-
1
-
-
63449139456
-
Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding
-
Aller, S. G., Yu, J., Ward, A., Weng, Y., Chittaboina, S., Zhuo, R., Harrell, P. M., Trinh, Y. T., Zhang, Q., Urbatsch, I. L., et al. (2009). Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science 323, 1718-1722.
-
(2009)
Science
, vol.323
, pp. 1718-1722
-
-
Aller, S.G.1
Yu, J.2
Ward, A.3
Weng, Y.4
Chittaboina, S.5
Zhuo, R.6
Harrell, P.M.7
Trinh, Y.T.8
Zhang, Q.9
Urbatsch, I.L.10
-
2
-
-
0033214124
-
Co-operative binding sites for transported substrates in the multiple drug resistance transporter Mdr1
-
Buxbaum, E. (1999). Co-operative binding sites for transported substrates in the multiple drug resistance transporter Mdr1. Eur. J. Biochem. 265, 64-70.
-
(1999)
Eur. J. Biochem.
, vol.265
, pp. 64-70
-
-
Buxbaum, E.1
-
3
-
-
0347683446
-
Molecular modeling correctly predicts the functional importance of Phe594 in transmembrane helix 11 of the multidrug resistance protein, MRP1 (ABCC1)
-
Campbell, J. D., Koike, K., Moreau, C., Sansom, M. S., Deeley, R. G., and Cole, S. P. (2004). Molecular modeling correctly predicts the functional importance of Phe594 in transmembrane helix 11 of the multidrug resistance protein, MRP1 (ABCC1). J. Biol. Chem. 279, 463-468.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 463-468
-
-
Campbell, J.D.1
Koike, K.2
Moreau, C.3
Sansom, M.S.4
Deeley, R.G.5
Cole, S.P.6
-
4
-
-
77956405769
-
Pharmacokinetics of bisphenol A in neonatal and adult rhesus monkeys
-
Doerge, D., Twaddle, N. C., Woodling, K. A., and Fisher, J. W. (2010). Pharmacokinetics of bisphenol A in neonatal and adult rhesus monkeys. Toxicol. Appl. Pharmacol. 248, 1-11.
-
(2010)
Toxicol. Appl. Pharmacol.
, vol.248
, pp. 1-11
-
-
Doerge, D.1
Twaddle, N.C.2
Woodling, K.A.3
Fisher, J.W.4
-
5
-
-
80052363545
-
Distribution of bisphenol A into tissues of adult, neonatal, and fetal Sprague-Dawley rats
-
Doerge, D. R., Twaddle, N. C., Vanlandingham, M., Brown, R. P., and Fisher, J. W. (2011a). Distribution of bisphenol A into tissues of adult, neonatal, and fetal Sprague-Dawley rats. Toxicol. Appl. Pharmacol. 255, 261-270.
-
(2011)
Toxicol. Appl. Pharmacol.
, vol.255
, pp. 261-270
-
-
Doerge, D.R.1
Twaddle, N.C.2
Vanlandingham, M.3
Brown, R.P.4
Fisher, J.W.5
-
6
-
-
80054678577
-
Pharmacokinetics of bisphenol A in neonatal and adult CD-1 mice: Interspecies comparisons with Sprague-Dawley rats and rhesus monkeys
-
Doerge, D. R., Twaddle, N. C., Vanlandingham, M., and Fisher, J. W. (2011b). Pharmacokinetics of bisphenol A in neonatal and adult CD-1 mice: Interspecies comparisons with Sprague-Dawley rats and rhesus monkeys. Toxicol. Lett. 207, 298-305.
-
(2011)
Toxicol. Lett.
, vol.207
, pp. 298-305
-
-
Doerge, D.R.1
Twaddle, N.C.2
Vanlandingham, M.3
Fisher, J.W.4
-
7
-
-
81255149595
-
Pharmacokinetic modeling: Prediction and evaluation of route dependent dosimetry of bisphenol A in monkeys with extrapolation to humans
-
Fisher, J. W., Twaddle, N. C., Vanlandingham, M., and Doerge, D. R. (2011). Pharmacokinetic modeling: Prediction and evaluation of route dependent dosimetry of bisphenol A in monkeys with extrapolation to humans. Toxicol. Appl. Pharmacol. 257, 122-136.
