-
1
-
-
0031732606
-
Penetration of dexamethasone into brain glucocorticoid targets is enhanced in mdr1A P-glycoprotein knockout mice
-
O. C. Meijer, E. C. de Lange, D. D. Breimer, A. G. de Boer, J. O. Workel, and E. R. de Kloet. Penetration of dexamethasone into brain glucocorticoid targets is enhanced in mdr1A P-glycoprotein knockout mice. Endocrinology 139:1789-1793 (1998).
-
(1998)
Endocrinology
, vol.139
, pp. 1789-1793
-
-
Meijer, O.C.1
De Lange, E.C.2
Breimer, D.D.3
De Boer, A.G.4
Workel, J.O.5
De Kloet, E.R.6
-
2
-
-
0035017246
-
Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain
-
A. M. Karssen, O. C. Meijer, I. C. van der Sandt, P. J. Lucassen, E. C. de Lange, A. G. de Boer, and E. R. de Kloet. Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain. Endocrinology 142: 2686-2694 (2001).
-
(2001)
Endocrinology
, vol.142
, pp. 2686-2694
-
-
Karssen, A.M.1
Meijer, O.C.2
Van Der Sandt, I.C.3
Lucassen, P.J.4
De Lange, E.C.5
De Boer, A.G.6
De Kloet, E.R.7
-
3
-
-
0033053170
-
Different absorption behaviors among steroid hormones due to possible interaction with P-glycoprotein in the rat small intestine
-
A. Nakayama, O. Eguchi, M. Hatakeyama, H. Saitoh, and M. Takada. Different absorption behaviors among steroid hormones due to possible interaction with P-glycoprotein in the rat small intestine. Biol. Pharm. Bull. 22:535-538 (1999).
-
(1999)
Biol. Pharm. Bull.
, vol.22
, pp. 535-538
-
-
Nakayama, A.1
Eguchi, O.2
Hatakeyama, M.3
Saitoh, H.4
Takada, M.5
-
4
-
-
0027214172
-
Expression of an mdr gene is associated with a new form of resistance to dexamethasone-induced apoptosis
-
S. Bourgeois, D. J. Gruol, R. F. Newby, and F. M. Rajah. Expression of an mdr gene is associated with a new form of resistance to dexamethasone- induced apoptosis. Mol. Endocrinol. 7: 840-851 (1993).
-
(1993)
Mol. Endocrinol.
, vol.7
, pp. 840-851
-
-
Bourgeois, S.1
Gruol, D.J.2
Newby, R.F.3
Rajah, F.M.4
-
5
-
-
0031058658
-
Chemosensitizing steroids: Glucocorticoid receptor agonists capable of inhibiting P-glycoprotein function
-
D. J. Gruoland S. Bourgeois. Chemosensitizing steroids: glucocorticoid receptor agonists capable of inhibiting P-glycoprotein function. Cancer Res. 57:720-727 (1997).
-
(1997)
Cancer Res.
, vol.57
, pp. 720-727
-
-
Gruoland, D.J.1
Bourgeois, S.2
-
6
-
-
0026487058
-
Human P-glycoprotein transports cortisol, aldosterone, and dexamethasone, but not progesterone
-
K. Ueda, N. Okamura, M. Hirai, Y. Tanigawara, T. Saeki, N. Kioka, T. Komano, and R. Hori. Human P-glycoprotein transports cortisol, aldosterone, and dexamethasone, but not progesterone. J. Biol. Chem. 267:24248-24252 (1992).
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 24248-24252
-
-
Ueda, K.1
Okamura, N.2
Hirai, M.3
Tanigawara, Y.4
Saeki, T.5
Kioka, N.6
Komano, T.7
Hori, R.8
-
7
-
-
0027502850
-
Cortisol is transported by the multidrug resistance gene product P-glycoprotein
-
C. K. van Kalken, H. J. Broxterman, H. M. Pinedo, N. Feller, H. Dekker, J. Lankelma, and G. Giaccone. Cortisol is transported by the multidrug resistance gene product P-glycoprotein. Br. J. Cancer 67:284-289 (1993).
