-
2
-
-
0344927562
-
Conjugate export pumps of the multidrug resistance protein (MRP) family: Localization, substrate specificity, and MRP2-mediated drug resistance
-
J. Konig, A. T. Nies, Y. Cui, I. Leier, and D. Keppler. Conjugate export pumps of the multidrug resistance protein (MRP) family: localization, substrate specificity, and MRP2-mediated drug resistance. Biochim. Biophys. Acta 1461:377-394 (1999).
-
(1999)
Biochim. Biophys. Acta
, vol.1461
, pp. 377-394
-
-
Konig, J.1
Nies, A.T.2
Cui, Y.3
Leier, I.4
Keppler, D.5
-
3
-
-
0034821939
-
The role of transport proteins in drug absorption, distribution and excretion
-
A. Ayrton and P. Morgan. The role of transport proteins in drug absorption, distribution and excretion. Xenobiotica 3:469-497 (2001).
-
(2001)
Xenobiotica
, vol.3
, pp. 469-497
-
-
Ayrton, A.1
Morgan, P.2
-
4
-
-
0033745088
-
Hepatic secretion of conjugated drugs and endogenous substances
-
D. Keppler and J. Konig. Hepatic secretion of conjugated drugs and endogenous substances. Semin. Liver Dis. 20:265-272 (2000).
-
(2000)
Semin. Liver Dis.
, vol.20
, pp. 265-272
-
-
Keppler, D.1
Konig, J.2
-
5
-
-
0034072174
-
Interactions of the human multidrug resistance proteins MRP1 and MRP2 with organic anions
-
E. Bakos, R. Evers, E. Sinko, A. Varadi, P. Borst, and B. Sarkadi. Interactions of the human multidrug resistance proteins MRP1 and MRP2 with organic anions. Mol. Pharmacol. 57:760-768 (2000).
-
(2000)
Mol. Pharmacol.
, vol.57
, pp. 760-768
-
-
Bakos, E.1
Evers, R.2
Sinko, E.3
Varadi, A.4
Borst, P.5
Sarkadi, B.6
-
6
-
-
0030753176
-
Methotrexate is excreted into the bile by canalicular multispecific organic anion transporter in rats
-
M. Masuda, Y. I'izuka, M. Yamazaki, R. Nishgaki, Y. Kato, K. Ni'inuma, H. Suzuki, and Y. Sugiyama. Methotrexate is excreted into the bile by canalicular multispecific organic anion transporter in rats. Cancer Res. 57:3506-3510 (1997).
-
(1997)
Cancer Res.
, vol.57
, pp. 3506-3510
-
-
Masuda, M.1
I'izuka, Y.2
Yamazaki, M.3
Nishgaki, R.4
Kato, Y.5
Ni'inuma, K.6
Suzuki, H.7
Sugiyama, Y.8
-
7
-
-
0030906434
-
Multiplicity of biliary excretion mechanisms for irinotecan, CPT-11, and its metabolites in rats
-
X. Y. Chu, Y. Kato, and Y. Sugiyama. Multiplicity of biliary excretion mechanisms for irinotecan, CPT-11, and its metabolites in rats. Cancer Res. 57:1934-1938 (1997).
-
(1997)
Cancer Res.
, vol.57
, pp. 1934-1938
-
-
Chu, X.Y.1
Kato, Y.2
Sugiyama, Y.3
-
9
-
-
0029026940
-
Different biliary excretion systems for glucuronide and sulfate of a model compound: Study using Eisai hyperbilirubinemic rats
-
O. Takenaka, T. Horie, H. Suzuki, and Y. Sugiyama. Different biliary excretion systems for glucuronide and sulfate of a model compound: study using Eisai hyperbilirubinemic rats. J. Pharmacol. Exp. Ther. 274:1362-1369 (1995).
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.274
, pp. 1362-1369
-
-
Takenaka, O.1
Horie, T.2
Suzuki, H.3
Sugiyama, Y.4
-
10
-
-
0033815393
-
Both cMOAT/MRP2 and another unknown transporter(s) are responsible for the biliary excretion of glucuronide conjugate of the nonpeptide angiotensin II antagonist, telmisaltan
-
Y. Kato, T. Igarashi, and Y. Sugiyama. Both cMOAT/MRP2 and another unknown transporter(s) are responsible for the biliary excretion of glucuronide conjugate of the nonpeptide angiotensin II antagonist, telmisaltan. Drug Metab. Disp. 28:1146-1148 (2000).
-
(2000)
Drug Metab. Disp.
, vol.28
, pp. 1146-1148
-
-
Kato, Y.1
Igarashi, T.2
Sugiyama, Y.3
-
11
-
-
0021804301
-
Hereditary chronic conjugated hyperbilirubinaemia in mutant rats caused by defective hepatic anion transport
-
P. L. M. Jansen, W. H. M. Peter, and W. H. Lamers. Hereditary chronic conjugated hyperbilirubinaemia in mutant rats caused by defective hepatic anion transport. Hepatology 5:573-579 (1985).