-
(2011)
Toxicol. Appl. Pharmacol.
, vol.257
, pp. 122-136
-
-
Fisher, J.W.1
Twaddle, N.C.2
Vanlandingham, M.3
Doerge, D.R.4
-
8
-
-
77649216536
-
Membrane transporters in drug development
-
Giacomini, K. M., Huang, S. M., Tweedie, D. J., Benet, L. Z., Brouwer, K. L., Chu, X., Dahlin, A., Evers, R., Fischer, V., Hillgren, K. M., et al. (2010). Membrane transporters in drug development. Nat. Rev. Drug Discov. 9, 215-236.
-
(2010)
Nat. Rev. Drug Discov.
, vol.9
, pp. 215-236
-
-
Giacomini, K.M.1
Huang, S.M.2
Tweedie, D.J.3
Benet, L.Z.4
Brouwer, K.L.5
Chu, X.6
Dahlin, A.7
Evers, R.8
Fischer, V.9
Hillgren, K.M.10
-
9
-
-
2542491777
-
The role of ABC transporters in drug resistance, metabolism and toxicity
-
Glavinas, H., Krajcsi, P., Cserepes, J., and Sarkadi, B. (2004). The role of ABC transporters in drug resistance, metabolism and toxicity. Curr. Drug Deliv. 1, 27-42.
-
(2004)
Curr. Drug Deliv.
, vol.1
, pp. 27-42
-
-
Glavinas, H.1
Krajcsi, P.2
Cserepes, J.3
Sarkadi, B.4
-
10
-
-
0025766958
-
A single amino acid substitution strongly modulates the activity and substrate specificity of the mouse mdr1 and mdr3 drug efflux pumps
-
Gros, P., Dhir, R., Croop, J., and Talbot, F. (1991). A single amino acid substitution strongly modulates the activity and substrate specificity of the mouse mdr1 and mdr3 drug efflux pumps. Proc. Natl. Acad. Sci. U.S.A. 88, 7289-7293.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 7289-7293
-
-
Gros, P.1
Dhir, R.2
Croop, J.3
Talbot, F.4
-
11
-
-
0032541975
-
Contribution to substrate specificity and transport of nonconserved residues in transmembrane domain 12 of human P-glycoprotein
-
Hafkemeyer, P., Dey, S., Ambudkar, S. V., Hrycyna, C. A., Pastan, I., and Gottesman, M. M. (1998). Contribution to substrate specificity and transport of nonconserved residues in transmembrane domain 12 of human P-glycoprotein. Biochemistry 37, 16400-16409.
-
(1998)
Biochemistry
, vol.37
, pp. 16400-16409
-
-
Hafkemeyer, P.1
Dey, S.2
Ambudkar, S.V.3
Hrycyna, C.A.4
Pastan, I.5
Gottesman, M.M.6
-
12
-
-
1242335471
-
The MRPrelated and BCRP/ABCG2 multidrug resistance proteins: Biology, substrate specificity and regulation
-
Haimeur, A., Conseil, G., Deeley, R. G., and Cole, S. P. (2004a). The MRPrelated and BCRP/ABCG2 multidrug resistance proteins: Biology, substrate specificity and regulation. Curr. Drug Metab. 5, 21-53.
-
(2004)
Curr. Drug Metab.
, vol.5
, pp. 21-53
-
-
Haimeur, A.1
Conseil, G.2
Deeley, R.G.3
Cole, S.P.4
-
13
-
-
2442660256
-
Mutations of charged amino acids in or near the transmembrane helices of the second membrane spanning domain differentially affect the substrate specificity and transport activity of the multidrug resistance protein MRP1 (ABCC1)
-
Haimeur, A., Conseil, G., Deeley, R. G., and Cole, S. P. (2004b). Mutations of charged amino acids in or near the transmembrane helices of the second membrane spanning domain differentially affect the substrate specificity and transport activity of the multidrug resistance protein MRP1 (ABCC1). Mol. Pharmacol. 65, 1375-1385.
-
(2004)
Mol. Pharmacol.