-
(1993)
Br. J. Cancer
, vol.67
, pp. 284-289
-
-
Van Kalken, C.K.1
Broxterman, H.J.2
Pinedo, H.M.3
Feller, N.4
Dekker, H.5
Lankelma, J.6
Giaccone, G.7
-
8
-
-
0030589989
-
Steroid treatment, accumulation, and antagonism of P-glycoprotein in multidrug-resistant cells
-
K. M. Barnes, B. Dickstein, G. B. Cutler Jr., T. Fojo, and S. E. Bates. Steroid treatment, accumulation, and antagonism of P-glycoprotein in multidrug-resistant cells. Biochemistry 35:4820-4827 (1996).
-
(1996)
Biochemistry
, vol.35
, pp. 4820-4827
-
-
Barnes, K.M.1
Dickstein, B.2
Cutler Jr., G.B.3
Fojo, T.4
Bates, S.E.5
-
9
-
-
0028825399
-
Absence of the mdr1a P-Glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A
-
A. H. Schinkel, E. Wagenaar, L. van Deemter, C. A. Mol, and P. Borst. Absence of the mdr1a P-Glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A. J. Clin. Invest. 96:1698-1705 (1995).
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 1698-1705
-
-
Schinkel, A.H.1
Wagenaar, E.2
Van Deemter, L.3
Mol, C.A.4
Borst, P.5
-
10
-
-
0024344261
-
Differential overexpression of three mdr gene family members in multidrug-resistant J774.2 mouse cells. Evidence that distinct P-glycoprotein precursors are encoded by unique mdr genes
-
S. I. Hsu, L. Lothstein, and S. B. Horwitz. Differential overexpression of three mdr gene family members in multidrug-resistant J774.2 mouse cells. Evidence that distinct P-glycoprotein precursors are encoded by unique mdr genes. J. Biol. Chem. 264:12053-12062 (1989).
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 12053-12062
-
-
Hsu, S.I.1
Lothstein, L.2
Horwitz, S.B.3
-
11
-
-
0027432409
-
Fluorescent cellular indicators are extruded by the multidrug resistance protein
-
L. Homolya, Z. Hollo, U. A. Germann, I. Pastan, M. M. Gottesman, and B. Sarkadi. Fluorescent cellular indicators are extruded by the multidrug resistance protein. J. Biol. Chem. 268:21493-21496 (1993).
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 21493-21496
-
-
Homolya, L.1
Hollo, Z.2
Germann, U.A.3
Pastan, I.4
Gottesman, M.M.5
Sarkadi, B.6
-
12
-
-
0029939665
-
Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemosensitisers
-
J. M. Ford. Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemosensitisers. Eur. J. Cancer 32A:991-1001 (1996).
-
(1996)
Eur. J. Cancer
, vol.32 A
, pp. 991-1001
-
-
Ford, J.M.1
-
13
-
-
0035066727
-
Time-variant increase in methylprednisolone clearance in patients with acute respiratory distress syndrome: A population pharmacokinetic study
-
C. R. Yates, A. Vysokanov, A. Mukherjee, T. M. Ludden, E. Tolley, G. U. Meduri, and J. T. Dalton. Time-variant increase in methylprednisolone clearance in patients with acute respiratory distress syndrome: a population pharmacokinetic study. J. Clin. Pharmacol. 41:415-424 (2001).
-
(2001)
J. Clin. Pharmacol.
, vol.41
, pp. 415-424
-
-
Yates, C.R.1
Vysokanov, A.2
Mukherjee, A.3
Ludden, T.M.4
Tolley, E.5
Meduri, G.U.6
Dalton, J.T.7
-
14
-
-
0027548454
-
A fast new approach to pharmacophore mapping and its application to dopaminergic and benzodiazepine agonists
-
Y. C. Martin, M. G. Bures, E. A. Danaher, J. DeLazzer, I. Lico, and P. A. Pavlik. A fast new approach to pharmacophore mapping and its application to dopaminergic and benzodiazepine agonists. J. Comput. Aided Mol. Des. 7:83-102 (1993).
