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dc.contributor.authorDalay, N
dc.contributor.authorAkisik, E
dc.date.accessioned2021-03-04T13:40:37Z
dc.date.available2021-03-04T13:40:37Z
dc.date.issued2004
dc.identifier.citationAkisik E., Dalay N., "Estrogen receptor codon 594 and HER2 codon 655 polymorphisms and breast cancer risk", EXPERIMENTAL AND MOLECULAR PATHOLOGY, cilt.76, sa.3, ss.260-263, 2004
dc.identifier.issn0014-4800
dc.identifier.otherav_7dadcb74-2c65-438d-9b22-eca32803c666
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/85853
dc.identifier.urihttps://doi.org/10.1016/j.yexmp.2003.12.005
dc.description.abstractThe estrogen receptor (ER) and the human epithelial growth factor receptor 2 (HER2) genes have been implicated in the development and prognosis of breast cancer. Several genetic polymorphic sites in these genes have been identified and associated with the risk of breast cancer. We have investigated the association between the estrogen receptor codon 594 (ACA to ACG) and HER2 codon 655 (ATC to GTC) polymorphisms and breast cancer risk. Genomic DNA from breast cancer patients and control subjects was analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-R-FLP). When allelic frequencies of the ER codon 594 and HER2 codon 655 gene were compared, no significant differences were observed between the patient and control groups. (P = 0.063, OR = 1.55, 95% CI = 0.25-9.41 and P = 0.949, OR = 1.01, 95% CI = 0.55-1.88, respectively). In conclusion, our results support the view that both the ER codon 594 and HER2 codon 655 polymorphisms are not associated with increased risk of breast cancer. (C) 2003 Elsevier Inc. All rights reserved.
dc.language.isoeng
dc.subjectPatoloji
dc.subjectTemel Bilimler
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.titleEstrogen receptor codon 594 and HER2 codon 655 polymorphisms and breast cancer risk
dc.typeMakale
dc.relation.journalEXPERIMENTAL AND MOLECULAR PATHOLOGY
dc.contributor.department, ,
dc.identifier.volume76
dc.identifier.issue3
dc.identifier.startpage260
dc.identifier.endpage263
dc.contributor.firstauthorID171707


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