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dc.contributor.authorStanford, MR
dc.contributor.authorMarshall, SE
dc.contributor.authorJewell, DP
dc.contributor.authorKanawati, CA
dc.contributor.authorFortune, F
dc.contributor.authorYang, X
dc.contributor.authorAhmad, T
dc.contributor.authorGogus, F
dc.contributor.authorWallace, GR
dc.contributor.authorMadanat, W
dc.date.accessioned2021-03-03T18:25:21Z
dc.date.available2021-03-03T18:25:21Z
dc.date.issued2004
dc.identifier.citationYang X., Ahmad T., Gogus F., Wallace G., Madanat W., Kanawati C., Stanford M., Fortune F., Jewell D., Marshall S., "Analysis of the CC chemokine receptor 5 (CCR5) Delta 32 polymorphism in Behcet's disease", EUROPEAN JOURNAL OF IMMUNOGENETICS, cilt.31, sa.1, ss.11-14, 2004
dc.identifier.issn0960-7420
dc.identifier.othervv_1032021
dc.identifier.otherav_4eed634c-5cf9-42b2-8028-9173e82cce85
dc.identifier.urihttp://hdl.handle.net/20.500.12627/56349
dc.identifier.urihttps://doi.org/10.1111/j.1365-2370.2004.00444.x
dc.description.abstractChemokines are important determinants of the early inflammatory response. The CC chemokine receptor 5 (CCR5) Delta32 variant results in a non-functional form of the chemokine receptor, and has been implicated in a variety of immune-mediated diseases. To investigate its role in the pathogenesis of Behcet's disease, we studied 350 patients and 519 healthy controls from three ethnic groups. While significant inter-ethnic variation in allele frequency was observed, no association was identified with disease, even when data were stratified by the known susceptibility gene HLA-B*51.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectTıp
dc.subjectİmmünoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleAnalysis of the CC chemokine receptor 5 (CCR5) Delta 32 polymorphism in Behcet's disease
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF IMMUNOGENETICS
dc.contributor.department, ,
dc.identifier.volume31
dc.identifier.issue1
dc.identifier.startpage11
dc.identifier.endpage14
dc.contributor.firstauthorID170961


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