Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin
Abstract
Defective membrane repair can contribute to the progression of muscular dystrophy. Although mutations in caveolin-3 (Cav3) and dysferlin are linked to muscular dystrophy in human patients, the molecular mechanism underlying the functional interplay between Cav3 and dysferlin in membrane repair of mu …
Keywords
National Center for Biotechnology Information
NCBI
NLM
MEDLINE
Mice
animals
humans
pubmed abstract
nih
national institutes of health
national library of medicine
research support
non-u.s. gov't
N.I.H.
Extramural
plasmids
mutation
transgenic
transfection
carrier proteins / genetics*
muscle
carrier proteins / metabolism
membrane proteins / metabolism
dna repair / genetics*
skeletal / pathology
skeletal / physiopathology
pmid:19380584
pmc2708885
doi:10.1074/jbc.m109.009589
chuanxi cai
noah weisleder
jianjie ma
caveolin 3 / genetics*
caveolin 3 / metabolism
dysferlin
membrane proteins / genetics*
muscle proteins / genetics*
muscle proteins / metabolism
muscular dystrophies / genetics*
muscular dystrophies / pathology
myoblasts / physiology
sarcolemma / physiology
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273954
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