Overexpression of Staufen1 in DM1 mouse skeletal muscle exacerbates dystrophic and atrophic features
Author:
Affiliation:
1. Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
2. Eric Poulin Centre for Neuromuscular Disease, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
Abstract
Funder
Association Française contre les Myopathies
Muscular Dystrophy Association
Rachel Fund
Canadian Institutes of Health Research
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddaa111/33460439/ddaa111.pdf
Reference67 articles.
1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
2. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992
3. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992
4. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues;Taneja;J. Cell Biol.,1995
5. Expansion of a CUG trinucleotide repeat in the 3′ untranslated region of myotonic dystrophy protein kinase transcripts results;Davis;Proc. Natl. Acad. Sci. U. S. A.,1997
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