Authors:
Smith, RA
Barbosa, J
Blum, CL
Bobko, MA
Caringal, YV
Dally, R
Johnson, JS
Katz, ME
Kennure, N
Kingery-Wood, J
Lee, W
Lowinger, TB
Lyons, J
Marsh, V
Rogers, DH
Swartz, S
Walling, T
Wild, H
Citation: Ra. Smith et al., Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: Identification of a second generation lead by a combinatorial chemistry approach, BIOORG MED, 11(20), 2001, pp. 2775-2778
Authors:
Redman, AM
Johnson, JS
Dally, R
Swartz, S
Wild, H
Paulsen, H
Caringal, Y
Gunn, D
Renick, J
Osterhout, M
Kingery-Wood, J
Smith, RA
Lee, W
Dumas, J
Wilhelm, SM
Housley, TJ
Bhargava, A
Ranges, GE
Shrikhande, A
Young, D
Bombara, M
Scott, WJ
Citation: Am. Redman et al., p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: Thienyl, furyl, and pyrrolyl ureas, BIOORG MED, 11(1), 2001, pp. 9-12
Authors:
Spencer-Smith, J
Wild, H
Innes-Ker, AH
Townsend, J
Duffy, C
Edwards, C
Ervin, K
Merritt, N
Paik, JW
Citation: J. Spencer-smith et al., Making faces: Creating three-dimensional parameterized models of facial expression, BEHAV RE ME, 33(2), 2001, pp. 115-123
Authors:
Matassova, NB
Rodnina, MV
Endermann, R
Kroll, HP
Pleiss, U
Wild, H
Wintermeyer, W
Citation: Nb. Matassova et al., Ribosomal RNA is the target for oxazolidinones, a novel class of translational inhibitors, RNA, 5(7), 1999, pp. 939-946