-
1
-
-
23844549244
-
2 terminus of P-glycoprotein
-
2 terminus of P-glycoprotein. Clin. Cancer Res., 2005, 11, 5833-5839
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 5833-5839
-
-
Rao, P.S.1
Govindarajan, R.2
Mallya, K.B.3
West, W.4
Rao, U.S.5
-
2
-
-
33745512111
-
Regulation of multidrug resistance by pro-inflammatory cytokines
-
DOI 10.2174/156800906777441753
-
Ho, E.A.; Piquette-Miller, M. Regulation of multidrug resistance by pro-inflammatory cytokines. Curr. Cancer Drug Targets, 2006, 6, 295-311. (Pubitemid 43961865)
-
(2006)
Current Cancer Drug Targets
, vol.6
, Issue.4
, pp. 295-311
-
-
Ho, E.A.1
Piquette-Miller, M.2
-
3
-
-
52449108379
-
Novel insight in structure-activity relationship and bioanalysis of P-glycoprotein targeting highly potent tetrakishydroxymethyl substituted 3,9-diazatetraasteranes
-
Coburger, C.; Wollmann, J.; Baumert, C.; Krug, M.; Molnar, J.; Lage, H.; Hilgeroth, A. Novel insight in structure-activity relationship and bioanalysis of P-glycoprotein targeting highly potent tetrakishydroxymethyl substituted 3,9-diazatetraasteranes. J. Med. Chem., 2008, 51, 5871-5874
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5871-5874
-
-
Coburger, C.1
Wollmann, J.2
Baumert, C.3
Krug, M.4
Molnar, J.5
Lage, H.6
Hilgeroth, A.7
-
4
-
-
41649119544
-
4-Biphenyl and 2-naphthyl substituted 6,7-dimethoxytetrahydroisoquinoline derivatives as potent P-gp modulators
-
DOI 10.1016/j.bmc.2008.01.055, PII S0968089608000916
-
Colabufo, N.A.; Berardi, F.; Cantore, M.; Perrone, M.G.; Contino, M.; Inglese, C.; Niso, M.; Perrone, R.; Azzariti, A.; Simone, G.M.; Paradiso, A. 4-Biphenyl and 2-naphthyl substituted 6,7-dimethoxytetrahydroisoquinoline derivatives as potent P-gp modulators. Bioorg. Med. Chem., 2008, 16, 3732-3743 (Pubitemid 351484037)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.7
, pp. 3732-3743
-
-
Colabufo, N.A.1
Berardi, F.2
Cantore, M.3
Perrone, M.G.4
Contino, M.5
Inglese, C.6
Niso, M.7
Perrone, R.8
Azzariti, A.9
Simone, G.M.10
Paradiso, A.11
-
5
-
-
27644467858
-
Characterization of the human MDR1 gene
-
Bodor, M.; Kelly, E.J.; Ho, R.J. Characterization of the human MDR1 gene. AAPS J., 2005, 7, E1-5.
-
(2005)
AAPS J.
, vol.7
-
-
Bodor, M.1
Kelly, E.J.2
Ho, R.J.3
-
6
-
-
13244265753
-
The dileucine motif at the COOH terminus of human multidrug resistance P-glycoprotein is important for folding but not activity
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. The dileucine motif at the COOH terminus of human multidrug resistance P-glycoprotein is important for folding but not activity. J. Biol. Chem., 2005, 280, 2522-2528
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 2522-2528
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
7
-
-
0023798439
-
Multidrug resistance during chemical carcinogenesis: A mechanism revealed?
-
Gottesman, M.M. Multidrug resistance during chemical carcinogenesis: a mechanism revealed? J. Natl. Cancer Inst., 1988, 80, 1352-1353
-
(1988)
J. Natl. Cancer Inst.
, vol.80
, pp. 1352-1353
-
-
Gottesman, M.M.1
-
8
-
-
0032900953
-
Biochemical, cellular, and pharmacological aspects of the multidrug transporter
-
Ambudkar, S.V.; Dey, S.; Hrycyna, C.A.; Ramachandra, M.; Pastan, I.; Gottesman, M.M. Biochemical, cellular, and pharmacological aspects of the multidrug transporter. Annu. Rev. Pharmacol. Toxicol., 1999, 39, 361-398
-
(1999)
Annu. Rev. Pharmacol. Toxicol.
, vol.39
, pp. 361-398
-
-
Ambudkar, S.V.1
Dey, S.2
Hrycyna, C.A.3
Ramachandra, M.4
Pastan, I.5
Gottesman, M.M.6
-
9
-
-
0034142125
-
Functional characterization of glycosylation-deficient human P-glycoprotein using a vaccinia virus expression system
-
Gribar, J.J.; Ramachandra, M.; Hrycyna, C.A.; Dey, S.; Ambudkar, S.V. Functional characterization of glycosylation-deficient human P-glycoprotein using a vaccinia virus expression system. J. Membr. Biol., 2000, 173, 203-214
-
(2000)
J. Membr. Biol.
, vol.173
, pp. 203-214
-
-
Gribar, J.J.1
Ramachandra, M.2
Hrycyna, C.A.3
Dey, S.4
Ambudkar, S.V.5
-
10
-
-
0033600861
-
Use of a peptide mimotope to guide the humanization of MRK-16, an anti-P-glycoprotein monoclonal antibody
-
Tang, Y.; Beuerlein, G.; Pecht, G.; Chilton, T.; Huse, W.D.; Watkins, J.D. Use of a peptide mimotope to guide the humanization of MRK-16, an anti-P-glycoprotein monoclonal antibody. J. Biol. Chem., 1999, 274, 27371-27378 (Pubitemid 129527777)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.39
, pp. 27371-27378
-
-
Tang, Y.1
Beuerlein, G.2
Pecht, G.3
Chilton, T.4
Huse, W.D.5
Watkins, J.D.6
-
11
-
-
0029954843
-
P-glycoprotein - A mediator of multidrug resistance in tumour cells
-
DOI 10.1016/0959-8049(96)00057-3
-
Germann, U.A. P-glycoprotein - a mediator of multidrug resistance in tumour cells. Eur. J. Cancer, 1996, 32A, 927-944 (Pubitemid 26191761)
-
(1996)
European Journal of Cancer Part a
, vol.32
, Issue.6
, pp. 927-944
-
-
Germann, U.A.1
-
12
-
-
14644425991
-
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?
-
Loo, T.W.; Clarke, D.M. Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"? Biochem. Biophys. Res. Commun., 2005, 329, 419-422
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.329
, pp. 419-422
-
-
Loo, T.W.1
Clarke, D.M.2
-
13
-
-
0032601621
-
Merck Frosst Award Lecture 1998. Molecular dissection of the human multidrug resistance Pglycoprotein
-
Loo, T.W.; Clarke, D.M. Merck Frosst Award Lecture 1998. Molecular dissection of the human multidrug resistance Pglycoprotein. Biochem. Cell Biol., 1999, 77, 11-23.
-
(1999)
Biochem. Cell Biol.
, vol.77
, pp. 11-23
-
-
Loo, T.W.1
Clarke, D.M.2
-
14
-
-
21844451868
-
The coupling mechanism of P-glycoprotein involves residue L339 in the sixth membrane spanning segment
-
DOI 10.1016/j.febslet.2005.06.030, PII S0014579305007611
-
Rothnie, A.; Storm, J.; McMahon, R.; Taylor, A.; Kerr, I.D.; Callaghan, R. The coupling mechanism of P-glycoprotein involves residue L339 in the sixth membrane spanning segment. FEBS Lett., 2005, 579, 3984-3990 (Pubitemid 40961900)
-
(2005)
FEBS Letters
, vol.579
, Issue.18
, pp. 3984-3990
-
-
Rothnie, A.1
Storm, J.2
McMahon, R.3
Taylor, A.4
Kerr, I.D.5
Callaghan, R.6
-
15
-
-
0033609856
-
The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surface
-
Loo, T.W.; Clarke, D.M. The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surface. J. Biol. Chem., 1999, 274, 24759-24765 (Pubitemid 129529362)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.35
, pp. 24759-24765
-
-
Loo, T.W.1
Clarke, D.M.2
-
16
-
-
0032510958
-
Superfolding of the partially unfolded core-glycosylated intermediate of human P-glycoprotein into the mature enzyme is promoted by substrate-induced transmembrane domain interactions
-
Loo, T.W.; Clarke, D.M. Superfolding of the partially unfolded core-glycosylated intermediate of human P-glycoprotein into the mature enzyme is promoted by substrate-induced transmembrane domain interactions. J. Biol. Chem., 1998, 273, 14671-14674
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 14671-14674
-
-
Loo, T.W.1
Clarke, D.M.2
-
17
-
-
27644456826
-
Targeting drug-efflux pumps -- A pharmacoinformatic approach
-
Pleban, K.; Kaiser, D.; Kopp, S.; Peer, M.; Chiba, P.; Ecker, G.F. Targeting drug-efflux pumps -- a pharmacoinformatic approach. Acta Biochim. Pol., 2005, 52, 737-740
-
(2005)
Acta Biochim. Pol.
