-
1
-
-
19444376971
-
Drug metabolism and variability among patients in drug response
-
Wilkinson GR. Drug metabolism and variability among patients in drug response. N Engl J Med 2005; 352: 2211-21.
-
(2005)
N Engl J Med
, vol.352
, pp. 2211-2221
-
-
Wilkinson, G.R.1
-
2
-
-
9044254525
-
P450 superfamily: Update on new sequences, gene mapping, accession numbers and nomenclature
-
Nelson DR, Koymans L, Kamataki T, Stegeman JJ, Feyereisen R, Waxman DJ, Waterman MR, Gotoh O, Coon MJ, Estabrook RW, Gunsalus IC, Nebert DW. P450 superfamily: update on new sequences, gene mapping, accession numbers and nomenclature. Pharmacogenetics 1996; 6: 1-42.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 1-42
-
-
Nelson, D.R.1
Koymans, L.2
Kamataki, T.3
Stegeman, J.J.4
Feyereisen, R.5
Waxman, D.J.6
Waterman, M.R.7
Gotoh, O.8
Coon, M.J.9
Estabrook, R.W.10
Gunsalus, I.C.11
Nebert, D.W.12
-
3
-
-
0026459382
-
Speculations on the substrate structure-activity relationship (SSAR) of cytochrome P450 enzymes
-
Smith DA, Jones BC. Speculations on the substrate structure-activity relationship (SSAR) of cytochrome P450 enzymes. Biochem Pharmacol 1992; 44: 2089-98.
-
(1992)
Biochem Pharmacol
, vol.44
, pp. 2089-2098
-
-
Smith, D.A.1
Jones, B.C.2
-
4
-
-
3242733232
-
Probing the world of cytochrome p450 enzymes
-
Frye RF. Probing the world of cytochrome p450 enzymes. Mol Interv 2004; 4: 157-62.
-
(2004)
Mol Interv
, vol.4
, pp. 157-162
-
-
Frye, R.F.1
-
5
-
-
0031841377
-
Cytochrome P4502C9: An enzyme of major importance in human drug metabolism
-
Miners JO, Birkett DJ. Cytochrome P4502C9: an enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 1998; 45: 525-38.
-
(1998)
Br J Clin Pharmacol
, vol.45
, pp. 525-538
-
-
Miners, J.O.1
Birkett, D.J.2
-
6
-
-
27744485315
-
A prospective, randomized pilot trial of model-based warfarin dose initiation using CYP2C9 genotype and clinical data
-
Hillman MA, Wilke RA, Yale SH, Vidaillet HJ, Caldwell MD, Glurich I, Berg RL, Schmelzer J, Burmester JK. A prospective, randomized pilot trial of model-based warfarin dose initiation using CYP2C9 genotype and clinical data. Clin Med 2005; 3: 137-45.
-
(2005)
Clin Med
, vol.3
, pp. 137-145
-
-
Hillman, M.A.1
Wilke, R.A.2
Yale, S.H.3
Vidaillet, H.J.4
Caldwell, M.D.5
Glurich, I.6
Berg, R.L.7
Schmelzer, J.8
Burmester, J.K.9
-
7
-
-
21444446714
-
Evaluation of phenytoin dosage regimens based on genotyping of CYP2C subfamily in routinely treated Japanese patients
-
Taguchi M, Hongou K, Yagi S, Miyawaki T, Takizawa M, Aiba T, Hashimoto Y. Evaluation of phenytoin dosage regimens based on genotyping of CYP2C subfamily in routinely treated Japanese patients. Drug Metab Pharmacokinet 2005; 20: 107-12.
-
(2005)
Drug Metab Pharmacokinet
, vol.20
, pp. 107-112
-
-
Taguchi, M.1
Hongou, K.2
Yagi, S.3
Miyawaki, T.4
Takizawa, M.5
Aiba, T.6
Hashimoto, Y.7
-
8
-
-
18844399403
-
Detection of a novel reactive metabolite of diclofenac: Evidence for CYP2C9-mediated bioactivation via arene oxides
-
Yan Z, Li J, Huebert N, Caldwell GW, Du Y, Zhong H. Detection of a novel reactive metabolite of diclofenac: evidence for CYP2C9-mediated bioactivation via arene oxides. Drug Metab Dispos 2005; 33: 706-13.
