Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear poly(A)-binding protein with a single-domain intracellular antibody

By Verheesen Peter   de Kluijver Anna   van Koningsbruggen Silvana   de Haard Hans J.   van Ommen Gert-Jan B.   van der Maarel Silvère M.   Verrips C. Theo  

Human Molecular Genetics, Vol. 15, Iss. 1, 2006-01 ,pp. : 105-111

Oxford University Press

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Over-expression of BCL2 rescues muscle weakness in a mouse model of oculopharyngeal muscular dystrophy

By Davies Janet E.   Rubinsztein David C.  

Human Molecular Genetics, Vol. 20, Iss. 6, 2011-03 ,pp. : 1154-1163

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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Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy

By Abu-Baker Aida  

Human Molecular Genetics, Vol. 12, Iss. 20, 2003-10 ,pp. : 2609-2623

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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