, vol.52
, pp. 737-740
-
-
Pleban, K.1
Kaiser, D.2
Kopp, S.3
Peer, M.4
Chiba, P.5
Ecker, G.F.6
-
18
-
-
4544254316
-
Processing mutations located throughout the human multidrug resistance P-glycoprotein disrupt interactions between the nucleotide binding domains
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Processing mutations located throughout the human multidrug resistance P-glycoprotein disrupt interactions between the nucleotide binding domains. J. Biol. Chem., 2004, 279, 38395-38401
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 38395-38401
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
19
-
-
33748040419
-
Gomisin A alters substrate interaction and reverses Pglycoprotein- mediated multidrug resistance in HepG2-DR cells
-
Wan, C.K.; Zhu, G.Y.; Shen, X.L.; Chattopadhyay, A.; Dey, S.; Fong, W.F. Gomisin A alters substrate interaction and reverses Pglycoprotein-mediated multidrug resistance in HepG2-DR cells. Biochem. Pharmacol., 2006, 72, 824-837
-
(2006)
Biochem. Pharmacol.
, vol.72
, pp. 824-837
-
-
Wan, C.K.1
Zhu, G.Y.2
Shen, X.L.3
Chattopadhyay, A.4
Dey, S.5
Fong, W.F.6
-
20
-
-
17444419056
-
A pharmacophore hypothesis for P-glycoprotein substrate recognition using GRIND-based 3D-QSAR
-
Cianchetta, G.; Singleton, R.W.; Zhang, M.; Wildgoose, M.; Giesing, D.; Fravolini, A.; Cruciani, G.; Vaz, R.J. A pharmacophore hypothesis for P-glycoprotein substrate recognition using GRIND-based 3D-QSAR. J. Med. Chem., 2005, 48, 2927-2935
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2927-2935
-
-
Cianchetta, G.1
Singleton, R.W.2
Zhang, M.3
Wildgoose, M.4
Giesing, D.5
Fravolini, A.6
Cruciani, G.7
Vaz, R.J.8
-
21
-
-
31844452412
-
Insight in eukaryotic ABC transporter function by mutation analysis
-
DOI 10.1016/j.febslet.2006.01.024, PII S0014579306000640, ABC Transporters
-
Frelet, A.; Klein, M. Insight in eukaryotic ABC transporter function by mutation analysis. FEBS Lett., 2006, 580, 1064-1084 (Pubitemid 43185287)
-
(2006)
FEBS Letters
, vol.580
, Issue.4
, pp. 1064-1084
-
-
Frelet, A.1
Klein, M.2
-
22
-
-
0036829647
-
The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence. J. Biol. Chem., 2002, 277, 41303-41306
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 41303-41306
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
23
-
-
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.; Ambudkar, S.V. 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, 2006, 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
-
24
-
-
0037085284
-
Structural and functional asymmetry of the nucleotide-binding domains of P-glycoprotein investigated by attenuated total reflection Fourier transform infrared spectroscopy
-
DOI 10.1074/jbc.M107928200
-
Vigano, C.; Julien, M.; Carrier, I.; Gros, P.; Ruysschaert, J.M. Structural and functional asymmetry of the nucleotide-binding domains of P-glycoprotein investigated by attenuated total reflection Fourier transform infrared spectroscopy. J. Biol. Chem., 2002, 277, 5008-5016 (Pubitemid 34968540)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.7
, pp. 5008-5016
-
-
Vigano, C.1
Julien, M.2
Carrier, I.3
Gros, P.4
Ruysschaert, J.-M.5
-
25
-
-
0005014240
-
P-glycoprotein and multidrug resistance
-
Gottesman, M.M.; Pastan, I.; Ambudkar, S.V. P-glycoprotein and multidrug resistance. Curr. Opin. Genet. Dev., 1996, 6, 610-617
-
(1996)
Curr. Opin. Genet. Dev.
, vol.6
, pp. 610-617
-
-
Gottesman, M.M.1
Pastan, I.2
Ambudkar, S.V.3
-
26
-
-
0030065776
-
Functional reconstitution of P-glycoprotein reveals an apparent near stoichiometric drug transport to ATP hydrolysis
-
Eytan, G.D.; Regev, R.; Assaraf, Y.G. Functional reconstitution of P-glycoprotein reveals an apparent near stoichiometric drug transport to ATP hydrolysis. J. Biol. Chem., 1996, 271, 3172-3178
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3172-3178
-
-
Eytan, G.D.1
Regev, R.2
Assaraf, Y.G.3
-
27
-
-
0035943691
-
Cross-linking of human multidrug resistance P-glycoprotein by the substrate, Tris-(2-maleimidoethyl)amine, is altered by ATP hydrolysis: Evidence for rotation of a transmembrane helix
-
DOI 10.1074/jbc.M103498200
-
Loo, T.W.; Clarke, D.M. Cross-linking of human multidrug resistance P-glycoprotein by the substrate, tris-(2-maleimidoethyl) amine, is altered by ATP hydrolysis. Evidence for rotation of a transmembrane helix. J. Biol. Chem., 2001, 276, 31800-31805 (Pubitemid 37384829)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.34
, pp. 31800-31805
-
-
Loo, T.W.1
Clarke, D.M.2
-
28
-
-
0035836608
-
P-glycoprotein-mediated colchicine resistance in different cell lines correlates with the effects of colchicine on P-glycoprotein conformation
-
Druley, T.E.; Stein, W.D.; Roninson, I.B. P-glycoprotein-mediated colchicine resistance in different cell lines correlates with the effects of colchicine on P-glycoprotein conformation. Biochemistry, 2001, 40, 4312-4322
-
(2001)
Biochemistry
, vol.40
, pp. 4312-4322
-
-
Druley, T.E.1
Stein, W.D.2
Roninson, I.B.3
-
29
-
-
52249103044
-
P-glycoprotein senses its substrates and the lateral membrane packing density: Consequences for the catalytic cycle
-
Aanismaa, P.; Gatlik-Landwojtowicz, E.; Seelig, A. P-glycoprotein senses its substrates and the lateral membrane packing density: consequences for the catalytic cycle. Biochemistry, 2008, 47, 10197-10207
-
(2008)
Biochemistry
, vol.47
, pp. 10197-10207
-
-
Aanismaa, P.1
Gatlik-Landwojtowicz, E.2
Seelig, A.3
-
30
-
-
0033969525
-
Analysis of the tangled relationships between P-glycoprotein-mediated multidrug resistance and the lipid phase of the cell membrane
-
DOI 10.1046/j.1432-1327.2000.01046.x
-
Ferté, J. Analysis of the tangled relationships between P-glycoprotein-mediated multidrug resistance and the lipid phase of the cell membrane. Eur. J. Biochem., 2000, 267, 277-294 (Pubitemid 30072888)
-
(2000)
European Journal of Biochemistry
, vol.267
, Issue.2
, pp. 277-294
-
-
Ferte, J.1
-
31
-
-
0032578434
-
Structural flexibility of the linker region of human P-glycoprotein permits ATP hydrolysis and drug transport
-
Hrycyna, C.A.; Airan, L.E.; Germann, U.A.; Ambudkar, S.V.; Pastan, I.; Gottesman, M.M. Structural flexibility of the linker region of human P-glycoprotein permits ATP hydrolysis and drug transport. Biochemistry, 1998, 37, 13660-13673
-
(1998)
Biochemistry
, vol.37
, pp. 13660-13673
-
-
Hrycyna, C.A.1
Airan, L.E.2
Germann, U.A.3
Ambudkar, S.V.4
Pastan, I.5
Gottesman, M.M.6
-
32
-
-
23044503311
-
ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein. Biochemistry, 2005, 44, 10250-10258
-
(2005)
Biochemistry
, vol.44
, pp. 10250-10258
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
33
-
-
0035813143
-
Determining the Dimensions of the Drug-binding Domain of Human P-glycoprotein Using Thiol Cross-linking Compounds as Molecular Rulers
-
DOI 10.1074/jbc.C100467200
-
Loo, T.W.; Clarke, D.M. Determining the dimensions of the drug-binding domain of human P-glycoprotein using thiol cross-linking compounds as molecular rulers. J. Biol. Chem., 2001, 276, 36877-36880 (Pubitemid 37384096)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.40
, pp. 36877-36880
-
-
Loo, T.W.1
Clarke, D.M.2
-
34
-
-
2442597224
-
Val133 and Cys137 in transmembrane segment 2 are close to Arg935 and Gly939 in transmembrane segment 11 of human P-glycoprotein
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Val133 and Cys137 in transmembrane segment 2 are close to Arg935 and Gly939 in transmembrane segment 11 of human P-glycoprotein. J. Biol. Chem., 2004, 279, 18232-18238
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18232-18238
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
35
-
-
33745008903
-
Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket
-
DOI 10.1042/BJ20060012
-
Loo, T.W.; Bartlettt, M.C.; Clarke, D.M. Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket. Biochem. J., 2006, 396, 537-545 (Pubitemid 44228168)
-
(2006)
Biochemical Journal
, vol.396
, Issue.3
, pp. 537-545
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
36
-
-
0035805573
-
Defining the Drug-binding Site in the Human Multidrug Resistance P-glycoprotein Using a Methanethiosulfonate Analog of Verapamil, MTS-verapamil
