Acronym Finder

Protein number 1 contains the second and bind to the nucleotide, a receptor is a protein that in humans is Gene "NOD1" code. This receiver, a bacteria identified and the reaction of immune stimulation.

This protein contain "the second card (CARD)" and is one of the family members, the receiver pseudo-NOD and also one of the receptors identified pattern within the cell....

Syndrome, or or the abbreviation PS, a group of genetic diseases are rare that person with your much older than the age at which. shows. So-called Syndrome , etc. is not necessarily the same . But your some kind of Syndrome .

this syndrome is very rare, and of every 8 million babies., the only one to be afflicted with it. This syndrome hereditary? i.e. gene in the parents causing the disease. but also due to a genetic mutation happens. People who have this syndrome. the first sign at the same time in neonates with things like weight, lack., the dimensions of the face and small jaw, the analysis has gone to update their. Later syndrome your skin, fill wrinkles, atherosclerosis, etc., kidney failure, etc. going. stiff and hardening of the skin in the body and hair loss show.

a few of these patients over 13 years of work and 90% of them result in a heart attack....

ZMPSTE24 is the name of a gene in humans. The protein that this gene is achieved. a is making A company.

in humans, mutations in this gene cause premature aging. Basically, the defects in the construction of the correct protein fairy A, caused a disruption in the regeneration of DNA....

Muscular dystrophy, Limbe , etc. (with the symbol abbreviations LGMD), a genetically reveal an important heterogeneity has been and symptoms of the disease includes weakness of the primary muscles of the hip and shoulder can be followed by the muscles of the part hands and feet are also involved. Analysis of continuity of genes to the disease in the families and in families with married families showed that at least 11 loci for different responsible for Muscular Dystrophy, Limb Girdle; these are Turtles In that proteins (Sarcoglycan) in the code are continuous with the disease. Bug in prevented from binding F-actin with the extracellular matrix by these tests are used and, finally, the muscle cells degenerated, and the ability of the muscles disappears....

Viewing the scheduled for a diagnosis of autism (ADOS) is an instrument for diagnosis and assessment of autism. It includes a series of acts structured and semi-structured that includes social interaction between the patient and the specialist. Expert behavior, the child's view. identifies and groups pre-specified assignment.

ADOS set of tests, structured and semi-structured, which is about 30 to 60 Minutes is all it takes. During this time, experimenter a series of positions to check the communication and social relations related to the diagnosis of autism provides.

each sample with one of the 4 methods below will be checked. Choose the appropriate method based on the developmental and language level of the person. The only group that can't be tested here. Teen, Teen and adult nonverbal.

ADOS should not be used for formal diagnosis with people who are blind, deaf, or seriously impaired sensory or motor (e.g., disorders such as cerebral palsy or muscular dystrophy). should not be used.

Method 1: for children who can't speak, or sentences short.

Method 2: people who can such Express, but not speak.
Method 3: larger samples that speak fluent
method 4: for, and, that the soul can speak.
since which in methods 1 and 2., the sample must be in the room., motor ability in them is essential.

examples of modules 1 or 2, response to name, Social smile, or the bubble game. Module 3 or 4, the game involves mutual communication and show empathy or express thoughts about the feelings of others....

Diss proxy verbal evolutionary or the abbreviation "DVD" is the name speech in childhood (CAS) and evolutionary speech (DAS) also known as? disorder in which the child on speech sounds, phonemes, syllables, and words is in trouble. The cause of this disorder, weakness or paralysis of muscle, but forms in the brain is not able between the members and the muscles related to speech (lips, jaws, etc. language, etc.) the harmony of creation. Babe knows what wants to say, but his brain could not between the movements of the muscles that to express words and letter, are essential., the harmony of creation. The real cause of this disorder is yet to be determined, but some evidence suggests that the reasons may be genetic. what that a lot of people in their families, etc. problems in verbal communication there is. The disease, treatment, definite, and complete. but with the use of appropriate interventions, etc., focused, and ongoing therapy, etc., verbal skills, people with this disorder of motor speech, as substantially be improved.
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FOXP2 as a complete protein Pi 2 box is a protein that in humans is Gene, "FOXP2" is coded. The gene name, such as "CAGH44 a", "SPCH1" or "TNRC10" are, and the direction of evolution, correct the power of speech and language learning in humans is essential. This gene in many other vertebrates, there is also in them, plays an important role in the creation of the connection (for example, creating the sound of the birds) plays.

FOXP2, the first gene is associated with language and the word was discovered. This gene on the long arm of chromosome 7 located in the brain, heart, lungs and intestines of the fetus and the adult human express. Also, making another of these genes in other mammals have been found and the map gene, complete it in hand. This gene in both of them more active than male, and this issue maybe is the reason for skills more learning language in women (compared to men).

in humans, mutations in this gene cause severe disorders of verbal and verbal. Since version similar of this gene in other vertebrates. there is a survey done on it in mice, and bird singers has shown that the existence of this gene for the flexibility of the neural circuits of the brain is essential. Apart from the brain. the presence of the gene for the natural evolution of the gut and the heart, too, is necessary.

FOXP2 "gene language" reputation. but it should be noted that gene, is another important in the evolution of verbal and language, human role, that of it among the can be to CNTNAP2, etc. CTBP1 and SRPX2 noted.

gene FOXP2 in humans and chimpanzees, only in 2 amino acid differences, but only one of these differences, dual, etc. specific human....

Protein FOXP3 that with the name "" (Scurfin) is also known. is a protein that in response, a safety device body involved. This molecule component of the protein family, FOX and is a main regulator in the process of organizing the expression of genes in the context of the evolution and function of lymphocytes, t-regulator can be considered. Lymphocytes, t-regulator, in total they reduce the immune response. In the flow of cancer, increase the activity of the lymphocytes caused by your body's immune system fails to well with the cancer cells fight. When the incidence of disease, autoimmune disease, reducing the activity of lymphocytes, t-regulator causes other immune cells to the tissue itself in the body, attacking.

although the exact mechanism of control and regulation of these molecules has not yet determined. the protein, FOX, themselves, belong to the large family system factors, transcription spiral winged/ that are probably the same verb can increase free radicals connection used in the flow regulating transcription of a DNA. used.

in the model, system, lymphocytes, t-regulator, transcription factor FOXP3, etc. the promoter gene involved in the performance of this type of lymphocytes has occupied, and possibly after stimulation, receptors, lymphocytes, t -, thereby transcribe genes, the main and most important in this field.

the gene coding FOXP3 has 11 exons and has been on the arm of the short chromosome X (in particular, the position Xp11.23) is located.

apart the role that FOXP3 in the field of differentiation of lymphocytes, t-regulator has the evidence several of the important role of this gene and in the creation of cancer there is. This gene is probably a gene repressive and tumor reducing activities that in the examples of breast cancer, prostate cancer and ovarian cancer have been reported.

protein, FOXP3 herself enzymes, antineoplastic, such as CD8 + and CD39. Hyperactivity CD39 in patients with melanoma, cancer, blood, cancer of the pancreas, colon cancer and ovarian cancer have been reported.

the mutation or disorder in the direction of the regulator Foxp3, leading to the occurrence of diseases autoimmune disease is specific to tissue, such as autoimmune or type 1....