Rodent carcinogenesis bioassay with oxisuran, a selective immunosuppressive agent
dc.contributor.author | de la Iglesia, Felix A. | en_US |
dc.contributor.author | McGuire, Edward J. | en_US |
dc.date.accessioned | 2006-04-07T18:38:45Z | |
dc.date.available | 2006-04-07T18:38:45Z | |
dc.date.issued | 1983-09 | en_US |
dc.identifier.citation | De 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.uri | http://www.sciencedirect.com/science/article/B6TCN-4777PHX-2N/2/0345f0ec6bc5ece559cd0a146760ab01 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/25114 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6688895&dopt=citation | en_US |
dc.description.abstract | The 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 < 0.01) contributed to an overall decrease in both benign tumors and in the combined benign and malignant tumor rates. | en_US |
dc.format.extent | 594477 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Rodent carcinogenesis bioassay with oxisuran, a selective immunosuppressive agent | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Pharmacy and Pharmacology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department 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.affiliationum | Department 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.pmid | 6688895 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/25114/1/0000547.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0300-483X(83)90102-6 | en_US |
dc.identifier.source | Toxicology | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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