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MYELOPEROXIDASE GENE PROMOTOR POLYMORPHYSM IN MOTHERS WHO HAVE A CHILD WITH NEURAL TUBE DEFECT

dc.contributor.authorBalat, Ozcan
dc.contributor.authorDikensoy, Ebru
dc.contributor.authorSever, Tugce
dc.contributor.authorPEHLİVAN, Sacide
dc.contributor.authorCebesoy, Fatma Bahar
dc.contributor.authorKarcin, Esin
dc.date.accessioned2022-02-18T09:45:35Z
dc.date.available2022-02-18T09:45:35Z
dc.date.issued2010
dc.identifier.citationDikensoy E., Sever T., PEHLİVAN S., Balat O., Cebesoy F. B. , Karcin E., "MYELOPEROXIDASE GENE PROMOTOR POLYMORPHYSM IN MOTHERS WHO HAVE A CHILD WITH NEURAL TUBE DEFECT", TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY, cilt.7, sa.2, ss.102-106, 2010
dc.identifier.othervv_1032021
dc.identifier.otherav_5b3bc2bf-779b-4ba4-a244-0a36fcdb6985
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177913
dc.description.abstractObjective: The inflammatory pathway genes myeloperoxidase (MPO) is involved with regulation of inflammation through reactions with hydrogen peroxide (H2O2). The MPO enzyme is expressed abundantly in neutrophils, in which its antimicrobial function converts (H2O2) to the bacterocidal and DNA-damaging hypochlorous acid. Our aim was in this study to investigate whether there is a relationship between MPO gene (rs 2333227) polymorphysm (-463G/A) and neural tube defects.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectObstetrics and Gynecology
dc.subjectHealth Sciences
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.titleMYELOPEROXIDASE GENE PROMOTOR POLYMORPHYSM IN MOTHERS WHO HAVE A CHILD WITH NEURAL TUBE DEFECT
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY
dc.contributor.departmentGaziantep Üniversitesi , ,
dc.identifier.volume7
dc.identifier.issue2
dc.identifier.startpage102
dc.identifier.endpage106
dc.contributor.firstauthorID3377901


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