Second Virtual Summer School: Alternative methods in science: Towards model complexity

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Published: Jul 19, 2021
DOI: https://doi.org/10.14573/altex.2106221

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Francesca Caloni
Università degli Studi di Milano, Department of Environmental Science and Policy (ESP), Milan, Italy
Alessandra Cazzaniga
Fondazione Alessandro Volta, Como, Italy
Teresa Coccini
Laboratory of Clinical and Experimental Toxicology – Toxicology Unit, Istituti Clinici Scientifici Maugeri S.p.A.-SB, IRCCS Pavia, Pavia, Italy
Arno C. Gutleb
Luxembourg Institute of Science and Technology, Environmental Research and Innovation (ERIN) Department, Luxembourg, Luxembourg
Helena Kandarova
Centre of Experimental Medicine (CEM), Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Bratislava, Slovakia; Faculty of Chemical and Food Technology (FChFT), Institute of Biochemistry and Microbiology, Slovak University of Technology (STU), Bratislava, Slovakia
Laura Ceriotti
VitroScreen, Milan, Italy
Hassan Rashidi
UCL Great Ormond Street Institute of Child Health, University College London, London, UK
Yula Sambuy
Cell Biologist, Rome, Italy
Sonja von Aulock
ALTEX – Alternatives to Animal Experimentation, Kreuzlingen, Switzerland
Doris Wilflingseder
Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, Austria

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How to Cite
Caloni, F., Cazzaniga, A., Coccini, T., Gutleb, A. C., Kandarova, H., Ceriotti, L., Rashidi, H., Sambuy, Y., von Aulock, S. and Wilflingseder, D. (2021) “Second Virtual Summer School: Alternative methods in science: Towards model complexity”, ALTEX - Alternatives to animal experimentation, 38(3), pp. 510–512. doi: 10.14573/altex.2106221.
Issue
Vol. 38 No. 3 (2021)
Section
Meeting Reports
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References

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Marescotti, D., Serchi, T., Luettich, K. et al. (2019). Added value of complexity: How complex should an in vitro model be? The experience on a 3D alveolar model. ALTEX 36, 388-402. doi:10.14573/altex.1811221

Rashidi, H., Luu, N. T., Alwahsh, S. et al. (2018). 3D human liver tissue from pluripotent stem cells displays stable phenotype in vitro and supports compromised liver function in vivo. Arch Toxicol 92, 3117-3129. doi:10.1007/s00204-018-2280-2