-
1
-
-
0030799001
-
The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
-
Obach RS, Baxter JG, Liston TE, et al. The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J Pharmacol Exp Ther. 1997;283(1):46-58.
-
(1997)
J Pharmacol Exp Ther
, vol.283
, Issue.1
, pp. 46-58
-
-
Obach, R.S.1
Baxter, J.G.2
Liston, T.E.3
-
2
-
-
0037364162
-
ADMET in silico modelling: towards prediction paradise?
-
van de Waterbeemd H, Gifford E. ADMET in silico modelling: towards prediction paradise? Nat Rev Drug Discov. 2003;2(3):192-204.
-
(2003)
Nat Rev Drug Discov
, vol.2
, Issue.3
, pp. 192-204
-
-
van de Waterbeemd, H.1
Gifford, E.2
-
3
-
-
27644596457
-
Predicting in vivo drug interactions from in vitro drug discovery data
-
Wienkers LC, Heath TG. Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov. 2005;4(10):825-833.
-
(2005)
Nat Rev Drug Discov
, vol.4
, Issue.10
, pp. 825-833
-
-
Wienkers, L.C.1
Heath, T.G.2
-
4
-
-
10744232330
-
The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
-
Bjornsson TD, Callaghan JT, Einolf HJ, et al. The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos. 2003;31(7):815-832.
-
(2003)
Drug Metab Dispos
, vol.31
, Issue.7
, pp. 815-832
-
-
Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
-
5
-
-
84946478501
-
Predicting clearance mechanism in drug discovery: extended clearance classification system (ECCS)
-
Varma MV, Steyn SJ, Allerton C, El-Kattan AF. Predicting clearance mechanism in drug discovery: extended clearance classification system (ECCS). Pharm Res. 2015;32(12):3785-3802.
-
(2015)
Pharm Res
, vol.32
, Issue.12
, pp. 3785-3802
-
-
Varma, M.V.1
Steyn, S.J.2
Allerton, C.3
El-Kattan, A.F.4
-
6
-
-
84905013159
-
Prediction of pharmacokinetics and drug-drug interactions when hepatic transporters are involved
-
Li R, Barton HA, Varma MV. Prediction of pharmacokinetics and drug-drug interactions when hepatic transporters are involved. Clin Pharmacokinet. 2014;53(8):659-678.
-
(2014)
Clin Pharmacokinet
, vol.53
, Issue.8
, pp. 659-678
-
-
Li, R.1
Barton, H.A.2
Varma, M.V.3
-
7
-
-
84872229531
-
Clinical significance of organic anion transporting polypeptides (OATPs) in drug disposition: their roles in hepatic clearance and intestinal absorption
-
Shitara Y, Maeda K, Ikejiri K, Yoshida K, Horie T, Sugiyama Y. Clinical significance of organic anion transporting polypeptides (OATPs) in drug disposition: their roles in hepatic clearance and intestinal absorption. Biopharm Drug Dispos. 2013;34(1):45-78.
-
(2013)
Biopharm Drug Dispos
, vol.34
, Issue.1
, pp. 45-78
-
-
Shitara, Y.1
Maeda, K.2
Ikejiri, K.3
Yoshida, K.4
Horie, T.5
Sugiyama, Y.6
-
8
-
-
0031430085
-
Organ clearance concepts: new perspectives on old principles
-
Sirianni GL, Pang KS. Organ clearance concepts: new perspectives on old principles. J Pharmacokinet Biopharm. 1997;25(4):449-470.
-
(1997)
J Pharmacokinet Biopharm
, vol.25
, Issue.4
, pp. 449-470
-
-
Sirianni, G.L.1
Pang, K.S.2
-
9
-
-
84872234822
-
Hepatic and intestinal drug transporters: prediction of pharmacokinetic effects caused by drug-drug interactions and genetic polymorphisms
-
Yoshida K, Maeda K, Sugiyama Y. Hepatic and intestinal drug transporters: prediction of pharmacokinetic effects caused by drug-drug interactions and genetic polymorphisms. Annu Rev Pharmacol Toxicol. 2013;53:581-612.
-
(2013)
Annu Rev Pharmacol Toxicol
, vol.53
, pp. 581-612
-
-
Yoshida, K.1
Maeda, K.2
Sugiyama, Y.3
-
11
-
-
33644847684
-
Transporters as a determinant of drug clearance and tissue distribution
-
Shitara Y, Horie T, Sugiyama Y. Transporters as a determinant of drug clearance and tissue distribution. Eur J Pharm Sci. 2006;27(5):425-446.
-
(2006)
Eur J Pharm Sci
, vol.27
, Issue.5
, pp. 425-446
-
-
Shitara, Y.1
Horie, T.2
Sugiyama, Y.3
-
12
-
-
79953901458
-
Organic anion transporting polypeptide 1B1: a genetically polymorphic transporter of major importance for hepatic drug uptake
-
Niemi M, Pasanen MK, Neuvonen PJ. Organic anion transporting polypeptide 1B1: a genetically polymorphic transporter of major importance for hepatic drug uptake. Pharmacol Rev. 2011;63(1):157-181.
-
(2011)
Pharmacol Rev
, vol.63
, Issue.1
, pp. 157-181
-
-
Niemi, M.1
Pasanen, M.K.2
Neuvonen, P.J.3
-
13
-
-
34547212999
-
Bosentan is a substrate of human OATP1B1 and OATP1B3: inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil
-
Treiber A, Schneiter R, Häusler S, Stieger B. Bosentan is a substrate of human OATP1B1 and OATP1B3: inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil. Drug Metab Dispos. 2007;35(8):1400-1407.
-
(2007)
Drug Metab Dispos
, vol.35
, Issue.8
, pp. 1400-1407
-
-
Treiber, A.1
Schneiter, R.2
Häusler, S.3
Stieger, B.4
-
14
-
-
33745231761
-
Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans
-
Yamashiro W, Maeda K, Hirouchi M, Adachi Y, Hu Z, Sugiyama Y. Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans. Drug Metab Dispos. 2006;34(7):1247-1254.
-
(2006)
Drug Metab Dispos
, vol.34
, Issue.7
, pp. 1247-1254
-
-
Yamashiro, W.1
Maeda, K.2
Hirouchi, M.3
Adachi, Y.4
Hu, Z.5
Sugiyama, Y.6
-
15
-
-
85027905060
-
-
EMA. Guideline on the Investigation of Drug Interactions. Committee for Human Medicinal Products (CHMP). London, UK; 2012.
