-
1
-
-
35148901576
-
An investigation of potential genetic determinants of propofol requirements and recovery from anaesthesia
-
Iohom, G., Ni Chonghaile, M., O'Brien, J. K., Cunningham, A. J., Fitzgerald, D. F. and Shields, D. C.: An investigation of potential genetic determinants of propofol requirements and recovery from anaesthesia. Eur. J. Anaesthesiol., 24: 912-929 (2007).
-
(2007)
Eur. J. Anaesthesiol.
, vol.24
, pp. 912-929
-
-
Iohom, G.1
Ni Chonghaile, M.2
O'Brien, J.K.3
Cunningham, A.J.4
Fitzgerald, D.F.5
Shields, D.C.6
-
2
-
-
0031955972
-
The influence of method of administration and covariates on the pharmacokinetics of propofol in adult volunteers
-
Schnider, T. W., Minto, C. F., Gambus, P. L., Andresen, C., Goodale, D. B., Shafer, S. L. and Youngs, E. J.: The influence of method of administration and covariates on the pharmacokinetics of propofol in adult volunteers. Anesthesiology, 88: 1170-1182 (1998).
-
(1998)
Anesthesiology
, vol.88
, pp. 1170-1182
-
-
Schnider, T.W.1
Minto, C.F.2
Gambus, P.L.3
Andresen, C.4
Goodale, D.B.5
Shafer, S.L.6
Youngs, E.J.7
-
3
-
-
84860268964
-
Influence of sex on propofol metabolism, a pilot study: Implications for propofol anesthesia
-
Loryan, I., Lindqvist, M., Johansson, I., Hiratsuka, M., van der Heiden, I., van Schaik, R. H., Jakobsson, J. and Ingelman-Sundberg, M.: Influence of sex on propofol metabolism, a pilot study: implications for propofol anesthesia. Eur. J. Clin. Pharmacol., 68: 397-406 (2012).
-
(2012)
Eur. J. Clin. Pharmacol.
, vol.68
, pp. 397-406
-
-
Loryan, I.1
Lindqvist, M.2
Johansson, I.3
Hiratsuka, M.4
Van Der Heiden, I.5
Van Schaik, R.H.6
Jakobsson, J.7
Ingelman-Sundberg, M.8
-
4
-
-
4143072423
-
Identification of common polymorphisms in the promoter of the UGT1A9 gene: Evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver
-
Girard, H., Court, M. H., Bernard, O., Fortier, L. C., Villeneuve, L., Hao, Q., Greenblatt, D. J., von Moltke, L. L., Perussed, L., et al.: Identification of common polymorphisms in the promoter of the UGT1A9 gene: evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver. Pharmacogenetics, 14: 501-515 (2004).
-
(2004)
Pharmacogenetics
, vol.14
, pp. 501-515
-
-
Girard, H.1
Court, M.H.2
Bernard, O.3
Fortier, L.C.4
Villeneuve, L.5
Hao, Q.6
Greenblatt, D.J.7
Von Moltke, L.L.8
Perussed, L.9
-
5
-
-
0035165506
-
Cytochrome P-450 2B6 is responsible for interindividual variability of propofol hydroxylation by human liver microsomes
-
Court, M. H., Duan, S. X., Hesse, L. M., Venkatakrishnan, K. and Greenblatt, D. J.: Cytochrome P-450 2B6 is responsible for interindividual variability of propofol hydroxylation by human liver microsomes. Anesthesiology, 94: 110-119 (2001).
-
(2001)
Anesthesiology
, vol.94
, pp. 110-119
-
-
Court, M.H.1
Duan, S.X.2
Hesse, L.M.3
Venkatakrishnan, K.4
Greenblatt, D.J.5
-
6
-
-
34548105118
-
Polymorphic CYP2B6: Molecular mechanisms and emerging clinical significance
-
Zanger, U. M., Klein, K., Saussele, T., Blievernicht, J., Hofmann, M. H. and Schwab, M.: Polymorphic CYP2B6: molecular mechanisms and emerging clinical significance. Pharmacogenomics, 8: 743-759 (2007).
-
(2007)
Pharmacogenomics
, vol.8
, pp. 743-759
-
-
Zanger, U.M.1
Klein, K.2
Saussele, T.3
Blievernicht, J.4
Hofmann, M.H.5
Schwab, M.6
-
7
-
-
84876078320
-
Pharmacogenetics of cytochrome P450 2B6 (CYP2B6): Advances on polymorphisms, mechanisms, and clinical relevance
-
Zanger, U. M. and Klein, K.: Pharmacogenetics of cytochrome P450 2B6 (CYP2B6): advances on polymorphisms, mechanisms, and clinical relevance. Front. Genet., 4: 24 (2013).
-
(2013)
Front. Genet.
, vol.4
, pp. 24
-
-
Zanger, U.M.1
Klein, K.2
-
8
-
-
80055078449
-
Individual differences in pharmacokinetics and pharmacodynamics of anesthetic agent propofol with regard to CYP2B6 and UGT1A9 genotype and patient age
-
Kansaku, F., Kumai, T., Sasaki, K., Yokozuka, M., Shimizu, M., Tateda, T., Murayama, N., Kobayashi, S. and Yamazaki, H.: Individual differences in pharmacokinetics and pharmacodynamics of anesthetic agent propofol with regard to CYP2B6 and UGT1A9 genotype and patient age. Drug Metab. Pharmacokinet., 26: 532-537 (2011).
-
(2011)
Drug Metab. Pharmacokinet.
