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3. PON1 M/L55 mutation protects high-risk patients against coronary artery disease. Oliveira SA; Mansur AP; Ribeiro CC; Ramires JA; Annichino-Bizzacchi JM Int J Cardiol; 2004 Mar; 94(1):73-7. PubMed ID: 14996478 [TBL] [Abstract][Full Text] [Related]
4. Hyperhomocysteinemia, paraoxonase activity and risk of coronary artery disease. Kerkeni M; Addad F; Chauffert M; Chuniaud L; Miled A; Trivin F; Maaroufi K Clin Biochem; 2006 Aug; 39(8):821-5. PubMed ID: 16875684 [TBL] [Abstract][Full Text] [Related]
5. [Relationship between paraoxonase 1 55 Met/Leu, paraoxonase 2 148 Ala/Gly genetic polymorphisms and coronary artery disease]. Chi DS; Ling WH; Ma J; Xia M; Hou MJ; Wang Q; Zhu HL; Tang ZH; Yu XP Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):289-93. PubMed ID: 16767666 [TBL] [Abstract][Full Text] [Related]
6. Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke. Can Demirdöğen B; Türkanoğlu A; Bek S; Sanisoğlu Y; Demirkaya S; Vural O; Arinç E; Adali O Clin Biochem; 2008 Jan; 41(1-2):1-9. PubMed ID: 17920578 [TBL] [Abstract][Full Text] [Related]
7. Synergistic effects between Q192R polymorphism of paraoxonase 1 gene and some conventional risk factors in premature coronary artery disease. Balcerzyk A; Zak I; Krauze J Arch Med Res; 2007 Jul; 38(5):545-50. PubMed ID: 17560461 [TBL] [Abstract][Full Text] [Related]
8. Association of homocysteine thiolactonase activity and PON1 polymorphisms with the severity of acute coronary syndrome. Koubaa N; Nakbi A; Hammami S; Attia N; Mehri S; Ben Hamda K; Ben Farhat M; Miled A; Hammami M Clin Biochem; 2009 Jun; 42(9):771-6. PubMed ID: 19269283 [TBL] [Abstract][Full Text] [Related]
9. [The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease]. Taşkiran P; Cam SF; Sekuri C; Tüzün N; Alioğlu E; Altintaş N; Berdeli A Turk Kardiyol Dern Ars; 2009 Oct; 37(7):473-8. PubMed ID: 20098041 [TBL] [Abstract][Full Text] [Related]
10. Combined impact of matrix metalloproteinase-3 and paraoxonase 1 55/192 gene variants on coronary artery disease in Turkish patients. Ozkök E; Aydin M; Babalik E; Ozbek Z; Ince N; Kara I Med Sci Monit; 2008 Oct; 14(10):CR536-42. PubMed ID: 18830194 [TBL] [Abstract][Full Text] [Related]
11. Age and hypertension related changes in genotypes of MTHFR 677C>T, 1298A>C and PON1 -108C>T SNPs in men with coronary artery disease (CAD). Strauss E; Głuszek J; Pawlak AL J Physiol Pharmacol; 2005 Mar; 56 Suppl 2():65-75. PubMed ID: 16077191 [TBL] [Abstract][Full Text] [Related]
12. Maternal exposure to floricultural work during pregnancy, PON1 Q192R polymorphisms and the risk of low birth weight. Moreno-Banda G; Blanco-Muñoz J; Lacasaña M; Rothenberg SJ; Aguilar-Garduño C; Gamboa R; Pérez-Méndez O Sci Total Environ; 2009 Oct; 407(21):5478-85. PubMed ID: 19646734 [TBL] [Abstract][Full Text] [Related]
13. [Smoking enhances the decrease of adiponectin level in patients with coronary artery disease, carriers of MTHFR 677T and PON1 55M alleles]. Strauss E; Radziemski A; Głuszek J; Pawlak A Przegl Lek; 2010; 67(10):859-65. PubMed ID: 21360915 [TBL] [Abstract][Full Text] [Related]
14. Interaction of paraoxonase-192 polymorphism with low HDL-cholesterol in coronary artery disease risk. Mendonça MI; Dos Reis RP; Freitas AI; Pereira A; Sousa AC; Freitas S; Ornelas I; Freitas C; Brehm A; Araújo JJ Rev Port Cardiol; 2010 Apr; 29(4):571-80. PubMed ID: 20734577 [TBL] [Abstract][Full Text] [Related]
15. Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated with coronary artery spasm. Ito T; Yasue H; Yoshimura M; Nakamura S; Nakayama M; Shimasaki Y; Harada E; Mizuno Y; Kawano H; Ogawa H Hum Genet; 2002 Jan; 110(1):89-94. PubMed ID: 11810302 [TBL] [Abstract][Full Text] [Related]
16. Paraoxonase polymorphisms PON1 192 and 55 and longevity in Italian centenarians and Irish nonagenarians. A pooled analysis. Rea IM; McKeown PP; McMaster D; Young IS; Patterson C; Savage MJ; Belton C; Marchegiani F; Olivieri F; Bonafe M; Franceschi C Exp Gerontol; 2004 Apr; 39(4):629-35. PubMed ID: 15050299 [TBL] [Abstract][Full Text] [Related]
17. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal). Freitas AI; Mendonça I; Guerra G; Brión M; Reis RP; Carracedo A; Brehm A Thromb Res; 2008; 122(5):648-56. PubMed ID: 18384842 [TBL] [Abstract][Full Text] [Related]
18. A preliminary study of human paraoxonase and PON 1 L/M55-PON 1 Q/R 192 polymorphisms in Turkish patients with coronary artery disease. Kaman D; Ilhan N; Metin K; Akbulut M; Ustündağ B Cell Biochem Funct; 2009 Mar; 27(2):88-92. PubMed ID: 19226538 [TBL] [Abstract][Full Text] [Related]
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20. Paraoxonase gene polymorphism and serum activity in progressive IgA nephropathy. Kovács TJ; Harris S; Vas TK; Seres I; Short CD; Wittmann IK; Paragh G; Mackness MI; Mackness B; Durrington PN; Nagy JM; Brenchley PE J Nephrol; 2006; 19(6):732-8. PubMed ID: 17173245 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]