HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy. - Wikidata - awgldk - TriplyDB

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

http://www.wikidata.org/entity/Q37674663

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Redox regulation of FoxO transcription factors Disrupted autophagy undermines skeletal muscle adaptation and integrity Longevity and skeletal muscle mass: the role of IGF signalling, the sirtuins, dietary restriction and protein intake Histone deacetylase inhibition protects hearing against acute ototoxicity by activating the Nf-κB pathway.Genome-wide identification of FoxO-dependent gene networks in skeletal muscle during C26 cancer cachexia.Inhibition of forkhead boxO-specific transcription prevents mechanical ventilation-induced diaphragm dysfunction.Identification of the Acetylation and Ubiquitin-Modified Proteome during the Progression of Skeletal Muscle Atrophy.Histone deacetylase inhibitors induce autophagy through FOXO1-dependent pathways.Denervation-Induced Activation of the Standard Proteasome and Immunoproteasome The histone deacetylase inhibitor butyrate improves metabolism and reduces muscle atrophy during aging.Differential expression of HDAC and HAT genes in atrophying skeletal muscle.Diminished anabolic signaling response to insulin induced by intramuscular lipid accumulation is associated with inflammation in aging but not obesity Microbiome, probiotics and neurodegenerative diseases: deciphering the gut brain axis.Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy.miR-181a increases FoxO1 acetylation and promotes granulosa cell apoptosis via SIRT1 downregulation.l-glutamine Improves Skeletal Muscle Cell Differentiation and Prevents Myotube Atrophy After Cytokine (TNF-α) Stress Via Reduced p38 MAPK Signal Transduction.Short- and Long-Term Hindlimb Immobilization and Reloading: Profile of Epigenetic Events in Gastrocnemius.Recent advances in mitochondrial turnover during chronic muscle disuse.Mechanistic Role of Reactive Oxygen Species and Therapeutic Potential of Antioxidants in Denervation- or Fasting-Induced Skeletal Muscle Atrophy.Epigenetic Regulation of Cytosolic Phospholipase A2 in SH-SY5Y Human Neuroblastoma Cells.The effects of Rpd3 on fly metabolism, health, and longevity.Trichostatin A, a histone deacetylase inhibitor, modulates unloaded-induced skeletal muscle atrophy.Emerging roles for histone deacetylases in age-related muscle atrophy.

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P2860

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

http://www.wikidata.org/entity/Q37674663

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 24 January 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@en

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@nl

type

label

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@en

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@nl

prefLabel

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@en

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@nl

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P1433

Journal of Cell Science

P1476

HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy.

@en

P2093

Adam W Beharry

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

Brandon M Roberts

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

Leonardo F Ferreira

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

Pooja B Sandesara

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

Sarah M Senf

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

P2860

Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor

Histone deacetylases specifically down-regulate p53-dependent gene activation

Acetylation of Foxo1 alters its DNA-binding ability and sensitivity to phosphorylation

MDM2-HDAC1-mediated deacetylation of p53 is required for its degradation

A role for histone deacetylase HDAC1 in modulating the transcriptional activity of MyoD: inhibition of the myogenic program

A role for histone deacetylase activity in HDAC1-mediated transcriptional repression

Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

Regulation of mammalian epithelial differentiation and intestine development by class I histone deacetylases

FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells

FoxO3 controls autophagy in skeletal muscle in vivo

P304

1441-1453

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scholarly article

P356

10.1242/JCS.136390

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P407

P433

Pt 7

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P478

127

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P577

2014-01-24T00:00:00Z

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259918424

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24463822

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3970557

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