Protective role of DDAH2 (rs805304) gene polymorphism in patients with myocardial infarction
Author:
Funder
Consejo Nacional de Ciencia y Tecnología
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Molecular Biology,Pathology and Forensic Medicine
Reference34 articles.
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2. Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes;Abhary;PLoS One,2010
3. Asymmetric dimethylarginine causes hypertension and cardiac dysfunction in humans and is actively metabolized by dimethylarginine dimethylamonohydrolase;Achan;Arterioscler. Thromb. Vasc. Biol.,2003
4. Diagnosis of acute coronary syndrome;Achar;Am. Fam. Physician,2005
5. Vascular mechanobiology: Endothelial cell responses to fluid shear stress;Ando;Circ. J.,2009
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1. Association of Variability in the DDAH1, DDAH2, AGXT2 and PRMT1 Genes with Circulating ADMA Concentration in Human Whole Blood;Journal of Clinical Medicine;2022-02-11
2. The Functional Polymorphism of DDAH2 rs9267551 Is an Independent Determinant of Arterial Stiffness;Frontiers in Cardiovascular Medicine;2022-01-03
3. Polymorphism (-499C/G) in DDAH2 promoter may act as a protective factor for metabolic syndrome: A case-control study in Azar-Cohort population;Archives of Endocrinology and Metabolism;2021-07-16
4. Sequence Variation in the DDAH1 Gene Predisposes for Delayed Cerebral Ischemia in Subarachnoidal Hemorrhage;Journal of Clinical Medicine;2020-12-01
5. A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients;Cardiovascular Diabetology;2019-08-13
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