Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy

Published:2012-04-20 Issue:14 Volume:21 Page:3237-3254
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Friedrich Felix W.,Wilding Brendan R.,Reischmann Silke,Crocini Claudia,Lang Patrick,Charron Philippe,Müller Oliver J.,McGrath Meagan J.,Vollert Ingra,Hansen Arne,Linke Wolfgang A.,Hengstenberg Christian,Bonne Gisèle,Morner Stellan,Wichter Thomas,Madeira Hugo,Arbustini Eloisa,Eschenhagen Thomas,Mitchell Christina A.,Isnard Richard,Carrier Lucie

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/14/3237/17256603/dds157.pdf

Reference63 articles.

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3. Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication;Brown;J. Biol. Chem.,1999

4. Skeletal muscle LIM protein 1 regulates integrin-mediated myoblast adhesion, spreading, and migration;Robinson;Am. J. Physiol. Cell Physiol.,2003

5. The transcriptional coactivator FHL2 transmits Rho signals from the cell membrane into the nucleus;Muller;EMBO J.,2002

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