Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25687
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dc.contributor.authorÖzgöz, Asuman-
dc.date.accessioned2022-04-11T07:00:19Z-
dc.date.available2022-04-11T07:00:19Z-
dc.date.issued2012-
dc.identifier.citationŞamlı, H. vd. (2012). "Vascular endothelial growth factor gene 1154 G/A, 2578 C/A, 460 C/T, 936 C/T polymorphisms and association with recurrent pregnancy losses". Genetics and Molecular Research, 11(4), 4739-4745.en_US
dc.identifier.issn1676-5680-
dc.identifier.urihttps://doi.org/10.4238/2012.December.17.6-
dc.identifier.urihttp://www.funpecrp.com.br/gmr/year2012/vol11-4/pdf/gmr2213.pdf-
dc.identifier.urihttp://hdl.handle.net/11452/25687-
dc.description.abstractVascular endothelial growth factor (VEGF) regulates endothelial cell proliferation, migration and differentiation. VEGF plays a critical role in angiogenesis during placenta formation. We investigated whether VEGF gene polymorphisms are associated with recurrent pregnancy loss. Thirty-eight women with recurrent pregnancy loss and 30 control women with live-born children were recruited from 2010 to 2011 in the region of Bursa, Turkey. VEGF gene polymorphisms were assessed with PCR-RFLP analysis of DNA samples obtained from leukocytes. DNA fragments were investigated by using appropriate primers. SNP scanning was performed using MnII, BgIII, BshI2361, Hsp92II restriction enzymes for 1154 G/A, 2578 C/A, 460 C/T, and 936 C/T polymorphisms, respectively. The frequencies of 2578 C/A, 460 C/T, 936 C/T polymorphisms were not significantly different between the controls and women with recurrent pregnancy loss. However, the prevalence of the 1154 G/A polymorphism A/A genotype was significantly higher in the recurrent pregnancy loss group (23.7 vs 3.4%). One of the four common polymorphisms of the VEGF gene was found to be more frequent in women with recurrent pregnancy loss. It is possible that disruption of VEGF function and placental angiogenesis can contribute to pregnancy loss in women with recurrent pregnancy loss.en_US
dc.language.isoenen_US
dc.publisherFunpec-Editoraen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBiochemistry & molecular biologyen_US
dc.subjectGenetics & heredityen_US
dc.subjectPolymorphismsen_US
dc.subjectRecurrent pregnancy lossen_US
dc.subjectVegfen_US
dc.subjectFactor vegfen_US
dc.subjectVasculogenesisen_US
dc.subjectAngiogenesisen_US
dc.subjectLethalityen_US
dc.subject.meshAbortion, habitualen_US
dc.subject.meshAdulten_US
dc.subject.meshBase sequenceen_US
dc.subject.meshCase-control studiesen_US
dc.subject.meshDna primersen_US
dc.subject.meshFemaleen_US
dc.subject.meshGenetic association studiesen_US
dc.subject.meshHumansen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshPolymorphism, restriction fragment lengthen_US
dc.subject.meshPolymorphism, single nucleotideen_US
dc.subject.meshPregnancyen_US
dc.subject.meshSequence analysis, dnaen_US
dc.subject.meshVascular endothelial growth factor aen_US
dc.subject.meshYoung adulten_US
dc.titleVascular endothelial growth factor gene 1154 G/A, 2578 C/A, 460 C/T, 936 C/T polymorphisms and association with recurrent pregnancy lossesen_US
dc.typeArticleen_US
dc.identifier.wos000313960500120tr_TR
dc.identifier.scopus2-s2.0-84885658924tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Veteriner Fakültesi/Genetik Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı.tr_TR
dc.relation.bapUAP(F)-2009/41tr_TR
dc.identifier.startpage4739tr_TR
dc.identifier.endpage4745tr_TR
dc.identifier.volume11tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalGenetics and Molecular Researchen_US
dc.contributor.buuauthorŞamlı, Hale-
dc.contributor.buuauthorÇetinkaya, Demir Bilge-
dc.contributor.buuauthorAtalay, Mehmet Aral-
dc.contributor.buuauthorUncu, Gürkan-
dc.contributor.researcheridAAH-9834-2021tr_TR
dc.contributor.researcheridAAH-6488-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed23315815tr_TR
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosGenetics & heredityen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.contributor.scopusid6507670789tr_TR
dc.contributor.scopusid36923039100tr_TR
dc.contributor.scopusid53863297800tr_TR
dc.contributor.scopusid6603716169tr_TR
dc.subject.scopusVascular Endothelial Growth Factor A; Restriction Fragment Length Polymorphisms; Polymorphismen_US
dc.subject.emtreePrimer dnaen_US
dc.subject.emtreeVasculotropin aen_US
dc.subject.emtreeVegfa protein, humanen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCase control studyen_US
dc.subject.emtreeDna sequenceen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGenetic associationen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeNucleotide sequenceen_US
dc.subject.emtreePregnancyen_US
dc.subject.emtreeRecurrent abortionen_US
dc.subject.emtreeRestriction fragment length polymorphismen_US
dc.subject.emtreeSingle nucleotide polymorphismen_US
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