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Journal of Medicinal Chemistry|December 27, 2021
Structure-Based and Knowledge-Informed Design of B-Raf Inhibitors Devoid of Deleterious PXR BindingMelanie Schneider, Vanessa Delfosse, Muriel Gelin, et al.
Toxicology and Applied Pharmacology|August 10, 2014
Selectivity of natural, synthetic and environmental estrogens for zebrafish estrogen receptorsCaroline Pinto, Marina Grimaldi, Abdelhay Boulahtouf, et al.
Nature Structural & Molecular Biology|June 15, 2010
A unique secondary-structure switch controls constitutive gene repression by retinoic acid receptorAlbane le Maire, Catherine Teyssier, Cathie Erb, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|March 5, 2014
Halogenated bisphenol-A analogs act as obesogens in zebrafish larvae (Danio rerio)Anne Riu, Catherine W McCollum, Caroline L Pinto, et al.
Journal of Medicinal Chemistry|November 3, 2020
A Novel N-Substituted Valine Derivative with Unique Peroxisome Proliferator-Activated Receptor γ Binding Properties and Biological ActivitiesFranck Peiretti, Roberta Montanari, Davide Capelli, et al.
Cells|July 12, 2020
The Anti-Cancer Drug Dabrafenib Is a Potent Activator of the Human Pregnane X ReceptorNicolas Creusot, Matthieu Gassiot, Elina Alaterre, et al.
Water Research|April 6, 2018
Analysis of endocrine activity in drinking water, surface water and treated wastewater from six countriesFrederic D L Leusch, Peta A Neale, Charlotte Arnal, et al.
Nature Communications|November 17, 2022
Cryo-EM structure of the agonist-bound Hsp90-XAP2-AHR cytosolic complexJakub Gruszczyk, Loïc Grandvuillemin, Josephine Lai-Kee-Him, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 19, 2025
Inter-laboratory validation study of an in vitro glucocorticoid receptor transactivation assay for testing potential endocrine disrupting chemicalsAndrea Rivero-Arze, Marina Grimaldi, Géraldine Maillet, et al.
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