DNA Probes
Nucleic Acid Hybridization
Molecular Probes
Oligonucleotide Probes
Base Sequence
DNA Probes, HLA
Digoxigenin
In Situ Hybridization, Fluorescence
Molecular Sequence Data
Blotting, Southern
Molecular Probe Techniques
Cloning, Molecular
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
DNA
Evaluation Studies as Topic
RNA Probes
Fluorescent Dyes
Species Specificity
Biotin
Sensitivity and Specificity
Heartwater Disease
Chromosome Mapping
Nucleic Acid Probes
DNA Restriction Enzymes
Chromosome Banding
Escherichia coli
Restriction Mapping
X Chromosome
Sequence Homology, Nucleic Acid
Amino Acid Sequence
Ehrlichia ruminantium
Genes
RNA, Messenger
Plasmids
In Situ Hybridization
Y Chromosome
RNA, Bacterial
Luminescent Measurements
Repetitive Sequences, Nucleic Acid
Genetic Markers
Shiga Toxin 1
Electrophoresis, Agar Gel
DNA, Recombinant
Reagent Kits, Diagnostic
Chromosome Aberrations
Oligonucleotides
Bacterial Toxins
Transcription, Genetic
RNA, Ribosomal, 16S
Sex Chromosome Aberrations
Genetic Linkage
DNA, Ribosomal
RNA, Ribosomal
Diarrhea
Oligonucleotide Array Sequence Analysis
DNA Primers
Chromosomes, Human, Pair 1
DNA, Satellite
Cytotoxins
Interphase
Sequence Analysis, DNA
Aneuploidy
Carbocyanines
Bacterial Typing Techniques
Campylobacter
Peptide Nucleic Acids
Feces
Mycobacterium avium Complex
Hybrid Cells
Biosensing Techniques
Colorimetry
DNA Fingerprinting
Deoxyribonucleases, Type II Site-Specific
Translocation, Genetic
Gene Amplification
Porphyromonas endodontalis
Nontuberculous Mycobacteria
Cattle
Bacteroides
Smegma
Serotyping
Deoxyribonuclease EcoRI
Fluorescence
Mycobacterium
Pedigree
Aneugens
Oligodeoxyribonucleotides
Water Microbiology
RNA
Chromosomes, Human
Blotting, Northern
Genomic Library
Chromosomes, Human, Pair 7
Enterotoxins
Chromosomes
Nucleic Acid Amplification Techniques
Bacteria
Mycobacterium avium
Cosmids
Streptavidin
Centromere
Gene Library
Collodion
Avidin
Environmental Microbiology
Gonorrhea
Europium
Cytogenetics
Deoxyribonuclease BamHI
Telomeric repeats on small polydisperse circular DNA (spcDNA) and genomic instability. (1/5773)
Small polydisperse circular DNA (spcDNA) is a heterogeneous population of extrachromosomal circular molecules present in a large variety of eukaryotic cells. Elevated amounts of total spcDNA are related to endogenous and induced genomic instability in rodent and human cells. We suggested spcDNA as a novel marker for genomic instability, and speculated that spcDNA might serve as a mutator. In this study, we examine the presence of telomeric sequences on spcDNA. We report for the first time the appearance of telomeric repeats in spcDNA molecules (tel-spcDNA) in rodent and human cells. Restriction enzyme analysis indicates that tel-spcDNA molecules harbor mostly, if not exclusively, telomeric repeats. In rodent cells, tel-spcDNA levels are higher in transformed than in normal cells and are enhanced by treatment with carcinogen. Tel-spcDNA is also detected in some human tumors and cell lines, but not in others. We suggest, that its levels in human cells may be primarily related to the amount of the chromosomal telomeric sequences. Tel-spcDNA may serve as a unique mutator, through specific mechanisms related to the telomeric repeats, which distinguish it from the total heterogeneous spcDNA population. It may affect telomere dynamics and genomic instability by clastogenic events, alterations of telomere size and sequestration of telomeric proteins. (+info)Polynucleotide probes that target a hypervariable region of 16S rRNA genes to identify bacterial isolates corresponding to bands of community fingerprints. (2/5773)
Temperature gradient gel electrophoresis (TGGE) is well suited for fingerprinting bacterial communities by separating PCR-amplified fragments of 16S rRNA genes (16S ribosomal DNA [rDNA]). A strategy was developed and was generally applicable for linking 16S rDNA from community fingerprints to pure culture isolates from the same habitat. For this, digoxigenin-labeled polynucleotide probes were generated by PCR, using bands excised from TGGE community fingerprints as a template, and applied in hybridizations with dot blotted 16S rDNA amplified from bacterial isolates. Within 16S rDNA, the hypervariable V6 region, corresponding to positions 984 to 1047 (Escherichia coli 16S rDNA sequence), which is a subset of the region used for TGGE (positions 968 to 1401), best met the criteria of high phylogenetic variability, required for sufficient probe specificity, and closely flanking conserved priming sites for amplification. Removal of flanking conserved bases was necessary to enable the differentiation of closely related species. This was achieved by 5' exonuclease digestion, terminated by phosphorothioate bonds which were synthesized into the primers. The remaining complementary strand was removed by single-strand-specific digestion. Standard hybridization with truncated probes allowed differentiation of bacteria which differed by only two bases within the probe target site and 1.2% within the complete 16S rDNA. However, a truncated probe, derived from an excised TGGE band of a rhizosphere community, hybridized with three phylogenetically related isolates with identical V6 sequences. Only one of the isolates comigrated with the excised band in TGGE, which was shown to be due to identical sequences, demonstrating the utility of a combined TGGE and V6 probe approach. (+info)The role of interleukin 12 in the development of atherosclerosis in ApoE-deficient mice. (3/5773)
