-
1
-
-
0038449770
-
-
57th ed. Montvale. NJ: Medical Economics Company
-
Physicians' Desk Reference, 57th ed. Montvale. NJ: Medical Economics Company; 2004.
-
(2004)
Physicians' Desk Reference
-
-
-
2
-
-
0028869086
-
Rapamune (sirolimus, rapamycin): An overview and mechanism of action
-
Sehgal SN. Rapamune (sirolimus, rapamycin): an overview and mechanism of action. Ther Drug Vonit. 1995;17:660-665.
-
(1995)
Ther. Drug Vonit.
, vol.17
, pp. 660-665
-
-
Sehgal, S.N.1
-
3
-
-
33646648946
-
-
United States Pharmacopeial Convention. Rockville, MD: United States Pharmacopeial Convention
-
United States Pharmacopeial Convention. USP Dictionary of USAN and International Drug Names. Rockville, MD: United States Pharmacopeial Convention.
-
USP Dictionary of USAN and International Drug Names
-
-
-
4
-
-
0025893168
-
Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes
-
Liu J, Farmer JD Jr, Lane WS, Friedman J, Weissman I, Schreiber SL. Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes. Cell. 1991;66:807-815.
-
(1991)
Cell
, vol.66
, pp. 807-815
-
-
Liu, J.1
Farmer Jr., J.D.2
Lane, W.S.3
Friedman, J.4
Weissman, I.5
Schreiber, S.L.6
-
5
-
-
0001940434
-
Immunomodulators: Immunosuppressive agents and immunostimulants
-
Hardman JG, Limbird LE, eds. 9th ed, New York. NY: McGraw-Hill
-
Diasio RB, LoBuglio AF. Immunomodulators: immunosuppressive agents and immunostimulants. In: Hardman JG, Limbird LE, eds. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 9th ed, New York. NY: McGraw-Hill; 1995:1291-1308.
-
(1995)
Goodman and Gilman's The Pharmacological Basis of Therapeutics
, pp. 1291-1308
-
-
Diasio, R.B.1
LoBuglio, A.F.2
-
6
-
-
0028950217
-
Isolation of a protein target of the FKBP 12-rapamycin complex in mammalian cells
-
Sabers CJ, Martin MM, Brunn GJ, et al. Isolation of a protein target of the FKBP 12-rapamycin complex in mammalian cells. J Biol Chem. 1995;270:815-822.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 815-822
-
-
Sabers, C.J.1
Martin, M.M.2
Brunn, G.J.3
-
7
-
-
0029842109
-
Structure of the FKBP12-rapamycin complex interacting with the binding domain of human FRAP
-
Choi J, Chen J, Schreiber SL, Clardy J. Structure of the FKBP12-rapamycin complex interacting with the binding domain of human FRAP. Science. 1996;273:239-242.
-
(1996)
Science
, vol.273
, pp. 239-242
-
-
Choi, J.1
Chen, J.2
Schreiber, S.L.3
Clardy, J.4
-
8
-
-
0028032355
-
Rapamycin selectively inhibits translation of mRNAs encoding elongation factors and ribosomal proteins
-
Terada N, Patel HR, Takase K, Kohno K, Nairn AC, Gelfand EW. Rapamycin selectively inhibits translation of mRNAs encoding elongation factors and ribosomal proteins. Proc Natl Acad Sci U S A. 1994;91:11477-11481.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 11477-11481
-
-
Terada, N.1
Patel, H.R.2
Takase, K.3
Kohno, K.4
Nairn, A.C.5
Gelfand, E.W.6
-
9
-
-
0028899974
-
Rapamycin selectively blocks interleukin-2 induced proliferating cell nuclear antigen gene expression in T lymphocyte
-
Feuerstein N, Huang D, Prystowsky MB. Rapamycin selectively blocks interleukin-2 induced proliferating cell nuclear antigen gene expression in T lymphocyte. J Biol Chem. 1995;270:9454-9458.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 9454-9458
-
-
Feuerstein, N.1
Huang, D.2
Prystowsky, M.B.3
-
10
-
-
0028172867
-
Interleukin-2-mediated elimination of the p27Kip1 cyclin-dependent kinase inhibitor prevented by rapamycin
-
Nourse J, Firpo E, Flanagan WM, et al. Interleukin-2-mediated elimination of the p27Kip1 cyclin-dependent kinase inhibitor prevented by rapamycin. Nature. 1994;372:570-573.
