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Items: 1 to 20 of 179

1.

Association between endothelial nitric oxide gene intron 4a4b VNTR polymorphism and plasma homocysteine concentrations in Tunisian male patients with myocardial infarction.

Jemaa R, Kallel A, Sediri Y, Abdessalem S, Mourali MS, Feki M, Mechmeche R, Kaabachi N.

Nutr Res. 2012 May;32(5):342-6. doi: 10.1016/j.nutres.2012.03.013. Epub 2012 Apr 27.

PMID:
22652373
2.

Association of a 27-bp repeat polymorphism in intron 4 of endothelial constitutive nitric oxide synthase gene with hypertension in a Tunisian population.

Jemaa R, Ben Ali S, Kallel A, Feki M, Elasmi M, Taieb SH, Sanhaji H, Omar S, Kaabachi N.

Clin Biochem. 2009 Jun;42(9):852-6. doi: 10.1016/j.clinbiochem.2008.12.002. Epub 2008 Dec 14.

PMID:
19111531
3.

Association of a 27-bp repeat polymorphism in intron 4 of endothelial constitutive nitric oxide synthase gene with myocardial infarction in Tunisian patients.

Jemaa R, Kallel A, Ben Ali S, Omar S, Chabrak S, Elasmi M, Haj Taieb S, Sanhaji H, Feki M, Mechmeche R, Kaabachi N.

Clin Chem Lab Med. 2007;45(11):1476-80.

PMID:
17970703
4.

Polymorphisms of the NOS3 gene and risk of myocardial infarction in the Tunisian population.

Kallel A, Sbaï MH, Sediri Y, Abdessalem S, Mourali MS, Feki M, Mechmeche R, Jemaa R, Kaabachi N.

Cytokine. 2013 Dec;64(3):646-51. doi: 10.1016/j.cyto.2013.09.005. Epub 2013 Oct 3.

PMID:
24095258
5.

Hyperhomocysteinemia, endothelial nitric oxide synthase polymorphism, and risk of coronary artery disease.

Kerkeni M, Addad F, Chauffert M, Myara A, Ben Farhat M, Miled A, Maaroufi K, Trivin F.

Clin Chem. 2006 Jan;52(1):53-8. Epub 2005 Nov 10.

6.

Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia.

Brown KS, Kluijtmans LA, Young IS, Woodside J, Yarnell JW, McMaster D, Murray L, Evans AE, Boreham CA, McNulty H, Strain JJ, Mitchell LE, Whitehead AS.

Arterioscler Thromb Vasc Biol. 2003 Jun 1;23(6):1014-20. Epub 2003 Apr 10.

7.

Influence of endothelial nitric oxide synthase gene polymorphisms (-786T>C, 4a4b, 894G>T) in Korean patients with coronary artery disease.

Kim IJ, Bae J, Lim SW, Cha DH, Cho HJ, Kim S, Yang DH, Hwang SG, Oh D, Kim NK.

Thromb Res. 2007;119(5):579-85. Epub 2006 Jul 13.

PMID:
16842840
8.

[Arterial blood pressure variations: homocysteine and nitric oxide synthase gene polymorphisms (NOS3)].

Rodríguez Esparragón FJ, Rodríguez Pérez JC, Macías Reyes A, Hernández Trujillo Y, González Leiza M, Caballero Hidalgo A.

Nefrologia. 2006;26(5):559-63. Spanish.

9.

Lack of consistent association between endothelial nitric oxide synthase gene polymorphisms, homocysteine levels and recurrent pregnancy loss in tunisian women.

Zammiti W, Mtiraoui N, Mahjoub T.

Am J Reprod Immunol. 2008 Feb;59(2):139-45. doi: 10.1111/j.1600-0897.2007.00551.x.

PMID:
18211539
10.

Endothelial nitric oxide synthase -786T>C, but not 894G>T and 4a4b, polymorphism influences plasma homocysteine concentrations in persons with normal vitamin status.

