A major dental enamel-forming protein found in mammals. In humans the protein is encoded by GENES found on both the X CHROMOSOME and the Y CHROMOSOME.
The proteins that are part of the dental enamel matrix.
A secreted matrix metalloproteinase that is the predominant proteolytic activity in the enamel matrix. The enzyme has a high specificity for dental enamel matrix protein AMELOGENIN.
The elaboration of dental enamel by ameloblasts, beginning with its participation in the formation of the dentino-enamel junction to the production of the matrix for the enamel prisms and interprismatic substance. (Jablonski, Dictionary of Dentistry, 1992).
A hard thin translucent layer of calcified substance which envelops and protects the dentin of the crown of the tooth. It is the hardest substance in the body and is almost entirely composed of calcium salts. Under the microscope, it is composed of thin rods (enamel prisms) held together by cementing substance, and surrounded by an enamel sheath. (From Jablonski, Dictionary of Dentistry, 1992, p286)
Cylindrical epithelial cells in the innermost layer of the ENAMEL ORGAN. Their functions include contribution to the development of the dentinoenamel junction by the deposition of a layer of the matrix, thus producing the foundation for the prisms (the structural units of the DENTAL ENAMEL), and production of the matrix for the enamel prisms and interprismatic substance. (From Jablonski's Dictionary of Dentistry, 1992)
An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
Spherical particles of nanometer dimensions.
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
The collective tissues from which an entire tooth is formed, including the DENTAL SAC; ENAMEL ORGAN; and DENTAL PAPILLA. (From Jablonski, Dictionary of Dentistry, 1992)
The process whereby calcium salts are deposited in the dental enamel. The process is normal in the development of bones and teeth. (Boucher's Clinical Dental Terminology, 4th ed, p43)
One of a set of bone-like structures in the mouth used for biting and chewing.
A group of phosphate minerals that includes ten mineral species and has the general formula X5(YO4)3Z, where X is usually calcium or lead, Y is phosphorus or arsenic, and Z is chlorine, fluorine, or OH-. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Epithelial cells surrounding the dental papilla and differentiated into three layers: the inner enamel epithelium, consisting of ameloblasts which eventually form the enamel, and the enamel pulp and external enamel epithelium, both of which atrophy and disappear before and upon eruption of the tooth, respectively.
Calcium salts of phosphoric acid. These compounds are frequently used as calcium supplements.
Large herbivorous tropical American lizards.
The most posterior teeth on either side of the jaw, totaling eight in the deciduous dentition (2 on each side, upper and lower), and usually 12 in the permanent dentition (three on each side, upper and lower). They are grinding teeth, having large crowns and broad chewing surfaces. (Jablonski, Dictionary of Dentistry, 1992, p821)
Validation of the SEX of an individual by inspection of the GONADS and/or by genetic tests.
Proteins obtained from species of REPTILES.
Any of the eight frontal teeth (four maxillary and four mandibular) having a sharp incisal edge for cutting food and a single root, which occurs in man both as a deciduous and a permanent tooth. (Jablonski, Dictionary of Dentistry, 1992, p820)
The mineral component of bones and teeth; it has been used therapeutically as a prosthetic aid and in the prevention and treatment of osteoporosis.
Nanometer-sized tubes composed of various substances including carbon (CARBON NANOTUBES), boron nitride, or nickel vanadate.
The process of TOOTH formation. It is divided into several stages including: the dental lamina stage, the bud stage, the cap stage, and the bell stage. Odontogenesis includes the production of tooth enamel (AMELOGENESIS), dentin (DENTINOGENESIS), and dental cementum (CEMENTOGENESIS).
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
Tissue, organ, or gamete donation intended for a designated recipient.
The mechanisms by which the SEX of an individual's GONADS are fixed.

Analysis of ancient DNA from a prehistoric Amerindian cemetery. (1/231)

The Norris Farms No. 36 cemetery in central Illinois has been the subject of considerable archaeological and genetic research. Both mitochondrial DNA (mtDNA) and nuclear DNA have been examined in this 700-year-old population. DNA preservation at the site was good, with about 70% of the samples producing mtDNA results and approximately 15% yielding nuclear DNA data. All four of the major Amerindian mtDNA haplogroups were found, in addition to a fifth haplogroup. Sequences of the first hypervariable region of the mtDNA control region revealed a high level of diversity in the Norris Farms population and confirmed that the fifth haplogroup associates with Mongolian sequences and hence is probably authentic. Other than a possible reduction in the number of rare mtDNA lineages in many populations, it does not appear as if European contact significantly altered patterns of Amerindian mtDNA variation, despite the large decrease in population size that occurred. For nuclear DNA analysis, a novel method for DNA-based sex identification that uses nucleotide differences between the X and Y copies of the amelogenin gene was developed and applied successfully in approximately 20 individuals. Despite the well-known problems of poor DNA preservation and the ever-present possibility of contamination with modern DNA, genetic analysis of the Norris Farms No. 36 population demonstrates that ancient DNA can be a fruitful source of new insights into prehistoric populations.  (+info)

Rapid quantification of mixed chimerism using multiplex amplification of short tandem repeat markers and fluorescence detection. (2/231)

