Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophyMolecular basis for impaired muscle differentiation in myotonic dystrophyIn vivo co-localisation of MBNL protein with DMPK expanded-repeat transcriptsEpigenetics and Triplet-Repeat Neurological DiseasesMuscle wasting in myotonic dystrophies: a model of premature agingRNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1Expression of evolutionarily conserved eye specification genes during Drosophila embryogenesisSix homeoproteins directly activate Myod expression in the gene regulatory networks that control early myogenesisThe sine oculis homeobox (SIX) family of transcription factors as regulators of development and diseaseSix4, a putative myogenin gene regulator, is not essential for mouse embryonal development.Lessons from human progeroid syndromes.Cat-Map: putting cataract on the mapDoes (CUG)n repeat in DMPK mRNA 'paint' chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: A new hypothesis of long-range cis autosomal inactivation.Cooperation between myogenic regulatory factors and SIX family transcription factors is important for myoblast differentiationDystrophia myotonia: why focus on foci?Increased SK3 expression in DM1 lens cells leads to impaired growth through a greater calcium-induced fragility.Clinical ramifications of the MHC family Fc receptor FcRn.Epigenetic mechanisms and genome stability.Myotonic dystrophy: RNA pathogenesis comes into focus.Changes in myotonic dystrophy protein kinase levels and muscle development in congenital myotonic dystrophyUncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem CellsAlternative splicing and muscular dystrophy.Neurodegeneration the RNA wayMisregulation of alternative splicing causes pathogenesis in myotonic dystrophy.The role of the lens actin cytoskeleton in fiber cell elongation and differentiation.Epigenetics in nucleotide repeat expansion disorders.Antisense oligonucleotides: rising stars in eliminating RNA toxicity in myotonic dystrophy.Dnmt1 deficiency promotes CAG repeat expansion in the mouse germlineRNA-mediated toxicity in neurodegenerative diseaseSine oculis, a member of the SIX family of transcription factors, directs eye formationNovel dominant-negative mutation within the six domain of the conserved eye specification gene sine oculis inhibits eye development in Drosophila.A Potent Inhibitor of Protein Sequestration by Expanded Triplet (CUG) Repeats that Shows Phenotypic Improvements in a Drosophila Model of Myotonic Dystrophy.Perinatal DDT Exposure Induces Hypertension and Cardiac Hypertrophy in Adult MicePathogenic mechanisms of myotonic dystrophyMyotonic dystrophy mouse models: towards rational therapy development.The lens in focus: a comparison of lens development in Drosophila and vertebrates.Epigenetic changes and non-coding expanded repeats.Repeat expansion disease: progress and puzzles in disease pathogenesisPerspectives on gene therapy in myotonic dystrophy type 1.The role of Six1 in the genesis of muscle cell and skeletal muscle development.
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P2860
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
description
2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մայիսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2000
@ast
im Mai 2000 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2000/05/01)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd op 2000/05/01)
@nl
наукова стаття, опублікована в травні 2000
@uk
name
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@ast
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@en
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@nl
type
label
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@ast
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@en
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@nl
prefLabel
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@ast
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@en
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@nl
P2093
P2860
P3181
P356
P1433
P1476
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
@en
P2093
E. C. Yuen
J. Adelman
J. I. Clark
P. Soriano
S. J. Tapscott
T. R. Klesert
P2860
P2888
P304
P3181
P356
10.1038/75490
P407
P577
2000-05-01T00:00:00Z