Altex-Alternatives to Animal Experimentation

Papers
(The median citation count of Altex-Alternatives to Animal Experimentation is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-11-01 to 2025-11-01.)
ArticleCitations
Alternative Methods in Science: Towards Fluidic Systems61
Application of high-throughput transcriptomics for mechanism-based biological read-across of short-chain carboxylic acid analogues of valproic acid_suppl137
Intestinal in vitro transport assay combined with physiologically based kinetic modeling as a tool to predict bile acid levels in vivo_suppl132
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl125
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl521
Sensitivity analysis and quality indicators for an in vitro oral irritation assay12
Validation of an Endopep-suspension immunoassay for the diagnostics of human botulism_suppl11
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency11
The effect of surfactants and film-forming polymers on pulmonary surfactant function measured in vitro is dose rate dependent_suppl11
Animal research ethics as interaction of research ethics, animal ethics, and (animal protection) law10
Validation of the monocyte activation test with three therapeutic monoclonal antibodies9
REACH out-numbered! The future of REACH and animal numbers8
Integrated skin sensitization assessment based on OECD methods (I): Deriving a point of departure for risk assessment8
Developmental neurotoxicity (DNT): A call for implementation of new approach methodologies for regulatory purposes: Summary of the 5th International Conference on DNT Testing8
Technical framework for enabling high-quality measurements in new approach methodologies (NAMs)8
Off to a good start? Review of the predictivity of reactivity methods modelling the molecular initiating event of skin sensitization8
Integrated skin sensitization assessment based on OECD methods (I): Deriving a point of departure for risk assessment_suppl48
Predicting Acute Oral Toxicity Using AcutoX: An Animal Product-Free and Metabolically Relevant Human Cell-Based Test7
Making safety decisions for a sunscreen active ingredient using next-generation risk assessment: Benzophenone-4 case study7
A sensitive cell-based assay for testing potency of Botulinum neurotoxin type A7
The long way from raw data to NAM-based information: Overview on data layers and processing steps7
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl47
Mapping out strategies to further develop human-relevant, new approach methodology (NAM)-based developmental neurotoxicity (DNT) testing7
E-validation – Unleashing AI for validation7
Chemical selection for the Thyroid Validation Study coordinated by EURL ECVAM and involving EU-NETVAL laboratories_suppl36
Microphysiological endothelial models to characterize subcutaneous drug absorption_suppl6
Exploring the synergy of CRISPR and microphysiological systems6
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl16
Mapping physiology: A systems biology approach for the development of alternative methods in toxicology6
Developing a global education hub for animal-free innovation_suppl6
Non-animal approaches – Concept, validation, and regulatory acceptance: The fourth Asian Congress of Alternatives to Animal Experiments (4ACAAE) and the seventh Annual Meeting of the Society for Alter5
3Rs: Progress or a fig leaf?5
Assessment of a 3D neural spheroid model to detect pharmaceutical-induced neurotoxicity5
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl65
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations5
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl25
Investigation of the publication rate of recent research projects using non-human primates in France5
COVID-19 through Adverse Outcome Pathways: Building networks to better understand the disease – 3rd CIAO AOP Design Workshop5
A human osteoarthritis mimicking goat cartilage explant-based disease model for drug screening_suppl5
AOP 460: Antagonism of Smoothened receptor leading to orofacial clefting_suppl15
Designing a national strategy to enable human-relevant research in India: A multistakeholder roundtable meeting report4
In vitro-based prediction of human plasma concentrations of food-related compounds_suppl14
ALTEX Proceedings TIERethik Corrigendum to Incorporating new approach methodologies into regulatory nonclinical pharmaceutical safety assessment4
Incorporating new approach methodologies into regulatory nonclinical pharmaceutical safety assessment4
The Alarming Consequences of Workforce Reductions at the FDA, EPA, NIH and CDC in the United States4
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl34
Integrated skin sensitization assessment based on OECD methods (II): Hazard and potency by combining kinetic peptide reactivity and the “2 out of 3” Defined Approach_suppl44
Role of standards and funding in accelerating the development and use of microphysiological systems4
Material-mediated pyrogens in medical devices: Myth or reality?_suppl24