-
(1994)
Nature
, vol.372
, pp. 570-573
-
-
Nourse, J.1
Firpo, E.2
Flanagan, W.M.3
-
13
-
-
4244174370
-
Sirolimus oral solution and tablets demonstrate equivalent safety and efficacy in renal allograft patients
-
Van Buren CT. Sirolimus oral solution and tablets demonstrate equivalent safety and efficacy in renal allograft patients. Transplantation. 2000;69(suppl):S153-S154.
-
(2000)
Transplantation
, vol.69
, Issue.SUPPL.
-
-
Van Buren, C.T.1
-
14
-
-
0033346578
-
The effect of a high-fat rneal on the oral bioavailability of the immunosuppressant sirolimus (rapamycin)
-
Zimmerman JJ, Ferron GM, Lim HK, Parker V. The effect of a high-fat rneal on the oral bioavailability of the immunosuppressant sirolimus (rapamycin). J Clin Pharmacol. 1999;39:1155-1161.
-
(1999)
J. Clin. Pharmacol.
, vol.39
, pp. 1155-1161
-
-
Zimmerman, J.J.1
Ferron, G.M.2
Lim, H.K.3
Parker, V.4
-
15
-
-
63549099427
-
The effect of ethnicity on the pharmacokinetics of sirolimus: A population pharmacokinetic analysis of phase 1 data
-
[abstract]. Abstract 2353
-
Pentikis H, Kriebel W, Reis P, Zimmerman JJ. The effect of ethnicity on the pharmacokinetics of sirolimus: a population pharmacokinetic analysis of phase 1 data [abstract]. AAPS Pharm Sci. 2003;5(S4):Abstract 2353.
-
(2003)
AAPS Pharm. Sci.
, Issue.5 SUPPL. 4
-
-
Pentikis, H.1
Kriebel, W.2
Reis, P.3
Zimmerman, J.J.4
-
16
-
-
85071409572
-
Safety and pharmacokinetics of ascending single doses of sirolimus (Rapamune®, rapamycin) in pediatric patients with stable chronic renal failure undergoing dialysis
-
In press
-
Tejani A, Alexander S, Ettengger R, et al. Safety and pharmacokinetics of ascending single doses of sirolimus (Rapamune®, rapamycin) in pediatric patients with stable chronic renal failure undergoing dialysis. Pediatr Transplant. In press.
-
Pediatr. Transplant.
-
-
Tejani, A.1
Alexander, S.2
Ettengger, R.3
-
17
-
-
0034080767
-
Introduction and overview (Advances in therapeutic drug monitoring for immunosuppressants: A review of sirolimus)
-
Shaw LM, Kaplan B, Brayman KL. Introduction and overview (Advances in therapeutic drug monitoring for immunosuppressants: a review of sirolimus). Clin Ther. 2000;22(suppl B):B1-B13.
-
(2000)
Clin. Ther.
, vol.22
, Issue.SUPPL. B
-
-
Shaw, L.M.1
Kaplan, B.2
Brayman, K.L.3
-
18
-
-
0034121591
-
An immunoassay for the measurement of sirolimus
-
Jones K, Saadat-Lajevardi S, Lee T, et al. An immunoassay for the measurement of sirolimus. Clin Ther. 2000;22(suppl B):B49-B61.
-
(2000)
Clin. Ther.
