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A Role for Heterozygosity of NF-kappa B1 rs28362491 Polymorphism in Patients with Idiopathic Oligospermia

dc.contributor.authorTuncdemir, Matem
dc.contributor.authorTek, Burak
dc.contributor.authorElcin, Pinar
dc.contributor.authorOzkara, Hamdi
dc.contributor.authorSultuybek, Gönül
dc.contributor.authorOnaran, Ilhan
dc.date.accessioned2021-03-05T08:07:53Z
dc.date.available2021-03-05T08:07:53Z
dc.date.issued2016
dc.identifier.citationTek B., Elcin P., Tuncdemir M., Onaran I., Ozkara H., Sultuybek G., "A Role for Heterozygosity of NF-kappa B1 rs28362491 Polymorphism in Patients with Idiopathic Oligospermia", ARCHIVES OF IRANIAN MEDICINE, cilt.19, ss.275-281, 2016
dc.identifier.issn1029-2977
dc.identifier.othervv_1032021
dc.identifier.otherav_975775ff-e1e2-48f7-b2d4-98dc868cbf9b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101867
dc.description.abstractBackground: Nuclear factor-kappa B (NF-kB) activation and its inhibition by NF-kB inhibitor (IkB) have been functionally linked to germ cell apoptosis, which may affect human infertility. We hypothesized a possible relationship between the NF-kappa B1-94insidel ATTG (rs28362491) and NF-kappa BIA 3'UTR A -> G (rs696) polymorphism, which are common polymorphisms and the susceptibility to oligospermia in the context of the sperm apoptosis.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.titleA Role for Heterozygosity of NF-kappa B1 rs28362491 Polymorphism in Patients with Idiopathic Oligospermia
dc.typeMakale
dc.relation.journalARCHIVES OF IRANIAN MEDICINE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume19
dc.identifier.issue4
dc.identifier.startpage275
dc.identifier.endpage281
dc.contributor.firstauthorID4895


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