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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Molecular mechanisms responsible for aberrant splicing of SERCA1 in myotonic dystrophy type 1

By Hino Shin-ichiro   Kondo Shinichi   Sekiya Hiroshi   Saito Atsushi   Kanemoto Soshi   Murakami Tomohiko   Chihara Kazuyasu   Aoki Yuri   Nakamori Masayuki   Takahashi Masanori P.   Imaizumi Kazunori  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2834-2843

Oxford University Press

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Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy

By Ho Thai H.   Bundman Donnie   Armstrong Dawna L.   Cooper Thomas A.  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1539-1547

Oxford University Press

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Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons

By Jiang Hong  

Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3079-3088

Oxford University Press

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Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca 2+ -ATPase in myotonic dystrophy type 1

By Kimura Takashi  

Human Molecular Genetics, Vol. 14, Iss. 15, 2005-08 ,pp. : 2189-2200

Oxford University Press

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