The cytokine profile of atherosclerotic aortas from apoE-deficient mice was assessed by reverse transcriptase-polymerase chain reaction. The results clearly showed that the expression of mRNA for IL-12p40 was evident in aortas from 3-month-old apoE-deficient mice. The mRNA for IL-10 was detected in aorta from these mice at the age of 6 months, indicating that expression of IL-12 is earlier than that of IL-10 in these animals. Concurrent with IL-12p40, the mRNA for the T-cell cytokine IFN-gamma, but not IL-4, was detected in aortas of mice at young and old ages. Both in situ hybridization and immunostaining further demonstrated the localization of IL-12 in macrophages of atherosclerotic lesions. Immunohistochemistry also demonstrated the expression of costimulatory molecules B7-1 and B7-2 in macrophages, suggesting that activation of T lymphocytes by macrophages may occur via surface antigens in lesions. When the immunoglobulin isotype of the antioxidized LDL antibodies in sera of apoE-deficient mice was determined, it revealed that both IgM and IgG were present. Furthermore, IgG2a is predominant and comprises approximately 50% of the antioxidized LDL IgG in sera from young mice (3 months), but decreased to lower levels (35%) in older mice (6 months). Daily administration of IL-12 led to an increase in serum levels of antioxidized LDL antibodies and accelerated atherosclerosis in young apoE-deficient mice compared with control mice injected with PBS alone. Taken together, these data suggest that IL-12 plays an active role in regulating the immune response during the early phase of atherosclerosis in apoE-deficient mice. (+info)Species identification and strain differentiation of dermatophyte fungi by analysis of ribosomal-DNA intergenic spacer regions. (4/5773)
Restriction fragment length polymorphisms (RFLPs) identified in the ribosomal-DNA (rDNA) repeat were used for molecular strain differentiation of the dermatophyte fungus Trichophyton rubrum. The polymorphisms were detected by hybridization of EcoRI-digested T. rubrum genomic DNAs with a probe amplified from the small-subunit (18S) rDNA and adjacent internal transcribed spacer (ITS) regions. The rDNA RFLPs mapped to the nontranscribed spacer (NTS) region of the rDNA repeat and appeared similar to those caused by short repetitive sequences in the intergenic spacers of other fungi. Fourteen individual RFLP patterns (DNA types A to N) were recognized among 50 random clinical isolates of T. rubrum. A majority of strains (19 of 50 [38%]) were characterized by one RFLP pattern (DNA type A), and four types (DNA types A to D) accounted for 78% (39 of 50) of all strains. The remaining types (DNA types E to N) were represented by one or two isolates only. A rapid and simple method was also developed for molecular species identification of dermatophyte fungi. The contiguous ITS and 5.8S rDNA regions were amplified from 17 common dermatophyte species by using the universal primers ITS 1 and ITS 4. Digestion of the amplified ITS products with the restriction endonuclease MvaI produced unique and easily identifiable fragment patterns for a majority of species. However, some closely related taxon pairs, such as T. rubrum-T. soudanense and T. quinkeanum-T. schoenlenii could not be distinguished. We conclude that RFLP analysis of the NTS and ITS intergenic regions of the rDNA repeat is a valuable technique both for molecular strain differentiation of T. rubrum and for species identification of common dermatophyte fungi. (+info)Identification of Mycobacterium kansasii by using a DNA probe (AccuProbe) and molecular techniques. (5/5773)
The newly formulated Mycobacterium kansasii AccuProbe was evaluated, and the results obtained with the new version were compared to the results obtained with the old version of this test by using 116 M. kansasii strains, 1 Mycobacterium gastri strain, and 19 strains of several mycobacterial species. The sensitivity of this new formulation was 97.4% and the specificity was 100%. Still, three M. kansasii strains were missed by this probe. To evaluate the variability within the species, genetic analyses of the hsp65 gene, the spacer sequence between the 16S and 23S rRNA genes, and the 16S rRNA gene of several M. kansasii AccuProbe-positive strains as well as all AccuProbe-negative strains were performed. Genetic analyses of the one M. gastri strain from the comparative assay and of two further M. gastri strains were included because of the identity of the 16S rRNA gene in M. gastri to that in M. kansasii. The data confirmed the genetic heterogeneity of M. kansasii. Furthermore, a subspecies with an unpublished hsp65 restriction pattern and spacer sequence was described. The genetic data indicate that all M. kansasii strains missed by the AccuProbe test belong to one subspecies, the newly described subspecies VI, as determined by the hsp65 restriction pattern and the spacer sequence. Since the M. kansasii strains that are missed are rare and all M. gastri strains are correctly negative, the new formulated AccuProbe provides a useful tool for the identification of M. kansasii. (+info)Development and characterization of complex DNA fingerprinting probes for the infectious yeast Candida dubliniensis. (6/5773)
Using a strategy to clone large genomic sequences containing repetitive elements from the infectious yeast Candida dubliniensis, the three unrelated sequences Cd1, Cd24, and Cd25, with respective molecular sizes of 15,500, 10,000, and 16,000 bp, were cloned and analyzed for their efficacy as DNA fingerprinting probes. Each generated a complex Southern blot hybridization pattern with endonuclease-digested genomic DNA. Cd1 generated an extremely variable pattern that contained all of the bands of the pattern generated by the repeat element RPS of Candida albicans. We demonstrated that Cd1 does not contain RPS but does contain a repeat element associated with RPS throughout the C. dubliniensis genome. The Cd1 pattern was the least stable over time both in vitro and in vivo and for that reason proved most effective in assessing microevolution. Cd24, which did not exhibit microevolution in vitro, was highly variable in vivo, suggesting in vivo-dependent microevolution. Cd25 was deemed the best probe for broad epidemiological studies, since it was the most stable over time, was the only truly C. dubliniensis-specific probe of the three, generated the most complex pattern, was distributed throughout all C. dubliniensis chromosomes, and separated a worldwide collection of 57 C. dubliniensis isolates into two distinct groups. The presence of a species-specific repetitive element in Cd25 adds weight to the already substantial evidence that C. dubliniensis represents a bona fide species. (+info)Molecular evidence for the existence of additional members of the order Chlamydiales. (7/5773)
