MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1

By de Haro María   Al-Ramahi Ismael   De Gouyon Beatrice   Ukani Lubna   Rosa Alberto   Faustino Nuno André   Ashizawa Tetsuo   Cooper Thomas A.   Botas Juan  

Human Molecular Genetics, Vol. 15, Iss. 13, 2006-07 ,pp. : 2138-2145

Oxford University Press

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CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1

By Ward Amanda J.   Rimer Mendell   Killian James M.   Dowling James J.   Cooper Thomas A.  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3614-3622

Oxford University Press

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Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1

By Koshelev Misha   Sarma Satyam   Price Roger E.   Wehrens Xander H.T.   Cooper Thomas A.  

Human Molecular Genetics, Vol. 19, Iss. 6, 2010-03 ,pp. : 1066-1075

Oxford University Press

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Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

By Lin Xiaoyan   Miller Jill W.   Mankodi Ami   Kanadia Rahul N.   Yuan Yuan   Moxley Richard T.   Swanson Maurice S.   Thornton Charles A.  

Human Molecular Genetics, Vol. 15, Iss. 13, 2006-07 ,pp. : 2087-2097

Oxford University Press

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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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