Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
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Unfolding the Role of Large Heat Shock Proteins: New Insights and Therapeutic ImplicationsHSP90 and HSP70: Implication in Inflammation Processes and Therapeutic Approaches for Myeloproliferative NeoplasmsHSP90 inhibition suppresses lipopolysaccharide-induced lung inflammation in vivoContribution of chaperones to STAT pathway signaling.Roles of Erythroid Differentiation Regulator 1 (Erdr1) on Inflammatory Skin DiseasesChemotherapeutic potential of 17-AAG against cutaneous leishmaniasis caused by Leishmania (Viannia) braziliensisHSP90 inhibition by 17-DMAG attenuates oxidative stress in experimental atherosclerosisHeat shock protein 90 regulates IκB kinase complex and NF-κB activation in angiotensin II-induced cardiac cell hypertrophy.Heat shock protein 90 inhibitors reduce trafficking of ATP-gated P2X1 receptors and human platelet responsiveness.Heat shock protein 90 inhibition by 17-DMAG lessens disease in the MRL/lpr mouse model of systemic lupus erythematosusHIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.Matrix metalloproteinases (MMP-2,9) and their tissue inhibitors (TIMP-1,2) as novel markers of stress response and atherogenesis in children with chronic kidney disease (CKD) on conservative treatment.Neutrophil gelatinase-associated lipocalin (NGAL) and matrix metalloproteinases as novel stress markers in children and young adults on chronic dialysis.Pharmacological induction of the 70-kDa heat shock protein protects against brain injuryRetinoblastoma protein modulates the inverse relationship between cellular proliferation and elastogenesisHeat shock protein 90 inhibition by 17-DMAG attenuates abdominal aortic aneurysm formation in miceInhibition of heat shock protein (molecular weight 90 kDa) attenuates proinflammatory cytokines and prevents lipopolysaccharide-induced liver injury in mice.Molecular chaperones and heat shock proteins in atherosclerosis.17-DMAG, an HSP90 Inhibitor, Ameliorates Multiple Organ Dysfunction Syndrome via Induction of HSP70 in Endotoxemic Rats.Heat shock protein 90 inhibition by 17-Dimethylaminoethylamino-17-demethoxygeldanamycin protects blood-brain barrier integrity in cerebral ischemic stroke.Opposing actions of heat shock protein 90 and 70 regulate nicotinamide adenine dinucleotide phosphate oxidase stability and reactive oxygen species production.Heat shock proteins: pathogenic role in atherosclerosis and potential therapeutic implications.Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approachHeat shock protein 70 and AMP-activated protein kinase contribute to 17-DMAG-dependent protection against heat stroke.Oxidized Low-Density Lipoprotein (OxLDL)-Treated Dendritic Cells Promote Activation of T Cells in Human Atherosclerotic Plaque and Blood, Which Is Repressed by Statins: microRNA let-7c Is Integral to the Effect.Heat shock proteins 60 and 70 specific proinflammatory and cytotoxic response of CD4+CD28null cells in chronic kidney disease.Down-regulation of hsa-miR-148b inhibits vascular smooth muscle cells proliferation and migration by directly targeting HSP90 in atherosclerosis.Inhibition of heat shock protein 90 improves pulmonary arteriole remodeling in pulmonary arterial hypertension.Anti-inflammatory properties and pharmacological induction of Hsp70 after brain injury.The role of heat shock protein 90 in modulating ischemia-reperfusion injury in the kidney.Molecular biology of atherosclerosis.Drug-Induced HSP90 Inhibition Alleviates Pain in Monoarthritic Rats and Alters the Expression of New Putative Pain Players at the DRG.HSP90 inhibition by 17-DMAG reduces inflammation in J774 macrophages through suppression of Akt and nuclear factor-κB pathways.FNDC4 acts as an anti-inflammatory factor on macrophages and improves colitis in mice.Genomic profiles and predictors of early allograft dysfunction after human liver transplantation.Hsp90 regulates NADPH oxidase activity and is necessary for superoxide but not hydrogen peroxide production.Mitochondrial heat shock protein-90 modulates vascular smooth muscle cell survival and the vascular injury response in vivo.Heat shock protein 90 is a potential therapeutic target for ameliorating skeletal muscle abnormalities in Parkinson's diseaseHeat effect induces production of inflammatory cytokines through heat shock protein 90 pathway in cornea cells.Effect of gedunin on acute articular inflammation and hypernociception in mice.
P2860
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P2860
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@en
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@nl
type
label
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@en
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@nl
prefLabel
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@en
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@nl
P2093
P2860
P356
P1476
Heat shock protein 90 inhibitors attenuate inflammatory responses in atherosclerosis.
@en
P2093
Begoña Muñoz-García
Jesus Egido
Jose Luis Martín-Ventura
Julio Madrigal-Matute
Luis Miguel Blanco-Colio
Luis Ortega
Oscar López-Franco
Priscila Ramos-Mozo
P2860
P304
P356
10.1093/CVR/CVQ046
P577
2010-02-12T00:00:00Z