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1 (+)-independent organic anion transporter 2 (Oatp2).
2 increased hepatic expression of Oatp1 and/or Oatp2.
3 may function as intracellular substrates for Oatp2.
4 .6-kilobase (kb) 5'-flanking region of mouse Oatp2.
6 lot analysis revealed abundant expression of OATP2 after incubation of cells for 48 h in zinc, wherea
10 Furthermore, the identification of oatp1 and OATP2 as pravastatin transporters suggests that they are
16 Interestingly, [(3)H]taurocholate uptake in Oatp2-expressing oocytes was also trans-stimulated when
17 ke of [(3)H]taurocholate or [(3)H]digoxin in Oatp2-expressing oocytes, indicating that the stimulator
19 1, uptake of 10 microM [(3)H]taurocholate in Oatp2-expressing Xenopus laevis oocytes was trans-stimul
20 in cell-associated [3H]bilirubin in induced (OATP2-expressing) as compared with uninduced cells (11.2
31 rs (bp) of the 5'-flanking region of the rat oatp2 gene were linked to the luciferase reporter gene a
34 s other members of the OATP family, i.e. rat oatp2, human OATP, and the prostaglandin transporter, di
35 the current study indicates that a role for OATP2 in hepatocyte bilirubin transport is unlikely, it
44 Taken together, the results indicate that Oatp2 mediates bidirectional transport of organic anions
47 gs, dibutyryl cAMP and 8-bromo-cAMP, induced Oatp2 mRNA expression in a time- and dose-dependent mann
49 Organic anion transporting polypeptide 2 (Oatp2) mRNA was decreased in pregnancy and increased pos
51 -deletion constructs derived from the 7.6-kb Oatp2 promoter reporter gene construct, as well as 7.6-k
52 and remained elevated, whereas the amount of Oatp2 protein increased throughout the 96-hour interval.
54 ffects of PCN treatment on the expression of Oatp2, rats were administered PCN, livers were extracted
55 ansporting polypeptides, Oatp1 (Slc21a1) and Oatp2 (Slc21a5), mediate hepatic uptake of cardiac glyco
56 at organic anion transporting polypeptide 2 (oatp2; Slc21a5) is a liver transporter that mediates the
58 ively, n = 5) We obtained similar results in OATP2-transfected HEK293 cells that were used in the ori
59 cells that had been stably transfected with OATP2 under regulation of a metallothionein promoter.
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