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Mutagenesis
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October 8, 2015
Genotoxicity of flubendazole and its metabolites in vitro and the impact of a new formulation on in vivo aneugenicity
David J Tweats, George E Johnson, Ivan Scandale, et al.
Regulatory Toxicology and Pharmacology : RTP
|
October 7, 2023
Nitrosamine acceptable intakes should consider variation in molecular weight: The implication of stoichiometric DNA damage
Jonathan Fine, Leonardo Allain, Joerg Schlingemann, et al.
Mutagenesis
|
June 10, 2021
Empirical comparison of genotoxic potency estimations: the in vitro DNA-damage ToxTracker endpoints versus the in vivo micronucleus assay
John W Wills, Elias Halkes-Wellstead, Huw D Summers, et al.
Environmental and Molecular Mutagenesis
|
September 26, 2017
Comparing BMD-derived genotoxic potency estimations across variants of the transgenic rodent gene mutation assay
John W Wills, George E Johnson, Hannah L Battaion, et al.
Environmental and Molecular Mutagenesis
|
January 11, 2021
The use of benchmark dose uncertainty measurements for robust comparative potency analyses
Ryan P Wheeldon, Stephen D Dertinger, Steven M Bryce, et al.
Archives of Toxicology
|
January 3, 2025
Critical comparison of BMD and TD<sub>50</sub> methods for the calculation of acceptable intakes for N-nitroso compounds
Robert Thomas, David J Ponting, Andrew Thresher, et al.
Environmental and Molecular Mutagenesis
|
September 14, 2020
Genotoxicity as a toxicologically relevant endpoint to inform risk assessment: A case study with ethylene oxide
Bala Bhaskar Gollapudi, Steave Su, Abby A Li, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
November 13, 2010
N-methylpurine DNA glycosylase plays a pivotal role in the threshold response of ethyl methanesulfonate-induced chromosome damage
Zoulikha M Zaïr, Gareth J Jenkins, Shareen H Doak, et al.
Environmental and Molecular Mutagenesis
|
January 27, 2020
Benchmark Dose Analysis of DNA Damage Biomarker Responses Provides Compound Potency and Adverse Outcome Pathway Information for the Topoisomerase II Inhibitor Class of Compounds
Ryan P Wheeldon, Derek T Bernacki, Stephen D Dertinger, et al.
Mutagenesis
|
December 22, 2015
Empirical analysis of BMD metrics in genetic toxicology part I: in vitro analyses to provide robust potency rankings and support MOA determinations
John W Wills, George E Johnson, Shareen H Doak, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 65) with videos related to
Sort By:
Page
of 7
Mutagenesis
|
October 8, 2015
Genotoxicity of flubendazole and its metabolites in vitro and the impact of a new formulation on in vivo aneugenicity
David J Tweats, George E Johnson, Ivan Scandale, et al.
Regulatory Toxicology and Pharmacology : RTP
|
October 7, 2023
Nitrosamine acceptable intakes should consider variation in molecular weight: The implication of stoichiometric DNA damage
Jonathan Fine, Leonardo Allain, Joerg Schlingemann, et al.
Mutagenesis
|
June 10, 2021
Empirical comparison of genotoxic potency estimations: the in vitro DNA-damage ToxTracker endpoints versus the in vivo micronucleus assay
John W Wills, Elias Halkes-Wellstead, Huw D Summers, et al.
Environmental and Molecular Mutagenesis
|
September 26, 2017
Comparing BMD-derived genotoxic potency estimations across variants of the transgenic rodent gene mutation assay
John W Wills, George E Johnson, Hannah L Battaion, et al.
Environmental and Molecular Mutagenesis
|
January 11, 2021
The use of benchmark dose uncertainty measurements for robust comparative potency analyses
Ryan P Wheeldon, Stephen D Dertinger, Steven M Bryce, et al.
Archives of Toxicology
|
January 3, 2025
Critical comparison of BMD and TD<sub>50</sub> methods for the calculation of acceptable intakes for N-nitroso compounds
Robert Thomas, David J Ponting, Andrew Thresher, et al.
Environmental and Molecular Mutagenesis
|
September 14, 2020
Genotoxicity as a toxicologically relevant endpoint to inform risk assessment: A case study with ethylene oxide
Bala Bhaskar Gollapudi, Steave Su, Abby A Li, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
November 13, 2010
N-methylpurine DNA glycosylase plays a pivotal role in the threshold response of ethyl methanesulfonate-induced chromosome damage
Zoulikha M Zaïr, Gareth J Jenkins, Shareen H Doak, et al.
Environmental and Molecular Mutagenesis
|
January 27, 2020
Benchmark Dose Analysis of DNA Damage Biomarker Responses Provides Compound Potency and Adverse Outcome Pathway Information for the Topoisomerase II Inhibitor Class of Compounds
Ryan P Wheeldon, Derek T Bernacki, Stephen D Dertinger, et al.
Mutagenesis
|
December 22, 2015
Empirical analysis of BMD metrics in genetic toxicology part I: in vitro analyses to provide robust potency rankings and support MOA determinations
John W Wills, George E Johnson, Shareen H Doak, et al.
Page
of 7