Ames concordance with the in vivo transgenic rodent (TGR) gene mutation assay for NDSRIs and relative in vivo TGR potency with nitrosamines with robust dose-response carcinogenicity data

Robert A. Jolly(Eli Lilly (United States)), Raechel Puglisi(Health and Environmental Sciences Institute), Sheroy Minocherhomji(University of Copenhagen), Mark W. Powley(Merck & Co., Inc., Rahway, NJ, USA (United States)), Raphael Nudelman(Applied Materials (Israel)), David J. Ponting, Joel P. Bercu(Gilead Sciences (United States)), Andreas Czich(Sanofi (Germany)), Rachael E. Tennant, Cheryl A. Hobbs(Pivot Bio (United States)), Zhanna Sobol(Pfizer (United States)), Connie L. Chen(Health and Environmental Sciences Institute), Andreas Zeller(Roche (Switzerland)), Patricia A. Escobar(Merck & Co., Inc., Rahway, NJ, USA (United States)), Anthony M. Lynch, Maik Schuler(Pfizer (United States)), George Johnson(Swansea University), Yi Hui Yang(AbbVie (United States)), Alejandra Trejo-Martin(Gilead Sciences (United States)), Paul B. White(Health Canada), Gregory R. Ott(Teva Pharmaceuticals (United States))
Regulatory Toxicology and Pharmacology
January 30, 2026
Cited by 3


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