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dc.contributor.authorErgul, E
dc.contributor.authorKara, I
dc.contributor.authorGuzelhan, Y
dc.contributor.authorKaya, G
dc.contributor.authorSazci, A
dc.date.accessioned2021-03-06T09:20:26Z
dc.date.available2021-03-06T09:20:26Z
dc.date.issued2003
dc.identifier.citationSazci A., Ergul E., Guzelhan Y., Kaya G., Kara I., "Methylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia", MOLECULAR BRAIN RESEARCH, cilt.117, ss.104-107, 2003
dc.identifier.issn0169-328X
dc.identifier.otherav_e52acc60-be6c-4321-b71a-138d50e50e2d
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/150784
dc.identifier.urihttps://doi.org/10.1016/s0169-328x(03)00327-9
dc.description.abstractTo investigate the role of methylenetetrahydrofolate reductase gene polymorphisms in schizophrenia, we analyzed the genotypes of MTHFR677 and MTHFR1298 of 130 schizophrenic patients and 226 controls, using a polymerase chain reaction restriction fragment length polymorphism method. The MTHFR T677 allele was significantly distributed (chi(2) = 7.900; P = 0.019), between schizophrenic cases and healthy controls. The T677T genotype was overrepresented in the schizophrenic patients (OR = 2.504; 95% CI = 1.276-4.915; 2 chi(2) = 7.477; P = 0.006). The T677T/A1298A, and C677T/C1298C compound genotypes were greater in the schizophrenic patients, (OR = 3.157; 95% CI = 1.522-6.545; chi(2) = 10.336; P = 0.001 and OR = 1.744; 95% CI = 0.108-28.121; chi(2) = 0.158; P = 0.691, respectively). The MTHFR T677 allele and T677T and T677T/A1298A genotypes are genetic risk factors for schizophrenia. (C) 2003 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri
dc.titleMethylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia
dc.typeMakale
dc.relation.journalMOLECULAR BRAIN RESEARCH
dc.contributor.department, ,
dc.identifier.volume117
dc.identifier.issue1
dc.identifier.startpage104
dc.identifier.endpage107
dc.contributor.firstauthorID169411


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