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Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A.
J Biol Chem. 1998 Jul 3;273(27):17073-8. doi: 10.1074/jbc.273.27.17073.
J Biol Chem. 1998.
PMID: 9642272
Free article.
Multiple molecular interactions implicate the connectin/titin N2A region as a modulating scaffold for p94/calpain 3 activity in skeletal muscle.
Hayashi C, Ono Y, Doi N, Kitamura F, Tagami M, Mineki R, Arai T, Taguchi H, Yanagida M, Hirner S, Labeit D, Labeit S, Sorimachi H.
Hayashi C, et al.
J Biol Chem. 2008 May 23;283(21):14801-14. doi: 10.1074/jbc.M708262200. Epub 2008 Feb 29.
J Biol Chem. 2008.
PMID: 18310072
Free article.
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