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Paraoxonase 1 Polymorphisms in Patients With Primary Glomerulonephritis A Single-center Study in Turkey

dc.contributor.authorTuglular, Serhan
dc.contributor.authorErgen, Arzu
dc.contributor.authorArikan, Hakki
dc.contributor.authorIsbir, Turgay
dc.contributor.authorAkoglu, Emel
dc.contributor.authorEren, Zehra
dc.contributor.authorKantarci, Gulcin
dc.contributor.authorBiyikli, Nese
dc.date.accessioned2021-03-03T20:55:40Z
dc.date.available2021-03-03T20:55:40Z
dc.date.issued2012
dc.identifier.citationEren Z., Kantarci G., Biyikli N., Arikan H., Tuglular S., Ergen A., Isbir T., Akoglu E., "Paraoxonase 1 Polymorphisms in Patients With Primary Glomerulonephritis A Single-center Study in Turkey", IRANIAN JOURNAL OF KIDNEY DISEASES, cilt.6, sa.3, ss.181-185, 2012
dc.identifier.issn1735-8582
dc.identifier.othervv_1032021
dc.identifier.otherav_5c7f8a94-d47f-4720-a078-e56c9685e702
dc.identifier.urihttp://hdl.handle.net/20.500.12627/64847
dc.description.abstractIntroduction. Human paraoxonase 1 (PON1) is an enzyme related with high-density lipoprotein cholesterol. The link between genetic polymorphisms of PON1 and hyperlipidemia and increased lipid oxidation may explain these complications in the course of glomerular diseases. In this study, we aimed to investigate PON1 192 and PON1 55 polymorphisms in patients with primary glomerulonephritis and healthy individuals.
dc.language.isoeng
dc.subjectNefroloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleParaoxonase 1 Polymorphisms in Patients With Primary Glomerulonephritis A Single-center Study in Turkey
dc.typeMakale
dc.relation.journalIRANIAN JOURNAL OF KIDNEY DISEASES
dc.contributor.departmentMarmara Üniversitesi , ,
dc.identifier.volume6
dc.identifier.issue3
dc.identifier.startpage181
dc.identifier.endpage185
dc.contributor.firstauthorID75617


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