-
-
-
-
16
-
-
85027905409
-
-
USFDA. Drug Interaction Studies—Study Design, Data Analysis, Implications for Dosing, and Labeling Recommendations. Center for Drug Evaluation and Research (CDER). Silver Spring, MD; 2012.
-
-
-
-
17
-
-
84875160515
-
Model-based approaches to predict drug-drug interactions associated with hepatic uptake transporters: preclinical, clinical and beyond
-
Barton HA, Lai Y, Goosen TC, et al. Model-based approaches to predict drug-drug interactions associated with hepatic uptake transporters: preclinical, clinical and beyond. Expert Opin Drug Metab Toxicol. 2013;9(4):459-472.
-
(2013)
Expert Opin Drug Metab Toxicol
, vol.9
, Issue.4
, pp. 459-472
-
-
Barton, H.A.1
Lai, Y.2
Goosen, T.C.3
-
18
-
-
33748042671
-
Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: drug-drug interactions and interindividual differences in transporter and metabolic enzyme functions
-
Shitara Y, Sugiyama Y. Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: drug-drug interactions and interindividual differences in transporter and metabolic enzyme functions. Pharmacol Ther. 2006;112(1):71-105.
-
(2006)
Pharmacol Ther
, vol.112
, Issue.1
, pp. 71-105
-
-
Shitara, Y.1
Sugiyama, Y.2
-
19
-
-
33846571368
-
Effect of OATP1B transporter inhibition on the pharmacokinetics of atorvastatin in healthy volunteers
-
Lau YY, Huang Y, Frassetto L, Benet LZ. Effect of OATP1B transporter inhibition on the pharmacokinetics of atorvastatin in healthy volunteers. Clin Pharmacol Ther. 2007;81(2):194-204.
-
(2007)
Clin Pharmacol Ther
, vol.81
, Issue.2
, pp. 194-204
-
-
Lau, Y.Y.1
Huang, Y.2
Frassetto, L.3
Benet, L.Z.4
-
20
-
-
0027327029
-
Altered disposition of pravastatin following concomitant drug therapy with cyclosporin A in transplant recipients
-
Regazzi MB, Iacona I, Campana C, et al. Altered disposition of pravastatin following concomitant drug therapy with cyclosporin A in transplant recipients. Transplant Proc. 1993;25(4):2732-2734.
-
(1993)
Transplant Proc
, vol.25
, Issue.4
, pp. 2732-2734
-
-
Regazzi, M.B.1
Iacona, I.2
Campana, C.3
-
21
-
-
11144354934
-
The effect of gemfibrozil on the pharmacokinetics of rosuvastatin
-
Schneck DW, Birmingham BK, Zalikowski JA, et al. The effect of gemfibrozil on the pharmacokinetics of rosuvastatin. Clin Pharmacol Ther. 2004;75(5):455-463.
-
(2004)
Clin Pharmacol Ther
, vol.75
, Issue.5
, pp. 455-463
-
-
Schneck, D.W.1
Birmingham, B.K.2
Zalikowski, J.A.3
-
22
-
-
84861349018
-
Transporter-mediated drug-drug interactions involving OATP substrates: predictions based on in vitro inhibition studies
-
Yoshida K, Maeda K, Sugiyama Y. Transporter-mediated drug-drug interactions involving OATP substrates: predictions based on in vitro inhibition studies. Clin Pharmacol Ther. 2012;91(6):1053-1064.
-
(2012)
Clin Pharmacol Ther
, vol.91
, Issue.6
, pp. 1053-1064
-
-
Yoshida, K.1
Maeda, K.2
Sugiyama, Y.3
-
23
-
-
33747841593
-
Use of cryopreserved human hepatocytes in sandwich culture to measure hepatobiliary transport
-
Bi Y-a, Kazolias D, Duignan DB. Use of cryopreserved human hepatocytes in sandwich culture to measure hepatobiliary transport. Drug Metab Dispos. 2006;34(9):1658-1665.
-
(2006)
Drug Metab Dispos
, vol.34
, Issue.9
, pp. 1658-1665
-
-
Y-a, B.1
Kazolias, D.2
Duignan, D.B.3
-
24
-
-
84879417097
-
In vitro methods to support transporter evaluation in drug discovery and development
-
Brouwer KL, Keppler D, Hoffmaster KA, et al. In vitro methods to support transporter evaluation in drug discovery and development. Clin Pharmacol Ther. 2013;94(1):95-112.
-
(2013)
Clin Pharmacol Ther
, vol.94
, Issue.1
, pp. 95-112
-
-
Brouwer, K.L.1
Keppler, D.2
Hoffmaster, K.A.3
-
25
-
-
84879416924
-
ITC recommendations for transporter kinetic parameter estimation and translational modeling of transport-mediated PK and DDIs in humans
-
Zamek-Gliszczynski MJ, Lee CA, Poirier A, et al. ITC recommendations for transporter kinetic parameter estimation and translational modeling of transport-mediated PK and DDIs in humans. Clin Pharmacol Ther. 2013;94(1):64-79.
-
(2013)
Clin Pharmacol Ther
, vol.94
, Issue.1
, pp. 64-79
-
-
Zamek-Gliszczynski, M.J.1
Lee, C.A.2
Poirier, A.3
-
26
-
-
76149124823
-
Investigation of the rate-determining process in the hepatic elimination of HMG-CoA reductase inhibitors in rats and humans
-
Watanabe T, Kusuhara H, Maeda K, et al. Investigation of the rate-determining process in the hepatic elimination of HMG-CoA reductase inhibitors in rats and humans. Drug Metab Dispos. 2010;38(2):215-222.
-
(2010)
Drug Metab Dispos
, vol.38
, Issue.2
, pp. 215-222
-
-
Watanabe, T.1
Kusuhara, H.2
Maeda, K.3
-
27
-
-
84861234645
-
Predicting human hepatic clearance from in vitro drug metabolism and transport data: a scientific and pharmaceutical perspective for assessing drug-drug interactions
-
Camenisch G, Umehara K. Predicting human hepatic clearance from in vitro drug metabolism and transport data: a scientific and pharmaceutical perspective for assessing drug-drug interactions. Biopharm Drug Dispos. 2012;33(4):179-194.
-
(2012)
Biopharm Drug Dispos
, vol.33
, Issue.4
, pp. 179-194
-
-
Camenisch, G.1
Umehara, K.2
-
28
-
-
84865191410
-
Use of mechanistic modeling to assess interindividual variability and interspecies differences in active uptake in human and rat hepatocytes
-
Menochet K, Kenworthy KE, Houston JB, Galetin A. Use of mechanistic modeling to assess interindividual variability and interspecies differences in active uptake in human and rat hepatocytes. Drug Metab Dispos. 2012;40(9):1744-1756.