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay4
The Virtual Human Platform for Safety Assessment (VHP4Safety) project: Next generation chemical safety assessment based on human data4
Assessment of developmental neurotoxicology-associated alterations in neuronal architecture and function using Caenorhabditis elegans_suppl4
From cellular perturbation to probabilistic risk assessments4
Women in Alternatives4
Linking nanomaterial-induced mitochondrial dysfunction to existing adverse outcome pathways for chemicals_suppl13
A path forward advancing microphysiological systems3
Transition to animal-free science: Phasing out animal experiments, phasing in innovation3
Evaluation of 147 perfluoroalkyl substances for immunotoxic and other (patho)physiological activities through phenotypic screening of human primary cells_suppl23
Beyond chemicals: Opportunities and challenges of integrating non-chemical stressors in adverse outcome pathways3
COVID-19 through Adverse Outcome Pathways: Building networks to better understand the disease – 3rd CIAO AOP Design Workshop_suppl3
Human relevant frontiers in drug safety and efficacy3
Identifying candidate reference chemicals for in vitro testing of the retinoid pathway for predictive developmental toxicity_suppl3
Grouping of UVCB substances with dose-response transcriptomics data from human cell-based assays_suppl3
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis_suppl13
Qualitative and quantitative concentration-response modelling of gene co-expression networks to unlock hepatotoxic mechanisms for next generation chemical safety assessment2
The SCAHT Adverse Outcome Pathway (AOP)_HUB: A hands-on platform for information exchange, sharing, and developing AOPs2
Integrated skin sensitization assessment based on OECD methods (II): Hazard and potency by combining kinetic peptide reactivity and the “2 out of 3” Defined Approach_suppl22
Proceedings of a workshop to address animal methods bias in scientific publishing_suppl2
Next-generation risk assessment of chemicals – Rolling out a human-centric testing strategy to drive 3R implementation: The RISK-HUNT3R project perspective2
Linking nanomaterial-induced mitochondrial dysfunction to existing adverse outcome pathways for chemicals_suppl22
Impact of in vitro experimental variation in kinetic parameters on physiologically based kinetic (PBK) model simulations_suppl12
Second scientific sessions and international conference of the Society for Alternatives to Animal Testing in Sri Lanka (SAAT-SL)2
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl62
How to formulate hypotheses and IATA to support grouping and read-across of nanoforms2
Building confidence in PBK model predictions in the absence of human kinetic data: Benzophenone-4 case study_suppl12
The need for epigenotoxicity testing2
Development of a network of carcinogenicity adverse outcome pathways and its employment as an evidence framework for safety assessment2
Virtual control groups in non-clinical toxicology – A replicability challenge2
Micro-replace systems2
Biology-inspired dynamic microphysiological system approaches to revolutionize basic research, healthcare and animal welfare2
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl72
Comparative evaluation of rat and human in vitro assays for evaluation of thyroid toxicity_suppl12
Novel prediction models for genotoxicity based on biomarker genes in human HepaRGTM cells_suppl22
AOP 460: Antagonism of Smoothened receptor leading to orofacial clefting2
Open-source human skin model with an in vivo-like barrier for drug testing_suppl2
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides_suppl22
Grouping of UVCB substances with dose-response transcriptomics data from human cell-based assays1
Towards NAM-based risk assessment for developmental neurotoxic effects, illustrated with chlorpyrifos1
Integrated skin sensitization assessment based on OECD methods (I): Deriving a point of departure for risk assessment_suppl31
Ready for regulatory use: NAMs and NGRA for chemical safety assurance1
Predictive performance of next generation human physiologically based kinetic (PBK) model predictions based on in vitro and in silico input data_suppl21
On the usefulness of animals as a model system (part II): Considering benefits within distinct use domains1
Building confidence in PBK model predictions in the absence of human kinetic data: Benzophenone-4 case study1
Exploration of the GARDskin applicability domain: Indirectly acting haptens, hydrophobic substances and UVCBs1
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl11
Perspectives on the evaluation and adoption of complex in vitro models in drug development: Workshop with the FDA and the pharmaceutical industry (IQ MPS Affiliate)1
Comparison of human recombinant protein coatings and fibroblast-ECM to Matrigel for induced pluripotent stem cell culture and renal podocyte differentiation_suppl11