-
DOI 10.1074/jbc.M100407200
-
Loo, T.W.; Clarke, D.M. Defining the drug-binding site in the human multidrug resistance P-glycoprotein using a methanethiosulfonate analog of verapamil, MTS-verapamil. J. Biol. Chem., 2001, 276, 14972-14979 (Pubitemid 37373379)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.18
, pp. 14972-14979
-
-
Loo, T.W.1
Clarke, D.M.2
-
37
-
-
33749985062
-
Transmembrane segment 7 of human P-glycoprotein forms part of the drug-binding pocket
-
DOI 10.1042/BJ20060715
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Transmembrane segment 7 of human P-glycoprotein forms part of the drug-binding pocket. Biochem. J., 2006, 399, 351-359 (Pubitemid 44570297)
-
(2006)
Biochemical Journal
, vol.399
, Issue.2
, pp. 351-359
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
38
-
-
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. J. Biol. Chem., 2003, 278, 39706-39710
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 39706-39710
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
39
-
-
0037687304
-
Substrate-induced conformational changes in the transmembrane segments of human Pglycoprotein. Direct evidence for the substrate-induced fit mechanism for drug binding
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Substrate-induced conformational changes in the transmembrane segments of human Pglycoprotein. Direct evidence for the substrate-induced fit mechanism for drug binding. J. Biol. Chem., 2003, 278, 13603-13606
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13603-13606
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
40
-
-
0037113961
-
Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein
-
DOI 10.1074/jbc.M208433200
-
Loo, T.W.; Clarke, D.M. Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein. J. Biol. Chem., 2002, 277, 44332-44338 (Pubitemid 36157868)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.46
, pp. 44332-44338
-
-
Loo, T.W.1
Clarke, D.M.2
-
41
-
-
12144262818
-
Interaction of LDS-751 with Pglycoprotein and mapping of the location of the R drug binding site
-
Lugo, M.R.; Sharom, F.J. Interaction of LDS-751 with Pglycoprotein and mapping of the location of the R drug binding site. Biochemistry, 2005, 44, 643-655
-
(2005)
Biochemistry
, vol.44
, pp. 643-655
-
-
Lugo, M.R.1
Sharom, F.J.2
-
42
-
-
1542320036
-
Disulfide cross-linking analysis shows that transmembrane segments 5 and 8 of human P glycoprotein are close together on the cytoplasmic side of the membrane
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Disulfide cross-linking analysis shows that transmembrane segments 5 and 8 of human P glycoprotein are close together on the cytoplasmic side of the membrane. J. Biol. Chem., 2004, 279, 7692-7697
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7692-7697
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
43
-
-
0042531543
-
A structural model for the open conformation of the mdr1 P-glycoprotein based on the MsbA crystal structure
-
DOI 10.1074/jbc.M302443200
-
Seigneuret, M.; Garnier-Suillerot, A. A structural model for the open conformation of the mdr1 P-glycoprotein based on the MsbA crystal structure. J. Biol. Chem., 2003, 278, 30115-30124 (Pubitemid 36962404)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.32
, pp. 30115-30124
-
-
Seigneuret, M.1
Garnier-Suillerot, A.2
-
44
-
-
0642272487
-
An atomic detail model for the human ATP binding cassette transporter P-glycoprotein derived from disulfide cross-linking and homology modeling
-
Stenham, D.R.; Campbell, J.D.; Sansom, M.S.; Higgins, C.F.; Kerr, I.D.; Linton, K.J. An atomic detail model for the human ATP binding cassette transporter P-glycoprotein derived from disulfide cross-linking and homology modeling. FASEB J., 2003, 17, 2287-2289
-
(2003)
FASEB J.
, vol.17
, pp. 2287-2289
-
-
Stenham, D.R.1
Campbell, J.D.2
Sansom, M.S.3
Higgins, C.F.4
Kerr, I.D.5
Linton, K.J.6
-
45
-
-
2342533129
-
Structure-Function Relationships of Multidrug Resistance P-Glycoprotein
-
DOI 10.1021/jm031009p
-
Pajeva, I.K.; Globisch, C.; Wiese, M. Structure-function relationships of multidrug resistance P-glycoprotein. J. Med. Chem., 2004, 47, 2523-2533 (Pubitemid 38580090)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.10
, pp. 2523-2533
-
-
Pajeva, I.K.1
Globisch, C.2
Wiese, M.3
-
46
-
-
0030971840
-
Structure of the multidrug resistance p-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis
-
DOI 10.1074/jbc.272.16.10685
-
Rosenberg, M.F.; Callaghan, R.; Ford, R.C.; Higgins, C.F. Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis. J. Biol. Chem., 1997, 272, 10685-10694 (Pubitemid 27181079)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.16
, pp. 10685-10694
-
-
Rosenberg, M.F.1
Callaghan, R.2
Ford, R.C.3
Higgins, C.F.4
-
47
-
-
0037424343
-
Three-dimensional structures of the mammalian multidrug resistance P-glycoprotein demonstrate major conformational changes in the transmembrane domains upon nucleotide binding
-
Rosenberg, M.F.; Kamis, A.B.; Callaghan, R.; Higgins, C.F.; Ford, R.C. Three-dimensional structures of the mammalian multidrug resistance P-glycoprotein demonstrate major conformational changes in the transmembrane domains upon nucleotide binding. J. Biol. Chem., 2003, 278, 8294-8299
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 8294-8299
-
-
Rosenberg, M.F.1
Kamis, A.B.2
Callaghan, R.3
Higgins, C.F.4
Ford, R.C.5
-
48
-
-
0037137614
-
Pharmacophore model of drugs involved in P-glycoprotein multidrug resistance: Explanation of structural variety (hypothesis)
-
DOI 10.1021/jm020941h
-
Pajeva, I.K.; Wiese, M. Pharmacophore model of drugs involved in P-glycoprotein multidrug resistance: explanation of structural variety (hypothesis). J. Med. Chem., 2002, 45, 5671-5686 (Pubitemid 35453760)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.26
, pp. 5671-5686
-
-
Pajeva, I.K.1
Wiese, M.2
-
49
-
-
33646029725
-
Predicting the three-dimensional structure of human P-glycoprotein in absence of ATP by computational techniques embodying crosslinking data: Insight into the mechanism of ligand migration and binding sites
-
Vandevuer, S.; Van Bambeke, F.; Tulkens, P.M.; Prévost, M. Predicting the three-dimensional structure of human P-glycoprotein in absence of ATP by computational techniques embodying crosslinking data: insight into the mechanism of ligand migration and binding sites. Proteins, 2006, 63, 466-478
-
(2006)
Proteins
, vol.63
, pp. 466-478
-
-
Vandevuer, S.1
Van Bambeke, F.2
Tulkens, P.M.3
Prévost, M.4
-
50
-
-
33646596002
-
The remarkable transport mechanism of P-glycoprotein: A multidrug transporter
-
DOI 10.1007/s10863-005-9497-5
-
Al-Shawi, M.K.; Omote, H. The remarkable transport mechanism of P-glycoprotein: a multidrug transporter. J. Bioenerg. Biomembr., 2005, 37, 489-496 (Pubitemid 43725181)
-
(2005)
Journal of Bioenergetics and Biomembranes
, vol.37
, Issue.6
, pp. 489-496
-
-
Al-Shawi, M.K.1
Omote, H.2
-
51
-
-
33748670458
-
Crystal structures of a multidrug transporter reveal a functionally rotating mechanism
-
Murakami, S.; Nakashima, R.; Yamashita, E.; Matsumoto, T.; Yamaguchi, A. Crystal structures of a multidrug transporter reveal a functionally rotating mechanism. Nature, 2006, 443, 173-179
-
(2006)
Nature
, vol.443
, pp. 173-179
-
-
Murakami, S.1
Nakashima, R.2
Yamashita, E.3
Matsumoto, T.4
Yamaguchi, A.5
-
52
-
-
0042167430
-
P-glycoprotein inhibitors and their screening: A perspective from bioavailability enhancement
-
DOI 10.1016/S1043-6618(03)00158-0
-
Varma, M.V.; Ashokraj, Y.; Dey, C.S.; Panchagnula, R. Pglycoprotein inhibitors and their screening: a perspective from bioavailability enhancement. Pharmacol. Res., 2003, 48, 347-359 (Pubitemid 36945333)
-
(2003)
Pharmacological Research
, vol.48
, Issue.4
, pp. 347-359
-
-
Varma, M.V.S.1
Ashokraj, Y.2
Dey, C.S.3
Panchagnula, R.4
-
53
-
-
0032791241
-
Modeling of P-glycoprotein-involved epithelial drug transport in MDCK cells
-
Ito, S.; Woodland, C.; Sarkadi, B.; Hockmann, G.; Walker, S.E.; Koren, G. Modeling of P-glycoprotein-involved epithelial drug transport in MDCK cells. Am. J. Physiol., 1999, 46, F84-96.