-
(2012)
Drug Metab Dispos
, vol.40
, Issue.9
, pp. 1744-1756
-
-
Menochet, K.1
Kenworthy, K.E.2
Houston, J.B.3
Galetin, A.4
-
29
-
-
84859910816
-
Mechanistic pharmacokinetic modeling for the prediction of transporter-mediated disposition in humans from sandwich culture human hepatocyte data
-
Jones HM, Barton HA, Lai Y, et al. Mechanistic pharmacokinetic modeling for the prediction of transporter-mediated disposition in humans from sandwich culture human hepatocyte data. Drug Metab Dispos. 2012;40(5):1007-1017.
-
(2012)
Drug Metab Dispos
, vol.40
, Issue.5
, pp. 1007-1017
-
-
Jones, H.M.1
Barton, H.A.2
Lai, Y.3
-
30
-
-
84907180162
-
Quantitative prediction of transporter- and enzyme-mediated clinical drug-drug interactions of organic anion-transporting polypeptide 1B1 substrates using a mechanistic net-effect model
-
Varma MV, Bi Y-a, Kimoto E, Lin J. Quantitative prediction of transporter- and enzyme-mediated clinical drug-drug interactions of organic anion-transporting polypeptide 1B1 substrates using a mechanistic net-effect model. J Pharmacol Exp Ther. 2014;351(1):214-223.
-
(2014)
J Pharmacol Exp Ther
, vol.351
, Issue.1
, pp. 214-223
-
-
Varma, M.V.1
Y-a, B.2
Kimoto, E.3
Lin, J.4
-
31
-
-
46449097700
-
Prediction of the pharmacokinetics of atorvastatin, cerivastatin, and indomethacin using kinetic models applied to isolated rat hepatocytes
-
Paine SW, Parker AJ, Gardiner P, Webborn PJ, Riley RJ. Prediction of the pharmacokinetics of atorvastatin, cerivastatin, and indomethacin using kinetic models applied to isolated rat hepatocytes. Drug Metab Dispos. 2008;36(7):1365-1374.
-
(2008)
Drug Metab Dispos
, vol.36
, Issue.7
, pp. 1365-1374
-
-
Paine, S.W.1
Parker, A.J.2
Gardiner, P.3
Webborn, P.J.4
Riley, R.J.5
-
32
-
-
72349089654
-
Prediction of pharmacokinetic profile of valsartan in human based on in vitro uptake transport data
-
Poirier A, Cascais AC, Funk C, Lave T. Prediction of pharmacokinetic profile of valsartan in human based on in vitro uptake transport data. J Pharmacokinet Pharmacodyn. 2009;36(6):585-611.
-
(2009)
J Pharmacokinet Pharmacodyn
, vol.36
, Issue.6
, pp. 585-611
-
-
Poirier, A.1
Cascais, A.C.2
Funk, C.3
Lave, T.4
-
33
-
-
59649130318
-
Physiologically based pharmacokinetic modeling to predict transporter-mediated clearance and distribution of pravastatin in humans
-
Watanabe T, Kusuhara H, Maeda K, Shitara Y, Sugiyama Y. Physiologically based pharmacokinetic modeling to predict transporter-mediated clearance and distribution of pravastatin in humans. J Pharmacol Exp Ther. 2009;328(2):652-662.
-
(2009)
J Pharmacol Exp Ther
, vol.328
, Issue.2
, pp. 652-662
-
-
Watanabe, T.1
Kusuhara, H.2
Maeda, K.3
Shitara, Y.4
Sugiyama, Y.5
-
34
-
-
84866708911
-
Physiologically based modeling of pravastatin transporter-mediated hepatobiliary disposition and drug-drug interactions
-
Varma MV, Lai Y, Feng B, Litchfield J, Goosen TC, Bergman A. Physiologically based modeling of pravastatin transporter-mediated hepatobiliary disposition and drug-drug interactions. Pharm Res. 2012;29(10):2860-2873.
-
(2012)
Pharm Res
, vol.29
, Issue.10
, pp. 2860-2873
-
-
Varma, M.V.1
Lai, Y.2
Feng, B.3
Litchfield, J.4
Goosen, T.C.5
Bergman, A.6
-
35
-
-
17644381224
-
Prediction of human drug clearance from in vitro and preclinical data using physiologically based and empirical approaches
-
Ito K, Houston JB. Prediction of human drug clearance from in vitro and preclinical data using physiologically based and empirical approaches. Pharm Res. 2005;22(1):103-112.
-
(2005)
Pharm Res
, vol.22
, Issue.1
, pp. 103-112
-
-
Ito, K.1
Houston, J.B.2
-
36
-
-
84904201004
-
A “middle-out” approach to human pharmacokinetic predictions for OATP substrates using physiologically-based pharmacokinetic modeling
-
Li R, Barton HA, Yates PD, et al. A “middle-out” approach to human pharmacokinetic predictions for OATP substrates using physiologically-based pharmacokinetic modeling. J Pharmacokinet Pharmacodyn. 2014;41(3):197-209.
-
(2014)
J Pharmacokinet Pharmacodyn
, vol.41
, Issue.3
, pp. 197-209
-
-
Li, R.1
Barton, H.A.2
Yates, P.D.3
-
37
-
-
4644364576
-
Contribution of OATP2 (OATP1B1) and OATP8 (OATP1B3) to the hepatic uptake of pitavastatin in humans
-
Hirano M, Maeda K, Shitara Y, Sugiyama Y. Contribution of OATP2 (OATP1B1) and OATP8 (OATP1B3) to the hepatic uptake of pitavastatin in humans. J Pharmacol Exp Ther. 2004;311(1):139-146.
-
(2004)
J Pharmacol Exp Ther
, vol.311
, Issue.1
, pp. 139-146
-
-
Hirano, M.1
Maeda, K.2
Shitara, Y.3
Sugiyama, Y.4
-
38
-
-
84927701275
-
Toward prospective prediction of pharmacokinetics in OATP1B1 genetic variant populations
-
Li R, Barton HA, Maurer TS. Toward prospective prediction of pharmacokinetics in OATP1B1 genetic variant populations. CPT Pharmacometr Syst Pharmacol. 2014;3:e151.
-
(2014)
CPT Pharmacometr Syst Pharmacol
, vol.3
-
-
Li, R.1
Barton, H.A.2
Maurer, T.S.3
-
39
-
-
84907588697
-
Physiologically based pharmacokinetic prediction of telmisartan in human
-
Li R, Ghosh A, Maurer TS, Kimoto E, Barton HA. Physiologically based pharmacokinetic prediction of telmisartan in human. Drug Metab Dispos. 2014;42(10):1646-1655.
