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dc.contributor.authorKarahalil, Bensu
dc.contributor.authorKarakaya, Ali
dc.contributor.authorCİVELEK, EREN
dc.contributor.authorKocabas, NA
dc.contributor.authorAlhayıroğlu, Ela
dc.contributor.authorŞardaş, Semra
dc.date.accessioned2021-03-02T21:35:43Z
dc.date.available2021-03-02T21:35:43Z
dc.identifier.citationKarahalil B., Şardaş S., Kocabas N., Alhayıroğlu E., Karakaya A., CİVELEK E., "Chromosomal aberrations under basal conditions and after treatment with X-ray in human lymphocytes as related to the GSTM1 genotype", MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, cilt.515, ss.135-140, 2002
dc.identifier.issn1383-5718
dc.identifier.othervv_1032021
dc.identifier.otherav_07ddd018-0d8a-4a24-9f9b-8766cb30c830
dc.identifier.urihttp://hdl.handle.net/20.500.12627/11108
dc.identifier.urihttps://doi.org/10.1016/s1383-5718(02)00003-7
dc.description.abstractThe frequency of chromosomal aberrations (CAs) was evaluated in blood lymphocytes from 18 healthy subjects. Basal CA frequencies were not significantly different in GSTM1 positive and GSTM1 null subjects (P > 0.05), whereas they were considerably higher in smokers than in non-smokers. After 1 Gy dose of X-ray challenge of blood samples, CA frequencies were significantly higher in GSTM1 null subjects, compared to GSTM1 positive subjects (P < 0.005), and in smokers, compared to non-smokers. These effects are ascribed to the influence of GSTM1 genotype and of smoking status on DNA repair capacities. As the induction of CAs are associated with carcinogenesis, the challenge assay is able to detect enhanced susceptibility for CA caused by genetic predisposition of DNA repair deficiency. (C) 2002 Published by Elsevier Science B.V
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOTEKNOLOJİ VE UYGULAMALI MİKROBİYOLOJİ
dc.subjectMikrobiyoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTOKSİKOLOJİ
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectEczacılık
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectYaşam Bilimleri
dc.subjectBiyoteknoloji
dc.subjectTemel Bilimler
dc.titleChromosomal aberrations under basal conditions and after treatment with X-ray in human lymphocytes as related to the GSTM1 genotype
dc.typeMakale
dc.relation.journalMUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
dc.contributor.department, ,
dc.identifier.volume515
dc.identifier.startpage135
dc.identifier.endpage140
dc.contributor.firstauthorID727096


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