Paraoxonase 1 Mutations in a Turkish Population
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Toxicology
Reference21 articles.
1. Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: Glutamine or arginine at position 192, for the respective A or B allozymes;Adkins;Am. J. Hum. Genet.,1993
2. The Gln-Arg192 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns;Antikainen;J. Clin. Invest.,1996
3. Arylamine N-acetyltransferase (NAT2) genotypes in a Turkish population;Aynacioglu;Pharmacogenetics,1997
4. High frequency of CYP1A1 mutations in a Turkish population;Aynacioglu;Arch. Toxicol.,1998
5. Paraoxonase polymorphism Met-Leu55 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetes;Blatter-Garin;J. Clin. Invest.,1997
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1. Paraoxonase 1 gene polymorphısms (Q192r and L55m) and assocıatıon wıth coronary slow flow;Turkish Journal of Clinics and Laboratory;2023-09-30
2. The Role of PON1 Variants in Disease Susceptibility in a Turkish Population;Global Medical Genetics;2020-08
3. Synergic predisposing effect of G894T (eNOS), 4G/5G (PAI) and T1131C (APOA5) polymorphisms to myocardial infarction;Gene Reports;2018-06
4. The genetic association between PON1 polymorphisms and osteonecrosis of femoral head;Medicine;2017-10
5. A pilot study assessing the association between paraoxonase 1 gene polymorphism and prostate cancer;Türk Üroloji Dergisi/Turkish Journal of Urology;2017-08-16
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