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Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion

Food and chemical toxicology, 2009-04, Vol.47 (4), p.760-768

2009

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Assessing the dose-dependency of allometric scaling performance using physiologically based pharmacokinetic modeling

Regulatory toxicology and pharmacology, 2003-12, Vol.38 (3), p.345-367

2003

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Biological and physiological factors involved in disposition of dioxin and related compounds

Chemosphere, 1992, Vol.25 (1), p.3-6

1992

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Cancer dose–response assessment for acrylonitrile based upon rodent brain tumor incidence: Use of epidemiologic, mechanistic, and pharmacokinetic support for nonlinearity

Regulatory toxicology and pharmacology, 2005-10, Vol.43 (1), p.85-103

2005

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Corrigendum to “pharmacokinetic modeling of 2,4-dichlorophenoxyacetic acid (2,4-d) in rat and in rabbit brain following single dose administration”

Toxicology letters, 1995-03, Vol.76 (2), p.185-185

1995

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Derivation of Noncancer Reference Values for Acrylonitrile

Risk analysis, 2008-10, Vol.28 (5), p.1375-1394

2008

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Determination of Tissue Partition Coefficients for Volatile Tissue-Reactive Chemicals: Acrylonitrile and Its Metabolite 2-Cyanoethylene Oxide

Toxicology and applied pharmacology, 1994-09, Vol.128 (1), p.92-96

1994

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Development of a physiologically based pharmacokinetic model for 2,4-dichlorophenoxyacetic acid dosimetry in discrete areas of the rabbit brain

Neurotoxicology and teratology, 1995-03, Vol.17 (2), p.111-120

1995

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Development of a physiologically based pharmacokinetic model for chloroform

Toxicology and applied pharmacology, 1990-05, Vol.103 (3), p.512-527

1990

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Development of a physiologically based pharmacokinetic model for risk assessment with 1,4-dioxane

Toxicology and applied pharmacology, 1990-08, Vol.105 (1), p.37-54

1990

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Erratum to: “Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion” [Food and Chemical Toxicology 47 (2009) 760–768]

Food and chemical toxicology, 2009-11, Vol.47 (11), p.2875-2875

2009

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Kinetic Analysis of Furan Biotransformation by F-344 Rats in Vivo and in Vitro

Toxicology and applied pharmacology, 1993-12, Vol.123 (2), p.274-282

1993

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Modeling Receptor-Mediated Processes with Dioxin: Implications for Pharmacokinetics and Risk Assessment

Risk analysis, 1993-02, Vol.13 (1), p.25-36

1993

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Pharmacokinetic modeling of 2, 4-dichlorophenoxyacetic acid (2,4-D) in rat and in rabbit brain following single dose administration

Toxicology letters, 1994-12, Vol.74 (3), p.189-201

1994

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A Physiological Toxicokinetic Model for Exogenous and Endogenous Ethylene and Ethylene Oxide in Rat, Mouse, and Human: Formation of 2-Hydroxyethyl Adducts with Hemoglobin and DNA

Toxicology and applied pharmacology, 2000-05, Vol.165 (1), p.1-26

2000

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A Physiologically Based Description of Ethylene Oxide Dosimetry in the Rat

Toxicology and industrial health, 1992-05, Vol.8 (3), p.121-140

1992

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A Physiologically Based Dosimetry Description of Acrylonitrile and Cyanoethylene Oxide in the Rat

Toxicology and applied pharmacology, 1995-10, Vol.134 (2), p.185-194

1995

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Physiologically based pharmacokinetics and the risk assessment process for methylene chloride

Toxicology and applied pharmacology, 1987-02, Vol.87 (2), p.185-205

1987

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A physiologically based toxicokinetic model for the uptake and disposition of waterborne organic chemicals in fish

Toxicology and applied pharmacology, 1990-12, Vol.106 (3), p.433-447

1990

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Relationship of hepatotoxicity and lethality with metabolic constants of BrCCl 3 in rats pretreated with chlordecone, phenobarbital and mirex

European journal of pharmacology, 1990, Vol.183 (4), p.1539-1539

1990

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Relationship of hepatotoxicity and lethality with metabolic constants of BrCCl3 in rats pretreated with chlordecone, phenobarbital and mirex

European journal of pharmacology, 1990-07, Vol.183 (4), p.1539

1990

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Response to, “ Reaction on Gargas et al.: Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion”, by Hogervorst et al

Food and chemical toxicology, 2009-11, Vol.47 (11), p.2873-2874

2009

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Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion

Assessing the dose-dependency of allometric scaling performance using physiologically based pharmacokinetic modeling

Biological and physiological factors involved in disposition of dioxin and related compounds

Cancer dose–response assessment for acrylonitrile based upon rodent brain tumor incidence: Use of epidemiologic, mechanistic, and pharmacokinetic support for nonlinearity

Corrigendum to “pharmacokinetic modeling of 2,4-dichlorophenoxyacetic acid (2,4-d) in rat and in rabbit brain following single dose administration”

Derivation of Noncancer Reference Values for Acrylonitrile

Determination of Tissue Partition Coefficients for Volatile Tissue-Reactive Chemicals: Acrylonitrile and Its Metabolite 2-Cyanoethylene Oxide

Development of a physiologically based pharmacokinetic model for 2,4-dichlorophenoxyacetic acid dosimetry in discrete areas of the rabbit brain

Development of a physiologically based pharmacokinetic model for chloroform

Development of a physiologically based pharmacokinetic model for risk assessment with 1,4-dioxane

Erratum to: “Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion” [Food and Chemical Toxicology 47 (2009) 760–768]

Kinetic Analysis of Furan Biotransformation by F-344 Rats in Vivo and in Vitro

Modeling Receptor-Mediated Processes with Dioxin: Implications for Pharmacokinetics and Risk Assessment

Pharmacokinetic modeling of 2, 4-dichlorophenoxyacetic acid (2,4-D) in rat and in rabbit brain following single dose administration

A Physiological Toxicokinetic Model for Exogenous and Endogenous Ethylene and Ethylene Oxide in Rat, Mouse, and Human: Formation of 2-Hydroxyethyl Adducts with Hemoglobin and DNA

A Physiologically Based Description of Ethylene Oxide Dosimetry in the Rat

A Physiologically Based Dosimetry Description of Acrylonitrile and Cyanoethylene Oxide in the Rat

Physiologically based pharmacokinetics and the risk assessment process for methylene chloride

A physiologically based toxicokinetic model for the uptake and disposition of waterborne organic chemicals in fish

Relationship of hepatotoxicity and lethality with metabolic constants of BrCCl 3 in rats pretreated with chlordecone, phenobarbital and mirex

Relationship of hepatotoxicity and lethality with metabolic constants of BrCCl3 in rats pretreated with chlordecone, phenobarbital and mirex

Response to, “ Reaction on Gargas et al.: Acrylamide: Consideration of species differences and nonlinear processes in estimating risk and safety for human ingestion”, by Hogervorst et al

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