Myotonic Dystrophy: The Role of RNA CUG Triplet Repeats
- 1 February 1999
- journal article
- review article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (2), 360-364
- https://doi.org/10.1086/302268
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Disruption of Splicing Regulated by a CUG-Binding Protein in Myotonic DystrophyScience, 1998
- Identification of HuR as a protein implicated in AUUUA-mediated mRNA decayThe EMBO Journal, 1997
- RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.Journal of Clinical Investigation, 1997
- Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathyNature Genetics, 1996
- Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in miceNature Genetics, 1996
- Overexpression of Myotonic Dystrophy Kinase in BC3H1 Cells Induces the Skeletal Muscle PhenotypePublished by Elsevier ,1996
- A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeatHuman Molecular Genetics, 1995
- Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationHuman Molecular Genetics, 1995
- A liver-enriched transcriptional activator protein, LAP, and a transcriptional inhibitory protein, LIP, are translated from the sam mRNACell, 1991
- Positive autoregulation of Sex-lethal by alternative splicing maintains the female determined state in DrosophilaCell, 1991