JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation. - Wikidata - awgldk - TriplyDB

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

http://www.wikidata.org/entity/Q37612678

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PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1 Disruption of a Regulatory Network Consisting of Neutrophils and Platelets Fosters Persisting Inflammation in Rheumatic Diseases NK Cells, Tumor Cell Transition, and Tumor Progression in Solid Malignancies: New Hints for NK-Based Immunotherapy?High Mobility Group B Proteins, Their Partners, and Other Redox Sensors in Ovarian and Prostate Cancer Novel Mechanisms of Herbal Therapies for Inhibiting HMGB1 Secretion or Action Stress sounds the alarmin: The role of the danger-associated molecular pattern HMGB1 in stress-induced neuroinflammatory priming Emerging roles for HMGB1 protein in immunity, inflammation, and cancer Extracellular high-mobility group box 1 protein (HMGB1) as a mediator of persistent pain Molecular mechanism and therapeutic modulation of high mobility group box 1 release and action: an updated review.Testosterone suppresses uropathogenic Escherichia coli invasion and colonization within prostate cells and inhibits inflammatory responses through JAK/STAT-1 signaling pathway.Diagnostic and prognostic biomarkers for malignant mesothelioma: an update.High mobility group box-1 (HMGB1) participates in the pathogenesis of alcoholic liver disease (ALD).Sequestering HMGB1 via DNA-conjugated beads ameliorates murine colitis HMGB1 in health and disease.The salutary effects of diphenyldifluoroketone EF24 in liver of a rat hemorrhagic shock model High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome.Axonal amphoterin mRNA is regulated by translational control and enhances axon outgrowth Bone marrow derived cells facilitate urinary bladder regeneration by attenuating tissue inflammatory responses.The brighter (and evolutionarily older) face of the metabolic syndrome: evidence from Trypanosoma cruzi infection in CD-1 mice An ongoing search for potential targets and therapies for lethal sepsis Activation of Plant Innate Immunity by Extracellular High Mobility Group Box 3 and Its Inhibition by Salicylic Acid.Extracorporeal liver assist device to exchange albumin and remove endotoxin in acute liver failure: Results of a pivotal pre-clinical study HMGB1 Is a Potential Biomarker for Severe Viral Hemorrhagic Fevers Endotoxin tolerance alleviates experimental acute liver failure via inhibition of high mobility group box 1.Serum Amyloid A Stimulates PKR Expression and HMGB1 Release Possibly through TLR4/RAGE Receptors Osteopontin facilitates tumor metastasis by regulating epithelial-mesenchymal plasticity Deacetylation-mediated interaction of SIRT1-HMGB1 improves survival in a mouse model of endotoxemia.Inhibition of HMGB1 release via salvianolic acid B-mediated SIRT1 up-regulation protects rats against non-alcoholic fatty liver disease.High Mobility Group Box Protein 1 (HMGB1): The Prototypical Endogenous Danger Molecule Characterization of the Inflammatory Properties of Actively Released HMGB1 in Juvenile Idiopathic Arthritis.HMGB1 and Its Hyperacetylated Isoform are Sensitive and Specific Serum Biomarkers to Detect Asbestos Exposure and to Identify Mesothelioma Patients.Leukocytes recruited by tumor-derived HMGB1 sustain peritoneal carcinomatosis Systemic HMGB1 Neutralization Prevents Postoperative Neurocognitive Dysfunction in Aged Rats.How macrophages ring the inflammation alarm Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription The expression of HMGB1 on microparticles released during cell activation and cell death in vitro and in vivo.Nucleic acid sensing and beyond: virtues and vices of high-mobility group box 1.The functions of HMGB1 depend on molecular localization and post-translational modifications.The Specific Roles of JAK/STAT Signaling Pathway in Sepsis.Therapeutic Opportunities in Damage-Associated Molecular Pattern-Driven Metabolic Diseases.

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JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

http://www.wikidata.org/entity/Q37612678

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on 27 January 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@en

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@nl

type

label

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@en

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@nl

prefLabel

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@en

JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

@nl

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PNAS.1316925111

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Proceedings of the National Academy of Sciences of the United States of America

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JAK/STAT1 signaling promotes HMGB1 hyperacetylation and nuclear translocation.

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Ben Lu

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

Daniel J Antoine

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

Hanna Schierbeck

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

Heidi Wähämaa

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

Helena Erlandsson-Harris

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

Huan Yang

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

Jianhua Li

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Kevin Kwan

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

Marieke A D Van Zoelen

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

Melissa Robinson

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

P2860

Novel role of PKR in inflammasome activation and HMGB1 release

Endogenous HMGB1 regulates autophagy

A critical cysteine is required for HMGB1 binding to Toll-like receptor 4 and activation of macrophage cytokine release

Regulation of HMGB1 release by inflammasomes

Non-canonical inflammasome activation targets caspase-11

HMGB proteins function as universal sentinels for nucleic-acid-mediated innate immune responses

Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion.

TLR4-mediated skin carcinogenesis is dependent on immune and radioresistant cells.

Molecular forms of HMGB1 and keratin-18 as mechanistic biomarkers for mode of cell death and prognosis during clinical acetaminophen hepatotoxicity

Tunable signal processing through modular control of transcription factor translocation.

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3068-3073

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scholarly article

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10.1073/PNAS.1316925111

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8

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111

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Peter Lundbäck

Kevin J. Tracey

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2014-01-27T00:00:00Z

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259956736

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24469805

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3939889

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