Fatini C, Sofi F, Gori AM, Sticchi E, Marcucci R, Lenti M, Casini A, Surrenti C, Abbate R, Gensini GF.

Clin Chem. 2005 Jul;51(7):1159-64. Epub 2005 May 19.

11.

Association of the genetic variants of endothelial nitric oxide synthase gene with angiographically defined coronary artery disease and myocardial infarction in South Indian patients with type 2 diabetes mellitus.

Narne P, Ponnaluri KC, Singh S, Siraj M, Ishaq M.

J Diabetes Complications. 2013 May-Jun;27(3):255-61. doi: 10.1016/j.jdiacomp.2012.10.009. Epub 2012 Nov 20.

PMID:
23182401
12.

Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease.

Kerkeni M, Addad F, Chauffert M, Myara A, Gerhardt M, Chevenne D, Trivin F, Farhat MB, Miled A, Maaroufi K.

Ann Clin Biochem. 2006 May;43(Pt 3):200-6.

PMID:
16704755
13.

Influence of endothelial nitric oxide synthase gene polymorphisms (G894T, 4a4b, T-786C) and hyperhomocysteinemia on the predisposition to acute coronary syndromes.

Fatini C, Sofi F, Sticchi E, Gensini F, Gori AM, Fedi S, Lapini I, Rostagno C, Comeglio M, Brogi D, Gensini G, Abbate R.

Am Heart J. 2004 Mar;147(3):516-21.

PMID:
14999203
14.

eNOS gene intron 4 a/b VNTR polymorphism is a risk factor for coronary artery disease in Southern Turkey.

Matyar S, Attila G, Acartürk E, Akpinar O, Inal T.

Clin Chim Acta. 2005 Apr;354(1-2):153-8. Epub 2005 Jan 25.

PMID:
15748612
15.

Association of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged men.

Kunnas TA, Ilveskoski E, Niskakangas T, Laippala P, Kajander OA, Mikkelsson J, Goebeler S, Penttilä A, Perola M, Nikkari ST, Karhunen PJ.

J Mol Med (Berl). 2002 Sep;80(9):605-9. Epub 2002 Jul 3.

PMID:
12226742
16.

Endothelial nitric oxide synthase gene Glu298Asp polymorphism in patients with coronary artery disease.

Salimi S, Firoozrai M, Zand H, Nakhaee A, Shafiee SM, Tavilani H, Mohebbi A.

Ann Saudi Med. 2010 Jan-Feb;30(1):33-7. doi: 10.4103/0256-4947.59370.

17.

Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients.

Jemaa R, Achouri A, Kallel A, Ben Ali S, Mourali S, Feki M, Elasmi M, Taieb SH, Sanhaji H, Omar S, Mechmeche R, Kaabachi N.

Clin Chem Lab Med. 2008;46(10):1364-8. doi: 10.1515/CCLM.2008.306.

PMID:
18844488
18.

Lack of association between endothelial nitric oxide synthase gene polymorphisms and risk of premature coronary artery disease in the Greek population.

Vasilakou M, Votteas V, Kasparian C, Pantazopoulos N, Dedoussis G, Deltas C, Nastos P, Nikolakis D, Lamnissou K.

Acta Cardiol. 2008 Oct;63(5):609-14.

PMID:
19014005
19.

Endothelial function and endothelial nitric oxide synthase intron 4a/b polymorphism in primary hyperparathyroidism.

Ekmekci A, Abaci N, Colak Ozbey N, Agayev A, Aksakal N, Oflaz H, Erginel-Unaltuna N, Erbil Y.

J Endocrinol Invest. 2009 Jul;32(7):611-6. doi: 10.3275/6400. Epub 2009 Jul 2.

PMID:
19574729
20.

Plasma nitric oxide concentrations and nitric oxide synthase gene polymorphisms in coronary artery disease.

Yoon Y, Song J, Hong SH, Kim JQ.

Clin Chem. 2000 Oct;46(10):1626-30. Erratum in: Clin Chem 2001 Jan;47(1):151.

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