Respiratory tract infections in man may be caused by several members of the genus Chlamydia and also by two Chlamydia-like strains, 'Simkania negevensis' (Z-agent) and 'Parachlamydia acanthamoebae' (Bng). To facilitate diagnostic procedures a PCR assay able to detect all known Chlamydiaceae sequences in one reaction was developed. For this purpose, primers were selected to amplify a fragment of the 16S rRNA gene. Characterization of the amplified fragments was done by hybridization with specific probes and by sequencing. PCR assays were carried out using DNA isolated from nose/throat specimens or from peripheral blood mononuclear cells of patients with respiratory tract infections, and from vessel wall specimens of abdominal aneurysms. Six of the 42 nose/throat swab specimens analysed yielded strong bands and one yielded a faint band. Three of these bands were identified as Chlamydia pneumoniae and one as Chlamydia trachomatis by sequencing. Analysis of the three other bands yielded two different new sequences. DNA isolated from peripheral blood mononuclear cells of one patient yielded a third new sequence. DNA isolated from peripheral blood mononuclear cells of four healthy controls was negative. One of the abdominal aneurysm specimens also yielded a strong band. Sequencing revealed a fourth new sequence. All negative controls included during specimen processing and PCR analysis remained negative. The typical secondary structure of microbial 16S genes was present in all four new sequences indicating the validity of the sequence data. All four new sequences were distinct from other bacteria and clustered together with known Chlamydiaceae sequences. Phylogenetic analysis suggested a new lineage, separating the four new sequences, 'S. negevensis' and 'P. acanthamoebae' from the genus Chlamydia with the four known chlamydial species. In conclusion, this study provides evidence for the existence of several new members of the order Chlamydiales. Since the source of the Chlamydia-like strains has not been identified and serological and/or molecular cross-reactivities may be expected, results of identification of infecting recognized organisms should be interpreted cautiously. (+info)Preimplantation diagnosis by fluorescence in situ hybridization using 13-, 16-, 18-, 21-, 22-, X-, and Y-chromosome probes. (8/5773)
PURPOSE: Our purpose was to select the proper chromosomes for preimplantation diagnosis based on aneuploidy distribution in abortuses and to carry out a feasibility study of preimplantation diagnosis for embryos using multiple-probe fluorescence in situ hybridization (FISH) on the selected chromosomes of biopsied blastomeres. METHODS: After determining the frequency distribution of aneuploidy found in abortuses, seven chromosomes were selected for FISH probes. Blastomeres were obtained from 33 abnormal or excess embryos. The chromosome complements of both the biopsied blastomeres and the remaining sibling blastomeres in each embryo were determined by FISH and compared to evaluate their preimplantation diagnostic potential. RESULTS: Chromosomes (16, 22, X, Y) and (13, 18, 21) were selected on the basis of the high aneuploid prevalence in abortuses for the former group and the presence of trisomy in the newborn for the latter. Thirty-six (72%) of 50 blastomeres gave signals to permit a diagnosis. Diagnoses made from biopsied blastomeres were consistent with the diagnoses made from the remaining sibling blastomeres in 18 embryos. In only 2 of 20 cases did the biopsied blastomere diagnosis and the embryo diagnosis not match. CONCLUSIONS: If FISH of biopsied blastomere was successful, a preimplantation diagnosis could be made with 10% error. When a combination of chromosome-13, -16, -18, -21, -22, -X, and -Y probes was used, up to 65% of the embryos destined to be aborted could be detected. (+info)The disease is characterized by fever, loss of appetite, weight loss, and swelling of the legs, neck, and head. It can progress to renal failure, anemia, and heart failure, leading to death within a few weeks. Diagnosis is based on clinical signs, laboratory tests, and observation of tick infestation.
Treatment is largely supportive and includes antibiotics to prevent secondary bacterial infections, fluid therapy, and restoration of electrolyte balance. Prevention involves controlling ticks and using acaricides, as well as vaccination with live or inactivated Cowdria vaccines.
In the medical field, Heartwater disease is a significant economic and public health concern in many parts of the world due to its high mortality rate and potential for transmission to humans through tick bites. It is important for veterinarians and physicians to be aware of this disease and take appropriate measures to prevent and control it.
There are several types of chromosome aberrations, including:
1. Chromosomal deletions: Loss of a portion of a chromosome.
2. Chromosomal duplications: Extra copies of a chromosome or a portion of a chromosome.
3. Chromosomal translocations: A change in the position of a chromosome or a portion of a chromosome.
4. Chromosomal inversions: A reversal of a segment of a chromosome.
5. Chromosomal amplifications: An increase in the number of copies of a particular chromosome or gene.
Chromosome aberrations can be detected through various techniques, such as karyotyping, fluorescence in situ hybridization (FISH), or array comparative genomic hybridization (aCGH). These tests can help identify changes in the chromosomal makeup of cells and provide information about the underlying genetic causes of disease.
Chromosome aberrations are associated with a wide range of diseases, including:
1. Cancer: Chromosome abnormalities are common in cancer cells and can contribute to the development and progression of cancer.
2. Birth defects: Many birth defects are caused by chromosome abnormalities, such as Down syndrome (trisomy 21), which is caused by an extra copy of chromosome 21.
3. Neurological disorders: Chromosome aberrations have been linked to various neurological disorders, including autism and intellectual disability.