Monitoring the engraftment of donor cells after allogeneic blood stem cell transplantation (BSCT) may be important for the early diagnosis of graft failure or relapse of disease. Several techniques have been reported for this purpose. PCR-based assays analyzing polymorphic short tandem repeat (STR) markers are attractive because they are sensitive and can be performed rapidly. The intent of the present study was to test a novel approach for the quantification of mixed chimerism using a commercial multiplex STR assay with fluorescence-based detection for forensic purposes. The feasibility of this assay and the accuracy of quantitative results was tested using serial cell mixtures of unrelated individuals. Sample preparation was optimized to obtain information from minute amounts of starting material, eg from patients with aplasia or from sorted cell populations. Using the STR-PCR, discrimination between donor and recipient was possible in all patients analyzed (n = 25). Cell dilution experiments showed a linear correlation between the cell numbers added and the proportions found, with the limit of detection for a minor cell population being 5%. Comparison of values obtained with standard FISH analysis in patients transplanted from sex-mismatched donors showed an excellent correlation with the STR-PCR results. Taken together, this procedure allows the rapid, versatile and accurate quantification of mixed chimerism, even with minuscule numbers of cells.  (+info)

An immunocytochemical study of amelogenin proteins in the developing tooth enamel of the gar-pike, Lepisosteus oculatus (Holostei, Actinopterygii). (3/231)

Previous studies have demonstrated the morphological similarity of the enamel-like layer found in the teeth of the coelacanth, lungfish and gar-pike to the enamel of tetrapods. In order to clarify the phylogenetic continuity between both structures, tooth germs of the gar-pike were immunocytochemically studied using an anti-bovine amelogenin polyclonal antibody. Intense immunoreaction was shown over the enamel-like matrix layer. Certain cell organelles associated with the secretory pathway of the ameloblasts were recognized as immunoreactive. These results indicate that the enamel-like layer of the gar-pike is a tissue homologous with the mammalian enamel because both possess a common, amelogenin-like substance.  (+info)

Histological analysis and ancient DNA amplification of human bone remains found in caius iulius polybius house in pompeii. (4/231)

Thirteen skeletons found in the Caius Iulius Polybius house, which has been the object of intensive study since its discovery in Pompeii 250 years ago, have provided an opportunity to study either bone diagenesis by histological investigation or ancient DNA by polymerase chain reaction analysis. DNA analysis was done by amplifying both X- and Y-chromosomes amelogenin loci and Y-specific alphoid repeat locus. The von Willebrand factor (vWF) microsatellite locus on chromosome 12 was also analyzed for personal identification in two individuals showing alleles with 10/11 and 12/12 TCTA repeats, respectively. Technical problems were the scarcity of DNA content from osteocytes, DNA molecule fragmentation, microbial contamination which change bone structure, contaminating human DNA which results from mishandling, and frequent presence of Taq DNA polymerase inhibiting molecules like polyphenols and heavy metals. The results suggest that the remains contain endogenous human DNA that can be amplified and analyzed. The amplifiability of DNA corresponds to the bone preservation and dynamics of the burial conditions subsequent to the 79 A.D. eruption.  (+info)

Proteinases in developing dental enamel. (5/231)

For almost three decades, proteinases have been known to reside within developing dental enamel. However, identification and characterization of these proteinases have been slow and difficult, because they are present in very small quantities and they are difficult to purify directly from the mineralizing enamel. Enamel matrix proteins such as amelogenin, ameloblastin, and enamelin are cleaved by proteinases soon after they are secreted, and their cleavage products accumulate in the deeper, more mature enamel layers, while the full-length proteins are observed only at the surface. These results suggest that proteinases are necessary for "activating" enamel proteins so the parent proteins and their cleavage products may perform different functions. A novel matrix metalloproteinase named enamelysin (MMP-20) was recently cloned from tooth tissues and was later shown to localize primarily within the most recently formed enamel. Furthermore, recombinant porcine enamelysin was demonstrated to cleave recombinant porcine amelogenin at virtually all of the sites that have previously been described in vivo. Therefore, enamelysin is at least one enzyme that may be important during early enamel development. As enamel development progresses to the later stages, a profound decrease in the enamel protein content is observed. Proteinases have traditionally been assumed to degrade the organic matrix prior to its removal from the enamel. Recently, a novel serine proteinase named enamel matrix serine proteinase-1 (EMSP1) was cloned from enamel organ epithelia. EMSP1 localizes primarily to the early maturation stage enamel and may, therefore, be involved in the degradation of proteins prior to their removal from the maturing enamel. Other, as yet unidentified, proteinases and proteinase inhibitors are almost certainly present within the forming enamel and await discovery.  (+info)

Identification of CCAAT/enhancer-binding protein alpha as a transactivator of the mouse amelogenin gene. (6/231)

