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dc.contributor.authorAkisik, Elif
dc.contributor.authorDalay, Nejat
dc.date.accessioned2021-03-03T12:39:04Z
dc.date.available2021-03-03T12:39:04Z
dc.date.issued2007
dc.identifier.citationAkisik E., Dalay N., "Functional polymorphism of thymidylate synthase, but not of the COMT and IL-1B genes, is associated with breast cancer", JOURNAL OF CLINICAL LABORATORY ANALYSIS, cilt.21, sa.2, ss.97-102, 2007
dc.identifier.issn0887-8013
dc.identifier.othervv_1032021
dc.identifier.otherav_2f48596f-6cf7-463b-aced-3acb60fa1f5d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/36309
dc.identifier.urihttps://doi.org/10.1002/jcla.20139
dc.description.abstractPolymorphic variations may affect the rate of gene transcription, the stability of the mRNA, or the quantity and activity of the resulting protein. In this study We evaluated the association between the interleukin-1B C-31T, catechol-O-methyltransferase Val158Met, and thymidylate synthase (TS) 1494del6 polymorphisms and breast cancer. Each genetic polymorphism was investigated by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis. No significant difference in either the genotype distribution or the allelic frequencies of the IL-1B and C : OMT gene polymorphisms was observed between the patient and control groups. For the TS 1494del6 polymorphism a significant difference was observed for both the genotypes (P=0.01) and the allele frequencies (P=0.0097), indicating a decreased risk associated with the variant allele. Our data do not provide evidence for an association between the polymorphic variants of the IL-1B and COMT genes and breast cancer risk. On the other hand, the TS 1494del6 polymorphism is associated with a significantly lower risk of breast cancer and may be a potential genetic marker.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectTIBBİ LABORATUVAR TEKNOLOJİSİ
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.titleFunctional polymorphism of thymidylate synthase, but not of the COMT and IL-1B genes, is associated with breast cancer
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL LABORATORY ANALYSIS
dc.contributor.department, ,
dc.identifier.volume21
dc.identifier.issue2
dc.identifier.startpage97
dc.identifier.endpage102
dc.contributor.firstauthorID180954


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