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Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome

dc.contributor.authorPehlivan, Sacide
dc.contributor.authorBÜYÜKÇELİK, MİTHAT
dc.contributor.authorOĞUZKAN BALCI, SİBEL
dc.contributor.authorKUL, SEVAL
dc.contributor.authorCol, Nilgun
dc.contributor.authorBalat, Ayse
dc.contributor.authorKILIÇ, BELTİNGE DEMİRCİOĞLU
dc.date.accessioned2021-03-05T09:20:59Z
dc.date.available2021-03-05T09:20:59Z
dc.date.issued2018
dc.identifier.citationKILIÇ B. D. , BÜYÜKÇELİK M., OĞUZKAN BALCI S., Pehlivan S., KUL S., Col N., Balat A., "Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome", PEDIATRIC NEPHROLOGY, cilt.33, ss.295-303, 2018
dc.identifier.issn0931-041X
dc.identifier.othervv_1032021
dc.identifier.otherav_9d713abb-52d8-48d2-8529-5ac4115bfb46
dc.identifier.urihttp://hdl.handle.net/20.500.12627/105781
dc.identifier.urihttps://doi.org/10.1007/s00467-017-3800-7
dc.description.abstractUteroglobin (UG) is a multifunctional protein with anti-inflammatory properties. The aim of this study was to first evaluate the role of UG gene G38A polymorphism in childhood idiopathic nephrotic syndrome (INS), and determine whether this variation may be related to the occurrence of INS or a steroid response.
dc.language.isoeng
dc.subjectNefroloji
dc.subjectKlinik Tıp (MED)
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.titleUteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome
dc.typeMakale
dc.relation.journalPEDIATRIC NEPHROLOGY
dc.contributor.departmentGaziantep Üniversitesi , Tıp Fakültesi , Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
dc.identifier.volume33
dc.identifier.issue2
dc.identifier.startpage295
dc.identifier.endpage303
dc.contributor.firstauthorID251192


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