-
(2014)
Drug Metab Dispos
, vol.42
, Issue.10
, pp. 1646-1655
-
-
Li, R.1
Ghosh, A.2
Maurer, T.S.3
Kimoto, E.4
Barton, H.A.5
-
40
-
-
84908003218
-
Predicting carrier-mediated hepatic disposition of rosuvastatin in man by scaling from individual transfected cell-lines in vitro using absolute transporter protein quantification and PBPK modeling
-
Bosgra S, Steeg EV, Vlaming ML, et al. Predicting carrier-mediated hepatic disposition of rosuvastatin in man by scaling from individual transfected cell-lines in vitro using absolute transporter protein quantification and PBPK modeling. Eur J Pharm Sci. 2014;65:156-166.
-
(2014)
Eur J Pharm Sci
, vol.65
, pp. 156-166
-
-
Bosgra, S.1
Steeg, E.V.2
Vlaming, M.L.3
-
41
-
-
84939781080
-
Meta-analysis of expression of hepatic organic anion-transporting polypeptide (OATP) transporters in cellular systems relative to human liver tissue
-
Badee J, Achour B, Rostami-Hodjegan A, Galetin A. Meta-analysis of expression of hepatic organic anion-transporting polypeptide (OATP) transporters in cellular systems relative to human liver tissue. Drug Metab Dispos. 2015;43(4): 424-432.
-
(2015)
Drug Metab Dispos
, vol.43
, Issue.4
, pp. 424-432
-
-
Badee, J.1
Achour, B.2
Rostami-Hodjegan, A.3
Galetin, A.4
-
42
-
-
84870539183
-
Characterization of organic anion transporting polypeptide (OATP) expression and its functional contribution to the uptake of substrates in human hepatocytes
-
Kimoto E, Yoshida K, Balogh LM, et al. Characterization of organic anion transporting polypeptide (OATP) expression and its functional contribution to the uptake of substrates in human hepatocytes. Mol Pharmacol. 2012;9(12):3535-3542.
-
(2012)
Mol Pharmacol
, vol.9
, Issue.12
, pp. 3535-3542
-
-
Kimoto, E.1
Yoshida, K.2
Balogh, L.M.3
-
43
-
-
84890663852
-
Interindividual variability in hepatic organic anion-transporting polypeptides and P-glycoprotein (ABCB1) protein expression: quantification by liquid chromatography tandem mass spectroscopy and influence of genotype, age, and sex
-
Prasad B, Evers R, Gupta A, et al. Interindividual variability in hepatic organic anion-transporting polypeptides and P-glycoprotein (ABCB1) protein expression: quantification by liquid chromatography tandem mass spectroscopy and influence of genotype, age, and sex. Drug Metab Dispos. 2014;42(1):78-88.
-
(2014)
Drug Metab Dispos
, vol.42
, Issue.1
, pp. 78-88
-
-
Prasad, B.1
Evers, R.2
Gupta, A.3
-
44
-
-
84876752739
-
Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicin
-
Varma MV, Lin J, Bi YA, et al. Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicin. Drug Metab Dispos. 2013;41(5):966-974.
-
(2013)
Drug Metab Dispos
, vol.41
, Issue.5
, pp. 966-974
-
-
Varma, M.V.1
Lin, J.2
Bi, Y.A.3
-
45
-
-
67650825002
-
Comparison of different algorithms for predicting clinical drug-drug interactions, based on the use of CYP3A4 in vitro data: predictions of compounds as precipitants of interaction
-
Fahmi OA, Hurst S, Plowchalk D, et al. Comparison of different algorithms for predicting clinical drug-drug interactions, based on the use of CYP3A4 in vitro data: predictions of compounds as precipitants of interaction. Drug Metab Dispos. 2009;37(8):1658-1666.
-
(2009)
Drug Metab Dispos
, vol.37
, Issue.8
, pp. 1658-1666
-
-
Fahmi, O.A.1
Hurst, S.2
Plowchalk, D.3
-
46
-
-
47949115175
-
A combined model for predicting CYP3A4 clinical net drug-drug interaction based on CYP3A4 inhibition, inactivation, and induction determined in vitro
-
Fahmi OA, Maurer TS, Kish M, Cardenas E, Boldt S, Nettleton D. A combined model for predicting CYP3A4 clinical net drug-drug interaction based on CYP3A4 inhibition, inactivation, and induction determined in vitro. Drug Metab Dispos. 2008;36(8):1698-1708.
-
(2008)
Drug Metab Dispos
, vol.36
, Issue.8
, pp. 1698-1708
-
-
Fahmi, O.A.1
Maurer, T.S.2
Kish, M.3
Cardenas, E.4
Boldt, S.5
Nettleton, D.6
-
47
-
-
84859346272
-
In vitro and in silico strategies to identify OATP1B1 inhibitors and predict clinical drug-drug interactions
-
Karlgren M, Ahlin G, Bergstrom CA, Svensson R, Palm J, Artursson P. In vitro and in silico strategies to identify OATP1B1 inhibitors and predict clinical drug-drug interactions. Pharm Res. 2012;29(2):411-426.
-
(2012)
Pharm Res
, vol.29
, Issue.2
, pp. 411-426
-
-
Karlgren, M.1
Ahlin, G.2
Bergstrom, C.A.3
Svensson, R.4
Palm, J.5
Artursson, P.6
-
48
-
-
84861494749
-
Classification of inhibitors of hepatic organic anion transporting polypeptides (OATPs): influence of protein expression on drug-drug interactions
-
Karlgren M, Vildhede A, Norinder U, et al. Classification of inhibitors of hepatic organic anion transporting polypeptides (OATPs): influence of protein expression on drug-drug interactions. J Med Chem. 2012;55(10):4740-4763.
-
(2012)
J Med Chem
, vol.55
, Issue.10
, pp. 4740-4763
-
-
Karlgren, M.1
Vildhede, A.2
Norinder, U.3
-
49
-
-
84940384444
-
Quantitative rationalization of gemfibrozil drug interactions: consideration of transporters-enzyme interplay and the role of circulating metabolite gemfibrozil 1-O-beta-glucuronide
-
Varma MV, Lin J, Bi YA, Kimoto E, Rodrigues AD. Quantitative rationalization of gemfibrozil drug interactions: consideration of transporters-enzyme interplay and the role of circulating metabolite gemfibrozil 1-O-beta-glucuronide. Drug Metab Dispos. 2015;43(7):1108-1118.