4. Immunodeficiency diseases: Some immunodeficiency diseases, such as X-linked severe combined immunodeficiency (SCID), are caused by chromosome abnormalities.
5. Infectious diseases: Chromosome aberrations can increase the risk of infection with certain viruses, such as human immunodeficiency virus (HIV).
6. Ageing: Chromosome aberrations have been linked to the ageing process and may contribute to the development of age-related diseases.
7. Radiation exposure: Exposure to radiation can cause chromosome abnormalities, which can increase the risk of cancer and other diseases.
8. Genetic disorders: Many genetic disorders are caused by chromosome aberrations, such as Turner syndrome (45,X), which is caused by a missing X chromosome.
9. Rare diseases: Chromosome aberrations can cause rare diseases, such as Klinefelter syndrome (47,XXY), which is caused by an extra copy of the X chromosome.
10. Infertility: Chromosome abnormalities can contribute to infertility in both men and women.
Understanding the causes and consequences of chromosome aberrations is important for developing effective treatments and improving human health.
Some common effects of chromosomal deletions include:
1. Genetic disorders: Chromosomal deletions can lead to a variety of genetic disorders, such as Down syndrome, which is caused by a deletion of a portion of chromosome 21. Other examples include Prader-Willi syndrome (deletion of chromosome 15), and Williams syndrome (deletion of chromosome 7).
2. Birth defects: Chromosomal deletions can increase the risk of birth defects, such as heart defects, cleft palate, and limb abnormalities.
3. Developmental delays: Children with chromosomal deletions may experience developmental delays, learning disabilities, and intellectual disability.
4. Increased cancer risk: Some chromosomal deletions can increase the risk of developing certain types of cancer, such as chronic myelogenous leukemia (CML) and breast cancer.
5. Reproductive problems: Chromosomal deletions can lead to reproductive problems, such as infertility or recurrent miscarriage.
Chromosomal deletions can be diagnosed through a variety of techniques, including karyotyping (examination of the chromosomes), fluorescence in situ hybridization (FISH), and microarray analysis. Treatment options for chromosomal deletions depend on the specific effects of the deletion and may include medication, surgery, or other forms of therapy.
Types of Sex Chromosome Aberrations:
1. Turner Syndrome: A condition where a female has only one X chromosome instead of two (45,X).
2. Klinefelter Syndrome: A condition where a male has an extra X chromosome (47,XXY) or an extra Y chromosome (47,XYYY).
3. XXX Syndrome: A rare condition where a female has three X chromosomes instead of two.
4. XYY Syndrome: A rare condition where a male has an extra Y chromosome (48,XYY).
5. Mosaicism: A condition where a person has a mixture of cells with different numbers of sex chromosomes.
Effects of Sex Chromosome Aberrations:
Sex chromosome aberrations can cause a range of physical and developmental abnormalities, such as short stature, infertility, and reproductive problems. They may also increase the risk of certain health conditions, including:
1. Congenital heart defects
2. Cognitive impairments
3. Learning disabilities
4. Developmental delays
5. Increased risk of infections and autoimmune disorders
Diagnosis of Sex Chromosome Aberrations:
Sex chromosome aberrations can be diagnosed through various methods, including:
1. Karyotyping: A test that involves analyzing the number and structure of an individual's chromosomes.
2. Fluorescence in situ hybridization (FISH): A test that uses fluorescent probes to detect specific DNA sequences on chromosomes.
3. Chromosomal microarray analysis: A test that looks for changes in the number or structure of chromosomes by analyzing DNA from blood or other tissues.
4. Next-generation sequencing (NGS): A test that analyzes an individual's entire genome to identify specific genetic variations, including sex chromosome aberrations.
Treatment and Management of Sex Chromosome Aberrations:
There is no cure for sex chromosome aberrations, but there are various treatments and management options available to help alleviate symptoms and improve quality of life. These may include:
1. Hormone replacement therapy (HRT): To address hormonal imbalances and related symptoms.
2. Assisted reproductive technologies (ART): Such as in vitro fertilization (IVF) or preimplantation genetic diagnosis (PGD), to help individuals with infertility or pregnancy complications.
3. Prenatal testing: To identify sex chromosome aberrations in fetuses, allowing parents to make informed decisions about their pregnancies.
4. Counseling and support: To help individuals and families cope with the emotional and psychological impact of a sex chromosome abnormality diagnosis.
5. Surgeries or other medical interventions: To address related health issues, such as infertility, reproductive tract abnormalities, or genital ambiguity.
It's important to note that each individual with a sex chromosome aberration may require a unique treatment plan tailored to their specific needs and circumstances. A healthcare provider can work with the individual and their family to develop a personalized plan that takes into account their medical, emotional, and social considerations.
In conclusion, sex chromosome aberrations are rare genetic disorders that can have significant implications for an individual's physical, emotional, and social well-being. While there is no cure for these conditions, advances in diagnostic testing and treatment options offer hope for improving the lives of those affected. With proper medical care, support, and understanding, individuals with sex chromosome aberrations can lead fulfilling lives.
There are several types of diarrhea, including:
1. Acute diarrhea: This type of diarrhea is short-term and usually resolves on its own within a few days. It can be caused by a viral or bacterial infection, food poisoning, or medication side effects.
2. Chronic diarrhea: This type of diarrhea persists for more than 4 weeks and can be caused by a variety of conditions, such as irritable bowel syndrome (IBS), inflammatory bowel disease (IBD), or celiac disease.
3. Diarrhea-predominant IBS: This type of diarrhea is characterized by frequent, loose stools and abdominal pain or discomfort. It can be caused by a variety of factors, including stress, hormonal changes, and certain foods.
4. Infectious diarrhea: This type of diarrhea is caused by a bacterial, viral, or parasitic infection and can be spread through contaminated food and water, close contact with an infected person, or by consuming contaminated food.
