Search Results - "SCHULTZ, Terry W"
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Identification and description of the uncertainty, variability, bias and influence in quantitative structure-activity relationships (QSARs) for toxicity prediction
Published in Regulatory toxicology and pharmacology (01-08-2019)“…Improving regulatory confidence in, and acceptance of, a prediction of toxicity from a quantitative structure-activity relationship (QSAR) requires assessment…”
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Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology
Published in Chemical reviews (13-04-2011)“…Schwobel et all examine the measurement and estimation of electrophilic reactivity for predictive toxicology…”
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Clustering a Chemical Inventory for Safety Assessment of Fragrance Ingredients: Identifying Read-Across Analogs to Address Data Gaps
Published in Chemical research in toxicology (20-07-2020)“…A valuable approach to chemical safety assessment is the use of read-across chemicals to provide safety data to support the assessment of structurally similar…”
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Integrated approach to testing and assessment for predicting rodent genotoxic carcinogenicity
Published in Journal of applied toxicology (01-12-2016)“…We investigated the performance of an integrated approach to testing and assessment (IATA), designed to cover different genotoxic mechanisms causing cancer and…”
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Equations for estimating binary mixture toxicity: 3-methyl-2-butanone with a series of electrophiles
Published in PloS one (03-07-2024)“…Mixture toxicity was determined for 32 binary combinations. One chemical was the non-reactive, non-polar narcotic 3-methyl-2-butanone (always chemical A) and…”
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Uncertainty in the results from oral repeated dose toxicity tests: Impact on regulatory classifications
Published in Regulatory toxicology and pharmacology (01-01-2024)“…The Lowest Observed (Adverse) Effect Level (LO(A)EL) values are point-of-departure (PoD) values that quantify repeat dose toxicity (RDT). Here, the uncertainty…”
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Lessons learned from read-across case studies for repeated-dose toxicity
Published in Regulatory toxicology and pharmacology (01-08-2017)“…A series of case studies designed to further acceptance of read-across predictions, especially for chronic health-related endpoints, have been evaluated with…”
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Estimating uncertainty in LLNA EC3 data and its impact on regulatory classifications
Published in Regulatory toxicology and pharmacology (01-03-2023)“…The murine Local Lymph Node Assay (LLNA) is a test that produces numerical results (EC3 values) quantifying the sensitization potency of chemicals. These…”
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An End Point-Specific Framework for Read-Across Analog Selection for Human Health Effects
Published in Chemical research in toxicology (19-12-2022)“…Integrating computational chemistry and toxicology can improve the read-across analog approach to fill data gaps in chemical safety assessment. In read-across,…”
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Automated read-across workflow for predicting acute oral toxicity: I. The decision scheme in the QSAR toolbox
Published in Regulatory toxicology and pharmacology (01-10-2021)“…A decision-scheme outlining the steps for identifying the appropriate chemical category and subsequently appropriate tested source analog(s) for data gap…”
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Determination of “fitness-for-purpose” of quantitative structure-activity relationship (QSAR) models to predict (eco-)toxicological endpoints for regulatory use
Published in Regulatory toxicology and pharmacology (01-07-2021)“…In silico models are used to predict toxicity and molecular properties in chemical safety assessment, gaining widespread regulatory use under a number of…”
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Chemical applicability domain of the Local Lymph Node Assay (LLNA) for skin sensitisation potency. Part 3. Apparent discrepancies between LLNA and GPMT sensitisation potential: False positives or differences in sensitivity?
Published in Regulatory toxicology and pharmacology (01-10-2016)“…The Local Lymph Node Assay (LLNA) is the gold standard regulatory toxicology test for skin sensitisation along with the guinea pig maximisation test (GPMT)…”
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Development of a Decision Tree for Mitochondrial Dysfunction: Uncoupling of Oxidative Phosphorylation
Published in Chemical research in toxicology (20-08-2018)“…Mitochondrial dysfunction is the result of a number of processes including the uncoupling of oxidative phosphorylation. This study outlines the development of…”
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Skin Sensitization QMM for HRIPT NOEL Data: Aldehyde Schiff-Base Domain
Published in Chemical research in toxicology (19-06-2017)“…The general chemistry principles underlying skin sensitization for Schiff base (SB) electrophiles may be used to develop a quantitative mechanistic model…”
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The implementation of RAAF in the OECD QSAR Toolbox
Published in Regulatory toxicology and pharmacology (01-07-2019)“…The Read-Across Assessment Framework (RAAF) was developed by the European Chemicals Agency (ECHA) as an internal tool providing a framework for a consistent,…”
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The Adverse Outcome Pathway for Skin Sensitisation: Moving Closer to Replacing Animal Testing
Published in Alternatives to laboratory animals (01-10-2016)“…This article outlines the work of the Organisation for Economic Co-operation and Development (OECD) that led to being jointly awarded the 2015 Lush Black Box…”
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Building up a QSAR model for toxicity toward Tetrahymena pyriformis by the Monte Carlo method: A case of benzene derivatives
Published in Environmental toxicology and pharmacology (01-03-2016)“…Graphical abstract…”
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Kinetic-Based Reactivity for Michael Acceptors: Structural Activity Relationships and Its Relationship to Excess Acute Fish Toxicity
Published in Bulletin of environmental contamination and toxicology (01-12-2016)“…Acute aquatic toxicity is divided into the “physical” mode governed by weak, non-covalent interactions and the “chemical” mode governed by covalent reactions…”
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A practical guidance for Cramer class determination
Published in Regulatory toxicology and pharmacology (01-12-2015)“…Expanded use of the Threshold of Toxicological Concern (TTC) methodology has brought into discussion the intent of the original questions used in the Cramer…”
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Mechanistic relationship between biodegradation and bioaccumulation. Practical outcomes
Published in Regulatory toxicology and pharmacology (01-10-2019)“…According to the REACH Regulation, for all substances manufactured or imported in amounts of 10 or more tons per year, that are not exempted from the…”
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