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Nat Rev Mol Cell Biol. 2006 Oct;7(10):762-73. Epub 2006 Sep 13.

Molecular mechanisms of muscular dystrophies: old and new players.

Author information

1
Department of Physiology, Anatomy and Genetics, MRC Functional Genetics Unit, South Parks Road, Oxford OX1 3QX, UK. kay.davies@human-anatomy.oxford.ac.uk

Abstract

The study of the muscle cell in the muscular dystrophies (MDs) has shown that mutant proteins result in perturbations of many cellular components. MDs have been associated with mutations in structural proteins, signalling molecules and enzymes as well as mutations that result in aberrant processing of mRNA or alterations in post-translational modifications of proteins. These findings have not only revealed important insights for cell biologists, but have also provided unexpected and exciting new approaches for therapy.

PMID:
16971897
DOI:
10.1038/nrm2024
[Indexed for MEDLINE]

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