-
(2015)
Drug Metab Dispos
, vol.43
, Issue.7
, pp. 1108-1118
-
-
Varma, M.V.1
Lin, J.2
Bi, Y.A.3
Kimoto, E.4
Rodrigues, A.D.5
-
50
-
-
84927679943
-
Physiologically based pharmacokinetic modeling in drug discovery and development: a pharmaceutical industry perspective
-
Jones HM, Chen Y, Gibson C, et al. Physiologically based pharmacokinetic modeling in drug discovery and development: a pharmaceutical industry perspective. Clin Pharmacol Ther. 2015;97(3):247-262.
-
(2015)
Clin Pharmacol Ther
, vol.97
, Issue.3
, pp. 247-262
-
-
Jones, H.M.1
Chen, Y.2
Gibson, C.3
-
51
-
-
84862777920
-
The role of physiologically based pharmacokinetic modeling in regulatory review
-
Huang SM, Rowland M. The role of physiologically based pharmacokinetic modeling in regulatory review. Clin Pharmacol Ther. 2012;91(3): 542-549.
-
(2012)
Clin Pharmacol Ther
, vol.91
, Issue.3
, pp. 542-549
-
-
Huang, S.M.1
Rowland, M.2
-
52
-
-
84862619047
-
Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: a marriage under the arch of systems pharmacology
-
Rostami-Hodjegan A. Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: a marriage under the arch of systems pharmacology. Clin Pharmacol Ther. 2012;92(1):50-61.
-
(2012)
Clin Pharmacol Ther
, vol.92
, Issue.1
, pp. 50-61
-
-
Rostami-Hodjegan, A.1
-
53
-
-
84858660647
-
From preclinical to human—prediction of oral absorption and drug-drug interaction potential using physiologically based pharmacokinetic (PBPK) modeling approach in an industrial setting: a workflow by using case example
-
Sinha VK, Snoeys J, Osselaer NV, Peer AV, Mackie C, Heald D. From preclinical to human—prediction of oral absorption and drug-drug interaction potential using physiologically based pharmacokinetic (PBPK) modeling approach in an industrial setting: a workflow by using case example. Biopharm Drug Dispos. 2012;33(2):111-121.
-
(2012)
Biopharm Drug Dispos
, vol.33
, Issue.2
, pp. 111-121
-
-
Sinha, V.K.1
Snoeys, J.2
Osselaer, N.V.3
Peer, A.V.4
Mackie, C.5
Heald, D.6
-
54
-
-
84862777396
-
Application of IVIVE and PBPK modeling in prospective prediction of clinical pharmacokinetics: strategy and approach during the drug discovery phase with four case studies
-
Chen Y, Jin JY, Mukadam S, Malhi V, Kenny JR. Application of IVIVE and PBPK modeling in prospective prediction of clinical pharmacokinetics: strategy and approach during the drug discovery phase with four case studies. Biopharm Drug Dispos. 2012;33(2):85-98.
-
(2012)
Biopharm Drug Dispos
, vol.33
, Issue.2
, pp. 85-98
-
-
Chen, Y.1
Jin, J.Y.2
Mukadam, S.3
Malhi, V.4
Kenny, J.R.5
-
55
-
-
84862634533
-
Best practice in the use of physiologically based pharmacokinetic modeling and simulation to address clinical pharmacology regulatory questions
-
Zhao P, Rowland M, Huang SM. Best practice in the use of physiologically based pharmacokinetic modeling and simulation to address clinical pharmacology regulatory questions. Clin Pharmacol Ther. 2012;92(1):17-20.
-
(2012)
Clin Pharmacol Ther
, vol.92
, Issue.1
, pp. 17-20
-
-
Zhao, P.1
Rowland, M.2
Huang, S.M.3
-
56
-
-
84878824845
-
Cyclosporine inhibition of hepatic and intestinal CYP3A4, uptake and efflux transporters: application of PBPK modeling in the assessment of drug-drug interaction potential
-
Gertz M, Cartwright CM, Hobbs MJ, et al. Cyclosporine inhibition of hepatic and intestinal CYP3A4, uptake and efflux transporters: application of PBPK modeling in the assessment of drug-drug interaction potential. Pharm Res. 2013;30(3):761-780.
-
(2013)
Pharm Res
, vol.30
, Issue.3
, pp. 761-780
-
-
Gertz, M.1
Cartwright, C.M.2
Hobbs, M.J.3
-
57
-
-
84866708911
-
-
Varma MV, Lai Y, Feng B, Litchfield J, Goosen TC, Bergman A. Physiologically based modeling of pravastatin transporter-mediated hepatobiliary disposition and drug-drug interactions. Pharm Res. 2012.
-
-
-
-
58
-
-
84876483882
-
Mechanistic modeling to predict the transporter- and enzyme-mediated drug-drug interactions of repaglinide
-
Varma MV, Lai Y, Kimoto E, Goosen TC, El-Kattan AF, Kumar V. Mechanistic modeling to predict the transporter- and enzyme-mediated drug-drug interactions of repaglinide. Pharm Res. 2013;30(4):1188-1199.
-
(2013)
Pharm Res
, vol.30
, Issue.4
, pp. 1188-1199
-
-
Varma, M.V.1
Lai, Y.2
Kimoto, E.3
Goosen, T.C.4
El-Kattan, A.F.5
Kumar, V.6
-
59
-
-
84877786965
-
Response to the comment on the article “Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions
-
Varma MV, Lai Y, Feng B, Litchfield J, Goosen TC, Bergman A. Response to the comment on the article “Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions.” Pharm Res. 2013;30(6):1469-1470.
-
(2013)
Pharm Res
, vol.30
, Issue.6
, pp. 1469-1470
-
-
Varma, M.V.1
Lai, Y.2
Feng, B.3
Litchfield, J.4
Goosen, T.C.5
Bergman, A.6
-
60
-
-
84903633472
-
Mechanism-based pharmacokinetic modeling to evaluate transporter-enzyme interplay in drug interactions and pharmacogenetics of glyburide
-
Varma MV, Scialis RJ, Lin J, et al. Mechanism-based pharmacokinetic modeling to evaluate transporter-enzyme interplay in drug interactions and pharmacogenetics of glyburide. AAPS J. 2014;16(4):736-748.
-
(2014)
AAPS J
, vol.16
, Issue.4
, pp. 736-748
-
-
Varma, M.V.1
Scialis, R.J.2
Lin, J.3
-
61
-
-
84891867228
-
A mechanistic framework for in vitro-in vivo extrapolation of liver membrane transporters: prediction of drug-drug interaction between rosuvastatin and cyclosporine
-
Jamei M, Bajot F, Neuhoff S, et al. A mechanistic framework for in vitro-in vivo extrapolation of liver membrane transporters: prediction of drug-drug interaction between rosuvastatin and cyclosporine. Clin Pharmacokinet. 2014;53(1):73-87.
