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 2022-05-01 to 2026-05-01.)
ArticleCitations
Alternative Methods in Science: Towards Fluidic Systems51
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl128
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl518
Sensitivity analysis and quality indicators for an in vitro oral irritation assay16
Validation of an Endopep-suspension immunoassay for the diagnostics of human botulism_suppl15
Animal research ethics as interaction of research ethics, animal ethics, and (animal protection) law13
The effect of surfactants and film-forming polymers on pulmonary surfactant function measured in vitro is dose rate dependent_suppl10
REACH out-numbered! The future of REACH and animal numbers9
Intestinal in vitro transport assay combined with physiologically based kinetic modeling as a tool to predict bile acid levels in vivo_suppl19
Predicting Acute Oral Toxicity Using AcutoX: An Animal Product-Free and Metabolically Relevant Human Cell-Based Test9
Off to a good start? Review of the predictivity of reactivity methods modelling the molecular initiating event of skin sensitization9
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency9
A sensitive cell-based assay for testing potency of Botulinum neurotoxin type A8
Mapping out strategies to further develop human-relevant, new approach methodology (NAM)-based developmental neurotoxicity (DNT) testing7
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl47
Chemical selection for the Thyroid Validation Study coordinated by EURL ECVAM and involving EU-NETVAL laboratories_suppl17
E-validation – Unleashing AI for validation7
Making safety decisions for a sunscreen active ingredient using next-generation risk assessment: Benzophenone-4 case study7
The long way from raw data to NAM-based information: Overview on data layers and processing steps6
Developing a global education hub for animal-free innovation_suppl6
Stakeholder input towards further refinement and consolidation of the alternative safety profiling algorithm (ASPA) for next generation risk assessment (NGRA)_suppl26
Developmental neurotoxicity (DNT): A call for implementation of new approach methodologies for regulatory purposes: Summary of the 5th International Conference on DNT Testing6
Validation study for the evaluation of MCTT HCE™ test method for eye safety assessment of medical devices6
Chemical selection for the Thyroid Validation Study coordinated by EURL ECVAM and involving EU-NETVAL laboratories_suppl35
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl15
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 Alter4
Lost in NAMs-lation: A review of animal-free science definitions4
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl64
3Rs: Progress or a fig leaf?4
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations4
Mapping physiology: A systems biology approach for the development of alternative methods in toxicology4
Investigation of the publication rate of recent research projects using non-human primates in France4
Exploring the synergy of CRISPR and microphysiological systems4
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays_suppl34
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl24
AOP 460: Antagonism of Smoothened receptor leading to orofacial clefting_suppl14
In vitro-based prediction of human plasma concentrations of food-related compounds_suppl13
Women in Alternatives3
The Alarming Consequences of Workforce Reductions at the FDA, EPA, NIH and CDC in the United States3
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays_suppl23
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay3
Low rejection rate for animal experiments in Germany despite legal reform3
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl33
The Virtual Human Platform for Safety Assessment (VHP4Safety) project: Next generation chemical safety assessment based on human data3
From cellular perturbation to probabilistic risk assessments2
ALTEX Proceedings TIERethik Corrigendum to Incorporating new approach methodologies into regulatory nonclinical pharmaceutical safety assessment2
Linking nanomaterial-induced mitochondrial dysfunction to existing adverse outcome pathways for chemicals_suppl12
The SCAHT Adverse Outcome Pathway (AOP)_HUB: A hands-on platform for information exchange, sharing, and developing AOPs2
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl72
Biology-inspired dynamic microphysiological system approaches to revolutionize basic research, healthcare and animal welfare2
Bridging the gap in chemical risk assessment: Leveraging metabolite similarity for enhanced read-across applications2
Transition to animal-free science: Phasing out animal experiments, phasing in innovation2
