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dc.contributor.authorSaruhan-Direskeneli, G
dc.contributor.authorYilmaz, V
dc.contributor.authorHajeer, AH
dc.contributor.authorUyar, FA
dc.contributor.authorGul, A
dc.contributor.authorDuymaz-Tozkir, J
dc.date.accessioned2021-03-05T18:00:13Z
dc.date.available2021-03-05T18:00:13Z
dc.date.issued2005
dc.identifier.citationDuymaz-Tozkir J., Yilmaz V., Uyar F., Hajeer A., Saruhan-Direskeneli G., Gul A., "Polymorphisms of the IL-8 and CXCR2 genes are not associated with Behcet's disease", JOURNAL OF RHEUMATOLOGY, cilt.32, ss.93-97, 2005
dc.identifier.issn0315-162X
dc.identifier.othervv_1032021
dc.identifier.otherav_c8463169-afc1-4b04-a461-66a025db0440
dc.identifier.urihttp://hdl.handle.net/20.500.12627/132721
dc.description.abstractObjective. Genetic susceptibility to Behcet's disease (BD) is well documented for HLA-B51; however, contribution of other genetic polymorphisms is estimated to be substantial. Interleukin 8 (IL-8), a potent chemoattractant for neutrophils, has been found to be elevated in BD serum, and the serum concentrations correlate with disease activity. Novel polymorphisms in IL-8 (CXCL8) and in one of its receptors, CXCR2 gene, may have a role in enhanced IL-8 activity in BD.
dc.language.isoeng
dc.subjectİmmünoloji ve Romatoloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titlePolymorphisms of the IL-8 and CXCR2 genes are not associated with Behcet's disease
dc.typeMakale
dc.relation.journalJOURNAL OF RHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume32
dc.identifier.issue1
dc.identifier.startpage93
dc.identifier.endpage97
dc.contributor.firstauthorID50951


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