-
(1993)
J. Comput. Aided Mol. Des.
, vol.7
, pp. 83-102
-
-
Martin, Y.C.1
Bures, M.G.2
Danaher, E.A.3
DeLazzer, J.4
Lico, I.5
Pavlik, P.A.6
-
15
-
-
0032576701
-
Quantitative analysis of the structural requirements for blockade of the N-methyl-D-aspartate receptor at the phencyclidine binding site
-
R. T. Kroemer, E. Koutsilieri, P. Hecht, K. R. Liedl, P. Riederer, and J. Kornhuber. Quantitative analysis of the structural requirements for blockade of the N-methyl-D-aspartate receptor at the phencyclidine binding site. J. Med. Chem. 41:393-400 (1998).
-
(1998)
J. Med. Chem.
, vol.41
, pp. 393-400
-
-
Kroemer, R.T.1
Koutsilieri, E.2
Hecht, P.3
Liedl, K.R.4
Riederer, P.5
Kornhuber, J.6
-
16
-
-
0026696669
-
Definition and display of steric, hydrophobic, and hydrogen-bonding properties of ligand binding sites in proteins using Lee and Richards accessible surface: Validation of a high-resolution graphical tool for drug design
-
R. S. Bohacek and C. McMartin. Definition and display of steric, hydrophobic, and hydrogen-bonding properties of ligand binding sites in proteins using Lee and Richards accessible surface: validation of a high-resolution graphical tool for drug design. J. Med. Chem. 35:1671-1684 (1992).
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1671-1684
-
-
Bohacek, R.S.1
McMartin, C.2
-
17
-
-
0027944195
-
Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity
-
G. Klebe, U. Abraham, and T. Mietzner. Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity. J. Med. Chem. 37: 4130-4146 (1994).
-
(1994)
J. Med. Chem.
, vol.37
, pp. 4130-4146
-
-
Klebe, G.1
Abraham, U.2
Mietzner, T.3
-
19
-
-
0033058419
-
The human multidrug resistance protein MRP1 translocates sphingolipid analogs across the plasma membrane
-
R. J. Raggers, A. van Helvoort, R. Evers, and G. van Meer. The human multidrug resistance protein MRP1 translocates sphingolipid analogs across the plasma membrane. J. Cell Sci. 112(Pt 3):415-422 (1999).
-
(1999)
J. Cell Sci.
, vol.112
, Issue.3 PART
, pp. 415-422
-
-
Raggers, R.J.1
Van Helvoort, A.2
Evers, R.3
Van Meer, G.4
-
20
-
-
0028242843
-
High lipophilicity decreases drug transport across intestinal epithelial cells
-
P. Wils, A. Warnery, V. Phung-Ba, S. Legrain, and D. Scherman. High lipophilicity decreases drug transport across intestinal epithelial cells. J. Pharmacol. Exp. Ther. 269:654-658 (1994).
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.269
, pp. 654-658
-
-
Wils, P.1
Warnery, A.2
Phung-Ba, V.3
Legrain, S.4
Scherman, D.5
-
21
-
-
0020321112
-
Mechanism of cholesterol efflux from cells. Effects of acceptor structure and concentration
-
G. H. Rothblat and M. C. Phillips. Mechanism of cholesterol efflux from cells. Effects of acceptor structure and concentration. J. Biol. Chem. 257:4775-4782 (1982).
-
(1982)
J. Biol. Chem.
, vol.257
, pp. 4775-4782
-
-
Rothblat, G.H.1
Phillips, M.C.2
-
22
-
-
0026447133
-
A new method for quantitating intracellular transport: Application to the thyroid hormone 3,5,3′-triiodothyronine
-
B. A. Luxonand R. A. Weisiger. A new method for quantitating intracellular transport: application to the thyroid hormone 3,5,3′- triiodothyronine. Am. J. Physiol. 263:G733-G741 (1992).
-
(1992)
Am. J. Physiol.
, vol.263
-
-
Luxonand, B.A.1
Weisiger, R.A.2
-
23
-
-
0027209171
-
The Probability of Chance Correlation Using Partial Least Squares (PLS)
-
M. Clarkand R. D. Cramer III. The Probability of Chance Correlation Using Partial Least Squares (PLS). Quant. Struct.-Act. Relat. 12:137-145 (1993).
-
(1993)
Quant. Struct.-Act. Relat.