, vol.22
, Issue.SUPPL. B
-
-
Jones, K.1
Saadat-Lajevardi, S.2
Lee, T.3
-
19
-
-
0141653840
-
Pharmacokinetic interactions between sirolimus and microemulsion cyclosporine when orally administered jointly and 4 hours apart
-
Zimmerman JJ, Harper D, Getsy J, Jusko WJ. Pharmacokinetic interactions between sirolimus and microemulsion cyclosporine when orally administered jointly and 4 hours apart. J Clin Pharmacol. 2003;43:1168-1176.
-
(2003)
J. Clin. Pharmacol.
, vol.43
, pp. 1168-1176
-
-
Zimmerman, J.J.1
Harper, D.2
Getsy, J.3
Jusko, W.J.4
-
20
-
-
0004282518
-
-
SAS Institute Inc. Cary, NC: SAS Institute Inc
-
SAS Institute Inc. SAS/STAT, User's Guide, Version 8. Cary, NC: SAS Institute Inc; 2000.
-
(2000)
SAS/STAT, User's Guide, Version 8
-
-
-
21
-
-
84946640223
-
Transformation of the independent variables
-
Box GEP, Tidwell PW. Transformation of the independent variables. Technometrics. 1962;4:531-550.
-
(1962)
Technometrics
, vol.4
, pp. 531-550
-
-
Box, G.E.P.1
Tidwell, P.W.2
-
22
-
-
0026662551
-
Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat
-
Sattler M, Guengerich FP, Yun CH, et al. Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat. Drug Metab Disp. 1992;20:753-761.
-
(1992)
Drug Metab. Disp.
, vol.20
, pp. 753-761
-
-
Sattler, M.1
Guengerich, F.P.2
Yun, C.H.3
-
23
-
-
0031863355
-
Metabolism and transport of the macrolide immunosuppressant sirolimus in the small intestine
-
Lampen A, Zhang Y, Hackbarth I, et al. Metabolism and transport of the macrolide immunosuppressant sirolimus in the small intestine. J Pharmacol Exp Ther. 1998;285:1104-1112.
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.285
, pp. 1104-1112
-
-
Lampen, A.1
Zhang, Y.2
Hackbarth, I.3
-
24
-
-
2042466413
-
14C-Rapamucin (sirolimus) in healthy male subjects after a single oral dose
-
[abstract]
-
14C-Rapamucin (sirolimus) in healthy male subjects after a single oral dose [abstract]. ISSX Proc. 1997;12:26.
-
(1997)
ISSX Proc.
, vol.12
, pp. 26
-
-
Leung, L.Y.1
Zimmerman, J.2
Lim, H.K.3
-
25
-
-
0031786057
-
In vitro and in situ absorption of SDZ-RAD using a human intestinal cell line (Caco-2) and a single pass perfusion model in rats: Comparison with rapamycin
-
Crowe A, Lemaire M. In vitro and in situ absorption of SDZ-RAD using a human intestinal cell line (Caco-2) and a single pass perfusion model in rats: comparison with rapamycin. Pharm Res. 1998;15:1666-1672.
-
(1998)
Pharm. Res.
, vol.15
, pp. 1666-1672
-
-
Crowe, A.1
Lemaire, M.2
-
26
-
-
0023447098
-
Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues
-
Thiebaut F, Tsuruo T, Hamada H, Gottesman MM, Pastan I, Willingham MC. Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. Proc Natl Acad Sci U S A. 1987;84:7735-7738.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 7735-7738
-
-
Thiebaut, F.1
Tsuruo, T.2
Hamada, H.3
Gottesman, M.M.4
Pastan, I.5
Willingham, M.C.6
-
27
-
-
0030581087
-
Active secretion and enterocytic drug metabolism barriers to drug absorption
-
Wacher VJ, Salphati L, Benet LZ. Active secretion and enterocytic drug metabolism barriers to drug absorption. Adv Drug Deliv Rev. 1996;20:99-112.
-
(1996)
Adv. Drug Deliv. Rev.
