The kyphoscoliosis ( ky ) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein

By van Mier P.  

Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 9-16

Oxford University Press

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The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression

By Kim Y-J.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1129-1139

Oxford University Press

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Temporal gene expression profiling of dystrophin-deficient ( mdx ) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy

By Porter John D.  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 257-269

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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Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres

By Trollet Capucine   Anvar Seyed Yahya   Venema Andrea   Hargreaves Iain P.   Foster Keith   Vignaud Alban   Ferry Arnaud   Negroni Elisa   Hourde Christophe   Baraibar Martin A.   't Hoen Peter A.C.   Davies Janet E.   Rubinsztein David C.   Heales Simon J.   Mouly Vincent   van der Maarel Silvre M.   Butler-Browne Gillian   Raz Vered   Dickson George  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2191-2207

Oxford University Press

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