ライフサイエンスコーパス: taurocholic acid

1 d-open conformation bound to two Na(+) and a taurocholic acid.

2 ganic anions such as sulfobromophthalein and taurocholic acid.

3 to promote C difficile colonization such as taurocholic acid.

4 ted in a markedly reduced uptake activity of taurocholic acid.

5 While 3alpha-NBD-taurocholic acid, 3beta-NBD-taurocholic acid, 3alpha-NBD-glycocholic acid, and 3beta

6 While 3alpha-NBD-taurocholic acid, 3beta-NBD-taurocholic acid, 3alpha-NBD

7 TM3 mutants demonstrates significant loss of taurocholic acid affinity for mutants S128C and L145C-T1

8 y, blood concentrations of total bile acids, taurocholic acid, an FXR ligand, and taurohyocholic acid

9 e acid composition showed marked increase of taurocholic acid and decrease of tauro-alpha and beta-mu

10 ze was increased in DKO mice, with increased taurocholic acid and decreased tauromuricholic acids.

11 pathway, which is consistent with decreased taurocholic acid and increased tauromuricholic acids in

12 Taurocholic acid and taurodeoxycholic acid decreased CYP

13 We found that taurocholic acid and taurohyodeoxycholic acid regulated

14 cles, sorafenib-glycyrrhizin and terbinafine-taurocholic acid both ex vivo and in vivo.

15 ce were fed a low-fat diet supplemented with taurocholic acid, but not with glycocholic acid, for exa

16 with primary open-angle glaucoma, increased taurocholic acid, decreased glutathione, and a reduction

17 Inhibition of [3H]-taurocholic acid efflux was observed after 30 minutes an

18 by the organic substrates MK571, probenecid, taurocholic acid, estrone sulfate, and bromosulfophthale

19 ctory response to all three cues (l-alanine, taurocholic acid, food cue) tested, suggesting that TFM

20 rn mice, with 50% +/- 9% TDC and 42% +/- 10% taurocholic acid in bile, as opposed to 2% +/- 1% and 80

21 rising only alpha subunits were sensitive to taurocholic acid in functional experiments using Xenopus

22 s showed that aductular sea lamprey secreted taurocholic acid into its intestinal lumen.

23 creatitis severity after infusion of TLCS or taurocholic acid into the pancreatic duct.

24 ometabolites as well as cyprinol sulfate and taurocholic acid, lysophospholipids, and a decrease in s

25 er CDR; whereas both Ruminiclostridium 5 and taurocholic acid prior to CDR were associated with NREM

26 Taurocholic acid regulation of ENaC was voltage-dependen

27 TUDCA, but not taurocholic acid, selectively induced translocation of t

28 (KA) iGluR agonists and odorants (glutamine, taurocholic acid) stimulated activity-dependent labeling

29 porter activity was directly assayed with 3H-taurocholic acid (TC) scintigraphy.

30 y solute transport, IBDUs were perfused with taurocholic acid (TCA) and bile acid uptake was calculat

31 with binding energies comparable to those of taurocholic acid (TCA) and GCA.

32 Treatment of primary mouse hepatocytes with taurocholic acid (TCA) increased the expression of MIP-2

33 proportion in bile increased by 2.6-fold and taurocholic acid (TCA) level reduced by 71%.

34 (TCDCA), glycochenodeoxycholic acid (GCDCA), taurocholic acid (TCA), glycocholic acid (GCA), and taur

35 Taurocholic acid (TCA), taurochenodeoxycholic acid (TCDC

36 on the findings of the absorption pathway of taurocholic acid (TCA)-linked heparin and docetaxel (DTX

37 [uptake of the prototypical hASBT substrate taurocholic acid (TCA)], and sensitivities to MTS exposu

38 Bile acids (deoxycholic acid, DCA; taurocholic acid, TCA) activated AKT and glycogen syntha

39 0-100, demonstrated levels of uptake of [14C]taurocholic acid that were increased as much as threefol

40 , OATP2, has been identified that transports taurocholic acid, the adrenal androgen dehydroepiandrost

41 Furthermore, sodium-dependent taurocholic acid uptake was inhibited by Myrcludex B in

42 olic acid uptake, whereas sodium-independent taurocholic acid uptake was unchanged.

43 patocytes showed absence of sodium-dependent taurocholic acid uptake, whereas sodium-independent taur