, vol.20
, pp. 99-112
-
-
Wacher, V.J.1
Salphati, L.2
Benet, L.Z.3
-
28
-
-
0035054725
-
The gut as a barrier to drug absorption: Combined role of cytochrome P450 3A and P-glycoprotein
-
Zhang Y, Benet LZ. The gut as a barrier to drug absorption: combined role of cytochrome P450 3A and P-glycoprotein. Clin Pharmacokinet. 2001;40:159-168.
-
(2001)
Clin. Pharmacokinet.
, vol.40
, pp. 159-168
-
-
Zhang, Y.1
Benet, L.Z.2
-
29
-
-
0035137211
-
Pharmacokinetic interaction between single oral doses of diltiazem and sirolimus in healthy volunteers
-
Bottiger Y, Sawe J, Brattstrom C, et al. Pharmacokinetic interaction between single oral doses of diltiazem and sirolimus in healthy volunteers. Clin Pharmacol Ther. 2001;69:32-40.
-
(2001)
Clin. Pharmacol. Ther.
, vol.69
, pp. 32-40
-
-
Bottiger, Y.1
Sawe, J.2
Brattstrom, C.3
-
30
-
-
0001319826
-
Sirolimus oral bioavailability increases eleven-fold with concomitant ketoconazole
-
[abstract]
-
Floren LC, Christians U, Zimmerman JJ, et al. Sirolimus oral bioavailability increases eleven-fold with concomitant ketoconazole [abstract]. Clin Pharmacol Ther. 1999;65:159.
-
(1999)
Clin. Pharmacol. Ther.
, vol.65
, pp. 159
-
-
Floren, L.C.1
Christians, U.2
Zimmerman, J.J.3
-
31
-
-
33646635854
-
Pharmacokinetic (PK) interaction study of sirolimus (SRL) and cyclosporine (CsA)
-
[abstract]
-
Patat A, Zimmerman JJ, Parks V, Richards J. Pharmacokinetic (PK) interaction study of sirolimus (SRL) and cyclosporine (CsA) [abstract]. Clin Pharmacol Ther. 2004;75:33.
-
(2004)
Clin. Pharmacol. Ther.
, vol.75
, pp. 33
-
-
Patat, A.1
Zimmerman, J.J.2
Parks, V.3
Richards, J.4
-
32
-
-
33646645259
-
Potential pharmacokinetic interactions between sirolimus and atorvastatin
-
eds. [abstract]. (Oct 6-11)
-
Zimmerman JJ, Harper D, Speth JT, Fruncillo RJ, Getsy J, eds. Potential pharmacokinetic interactions between sirolimus and atorvastatin [abstract]. ESOT. 2001;(Oct 6-11):145.
-
(2001)
ESOT
, pp. 145
-
-
Zimmerman, J.J.1
Harper, D.2
Speth, J.T.3
Fruncillo, R.J.4
Getsy, J.5
-
33
-
-
0006562890
-
Potential pharmacokinetic interactions between sirolimus and tacrolimus
-
[abstract]
-
Zimmerman JJ, Patat A, Souan J-L, Paty I, Cadieu G. Potential pharmacokinetic interactions between sirolimus and tacrolimus [abstract]. Am J Transplant. 2001;1(suppl 1):384.
-
(2001)
Am. J. Transplant.
, vol.1
, Issue.SUPPL. 1
, pp. 384
-
-
Zimmerman, J.J.1
Patat, A.2
Souan, J.-L.3
Paty, I.4
Cadieu, G.5
-
34
-
-
0025168996
-
Identification of the rabbit and human cytochromes P-450IIIA as the major enzymes involved in the N-demethylation of diltiazem
-
Pichard L, Gillet G, Fabre I, et al. Identification of the rabbit and human cytochromes P-450IIIA as the major enzymes involved in the N-demethylation of diltiazem. Drug Metab Dispos. 1990;18:711-719.
-
(1990)
Drug Metab. Dispos.