Incorporating new approach methodologies into regulatory nonclinical pharmaceutical safety assessment2
Assessment of developmental neurotoxicology-associated alterations in neuronal architecture and function using Caenorhabditis elegans_suppl2
Material-mediated pyrogens in medical devices: Myth or reality?_suppl22
Comparative evaluation of rat and human in vitro assays for evaluation of thyroid toxicity_suppl12
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl62
Qualitative and quantitative concentration-response modelling of gene co-expression networks to unlock hepatotoxic mechanisms for next generation chemical safety assessment2
Human relevant frontiers in drug safety and efficacy2
Beyond chemicals: Opportunities and challenges of integrating non-chemical stressors in adverse outcome pathways2
A path forward advancing microphysiological systems2
Role of standards and funding in accelerating the development and use of microphysiological systems2
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis_suppl12
Building confidence in PBK model predictions in the absence of human kinetic data: Benzophenone-4 case study_suppl12
Second scientific sessions and international conference of the Society for Alternatives to Animal Testing in Sri Lanka (SAAT-SL)2
Micro-replace systems2
Towards NAM-based risk assessment for developmental neurotoxic effects, illustrated with chlorpyrifos1
International conference and workshop on “New Approach Methodologies (NAMs) in Pharmacology and Toxicology”1
Phase-out planning for animal experimentation: A definition, an argument, and seven action points1
Phasing in human-relevant science: Why the UK’s roadmap matters – and how to make it work1
Advancing humane and human-relevant science: The 8th Annual Conference of the Society for Alternatives to Animal Experiments – India (SAAE-I 2025)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
Guidance for Good In Vitro Reporting Standards (GIVReSt) – A draft for stakeholder discussion and background documentation1
Fish Count, Too – The Animal Toll of REACH Aquatic Toxicity Tests_suppl21
AOP 460: Antagonism of Smoothened receptor leading to orofacial clefting1
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides_suppl21
Virtual control groups in non-clinical toxicology – A replicability challenge1
The benefits of validation of methods for toxicity testing outweigh its costs1
Advancing skin sensitization potency categorization using U-SENS™ in OECD TG 4971
3 Days for 3Rs 2023: Refinement, reduction, replacement1
Ways to broaden the awareness, consideration and adoption of new approach methodologies (NAMs)1
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis1
Linking nanomaterial-induced mitochondrial dysfunction to existing adverse outcome pathways for chemicals_suppl21
A sensitive cell-based assay for testing potency of Botulinum neurotoxin type A_suppl1
The need for epigenotoxicity testing1
A call for a Human Exposome Project0
The importance of variations in in vitro dosimetry to support risk assessment of inhaled toxicants_suppl10
Report on the 5th and 6th Mystery of Reactive Oxygen Species Conferences0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_suppl20
Biology-inspired dynamic microphysiological system approaches to revolutionize basic research, healthcare and animal welfare_suppl0
The probable future of toxicology - probabilistic risk assessment0
Serum-free in vitro assessment of receptor-mediated endocrine activity including Phase-1 metabolism_suppl0
Developing a global education hub for animal-free innovation0
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_suppl30
An Alternative Safety Profiling Algorithm (ASPA) to transform next generation risk assessment into a structured and transparent process_suppl0
Intestinal in vitro transport assay combined with physiologically based kinetic modeling as a tool to predict bile acid levels in vivo_suppl20
Organizing shipping studies to evaluate the transferability of cell- and tissue-based test systems and reagents: An end user perspective0
Considerations from the pharmaceutical industry (IQ MPS affiliate) workshop on animal microphysiological systems and 3Rs in drug development0
Estimation of bioavailable concentration of endogenously formed N-nitrosamines by physiologically based kinetic modelling0
Revolutionizing developmental neurotoxicity testing – a journey from animal models to advanced in vitro systems0
Determination of U-SENS™ borderline range thresholds to address uncertainty for skin sensitization assessment in a regulatory context_suppl10
A survey to assess animal methods bias in scientific publishing_suppl30
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl10
Possible applications of new approach methodologies (NAMs) in ecotoxicology0