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis1
Guidance for Good In Vitro Reporting Standards (GIVReSt) – A draft for stakeholder discussion and background documentation1
Phase-out planning for animal experimentation: A definition, an argument, and seven action points1
3 Days for 3Rs 2023: Refinement, reduction, replacement1
International conference and workshop on “New Approach Methodologies (NAMs) in Pharmacology and Toxicology”1
Fish Count, Too – The Animal Toll of REACH Aquatic Toxicity Tests_suppl21
The turning point: April 2025 marks historic shift in US animal testing policy1
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl31
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective_suppl11
Ways to broaden the awareness, consideration and adoption of new approach methodologies (NAMs)1
Material-mediated pyrogens in medical devices: Myth or reality?_suppl11
Impact of gut permeability on estimation of oral bioavailability for chemicals in commerce and the environment1
A sensitive cell-based assay for testing potency of Botulinum neurotoxin type A_suppl1
The benefits of validation of methods for toxicity testing outweigh its costs1
Novel prediction models for genotoxicity based on biomarker genes in human HepaRGTM cells_suppl11
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl21
Amplifying the impact of kidney microphysiological systems: predicting renal drug clearance using mechanistic modelling based on reconstructed drug secretion_suppl1
Predictive alternative methods for assessing biocompatibility of dental materials: A NIST-NIDCR workshop report1
Integrated skin sensitization assessment based on OECD methods (II): Hazard and potency by combining kinetic peptide reactivity and the “2 out of 3” Defined Approach_suppl31
The impact of biostatistics on hazard characterization using in vitro developmental neurotoxicity assays1
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl10
The importance of variations in in vitro dosimetry to support risk assessment of inhaled toxicants_suppl30
Improved identification of human hepatotoxic potential by summary variables of gene expression_suppl0
New approach methodologies (NAMs): The strategic vision in science0
Dog as the experimental model: Laboratory uses of dogs in the United States0
Application of high-throughput transcriptomics for mechanism-based biological read-across of short-chain carboxylic acid analogues of valproic acid_suppl20
The GARD™skin assay: Investigation of the applicability domain for metals_suppl0
Off to a good start? Review of the predictivity of reactivity methods modelling the molecular initiating event of skin sensitization_suppl10
Novel prediction models for genotoxicity based on biomarker genes in human HepaRGTM cells0
No more secrets: Enhancing transparency in animal research0
60 Years of the 3Rs symposium: Lessons learned and the road ahead0
A human osteoarthritis mimicking goat cartilage explant-based disease model for drug screening0
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl40
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl10
Integrated skin sensitization assessment based on OECD methods (II): Hazard and potency by combining kinetic peptide reactivity and the “2 out of 3” Defined Approach0
Challenges and opportunities for validation of AI-based new approach methods0
Possible applications of new approach methodologies (NAMs) in ecotoxicology0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl60
Workshop report on the evaluation of the updated and expanded carcinogen database to support derivation of threshold of toxicological concern values for DNA reactive carcinogens0
InViTe2 Retreat: Advancing new approach methodologies in chemical safety testing and drug discovery0
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl50
Mapping physiology: A systems biology approach for the development of alternative methods in toxicology_suppl0
Organoid intelligence (OI) – The ultimate functionality of a brain microphysiological system0
An Alternative Safety Profiling Algorithm (ASPA) to transform next generation risk assessment into a structured and transparent process0
Pollutant exposure and myocardial injury: Protocol and progress report for a toxicological systematic mapping review_Supplement0
Identifying candidate reference chemicals for in vitro testing of the retinoid pathway for predictive developmental toxicity_suppl20
Determination of U-SENS™ borderline range thresholds to address uncertainty for skin sensitization assessment in a regulatory context_suppl10
Performance of the DASF compared to other combinations of OECD NAMs for eye hazard identification of surfactants0
Material-mediated pyrogens in medical devices: Myth or reality?0
Comparison of structural equation modeling and Bayesian network for de novo construction of a quantitative adverse outcome pathway network0
A proof-of-concept rat toxicity study highlights the potential utility and challenges of virtual control groups_suppl0