Amelogenin expression is ameloblast-specific and developmentally regulated at the temporal and spatial levels. In a previous transgenic mouse analysis, the expression pattern of the endogenous amelogenin gene was recapitulated by a reporter gene driven by a 2. 2-kilobase mouse amelogenin proximal promoter. To understand the molecular mechanisms underlying the spatiotemporal expression of the amelogenin gene during odontogenesis, the mouse amelogenin promoter was systematically analyzed in mouse ameloblast-like LS8 cells. Deletion analysis identified a minimal promoter (-70/+52) containing a CCAAT/enhancer-binding protein (C/EBP)-binding site upstream of the TATA box. In transient transfection assays, C/EBPalpha up-regulated the promoter activity in a dose-dependent manner. The C/EBP-binding site was necessary for both C/EBPalpha-mediated transactivation and basal promoter activity. Electrophoresis mobility shift assays demonstrated that C/EBPalpha bound to its cognate site in the amelogenin promoter and that the binding was specific. Endogenous C/EBPalpha was detected in LS8 cells, and overexpression of exogenous C/EBPalpha in LS8 cells was able to increase the expression level of the endogenous amelogenin protein. The activity of the amelogenin promoter in rat parotid Pa-4 cells and Madin-Darby canine kidney cells was minimal, ranging from 20 to 30% of the activity in ameloblast-like cells. Transient transfection experiments showed that C/EBPalpha transactivated the mouse amelogenin reporter gene in Pa-4 cells, but not in Madin-Darby canine kidney cells. Taken together, these data indicate that C/EBPalpha is a bona fide transcriptional activator of the mouse amelogenin gene in a cell type-specific manner.  (+info)

Functional antagonism between Msx2 and CCAAT/enhancer-binding protein alpha in regulating the mouse amelogenin gene expression is mediated by protein-protein interaction. (7/231)

Ameloblast-specific amelogenin gene expression is spatiotemporally regulated during tooth development. In a previous study, the CCAAT/enhancer-binding protein alpha (C/EBPalpha) was identified as a transcriptional activator of the mouse amelogenin gene in a cell type-specific manner. Here, Msx2 is shown to repress the promoter activity of amelogenin-promoter reporter constructs independent of its intrinsic DNA binding activity. In transient cotransfection assays, Msx2 and C/EBPalpha antagonize each other in regulating the expression of the mouse amelogenin gene. Electrophoresis mobility shift assays demonstrate that Msx2 interferes with the binding of C/EBPalpha to its cognate site in the mouse amelogenin minimal promoter, although Msx2 itself does not bind to the same promoter fragment. Protein-protein interaction between Msx2 and C/EBPalpha is identified with co-immunoprecipitation analyses. Functional antagonism between Msx2 and C/EBPalpha is also observed on the stably transfected 2.2-kilobase mouse amelogenin promoter in ameloblast-like LS8 cells. Furthermore, the carboxyl-terminal residues 183-267 of Msx2 are required for protein-protein interaction, whereas the amino-terminal residues 2-97 of Msx2 play a less critical role. Among three family members tested (C/EBPalpha, -beta, and -gamma), Msx2 preferentially interacts with C/EBPalpha. Taken together, these data indicate that protein-protein interaction rather than competition for overlapping binding sites results in the functional antagonism between Msx2 and C/EBPalpha in regulating the mouse amelogenin gene expression.  (+info)

Time-related changes of developing enamel crystals after exposure to the tissue fluid in vivo: analysis of a subcutaneously implanted rat incisor. (8/231)

To investigate the effects of tissue fluid on the growth of enamel crystals, upper and lower incisors extracted from 3-week-old Wistar rats were removed of the enamel organ, implanted subcutaneously in the dorsal portion of animals from the same litter, and harvested at 72 h or 1 week after implantation. The grafts were chemically fixed with surrounding tissues and prepared for light and electron microscopy, X-ray microanalysis, or for the immunohistochemistry of amelogenin. Mineralization of implanted enamel layers was examined by contact X-ray microradiography. The immunoreactivities for 25 kD amelogenin in immature enamel decreased sequentially, starting from the surface to the deeper layers; by 1 week after implantation, no positive reactivities remained in the entire enamel layers at the stages of matrix formation and early maturation. In accordance with the loss of enamel proteins, immature enamel gained mineral density until it attained higher radio opacity than that of the adjacent dentin by 1 week. In contrast, the radio opacity of the full thickness of the enamel at early maturation remained low except for a superficial thin layer. Electron microscopy revealed no sign of growth of original enamel crystals, but showed heavy precipitation of electron-dense fine granules of calcium phosphate in all layers of the secretory enamel and the superficial layer of enamel at early maturation, which showed high radio opacity. The Ca/P ratio and electron diffraction patterns of the granular materials precipitated between intrinsic enamel crystals indicated the property of hydroxy apatite or octacalcium phosphate though a characteristic ribbon-like profile of enamel crystals was lacking. These data indicate that the enamel organ blocks exogenous mineral precipitates in growing enamel during the stage of matrix formation and plays an essential regulatory role for fine enamel crystallites to grow into large hexagonal crystals.  (+info)

Amelogenin is a protein that plays a crucial role in the formation and mineralization of enamel, which is the hard, calcified tissue that covers the outer surface of teeth. It is expressed during tooth development and is secreted by ameloblasts, the cells responsible for producing enamel.

Amelogenin makes up approximately 90% of the organic matrix of developing enamel and guides the growth and organization of hydroxyapatite crystals, which are the primary mineral component of enamel. The protein is subsequently degraded and removed as the enamel matures and becomes fully mineralized.

