Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins

By Voit T.  

Human Molecular Genetics, Vol. 12, Iss. 19, 2003-10 ,pp. : 2467-2479

Oxford University Press

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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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Autosomal Glycogenosis of Liver and Muscle Due to Phosphorylase Kinase Deficiency is Caused by Mutations in the Phosphorylase Kinase β Subunit ( PHKB )

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Human Molecular Genetics, Vol. 6, Iss. 7, 1997-01 ,pp. : 1109-1115

Oxford University Press

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

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

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An Actn3 knockout mouse provides mechanistic insights into the association between -actinin-3 deficiency and human athletic performance

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Human Molecular Genetics, Vol. 17, Iss. 8, 2008-04 ,pp. : 1076-1086

Oxford University Press

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