, vol.26
, pp. 532-537
-
-
Kansaku, F.1
Kumai, T.2
Sasaki, K.3
Yokozuka, M.4
Shimizu, M.5
Tateda, T.6
Murayama, N.7
Kobayashi, S.8
Yamazaki, H.9
-
9
-
-
84880312309
-
Sex difference in formation of propofol metabolites: A replication study
-
Choong, E., Loryan, I., Lindqvist, M., Nordling, A., El Bouazzaoui, S., van Schaik, R. H., Johansson, I., Jakobsson, J. and Ingelman-Sundberg, M.: Sex difference in formation of propofol metabolites: A replication study. Basic Clin. Pharmacol. Toxicol., 113: 126-131 (2013).
-
(2013)
Basic Clin. Pharmacol. Toxicol.
, vol.113
, pp. 126-131
-
-
Choong, E.1
Loryan, I.2
Lindqvist, M.3
Nordling, A.4
El Bouazzaoui, S.5
Van Schaik, R.H.6
Johansson, I.7
Jakobsson, J.8
Ingelman-Sundberg, M.9
-
10
-
-
0034948077
-
Extensive genetic polymorphism in the human CYP2B6 gene with impact on expression and function in human liver
-
Lang, T., Klein, K., Fischer, J., Nüssler, A. K., Neuhaus, P., Hofmann, U., Eichelbaum, M., Schwab, M. and Zanger, U. M.: Extensive genetic polymorphism in the human CYP2B6 gene with impact on expression and function in human liver. Pharmacogenetics, 11: 399-415 (2001).
-
(2001)
Pharmacogenetics
, vol.11
, pp. 399-415
-
-
Lang, T.1
Klein, K.2
Fischer, J.3
Nüssler, A.K.4
Neuhaus, P.5
Hofmann, U.6
Eichelbaum, M.7
Schwab, M.8
Zanger, U.M.9
-
11
-
-
34250764311
-
Impact of CYP2B6 polymorphism on heaptic efavirenz metabolism in vitro
-
Desta, Z., Saussele, T., Ward, B., Blievernicht, J., Li, L., Klein, K., Flockhart, D. A. and Zanger, U. M.: Impact of CYP2B6 polymorphism on heaptic efavirenz metabolism in vitro. Pharmacogenomics, 8: 547-558 (2007).
-
(2007)
Pharmacogenomics
, vol.8
, pp. 547-558
-
-
Desta, Z.1
Saussele, T.2
Ward, B.3
Blievernicht, J.4
Li, L.5
Klein, K.6
Flockhart, D.A.7
Zanger, U.M.8
-
12
-
-
41149132905
-
Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B6*6, is responsible for decreased expression and activity of CYP2B6 in the liver
-
Hofmann, M. H., Blievernicht, J. K., Klein, K., Saussele, T., Schaeffeler, E., Schwab, M. and Zanger, U. M.: Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B6*6, is responsible for decreased expression and activity of CYP2B6 in the liver. J. Pharmacol. Exp. Ther., 325: 284-292 (2008).
-
(2008)
J. Pharmacol. Exp. Ther.
, vol.325
, pp. 284-292
-
-
Hofmann, M.H.1
Blievernicht, J.K.2
Klein, K.3
Saussele, T.4
Schaeffeler, E.5
Schwab, M.6
Zanger, U.M.7
-
13
-
-
0036257688
-
Propofol metabolites in man following propofol induction and maintenance
-
Favetta, P., Degoute, C.-S., Perdrix, J.-P., Dufresne, C., Boulieu, R. and Guitton, J.: Propofol metabolites in man following propofol induction and maintenance. Br. J. Anaesth., 88: 653-658 (2002).
-
(2002)
Br. J. Anaesth.
, vol.88
, pp. 653-658
-
-
Favetta, P.1
Degoute, C.-S.2
Perdrix, J.-P.3
Dufresne, C.4
Boulieu, R.5
Guitton, J.6
-
14
-
-
33745242349
-
The novel UGT1A9 intronic I399 polymorphism appears as a predictor of 7-ethyl-10-hydroxycamptothecin glucuronidation levels in the liver
-
Girard, H., Villeneuve, L., Court, M. H., Fortier, L.-C., Caron, P., Hao, Q., von Moltke, L. L., Greenblatt, D. J. and Guillemette, C.: The novel UGT1A9 intronic I399 polymorphism appears as a predictor of 7-ethyl-10- hydroxycamptothecin glucuronidation levels in the liver. Drug Metab. Dispos., 34: 1220-1228 (2006).
-
(2006)
Drug Metab. Dispos.
, vol.34
, pp. 1220-1228
-
-
Girard, H.1
Villeneuve, L.2
Court, M.H.3
Fortier, L.-C.4
Caron, P.5
Hao, Q.6
Von Moltke, L.L.7
Greenblatt, D.J.8
Guillemette, C.9
-
15
-
-
47649127415
-
Effect of D256N and Y483D on propofol glucuronidation by human uridine 5′-diphosphate glucuronosyltransferase (UGT1A9)
-
Takahashi, H., Maruo, Y., Mori, A., Iwai, M., Sato, H. and Takeuchi, Y.: Effect of D256N and Y483D on propofol glucuronidation by human uridine 5′-diphosphate glucuronosyltransferase (UGT1A9). Basic Clin. Pharmacol. Toxicol., 103: 131-136 (2008).
-
(2008)
Basic Clin. Pharmacol. Toxicol.
, vol.103
, pp. 131-136
-
-
Takahashi, H.1
Maruo, Y.2
Mori, A.3
Iwai, M.4
Sato, H.5
Takeuchi, Y.6
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