Symptoms of diarrhea may include:
* Frequent, loose, and watery stools
* Abdominal cramps and pain
* Bloating and gas
* Nausea and vomiting
* Fever and chills
* Headache
* Fatigue and weakness
Diagnosis of diarrhea is typically made through a physical examination, medical history, and laboratory tests to rule out other potential causes of the symptoms. Treatment for diarrhea depends on the underlying cause and may include antibiotics, anti-diarrheal medications, fluid replacement, and dietary changes. In severe cases, hospitalization may be necessary to monitor and treat any complications.
Prevention of diarrhea includes:
* Practicing good hygiene, such as washing hands frequently and thoroughly, especially after using the bathroom or before preparing food
* Avoiding close contact with people who are sick
* Properly storing and cooking food to prevent contamination
* Drinking safe water and avoiding contaminated water sources
* Avoiding raw or undercooked meat, poultry, and seafood
* Getting vaccinated against infections that can cause diarrhea
Complications of diarrhea can include:
* Dehydration: Diarrhea can lead to a loss of fluids and electrolytes, which can cause dehydration. Severe dehydration can be life-threatening and requires immediate medical attention.
* Electrolyte imbalance: Diarrhea can also cause an imbalance of electrolytes in the body, which can lead to serious complications.
* Inflammation of the intestines: Prolonged diarrhea can cause inflammation of the intestines, which can lead to abdominal pain and other complications.
* Infections: Diarrhea can be a symptom of an infection, such as a bacterial or viral infection. If left untreated, these infections can lead to serious complications.
* Malnutrition: Prolonged diarrhea can lead to malnutrition and weight loss, which can have long-term effects on health and development.
Treatment of diarrhea will depend on the underlying cause, but may include:
* Fluid replacement: Drinking plenty of fluids to prevent dehydration and replace lost electrolytes.
* Anti-diarrheal medications: Over-the-counter or prescription medications to slow down bowel movements and reduce diarrhea.
* Antibiotics: If the diarrhea is caused by a bacterial infection, antibiotics may be prescribed to treat the infection.
* Rest: Getting plenty of rest to allow the body to recover from the illness.
* Dietary changes: Avoiding certain foods or making dietary changes to help manage symptoms and prevent future episodes of diarrhea.
It is important to seek medical attention if you experience any of the following:
* Severe diarrhea that lasts for more than 3 days
* Diarrhea that is accompanied by fever, blood in the stool, or abdominal pain
* Diarrhea that is severe enough to cause dehydration or electrolyte imbalances
* Diarrhea that is not responding to treatment
Prevention of diarrhea includes:
* Good hand hygiene: Washing your hands frequently, especially after using the bathroom or before preparing food.
* Safe food handling: Cooking and storing food properly to prevent contamination.
* Avoiding close contact with people who are sick.
* Getting vaccinated against infections that can cause diarrhea, such as rotavirus.
Overall, while diarrhea can be uncomfortable and disruptive, it is usually a minor illness that can be treated at home with over-the-counter medications and plenty of fluids. However, if you experience severe or persistent diarrhea, it is important to seek medical attention to rule out any underlying conditions that may require more formal treatment.
There are several types of aneuploidy, including:
1. Trisomy: This is the presence of an extra copy of a chromosome. For example, Down syndrome is caused by an extra copy of chromosome 21 (trisomy 21).
2. Monosomy: This is the absence of a chromosome.
3. Mosaicism: This is the presence of both normal and abnormal cells in the body.
4. Uniparental disomy: This is the presence of two copies of a chromosome from one parent, rather than one copy each from both parents.
Aneuploidy can occur due to various factors such as errors during cell division, exposure to certain chemicals or radiation, or inheritance of an abnormal number of chromosomes from one's parents. The risk of aneuploidy increases with age, especially for women over the age of 35, as their eggs are more prone to errors during meiosis (the process by which egg cells are produced).
Aneuploidy can be diagnosed through various methods such as karyotyping (examining chromosomes under a microscope), fluorescence in situ hybridization (FISH) or quantitative PCR. Treatment for aneuploidy depends on the underlying cause and the specific health problems it has caused. In some cases, treatment may involve managing symptoms, while in others, it may involve correcting the genetic abnormality itself.
In summary, aneuploidy is a condition where there is an abnormal number of chromosomes present in a cell, which can lead to various developmental and health problems. It can occur due to various factors and can be diagnosed through different methods. Treatment depends on the underlying cause and the specific health problems it has caused.
https://www.medicinenet.com › Medical Dictionary › G
A genetic translocation is a change in the number or arrangement of the chromosomes in a cell. It occurs when a portion of one chromosome breaks off and attaches to another chromosome. This can result in a gain or loss of genetic material, which can have significant effects on the individual.
Genetic Translocation | Definition & Facts | Britannica
https://www.britannica.com › science › Genetic-tr...
Genetic translocation, also called chromosomal translocation, a type of chromosomal aberration in which a portion of one chromosome breaks off and attaches to another chromosome. This can result in a gain or loss of genetic material. Genetic translocations are often found in cancer cells and may play a role in the development and progression of cancer.
Translocation, Genetic | health Encyclopedia - UPMC
https://www.upmc.com › health-library › gene...
A genetic translocation is a change in the number or arrangement of the chromosomes in a cell. It occurs when a portion of one chromosome breaks off and attaches to another chromosome. This can result in a gain or loss of genetic material, which can have significant effects on the individual.
Genetic Translocation | Genetics Home Reference - NIH
https://ghr.nlm.nih.gov › condition › ge...
A genetic translocation is a change in the number or arrangement of the chromosomes in a cell. It occurs when a portion of one chromosome breaks off and attaches to another chromosome. This can result in a gain or loss of genetic material, which can have significant effects on the individual.