-
(2005)
Drug Metab Dispos
, vol.33
, pp. 706-713
-
-
Yan, Z.1
Li, J.2
Huebert, N.3
Caldwell, G.W.4
Du, Y.5
Zhong, H.6
-
9
-
-
0036736497
-
Glyburide and glimepiride pharmacokinetics in subjects with different CYP2C9 genotypes
-
Niemi M, Cascorbi I, Timm R, Kroemer HK, Neuvonen PJ, Kivisto KT. Glyburide and glimepiride pharmacokinetics in subjects with different CYP2C9 genotypes. Clin Pharmacol Ther 2002; 72: 326-32.
-
(2002)
Clin Pharmacol Ther
, vol.72
, pp. 326-332
-
-
Niemi, M.1
Cascorbi, I.2
Timm, R.3
Kroemer, H.K.4
Neuvonen, P.J.5
Kivisto, K.T.6
-
10
-
-
11844304376
-
Clinical consequences of cytochrome P450 2C9 polymorphisms
-
Kirchheiner J, Brockmoller J. Clinical consequences of cytochrome P450 2C9 polymorphisms. Clin Pharmacol Ther 2005; 77: 1-16.
-
(2005)
Clin Pharmacol Ther
, vol.77
, pp. 1-16
-
-
Kirchheiner, J.1
Brockmoller, J.2
-
11
-
-
0038293267
-
Differences in flurbiprofen pharmacokinetics between CYP2C9*1/*1, *1/*2, and *1/*3 genotypes
-
Lee CR, Pieper JA, Frye RF, Hinderliter AL, Blaisdell JA, Goldstein JA. Differences in flurbiprofen pharmacokinetics between CYP2C9*1/*1, *1/*2, and *1/*3 genotypes. Eur J Clin Pharmacol 2003; 58: 791-4.
-
(2003)
Eur J Clin Pharmacol
, vol.58
, pp. 791-794
-
-
Lee, C.R.1
Pieper, J.A.2
Frye, R.F.3
Hinderliter, A.L.4
Blaisdell, J.A.5
Goldstein, J.A.6
-
12
-
-
0034007388
-
Phenotyping of drug-metabolizing enzymes in adults: A review of in-vivo cytochrome P450 phenotyping probes
-
Streetman DS, Bertino JS Jr, Nafziger AN. Phenotyping of drug-metabolizing enzymes in adults: a review of in-vivo cytochrome P450 phenotyping probes. Pharmacogenetics 2000; 10: 187-216.
-
(2000)
Pharmacogenetics
, vol.10
, pp. 187-216
-
-
Streetman, D.S.1
Bertino Jr, J.S.2
Nafziger, A.N.3
-
13
-
-
0031909513
-
Use of chlorzoxazone as an in vivo probe of cytochrome P450 2E1: Choice of dose and phenotypic trait measure
-
Frye RF, Adedoyin A, Mauro K, Matzke GR, Branch RA. Use of chlorzoxazone as an in vivo probe of cytochrome P450 2E1: choice of dose and phenotypic trait measure. J Clin Pharmacol 1998; 38: 82-9.
-
(1998)
J Clin Pharmacol
, vol.38
, pp. 82-89
-
-
Frye, R.F.1
Adedoyin, A.2
Mauro, K.3
Matzke, G.R.4
Branch, R.A.5
-
14
-
-
2942620708
-
Cytochrome P450 2C9 phenotyping using low-dose tolbutamide
-
Jetter A, Kinzig-Schippers M, Skott A, Lazar A, Tomalik-Scharte D, Kirchheiner J, Walchner-Bonjean M, Hering U, Jakob V, Rodamer M, Jabrane W, Kasel D, Brockmoller J, Fuhr U, Sorgel F. Cytochrome P450 2C9 phenotyping using low-dose tolbutamide. Eur J Clin Pharmacol 2004; 60: 165-71.
-
(2004)
Eur J Clin Pharmacol
, vol.60
, pp. 165-171
-
-
Jetter, A.1
Kinzig-Schippers, M.2
Skott, A.3
Lazar, A.4
Tomalik-Scharte, D.5
Kirchheiner, J.6
Walchner-Bonjean, M.7
Hering, U.8
Jakob, V.9
Rodamer, M.10
Jabrane, W.11
Kasel, D.12
Brockmoller, J.13
Fuhr, U.14
Sorgel, F.15
-
15
-
-
0029951216
-
Limited value of the urinary phenytoin metabolic ratio for the assessment of cytochrome P4502C9 activity in vivo
-
Tassaneeyakul W, Birkett DJ, Pass MC, Miners JO. Limited value of the urinary phenytoin metabolic ratio for the assessment of cytochrome P4502C9 activity in vivo. Br J Clin Pharmacol 1996; 42: 774-8.
