Paraoxonase 1 Mutations in a Turkish Population

Author:

Aynacioglu A.Sükrü,Cascorbi Ingolf,Mrozikiewicz Przemyslaw M.,Nacak Muradiye,Tapanyigit E.Ebru,Roots Ivar

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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