistant strains.

When prescribing combination drug therapy, healthcare providers must carefully consider factors such as potential drug interactions, dosing schedules, adverse effects, and contraindications to ensure safe and effective treatment. Regular monitoring of patients is essential to assess treatment response, manage side effects, and adjust the treatment plan as needed.

Insect bites and stings refer to the penetration of the skin by insects, such as mosquitoes, fleas, ticks, or bees, often resulting in localized symptoms including redness, swelling, itching, and pain. The reaction can vary depending on the individual's sensitivity and the type of insect. In some cases, systemic reactions like anaphylaxis may occur, which requires immediate medical attention. Treatment typically involves relieving symptoms with topical creams, antihistamines, or in severe cases, epinephrine. Prevention measures include using insect repellent and protective clothing.

"Saimiri" is the genus name for the group of primates known as squirrel monkeys. These small, agile New World monkeys are native to Central and South America and are characterized by their slim bodies, long limbs, and distinctive hairless faces with large eyes. They are omnivorous and known for their active, quick-moving behavior in the trees. There are several species of squirrel monkey, including the Central American squirrel monkey (Saimiri oerstedii) and the much more widespread common squirrel monkey (Saimiri sciureus).

Aminoquinolines are a class of drugs that contain a quinoline chemical structure and an amino group. They are primarily used as antimalarial agents, with the most well-known members of this class being chloroquine and hydroxychloroquine. These drugs work by inhibiting the parasite's ability to digest hemoglobin in the red blood cells, which is necessary for its survival and reproduction.

In addition to their antimalarial properties, aminoquinolines have also been studied for their potential anti-inflammatory and immunomodulatory effects. They have been investigated as a treatment for various autoimmune diseases, such as rheumatoid arthritis and lupus, although their use in these conditions is not yet widely accepted.

It's important to note that aminoquinolines can have significant side effects, including gastrointestinal symptoms, retinopathy, and cardiac toxicity. They should only be used under the close supervision of a healthcare provider, and their use may be contraindicated in certain populations, such as pregnant women or individuals with preexisting heart conditions.

An allele is a variant form of a gene that is located at a specific position on a specific chromosome. Alleles are alternative forms of the same gene that arise by mutation and are found at the same locus or position on homologous chromosomes.

Each person typically inherits two copies of each gene, one from each parent. If the two alleles are identical, a person is said to be homozygous for that trait. If the alleles are different, the person is heterozygous.

For example, the ABO blood group system has three alleles, A, B, and O, which determine a person's blood type. If a person inherits two A alleles, they will have type A blood; if they inherit one A and one B allele, they will have type AB blood; if they inherit two B alleles, they will have type B blood; and if they inherit two O alleles, they will have type O blood.

Alleles can also influence traits such as eye color, hair color, height, and other physical characteristics. Some alleles are dominant, meaning that only one copy of the allele is needed to express the trait, while others are recessive, meaning that two copies of the allele are needed to express the trait.

Membrane proteins are a type of protein that are embedded in the lipid bilayer of biological membranes, such as the plasma membrane of cells or the inner membrane of mitochondria. These proteins play crucial roles in various cellular processes, including:

1. Cell-cell recognition and signaling
2. Transport of molecules across the membrane (selective permeability)
3. Enzymatic reactions at the membrane surface
4. Energy transduction and conversion
5. Mechanosensation and signal transduction

Membrane proteins can be classified into two main categories: integral membrane proteins, which are permanently associated with the lipid bilayer, and peripheral membrane proteins, which are temporarily or loosely attached to the membrane surface. Integral membrane proteins can further be divided into three subcategories based on their topology:

1. Transmembrane proteins, which span the entire width of the lipid bilayer with one or more alpha-helices or beta-barrels.
2. Lipid-anchored proteins, which are covalently attached to lipids in the membrane via a glycosylphosphatidylinositol (GPI) anchor or other lipid modifications.
3. Monotopic proteins, which are partially embedded in the membrane and have one or more domains exposed to either side of the bilayer.

Membrane proteins are essential for maintaining cellular homeostasis and are targets for various therapeutic interventions, including drug development and gene therapy. However, their structural complexity and hydrophobicity make them challenging to study using traditional biochemical methods, requiring specialized techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and single-particle cryo-electron microscopy (cryo-EM).

Genetic variation refers to the differences in DNA sequences among individuals and populations. These variations can result from mutations, genetic recombination, or gene flow between populations. Genetic variation is essential for evolution by providing the raw material upon which natural selection acts. It can occur within a single gene, between different genes, or at larger scales, such as differences in the number of chromosomes or entire sets of chromosomes. The study of genetic variation is crucial in understanding the genetic basis of diseases and traits, as well as the evolutionary history and relationships among species.

Recombinant proteins are artificially created proteins produced through the use of recombinant DNA technology. This process involves combining DNA molecules from different sources to create a new set of genes that encode for a specific protein. The resulting recombinant protein can then be expressed, purified, and used for various applications in research, medicine, and industry.

Recombinant proteins are widely used in biomedical research to study protein function, structure, and interactions. They are also used in the development of diagnostic tests, vaccines, and therapeutic drugs. For example, recombinant insulin is a common treatment for diabetes, while recombinant human growth hormone is used to treat growth disorders.

The production of recombinant proteins typically involves the use of host cells, such as bacteria, yeast, or mammalian cells, which are engineered to express the desired protein. The host cells are transformed with a plasmid vector containing the gene of interest, along with regulatory elements that control its expression. Once the host cells are cultured and the protein is expressed, it can be purified using various chromatography techniques.

Overall, recombinant proteins have revolutionized many areas of biology and medicine, enabling researchers to study and manipulate proteins in ways that were previously impossible.

Heme proteins are a type of protein that contain a heme group, which is a prosthetic group composed of an iron atom contained in the center of a large organic ring called a porphyrin. The heme group gives these proteins their characteristic red color. Hemeproteins have various important functions in biological systems, including oxygen transport (e.g., hemoglobin), electron transfer (e.g., cytochromes), and enzymatic catalysis (e.g., peroxidases and catalases). The heme group can bind and release gases, such as oxygen and carbon monoxide, and can participate in redox reactions due to the ease with which iron can change its oxidation state.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

I'm sorry for any confusion, but "French Guiana" is not a medical term or concept. It's a geographical location, specifically an overseas department and region of France, located on the northeastern coast of South America. If you have any questions about geographical places, I'd be happy to try to help answer those, but for medical inquiries, please provide a medical term or concept and I will do my best to provide a definition or explanation.

Surface antigens are molecules found on the surface of cells that can be recognized by the immune system as being foreign or different from the host's own cells. Antigens are typically proteins or polysaccharides that are capable of stimulating an immune response, leading to the production of antibodies and activation of immune cells such as T-cells.

Surface antigens are important in the context of infectious diseases because they allow the immune system to identify and target infected cells for destruction. For example, viruses and bacteria often display surface antigens that are distinct from those found on host cells, allowing the immune system to recognize and attack them. In some cases, these surface antigens can also be used as targets for vaccines or other immunotherapies.

In addition to their role in infectious diseases, surface antigens are also important in the context of cancer. Tumor cells often display abnormal surface antigens that differ from those found on normal cells, allowing the immune system to potentially recognize and attack them. However, tumors can also develop mechanisms to evade the immune system, making it difficult to mount an effective response.

Overall, understanding the properties and behavior of surface antigens is crucial for developing effective immunotherapies and vaccines against infectious diseases and cancer.

DNA Sequence Analysis is the systematic determination of the order of nucleotides in a DNA molecule. It is a critical component of modern molecular biology, genetics, and genetic engineering. The process involves determining the exact order of the four nucleotide bases - adenine (A), guanine (G), cytosine (C), and thymine (T) - in a DNA molecule or fragment. This information is used in various applications such as identifying gene mutations, studying evolutionary relationships, developing molecular markers for breeding, and diagnosing genetic diseases.

The process of DNA Sequence Analysis typically involves several steps, including DNA extraction, PCR amplification (if necessary), purification, sequencing reaction, and electrophoresis. The resulting data is then analyzed using specialized software to determine the exact sequence of nucleotides.

In recent years, high-throughput DNA sequencing technologies have revolutionized the field of genomics, enabling the rapid and cost-effective sequencing of entire genomes. This has led to an explosion of genomic data and new insights into the genetic basis of many diseases and traits.

Synthetic vaccines are artificially produced, designed to stimulate an immune response and provide protection against specific diseases. Unlike traditional vaccines that are derived from weakened or killed pathogens, synthetic vaccines are created using synthetic components, such as synthesized viral proteins, DNA, or RNA. These components mimic the disease-causing agent and trigger an immune response without causing the actual disease. The use of synthetic vaccines offers advantages in terms of safety, consistency, and scalability in production, making them valuable tools for preventing infectious diseases.

Placental diseases, also known as placental pathologies, refer to a group of conditions that affect the development and function of the placenta during pregnancy. The placenta is an organ that develops in the uterus during pregnancy and provides oxygen and nutrients to the developing fetus while removing waste products.

Placental diseases can have serious consequences for both the mother and the fetus, including preterm labor, growth restriction, stillbirth, and long-term health problems for the child. Some common placental diseases include:

1. Placental abruption: This occurs when the placenta separates from the uterine wall before delivery, causing bleeding and potentially harming the fetus.
2. Placental previa: This is a condition where the placenta implants in the lower part of the uterus, covering the cervix. It can cause bleeding and may require cesarean delivery.
3. Preeclampsia: This is a pregnancy-related disorder characterized by high blood pressure and damage to organs such as the liver and kidneys. Placental dysfunction is thought to play a role in its development.
4. Intrauterine growth restriction (IUGR): This occurs when the fetus does not grow properly due to poor placental function, leading to low birth weight and potential health problems.
5. Chorioamnionitis: This is an infection of the membranes surrounding the fetus, which can lead to preterm labor and other complications.
6. Placental infarction: This occurs when a portion of the placenta dies due to a lack of blood flow, which can lead to growth restriction or stillbirth.

Prompt diagnosis and treatment of placental diseases are essential for ensuring the best possible outcomes for both the mother and the fetus.

Anemia is a medical condition characterized by a lower than normal number of red blood cells or lower than normal levels of hemoglobin in the blood. Hemoglobin is an important protein in red blood cells that carries oxygen from the lungs to the rest of the body. Anemia can cause fatigue, weakness, shortness of breath, and a pale complexion because the body's tissues are not getting enough oxygen.

Anemia can be caused by various factors, including nutritional deficiencies (such as iron, vitamin B12, or folate deficiency), blood loss, chronic diseases (such as kidney disease or rheumatoid arthritis), inherited genetic disorders (such as sickle cell anemia or thalassemia), and certain medications.

There are different types of anemia, classified based on the underlying cause, size and shape of red blood cells, and the level of hemoglobin in the blood. Treatment for anemia depends on the underlying cause and may include dietary changes, supplements, medication, or blood transfusions.

I'm sorry for any confusion, but "Madagascar" is not a medical term. It is actually the fourth-largest island country in the world, located in the Indian Ocean, off the southeastern coast of Africa. If you have any questions about medical terms or concepts, I'd be happy to help answer those!

Cytochromes b are a group of electron transport proteins that contain a heme c group, which is the prosthetic group responsible for their redox activity. They play a crucial role in the electron transport chain (ETC) located in the inner mitochondrial membrane of eukaryotic cells and in the plasma membrane of prokaryotic cells.

The cytochromes b are part of Complex III, also known as the cytochrome bc1 complex or ubiquinol-cytochrome c reductase, in the ETC. In this complex, they function as electron carriers between ubiquinone (Q) and cytochrome c, participating in the process of oxidative phosphorylation to generate ATP.

There are multiple isoforms of cytochromes b found in various organisms, with different numbers of subunits and structures. However, they all share a common function as essential components of the electron transport chain, facilitating the transfer of electrons during cellular respiration and energy production.

"Multiple drug resistance" (MDR) is a term used in medicine to describe the condition where a patient's infection becomes resistant to multiple antimicrobial drugs. This means that the bacteria, virus, fungus or parasite that is causing the infection has developed the ability to survive and multiply despite being exposed to medications that were originally designed to kill or inhibit its growth.

In particular, MDR occurs when an organism becomes resistant to at least one drug in three or more antimicrobial categories. This can happen due to genetic changes in the microorganism that allow it to survive in the presence of these drugs. The development of MDR is a significant concern for public health because it limits treatment options and can make infections harder, if not impossible, to treat.

MDR can develop through several mechanisms, including mutations in the genes that encode drug targets or enzymes involved in drug metabolism, as well as the acquisition of genetic elements such as plasmids and transposons that carry resistance genes. The overuse and misuse of antimicrobial drugs are major drivers of MDR, as they create selective pressure for the emergence and spread of resistant strains.

MDR infections can occur in various settings, including hospitals, long-term care facilities, and communities. They can affect people of all ages and backgrounds, although certain populations may be at higher risk, such as those with weakened immune systems or chronic medical conditions. Preventing the spread of MDR requires a multifaceted approach that includes surveillance, infection control, antimicrobial stewardship, and research into new therapies and diagnostics.

Phenanthrenes are not typically defined in a medical context, but they are a class of organic compounds that have a polycyclic aromatic hydrocarbon structure consisting of three benzene rings fused together. They can be found in some natural products and have been studied for their potential pharmacological properties. Some phenanthrenes have shown anti-inflammatory, antioxidant, and cytotoxic activities, among others. However, more research is needed to fully understand their therapeutic potential and safety profile.

Prevalence, in medical terms, refers to the total number of people in a given population who have a particular disease or condition at a specific point in time, or over a specified period. It is typically expressed as a percentage or a ratio of the number of cases to the size of the population. Prevalence differs from incidence, which measures the number of new cases that develop during a certain period.

The Duffy blood group system is a system of identifying blood types based on the presence or absence of certain antigens on the surface of red blood cells. The antigens in this system are proteins called Duffy antigens, which are receptors for the malarial parasite Plasmodium vivax.

There are two major Duffy antigens, Fya and Fyb, and individuals can be either positive or negative for each of these antigens. This means that there are four main Duffy blood types: Fy(a+b-), Fy(a-b+), Fy(a+b+), and Fy(a-b-).

The Duffy blood group system is important in blood transfusions to prevent a potentially dangerous immune response known as a transfusion reaction. If a person receives blood that contains antigens that their body recognizes as foreign, their immune system may attack the transfused red blood cells, leading to symptoms such as fever, chills, and in severe cases, kidney failure or even death.

Additionally, the Duffy blood group system has been found to be associated with susceptibility to certain diseases. For example, individuals who are negative for both Fya and Fyb antigens (Fy(a-b-)) are resistant to infection by Plasmodium vivax, one of the malarial parasites that causes malaria in humans. This is because the Duffy antigens serve as receptors for the parasite to enter and infect red blood cells.

