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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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Autors principals: Yue, Yongping, Skimming, Jeffrey W., Liu, Mingju, Strawn, Tammy, Duan, Dongsheng
Format: Artigo
Idioma:Inglês
Publicat: 2004
Matèries:
Accés en línia: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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