Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29153
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dc.contributor.authorÖzçimen, Ahmet Ata-
dc.date.accessioned2022-10-20T05:48:53Z-
dc.date.available2022-10-20T05:48:53Z-
dc.date.issued2013-10-
dc.identifier.citationYücel, A. vd. (2013). "Interleukin-2 gene polymorphism in Turkish patients with Behcet's disease and its association with ocular involvement". International Journal of Immunogenetics, 40(5), 349-355.en_US
dc.identifier.issn1744-3121-
dc.identifier.urihttps://doi.org/10.1111/iji.12039-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1111/iji.12039-
dc.identifier.urihttp://hdl.handle.net/11452/29153-
dc.description.abstractBehcet's disease (BD) is a chronic immune-mediated systemic disease, characterized by oral and genital lesions and ocular inflammation. Several cytokine genes may play crucial roles in host susceptibility to BD, because the cytokine production capacity varies among individuals and depends on the cytokine gene polymorphisms. The association of the interleukin (IL)-2 gene polymorphisms with the susceptibility to BD was investigated in this study. DNA samples were obtained from a Turkish population of 97 patients with BD and 76 healthy control subjects. Polymorphisms of IL-2 gene at position -330 and +166 were determined using the polymerase chain reaction with sequence-specific primers. In the patients with BD, there was a significantly increased frequency of IL-2 -330 GT genotype. Interestingly, we demonstrated that the frequencies of IL-2 -330 GT and IL-2+166 GG genotypes were increased in BD patients with ocular involvement, whilst IL-2 -330 TT genotype was significantly decreased. Also, analysis of allele frequency demonstrated that the presence of G allele at position +166 of IL-2 seems to be a risk factor for ocular involvement. These results reveal that IL-2 -330 GT genotype may be a susceptibility factor for BD, whereas IL-2 -330 TT genotype seems to display a protective association with BD. Additionally, IL-2 gene polymorphisms might be associated with ocular involvement in BD.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGenetics & heredityen_US
dc.subjectImmunologyen_US
dc.subjectSystemic-lupus-erythematosusen_US
dc.subjectHan chinese populationen_US
dc.subjectMultiple-sclerosisen_US
dc.subjectIl-2 geneen_US
dc.subjectT-cellsen_US
dc.subjectOnline databasesen_US
dc.subjectFactor-Ven_US
dc.subjectInfectionen_US
dc.subjectCytokinesen_US
dc.subjectTurkeyen_US
dc.subject.meshBehcet syndromeen_US
dc.subject.meshDNAen_US
dc.subject.meshEyeen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene frequencyen_US
dc.subject.meshGenetic predisposition to diseaseen_US
dc.subject.meshGenotypeen_US
dc.subject.meshHumansen_US
dc.subject.meshInflammationen_US
dc.subject.meshInterleukin-2en_US
dc.subject.meshLymphocytesen_US
dc.subject.meshMaleen_US
dc.subject.meshNeutrophilsen_US
dc.subject.meshPolymorphism, single nucleotideen_US
dc.subject.meshTurkeyen_US
dc.titleInterleukin-2 gene polymorphism in Turkish patients with Behcet's disease and its association with ocular involvementen_US
dc.typeArticleen_US
dc.identifier.wos000324023400001tr_TR
dc.identifier.scopus2-s2.0-84883650660tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Göz Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Kalp Damar Cerrahisi Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı.tr_TR
dc.relation.bapT-2004/59tr_TR
dc.contributor.orcid0000-0003-0463-6818tr_TR
dc.identifier.startpage349tr_TR
dc.identifier.endpage355tr_TR
dc.identifier.volume40tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalInternational Journal of Immunogeneticsen_US
dc.contributor.buuauthorYücel, Ali-
dc.contributor.buuauthorDilek, Kamil-
dc.contributor.buuauthorSaba, Davit-
dc.contributor.buuauthorYurtkuran, Mustafa Abbas-
dc.contributor.buuauthorOral, Haluk Barbaros-
dc.contributor.researcheridK-7285-2012tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed23331481tr_TR
dc.subject.wosGenetics & heredityen_US
dc.subject.wosImmunologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid57225839918tr_TR
dc.contributor.scopusid56005080200tr_TR
dc.contributor.scopusid55987378200tr_TR
dc.contributor.scopusid7003389525tr_TR
dc.contributor.scopusid7004498001tr_TR
dc.subject.scopusFluorescence Lifetime; Esterases; Optical Imagingen_US
dc.subject.emtreeGenomic DNAen_US
dc.subject.emtreeInterleukin 2en_US
dc.subject.emtreeAlleleen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBehcet diseaseen_US
dc.subject.emtreeClinical featureen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCytokine productionen_US
dc.subject.emtreeDNA polymorphismen_US
dc.subject.emtreeGene frequencyen_US
dc.subject.emtreeGene sequenceen_US
dc.subject.emtreeGenetic associationen_US
dc.subject.emtreeGenotypeen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreePolymerase chain reactionen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRisk factoren_US
dc.subject.emtreeTurkey (republic)en_US
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