Authors:
AMIN D
RUTLEDGE RZ
NEEDLE SN
GALCZENSKI HF
NEUENSCHWANDER K
SCOTESE AC
MAGUIRE MP
BUSH RC
HELE DJ
BILDER GE
PERRONE MH
Citation: D. Amin et al., RPR-107393, A POTENT SQUALENE SYNTHASE INHIBITOR AND ORALLY EFFECTIVECHOLESTEROL-LOWERING AGENT - COMPARISON WITH INHIBITORS OF HMG-COA REDUCTASE, The Journal of pharmacology and experimental therapeutics, 281(2), 1997, pp. 746-752
Authors:
SMITH C
ASHTON MJ
BUSH RC
FACCHINI V
HARRIS NV
HART TW
JORDAN R
MACKENZIE R
RIDDELL D
Citation: C. Smith et al., RP-73163 - A BIOAVAILABLE ALKLYSULFINYL-DIPHENYLIMIDAZOLE ACAT INHIBITOR, Bioorganic & medicinal chemistry letters, 6(1), 1996, pp. 47-50
Authors:
AMIN D
RUTLEDGE RZ
NEEDLE SJ
HELE DJ
NEUENSWANDER K
BUSH RC
BILDER GE
PERRONE MH
Citation: D. Amin et al., RPR101821, A NEW POTENT CHOLESTEROL-LOWERING AGENT - INHIBITION OF SQUALENE SYNTHASE AND 7-DEHYDROCHOLESTEROL REDUCTASE, Naunyn-Schmiedeberg's archives of pharmacology, 353(2), 1996, pp. 233-240
Citation: Rc. Bush, EMBRACING CHANGE - POSTMODERN INTERPRETATIONS OF THE I-CHING FROM A CHRISTIAN PERSPECTIVE - LEE,JY, Journal of ecumenical studies, 33(2), 1996, pp. 280-280
Authors:
RIDDELL D
BRIGHT CP
BURTON BJ
BUSH RC
HARRIS NV
HELE D
MOORE UM
NAIK K
PARROTT DP
SMITH C
WILLIAMS RJ
Citation: D. Riddell et al., HYPOLIPEMIC PROPERTIES OF A POTENT AND BIOAVAILABLE ALKLYSULFINYL-DIPHENYLIMIDAZOLE ACAT INHIBITOR (RP-73163) IN ANIMALS FED DIETS LOW IN CHOLESTEROL, Biochemical pharmacology, 52(8), 1996, pp. 1177-1186
Authors:
BELLO AA
BRIGHT C
BURTON BJ
BUSH RC
CASEY JH
DRON DI
FACCHINI V
JOANNOU PP
PARROTT DP
RIDDELL D
ROBERTS SA
WILLIAMS RJ
Citation: Aa. Bello et al., RP-64477 - A POTENT INHIBITOR OF ACYL-COENZYME-A - CHOLESTEROL O-ACYLTRANSFERASE WITH LOW SYSTEMIC BIOAVAILABILITY, Biochemical pharmacology, 51(4), 1996, pp. 413-421
Authors:
HELE DJ
BIRRELL M
BUSH RC
FLYNN DA
BROWN TJ
ROACH AG
Citation: Dj. Hele et al., SELECTIVE ETA AND MIXED ETA ETB RECEPTOR ANTAGONISTS INHIBIT BALLOON CATHETER-INDUCED SMOOTH-MUSCLE CELL-PROLIFERATION IN THE RAT THORACIC AORTA, British Journal of Pharmacology, 114, 1995, pp. 199-199