Sulfanilamides are a group of synthetic antibacterial agents that are chemically related to sulfanilic acid. They work by inhibiting the growth of bacteria, particularly Gram-positive cocci, and have been used in the treatment of various bacterial infections such as pneumonia, meningitis, and urinary tract infections.

Sulfanilamides are absorbed well from the gastrointestinal tract and are distributed widely throughout the body tissues. They are excreted mainly in the urine, and their action is enhanced by acidic urine. Common side effects of sulfonamides include skin rashes, nausea, vomiting, and headache. Rare but serious side effects include blood disorders, liver damage, and Stevens-Johnson syndrome.

Sulfanilamides have been largely replaced by newer antibiotics due to the emergence of drug-resistant bacteria and the availability of safer and more effective alternatives. However, they are still used in some cases, particularly for the treatment of certain parasitic infections and as topical agents for skin infections.

I'm sorry for any confusion, but "seasons" is not a term that has a medical definition. Seasons refer to the four divisions of the year (spring, summer, autumn or fall, and winter) based on the position of the earth in its orbit around the sun. If you have any questions related to health or medicine, I'd be happy to try to help answer those!

In genetics, sequence alignment is the process of arranging two or more DNA, RNA, or protein sequences to identify regions of similarity or homology between them. This is often done using computational methods to compare the nucleotide or amino acid sequences and identify matching patterns, which can provide insight into evolutionary relationships, functional domains, or potential genetic disorders. The alignment process typically involves adjusting gaps and mismatches in the sequences to maximize the similarity between them, resulting in an aligned sequence that can be visually represented and analyzed.

I'm sorry for any confusion, but there seems to be a mistake in your question. Avian malaria is a disease that affects birds, not humans. It is caused by parasites from the genus Plasmodium, which are different than the ones causing human malaria (Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, and Plasmodium malariae).

Avian malaria is not a significant public health concern, and it's not transmitted to humans through mosquitoes or any other means. However, it can have serious impacts on bird populations.

Sickle cell trait is a genetic condition where an individual inherits one abnormal gene for hemoglobin S (HbS) from one parent and one normal gene for hemoglobin A (HbA) from the other parent. Hemoglobin is a protein in red blood cells that carries oxygen throughout the body.

People with sickle cell trait do not have sickle cell disease, but they can pass the abnormal HbS gene on to their children. In certain situations, such as high altitude, low oxygen levels, or intense physical exertion, individuals with sickle cell trait may experience symptoms similar to those of sickle cell disease, such as fatigue, pain, and shortness of breath. However, these symptoms are typically milder and less frequent than in people with sickle cell disease.

It is important for individuals who know they have sickle cell trait to inform their healthcare providers, especially if they become pregnant or plan to engage in activities that may cause low oxygen levels, such as scuba diving or high-altitude climbing.

Sequence homology, amino acid, refers to the similarity in the order of amino acids in a protein or a portion of a protein between two or more species. This similarity can be used to infer evolutionary relationships and functional similarities between proteins. The higher the degree of sequence homology, the more likely it is that the proteins are related and have similar functions. Sequence homology can be determined through various methods such as pairwise alignment or multiple sequence alignment, which compare the sequences and calculate a score based on the number and type of matching amino acids.

Quinolines are a class of organic compounds that consist of a bicyclic structure made up of a benzene ring fused to a piperidine ring. They have a wide range of applications, but they are perhaps best known for their use in the synthesis of various medications, including antibiotics and antimalarial drugs.

Quinolone antibiotics, such as ciprofloxacin and levofloxacin, work by inhibiting the bacterial enzymes involved in DNA replication and repair. They are commonly used to treat a variety of bacterial infections, including urinary tract infections, pneumonia, and skin infections.

Quinoline-based antimalarial drugs, such as chloroquine and hydroxychloroquine, work by inhibiting the parasite's ability to digest hemoglobin in the red blood cells. They are commonly used to prevent and treat malaria.

It is important to note that quinolines have been associated with serious side effects, including tendinitis and tendon rupture, nerve damage, and abnormal heart rhythms. As with any medication, it is important to use quinolines only under the supervision of a healthcare provider, and to follow their instructions carefully.

I'm sorry for any confusion, but "Peru" is not a medical term. It is a country located in South America, known for its rich history, diverse culture, and beautiful landscapes. If you have any questions about medical terms or concepts, I would be happy to help answer those!

Hemoglobin (Hb or Hgb) is the main oxygen-carrying protein in the red blood cells, which are responsible for delivering oxygen throughout the body. It is a complex molecule made up of four globin proteins and four heme groups. Each heme group contains an iron atom that binds to one molecule of oxygen. Hemoglobin plays a crucial role in the transport of oxygen from the lungs to the body's tissues, and also helps to carry carbon dioxide back to the lungs for exhalation.

There are several types of hemoglobin present in the human body, including:

* Hemoglobin A (HbA): This is the most common type of hemoglobin, making up about 95-98% of total hemoglobin in adults. It consists of two alpha and two beta globin chains.
* Hemoglobin A2 (HbA2): This makes up about 1.5-3.5% of total hemoglobin in adults. It consists of two alpha and two delta globin chains.
* Hemoglobin F (HbF): This is the main type of hemoglobin present in fetal life, but it persists at low levels in adults. It consists of two alpha and two gamma globin chains.
* Hemoglobin S (HbS): This is an abnormal form of hemoglobin that can cause sickle cell disease when it occurs in the homozygous state (i.e., both copies of the gene are affected). It results from a single amino acid substitution in the beta globin chain.
* Hemoglobin C (HbC): This is another abnormal form of hemoglobin that can cause mild to moderate hemolytic anemia when it occurs in the homozygous state. It results from a different single amino acid substitution in the beta globin chain than HbS.

Abnormal forms of hemoglobin, such as HbS and HbC, can lead to various clinical disorders, including sickle cell disease, thalassemia, and other hemoglobinopathies.

Hypoxanthine is a purine derivative and an intermediate in the metabolic pathways of nucleotide degradation, specifically adenosine to uric acid in humans. It is formed from the oxidation of xanthine by the enzyme xanthine oxidase. In the body, hypoxanthine is converted to xanthine and then to uric acid, which is excreted in the urine. Increased levels of hypoxanthine in the body can be indicative of various pathological conditions, including tissue hypoxia, ischemia, and necrosis.

I'm not aware of any medical definitions associated with the term "Benin." Benin is a country located in West Africa, and its name is used in medical literature to describe conditions or issues related to that country, such as diseases prevalent there. However, without additional context, it's difficult to provide a specific medical definition for 'Benin.'

I'm not aware of any medical definitions associated with the term "Angola." Angola is a country located in Southern Africa, known officially as the Republic of Angola. It does not have any specific relevance to medical terminology or healthcare. If you have more context or information about why you are looking for a medical definition of Angola, I may be able to provide a more helpful response.

I'm sorry for any confusion, but "Liberia" is not a medical term. It is a country in West Africa, bordering the North Atlantic Ocean, between Côte d'Ivoire and Sierra Leone. Established in 1847, it was the first African republic to proclaim its independence, and is known for its unique history of being settled by freed slaves from the United States. Is there a different term or concept you would like me to define or provide information about?

Chondroitin sulfates are a type of complex carbohydrate molecules known as glycosaminoglycans (GAGs). They are a major component of cartilage, the tissue that cushions and protects the ends of bones in joints. Chondroitin sulfates are composed of repeating disaccharide units made up of glucuronic acid and N-acetylgalactosamine, which can be sulfated at various positions.

Chondroitin sulfates play a crucial role in the biomechanical properties of cartilage by attracting water and maintaining the resiliency and elasticity of the tissue. They also interact with other molecules in the extracellular matrix, such as collagen and proteoglycans, to form a complex network that provides structural support and regulates cell behavior.

Chondroitin sulfates have been studied for their potential therapeutic benefits in osteoarthritis, a degenerative joint disease characterized by the breakdown of cartilage. Supplementation with chondroitin sulfate has been shown to reduce pain and improve joint function in some studies, although the evidence is not consistent across all trials. The mechanism of action is thought to involve inhibition of enzymes that break down cartilage, as well as stimulation of cartilage repair and synthesis.

I'm sorry for any confusion, but "Melanesia" is not a medical term. It is a geographical region in the southwestern Pacific Ocean, consisting of an island group including New Guinea, the Bismarck Archipelago, the Solomon Islands, Vanuatu, New Caledonia, and the Fiji islands. The term "Melanesia" comes from the Greek words "melas," meaning black, and "nesos," meaning island, referring to the dark skin of the inhabitants. It's primarily used in anthropological, geographical, and cultural contexts.

Sensitivity and specificity are statistical measures used to describe the performance of a diagnostic test or screening tool in identifying true positive and true negative results.

* Sensitivity refers to the proportion of people who have a particular condition (true positives) who are correctly identified by the test. It is also known as the "true positive rate" or "recall." A highly sensitive test will identify most or all of the people with the condition, but may also produce more false positives.
* Specificity refers to the proportion of people who do not have a particular condition (true negatives) who are correctly identified by the test. It is also known as the "true negative rate." A highly specific test will identify most or all of the people without the condition, but may also produce more false negatives.

In medical testing, both sensitivity and specificity are important considerations when evaluating a diagnostic test. High sensitivity is desirable for screening tests that aim to identify as many cases of a condition as possible, while high specificity is desirable for confirmatory tests that aim to rule out the condition in people who do not have it.

It's worth noting that sensitivity and specificity are often influenced by factors such as the prevalence of the condition in the population being tested, the threshold used to define a positive result, and the reliability and validity of the test itself. Therefore, it's important to consider these factors when interpreting the results of a diagnostic test.

I'm sorry for any confusion, but "Malawi" is not a medical term. It is the name of a country located in southeastern Africa. If you have any questions about medical terminology or health-related topics, I would be happy to help with those!

I'm not aware of any medical definition for "Comoros." The term "Comoros" most commonly refers to the Comoros Union, which is a country made up of three main islands (Grande Comore, Anjouan, and Mohéli) located in the Indian Ocean, north of Madagascar. It is possible that you may have heard this term in a medical context, such as in reference to a specific disease outbreak or medical research conducted in the country. However, without more information, it is difficult for me to provide a more precise definition.

I'm sorry for any confusion, but "New Guinea" is not a medical term. It is the second largest island in the world, located in the southwest Pacific Ocean, northeast of Australia. The island is divided politically between the independent nation of Papua New Guinea to the east and the Indonesian provinces of Papua and West Papua to the west.

If you have any medical questions or terms that you would like defined, I'd be happy to help!

I'm sorry for any confusion, but "Nigeria" is not a medical term. It is a country located in West Africa, and it is the most populous country in Africa. If you have any questions about medical conditions or terms, I would be happy to help clarify those for you.

I'm sorry for any confusion, but "Uganda" is not a medical term or concept. It is the name of a country located in East Africa, known officially as the Republic of Uganda. If you have any questions about medical terms or concepts, I would be happy to help with those!

I'm sorry for any confusion, but "Honduras" is not a medical term or concept. It is the name of a country located in Central America, bordered by Guatemala to the west, El Salvador to the southwest, Nicaragua to the southeast, and the Caribbean Sea to the north, and the Pacific Ocean to the southwest. If you have any questions about medical terms or concepts, I would be happy to help with those!

A haplotype is a group of genes or DNA sequences that are inherited together from a single parent. It refers to a combination of alleles (variant forms of a gene) that are located on the same chromosome and are usually transmitted as a unit. Haplotypes can be useful in tracing genetic ancestry, understanding the genetic basis of diseases, and developing personalized medical treatments.

In population genetics, haplotypes are often used to study patterns of genetic variation within and between populations. By comparing haplotype frequencies across populations, researchers can infer historical events such as migrations, population expansions, and bottlenecks. Additionally, haplotypes can provide information about the evolutionary history of genes and genomic regions.

In clinical genetics, haplotypes can be used to identify genetic risk factors for diseases or to predict an individual's response to certain medications. For example, specific haplotypes in the HLA gene region have been associated with increased susceptibility to certain autoimmune diseases, while other haplotypes in the CYP450 gene family can affect how individuals metabolize drugs.

Overall, haplotypes provide a powerful tool for understanding the genetic basis of complex traits and diseases, as well as for developing personalized medical treatments based on an individual's genetic makeup.

The placenta is an organ that develops in the uterus during pregnancy and provides oxygen and nutrients to the growing baby through the umbilical cord. It also removes waste products from the baby's blood. The placenta attaches to the wall of the uterus, and the baby's side of the placenta contains many tiny blood vessels that connect to the baby's circulatory system. This allows for the exchange of oxygen, nutrients, and waste between the mother's and baby's blood. After the baby is born, the placenta is usually expelled from the uterus in a process called afterbirth.

Dapsone is a medication that belongs to a class of drugs called sulfones. It is primarily used to treat bacterial skin infections such as leprosy and dermatitis herpetiformis (a skin condition associated with coeliac disease). Dapsone works by killing the bacteria responsible for these infections.

In addition, dapsone has anti-inflammatory properties and is sometimes used off-label to manage inflammatory conditions such as vasculitis, bullous pemphigoid, and chronic urticaria. It is available in oral tablet form and topical cream or gel form.

Like all medications, dapsone can cause side effects, which may include nausea, loss of appetite, and headache. More serious side effects, such as methemoglobinemia (a blood disorder that affects the body's ability to transport oxygen), peripheral neuropathy (nerve damage that causes pain, numbness, or weakness in the hands and feet), and liver damage, can occur but are less common.

It is important for patients taking dapsone to be monitored by a healthcare provider to ensure safe and effective use of the medication.

Naphthoquinones are a type of organic compound that consists of a naphthalene ring (two benzene rings fused together) with two ketone functional groups (=O) at the 1 and 2 positions. They exist in several forms, including natural and synthetic compounds. Some well-known naphthoquinones include vitamin K1 (phylloquinone) and K2 (menaquinone), which are important for blood clotting and bone metabolism. Other naphthoquinones have been studied for their potential medicinal properties, including anticancer, antibacterial, and anti-inflammatory activities. However, some naphthoquinones can also be toxic or harmful to living organisms, so they must be used with caution.

Vacuoles are membrane-bound organelles found in the cells of most eukaryotic organisms. They are essentially fluid-filled sacs that store various substances, such as enzymes, waste products, and nutrients. In plants, vacuoles often contain water, ions, and various organic compounds, while in fungi, they may store lipids or pigments. Vacuoles can also play a role in maintaining the turgor pressure of cells, which is critical for cell shape and function.

In animal cells, vacuoles are typically smaller and less numerous than in plant cells. Animal cells have lysosomes, which are membrane-bound organelles that contain digestive enzymes and break down waste materials, cellular debris, and foreign substances. Lysosomes can be considered a type of vacuole, but they are more specialized in their function.

Overall, vacuoles are essential for maintaining the health and functioning of cells by providing a means to store and dispose of various substances.

