A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay-Reference-Cited by-同舟云学术

A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay

Published:2007-02 Issue:2 Volume:17 Page:148-156
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Milic Astrid,Daniele Nathalie,Lochmüller Hanns,Mora Marina,Comi Giacomo P.,Moggio Maurizio,Noulet Fanny,Walter Maggie C.,Morandi Lucia,Poupiot Jérôme,Roudaut Carinne,Bittner Reginald E.,Bartoli Marc,Richard Isabelle

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference24 articles.

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2. The frequency of limb girdle muscular dystrophy 2A in Northeastern Italy;Fanin;Neuromuscul Disord,2005

3. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995

4. Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A;Ono;J Biol Chem,1998

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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