Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes.
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Regulatory factor for X-box family proteins differentially interact with histone deacetylases to repress collagen alpha2(I) gene (COL1A2) expressionICBP90, a novel methyl K9 H3 binding protein linking protein ubiquitination with heterochromatin formationMechanism of histone lysine methyl transfer revealed by the structure of SET7/9-AdoMet.Herpesviral latency-associated transcript gene promotes assembly of heterochromatin on viral lytic-gene promoters in latent infection.Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatinAllele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes.Tissue-specific and imprinted epigenetic modifications of the human NDN geneStructure of the Neurospora SET domain protein DIM-5, a histone H3 lysine methyltransferaseHistone modifications and nuclear architecture: a reviewSet9, a novel histone H3 methyltransferase that facilitates transcription by precluding histone tail modifications required for heterochromatin formation.Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosomeA novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silencedG9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesisLysine methylation within the globular domain of histone H3 by Dot1 is important for telomeric silencing and Sir protein associationSETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteinsNormal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteinsAssembly and characterization of heterochromatin and euchromatin on human artificial chromosomesThe Polycomb group protein Eed protects the inactive X-chromosome from differentiation-induced reactivation.Higher order chromatin organization in cancerTranscriptional regulation by the Set7 lysine methyltransferaseRestricting dosage compensation complex binding to the X chromosomes by H2A.Z/HTZ-1Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae.Effect of phenylhexyl isothiocyanate on aberrant histone H3 methylation in primary human acute leukemiaIdentification and characterization of Smyd2: a split SET/MYND domain-containing histone H3 lysine 36-specific methyltransferase that interacts with the Sin3 histone deacetylase complexMouse polycomb proteins bind differentially to methylated histone H3 and RNA and are enriched in facultative heterochromatinEvolution from XIST-independent to XIST-controlled X-chromosome inactivation: epigenetic modifications in distantly related mammalsComparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locusMethylation of histone H3 Lys 4 in coding regions of active genesMeiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegans.RNAi-dependent H3K27 methylation is required for heterochromatin formation and DNA elimination in Tetrahymena.Involvement of histone methylation and phosphorylation in regulation of transcription by thyroid hormone receptor.Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression.A nonenzymatic modification of the amino-terminal domain of histone H3 by bile acid acyl adenylate.CXXC finger protein 1 restricts the Setd1A histone H3K4 methyltransferase complex to euchromatin.A novel tRNA variable number tandem repeat at human chromosome 1q23.3 is implicated as a boundary element based on conservation of a CTCF motif in mouse.Heterochromatin on the inactive X chromosome delays replication timing without affecting origin usageATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells.Chromatin regulation and sumoylation in the inhibition of Ras-induced vulval development in Caenorhabditis elegans.The Mbd1-Atf7ip-Setdb1 pathway contributes to the maintenance of X chromosome inactivation.Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expression
P2860
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P2860
Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Differentially methylated form ...... inactive human X chromosomes.
@en
Differentially methylated form ...... inactive human X chromosomes.
@nl
type
label
Differentially methylated form ...... inactive human X chromosomes.
@en
Differentially methylated form ...... inactive human X chromosomes.
@nl
prefLabel
Differentially methylated form ...... inactive human X chromosomes.
@en
Differentially methylated form ...... inactive human X chromosomes.
@nl
P2093
P356
P1433
P1476
Differentially methylated form ...... inactive human X chromosomes.
@en
P2093
A Craig Chinault
Barbara A Boggs
C David Allis
David L Spector
Edith Heard
Peter Cheung
P2888
P356
10.1038/NG787
P407
P577
2001-12-10T00:00:00Z
P5875
P6179
1012808229