Molecular cloning is a laboratory technique used to create multiple copies of a specific DNA sequence. This process involves several steps:

1. Isolation: The first step in molecular cloning is to isolate the DNA sequence of interest from the rest of the genomic DNA. This can be done using various methods such as PCR (polymerase chain reaction), restriction enzymes, or hybridization.
2. Vector construction: Once the DNA sequence of interest has been isolated, it must be inserted into a vector, which is a small circular DNA molecule that can replicate independently in a host cell. Common vectors used in molecular cloning include plasmids and phages.
3. Transformation: The constructed vector is then introduced into a host cell, usually a bacterial or yeast cell, through a process called transformation. This can be done using various methods such as electroporation or chemical transformation.
4. Selection: After transformation, the host cells are grown in selective media that allow only those cells containing the vector to grow. This ensures that the DNA sequence of interest has been successfully cloned into the vector.
5. Amplification: Once the host cells have been selected, they can be grown in large quantities to amplify the number of copies of the cloned DNA sequence.

Molecular cloning is a powerful tool in molecular biology and has numerous applications, including the production of recombinant proteins, gene therapy, functional analysis of genes, and genetic engineering.

Pregnancy is a physiological state or condition where a fertilized egg (zygote) successfully implants and grows in the uterus of a woman, leading to the development of an embryo and finally a fetus. This process typically spans approximately 40 weeks, divided into three trimesters, and culminates in childbirth. Throughout this period, numerous hormonal and physical changes occur to support the growing offspring, including uterine enlargement, breast development, and various maternal adaptations to ensure the fetus's optimal growth and well-being.

Asymptomatic infections are those in which an individual carries and may transmit a pathogen, such as a virus or bacteria, but does not develop any symptoms associated with the infection. These individuals are often referred to as being "asymptomatically infected" or "asymptomatic carriers."

Asymptomatic infections can occur with various infectious diseases, including COVID-19, HIV, hepatitis B, and some sexually transmitted infections. In many cases, asymptomatic individuals may not realize they are infected and unknowingly transmit the pathogen to others. This makes identifying and controlling asymptomatic infections crucial for preventing outbreaks and limiting the spread of infectious diseases.

It's important to note that while asymptomatic individuals do not experience symptoms, they can still develop immunity to the infection, similar to those who experienced symptoms. Additionally, some asymptomatic infections may progress to symptomatic illness over time or upon subsequent exposures to the pathogen.

An epitope is a specific region on the surface of an antigen (a molecule that can trigger an immune response) that is recognized by an antibody, B-cell receptor, or T-cell receptor. It is also commonly referred to as an antigenic determinant. Epitopes are typically composed of linear amino acid sequences or conformational structures made up of discontinuous amino acids in the antigen. They play a crucial role in the immune system's ability to differentiate between self and non-self molecules, leading to the targeted destruction of foreign substances like viruses and bacteria. Understanding epitopes is essential for developing vaccines, diagnostic tests, and immunotherapies.

Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency is a genetic disorder that affects the normal functioning of an enzyme called G6PD. This enzyme is found in red blood cells and plays a crucial role in protecting them from damage.

In people with G6PD deficiency, the enzyme's activity is reduced or absent, making their red blood cells more susceptible to damage and destruction, particularly when they are exposed to certain triggers such as certain medications, infections, or foods. This can lead to a condition called hemolysis, where the red blood cells break down prematurely, leading to anemia, jaundice, and in severe cases, kidney failure.

G6PD deficiency is typically inherited from one's parents in an X-linked recessive pattern, meaning that males are more likely to be affected than females. While there is no cure for G6PD deficiency, avoiding triggers and managing symptoms can help prevent complications.

CD36 is a type of protein found on the surface of certain cells in the human body, including platelets, white blood cells (monocytes and macrophages), and fat (adipose) cells. It is a type of scavenger receptor that plays a role in various biological processes, such as:

1. Fatty acid uptake and metabolism: CD36 helps facilitate the transport of long-chain fatty acids into cells for energy production and storage.
2. Inflammation and immune response: CD36 is involved in the recognition and clearance of foreign substances (pathogens) and damaged or dying cells, which can trigger an immune response.
3. Angiogenesis: CD36 has been implicated in the regulation of blood vessel formation (angiogenesis), particularly during wound healing and tumor growth.
4. Atherosclerosis: CD36 has been associated with the development and progression of atherosclerosis, a condition characterized by the buildup of fats, cholesterol, and other substances in and on the artery walls. This is due to its role in the uptake of oxidized low-density lipoprotein (oxLDL) by macrophages, leading to the formation of foam cells and the development of fatty streaks in the arterial wall.
5. Infectious diseases: CD36 has been identified as a receptor for various pathogens, including malaria parasites, HIV, and some bacteria, which can use this protein to gain entry into host cells.

As an antigen, CD36 is a molecule that can be targeted by the immune system to produce an immune response. Antibodies against CD36 have been found in various diseases, such as autoimmune disorders and certain infections. Modulation of CD36 activity has been suggested as a potential therapeutic strategy for several conditions, including atherosclerosis, diabetes, and infectious diseases.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

A mutation is a permanent change in the DNA sequence of an organism's genome. Mutations can occur spontaneously or be caused by environmental factors such as exposure to radiation, chemicals, or viruses. They may have various effects on the organism, ranging from benign to harmful, depending on where they occur and whether they alter the function of essential proteins. In some cases, mutations can increase an individual's susceptibility to certain diseases or disorders, while in others, they may confer a survival advantage. Mutations are the driving force behind evolution, as they introduce new genetic variability into populations, which can then be acted upon by natural selection.

To the best of my knowledge, "Côte d'Ivoire" is not a medical term or concept. It is the name of a country, which is officially known as the Republic of Côte d'Ivoire. The country is located in West Africa and is bordered by countries such as Ghana, Mali, Burkina Faso, and Liberia.

Côte d'Ivoire was once a French colony and gained its independence in 1960. The country has a diverse population and a developing economy, with agriculture being a major contributor to its GDP. The capital city of Côte d'Ivoire is Yamoussoukro, while the largest city is Abidjan.

It's important to note that medical terminology and concepts are typically related to anatomy, physiology, diseases, treatments, and other health-related topics. Therefore, it's unlikely that a country name like Côte d'Ivoire would have a direct medical definition or application.

I'm sorry for any confusion, but "Sulfalene" does not appear to be a valid or recognized term in medical or pharmaceutical literature. It's possible that there may be a spelling error or it could be a regional or outdated term for a specific medication. If you have more context or details, I'd be happy to help further!

Tertiary protein structure refers to the three-dimensional arrangement of all the elements (polypeptide chains) of a single protein molecule. It is the highest level of structural organization and results from interactions between various side chains (R groups) of the amino acids that make up the protein. These interactions, which include hydrogen bonds, ionic bonds, van der Waals forces, and disulfide bridges, give the protein its unique shape and stability, which in turn determines its function. The tertiary structure of a protein can be stabilized by various factors such as temperature, pH, and the presence of certain ions. Any changes in these factors can lead to denaturation, where the protein loses its tertiary structure and thus its function.

Rosette formation is a term used in pathology and histology, which refers to the circular arrangement of cells or structures around a central point, creating a pattern that resembles a rose flower. This phenomenon can be observed in various tissues and diseases. For example, in the context of cancer, rosette formation may be seen in certain types of tumors, such as medulloblastomas or retinoblastomas, where cancer cells cluster around blood vessels or form distinctive arrangements that are characteristic of these malignancies. In some cases, rosette formation can provide valuable clues for the diagnosis and classification of neoplasms. However, it is essential to consider other histological features and clinical context when interpreting rosette formation in diagnostic pathology.

Restriction Fragment Length Polymorphism (RFLP) is a term used in molecular biology and genetics. It refers to the presence of variations in DNA sequences among individuals, which can be detected by restriction enzymes. These enzymes cut DNA at specific sites, creating fragments of different lengths.

In RFLP analysis, DNA is isolated from an individual and treated with a specific restriction enzyme that cuts the DNA at particular recognition sites. The resulting fragments are then separated by size using gel electrophoresis, creating a pattern unique to that individual's DNA. If there are variations in the DNA sequence between individuals, the restriction enzyme may cut the DNA at different sites, leading to differences in the length of the fragments and thus, a different pattern on the gel.

These variations can be used for various purposes, such as identifying individuals, diagnosing genetic diseases, or studying evolutionary relationships between species. However, RFLP analysis has largely been replaced by more modern techniques like polymerase chain reaction (PCR)-based methods and DNA sequencing, which offer higher resolution and throughput.

Alpha-thalassemia is a genetic disorder that affects the production of hemoglobin, a protein in red blood cells that carries oxygen throughout the body. It is caused by deletions or mutations in the genes that produce the alpha-globin chains of hemoglobin.

There are several types of alpha-thalassemia, ranging from mild to severe. The most severe form, called hydrops fetalis, occurs when all four alpha-globin genes are deleted or mutated. This can cause stillbirth or death shortly after birth due to heart failure and severe anemia.

Less severe forms of alpha-thalassemia can cause mild to moderate anemia, which may be asymptomatic or associated with symptoms such as fatigue, weakness, and jaundice. These forms of the disorder are more common in people from Mediterranean, Southeast Asian, and African backgrounds.

Treatment for alpha-thalassemia depends on the severity of the condition and may include blood transfusions, iron chelation therapy, or occasionally stem cell transplantation.

'Diagnostic tests, routine' is a medical term that refers to standard or commonly used tests that are performed to help diagnose, monitor, or manage a patient's health condition. These tests are typically simple, non-invasive, and safe, and they may be ordered as part of a regular check-up or when a patient presents with specific symptoms.

Routine diagnostic tests may include:

1. Complete Blood Count (CBC): A test that measures the number of red and white blood cells, platelets, and hemoglobin in the blood. It can help diagnose conditions such as anemia, infection, and inflammation.
2. Urinalysis: A test that examines a urine sample for signs of infection, kidney disease, or other medical conditions.
3. Blood Chemistry Tests: Also known as a chemistry panel or comprehensive metabolic panel, this test measures various chemicals in the blood such as glucose, electrolytes, and enzymes to evaluate organ function and overall health.
4. Electrocardiogram (ECG): A test that records the electrical activity of the heart, which can help diagnose heart conditions such as arrhythmias or heart attacks.
5. Chest X-ray: An imaging test that creates pictures of the structures inside the chest, including the heart, lungs, and bones, to help diagnose conditions such as pneumonia or lung cancer.
6. Fecal Occult Blood Test (FOBT): A test that checks for hidden blood in the stool, which can be a sign of colon cancer or other gastrointestinal conditions.
7. Pap Smear: A test that collects cells from the cervix to check for abnormalities that may indicate cervical cancer or other gynecological conditions.

These are just a few examples of routine diagnostic tests that healthcare providers may order. The specific tests ordered will depend on the patient's age, sex, medical history, and current symptoms.

I'm sorry for any confusion, but "India" is not a medical term or concept. It is a country in South Asia, the second-most populous country in the world, known for its rich history, diverse culture, and numerous contributions to various fields including medicine. If you have any questions related to medical topics, I would be happy to help answer them!

Phylogeny is the evolutionary history and relationship among biological entities, such as species or genes, based on their shared characteristics. In other words, it refers to the branching pattern of evolution that shows how various organisms have descended from a common ancestor over time. Phylogenetic analysis involves constructing a tree-like diagram called a phylogenetic tree, which depicts the inferred evolutionary relationships among organisms or genes based on molecular sequence data or other types of characters. This information is crucial for understanding the diversity and distribution of life on Earth, as well as for studying the emergence and spread of diseases.

Microsatellite repeats, also known as short tandem repeats (STRs), are repetitive DNA sequences made up of units of 1-6 base pairs that are repeated in a head-to-tail manner. These repeats are spread throughout the human genome and are highly polymorphic, meaning they can have different numbers of repeat units in different individuals.

Microsatellites are useful as genetic markers because of their high degree of variability. They are commonly used in forensic science to identify individuals, in genealogy to trace ancestry, and in medical research to study genetic diseases and disorders. Mutations in microsatellite repeats have been associated with various neurological conditions, including Huntington's disease and fragile X syndrome.

Triazines are not a medical term, but a class of chemical compounds. They have a six-membered ring containing three nitrogen atoms and three carbon atoms. Some triazine derivatives are used in medicine as herbicides, antimicrobials, and antitumor agents.

Asexual reproduction in a medical context refers to a type of reproduction that does not involve the fusion of gametes (sex cells) or the exchange of genetic material between two parents. In asexual reproduction, an organism creates offspring that are genetically identical to itself. This can occur through various mechanisms, such as budding, binary fission, fragmentation, or vegetative reproduction. Asexual reproduction is common in some plants, fungi, and unicellular organisms, but it also occurs in certain animals, such as starfish and some types of flatworms. This mode of reproduction allows for rapid population growth and can be advantageous in stable environments where genetic diversity is not essential for survival.

Gravidity is a medical term that refers to the number of times a woman has been pregnant, regardless of the outcome of the pregnancies. It's a way to quantify a woman's childbearing experience and is often used in obstetrics and gynecology to assess potential risks and complications during pregnancy and childbirth.

For example, a woman who has been pregnant once before would have a gravidity of 1, while a woman who has been pregnant twice would have a gravidity of 2. This term is distinct from parity, which refers to the number of pregnancies that have reached a viable gestational age and resulted in a live birth.

I'm sorry for any confusion, but "Laos" is not a medical term. It is the name of a country, the Lao People's Democratic Republic, located in Southeast Asia. If you have any questions about medical terms or health-related topics, I'd be happy to try and help answer them!

Cinchona alkaloids are a group of naturally occurring chemical compounds that are found in the bark of Cinchona trees, which are native to South America. These alkaloids have been used for centuries in traditional medicine to treat various ailments, most notably malaria. The main cinchona alkaloids include quinine, quinidine, cinchonine, and cinchonidine.

Quinine is the most well-known of these alkaloids and has been used for centuries as an effective antimalarial agent. It works by interfering with the reproduction of the malaria parasite in the red blood cells. Quinine is also used to treat other medical conditions, such as leg cramps and restless legs syndrome.

Quinidine is another important cinchona alkaloid that is used primarily as an antiarrhythmic agent to treat irregular heart rhythms. It works by slowing down the electrical conduction in the heart and stabilizing its rhythm.

Cinchonine and cinchonidine have more limited medical uses, mainly as bitter-tasting ingredients in tonics and other beverages. However, they also have some medicinal properties, such as being used as antimalarial agents and antiarrhythmic drugs in some countries.

It is important to note that cinchona alkaloids can have serious side effects if not used properly, so they should only be taken under the supervision of a healthcare professional.

18S rRNA (ribosomal RNA) is the smaller subunit of the eukaryotic ribosome, which is the cellular organelle responsible for protein synthesis. The "18S" refers to the sedimentation coefficient of this rRNA molecule, which is a measure of its rate of sedimentation in a centrifuge and is expressed in Svedberg units (S).

