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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The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation

By Amack J.D.   Mahadevan M.S.  

Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1879-1887

Oxford University Press

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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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Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2

By Schalling M.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2165-2170

Oxford University Press

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Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat

By Alwazzan Madawi   Newman Emma   Hamshere Marion G.   Brook J. David   Harper P.   Brook J.D.   Fu Y.-H.   Mahadevan M.   Harley H.G.   Alwazzan M.   Boucher C.A.   Shaw D.J.   Jansen G.   Klesert T.R.   Thornton C.A.   Hamshere M.G.   Harley H.G.   Neville C.E.   Davis B.M.   Wang Y.H.   Wang Y.H.   Otten A.D.   Pearson C.E.   Jansen G.   Phillips A.V.   Maniatis T.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1491-1497

Oxford University Press

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