Mutations in the gene that encodes amelogenin (AMELX on the X chromosome) can lead to various inherited enamel defects, such as amelogenesis imperfecta, which is characterized by thin, soft, or poorly formed enamel. Additionally, because of its high expression in developing teeth and unique size and structure, amelogenin has been widely used as a marker in forensic dentistry for human identification and sex determination.

Dental enamel is the hard, outermost layer of a tooth that protects the dentin and pulp inside. It is primarily made up of minerals, mainly hydroxyapatite, and contains very little organic material. However, during the formation of dental enamel, proteins are synthesized and secreted by ameloblast cells, which help in the development and mineralization of the enamel. These proteins play a crucial role in the proper formation and structure of the enamel.

Some of the main dental enamel proteins include:

1. Amelogenin: This is the most abundant protein found in developing enamel, accounting for about 90% of the organic matrix. Amelogenin helps regulate the growth and organization of hydroxyapatite crystals during mineralization. It also plays a role in determining the final hardness and structure of the enamel.

2. Enamelin: This protein is the second most abundant protein in developing enamel, accounting for about 5-10% of the organic matrix. Enamelin is involved in the elongation and thickening of hydroxyapatite crystals during mineralization. It also helps maintain the stability of the enamel structure.

3. Ameloblastin: This protein is produced by ameloblast cells and is essential for proper enamel formation. Ameloblastin plays a role in regulating crystal growth, promoting adhesion between crystals, and maintaining the structural integrity of the enamel.

4. Tuftelin: This protein is found in both dentin and enamel but is more abundant in enamel. Tuftelin is involved in the initiation of mineralization and helps regulate crystal growth during this process.

5. Dentin sialophosphoprotein (DSPP): Although primarily associated with dentin formation, DSPP is also found in developing enamel. It plays a role in regulating crystal growth and promoting adhesion between crystals during mineralization.

After the formation of dental enamel is complete, these proteins are largely degraded and removed, leaving behind the highly mineralized and hard tissue that characterizes mature enamel. However, traces of these proteins may still be present in the enamel and could potentially play a role in its structure and properties.

Matrix metalloproteinase-20 (MMP-20) is a type of enzyme that belongs to the matrix metalloproteinase (MMP) family. MMPs are involved in the breakdown and remodeling of extracellular matrix components, such as collagen and elastin.

MMP-20, also known as Enamelysin, is primarily expressed in developing teeth and plays a crucial role in tooth development and mineralization. It is responsible for the degradation of enamel proteins during tooth formation, helping to shape and harden the enamel matrix. MMP-20 is secreted by ameloblasts, which are the cells that produce enamel.

Defects in MMP-20 have been associated with dental disorders such as Amelogenesis imperfecta, a group of genetic conditions characterized by abnormalities in tooth enamel formation and structure.

Amelogenesis is the biological process of forming enamel, which is the hard and highly mineralized outer layer of teeth. Enamel is primarily made up of calcium and phosphate minerals and is the toughest substance in the human body. Amelogenesis involves the synthesis, secretion, and maturation of enamel proteins by specialized cells called ameloblasts.

The medical definition of 'Amelogenesis' refers to a genetic disorder that affects the development and formation of tooth enamel. This condition is also known as Amelogenesis Imperfecta (AI) and can result in teeth that are discolored, sensitive, and prone to decay. There are several types of Amelogenesis Imperfecta, each with its own set of symptoms and genetic causes.

In summary, 'Amelogenesis' is the biological process of enamel formation, while 'Amelogenesis Imperfecta' is a genetic disorder that affects this process, leading to abnormal tooth enamel development.

Dental enamel is the hard, white, outermost layer of a tooth. It is a highly mineralized and avascular tissue, meaning it contains no living cells or blood vessels. Enamel is primarily composed of calcium and phosphate minerals and serves as the protective covering for the crown of a tooth, which is the portion visible above the gum line.

Enamel is the hardest substance in the human body, and its primary function is to provide structural support and protection to the underlying dentin and pulp tissues of the tooth. It also plays a crucial role in chewing and biting by helping to distribute forces evenly across the tooth surface during these activities.

Despite its hardness, dental enamel can still be susceptible to damage from factors such as tooth decay, erosion, and abrasion. Once damaged or lost, enamel cannot regenerate or repair itself, making it essential to maintain good oral hygiene practices and seek regular dental checkups to prevent enamel damage and protect overall oral health.

Ameloblasts are the specialized epithelial cells that are responsible for the formation of enamel, which is the hard, outermost layer of a tooth. These cells are a part of the dental lamina and are present in the developing tooth's crown region. They align themselves along the surface of the developing tooth and secrete enamel proteins and minerals to form the enamel rods and interrod enamel. Once the enamel formation is complete, ameloblasts undergo programmed cell death, leaving behind the hard, mineralized enamel matrix. Any damage or abnormality in the functioning of ameloblasts can lead to developmental defects in the enamel, such as hypoplasia or hypocalcification, which may affect the tooth's structure and function.

