Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy-Reference-Cited by-同舟云学术

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy

Published:2011-05-29 Issue:6 Volume:17 Page:720-725
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Fugier Charlotte,Klein Arnaud F,Hammer Caroline,Vassilopoulos Stéphane,Ivarsson Ylva,Toussaint Anne,Tosch Valérie,Vignaud Alban,Ferry Arnaud,Messaddeq Nadia,Kokunai Yosuke,Tsuburaya Rie,de la Grange Pierre,Dembele Doulaye,Francois Virginie,Precigout Guillaume,Boulade-Ladame Charlotte,Hummel Marie-Christine,de Munain Adolfo Lopez,Sergeant Nicolas,Laquerrière Annie,Thibault Christelle,Deryckere François,Auboeuf Didier,Garcia Luis,Zimmermann Pascale,Udd Bjarne,Schoser Benedikt,Takahashi Masanori P,Nishino Ichizo,Bassez Guillaume,Laporte Jocelyn,Furling Denis,Charlet-Berguerand Nicolas

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2374.pdf

Reference40 articles.

1. Brook, J.D. et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68, 799–808 (1992).

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. Philips, A.V., Timchenko, L.T. & Cooper, T.A. Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. Science 280, 737–741 (1998).

Cited by 279 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. SRSF2 is a key player in orchestrating the directional migration and differentiation of MyoD progenitors during skeletal muscle development;eLife;2024-09-09

2. SRSF2 is a key player in orchestrating the directional migration and differentiation of MyoD progenitors during skeletal muscle development;eLife;2024-09-09

3. RNA mis-splicing in children with myotonic dystrophy is associated with physical function;2024-07-03

4. SRSF2 is a key player in orchestrating the directional migration and differentiation of MyoD progenitors during skeletal muscle development;2024-06-03

5. Amphiphysin-2 (BIN1) functions and defects in cardiac and skeletal muscle;Trends in Molecular Medicine;2024-06