Acronym Finder

Ruin, stain, yellow, or macular degeneration, etc., the most common cause of blindness in the elderly. In this condition, the macula, or yellow stains destruction. The macula, the part light-sensitive retina and is responsible for the direct sight and it is obvious that for the exact jobs like reading and driving required.

ruin the yellow stains on two types: dry (Dry) and (Wet). Dry type Common has been about 90% of patients to this type of suffering. Type more usually, with the decline more severe and more serious is associated.

ruin the yellow stains in people over 65 years, Common have and more women to this disease. Most cases of this disease with increasing age, arise. This disease can be a complication of some medications as well. Also, it seems inheritance is also susceptible to this disease involved....

(lacquer heparin), a medical instruments auxiliaries, is mainly used as the path and the port injection are used and widely by medical institutions has been approved. Use when with or catheter within the venous goes to work and plays an important role. has many advantages, including: the safety, health, usability a few times, hole. size. easy to use, the price, and the best advantage it relieve the pain/ wound of the patient during the infusion.

features:
usable with catheters or vein thrombosis
made of excellent material (feet grade medical) and a perforation easily
having, or lacking,
sterile
certified by CE and ISO 13485
useful life of 5 years...

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....