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The assessment of the relationship between variations in the apelin gene and coronary artery disease in Turkish population

dc.contributor.authorCoskunpinar, Ender
dc.contributor.authorCakmak, Huseyin Altug
dc.contributor.authorOltulu, Yasemin Musteri
dc.contributor.authorIkitimur, Barış
dc.contributor.authorVural, Vural Ali
dc.contributor.authorSaglam, Zumrut Mine Isik
dc.contributor.authorKarimova, Ayla
dc.contributor.authorPakizeh, Ebrahim
dc.date.accessioned2021-03-03T11:25:46Z
dc.date.available2021-03-03T11:25:46Z
dc.date.issued2015
dc.identifier.citationPakizeh E., Coskunpinar E., Oltulu Y. M. , Cakmak H. A. , Ikitimur B., Saglam Z. M. I. , Karimova A., Vural V. A. , "The assessment of the relationship between variations in the apelin gene and coronary artery disease in Turkish population", ANATOLIAN JOURNAL OF CARDIOLOGY, cilt.15, sa.9, ss.716-721, 2015
dc.identifier.issn2149-2263
dc.identifier.othervv_1032021
dc.identifier.otherav_27dbd7a1-665b-466c-8e4d-8f0228f6705c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/31644
dc.identifier.urihttps://doi.org/10.5152/akd.2014.5685
dc.description.abstractObjective: Apelin is a novel endogenous peptide with inotropic and vasodilatory properties and is the ligand for the angiotensin receptor-like 1 (APJ) receptor. The aim of the study was to investigate the association of 2 single-nucleotide polymorphisms (SNPs) in the apelin gene with susceptibility to coronary artery disease (CAD) in the Turkish population.
dc.language.isoeng
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectKardiyoloji
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectKlinik Tıp
dc.titleThe assessment of the relationship between variations in the apelin gene and coronary artery disease in Turkish population
dc.typeMakale
dc.relation.journalANATOLIAN JOURNAL OF CARDIOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume15
dc.identifier.issue9
dc.identifier.startpage716
dc.identifier.endpage721
dc.contributor.firstauthorID89685


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