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1 C1 (multidrug resistant protein 1) or ABCG2 (breast cancer resistance protein).
2 sporters, multidrug resistance protein 2 and breast cancer resistance protein.
3 ABC) transporter proteins, P-glycoprotein or breast cancer resistance protein.
4 ated with enhanced expression of Pgp but not breast cancer resistance protein.
5 e membrane vesicles expressing human MRP2 or breast cancer resistance protein.
6 ate for the ATP-binding cassette transporter breast cancer resistance protein.
9 33342 from these cell lines defined a human breast cancer-resistance protein 1-expressing, verapamil
10 so known as mitoxantrone resistance protein, breast cancer-resistance protein, ABC placenta) is a mem
11 s of compounds was found to also inhibit the breast cancer resistance protein ABCG2 but with totally
12 ional activity of P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) efflux transpor
13 multidrug resistance protein 1 (ABCC1), and breast cancer resistance protein (ABCG2) play an importa
16 resistance associated protein 4 (ABCC4) and breast cancer resistance protein (ABCG2), are important
17 flux transport by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2), thereby limiti
19 PBX1 ALL, significantly higher expression of breast cancer resistance protein (ABCG2, an MTX efflux t
21 cassette subfamily B, member 1 [ABCB1]) and breast cancer resistance protein (adenosine triphosphate
23 ce protein 1 (MRP1), P-glycoprotein, and the breast cancer resistance protein are each present in a p
24 multidrug resistance-associated protein, and breast cancer resistance protein are known to transport
25 er of stem and progenitor cells known as the breast cancer resistance protein (BCRP or ABCG2) confers
26 ssette transporters P-glycoprotein (Pgp) and breast cancer resistance protein (BCRP) are 2 major gate
27 resistance-associated protein 2 (Mrp2), and breast cancer resistance protein (BCRP) expression in ra
28 -response elements and significantly induced breast cancer resistance protein (BCRP) gene transcripti
29 ation of pioglitazone, whereas inhibition of breast cancer resistance protein (BCRP) has little effec
30 ole for the ATP-binding cassette transporter breast cancer resistance protein (BCRP) in MTX resistanc
37 ransporters (e.g., P-glycoprotein (P-gp) and breast cancer resistance protein (Bcrp)) at the BBB limi
38 rostate cancer, are defined by expression of breast cancer resistance protein (BCRP), a marker of plu
39 strated that T98G and HCT8 cells express the breast cancer resistance protein (BCRP), a recently clon
42 ncluding multidrug resistance protein (MRP), breast cancer resistance protein (BCRP), and/or Pgp.
43 ransporters, e.g., P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), at the blood-br
45 g-resistance associated protein 4 (MRP4) and breast cancer resistance protein (BCRP), located on endo
47 The gene encoding a novel transporter, the breast cancer resistance protein (BCRP), was recently fo
48 doxorubicin and mitoxantrone are effluxed by breast cancer resistance protein (BCRP), we assessed whe
49 resistance-associated protein 1 (MRP1), and breast cancer resistance protein (BCRP), which may serve
55 ance-associated protein 1 (MRP1, ABCC1), and breast cancer resistance protein (BCRP, ABCG2) are the t
57 function and substrate specificity of human breast cancer resistance protein (BCRP, ABCG2) in the ab
60 otein (P-gp, official gene symbol ABCB1) and breast cancer resistance protein (BCRP, official gene sy
61 tandem mass spectrometry (LC-MS/MS) mediated breast cancer resistance protein (BCRP/ABCG2) and bile s
69 in the transport process, in particular for breast cancer resistance protein (BCRP/ABCG2), there is
70 ase inhibitor, is effluxed from cells by the breast cancer resistance protein (BCRP/ABCG2), yet publi
72 ance-associated proteins (MRP1-MRP6), or the breast cancer resistance protein (BCRP/MXR), the (67)Ga-
74 port by P-glycoprotein (P-gp; ABCB1) and the breast cancer resistance protein (BCRP; ABCG2) was teste
75 the ATP-binding cassette (ABC) transporters: breast cancer resistance protein (BCRP; ABCG2), multidru
77 several membrane transporters, in particular breast-cancer resistance protein (BCRP), to exit the BBB
78 triphosphate-binding cassette protein ABCG2 (breast cancer resistance protein [BCRP], mitoxantrone re
79 nvestigate transcriptional activation of the breast cancer resistance protein gene (BCRP/ABCG2), we e
80 d BAALC, ERG and MN1 genes and expression of breast cancer resistance protein have been shown to conf
81 such as lung-resistance protein, bcl-2, and breast cancer-resistance protein, have been described in
82 tinib with the multidrug efflux transporters breast cancer resistance protein (humans, ABCG2; rodents
83 ltidrug resistance-associated protein 1, and breast cancer resistance protein (i.e., ABCG2) consisten
84 brevianamide F analogues possess interesting breast cancer resistance protein inhibitory activity.
85 dihydroxychalcone (2',5'-DHC) to induce both breast cancer resistance protein-mediated export of glut
86 tified in small cell lung cancer followed by breast cancer resistance protein (mitoxantrone resistanc
88 otein)- and ABC subfamily G member 2 (ABCG2; breast cancer resistance protein/mitoxantrone resistance
89 1, multidrug resistance-related protein, and breast cancer resistance protein occurred after treatmen
91 ated protein 1, lung resistance protein, and breast cancer resistance protein, were comparable in the
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