-
(2014)
Clin Pharmacokinet
, vol.53
, Issue.1
, pp. 73-87
-
-
Jamei, M.1
Bajot, F.2
Neuhoff, S.3
-
62
-
-
0035857020
-
New drug targets for type 2 diabetes and the metabolic syndrome
-
Moller DE. New drug targets for type 2 diabetes and the metabolic syndrome. Nature. 2001;414(6865):821-827.
-
(2001)
Nature
, vol.414
, Issue.6865
, pp. 821-827
-
-
Moller, D.E.1
-
63
-
-
0028929401
-
Pharmacology of competitive inhibitors of HMG-CoA reductase
-
Corsini A, Maggi FM, Catapano AL. Pharmacology of competitive inhibitors of HMG-CoA reductase. Pharmacol Res. 1995;31(1):9-27.
-
(1995)
Pharmacol Res
, vol.31
, Issue.1
, pp. 9-27
-
-
Corsini, A.1
Maggi, F.M.2
Catapano, A.L.3
-
64
-
-
84863115976
-
Discovery of (S)-6-(3-cyclopentyl-2-(4-(trifluoromethyl)-1 H-imidazol-1-yl) propanamido) nicotinic acid as a hepatoselective glucokinase activator clinical candidate for treating type 2 diabetes mellitus
-
Pfefferkorn JA, Guzman-Perez A, Litchfield J, et al. Discovery of (S)-6-(3-cyclopentyl-2-(4-(trifluoromethyl)-1 H-imidazol-1-yl) propanamido) nicotinic acid as a hepatoselective glucokinase activator clinical candidate for treating type 2 diabetes mellitus. J Med Chem. 2012;55(3):1318-1333.
-
(2012)
J Med Chem
, vol.55
, Issue.3
, pp. 1318-1333
-
-
Pfefferkorn, J.A.1
Guzman-Perez, A.2
Litchfield, J.3
-
65
-
-
79960632377
-
Development of a liver-targeted stearoyl-CoA desaturase (SCD) inhibitor (MK-8245) to establish a therapeutic window for the treatment of diabetes and dyslipidemia
-
Oballa RM, Belair L, Black WC, et al. Development of a liver-targeted stearoyl-CoA desaturase (SCD) inhibitor (MK-8245) to establish a therapeutic window for the treatment of diabetes and dyslipidemia. J Med Chem. 2011;54(14):5082-5096.
-
(2011)
J Med Chem
, vol.54
, Issue.14
, pp. 5082-5096
-
-
Oballa, R.M.1
Belair, L.2
Black, W.C.3
-
66
-
-
84879343782
-
Intracellular drug concentrations and transporters: measurement, modeling, and implications for the liver
-
Chu X, Korzekwa K, Elsby R, et al. Intracellular drug concentrations and transporters: measurement, modeling, and implications for the liver. Clin Pharmacol Ther. 2013;94(1):126-141.
-
(2013)
Clin Pharmacol Ther
, vol.94
, Issue.1
, pp. 126-141
-
-
Chu, X.1
Korzekwa, K.2
Elsby, R.3
-
67
-
-
84905370710
-
Application of a physiologically based pharmacokinetic model to predict OATP1B1-related variability in pharmacodynamics of rosuvastatin
-
Rose RH, Neuhoff S, Abduljalil K, Chetty M, Rostami-Hodjegan A, Jamei M. Application of a physiologically based pharmacokinetic model to predict OATP1B1-related variability in pharmacodynamics of rosuvastatin. CPT: Pharmacometrics Syst Pharmacol. 2014;3:e124.
-
(2014)
CPT: Pharmacometrics Syst Pharmacol
, vol.3
-
-
Rose, R.H.1
Neuhoff, S.2
Abduljalil, K.3
Chetty, M.4
Rostami-Hodjegan, A.5
Jamei, M.6
-
68
-
-
78751500357
-
Clinical pharmacokinetics of metformin
-
Graham GG, Punt J, Arora M, et al. Clinical pharmacokinetics of metformin. Clin Pharmacokinet. 2011;50(2):81-98.
-
(2011)
Clin Pharmacokinet
, vol.50
, Issue.2
, pp. 81-98
-
-
Graham, G.G.1
Punt, J.2
Arora, M.3
-
69
-
-
69449098951
-
The effects of genetic polymorphisms in the organic cation transporters OCT1, OCT2, and OCT3 on the renal clearance of metformin
-
Tzvetkov MV, Vormfelde SV, Balen D, et al. The effects of genetic polymorphisms in the organic cation transporters OCT1, OCT2, and OCT3 on the renal clearance of metformin. Clin Pharmacol Ther. 2009;86(3):299-306.
-
(2009)
Clin Pharmacol Ther
, vol.86
, Issue.3
, pp. 299-306
-
-
Tzvetkov, M.V.1
Vormfelde, S.V.2
Balen, D.3
-
70
-
-
84953356353
-
Steady-state pharmacokinetics of metformin is independent of the OCT1 genotype in healthy volunteers
-
Christensen MM, Hojlund K, Hother-Nielsen O, et al. Steady-state pharmacokinetics of metformin is independent of the OCT1 genotype in healthy volunteers. Eur J Clin Pharmacol. 2015;71(6):691-697.
-
(2015)
Eur J Clin Pharmacol
, vol.71
, Issue.6
, pp. 691-697
-
-
Christensen, M.M.1
Hojlund, K.2
Hother-Nielsen, O.3
-
71
-
-
38349085099
-
Effect of genetic variation in the organic cation transporter 1, OCT1, on metformin pharmacokinetics
-
Shu Y, Brown C, Castro RA, et al. Effect of genetic variation in the organic cation transporter 1, OCT1, on metformin pharmacokinetics. Clin Pharmacol Ther. 2008;83(2):273-280.
-
(2008)
Clin Pharmacol Ther
, vol.83
, Issue.2
, pp. 273-280
-
-
Shu, Y.1
Brown, C.2
Castro, R.A.3
-
72
-
-
81055140250
-
The pharmacogenetics of metformin and its impact on plasma metformin steady-state levels and glycosylated hemoglobin A1c
-
Christensen MM, Brasch-Andersen C, Green H, et al. The pharmacogenetics of metformin and its impact on plasma metformin steady-state levels and glycosylated hemoglobin A1c. Pharmacogenet Genomics. 2011;21(12):837-850.
