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Dystrophin

More information in Books or onNLM PubMed
Definition: A muscle protein localized in surface membranes which is the product of the Duchenne/Becker muscular dystrophy gene. Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while those with Becker muscular dystrophy have dystrophin of an altered size. It shares features with other cytoskeletal proteins such as SPECTRIN and alpha-actinin but the precise function of dystrophin is not clear. One possible role might be to preserve the integrity and alignment of the plasma membrane to the myofibrils during muscle contraction and relaxation. MW 400 kDa.  a muscle protein: see MeSH definition for relation to musc dystrophy; /biosyn /drug eff /physiol /ultrastruct permitted   
See Also Mice, Inbred mdx; Muscular Dystrophy, Duchenne
 
SubstanceCAS Registry & nameCategoriesSourceDrugs*
Dp260 protein, mouse  0   *Dystrophin.
DMD protein, human  0   *Dystrophin.
dys-1 protein, C elegans  0   *Dystrophin *Caenorhabditis elegans Proteins. Neurogenetics 1998 Dec;2(1):61-72
Dp260 protein, rat  0   *Dystrophin. Hum Mol Genet 1995 May;4(5):837-42
140-kDa dystrophin  0   *Dystrophin. Hum Mol Genet 1995 Mar;4(3):329-35
Dmd protein, rat  0   *Dystrophin. Hum Mol Genet 1994 Aug;3(8):1309-16
apo-dystrophin 1  0   *Dystrophin. Hum Mol Genet 1993 Nov;2(11):1883-8

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
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