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1 ug efflux pump similar to P-glycoprotein and multidrug resistance-associated protein.
2 tivity has recently been associated with the multidrug resistance-associated protein.
3 P-glycoprotein multidrug-resistance gene or multidrug resistance-associated protein.
4 on transporting polypeptides and basolateral multidrug resistance associated proteins.
5 ther Notch1 is involved in the expression of multidrug resistance-associated protein 1 (ABCC1/MRP1; h
9 ivered IgGs can inhibit the drug efflux pump multidrug resistance-associated protein 1 (MRP1) and the
10 by estrogen encoded the chick homolog of the multidrug resistance-associated protein 1 (MRP1) gene.
15 cytometry and immunostaining have shown that multidrug resistance-associated protein 1 (MRP1) is prev
16 regulates the cell surface expression of the multidrug resistance-associated protein 1 (MRP1) transpo
17 BD1 and the Tyr1302 residue in NBD2 of human multidrug resistance-associated protein 1 (MRP1) was mut
18 g cassette (ABC) transporters, such as P-gp, multidrug resistance-associated protein 1 (MRP1), and br
19 on a known ATP-binding cassette transporter, multidrug resistance-associated protein 1 (MRP1), and fo
20 drug efflux pumps, P-glycoprotein (Pgp) and multidrug resistance-associated protein 1 (MRP1), correl
21 resistance gene-1 P-glycoprotein (MDR1) and multidrug resistance-associated protein 1 (MRP1), has be
22 hat the function of Ycf1p, yeast ortholog of multidrug resistance-associated protein 1 (MRP1), is reg
23 GSH) and that the GSH-conjugate transporter, multidrug resistance-associated protein 1 (MRP1), mediat
24 across erythrocyte membranes is inhibited by multidrug resistance-associated protein 1 (MRP1)-specifi
28 th respect to potency and selectivity toward multidrug resistance-associated protein 1 (MRP1, ABCC1).
30 ctions of flavonoids with P-glycoprotein and multidrug resistance-associated protein 1 have been repo
31 onferring multidrug resistance such as MRP1 (multidrug resistance-associated protein 1) and LRP (lung
32 ved in drug resistance, namely GST and MRP1 (multidrug resistance-associated protein 1), are critical
33 emia, with permeability glycoprotein (P-gp), multidrug resistance-associated protein 1, and breast ca
34 es expressing high levels of P-glycoprotein, multidrug resistance-associated protein 1, or ABCG2, PhA
35 hree major drug transporters P-glycoprotien, multidrug resistance-associated protein 1, or ATP-bindin
38 ate a facile induction of mRNAs for mRFC and multidrug resistance-associated proteins 1 and 3 in inte
40 erase P1 (3.74-fold, 1.3-33.1, p<0.0001) and multidrug resistance associated protein-1 (4.06-fold, 1.
43 dramatic UL138-mediated loss of cell surface multidrug resistance-associated protein-1 (MRP1) and the
44 ts ATP binding cassette subfamily C member 2/multidrug resistance associated protein 2 (ABCC2/MRP2),
46 s of the canalicular organic ion transporter multidrug resistance associated protein 2 (Mrp2) on chlo
47 suppressed the ability of CAR to induce the multidrug resistance associated protein 2 (MRP2), a bili
50 ane cholesterol on the transport kinetics of multidrug resistance-associated protein 2 (MRP2) and of
51 ic retrieval and function of the canalicular multidrug resistance-associated protein 2 (Mrp2) and the
52 breast cancer resistance protein (BCRP), and multidrug resistance-associated protein 2 (MRP2) at the
53 holate cotransporting polypeptide (NTCP) and multidrug resistance-associated protein 2 (MRP2) by conv
54 eval of the bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2) from th
57 n of the ATP-dependent conjugate export pump multidrug resistance-associated protein 2 (Mrp2) is dimi
60 ) as a positive regulator of P-glycoprotein, multidrug resistance-associated protein 2 (Mrp2), and br
61 1A1 (Oatp1a1), the hepatobiliary transporter multidrug resistance-associated protein 2 (Mrp2), and th
69 0 administration significantly induced renal multidrug resistance-associated protein 2 and 4, peroxis
71 f 3 xenobiotic efflux pumps, P-glycoprotein, multidrug resistance-associated protein 2, and breast ca
73 tes, has been reported to selectively tether multidrug-resistance-associated protein 2 to the apical
74 luorescence showed that apical transporters (multidrug-resistance-associated protein 2, bile salt exp
75 rting polypeptides 1 and 2 (Oatp1 and 2) and multidrug resistance associated protein-2 (Mrp2) in preg
76 b, the bile salt export pump (Bsep), and the multidrug resistance-associated protein-2 (Mrp2) in medi
77 ycoprotein, ATP binding cassette b1 (Abcb1); multidrug resistance-associated protein-2 (Mrp2), Abcc2;
78 nofluorescence analyses confirmed that MRP3 (multidrug resistance associated protein 3), which was hi
79 ic basolateral membrane export transporters, multidrug resistance-associated protein 3 (Mrp3) and Mrp
80 ction of the cytochrome p450 CYP3A11 and the multidrug resistance-associated protein 3 transporter, w
81 blood-brain barrier, P-glycoprotein (ABCB1), multidrug resistance associated protein 4 (ABCC4) and br
82 polypeptide (NTCP) expression and activity, multidrug resistance-associated protein 4 (MRP4) overexp