-
(1985)
Hepatology
, vol.5
, pp. 573-579
-
-
Jansen, P.L.M.1
Peter, W.H.M.2
Lamers, W.H.3
-
12
-
-
0000053197
-
The character of a new mutant in rats with hyperbilirubinuria syndrome
-
T. Mimaki, T. Nozaki, O. Tagaya, S. Hosokawa, T. Nakura, H. Mori, S. Kondou, Y. Matsubara, and T. Ougoh. The character of a new mutant in rats with hyperbilirubinuria syndrome. Congen. Anom. 26:250-251 (1986).
-
(1986)
Congen. Anom.
, vol.26
, pp. 250-251
-
-
Mimaki, T.1
Nozaki, T.2
Tagaya, O.3
Hosokawa, S.4
Nakura, T.5
Mori, H.6
Kondou, S.7
Matsubara, Y.8
Ougoh, T.9
-
13
-
-
0031031247
-
Molecular cloning of canaliculiar multispecific organic anion transporter defective in EHBR
-
K. Ito, H. Suzuki, T. Hirohashi, K. Kume, T. Shimizu, and Y. Sugiyama. Molecular cloning of canaliculiar multispecific organic anion transporter defective in EHBR. Am. J. Physiol. 272:G16-G22 (1997).
-
(1997)
Am. J. Physiol.
, vol.272
-
-
Ito, K.1
Suzuki, H.2
Hirohashi, T.3
Kume, K.4
Shimizu, T.5
Sugiyama, Y.6
-
14
-
-
0030951558
-
Temocaprilat, a novel angiotensin-converting enzyme inhibitor, is excreted in bile via an ATP-dependent active transporter (cMOAT) that is deficient in Eisai hyperbilirubinemic mutant rats (EHBR)
-
H. Ishizuka, K. Konno, H. Naganuma, K. Sasahara, Y. Kawahara, K. Ninuma, H. Suzuki, and Y. Sugiyama. Temocaprilat, a novel angiotensin-converting enzyme inhibitor, is excreted in bile via an ATP-dependent active transporter (cMOAT) that is deficient in Eisai hyperbilirubinemic mutant rats (EHBR). J. Pharmacol. Exp. Ther. 280:1304-1311 (1997).
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.280
, pp. 1304-1311
-
-
Ishizuka, H.1
Konno, K.2
Naganuma, H.3
Sasahara, K.4
Kawahara, Y.5
Ninuma, K.6
Suzuki, H.7
Sugiyama, Y.8
-
15
-
-
0030862073
-
Biliary excretion of pravastatin in rats: Contribution of the excretion pathways mediated by the canalicular multispecific organic anion transporter (cMOAT)
-
M. Yamazaki, S. Akiyama, K. Ni'inuma, R. Nishigaki, and Y. Sugiyama. Biliary excretion of pravastatin in rats: contribution of the excretion pathways mediated by the canalicular multispecific organic anion transporter (cMOAT). Drug Metab. Disp. 25:1123-1129 (1997).
-
(1997)
Drug Metab. Disp.
, vol.25
, pp. 1123-1129
-
-
Yamazaki, M.1
Akiyama, S.2
Ni'inuma, K.3
Nishigaki, R.4
Sugiyama, Y.5
-
16
-
-
0033623722
-
Biliary excretion of 17β-estradiol 17β-D-glucuronide is predominantly mediated by cMOAT/MRP 2
-
A. Morikawa, Y. Goto, H. Suzuki, T. Hirohashi, and Y. Sugiyama. Biliary excretion of 17β-estradiol 17β-D-glucuronide is predominantly mediated by cMOAT/MRP2. Pharm. Res. 17:546-552 (2000).
-
(2000)
Pharm. Res.
, vol.17
, pp. 546-552
-
-
Morikawa, A.1
Goto, Y.2
Suzuki, H.3
Hirohashi, T.4
Sugiyama, Y.5
-
17
-
-
0034119967
-
Expression and localization of multidrug resistant protein mrp 2 in rat small intestine
-
A. D. Mottino, T. Hoffman, L. Jennes, and M. Vore. Expression and localization of multidrug resistant protein mrp2 in rat small intestine. J. Pharmacol. Exp. Ther. 293:717-723 (2000).
