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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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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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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Muscle-specific BCL2 expression ameliorates muscle disease in laminin α2-deficient, but not in dystrophin-deficient, mice

By Dominov Janice A.   Kravetz Amanda J.   Ardelt Magdalena   Kostek Christine A.   Beermann Mary Lou   Miller Jeffrey B.  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1029-1040

Oxford University Press

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Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin

By Gilbert Rénald  

Human Molecular Genetics, Vol. 12, Iss. 11, 2003-06 ,pp. : 1287-1299

Oxford University Press

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