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25. Loss of high frequency of sister chromatid exchanges in Epstein-Barr virus-established lymphoblastoid cell lines from two patients with Bloom's syndrome. Hashimoto T, Gamo S, Furuyama J, Chiyo H. Hum Genet; 1983; 63(1):75-6. PubMed ID: 6299928 [Abstract] [Full Text] [Related]
27. A unique human mutant B-lymphoblastoid cell line (ataxia telangiectasia) which exhibits increased sister-chromatid exchange retaining hypersensitivity to neocarzinostatin and bleomycin. Li MJ, Shiraishi Y. Mutat Res; 1990 Jun; 230(2):167-75. PubMed ID: 1695711 [Abstract] [Full Text] [Related]
28. The effects of incorporated tritium and bromodeoxyuridine on the frequency of sister chromatid exchanges. Bianchi NO, Larramendy ML. Chromosoma; 1983 Jun; 88(1):11-5. PubMed ID: 6884153 [Abstract] [Full Text] [Related]
31. Bloom's syndrome and EM9 cells in BrdU-containing medium exhibit similarly elevated frequencies of sister chromatid exchange but dissimilar amounts of cellular proliferation and chromosome disruption. Ray JH, German J. Chromosoma; 1984 Jun; 90(5):383-8. PubMed ID: 6510115 [Abstract] [Full Text] [Related]
35. Cell cycle rate and sister chromatid exchange profile in polyethylene glycol-exposed/unexposed Bloom syndrome and normal cells. A co-culture study. Bamezai R, Shiraishi Y. Hum Genet; 1987 Apr; 75(4):356-8. PubMed ID: 3570291 [Abstract] [Full Text] [Related]
36. Induction of sister-chromatid exchanges (SCEs) by 5-fluorodeoxyuridine. The role of 5-bromodeoxyuridine incorporated into parental DNA. Escalza P, Cortés F, Schvartzman JB. Mutat Res; 1985 Aug; 151(1):77-82. PubMed ID: 3160947 [Abstract] [Full Text] [Related]
40. Dependency of the yield of sister-chromatid exchanges induced by alkylating agents on fixation time. Possible involvement of secondary lesions in sister-chromatid exchange induction. Kaina B, Aurich O. Mutat Res; 1985 May; 149(3):451-61. PubMed ID: 3990696 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]