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.293
, pp. 717-723
-
-
Mottino, A.D.1
Hoffman, T.2
Jennes, L.3
Vore, M.4
-
18
-
-
0033958156
-
Involvement of an organic anion transporter (canalicular multispecific organic anion transporter/multidrug resistance-associated protein 2) in gastrointestinal secretion of glutathione conjugates in rats
-
Y. Gotoh, H. Suzuki, S. Kinoshita, T. Hirohashi, Y. Kato, and Y. Sugiyama. Involvement of an organic anion transporter (canalicular multispecific organic anion transporter/multidrug resistance-associated protein 2) in gastrointestinal secretion of glutathione conjugates in rats. J. Pharmacol. Exp. Ther. 292:433-439 (2000).
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.292
, pp. 433-439
-
-
Gotoh, Y.1
Suzuki, H.2
Kinoshita, S.3
Hirohashi, T.4
Kato, Y.5
Sugiyama, Y.6
-
19
-
-
0035034532
-
Increased bioavailability of the food-derived carcinogen 2-amino-1-methyl-6-pheylimidazo[4,5-b]pyridine in Mrp-2-deficient rats
-
C. G. Dietrich, D. R. D. Waart, R. Ottenhoff, and I. G. Schoots. Increased bioavailability of the food-derived carcinogen 2-amino-1-methyl-6-pheylimidazo[4,5-b]pyridine in Mrp-2-deficient rats. Mol. Pharmacol. 59:974-980 (2001).
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 974-980
-
-
Dietrich, C.G.1
Waart, D.R.D.2
Ottenhoff, R.3
Schoots, I.G.4
-
21
-
-
3543011948
-
Pharmacokinetic and pharmacodynamic changes of furosemide after intravenous and oral administration to rats with alloxan-induced diabetes mellitus
-
J. H. Park, W. I. Lee, W. H. Yoon, Y. D. Park, J. S. Lee, and M. G. Lee. Pharmacokinetic and pharmacodynamic changes of furosemide after intravenous and oral administration to rats with alloxan-induced diabetes mellitus. Biopharm. Drug Disp. 19:357-364 (1998).
-
(1998)
Biopharm. Drug Disp.
, vol.19
, pp. 357-364
-
-
Park, J.H.1
Lee, W.I.2
Yoon, W.H.3
Park, Y.D.4
Lee, J.S.5
Lee, M.G.6
-
22
-
-
0016238366
-
Excretion of probenecid and its metabolites in bile and urine of rats
-
W. D. Conway and S. Melethil. Excretion of probenecid and its metabolites in bile and urine of rats. J. Pharm. Sci. 63:1551-1554 (1974).
-
(1974)
J. Pharm. Sci.
, vol.63
, pp. 1551-1554
-
-
Conway, W.D.1
Melethil, S.2
-
24
-
-
0034071009
-
Species difference in oral bioavailability of methotrexate between rats and monkeys
-
T. Kuroda, K. Namba, T. Torimaru, K. Kawashima, and M. Hayashi. Species difference in oral bioavailability of methotrexate between rats and monkeys. Biol. Pharm. Bull. 23:334-338 (2000).
-
(2000)
Biol. Pharm. Bull.
, vol.23
, pp. 334-338
-
-
Kuroda, T.1
Namba, K.2
Torimaru, T.3
Kawashima, K.4
Hayashi, M.5
-
25
-
-
0035149324
-
Development of an in vitro preclinical screen model to estimate absorption and bioavailability of xenobiotics
-
K. W. Ward, J. W. Proksch, M. A. Levy, and B. R. Smith. Development of an in vitro preclinical screen model to estimate absorption and bioavailability of xenobiotics. Drug Metab. Disp. 28:82-88 (2001).
-
(2001)
Drug Metab. Disp.
, vol.28
, pp. 82-88
-
-
Ward, K.W.1
Proksch, J.W.2
Levy, M.A.3
Smith, B.R.4
-
26
-
-
0035012079
-
Inhibition of biliary excretion of methotrexate by probenecid in rats: Quantitative prediction of interaction from in vitro data
-
K. Ueda, K. Kato, K. Komatsu, and Y. Sugiyama. Inhibition of biliary excretion of methotrexate by probenecid in rats: quantitative prediction of interaction from in vitro data. J. Pharmacol. Exp. Ther 297:1036-1043 (2001)
-
(2001)
J. Pharmacol. Exp. Ther
, vol.297
, pp. 1036-1043
-
-
Ueda, K.1
Kato, K.2
Komatsu, K.3
Sugiyama, Y.4
-
27
-
-
0034747783
-
Effect of probenecid on fluorescein transport in the central nervous system using in vitro and in vivo models
-
H. Sun, D. W. Miller, and W. F. Elmquist. Effect of probenecid on fluorescein transport in the central nervous system using in vitro and in vivo models. Pharm. Res. 18:1542-1549 (2001).
-
(2001)
Pharm. Res.
, vol.18
, pp. 1542-1549
-
-
Sun, H.1
Miller, D.W.2
Elmquist, W.F.3
|