In conclusion, Genetic Translocation is an abnormality in the number or arrangement of chromosomes in a cell. It occurs when a portion of one chromosome breaks off and attaches to another chromosome, resulting in a gain or loss of genetic material that can have significant effects on the individual.
Here are some common types of E. coli infections:
1. Urinary tract infections (UTIs): E. coli is a leading cause of UTIs, which occur when bacteria enter the urinary tract and cause inflammation. Symptoms include frequent urination, burning during urination, and cloudy or strong-smelling urine.
2. Diarrheal infections: E. coli can cause diarrhea, abdominal cramps, and fever if consumed through contaminated food or water. In severe cases, this type of infection can lead to dehydration and even death, particularly in young children and the elderly.
3. Septicemia (bloodstream infections): If E. coli bacteria enter the bloodstream, they can cause septicemia, a life-threatening condition that requires immediate medical attention. Symptoms include fever, chills, rapid heart rate, and low blood pressure.
4. Meningitis: In rare cases, E. coli infections can spread to the meninges, the protective membranes covering the brain and spinal cord, causing meningitis. This is a serious condition that requires prompt treatment with antibiotics and supportive care.
5. Hemolytic-uremic syndrome (HUS): E. coli infections can sometimes cause HUS, a condition where the bacteria destroy red blood cells, leading to anemia, kidney failure, and other complications. HUS is most common in young children and can be fatal if not treated promptly.
Preventing E. coli infections primarily involves practicing good hygiene, such as washing hands regularly, especially after using the bathroom or before handling food. It's also essential to cook meat thoroughly, especially ground beef, to avoid cross-contamination with other foods. Avoiding unpasteurized dairy products and drinking contaminated water can also help prevent E. coli infections.
If you suspect an E. coli infection, seek medical attention immediately. Your healthcare provider may perform a urine test or a stool culture to confirm the diagnosis and determine the appropriate treatment. In mild cases, symptoms may resolve on their own within a few days, but antibiotics may be necessary for more severe infections. It's essential to stay hydrated and follow your healthcare provider's recommendations to ensure a full recovery.
Symptoms of gonorrhea in men include:
* A burning sensation when urinating
* Discharge from the penis
* Painful or swollen testicles
* Painful urination
Symptoms of gonorrhea in women include:
* Increased vaginal discharge
* Painful urination
* Painful intercourse
* Abnormal vaginal bleeding
Gonorrhea can be diagnosed through a physical exam and laboratory tests, such as a urine test or a swab of the affected area. It is typically treated with antibiotics.
If left untreated, gonorrhea can cause serious complications, including:
* Pelvic inflammatory disease (PID) in women
* Epididymitis (inflammation of the tube that carries sperm) in men
* Infertility
* Chronic pain
* Increased risk of HIV transmission
Gonorrhea is a reportable disease, meaning that healthcare providers are required by law to report cases to public health authorities. This helps to track and prevent the spread of the infection.
Prevention methods for gonorrhea include:
* Safe sex practices, such as using condoms or dental dams
* Avoiding sexual contact with someone who has gonorrhea
* Getting regularly tested for STIs
* Using pre-exposure prophylaxis (PrEP) for HIV prevention
It is important to note that gonorrhea can be asymptomatic, meaning that individuals may not experience any symptoms even if they have the infection. Therefore, regular testing is important for early detection and treatment.
Sigma-Aldrich
Jane A. Langdale
Xiaoliang Sunney Xie
Chromogenic in situ hybridization
Molecular Inversion Probe
So-Jung Park
9q34.3 deletion syndrome
Nude in the Nettles
Roman Baths (Bath)
Thermae Bath Spa
Streptococcus pseudopneumoniae
List of solved missing person cases: pre-2000
DAPI
Black Hole Quencher 1
Z-DNA
HARS
RNA therapeutics
Patent
Brazilians
Race and ethnicity in Brazil
Branched DNA assay
Eastern blot
White Brazilians
Brown (racial classification)
Macro-haplogroup L (mtDNA)
Tom Brown (chemist)
Kesara Margrét Anamthawat-Jónsson
Locked nucleic acid
Grand Masti
Nucleic acid test
Killing of Jennifer Laude
2010 Mirchpur caste violence
2017 Mengalum Island boat accident
Salvia
List of political self-immolations
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Browsing by Subject "DNA Probes"
High Salt Lysates: a Simple Method to Store Blood Samples Without Refrigeration for Subsequent Use with DNA Probes in: The...
Browsing by Subject "HPV-DNA Probes"
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DNA probes :
› WHO HQ Library catalog
Dna probes industry status and prospects professional Worldwide Market Reports
Vysis CEP 8 DNA Probe Kit | Abbott Molecular
Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot...
High Resolution Imaging of DNA Origami with Encased Cantilevers | Scuba Probe Technologies
Course Content - #94554: Tuberculosis: An Update - NetCE
Protocols for 16S rDNA Array Analyses of Microbial Communities by Sequence-Specific Labeling of DNA Probes - Nofima
Pulmonary versus Nonpulmonary Nontuberculous Mycobacteria, Ontario, Canada - Volume 23, Number 11-November 2017 - Emerging...
Supplementary figure S2. Electrochemical methods for probing DNA damage mechanisms and designing cisplatin-based combination...
Quantification of purified endogenous miRNAs with high sensitivity and specificity | Nature Communications
A novel means to develop strain-specific DNA probes for detecting bacteria in the environment. Pristine environments harbor a...
510(k) Premarket Notification
Interpol: All Dubai assassins wanted
Identity of active methanotrophs in landfill cover soil as revealed by DNA-stable isotope probing<...
Article - Billing and Coding: Gastrointestinal Pathogen (GIP) Panels Utilizing Multiplex Nucleic Acid Amplification Techniques ...
