-
1
-
-
38749113348
-
Kinetic identification of membrane transporters that assist P-glycoprotein-mediated transport of digoxin and loperamide through a confluent monolayer of MDCKII-hMDR1 cells
-
Acharya P., O'Connor M.P., Polli J.W., Ayrton A., Ellens H., Bentz J. Kinetic identification of membrane transporters that assist P-glycoprotein-mediated transport of digoxin and loperamide through a confluent monolayer of MDCKII-hMDR1 cells. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2008, 36:452-460.
-
(2008)
Drug Metabolism and Disposition: The Biological Fate of Chemicals
, vol.36
, pp. 452-460
-
-
Acharya, P.1
O'Connor, M.P.2
Polli, J.W.3
Ayrton, A.4
Ellens, H.5
Bentz, J.6
-
2
-
-
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., et al. Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science 2009, 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
-
3
-
-
33745653136
-
Development and characterization of LLC-PK1 cells containing Sprague-Dawley rat Abcb1a (Mdr1a): comparison of rat P-glycoprotein transport to human and mouse
-
Booth-Genthe C.L., Louie S.W., Carlini E.J., Li B., Leake B.F., Eisenhandler R., et al. Development and characterization of LLC-PK1 cells containing Sprague-Dawley rat Abcb1a (Mdr1a): comparison of rat P-glycoprotein transport to human and mouse. Journal of Pharmacological and Toxicological Methods 2006, 54:78-89.
-
(2006)
Journal of Pharmacological and Toxicological Methods
, vol.54
, pp. 78-89
-
-
Booth-Genthe, C.L.1
Louie, S.W.2
Carlini, E.J.3
Li, B.4
Leake, B.F.5
Eisenhandler, R.6
-
4
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 1976, 72:248-254.
-
(1976)
Analytical Biochemistry
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
5
-
-
31844448665
-
The translocation mechanism of P-glycoprotein
-
Callaghan R., Ford R.C., Kerr I.D. The translocation mechanism of P-glycoprotein. FEBS Letters 2006, 580:1056-1063.
-
(2006)
FEBS Letters
, vol.580
, pp. 1056-1063
-
-
Callaghan, R.1
Ford, R.C.2
Kerr, I.D.3
-
6
-
-
0023874147
-
A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases
-
Chifflet S., Torriglia A., Chiesa R., Tolosa S. A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases. Analytical Biochemistry 1988, 168:1-4.
-
(1988)
Analytical Biochemistry
, vol.168
, pp. 1-4
-
-
Chifflet, S.1
Torriglia, A.2
Chiesa, R.3
Tolosa, S.4
-
7
-
-
84859430407
-
Determination of the inhibitory potencies of p-glycoprotein inhibitors by transcellular permeability of Caco-2 cells
-
Dickens D., Owen A., Alfirevic A., Pirmohamed M. Determination of the inhibitory potencies of p-glycoprotein inhibitors by transcellular permeability of Caco-2 cells. Proceedings of the British Pharmacological Society 2009, http://pa2online.org/abstracts/Vol7Issue4abst092P.pdf.
-
(2009)
Proceedings of the British Pharmacological Society
-
-
Dickens, D.1
Owen, A.2
Alfirevic, A.3
Pirmohamed, M.4
-
8
-
-
33947401100
-
P-glycoprotein (ABCB1) interacts directly with lipid-based anti-cancer drugs and platelet-activating factors
-
Eckford P.D., Sharom F.J. P-glycoprotein (ABCB1) interacts directly with lipid-based anti-cancer drugs and platelet-activating factors. Biochemistry and Cell Biology 2006, 84:1022-1033.
-
(2006)
Biochemistry and Cell Biology
, vol.84
, pp. 1022-1033
-
-
Eckford, P.D.1
Sharom, F.J.2
-
9
-
-
67650685020
-
ABC efflux pump-based resistance to chemotherapy drugs
-
Eckford P.D., Sharom F.J. ABC efflux pump-based resistance to chemotherapy drugs. Chemical Reviews 2009, 109:2989-3011.
