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Rodent carcinogenesis bioassay with oxisuran, a selective immunosuppressive agent

dc.contributor.authorde la Iglesia, Felix A.en_US
dc.contributor.authorMcGuire, Edward J.en_US
dc.date.accessioned2006-04-07T18:38:45Z
dc.date.available2006-04-07T18:38:45Z
dc.date.issued1983-09en_US
dc.identifier.citationDe La Iglesia, Felix A., McGuire, Edward J. (1983/09)."Rodent carcinogenesis bioassay with oxisuran, a selective immunosuppressive agent." Toxicology 28(1-2): 17-28. <http://hdl.handle.net/2027.42/25114>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TCN-4777PHX-2N/2/0345f0ec6bc5ece559cd0a146760ab01en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25114
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6688895&dopt=citationen_US
dc.description.abstractThe carcinogenic potential of oxisuran, a synthetic immunosuppressive agent, was studied for 80 weeks and 104 weeks in mice and rats, respectively. Groups of 50 mice and 70 rats of each sex received oxisuran at doses of 600, 240, and 40 mg/kg/day as dietary admixtures over the entire experimental period. Adequate survival rates allowed accurate statistical analysis of diagnosed neoplasia. Increased susceptibility to tumor development was not clearly demonstrated. In mice the only statistically significant increase in the incidence of malignancy was lung carcinomas in high dose females (P P P P &lt; 0.01) contributed to an overall decrease in both benign tumors and in the combined benign and malignant tumor rates.en_US
dc.format.extent594477 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleRodent carcinogenesis bioassay with oxisuran, a selective immunosuppressive agenten_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology and Experimental Toxicology, Warner-Lambert/Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, MI 48105, USA; Department of Environmental and Industrial Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Pathology and Experimental Toxicology, Warner-Lambert/Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, MI 48105, USA; Department of Environmental and Industrial Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.identifier.pmid6688895en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25114/1/0000547.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0300-483X(83)90102-6en_US
dc.identifier.sourceToxicologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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