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 774-778
-
-
Tassaneeyakul, W.1
Birkett, D.J.2
Pass, M.C.3
Miners, J.O.4
-
16
-
-
0031807762
-
Metabolism of warfarin enantiomers in Japanese patients with heart disease having different CYP2C9 and CYP2C19 genotypes
-
Takahashi H, Kashima T, Nomizo Y, Muramoto N, Shimizu T, Nasu K, Kubota T, Kimura S, Echizen H. Metabolism of warfarin enantiomers in Japanese patients with heart disease having different CYP2C9 and CYP2C19 genotypes. Clin Pharmacol Ther 1998; 63: 519-28.
-
(1998)
Clin Pharmacol Ther
, vol.63
, pp. 519-528
-
-
Takahashi, H.1
Kashima, T.2
Nomizo, Y.3
Muramoto, N.4
Shimizu, T.5
Nasu, K.6
Kubota, T.7
Kimura, S.8
Echizen, H.9
-
17
-
-
0028242015
-
Stereoselective disposition of flurbiprofen in healthy subjects following administration of the single enantiomers
-
Geisslinger G, Lotsch J, Menzel S, Kobal G, Brune K. Stereoselective disposition of flurbiprofen in healthy subjects following administration of the single enantiomers. Br J Clin Pharmacol 1994; 37: 392-4.
-
(1994)
Br J Clin Pharmacol
, vol.37
, pp. 392-394
-
-
Geisslinger, G.1
Lotsch, J.2
Menzel, S.3
Kobal, G.4
Brune, K.5
-
18
-
-
0026539055
-
Stereoselective disposition of flurbiprofen in normal volunteers
-
Knadler MP, Brater DC, Hall SD. Stereoselective disposition of flurbiprofen in normal volunteers. Br J Clin Pharmacol 1992; 33: 369-75.
-
(1992)
Br J Clin Pharmacol
, vol.33
, pp. 369-375
-
-
Knadler, M.P.1
Brater, D.C.2
Hall, S.D.3
-
19
-
-
0028984776
-
Clinical pharmacokinetics of flurbiprofen and its enantiomers
-
Davies NM. Clinical pharmacokinetics of flurbiprofen and its enantiomers. Clin Pharmacokinet 1995; 28: 100-14.
-
(1995)
Clin Pharmacokinet
, vol.28
, pp. 100-114
-
-
Davies, N.M.1
-
20
-
-
4143143372
-
The structure of human cytochrome P450 2C9 complexed with flurbiprofen at 2.0-A resolution
-
Wester MR, Yano JK, Schoch GA, Yang C, Griffin KJ, Stout CD, Johnson EF. The structure of human cytochrome P450 2C9 complexed with flurbiprofen at 2.0-A resolution. J Biol Chem 2004; 279: 35630-7.
-
(2004)
J Biol Chem
, vol.279
, pp. 35630-35637
-
-
Wester, M.R.1
Yano, J.K.2
Schoch, G.A.3
Yang, C.4
Griffin, K.J.5
Stout, C.D.6
Johnson, E.F.7
-
21
-
-
0029010518
-
Role of cytochrome P450 2C9 and an allelic variant in the 4?-hydroxylation of (R)- and (S)-flurbiprofen
-
Tracy TS, Rosenbluth BW, Wrighton SA, Gonzalez FJ, Korzekwa KR. Role of cytochrome P450 2C9 and an allelic variant in the 4?-hydroxylation of (R)- and (S)-flurbiprofen. Biochem Pharmacol 1995; 49: 1269-75.
-
(1995)
Biochem Pharmacol
, vol.49
, pp. 1269-1275
-
-
Tracy, T.S.1
Rosenbluth, B.W.2
Wrighton, S.A.3
Gonzalez, F.J.4
Korzekwa, K.R.5
-
22
-
-
0030601837
-
Studies of flurbiprofen 4′-hydroxylation. Additional evidence suggesting the sole involvement of cytochrome P450 2C9
-
Tracy TS, Marra C, Wrighton SA, Gonzalez FJ, Korzekwa KR. Studies of flurbiprofen 4′-hydroxylation. Additional evidence suggesting the sole involvement of cytochrome P450 2C9. Biochem Pharmacol 1996; 52: 1305-9.