Material-mediated pyrogens in medical devices: Myth or reality?0
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides_suppl10
Erratum to National Workshop on Alternatives to Higher Animals in Toxicology and Biomedical Science0
Characterization of the C17.2 cell line as testing system for endocrine disruption-induced developmental neurotoxicity_suppl0
Mapping physiology: A systems biology approach for the development of alternative methods in toxicology_suppl0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl40
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl30
Have the non-technical summaries of animal experiments in Europe improved? An update0
Low rejection rate for animal experiments in Germany despite legal reform_suppl0
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl30
Assessing proarrhythmic potential of environmental chemicals using a high throughput in vitro-in silico model with human induced pluripotent stem cell-derived cardiomyocytes0
Serum-free in vitro assessment of receptor-mediated endocrine activity including Phase-1 metabolism0
In vitro model of neurotrauma using the chick embryo to test regenerative bioimplantation0
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective0
The turning point: April 2025 marks historic shift in US animal testing policy0
Identifying candidate reference chemicals for in vitro testing of the retinoid pathway for predictive developmental toxicity_suppl20
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals_suppl20
In vitro-based prediction of human plasma concentrations of food-related compounds0
Challenges and opportunities for validation of AI-based new approach methods0
Building confidence in PBK model predictions in the absence of human kinetic data: Benzophenone-4 case study0
Development of physiologically based gut absorption model for probabilistic prediction of environmental chemical bioavailability0
Moving towards making (quantitative) structure-activity relationships ((Q)SARs) for toxicity-related endpoints findable, accessible, interoperable and reusable (FAIR)0
Investigation of the potential of bisphenol A substitutes to induce allergic contact sensitization using OECD defined approaches0
Custom GPTs to aid in compliance checking for reporting standards in academic publishing0
Argentina's progress towards adopting new alternative methods in safety testing: The role of the Laboratorio de Métodos Alternativos0
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl10
Cardiotoxicity of chemicals: Current regulatory guidelines, knowledge gaps, and needs0
Determination of U-SENS™ borderline range thresholds to address uncertainty for skin sensitization assessment in a regulatory context_suppl20
Software tools for systematic review literature screening and data extraction: Qualitative user experiences from succinct formal tests0
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective_suppl10
Data-driven derivation of an adverse outcome pathway linking vascular endothelial growth factor receptor (VEGFR), endocrine disruption, and atherosclerosis_suppl20
National workshop on alternatives to higher animals in toxicology and biomedical science0
3D bioprinting of human skin and squamous cell tumors (SCCs) as advanced models for precision medicine (BIOSQIN)0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl80
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl20
Advancing skin sensitization potency categorization using U-SENS™ in OECD TG 497_suppl0
Implementation of reduction and refinement-related parameters in repeated dose toxicity studies0
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl10
Bridging the gap in chemical risk assessment: Leveraging metabolite similarity for enhanced read-across applications_suppl10
National workshop on non-mammalian models in research with emphasis on the 3Rs principle0
Comparing translational success rates across medical research fields - A combined analysis of literature and clinical trial data0
The effect of surfactants and film-forming polymers on pulmonary surfactant function measured in vitro is dose rate dependent0
Multiparametric evaluation of different FBS-free replacement media for widely used human cancer cell lines_Suppl50
In vitro evaluation of the carcinogenic potential of perfluorinated chemicals0
A survey to assess animal methods bias in scientific publishing_suppl20
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl20
The validation of regulatory test methods – Conceptual, ethical, and philosophical foundations0
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays0
Stakeholder input towards further refinement and consolidation of the alternative safety profiling algorithm (ASPA) for next generation risk assessment (NGRA)0
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl30
