Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

Clicks: 269
ID: 273954
2009
Free PDF
Article Quality & Performance Metrics
Overall Quality Improving Quality
0.0 /100
Combines engagement data with AI-assessed academic quality
AI Quality Assessment
Not analyzed
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 …
Reference Key
c2009themembrane Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Cai C;Weisleder N;Ko JK;Komazaki S;Sunada Y;Nishi M;Takeshima H;Ma J;;
Journal The Journal of biological chemistry
Year 2009
DOI
DOI not found
URL
https://www.ncbi.nlm.nih.gov/pubmed/19380584
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

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.