SCE frequencies in rabbit lymphocytes as a function of time after an acute dose of cyclophosphamide
Author:
Publisher
Elsevier BV
Subject
Health, Toxicology and Mutagenesis,Genetics,Molecular Biology
Reference20 articles.
1. Metabolism of cyclophosphamide;Brock;Cancer,1967
2. A comparison of chromosome aberration yields in rabbit blood lymphocytes irradiated in vitro and in vivo;Clemenger;Int. J. Radiation Biol.,1973
3. Lymphocyte lifetime in the rabbit measured by the decline in radiation-induced chromosome damage;Decat;Int. J. Radiation Biol.,1980
4. Kinetics of cyclophosphamide biotransformation in vivo;Domeyer;Cancer Res.,1980
5. Cyclophosphamide induced SCEs in rabbit lymphocytes;DuFrain;Environ. Mutagen.,1979
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1. Relationship between the duration and number of cell cycles after mutagenic exposure and the incidence of sister chromatid exchanges;Bulletin of Experimental Biology and Medicine;1998-02
2. Persistence during G1 of gamma ray- or mitomycin C-induced lesions eliciting SCE in murine salivary gland cells in vivo;Somatic Cell and Molecular Genetics;1995-01
3. Persistence of chromosomal lesions induced in actively proliferating bone marrow cells of the mouse;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1992-09
4. Fate of DNA lesions that elicit sister-chromatid exchanges;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1990-09
5. Time course of frequency of sister chromatid exchanges after exposure to thiophosphamide in vivo;Bulletin of Experimental Biology and Medicine;1989-01
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