Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference125 articles.
1. Report on the 12th ENMC sponsored international workshop—The “limb-girdle” muscular dystrophies;Bushby;Neuromuscul. Disord.,1992
2. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995
3. Calpain 3 cleaves filamin C and regulates its ability to interact with gamma- and delta-sarcoglycans;Guyon;Muscle Nerve,2003
4. Calpain 3 participates in muscle remodeling by acting upstream of the ubiquitin-proteasome pathway;Kramerova;Hum. Mol. Genet.,2005
5. Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components;Taveau;Mol. Cell. Biol.,2003
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