Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle

By Kramerova Irina   Kudryashova Elena   Wu Benjamin   Germain Sean   Vandenborne Krista   Romain Nadine   Haller Ronald G.   Verity M. Anthony   Spencer Melissa J.  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3194-3205

Oxford University Press

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In vivo electrotransfer of the cardiotrophin-1 gene into skeletal muscle slows down progression of motor neuron degeneration in pmn mice

By Lesbordes J-C.  

Human Molecular Genetics, Vol. 11, Iss. 14, 2002-07 ,pp. : 1615-1625

Oxford University Press

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Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice

By Wong Margaret   Martin Lee J.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2284-2302

Oxford University Press

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Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration

By Vlachantoni Dafni   Bramall Alexa N.   Murphy Michael P.   Taylor Robert W.   Shu Xinhua   Tulloch Brian   Van Veen Theo   Turnbull Douglass M.   McInnes Roderick R.   Wright Alan F.  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 322-335

Oxford University Press

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The asthma-associated ORMDL3 gene product regulates endoplasmic reticulum-mediated calcium signaling and cellular stress

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Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 111-121

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