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ACS Medicinal Chemistry Letters|June 6, 2014
Discovery and Biological Profiling of Potent and Selective mTOR Inhibitor GDC-0349Zhonghua Pei, Elizabeth Blackwood, Lichuan Liu, et al.
ACS Medicinal Chemistry Letters|June 20, 2014
Structure-Guided Rescaffolding of Selective Antagonists of BCL-XLMichael F T Koehler, Philippe Bergeron, Edna F Choo, et al.
Journal of Biomolecular Techniques : JBT|March 9, 2006
The SNPlex genotyping system: a flexible and scalable platform for SNP genotypingAndreas R Tobler, Sabine Short, Mark R Andersen, et al.
Nature|May 4, 2018
Structural basis for dual-mode inhibition of the ABC transporter MsbAHoangdung Ho, Anh Miu, Mary Kate Alexander, et al.
Bioorganic & Medicinal Chemistry Letters|September 1, 2009
GDC-0449-a potent inhibitor of the hedgehog pathwayKirk D Robarge, Shirley A Brunton, Georgette M Castanedo, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2024
Discovery of potent dihydro-oxazinoquinolinone inhibitors of GuaB for the treatment of tuberculosisYuebiao Zhou, Ignacio Aliagas, Shumei Wang, et al.
Analytical Chemistry|November 5, 2013
Multiplexed target detection using DNA-binding dye chemistry in droplet digital PCRGeoffrey P McDermott, Duc Do, Claudia M Litterst, et al.
Journal of Medicinal Chemistry|June 16, 2012
Discovery and optimization of C-2 methyl imidazopyrrolopyridines as potent and orally bioavailable JAK1 inhibitors with selectivity over JAK2Mark Zak, Rohan Mendonca, Mercedesz Balazs, et al.
ACS Medicinal Chemistry Letters|October 15, 2014
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo ActivityZhi-Fu Tao, Lisa Hasvold, Le Wang, et al.
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