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Pharmacokinetics and molecular detoxication.
Cashman JR, Perotti BY, Berkman CE, Lin J.
Environ Health Perspect. 1996 Mar;104 Suppl 1:23-40. Review.PMID: 8722108 [PubMed - indexed for MEDLINE]Related articlesFree article
Biotransformation of organophosphorus compounds.
Jokanović M.
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Sources, pathways, and relative risks of contaminants in surface water and groundwater: a perspective prepared for the Walkerton inquiry.
Ritter L, Solomon K, Sibley P, Hall K, Keen P, Mattu G, Linton B.
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Incorporating human interindividual biotransformation variance in health risk assessment.
Lipscomb JC, Kedderis GL.
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Detoxication of paraoxon by rat liver homogenate and serum carboxylesterases and A-esterases.
Tang J, Chambers JE.
J Biochem Mol Toxicol. 1999;13(5):261-8.PMID: 10402560 [PubMed - indexed for MEDLINE]Related articles
Human hepatic cell cultures: in vitro and in vivo drug metabolism.
Gómez-Lechón MJ, Donato T, Ponsoda X, Castell JV.
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Risk management frameworks for human health and environmental risks.
Jardine C, Hrudey S, Shortreed J, Craig L, Krewski D, Furgal C, McColl S.
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Applications of carboxylesterase activity in environmental monitoring and toxicity identification evaluations (TIEs).
Wheelock CE, Phillips BM, Anderson BS, Miller JL, Miller MJ, Hammock BD.
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Cytochrome P450 catalysed insecticide metabolism: chemical and theoretical models.
Keserü GM.
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Application of in vitro biotransformation data and pharmacokinetic modeling to risk assessment.
Kedderis GL, Lipscomb JC.
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Mechanistic aspects of organophosphorothionate toxicity in fish and humans.
Vittozzi L, Fabrizi L, Di Consiglio E, Testai E.
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Mediation of pyrethroid insecticide toxicity to honey bees (Hymenoptera: Apidae) by cytochrome P450 monooxygenases.
Johnson RM, Wen Z, Schuler MA, Berenbaum MR.
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Preclinical pharmacokinetics: an approach towards safer and efficacious drugs.
Singh SS.
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Human drug metabolism and the cytochromes P450: application and relevance of in vitro models.
Venkatakrishnan K, Von Moltke LL, Greenblatt DJ.
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Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition.
Poulin P, Theil FP.
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Glutathione S-transferase conjugation of organophosphorus pesticides yields S-phospho-, S-aryl-, and S-alkylglutathione derivatives.
Fujioka K, Casida JE.
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An overview of human exposure modeling activities at the USEPA's National Exposure Research Laboratory.
Furtaw EJ Jr.
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Enzymes involved in the metabolism of the carcinogen 2-nitroanisole: evidence for its oxidative detoxication by human cytochromes P450.
Miksanová M, Sulc M, Rýdlová H, Schmeiser HH, Frei E, Stiborová M.
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Genetic variability in the cytochrome P450-paraoxonase 1 (PON1) pathway for detoxication of organophosphorus compounds.
Furlong CE.
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Prediction of interindividual variation in drug plasma levels in vivo from individual enzyme kinetic data and physiologically based pharmacokinetic modeling.
Bogaards JJ, Hissink EM, Briggs M, Weaver R, Jochemsen R, Jackson P, Bertrand M, van Bladeren PJ.
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