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Browsing "Pharmacology" by Author Sallustio, B.

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PreviewIssue DateTitleAuthor(s)
2004A new simple diagnostic assay for the identification of the major CYP2D6 genotypes by DNA sequencing analysisJames, H.; Coller, J.; Gillis, D.; Bahnisch, J.; Sallustio, B.; Somogyi, A.
1999Assessment of interlaboratory performance in the provision of perhexiline therapeutic drug monitoring services in Australia.Sallustio, B.; Morris, R.
2006Bioactivation of carboxylic acid compounds by UDP-glucuronosyltransferases to DNA-damaging intermediates: Role of glycoxidation and oxidative stress in genotoxicitySallustio, B.; DeGraaf, Y.; Weekley, J.; Burcham, P.
1995Biosynthesis, characterisation and direct high-performance liquid chromatographic analysis of gemfibrozil 1-O-β-acylglucuronideSallustio, B.; Fairchild, B.
2007Carboxylic acid drug-induced DNA nicking in HEK293 cells expressing human UDP-glucuronosyltransferases: Role of acyl glucuronide metabolites and glycation pathwaysSouthwood, H.; DeGraaf, Y.; MacKenzie, P.; Miners, J.; Burcham, P.; Sallustio, B.
2004Clinical inhibition of CYP2D6-catalysed metabolism by the antianginal agent perhexilineDavies, B.; Coller, J.; James, H.; Gillis, D.; Somogyi, A.; Horowitz, J.; Morris, R.; Sallustio, B.
2011Comparison of blood sirolimus, tacrolimus and everolimus concentrations measured by LC-MS/MS, HPLC-UV and immunoassay methodsSallustio, B.; Noll, B.; Morris, R.
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.
2007CYP2B6 CYP2D6 and CYP3A4 catalyze the primary oxidative metabolism of perhexiline enantiomers by human liver microsomesDavies, B.; Coller, J.; Somogyi, A.; Milne, R.; Sallustio, B.
2018CYP3A5*3 and ABCB1 61A>G significantly influence dose-adjusted trough blood tacrolimus concentrations in the first three months post-kidney transplantationHu, R.; Barratt, D.; Coller, J.; Sallustio, B.; Somogyi, A.
2004Determination of perhexiline and hydroxyperhexiline in plasma by liquid chromatography-mass spectrometryBeck, O.; Stephanson, N.; Morris, R.; Sallustio, B.; Hjemdahl, P.
2006Determination of the 4-monohydroxy metabolites of perhexiline in human plasma, urine and liver microsomes by liquid chromatographyDavies, B.; Herbert, M.; Coller, J.; Somogyi, A.; Milne, R.; Sallustio, B.
1996Disposition of gemfibrozil and gemfibrozil acyl glucuronide in the rat isolated perfused liverSallustio, B.; Fairchild, B.; Shanahan, K.; Evans, A.; Nation, R.
2007Effect of CYP2D6 metabolizer status on the disposition of the (+) and (-) enantiomers of perhexiline in patients with myocardial ischaemiaInglis, S.; Herbert, M.; Davies, B.; Coller, J.; James, H.; Horowitz, J.; Morris, R.; Milne, R.; Somogyi, A.; Sallustio, B.
1997Effects of gemfribozil and clofibric acid on the uptake of taurocholate by isolated rat hepatocytesSabordo, L.; Sallustio, B.
2006Enantioselective assay for the determination of perhexiline enantiomers in human plasma by liquid chromatographyDavies, B.; Herbert, M.; Culbert, J.; Pyke, S.; Coller, J.; Somogyi, A.; Milne, R.; Sallustio, B.
2005Evaluation of the immunotech cyclosporine direct radioimmunoassay for the determination of whole-blood cyclosporine in renal transplant patientsWesley, I.; Sallustio, B.; Morris, R.
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.
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.
2008Glucuronidation of mycophenolic acid by Wistar and Mrp2-deficient TR- rat liver microsomesWestley, I.; Morris, R.; Evans, A.; Sallustio, B.
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