-
(2011)
Pharmacogenet Genomics
, vol.21
, Issue.12
, pp. 837-850
-
-
Christensen, M.M.1
Brasch-Andersen, C.2
Green, H.3
-
73
-
-
49949104757
-
SLCO1B1 variants and statin-induced myopathy-a genomewide study
-
Group SC, Link E, Parish S, et al. SLCO1B1 variants and statin-induced myopathy-a genomewide study. N Engl J Med. 2008;359(8):789-799.
-
(2008)
N Engl J Med
, vol.359
, Issue.8
, pp. 789-799
-
-
Group, S.C.1
Link, E.2
Parish, S.3
-
74
-
-
72849141790
-
Transporter pharmacogenetics and statin toxicity
-
Niemi M. Transporter pharmacogenetics and statin toxicity. Clin Pharmacol Ther. 2010;87(1):130-133.
-
(2010)
Clin Pharmacol Ther
, vol.87
, Issue.1
, pp. 130-133
-
-
Niemi, M.1
-
75
-
-
36148953896
-
Different effects of SLCO1B1 polymorphism on the pharmacokinetics of atorvastatin and rosuvastatin
-
Pasanen MK, Fredrikson H, Neuvonen PJ, Niemi M. Different effects of SLCO1B1 polymorphism on the pharmacokinetics of atorvastatin and rosuvastatin. Clin Pharmacol Ther. 2007;82(6):726-733.
-
(2007)
Clin Pharmacol Ther
, vol.82
, Issue.6
, pp. 726-733
-
-
Pasanen, M.K.1
Fredrikson, H.2
Neuvonen, P.J.3
Niemi, M.4
-
76
-
-
84878019391
-
Lack of association between SLCO1B1 polymorphism and the lipid-lowering effects of atorvastatin and simvastatin in Chinese individuals
-
Fu Q, Li YP, Gao Y, et al. Lack of association between SLCO1B1 polymorphism and the lipid-lowering effects of atorvastatin and simvastatin in Chinese individuals. Eur J Clin Pharmacol. 2013;69(6):1269-1274.
-
(2013)
Eur J Clin Pharmacol
, vol.69
, Issue.6
, pp. 1269-1274
-
-
Fu, Q.1
Li, Y.P.2
Gao, Y.3
-
77
-
-
3242808852
-
High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)
-
Niemi M, Schaeffeler E, Lang T, et al. High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1). Pharmacogenetics. 2004;14(7):429-440.
-
(2004)
Pharmacogenetics
, vol.14
, Issue.7
, pp. 429-440
-
-
Niemi, M.1
Schaeffeler, E.2
Lang, T.3
-
78
-
-
34447335619
-
Effect of drug transporter genotypes on pravastatin disposition in European- and African-American participants
-
Ho RH, Choi L, Lee W, et al. Effect of drug transporter genotypes on pravastatin disposition in European- and African-American participants. Pharmacogenet Genomics. 2007;17(8):647-656.
-
(2007)
Pharmacogenet Genomics
, vol.17
, Issue.8
, pp. 647-656
-
-
Ho, R.H.1
Choi, L.2
Lee, W.3
-
79
-
-
33749049136
-
SLCO1B1 polymorphism and sex affect the pharmacokinetics of pravastatin but not fluvastatin
-
Niemi M, Pasanen MK, Neuvonen PJ. SLCO1B1 polymorphism and sex affect the pharmacokinetics of pravastatin but not fluvastatin. Clin Pharmacol Ther. 2006;80(4):356-366.
-
(2006)
Clin Pharmacol Ther
, vol.80
, Issue.4
, pp. 356-366
-
-
Niemi, M.1
Pasanen, M.K.2
Neuvonen, P.J.3
-
80
-
-
84855499159
-
The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin
-
Martin NG, Li KW, Murray H, Putt W, Packard CJ, Humphries SE. The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. Br J Clin Pharmacol. 2012;73(2):303-306.
-
(2012)
Br J Clin Pharmacol
, vol.73
, Issue.2
, pp. 303-306
-
-
Martin, N.G.1
Li, K.W.2
Murray, H.3
Putt, W.4
Packard, C.J.5
Humphries, S.E.6
-
81
-
-
77955857999
-
Hepatic metabolism and transporter gene variants enhance response to rosuvastatin in patients with acute myocardial infarction: the GEOSTAT-1 Study
-
Bailey KM, Romaine SP, Jackson BM, et al. Hepatic metabolism and transporter gene variants enhance response to rosuvastatin in patients with acute myocardial infarction: the GEOSTAT-1 Study. Circ Cardiovasc Genet. 2010;3(3):276-285.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, Issue.3
, pp. 276-285
-
-
Bailey, K.M.1
Romaine, S.P.2
Jackson, B.M.3
-
82
-
-
25844458977
-
Rosuvastatin pharmacokinetics and pharmacogenetics in white and Asian subjects residing in the same environment
-
Lee E, Ryan S, Birmingham B, et al. Rosuvastatin pharmacokinetics and pharmacogenetics in white and Asian subjects residing in the same environment. Clin Pharmacol Ther. 2005;78(4):330-341.
-
(2005)
Clin Pharmacol Ther
, vol.78
, Issue.4
, pp. 330-341
-
-
Lee, E.1
Ryan, S.2
Birmingham, B.3
-
83
-
-
84882247785
-
Effects of polymorphisms in ABCG2, SLCO1B1, SLC10A1 and CYP2C9/19 on plasma concentrations of rosuvastatin and lipid response in Chinese patients
-
Lee HK, Hu M, Lui S, Ho CS, Wong CK, Tomlinson B. Effects of polymorphisms in ABCG2, SLCO1B1, SLC10A1 and CYP2C9/19 on plasma concentrations of rosuvastatin and lipid response in Chinese patients. Pharmacogenomics. 2013;14(11):1283-1294.
-
(2013)
Pharmacogenomics
, vol.14
, Issue.11
, pp. 1283-1294
-
-
Lee, H.K.1
Hu, M.2
Lui, S.3
Ho, C.S.4
Wong, C.K.5
Tomlinson, B.6
-
84
-
-
33751096467
-
SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid
-
Pasanen MK, Neuvonen M, Neuvonen PJ, Niemi M. SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid. Pharmacogenet Genomics. 2006;16(12): 873-879.