-
(2009)
Chemical Reviews
, vol.109
, pp. 2989-3011
-
-
Eckford, P.D.1
Sharom, F.J.2
-
10
-
-
38749087222
-
In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system
-
Feng B., Mills J.B., Davidson R.E., Mireles R.J., Janiszewski J.S., Troutman M.D., et al. In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2008, 36:268-275.
-
(2008)
Drug Metabolism and Disposition: The Biological Fate of Chemicals
, vol.36
, pp. 268-275
-
-
Feng, B.1
Mills, J.B.2
Davidson, R.E.3
Mireles, R.J.4
Janiszewski, J.S.5
Troutman, M.D.6
-
11
-
-
58549088199
-
Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug
-
Fenner K.S., Troutman M.D., Kempshall S., Cook J.A., Ware J.A., Smith D.A., et al. Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug. Clinical Pharmacology and Therapeutics 2009, 85:173-181.
-
(2009)
Clinical Pharmacology and Therapeutics
, vol.85
, pp. 173-181
-
-
Fenner, K.S.1
Troutman, M.D.2
Kempshall, S.3
Cook, J.A.4
Ware, J.A.5
Smith, D.A.6
-
12
-
-
77649216536
-
Membrane transporters in drug development
-
Giacomini K.M., Huang S.M., Tweedie D.J., Benet L.Z., Brouwer K.L., Chu X., et al. Membrane transporters in drug development. Nature Reviews in Drug Discovery 2010, 9:215-236.
-
(2010)
Nature Reviews in Drug Discovery
, 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
-
13
-
-
84859429838
-
-
New tariquidar-like ABCB1 modulators in cancer chemotherapy: Preclinical pharmacokinetic/pharmacodynamic investigations and computational studies. Ph.D. Dissertation: Universität Regensburg.
-
Höcheri, P. (2010). New tariquidar-like ABCB1 modulators in cancer chemotherapy: Preclinical pharmacokinetic/pharmacodynamic investigations and computational studies. Ph.D. Dissertation: Universität Regensburg.
-
(2010)
-
-
Höcheri, P.1
-
14
-
-
62149110091
-
Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators
-
Klinkhammer W., Muller H., Globisch C., Pajeva I.K., Wiese M. Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators. Bioorganic and Medicinal Chemistry 2009, 17:2524-2535.
-
(2009)
Bioorganic and Medicinal Chemistry
, vol.17
, pp. 2524-2535
-
-
Klinkhammer, W.1
Muller, H.2
Globisch, C.3
Pajeva, I.K.4
Wiese, M.5
-
16
-
-
17544368685
-
Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense
-
Leslie E.M., Deeley R.G., Cole S.P.C. Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense. Toxicology and Applied Pharmacology 2005, 204:216-237.
-
(2005)
Toxicology and Applied Pharmacology
, vol.204
, pp. 216-237
-
-
Leslie, E.M.1
Deeley, R.G.2
Cole, S.P.C.3
-
17
-
-
0029840320
-
Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains
-
Liu R., Sharom F.J. Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains. Biochemistry 1996, 35:11865-11873.
-
(1996)
Biochemistry
, vol.35
, pp. 11865-11873
-
-
Liu, R.1
Sharom, F.J.2
-
18
-
-
0034610402
-
Intrinsic fluorescence of the P-glycoprotein multidrug transporter: sensitivity of tryptophan residues to binding of drugs and nucleotides
-
Liu R., Siemiarczuk A., Sharom F.J. Intrinsic fluorescence of the P-glycoprotein multidrug transporter: sensitivity of tryptophan residues to binding of drugs and nucleotides. Biochemistry 2000, 39:14927-14938.
-
(2000)
Biochemistry
, vol.39
, pp. 14927-14938
-
-
Liu, R.1
Siemiarczuk, A.2
Sharom, F.J.3
-
19
-
-
0141994817
-
Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein
-
Loo T.W., Bartlett M.C., Clarke D.M. Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein. Journal of Biological Chemistry 2003, 278:39706-39710.
