Show simple item record

dc.contributor.authorBozkurt, Nilufer
dc.contributor.authorIsbir, Turgay
dc.contributor.authorBerber, Ibrahim
dc.contributor.authorTitiz, Izzet
dc.contributor.authorYigit, Bulent
dc.date.accessioned2021-03-03T16:28:02Z
dc.date.available2021-03-03T16:28:02Z
dc.date.issued2007
dc.identifier.citationYigit B., Bozkurt N., Berber I., Titiz I., Isbir T., "Analysis of CC chemokine receptor 5 and 2 polymorphisms and renal transplant survival", CELL BIOCHEMISTRY AND FUNCTION, cilt.25, sa.4, ss.423-426, 2007
dc.identifier.issn0263-6484
dc.identifier.othervv_1032021
dc.identifier.otherav_4464e260-f3a9-40ed-bd1d-093ece68709c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/49670
dc.identifier.urihttps://doi.org/10.1002/cbf.1322
dc.description.abstractChronic rejection is an immune process leading to graft failure. By regulating the trafficking of leukocytes, chemokines and chemokine receptors are thought to be one of the reasons causing acute renal rejection (ARE), which increases the possibility of chronic rejection and organ destruction. This study was designed to investigate, in the Turkish population, an association of chemokine receptor genetic variants, CCR2V641, CCR5-59029-A/G, CCR5-A32 and acute renal rejection after renal transplant surgery. We carried out our study in 85 Turkish renal transplant patients (45 men, 40 women; mean age 39 2 years) by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) techniques. We found no significant difference in the incidence of rejection among patients possessing or lacking CCR5-A32. For the groups with and without acute renal rejection, we found a significant difference between the groups in A and G allele distribution in both CCR2V641 and CCR559029 gene variants (p = 0.003 and p = 0.003, respectively). According to our findings, the risk of acute rejection in renal transplantation may be associated with genetic variation in the chemokine receptor genes CCR559029 and CCR2V641 in Turkey, and studies on these gene polymorphisms could be an ideal target for future interventions intended to prevent renal transplant loss. Copyright (C) 2006 John Wiley & Sons, Ltd.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectTemel Tıp Bilimleri
dc.subjectHistoloji-Embriyoloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectHÜCRE BİYOLOJİSİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleAnalysis of CC chemokine receptor 5 and 2 polymorphisms and renal transplant survival
dc.typeMakale
dc.relation.journalCELL BIOCHEMISTRY AND FUNCTION
dc.contributor.department, ,
dc.identifier.volume25
dc.identifier.issue4
dc.identifier.startpage423
dc.identifier.endpage426
dc.contributor.firstauthorID183309


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record