-
(1999)
Am. J. Physiol.
, vol.46
-
-
Ito, S.1
Woodland, C.2
Sarkadi, B.3
Hockmann, G.4
Walker, S.E.5
Koren, G.6
-
54
-
-
11244309507
-
The elementary mass action rate constants of P-gp transport for a confluent monolayer of MDCKII-hMDR1 cells
-
DOI 10.1529/biophysj.104.045633
-
Tran, T.T.; Mittal, A.; Aldinger, T.; Polli, J.W.; Ayrton, A.; Ellens, H.; Bentz, J. The elementary mass action rate constants of P-gp transport for a confluent monolayer of MDCKII-hMDR1 cells. Biophys. J., 2005, 88, 715-738 (Pubitemid 40070714)
-
(2005)
Biophysical Journal
, vol.88
, Issue.1
, pp. 715-738
-
-
Tran, T.T.1
Mittal, A.2
Aldinger, T.3
Polli, J.W.4
Ayrton, A.5
Ellens, H.6
Bentz, J.7
-
55
-
-
25144511902
-
m
-
DOI 10.1007/s11095-005-6627-z
-
Bentz, J.; Tran, T.T.; Polli, J.W.; Ayrton, A.; Ellens, H. The steady-state Michaelis-Menten analysis of P-glycoprotein mediated transport through a confluent cell monolayer cannot predict the correct Michaelis constant Km. Pharm. Res., 2005, 22, 1667-1677 (Pubitemid 41355906)
-
(2005)
Pharmaceutical Research
, vol.22
, Issue.10
, pp. 1667-1677
-
-
Bentz, J.1
Thuy, T.T.2
Polli, J.W.3
Ayrton, A.4
Ellens, H.5
-
56
-
-
0032556517
-
Kinetic analysis of the mechanism of action of the multidrug transporter
-
DOI 10.1006/jtbi.1998.0787
-
Ashida, H.; Oonishi, T.; Uyesaka, N. Kinetic analysis of the mechanism of action of the multidrug transporter. J. Theor. Biol., 1998, 195, 219-232 (Pubitemid 28528827)
-
(1998)
Journal of Theoretical Biology
, vol.195
, Issue.2
, pp. 219-232
-
-
Ashida, H.1
Oonishi, T.2
Uyesaka, N.3
-
57
-
-
0027432409
-
Fluorescent cellular indicators are extruded by the multidrug resistance protein
-
Homolya, L.; Hollo, Z.; Germann, U.A.; Pastan, I.; Gottesman, M.M.; Sarkadi, B. Fluorescent cellular indicators are extruded by the multidrug resistance protein. J. Biol. Chem., 1993, 268, 21493-21496 (Pubitemid 23320634)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.29
, pp. 21493-21496
-
-
Homolya, L.1
Hollo, Z.2
Germann, U.A.3
Pastan, I.4
Gottesman, M.M.5
Sarkadi, B.6
-
58
-
-
0025193531
-
Photosensitized labeling of a functinal multidrug transporter in living drug-resistant tumor cells
-
Raviv, Y.; Pollard, H.B.; Bruggemann, E.P.; Pastan, I.; Gottesman, M.M. Photosensitized labeling of a functional multidrug transporter in living drug-resistant tumor cells. J. Biol. Chem., 1990, 265, 3975-3980 (Pubitemid 20096035)
-
(1990)
Journal of Biological Chemistry
, vol.265
, Issue.7
, pp. 3975-3980
-
-
Raviv, Y.1
Pollard, H.B.2
Bruggemann, E.P.3
Pastan, I.4
Gottesman, M.M.5
-
59
-
-
0037449746
-
Drug binding in human Pglycoprotein causes conformational changes in both nucleotidebinding domains
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Drug binding in human Pglycoprotein causes conformational changes in both nucleotidebinding domains. J. Biol. Chem., 2003, 278, 1575-1578
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 1575-1578
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
60
-
-
0033544851
-
Identification of residues in the drug-binding domain of human P-glycoprotein. Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimane
-
Loo, T.W.; Clarke, D.M. Identification of residues in the drug-binding domain of human P-glycoprotein. Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimane. J. Biol. Chem., 1999, 274, 35388-35392
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 35388-35392
-
-
Loo, T.W.1
Clarke, D.M.2
-
61
-
-
1242272074
-
Synergy between conserved ABC signature Ser residues in Pglycoprotein catalysis
-
Tombline, G.; Bartholomew, L.; Gimi, K.; Tyndall, G.A.; Senior, A.E. Synergy between conserved ABC signature Ser residues in Pglycoprotein catalysis. J. Biol. Chem., 2004, 279, 5363-5373
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 5363-5373
-
-
Tombline, G.1
Bartholomew, L.2
Gimi, K.3
Tyndall, G.A.4
Senior, A.E.5
-
62
-
-
0037180390
-
Importance of the conserved Walker B glutamate residues, 556 and 1201, for the completion of the catalytic cycle of ATP hydrolysis by human P-glycoprotein (ABCB1)
-
Sauna, Z.E.; Muller, M.; Peng, X.H.; Ambudkar, S.V. Importance of the conserved Walker B glutamate residues, 556 and 1201, for the completion of the catalytic cycle of ATP hydrolysis by human P-glycoprotein (ABCB1). Biochemistry, 2002, 41, 13989-14000
-
(2002)
Biochemistry
, vol.41
, pp. 13989-14000
-
-
Sauna, Z.E.1
Muller, M.2
Peng, X.H.3
Ambudkar, S.V.4
-
63
-
-
0038419822
-
Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drug-binding site
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drug-binding site. J. Biol. Chem., 2003, 278, 20449-20452
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20449-20452
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
64
-
-
0347379911
-
Methanethiosulfonate derivatives of rhodamine and verapamil activate human Pglycoprotein at different sites
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Methanethiosulfonate derivatives of rhodamine and verapamil activate human Pglycoprotein at different sites. J. Biol. Chem., 2003, 278, 50136-50141
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 50136-50141
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
65
-
-
13244292479
-
Three-dimensional structure of P-glycoprotein: The transmembrane regions adopt an asymmetric configuration in the nucleotidebound state
-
Rosenberg, M.F.; Callaghan, R.; Modok, S.; Higgins, C.F.; Ford, R.C. Three-dimensional structure of P-glycoprotein: the transmembrane regions adopt an asymmetric configuration in the nucleotidebound state. J. Biol. Chem., 2005, 280, 2857-2862
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 2857-2862
-
-
Rosenberg, M.F.1
Callaghan, R.2
Modok, S.3
Higgins, C.F.4
Ford, R.C.5
-
66
-
-
0037133616
-
Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site
-
Loo, T.W.; Clarke, D.M. Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site. Proc. Natl. Acad. Sci. U S A, 2002, 99, 3511-3516
-
Proc. Natl. Acad. Sci. U S A, 2002
, vol.99
, pp. 3511-3516
-
-
Loo, T.W.1
Clarke, D.M.2
-
67
-
-
0035853686
-
Characterization of the catalytic cycle of ATP hydrolysis by human P-glycoprotein. the two ATP hydrolysis events in a single catalytic cycle are kinetically similar but affect different functional outcomes
-
DOI 10.1074/jbc.M011294200
-
Sauna, Z.E.; Ambudkar, S.V. Characterization of the catalytic cycle of ATP hydrolysis by human P-glycoprotein. The two ATP hydrolysis events in a single catalytic cycle are kinetically similar but affect different functional outcomes. J. Biol. Chem., 2001, 276, 11653-11661 (Pubitemid 37385318)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.15
, pp. 11653-11661
-
-
Sauna, Z.E.1
Ambudkar, S.V.2
-
68
-
-
32044453808
-
Recent progress in understanding the mechanism of P-glycoprotein-mediated drug efflux
-
Loo, T.W.; Clarke, D.M. Recent progress in understanding the mechanism of P-glycoprotein-mediated drug efflux. J. Membr. Biol., 2005, 206, 173-185
-
(2005)
J. Membr. Biol.
, vol.206
, pp. 173-185
-
-
Loo, T.W.1
Clarke, D.M.2
-
69
-
-
33748747880
-
Exploiting reaction intermediates of the ATPase reaction to elucidate the mechanism of transport by P-glycoprotein (ABCB1)
-
Sauna, Z.E.; Nandigama, K.; Ambudkar, S.V. Exploiting reaction intermediates of the ATPase reaction to elucidate the mechanism of transport by P-glycoprotein (ABCB1). J. Biol. Chem., 2006, 281, 26501-26511
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 26501-26511
-
-
Sauna, Z.E.1
Nandigama, K.2
Ambudkar, S.V.3
-
70
-
-
17944370228
-
Repacking of the transmembrane domains of Pglycoprotein during the transport ATPase cycle
-
Rosenberg, M.F.; Velarde, G.; Ford, R.C.; Martin, C.; Berridge, G.; Kerr, I.D.; Callaghan, R.; Schmidlin, A.; Wooding, C.; Linton, K.J.; Higgins, C.F. Repacking of the transmembrane domains of Pglycoprotein during the transport ATPase cycle. EMBO J., 2001, 20, 5615-5625
-
(2001)
EMBO J.
