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Plos One|August 3, 2017
Progress towards a public chemogenomic set for protein kinases and a call for contributionsDavid H Drewry, Carrow I Wells, David M Andrews, et al.Anti-Cancer Drugs|August 16, 2020
A novel screening approach comparing kinase activity of small molecule inhibitors with similar molecular structures and distinct biologic effects in triple-negative breast cancer to identify targetable signaling pathwaysMargarite D Matossian, Hope E Burks, Steven Elliott, et al.Journal of Virology|May 15, 2009
Human immunodeficiency virus type 1 elite neutralizers: individuals with broad and potent neutralizing activity identified by using a high-throughput neutralization assay together with an analytical selection algorithmMelissa D Simek, Wasima Rida, Frances H Priddy, et al.Cells|January 21, 2023
SGC-CAMKK2-1: A Chemical Probe for CAMKK2Carrow Wells, Yi Liang, Thomas L Pulliam, et al.Alzheimer'S & Dementia (New York, N. Y.)|April 27, 2022
AD Informer Set: Chemical tools to facilitate Alzheimer's disease drug discoveryFrances M Potjewyd, Joel K Annor-Gyamfi, Jeffrey Aubé, et al.Alzheimer'S & Dementia (New York, N. Y.)|April 18, 2022
Use of AD Informer Set compounds to explore validity of novel targets in Alzheimer's disease pathologyFrances M Potjewyd, Joel K Annor-Gyamfi, Jeffrey Aubé, et al.Journal of Medicinal Chemistry|July 15, 2021
Hinge Binder Scaffold Hopping Identifies Potent Calcium/Calmodulin-Dependent Protein Kinase Kinase 2 (CAMKK2) Inhibitor ChemotypesBenjamin J Eduful, Sean N O'Byrne, Louisa Temme, et al.Journal of Medicinal Chemistry|July 18, 2024
Discovery of Two Highly Selective Structurally Orthogonal Chemical Probes for Activin Receptor-like Kinases 1 and 2Václav Němec, Marek Remeš, Petr Beňovský, et al.Cell Chemical Biology|November 28, 2017
Quantitative, Wide-Spectrum Kinase Profiling in Live Cells for Assessing the Effect of Cellular ATP on Target EngagementJames D Vasta, Cesear R Corona, Jennifer Wilkinson, et al.Nature Chemical Biology|March 26, 2013
Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding groupMercedes Lobera, Kevin P Madauss, Denise T Pohlhaus, et al.Pageof 18