Dental enamel hypoplasia is a condition characterized by the deficiency or reduction in the thickness of the tooth's enamel surface. This results in the enamel being thin, weak, and prone to wear, fractures, and dental cavities. The appearance of teeth with enamel hypoplasia may be yellowish, brownish, or creamy white, and they can have pits, grooves, or bands of varying widths and shapes.

Enamel hypoplasia can occur due to various factors, including genetics, premature birth, low birth weight, malnutrition, infections during childhood (such as measles or chickenpox), trauma, exposure to environmental toxins, and certain medical conditions that affect enamel formation.

The condition is usually diagnosed through a dental examination, where the dentist can observe and assess the appearance and structure of the teeth. Treatment options depend on the severity of the hypoplasia and may include fluoride treatments, sealants, fillings, crowns, or extractions in severe cases. Preventive measures such as maintaining good oral hygiene, a balanced diet, and regular dental check-ups can help reduce the risk of developing enamel hypoplasia.

Nanospheres are defined in the medical context as tiny, spherical particles that have a diameter in the nanometer range (typically between 1 to 1000 nm). They can be made up of various materials such as polymers, lipids, metals or ceramics. Nanospheres have unique properties due to their small size and large surface area, making them useful for a variety of medical applications including drug delivery, diagnostic imaging, and tissue engineering.

In the field of drug delivery, nanospheres can be used to encapsulate drugs and deliver them to specific sites in the body, improving the efficacy and safety of treatments. They can also be designed to target certain cell types or release their cargo in response to specific stimuli. Additionally, nanospheres can be used as contrast agents for medical imaging techniques such as magnetic resonance imaging (MRI) and computed tomography (CT).

Overall, nanospheres are a promising tool in the development of new medical technologies and therapies.

Amelogenesis Imperfecta is a group of inherited dental disorders that affect the structure and appearance of tooth enamel. It is caused by mutations in various genes involved in the development and formation of enamel. The condition can be characterized by small, discolored, and poorly formed teeth that are prone to rapid wear, decay, and sensitivity. There are several types of Amelogenesis Imperfecta, which vary in their severity and the specific symptoms they present. Treatment typically focuses on managing the symptoms and improving the appearance and function of the teeth through restorative dental procedures.

A tooth germ is a small cluster of cells that eventually develop into a tooth. It contains the dental papilla, which will become the dentin and pulp of the tooth, and the dental follicle, which will form the periodontal ligament, cementum, and alveolar bone. The tooth germ starts as an epithelial thickening called the dental lamina, which then forms a bud, cap, and bell stage before calcification occurs and the tooth begins to erupt through the gums. It is during the bell stage that the enamel organ, which will form the enamel of the tooth, is formed.

Tooth calcification, also known as dental calculus or tartar formation, refers to the hardening of plaque on the surface of teeth. This process occurs when minerals from saliva combine with bacterial deposits and dental plaque, resulting in a hard, calcified substance that adheres to the tooth surface. Calcification can occur both above and below the gum line, and if not removed through professional dental cleanings, it can lead to periodontal disease, tooth decay, and other oral health issues.

A tooth is a hard, calcified structure found in the jaws (upper and lower) of many vertebrates and used for biting and chewing food. In humans, a typical tooth has a crown, one or more roots, and three layers: the enamel (the outermost layer, hardest substance in the body), the dentin (the layer beneath the enamel), and the pulp (the innermost layer, containing nerves and blood vessels). Teeth are essential for proper nutrition, speech, and aesthetics. There are different types of teeth, including incisors, canines, premolars, and molars, each designed for specific functions in the mouth.

Apatite is a group of phosphate minerals, primarily consisting of fluorapatite, chlorapatite, and hydroxylapatite. They are important constituents of rocks and bones, and they have a wide range of applications in various industries. In the context of medicine, apatites are most notable for their presence in human teeth and bones.

Hydroxylapatite is the primary mineral component of tooth enamel, making up about 97% of its weight. It provides strength and hardness to the enamel, enabling it to withstand the forces of biting and chewing. Fluorapatite, a related mineral that contains fluoride ions instead of hydroxyl ions, is also present in tooth enamel and helps to protect it from acid erosion caused by bacteria and dietary acids.

Chlorapatite has limited medical relevance but can be found in some pathological calcifications in the body.

In addition to their natural occurrence in teeth and bones, apatites have been synthesized for various medical applications, such as bone graft substitutes, drug delivery systems, and tissue engineering scaffolds. These synthetic apatites are biocompatible and can promote bone growth and regeneration, making them useful in dental and orthopedic procedures.

The enamel organ is a structure found in the developing teeth of vertebrates. It is responsible for the formation of enamel, which is the hard, outermost layer of the tooth crown. The enamel organ is derived from the dental papilla and is composed of several layers: the outer enamel epithelium, the stellate reticulum, the stratum intermedium, and the inner enamel epithelium. These layers work together to produce the enamel matrix, which is then mineralized to form the hard tissue that covers the tooth's crown. The enamel organ disappears after the formation of enamel is complete, leaving only the hardened enamel layer behind.