, vol.20
, pp. 5615-5625
-
-
Rosenberg, M.F.1
Velarde, G.2
Ford, R.C.3
Martin, C.4
Berridge, G.5
Kerr, I.D.6
Callaghan, R.7
Schmidlin, A.8
Wooding, C.9
Linton, K.J.10
Higgins, C.F.11
-
71
-
-
4644265234
-
The drug-binding pocket of the human multidrug resistance P-glycoprotein is accessible to the aqueous medium
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. The drug-binding pocket of the human multidrug resistance P-glycoprotein is accessible to the aqueous medium. Biochemistry, 2004, 43, 12081-12089
-
(2004)
Biochemistry
, vol.43
, pp. 12081-12089
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
72
-
-
33749570969
-
Insertion of an arginine residue into the transmembrane segments corrects protein misfolding
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Insertion of an arginine residue into the transmembrane segments corrects protein misfolding. J. Biol. Chem., 2006, 281, 29436-29440
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 29436-29440
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
73
-
-
33846419807
-
How can we best use structural information on P-glycoprotein to design inhibitors?
-
McDevitt, C.A.; Callaghan, R. How can we best use structural information on P-glycoprotein to design inhibitors? Pharmacol. Ther., 2007, 113, 429-441
-
(2007)
Pharmacol. Ther.
, vol.113
, pp. 429-441
-
-
McDevitt, C.A.1
Callaghan, R.2
-
74
-
-
1542268189
-
Synthesis and evaluation of dihydropyrroloquinolines that selectively antagonize P-glycoprotein
-
Lee, B.D.; Li, Z.; French, K.J.; Zhuang, Y.; Xia, Z.; Smith, C.D. Synthesis and evaluation of dihydropyrroloquinolines that selectively antagonize P-glycoprotein. J. Med. Chem., 2004, 47, 1413-1422
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1413-1422
-
-
Lee, B.D.1
Li, Z.2
French, K.J.3
Zhuang, Y.4
Xia, Z.5
Smith, C.D.6
-
75
-
-
34249324102
-
The pharmacology of cancer resistance
-
O'Connor, R. The pharmacology of cancer resistance. Anticancer Res., 2007, 27, 1267-1272
-
(2007)
Anticancer Res.
, vol.27
, pp. 1267-1272
-
-
O'Connor, R.1
-
76
-
-
0037358040
-
Overcoming multidrug resistance in cancer: An update on the clinical strategy of inhibiting pglycoprotein
-
Thomas, H.; Coley, H.M. Overcoming multidrug resistance in cancer: an update on the clinical strategy of inhibiting pglycoprotein. Cancer Control, 2003, 10, 159-165
-
(2003)
Cancer Control
, vol.10
, pp. 159-165
-
-
Thomas, H.1
Coley, H.M.2
-
77
-
-
33748747119
-
(+/-)-3′-O,4′-Odicynnamoyl-cis-khellactone, a derivative of (+/-)-praeruptorin A, reverses P-glycoprotein mediated multidrug resistance in cancer cells
-
Shen, X.L.; Chen, G.Y.; Zhu, G.Y.; Fong, W.F. (+/-)-3′-O,4′- Odicynnamoyl-cis-khellactone, a derivative of (+/-)-praeruptorin A, reverses P-glycoprotein mediated multidrug resistance in cancer cells. Bioorg. Med. Chem., 2006, 14, 7138-7145
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 7138-7145
-
-
Shen, X.L.1
Chen, G.Y.2
Zhu, G.Y.3
Fong, W.F.4
-
78
-
-
46449133480
-
Reversal of multidrug resistance by synthetic and natural compounds in drug-resistant MCF-7 cell lines
-
DOI 10.1159/000140462
-
Kars, M.D.; Iseri, O.D.; Gunduz, U.; Molnar, J. Reversal of multidrug resistance by synthetic and natural compounds in drug-resistant MCF-7 cell lines. Chemotherapy, 2008, 54, 194-200. (Pubitemid 351929270)
-
(2008)
Chemotherapy
, vol.54
, Issue.3
, pp. 194-200
-
-
Kars, M.D.1
Iseri, O.D.2
Gunduz, U.3
Molnar, J.4
-
79
-
-
51049115157
-
Overcoming multidrug resistance in human carcinoma cells by an antisense oligodeoxynucleotide - doxorubicin conjugate in vitro and in vivo
-
Ren, Y.; Wang, Y.; Zhang, Y.; Wei, D. Overcoming multidrug resistance in human carcinoma cells by an antisense oligodeoxynucleotide - doxorubicin conjugate in vitro and in vivo. Mol. Pharm., 2008, 5, 579-587
-
(2008)
Mol. Pharm.
, vol.5
, pp. 579-587
-
-
Ren, Y.1
Wang, Y.2
Zhang, Y.3
Wei, D.4
-
80
-
-
41549157906
-
Levistolide a overcomes P-glycoprotein-mediated drug resistance in human breast carcinoma cells
-
DOI 10.1111/j.1745-7254.2008.00719.x
-
Chen, F.; Wang, T.; Wang, J.; Wang, Z.Q.; Qian, M. Levistolide A overcomes P-glycoprotein-mediated drug resistance in human breast carcinoma cells. Acta Pharmacol. Sin., 2008, 29, 458-464 (Pubitemid 351465503)
-
(2008)
Acta Pharmacologica Sinica
, vol.29
, Issue.4
, pp. 458-464
-
-
Chen, F.1
Wang, T.2
Wang, J.3
Wang, Z.-Q.4
Qian, M.5
-
81
-
-
39549123404
-
The synergistic reversal effect of multidrug resistance by quercetin and hyperthermia in doxorubicin-resistant human myelogenous leukemia cells
-
DOI 10.1080/02656730701843109, PII 789606311
-
Shen, J.; Zhang, W.; Wu, J.; Zhu, Y. The synergistic reversal effect of multidrug resistance by quercetin and hyperthermia in doxorubicin-resistant human myelogenous leukemia cells. Int. J. Hyperthermia, 2008, 24, 151-159 (Pubitemid 351279955)
-
(2008)
International Journal of Hyperthermia
, vol.24
, Issue.2
, pp. 151-159
-
-
Shen, J.1
Zhang, W.2
Wu, J.3
Zhu, Y.4
-
82
-
-
50149102163
-
Impact of highly active antiretroviral therapy on ophthalmic manifestations in human immunodeficiency virus / acquired immune deficiency syndrome
-
Venkatesh, K.K.; Biswas, J.; Kumarasamy, N. Impact of highly active antiretroviral therapy on ophthalmic manifestations in human immunodeficiency virus / acquired immune deficiency syndrome. Indian J. Ophthalmol., 2008, 56, 391-393
-
(2008)
Indian J. Ophthalmol.
, vol.56
, pp. 391-393
-
-
Venkatesh, K.K.1
Biswas, J.2
Kumarasamy, N.3
-
83
-
-
58149393061
-
Association of complementary and alternative medicine use with highly active antiretroviral therapy initiation
-
Merenstein, D.; Yang, Y.; Schneider, M.F.; Goparaju, L.; Weber, K.; Sharma, A.; Levine, A.M.; Sharp, G.B.; Gandhi, M.; Liu, C. Association of complementary and alternative medicine use with highly active antiretroviral therapy initiation. Altern. Ther. Health Med., 2008, 14, 18-22.
-
(2008)
Altern. Ther. Health Med.
, vol.14
, pp. 18-22
-
-
Merenstein, D.1
Yang, Y.2
Schneider, M.F.3
Goparaju, L.4
Weber, K.5
Sharma, A.6
Levine, A.M.7
Sharp, G.B.8
Gandhi, M.9
Liu, C.10
-
84
-
-
9644257647
-
An MDR-EGFP gene fusion allows for direct cellular localization, function and stability assessment of P-glycoprotein
-
Petriz, J.; Gottesman, M.M.; Aran, J.M. An MDR-EGFP gene fusion allows for direct cellular localization, function and stability assessment of P-glycoprotein. Curr. Drug Deliv., 2004, 1, 43-56.
-
(2004)
Curr. Drug Deliv.
