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Jernigan, James D., Harbison, Raymond D. (1982) Role of biotransformation in the potentiation of halocarbon hepatotoxicity by 2,5‐hexanedione. Journal of Toxicology and Environmental Health, 9. 761-781 doi:10.1080/15287398209530202

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Reference TypeJournal (article/letter/editorial)
TitleRole of biotransformation in the potentiation of halocarbon hepatotoxicity by 2,5‐hexanedione
JournalJournal of Toxicology and Environmental Health
AuthorsJernigan, James D.Author
Harbison, Raymond D.Author
Year1982 (May)Volume9
PublisherInforma UK Limited
DOIdoi:10.1080/15287398209530202Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID9731667Long-form Identifiermindat:1:5:9731667:7
GUID0
Full ReferenceJernigan, James D., Harbison, Raymond D. (1982) Role of biotransformation in the potentiation of halocarbon hepatotoxicity by 2,5‐hexanedione. Journal of Toxicology and Environmental Health, 9. 761-781 doi:10.1080/15287398209530202
Plain TextJernigan, James D., Harbison, Raymond D. (1982) Role of biotransformation in the potentiation of halocarbon hepatotoxicity by 2,5‐hexanedione. Journal of Toxicology and Environmental Health, 9. 761-781 doi:10.1080/15287398209530202
In(n.d.) Journal of Toxicology and Environmental Health Vol. 9. Informa UK Limited

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Raymond, Pierre, Plaa, Gabriel L. (1996) Ketone Potentiation of Haloalkane-Induced Hepatotoxicity: CCl4 and Ketone Treatment on Hepatic Membrane Integrity. Journal of Toxicology and Environmental Health, 49. 285-300 doi:10.1080/00984108.1996.11667602
Gilbert, Steven G., Maurissen, Jacques P. J. (1982) Assessment of the effects of acrylamide, methylmercury, and 2,5‐hexanedione on motor functions in mice. Journal of Toxicology and Environmental Health, 10. 31-41 doi:10.1080/15287398209530228
Roberts, Stephen M., Harbison, Raymond D., Roth, Lois, James, Robert C. (1994) Methyphenidate-induced hepatotoxicity in mice and its potentiation by β-adrenergic agonist drugs. Life Sciences, 55 (4) 269-281 doi:10.1016/0024-3205(94)00729-2
Raje, Ravindra R. (1983) In vitrotoxicity ofn‐hexane and 2,5‐hexanedione using isolated perfused rabbit heart. Journal of Toxicology and Environmental Health, 11. 879-884 doi:10.1080/15287398309530391
Scales, M. D. G., Timbrell, J. A. (1982) Studies on hydrazine hepatotoxicity. 1. Pathological findings. Journal of Toxicology and Environmental Health, 10. 941-953 doi:10.1080/15287398209530308
Gibson, James E. (1984) Comments on “formaldehyde and hepatotoxicity” by Beall and Ulsamer. Journal of Toxicology and Environmental Health, 14. 465-467 doi:10.1080/15287398409530593
Johnson, D. R. (1982) Role of renal cortical sulfhydryl groups in development of mercury‐induced renal toxicity. Journal of Toxicology and Environmental Health, 9. 119-126 doi:10.1080/15287398209530147
Timbretl, J. A., Scales, M. D. C., Streeter, A. J. (1982) Studies on hydrazine hepatotoxicity. 2. Biochemical findings. Journal of Toxicology and Environmental Health, 10. 955-968 doi:10.1080/15287398209530309
Jortner, Bernard S., Ehrich, Marion (1993) Comparison of toxicities of acrylamide and 2,5‐hexanedione in hens and rats on 3‐week dosing regimens. Journal of Toxicology and Environmental Health, 39. 417-428 doi:10.1080/15287399309531762
Graham, Doyle G., Abou‐Donia, Mohamed B. (1980) Studies of the molecular pathogenesis of hexane neuropathy. I. Evaluation of the inhibition of glyceraldehyde‐3‐phosphate dehydrogenase by 2,5‐hexanedione. Journal of Toxicology and Environmental Health, 6. 621-631 doi:10.1080/15287398009529880
Gandy, Jay, Millner, Glenn C., Bates, Hudson K., Casciano, Daniel A., Harbison, Raymond D. (1990) Effects of selected chemicals on the glutathione status in the male reproductive system of rats. Journal of Toxicology and Environmental Health, 29. 45-57 doi:10.1080/15287399009531370
 
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