Hdac3 is essential for the maintenance of chromatin structure and genome stability. - Wikidata - awgldk - TriplyDB

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

http://www.wikidata.org/entity/Q34417264

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Replication Stress: A Lifetime of Epigenetic Change Epigenetic mechanisms underlying the link between non-alcoholic fatty liver diseases and nutrition Targeting histone deacetylases for cancer therapy: from molecular mechanisms to clinical implications Metabolic reprogramming by class I and II histone deacetylases New and emerging HDAC inhibitors for cancer treatment Touch and go: nuclear proteolysis in the regulation of metabolic genes and cancer Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells Dosage-dependent tumor suppression by histone deacetylases 1 and 2 through regulation of c-Myc collaborating genes and p53 function Inhibition of histone deacetylase 3 causes replication stress in cutaneous T cell lymphoma Histone deacetylase 3 (HDAC3) participates in the transcriptional repression of the p16 (INK4a) gene in mammary gland of the female rat offspring exposed to an early-life high-fat diet Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's disease Quantitative proteomic analysis of histone modifications A conserved histone deacetylase with a role in the regulation of cytokinesis in Schizosaccharomyces pombe.Setd5 is essential for mammalian development and the co-transcriptional regulation of histone acetylation.B1, a novel HDAC inhibitor, induces apoptosis through the regulation of STAT3 and NF-κB.Mutations of Chromatin Structure Regulating Genes in Human Malignancies.The therapeutic potential of class I selective histone deacetylase inhibitors in ovarian cancer Histone deacetylase inhibitor (HDACI) mechanisms of action: emerging insights.Nuclear localization signal domain of HDAC3 is necessary and sufficient for the expression regulation of MDR1.Histone deacetylase inhibitor treatment induces 'BRCAness' and synergistic lethality with PARP inhibitor and cisplatin against human triple negative breast cancer cells Deleted in Breast Cancer 1 regulates cellular senescence during obesity Ketone bodies as signaling metabolites.Chromatin replication and epigenome maintenance.Cancer genetics and epigenetics: two sides of the same coin?Histone deacetylase 3 (HDAC3) plays an important role in retinal ganglion cell death after acute optic nerve injury.Nuclear receptor corepressor complexes in cancer: mechanism, function and regulation Changes in nucleosome occupancy associated with metabolic alterations in aged mammalian liver.Histone deacetylases 9 and 10 are required for homologous recombination.Identification of highly selective and potent histone deacetylase 3 inhibitors using click chemistry-based combinatorial fragment assembly.Analysis of protein dynamics at active, stalled, and collapsed replication forks.Suberoylanilide hydroxamic acid (SAHA) enhances olaparib activity by targeting homologous recombination DNA repair in ovarian cancer.Selective inhibition of protein arginine methyltransferase 5 blocks initiation and maintenance of B-cell transformation Integrative network analysis identifies key genes and pathways in the progression of hepatitis C virus induced hepatocellular carcinoma.β-hydroxybutyrate: much more than a metabolite The DNA damage mark pH2AX differentiates the cytotoxic effects of small molecule HDAC inhibitors in ovarian cancer cells HPV16 Down-Regulates the Insulin-Like Growth Factor Binding Protein 2 to Promote Epithelial Invasion in Organotypic Cultures.PPARγ contributes to PKM2 and HK2 expression in fatty liver Histone Deacetylase 3 Is Required for T Cell Maturation The nuclear envelope protein emerin binds directly to histone deacetylase 3 (HDAC3) and activates HDAC3 activity.Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma.

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Hdac3 is essential for the maintenance of chromatin structure and genome stability.

http://www.wikidata.org/entity/Q34417264

description

2010 nî lūn-bûn

@nan

2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@ast

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@en

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@nl

type

label

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@ast

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@en

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@nl

prefLabel

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@ast

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@en

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@nl

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J.CCR.2010.10.022

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P1476

Hdac3 is essential for the maintenance of chromatin structure and genome stability.

@en

P2093

Alyssa R Bonine-Summers

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

Andrew J Wilson

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

Ashwini Yenamandra

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

Christina E Wells

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

Dineo Khabele

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

Edward B Holson

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

Fen Xia

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

Florence F Wagner

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

Guochun Jiang

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

Jia-Ling Yuan

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

P2860

Crystal structure of the nucleosome core particle at 2.8 A resolution

Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

Nucleosome assembly by a complex of CAF-1 and acetylated histones H3/H4

Insight into hepatocellular carcinogenesis at transcriptome level by comparing gene expression profiles of hepatocellular carcinoma with those of corresponding noncancerous liver

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

The S. cerevisiae SET3 complex includes two histone deacetylases, Hos2 and Hst1, and is a meiotic-specific repressor of the sporulation gene program.

Histone deacetylase Rpd3 antagonizes Sir2-dependent silent chromatin propagation

Esa1p is an essential histone acetyltransferase required for cell cycle progression.

Acetylation of lysine 56 of histone H3 catalyzed by RTT109 and regulated by ASF1 is required for replisome integrity.

Human class I histone deacetylase complexes show enhanced catalytic activity in the presence of ATP and co-immunoprecipitate with the ATP-dependent chaperone protein Hsp70

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436-447

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scholarly article

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10.1016/J.CCR.2010.10.022

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5

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18

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2010-11-01T00:00:00Z

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47790740

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21075309

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3004468

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