Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle. - Wikidata - wikimedia - TriplyDB

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

http://www.wikidata.org/entity/Q35312286

about

Histone deacetylase signaling in cardioprotection Metabolic reprogramming by class I and II histone deacetylases Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice Histone deacetylase 3 modulates Tbx5 activity to regulate early cardiogenesis Transcriptional coregulators: fine-tuning metabolism.Linking epigenetics to lipid metabolism: focus on histone deacetylases.Energizing Genetics and Epi-genetics: Role in the Regulation of Mitochondrial Function.FOXP3+ regulatory T cell development and function require histone/protein deacetylase 3.Readers, writers, and erasers: chromatin as the whiteboard of heart disease Histone deacetylase 3 regulates smooth muscle differentiation in neural crest cells and development of the cardiac outflow tract Histone deacetylase 3 is an epigenomic brake in macrophage alternative activation.Non-sirtuin histone deacetylases in the control of cardiac aging Histone deacetylase 3 is required for maintenance of bone mass during aging A novel adipose-specific gene deletion model demonstrates potential pitfalls of existing methods.Nuclear receptor co-repressors are required for the histone-deacetylase activity of HDAC3 in vivo.Hdac3 Deficiency Increases Marrow Adiposity and Induces Lipid Storage and Glucocorticoid Metabolism in Osteochondroprogenitor Cells Inhibition of class I histone deacetylases unveils a mitochondrial signature and enhances oxidative metabolism in skeletal muscle and adipose tissue Improving insulin sensitivity with HDAC inhibitor Histone deacetylase 3 suppression increases PH domain and leucine-rich repeat phosphatase (Phlpp)1 expression in chondrocytes to suppress Akt signaling and matrix secretion Aldose Reductase Acts as a Selective Derepressor of PPARγ and the Retinoic Acid Receptor.Emerging roles of the corepressors NCoR1 and SMRT in homeostasis.HDAC3 is essential for DNA replication in hematopoietic progenitor cells.Expression of histone deacetylase 3 instructs alveolar type I cell differentiation by regulating a Wnt signaling niche in the lung.Management and therapy for cardiomyopathy in Friedreich's ataxia.HDAC3-Dependent Epigenetic Pathway Controls Lung Alveolar Epithelial Cell Remodeling and Spreading via miR-17-92 and TGF-β Signaling Regulation.Physical exercise and epigenetic adaptations of the cardiovascular system.Protein acetylation in metabolism - metabolites and cofactors.The opposite roles of agdA and glaA on citric acid production in Aspergillus niger.Nutrition Modulation of Cardiotoxicity and Anticancer Efficacy Related to Doxorubicin Chemotherapy by Glutamine and ω-3 Polyunsaturated Fatty Acids.HDAC3 is a molecular brake of the metabolic switch supporting white adipose tissue browning Histone deacetylase 3 prepares brown adipose tissue for acute thermogenic challenge.The Role of Eif6 in Skeletal Muscle Homeostasis Revealed by Endurance Training Co-expression Networks.Genome-Nuclear Lamina Interactions Regulate Cardiac Stem Cell Lineage Restriction.Manifestations and mechanisms of myocardial lipotoxicity in obesity.The fate of sulfate in chronic heart failure.Pattern of change in histone 3 lysine 9 acetylation and histone deacetylases in development of zebrafish embryo.Exposure to Penicillium mycotoxins alters gene expression of enzymes involved in the epigenetic regulation of bovine macrophages (BoMacs).Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure

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P2860

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

http://www.wikidata.org/entity/Q35312286

description

2011 nî lūn-bûn

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2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@ast

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@en

type

label

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@ast

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@en

prefLabel

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@ast

Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@en

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JBC.M111.277707

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Journal of Biological Chemistry

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Diet-induced lethality due to deletion of the Hdac3 gene in heart and skeletal muscle.

@en

P2093

Jonathan A Epstein

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

Li Li

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

Lijun Yuan

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

Logan J Everett

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

Mitchell A Lazar

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

Nikhil Singh

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

Shannon E Mullican

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Xi Liu

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Zheng Sun

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P2860

A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness

The N-CoR-HDAC3 nuclear receptor corepressor complex inhibits the JNK pathway through the integral subunit GPS2

Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3

Significance analysis of microarrays applied to the ionizing radiation response

Mitochondria in the diabetic heart

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

Class II histone deacetylases act as signal-responsive repressors of cardiac hypertrophy

Clinical development of histone deacetylase inhibitors as anticancer agents

The cardiac phenotype induced by PPARalpha overexpression mimics that caused by diabetes mellitus

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10.1074/JBC.M111.277707

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3190900

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