, vol.65
, pp. 1375-1385
-
-
Haimeur, A.1
Conseil, G.2
Deeley, R.G.3
Cole, S.P.4
-
14
-
-
70349282243
-
Construction of triple-transfected cells organic anion-transporting polypeptide (OATP) 1B1/multidrug resistance-associated protein (MRP) 2/MRP3 and OATP1B1/MRP2/MRP4 for analysis of the sinusoidal function of MRP3 and MRP4
-
Hirouchi, M., Kusuhara, H., Onuki, R., Ogilvie, B. W., Parkinson, A., and Sugiyama, Y. (2009). Construction of triple-transfected cells organic anion-transporting polypeptide (OATP) 1B1/multidrug resistance-associated protein (MRP) 2/MRP3 and OATP1B1/MRP2/MRP4 for analysis of the sinusoidal function of MRP3 and MRP4. Drug Metab. Dispos. 37, 2103-2111.
-
(2009)
Drug Metab. Dispos.
, vol.37
, pp. 2103-2111
-
-
Hirouchi, M.1
Kusuhara, H.2
Onuki, R.3
Ogilvie, B.W.4
Parkinson, A.5
Sugiyama, Y.6
-
15
-
-
0037671242
-
Bisphenol A glucuronidation and absorption in rat intestine
-
Inoue, H., Yuki, G., Yokota, H., and Kato, S. (2003). Bisphenol A glucuronidation and absorption in rat intestine. Drug Metab. Dispos. 31, 140-144.
-
(2003)
Drug Metab. Dispos.
, vol.31
, pp. 140-144
-
-
Inoue, H.1
Yuki, G.2
Yokota, H.3
Kato, S.4
-
16
-
-
17044373986
-
Effect of bisphenol A on drug efflux in BeWo, a human trophoblast-like cell line
-
Jin, H., and Audus, K. L. (2005). Effect of bisphenol A on drug efflux in BeWo, a human trophoblast-like cell line. Placenta 26, S96-S103.
-
(2005)
Placenta
, vol.26
-
-
Jin, H.1
Audus, K.L.2
-
17
-
-
33745174833
-
The conserved tyrosine residues 401 and 1044 in ATP sites of human P-glycoprotein are critical for ATP binding and hydrolysis: Evidence for a conserved subdomain, the A-loop in the ATP-binding cassette
-
Kim, I. W., Peng, X. H., Sauna, Z. E., FitzGerald, P. C., Xia, D., Muller, M., Nandigama, K., and Ambudkar, S. V. (2006). The conserved tyrosine residues 401 and 1044 in ATP sites of human P-glycoprotein are critical for ATP binding and hydrolysis: Evidence for a conserved subdomain, the A-loop in the ATP-binding cassette. Biochemistry 45, 7605-7616.
-
(2006)
Biochemistry
, vol.45
, pp. 7605-7616
-
-
Kim, I.W.1
Peng, X.H.2
Sauna, Z.E.3
FitzGerald, P.C.4
Xia, D.5
Muller, M.6
Nandigama, K.7
Ambudkar, S.V.8
-
18
-
-
1242267914
-
Identification of proline residues in the core cytoplasmic and transmembrane regions of multidrug resistance protein 1 (MRP1/ABCC1) important for transport function, substrate specificity, and nucleotide interactions
-
Koike, K., Conseil, G., Leslie, E. M., Deeley, R. G., and Cole, S. P. (2004). Identification of proline residues in the core cytoplasmic and transmembrane regions of multidrug resistance protein 1 (MRP1/ABCC1) important for transport function, substrate specificity, and nucleotide interactions. J. Biol. Chem. 279, 12325-12336.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 12325-12336
-
-
Koike, K.1
Conseil, G.2
Leslie, E.M.3
Deeley, R.G.4
Cole, S.P.5
-
19
-
-
34748895120
-
Prediction of metabolic clearance of bisphenol A (4,4 '-dihydroxy-2,2-diphenylpropane) using cryopreserved human hepatocytes
-
Kuester, R. K., and Sipes, I. G. (2007). Prediction of metabolic clearance of bisphenol A (4,4 '-dihydroxy-2,2-diphenylpropane) using cryopreserved human hepatocytes. Drug Metab. Dispos. 35, 1910-1915.
