Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/1015
Title: Importance of NOS3 Genetic Polymorphisms in the Risk of Development of Ischemic Stroke in the Turkish Population
Authors: Özçelik, Aysun Türkanoğlu
Can Demirdöğen, Birsen
Demirkaya, Şeref
Adalı, Orhan
Keywords: l-arginine
ecnos gene
coronary-artery-disease
nitric-oxide synthase
myocardial-infarction
enos gene
repeat polymorphism
chinese population
korean patients
glu298asp polymorphism
Publisher: Mary Ann Liebert, Inc
Source: Türkanoğlu Özçelik, A., Can Demirdöğen, B., Demirkaya, Ş., & Adalı, O. (2014). Importance of NOS3 genetic polymorphisms in the risk of development of ischemic stroke in the Turkish population. Genetic testing and molecular biomarkers, 18(12), 797-803.
Abstract: In the present study, we aimed to investigate the relationship between endothelial nitric oxide synthase 3 (NOS3) G894T, T-786C, and intron 4 variable number of tandem repeat (VNTR) variants, alone or in combination, and the risk of incidence of ischemic stroke in the Turkish population. The genotypes for all polymorphisms were determined by polymerase chain reaction/restriction fragment length polymorphism techniques on 245 ischemic stroke patients and 145 controls. In the case-control analysis, no significant difference was observed between stroke patients and controls with respect to NOS3 G894T, T-786C, and intron 4 VNTR polymorphisms genotype and allele frequency distribution. However, the copresence of G894T and intron 4 VNTR risk-elevating genotypes in the same individual increased the risk of stroke seven times (odds ratio=7.083, 95% confidence interval=0.866-57.963, p=0.029).
URI: https://hdl.handle.net/20.500.11851/1015
ISSN: 1945-0265
Appears in Collections:Biyomedikal Mühendisliği Bölümü / Department of Biomedical Engineering
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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