-
(1996)
Biochem Pharmacol
, vol.52
, pp. 1305-1309
-
-
Tracy, T.S.1
Marra, C.2
Wrighton, S.A.3
Gonzalez, F.J.4
Korzekwa, K.R.5
-
23
-
-
0025195884
-
Influence of H2 receptor antagonists on the disposition of flurbiprofen enantiomers
-
Small RE, Cox SR, Adams WJ. Influence of H2 receptor antagonists on the disposition of flurbiprofen enantiomers. J Clin Pharmacol 1990; 30: 660-4.
-
(1990)
J Clin Pharmacol
, vol.30
, pp. 660-664
-
-
Small, R.E.1
Cox, S.R.2
Adams, W.J.3
-
24
-
-
0027159323
-
Single-dose disulfiram inhibition of chlorzoxazone metabolism: A clinical probe for P450 2E1
-
Kharasch ED, Thummel KE, Mhyre J, Lillibridge JH. Single-dose disulfiram inhibition of chlorzoxazone metabolism: a clinical probe for P450 2E1. Clin Pharmacol Ther 1993; 53: 643-50.
-
(1993)
Clin Pharmacol Ther
, vol.53
, pp. 643-650
-
-
Kharasch, E.D.1
Thummel, K.E.2
Mhyre, J.3
Lillibridge, J.H.4
-
25
-
-
0034004083
-
Effects of the antifungal agents on oxidative drug metabolism: Clinical relevance
-
Venkatakrishnan K, Von Moltke LL, Greenblatt DJ. Effects of the antifungal agents on oxidative drug metabolism: clinical relevance. Clin Pharmacokinet 2000; 38: 111-80.
-
(2000)
Clin Pharmacokinet
, vol.38
, pp. 111-180
-
-
Venkatakrishnan, K.1
Von Moltke, L.L.2
Greenblatt, D.J.3
-
26
-
-
0036451138
-
The effect of fluconazole on the pharmacokinetics of rosuvastatin
-
Cooper KJ, Martin PD, Dane AL, Warwick MJ, Schneck DW, Cantarini MV. The effect of fluconazole on the pharmacokinetics of rosuvastatin. Eur J Clin Pharmacol 2002; 58: 527-31.
-
(2002)
Eur J Clin Pharmacol
, vol.58
, pp. 527-531
-
-
Cooper, K.J.1
Martin, P.D.2
Dane, A.L.3
Warwick, M.J.4
Schneck, D.W.5
Cantarini, M.V.6
-
27
-
-
0034014319
-
Major role of human liver microsomal cytochrome P450 2C9 (CYP2C9) in the oxidative metabolism of celecoxib, a novel cyclooxygenase-II inhibitor
-
Tang C, Shou M, Mei Q, Rushmore TH, Rodrigues AD. Major role of human liver microsomal cytochrome P450 2C9 (CYP2C9) in the oxidative metabolism of celecoxib, a novel cyclooxygenase-II inhibitor. J Pharmacol Exp Ther 2000; 293: 453-9.
-
(2000)
J Pharmacol Exp Ther
, vol.293
, pp. 453-459
-
-
Tang, C.1
Shou, M.2
Mei, Q.3
Rushmore, T.H.4
Rodrigues, A.D.5
-
28
-
-
24944576037
-
Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes
-
Niwa T, Shiraga T, Takagi A. Effect of antifungal drugs on cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 activities in human liver microsomes. Biol Pharm Bull 2005; 28: 1805-8.
-
(2005)
Biol Pharm Bull
, vol.28
, pp. 1805-1808
-
-
Niwa, T.1
Shiraga, T.2
Takagi, A.3
-
29
-
-
0025760346
-
Effect of fluconazole on the disposition of phenytoin
-
Blum RA, Wilton JH, Hilligoss DM, Gardner MJ, Henry EB, Harrison NJ, Schentag JJ. Effect of fluconazole on the disposition of phenytoin. Clin Pharmacol Ther 1991; 49: 420-5.
