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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Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx mice

By Kim Michelle H.   Kay Danielle I.   Rudra Renuka T.   Chen Bo Ming   Hsu Nigel   Izumiya Yasuhiro   Martinez Leonel   Spencer Melissa J.   Walsh Kenneth   Grinnell Alan D.   Crosbie Rachelle H.  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1324-1338

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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Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice

By Ito Kaori   Kimura Shigemi   Ozasa Shiro   Matsukura Makoto   Ikezawa Makoto   Yoshioka Kowashi   Ueno Hiroe   Suzuki Misao   Araki Kimi   Yamamura Ken-ichi   Miwa Takeshi   Dickson George   Thomas Gail D.   Miike Teruhisa  

Human Molecular Genetics, Vol. 15, Iss. 14, 2006-07 ,pp. : 2266-2275

Oxford University Press

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Delivery of a read-through inducing compound, TC007, lessens the severity of a spinal muscular atrophy animal model

By Mattis Virginia B.   Ebert Allison D.   Fosso Marina Y.   Chang Cheng-Wei   Lorson Christian L.  

Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3906-3913

Oxford University Press

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