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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|May 2, 2013
Elucidation of the biochemical basis for a clinical drug-drug interaction between atorvastatin and 5-(N-(4-((4-ethylbenzyl)thio)phenyl)sulfamoyl)-2-methyl benzoic acid (CP-778875), a subtype selective agonist of the peroxisome proliferator-activated receptor alphaAmit S Kalgutkar, Danny Chen, Manthena V Varma, et al.The Journal of Pharmacology and Experimental Therapeutics|December 17, 2020
Discovery of M5049: A Novel Selective Toll-Like Receptor 7/8 Inhibitor for Treatment of AutoimmunityJaromir Vlach, Andrew T Bender, Melinda Przetak, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 1, 2018
Considerations from the Innovation and Quality Induction Working Group in Response to Drug-Drug Interaction Guidances from Regulatory Agencies: Focus on CYP3A4 mRNA In Vitro Response Thresholds, Variability, and Clinical RelevanceJane R Kenny, Diane Ramsden, David B Buckley, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 7, 2015
Contribution of metabolites to P450 inhibition-based drug-drug interactions: scholarship from the drug metabolism leadership group of the innovation and quality consortium metabolite groupHongbin Yu, Suresh K Balani, Weichao Chen, et al.Toxicological Sciences : an Official Journal of the Society of Toxicology|November 6, 2013
Early prediction of polymyxin-induced nephrotoxicity with next-generation urinary kidney injury biomarkersNatalie D Keirstead, Matthew P Wagoner, Patricia Bentley, et al.Pageof 3