-
(1991)
Clin Pharmacol Ther
, vol.49
, pp. 420-425
-
-
Blum, R.A.1
Wilton, J.H.2
Hilligoss, D.M.3
Gardner, M.J.4
Henry, E.B.5
Harrison, N.J.6
Schentag, J.J.7
-
30
-
-
0029877219
-
Warfarin-fluconazole. I. Inhibition of the human cytochrome P450-dependent metabolism of warfarin by fluconazole: In vitro studies
-
Kunze KL, Wienkers LC, Thummel KE, Trager WF. Warfarin-fluconazole. I. Inhibition of the human cytochrome P450-dependent metabolism of warfarin by fluconazole: in vitro studies. Drug Metab Dispos 1996; 24: 414-21.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 414-421
-
-
Kunze, K.L.1
Wienkers, L.C.2
Thummel, K.E.3
Trager, W.F.4
-
31
-
-
0029996292
-
Warfarin-fluconazole. II. A metabolically based drug interaction: In vivo studies
-
Black DJ, Kunze KL, Wienkers LC, Gidal BE, Seaton TL, McDonnell ND, Evans JS, Bauwens JE, Trager WF. Warfarin-fluconazole. II. A metabolically based drug interaction: in vivo studies. Drug Metab Dispos 1996; 24: 422-8.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 422-428
-
-
Black, D.J.1
Kunze, K.L.2
Wienkers, L.C.3
Gidal, B.E.4
Seaton, T.L.5
McDonnell, N.D.6
Evans, J.S.7
Bauwens, J.E.8
Trager, W.F.9
-
32
-
-
0029914380
-
Warfarin-fluconazole. III. A rational approach to management of a metabolically based drug interaction
-
Kunze KL, Trager WF. Warfarin-fluconazole. III. A rational approach to management of a metabolically based drug interaction. Drug Metab Dispos 1996; 24: 429-35.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 429-435
-
-
Kunze, K.L.1
Trager, W.F.2
-
33
-
-
0031957174
-
Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174
-
Kaukonen KM, Olkkola KT, Neuvonen PJ. Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174. Eur J Clin Pharmacol 1998; 53: 445-9.
-
(1998)
Eur J Clin Pharmacol
, vol.53
, pp. 445-449
-
-
Kaukonen, K.M.1
Olkkola, K.T.2
Neuvonen, P.J.3
-
34
-
-
30444445695
-
Interaction of flurbiprofen with cranberry juice, grape juice, tea, and fluconazole: In vitro and clinical studies
-
Greenblatt DJ, Von Moltke LL, Perloff ES, Luo Y, Harmatz JS, Zinny MA. Interaction of flurbiprofen with cranberry juice, grape juice, tea, and fluconazole: in vitro and clinical studies. Clin Pharmacol Ther 2006; 79: 125-33.
-
(2006)
Clin Pharmacol Ther
, vol.79
, pp. 125-133
-
-
Greenblatt, D.J.1
Von Moltke, L.L.2
Perloff, E.S.3
Luo, Y.4
Harmatz, J.S.5
Zinny, M.A.6
-
35
-
-
0034634555
-
Sensitive and specific high-performance liquid chromatographic assay for 4′-hydroxyflurbiprofen and flurbiprofen in human urine and plasma
-
Hutzler JM, Frye RF, Tracy TS. Sensitive and specific high-performance liquid chromatographic assay for 4′-hydroxyflurbiprofen and flurbiprofen in human urine and plasma. J Chromatogr B Biomed Sci Appl 2000; 749: 119-25.
-
(2000)
J Chromatogr B Biomed Sci Appl
, vol.749
, pp. 119-125
-
-
Hutzler, J.M.1
Frye, R.F.2
Tracy, T.S.3
-
36
-
-
0030712276
-
Validation of the five-drug 'Pittsburgh cocktail' approach for assessment of selective regulation of drug-metabolizing enzymes
-
Frye RF, Matzke GR, Adedoyin A, Porter JA, Branch RA. Validation of the five-drug 'Pittsburgh cocktail' approach for assessment of selective regulation of drug-metabolizing enzymes. Clin Pharmacol Ther 1997; 62: 365-76.
-
(1997)
Clin Pharmacol Ther
, vol.62
, pp. 365-376
-
-
Frye, R.F.1
Matzke, G.R.2
Adedoyin, A.3
Porter, J.A.4
Branch, R.A.5
-
38
-
-
0034807892
-
Optimizing drug development: Strategies to assess drug metabolism/transporter interaction potential - toward a consensus
-
Tucker GT, Houston JB, Huang SM. Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential - toward a consensus. Pharm Res 2001; 18: 1071-80.
