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Mutation Research|December 1, 1981
Induction of petite formation in Saccharomyces cerevisiae by experimental antitumour agents. Structure--activity relationships for 9-anilinoacridinesL R Ferguson, B C BaguleyMutation Research|June 1, 1981
The relationship between frameshift mutagenicity and DNA-binding affinity in a series of acridine-substituted derivatives of the experimental antitumour drug 4'-(9-acridinylamino)methanesulphonanilide (AMSA)L R Ferguson, B C BaguleyMutation Research|August 17, 1996
Mutagenicity of anticancer drugs that inhibit topoisomerase enzymesL R Ferguson, B C BaguleyMutation Research|September 1, 1988
Verapamil as a co-mutagen in the Salmonella/mammalian microsome mutagenicity testL R Ferguson, B C BaguleyMutation Research|October 1, 1993
Induction of mitotic crossing-over by the topoisomerase II poison DACA (N-[2-dimethylamino)ethyl]acridine-4-carboxamide) in Saccharomyces cerevisiaeL R Ferguson, P M Turner, B C BaguleyMutation Research|February 1, 1988
Comparison of the mutagenicity of amsacrine with that of a new clinical analogue, CI-921L R Ferguson, P van Zijl, B C BaguleyMutation Research|July 1, 1992
Photo-enhancement of the mutagenicity of 9-anilinoacridine derivatives related to the antitumour agent amsacrineY Iwamoto, L R Ferguson, A Pearson, et al.Mutation Research|August 1, 1990
Mutagenic and recombinogenic consequences of DNA-repair inhibition during treatment with 1,3-bis(2-chloroethyl)-1-nitrosourea in Saccharomyces cerevisiaeL R FergusonPageof 7