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The AAPS Journal|May 13, 2022
When to Extend Monitoring of Anti-drug Antibodies for High-risk Biotherapeutics in Clinical Trials: an Opinion from the European Immunogenicity PlatformGregor P Lotz, Karin Benstein, Karien Bloem, et al.Bioanalysis|July 29, 2022
Biomarker context-of-use: how organizational design can impact the implementation of the appropriate biomarker assay strategyKyra J Cowan, Michaela Golob, Joanne Goodman, et al.Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Synthetic LXR ligand inhibits the development of atherosclerosis in miceSean B Joseph, Elaine McKilligin, Liming Pei, et al.Bioanalysis|August 9, 2024
Re-thinking the current paradigm for clinical immunogenicity assessment: an update from the discussion in the European Bioanalysis ForumJoanne Goodman, Kyra J Cowan, Michaela Golob, et al.Scientific Reports|December 21, 2016
Engineering the surface properties of a human monoclonal antibody prevents self-association and rapid clearance in vivoClaire L Dobson, Paul W A Devine, Jonathan J Phillips, et al.The AAPS Journal|December 2, 2021
Anti-drug Antibody Validation Testing and Reporting HarmonizationHeather Myler, João Pedras-Vasconcelos, Kelli Phillips, et al.Pageof 3