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

By Davies Janet E.   Sarkar Sovan   Rubinsztein David C.  

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

Oxford University Press

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Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy

By Kayali Refik   Ku Jin-Mo   Khitrov Gregory   Jung Michael E.   Prikhodko Olga   Bertoni Carmen  

Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4007-4020

Oxford University Press

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Prevention of oculopharyngeal muscular dystrophy by muscular expression of Llama single-chain intrabodies in vivo

By Chartier Aymeric   Raz Vered   Sterrenburg Ellen   Verrips C. Theo   van der Maarel Silvre M.   Simonelig Martine  

Human Molecular Genetics, Vol. 18, Iss. 10, 2009-05 ,pp. : 1849-1859

Oxford University Press

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