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Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice

  • Published:2012-07-13 Issue:20 Volume:21 Page:4378-4393
  • ISSN:1460-2083
  • Container-title:Human Molecular Genetics
  • language:en
  • Short-container-title:

Author:

Marshall Jamie L.,Chou Eric,Oh Jennifer,Kwok Allan,Burkin Dean J.,Crosbie-Watson Rachelle H.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference80 articles.

1. Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies;Bonnemann;Semin. Pediatr. Neurol.,2002

2. Cell-matrix interactions in muscle disease;Carmignac;J. Pathol.,2012

3. Dystrophin, its interactions with other proteins, and implications for muscular dystrophy;Ervasti;Biochem. Biophys. Acta,2007

4. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix;Ibraghimov-Beskrovnaya;Nature,1992

5. Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization;Ibraghimov-Beskrovnaya;Hum. Mol. Genet.,1993
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