X-chromosome inactivation: molecular mechanisms from the human perspective.
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The demoiselle of X-inactivation: 50 years old and as trendy and mesmerising as everDisruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderUnderstanding the Functions of Long Non-Coding RNAs through Their Higher-Order StructuresThree-dimensional super-resolution microscopy of the inactive X chromosome territory reveals a collapse of its active nuclear compartment harboring distinct Xist RNA foci.DaVIE: Database for the Visualization and Integration of Epigenetic data.A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data.Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domainsVariable escape from X-chromosome inactivation: identifying factors that tip the scales towards expressionCoupling of X-chromosome reactivation with the pluripotent stem cell state.Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome.The human sex ratio from conception to birth.X-chromosome inactivation in rett syndrome human induced pluripotent stem cells.Finding a balance: how diverse dosage compensation strategies modify histone h4 to regulate transcriptionImpact of flanking chromosomal sequences on localization and silencing by the human non-coding RNA XIST.Targeting of >1.5 Mb of human DNA into the mouse X chromosome reveals presence of cis-acting regulators of epigenetic silencing.X-linked Christianson syndrome: heterozygous female Slc9a6 knockout mice develop mosaic neuropathological changes and related behavioral abnormalitiesDe Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations45,X mosaicism in northeast China: a clinical report and review of the literature.XIST-induced silencing of flanking genes is achieved by additive action of repeat a monomers in human somatic cellsTumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias.Disruption of HDX gene in premature ovarian failure.Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region.Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.Reanalysis of Ohno's hypothesis on conservation of the size of the X chromosome in mammalsLong non-coding RNA: its evolutionary relics and biological implications in mammals: a review
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X-chromosome inactivation: molecular mechanisms from the human perspective.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 07 May 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
X-chromosome inactivation: molecular mechanisms from the human perspective.
@en
X-chromosome inactivation: molecular mechanisms from the human perspective.
@nl
type
label
X-chromosome inactivation: molecular mechanisms from the human perspective.
@en
X-chromosome inactivation: molecular mechanisms from the human perspective.
@nl
prefLabel
X-chromosome inactivation: molecular mechanisms from the human perspective.
@en
X-chromosome inactivation: molecular mechanisms from the human perspective.
@nl
P2093
P2860
P1433
P1476
X-chromosome inactivation: molecular mechanisms from the human perspective.
@en
P2093
Andrew G Chapman
Angela D Kelsey
Christine Yang
Jakub Minks
P2860
P2888
P304
P356
10.1007/S00439-011-0994-9
P577
2011-05-07T00:00:00Z