, vol.18
, pp. 711-719
-
-
Pichard, L.1
Gillet, G.2
Fabre, I.3
-
35
-
-
0025134337
-
Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A Oxidase) in primary cultures of human hepatocytes and liver microsomes
-
Pichard L, Fabre I, Fabre G, et al. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A Oxidase) in primary cultures of human hepatocytes and liver microsomes. Drug Metab Dispos. 1990;18:595-606.
-
(1990)
Drug Metab. Dispos.
, vol.18
, pp. 595-606
-
-
Pichard, L.1
Fabre, I.2
Fabre, G.3
-
36
-
-
0027309055
-
P-glycoprotein-mediated transcellular transport of MDR-reversing agents
-
Saeki T, Ueda K, Tanigawara Y, Hori R, Komano T. P-glycoprotein-mediated transcellular transport of MDR-reversing agents. Fed Europ Biochem Soc. 1993;324:99-102.
-
(1993)
Fed. Europ. Biochem. Soc.
, vol.324
, pp. 99-102
-
-
Saeki, T.1
Ueda, K.2
Tanigawara, Y.3
Hori, R.4
Komano, T.5
-
37
-
-
0031900997
-
Role of P-glycoprotein as a secretory mechanism in quinidine absorption from rat small intestine
-
Emi Y, Tsunashima D, Ogawara K-I, Higaki K, Kimura T. Role of P-glycoprotein as a secretory mechanism in quinidine absorption from rat small intestine. J Pharm Sci. 1998;87:295-299.
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 295-299
-
-
Emi, Y.1
Tsunashima, D.2
Ogawara, K.-I.3
Higaki, K.4
Kimura, T.5
-
38
-
-
0027295760
-
Identification of P450 enzymes involved in metabolism of verapamil in humans
-
Kroemer HK, Gautier J-C, Beaune P, Henderson C, Wolf CR, Eichelbaum M. Identification of P450 enzymes involved in metabolism of verapamil in humans. Arch Pharmacol. 1993;348:332-337.
-
(1993)
Arch. Pharmacol.
, vol.348
, pp. 332-337
-
-
Kroemer, H.K.1
Gautier, J.-C.2
Beaune, P.3
Henderson, C.4
Wolf, C.R.5
Eichelbaum, M.6
-
39
-
-
0021825310
-
Inhibition of hepatic microsomal drug metabolism by the calcium channel blockers diltiazem and verapamil
-
Renton KW. Inhibition of hepatic microsomal drug metabolism by the calcium channel blockers diltiazem and verapamil. Biochem Pharmacol. 1985;34:2533-2549.
-
(1985)
Biochem. Pharmacol.
, vol.34
, pp. 2533-2549
-
-
Renton, K.W.1
-
40
-
-
0024421664
-
Reversal mechanism of multidrug resistance by verapamil: Direct binding of verapamil to P-glycoprotein on specific sites and transport of verapamil outward across the plasma membrane of K562/ADM cells
-
Yusa K, Tsurua T. Reversal mechanism of multidrug resistance by verapamil: direct binding of verapamil to P-glycoprotein on specific sites and transport of verapamil outward across the plasma membrane of K562/ADM cells. Cancer Res. 1989;49:5002-5006.
-
(1989)
Cancer Res.
, vol.49
, pp. 5002-5006
-
-
Yusa, K.1
Tsurua, T.2
-
41
-
-
0026654583
-
Stereoisomers of calcium antagonists which differ markedly in their potencies as calcium blockers are equally effective in modulating drug transport by P-glycoprotein
-
Hollt V, Kouba M, Dietel M, Vogt G. Stereoisomers of calcium antagonists which differ markedly in their potencies as calcium blockers are equally effective in modulating drug transport by P-glycoprotein. Biochem Pharmacol. 1992;43:2601-2608.
