Absence of α7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy

By Guo Chun   Willem Michael   Raivich Gennadij   Emerson Michael   Neyses Ludwig   Mayer Ulrike  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 989-998

Oxford University Press

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Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy

By Kimura En   Han Jay J.   Li Sheng   Fall Brent   Ra Jennifer   Haraguchi Miki   Tapscott Stephen J.   Chamberlain Jeffrey S.  

Human Molecular Genetics, Vol. 17, Iss. 16, 2008-08 ,pp. : 2507-2517

Oxford University Press

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Animal models for muscular dystrophy: valuable tools for the development of therapies

By Allamand Valérie   Campbell KevinP.  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2459-2467

Oxford University Press

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Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for Duchenne muscular dystrophy

By Ahmad A.  

Human Molecular Genetics, Vol. 9, Iss. 17, 2000-10 ,pp. : 2507-2515

Oxford University Press

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Temporal gene expression profiling of dystrophin-deficient ( mdx ) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy

By Porter John D.  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 257-269

Oxford University Press

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