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Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy.

Mutations in genes coding for dystrophin, for alpha, beta, gamma, and delta-sarcoglycans, or for the alpha2 chain of the basement membrane component merosin (laminin-2/4) cause various forms of muscular dystrophy. Analyses of integrins showed an abnormal expression and localization of alpha7beta1 is...

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Detalhes bibliográficos
Main Authors: Vachon, P H, Xu, H, Liu, L, Loechel, F, Hayashi, Y, Arahata, K, Reed, J C, Wewer, U M, Engvall, E
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC508374/
https://ncbi.nlm.nih.gov/pubmed/9312189
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