-
(2001)
Pharm Res
, vol.18
, pp. 1071-1080
-
-
Tucker, G.T.1
Houston, J.B.2
Huang, S.M.3
-
39
-
-
0025264682
-
Validation of the tolbutamide metabolic ratio for population screening with use of sulfaphenazole to produce model phenotypic poor metabolizers
-
Veronese ME, Miners JO, Randles D, Gregov D, Birkett DJ. Validation of the tolbutamide metabolic ratio for population screening with use of sulfaphenazole to produce model phenotypic poor metabolizers. Clin Pharmacol Ther 1990; 47: 403-11.
-
(1990)
Clin Pharmacol Ther
, vol.47
, pp. 403-411
-
-
Veronese, M.E.1
Miners, J.O.2
Randles, D.3
Gregov, D.4
Birkett, D.J.5
-
40
-
-
0019515321
-
Debrisoquine hydroxylation capacity: Problems of assessment in two populations
-
Inaba T, Otton SV, Kalow W. Debrisoquine hydroxylation capacity: problems of assessment in two populations. Clin Pharmacol Ther 1981; 29: 218-23.
-
(1981)
Clin Pharmacol Ther
, vol.29
, pp. 218-223
-
-
Inaba, T.1
Otton, S.V.2
Kalow, W.3
-
41
-
-
0037214177
-
Tolbutamide, flurbiprofen, and losartan as probes of CYP2C9 activity in humans
-
Lee CR, Pieper JA, Frye RF, Hinderliter AL, Blaisdell JA, Goldstein JA. Tolbutamide, flurbiprofen, and losartan as probes of CYP2C9 activity in humans. J Clin Pharmacol 2003; 43: 84-91.
-
(2003)
J Clin Pharmacol
, vol.43
, pp. 84-91
-
-
Lee, C.R.1
Pieper, J.A.2
Frye, R.F.3
Hinderliter, A.L.4
Blaisdell, J.A.5
Goldstein, J.A.6
-
42
-
-
0023853493
-
Pharmacokinetics of ibuprofen enantiomers in humans following oral administration of tablets with different absorption rates
-
Jamali F, Singh NN, Pasutto FM, Russell AS, Coutts RT. Pharmacokinetics of ibuprofen enantiomers in humans following oral administration of tablets with different absorption rates. Pharm Res 1988; 5: 40-3.
-
(1988)
Pharm Res
, vol.5
, pp. 40-43
-
-
Jamali, F.1
Singh, N.N.2
Pasutto, F.M.3
Russell, A.S.4
Coutts, R.T.5
-
43
-
-
0021740808
-
Determination of flurbiprofen in human serum by reverse-phase high-performance liquid chromatography with fluorescence detection
-
Albert KS, Gillespie WR, Raabe A, Garry M. Determination of flurbiprofen in human serum by reverse-phase high-performance liquid chromatography with fluorescence detection. J Pharm Sci 1984; 73: 1823-5.
-
(1984)
J Pharm Sci
, vol.73
, pp. 1823-1825
-
-
Albert, K.S.1
Gillespie, W.R.2
Raabe, A.3
Garry, M.4
-
44
-
-
0023248628
-
Pharmacokinetics of flurbiprofen in man. I. Area/dose relationships
-
Szpunar GJ, Albert KS, Bole GG, Dreyfus JN, Lockwood GF, Wagner JG. Pharmacokinetics of flurbiprofen in man. I. Area/dose relationships. Biopharm Drug Dispos 1987; 8: 273-83.
-
(1987)
Biopharm Drug Dispos
, vol.8
, pp. 273-283
-
-
Szpunar, G.J.1
Albert, K.S.2
Bole, G.G.3
Dreyfus, J.N.4
Lockwood, G.F.5
Wagner, J.G.6
-
45
-
-
0024406057
-
Single-dose pharmacokinetics of flurbiprofen granules and tablets in healthy volunteers
-
Benvenuti C, Gambaro V, Lodi F, Scaroni C, Bandi G, Valenti M. Single-dose pharmacokinetics of flurbiprofen granules and tablets in healthy volunteers. Int J Clin Pharmacol Ther Toxicol 1989; 27: 334-7.