-
(2003)
Journal of Biological Chemistry
, vol.278
, pp. 39706-39710
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
20
-
-
0034818922
-
Drug transport by reconstituted P-glycoprotein in proteoliposomes. Effect of substrates and modulators, and dependence on bilayer phase state
-
Lu P., Liu R., Sharom F.J. Drug transport by reconstituted P-glycoprotein in proteoliposomes. Effect of substrates and modulators, and dependence on bilayer phase state. European Journal of Biochemistry 2001, 268:1687-1697.
-
(2001)
European Journal of Biochemistry
, vol.268
, pp. 1687-1697
-
-
Lu, P.1
Liu, R.2
Sharom, F.J.3
-
21
-
-
27144451192
-
Interaction of LDS-751 and rhodamine 123 with P-glycoprotein: evidence for simultaneous binding of both drugs
-
Lugo M.R., Sharom F.J. Interaction of LDS-751 and rhodamine 123 with P-glycoprotein: evidence for simultaneous binding of both drugs. Biochemistry 2005, 44:14020-14029.
-
(2005)
Biochemistry
, vol.44
, pp. 14020-14029
-
-
Lugo, M.R.1
Sharom, F.J.2
-
22
-
-
0033862765
-
Communication between multiple drug binding sites on P-glycoprotein
-
Martin C., Berridge G., Higgins C.F., Mistry P., Charlton P., Callaghan R. Communication between multiple drug binding sites on P-glycoprotein. Molecular Pharmacology 2000, 58:624-632.
-
(2000)
Molecular Pharmacology
, vol.58
, pp. 624-632
-
-
Martin, C.1
Berridge, G.2
Higgins, C.F.3
Mistry, P.4
Charlton, P.5
Callaghan, R.6
-
23
-
-
79951973326
-
Molecular dissection of dual pseudosymmetric solute translocation pathways in human P-glycoprotein
-
Parveen Z., Stockner T., Bentele C., Pferschy S., Kraupp M., Freissmuth M., et al. Molecular dissection of dual pseudosymmetric solute translocation pathways in human P-glycoprotein. Molecular Pharmacology 2011, 79:443-452.
-
(2011)
Molecular Pharmacology
, vol.79
, pp. 443-452
-
-
Parveen, Z.1
Stockner, T.2
Bentele, C.3
Pferschy, S.4
Kraupp, M.5
Freissmuth, M.6
-
24
-
-
0034763005
-
Rational use of in vitro P-glycoprotein assays in drug discovery
-
Polli J.W., Wring S.A., Humphreys J.E., Huang L.Y., Morgan J.B., Webster L.O., et al. Rational use of in vitro P-glycoprotein assays in drug discovery. Journal of Pharmacology and Experimental Therapeutics 2001, 299:620-628.
-
(2001)
Journal of Pharmacology and Experimental Therapeutics
, vol.299
, pp. 620-628
-
-
Polli, J.W.1
Wring, S.A.2
Humphreys, J.E.3
Huang, L.Y.4
Morgan, J.B.5
Webster, L.O.6
-
25
-
-
33645805657
-
In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: A recommendation for probe substrates
-
Rautio J., Humphreys J.E., Webster L.O., Balakrishnan A., Keogh J.P., Kunta J.R., et al. In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: A recommendation for probe substrates. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2006, 34:786-792.
-
(2006)
Drug Metabolism and Disposition: The Biological Fate of Chemicals
, vol.34
, pp. 786-792
-
-
Rautio, J.1
Humphreys, J.E.2
Webster, L.O.3
Balakrishnan, A.4
Keogh, J.P.5
Kunta, J.R.6
-
26
-
-
78951479924
-
Rifampin's acute inhibitory and chronic inductive drug interactions: experimental and model-based approaches to drug-drug interaction trial design
-
Reitman M.L., Chu X., Cai X., Yabut J., Venkatasubramanian R., Zajic S., et al. Rifampin's acute inhibitory and chronic inductive drug interactions: experimental and model-based approaches to drug-drug interaction trial design. Clinical Pharmacology and Therapeutics 2011, 89:234-242.
-
(2011)
Clinical Pharmacology and Therapeutics
, vol.89
, pp. 234-242
-
-
Reitman, M.L.1
Chu, X.2
Cai, X.3
Yabut, J.4
Venkatasubramanian, R.5
Zajic, S.6
-
27
-
-
0030757153
-
Interaction of P-glycoprotein with defined phospholipid bilayers: a differential scanning calorimetric study
-
Romsicki Y., Sharom F.J. Interaction of P-glycoprotein with defined phospholipid bilayers: a differential scanning calorimetric study. Biochemistry 1997, 36:9807-9815.
