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The AAPS Journal|July 28, 2025
Double-humanized Rats for CYP3A and PXR as an Improved Model for Analyzing Drug-drug Interactions Mediated by CYP3A4Kaoru Kobayashi, Genki Minegishi, Kanako Kazuki, et al.
The AAPS Journal|July 28, 2025
Machine Learning Predicts Drug Release Profiles and Kinetic Parameters Based on Tablets' FormulationsChrystalla Protopapa, Angeliki Siamidi, Amelia Adibe Eneli, et al.
The AAPS Journal|September 13, 2013
Impact of genetic polymorphism on drug-drug interactions mediated by cytochromes: a general approachMichel Tod, Christina Nkoud-Mongo, François Gueyffier
The AAPS Journal|July 26, 2014
Next generation ligand binding assays-review of emerging real-time measurement technologiesStephanie Fraser, Mark Cameron, Edward O'Connor, et al.
The AAPS Journal|August 31, 2013
Radionuclide decorporation: matching the biokinetics of actinides by transdermal delivery of pro-chelatorsYong Zhang, Matthew P Sadgrove, Russell J Mumper, et al.
The AAPS Journal|December 7, 2013
Automation practices in large molecule bioanalysis: recommendations from group L5 of the global bioanalytical consortiumAgo Ahene, Claudio Calonder, Scott Davis, et al.
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