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1 4) is transferred to its export carrier, the multidrug resistance protein-1.
2 toplasmic side of the membrane for export by multidrug resistance protein-1.
3 efflux pumps such as P-glycoprotein (ABCB1), multidrug resistance protein 1 (ABCC1), and breast cance
4 ne domains but some, including SUR and MRP1 (multidrug resistance protein 1), contain an extra N-term
5 ciated protein 2, bile salt export pump, and multidrug-resistance protein 1) dissociated from their n
6 mium resistance by serving as a cofactor for multidrug resistance protein 1/GS-X pump-mediated cadmiu
8 led to increased expression and activity of multidrug resistance protein 1 (MDR-1), a membrane trans
9 lar cAMP or inhibit non-CFTR Cl(-) channels, multidrug resistance protein-1 (MDR-1), ATP-sensitive K(
11 ociated proteins caveolin-1, syntaxin-6, and multidrug resistance protein 1 (MDR1) in brain endotheli
13 ers breast cancer resistance protein (BCRP), multidrug-resistance protein 1 (MDR1), and multidrug-res
18 ions, and the role of P-glycoprotein (P-gp), multidrug resistance protein 1 (mrp1) and organic anion
19 histochemical expression of bronchopulmonary multidrug resistance protein 1 (MRP1) and permeability g
22 of multidrug resistance protein 1 (MDR1) and multidrug resistance protein 1 (MRP1) gene products is a
24 eans to overcome resistance by silencing the multidrug resistance protein 1 (MRP1), before chemothera
26 reports, no consistent relationship between multidrug resistance protein 1 (MRP1, ABCC1) expression
27 ned against P-glycoprotein (P-gp, ABCB1) and multidrug resistance protein 1 (MRP1, ABCC1) to confirm
29 The ATP-binding cassette (ABC) transporter multidrug resistance protein 1 (MRP1/ABCC1) is responsib
30 uman ATP-binding cassette (ABC) transporter, multidrug resistance protein 1 (MRP1/ABCC1), confers res
31 not for the MDR1 P-glycoprotein (ABCB1/Pgp), multidrug resistance protein 1 (MRP1/ABCC1), or multidru
33 und that human endothelial cells express the multidrug resistance protein-1 (MRP1) and use this as th
34 thiol/disulfide balance, greater extents of multidrug resistance protein-1 (MRP1) expression, and gr
35 calcein, a membrane-impermeant substrate of multidrug resistance protein-1 (MRP1), into HEK-MRP1 cel
37 l-time PCR to measure the mRNA expression of multidrug resistance protein 1, multidrug resistance-rel
38 her conferred by the classic P-glycoprotein (multidrug resistance protein 1) or by other mechanisms,
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