about
Triggering role of acid sphingomyelinase in endothelial lysosome-membrane fusion and dysfunction in coronary arteries.N-acetylcysteine-induced vasodilation involves voltage-gated potassium channels in rat aorta.Different biomechanical properties of medial and adventitial layers of thoracic aorta in Wistar-Kyoto and spontaneously hypertensive rats.Visfatin-induced lipid raft redox signaling platforms and dysfunction in glomerular endothelial cells.SNARE-mediated rapid lysosome fusion in membrane raft clustering and dysfunction of bovine coronary arterial endothelium.Reversal by growth hormone of homocysteine-induced epithelial-to-mesenchymal transition through membrane raft-redox signaling in podocytesRequirement of translocated lysosomal V1 H(+)-ATPase for activation of membrane acid sphingomyelinase and raft clustering in coronary endothelial cells.Overexpression of HIF prolyl-hydoxylase-2 transgene in the renal medulla induced a salt sensitive hypertensionHypoxia-inducible factor prolyl-hydroxylase-2 mediates transforming growth factor beta 1-induced epithelial-mesenchymal transition in renal tubular cells.Association of a SNP in SLC35F3 Gene with the Risk of Hypertension in a Chinese Han PopulationContributory role of endothelium and voltage-gated potassium channels in apocynin-induced vasorelaxations.Changes in the composition of the thoracic aortic wall in spontaneously hypertensive rats treated with losartan or spironolactone.Ca2+ -regulated lysosome fusion mediates angiotensin II-induced lipid raft clustering in mesenteric endothelial cells.Protease-activated receptor 1 and 2 contribute to angiotensin II-induced activation of adventitial fibroblasts from rat aorta.Membrane rafts-redox signalling pathway contributes to renal fibrosis via modulation of the renal tubular epithelial-mesenchymal transitionMembrane raft redox signalling contributes to endothelial dysfunction and vascular remodelling of thoracic aorta in angiotensin II-infused rats
P50
Q30493665-1ECF606C-D611-43E2-994B-A6F2F2B92CB9Q33415766-9011E2FE-C99C-4E3E-B69E-F533BFBA7EBDQ33577616-C8E1A644-882E-4A25-8D69-8BDA75E67278Q34235479-70506512-4E9C-4FFC-AA1E-F64C169C7490Q35543506-2D1ABFC9-85B9-4CCB-BEAB-803E4E7A59C8Q35564803-7AF1F44D-DF65-4C33-B3EE-F2814CE9ED4AQ35891203-3EB764CB-9ADF-4956-BCB3-F436AFEABEF6Q36288683-DE995C7A-F01D-4BBE-B9CE-357A8275582CQ36780416-C2BC67DA-DE35-4A2C-974A-4B0BB5E3F037Q37018912-89824CE3-AD81-48FA-BC21-E713EFB3393FQ42938873-6A5E1515-97B0-4FF5-A049-37169CF4E4F8Q43293136-C4FC18BB-095C-4063-948D-51C999793705Q53210411-CBA59691-0B81-4032-A1AD-F509881CC297Q53783839-D7110594-A959-4F3E-BE3D-106C39382103Q88972845-A44DD203-0301-4942-B83C-AD9C8DCAC58BQ92693256-7883AAE4-9DDA-40EB-854B-02C3D4939063
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Wei-qing Han
@ast
Wei-qing Han
@en
Wei-qing Han
@es
Wei-qing Han
@nl
Wei-qing Han
@sl
type
label
Wei-qing Han
@ast
Wei-qing Han
@en
Wei-qing Han
@es
Wei-qing Han
@nl
Wei-qing Han
@sl
prefLabel
Wei-qing Han
@ast
Wei-qing Han
@en
Wei-qing Han
@es
Wei-qing Han
@nl
Wei-qing Han
@sl
P106
P1153
34769971700
P31
P496
0000-0001-9702-0523