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Structure (London, England : 1993)|November 15, 2016
Crystal Structure and Conformational Change Mechanism of a Bacterial Nramp-Family Divalent Metal TransporterAaron T Bozzi, Lukas B Bane, Wilhelm A Weihofen, et al.
Structure (London, England : 1993)|August 24, 2024
Scorpion α-toxin LqhαIT specifically interacts with a glycan at the pore domain of voltage-gated sodium channelsSwastik Phulera, Callum J Dickson, Christopher J Schwalen, et al.
The Journal of Biological Chemistry|January 1, 2010
Characterization and structural studies of the Plasmodium falciparum ubiquitin and Nedd8 hydrolase UCHL3Katerina Artavanis-Tsakonas, Wilhelm A Weihofen, John M Antos, et al.
Plos Biology|April 7, 2011
Enzymatic blockade of the ubiquitin-proteasome pathwayRobert Ernst, Jasper H L Claessen, Britta Mueller, et al.
Scientific Reports|September 16, 2017
A NMDA-receptor calcium influx assay sensitive to stimulation by glutamate and glycine/D-serineHongqiu Guo, L Miguel Camargo, Fred Yeboah, et al.
ACS Medicinal Chemistry Letters|November 22, 2019
Scaffold Morphing Identifies 3-Pyridyl Azetidine Ureas as Inhibitors of Nicotinamide Phosphoribosyltransferase (NAMPT)Daniel S Palacios, Erik L Meredith, Toshio Kawanami, et al.
Nature Chemical Biology|January 16, 2019
Discovery of a ZIP7 inhibitor from a Notch pathway screenErin Nolin, Sara Gans, Luis Llamas, et al.
Nature Chemical Biology|December 11, 2019
CPSF3-dependent pre-mRNA processing as a druggable node in AML and Ewing's sarcomaNathan T Ross, Felix Lohmann, Seth Carbonneau, et al.
Nature Chemical Biology|March 7, 2020
Author Correction: CPSF3-dependent pre-mRNA processing as a druggable node in AML and Ewing's sarcomaNathan T Ross, Felix Lohmann, Seth Carbonneau, et al.
Journal of Medicinal Chemistry|June 20, 2020
Structure-Based Design and Preclinical Characterization of Selective and Orally Bioavailable Factor XIa Inhibitors: Demonstrating the Power of an Integrated S1 Protease Family ApproachEdwige Lorthiois, James Roache, David Barnes-Seeman, et al.
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