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1 d-open conformation bound to two Na(+) and a taurocholic acid.
2 ganic anions such as sulfobromophthalein and taurocholic acid.
3 ted in a markedly reduced uptake activity of taurocholic acid.
4 TM3 mutants demonstrates significant loss of taurocholic acid affinity for mutants S128C and L145C-T1
5 y, blood concentrations of total bile acids, taurocholic acid, an FXR ligand, and taurohyocholic acid
6 e acid composition showed marked increase of taurocholic acid and decrease of tauro-alpha and beta-mu
7  pathway, which is consistent with decreased taurocholic acid and increased tauromuricholic acids in
8                                              Taurocholic acid and taurodeoxycholic acid decreased CYP
9 ce were fed a low-fat diet supplemented with taurocholic acid, but not with glycocholic acid, for exa
10                           Inhibition of [3H]-taurocholic acid efflux was observed after 30 minutes an
11 by the organic substrates MK571, probenecid, taurocholic acid, estrone sulfate, and bromosulfophthale
12 ctory response to all three cues (l-alanine, taurocholic acid, food cue) tested, suggesting that TFM
13 rn mice, with 50% +/- 9% TDC and 42% +/- 10% taurocholic acid in bile, as opposed to 2% +/- 1% and 80
14 s showed that aductular sea lamprey secreted taurocholic acid into its intestinal lumen.
15 creatitis severity after infusion of TLCS or taurocholic acid into the pancreatic duct.
16 ometabolites as well as cyprinol sulfate and taurocholic acid, lysophospholipids, and a decrease in s
17                               TUDCA, but not taurocholic acid, selectively induced translocation of t
18 (KA) iGluR agonists and odorants (glutamine, taurocholic acid) stimulated activity-dependent labeling
19 porter activity was directly assayed with 3H-taurocholic acid (TC) scintigraphy.
20 y solute transport, IBDUs were perfused with taurocholic acid (TCA) and bile acid uptake was calculat
21  Treatment of primary mouse hepatocytes with taurocholic acid (TCA) increased the expression of MIP-2
22 proportion in bile increased by 2.6-fold and taurocholic acid (TCA) level reduced by 71%.
23 (TCDCA), glycochenodeoxycholic acid (GCDCA), taurocholic acid (TCA), glycocholic acid (GCA), and taur
24                                              Taurocholic acid (TCA), taurochenodeoxycholic acid (TCDC
25 on the findings of the absorption pathway of taurocholic acid (TCA)-linked heparin and docetaxel (DTX
26  [uptake of the prototypical hASBT substrate taurocholic acid (TCA)], and sensitivities to MTS exposu
27           Bile acids (deoxycholic acid, DCA; taurocholic acid, TCA) activated AKT and glycogen syntha
28 0-100, demonstrated levels of uptake of [14C]taurocholic acid that were increased as much as threefol
29 , OATP2, has been identified that transports taurocholic acid, the adrenal androgen dehydroepiandrost
30                Furthermore, sodium-dependent taurocholic acid uptake was inhibited by Myrcludex B in
31 olic acid uptake, whereas sodium-independent taurocholic acid uptake was unchanged.
32 patocytes showed absence of sodium-dependent taurocholic acid uptake, whereas sodium-independent taur

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