Over-expression of BCL2 rescues muscle weakness in a mouse model of oculopharyngeal muscular dystrophy

By Davies Janet E.   Rubinsztein David C.  

Human Molecular Genetics, Vol. 20, Iss. 6, 2011-03 ,pp. : 1154-1163

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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A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

By Malicdan May Christine V.   Noguchi Satoru   Nonaka Ikuya   Hayashi Yukiko K.   Nishino Ichizo  

Human Molecular Genetics, Vol. 16, Iss. 2, 2007-01 ,pp. : 115-128

Oxford University Press

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Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

By Wang Yuexia   Herron Alan J.   Worman Howard J.  

Human Molecular Genetics, Vol. 15, Iss. 16, 2006-08 ,pp. : 2479-2489

Oxford University Press

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Ku70 regulates Bax-mediated pathogenesis in laminin-2-deficient human muscle cells and mouse models of congenital muscular dystrophy

By Vishnudas Vivek K.   Miller Jeffrey Boone  

Human Molecular Genetics, Vol. 18, Iss. 23, 2009-12 ,pp. : 4467-4477

Oxford University Press

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