Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts
- 1 November 2001
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 11 (8) , 728-735
- https://doi.org/10.1016/s0960-8966(01)00226-7
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionHuman Molecular Genetics, 1999
- Disruption of Splicing Regulated by a CUG-Binding Protein in Myotonic DystrophyScience, 1998
- Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHPNature Genetics, 1997
- Expansion of a CUG trinucleotide repeat in the 3′ untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcriptsProceedings of the National Academy of Sciences, 1997
- Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genesProceedings of the National Academy of Sciences, 1997
- Identification of a (CUG)n Triplet Repeat RNA-Binding Protein and Its Expression in Myotonic DystrophyNucleic Acids Research, 1996
- Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.The Journal of cell biology, 1995
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the GeneScience, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,1992