Targeting and Regulation of Reactive Oxygen Species Generation by Nox Family NADPH Oxidases-Reference-Cited by-同舟云学术

Targeting and Regulation of Reactive Oxygen Species Generation by Nox Family NADPH Oxidases

Published:2009-10 Issue:10 Volume:11 Page:2607-2619
ISSN:1523-0864
Container-title:Antioxidants & Redox Signaling
language:en
Short-container-title:Antioxidants & Redox Signaling

Author:

Leto Thomas L.¹,Morand Stanislas¹,Hurt Darrell²,Ueyama Takehiko³

Affiliation:

1. Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.

2. Bioinformatics and Computational Biosciences Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.

3. Laboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe, Japan.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry,Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry

Link

http://www.liebertpub.com/doi/pdf/10.1089/ars.2009.2637

Reference113 articles.

1. Activation of the NADPH oxidase involves the small GTP-binding protein p21rac1

2. Mechanism for Phosphorylation-induced Activation of the Phagocyte NADPH Oxidase Protein p47

3. Direct Interaction of the Novel Nox Proteins with p22phox Is Required for the Formation of a Functionally Active NADPH Oxidase

4. Dual Oxidase-2 Has an Intrinsic Ca2+-dependent H2O2-generating Activity

5. CD18-dependent activation of the neutrophil NADPH oxidase during phagocytosis of Escherichia coli or Staphylococcus aureus is regulated by class III but not class I or II PI3Ks

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