Histone H2A.Z is essential for estrogen receptor signaling. - Test2 - elhamkhani - TriplyDB

Histone H2A.Z is essential for estrogen receptor signaling.

Histone H2A.Z is essential for estrogen receptor signaling.

http://www.wikidata.org/entity/Q37247116

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Essential role of p18Hamlet/SRCAP-mediated histone H2A.Z chromatin incorporation in muscle differentiation H3K27 demethylation by JMJD3 at a poised enhancer of anti-apoptotic gene BCL2 determines ERα ligand dependency The euchromatic and heterochromatic landscapes are shaped by antagonizing effects of transcription on H2A.Z deposition TIP48/Reptin and H2A.Z requirement for initiating chromatin remodeling in estrogen-activated transcription Expression and functionality of histone H2A variants in cancer H2A.Z: a molecular rheostat for transcriptional control Histone variants and their post-translational modifications in primary human fat cells Gene reactivation by 5-aza-2'-deoxycytidine-induced demethylation requires SRCAP-mediated H2A.Z insertion to establish nucleosome depleted regions Dissecting epigenetic silencing complexity in the mouse lung cancer suppressor gene Cadm1 Insulin-dependent transcriptional control in L6 rat myotubes is associated with modulation of histone acetylation and accumulation of the histone variant H2A.Z in the proximity of the transcriptional start site Histone variants and epigenetics.Characterization of the histone H2A.Z-1 and H2A.Z-2 isoforms in vertebrates.VAP: a versatile aggregate profiler for efficient genome-wide data representation and discovery The E1A-associated p400 protein modulates cell fate decisions by the regulation of ROS homeostasis.ChIP on Chip: surprising results are often artifacts.Histone variants: emerging players in cancer biology.Histones and their modifications in ovarian cancer - drivers of disease and therapeutic targets.Location analysis for the estrogen receptor-alpha reveals binding to diverse ERE sequences and widespread binding within repetitive DNA elements.Histone variant H3F3A promotes lung cancer cell migration through intronic regulation Genome-wide analysis reveals PADI4 cooperates with Elk-1 to activate c-Fos expression in breast cancer cells.Histone H2A.Z deregulation in prostate cancer. Cause or effect?Changes in H2A.Z occupancy and DNA methylation during B-cell lymphomagenesis The FRIGIDA complex activates transcription of FLC, a strong flowering repressor in Arabidopsis, by recruiting chromatin modification factors.The Tnt1 retrotransposon escapes silencing in tobacco, its natural host.PRC1 and PRC2 are not required for targeting of H2A.Z to developmental genes in embryonic stem cells.Targeting DNA methylation for epigenetic therapy.Activation of p21 by HDAC inhibitors requires acetylation of H2A.Z.USP10 deubiquitylates the histone variant H2A.Z and both are required for androgen receptor-mediated gene activation Chromatin higher-order structures and gene regulation Loss of H2A.Z Is Not Sufficient to Determine Transcriptional Activity of Snf2-Related CBP Activator Protein or p400 Complexes Direct regulation of nucleosome density by the conserved AAA-ATPase Yta7 Regulation of u-PAR gene expression by H2A.Z is modulated by the MEK-ERK/AP-1 pathway.Effective Targeting of Estrogen Receptor-Negative Breast Cancers with the Protein Kinase D Inhibitor CRT0066101.Acetylation of H2A.Z is a key epigenetic modification associated with gene deregulation and epigenetic remodeling in cancer.Foxa1 and Foxa2 are essential for sexual dimorphism in liver cancer Genetic and epigenetic underpinnings of sex differences in the brain and in neurological and psychiatric disease susceptibility Histone H3 Variant Regulates RNA Polymerase II Transcription Termination and Dual Strand Transcription of siRNA Loci in Trypanosoma brucei Analysis of chromatin dynamics during glucocorticoid receptor activation A conserved function for the H2A.Z C terminus.Functional and therapeutic significance of protein kinase D enzymes in invasive breast cancer.

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Histone H2A.Z is essential for estrogen receptor signaling.

http://www.wikidata.org/entity/Q37247116

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 10 June 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Histone H2A.Z is essential for estrogen receptor signaling.

@en

Histone H2A.Z is essential for estrogen receptor signaling.

@nl

type

label

Histone H2A.Z is essential for estrogen receptor signaling.

@en

Histone H2A.Z is essential for estrogen receptor signaling.

@nl

prefLabel

Histone H2A.Z is essential for estrogen receptor signaling.

@en

Histone H2A.Z is essential for estrogen receptor signaling.

@nl

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Genes & Development

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Histone H2A.Z is essential for estrogen receptor signaling.

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Amy Svotelis

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

François Robert

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

Liette Laflamme

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

Luc Gaudreau

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

Nicolas Gévry

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

Pierre-Etienne Jacques

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

Sara Hardy

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

P2860

Variant histone H2A.Z is globally localized to the promoters of inactive yeast genes and regulates nucleosome positioning.

Identification of a novel SNF2/SWI2 protein family member, SRCAP, which interacts with CREB-binding protein

Synergy between estrogen receptor alpha activation functions AF1 and AF2 mediated by transcription intermediary factor TIF2.

Core transcriptional regulatory circuitry in human embryonic stem cells

Preferential occupancy of histone variant H2AZ at inactive promoters influences local histone modifications and chromatin remodeling

TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes

BRG-1 is recruited to estrogen-responsive promoters and cooperates with factors involved in histone acetylation

The p400 E1A-associated protein is a novel component of the p53 --> p21 senescence pathway

FoxA1 translates epigenetic signatures into enhancer-driven lineage-specific transcription

Estrogen receptors and human disease

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1522-1533

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scholarly article

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10.1101/GAD.1787109

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13

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23

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2009-06-10T00:00:00Z

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19515975

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2704467

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