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Citation: J. Dong et al., Probing inhibitors binding to human urokinase crystals by Raman microscopy: Implications for compound screening, BIOCHEM, 40(33), 2001, pp. 9751-9757

Authors: Nienaber, VL Richardson, PL Klighofer, V Bouska, JJ Giranda, VL Greer, J

Citation: Vl. Nienaber et al., Discovering novel ligands for macromolecules using X-ray crystallographic screening, NAT BIOTECH, 18(10), 2000, pp. 1105-1108

Authors: Nienaber, VL Davidson, D Edalji, R Giranda, VL Klinghofer, V Henkin, J Magdalinos, P Mantei, R Merrick, S Severin, JM Smith, RA Stewart, K Walter, K Wang, JY Wendt, M Weitzberg, M Zhao, XM Rockway, T

Citation: Vl. Nienaber et al., Structure-directed discovery of potent non-peptidic inhibitors of human urokinase that access a novel binding subsite, STRUCT F D, 8(5), 2000, pp. 553-563

Authors: Muchmore, SW Olson, J Jones, R Pan, J Blum, M Greer, J Merrick, SM Magdalinos, P Nienaber, VL

Citation: Sw. Muchmore et al., Automated crystal mounting and data collection for protein crystallography, STRUCTURE, 8(12), 2000, pp. R243-R246

Authors: Nienaber, VL Boxrud, PD Berliner, LJ

Citation: Vl. Nienaber et al., Thrombin inhibitor design: X-ray and solution studies provide a novel P1 determinant, J PROTEIN C, 19(4), 2000, pp. 327-333

Authors: Nienaber, VL Berliner, LJ

Citation: Vl. Nienaber et Lj. Berliner, Atomic structures of two nitroxide spin labels complexed with human thrombin: Comparison with solution studies, J PROTEIN C, 19(2), 2000, pp. 129-137