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Article

Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis

1 Jun 1994

Abstract excerpt

Duchenne muscular dystrophy (DMD) and the myopathy seen in the mdx mouse both result from absence of the protein dystrophin. Structural similarities between dystrophin and other cytoskeletal proteins, its enrichment at myotendinous junctions, and its indirect association with laminin mediated by a transmembrane glycoprotein complex suggest that one of dystrophin's functions in normal muscle is to form one of the...

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PMID: 7962191
DOI: 10.1242/jcs.107.6.1477

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Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosisPMID 7962191Read ↗

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