y+ LAT-1 mediates transport of the potent and selective iNOS inhibitor, GW274150, in control J774 macrophages-Reference-Cited by-同舟云学术

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y+ LAT-1 mediates transport of the potent and selective iNOS inhibitor, GW274150, in control J774 macrophages

Published:2006-05-15 Issue:2 Volume:31 Page:101-109
ISSN:0939-4451
Container-title:Amino Acids
language:en
Short-container-title:Amino Acids

Author:

Baydoun A. R.,Bertran J.,Thakur S.,Dawson J.,Palacín M.,Knowles R. G.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s00726-005-0311-9.pdf

Reference53 articles.

1. Nitric oxide synthases: structure, function and inhibition

2. Amino acid transport system y+L of human erythrocytes: Specificity and cation dependence of the translocation step

3. Design of isoform-selective inhibitors of nitric oxide synthase

4. Selective Targeting of Nitric Oxide Synthase Inhibitors to System y+ in Activated Macrophages

5. Discrimination between citrulline and arginine transport in activated murine macrophages: inefficient synthesis of NO from recycling of citrulline to arginine

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1. There is no direct competition between arginase and nitric oxide synthase for the common substrate l-arginine;Nitric Oxide;2022-12

2. Nitric Oxide Synthase Inhibitors into the Clinic at Last;Reactive Oxygen Species;2020

3. Decoding the Substrate Supply to Human Neuronal Nitric Oxide Synthase;PLoS ONE;2013-07-09

4. Genetic and Pharmacological Inhibition of Dimethylarginine Dimethylaminohydrolase 1 Is Protective in Endotoxic Shock;Arteriosclerosis, Thrombosis, and Vascular Biology;2012-11

5. Arginine-Based Inhibitors of Nitric Oxide Synthase: Therapeutic Potential and Challenges;Mediators of Inflammation;2012

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