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Bioorganic & Medicinal Chemistry Letters|January 30, 2008
Tyramine fragment binding to BACE-1Andreas Kuglstatter, Martin Stahl, Jens-Uwe Peters, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 4, 2011
Molecular recognition at the active site of catechol-O-methyltransferase (COMT): adenine replacements in bisubstrate inhibitorsManuel Ellermann, Ralph Paulini, Roland Jakob-Roetne, et al.
Mabs|June 2, 2012
Generation, characterization and structural data of chymase binding proteins based on the human Fyn kinase SH3 domainDaniel Schlatter, Simon Brack, David W Banner, et al.
Chemmedchem|March 28, 2009
Design and biological evaluation of novel, balanced dual PPARalpha/gamma agonistsUwe Grether, Agnes Bénardeau, Jörg Benz, et al.
The Journal of Biological Chemistry|April 23, 2020
Small molecule AX-024 reduces T cell proliferation independently of CD3ϵ/Nck1 interaction, which is governed by a domain swap in the Nck1-SH3.1 domainKirsten Richter, Arne C Rufer, Magali Muller, et al.
Journal of Surgical Orthopaedic Advances|May 2, 2017
How High Can You Go?: Retrograde Nailing of Proximal Femur FracturesKevin M Kuhn, Lisa K Cannada, J Tracy Watson, et al.
Bioorganic & Medicinal Chemistry Letters|April 8, 2009
Aleglitazar, a new, potent, and balanced dual PPARalpha/gamma agonist for the treatment of type II diabetesAgnes Bénardeau, Jörg Benz, Alfred Binggeli, et al.
European Journal of Medicinal Chemistry|February 10, 2009
Design of novel aminopyrrolidine factor Xa inhibitors from a screening hitKatrin Groebke Zbinden, Lilli Anselm, David W Banner, et al.
Ebiomedicine|September 20, 2017
Potent and Selective BACE-1 Peptide Inhibitors Lower Brain Aβ Levels Mediated by Brain Shuttle TransportNadine Ruderisch, Daniel Schlatter, Andreas Kuglstatter, et al.
Acta Crystallographica. Section D, Biological Crystallography|May 23, 2013
Mapping the conformational space accessible to BACE2 using surface mutants and cocrystals with Fab fragments, Fynomers and XaperonesDavid W Banner, Bernard Gsell, Jörg Benz, et al.
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