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 2601-2608
-
-
Hollt, V.1
Kouba, M.2
Dietel, M.3
Vogt, G.4
-
43
-
-
0345411341
-
P-glycoprotein and cytochrome P-450 3A inhibition: Dissociation of inhibitory potencies
-
Wandel C, Kim RB, Kajiji S, Guengerich FP, Wilkinson GR, Wood AJJ. P-glycoprotein and cytochrome P-450 3A inhibition: dissociation of inhibitory potencies. Cancer Res. 1999;3944-3948.
-
(1999)
Cancer Res.
, pp. 3944-3948
-
-
Wandel, C.1
Kim, R.B.2
Kajiji, S.3
Guengerich, F.P.4
Wilkinson, G.R.5
Wood, A.J.J.6
-
44
-
-
0027418815
-
Human P-glycoprotein transports cyclosporin A and FK506
-
Saeki T, Ueda K, Tanigawara Y, Hori R, Komano T. Human P-glycoprotein transports cyclosporin A and FK506. J Biol Chem. 1993;268:6077-6080.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 6077-6080
-
-
Saeki, T.1
Ueda, K.2
Tanigawara, Y.3
Hori, R.4
Komano, T.5
-
45
-
-
0026601064
-
Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol
-
Hunt CM, Watkins PB, Saenger P, et al. Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol. Clin Pharmacol Ther. 1992;51:18-23.
-
(1992)
Clin. Pharmacol. Ther.
, vol.51
, pp. 18-23
-
-
Hunt, C.M.1
Watkins, P.B.2
Saenger, P.3
-
46
-
-
0020575075
-
Effects of erythromycin on hepatic drug-metabolizing enzymes in humans
-
Larrey D, Funck-Brentano C, Breil P, et al. Effects of erythromycin on hepatic drug-metabolizing enzymes in humans. Biochem Pharmacol. 1983;32:1063-1068.
-
(1983)
Biochem. Pharmacol.
, vol.32
, pp. 1063-1068
-
-
Larrey, D.1
Funck-Brentano, C.2
Breil, P.3
-
47
-
-
0032907322
-
Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein
-
Kim RB, Wandel C, Leake B, et al. Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharm Res. 1999;16:408-413.
-
(1999)
Pharm. Res.
, vol.16
, pp. 408-413
-
-
Kim, R.B.1
Wandel, C.2
Leake, B.3
-
48
-
-
0024381034
-
Reversal of drug resistance by erythromycin: Erythromycin increases the accumulation of actinomycin D and doxorubicin in multidrug-resistant cells
-
Hofsli E, Nissen-Meyer J. Reversal of drug resistance by erythromycin: erythromycin increases the accumulation of actinomycin D and doxorubicin in multidrug-resistant cells. Int J Cancer. 1989;44:149-154.
-
(1989)
Int. J. Cancer
, vol.44
, pp. 149-154
-
-
Hofsli, E.1
Nissen-Meyer, J.2
-
49
-
-
0028970047
-
Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9
-
Baldwin SJ, Bloomer JC, Smith GJ, Ayrton AD, Clarke SE, Chenery RJ. Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9. Xenobiotica. 1995;25:261-270.
-
(1995)
Xenobiotica
, vol.25
, pp. 261-270
-
-
Baldwin, S.J.1
Bloomer, J.C.2
Smith, G.J.3
Ayrton, A.D.4
Clarke, S.E.5
Chenery, R.J.6
-
50
-
-
0028098101
-
Ketoconazole effectively reverses multidrug resistance in highly resistant KB cell
-
Siegmund MJ, Cardarelli C, Aksenriwevich I, Sugimoto Y, Pastan I, Gottesman MM. Ketoconazole effectively reverses multidrug resistance in highly resistant KB cell. J Urol. 1994;151:485-491.