The 18S rRNA is a component of the 40S subunit of the ribosome, and it plays a crucial role in the decoding of messenger RNA (mRNA) during protein synthesis. Specifically, the 18S rRNA helps to form the structure of the ribosome and contains several conserved regions that are involved in binding to mRNA and guiding the movement of transfer RNAs (tRNAs) during translation.

The 18S rRNA is also a commonly used molecular marker for evolutionary studies, as its sequence is highly conserved across different species and can be used to infer phylogenetic relationships between organisms. Additionally, the analysis of 18S rRNA gene sequences has been widely used in various fields such as ecology, environmental science, and medicine to study biodiversity, biogeography, and infectious diseases.

L-Lactate Dehydrogenase (LDH) is an enzyme found in various tissues within the body, including the heart, liver, kidneys, muscles, and brain. It plays a crucial role in the process of energy production, particularly during anaerobic conditions when oxygen levels are low.

In the presence of the coenzyme NADH, LDH catalyzes the conversion of pyruvate to lactate, generating NAD+ as a byproduct. Conversely, in the presence of NAD+, LDH can convert lactate back to pyruvate using NADH. This reversible reaction is essential for maintaining the balance between lactate and pyruvate levels within cells.

Elevated blood levels of LDH may indicate tissue damage or injury, as this enzyme can be released into the circulation following cellular breakdown. As a result, LDH is often used as a nonspecific biomarker for various medical conditions, such as myocardial infarction (heart attack), liver disease, muscle damage, and certain types of cancer. However, it's important to note that an isolated increase in LDH does not necessarily pinpoint the exact location or cause of tissue damage, and further diagnostic tests are usually required for confirmation.

Cross reactions, in the context of medical diagnostics and immunology, refer to a situation where an antibody or a immune response directed against one antigen also reacts with a different antigen due to similarities in their molecular structure. This can occur in allergy testing, where a person who is allergic to a particular substance may have a positive test result for a different but related substance because of cross-reactivity between them. For example, some individuals who are allergic to birch pollen may also have symptoms when eating certain fruits, such as apples, due to cross-reactive proteins present in both.

Fever, also known as pyrexia or febrile response, is a common medical sign characterized by an elevation in core body temperature above the normal range of 36.5-37.5°C (97.7-99.5°F) due to a dysregulation of the body's thermoregulatory system. It is often a response to an infection, inflammation, or other underlying medical conditions, and it serves as a part of the immune system's effort to combat the invading pathogens or to repair damaged tissues.

Fevers can be classified based on their magnitude:

* Low-grade fever: 37.5-38°C (99.5-100.4°F)
* Moderate fever: 38-39°C (100.4-102.2°F)
* High-grade or severe fever: above 39°C (102.2°F)

It is important to note that a single elevated temperature reading does not necessarily indicate the presence of a fever, as body temperature can fluctuate throughout the day and can be influenced by various factors such as physical activity, environmental conditions, and the menstrual cycle in females. The diagnosis of fever typically requires the confirmation of an elevated core body temperature on at least two occasions or a consistently high temperature over a period of time.

While fevers are generally considered beneficial in fighting off infections and promoting recovery, extremely high temperatures or prolonged febrile states may necessitate medical intervention to prevent potential complications such as dehydration, seizures, or damage to vital organs.

I'm sorry for any confusion, but "Vietnam" is not a medical term. It is the name of a country located in Southeast Asia. If you have any questions about medical conditions or terminology, I would be happy to help clarify those for you.

Molecular models are three-dimensional representations of molecular structures that are used in the field of molecular biology and chemistry to visualize and understand the spatial arrangement of atoms and bonds within a molecule. These models can be physical or computer-generated and allow researchers to study the shape, size, and behavior of molecules, which is crucial for understanding their function and interactions with other molecules.

Physical molecular models are often made up of balls (representing atoms) connected by rods or sticks (representing bonds). These models can be constructed manually using materials such as plastic or wooden balls and rods, or they can be created using 3D printing technology.

Computer-generated molecular models, on the other hand, are created using specialized software that allows researchers to visualize and manipulate molecular structures in three dimensions. These models can be used to simulate molecular interactions, predict molecular behavior, and design new drugs or chemicals with specific properties. Overall, molecular models play a critical role in advancing our understanding of molecular structures and their functions.

A newborn infant is a baby who is within the first 28 days of life. This period is also referred to as the neonatal period. Newborns require specialized care and attention due to their immature bodily systems and increased vulnerability to various health issues. They are closely monitored for signs of well-being, growth, and development during this critical time.

Genetically modified organisms (GMOs) are organisms whose genetic material has been altered using genetic engineering techniques. This can include the insertion, deletion, or modification of specific genes to achieve desired traits. In the context of medical definitions, GMOs are often used in research, biomedicine, and pharmaceutical production.

For example, genetically modified bacteria or yeast can be used to produce therapeutic proteins, such as insulin or vaccines. Genetic modification can also be used to create animal models of human diseases, allowing researchers to study disease mechanisms and test new therapies in a controlled setting. Additionally, GMOs are being explored for their potential use in gene therapy, where they can be engineered to deliver therapeutic genes to specific cells or tissues in the body.

It's important to note that while genetically modified organisms have shown great promise in many areas of medicine and biotechnology, there are also concerns about their potential impacts on human health and the environment. Therefore, their development and use are subject to strict regulations and oversight.

Protein binding, in the context of medical and biological sciences, refers to the interaction between a protein and another molecule (known as the ligand) that results in a stable complex. This process is often reversible and can be influenced by various factors such as pH, temperature, and concentration of the involved molecules.

In clinical chemistry, protein binding is particularly important when it comes to drugs, as many of them bind to proteins (especially albumin) in the bloodstream. The degree of protein binding can affect a drug's distribution, metabolism, and excretion, which in turn influence its therapeutic effectiveness and potential side effects.

Protein-bound drugs may be less available for interaction with their target tissues, as only the unbound or "free" fraction of the drug is active. Therefore, understanding protein binding can help optimize dosing regimens and minimize adverse reactions.

Species specificity is a term used in the field of biology, including medicine, to refer to the characteristic of a biological entity (such as a virus, bacterium, or other microorganism) that allows it to interact exclusively or preferentially with a particular species. This means that the biological entity has a strong affinity for, or is only able to infect, a specific host species.

For example, HIV is specifically adapted to infect human cells and does not typically infect other animal species. Similarly, some bacterial toxins are species-specific and can only affect certain types of animals or humans. This concept is important in understanding the transmission dynamics and host range of various pathogens, as well as in developing targeted therapies and vaccines.

Treatment failure is a term used in medicine to describe the situation when a prescribed treatment or intervention is not achieving the desired therapeutic goals or objectives. This may occur due to various reasons, such as:

1. Development of drug resistance by the pathogen or disease being treated.
2. Inadequate dosage or frequency of the medication.
3. Poor adherence or compliance to the treatment regimen by the patient.
4. The presence of underlying conditions or comorbidities that may affect the efficacy of the treatment.
5. The severity or progression of the disease despite appropriate treatment.

When treatment failure occurs, healthcare providers may need to reassess the patient's condition and modify the treatment plan accordingly, which may include adjusting the dosage, changing the medication, adding new medications, or considering alternative treatments.

Treatment outcome is a term used to describe the result or effect of medical treatment on a patient's health status. It can be measured in various ways, such as through symptoms improvement, disease remission, reduced disability, improved quality of life, or survival rates. The treatment outcome helps healthcare providers evaluate the effectiveness of a particular treatment plan and make informed decisions about future care. It is also used in clinical research to compare the efficacy of different treatments and improve patient care.

A point mutation is a type of genetic mutation where a single nucleotide base (A, T, C, or G) in DNA is altered, deleted, or substituted with another nucleotide. Point mutations can have various effects on the organism, depending on the location of the mutation and whether it affects the function of any genes. Some point mutations may not have any noticeable effect, while others might lead to changes in the amino acids that make up proteins, potentially causing diseases or altering traits. Point mutations can occur spontaneously due to errors during DNA replication or be inherited from parents.

I'm sorry for any confusion, but "geography" is not a term that has a medical definition. Geography is a field of study that deals with the location and distribution of physical and cultural features on Earth's surface, as well as how humans interact with and affect those features. It is not a concept that is typically used in a medical context. If you have any questions related to medicine or healthcare, I would be happy to try to help answer them for you!

DNA primers are short single-stranded DNA molecules that serve as a starting point for DNA synthesis. They are typically used in laboratory techniques such as the polymerase chain reaction (PCR) and DNA sequencing. The primer binds to a complementary sequence on the DNA template through base pairing, providing a free 3'-hydroxyl group for the DNA polymerase enzyme to add nucleotides and synthesize a new strand of DNA. This allows for specific and targeted amplification or analysis of a particular region of interest within a larger DNA molecule.

Southeast Asia is a geographical region that consists of the countries that are located at the southeastern part of the Asian continent. The definition of which countries comprise Southeast Asia may vary, but it generally includes the following 11 countries:

* Brunei
* Cambodia
* East Timor (Timor-Leste)
* Indonesia
* Laos
* Malaysia
* Myanmar (Burma)
* Philippines
* Singapore
* Thailand
* Vietnam

Southeast Asia is known for its rich cultural diversity, with influences from Hinduism, Buddhism, Islam, and Christianity. The region is also home to a diverse range of ecosystems, including rainforests, coral reefs, and mountain ranges. In recent years, Southeast Asia has experienced significant economic growth and development, but the region still faces challenges related to poverty, political instability, and environmental degradation.

The Democratic Republic of the Congo (DRC) is a country located in Central Africa. It is named after the Congo River, which flows through the country. The DRC is the second-largest country in Africa by area and the eleventh-largest in the world. It is home to a diverse population of more than 80 million people, making it one of the most populous countries on the continent.

The DRC is a democratic republic, which means that it is a form of government in which the people have the power to choose their leaders through free and fair elections. The country has a presidential system of government, in which the president serves as both the head of state and the head of government. The current president of the DRC is Félix Tshisekedi, who took office in January 2019.

The DRC is a federal republic, meaning that it is divided into several provinces, each with its own elected government. The country has a total of 26 provinces, which are further divided into districts and sectors.

The DRC is a member of various international organizations, including the United Nations, the African Union, and the Southern African Development Community. It is also a party to several international treaties and agreements, such as the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) and the Paris Agreement on climate change.

The DRC has a mixed economy, with both private and public sectors playing important roles. The country is rich in natural resources, including minerals such as copper, diamonds, gold, and tin. It also has large areas of fertile land that are suitable for agriculture. However, the DRC faces significant challenges, including poverty, corruption, and conflict. Despite these challenges, the country has made progress in recent years in terms of economic growth and development.

I'm sorry for any confusion, but "Mauritania" is not a medical term. It's actually the name of a country located in Northwest Africa, known officially as the Islamic Republic of Mauritania. If you have any questions about medical terms or conditions, I'd be happy to help with those!

Fosfomycin is an antibiotic that is primarily used to treat uncomplicated lower urinary tract infections. It works by inhibiting the bacterial enzyme responsible for the synthesis of the cell wall. The chemical name for fosfomycin is (E)-1,2-epoxypropylphosphonic acid.

Fosfomycin is available as an oral tablet and as a granule that can be dissolved in water for oral administration. It has a broad spectrum of activity against both gram-positive and gram-negative bacteria, including some strains that are resistant to other antibiotics.

Common side effects of fosfomycin include diarrhea, nausea, and headache. It is generally well tolerated and can be used in patients with impaired renal function. However, it should be avoided in people who have a history of allergic reactions to fosfomycin or any of its components.

It's important to note that the use of antibiotics like fosfomycin can lead to the development of bacterial resistance, so they should only be used when necessary and under the guidance of a healthcare professional.

Cell adhesion refers to the binding of cells to extracellular matrices or to other cells, a process that is fundamental to the development, function, and maintenance of multicellular organisms. Cell adhesion is mediated by various cell surface receptors, such as integrins, cadherins, and immunoglobulin-like cell adhesion molecules (Ig-CAMs), which interact with specific ligands in the extracellular environment. These interactions lead to the formation of specialized junctions, such as tight junctions, adherens junctions, and desmosomes, that help to maintain tissue architecture and regulate various cellular processes, including proliferation, differentiation, migration, and survival. Disruptions in cell adhesion can contribute to a variety of diseases, including cancer, inflammation, and degenerative disorders.

Immunization is defined medically as the process where an individual is made immune or resistant to an infectious disease, typically through the administration of a vaccine. The vaccine stimulates the body's own immune system to recognize and fight off the specific disease-causing organism, thereby preventing or reducing the severity of future infections with that organism.

Immunization can be achieved actively, where the person is given a vaccine to trigger an immune response, or passively, where antibodies are transferred to the person through immunoglobulin therapy. Immunizations are an important part of preventive healthcare and have been successful in controlling and eliminating many infectious diseases worldwide.

I apologize, but "Brazil" is not a medical term or condition. It is the largest country in both South America and Latin America by land area and population. If you have any questions related to medical terminology or health concerns, please provide more information and I will do my best to help.

An epitope is a specific region on an antigen (a substance that triggers an immune response) that is recognized and bound by an antibody or a B-lymphocyte (a type of white blood cell that produces antibodies). Epitopes are also sometimes referred to as antigenic determinants.

B-lymphocytes, or B cells, are a type of immune cell that plays a key role in the humoral immune response. They produce and secrete antibodies, which are proteins that recognize and bind to specific epitopes on antigens. When a B cell encounters an antigen, it binds to the antigen at its surface receptor, which recognizes a specific epitope on the antigen. This binding activates the B cell, causing it to divide and differentiate into plasma cells, which produce and secrete large amounts of antibody that is specific for the epitope on the antigen.

The ability of an antibody or a B cell to recognize and bind to a specific epitope is determined by the structure of the variable region of the antibody or B cell receptor. The variable region is made up of several loops of amino acids, called complementarity-determining regions (CDRs), that form a binding site for the antigen. The CDRs are highly variable in sequence and length, allowing them to recognize and bind to a wide variety of different epitopes.

In summary, an epitope is a specific region on an antigen that is recognized and bound by an antibody or a B-lymphocyte. The ability of an antibody or a B cell to recognize and bind to a specific epitope is determined by the structure of the variable region of the antibody or B cell receptor.

Reagent kits, diagnostic are prepackaged sets of chemical reagents and other components designed for performing specific diagnostic tests or assays. These kits are often used in clinical laboratories to detect and measure the presence or absence of various biomarkers, such as proteins, antibodies, antigens, nucleic acids, or small molecules, in biological samples like blood, urine, or tissues.

Diagnostic reagent kits typically contain detailed instructions for their use, along with the necessary reagents, controls, and sometimes specialized equipment or supplies. They are designed to simplify the testing process, reduce human error, and increase standardization, ensuring accurate and reliable results. Examples of diagnostic reagent kits include those used for pregnancy tests, infectious disease screening, drug testing, genetic testing, and cancer biomarker detection.

