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dc.contributor.authorHATEMI, AC
dc.contributor.authorCINE, Naci
dc.contributor.authorErginel-Unaltuna, Nihan
dc.date.accessioned2021-03-03T15:42:14Z
dc.date.available2021-03-03T15:42:14Z
dc.date.issued2002
dc.identifier.citationCINE N., HATEMI A., Erginel-Unaltuna N., "Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients", CLINICAL GENETICS, cilt.61, sa.1, ss.66-70, 2002
dc.identifier.issn0009-9163
dc.identifier.otherav_405c34d5-c3d1-4dc4-9da6-ac35ca5c0907
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/47043
dc.identifier.urihttps://doi.org/10.1034/j.1399-0004.2002.610113.x
dc.description.abstractIn this study we examined a possible association between a 27 base pair (bp)-repeat polymorphism in intron 4 of the ecNOS gene and myocardial infarction (MI) in a subgroup of the Turkish population. We compared MI and control groups for the frequencies of the ecNOS alleles and their genotypes. The frequency of the ecNOS 4a/a and 4a/b genotypes was found to be significantly higher in the MI group than in the control group. Interestingly, the frequency of the ecNOS 4a/b polymorphism was found to be significantly higher in the selected MI group (patients with no known secondary risk factors) than in the control and non-selected MI group. We found that the patients with MI had the frequency of the a/a genotype 4.3%, of the a/b genotype 26.6% and the b/b genotype 69.1%, The controls, however, showed only 0.6% for a/a, 18.0% for a/b and 81.4% for the b/b genotype (P<0.001; &chi;(2)=13.626). In this study, we show that myocardial infarction is associated with one subtype of ecNOS gene polymorphism.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleAssociation of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients
dc.typeMakale
dc.relation.journalCLINICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume61
dc.identifier.issue1
dc.identifier.startpage66
dc.identifier.endpage70
dc.contributor.firstauthorID28681


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