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Journal of Medicinal Chemistry|December 19, 2009
Evaluation of substituted N,N'-diarylsulfonamides as activators of the tumor cell specific M2 isoform of pyruvate kinaseMatthew B Boxer, Jian-kang Jiang, Matthew G Vander Heiden, et al.
Biochemistry|July 8, 2009
Identification of aminothienopyridazine inhibitors of tau assembly by quantitative high-throughput screeningAlex Crowe, Wenwei Huang, Carlo Ballatore, et al.
Environmental Health Perspectives|January 27, 2015
Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening studyNour Abdo, Menghang Xia, Chad C Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2012
Identification of benzodiazepine Ro5-3335 as an inhibitor of CBF leukemia through quantitative high throughput screen against RUNX1-CBFβ interactionLea Cunningham, Steven Finckbeiner, R Katherine Hyde, et al.
Antimicrobial Agents and Chemotherapy|November 7, 2012
A class of tricyclic compounds blocking malaria parasite oocyst development and transmissionRichard T Eastman, Sittiporn Pattaradilokrat, Dipak K Raj, et al.
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