Lung tumor microphysiological system with 3D endothelium to evaluate modulators of T-cell migration0
Opportunities and challenges for human microphysiological systems in drug development0
Indian Society for Alternatives to Animal Experiments: Sixth annual meeting and international conference0
Multiparametric evaluation of different FBS-free replacement media for widely used human cancer cell lines_Suppl30
Fish Count, Too – The Animal Toll of REACH Aquatic Toxicity Tests_suppl10
Development of a Monoclonal Antibody Sandwich ELISA for the Determination of Antigen Content and Quality in Human and Animal Tetanus Vaccines0
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
Statistical derivation of cut-off values for in vitro assays0
Characterization and optimization of variability in a human colonic epithelium culture model0
The road to virtual control groups and the importance of proper body-weight selection0
Impact of gut permeability on estimation of oral bioavailability for chemicals in commerce and the environment_suppl20
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl20
A proof-of-concept rat toxicity study highlights the potential utility and challenges of virtual control groups_suppl0
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl20
Bridging the gap in chemical risk assessment: Leveraging metabolite similarity for enhanced read-across applications_suppl20
Tracing progress: The evolution of a protocol for relative metal release in surrogate gastric fluid_suppl0
ToxAIcology - The evolving role of artificial intelligence in advancing toxicology and modernizing regulatory science0
State of the science on assessing developmental neurotoxicity using new approach methods0
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment_suppl10
Pyrogen testing at a turning point – On occasion of the 30th anniversary of the whole blood monocyte activation test0
Elements and development processes for test methods in toxicology and human health-relevant life science research0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl50
Performance of the DASF compared to other combinations of OECD NAMs for eye hazard identification of surfactants0
EU roadmap for phasing out animal testing for chemical safety assessments: Recommendations from a multi-stakeholder roundtable0
Validation study for the evaluation of MCTT HCE™ test method for eye safety assessment of medical devices_Suppl10
Trust your gut: Establishing confidence in gastrointestinal models - An overview of the state of the science and contexts of use0
Report of the 3rd and 4th Mystery of Reactive Oxygen Species Conference0
Pollutant exposure and myocardial injury: Protocol and progress report for a toxicological systematic mapping review_Supplement0
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays _suppl10
A survey to assess animal methods bias in scientific publishing_suppl50
A human iPSC-based in vitro neural network formation assay to investigate neurodevelopmental toxicity of pesticides0
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl70
Trends in the use of animals and non-animal methods over the last 20 years0
Towards NAM-based risk assessment for developmental neurotoxic effects, illustrated with chlorpyrifos_suppl10
Protectiveness of NAM-based hazard assessment – which testing scope is required?_suppl30
Characterization of the C17.2 cell line as testing system for endocrine disruption-induced developmental neurotoxicity0
Perception and power: Barriers to animal-free research - Animalfree Research Forum 20250
Acceptance criteria for new approach methods in toxicology and human health-relevant life science research – part I0
Determining a point of departure for skin sensitization potency and quantitative risk assessment of fragrance ingredients using the GARDskin dose-response assay_suppl20
Beyond Animal Testing Index: Benchmarking tool for a world beyond animal testing_suppl50
Review on organ-on-chips for medicines safety assessment: A European regulatory perspective_suppl20
The Implementation Moonshot Project for Alternative Chemical Testing (IMPACT) toward a Human Exposome Project0
Investigation of the publication rate of recent research projects using non-human primates in France_suppl10
Making safety decisions for a sunscreen active ingredient using next-generation risk assessment: Benzophenone-4 case study_suppl20
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_Suppl60
Sensitivity analysis and quality indicators for an in vitro oral irritation assay_suppl0
Systematic analysis of read-across adaptations in testing proposal evaluations by the European Chemicals Agency_suppl40
Improved identification of human hepatotoxic potential by summary variables of gene expression_suppl0
