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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Özçimen, Ahmet Ata | - |
dc.date.accessioned | 2021-12-23T11:03:20Z | - |
dc.date.available | 2021-12-23T11:03:20Z | - |
dc.date.issued | 2011-08 | - |
dc.identifier.citation | Özçimen, A. A. vd. (2011). "IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease". International Journal of Immunogenetics, 38(4), 295-301. | en_US |
dc.identifier.issn | 1744-3121 | - |
dc.identifier.uri | https://doi.org/10.1111/j.1744-313X.2011.01006.x | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01006.x | - |
dc.identifier.uri | http://hdl.handle.net/11452/23505 | - |
dc.description.abstract | Several cytokine genes may play crucial roles in host susceptibility to Behcet's Disease (BD), since the cytokine production capacity varies among individuals and depends on the cytokine gene polymorphisms. The association of the IL-1 cluster gene polymorphisms with the development of BD was investigated in this study. DNA samples were obtained from a Turkish population of 97 patients with BD, and 77 healthy control subjects. All genotyping (IL-1 alpha, IL-1 beta, IL-1R and IL-1Ra) experiments were performed using sequence specific primers PCR (PCR-SSP). When compared to the healthy controls, the frequencies of IL-1Ra IL-1 alpha and IL-1R gene polymorphisms were not significantly different in BD patients. The frequency of IL-1 beta -511 TT genotype was higher in the BD group in comparison to the control group. Interestingly, we demonstrated that IL-1 beta +3962 gene polymorphism seems to be associated with the presence of Erythema nodosum in BD patients. Our data suggest that polymorphisms in IL-1 beta gene may affect host susceptibility to BD. In order to confirm the biological significance of our results, further studies should be performed in a large-scale study and/or in different ethnic groups. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Immunology | en_US |
dc.subject | Interleukin-1 receptor antagonist | en_US |
dc.subject | Inflammatory-bowel-disease | en_US |
dc.subject | Ifn-gamma gene | en_US |
dc.subject | In-vitro | en_US |
dc.subject | Nucleotide-sequence | en_US |
dc.subject | Cytokine production | en_US |
dc.subject | Online databases | en_US |
dc.subject | Long arm | en_US |
dc.subject | Association | en_US |
dc.subject | Risk | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Behcet syndrome | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Gene frequency | en_US |
dc.subject.mesh | Genetic predisposition to disease | en_US |
dc.subject.mesh | Genotype | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interleukin-1 | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Multigene Family | en_US |
dc.subject.mesh | Polymorphism, genetic | en_US |
dc.subject.mesh | Polymorphism, single nucleotide | en_US |
dc.subject.mesh | Turkey | en_US |
dc.title | IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000292335800005 | tr_TR |
dc.identifier.scopus | 2-s2.0-79959944004 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı. | tr_TR |
dc.relation.bap | T-2004/59 | tr_TR |
dc.contributor.orcid | 0000-0003-0463-6818 | tr_TR |
dc.contributor.orcid | 0000-0003-4436-3797 | tr_TR |
dc.identifier.startpage | 295 | tr_TR |
dc.identifier.endpage | 301 | tr_TR |
dc.identifier.volume | 38 | tr_TR |
dc.identifier.issue | 4 | tr_TR |
dc.relation.journal | International Journal of Immunogenetics | en_US |
dc.contributor.buuauthor | Dilek, Kamil | - |
dc.contributor.buuauthor | Bingöl, Ümit | - |
dc.contributor.buuauthor | Sarıcaoğlu, Hayriye | - |
dc.contributor.buuauthor | Sarandöl, Aslı | - |
dc.contributor.buuauthor | Taşkapılıoğlu, Özlem | - |
dc.contributor.buuauthor | Yurtkuran, Merih M. | - |
dc.contributor.buuauthor | Yurtkuran, Mustafa Abbas | - |
dc.contributor.buuauthor | Oral, Haluk Barbaros | - |
dc.contributor.researcherid | AAK-6623-2020 | tr_TR |
dc.contributor.researcherid | K-7285-2012 | tr_TR |
dc.contributor.researcherid | X-4479-2018 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 21418526 | tr_TR |
dc.subject.wos | Genetics & heredity | en_US |
dc.subject.wos | Immunology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q4 | en_US |
dc.contributor.scopusid | 56005080200 | tr_TR |
dc.contributor.scopusid | 6507727900 | tr_TR |
dc.contributor.scopusid | 6603722836 | tr_TR |
dc.contributor.scopusid | 14020405100 | tr_TR |
dc.contributor.scopusid | 23037226400 | tr_TR |
dc.contributor.scopusid | 55408539300 | tr_TR |
dc.contributor.scopusid | 7003389525 | tr_TR |
dc.contributor.scopusid | 7004498001 | tr_TR |
dc.subject.scopus | Behcet Syndrome; Uveitis; Infliximab | en_US |
dc.subject.emtree | Interleukin 1 receptor | en_US |
dc.subject.emtree | Interleukin 1 receptor blocking agent | en_US |
dc.subject.emtree | Interleukin 1alpha | en_US |
dc.subject.emtree | Interleukin 1beta | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Behcet disease | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Disease association | en_US |
dc.subject.emtree | Disease course | en_US |
dc.subject.emtree | Disease predisposition | en_US |
dc.subject.emtree | DNA polymorphism | en_US |
dc.subject.emtree | Erythema nodosum | en_US |
dc.subject.emtree | Ethnic difference | en_US |
dc.subject.emtree | Ethnic group | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Gene cluster | en_US |
dc.subject.emtree | Gene frequency | en_US |
dc.subject.emtree | Genetic susceptibility | en_US |
dc.subject.emtree | Genotype | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Turkey (republic) | en_US |
Appears in Collections: | Scopus Web of Science |
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