"Physarum" is not a term that has a specific medical definition. It is a genus of slime molds, which are single-celled organisms that can behave as multicellular entities under certain conditions. They are often studied in biological research for their unique behaviors and abilities, but they do not have direct relevance to human medicine.

Glycosylphosphatidylinositols (GPIs) are complex glycolipids that are attached to the outer leaflet of the cell membrane. They play a role in anchoring proteins to the cell surface by serving as a post-translational modification site for certain proteins, known as GPI-anchored proteins.

The structure of GPIs consists of a core glycan backbone made up of three mannose and one glucosamine residue, which is linked to a phosphatidylinositol (PI) anchor via a glycosylphosphatidylinositol anchor addition site. The PI anchor is composed of a diacylglycerol moiety and a phosphatidylinositol headgroup.

GPIs are involved in various cellular processes, including signal transduction, protein targeting, and cell adhesion. They have also been implicated in several diseases, such as cancer and neurodegenerative disorders.

'Mosquito Control' is not a medical term per se, but it is a public health concept that refers to the systematic reduction or elimination of mosquito populations through various methods to prevent or minimize the transmission of mosquito-borne diseases. This multidisciplinary field involves entomologists, ecologists, engineers, and public health professionals working together to manage mosquito habitats, apply insecticides, and educate communities about personal protection measures. By controlling mosquito populations, we can significantly reduce the risk of contracting vector-borne illnesses such as malaria, dengue fever, yellow fever, Zika virus, and West Nile virus, among others.

BALB/c is an inbred strain of laboratory mouse that is widely used in biomedical research. The strain was developed at the Institute of Cancer Research in London by Henry Baldwin and his colleagues in the 1920s, and it has since become one of the most commonly used inbred strains in the world.

BALB/c mice are characterized by their black coat color, which is determined by a recessive allele at the tyrosinase locus. They are also known for their docile and friendly temperament, making them easy to handle and work with in the laboratory.

One of the key features of BALB/c mice that makes them useful for research is their susceptibility to certain types of tumors and immune responses. For example, they are highly susceptible to developing mammary tumors, which can be induced by chemical carcinogens or viral infection. They also have a strong Th2-biased immune response, which makes them useful models for studying allergic diseases and asthma.

BALB/c mice are also commonly used in studies of genetics, neuroscience, behavior, and infectious diseases. Because they are an inbred strain, they have a uniform genetic background, which makes it easier to control for genetic factors in experiments. Additionally, because they have been bred in the laboratory for many generations, they are highly standardized and reproducible, making them ideal subjects for scientific research.

Antiprotozoal agents are a type of medication used to treat protozoal infections, which are infections caused by microscopic single-celled organisms called protozoa. These agents work by either killing the protozoa or inhibiting their growth and reproduction. They can be administered through various routes, including oral, topical, and intravenous, depending on the type of infection and the severity of the illness.

Examples of antiprotozoal agents include:

* Metronidazole, tinidazole, and nitazoxanide for treating infections caused by Giardia lamblia and Entamoeba histolytica.
* Atovaquone, clindamycin, and pyrimethamine-sulfadoxine for treating malaria caused by Plasmodium falciparum or other Plasmodium species.
* Pentamidine and suramin for treating African trypanosomiasis (sleeping sickness) caused by Trypanosoma brucei gambiense or T. b. rhodesiense.
* Nitroimidazoles, such as benznidazole and nifurtimox, for treating Chagas disease caused by Trypanosoma cruzi.
* Sodium stibogluconate and paromomycin for treating leishmaniasis caused by Leishmania species.

Antiprotozoal agents can have side effects, ranging from mild to severe, depending on the drug and the individual patient's response. It is essential to follow the prescribing physician's instructions carefully when taking these medications and report any adverse reactions promptly.

Hemoglobin C is a type of hemoglobin variant, which is the oxygen-carrying protein in red blood cells. Hemoglobin C is caused by a specific genetic mutation that results in the substitution of lysine for glutamic acid at position 6 on the beta globin chain of the hemoglobin molecule.

This variant is often associated with a benign condition known as hemoglobin C trait, where an individual inherits one copy of the mutated gene from one parent and one normal gene from the other parent. People with this trait usually have no symptoms or only mild anemia, if any. However, if an individual inherits two copies of the Hemoglobin C gene (one from each parent), they will have a more severe form of hemoglobin disorder called Hemoglobin CC disease, which can cause mild to moderate hemolytic anemia and other complications.

It's important to note that Hemoglobin C is most commonly found in people of West African descent, but it can also occur in other populations with African ancestry.

Coinfection is a term used in medicine to describe a situation where a person is infected with more than one pathogen (infectious agent) at the same time. This can occur when a person is infected with two or more viruses, bacteria, parasites, or fungi. Coinfections can complicate the diagnosis and treatment of infectious diseases, as the symptoms of each infection can overlap and interact with each other.

Coinfections are common in certain populations, such as people who are immunocompromised, have chronic illnesses, or live in areas with high levels of infectious agents. For example, a person with HIV/AIDS may be more susceptible to coinfections with tuberculosis, hepatitis, or pneumocystis pneumonia. Similarly, a person who has recently undergone an organ transplant may be at risk for coinfections with cytomegalovirus, Epstein-Barr virus, or other opportunistic pathogens.

Coinfections can also occur in people who are otherwise healthy but are exposed to multiple infectious agents at once, such as through travel to areas with high levels of infectious diseases or through close contact with animals that carry infectious agents. For example, a person who travels to a tropical area may be at risk for coinfections with malaria and dengue fever, while a person who works on a farm may be at risk for coinfections with influenza and Q fever.

Effective treatment of coinfections requires accurate diagnosis and appropriate antimicrobial therapy for each pathogen involved. In some cases, treating one infection may help to resolve the other, but in other cases, both infections may need to be treated simultaneously to achieve a cure. Preventing coinfections is an important part of infectious disease control, and can be achieved through measures such as vaccination, use of personal protective equipment, and avoidance of high-risk behaviors.

Equatorial Guinea is a country located in Central Africa, straddling the equator. It is not a medical term but a geographical and political designation. The country is composed of two main parts: Río Muni, which is the mainland and makes up about 10% of the country's total area, and Bioko, a tropical island in the Bight of Bonny, along with several smaller islands including Annobón, Corisco, and Elobey.

The capital city, Malabo, is located on Bioko Island. The official languages are Spanish and French, with Portuguese also recognized as an official language due to its membership in the Community of Portuguese Language Countries (CPLP).

Equatorial Guinea has a population of approximately 1.4 million people and is one of the smallest countries in Africa by land area. It gained independence from Spain in 1968, and since then, it has faced numerous challenges related to political instability, human rights abuses, and socio-economic development.

In terms of medical aspects, Equatorial Guinea faces various health issues, such as high infant mortality rates, malaria, HIV/AIDS, and other infectious diseases. The country also struggles with providing adequate healthcare services to its population due to limited resources, infrastructure, and healthcare personnel.

A disease vector is a living organism that transmits infectious pathogens from one host to another. These vectors can include mosquitoes, ticks, fleas, and other arthropods that carry viruses, bacteria, parasites, or other disease-causing agents. The vector becomes infected with the pathogen after biting an infected host, and then transmits the infection to another host through its saliva or feces during a subsequent blood meal.

Disease vectors are of particular concern in public health because they can spread diseases rapidly and efficiently, often over large geographic areas. Controlling vector-borne diseases requires a multifaceted approach that includes reducing vector populations, preventing bites, and developing vaccines or treatments for the associated diseases.

"Africa South of the Sahara" is a term commonly used in medical and scientific literature to refer to the region of the African continent that lies south of the Sahara Desert. This region includes 48 countries, with a population of over 1 billion people, and is characterized by its tropical or subtropical climate, diverse cultures, and unique health challenges.

The term "South of the Sahara" is used to distinguish this region from North Africa, which is predominantly Arab and Berber in culture and has closer ties to the Middle East than to Sub-Saharan Africa. The Sahara Desert serves as a natural geographical boundary between these two regions.

In medical terms, "Africa South of the Sahara" encompasses a wide range of health issues, including infectious diseases such as HIV/AIDS, malaria, tuberculosis, and Ebola, which are prevalent in many parts of the region. The area also faces challenges related to maternal and child health, nutrition, water and sanitation, and non-communicable diseases such as cancer, diabetes, and cardiovascular disease.

Medical research and interventions focused on "Africa South of the Sahara" aim to address these unique health challenges and improve the overall health outcomes of the population in this region.

Antibody specificity refers to the ability of an antibody to bind to a specific epitope or antigenic determinant on an antigen. Each antibody has a unique structure that allows it to recognize and bind to a specific region of an antigen, typically a small portion of the antigen's surface made up of amino acids or sugar residues. This highly specific binding is mediated by the variable regions of the antibody's heavy and light chains, which form a pocket that recognizes and binds to the epitope.

The specificity of an antibody is determined by its unique complementarity-determining regions (CDRs), which are loops of amino acids located in the variable domains of both the heavy and light chains. The CDRs form a binding site that recognizes and interacts with the epitope on the antigen. The precise fit between the antibody's binding site and the epitope is critical for specificity, as even small changes in the structure of either can prevent binding.

Antibody specificity is important in immune responses because it allows the immune system to distinguish between self and non-self antigens. This helps to prevent autoimmune reactions where the immune system attacks the body's own cells and tissues. Antibody specificity also plays a crucial role in diagnostic tests, such as ELISA assays, where antibodies are used to detect the presence of specific antigens in biological samples.

Triclosan is an antimicrobial agent that has been used in various consumer products, such as soaps, toothpastes, and cosmetics, to reduce or prevent bacterial contamination. It works by inhibiting the growth of bacteria and other microorganisms. The chemical formula for triclosan is 5-chloro-2-(2,4-dichlorophenoxy)phenol.

It's worth noting that in recent years, there has been some controversy surrounding the use of triclosan due to concerns about its potential health effects and environmental impact. Some studies have suggested that triclosan may interfere with hormone regulation and contribute to antibiotic resistance. As a result, the U.S. Food and Drug Administration (FDA) banned the use of triclosan in over-the-counter consumer antiseptic washes in 2016, citing concerns about its safety and effectiveness. However, it is still allowed in other products such as toothpaste.

Peptides are short chains of amino acid residues linked by covalent bonds, known as peptide bonds. They are formed when two or more amino acids are joined together through a condensation reaction, which results in the elimination of a water molecule and the formation of an amide bond between the carboxyl group of one amino acid and the amino group of another.

Peptides can vary in length from two to about fifty amino acids, and they are often classified based on their size. For example, dipeptides contain two amino acids, tripeptides contain three, and so on. Oligopeptides typically contain up to ten amino acids, while polypeptides can contain dozens or even hundreds of amino acids.

Peptides play many important roles in the body, including serving as hormones, neurotransmitters, enzymes, and antibiotics. They are also used in medical research and therapeutic applications, such as drug delivery and tissue engineering.

I'm sorry for any confusion, but "Haiti" is not a medical term. It is a country located in the Caribbean, specifically on the island of Hispaniola. If you have any questions about medical conditions or terminology, I would be happy to help clarify those for you.

I'm sorry for any confusion, but "Guyana" is not a medical term. It's actually the name of a country located in South America, known for its diverse wildlife, rainforests, and unique cultural heritage. If you have any questions about medical terms or concepts, I'd be happy to help answer those for you!