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1910-1915
-
-
Kuester, R.K.1
Sipes, I.G.2
-
20
-
-
0035996051
-
Disposition of a low dose of bisphenol A in male and female cynomolgus monkeys
-
Kurebayashi, H., Harada, R., Stewart, R. K., Numata, H., and Ohno, Y. (2002). Disposition of a low dose of bisphenol A in male and female cynomolgus monkeys. Toxicol. Sci. 68, 32-42.
-
(2002)
Toxicol. Sci.
, vol.68
, pp. 32-42
-
-
Kurebayashi, H.1
Harada, R.2
Stewart, R.K.3
Numata, H.4
Ohno, Y.5
-
21
-
-
17544368685
-
Multidrug resistance proteins: Role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense
-
Leslie, E. M., Deeley, R. G., and Cole, S. (2005). Multidrug resistance proteins: Role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense. Toxicol. Appl. Pharmacol. 204, 216-237.
-
(2005)
Toxicol. Appl. Pharmacol.
, vol.204
, pp. 216-237
-
-
Leslie, E.M.1
Deeley, R.G.2
Cole, S.3
-
22
-
-
58149465922
-
Absolute difference of hepatobiliary transporter multidrug resistance-associated protein (MRP2/Mrp2) in liver tissues and isolated hepatocytes from rat, dog, monkey, and human
-
Li, N., Zhang, Y., Hua, F., and Lai, Y. (2009). Absolute difference of hepatobiliary transporter multidrug resistance-associated protein (MRP2/Mrp2) in liver tissues and isolated hepatocytes from rat, dog, monkey, and human. Drug Metab. Dispos. 37, 66-73.
-
(2009)
Drug Metab. Dispos.
, vol.37
, pp. 66-73
-
-
Li, N.1
Zhang, Y.2
Hua, F.3
Lai, Y.4
-
23
-
-
0027997698
-
Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1994). Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein. Biochemistry 33, 14049-14057.
-
(1994)
Biochemistry
, vol.33
, pp. 14049-14057
-
-
Loo, T.W.1
Clarke, D.M.2
-
24
-
-
0038419822
-
Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drugbinding site
-
Loo, T. W., Bartlett, C., and Clarke, D. M. (2003). Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drugbinding site. J. Biol. Chem. 278, 20449-20452.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20449-20452
-
-
Loo, T.W.1
Bartlett, C.2
Clarke, D.M.3
-
25
-
-
78649530850
-
Differences between human and rat intestinal and hepatic bisphenol A glucuronidation and the influence of alamethicin on in vitro kinetic measurements
-
Mazur, C. S., Kenneke, J. F., Hess-Wilson, J. K., and Lipscomb, J. C. (2010). Differences between human and rat intestinal and hepatic bisphenol A glucuronidation and the influence of alamethicin on in vitro kinetic measurements. Drug Metab. Dispos. 38, 2232-2238.
-
(2010)
Drug Metab. Dispos.
, vol.38
, pp. 2232-2238
-
-
Mazur, C.S.1
Kenneke, J.F.2
Hess-Wilson, J.K.3
Lipscomb, J.C.4
-
26
-
-
77954089848
-
Placental transport and in vitro effects of bisphenol A
-
Mørck, T. J., Sorda, G., Bechi, N., Rasmussen, B. S., Nielsen, J. B., Ietta, F., Rytting, E., Mathiesen, L., Paulesu, L., and Knudsen, L. E. (2010). Placental transport and in vitro effects of bisphenol A. Reprod. Toxicol. 30, 131-137.
-
(2010)
Reprod. Toxicol.
, vol.30
, pp. 131-137
-
-
Mørck, T.J.1
Sorda, G.2
Bechi, N.3
Rasmussen, B.S.4
Nielsen, J.B.5
Ietta, F.6
Rytting, E.7
Mathiesen, L.8
Paulesu, L.9
Knudsen, L.E.10
-
27
-
-
0034623005
-
T-coffee: A novel method for fast and accurate multiple sequence alignment
-
Notredame, C., Higgins, D. G., and Heringa, J. (2000). T-coffee: A novel method for fast and accurate multiple sequence alignment. J. Mol. Biol. 302, 205-217.
