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Chromosomal aberrations in mouse lymphocytes exposed in vivo and in vitro to aliphatic epoxides

dc.contributor.authorDas, L.en_US
dc.contributor.authorDas, Salil K.en_US
dc.contributor.authorChu, Ernest H. Y.en_US
dc.contributor.authorSinsheimer, Joseph E.en_US
dc.date.accessioned2006-04-10T15:50:45Z
dc.date.available2006-04-10T15:50:45Z
dc.date.issued1993-03en_US
dc.identifier.citationDas, L., Das, S. K., Chu, E. H. Y., Sinsheimer, J. E. (1993/03)."Chromosomal aberrations in mouse lymphocytes exposed in vivo and in vitro to aliphatic epoxides." Mutation Research/Genetic Toxicology 299(1): 19-24. <http://hdl.handle.net/2027.42/30912>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B73FB-474WXNM-1C/2/6274c619e825054adddc3272e200e216en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30912
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7679188&dopt=citationen_US
dc.description.abstractMouse lymphocytes in vivo or in vitro were exposed for 24 h to 4 aliphatic epoxides, glycidyl 1-naphthyl ether, glycidyl 4-nitrophenyl ether, 1-naphthylpropylene oxide and trichloropropylene oxide (TCPO), and tested for the induction of chromosomal aberrations (CA). These epoxides were among the most genotoxic aliphatic epoxides in our previous studies. With the exception of TCPO, the test epoxides caused significant increases in CA in vivo compared to a negative control. There were concentration related increases in CA for all 4 epoxides in vitro and TCPO produced the greatest cellular toxicity and genotoxic effects towards cultured lymphocytes. The difference in the order of genotoxicity for the two test systems can be explained on the basis of a much shorter half-life for TCPO than for the other epoxides.en_US
dc.format.extent403478 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleChromosomal aberrations in mouse lymphocytes exposed in vivo and in vitro to aliphatic epoxidesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.identifier.pmid7679188en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30912/1/0000581.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0165-1218(93)90114-Sen_US
dc.identifier.sourceMutation Research/Genetic Toxicologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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