Acronym Finder

Bank data, global protein, which briefly \"wwPDB\", also called the agency that archives the structure of the macromolecule, have maintenance and updated. Mission it is the management and maintenance of an Archive database, the protein isolated from the data, the structural macromolecule is to be public and free available community.

organization in 2003 (ad) has been established and the establishment of the manufacturers, it is the committee collaboration research for the database bioinformatics, structural (United States), bank data protein in Europe, and bank data protein Japan have been. In 2006, the bank data of the resonance magnetic bio (from the USA) to the organization joined. The base and the each of the members can be given the structural accepted and Case Processing. Data processed to the holder of the archive are sent. Now, workgroup collaboration research for the database bioinformatics, structural as the holder of the archive activity. The issue of ensuring part of it is just a version of that data for all users is identical. Database modified, then available to other members placed. Then, each of the members, records the structural result through your site, at the disposal of the public. The information on the site is the only link to the site, members is accessible. Site, members, something over the site, The Mirror holder of the archive (the Working Group on a research collaboration for the database bioinformatics, structural). because the members on the site, different devices for the analysis and review of data, the database can provide....

The second card (CARD domain), or "the second, absorption " or "the second, absorption, and strengthen the " that refer to "CARDs". the motif of the Interactive an important that are in a range of proteins (especially the ones in inflammation and apoptosis play a role) are found.

This is the second, in forming the building complex in the protein, through the interplay between CARDs. effective.

second, the CARD in a wide range of proteins, such as the " a", " a", ", a", "" and other factors, cytoplasmic are found....

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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