VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q50086103 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235918.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q50086103‏
024 ‎‡a 0000-0002-5594-0791‏ ‎‡2 orcid‏
024 ‎‡a 36771089400‏ ‎‡2 scopus‏
024 ‎‡a 36771089900‏ ‎‡2 scopus‏
024 ‎‡a 57196647475‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q50086103‏
100 0 ‎‡a William R. Foster‏ ‎‡9 es‏ ‎‡9 sl‏ ‎‡9 ast‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a উইলিয়াম আর ফস্টার‏ ‎‡9 bn‏
400 0 ‎‡a William R. Foster‏ ‎‡c researcher‏ ‎‡9 en‏
400 0 ‎‡a William R. Foster‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A retrospective analysis of toxicogenomics in the safety assessment of drug candidates.‏
670 ‎‡a Author's Current themes in microarray experimental design and analysis‏
670 ‎‡a Author's Discovery of a small molecule antagonist of the parathyroid hormone receptor by using an N-terminal parathyroid hormone peptide probe‏
670 ‎‡a Author's Discovery of the CCR1 antagonist, BMS-817399, for the treatment of rheumatoid arthritis‏
670 ‎‡a Author's Drug safety is a barrier to the discovery and development of new androgen receptor antagonists.‏
670 ‎‡a Author's Identification of bicyclic hexafluoroisopropyl alcohol sulfonamides as retinoic acid receptor-related orphan receptor gamma‏
670 ‎‡a Author's 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
670 ‎‡a Author's Identification of sequence determinants that direct different intracellular folding pathways for aquaporin-1 and aquaporin-4.‏
670 ‎‡a Author's Interlaboratory evaluation of genomic signatures for predicting carcinogenicity in the rat.‏
670 ‎‡a Author's p53-independent induction of rat hepatic Mdm2 following administration of phenobarbital and pregnenolone 16 Alpha -carbonitrile.‏
670 ‎‡a Author's The discovery of BMS-457, a potent and selective CCR1 antagonist.‏
670 ‎‡a Author's Transcriptional profiling of liver and effect of glucocorticoids in a rat adjuvant-induced arthritis model.‏
670 ‎‡a Author's Urine acidification has no effect on peroxisome proliferator-activated receptor‏
670 ‎‡a Author's Urine acidification has no effect on peroxisome proliferator-activated receptor (PPAR) signaling or epidermal growth factor (EGF) expression in rat urinary bladder urothelium‏
909 ‎‡a (scopus) 36771089400‏ ‎‡9 1‏
909 ‎‡a (scopus) 57196647475‏ ‎‡9 1‏
909 ‎‡a (scopus) 36771089900‏ ‎‡9 1‏
909 ‎‡a (orcid) 0000000255940791‏ ‎‡9 1‏
919 ‎‡a retrospectiveanalysisoftoxicogenomicsinthesafetyassessmentofdrugcandidates‏ ‎‡A A retrospective analysis of toxicogenomics in the safety assessment of drug candidates.‏ ‎‡9 1‏
919 ‎‡a currentthemesinmicroarrayexperimentaldesignandanalysis‏ ‎‡A Current themes in microarray experimental design and analysis‏ ‎‡9 1‏
919 ‎‡a discoveryofasmallmoleculeantagonistoftheparathyroidhormonereceptorbyusingannterminalparathyroidhormonepeptideprobe‏ ‎‡A Discovery of a small molecule antagonist of the parathyroid hormone receptor by using an N-terminal parathyroid hormone peptide probe‏ ‎‡9 1‏
919 ‎‡a discoveryoftheccr1antagonistbms817399forthetreatmentofrheumatoidarthritis‏ ‎‡A Discovery of the CCR1 antagonist, BMS-817399, for the treatment of rheumatoid arthritis‏ ‎‡9 1‏
919 ‎‡a drugsafetyisabarriertothediscoveryanddevelopmentofnewandrogenreceptorantagonists‏ ‎‡A Drug safety is a barrier to the discovery and development of new androgen receptor antagonists.‏ ‎‡9 1‏
919 ‎‡a identificationofbicyclichexafluoroisopropylalcoholsulfonamidesasretinoicacidreceptorrelatedorphanreceptorgammarorγrorcinverseagonistsemployingstructurebaseddrugdesigntoimprovepregnane10receptorpxrselectivity‏ ‎‡A 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 ‎‡9 1‏
919 ‎‡a identificationofsequencedeterminantsthatdirectdifferentintracellularfoldingpathwaysforaquaporin1andaquaporin4‏ ‎‡A Identification of sequence determinants that direct different intracellular folding pathways for aquaporin-1 and aquaporin-4.‏ ‎‡9 1‏
919 ‎‡a interlaboratoryevaluationofgenomicsignaturesforpredictingcarcinogenicityintherat‏ ‎‡A Interlaboratory evaluation of genomic signatures for predicting carcinogenicity in the rat.‏ ‎‡9 1‏
919 ‎‡a p53independentinductionofrathepaticmdm2followingadministrationofphenobarbitalandpregnenolone16 Alpha carbonitrile‏ ‎‡A p53-independent induction of rat hepatic Mdm2 following administration of phenobarbital and pregnenolone 16 Alpha -carbonitrile.‏ ‎‡9 1‏
919 ‎‡a discoveryofbms457apotentandselectiveccr1antagonist‏ ‎‡A The discovery of BMS-457, a potent and selective CCR1 antagonist.‏ ‎‡9 1‏
919 ‎‡a transcriptionalprofilingofliverandeffectofglucocorticoidsinaratadjuvantinducedarthritismodel‏ ‎‡A Transcriptional profiling of liver and effect of glucocorticoids in a rat adjuvant-induced arthritis model.‏ ‎‡9 1‏
919 ‎‡a urineacidificationhasnoeffectonperoxisomeproliferatoractivatedreceptor‏ ‎‡A Urine acidification has no effect on peroxisome proliferator-activated receptor‏ ‎‡9 1‏
919 ‎‡a urineacidificationhasnoeffectonperoxisomeproliferatoractivatedreceptorpparsignalingorepidermalgrowthfactoregfexpressioninraturinarybladderurothelium‏ ‎‡A Urine acidification has no effect on peroxisome proliferator-activated receptor (PPAR) signaling or epidermal growth factor (EGF) expression in rat urinary bladder urothelium‏ ‎‡9 1‏
919 ‎‡a identificationofbicyclichexafluoroisopropylalcoholsulfonamidesasretinoicacidreceptorrelatedorphanreceptorgamma‏ ‎‡A Identification of bicyclic hexafluoroisopropyl alcohol sulfonamides as retinoic acid receptor-related orphan receptor gamma‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