SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
about
Facioscapulohumeral dystrophy: the path to consensus on pathophysiologyA quantitative telomeric chromatin isolation protocol identifies different telomeric statesThe Trithorax group protein Ash2l and Saf-A are recruited to the inactive X chromosome at the onset of stable X inactivationAn integrated approach for experimental target identification of hypoxia-induced miR-210Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathiesAdvances in understanding chromosome silencing by the long non-coding RNA XistInteraction of Rab31 and OCRL-1 in oligodendrocytes: its role in transport of mannose 6-phosphate receptorsEpigenetic functions of smchd1 repress gene clusters on the inactive X chromosome and on autosomesA stepwise pathway for biogenesis of 24-nt secondary siRNAs and spreading of DNA methylationThe FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development.SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophyChild health, developmental plasticity, and epigenetic programmingHistone variant macroH2A confers resistance to nuclear reprogramming.A system for imaging the regulatory noncoding Xist RNA in living mouse embryonic stem cells.GMI1, a structural-maintenance-of-chromosomes-hinge domain-containing protein, is involved in somatic homologous recombination in Arabidopsis.Epigenetic characterization of the growth hormone gene identifies SmcHD1 as a regulator of autosomal gene clusters.An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouseThe Mbd1-Atf7ip-Setdb1 pathway contributes to the maintenance of X chromosome inactivation.X-inactivation normalizes O-GlcNAc transferase levels and generates an O-GlcNAc-depleted Barr body.Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expressionGenome-wide DNA methylation analysis in cohesin mutant human cell lines.Modifier genes and the plasticity of genetic networks in mice.Nuclear organization and dosage compensation.Normal DNA methylation dynamics in DICER1-deficient mouse embryonic stem cellsChromosomes. A comprehensive Xist interactome reveals cohesin repulsion and an RNA-directed chromosome conformationIdentification of Spen as a Crucial Factor for Xist Function through Forward Genetic Screening in Haploid Embryonic Stem Cells.A review of 18p deletions.Transcriptional gene silencing in humans.X marks the spot: does it matter that O-GlcNAc transferase is an X-linked gene?Structural maintenance of chromosomes flexible hinge domain containing 1 (SMCHD1) promotes non-homologous end joining and inhibits homologous recombination repair upon DNA damageIdentification of two novel SMCHD1 sequence variants in families with FSHD-like muscular dystrophy.A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in developmentInter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.Xist regulation and function explored.Evolutionary diversity and developmental regulation of X-chromosome inactivation.The A-repeat links ASF/SF2-dependent Xist RNA processing with random choice during X inactivationReduced dosage of the modifiers of epigenetic reprogramming Dnmt1, Dnmt3L, SmcHD1 and Foxo3a has no detectable effect on mouse telomere length in vivo.
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P2860
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
description
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2008
@ast
im Mai 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/05/01)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/05/01)
@nl
наукова стаття, опублікована в травні 2008
@uk
name
SmcHD1, containing a structura ...... ritical role in X inactivation
@ast
SmcHD1, containing a structura ...... ritical role in X inactivation
@en
SmcHD1, containing a structura ...... ritical role in X inactivation
@nl
type
label
SmcHD1, containing a structura ...... ritical role in X inactivation
@ast
SmcHD1, containing a structura ...... ritical role in X inactivation
@en
SmcHD1, containing a structura ...... ritical role in X inactivation
@nl
prefLabel
SmcHD1, containing a structura ...... ritical role in X inactivation
@ast
SmcHD1, containing a structura ...... ritical role in X inactivation
@en
SmcHD1, containing a structura ...... ritical role in X inactivation
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
SmcHD1, containing a structura ...... ritical role in X inactivation
@en
P2093
Anwyn Apedaile
Emma Whitelaw
Graham F Kay
Marnie E Blewitt
Nadia Whitelaw
Zhenyi Pang
P2860
P2888
P304
P3181
P356
10.1038/NG.142
P407
P50
P577
2008-04-20T00:00:00Z