... is a unicellular protozoan parasite of humans, and the deadliest species of Plasmodium that causes ... In 1897, William H. Welch created the name Plasmodium falciparum, which ICZN formally adopted in 1954. P. falciparum assumes ... Bousema, T.; Drakeley, C. (2011). "Epidemiology and Infectivity of Plasmodium falciparum and Plasmodium vivax Gametocytes in ... The Plasmodium Genome Resource UCSC Plasmodium Falciparum Browser Gene info at Kyoto University (CS1 errors: periodical ignored ...
... (PfEMP1) is a family of proteins present on the membrane surface of red ... Zhang Y, Jiang N, Chang Z, Wang H, Lu H, Wahlgren M, Chen Q (2014). "The var3 genes of Plasmodium falciparum 3D7 strain are ... In humans, malaria can be caused by five Plasmodium parasites, namely P. falciparum, P. vivax, P. malariae, P. ovale and P. ... Hviid, Lars; Jensen, Anja T.R. (2015). "PfEMP1 - A Parasite Protein Family of Key Importance in Plasmodium falciparum Malaria ...
Plasmodium Falciparum; in collaboration with Amico Bignami, 1900. Considerations on the treatment of malaria, 1933. On the ... called terzana maligna was attributed to Plasmodium falciparum, while a milder form of the disease called terzana benigna was ... they could therefore describe all the phases of the sporogonic cycle of Plasmodium Vivax from the Cocists stage of 42 hours ... and together with Bastianelli and Bignami he clarified the biological pattern of plasmodia from Anopheles mosquito to man in ...
The DNA of Plasmodium falciparum shows the same pattern of diversity as its human hosts, with greater diversity in Africa than ... Shortt HE, Fairley NH, Covell G, Shute PG, Garnham PC (1948). "Pre-erythrocytic Stage of Plasmodium Falciparum". Br Med J. 2 ( ... Nerlich AG, Schraut B, Dittrich S, Jelinek T, Zink AR (2008). "Plasmodium falciparum in Ancient Egypt". Emerg Infect Dis. 14 (8 ... Humans may have originally caught P. falciparum from gorillas. P. vivax, another malarial Plasmodium species among the six that ...
Rubio, J P; Thompson, J K; Cowman, A F (1 August 1996). "The var genes of Plasmodium falciparum are located in the subtelomeric ... The advantages of subtelomeres have been studied in different species such as Plasmodium falciparum, Drosophila melanogaster, ... Scherf, Artur; Lopez-Rubio, Jose Juan; Riviere, Loïc (October 2008). "Antigenic Variation in Plasmodium falciparum". Annual ... The subtelomeres of such diverse species as humans, Plasmodium falciparum, Drosophila melanogaster, and Saccharomyces ...
Dalexandri, F.; Kimura, E.; Peres, V.; Katzin, A. (2006). "Protein dolichylation in Plasmodium falciparum". FEBS Letters. 580 ( ... including the malarial parasite Plasmodium falciparum. Hjertman, M.; Wejde, J.; Dricu, A.; Carlberg, M.; Griffiths, W. J.; ...
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Glycophorin B acts as a receptor for erythrocyte binding Ligand (EBl-1) of Plasmodium falciparum involved in malaria. Both the ... Field SP, Hempelmann E, Mendelow BV, Fleming AF (February 1994). "Glycophorin variants and Plasmodium falciparum: protective ... Facer CA (1983). "Erythrocyte sialoglycoproteins and Plasmodium falciparum invasion". Trans. R. Soc. Trop. Med. Hyg. 77 (4): ... "Glycophorin B as an EBA-175 independent Plasmodium falciparum receptor of human erythrocytes". Mol. Biochem. Parasitol. 64 (1 ...
... durae Plasmodium egerniae Plasmodium elongatum Plasmodium eylesi Plasmodium fairchildi Plasmodium falciparum Plasmodium fallax ... Plasmodium cynomolgi, Plasmodium fragile, Plasmodium inui, Plasmodium fieldi, Plasmodium hylobati, Plasmodium inui, Plasmodium ... Plasmodium adunyinkai Plasmodium bitis Plasmodium bowiei Plasmodium brasiliense Plasmodium brucei Plasmodium bufoni Plasmodium ... Plasmodium accipiteris Plasmodium achiotense Plasmodium achromaticum Plasmodium acuminatum Plasmodium adleri Plasmodium ...
"Plasmodium falciparum (ID 33) - Genome - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-12-30. "Index of /genomes/refseq/protozoa/ ... "Index of /genomes/refseq/protozoa/Plasmodium_falciparum/latest_assembly_versions/GCF_000002765.5_GCA_000002765". ftp.ncbi.nih. ...
Treatment of Uncomplicated Plasmodium falciparum Malaria. World Health Organization. 2015-01-01. Archived from the original on ... Artemether is an antimalarial drug for uncomplicated malaria caused by P. falciparum (and chloroquine-resistant P. falciparum) ... "Efficacy and safety of artemether-lumefantrine compared with quinine in pregnant women with uncomplicated Plasmodium falciparum ... The World Health Organization (WHO) recommends the treatment of uncomplicated P. falciparum with artemisinin-based combination ...
Dongare, H. C.; Khatib, K. I. (2016). "JCDR - Exchange blood transfusion, Malaria, Plasmodium falciparum". Journal of Clinical ...
Plasmodium falciparum is the species responsible for more than 95% deaths caused by malaria. The WHO estimates there were 247 ... August 2018). "Plasmodium falciparum Sporozoite Vaccine in Tanzanian Adults". The American Journal of Tropical Medicine and ... Sanaria has developed the technology to grow and harvest aseptic, purified Plasmodium falciparum (Pf) SPZ and formulate them as ... May 2017). "Safety and efficacy of PfSPZ Vaccine against Plasmodium falciparum via direct venous inoculation in healthy malaria ...
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Tilley L, Straimer J, Gnädig NF, Ralph SA, Fidock DA (2016). "Artemisinin Action and Resistance in Plasmodium falciparum". ... Wicht KJ, Mok S, Fidock DA (September 2020). "Molecular Mechanisms of Drug Resistance in Plasmodium falciparum Malaria". Annual ... Ouji M, Augereau JM, Paloque L, Benoit-Vical F (2018). "Plasmodium falciparum resistance to artemisinin-based combination ... 2014). "Spread of artemisinin resistance in Plasmodium falciparum malaria". The New England Journal of Medicine. 371 (5): 411- ...
Krishna has made significant contributions to the understanding of membrane transporters in Plasmodium falciparum, a parasite ... July 2004). "Mefloquine resistance in Plasmodium falciparum and increased pfmdr1 gene copy number". The Lancet. 364 (9432): 438 ... August 2003). "Artemisinins target the SERCA of Plasmodium falciparum". Nature. 424 (6951): 957-961. Bibcode:2003Natur.424.. ... August 2006). "Decreasing pfmdr1 Copy Number in Plasmodium falciparum Malaria Heightens Susceptibility to Mefloquine, ...
... s are membranous structures seen in the red blood cell during infection with Plasmodium falciparum. The function ... Mundwiler-Pachlatko E, Beck HP (December 2013). "Maurer's clefts, the enigma of Plasmodium falciparum". Proceedings of the ... they appear to play a role in trafficking of Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) and other adhesins ... Maurer's clefts appear in the cytosol of red blood cells 2 to 4 hours after invasion by P. falciparum. They originally appear ...
Arnou B, Montigny C, Morth JP, Nissen P, Jaxel C, Møller JV, Maire M (June 2011). "The Plasmodium falciparum Ca(2+)-ATPase ... Kimura M, Yamaguchi Y, Takada S, Tanabe K (April 1993). "Cloning of a Ca(2+)-ATPase gene of Plasmodium falciparum and ... PfATP6, also known as PfSERCA or PfATPase6, is a calcium ATPase gene encoded by the malaria parasite Plasmodium falciparum. The ... December 2005). "Resistance of Plasmodium falciparum field isolates to in-vitro artemether and point mutations of the SERCA- ...
Hempelmann E, Marques HM (September 1994). "Analysis of malaria pigment from Plasmodium falciparum". J Pharmacol Toxicol ... Hempelmann E (2007). "Hemozoin biocrystallization in Plasmodium falciparum and the antimalarial activity of crystallization ... "Protein complex directs hemoglobin-to-hemozoin formation in Plasmodium falciparum". Proc Natl Acad Sci U S A. 110 (14): 5392-7 ... During its intraerythrocytic asexual reproduction cycle Plasmodium falciparum consumes up to 80% of the host cell hemoglobin. ...
Plasmodium falciparum causes the majority of infections. Of the 20 countries with the highest incidence of maternal mortality, ...
Eight months after the MDA, Plasmodium falciparum prevalence had decreased from 14% to 1%. The only reported project with an ... Eyles DE, Hoo CC, Warren M, Sandosham AA (November 1963). "Plasmodium falciparum resistant to chloroquine in Cambodia". Am. J. ... Payne D (April 1988). "Did medicated salt hasten the spread of chloroquine resistance in Plasmodium falciparum?". Parasitol. ... Kondrashin AV, Sanyal MC (December 1985). "Mass drug administration in Andhra Pradesh in areas under Plasmodium falciparum ...
2009). Artemisinin Resistance in Plasmodium falciparum Malaria. New England Journal Of Medicine, 361, 455-467. Doliwa C, ... and as of 2012 artemisinin-resistant Plasmodium falciparum has emerged in western Cambodia and western Thailand.Toxoplasma ... Plasmodium vivax has become chloroquine and sulfadoxine-pyrimethamine resistant a few decades ago, ...
Malaria is caused by apicomplexans, primarily Plasmodium falciparum, which largely reside in red blood cells and itself ... "Artemisinin Action and Resistance in Plasmodium falciparum". Trends in Parasitology. 32 (9): 682-696. doi:10.1016/j.pt.2016.05. ... "Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria" (PDF). The Cochrane Database of ... 2009). "Artemether‐Lumefantrine versus Dihydroartemisinin‐Piperaquine for Falciparum Malaria: A Longitudinal, Randomized Trial ...
Hempelmann E, Marques HM (September 1994). "Analysis of malaria pigment from Plasmodium falciparum". J Pharmacol Toxicol ... Heme biocrystallization has been found in blood feeding organisms of great medical importance including Plasmodium, Rhodnius ...
Azithromycin monotherapy or combination therapy has not shown effectiveness in treating Plasmodium falciparum or Plasmodium ... Severe malaria is usually caused by P. falciparum (often referred to as falciparum malaria). Symptoms of falciparum malaria ... Five species of Plasmodium can infect and be spread by humans. Most deaths are caused by P. falciparum, whereas P. vivax, P. ... It binds the Plasmodium falciparum circumsporozoite protein (CSP-1), essential to disease, and makes it ineffective. Drug ...
Malaria due to Plasmodium falciparum is a major selective factor in human evolution. It has influenced mutations in HBB in ... Verra F, Mangano VD, Modiano D (2009). "Genetics of susceptibility to Plasmodium falciparum: from classical malaria resistance ... HbC provides near full protection against Plasmodium falciparum in homozygous (CC) individuals and intermediate protection in ... "Haemoglobin C and S in natural selection against Plasmodium falciparum malaria: a plethora or a single shared adaptive ...
Plasmodium falciparum resistance to piperaquine driven by PfCRT. Lancet Infect Dis 19: 1168-9. Structure and drug resistance of ... Covalent Plasmodium falciparum-selective proteasome inhibitors exhibit a low propensity for generating resistance in vitro and ... Cell Chem Biol (in press). Plasmodium falciparum K13 mutations in Africa and Asia impact artemisinin resistance and parasite ... Dhingra, Satish K.; Small-Saunders, Jennifer L.; Ménard, Didier; Fidock, David A. (2019-11-01). "Plasmodium falciparum ...
"Plasmodium falciparum Apicoplast Drugs: Targets or Off-Targets?". Chemical Reviews. 112 (3): 1269-83. doi:10.1021/cr200258w. ... "Chemical Rescue of Malaria Parasites Lacking an Apicoplast Defines Organelle Function in Blood-Stage Plasmodium falciparum". ... Parasites in the apicomplexan genus Plasmodium are the causative agents of malaria. Studies of C. velia and V. brassicaformis ... Silico Search for Target Similarity Identifies Several Approved Drugs with Potential Activity against the Plasmodium falciparum ...
Plasmodium falciparum was probably not able to gain a foothold among African populations until larger sedentary communities ... Cortés A, Mellombo M, Mgone CS, Beck HP, Reeder JC, Cooke BM (2005). "Adhesion of Plasmodium falciparum-infected red blood ... Rihet P, Flori L, Tall F, Traore AS, Fumoux F (2004). "Hemoglobin C is associated with reduced Plasmodium falciparum ... Brenda AkinyiI Webala, "Prevalence of Fetal Hemoglobin and Antibody Responses to Plasmodium falciparum Antigens in Sickle Cell ...
Plasmodium falciparum is the major cause of infection. Senegal has made significant progress against malaria and remains a ...
Plasmodium falciparum is a unicellular protozoan parasite of humans, and the deadliest species of Plasmodium that causes ... In 1897, William H. Welch created the name Plasmodium falciparum, which ICZN formally adopted in 1954. P. falciparum assumes ... Bousema, T.; Drakeley, C. (2011). "Epidemiology and Infectivity of Plasmodium falciparum and Plasmodium vivax Gametocytes in ... The Plasmodium Genome Resource UCSC Plasmodium Falciparum Browser Gene info at Kyoto University (CS1 errors: periodical ignored ...
Here we provide biochemical and cellular evidence that artemisinins are potent inhibitors of Plasmodium falciparum ... kinase and increase of the lipid product phosphatidylinositol-3-phosphate induces resistance in Plasmodium falciparum. The ... In resistant clinical strains, increased PfPI3K was associated with the C580Y mutation in P. falciparum Kelch13 (PfKelch13), a ... Identification of a Plasmodium falciparum phospholipid transfer protein. J. Biol. Chem.. 288, 31971-31983 (2013) ...
PF3D7_1409100 [Plasmodium falciparum 3D7] PF3D7_1409100 [Plasmodium falciparum 3D7]. Gene ID:811669 ... Genome sequence of the human malaria parasite Plasmodium falciparum. Gardner MJ, et al. Nature, 2002 Oct 3. PMID 12368864, Free ... A protein interaction network of the malaria parasite Plasmodium falciparum. LaCount DJ, et al. Nature, 2005 Nov 3. PMID ... Plasmodium falciparum 3D7 (isolate: 3D7) Lineage. Eukaryota; Sar; Alveolata; Apicomplexa; Aconoidasida; Haemosporida; ...
New research synthesizes information from many different studies that attempt to link specific antibody responses to Plasmodium ... falciparum with protection from clinical malaria and comes to important conclusions about which antigens might be worth ... June 19, 2019 New high-resolution maps show the global burden of Plasmodium falciparum and Plasmodium vivax, the two parasites ... Relationship between anti-merozoite antibodies and incidence of Plasmodium falciparum malaria. Date:. January 22, 2010. Source: ...
Binding site differences revealed by crystal structures of Plasmodium falciparum and bovine acyl-CoA binding protein.. van ... The biochemical properties of Plasmodium falciparum ACBP are described together with the 2.0 A resolution crystal structures of ... The biochemical properties of Plasmodium falciparum ACBP are described together with the 2.0 A resolution crystal structures of ... Acyl-CoA binding protein from Plasmodium falciparum. *PDB DOI: https://doi.org/10.2210/pdb1HBK/pdb ...
The malaria parasite Plasmodium falciparum relies on an exchange of metabolites with the host for proliferation. Here we ... Host-parasite interactions revealed by Plasmodium falciparum metabolomics Cell Host Microbe. 2009 Feb 19;5(2):191-9. doi: ... The malaria parasite Plasmodium falciparum relies on an exchange of metabolites with the host for proliferation. Here we ... To identify the biochemical basis for this effect, we disrupted the plasmodium arginase gene in the rodent malaria model P. ...
... with Quinidine Gluconate: Discontinuation of Parenteral ... CDC has recently reviewed data on the reported incidence in the United States of Plasmodium falciparum malaria and has ... Notices to Readers Treatment of Severe Plasmodium falciparum Malaria with Quinidine Gluconate: Discontinuation of Parenteral ... An expanded report on the use of quinidine gluconate for the treatment of P. falciparum malaria will be published in an MMWR ...
Plasmodium falciparum life cycle. Figure 2. Plasmodium falciparum.[http://www.parasitesinhumans.org/plasmodium-falciparum- ... Legend/credit: Plasmodium falciparum life cycle [1]. Closed double brackets: ]] Other examples: Bold Italic Subscript: H2O ... talk , contribs) (→‎Plasmodium falciparum life cycle). (diff) ← Older revision , Latest revision (diff) , Newer revision → ( ... Chloroquine Resistance in Plasmodium falciparum. From MicrobeWiki, the student-edited microbiology resource ...
