Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study
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Soluble epoxide hydrolase: gene structure, expression and deletionAttenuation of cisplatin-induced renal injury by inhibition of soluble epoxide hydrolase involves nuclear factor κB signalingDysregulation of soluble epoxide hydrolase and lipidomic profiles in anorexia nervosaVariation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary interventionPharmacological inhibition of soluble epoxide hydrolase ameliorates diet-induced metabolic syndrome in ratsAdenosine A2A receptor modulates vascular response in soluble epoxide hydrolase-null mice through CYP-epoxygenases and PPARγInhibition of soluble epoxide hydrolase preserves cardiomyocytes: role of STAT3 signalingEpoxyeicosanoid signaling in CNS function and diseaseDisrupting Dimerization Translocates Soluble Epoxide Hydrolase to PeroxisomesGenetics in arterial calcification: pieces of a puzzle and cogs in a wheel.The relationship between race, cigarette smoking and carotid intimal medial thickness in systemic lupus erythematosus.The genetics of vascular complications in diabetes mellitus.The role of epoxide hydrolases in health and disease.Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications.Soluble epoxide hydrolase dimerization is required for hydrolase activity.Genome-wide transcriptional analysis of differentially expressed genes in diabetic, healing corneal epithelial cells: hyperglycemia-suppressed TGFβ3 expression contributes to the delay of epithelial wound healing in diabetic corneas.Synergistic Effect of the MTHFR C677T and EPHX2 G860A Polymorphism on the Increased Risk of Ischemic Stroke in Chinese Type 2 Diabetic Patients.Reno-protective mechanisms of epoxyeicosatrienoic acids in cardiovascular disease.Design and discovery of soluble epoxide hydrolase inhibitors for the treatment of cardiovascular diseases.Integrating multi-omics biomarkers and postprandial metabolism to develop personalized treatment for anorexia nervosa.1-(1-acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia
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P2860
Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@ast
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@en
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
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type
label
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@ast
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@en
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@nl
prefLabel
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@ast
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@en
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@nl
P2093
P2860
P3181
P356
P1476
Genetic analysis of the solubl ...... se in the Diabetes Heart Study
@en
P2093
Allison B Lehtinen
Barry I Freedman
Carl D Langefeld
David Herrington
Donald W Bowden
J Jeffrey Carr
Stephen S Rich
P2860
P304
P3181
P356
10.3132/DVDR.2008.021
P407
P577
2008-06-01T00:00:00Z