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http://hdl.handle.net/11452/25687
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DC Field | Value | Language |
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dc.contributor.author | Özgöz, Asuman | - |
dc.date.accessioned | 2022-04-11T07:00:19Z | - |
dc.date.available | 2022-04-11T07:00:19Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | Şamlı, 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.issn | 1676-5680 | - |
dc.identifier.uri | https://doi.org/10.4238/2012.December.17.6 | - |
dc.identifier.uri | http://www.funpecrp.com.br/gmr/year2012/vol11-4/pdf/gmr2213.pdf | - |
dc.identifier.uri | http://hdl.handle.net/11452/25687 | - |
dc.description.abstract | Vascular 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.iso | en | en_US |
dc.publisher | Funpec-Editora | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Biochemistry & molecular biology | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Polymorphisms | en_US |
dc.subject | Recurrent pregnancy loss | en_US |
dc.subject | Vegf | en_US |
dc.subject | Factor vegf | en_US |
dc.subject | Vasculogenesis | en_US |
dc.subject | Angiogenesis | en_US |
dc.subject | Lethality | en_US |
dc.subject.mesh | Abortion, habitual | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Base sequence | en_US |
dc.subject.mesh | Case-control studies | en_US |
dc.subject.mesh | Dna primers | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetic association studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Polymorphism, restriction fragment length | en_US |
dc.subject.mesh | Polymorphism, single nucleotide | en_US |
dc.subject.mesh | Pregnancy | en_US |
dc.subject.mesh | Sequence analysis, dna | en_US |
dc.subject.mesh | Vascular endothelial growth factor a | en_US |
dc.subject.mesh | Young adult | en_US |
dc.title | Vascular endothelial growth factor gene 1154 G/A, 2578 C/A, 460 C/T, 936 C/T polymorphisms and association with recurrent pregnancy losses | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000313960500120 | tr_TR |
dc.identifier.scopus | 2-s2.0-84885658924 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Veteriner Fakültesi/Genetik Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı. | tr_TR |
dc.relation.bap | UAP(F)-2009/41 | tr_TR |
dc.identifier.startpage | 4739 | tr_TR |
dc.identifier.endpage | 4745 | tr_TR |
dc.identifier.volume | 11 | tr_TR |
dc.identifier.issue | 4 | tr_TR |
dc.relation.journal | Genetics and Molecular Research | en_US |
dc.contributor.buuauthor | Şamlı, Hale | - |
dc.contributor.buuauthor | Çetinkaya, Demir Bilge | - |
dc.contributor.buuauthor | Atalay, Mehmet Aral | - |
dc.contributor.buuauthor | Uncu, Gürkan | - |
dc.contributor.researcherid | AAH-9834-2021 | tr_TR |
dc.contributor.researcherid | AAH-6488-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 23315815 | tr_TR |
dc.subject.wos | Biochemistry & molecular biology | en_US |
dc.subject.wos | Genetics & heredity | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.contributor.scopusid | 6507670789 | tr_TR |
dc.contributor.scopusid | 36923039100 | tr_TR |
dc.contributor.scopusid | 53863297800 | tr_TR |
dc.contributor.scopusid | 6603716169 | tr_TR |
dc.subject.scopus | Vascular Endothelial Growth Factor A; Restriction Fragment Length Polymorphisms; Polymorphism | en_US |
dc.subject.emtree | Primer dna | en_US |
dc.subject.emtree | Vasculotropin a | en_US |
dc.subject.emtree | Vegfa protein, human | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Case control study | en_US |
dc.subject.emtree | Dna sequence | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Genetic association | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Nucleotide sequence | en_US |
dc.subject.emtree | Pregnancy | en_US |
dc.subject.emtree | Recurrent abortion | en_US |
dc.subject.emtree | Restriction fragment length polymorphism | en_US |
dc.subject.emtree | Single nucleotide polymorphism | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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