Cutting edge: direct interaction of TLR4 with NAD(P)H oxidase 4 isozyme is essential for lipopolysaccharide-induced production of reactive oxygen species and activation of NF-kappa B
about
GRIM-19 interacts with nucleotide oligomerization domain 2 and serves as downstream effector of anti-bacterial function in intestinal epithelial cellsAutophagy protein Rubicon mediates phagocytic NADPH oxidase activation in response to microbial infection or TLR stimulationDynein light chain LC8 negatively regulates NF-kappaB through the redox-dependent interaction with IkappaBalphaPersistent nuclear factor-kappa B activation in Ucp2-/- mice leads to enhanced nitric oxide and inflammatory cytokine productionNovel redox-dependent regulation of NOX5 by the tyrosine kinase c-AblOxidative innate immune defenses by Nox/Duox family NADPH oxidasesRedox warfare between airway epithelial cells and Pseudomonas: dual oxidase versus pyocyaninProthrombin Kringle-2: A Potential Inflammatory Pathogen in the Parkinsonian Dopaminergic SystemThe Reactive Oxygen Species in Macrophage Polarization: Reflecting Its Dual Role in Progression and Treatment of Human DiseasesThe Toll of Vascular Insufficiency: Implications for the Management of Peripheral Arterial DiseaseThe Role of NADPH Oxidases (NOXs) in Liver Fibrosis and the Activation of MyofibroblastsEvolution of NADPH Oxidase Inhibitors: Selectivity and Mechanisms for Target EngagementBacterial and fungal pattern recognition receptors in homologous innate signaling pathways of insects and mammalsInterplay between Inflammation and Cellular Stress Triggered by Flaviviridae VirusesBiochemistry, physiology, and pathophysiology of NADPH oxidases in the cardiovascular systemRole of microglia in oxidative toxicity associated with encephalomycarditis virus infection in the central nervous systemSpatially-resolved intracellular sensing of hydrogen peroxide in living cellsModeling host genetic regulation of influenza pathogenesis in the collaborative crossHepatitis C Virus (HCV) Proteins Induce NADPH Oxidase 4 Expression in a Transforming Growth Factor -Dependent Manner: a New Contributor to HCV-Induced Oxidative StressCysteine S-Nitrosylation Protects Protein-tyrosine Phosphatase 1B against Oxidation-induced Permanent InactivationCellular stress response and innate immune signaling: integrating pathways in host defense and inflammation.A potential therapeutic role for aldose reductase inhibitors in the treatment of endotoxin-related inflammatory diseasesChronic LPS inhalation causes emphysema-like changes in mouse lung that are associated with apoptosisIron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseasesBasic principles and emerging concepts in the redox control of transcription factorsThe potential interplay of adipokines with toll-like receptors in the development of hepatocellular carcinomaReactive oxygen species in inflammation and tissue injuryHost genetic determinants of influenza pathogenicity.Selenoproteins regulate macrophage invasiveness and extracellular matrix-related gene expression.Role of NADPH oxidases in liver fibrosis.NOX enzymes and pulmonary disease.Potentiation of epithelial innate host responses by intercellular communication.Pulmonary endothelial cell NOXPeroxynitrite generated by inducible nitric oxide synthase and NADPH oxidase mediates microglial toxicity to oligodendrocytes.Oxidative stress and hepatic Nox proteins in chronic hepatitis C and hepatocellular carcinoma.Myofiber stress-response in myositis: parallel investigations on patients and experimental animal models of muscle regeneration and systemic inflammation.Mitochondria contribute to LPS-induced MAPK activation via uncoupling protein UCP2 in macrophagesDAMPening inflammation by modulating TLR signalling.S-glutathionylation activates STIM1 and alters mitochondrial homeostasis.Candesartan reduces the innate immune response to lipopolysaccharide in human monocytes
