Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy

By Hino Hirotake  

Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 181-190

Oxford University Press

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Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy

By Mitsuhashi Hiroaki   Mitsuhashi Satomi   Lynn-Jones Taylor   Kawahara Genri   Kunkel Louis M.  

Human Molecular Genetics, Vol. 22, Iss. 3, 2013-02 ,pp. : 568-577

Oxford University Press

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Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy

By Homma Sachiko   Beermann Mary Lou   Miller Jeffrey Boone  

Human Molecular Genetics, Vol. 20, Iss. 13, 2011-07 ,pp. : 2662-2672

Oxford University Press

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Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

By Baker Naomi L.  

Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 279-293

Oxford University Press

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Absence of α7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy

By Guo Chun   Willem Michael   Raivich Gennadij   Emerson Michael   Neyses Ludwig   Mayer Ulrike  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 989-998

Oxford University Press

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