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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Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila

By Houseley Jonathan M.  

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 873-883

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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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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Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts

By Machuca-Tzili Laura   Thorpe Helena   Robinson Thelma   Sewry Caroline   Brook J.  

Human Genetics, Vol. 120, Iss. 4, 2006-11 ,pp. : 487-499

Springer Publishing Company

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