Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy

By Kayali Refik   Ku Jin-Mo   Khitrov Gregory   Jung Michael E.   Prikhodko Olga   Bertoni Carmen  

Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4007-4020

Oxford University Press

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Dissection of temporal gene expression signatures of affected and spared muscle groups in dystrophin-deficient ( mdx ) mice

By Porter J.D.  

Human Molecular Genetics, Vol. 12, Iss. 15, 2003-08 ,pp. : 1813-1821

Oxford University Press

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A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice

By Andrade F.H.  

Human Molecular Genetics, Vol. 11, Iss. 3, 2002-02 ,pp. : 263-272

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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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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