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: Wang, JY Lou, PP Henkin, J

Citation: Jy. Wang et al., Selective inhibition of endothelial cell proliferation by fumagillin is not due to differential expression of methionine aminopeptidases, J CELL BIOC, 77(3), 2000, pp. 465-473

Authors: Henkin, J

Citation: J. Henkin, 'Driving Range', N AM REV, 285(3-4), 2000, pp. 37-41

Authors: Nienaber, V Wang, JY Davidson, D Henkin, J

Citation: V. Nienaber et al., Re-engineering of human urokinase provides a system for structure-based drug design at high resolution and reveals a novel structural subsite, J BIOL CHEM, 275(10), 2000, pp. 7239-7248

Authors: Schlesinger, Z Vered, Z Friedenson, A Reisin, L Jafari, J Flieb, T Sclarovsky, S Friedman, Y Ostfeld, B Solodky, A Abinader, E Rochfleish, S Palant, A Schneider, H Rosenfeld, T Khalid, S Wolfson, E Kishon, Y Narinsky, R Rotzak, R Davidov, A Levine, G Zahavi, I Vitrai, J Diker, D Pelled, B Pardu, J Galamidi, J Majadla, R Laniado, S Sherf, L Braun, S Eschar, Y Caspi, A Arditi, A Botwin, S Arkavi, L Ziv, M David, D Weisenberg, D Kohanovski, M Meisel, S Rougin, N Yahalom, M Glusman-Vazan, A Markiewitz, W Motlak, D Lessick, J Kagan, G Marmour, A Flich, M Solomon, R Tzivoni, D Zion, M Balkin, J Rabinowitz, B Barasch, E Brill, Z Aharon, L Asman, A Battler, A Gueron, M Cristal, N Liel, N Tsatskis, B Henkin, J

Citation: Z. Schlesinger et al., Secondary prevention by raising HDL cholesterol and reducing triglyceridesin patients with coronary artery disease - The bezafibrate infarction prevention (BIP) study, CIRCULATION, 102(1), 2000, pp. 21-27

Authors: Dawson, DW Volpert, OV Pearce, SFA Schneider, AJ Silverstein, RL Henkin, J Bouck, NP

Citation: Dw. Dawson et al., Three distinct D-amino acid substitutions confer potent antiangiogenic activity on an inactive peptide derived from a thrombospondin-1 type 1 repeat, MOLEC PHARM, 55(2), 1999, pp. 332-338