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Methods in Molecular Biology (Clifton, N.J.)|February 22, 2012
Analysing properties of proteasome inhibitors using kinetic and X-ray crystallographic studiesNerea Gallastegui, Michael GrollTrends in Biochemical Sciences|June 15, 2010
The 26S proteasome: assembly and function of a destructive machineNerea Gallastegui, Michael GrollStructure (London, England : 1993)|October 20, 2009
How ATPases unravel a mysteryNerea Gallastegui, Michael GrollTrends in Biochemical Sciences|December 16, 2014
Advances in our structural understanding of orphan nuclear receptorsNerea Gallastegui, Jonathan A G Mackinnon, Robert J Fletterick, et al.Angewandte Chemie (International Ed. in English)|November 29, 2013
Omuralide and vibralactone: differences in the proteasome- β-lactone-γ-lactam binding scaffold alter target preferencesAnja List, Evelyn Zeiler, Nerea Gallastegui, et al.Molecular and Cellular Endocrinology|June 10, 2014
Allosteric mechanisms of nuclear receptors: insights from computational simulationsJonathan A G Mackinnon, Nerea Gallastegui, David J Osguthorpe, et al.Journal of Medicinal Chemistry|April 2, 2013
Dimerized linear mimics of a natural cyclopeptide (TMC-95A) are potent noncovalent inhibitors of the eukaryotic 20S proteasomeAudrey Desvergne, Emilie Genin, Xavier Maréchal, et al.Journal of Medicinal Chemistry|November 23, 2012
Peptido sulfonyl fluorides as new powerful proteasome inhibitorsArwin J Brouwer, Anika Jonker, Paul Werkhoven, et al.Nature Communications|February 7, 2017
Structure of the homodimeric androgen receptor ligand-binding domainMarta Nadal, Stefan Prekovic, Nerea Gallastegui, et al.Journal of Medicinal Chemistry|January 17, 2013
Incorporation of non-natural amino acids improves cell permeability and potency of specific inhibitors of proteasome trypsin-like sitesPaul P Geurink, Wouter A van der Linden, Anne C Mirabella, et al.Pageof 1