Hammerhead ribozyme-mediated destruction of nuclear foci in myotonic dystrophy myoblasts
Open Access
- 1 May 2003
- journal article
- research article
- Published by Elsevier in Molecular Therapy
- Vol. 7 (5) , 670-680
- https://doi.org/10.1016/s1525-0016(03)00068-6
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblastsNeuromuscular Disorders, 2001
- Reconstructing Myotonic DystrophyScience, 2001
- Deconstructing Myotonic DystrophyScience, 2000
- Myotonic Dystrophy and Myotonic Dystrophy Protein KinaseProgress in Histochemistry and Cytochemistry, 2000
- 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
- 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
- Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytesAnnals of Neurology, 1994
- Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the GeneScience, 1992