-
(2006)
Pharmacogenet Genomics
, vol.16
, Issue.12
, pp. 873-879
-
-
Pasanen, M.K.1
Neuvonen, M.2
Neuvonen, P.J.3
Niemi, M.4
-
85
-
-
67651172794
-
ABCG2 polymorphism markedly affects the pharmacokinetics of atorvastatin and rosuvastatin
-
Keskitalo JE, Zolk O, Fromm MF, Kurkinen KJ, Neuvonen PJ, Niemi M. ABCG2 polymorphism markedly affects the pharmacokinetics of atorvastatin and rosuvastatin. Clin Pharmacol Ther. 2009;86(2):197-203.
-
(2009)
Clin Pharmacol Ther
, vol.86
, Issue.2
, pp. 197-203
-
-
Keskitalo, J.E.1
Zolk, O.2
Fromm, M.F.3
Kurkinen, K.J.4
Neuvonen, P.J.5
Niemi, M.6
-
86
-
-
84898854013
-
Association between statin-induced creatine kinase elevation and genetic polymorphisms in SLCO1B1, ABCB1 and ABCG2
-
Ferrari M, Guasti L, Maresca A, et al. Association between statin-induced creatine kinase elevation and genetic polymorphisms in SLCO1B1, ABCB1 and ABCG2. Eur J Clin Pharmacol. 2014;70(5):539-547.
-
(2014)
Eur J Clin Pharmacol
, vol.70
, Issue.5
, pp. 539-547
-
-
Ferrari, M.1
Guasti, L.2
Maresca, A.3
-
87
-
-
84885171127
-
Do MDR1 and SLCO1B1 polymorphisms influence the therapeutic response to atorvastatin? A study on a cohort of Egyptian patients with hypercholesterolemia
-
Shabana MF, Mishriki AA, Issac MS, Bakhoum SW. Do MDR1 and SLCO1B1 polymorphisms influence the therapeutic response to atorvastatin? A study on a cohort of Egyptian patients with hypercholesterolemia. Mol Diagnosis Ther. 2013;17(5):299-309.
-
(2013)
Mol Diagnosis Ther
, vol.17
, Issue.5
, pp. 299-309
-
-
Shabana, M.F.1
Mishriki, A.A.2
Issac, M.S.3
Bakhoum, S.W.4
-
88
-
-
84898619731
-
The effect of CYP3A4*1G allele on the pharmacokinetics of atorvastatin in Chinese Han patients with coronary heart disease
-
He BX, Shi L, Qiu J, Zeng XH, Zhao SJ. The effect of CYP3A4*1G allele on the pharmacokinetics of atorvastatin in Chinese Han patients with coronary heart disease. J Clin Pharmacol. 2014;54(4):462-467.
-
(2014)
J Clin Pharmacol
, vol.54
, Issue.4
, pp. 462-467
-
-
He, B.X.1
Shi, L.2
Qiu, J.3
Zeng, X.H.4
Zhao, S.J.5
-
89
-
-
50849097843
-
CYP3A4*1G polymorphism is associated with lipid-lowering efficacy of atorvastatin but not of simvastatin
-
Gao Y, Zhang LR, Fu Q. CYP3A4*1G polymorphism is associated with lipid-lowering efficacy of atorvastatin but not of simvastatin. Eur J Clin Pharmacol. 2008;64(9):877-882.
-
(2008)
Eur J Clin Pharmacol
, vol.64
, Issue.9
, pp. 877-882
-
-
Gao, Y.1
Zhang, L.R.2
Fu, Q.3
-
90
-
-
0346433752
-
CYP3A4 genotypes and plasma lipoprotein levels before and after treatment with atorvastatin in primary hypercholesterolemia
-
Kajinami K, Brousseau ME, Ordovas JM, Schaefer EJ. CYP3A4 genotypes and plasma lipoprotein levels before and after treatment with atorvastatin in primary hypercholesterolemia. Am J Cardiol. 2004;93(1):104-107.
-
(2004)
Am J Cardiol
, vol.93
, Issue.1
, pp. 104-107
-
-
Kajinami, K.1
Brousseau, M.E.2
Ordovas, J.M.3
Schaefer, E.J.4
-
91
-
-
70649110001
-
Different effects of the ABCG2 c.421C>A SNP on the pharmacokinetics of fluvastatin, pravastatin and simvastatin
-
Keskitalo JE, Pasanen MK, Neuvonen PJ, Niemi M. Different effects of the ABCG2 c.421C>A SNP on the pharmacokinetics of fluvastatin, pravastatin and simvastatin. Pharmacogenomics. 2009;10(10):1617-1624.
-
(2009)
Pharmacogenomics
, vol.10
, Issue.10
, pp. 1617-1624
-
-
Keskitalo, J.E.1
Pasanen, M.K.2
Neuvonen, P.J.3
Niemi, M.4
-
92
-
-
84925496475
-
Impact of ABCG2 and SLCO1B1 polymorphisms on pharmacokinetics of rosuvastatin, atorvastatin and simvastatin acid in Caucasian and Asian subjects: a class effect?
-
Birmingham BK, Bujac SR, Elsby R, et al. Impact of ABCG2 and SLCO1B1 polymorphisms on pharmacokinetics of rosuvastatin, atorvastatin and simvastatin acid in Caucasian and Asian subjects: a class effect? Eur J Clin Pharmacol. 2015;71(3):341-355.
-
(2015)
Eur J Clin Pharmacol
, vol.71
, Issue.3
, pp. 341-355
-
-
Birmingham, B.K.1
Bujac, S.R.2
Elsby, R.3
-
93
-
-
77951499767
-
ABCG2 polymorphism is associated with the low-density lipoprotein cholesterol response to rosuvastatin
-
Tomlinson B, Hu M, Lee VW, et al. ABCG2 polymorphism is associated with the low-density lipoprotein cholesterol response to rosuvastatin. Clin Pharmacol Ther. 2010;87(5):558-562.
-
(2010)
Clin Pharmacol Ther
, vol.87
, Issue.5
, pp. 558-562
-
-
Tomlinson, B.1
Hu, M.2
Lee, V.W.3
-
94
-
-
84875830097
-
ABCB1 gene polymorphisms, ABCB1 haplotypes and ABCG2 c.421c>A are determinants of inter-subject variability in rosuvastatin pharmacokinetics
-
Zhou Q, Ruan ZR, Yuan H, Xu DH, Zeng S. ABCB1 gene polymorphisms, ABCB1 haplotypes and ABCG2 c.421c>A are determinants of inter-subject variability in rosuvastatin pharmacokinetics. Pharmazie. 2013;68(2):129-134.
-
(2013)
Pharmazie
, vol.68
, Issue.2
, pp. 129-134
-
-
Zhou, Q.1
Ruan, Z.R.2
Yuan, H.3
Xu, D.H.4
Zeng, S.5
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