Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy-Reference-Cited by-同舟云学术

Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy

Published:2013-05-28 Issue:6 Volume:136 Page:1718-1731
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Ottenheijm Coen A. C.,Buck Danielle,de Winter Josine M.,Ferrara Claudia,Piroddi Nicoletta,Tesi Chiara,Jasper Jeffrey R.,Malik Fady I.,Meng Hui,Stienen Ger J. M.,Beggs Alan H.,Labeit Siegfried,Poggesi Corrado,Lawlor Michael W.,Granzier Henk

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/136/6/1718/11140667/awt113.pdf

Reference48 articles.

1. Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene;Anderson;Hum Genet,2004

2. Nebulin plays a direct role in promoting strong actin-myosin interactions;Bang;FASEB J,2009

3. Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle;Bang;J Cell Biol,2006

4. Rate of force generation in muscle: correlation with actomyosin ATPase activity in solution;Brenner;Proc Natl Acad Sci USA,1986

5. Differential splicing of the large sarcomeric protein nebulin during skeletal muscle development;Buck;J Struct Biol,2010

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