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Literature DB >> 11486078

Biomedicine. Reconstructing myotonic dystrophy.

S J Tapscott¹, C A Thornton.

Abstract

Entities: Chemical Disease

Mesh：

Substances：

Year: 2001 PMID： 11486078 DOI： 10.1126/science.1063517

Source DB: PubMed Journal: Science ISSN： 0036-8075 Impact factor: 47.728

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Cited

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11 in total

Review 1. Structures of trinucleotide repeats in human transcripts and their functional implications.

Authors: Anna Jasinska; Gracjan Michlewski; Mateusz de Mezer; Krzysztof Sobczak; Piotr Kozlowski; Marek Napierala; Wlodzimierz J Krzyzosiak
Journal: Nucleic Acids Res Date: 2003-10-01 Impact factor: 16.971

Review 2. Pathogenesis of spinocerebellar ataxias viewed from the RNA perspective.

Authors: Gracjan Michlewski; Wlodzimierz J Krzyzosiak
Journal: Cerebellum Date: 2005 Impact factor: 3.847

Review 3. Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.

Authors: Laura P W Ranum; John W Day
Journal: Curr Neurol Neurosci Rep Date: 2002-09 Impact factor: 5.081

4. RNA structure of trinucleotide repeats associated with human neurological diseases.

Authors: Krzysztof Sobczak; Mateusz de Mezer; Gracjan Michlewski; Jacek Krol; Wlodzimierz J Krzyzosiak
Journal: Nucleic Acids Res Date: 2003-10-01 Impact factor: 16.971

5. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.

Authors: Yoshio Ikeda; Joline C Dalton; Melinda L Moseley; Kathy L Gardner; Thomas D Bird; Tetsuo Ashizawa; William K Seltzer; Massimo Pandolfo; Aubrey Milunsky; Nicholas T Potter; Mikio Shoji; John B Vincent; John W Day; Laura P W Ranum
Journal: Am J Hum Genet Date: 2004-05-19 Impact factor: 11.025

Biomedicine. Reconstructing myotonic dystrophy.

Review 1. Structures of trinucleotide repeats in human transcripts and their functional implications.

Review 2. Pathogenesis of spinocerebellar ataxias viewed from the RNA perspective.

Review 3. Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.

4. RNA structure of trinucleotide repeats associated with human neurological diseases.

5. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.

6. RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression.

7. The evolution of infrahissian conduction time in myotonic dystrophy patients: clinical implications.

8. CAG repeats mimic CUG repeats in the misregulation of alternative splicing.

9. Mutant DMPK 3'-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD.

10. RNA toxicity is a component of ataxin-3 degeneration in Drosophila.