-
(1997)
Biochemistry
, vol.36
, pp. 9807-9815
-
-
Romsicki, Y.1
Sharom, F.J.2
-
28
-
-
0035849506
-
Phospholipid flippase activity of the reconstituted P-glycoprotein multidrug transporter
-
Romsicki Y., Sharom F.J. Phospholipid flippase activity of the reconstituted P-glycoprotein multidrug transporter. Biochemistry 2001, 40:6937-6947.
-
(2001)
Biochemistry
, vol.40
, pp. 6937-6947
-
-
Romsicki, Y.1
Sharom, F.J.2
-
30
-
-
0030782511
-
Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities
-
Shapiro A.B., Ling V. Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities. European Journal of Biochemistry 1997, 250:130-137.
-
(1997)
European Journal of Biochemistry
, vol.250
, pp. 130-137
-
-
Shapiro, A.B.1
Ling, V.2
-
31
-
-
0031455482
-
The P-glycoprotein efflux pump: how does it transport drugs?
-
Sharom F.J. The P-glycoprotein efflux pump: how does it transport drugs?. Journal of Membrane Biology 1997, 160:161-175.
-
(1997)
Journal of Membrane Biology
, vol.160
, pp. 161-175
-
-
Sharom, F.J.1
-
32
-
-
40949121607
-
ABC multidrug transporters: structure, function and role in chemoresistance
-
Sharom F.J. ABC multidrug transporters: structure, function and role in chemoresistance. Pharmacogenomics 2008, 9:105-127.
-
(2008)
Pharmacogenomics
, vol.9
, pp. 105-127
-
-
Sharom, F.J.1
-
35
-
-
0030769833
-
Pharmacological characterization of LY335979: a potent cyclopropyldibenzosuberane modulator of P-glycoprotein
-
Starling J.J., Shepard R.L., Cao J., Law K.L., Norman B.H., Kroin J.S., et al. Pharmacological characterization of LY335979: a potent cyclopropyldibenzosuberane modulator of P-glycoprotein. Advances in Enzyme Regulation 1997, 37:335-347.
-
(1997)
Advances in Enzyme Regulation
, vol.37
, pp. 335-347
-
-
Starling, J.J.1
Shepard, R.L.2
Cao, J.3
Law, K.L.4
Norman, B.H.5
Kroin, J.S.6
-
36
-
-
33846448814
-
-
U.S.Department of Health and Human Services Food and Drug Administration (FDA), [Electronic version], Available from:
-
U.S.Department of Health and Human Services Food and Drug Administration (FDA) Guidance for industry: Drug interaction studies - study design, data analysis, and implications for dosing and labelling 2006, [Electronic version], Available from:. http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm072101.pdf.
-
(2006)
Guidance for industry: Drug interaction studies - study design, data analysis, and implications for dosing and labelling
-
-
-
37
-
-
31044448805
-
Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: f2 values
-
Weiss J., Haefeli W.E. Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: f2 values. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2006, 34:203-207.
-
(2006)
Drug Metabolism and Disposition: The Biological Fate of Chemicals
, vol.34
, pp. 203-207
-
-
Weiss, J.1
Haefeli, W.E.2
-
38
-
-
79958829984
-
Substrate- and species-dependent inhibition of P-glycoprotein-mediated transport: implications for predicting in vivo drug interactions
-
Zolnerciks J.K., Booth-Genthe C.L., Gupta A., Harris J., Unadkat J.D. Substrate- and species-dependent inhibition of P-glycoprotein-mediated transport: implications for predicting in vivo drug interactions. Journal of Pharmaceutical Sciences 2011, 100:3055-3061.
-
(2011)
Journal of Pharmaceutical Sciences
, vol.100
, pp. 3055-3061
-
-
Zolnerciks, J.K.1
Booth-Genthe, C.L.2
Gupta, A.3
Harris, J.4
Unadkat, J.D.5
|