Evaluation of 147 perfluoroalkyl substances for immunotoxic and other (patho)physiological activities through phenotypic screening of human primary cells_suppl40
Considerations from the pharmaceutical industry (IQ MPS affiliate) workshop on animal microphysiological systems and 3Rs in drug development0
Development of physiologically based gut absorption model for probabilistic prediction of environmental chemical bioavailability0
Comparison of pyrogen assays by testing products exhibiting low endotoxin recovery_suppl0
Cardiotoxicity of chemicals: Current regulatory guidelines, knowledge gaps, and needs0
The road to virtual control groups and the importance of proper body-weight selection0
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl30
4.2 million and counting… The animal toll for REACH systemic toxicity studies0
Trust your gut: Establishing confidence in gastrointestinal models - An overview of the state of the science and contexts of use0
Practical workshop on replacing fetal bovine serum (FBS) in life science research: From theory into practice0
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective_suppl20
How to formulate hypotheses and IATA to support grouping and read-across of nanoforms_suppl0
Application of Immunocompetent Microphysiological Systems in Drug Development: Current Perspective and Recommendations0
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides_suppl10
Animal pilot studies should not be used to estimate sample size if effect size and population variance are unknown0
Leveraging biomarkers and translational medicine for preclinical safety - Lessons for advancing the validation of alternatives to animal testing0
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals0
Zebrafish embryo neonicotinoid developmental neurotoxicity in the FET test and behavioral assays0
The future of Parkinson’s disease research: A new paradigm of human-specific investigation is necessary… and possible0
Intestinal in vitro transport assay combined with physiologically based kinetic modeling as a tool to predict bile acid levels in vivo_suppl20
Development of an Evidence-Based Risk Assessment Framework0
Impact of in vitro experimental variation in kinetic parameters on physiologically based kinetic (PBK) model simulations0
Validation of the monocyte activation test with three therapeutic monoclonal antibodies_suppl0
The use of categorical regression in evidence integration_suppl0
National workshop on alternatives to higher animals in toxicology and biomedical science0
Applications of microphysiological systems to disease models in the biopharmaceutical industry: Opportunities and challenges0
Revolutionizing developmental neurotoxicity testing – a journey from animal models to advanced in vitro systems0
How evidence-based methodologies can help identify and reduce uncertainty in chemical risk assessment0
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl30
A microfluidic thyroid-liver platform to assess chemical safety in humans0
In vitro-based prediction of human plasma concentrations of food-related compounds0
Development of a Monoclonal Antibody Sandwich ELISA for the Determination of Antigen Content and Quality in Human and Animal Tetanus Vaccines0
Application of microphysiological systems for nonclinical evaluation of cell therapies0
The importance of variations in in vitro dosimetry to support risk assessment of inhaled toxicants_suppl10
Erratum to National Workshop on Alternatives to Higher Animals in Toxicology and Biomedical Science0
Argentina's progress towards adopting new alternative methods in safety testing: The role of the Laboratorio de Métodos Alternativos0
Fish count, too – The animal toll of REACH aquatic toxicity tests0
EU roadmap for phasing out animal testing for chemical safety assessments: Recommendations from a multi-stakeholder roundtable0
Have the non-technical summaries of animal experiments in Europe improved? An update0
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl20
KoCVAM-led validation of KeraSkin™ Phototoxicity Assay for inclusion in OECD TG 4980
Third Virtual Summer School 3Rs for ONE Science: Alternative methods: From complexity to predictivity0
Non-animal models: Complexity for interactions…Connecting science0
A proof-of-concept rat toxicity study highlights the potential utility and challenges of virtual control groups0
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment0
Application of high-throughput transcriptomics for mechanism-based biological read-across of short-chain carboxylic acid analogues of valproic acid0
AOPs to connect food additives’ effects on gut microbiota to health outcomes0
Chemical selection for the Thyroid Validation Study coordinated by EURL ECVAM and involving EU-NETVAL laboratories_suppl20
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl20
Estimation of bioavailable concentration of endogenously formed N-nitrosamines by physiologically based kinetic modelling_suppl0
