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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Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

By Calado Angelo   Tomé Fernando M.S.  

Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2321-2328

Oxford University Press

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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

By Tagawa Kazuhiko  

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

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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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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