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Michael H Court
Michael H Court
William R. Jones Professor of Pharmacogenomics
Dirección de correo verificada de wsu.edu - Página principal
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CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants
LM Hesse, K Venkatakrishnan, C MH, von Moltke LL, D SX, S RI, ...
Drug Metab Dispos 28 (10), 1176-1183, 2000
463*2000
Nonsteroidal anti-inflammatory drugs in cats: a review
BDX Lascelles, MH Court, EM Hardie, SA Robertson
Veterinary anaesthesia and analgesia 34 (4), 228-250, 2007
2592007
Pharmacogenetic determinants of interindividual variability in bupropion hydroxylation by cytochrome P450 2B6 in human liver microsomes
MH Hesse, L. M., He, P., Krishnaswamy, S., Hao, Q., Hogan, K., von Moltke, L ...
Pharmacogenetics and genomics 14 (4), 225-238, 2004
2332004
Curcuminoids inhibit multiple human cytochromes P450, UDP-glucuronosyltransferase, and sulfotransferase enzymes, whereas piperine is a relatively selective CYP3A4 inhibitor
LP Volak, S Ghirmai, JR Cashman
Drug metabolism and disposition 36 (8), 1594-1605, 2008
2272008
Evaluation of 3′-azido-3′-deoxythymidine, morphine, and codeine as probe substrates for UDP-glucuronosyltransferase 2B7 (UGT2B7) in human liver microsomes: specificity and …
S Krishnaswamy, Q Hao, SX Duan, CJ Patten, LL Von Moltke, ...
Drug Metabolism and Disposition 31 (9), 1125-1133, 2003
1862003
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for UGT1A1 and Atazanavir Prescribing
RS Gammal, MH Court, CE Haidar, OF Iwuchukwu, AH Gaur, M Alvarellos, ...
Clinical Pharmacology & Therapeutics 99 (4), 363-369, 2016
1802016
Court, MH, & Dixon, R.(1987). Investigation into the use of narcotic antagonists in the treatment of a stereotypic behavior pattern (crib-biting) in the horse
NH Dodman, L Shuster
American Journal of Veterinary Research 48 (2), 311-318, 1987
180*1987
Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as …
K Venkatakrishnan, LL von Moltke, JS Harmatz, CL Crespi, DJ Greenblatt
Drug metabolism and disposition 28 (12), 1493-1504, 2000
1702000
CYP2B6, CYP2A6 and UGT2B7 genetic polymorphisms are predictors of efavirenz mid-dose concentration in HIV-infected patients
A Kwara, M Lartey, KWC Sagoe, E Kenu
Aids 23 (16), 2101-2106, 2009
1672009
Genotype‐phenotype associations of cytochrome P450 3A4 and 3A5 polymorphism with midazolam clearance in vivo
P He, MH Court, DJ Greenblatt, LL Von Moltke
Clinical Pharmacology & Therapeutics 77 (5), 373-387, 2005
1632005
Quantitative distribution of mRNAs encoding the 19 human UDP-glucuronosyltransferase enzymes in 26 adult and 3 fetal tissues
MH Court, X Zhang, X Ding, KK Yee, LM Hesse, M Finel
Xenobiotica 42 (3), 266-277, 2012
1622012
CYP2B6 (c.516G→T) and CYP2A6 (*9B and/or *17) polymorphisms are independent predictors of efavirenz plasma concentrations in HIV‐infected patients
A Kwara, M Lartey, KW Sagoe, NL Rzek, MH Court
British journal of clinical pharmacology 67 (4), 427-436, 2009
1522009
Validation of serotonin (5-hydroxtryptamine) as an in vitro substrate probe for human UDP-glucuronosyltransferase (UGT) 1A6
S Krishnaswamy, SX Duan, LL Von Moltke, DJ Greenblatt
Drug Metabolism and Disposition 31 (1), 133-139, 2003
1522003
Court, MH, Yan, B., & Akhlaghi, F.(2011). Significantly reduced cytochrome P450 3A4 expression and activity in liver from humans with diabetes mellitus
M Dostalek
British Journal of Pharmacology 163 (5), 937-947, 2011
148*2011
Cytochrome P-450 2B6 is responsible for interindividual variability of propofol hydroxylation by human liver microsomes
MH Court, SX Duan, LM Hesse, K Venkatakrishnan, DJ Greenblatt
The Journal of the American Society of Anesthesiologists 94 (1), 110-119, 2001
1452001
Significantly reduced cytochrome P450 3A4 expression and activity in liver from humans with diabetes mellitus
M Dostalek, MH Court, B Yan, F Akhlaghi
British journal of pharmacology 163 (5), 937-947, 2011
1432011
UDP glucuronosyltransferase (UGT) 1A6 pharmacogenetics: II. Functional impact of the three most common nonsynonymous UGT1A6 polymorphisms (S7A, T181A, and R184S)
S Krishnaswamy, Q Hao, A Al-Rohaimi, LM Hesse, LL von Moltke, ...
Journal of Pharmacology and Experimental Therapeutics 313 (3), 1340-1346, 2005
1432005
COURT MH, DIAAN SX, HARMATZ JS, SHADER RI (1995) Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective …
V MOLTKE, DJ Greenblatt
J Clin Psychopharmacol 15, 125-131, 1995
143*1995
Midazolam and triazolam biotransformation in mouse and human liver microsomes: relative contribution of CYP3A and CYP2C isoforms
MD Perloff, LL von Moltke, T Kotegawa, RI Shader, DJ Greenblatt
Journal of Pharmacology and Experimental Therapeutics 292 (2), 618-628, 2000
1402000
Court MH, Duan SX, Harmatz JS, Shader RI. Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective …
LL Von Moltke, DJ Greenblatt
J Clin Psychopharmacol 15 (2), 125-131, 1995
1401995
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