Calcium phosphates are a group of minerals that are important components of bones and teeth. They are also found in some foods and are used in dietary supplements and medical applications. Chemically, calcium phosphates are salts of calcium and phosphoric acid, and they exist in various forms, including hydroxyapatite, which is the primary mineral component of bone tissue. Other forms of calcium phosphates include monocalcium phosphate, dicalcium phosphate, and tricalcium phosphate, which are used as food additives and dietary supplements. Calcium phosphates are important for maintaining strong bones and teeth, and they also play a role in various physiological processes, such as nerve impulse transmission and muscle contraction.

Iguanas are not a medical term. They refer to a type of large, herbivorous lizard that is native to Central and South America, as well as the Caribbean. Some species of iguanas are also found in Mexico and parts of the southern United States. The green iguana is the most common species kept as pets. If you're looking for a medical definition, it might be a case of mistaken identity or misspelling, please make sure the term is correct.

In the context of dentistry, a molar is a type of tooth found in the back of the mouth. They are larger and wider than other types of teeth, such as incisors or canines, and have a flat biting surface with multiple cusps. Molars are primarily used for grinding and chewing food into smaller pieces that are easier to swallow. Humans typically have twelve molars in total, including the four wisdom teeth.

In medical terminology outside of dentistry, "molar" can also refer to a unit of mass in the apothecaries' system of measurement, which is equivalent to 4.08 grams. However, this usage is less common and not related to dental or medical anatomy.

Sex determination analysis is a medical or biological examination used to establish the genetic or phenotypic sex of an individual. This can be done through various methods, including:

1. Genetic testing: Examination of an individual's DNA to identify the presence of specific sex chromosomes (XX for females and XY for males). This is typically performed through a blood or tissue sample.
2. Chromosomal analysis: Microscopic examination of an individual's chromosomes to determine their number and structure. In humans, females typically have 46 chromosomes, including two X chromosomes (46,XX), while males typically have 46 chromosomes, including one X and one Y chromosome (46,XY).
3. Phenotypic analysis: Observation of an individual's physical characteristics, such as the presence or absence of certain sex organs or secondary sexual characteristics, to determine their phenotypic sex.

Sex determination analysis is used in various medical and research contexts, including prenatal testing, diagnosis of disorders of sex development (DSDs), forensic investigations, and population studies. It's important to note that while sex determination analysis can provide information about an individual's genetic or phenotypic sex, it does not necessarily reflect their gender identity, which is a personal sense of being male, female, or something else.

I'm sorry for any confusion, but the term "Reptilian Proteins" does not have a specific or established medical or scientific meaning. The term "reptilian" generally refers to characteristics of reptiles, and proteins are complex molecules that perform various functions within all living organisms, including reptiles. However, there isn't a recognized category or classification called "Reptilian Proteins" in the field of medicine or biology. If you have any questions about specific reptile-related proteins or reptile physiology, I would be happy to try and help with those!

An incisor is a type of tooth that is primarily designed for biting off food pieces rather than chewing or grinding. They are typically chisel-shaped, flat, and have a sharp cutting edge. In humans, there are eight incisors - four on the upper jaw and four on the lower jaw, located at the front of the mouth. Other animals such as dogs, cats, and rodents also have incisors that they use for different purposes like tearing or gnawing.

Dura Mater: The tough, outer membrane that covers the brain and spinal cord.

Hydroxyapatite: A naturally occurring mineral form of calcium apatite, also known as dahllite, with the formula Ca5(PO4)3(OH), is the primary mineral component of biological apatites found in bones and teeth.

Therefore, "Durapatite" isn't a recognized medical term, but it seems like it might be a combination of "dura mater" and "hydroxyapatite." If you meant to ask about a material used in medical or dental applications that combines properties of both dura mater and hydroxyapatite, please provide more context.

Nanotubes, in the context of nanotechnology and materials science, refer to hollow cylindrical structures with extremely small diameters, measured in nanometers (nm). They are typically composed of carbon atoms arranged in a hexagonal lattice structure, similar to graphene. The most common types of nanotubes are single-walled nanotubes (SWNTs) and multi-walled nanotubes (MWNTs).

In the field of medicine, nanotubes have been studied for their potential applications in drug delivery, tissue engineering, and medical devices. For example, researchers have explored the use of nanotubes as drug carriers, where drugs can be loaded into the hollow interior of the tube and released in a controlled manner at the target site. Additionally, nanotubes have been used to create conductive scaffolds for tissue engineering, which may help promote nerve regeneration or muscle growth.

However, it's important to note that while nanotubes have shown promise in preclinical studies, their potential use in medical applications is still being researched and developed. There are concerns about the potential toxicity of nanotubes, as well as challenges related to their large-scale production and functionalization for specific medical applications.

Odontogenesis is the process of tooth development that involves the formation and calcification of teeth. It is a complex process that requires the interaction of several types of cells, including epithelial cells, mesenchymal cells, and odontoblasts. The process begins during embryonic development with the formation of dental lamina, which gives rise to the tooth bud. As the tooth bud grows and differentiates, it forms the various structures of the tooth, including the enamel, dentin, cementum, and pulp. Odontogenesis is completed when the tooth erupts into the oral cavity. Abnormalities in odontogenesis can result in developmental dental anomalies such as tooth agenesis, microdontia, or odontomas.