Organoid intelligence (OI) – The ultimate functionality of a brain microphysiological system0
Making safety decisions for a sunscreen active ingredient using next-generation risk assessment: Benzophenone-4 case study_suppl10
Potential value of animal microphysiological systems0
Off to a good start? Review of the predictivity of reactivity methods modelling the molecular initiating event of skin sensitization_suppl10
Fish count, too – The animal toll of REACH aquatic toxicity tests0
Incorporating new approach methodologies into regulatory nonclinical pharmaceutical safety assessment_suppl0
InViTe2 Retreat: Advancing new approach methodologies in chemical safety testing and drug discovery0
The importance of variations in in vitro dosimetry to support risk assessment of inhaled toxicants_suppl20
Statistical derivation of cut-off values for in vitro assays_suppl0
KoCVAM-led validation of KeraSkin™ Phototoxicity Assay for inclusion in OECD TG 4980
Risk-based prioritization of PFAS using phenotypic and transcriptomic data from human induced pluripotent stem cell-derived hepatocytes and cardiomyocytes_suppl30
Russell and Burch’s 3Rs then and now: The case of Switzerland0
Pollutant exposure and myocardial injury: Protocol and progress report for a toxicological systematic mapping review0
The impact of biostatistics on hazard characterization using in vitro developmental neurotoxicity assays_suppl0
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals0
Impact of gut permeability on estimation of oral bioavailability for chemicals in commerce and the environment_suppl10
Tracing progress: The evolution of a protocol for relative metal release in surrogate gastric fluid0
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl80
Integrated skin sensitization assessment based on OECD methods (III): Adding human data to the assessment0
Toward implementing virtual control groups in nonclinical safety studies0
Performance of the DASF compared to other combinations of OECD NAMs for eye hazard identification of surfactants_suppl0
Challenges integrating skin sensitization data for assessment of difficult to test substances_suppl0
Multiparametric evaluation of different FBS-free replacement media for widely used human cancer cell lines0
Animal pilot studies should not be used to estimate sample size if effect size and population variance are unknown0
Development of a defined approach for eye hazard identification of solid chemicals according to the three UN GHS categories0
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays_suppl50
60 Years of the 3Rs symposium: Lessons learned and the road ahead0
The impact of biostatistics on hazard characterization using in vitro developmental neurotoxicity assays0
An Alternative Safety Profiling Algorithm (ASPA) to transform next generation risk assessment into a structured and transparent process0
AOPs to connect food additives’ effects on gut microbiota to health outcomes0
Validation study for the evaluation of MCTT HCE™ test method for eye safety assessment of medical devices_Suppl20
Assessment of developmental neurotoxicology-associated alterations in neuronal architecture and function using Caenorhabditis elegans0
What does “success” look like in compliance check decisions by the European Chemicals Agency? The curious cases of accepted read-across adaptations_suppl50
Leveraging biomarkers and translational medicine for preclinical safety - Lessons for advancing the validation of alternatives to animal testing0
Estimation of bioavailable concentration of endogenously formed N-nitrosamines by physiologically based kinetic modelling_suppl0
Determination of U-SENS™ borderline range thresholds to address uncertainty for skin sensitization assessment in a regulatory context0
Applications of microphysiological systems to disease models in the biopharmaceutical industry: Opportunities and challenges0
Chemical fate in vitro: A physiological biokinetic (PBK) model for cell-based assays_suppl40
Chemical selection for the Thyroid Validation Study coordinated by EURL ECVAM and involving EU-NETVAL laboratories_suppl20
Comparative evaluation of rat and human in vitro assays for evaluation of thyroid toxicity0
Evaluation of a high-throughput in-vitro-to-in-vivo extrapolation (IVIVE) workflow for the prioritization of potential developmental toxicity of chemicals_suppl10
Comparing translational success rates across medical research fields - A combined analysis of literature and clinical trial data_suppl10
Multiparametric evaluation of different FBS-free replacement media for widely used human cancer cell lines_Suppl20
New approach methodologies (NAMs): The strategic vision in science0
4.2 million and counting… The animal toll for REACH systemic toxicity studies_suppl0
0.12813210487366