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Full-length dystrophin expression in half of the heart cells ameliorates β-isoproterenol-induced cardiomyopathy in mdx mice

Gene therapy holds great promise for curing Duchenne muscular dystrophy (DMD), the most common fatal inherited childhood muscle disease. Success of DMD gene therapy depends upon functional improvement in both skeletal and cardiac muscle. Numerous gene transfer studies have been performed to correct...

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Detalhes bibliográficos
Main Authors: Yue, Yongping, Skimming, Jeffrey W., Liu, Mingju, Strawn, Tammy, Duan, Dongsheng
Formato: Artigo
Idioma:Inglês
Publicado em: 2004
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2431460/
https://ncbi.nlm.nih.gov/pubmed/15190010
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddh174
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