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Publication : A muscleblind knockout model for myotonic dystrophy.

First Author  Kanadia RN Year  2003
Journal  Science Volume  302
Issue  5652 Pages  1978-80
PubMed ID  14671308 Mgi Jnum  J:86903
Mgi Id  MGI:2682447 Doi  10.1126/science.1088583
Citation  Kanadia RN, et al. (2003) A muscleblind knockout model for myotonic dystrophy. Science 302(5652):1978-80
abstractText  The neuromuscular disease myotonic dystrophy (DM) is caused by microsatellite repeat expansions at two different genomic loci. Mutant DM transcripts are retained in the nucleus together with the muscleblind (Mbnl) proteins, and these abnormal RNAs somehow interfere with pre-mRNA splicing regulation. Here, we show that disruption of the mouse Mbnl1 gene leads to muscle, eye, and RNA splicing abnormalities that are characteristic of DM disease. Our results support the hypothesis that manifestations of DM can result from sequestration of specific RNA binding proteins by a repetitive element expansion in a mutant RNA.
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