-
(1989)
Int J Clin Pharmacol Ther Toxicol
, vol.27
, pp. 334-337
-
-
Benvenuti, C.1
Gambaro, V.2
Lodi, F.3
Scaroni, C.4
Bandi, G.5
Valenti, M.6
-
46
-
-
0036206152
-
Polymorphic variants (CYP2C9*3 and CYP2C9*5) and the F114L active site mutation of CYP2C9: Effect on atypical kinetic metabolism profiles
-
Tracy TS, Hutzler JM, Haining RL, Rettie AE, Hummel MA, Dickmann LJ. Polymorphic variants (CYP2C9*3 and CYP2C9*5) and the F114L active site mutation of CYP2C9: effect on atypical kinetic metabolism profiles. Drug Metab Dispos 2002; 30: 385-90.
-
(2002)
Drug Metab Dispos
, vol.30
, pp. 385-390
-
-
Tracy, T.S.1
Hutzler, J.M.2
Haining, R.L.3
Rettie, A.E.4
Hummel, M.A.5
Dickmann, L.J.6
-
47
-
-
33344478229
-
Quantitative prediction of in vivo inhibitory interactions involving glucuronidated drugs from in vitro data: The effect of fluconazole on zidovudine glucuronidation
-
Uchaipichat V, Winner LK, MacKenzie PI, Elliot DJ, Williams JA, Miners JO. Quantitative prediction of in vivo inhibitory interactions involving glucuronidated drugs from in vitro data: the effect of fluconazole on zidovudine glucuronidation. Br J Clin Pharmacol 2006; 61: 427-39.
-
(2006)
Br J Clin Pharmacol
, vol.61
, pp. 427-439
-
-
Uchaipichat, V.1
Winner, L.K.2
MacKenzie, P.I.3
Elliot, D.J.4
Williams, J.A.5
Miners, J.O.6
-
48
-
-
22344442057
-
Glucuronidation of nonsteroidal anti-inflammatory drugs: Identifying the enzymes responsible in human liver microsomes
-
Kuehl GE, Lampe JW, Potter JD, Bigler J. Glucuronidation of nonsteroidal anti-inflammatory drugs: identifying the enzymes responsible in human liver microsomes. Drug Metab Dispos 2005; 33: 1027-35.
-
(2005)
Drug Metab Dispos
, vol.33
, pp. 1027-1035
-
-
Kuehl, G.E.1
Lampe, J.W.2
Potter, J.D.3
Bigler, J.4
-
49
-
-
7744245748
-
Carboxyl nonsteroidal anti-inflammatory drugs are efficiently glucuronidated by microsomes of the human gastrointestinal tract
-
Sabolovic N, Heydel JM, Li X, Little JM, Humbert AC, Radominska-Pandya A, Magdalou J. Carboxyl nonsteroidal anti-inflammatory drugs are efficiently glucuronidated by microsomes of the human gastrointestinal tract. Biochim Biophys Acta 2004; 1675: 120-9.
-
(2004)
Biochim Biophys Acta
, vol.1675
, pp. 120-129
-
-
Sabolovic, N.1
Heydel, J.M.2
Li, X.3
Little, J.M.4
Humbert, A.C.5
Radominska-Pandya, A.6
Magdalou, J.7
-
50
-
-
0041524274
-
Kiiv, an in vivo parameter for predicting the magnitude of a drug interaction arising from competitive enzyme inhibition
-
Neal JM, Kunze KL, Levy RH, O'Reilly RA, Trager WF. Kiiv, an in vivo parameter for predicting the magnitude of a drug interaction arising from competitive enzyme inhibition. Drug Metab Dispos 2003; 31: 1043-8.
-
(2003)
Drug Metab Dispos
, vol.31
, pp. 1043-1048
-
-
Neal, J.M.1
Kunze, K.L.2
Levy, R.H.3
O'Reilly, R.A.4
Trager, W.F.5
-
51
-
-
0029974530
-
Caffeine urinary metabolite ratios as markers of enzyme activity: A theoretical assessment
-
Rostami-Hodjegan A, Nurminen S, Jackson PR, Tucker GT. Caffeine urinary metabolite ratios as markers of enzyme activity: a theoretical assessment. Pharmacogenetics 1996; 6: 121-49.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 121-149
-
-
Rostami-Hodjegan, A.1
Nurminen, S.2
Jackson, P.R.3
Tucker, G.T.4
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