p47phox Associates With the Cytoskeleton Through Cortactin in Human Vascular Smooth Muscle Cells-Reference-Cited by-同舟云学术

p47phox Associates With the Cytoskeleton Through Cortactin in Human Vascular Smooth Muscle Cells

Published:2005-03 Issue:3 Volume:25 Page:512-518
ISSN:1079-5642
Container-title:Arteriosclerosis, Thrombosis, and Vascular Biology
language:en
Short-container-title:ATVB

Author:

Touyz R.M.¹,Yao G.¹,Quinn M.T.¹,Pagano P.J.¹,Schiffrin E.L.¹

Affiliation:

1. From Multidisciplinary Research Group on Hypertension (R.M.T., G.Y., E.L.S.), Clinical Research Institute of Montreal, University of Montreal, Canada; Department of Veterinary Molecular Biology (M.T.Q.), Montana State University, Bozeman; Hypertension and Vascular Research Division and Biostatistics Department (P.J.P.), Henry Ford Hospital, Detroit, Mich.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference48 articles.

1. Redox-dependent signalling by angiotensin II and vascular remodelling in hypertension

2. Vascular NAD(P)H oxidases: specific features, expression, and regulation

3. Redox signaling and the MAP kinase pathways

4. Role of p22phox in angiotensin�II and platelet-derived growth factor AA induced activator protein 1 activation in vascular smooth muscle cells

5. Oxidative stress is a critical mediator of the angiotensin II signal in human neutrophils: involvement of mitogen-activated protein kinase, calcineurin, and the transcription factor NF-κB

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