An encyclopedia is a comprehensive reference work containing articles on various topics, usually arranged in alphabetical order. In the context of medicine, a medical encyclopedia is a collection of articles that provide information about a wide range of medical topics, including diseases and conditions, treatments, tests, procedures, and anatomy and physiology. Medical encyclopedias may be published in print or electronic formats and are often used as a starting point for researching medical topics. They can provide reliable and accurate information on medical subjects, making them useful resources for healthcare professionals, students, and patients alike. Some well-known examples of medical encyclopedias include the Merck Manual and the Stedman's Medical Dictionary.

Directed tissue donation is the process by which a person designates a specific individual as the recipient of their donated tissues, such as corneas, heart valves, or skin, after their death. This allows the donor to make a direct and meaningful impact on the life of someone they know or are related to who may be in need of a tissue transplant. It is important to note that the final determination of whether the tissues are suitable for transplantation will be made by medical professionals at the time of donation, taking into account various factors such as the donor's medical history and cause of death. Directed tissue donation can provide comfort and solace to both the donor and their loved ones, knowing that they have been able to help someone in need even after their passing.

"Sex determination processes" refer to the series of genetic and biological events that occur during embryonic and fetal development which lead to the development of male or female physical characteristics. In humans, this process is typically determined by the presence or absence of a Y chromosome in the fertilized egg. If the egg has a Y chromosome, it will develop into a male (genetically XY) and if it does not have a Y chromosome, it will develop into a female (genetically XX).

The sex determination process involves the activation and repression of specific genes on the sex chromosomes, which direct the development of the gonads (ovaries or testes) and the production of hormones that influence the development of secondary sexual characteristics. This includes the development of internal and external genitalia, as well as other sex-specific physical traits.

It is important to note that while sex is typically determined by genetics and biology, gender identity is a separate construct that can be self-identified and may not align with an individual's biological sex.

