Asymmetric Dimethylarginine Limits the Efficacy of Simvastatin Activating Endothelial Nitric Oxide Synthase-Reference-Cited by-同舟云学术

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Asymmetric Dimethylarginine Limits the Efficacy of Simvastatin Activating Endothelial Nitric Oxide Synthase

Published:2016-04-03 Issue:4 Volume:5 Page:
ISSN:2047-9980
Container-title:Journal of the American Heart Association
language:en
Short-container-title:JAHA

Author:

Hsu Chiao‐Po¹²,Zhao Jin‐Feng³,Lin Shing‐Jong⁴⁵,Shyue Song‐Kun⁶,Guo Bei‐Chia³,Lu Tse‐Min¹⁵,Lee Tzong‐Shyuan³

Affiliation:

1. Faculty of Medicine, School of Medicine, National Yang‐Ming University, Taipei, Taiwan

2. Division of Cardiovascular Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, Taiwan

3. Department of Physiology, Genome Research Center, National Yang‐Ming University, Taipei, Taiwan

4. Institute of Clinical Medicine, National Yang‐Ming University, Taipei, Taiwan

5. Division of Cardiology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei, Taiwan

6. Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference63 articles.

1. Changes in Lipoprotein Particle Number With Ezetimibe/Simvastatin Coadministered With Extended‐Release Niacin in Hyperlipidemic Patients

2. Comparing Guidelines for Statin Treatment in Canada and the United States

3. The HMG-CoA reductase inhibitor simvastatin activates the protein kinase Akt and promotes angiogenesis in normocholesterolemic animals.

4. Endothelium-Dependent Effects of Statins

5. Relations of Change in Plasma Levels of LDL‐C, Non‐HDL‐C and apoB With Risk Reduction From Statin Therapy: A Meta‐Analysis of Randomized Trials

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4. Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation;Nature Communications;2022-01-10

5. Hyperuricemia induces endothelial dysfunction and accelerates atherosclerosis by disturbing the asymmetric dimethylarginine/dimethylarginine dimethylaminotransferase 2 pathway;Redox Biology;2021-10

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