, vol.12
, pp. 137-145
-
-
Clarkand, M.1
Cramer III, R.D.2
-
24
-
-
0033213781
-
Profound differences in the transport of steroids by two mouse P-glycoproteins
-
D. J. Gruol, Q. D. Vo, and M. C. Zee. Profound differences in the transport of steroids by two mouse P-glycoproteins. Biochem. Pharmacol. 58:1191-1199 (1999).
-
(1999)
Biochem. Pharmacol.
, vol.58
, pp. 1191-1199
-
-
Gruol, D.J.1
Vo, Q.D.2
Zee, M.C.3
-
25
-
-
18344390872
-
Three-dimensional quantitative structure-activity relationships of inhibitors of P-glycoprotein
-
S. Ekins, R. B. Kim, B. F. Leake, A. H. Dantzig, E. G. Schuetz, L. B. Lan, K. Yasuda, R. L. Shepard, M. A. Winter, J. D. Schuetz, J. H. Wikel, and S. A. Wrighton. Three-dimensional quantitative structure-activity relationships of inhibitors of P-glycoprotein. Mol. Pharmacol. 61:964-973 (2002).
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 964-973
-
-
Ekins, S.1
Kim, R.B.2
Leake, B.F.3
Dantzig, A.H.4
Schuetz, E.G.5
Lan, L.B.6
Yasuda, K.7
Shepard, R.L.8
Winter, M.A.9
Schuetz, J.D.10
Wikel, J.H.11
Wrighton, S.A.12
-
26
-
-
18344364851
-
Application of three-dimensional quantitative structure-activity relationships of P-glycoprotein inhibitors and substrates
-
S. Ekins, R. B. Kim, B. F. Leake, A. H. Dantzig, E. G. Schuetz, L. B. Lan, K. Yasuda, R. L. Shepard, M. A. Winter, J. D. Schuetz, J. H. Wikel, and S. A. Wrighton. Application of three-dimensional quantitative structure-activity relationships of P-glycoprotein inhibitors and substrates. Mol. Pharmacol. 61:974-981 (2002).
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 974-981
-
-
Ekins, S.1
Kim, R.B.2
Leake, B.F.3
Dantzig, A.H.4
Schuetz, E.G.5
Lan, L.B.6
Yasuda, K.7
Shepard, R.L.8
Winter, M.A.9
Schuetz, J.D.10
Wikel, J.H.11
Wrighton, S.A.12
-
27
-
-
0031938630
-
Involvement of intestinal P-glycoprotein in the restricted absorption of methylprednisolone from rat small intestine
-
H. Saitoh, M. Hatakeyama, O. Eguchi, M. Oda, and M. Takada. Involvement of intestinal P-glycoprotein in the restricted absorption of methylprednisolone from rat small intestine. J. Pharm. Sci. 87:73-75 (1998).
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 73-75
-
-
Saitoh, H.1
Hatakeyama, M.2
Eguchi, O.3
Oda, M.4
Takada, M.5
-
28
-
-
0033961357
-
Spinal cord bioavailability of methylprednisolone after intravenous and intrathecal administration: The role of P-glycoprotein
-
K. L. Koszdin, D. D. Shen, and C. M. Bernards. Spinal cord bioavailability of methylprednisolone after intravenous and intrathecal administration: the role of P-glycoprotein. Anesthesiology 92:156-163 (2000).
-
(2000)
Anesthesiology
, vol.92
, pp. 156-163
-
-
Koszdin, K.L.1
Shen, D.D.2
Bernards, C.M.3
-
29
-
-
0015030515
-
Structural approach to partitioning: Estimation of steroid partition coefficients based upon molecular constitution
-
G. L. Flynn. Structural approach to partitioning: Estimation of steroid partition coefficients based upon molecular constitution. J. Pharm. Sci. 60:345-353 (1971).
-
(1971)
J. Pharm. Sci.
, vol.60
, pp. 345-353
-
-
Flynn, G.L.1
-
30
-
-
8644243613
-
Partition coefficients and their uses
-
A. Leo, C. Hansch, and D. Elkins. Partition coefficients and their uses. Chem. Rev. 71:525-616 (1971).
-
(1971)
Chem. Rev.
, vol.71
, pp. 525-616
-
-
Leo, A.1
Hansch, C.2
Elkins, D.3
|