-
(1994)
J. Urol.
, vol.151
, pp. 485-491
-
-
Siegmund, M.J.1
Cardarelli, C.2
Aksenriwevich, I.3
Sugimoto, Y.4
Pastan, I.5
Gottesman, M.M.6
-
51
-
-
0026464616
-
Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes
-
Kolars JC, Schmiedlin-Ren P, Schuetz JD, Fang C, Watkins PB. Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. J Clin Invest. 1992;90:1871-1878.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 1871-1878
-
-
Kolars, J.C.1
Schmiedlin-Ren, P.2
Schuetz, J.D.3
Fang, C.4
Watkins, P.B.5
-
52
-
-
0033753435
-
Induction of P-glycoprotein by rifampin increases intestinal secretion of talinolol in human beings: A new type of drug/drug interaction
-
Westphal K, Weinbrenner A, Zschiesche M, et al. Induction of P-glycoprotein by rifampin increases intestinal secretion of talinolol in human beings: a new type of drug/drug interaction. Clin Pharmacol Ther. 2000;68:345-355.
-
(2000)
Clin. Pharmacol. Ther.
, vol.68
, pp. 345-355
-
-
Westphal, K.1
Weinbrenner, A.2
Zschiesche, M.3
-
53
-
-
0033783036
-
Lactonization is the critical first step in the disposition of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor atorvastatin
-
Jacobsen W, Kuhn B, Soldner A, et al. Lactonization is the critical first step in the disposition of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor atorvastatin. Drug Metab Dispos. 2000;28:1369-1378.
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 1369-1378
-
-
Jacobsen, W.1
Kuhn, B.2
Soldner, A.3
-
54
-
-
0033678688
-
Atorvastatin coadministration may increase digoxin concentrations by inhibition of intestinal P-glycoprotein-mediated secretion
-
Boyd RA, Stern RH, Stewart BH, et al. Atorvastatin coadministration may increase digoxin concentrations by inhibition of intestinal P-glycoprotein-mediated secretion. J Clin Pharmacol. 2000;40:91-98.
-
(2000)
J. Clin. Pharmacol.
, vol.40
, pp. 91-98
-
-
Boyd, R.A.1
Stern, R.H.2
Stewart, B.H.3
-
55
-
-
0027102401
-
The MDR1 gene product, p-glycoprotein, mediates the transport of the cardiac glycoside, digoxin
-
De Lannoy IA, Silverman M. The MDR1 gene product, p-glycoprotein, mediates the transport of the cardiac glycoside, digoxin. Biochem Biophys Res Commun. 1992;189:51-557.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.189
, pp. 51-557
-
-
De Lannoy, I.A.1
Silverman, M.2
-
56
-
-
0025646757
-
Catalytic activities of human liver cytochrome P-450 IIIA4 expressed in saccharomyces cerevisiae
-
Brian WR, Sari M-A, Iwasaki M, Shimada T, Kaminsky LS, Guengerich FP. Catalytic activities of human liver cytochrome P-450 IIIA4 expressed in saccharomyces cerevisiae. Biochemistry. 1990;29:11280-11292.
-
(1990)
Biochemistry
, vol.29
, pp. 11280-11292
-
-
Brian, W.R.1
Sari, M.-A.2
Iwasaki, M.3
Shimada, T.4
Kaminsky, L.S.5
Guengerich, F.P.6
-
57
-
-
0025860978
-
Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrome P-450 IIIA4
-
Guengerich FP, Brian WR, Iwasaki M, Sari M-A, Baarnhielm C, Berntsson P. Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrome P-450 IIIA4. J Med Chem. 1991;34:1838-1844.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1838-1844
-
-
Guengerich, F.P.1
Brian, W.R.2
Iwasaki, M.3
Sari, M.-A.4
Baarnhielm, C.5
Berntsson, P.6
-
58
-
-
0026722491
-
Immunosuppressants FK506 and rapamycin function as reversal agents of the multidrug resistance phenotype
-
Arceci RJ, Stieglitz K, Bierer BE. Immunosuppressants FK506 and rapamycin function as reversal agents of the multidrug resistance phenotype. Blood. 1992;80:1528-1536.
-
(1992)
Blood
, vol.80
, pp. 1528-1536
-
-
Arceci, R.J.1
Stieglitz, K.2
Bierer, B.E.3
|