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Journal of Medicinal Chemistry|September 3, 2021
Optimization of an Imidazo[1,2-<i>a</i>]pyridine Series to Afford Highly Selective Type I1/2 Dual Mer/Axl Kinase Inhibitors with <i>In Vivo</i> EfficacyWilliam McCoull, Scott Boyd, Martin R Brown, et al.Journal of Medicinal Chemistry|February 2, 2023
Discovery of a Potent and Orally Bioavailable Zwitterionic Series of Selective Estrogen Receptor Degrader-AntagonistsJames S Scott, Darren Stead, Bernard Barlaam, et al.Journal of Medicinal Chemistry|September 17, 2025
Fragment-Based Discovery and Structure-Led Optimization of MSC778, the First Potent, Selective, and Orally Bioavailable FEN1 InhibitorSam E Mann, Julien Lefranc, Omar Alkhatib, et al.Journal of Medicinal Chemistry|September 10, 2020
Discovery of AZD9833, a Potent and Orally Bioavailable Selective Estrogen Receptor Degrader and AntagonistJames S Scott, Thomas A Moss, Amber Balazs, et al.Molecular Vision|February 10, 2018
A genome-wide association study of corneal astigmatism: The CREAM ConsortiumRupal L Shah, Qing Li, Wanting Zhao, et al.Communications Biology|March 21, 2020
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive errorQiao Fan, Alfred Pozarickij, Nicholas Y Q Tan, et al.Pageof 14