Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A

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Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1393-1402

Oxford University Press

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Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy

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Human Molecular Genetics, Vol. 15, Iss. 1, 2006-01 ,pp. : 23-31

Oxford University Press

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Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1

By Catoire Hlne   Pasco Matthieu Y.   Abu-Baker Aida   Holbert Sbastien   Tourette Cendrine   Brais Bernard   Rouleau Guy A.   Parker J. Alex   Nri Christian  

Human Molecular Genetics, Vol. 17, Iss. 14, 2008-07 ,pp. : 2108-2117

Oxford University Press

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The zebrafish as a model for muscular dystrophy and congenital myopathy

By Bassett David I.   Currie Peter D.  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 265-270

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

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

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