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Lookup NU author(s): Dr Louise VB Anderson
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The zebrafish is an established model of vertebrate development and is also receiving increasing attention in terms of human disease modelling. In order to provide experimental support to realize this modelling potential, we report here the identification of apparent orthologues of many critical members of the dystrophin-associated glycoprotein complex (DGC) that have been implicated in a diverse range of neuromuscular disorders. In addition, immunohistochemical studies show the localization of the DGC to the sarcolemma of adult zebrafish muscle and in particular the myosepta. Together, these data suggest that the DGC in adult zebrafish may play a highly conserved functional role in muscle architecture that, when disrupted, could offer insight into human neuromuscular disease processes. © 2003 Elsevier Science (USA). All rights reserved.
Author(s): Chambers SP, Anderson LVB, Maguire GM, Dodd A, Love DR
Publication type: Article
Publication status: Published
Journal: Biochemical and Biophysical Research Communications
Year: 2003
Volume: 303
Issue: 2
Pages: 488-495
ISSN (print): 0006-291X
ISSN (electronic): 1090-2104
Publisher: Academic Press
URL: http://dx.doi.org/10.1016/S0006-291X(03)00355-3
DOI: 10.1016/S0006-291X(03)00355-3
PubMed id: 12659844
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