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Results: 1-8 |
Results: 8
Blocking CHK1 expression induces apoptosis and abrogates the G2 checkpointmechanism
Authors: Luo, Y Rockow-Magnone, SK Kroeger, PE Frost, L Chen, ZH Han, EKH Ng, SC Simmer, RL Giranda, VL
Citation: Y. Luo et al., Blocking CHK1 expression induces apoptosis and abrogates the G2 checkpointmechanism, NEOPLASIA, 3(5), 2001, pp. 411-419
Downregulation of Akt1 inhibits anchorage-independent cell growth and induces apoptosis in cancer cells
Authors: Liu, XS Shi, Y Han, EKH Chen, ZH Rosenberg, SH Giranda, VL Luo, Y Ng, SC
Citation: Xs. Liu et al., Downregulation of Akt1 inhibits anchorage-independent cell growth and induces apoptosis in cancer cells, NEOPLASIA, 3(4), 2001, pp. 278-286
Abrogation of G2 checkpoint specifically sensitize p53 defective cells to cancer chemotherapeutic agents
Authors: Luo, Y Rockow-Magnone, SK Joseph, MK Bradner, J Butler, CC Tahir, SK Han, EKH Ng, SC Severin, JM Gubbins, EJ Reilly, RM Rueter, A Simmer, RL Holzman, TF Giranda, VL
Citation: Y. Luo et al., Abrogation of G2 checkpoint specifically sensitize p53 defective cells to cancer chemotherapeutic agents, ANTICANC R, 21(1A), 2001, pp. 23-28
Species specificity of amidine-based urokinase inhibitors
Authors: Klinghofer, V Stewart, K McGonigal, T Smith, R Sarthy, A Nienaber, V Butler, C Dorwin, S Richardson, P Weitzberg, M Wendt, M Rockway, T Zhao, XM Hulkower, KI Giranda, VL
Citation: V. Klinghofer et al., Species specificity of amidine-based urokinase inhibitors, BIOCHEM, 40(31), 2001, pp. 9125-9131
Discovering novel ligands for macromolecules using X-ray crystallographic screening
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
Structure-directed discovery of potent non-peptidic inhibitors of human urokinase that access a novel binding subsite
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
Fluorescent microplate assay for cancer cell-associated cathepsin B
Authors: Hulkower, KI Butler, CC Linebaugh, BE Klaus, JL Keppler, D Giranda, VL Sloane, BF
Citation: Ki. Hulkower et al., Fluorescent microplate assay for cancer cell-associated cathepsin B, EUR J BIOCH, 267(13), 2000, pp. 4165-4170
Structure of the E2 DNA-binding domain from human papillomavirus serotype 31 at 2.4 angstrom
Authors: Bussiere, DE Kong, XP Egan, DA Walter, K Holzman, TF Lindh, F Robins, T Giranda, VL
Citation: De. Bussiere et al., Structure of the E2 DNA-binding domain from human papillomavirus serotype 31 at 2.4 angstrom, ACT CRYST D, 54, 1998, pp. 1367-1376
Risultati: 1-8 |