Software tools for systematic review literature screening and data extraction: Qualitative user experiences from succinct formal tests0
A novel coculture system for assessing respiratory sensitizing potential by IL-4 in T cells_suppl0
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl20
In vitro model of neurotrauma using the chick embryo to test regenerative bioimplantation0
Statistical derivation of cut-off values for in vitro assays0
Beyond pharmaceuticals: Fit-for-purpose new approach methodologies for environmental cardiotoxicity testing0
Cross-industrial applications of organotypic models0
In vitro models of the canine digestive tract as an alternative to in vivo assays: Advances and current challenges0
Sensitivity analysis and quality indicators for an in vitro oral irritation assay_suppl0
In vitro evaluation of the carcinogenic potential of perfluorinated chemicals0
A survey to assess animal methods bias in scientific publishing_suppl50
The Implementation Moonshot Project for Alternative Chemical Testing (IMPACT) toward a Human Exposome Project0
Evaluation of 147 perfluoroalkyl substances for immunotoxic and other (patho)physiological activities through phenotypic screening of human primary cells_suppl50
Predictive performance of next generation human physiologically based kinetic (PBK) model predictions based on in vitro and in silico input data_suppl10
Comparative evaluation of rat and human in vitro assays for evaluation of thyroid toxicity0
Challenges integrating skin sensitization data for assessment of difficult to test substances_suppl0
Assessing proarrhythmic potential of environmental chemicals using a high throughput in vitro-in silico model with human induced pluripotent stem cell-derived cardiomyocytes0
Development of an Evidence-Based Risk Assessment Framework0
3D bioprinting of human skin and squamous cell tumors (SCCs) as advanced models for precision medicine (BIOSQIN)0
Characterization of the C17.2 cell line as testing system for endocrine disruption-induced developmental neurotoxicity0
State of the science on assessing developmental neurotoxicity using new approach methods0
Statistical derivation of cut-off values for in vitro assays_suppl0
Biology-inspired dynamic microphysiological system approaches to revolutionize basic research, healthcare and animal welfare_suppl0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl50
A call for a Human Exposome Project0
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective0
Pollutant exposure and myocardial injury: Protocol and progress report for a toxicological systematic mapping review0
A survey to assess animal methods bias in scientific publishing_suppl20
The probable future of toxicology - probabilistic risk assessment0
Impact of gut permeability on estimation of oral bioavailability for chemicals in commerce and the environment_suppl10
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_suppl30
On the usefulness of animals as a model system (part I): Overview of criteria and focus on robustness0
Integrated skin sensitization assessment based on OECD methods (I): Deriving a point of departure for risk assessment_suppl10
Performance of the DASF compared to other combinations of OECD NAMs for eye hazard identification of surfactants_suppl0
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals_suppl20
Application of evidence-based methods to construct mechanism-driven chemical assessment frameworks0
A rodent thyroid-liver chip to capture thyroid toxicity on organ functional level_suppl0
Comparing translational success rates across medical research fields - A combined analysis of literature and clinical trial data0
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides0
Opportunities and challenges for human microphysiological systems in drug development0
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals_suppl10
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl20
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis_suppl20
Identifying candidate reference chemicals for in vitro testing of the retinoid pathway for predictive developmental toxicity0
ToxAIcology - The evolving role of artificial intelligence in advancing toxicology and modernizing regulatory science0
Trends in the use of animals and non-animal methods over the last 20 years0
4.2 million and counting… The animal toll for REACH systemic toxicity studies_suppl0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_suppl20
Dog as the experimental model: Laboratory uses of dogs in the United States_suppl0
Evaluation of 147 perfluoroalkyl substances for immunotoxic and other (patho)physiological activities through phenotypic screening of human primary cells_suppl60
The effect of surfactants and film-forming polymers on pulmonary surfactant function measured in vitro is dose rate dependent0
Making safety decisions for a sunscreen active ingredient using next-generation risk assessment: Benzophenone-4 case study_suppl20
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