NOX Activation by Subunit Interaction and Underlying Mechanisms in Disease-Reference-Cited by-同舟云学术

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NOX Activation by Subunit Interaction and Underlying Mechanisms in Disease

Published:2017-01-10 Issue: Volume:10 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Rastogi Radhika,Geng Xiaokun,Li Fengwu,Ding Yuchuan

Funder

American Heart Association

Rehabilitation Research and Development Service

National Natural Science Foundation of China

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Reference106 articles.

1. β-amyloid peptides induce mitochondrial dysfunction and oxidative stress in astrocytes and death of neurons through activation of NADPH oxidase;Abramov;J. Neurosci.,2004

2. Phosphorylation of p47phox directs phox homology domain from SH3 domain toward phosphoinositides, leading to phagocyte NADPH oxidase activation;Ago;Proc. Natl. Acad. Sci. U S A,2003

3. Mechanism for phosphorylation-induced activation of the phagocyte NADPH oxidase protein p47phox. Triple replacement of serines 303, 304, and 328 with aspartates disrupts the SH3 domain-mediated intramolecular interaction in p47phox, thereby activating the oxidase;Ago;J. Biol. Chem.,1999

4. Nicotinamide adenine dinucleotide phosphate oxidase (NOX) in experimental liver fibrosis: GKT137831 as a novel potential therapeutic agent;Aoyama;Hepatology,2012

5. Intracranial atherosclerosis and inflammation: lessons from the East and the West;Arenillas;Brain Circ.,2015

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