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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Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle

By Dickson G.  

Human Molecular Genetics, Vol. 11, Iss. 15, 2002-07 ,pp. : 1719-1730

Oxford University Press

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Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice

By Verma Mayank   Asakura Yoko   Hirai Hiroyuki   Watanabe Shuichi   Tastad Christopher   Fong Guo-Hua   Ema Masatsugu   Call Jarrod A.   Lowe Dawn A.   Asakura Atsushi  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4145-4159

Oxford University Press

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SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

By Riessland Markus   Ackermann Bastian   Frster Anja   Jakubik Miriam   Hauke Jan   Garbes Lutz   Fritzsche Ina   Mende Ylva   Blumcke Ingmar   Hahnen Eric   Wirth Brunhilde  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1492-1506

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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