-
(2000)
J. Mol. Biol.
, vol.302
, pp. 205-217
-
-
Notredame, C.1
Higgins, D.G.2
Heringa, J.3
-
28
-
-
35648940290
-
Transportermediated uptake into cellular compartments
-
Oswald, S., Grube, M., Siegmund, W., and Kroemer, H. K. (2007). Transportermediated uptake into cellular compartments. Xenobiotica 37, 1171-1195.
-
(2007)
Xenobiotica
, vol.37
, pp. 1171-1195
-
-
Oswald, S.1
Grube, M.2
Siegmund, W.3
Kroemer, H.K.4
-
29
-
-
71949127231
-
Interplay of transporters and enzymes in drug and metabolite processing
-
Pang, K. S., Maeng, H. J., and Fan, J. (2009). Interplay of transporters and enzymes in drug and metabolite processing. Mol. Pharm. 6, 1734-1755.
-
(2009)
Mol. Pharm.
, vol.6
, pp. 1734-1755
-
-
Pang, K.S.1
Maeng, H.J.2
Fan, J.3
-
30
-
-
0034102209
-
The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration
-
Pottenger, L. H., Domoradzki, J. Y., Markham, D. A., Hansen, S. C., Cagen, S. Z., and Waechter, J. M., Jr. (2000). The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration. Toxicol. Sci. 54, 3-18.
-
(2000)
Toxicol. Sci.
, vol.54
, pp. 3-18
-
-
Pottenger, L.H.1
Domoradzki, J.Y.2
Markham, D.A.3
Hansen, S.C.4
Cagen, S.Z.5
Waechter Jr., J.M.6
-
31
-
-
0036841276
-
Metabolism of bisphenol A in primary cultured hepatocytes from mice, rats, and humans
-
Pritchett, J. J., Kuester, R. K., and Sipes, I. G. (2002). Metabolism of bisphenol A in primary cultured hepatocytes from mice, rats, and humans. Drug Metab. Dispos. 30, 1180-1185.
-
(2002)
Drug Metab. Dispos.
, vol.30
, pp. 1180-1185
-
-
Pritchett, J.J.1
Kuester, R.K.2
Sipes, I.G.3
-
32
-
-
77957122945
-
The role of the placenta in fetal exposure to xenobiotics: Importance of membrane transporters and human models for transfer studies
-
Prouillac, C., and Lecoeur, S. (2010). The role of the placenta in fetal exposure to xenobiotics: Importance of membrane transporters and human models for transfer studies. Drug Metab. Dispos. 38, 1623.
-
(2010)
Drug Metab. Dispos.
, vol.38
, pp. 1623
-
-
Prouillac, C.1
Lecoeur, S.2
-
33
-
-
0035933744
-
Glutathione-dependent binding of a photoaffinity analog of agosterol A to the C-terminal half of human multidrug resistance protein
-
Ren, X.Q., Furukawa, T., Aoki, S., Nakajima, T., Sumizawa, T., Haraguchi, M., Chen, Z., Kobayashi, M., and Akiyama, S. (2001). Glutathione-dependent binding of a photoaffinity analog of agosterol A to the C-terminal half of human multidrug resistance protein. J. Biol. Chem. 276, 23197-23206.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 23197-23206
-
-
Ren, X.Q.1
Furukawa, T.2
Aoki, S.3
Nakajima, T.4
Sumizawa, T.5
Haraguchi, M.6
Chen, Z.7
Kobayashi, M.8
Akiyama, S.9
-
34
-
-
0026722467
-
Expression of the human multidrug resistance cDNA in insect cells generates a high activity drug-stimulated membrane ATPase
-
Sarkadi, B., Price, E. M., Boucher, R. C., Germann, U. A., and Scarborough, G. A. (1992). Expression of the human multidrug resistance cDNA in insect cells generates a high activity drug-stimulated membrane ATPase. J. Biol. Chem. 267, 4854-4858.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 4854-4858
-
-
Sarkadi, B.1
Price, E.M.2
Boucher, R.C.3
Germann, U.A.4
Scarborough, G.A.5
-
35
-
-
0028961304
-
Human (MDR1) and mouse (mdr1, mdr3) P-glycoproteins can be distinguished by their respective drug resistance profiles and sensitivity to modulators
-
Tang-Wai, D. F., Kajiji, S., DiCapua, F., de Graaf, D., Roninson, I. B., and Gros, P. (1995). Human (MDR1) and mouse (mdr1, mdr3) P-glycoproteins can be distinguished by their respective drug resistance profiles and sensitivity to modulators. Biochemistry 34, 32-39.