2019 AACC: Exhibitors
Mitochondrial DNA | Office of Justice Programs
Recommendations for the Prevention and Management of Chlamydia trachomatis Infections, 1993
1,100+ Pap Smear Illustrations, Royalty-Free Vector Graphics & Clip Art - iStock
TRIC J R
FBI Insider Trading Probe Targets Senator Grassley's Aide
Faculty Trainers | Therapeutic Sciences Graduate Program | Brown University
Dynamic Twists and Supercoiling Loops Can Enable DNA To Adjust Its Function
LOINC 85546-0 PRRSV European strain RNA [Presence] in Specimen by NAA with probe detection
Molecular1
- DNA stores a cell's genetic information in a stable and protected form that is readily accessible for the cell to carry on its activities," said corresponding author Dr. Lynn Zechiedrich, Kyle and Josephine Morrow Chair in molecular virology and microbiology at Baylor. (scitechdaily.com)
Sequences7
- The parasite DNA was found to be undegraded, as shown by the unaltered pattern of repetitive sequences obtained after storage of up to 1 month at 37°C, due to the inhibition of DNA degrading enzymes by the cesium salt. (ajtmh.org)
- The means to develop strain-specific DNA probes for detecting bacteria in the environment was examined using the polymerase chain reaction (PCR) amplification of target sequences. (readabstracts.com)
- The openings expose that particular DNA code, making it accessible to proteins looking for specific sequences to interact with the DNA, for instance, to repair it or make a copy of it. (scitechdaily.com)
- Our findings stimulate future work on how DNA may use its shape to govern accessibility to specific sequences in a variety of situations, like in response to drugs, infection or points in the cell cycle. (scitechdaily.com)
- Fluorescently labeled probes detect the amount of specific double-stranded DNA sequences. (cdc.gov)
- The RAPD (Random Amplification Polymorphic DNA) allows the amplification of DNA sequences and is a simple and quick technique that does not require prior knowledge on the genomes to characterize organisms, using one randomly determined (usually a decamer) primer 17 . (bvsalud.org)
- RNA or DNA) sequences of interest in organisms present in a clinical specimen. (cdc.gov)
Amplification4
- The universally conserved regions are used for PCR amplification primers, while the variable regions are used for the specific probes. (nofima.com)
- Microelectrophoretic approaches borrow microfabrication techniques from the semiconductor industry to miniaturize and integrate the amplification, purification and electrophoretic sequencing of DNA. (nature.com)
- The GEN-PROBE APTIMA trichomonas vaginalis assay combines the technologies of target capture, Transcription-Mediated Amplification (TMA), and Dual Kinetic Assay (DKA). (cdc.gov)
- A technique that amplifies (copies) DNA or RNA segments, in Amplification (NAA) order to directly identify microorganisms in sputum specimens. (cdc.gov)
Hybridization2
- In these protocols, the specificity obtained by sequence-specific labeling of DNA probes is combined with the possibility of detecting several different probes simultaneously by DNA array hybridization. (nofima.com)
- DNA was extracted using the alkaline-lysis and the production of extended-spectrum - method of Birnboim and Doly [16] and was lactamases by multidrug resistant E.coli has used in dot blot hybridization. (who.int)
Specific9
- Blood specimens to be tested for the presence of Plasmodium falciparum using specific DNA probes can be stored as high salt lysates (HSL) without refrigeration. (ajtmh.org)
- The Vysis CEP 8 SpectrumOrange DNA Probe Kit is a SpectrumOrange labeled probe specific for the alpha satellite (centromeric) region, 8p11.1-q11.1. (molecular.abbott)
- In multi-site clinical trials, the CEP 8 SpectrumOrange DNA Probe Kit for interphase analysis was 96% sensitive and 98% specific as compared to traditional cytogenetic analysis. (molecular.abbott)
- A novel means to develop strain-specific DNA probes for detecting bacteria in the environment. (readabstracts.com)
- The stress can promote the separation of the strands of the double helix at specific distant sites, exposing the DNA bases, which may facilitate repair, replication, transcription, or other aspects of DNA function. (scitechdaily.com)
- The GEN-PROBE TMA reaction replicates a specific region of the small ribosomal subunit from trichomonas vaginalis via DNA and RNA intermediates and generates RNA amplicon molecules. (cdc.gov)
- Therefore, in our study, E. coli complex, multi-factorial mechanism involv- isolates from diarrhoeal cases were ana- ing a large number of virulence factors that lysed using specific DNA probes for genes vary with pathotype. (who.int)
- Specific probes bind to the DNA, in order to determine what type of polio present. (cdc.gov)
- DNA probes specific for the identification of human papilloma virus. (bvsalud.org)
Single-stranded2
- A single-stranded chemiluminescent DNA probe, which is complementary to a region of the target amplicon, is labeled with different acridinium ester molecule. (cdc.gov)
- A piece of single-stranded nucleic acid that hybridizes specifically to the complementary sequence of RNA or DNA in the sample. (cdc.gov)
Sequencing2
- These aim to reduce the cost of DNA sequencing by several orders of magnitude. (nature.com)
- Nearly three decades have passed since the invention of electrophoretic methods for DNA sequencing. (nature.com)
Detection3
- During the detection step, light emitted from the labeled RNA: DNA hybrids is measured as photon signals in a luminometer, and are reported as Relative Light Units (RLU). (cdc.gov)
- Detection of PCR products in real time can be accomplished by using fluorescent dyes or probes. (cdc.gov)
- While fluorescent dyes detect only the amount of double-stranded DNA, in this video we are going to look at the principles behind fluorescent dye-based detection method. (cdc.gov)
Gene1
- We propose that variations in these novel DNA shapes could have potential nanotechnology applications, such as gene therapy. (scitechdaily.com)
Assay1
- We examined DNA methylation levels at more than 472,506 CpG probes through the Illumina Infinium HumanMethylation450 BeadChip assay. (cdc.gov)