Although the precise role of amelogenin(s) in regulating the mineralization process is unknown, it is known that amelogenins ... Developing human enamel contains about 70% protein, 90% of which are amelogenins. Amelogenins are believed to be involved in ... "deleted-amelogenin males" (DAMs). In response the authors suggested that while the amelogenin sex test may be accurate in ... The amelogenin gene has been most widely studied in humans, where it is a single copy gene, located on the X and Y chromosomes ...
Dr. Hugh Flax, one of the cover authors of Dentistry Todays January/February issue, stopped by our booth at the Chicago Dental Society Midwinter Meeting to visit and take a picture with James Radcliffe. ...
sex is determined by the amelogenin sex gene and is analysed in most types of DNA tests ... Amelogenin. Headway Services This Amelogenin gene is responsible for determining sex in an individual and is found on both the ... In very rare cases in males, there is what is known as a deletion on the Y chromosome of the amelogenin gene; this means that ... However, out of these 21 loci, one of them is the amelogenin gene which is tested as a precautionary measure and as a way to ...
Effects of Amelogenin phosphorylation on Carbonic Anhydrases MS Thesis Defense presentation by Lasya Bhogadi, BDS University of ... Effects of Amelogenin phosphorylation on Carbonic Anhydrases Effects of Amelogenin phosphorylation on Carbonic Anhydrases ... Effects of Amelogenin phosphorylation on Carbonic Anhydrases. MS Thesis Defense presentation by Lasya Bhogadi, BDS. University ... Effects of Amelogenin phosphorylation on Carbonic Anhydrases This is a past event. ...
The Non-Amelogenins: Ameloblastin and Enamelin. - Pp. 42-55 (14). Yong-Hee P. Chun, Jan C-C Hu, James P. Simmer. View Abstract ... Amelogenin Exons 8 and 9. - Pp. 163-173 (11). Wu Li, Jean Yves-Sire, Yoshiro Takano, Mary MacDougall, Michel Goldberg, Pamela ... Amelogenins: Multifaceted Proteins for Dental and Bone Formation and Repair Volume 1. eBook: US $99 Special Offer (PDF + ... Amelogenins: A Review of Formative and Degradative Aspects, and Transgene Expression in Bone Cells. - Pp. 32-41 (10). Rima ...
In humans, the amelogenin gene is present on both the X and the Y chromosomes. However, there are size differences in this gene ... The aim of the present study was to evaluate the application of the amelogenin gene for assessment of chimerism in PBL and/or ... Material and Methods: PCR techniques using a set of amelogenin gene primer were preformed on whole WBC and/or BMA samples, and ... In humans, the amelogenin gene is present on both the X and the Y chromosomes. However, there are size differences in this gene ...
The AMELX gene provides instructions for making a protein called amelogenin, which is essential for normal tooth development. ... The copy of the amelogenin gene on the Y chromosome, AMELY, makes very little amelogenin and is not needed for enamel formation ... Amelogenin is involved in the formation of enamel, which is the hard, white material that forms the protective outer layer of ... One copy of the amelogenin gene is located on each of the sex chromosomes (the X and Y chromosomes). The AMELX gene, which is ...
... ... Pseudogenized Amelogenin Reveals Early Tooth Loss in True Toads (Anura: Bufonidae). Academic Article * ... between the lack of teeth in edentulous vertebrates and the pseudogenization of the major tooth enamel gene amelogenin (AMEL) ...
Amelogenin. A gene present on the X and Y sex chromosomes that is used in DNA identification testing to determine the gender of ...
The Dynamic Interactions of a Multitargeting Domain in Ameloblastin Protein with Amelogenin and Membrane.. Kegulian, Natalie C ... amelogenin (Amel), and Ambn. Vesicle clearance and leakage assays indicated that peptide-membrane interactions were independent ...
Efficacy of amelogenin-chitosan hydrogel in biomimetic repair of human enamel in pH-cycling systems ... Amelogenin-chitosan (CS-AMEL) hydrogel has shown great potential for the prevention, restoration, and treatment of defective ... Efficacy of amelogenin-chitosan hydrogel in biomimetic repair of human enamel in pH-cycling systems. ...
RC is a cell line with isolated from the pleural effusion of a female with lymphoma. It can be used for immunology research.
Amelogenin: X,Y. CSF1PO: 11. D13S317: 13,14. D16S539: 9,12. D5S818: 10 ...
Including 27 Au-STRs, 25 Y-STRs and Amelogenin in a single reaction provides a higher expected likelihood ratio than most ... The combination of STR loci and Amelogenin is an effective tool for human identification ...
2009). To understand amelogenin molecular evolution, we cloned and characterized a number of reptilian and amphibian amelogenin ... How do amelogenin molecules evolve to modulate enamel physical properties?. To address the question of the non-mineralized ... Wang, X., Xing, Z., Zhang, X., and Diekwisch, T.G.H. (2013). Alternative splicing of the amelogenin gene in a caudate amphibian ... Diekwisch, T.G.H., Jin, T., Wang, X., Ito, Y., Schmidt, M.K., Druzinsky, R., Yamane, A., and Luan, X. (2009). Amelogenin ...
STR-PCR Data: Amelogenin: X. CSF1PO: 10,11. D13S317: 13,14. D16S539: 10,13. D5S818: 7,12 D7S820: 11 THO1: 7,9.3. TPOX: 8,9. vWA ...
STR-PCR Data: Amelogenin: X CSF1PO: 12 D13S317: 12,13. D16S539: 11,13. D5S818: 11,13. D7S820: 12. THO1: 9.3. TPOX: 8. vWA: 17, ...
Mutations in amelogenin gene which plays role in enamel formation during development.Causes enamel is abnormally thing. Yellow ...
Amelogenin nanoparticles in suspension: deviations from spherical shape and pH-dependent aggregation. Biomacromolecules 11 (2 ...
Amyloid-like amelogenin nanoribbons template mineralization via a low-energy interface of ion binding sites ( Read More ) ...
... amelogenin. In all amplification reactions, positive and a negative PCR controls were used. ...
Molekulární biologie se zabývá studiem buněčných procesů na molekulární úrovni. Genetika se zabývá dědičností a proměnlivostí organismů a populací a jejími příčinami. Náplní první části předmětu je popis základů genetiky a struktury a funkce biologických makromolekul podílejících se na dědičnosti organismů (DNA, RNA, proteinů), jejich vzájemné interakce a regulace jejich funkce. Druhou polovinu předmětu představuje výklad a praktický nácvik základních experimentálních molekulárních metodik ...
Adding MMP20 to amelogenin-chitosan hydrogel improves biomimetic enamel repair. S. Prajapati, Q. RUAN, K. Mukherjee, J. ... Investigating the Cooperative Interaction of Amelotin and Amelogenin for Mineralization. University of Toronto, Faculty of ...
Segments of the SRY and Amelogenin X/Y genes for sex determination, additionally species-specific cytochrome b regions for ... AmelY Ce: Amelogenin Y marker specific for red deer, AmelY Cc Dd: Amelogenin Y marker specific for roe deer and fallow deer, ... AmelY Ce: Amelogenin Y marker specific for red deer, AmelY Cc Dd: Amelogenin Y marker specific for roe deer and fallow deer, ... Amelogenin X and Y alleles were separated on 2.5% agarose gel, the selected allele bands were cut from the gel and purified ...
On a family-relationship DNA test report, this is called the amelogenin gene. ...
Amelogenins: Multifaceted Proteins for Dental and Bone Formation and Repair. Frontiers in Protein and Peptide Sciences ...
8, 9, 26] Adamantinomatous craniopharyngiomas also express various enamel proteins, including amelogenin, enamelin, and ...
Requires amplification of intron 1 of amelogenin gene. *Amelogenin gene, found on X-Y homologous chromosomes, contains a 184 ...
... the first 8-dye STR multiplex and allows co-amplification and fluorescent detection of the 20 CODIS core loci plus Amelogenin ... Consists of Amelogenin, 23 autosomal STR loci, 11 Y-STR loci and two quality indicators in a single multiplex ... the first 8-dye STR multiplex and allows co-amplification and fluorescent detection of the 20 CODIS core loci plus Amelogenin ...
We examined 12 noncoding STR loci and the gender-specific amelogenin locus, labeled with 3 different dyes (6-FAM, BTG, or BTY ...

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