Polymorphism of the Methylenetetrahydrofolate Reductase C677T Gene With Chronic Allograft Nephropathy in Renal Transplant Recipientsw

dc.contributor.authorAzarpira, Negar
dc.contributor.authorDarai, Masumeh
dc.contributor.authorRaisjalali, Ghanbar
dc.date.accessioned2025-11-18T12:53:43Z
dc.date.issued2008-03
dc.description.abstractObjectives: This study sought to investigate the frequency of the 5, 10-methylenetetrahydrofolate reductase gene (MTHFR C677T) in 127 patients (77 with chronic allograft nephropathy and 50 with normal renal function) who had undergone a renal transplant at least 20 months earlier to define the risk factors for chronic allograft dysfunction. Fifty healthy subjects served as controls. Materials and Methods: Genotypes were de­termined using polymerase chain reaction followed by restriction fragment length poly­morphism analysis. The restriction enzyme for the MTHFR C677T variants was HinfI. Results: No statistically significant differences were seen between the allelic and genotypic distribution of the MTHFR polymorphism. Conclusions: Additional studies with larger sample sizes are needed to define the influence of MTHFR C677T genotyping on clinical outcomes in renal allograft recipients.
dc.identifier.citationExperimental and Clinical Transplantation, Cilt 6, Sayı 1, 2008, ss. 54-58en
dc.identifier.eissn2146-8427en
dc.identifier.issn1304-0855
dc.identifier.issue1en
dc.identifier.urihttps://hdl.handle.net/11727/13909
dc.identifier.volume6en
dc.language.isoen_US
dc.publisherBaşkent Üniversitesi
dc.sourceExperimental and Clinical Transplantationen
dc.subjectMTHFR
dc.subjectAssociation
dc.subjectChronic allograft dysfunction
dc.subjectIranian
dc.subjectGenetic
dc.titlePolymorphism of the Methylenetetrahydrofolate Reductase C677T Gene With Chronic Allograft Nephropathy in Renal Transplant Recipientsw
dc.typeArticle

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