Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F

Author:

Peter Angela K.,Miller Gaynor,Capote Joana,DiFranco Marino,Solares-Pérez Alhondra,Wang Emily L.,Heighway Jim,Coral-Vázquez Ramón M.,Vergara Julio,Crosbie-Watson Rachelle H.

Funder

NIH NIGMS

American Heart Association

Muscular Dystrophy Association

NIH

National Institutes of Health

Consejo Nacional de Investigaciones Científicas y Técnicas

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Orthopedics and Sports Medicine

Reference51 articles.

1. Crosbie RH, Heighway J, Venzke DP, Lee JC, Campbell KP. Sarcospan: the 25 kDa transmembrane component of the dystrophin-glycoprotein complex. J Biol Chem. 1997;272:31221–4.

2. Ervasti JM, Campbell KP. Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy. Mol Cell Biol Hum Dis Ser. 1993;3:139–66.

3. Campbell KP, Kahl SD. Association of dystrophin and an integral membrane glycoprotein. Nature. 1989;338:259–62.

4. Ervasti JM, Kahl SD, Campbell KP. Purification of dystrophin from skeletal muscle. J Biol Chem. 1991;266:9161–5.

5. Ervasti JM, Ohlendieck K, Kahl SD, Gaver MG, Campbell KP. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature. 1990;345:315–9.

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