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Literature DB >> 1568252

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

J D Brook, M E McCurrach, H G Harley, A J Buckler, D Church, H Aburatani, K Hunter, V P Stanton, J P Thirion, T Hudson.

Abstract

Entities: Chemical Disease

Mesh：

Substances：
Protein Kinases

Year: 1992 PMID： 1568252 DOI： 10.1016/0092-8674(92)90418-c

Source DB: PubMed Journal: Cell ISSN： 0092-8674 Impact factor: 41.582

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Cited

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143 in total

1. Cancer risk among patients with myotonic muscular dystrophy.

Authors: Shahinaz M Gadalla; Marie Lund; Ruth M Pfeiffer; Sanne Gørtz; Christine M Mueller; Richard T Moxley; Sigurdur Y Kristinsson; Magnus Björkholm; Fatma M Shebl; James E Hilbert; Ola Landgren; Jan Wohlfahrt; Mads Melbye; Mark H Greene
Journal: JAMA Date: 2011-12-14 Impact factor: 56.272

Review 2. Neurodegeneration the RNA way.

Authors: Abigail J Renoux; Peter K Todd
Journal: Prog Neurobiol Date: 2011-11-03 Impact factor: 11.685

Review 3. Epigenetics in nucleotide repeat expansion disorders.

Authors: Fang He; Peter K Todd
Journal: Semin Neurol Date: 2012-01-21 Impact factor: 3.420

Review 4. Role of noncoding RNAs in trinucleotide repeat neurodegenerative disorders.

Authors: Huiping Tan; Zihui Xu; Peng Jin
Journal: Exp Neurol Date: 2012-01-27 Impact factor: 5.330

Review 5. The Role of RNA in Biological Phase Separations.

Authors: Marta M Fay; Paul J Anderson
Journal: J Mol Biol Date: 2018-05-10 Impact factor: 5.469

Review 6. CELFish ways to modulate mRNA decay.

Authors: Irina Vlasova-St Louis; Alexa M Dickson; Paul R Bohjanen; Carol J Wilusz
Journal: Biochim Biophys Acta Date: 2013-01-15

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1. Cancer risk among patients with myotonic muscular dystrophy.

Review 2. Neurodegeneration the RNA way.

Review 3. Epigenetics in nucleotide repeat expansion disorders.

Review 4. Role of noncoding RNAs in trinucleotide repeat neurodegenerative disorders.

Review 5. The Role of RNA in Biological Phase Separations.

Review 6. CELFish ways to modulate mRNA decay.

7. Heart rate variability declines with increasing age and CTG repeat length in patients with myotonic dystrophy type 1.

Review 8. Antisense oligonucleotides: rising stars in eliminating RNA toxicity in myotonic dystrophy.

9. Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise.

10. Age-dependent chloride channel expression in skeletal muscle fibres of normal and HSA(LR) myotonic mice.