Myotonic dystrophy: the role of RNA CUG triplet repeats. - Wikidata - wikimedia - TriplyDB

Myotonic dystrophy: the role of RNA CUG triplet repeats.

Myotonic dystrophy: the role of RNA CUG triplet repeats.

http://www.wikidata.org/entity/Q34068475

about

Molecular basis for impaired muscle differentiation in myotonic dystrophy Untranslated regions of mRNAs.Structural basis for the sequence-specific RNA-recognition mechanism of human CUG-BP1 RRM3 RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1 Novel role for RNA-binding protein CUGBP2 in mammalian RNA editing. CUGBP2 modulates C to U editing of apolipoprotein B mRNA by interacting with apobec-1 and ACF, the apobec-1 complementation factor Inherited conduction system abnormalities--one group of diseases, many genes Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy Myotonic dystrophies 1 and 2: complex diseases with complex mechanisms.Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.Daytime sleepiness and REM sleep characteristics in myotonic dystrophy: a case-control study.RNA structure of trinucleotide repeats associated with human neurological diseases.Cardiac complications of childhood myopathies.RNA Foci, CUGBP1, and ZNF9 are the primary targets of the mutant CUG and CCUG repeats expanded in myotonic dystrophies type 1 and type 2 Reduction of toxic RNAs in myotonic dystrophies type 1 and type 2 by the RNA helicase p68/DDX5 GSK3β mediates muscle pathology in myotonic dystrophy Reduction of the rate of protein translation in patients with myotonic dystrophy 2 Molecular mechanisms of muscle atrophy in myotonic dystrophies.GSK3β is a new therapeutic target for myotonic dystrophy type 1.Repeat expansion disease: progress and puzzles in disease pathogenesis Daytime sleepiness and myotonic dystrophy.Selectable system for monitoring the instability of CTG/CAG triplet repeats in mammalian cells.Biological implications of the DNA structures associated with disease-causing triplet repeats.Correction of GSK3β at young age prevents muscle pathology in mice with myotonic dystrophy type 1.Highlights of alternative splicing regulation session: yes, no, maybe--a history of paradigm shifts.

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P2860

Myotonic dystrophy: the role of RNA CUG triplet repeats.

http://www.wikidata.org/entity/Q34068475

description

1999 nî lūn-bûn

@nan

1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

@zh-mo

1999年論文

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1999年论文

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name

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@ast

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@en

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@nl

type

label

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@ast

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@en

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@nl

prefLabel

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@ast

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@en

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@nl

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American Journal of Human Genetics

P1476

Myotonic dystrophy: the role of RNA CUG triplet repeats.

@en

P2093

Timchenko LT

http://www.w3.org/2001/XMLSchema#string

P2860

Cardiac elav-type RNA-binding protein (ETR-3) binds to RNA CUG repeats expanded in myotonic dystrophy

Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy

Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy

Identification of two nuclear proteins which bind to RNA CUG repeats: significance for myotonic dystrophy

Cloning of the essential myotonic dystrophy region and mapping of the putative defect.

Identification of HuR as a protein implicated in AUUUA-mediated mRNA decay.

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

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

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360-364

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10.1086/302268

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