On August 9, a thin blood smear obtained at the time of admission was reported to show Plasmodium falciparum malaria with 3.2% ... Notes from the Field: Locally Acquired Mosquito-Transmitted (Autochthonous) Plasmodium falciparum Malaria - National Capital ... Notes from the Field: Locally Acquired Mosquito-Transmitted (Autochthonous) Plasmodium falciparum Malaria - National Capital ... In mid-2023, eight autochthonous malaria cases (Plasmodium vivax) were identified in Florida and Texas (3); in both states, the ...
... Nature. 2015 Oct 8;526(7572):207-211. ... We found that Plasmodium falciparum infection prevalence in endemic Africa halved and the incidence of clinical disease fell by ...
Plasmodium falciparum 3D7). Find diseases associated with this biological target and compounds tested against it in bioassay ...
CSourtesy of the CDC and Coatney GR, Collins WE, Warren M, Contacos PG. The Primate Malarias. U.S. Department of Health, Education and Welfare, Bethesda, 1971. ...
... proteins from Plasmodium parasites, and identifies a PfRH5 sequence variant that can be used for clinical production of a non- ... falciparum parasite. The antibodies induced by one protein variant were shown to be qualitatively similar to responses induced ... The Plasmodium falciparum reticulocyte-binding protein homolog 5 (PfRH5) has recently emerged as a leading candidate antigen ... Hjerrild, K., Jin, J., Wright, K. et al. Production of full-length soluble Plasmodium falciparum RH5 protein vaccine using a ...
BioAssay record AID 1077509 submitted by ChEMBL: Antimicrobial activity against Plasmodium falciparum NF54.
Plasmodium falciparum life cycle. Figure 2. Plasmodium falciparum.[http://www.parasitesinhumans.org/plasmodium-falciparum- ... Legend/credit: Plasmodium falciparum life cycle [1]. Closed double brackets: ]] Other examples: Bold Italic Subscript: H2O ... right,Figure 2. ,i,Plasmodium falciparum,/i,.[http://www.parasitesinhumans.org/plasmodium-falciparum-malaria.html]] ... right,Figure 2. ,i,Plasmodium falciparum,/i,.[http://www.parasitesinhumans.org/plasmodium-falciparum-malaria.html]] ...
To date, it is still poorly understood whether Anopheles mosquitoes that get infected with P. falciparum suffer fitness costs. ... However, in field experiments infecting a related species, Anopheles coluzzii, with P. falciparum using blood from donors in ... falciparum, with no impacts on the parasite. The results of our study suggest that pathways triggered by mating may help ... falciparum infection, and that the mating status of the mosquitoes does not impact the parasite. ...
Sequence of Plasmodium falciparum chromosomes 2, 10, 11 and 14. Gardner MJ, Shallom SJ, Carlton JM, Salzberg SL, Nene V, ... To stimulate basic research and facilitate the development of new drugs and vaccines, the genome of Plasmodium falciparum clone ... The mosquito-borne malaria parasite Plasmodium falciparum kills an estimated 0.7-2.7 million people every year, primarily ... These chromosomes represent about 35% of the 23-megabase P. falciparum genome. ...
Microscope slide showing the parasitic protozoan Plasmodium falciparum in human blood.. To learn more about this organism, ... please visit the CDCs article about the stages of Plasmodium falciparum in blood: https://www.cdc.gov/dpdx/resources/pdf/ ...
Plasmodium Falciparum And Vivax 6- Oxopurine Phosphoribosyltransferases And Their Pro-drugs As Antimalarial Agents. ...
DNA dynamics in the unusual cell cycle of the malaria parasite Plasmodium falciparum. ... DNA dynamics in the unusual cell cycle of the malaria parasite Plasmodium falciparum). Okres sprawozdawczy: 2021-06-01 do 2022- ... falciparum and one on the dynamics of schizogony in P. falciparum as compared with P. knowlesi.. Aim 2: to study replication- ... reviewing the state of the Plasmodium cell cycle field. (Checks and Balances? DNA replication and the cell cycle in Plasmodium ...
Structure of the Plasmodium falciparum SIP2 DNA-binding AP2 tandem repeat in complex with two SPE2 half-sites ... Structure of the Plasmodium falciparum SIP2 DNA-binding AP2 tandem repeat in complex with two SPE2 half-sites. *PDB DOI: https ... Structural and functional analysis of the Plasmodium falciparum SIP2 DNA binding domain. Niederwieser, I., Reiter, D., Kantsadi ... Plasmodium falciparum 3D7. Mutation(s): 0 Gene Names: PF3D7_0604100. UniProt. Find proteins for C6KSN9 (Plasmodium falciparum ( ...
You searched for: Subject Plasmodium falciparum ✖ Remove constraint Subject: Plasmodium falciparum Start Over ... MetabolismPlasmodium falciparumPathologyImmunology 9. Exploring the Plasmodium falciparum Transcriptome Using Hypergeometric ... PreventionChloroquinePlasmodium falciparum 7. Evidence of a Mild Mutator Phenotype in Cambodian Plasmodium falciparum Malaria ... MalariaMalaria--Environmental aspectsMalaria--EpidemiologyClimatic changesPlasmodium falciparumPlasmodium vivax 4. Dissecting ...
Patzewitz, Eva-Maria (2009) Glutathione metabolism of Plasmodium falciparum. PhD thesis, University of Glasgow. ... Plasmodium falciparum, glutathione, gamma-glutamylcysteine synthetase, glutathione synthetase, chloroquine resistance, ... Five different Plasmodium species can cause malaria in humans, leading to a total of approximately 500 million cases each year ... To address this question, the knockout of both genes encoding the enzymes of the GSH biosynthesis pathway in P. falciparum was ...
... how do Plasmodium falciparum and other forms of malaria find new hosts? and find homework help for other Plagues and Peoples ... "According to Plagues and People, how do Plasmodium falciparum and other forms of malaria find new hosts?" eNotes Editorial, 7 ... According to Plagues and People, how do Plasmodium falciparum and other forms of malaria find new hosts? ... www.enotes.com/homework-help/how-do-plasmodium-falciparum-other-forms-malaria-376584. Accessed 30 Nov. 2023. ...
The paradigm for heterochromatin function is the regulation of development and P. falciparum does use heterochromatin to ... The genome of the malaria parasite Plasmodium falciparum is maintained primarily as transcriptionally competent, euchromatin ... Chromatin structure and epigenetics in Plasmodium falciparum. Eucalyptus Seminar Room, Rm S205, Level 2, RN Robertson Building ... The genome of the malaria parasite Plasmodium falciparum is maintained primarily as transcriptionally competent, euchromatin ...
Abs that inhibit Plasmodium falciparum invasion of erythrocytes form an important component of human immunity against malaria, ... Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade ... Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and... ... Phenotypic variation by P. falciparum mediates the evasion of inhibitory Abs, contributing to the capacity of P. falciparum to ...
We evaluated the efficacy of a new combined Plasmodium falciparum-Plasmodim vivax immunochromatographic test (ICT Malaria Pf/Pv ... When P. falciparum parasitemia rates were , 500/microL, the sensitivity of the diagnosis was only 23.3%, with a positive ... The ICT Malaria Pf/Pv test was both sensitive (100.0%) and specific (99.7 %) for the diagnosis of falciparum malaria with ... A Suspected Case of Mixed Infection of Plasmodium vivax with Plasmodium falciparum: A Diagnostic Conundrum due to Pre- ...
Antimalarial Drug Trials on a Multiresistant Strain of Plasmodium Falciparum published on Nov 1963 by The American Society of ... failed to suppress mosquito-induced infections with a Thailand strain of Plasmodium falciparum. In one of the two cases ... The observations confirm and extend the reports of resistance of this strain of P. falciparum to normally suppressive or ...
  • malignant tertian malaria was caused by Laverania malariae (now P. falciparum), benign tertian malaria by Haemamoeba vivax (now P. vivax), and quartan malaria by Haemamoeba malariae (now P. malariae). (wikipedia.org)
  • Field evaluation of the ICT Malaria Pf/Pv immunochromatographic test for the detection of asymptomatic malaria in a Plasmodium falciparum/vivax endemic area in Thailand. (ajtmh.org)
  • We evaluated the efficacy of a new combined Plasmodium falciparum-Plasmodim vivax immunochromatographic test (ICT Malaria Pf/Pv) in a cross-sectional malaria survey of the village of Ban Kong Mong Tha, Kanchanaburi Provice, Thailand, from August to December 2000. (ajtmh.org)
  • darlingi were found infected with Plasmodium falciparum, Plasmodium vivax or Plasmodium malariae. (scielo.br)
  • Primaquine should be given if Plasmodium vivax or Plasmodium ovale is suspected after checking for the presence of glucose-6-phosphate dehydrogenase (G6PD) deficiency. (medscape.com)
  • Association of reduced glutathione levels with Plasmodium falciparum and Plasmodium vivax malaria: a systematic review and meta-analysis. (bvsalud.org)
  • Additionally, there was no significant difference in GSH levels between Plasmodium falciparum malaria and P. vivax malaria (P = 0.80, Hedges g 0.11, 95% CI - 0.76 to 0.98, I2 93.23%, three studies). (bvsalud.org)
  • AAH examined 35 608 blood films and diagnosed malaria in 4443 samples comprised of 2667 Plasmodium falciparum (Pf) and 1776 Plasmodium vivax (Pv). (who.int)
  • We found that Plasmodium falciparum infection prevalence in endemic Africa halved and the incidence of clinical disease fell by 40% between 2000 and 2015. (nih.gov)
  • Objectives: The overall aim was therefore, to elucidate the impact of S. mansoni infection on protective T helper immune responses on P. falciparum and S. mansoni co-infection. (scirp.org)
  • Methodology: This study evaluated the T helper immune responses in individuals with independent S. mansoni infection, independent P. falciparum infection, co-infection and non-infection in school attending children in a co-endemic area along Lake Victoria shores, Uganda. (scirp.org)
  • S. mansoni infection is a major contributor of a reduced effective T helper immune response against P. falciparum in P. falciparum and S. mansoni co-infection. (scirp.org)
  • A major part of virulence for Plasmodium falciparum malaria infection, the most lethal parasitic disease of humans, results from increased rigidity and adhesiveness of infected host red cells. (gla.ac.uk)
  • We investigate the variation of malaria cases, parasite density and the multiplicity of Plasmodium falciparum infection throughout the year in Brazzaville. (biomedcentral.com)
  • Infection with P. falciparum causes by far the highest morbidity of all human Plasmodium species. (biomedcentral.com)
  • Therefore, this systematic review and meta-analysis investigated the differences in GSH levels in relation to Plasmodium infection . (bvsalud.org)
  • Malaria is infection of red blood cells with one of five species of the protozoa Plasmodium . (msdmanuals.com)
  • Malaria is a potentially life-threatening disease caused by infection with Plasmodium protozoa transmitted by an infective female Anopheles mosquito. (medscape.com)
  • Plasmodium falciparum infection carries a poor prognosis with a high mortality if untreated, but it has an excellent prognosis if diagnosed early and treated appropriately. (medscape.com)
  • Although the preva- malaria and pregnant women are more like- lence and density of P. falciparum parasites ly to develop clinical attacks of malaria and are higher in pregnant women than in non- serious complications than non-pregnant pregnant women, most infections remain women of the same age. (who.int)
  • This work identifies Drosophila S2 cells as a clinically-relevant platform suited for the production of 'difficult-to-make' proteins from Plasmodium parasites, and identifies a PfRH5 sequence variant that can be used for clinical production of a non-glycosylated, soluble full-length protein vaccine immunogen. (nature.com)
  • Plasmodium falciparum parasites are the causative agent of the most severe form of human malaria, and the development of an effective vaccine remains a key strategic goal to aid the control, local elimination and eventual eradication of this disease. (nature.com)
  • Timecourses have been conducted to quantify the number and type of replicating nuclei, together with other cell-biological features, in P. falciparum parasites across the course of both erythrocytic schizogony and gametogenesis. (europa.eu)
  • Apicomplexan parasites of the genus Plasmodium are the causative agent of malaria, one of the most prevalent infectious diseases worldwide. (gla.ac.uk)
  • P. falciparum and S. mansoni infections initiate a T helper immune response [4] [5] , which links the innate and adaptive immune responses against the parasites. (scirp.org)
  • Human microRNAs translocate from host erythrocytes to Plasmodium falciparum parasites. (jove.com)
  • P. falciparum is transmitted by mosquitoes, so drugs that prevent the spread of the parasites into the mosquito host (transmission inhibitors) are considered essential for malaria control. (nagasaki-u.ac.jp)
  • We investigated the inhibitory effects of dihydroartemisinin (DHA), methoxyamino chalcone (C3), and iron chelators including deferiprone (DFP), 1-( N -acety1-6-aminohexyl)-3-hydroxy-2-methylpyridin-4-one (CM1) and deferiprone-resveratrol hybrid (DFP-RVT) against the growth of wild-type (WT) P. falciparum parasites and those with k13 and fd mutations. (biorxiv.org)
  • ART-resistant P. falciparum parasites emerged in Western Cambodia in the 2000s showing a slow clearance phenotype in malaria patients and an increased ring survival rate [ 2 , 3 ]. (biorxiv.org)
  • The cytoadherent properties of P. falciparum parasites may thus be a virulence factor in human falciparum malaria. (tropmedres.ac)
  • Intraerythrocytic sexual stages of human malaria parasites are essential for the transmission of Plasmodium falciparum from human host to mosquito. (biomedcentral.com)
  • In contrast to the 48-hour blood stage life cycle of asexual parasites, it takes 9-12 days for P. falciparum gametocytes to fully develop inside human red blood cells (RBCs). (biomedcentral.com)
  • Schistosoma mansoni is one of the causative agents of intestinal schistosomiasis and Plasmodium falciparum is the major causative agent of malaria. (scirp.org)
  • Background: Of the 5,484 predicted proteins of Plasmodium falciparum, the main causative agent of malaria, about 60\% do not have sufficient sequence similarity with proteins in other organisms to warrant provision of functional assignments. (cnrs.fr)
  • Three cases of uncomplicated Plasmodium falciparum malaria in Sokoto, Nigeria, between June and July 2006, apparently failed treatment with artesunate monotherapy. (scialert.net)
  • Artemisinin-based combination therapy (ACT) has been adopted by the World Health Organization as a first-line treatment for uncomplicated Plasmodium falciparum malaria. (biomedcentral.com)
  • Progressive increase in point mutations associated with chloroquine resistance in Plasmodium falciparum isolates from India. (cdc.gov)
  • Artemisinin resistance in Plasmodium falciparum malaria. (nature.com)
  • Hence, to enable our search for novel antimalarial drugs, we implemented and examined assay conditions and validated the PfLDH-based method in our laboratory using a reference set of standard antimalarial drugs with known activity against Plasmodium falciparum strains. (mmv.org)
  • Specifically, in people with antibodies to the merozoite proteins MSP-3 and MSP-119, the risk of developing P. falciparum malaria was reduced by 54% and 18%, respectively, compared to people without antibodies to these antigens. (sciencedaily.com)
  • This transgenic P. falciparum reporter line constantly expresses two reporter proteins, GFP and NanoLuc, at high levels in two different hosts, human and mosquito. (nagasaki-u.ac.jp)
  • By utilising the expression of these two reporter proteins, P. falciparum can be successfully visualised and quantified with high sensitivity. (nagasaki-u.ac.jp)
  • We have created a transgenic P. falciparum that expresses two reporter proteins, GFP and NanoLuc, at high levels in both the human- and the vector mosquito stage. (nagasaki-u.ac.jp)
  • We are targeting multiple proteins of P. falciparum which are found only on the surfaces of the sexual forms of the parasite and where antibodies against these proteins have been shown to block the progression of the parasite's life cycle in the mosquito and thus block transmission to the next human host. (ru.nl)