, vol.1
, pp. 43-56
-
-
Petriz, J.1
Gottesman, M.M.2
Aran, J.M.3
-
85
-
-
35548933763
-
P-glycoprotein-mediated active efflux of the anti-HIV1 nucleoside abacavir limits cellular accumulation and brain distribution
-
Shaik, N.; Giri, N.; Pan, G.; Elmquist, W.F. P-glycoprotein-mediated active efflux of the anti-HIV1 nucleoside abacavir limits cellular accumulation and brain distribution. Drug Metab. Dispos., 2007, 35, 2076-2085
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 2076-2085
-
-
Shaik, N.1
Giri, N.2
Pan, G.3
Elmquist, W.F.4
-
86
-
-
0034121122
-
Pharmacological inhibition of Pglycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes
-
Choo, E.F.; Leake, B.; Wandel, C.; Imamura, H.; Wood, A.J.J.; Wilkinson, G.R.; Kim, R.B. Pharmacological inhibition of Pglycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes. Drug Metab. Dispos., 2000, 28, 655-660
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 655-660
-
-
Choo, E.F.1
Leake, B.2
Wandel, C.3
Imamura, H.4
Wood, A.J.J.5
Wilkinson, G.R.6
Kim, R.B.7
-
87
-
-
18444373524
-
Effect of chronic administration of ritonavir on function of cytochrome P450 3A and P-glycoprotein in rats
-
DOI 10.1248/bpb.28.130
-
Kageyama, M.; Namiki, H.; Fukushima, H.; Terasaka, S.; Togawa, T.; Tanaka, A.; Ito, Y.; Shibata, N.; Takada, K. Effect of chronic administration of ritonavir on function of cytochrome P450 3A and P-glycoprotein in rats. Biol. Pharm. Bull., 2005, 28, 130-137 (Pubitemid 40879797)
-
(2005)
Biological and Pharmaceutical Bulletin
, vol.28
, Issue.1
, pp. 130-137
-
-
Kageyama, M.1
Namiki, H.2
Fukushima, H.3
Terasaka, S.4
Togawa, T.5
Tanaka, A.6
Ito, Y.7
Shibata, N.8
Takada, K.9
-
88
-
-
33747352798
-
MDR- And CYP3A4-mediated drug-drug interactions
-
Pal, D.; Mitra, A.K. MDR- and CYP3A4-mediated drug-drug interactions. J. Neuroimmune Pharmacol., 2006, 1, 323-339
-
(2006)
J. Neuroimmune Pharmacol.
, vol.1
, pp. 323-339
-
-
Pal, D.1
Mitra, A.K.2
-
89
-
-
42049093456
-
HIV-1 integrase inhibitors are substrates for the multidrug transporter MDR1-P-glycoprotein
-
Cianfriglia, M.; Dupuis, M.L.; Molinari, A.; Verdoliva, A.; Costi, R.; Galluzzo, C.M.; Andreotti, M.; Cara, A.; Di Santo, R.; Palmisano, L. HIV-1 integrase inhibitors are substrates for the multidrug transporter MDR1-P-glycoprotein. Retrovirology, 2007, 4, 17.
-
(2007)
Retrovirology
, vol.4
, pp. 17
-
-
Cianfriglia, M.1
Dupuis, M.L.2
Molinari, A.3
Verdoliva, A.4
Costi, R.5
Galluzzo, C.M.6
Andreotti, M.7
Cara, A.8
Di Santo, R.9
Palmisano, L.10
-
90
-
-
19944426763
-
P-glycoprotein expression affects the intracellular concentration and antiviral activity of the protease inhibitor saquinavir in a T cell line
-
Maffeo, A.; Bellomi, F.; Solimeo, I.; Bambacioni, F.; Scagnolari, C.; De Pisa, F.; Dupuis, M.L.; Cianfriglia, M.; Antonelli, G.; Turriziani, O. P-glycoprotein expression affects the intracellular concentration and antiviral activity of the protease inhibitor saquinavir in a T cell line. New Microbiol., 2004, 27, 119-126 (Pubitemid 40090999)
-
(2004)
New Microbiologica
, vol.27
, Issue.2 SUPPL. 1
, pp. 119-126
-
-
Maffeo, A.1
Bellomi, F.2
Solimeo, I.3
Bambacioni, F.4
Scagnolari, C.5
De Pisa, F.6
Dupuis, M.L.7
Cianfriglia, M.8
Antonelli, G.9
Turriziani, O.10
-
91
-
-
34250685774
-
An analysis of the population genetics of potential multi-drug resistance in Wuchereria bancrofti due to combination chemotherapy
-
DOI 10.1017/S0031182007002363, PII S0031182007002363
-
Schwab, A.E.; Churcher, T.S.; Schwab, A.J.; Basáñez, M.G.; Prichard, R.K. An analysis of the population genetics of potential multi-drug resistance in Wuchereria bancrofti due to combination chemotherapy. Parasitology, 2007, 134, 1025-1040 (Pubitemid 46933278)
-
(2007)
Parasitology
, vol.134
, Issue.7
, pp. 1025-1040
-
-
Schwab, A.E.1
Churcher, T.S.2
Schwab, A.J.3
Basanez, M.-G.4
Prichard, R.K.5
-
92
-
-
33847132229
-
Chemotherapeutic strategies against Trypanosoma brucei: Drug targets vs. drug targeting
-
DOI 10.2174/138161207780162809
-
Lüscher, A.; de Koning, H.P.; Mäser, P. Chemotherapeutic strategies against Trypanosoma brucei: drug targets vs. drug targeting. Curr. Pharm. Des., 2007, 13, 555-567 (Pubitemid 46477743)
-
(2007)
Current Pharmaceutical Design
, vol.13
, Issue.6
, pp. 555-567
-
-
Luscher, A.1
De Koning, H.P.2
Maser, P.3
-
93
-
-
0041331790
-
P-glycoprotein in helminths: Function and perspectives for anthelmintic treatment and reversal of resistance
-
Kerboeuf, D.; Blackhall, W.; Kaminsky, R.; von Samson-Himmelstjerna, G. P-glycoprotein in helminths: function and perspectives for anthelmintic treatment and reversal of resistance. Int. J. Antimicrob. Agents, 2003, 22, 332-346
-
(2003)
Int. J. Antimicrob. Agents
, vol.22
, pp. 332-346
-
-
Kerboeuf, D.1
Blackhall, W.2
Kaminsky, R.3
Von Samson-Himmelstjerna, G.4
-
94
-
-
23844456921
-
Dihidro-beta-agarofuran sesquiterpenes: A new class of reversal agents of the multidrug resistance phenotype mediated by P-glycoprotein in the protozoan parasite Leishmania
-
DOI 10.2174/1381612054864920
-
Cortés-Selva, F.; Jiménez, I.A.; Munoz-Martínez, F.; Campillo, M.; Bazzocchi, I.L.; Pardo, L.; Ravelo, A.G.; Castanys, S.; Gamarro, F. Dihydro-beta-agarofuran sesquiterpenes: a new class of reversal agents of the multidrug resistance phenotype mediated by Pglycoprotein in the protozoan parasite Leishmania. Curr. Pharm. Des., 2005, 11, 3125-3139 (Pubitemid 41149929)
-
(2005)
Current Pharmaceutical Design
, vol.11
, Issue.24
, pp. 3125-3159
-
-
Cortes-Selva, F.1
Jimenez, I.A.2
Munoz-Martinez, F.3
Campillo, M.4
Bazzocchi, I.L.5
Pardo, L.6
Ravelo, A.G.7
Castanys, S.8
Gamarro, F.9
-
95
-
-
55149107169
-
Update on gene modifiers in cystic fibrosis
-
Collaco, J.M.; Cutting, G.R. Update on gene modifiers in cystic fibrosis. Curr. Opin. Pulm. Med., 2008, 14, 559-566
-
(2008)
Curr. Opin. Pulm. Med.
, vol.14
, pp. 559-566
-
-
Collaco, J.M.1
Cutting, G.R.2
-
96
-
-
55549094466
-
Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating
-
He, L.; Aleksandrov, A.A.; Serohijos, A.W.; Hegedus, T.; Aleksandrov, L.A.; Cui, L.; Dokholyan, N.V.; Riordan, J.R. Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating. J. Biol. Chem., 2008, 283, 26383-26390
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 26383-26390
-
-
He, L.1
Aleksandrov, A.A.2
Serohijos, A.W.3
Hegedus, T.4
Aleksandrov, L.A.5
Cui, L.6
Dokholyan, N.V.7
Riordan, J.R.8
-
97
-
-
33646578825
-
Rescue of folding defects in ABC transporters using pharmacological chaperones
-
Loo, T.W.; Bartlett, M.C.; Clarke, D.M. Rescue of folding defects in ABC transporters using pharmacological chaperones. J. Bioenerg. Biomembr., 2005, 37, 501-507
-
(2005)
