Proteasome Inhibitor (MG-132) Treatment of mdx Mice Rescues the Expression and Membrane Localization of Dystrophin and Dystrophin-Associated Proteins-Reference-Cited by-同舟云学术

Proteasome Inhibitor (MG-132) Treatment of mdx Mice Rescues the Expression and Membrane Localization of Dystrophin and Dystrophin-Associated Proteins

Published:2003-10 Issue:4 Volume:163 Page:1663-1675
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Bonuccelli Gloria,Sotgia Federica,Schubert William,Park David S.,Frank Philippe G.,Woodman Scott E.,Insabato Luigi,Cammer Michael,Minetti Carlo,Lisanti Michael P.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference45 articles.

1. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

2. Membrane organization of the dystrophin-glycoprotein complex;Ervasti;Cell,1991

3. Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy;Brenman;Cell,1995

4. Caveolin-3 is not an essential component of the dystrophin glycoprotein complex;Crosbie;FEBS Lett,1998

5. 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

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