Nox isoforms in vascular pathophysiology: insights from transgenic and knockout mouse models

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Redox Report

• Publication date

  2010-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1179/174329210X12650506623401PMID 20500986PMCID PMC7067321
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2008cited by this paper
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• Point Mutations in the Proline-rich Region of p22phox Are Dominant Inhibitors of Nox1- and Nox2-dependent Reactive Oxygen Generation*

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  2005cited by this paper
• Nox1 Overexpression Potentiates Angiotensin II-Induced Hypertension and Vascular Smooth Muscle Hypertrophy in Transgenic Mice

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• Differential effects of diabetes on the expression of the gp91phox homologues nox1 and nox4.

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• gp91phox-Containing NADPH Oxidase Mediates Endothelial Dysfunction in Renovascular Hypertension

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• Distinct Subcellular Localizations of Nox1 and Nox4 in Vascular Smooth Muscle Cells

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• Nox4 as the Major Catalytic Component of an Endothelial NAD(P)H Oxidase

  2004cited by this paper
• Decreased neointimal formation in Nox2-deficient mice reveals a direct role for NADPH oxidase in the response to arterial injury.

  2004cited by this paper
• Direct Interaction of the Novel Nox Proteins with p22phox Is Required for the Formation of a Functionally Active NADPH Oxidase*

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• Functional association of nox1 with p22phox in vascular smooth muscle cells.

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• Gp91phox contributes to NADPH oxidase activity in aortic fibroblasts but not smooth muscle cells.

  2003cited by this paper
• Novel isoforms of NADPH oxidase in vascular physiology and pathophysiology

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• Two Novel Proteins Activate Superoxide Generation by the NADPH Oxidase NOX1*

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

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• Chronic granulomatous disease.

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• Expression of a Functionally Active gp91phox-Containing Neutrophil-Type NAD(P)H Oxidase in Smooth Muscle Cells From Human Resistance Arteries: Regulation by Angiotensin II

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• NADPH oxidase is involved in prostaglandin F2alpha-induced hypertrophy of vascular smooth muscle cells: induction of NOX1 by PGF2alpha.

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