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PreviewIssue DateTitleAuthor(s)
2004Evidence that unsaturated fatty acids are potent inhibitors of renal UDP-glucuronosyltransferases (UGT): kinetic studies using human kidney cortical microsomes and recombinant UGT1A9 and UGT2B7Toutsikos, P.; Miners, J.; Stapleton, A.; Thomas, A.; Sallustio, B.; Knights, K.
2003UDP-glucuronosyltransferase-dependent bioactivation of clofibric acid to a DNA-damaging intermediate in mouse hepatocytesGhaoui, R.; Sallustio, B.; Burcham, P.; Fontaine, F.
2000In vitro covalent binding of Nafenopin-CoA to human liver proteinsSallustio, B.; Nunthasomboon, S.; Drogemuller, C.; Knights, K.
2005Evaluation of the immunotech cyclosporine direct radioimmunoassay for the determination of whole-blood cyclosporine in renal transplant patientsWesley, I.; Sallustio, B.; Morris, R.
2005Validation of a high-performance liquid chromatography method for the measurement of mycophenolic acid and its glucuronide metabolites in plasmaWestley, I.; Sallustio, B.; Morris, R.
2000Hepatic disposition of electrophilic acyl glucuronide conjugatesSallustio, B.; Sabordo, L.; Evans, A.; Nation, R.
1997Genotoxicity of acyl glucurodine metabolites formed from clofibric acid and gemfibrozil: a novel role for phase II-mediated bioactivation in the hepatocarcinogenicity of the parent aglycones?Sallustio, B.; Harkin, L.; Mann, M.; Krivickas, S.; Burcham, P.
1996Disposition of gemfibrozil and gemfibrozil acyl glucuronide in the rat isolated perfused liverSallustio, B.; Fairchild, B.; Shanahan, K.; Evans, A.; Nation, R.
1995Biosynthesis, characterisation and direct high-performance liquid chromatographic analysis of gemfibrozil 1-O-β-acylglucuronideSallustio, B.; Fairchild, B.
2015Comparison of CYP2D metabolism and hepatotoxicity of the myocardial metabolic agent perhexiline in Sprague-Dawley and Dark Agouti ratsLicari, G.; Somogyi, A.; Milne, R.; Sallustio, B.