83 malignant lesions, we aim to investigate the multidrug resistance-associated protein 4 (MRP4)-depende
85 cassette (ABC) family, P-glycoprotein (Pgp), multidrug-resistance associated protein 4 (MRP4) and bre
88 te-binding cassette family of genes, encodes multidrug resistance-associated protein 6, a putative tr
89 g on the transcriptional regulation of MRP7 (multidrug resistance associated protein 7) gene expressi
91 e transporters such as P-glycoprotein (Pgp), multidrug resistance-associated protein, and breast canc
93 Verapamil and cyclosporin A, blockers of the multidrug resistance-associated protein, decreased UVA-i
95 nd expression of Mrp3, another member of the multidrug resistance-associated protein family, in norma
96 g for glutathione S-transferase Pi (GST-Pi), multidrug resistance-associated protein genes (MRP1/MRP2
97 hout overexpression of P-glycoprotein or the multidrug-resistance associated protein have raised the
98 ium taurocholate cotransporting polypeptide, multidrug resistance-associated protein (Mdr) 2, and bil
99 (99m)Tc-mebrofenin, and efflux transporters (multidrug resistance-associated proteins) mediating its
101 istance is accompanied by mislocalization of multidrug resistance associated protein (MRP) 1 and othe
102 fflux transporter genes with homology to the multidrug resistance associated protein (mrp) and permea
103 P2, were highly homologous to members of the multidrug resistance associated protein (MRP) subfamily.
104 ent studies implicate a role for some of the multidrug resistance associated proteins (MRP), includin
105 One major group of transporters is known as multidrug resistance associated proteins (MRP; ABCC gene
106 breast cancer resistance protein (Bcrp), and multidrug resistance-associated protein (Mrp) 4 in isola
111 ma led us to investigate a possible role for multidrug resistance-associated protein (MRP) as a cause
112 w that maize lpa1 mutants are defective in a multidrug resistance-associated protein (MRP) ATP-bindin
113 at export of glutathione-LDE-adducts through multidrug resistance-associated protein (MRP) channels i
115 n transporting polypeptide (OATP, SLC21) and multidrug resistance-associated protein (MRP) families.
116 dentified cDNA that has been assigned to the multidrug resistance-associated protein (MRP) family of
117 nding cassette transporters belonging to the multidrug resistance-associated protein (MRP) family.
118 The ABCC6 gene encodes MRP6, a member of the multidrug resistance-associated protein (MRP) family.
120 otection assay, we provide evidence that the multidrug resistance-associated protein (MRP) gene, whic
123 is associated with the overexpression of (a) multidrug resistance-associated protein (MRP) responsibl
124 cf1p is the prototypical member of the yeast multidrug resistance-associated protein (MRP) subfamily
125 inary experiments indicating that some plant multidrug resistance-associated protein (MRP) subfamily
126 vesicles prepared from cells expressing the multidrug resistance-associated protein (MRP) transport
127 resulted in elevated expression of mRNA for multidrug resistance-associated protein (MRP) within the
129 ), effectively inhibits growth and regresses multidrug resistance-associated protein (MRP)-overexpres
134 n this study, we examined the involvement of multidrug resistance-associated protein (MRP)4 (ABCC4) i
136 curonosyl-transferase (Ugt) 1a6 and 2b5, and multidrug resistance-associated proteins (Mrp) 2 and 3 m
139 , multidrug-resistance protein 1 (MDR1), and multidrug-resistance-associated protein (MRP) 2 and 3 el
140 sistance mediated by P-glycoprotein (Pgp) or multidrug-resistance-associated protein (MRP) remains a
141 transporters (bile salt export pump [BSEP], multidrug resistance-associated protein [MRP] 2) were un
142 other drug resistance proteins, notably the multidrug resistance-associated protein, MRP, and the lu
143 th MDR, including P-glycoprotein (P-gp), the multidrug resistance associated protein (MRP1), the lung
144 lastoma (NB), the level of expression of the multidrug resistance-associated protein (MRP1) gene is s
147 estigated a high-throughput assay to measure multidrug resistance-associated protein (MRP1)-mediated
150 variety of cells stably expressing MDR1 Pgp, multidrug resistance-associated proteins (MRP1-MRP6), or
152 CPE cells whereas MK-571, a pan-inhibitor of multidrug resistance associated proteins (MRPs), abolish
154 njugate transport, and possible mediation by multidrug resistance-associated proteins (MRPs) have bee
155 Additional drug transporters, such as the multidrug resistance-associated proteins (MRPs), have al
157 is, and the present study indicates that the multidrug resistance-associated proteins (MRPs/ABCC) are
158 as well as substrates of the plasma membrane multidrug resistance-associated proteins on the uptake o
159 Here we disrupted a gene encoding a putative multidrug resistance-associated protein (PfMRP) that was
160 o AP2 transcription factors and the P. vivax multidrug resistance-associated protein (PvMRP1), an ABC
161 an increase in the activity of pre-existing multidrug resistance-associated protein transporter carr