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Titlebook: Comparative Genetic Toxicology; J. M. Parry,C. F. Arlett Book 1985 Palgrave Macmillan, a division of Macmillan Publishers Limited 1985 com

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Design of the Study ‘Scientific Rationale and Chemical Selection’fferent phyla. Both of these objectives were of prime relevance to the science of environmental mutagenesis and carcinogenesis: the extrapolation to mammals of genotoxity data generated in experimental systems, in particular, to man (Ashby, 1983).
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Iyad Obeid,Ivan Selesnick,Joseph Piconer microgram of BZD, DAT and CDA. DAB had the weakest mutagenic activity, demonstrable only with rat-Aroclor and guinea pig-MC S9. DAT was the only compound which was active in the absence of metabolic activation.
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The Genotoxicity of Benzidine and 4-Dimethylaminoazobenzene: A Survey of the Literature has in excess of 200 listings. A summary to illustrate the range of assay systems which have been used to investigate the genotoxicity of these compounds was compiled and has been used to generate tables 1 and 2. The classification of the genetic system was basically that used by EMIC for its assay system/biological endpoint category.
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