Absorption, distribution, metabolism and excretion of daily oral doses of [14C]methyl parathion in hens.

[1]  M. Abou‐Donia,et al.  Inhibition and recovery of maternal and fetal cholinesterase enzyme activity following a single cutaneous dose of methyl parathion and diazinon, alone and in combination, in pregnant rats , 2001, Journal of applied toxicology : JAT.

[2]  M. Abou‐Donia,et al.  INHIBITION OF CHOLINESTERASE ENZYMES FOLLOWING A SINGLE DERMAL DOSE OF CHLORPYRIFOS AND METHYL PARATHION, ALONE AND IN COMBINATION, IN PREGNANT RATS , 2001, Journal of toxicology and environmental health. Part A.

[3]  D. Ray,et al.  The potential for toxic effects of chronic, low-dose exposure to organophosphates. , 2001, Toxicology letters.

[4]  M. Abou‐Donia,et al.  Urinary excretion of metabolites following a single dermal dose of [14C]methyl parathion in pregnant rats. , 2000, Toxicology.

[5]  M. Abou‐Donia,et al.  Placental transfer and pharmacokinetics of a single oral dose of [14C]p-nitrophenol in rats , 2000, Archives of Toxicology.

[6]  R. Trump,et al.  Depression among victims of south Mississippi's methyl parathion disaster. , 2000, Health & social work.

[7]  M. Abou‐Donia,et al.  Placental transfer and pharmacokinetics of a single dermal dose of [14C]methyl parathion in rats. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[8]  J. Kowalik,et al.  Effect of paraoxon‐methyl and parathion‐methyl on DNA in human lymphocytes and protective action of vitamin C , 1999 .

[9]  R. Gupta,et al.  Cytochrome P450 enzymes in chickens: characteristics and induction by xenobiotics. , 1998, Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.

[10]  L. Sultatos,et al.  Glutathione-dependent biotransformation of methyl parathion by mouse liver in vitro. , 1993, Toxicology letters.

[11]  I. Kraul,et al.  Disposition of parathion in neonatal and young pigs. , 1991, Pharmacology & toxicology.

[12]  R. Gupta,et al.  Mechanisms of joint neurotoxicity of n-hexane, methyl isobutyl ketone and O-ethyl O-4-nitrophenyl phenylphosphonothioate in hens. , 1991, The Journal of pharmacology and experimental therapeutics.

[13]  L. Sultatos,et al.  Biotransformation of the organophosphorus insecticides parathion and methyl parathion in male and female rat livers perfused in situ. , 1991, Drug metabolism and disposition: the biological fate of chemicals.

[14]  J. Snawder,et al.  Target site bioactivation of the neurotoxic organophosphorus insecticide parathion in partially hepatectomized rats. , 1991, Life sciences.

[15]  A. Nomeir,et al.  Absorption, distribution, and elimination of a single oral dose of [14C]tri-o-cresyl phosphate in hens. , 1990, Toxicology.

[16]  L. Sultatos.  The role of the liver in mediating the acute toxicity of the pesticide methyl parathion in the mouse. , 1987, Drug metabolism and disposition: the biological fate of chemicals.

[17]  W. Dauterman,et al.  Biotransformation of methyl parathion by human foetal liver glutathione S-transferases: an in vitro study. , 1987, Xenobiotica; the fate of foreign compounds in biological systems.

[18]  A. Nomeir,et al.  The role of pharmacokinetics and metabolism in species sensitivity to neurotoxic agents. , 1986, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[19]  M. Abou‐Donia,et al.  Distribution and metabolism of O-Ethyl O-4-nitrophenyl phenylphosphonothioate after a single oral dose in one-week old chicks , 1983, Archives of Toxicology.

[20]  H. Kay.  Environmental Health Criteria , 1980 .

[21]  R. A. Neal,et al.  Examination of the metabolism in vitro of parathion (diethyl p-nitrophenyl phosphorothionate) by rat lung and brain. , 1976, Biochemical pharmacology.

[22]  T B Gaines,et al.  Acute toxicity of pesticides. , 1969, Toxicology and applied pharmacology.

[23]  R. Metcalf,et al.  The selectivity of Sumithion compared with methyl parathion. Metabolism in the white mouse. , 1967 .

[24]  Thomas B. Gaines,et al.  The acute toxicity of pesticides to rats , 1960 .

[25]  B. Scribner,et al.  Non-ionic diffusion and the excretion of weak acids and bases. , 1958, The American journal of medicine.