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Current Opinion in Pharmacology|July 25, 2018
Predicting how drug molecules bind to their protein targetsMoira M Rachman, Xavier Barril, Roderick E HubbardAnalytical Biochemistry|October 27, 2012
MTSA--a Matlab program to fit thermal shift dataMichèle N Schulz, Jens Landström, Roderick E HubbardAnalytical Chemistry|February 15, 2011
Comparative assessment of different histidine-tags for immobilization of protein onto surface plasmon resonance sensorchipsMarcus Fischer, Andrew P Leech, Roderick E HubbardJournal of Chemical Information and Modeling|May 3, 2011
Predicting fragment binding poses using a combined MCSS MM-GBSA approachMuhammad K Haider, Hugues-Olivier Bertrand, Roderick E HubbardNucleic Acids Research|July 18, 2006
sgTarget: a target selection resource for structural genomicsAna P C Rodrigues, Barry J Grant, Roderick E HubbardCurrent Topics in Medicinal Chemistry|November 6, 2007
The SeeDs approach: integrating fragments into drug discoveryRoderick E Hubbard, Ben Davis, Ijen Chen, et al.Topics in Current Chemistry|June 8, 2011
Hsp90 inhibitors and drugs from fragment and virtual screeningStephen Roughley, Lisa Wright, Paul Brough, et al.International Journal of Molecular Sciences|July 30, 2020
Exploring IDP-Ligand Interactions: tau K18 as A Test CaseDarius Vagrys, James Davidson, Ijen Chen, et al.Trends in Microbiology|July 27, 2010
Caught in a TRAP: substrate-binding proteins in secondary transportMarcus Fischer, Qian Yi Zhang, Roderick E Hubbard, et al.Nature Reviews. Drug Discovery|July 16, 2016
Twenty years on: the impact of fragments on drug discoveryDaniel A Erlanson, Stephen W Fesik, Roderick E Hubbard, et al.Pageof 8