Purification1
- Protocols are presented for DNA purification, probe construction, probe labeling, and DNA array hybridizations. (nofima.com)
Genes2
- These results were supported by analysis of mmoX genes in (13)C-DNA. (elsevier.com)
- Isolates were screened for presence different toxins and 2 (2.2%) isolates were of genes encoding LT and ST enterotoxins, positive with all 4 DNA probes. (who.int)
20211
- Reference: "Supercoiling and looping promote DNA base accessibility and coordination among distant sites" by Jonathan M. Fogg, Allison K. Judge, Erik Stricker, Hilda L. Chan and Lynn Zechiedrich, 28 September 2021, Nature Communication . (scitechdaily.com)
Visualize1
- To visualize the detailed structure of DNA origami assemblies, gentle imaging conditions are required. (scubaprobe.com)
Reveal2
- Results reveal that the probes can be developed and utilized without prior knowledge of the host strain and that DNA probe sensitivity and selectivity observed conform with those in other PCR-based methods. (readabstracts.com)
- Studying linear DNA does not capture this phenomenon, but our supercoiled minicircles reveal these dynamic properties of DNA as it is found in cells. (scitechdaily.com)
Viral1
- In the instrument, viral RNA is copied into DNA and then the DNA is amplified. (cdc.gov)
Methods1
- In recent decades, traditional methods of microorganism phenotyping have been replaced or added by the procedures associated to recombinant DNA 12-14 . (bvsalud.org)
Sequence1
- The method was used without imposing the need to determine the nucleic acid sequence of the probe to produce the PCR primers. (readabstracts.com)
Organisms1
- Organisms achieve this seemingly paradoxical goal by storing DNA in supercoiled loops. (scitechdaily.com)
Involves1
- As part of a widening insider trading probe that involves the U.S. Congress, the Federal Bureau of Investigation is trying to determine if an aide to Sen. Charles Grassley's played a part in illegally divulging a key government decision to private corporations this spring, the Wall Street Journal reported on Monday. (ibtimes.com)
Stable2
- The identity of active methanotrophs in Roscommon landfill cover soil, a slightly acidic peat soil, was assessed by DNA-stable isotope probing (SIP). (elsevier.com)
- The labeled DNA probe combines with amplicon to form stable RNA: DNA hybrids. (cdc.gov)
Order2
- I challenge Israel to bring the suspects there in order to undergo a DNA test and compare them with the samples we have," he said in an interview to the UAE-based al-Khaleej newspaper. (ynetnews.com)
- Australian investigators arrived in Israel last week in order to probe the use of Australian passports belonging to three Israelis during the Dubai operation. (ynetnews.com)
Results2
Analysis2
- The identity of active methanotrophs was revealed by analysis of (13)C-labelled DNA fractions. (elsevier.com)
- The purified fragments analysis showed that 92 (46.0%) of the were used as probes after labelling with a 200 isolates examined were toxigenic. (who.int)
Study3
- In the current study, we investigated how supercoiling and looping modulate DNA activity. (scitechdaily.com)
- Our study rebrands DNA from a passive biomolecule to an active one," said co-author Hilda Chan, graduate student in the Medical Scientist Training Program. (scitechdaily.com)
- For two decades, scientists have been comparing every person's full set of DNA they study to a template that relies mostly on genetic material from one man affectionately known as "the guy from Buffalo. (cbs42.com)
Buffer1
- Here we show a high resolution tapping mode AFM image of a 2D DNA origami rectangle in a TAE buffer obtained using an encased cantilever. (scubaprobe.com)
Biology1
- Our cells have created many complex processes to deal with storing and using DNA, and the shape of that DNA affects all of them," said co-author Allison Judge, graduate student in the Department of Pharmacology and Chemical Biology. (scitechdaily.com)
Target1
- It is carried out by hybridizing target DNA to high-density microarrays that are designed to query the identity of individual bases. (nature.com)
Official1
- Congressional aides are rarely targeted in federal probes, as the official duties of legislative-branch employees are protected under the Constitution. (ibtimes.com)
Reach1
- The global DNA Probes market is expected to reach US$ XX Million by 2028, with a CAGR of XX% from 2023 to 2028, based on HNY Research newly published report. (worldwidemarketreports.com)
Samples1
- The investigation into the Mabhouh assassination has yet to yield new findings, although the Dubai police insist that they have obtained DNA samples of the assassins. (ynetnews.com)
Present1
- Zechiedrich and her collaborators began by making small pieces of supercoiled DNA, like those present in living cells. (scitechdaily.com)
Repair1
- 1982. Activity of organophosphorus insecticides in bacterial tests for mutagenicity and DNA repair. (cdc.gov)
Access1
- Here we showed that no protein is needed to access DNA, it can make itself accessible on its own," Zechiedrich said. (scitechdaily.com)
Human1
- FILE - This undated image made available by the National Human Genome Research Institute shows the output from a DNA sequencer. (cbs42.com)
Clear2
- Interpol Secretary-General Ronald Noble said that a thorough investigation by the Dubai police established a clear link between the passport records and the security footage, as well as DNA, evidence from eyewitnesses, credit card records and phone calls. (ynetnews.com)
- This supercoiling and looping are known to influence every aspect of DNA activity, but how this happens has not been clear. (scitechdaily.com)
Site1
- The effects of supercoiling stress at one site of the loop can be transmitted along the DNA backbone to a distant site. (scitechdaily.com)
Models2
- It was unexpected because the models indicate that supercoiled DNA circles would behave more like a twisted rubber band. (scitechdaily.com)
- We conducted separate linear mixed models to examine associations of DNA methylation levels at each CpG with AC and DC. (cdc.gov)