J. Bioenerg. Biomembr.
, vol.37
, pp. 501-507
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
98
-
-
23944447796
-
P-glycoprotein expression increases ATP release in respiratory cystic fibrosis cells
-
DOI 10.1016/j.jcf.2005.05.003, PII S1569199305000494
-
Naumann, N.; Siratska, O.; Gahr, M.; Rosen-Wolff, A. Pglycoprotein expression increases ATP release in respiratory cystic fibrosis cells. J. Cyst. Fibros., 2005, 4, 157-168 (Pubitemid 41200477)
-
(2005)
Journal of Cystic Fibrosis
, vol.4
, Issue.3
, pp. 157-168
-
-
Naumann, N.1
Siratska, O.2
Gahr, M.3
Rosen-Wolff, A.4
-
99
-
-
44349140031
-
Comment on: 'Antidepressant medications and other treatments of depressive disorders: a CINP Task Force report based on a review of evidence'
-
DOI 10.1017/S1461145708008705, PII S1461145708008705
-
Bauer, B. Comment on: 'antidepressant medications and other treatments of depressive disorders: a CINP Task Force report based on a review of evidence'. Int. J. Neuropsychopharmacol., 2008, 11, 577-578 (Pubitemid 351744815)
-
(2008)
International Journal of Neuropsychopharmacology
, vol.11
, Issue.4
, pp. 577-578
-
-
Belmaker, R.H.1
-
100
-
-
27644489474
-
Pglycoprotein deficiency at the blood-brain barrier increases amyloid-beta deposition in an Alzheimer disease mouse model
-
Cirrito, J.R.; Deane, R.; Fagan, A.M.; Spinner, M.L.; Parsadanian, M.; Finn, M.B.; Jiang, H.; Prior, J.L.; Sagare, A.; Bales, K.R.; Paul, S.M.; Zlokovic, B.V.; Piwnica-Worms, D.; Holtzman, D.M. Pglycoprotein deficiency at the blood-brain barrier increases amyloid-beta deposition in an Alzheimer disease mouse model. J. Clin. Invest., 2005, 115, 3285-3290
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 3285-3290
-
-
Cirrito, J.R.1
Deane, R.2
Fagan, A.M.3
Spinner, M.L.4
Parsadanian, M.5
Finn, M.B.6
Jiang, H.7
Prior, J.L.8
Sagare, A.9
Bales, K.R.10
Paul, S.M.11
Zlokovic, B.V.12
Piwnica-Worms, D.13
Holtzman, D.M.14
-
101
-
-
27744562662
-
MRP3, BCRP, and P-glycoprotein activities are prognostic factors in adult acute myeloid leukemia
-
Benderra, Z.; Faussat, A.M.; Sayada, L.; Perrot, J.Y.; Tang, R.P.; Chaoui, D.; Morjani, H.; Marzac, C.; Marie, J.P.; Legrand, O. MRP3, BCRP, and P-glycoprotein activities are prognostic factors in adult acute myeloid leukemia. Clin. Cancer Res., 2005, 11, 7764-7772
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 7764-7772
-
-
Benderra, Z.1
Faussat, A.M.2
Sayada, L.3
Perrot, J.Y.4
Tang, R.P.5
Chaoui, D.6
Morjani, H.7
Marzac, C.8
Marie, J.P.9
Legrand, O.10
-
102
-
-
5744228959
-
Modulation of drug resistance transporters as a strategy for treating myelodysplastic syndrome
-
Ross, D.D. Modulation of drug resistance transporters as a strategy for treating myelodysplastic syndrome. Best Pract. Res. Clin. Haematol., 2004, 17, 641-651
-
(2004)
Best Pract. Res. Clin. Haematol.
, vol.17
, pp. 641-651
-
-
Ross, D.D.1
-
103
-
-
21544479109
-
Cardiomyocytes of chronically ischemic pig hearts express the MDR-1 gene-encoded P-glycoprotein
-
Lazarowski, A.J.; Rivello, H.J.G.; Janavel, G.L.V.; Cuniberti, L.A.; Meckert, P.M.C.; Yannarelli, G.G.; Mele, A.; Crottogini, A.J.; Laguens, R.P. Cardiomyocytes of chronically ischemic pig hearts express the MDR-1 gene-encoded P-glycoprotein. J. Histochem. Cytochem., 2005, 53, 845-850
-
(2005)
J. Histochem. Cytochem.
, vol.53
, pp. 845-850
-
-
Lazarowski, A.J.1
Rivello, H.J.G.2
Janavel, G.L.V.3
Cuniberti, L.A.4
Meckert, P.M.C.5
Yannarelli, G.G.6
Mele, A.7
Crottogini, A.J.8
Laguens, R.P.9
-
104
-
-
20344386201
-
Intestinal inflammation induces adaptation of P-glycoprotein expression and activity
-
Buyse, M.; Radeva, G.; Bado, A.; Farinotti, R. Intestinal inflammation induces adaptation of P-glycoprotein expression and activity. Biochem. Pharmacol., 2005, 69, 1745-1754
-
(2005)
Biochem. Pharmacol.
, vol.69
, pp. 1745-1754
-
-
Buyse, M.1
Radeva, G.2
Bado, A.3
Farinotti, R.4
-
105
-
-
0036104334
-
Functional polymorphisms of the human multidrug resistance (MDR1) gene: Correlation with P glycoprotein expression and activity in vivo
-
Brinkmann, U. Functional polymorphisms of the human multidrug resistance (MDR1) gene: correlation with P glycoprotein expression and activity in vivo. Novartis Found Symp., 2002, 243, 207-210
-
Novartis Found Symp., 2002
, vol.243
, pp. 207-210
-
-
Brinkmann, U.1
-
106
-
-
0034724324
-
Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo
-
Hoffmeyer, S.; Burk, O.; von Richter, O.; Arnold, H.P.; Brockmöller, J.; Johne, A.; Cascorbi, I.; Gerloff, T.; Roots, I.; Eichelbaum, M.; Brinkmann, U. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc. Natl. Acad. Sci. USA., 2000, 97, 3473-3478
-
Proc. Natl. Acad. Sci. USA., 2000
, vol.97
, pp. 3473-3478
-
-
Hoffmeyer, S.1
Burk, O.2
Von Richter, O.3
Arnold, H.P.4
Brockmöller, J.5
Johne, A.6
Cascorbi, I.7
Gerloff, T.8
Roots, I.9
Eichelbaum, M.10
Brinkmann, U.11
-
107
-
-
33947417310
-
Shedding light on drug transport: Structure and function of the P-glycoprotein multidrug transporter (ABCB1)
-
Sharom FJ. Shedding light on drug transport: structure and function of the P-glycoprotein multidrug transporter (ABCB1). Biochem. Cell Biol., 2006, 84, 979-992
-
(2006)
Biochem. Cell Biol.
, vol.84
, pp. 979-992
-
-
Sharom, F.J.1
-
108
-
-
3042767682
-
Functional implications of genetic polymorphisms in the multidrug resistance gene MDR1 (ABCB1)
-
Pauli-Magnus, C.; Kroetz, D.L. Functional implications of genetic polymorphisms in the multidrug resistance gene MDR1 (ABCB1). Pharm. Res., 2004, 21, 904-913
-
(2004)
Pharm. Res.
, vol.21
, pp. 904-913
-
-
Pauli-Magnus, C.1
Kroetz, D.L.2
-
109
-
-
0037131893
-
The influence of MDR1 polymorphisms on Pglycoprotein expression and function in humans
-
Fromm, M.F. The influence of MDR1 polymorphisms on Pglycoprotein expression and function in humans. Adv. Drug Deliv. Rev., 2002, 54, 1295-1310.
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 1295-1310
-
-
Fromm, M.F.1
-
110
-
-
67249130775
-
Clinical impact of polymorphisms of transport proteins and enzymes involved in the metabolism of immunosuppressive drugs
-
Rosso Felipe, C.; de Sandes, T.V.; Sampaio, E.L.; Park, S.I.; Silva, H.T. Jr.; Medina Pestana, J.O. Clinical impact of polymorphisms of transport proteins and enzymes involved in the metabolism of immunosuppressive drugs. Transplant Proc., 2009, 41, 1441-1455
-
Transplant Proc., 2009
, vol.41
, pp. 1441-1455
-
-
Rosso Felipe, C.1
De Sandes, T.V.2
Sampaio, E.L.3
Park, S.I.4
Silva Jr., H.T.5
Medina Pestana, J.O.6
-
111
-
-
58549112368
-
An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment
-
Ekhart, C.; Rodenhuis, S.; Smits, P.H.; Beijnen, J.H.; Huitema, A.D. An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment. Cancer Treat. Rev., 2009, 35, 18-31.
-
(2009)
Cancer Treat. Rev.
, vol.35
, pp. 18-31
-
-
Ekhart, C.1
Rodenhuis, S.2
Smits, P.H.3
Beijnen, J.H.4
Huitema, A.D.5
-
112
-
-
56149110125
-
Impact of genetic polymorphisms of transporters on the pharmacokinetic, pharmacodynamic and toxicological properties of anionic drugs
-
Maeda, K.; Sugiyama, Y. Impact of genetic polymorphisms of transporters on the pharmacokinetic, pharmacodynamic and toxicological properties of anionic drugs. Drug Metab. Pharmacokinet., 2008, 23, 223-235
-
(2008)
Drug Metab. Pharmacokinet.
