The artificial gene Jazz, a transcriptional regulator of utrophin, corrects the dystrophic pathology in mdx mice

By Di Certo Maria Grazia   Corbi Nicoletta   Strimpakos Georgios   Onori Annalisa   Luvisetto Siro   Severini Cinzia   Guglielmotti Angelo   Batassa Enrico Maria   Pisani Cinzia   Floridi Aristide   Benassi Barbara   Fanciulli Maurizio   Magrelli Armando   Mattei Elisabetta   Passananti Claudio  

Human Molecular Genetics, Vol. 19, Iss. 5, 2010-03 ,pp. : 752-760

Oxford University Press

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Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice

By Enwere Emeka K.   Boudreault Louise   Holbrook Janelle   Timusk Kristen   Earl Nathalie   LaCasse Eric   Renaud Jean-Marc   Korneluk Robert G.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 867-878

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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Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology

By Spencer M.J.  

Human Molecular Genetics, Vol. 11, Iss. 21, 2002-10 ,pp. : 2645-2655

Oxford University Press

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Targeted inhibition of Ca 2+ /calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle

By Chakkalakal Joe V.   Michel Stephanie A.   Chin Eva R.   Michel Robin N.   Jasmin Bernard J.  

Human Molecular Genetics, Vol. 15, Iss. 9, 2006-05 ,pp. : 1423-1435

Oxford University Press

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