Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy-Reference-Cited by-同舟云学术

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy

Published:2011-06-19 Issue:7 Volume:18 Page:840-845
ISSN:1545-9993
Container-title:Nature Structural & Molecular Biology
language:en
Short-container-title:Nat Struct Mol Biol

Author:

Rau Frédérique,Freyermuth Fernande,Fugier Charlotte,Villemin Jean-Philippe,Fischer Marie-Christine,Jost Bernard,Dembele Doulaye,Gourdon Geneviève,Nicole Annie,Duboc Denis,Wahbi Karim,Day John W,Fujimura Harutoshi,Takahashi Masanori P,Auboeuf Didier,Dreumont Natacha,Furling Denis,Charlet-Berguerand Nicolas

Publisher

Springer Science and Business Media LLC

Subject

Molecular Biology,Structural Biology

Link

http://www.nature.com/articles/nsmb.2067.pdf

Reference60 articles.

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2. Fu, Y.H. et al. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science 255, 1256–1258 (1992).

3. Mahadevan, M. et al. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene. Science 255, 1253–1255 (1992).

4. Liquori, C.L. et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 293, 864–867 (2001).

5. Miller, J.W. et al. Recruitment of human muscleblind proteins to (CUG)n expansions associated with myotonic dystrophy. EMBO J. 19, 4439–4448 (2000).

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