-
(1995)
Biochemistry
, vol.34
, pp. 32-39
-
-
Tang-Wai, D.F.1
Kajiji, S.2
DiCapua, F.3
de Graaf, D.4
Roninson, I.B.5
Gros, P.6
-
36
-
-
20744460349
-
Evaluation of oral and intravenous route pharmacokinetics, plasma protein binding, and uterine tissue dose metrics of bisphenol A: A physiologically based pharmacokinetic approach
-
Teeguarden, J. G., Waechter, J. M., Jr, Clewell, H. J., III, Covington, T. R., and Barton, H. A. (2005). Evaluation of oral and intravenous route pharmacokinetics, plasma protein binding, and uterine tissue dose metrics of bisphenol A: A physiologically based pharmacokinetic approach. Toxicol. Sci. 85, 823-838.
-
(2005)
Toxicol. Sci.
, vol.85
, pp. 823-838
-
-
Teeguarden, J.G.1
Waechter Jr., J.M.2
Clewell III, H.J.3
Covington, T.R.4
Barton, H.A.5
-
37
-
-
0036802304
-
Metabolism and kinetics of bisphenol A in humans at low doses following oral administration
-
Volkel, W., Colnot, T., Csanady, G. A., Filser, J. G., and Dekant, W. (2002). Metabolism and kinetics of bisphenol A in humans at low doses following oral administration. Chem. Res. Toxicol. 15, 1281-1287.
-
(2002)
Chem. Res. Toxicol.
, vol.15
, pp. 1281-1287
-
-
Volkel, W.1
Colnot, T.2
Csanady, G.A.3
Filser, J.G.4
Dekant, W.5
-
38
-
-
0344629891
-
Identification of the structural and functional boundaries of the multidrug resistance protein 1 cytoplasmic loop 3
-
Westlake, C. J., Qian, Y. M., Gao, M., Vasa, M., Cole, S. P., and Deeley, R. G. (2003). Identification of the structural and functional boundaries of the multidrug resistance protein 1 cytoplasmic loop 3. Biochemistry 42, 14099-14113.
-
(2003)
Biochemistry
, vol.42
, pp. 14099-14113
-
-
Westlake, C.J.1
Qian, Y.M.2
Gao, M.3
Vasa, M.4
Cole, S.P.5
Deeley, R.G.6
-
39
-
-
0036783364
-
Permeability characteristics of endocrine-disrupting chemicals using an in vitro cell culture model, Caco-2 cells
-
Yoshikawa, Y., Hayashi, A., Iani, M., Matsuhita, A., Shibata, N., and Takada, K. (2002). Permeability characteristics of endocrine-disrupting chemicals using an in vitro cell culture model, Caco-2 cells. Curr. Drug Metab. 3, 551-557.
-
(2002)
Curr. Drug Metab.
, vol.3
, pp. 551-557
-
-
Yoshikawa, Y.1
Hayashi, A.2
Iani, M.3
Matsuhita, A.4
Shibata, N.5
Takada, K.6
-
40
-
-
80053141975
-
Efflux transport is an important determinant of ethinylestradiol glucuronide and ethinylestradiol sulfate pharmacokinetics
-
Zamek-Gliszczynski, M. J., Day, J. S., Hillgren, K. M., and Phillip, D. L. (2011). Efflux transport is an important determinant of ethinylestradiol glucuronide and ethinylestradiol sulfate pharmacokinetics. Drug Metab. Dispos. 39, 1794.
-
(2011)
Drug Metab. Dispos.
, vol.39
, pp. 1794
-
-
Zamek-Gliszczynski, M.J.1
Day, J.S.2
Hillgren, K.M.3
Phillip, D.L.4
|