Stra13 regulates oxidative stress mediated skeletal muscle degeneration

By Vercherat Ccile   Chung Teng-Kai   Yalcin Safak   Gulbagci Neriman   Gopinadhan Suma   Ghaffari Saghi   Taneja Reshma  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4304-4316

Oxford University Press

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Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle

By Kramerova Irina   Kudryashova Elena   Wu Benjamin   Ottenheijm Coen   Granzier Henk   Spencer Melissa J.  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3271-3280

Oxford University Press

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Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

By Diaz Francisca  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2737-2748

Oxford University Press

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-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle

By Quinlan Kate G.R.   Seto Jane T.   Turner Nigel   Vandebrouck Aurelie   Floetenmeyer Matthias   Macarthur Daniel G.   Raftery Joanna M.   Lek Monkol   Yang Nan   Parton Robert G.   Cooney Gregory J.   North Kathryn N.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1335-1346

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Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis

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Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 303-314

Oxford University Press

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