, vol.23
, pp. 223-235
-
-
Maeda, K.1
Sugiyama, Y.2
-
113
-
-
64649101364
-
A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function
-
Fung, K.L.; Gottesman, M.M. A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function. Biochim. Biophys. Acta, 2009, 1794, 860-871
-
(2009)
Biochim. Biophys. Acta
, vol.1794
, pp. 860-871
-
-
Fung, K.L.1
Gottesman, M.M.2
-
114
-
-
70350663033
-
Association between Genetic Polymorphism of Multidrug Resistance 1 Gene and Sasang Constitutions
-
Kim, H.J.; Hwang, S.Y.; Kim, J.H,.; Park, H.J.; Lee, S.G.; Lee, S.W.; Joo, J.C.; Kim, Y.K. Association between Genetic Polymorphism of Multidrug Resistance 1 Gene and Sasang Constitutions. Evid. Based Complement Alternat. Med., 2009, Suppl 1, 73-80.
-
(2009)
Evid. Based Complement Alternat. Med.
, Issue.SUPPL. 1
, pp. 73-80
-
-
Kim, H.J.1
Hwang, S.Y.2
Kim, J.H.3
Park, H.J.4
Lee, S.G.5
Lee, S.W.6
Joo, J.C.7
Kim, Y.K.8
-
115
-
-
0036667953
-
C3435T polymorphism in the MDR1 gene affects the enterocyte expression level of CYP3A4 rather than Pgp in recipients living donor liver transplantation
-
Goto, M.; Masuda, S.; Saito, H.; Uemoto, S.; Kiuchi, T.; Tanaka, K. C3435T polymorphism in the MDR1 gene affects the enterocyte expression level of CYP3A4 rather than Pgp in recipients living donor liver transplantation. Pharmacogenetics, 2002, 12, 451-457
-
(2002)
Pharmacogenetics
, vol.12
, pp. 451-457
-
-
Goto, M.1
Masuda, S.2
Saito, H.3
Uemoto, S.4
Kiuchi, T.5
Tanaka, K.6
-
116
-
-
58949089716
-
A MDR1 (ABCB1) gene single nucleotide polymorphism predicts outcome of temozolomide treatment in glioblastoma patients
-
Schaich, M,.; Kestel, L.; Pfirrmann, M.; Robel, K.; Illmer, T.; Kramer, M,.; Dill, C.; Ehninger, G.; Schackert, G.; Krex, D. A MDR1 (ABCB1) gene single nucleotide polymorphism predicts outcome of temozolomide treatment in glioblastoma patients. Ann. Oncol., 2009, 20, 175-181
-
(2009)
Ann. Oncol.
, vol.20
, pp. 175-181
-
-
Schaich, M.1
Kestel, L.2
Pfirrmann, M.3
Robel, K.4
Illmer, T.5
Kramer, M.6
Dill, C.7
Ehninger, G.8
Schackert, G.9
Krex, D.10
-
117
-
-
43049162139
-
Do polymorphisms in ABC transporter genes influence risk of childhood acute lymphoblastic leukemia?
-
Jamroziak, K.; Robak, T. Do polymorphisms in ABC transporter genes influence risk of childhood acute lymphoblastic leukemia? Leuk. Res., 2008, 32, 1173-1175
-
(2008)
Leuk. Res.
, vol.32
, pp. 1173-1175
-
-
Jamroziak, K.1
Robak, T.2
-
118
-
-
33751214491
-
Genetics of inflammatory bowel disease: Current status and future directions
-
Walters, T.D.; Silverberg, M.S. Genetics of inflammatory bowel disease: current status and future directions. Can. J. Gastroenterol., 2006, 20, 633-639
-
(2006)
Can. J. Gastroenterol.
, vol.20
, pp. 633-639
-
-
Walters, T.D.1
Silverberg, M.S.2
-
119
-
-
33745457857
-
Multidrug resistance 1 gene in inflammatory bowel disease: A meta-analysis
-
Annese, V.; Valvano, M.R.; Palmieri, O.; Latiano, A.; Bossa, F.; Andriulli, A. Multidrug resistance 1 gene in inflammatory bowel disease: a meta-analysis. World J. Gastroenterol., 2006, 12, 3636-3644 (Pubitemid 43950939)
-
(2006)
World Journal of Gastroenterology
, vol.12
, Issue.23
, pp. 3636-3644
-
-
Annese, V.1
Valvano, M.R.2
Palmieri, O.3
Latiano, A.4
Bossa, F.5
Andriulli, A.6
-
120
-
-
69349104835
-
A combination of proatherogenic single-nucleotide polymorphisms is associated with increased risk of coronary artery disease and myocardial infarction in Asian Indians
-
Poduri, A.; Khullar, M.; Bahl, A.; Sharma, Y.P.; Talwar, K.K. A combination of proatherogenic single-nucleotide polymorphisms is associated with increased risk of coronary artery disease and myocardial infarction in Asian Indians. DNA Cell Biol., 2009, 28, 451-460
-
(2009)
DNA Cell Biol.
, vol.28
, pp. 451-460
-
-
Poduri, A.1
Khullar, M.2
Bahl, A.3
Sharma, Y.P.4
Talwar, K.K.5
-
121
-
-
66849121735
-
MDR1/ABCB1 polymorphisms and multidrug resistance in epilepsy: In and out of fashion
-
Löscher, W.; Delanty, N. MDR1/ABCB1 polymorphisms and multidrug resistance in epilepsy: in and out of fashion. Pharmacogenomics, 2009, 10, 711-713
-
(2009)
Pharmacogenomics
, vol.10
, pp. 711-713
-
-
Löscher, W.1
Delanty, N.2
-
122
-
-
67449091266
-
Association of a polymorphism in the ABCB1 gene with Parkinson's disease
-
Westerlund M, Belin AC, Anvret A, Håkansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Association of a polymorphism in the ABCB1 gene with Parkinson's disease. Parkinsonism Relat. Disord., 2009, 15, 422-424
-
(2009)
Parkinsonism Relat. Disord.
, vol.15
, pp. 422-424
-
-
Westerlund, M.1
Belin, A.C.2
Anvret, A.3
Håkansson, A.4
Nissbrandt, H.5
Lind, C.6
Sydow, O.7
Olson, L.8
Galter, D.9
-
123
-
-
35448992847
-
Silent polymorphisms speak: How they affect pharmacogenomics and the treatment of cancer
-
Sauna, Z.E.; Kimchi-Sarfaty, C.; Ambudkar, S.V.; Gottesman, M.M. Silent polymorphisms speak: how they affect pharmacogenomics and the treatment of cancer. Cancer Res., 2007, 67, 9609-9612
-
(2007)
Cancer Res.
, vol.67
, pp. 9609-9612
-
-
Sauna, Z.E.1
Kimchi-Sarfaty, C.2
Ambudkar, S.V.3
Gottesman, M.M.4
-
124
-
-
56949102507
-
Polymorphisms and haplotypes in the multidrug resistance 1 gene (MDR1/ABCB1) and risk of multiple myeloma
-
Jamroziak, K.; Balcerczak, E.; Calka, K.; Piaskowski, S.; Urbanska-Rys, H.; Salagacka, A.; Mirowski, M.; Robak, T. Polymorphisms and haplotypes in the multidrug resistance 1 gene (MDR1/ABCB1) and risk of multiple myeloma. Leuk. Res., 2009, 33, 332-335
-
(2009)
Leuk. Res.
, vol.33
, pp. 332-335
-
-
Jamroziak, K.1
Balcerczak, E.2
Calka, K.3
Piaskowski, S.4
Urbanska-Rys, H.5
Salagacka, A.6
Mirowski, M.7
Robak, T.8
-
125
-
-
58549112368
-
An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment
-
Ekhart, C.; Rodenhuis, S.; Smits, P.H.; Beijnen, J.H.; Huitema, A.D. An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment. Cancer Treat. Rev., 2009, 35, 18-31.
-
(2009)
Cancer Treat. Rev.
, vol.35
, pp. 18-31
-
-
Ekhart, C.1
Rodenhuis, S.2
Smits, P.H.3
Beijnen, J.H.4
Huitema, A.D.5
-
126
-
-
84934436050
-
Pharmacogenomics of drug-metabolizing enzymes and drug transporters in chemotherapy
-
Bosch, T.M. Pharmacogenomics of drug-metabolizing enzymes and drug transporters in chemotherapy. Methods Mol. Biol., 2008, 448, 63-76.
-
(2008)
Methods Mol. Biol.
, vol.448
, pp. 63-76
-
-
Bosch, T.M.1
-
127
-
-
33646428345
-
Impact of extracellular acidity on the activity of P-glycoprotein and the cytotoxicity of chemotherapeutic drugs
-
Thews, O.; Gassner, B.; Kelleher, D.K.; Schwerdt, G.; Gekle, M. Impact of extracellular acidity on the activity of P-glycoprotein and the cytotoxicity of chemotherapeutic drugs. Neoplasia, 2006, 8, 143-152
-
(2006)
Neoplasia
, vol.8
, pp. 143-152
-
-
Thews, O.1
Gassner, B.2
Kelleher, D.K.3
Schwerdt, G.4
Gekle, M.5
|