Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model.
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M. Mahadevan | J. Amack | A. Paguio | J D Amack | A P Paguio | M S Mahadevan | Aileen Paguio | Jeffrey D. Amack
[1] R. Gibbs,et al. Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy. , 1993, Science.
[2] W. Kingston. Myotonic Dystrophy, 2nd Ed. , 1990, Neurology.
[3] David E. Housman,et al. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member , 1992, Cell.
[4] A. Fulton,et al. Transdifferentiation of chicken embryonic cells into muscle cells by the 3' untranslated region of muscle tropomyosin. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[5] M. Perryman,et al. Identification, Tissue-specific Expression, and Subcellular Localization of the 80- and 71-kDa Forms of Myotonic Dystrophy Kinase Protein (*) , 1995, The Journal of Biological Chemistry.
[6] H. Blau,et al. Tumor suppression by RNA from the 3' untranslated region of alpha-tropomyosin. , 1993, Cell.
[7] M. Swanson,et al. Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy. , 1996, Nucleic acids research.
[8] C. Caskey,et al. Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy. , 1996, Human molecular genetics.
[9] T. Cooper,et al. Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. , 1998, Science.
[10] E. Hoffman,et al. Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation. , 1995, Human molecular genetics.
[11] Keiichi Ohshima,et al. Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli , 1995, Nature Genetics.
[12] C. Junien,et al. Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele. , 1993, Human molecular genetics.
[13] E. Schultz,et al. Skeletal muscle satellite cells. , 1994, Reviews of physiology, biochemistry and pharmacology.
[14] C. Amemiya,et al. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. , 1992, Science.
[15] D. Housman,et al. Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[16] J. Barbet,et al. Immaturity of muscle fibers in the congenital form of myotonic dystrophy: Its consequences and its origin , 1988, Journal of the Neurological Sciences.
[17] N. Henderson,et al. Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[18] D. Housman,et al. Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy , 1996, Nature Genetics.
[19] Helen M. Blau,et al. Tumor suppression by RNA from the 3′ untranslated region of α-tropomyosin , 1993, Cell.
[20] T. Ashizawa,et al. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. , 1992, Science.
[21] M. Crespi,et al. enod40, a gene expressed during nodule organogenesis, codes for a non‐translatable RNA involved in plant growth. , 1994, The EMBO journal.
[22] S. Shafiq,et al. (CTG)n repeats markedly inhibit differentiation of the C2C12 myoblast cell line: implications for congenital myotonic dystrophy. , 1999, Biochimica et biophysica acta.
[23] H. Leffert,et al. Giant hairpins formed by CUG repeats in myotonic dystrophy messenger RNAs might sterically block RNA export through nuclear pores. , 1998, Journal of theoretical biology.
[24] K. Suzuki,et al. Expanded CTG repeats in myotonin protein kinase suppresses myogenic differentiation , 1997, Neuroreport.
[25] Helen M. Blau,et al. Genetic complementation reveals a novel regulatory role for 3′ untranslated regions in growth and differentiation , 1993, Cell.
[26] D. Housman,et al. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues , 1995, The Journal of cell biology.
[27] L. Surh,et al. Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene , 1993, Nature Genetics.
[28] H. Blau,et al. Plasticity of the differentiated state. , 1985, Science.
[29] H. Sarnat,et al. Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathologic study of four cases. , 1976, Archives of neurology.
[30] J. Brook,et al. Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[31] K. Taneja. Localization of trinucleotide repeat sequences in myotonic dystrophy cells using a single fluorochrome-labeled PNA probe. , 1998, BioTechniques.
[32] J. Wright,et al. Suppression of malignancy by the 3' untranslated regions of ribonucleotide reductase R1 and R2 messenger RNAs. , 1996, Cancer research.
[33] V. Funanage,et al. Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy. , 1993, Genomics.
[34] D. Watt,et al. Over expression of the murine myotonic dystrophy protein kinase in the mouse myogenic C2C12 cell line leads to inhibition of terminal differentiation. , 1998, Biochemical and biophysical research communications.
[35] D. Housman,et al. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model. , 1999, The Journal of clinical investigation.
[36] V. Sahgal,et al. Skeletal muscle in preterm infants with congenital myotonic dystrophy Morphologic and histochemical study , 1983, Journal of the Neurological Sciences.
[37] A. Berns,et al. Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice , 1996, Nature Genetics.
[38] S. Bodine‐Fowler,et al. Skeletal muscle regeneration after injury: an overview. , 1994, Journal of voice : official journal of the Voice Foundation.
[39] J. Watson,et al. In vitro activation of the interferon-induced, double-stranded RNA-dependent protein kinase PKR by RNA from the 3' untranslated regions of human alpha-tropomyosin. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[40] E. Roeder,et al. Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. , 1995, Genomics.
[41] K. Tamai,et al. Overexpression of 3′-Untranslated Region of the Myotonic Dystrophy Kinase cDNA Inhibits Myoblast Differentiation in Vitro* , 1997, The Journal of Biological Chemistry.
[42] S. Bhagavati,et al. Normal levels of DM RNA and myotonin protein kinase in skeletal muscle from adult myotonic dystrophy (DM) patients. , 1996, Biochimica et biophysica acta.
[43] B. Wieringa,et al. Expanding complexity in myotonic dystrophy , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.
[44] E. Hoffman,et al. RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance. , 1997, The Journal of clinical investigation.