Caveolinopathy – New mutations and additional symptoms-Reference-Cited by-同舟云学术

Caveolinopathy – New mutations and additional symptoms

Published:2008-07 Issue:7 Volume:18 Page:572-578
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Aboumousa Ahmed,Hoogendijk Jessica,Charlton Richard,Barresi Rita,Herrmann Ralf,Voit Thomas,Hudson Judith,Roberts Mark,Hilton-Jones David,Eagle Michelle,Bushby Kate,Straub Volker

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference27 articles.

1. Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy;Minetti;Nat Genet,1998

2. Identification of peptide and protein ligands for the caveolin-scaffolding domain. Implications for the interaction of caveolin with caveolae-associated proteins;Couet;J Biol Chem,1997

3. Caveolae and caveolin-3 in muscular dystrophy;Galbiati;Trends Mol Med,2001

4. Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarcolemma and co-fractionates with dystrophin and dystrophin-associated glycoproteins;Song;J Biol Chem,1996

5. Caveolin-3 directly interacts with the C-terminal tail of beta –dystroglycan. Identification of a central WW-like domain within caveolin family members;Sotgia;J Biol Chem,2000

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