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Journal of Medicinal Chemistry|February 20, 2015
Identification of novel aldose reductase inhibitors based on carboxymethylated mercaptotriazinoindole scaffoldMilan Stefek, Marta Soltesova Prnova, Magdalena Majekova, et al.Journal of Molecular Biology|October 24, 2007
Glutamate versus glutamine exchange swaps substrate selectivity in tRNA-guanine transglycosylase: insight into the regulation of substrate selectivity by kinetic and crystallographic studiesNaomi Tidten, Bernhard Stengl, Andreas Heine, et al.Biological Chemistry|December 18, 2012
Expression in non-melanogenic systems and purification of soluble variants of human tyrosinasePetra Cordes, Wei Sun, Rainer Wolber, et al.International Journal of Molecular Sciences|August 20, 2015
Structure-Based Optimization of Inhibitors of the Aspartic Protease EndothiapepsinAlwin M Hartman, Milon Mondal, Nedyalka Radeva, et al.Proteins|September 7, 2006
Physicochemical descriptors to discriminate protein-protein interactions in permanent and transient complexes selected by means of machine learning algorithmsPeter Block, Juri Paern, Eyke Hüllermeier, et al.Chemmedchem|August 23, 2008
Targeting the open-flap conformation of HIV-1 protease with pyrrolidine-based inhibitorsJark Böttcher, Andreas Blum, Stefanie Dörr, et al.Journal of Molecular Biology|April 10, 2007
Evidence for a novel binding site conformer of aldose reductase in ligand-bound stateHolger Steuber, Matthias Zentgraf, Concettina La Motta, et al.Archiv Der Pharmazie|September 14, 2004
Non-thiol farnesyltransferase inhibitors: utilization of the far aryl binding site by 5-cinnamoylaminobenzophenonesAndreas Mitsch, Pia Wissner, Markus Böhm, et al.International Journal of Pharmaceutics|July 21, 2012
Biophysical and biological investigation of DNA nano-complexes with a non-toxic, biodegradable amine-modified hyperbranched polyesterRegina Reul, Juliane Nguyen, Adam Biela, et al.Journal of Chemical Information and Modeling|November 28, 2006
3D QSAR selectivity analyses of carbonic anhydrase inhibitors: insights for the design of isozyme selective inhibitorsAlexander Weber, Markus Böhm, Claudiu T Supuran, et al.Pageof 25