P2860
Q24297555-993165F8-A05F-4C19-A1D7-B2CE1B0041CDQ24307761-C8626BA9-A2F7-4336-BC56-82B56C4F859BQ24329159-0ED79CCD-B3B5-41DF-8FF3-4FA72BDFDAC4Q24541307-5F3510A2-49AF-4D14-A841-52EF66E1970AQ24647638-02983AA0-7A37-4E8D-8710-31C995419E75Q24657408-F282FA27-B291-49FE-B294-0EA74578031FQ24657425-CF4351E3-BB5C-4367-B712-8F85FA04B697Q26738336-34D7DD12-A02F-43FD-8FFC-C72D7862B564Q26752888-69B49792-BE25-4B60-A09E-2098C613FAFEQ26753079-42CFAB8F-315E-45FC-B10A-21C2B94833DFQ26766479-1EFCF206-9F0F-49EE-BBA6-3D67809BAEB5Q26861119-DCBD3A28-7D31-44A4-B5CF-EF0BCF61B246Q26866418-851D05C7-9925-407D-AD38-30BB1EDFCEB4Q26970803-15171105-1FDD-492E-A181-6CBB5041BE31Q26991619-1F686645-A2A9-4C2C-B823-D0CFA033C25DQ27026361-83E28824-C2A5-4E3B-A905-A75A46C52015Q27305361-49A4F78C-241C-4616-9B45-1F56E828AC1DQ27336134-17CAB07C-F103-4F3C-B19D-7B30C02BB65DQ27490473-96E2C0E0-5558-4033-BD75-45F9EEA7B813Q27652444-82A91DD0-FCEE-40C6-84A7-2E20C630BF71Q27692108-DF3E3275-491D-4627-8678-D58309A1D104Q28382891-C3E631DD-66A1-4A91-B4D4-3791176D626BQ28386104-A70EA4CE-11D9-424C-AE86-76F90EA2492CQ28388335-E987DDFF-61E2-431D-AB93-84E698096E40Q28391506-475BC2A2-8191-425A-A090-ACF043090AC8Q28392224-58F8FDF2-A9DA-4373-951E-F19448AC3133Q28396273-839855F4-8DC5-4458-9654-040C409EFC76Q30352727-422F02CF-9DA2-462C-8F21-0F5B89A9E987Q33513325-04803210-DD27-4163-A23C-F0383C9B8934Q33632736-690A6DCB-C774-4EC7-A023-1C1D6CD73971Q33649864-79C68853-68F3-4D1A-896E-ADE183D52933Q33761401-7936EB7E-2802-42F0-A935-D9C032AB4F42Q33769358-1BA40F39-3F3D-4BA5-8061-035619388F55Q33895965-D235029C-A292-40F5-B2C4-D9CFE2A31998Q33904328-8E1B64A1-C5F3-465A-8E57-24D5093D23B5Q33923345-4DCAA58E-3AB7-41D4-AEFB-198C30726315Q34000569-AE43EC74-1DAA-469A-976F-DD16FC438B97Q34035570-AAE483CE-278A-43E6-9AE6-61C5DF2A311AQ34069961-B8309BF6-F76E-4A2E-8BF5-5FCBE06950E9Q34087095-F3642BF4-2796-41F8-8EA6-CAE94C2F1DC0
P2860
Cutting edge: direct interaction of TLR4 with NAD(P)H oxidase 4 isozyme is essential for lipopolysaccharide-induced production of reactive oxygen species and activation of NF-kappa B
description
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2004
@ast
im September 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2004/09/15)
@sk
vědecký článek publikovaný v roce 2004
@cs
wetenschappelijk artikel (gepubliceerd op 2004/09/15)
@nl
наукова стаття, опублікована у вересні 2004
@uk
مقالة علمية (نشرت في 15-9-2004)
@ar
name
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@ast
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@en
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@nl
type
label
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@ast
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@en
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@nl
prefLabel
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@ast
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@en
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@nl
P2093
P3181
P1476
Cutting edge: direct interacti ...... s and activation of NF-kappa B
@en
P2093
Eun Young Park
Hye Sun Park
Hye Young Jung
Jaesang Kim
Won Jae Lee
Yun Soo Bae
P304
P3181
P356
10.4049/JIMMUNOL.173.6.3589
P407
P577
2004-09-15T00:00:00Z