Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21113
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dc.date.accessioned2021-07-06T08:29:22Z-
dc.date.available2021-07-06T08:29:22Z-
dc.date.issued1998-
dc.identifier.citationÇeçener, G. vd. (1998). "Common fragile site expression and genetic predisposition to breast cancer". Teratogenesis Carcinogenesis and Mutagenesis, 18(6), 279-291.en_US
dc.identifier.issn0270-3211-
dc.identifier.urihttps://doi.org/10.1002/(SICI)1520-6866(1998)18:6<279::AID-TCM2>3.3.CO;2-L-
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/10052563-
dc.identifier.urihttp://hdl.handle.net/11452/21113-
dc.description.abstractThe expression of common fragile sites induced by aphidicolin and caffeine was evaluated on prometaphase obtained from the peripheral blood lymphocytes of 35 women with breast cancer, their 35 clinically healthy female family members, and 20 sex- and age-matched normal controls. As a result of the cytogenetic and statistical evaluation, the number of damaged cells, chromosomal aberrations, and expression frequencies of fragile sites detected in patients with breast cancer and their first-degree relatives were found to be significantly higher than those in the control group. Our findings indicate an increased genetic instability in women with breast carcinomas and their relatives. Therefore, fragile sites may be used as a reliable marker for defining genetic susceptibility to cancer in general.en_US
dc.language.isoenen_US
dc.publisherWiley-Lissen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOncologyen_US
dc.subjectGenetics & heredityen_US
dc.subjectToxicologyen_US
dc.subjectBreast canceren_US
dc.subjectAphidicolinen_US
dc.subjectCaffeineen_US
dc.subjectFragile sitesen_US
dc.subjectGenetic susceptibilityen_US
dc.subjectChromosomal abnormalitiesen_US
dc.subjectLung cancersen_US
dc.subjectChromosome breakpointsen_US
dc.subjectAphidicolinen_US
dc.subjectLymphocytesen_US
dc.titleCommon fragile site expression and genetic predisposition to breast canceren_US
dc.typeArticleen_US
dc.identifier.wos000078642200002tr_TR
dc.identifier.scopus2-s2.0-0032463423tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-3820-424Xtr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.identifier.startpage279tr_TR
dc.identifier.endpage291tr_TR
dc.identifier.volume18tr_TR
dc.identifier.issue6tr_TR
dc.relation.journalTeratogenesis Carcinogenesis and Mutagenesisen_US
dc.contributor.buuauthorÇeçener, Gülşah-
dc.contributor.buuauthorEgeli, Ünal-
dc.contributor.buuauthorTaşdelen, İsmet-
dc.contributor.buuauthorTunca, Berrin-
dc.contributor.buuauthorDuman, H.-
dc.contributor.buuauthorKızıl, Ayhan-
dc.contributor.researcheridAAP-9988-2020tr_TR
dc.contributor.researcheridABI-6078-2020tr_TR
dc.identifier.pubmed10052563tr_TR
dc.subject.wosOncologyen_US
dc.subject.wosGenetics & heredityen_US
dc.subject.wosToxicologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
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