  • In Africa each year around 24 million wom- women have acquired substantial protec- en become pregnant in malaria-endemic ar- tive immunity to malaria through repeated eas. (who.int)
  • Schistosoma mansoni and Plasmodium falciparum are co-endemic in Uganda and are the leading parasitic causes of public health problems across sub-Saharan Africa. (scirp.org)
  • This study aims to analyse the impact that the use of ACT has had compared to two classic treatments (quinine sulfate and doxycycline/clindamycin or atovaquone-proguanil) to treat patients admitted with uncomplicated malaria from P. falciparum to a hospital in a non-endemic area. (biomedcentral.com)
  • In resistant clinical strains, increased PfPI3K was associated with the C580Y mutation in P. falciparum Kelch13 (PfKelch13), a primary marker of artemisinin resistance. (nature.com)
  • Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and. (edu.au)
  • Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade naturally acquired immunity. (edu.au)
  • Using this drug platform, we identified a new compound, OU0074008, which kills the asexual blood stages of P. falciparum from a library of 1920 compounds provided by Osaka University. (nagasaki-u.ac.jp)
  • Malaria symptoms such as fever and chills are caused by the multiplication of P. falciparum in human red blood cells (asexual blood stage). (nagasaki-u.ac.jp)
  • The life cycle of P. falciparum was recapitulated in the laboratory, and the expression of GFP was confirmed in the asexual blood-, gametocyte-, oocyst-, sporozoite- and liver stages (Fig. 2). (nagasaki-u.ac.jp)
  • Artemisinin and derivatives (ARTs) are sesquiterpene lactones with an endoperoxide bridge that can quickly and effectively kill the Plasmodium parasite during the pathogenic asexual blood stage. (elifesciences.org)
  • Here the lipid profiles of red blood cells infected with the five different sexual stages of Plasmodium falciparum were analysed by mass spectrometry and compared to those from uninfected and asexual trophozoite infected erythrocytes. (biomedcentral.com)
  • Nearly all malarial deaths are caused by P. falciparum, and 95% of such cases occur in Africa. (wikipedia.org)
  • In Sub-Saharan Africa, almost 100% of cases were due to P. falciparum, whereas in most other malarial countries, other, less virulent plasmodial species predominate. (wikipedia.org)
  • The mosquito-borne malaria parasite Plasmodium falciparum kills an estimated 0.7-2.7 million people every year, primarily children in sub-Saharan Africa. (jcvi.org)
  • Information regarding treatment of P. falciparum malaria is available from the Malaria Branch, Division of Parasitic Diseases, Center for Infectious Diseases, CDC, telephone (404) 488-4046. (cdc.gov)
  • Microscope slide showing the parasitic protozoan Plasmodium falciparum in human blood. (boreal.com)
  • Thus, P. falciparum has a very sophisticated parasitic strategy for infecting two hosts, humans and mosquitoes (Fig.1). (nagasaki-u.ac.jp)
  • Molecular surveillance of mutations in dihydrofolate reductase and dihydropteroate synthase genes of Plasmodium falciparum in Ethiopia. (cdc.gov)
  • Moreover, amplification of the P . falciparum GTP cyclohydrolase 1 ( pfgch1 ) GCN is linked to upregulation of the Plasmodium falciparum dihydrofolate reductase ( pfdhfr ) and P . falciparum dihydropteroate synthase ( pfdhps ) genes, which are associated with sulfadoxine-pyrimethamine resistance in Southeast Asia [ 9 , 10 ]. (researchsquare.com)
  • To address this question, the knockout of both genes encoding the enzymes of the GSH biosynthesis pathway in P. falciparum was attempted. (gla.ac.uk)
  • We evaluated the invasion-inhibitory activity of acquired Abs from malaria-exposed children and adults from Kenya, using P. falciparum with disruption of genes encoding EBA140, EBA175, and EBA181, either individually or combined as EBA140/EBA175 or EBA175/EBA181 double knockouts. (edu.au)
  • Copy number variations (CNVs) of the Plasmodium falciparum multidrug resistance 1 ( pfmdr1 ), P. falciparum pfplasmepsin2 ( pfplasmepsin2 ) and P. falciparum GTP cyclohydrolase 1 ( pfgch1 ) genes are associated with antimalarial drug resistance in P. falciparum malaria. (researchsquare.com)
  • The aim of the present study was to develop and validate ddPCR assays for detection of the CNVs of P. falciparum genes associated with resistance to antimalarial drugs. (researchsquare.com)
  • The developed ddPCR assays are simple, accurate, precise and cost-effective tools for detection of the CNVs in the pfmdr1 , pfplasmepsin2 and pfgch1 genes of P. falciparum . (researchsquare.com)
  • Method: We present PlasmoDraft, a database of Gene Ontology (GO) annotation predictions for P. falciparum genes based on postgenomic data. (cnrs.fr)
  • Results: Gonna has been applied to all P. falciparum genes using most publicly available transcriptome, proteome and interactome data sources. (cnrs.fr)
  • To identify the biochemical basis for this effect, we disrupted the plasmodium arginase gene in the rodent malaria model P. berghei. (nih.gov)
  • Molecular surveillance is needed not only for the detection of mutations to the P . falciparum kelch gene, which are associated with artemisinin resistance [ 3 ], but also molecular markers associated with the efficacy of other antimalarial drugs. (researchsquare.com)
  • Regulation of gene expression in Plasmodium falciparum (Pf) remains poorly understood. (biomedcentral.com)
  • Active constituents showed differentiated activity towards Giardia lamblia, Trypanosoma cruzi, several Leishmania strains, Plasmodium falciparum and cytotoxicity against HeLa cells. (lu.se)
  • Plasmodium falciparum is a unicellular protozoan parasite of humans, and the deadliest species of Plasmodium that causes malaria in humans. (wikipedia.org)
  • P. falciparum is therefore regarded as the deadliest parasite in humans. (wikipedia.org)
  • Around the same time, Grassi demonstrated that P. falciparum was transmitted in humans only by female anopheline mosquito (in his case Anopheles claviger). (wikipedia.org)
  • Five different Plasmodium species can cause malaria in humans, leading to a total of approximately 500 million cases each year and of these, P. falciparum causes the most deadly form of the disease and is responsible for more than 1 million deaths annually. (gla.ac.uk)
  • Thus, by behaving differently in mosquitos and in humans, plasmodia are able to find new hosts. (enotes.com)
  • An increase in the P . falciparum multidrug resistance 1 ( pfmdr1 ) GCN is associated with mefloquine resistance [ 6 ], while an increase in the P . falciparum plasmepsin2 ( pfplasmepsin2 ) GCN is associated with piperaquine resistance [ 7 , 8 ]. (researchsquare.com)
  • Clinical correlates of in vitro Plasmodium falciparum cytoadherence. (tropmedres.ac)
  • To determine whether isolates of Plasmodium falciparum have intrinsically different cytoadherent properties and whether these differences contribute to the clinical severity of human falciparum malaria, we studied the cytoadherence to C32 melanoma cells in vitro of 59 parasite isolates from patients with naturally acquired infections in Thailand. (tropmedres.ac)
  • Quantitative assessment of the interactions and activity of combinations of antimalarial agents in continuous in vitro culture of Plasmodium falciparum / by Wilbur K. Milhous. (who.int)
  • Studies on resistance to chloroquine by Plasmodium falciparum with potential application to the development of a modified in vitro susceptibility test / by Michael Davis Rogers. (who.int)
  • Fig.2 GFP expression in P. falciparum in the multiple stages of the life cycle. (nagasaki-u.ac.jp)
  • In this study, we bridge this disconnect by measuring genome-wide translation using ribosome profiling, through five stages of the P. falciparum blood phase developmental cycle. (datadryad.org)
  • Protein tyrosine kinase activity was found to be distributed in all the stages of P. falciparum parasite maturation. (niscair.res.in)
  • CDC has recently reviewed data on the reported incidence in the United States of Plasmodium falciparum malaria and has evaluated information on the effective management of severe life-threatening infections. (cdc.gov)
  • New research synthesizes information from many different studies that attempt to link specific antibody responses to Plasmodium falciparum with protection from clinical malaria and comes to important conclusions about which antigens might be worth advancing as vaccine candidates. (sciencedaily.com)
  • This knowledge will help to advance malaria vaccine development and suggests that multiple invasion ligands need to be targeted to overcome the capacity of P. falciparum for immune evasion. (edu.au)
  • To evaluate the six-dose regimen of artemether-lumefantrine for treating uncomplicated falciparum malaria. (bvsalud.org)
  • A protein interaction network of the malaria parasite Plasmodium falciparum. (nih.gov)
  • The Plasmodium falciparum reticulocyte-binding protein homolog 5 (PfRH5) has recently emerged as a leading candidate antigen against the blood-stage human malaria parasite. (nature.com)
  • In this study, we genetically modified P. falciparum to simultaneously express GFP, a fluorescent protein, and NanoLuc, a luciferase. (nagasaki-u.ac.jp)
  • Resistance of Plasmodium falciparum to artemisinin, which has become a threat to malaria control, has been linked to mutations in the parasite protein K13. (elifesciences.org)
  • Epidemiology and control of Falciparum malaria in the Americas. (who.int)
  • It aims to transform our understanding of the basic biology of Plasmodium, and of how that biology affects virulence. (europa.eu)
  • The parasite is transmitted through the bite of a female Anopheles mosquito and causes the disease's most dangerous form, falciparum malaria. (wikipedia.org)
  • 8 kms] of the patient's residence) during the preceding month were identified, and although Anopheles mosquitoes were present near the patient's home, none of the 21 Anopheles mosquitoes tested at CDC was positive for P. falciparum . (cdc.gov)
  • ACT treatment of admitted hospital patients with imported uncomplicated malaria from P. falciparum reduced the days spent hospitalized as well as producing a more rapid parasite clearance compared to classic treatment. (biomedcentral.com)
  • The cytokines tumor necrosis factor, interleukin-1, and gamma interferon, which have been implicated in the pathogenesis of cerebral malaria and are known to promote intercellular adhesion in other systems, did not enhance the cytoadherence of P. falciparum isolates to C32 melanoma cells. (tropmedres.ac)
  • Severity of Plasmodium falciparum malaria is strongly correlated to the ABO blood group of the patient. (lu.se)
  • Genome sequence of the human malaria parasite Plasmodium falciparum. (nih.gov)
  • To stimulate basic research and facilitate the development of new drugs and vaccines, the genome of Plasmodium falciparum clone 3D7 has been sequenced using a chromosome-by-chromosome shotgun strategy. (jcvi.org)
  • These chromosomes represent about 35% of the 23-megabase P. falciparum genome. (jcvi.org)
  • Among many, the Plasmodium falciparum lactate dehydrogenase (PfLDH) assay has acceptable demand on equipment, labour, technical skills and affordability and offers a good opportunity for scientists in low- and middle-income countries to participate in the global effort of discovering future antimalarial drugs. (mmv.org)
  • The spread of artemisinin (ART)-resistant Plasmodium falciparum threatens the control of malaria and mutations in the propeller domains of P. falciparum Kelch13 ( k13 ) are strongly associated with the resistance. (biorxiv.org)
  • Abs that inhibit Plasmodium falciparum invasion of erythrocytes form an important component of human immunity against malaria, but key target Ags are largely unknown. (edu.au)
  • Here, the techniques used to transfect synthetic microRNAs into host erythrocytes and isolate all RNAs from P. falciparum are described. (jove.com)
  • Plasmodium falciparum in G6PD normal and G6PD-deficient erythrocytes : the parasite cycle and adaptive phenomena / by Esien Archibong Usanga. (who.int)
  • As a result of this review, CDC has concluded that the drug of choice in the United States for treatment of complicated P. falciparum infections is parenteral quinidine gluconate. (cdc.gov)
  • Weekly doses of amodiaquine (0.3 g) and pyrimethamine (0.05 g) failed to suppress mosquito-induced infections with a Thailand strain of Plasmodium falciparum . (ajtmh.org)
  • Results: We observed an up regulated Th1 T helper subpopulation in independent P. falciparum infections compared to the uninfected group. (scirp.org)
  • Phenotypic variation by P. falciparum mediates the evasion of inhibitory Abs, contributing to the capacity of P. falciparum to cause repeat and chronic infections. (edu.au)
  • Artemisinin (ART)-based combination therapy is recommended by the World Health Organization for the first-line treatment of malaria in uncomplicated Plasmodium falciparum infections. (biorxiv.org)
  • This study has generated a new genetically modified Plasmodium falciparum reporter line that could contribute to developing new anti-malarial drugs. (nagasaki-u.ac.jp)
  • This study suggests that a drug discovery platform using P. falciparum expressing NanoLuc will greatly advance the development of anti-malarial drugs. (nagasaki-u.ac.jp)
  • Fig.1 The whole life cycle of P. falciparum and desired anti-malarial drugs. (nagasaki-u.ac.jp)
  • The plasmodium stays in the mosquito's stomach and does not do anything that harms the mosquito. (enotes.com)
  • When it does this, the person becomes very sick, but the plasmodia are moving freely in the blood stream and can easily be sucked up by a mosquito and transferred to a new host. (enotes.com)
  • Plasmodium falciparum is transmitted to a new host after completing its sexual cycle within a mosquito. (ru.nl)
  • Numerous studies have been performed on human antibody responses to P. falciparum merozoite antigens, but they have given conflicting results. (sciencedaily.com)
  • Remarkably little is known about Plasmodium cell cycles, despite a wealth of knowledge on the subject in human cells. (europa.eu)
  • This project will reveal, with unprecedented resolution, how DNA replication is organised in Plasmodium and how it can be affected by changing conditions in the human host and exposure to antimalarial drugs. (europa.eu)
  • In this study, we used novel approaches to determine the importance of P. falciparum erythrocyte-binding Ags (EBAs), which are important invasion ligands, as targets of human invasion-inhibitory Abs and define their role in contributing to immune evasion through variation in function. (edu.au)
  • Plasmodium falciparum infects two types of hosts, human and vector mosquitoes. (nagasaki-u.ac.jp)
  • Several antibody-based rapid diagnostic tests (RDTs) are available for diagnosing malaria, but they cover only four of the five species that cause human malaria (all except Plasmodium knowlesi ). (medscape.com)
  • On August 9, a thin blood smear obtained at the time of admission was reported to show Plasmodium falciparum malaria with 3.2% parasitemia. (cdc.gov)
  • In the P. falciparum field samples, pfmdr1 and pfplasmepsin2 GCNs were amplified in 15% and 27% of samples from Ubon Ratchathani, Thailand, while pfgch1 GCN was amplified in 50% of samples from Yala, Thailand. (researchsquare.com)
  • The characterization of the transcriptome and proteome of Plasmodium falciparum has been a tremendous resource for the understanding of the molecular physiology of this parasite. (datadryad.org)
  • Artemisinin-based combination therapies (ACTs) are recommended as front-line treatments for Plasmodium falciparum malaria, which remains an important infectious disease in tropical regions. (researchsquare.com)
  • The prolonged duration of gametocyte maturation is a unique feature of only a few Plasmodium species infecting higher primates ( P. falciparum and P. reichenowi ) [ 1 , 2 ]. (biomedcentral.com)