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dc.contributor.authorÖzel, Mavi Deniz
dc.contributor.authorÖnder, Mehmet Emin
dc.contributor.authorSazcı, Ali
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:36:56Z
dc.date.available10.07.201910:49:14
dc.date.available2019-07-10T19:36:56Z
dc.date.issued2016en_US
dc.identifier.citationÖzel, M. D., Önder, M. E. ve Sazcı, A. (2016). Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder. Biomedical Reports, 5(4), 506-510. https://dx.doi.org/10.3892/br.2016.742en_US
dc.identifier.issn2049-9434
dc.identifier.urihttps://hdl.handle.net/20.500.12511/1290
dc.identifier.urihttps://dx.doi.org/10.3892/br.2016.742
dc.description.abstractThe transcription factor 4 (TCF4) gene encodes a helix-loop-helix transcription factor protein, which initiates neuronal differentiation and is primarily expressed during nervous system development. The aim of the present study is to investigate the association of the TCF4 rs9960767 polymorphism and bipolar disorder, which is highly heritable. DNA isolation was performed on 95 patients with bipolar disorder and 108 healthy control subjects to examine the TCF4 rs9960767 polymorphism. Genotypic and allelic frequencies were determined using the polymerase chain reaction-restriction fragment length polymorphism method designed in our laboratory. Statistical analysis was performed using ?2 test within the 95% confidence interval. Odds ratios were calculated and Hardy-Weinberg equilibrium (HWE) was verified for all control subjects and patients. The A allele frequency was 95.8% in the patients and 94.4% in the control subjects, and 4.2% in the patients and 5.6% in the control subjects for the C allele. The genotype frequencies of the TCF4 gene rs9960767 variant were as follows: AA, 91.6% and AC, 8.4% in patients with bipolar (CC genotype was not observed in cases); AA, 89.8%; AC, 9.3% and CC, 0.9% in the control subjects. No statistically significant difference was identified between the patients and control subjects (?2=0.937; P=0.626). In addition, gender specific analysis was performed, although no significant association was found according to the gender distrubition. All patients and control subjects were in HWE (P>0.05). Statistical analysis of the data indicates that the TCF4 gene rs9960767 polymorphism is not an independent risk factor for bipolar disorder in the overall population or in terms of gender; however, an increased population size would improve the statistical power. Furthermore, additional gene variants that are specifically involved in neuronal development may be analyzed for revealing the complex genetic architecture of bipolar disorder. An improved approach would be better to evaluate the TCF4 gene in a pathway specific manner due to its role as a transcription factor.en_US
dc.description.sponsorshipKocaeli Universityen_US
dc.language.isoengen_US
dc.publisherSpandidos Publicationsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBipolar Disorderen_US
dc.subjectPolymorphismen_US
dc.subjectRs9960767en_US
dc.subjectSingle Nucleotide Polymorphismen_US
dc.subjectTranscription Factor 4 Geneen_US
dc.titleTranscription factor 4 gene rs9960767 polymorphism in bipolar disorderen_US
dc.typearticleen_US
dc.relation.ispartofBiomedical Reportsen_US
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalıen_US
dc.identifier.volume5en_US
dc.identifier.issue4en_US
dc.identifier.startpage506en_US
dc.identifier.endpage510en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.3892/br.2016.742en_US
dc.identifier.scopusqualityQ1en_US


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