about
Discovery of the CCR1 antagonist, BMS-817399, for the treatment of rheumatoid arthritisp53-independent induction of rat hepatic Mdm2 following administration of phenobarbital and pregnenolone 16alpha-carbonitrile.Drug safety is a barrier to the discovery and development of new androgen receptor antagonists.The discovery of BMS-457, a potent and selective CCR1 antagonist.Discovery of a small molecule antagonist of the parathyroid hormone receptor by using an N-terminal parathyroid hormone peptide probeA retrospective analysis of toxicogenomics in the safety assessment of drug candidates.Interlaboratory evaluation of genomic signatures for predicting carcinogenicity in the rat.Transcriptional profiling of liver and effect of glucocorticoids in a rat adjuvant-induced arthritis model.Identification of bicyclic hexafluoroisopropyl alcohol sulfonamides as retinoic acid receptor-related orphan receptor gamma (RORγ/RORc) inverse agonists. Employing structure-based drug design to improve pregnane X receptor (PXR) selectivity.Urine acidification has no effect on peroxisome proliferator-activated receptor (PPAR) signaling or epidermal growth factor (EGF) expression in rat urinary bladder urothelium.Identification of sequence determinants that direct different intracellular folding pathways for aquaporin-1 and aquaporin-4.Current themes in microarray experimental design and analysis
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
William R. Foster
@ast
William R. Foster
@en
William R. Foster
@es
William R. Foster
@nl
William R. Foster
@sl
type
label
William R. Foster
@ast
William R. Foster
@en
William R. Foster
@es
William R. Foster
@nl
William R. Foster
@sl
prefLabel
William R. Foster
@ast
William R. Foster
@en
William R. Foster
@es
William R. Foster
@nl
William R. Foster
@sl
P1153
P106
P1153
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36771089900
57196647475
P21
P31
P496
0000-0002-5594-0791