ライフサイエンスコーパス: choleretic

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1 activation markedly inhibits the growth and choleretic activity of the biliary tree in the bile duct

2 t, hepatic transport, biotransformation, and choleretic activity were defined; intestinal absorption

3 d, was partly glucuronidated, and had normal choleretic activity.

4 he amF conjugate of cholylglycine had normal choleretic activity; other compounds were hypocholeretic

5 In the absence of an osmotic gradient, choleretic agents (secretin and forskolin) and a cholest

6 osure of isolated hepatocytes to glucagon, a choleretic agonist, significantly increased the expressi

7 Interestingly, both choleretic and cholestatic agents activate the same intr

8 Choleretic and cholestatic agents affect bile formation,

9 An emerging theme is that choleretic and cholestatic effects may be mediated by di

10 , cPKCalpha and nPKCdelta may be involved in choleretic, cholestatic, and anticholestatic effects by

11 cise cellular mechanisms accounting for this choleretic effect are unknown.

12 was 2.3-fold lower than in normals, but the choleretic effect of dibutyryl cGMP was only slightly re

13 egnane X receptor (PXR) target genes and the choleretic effect of diosgenin was reduced by approximat

14 Moreover, the choleretic effect of tauroursodeoxycholic acid (TUDCA) w

15 and suggest a novel mechanism explaining the choleretic effect of UDCA.

16 aPKCzeta may mediate choleretic effects by inserting NTCP into the plasma mem

17 Moreover, the choleretic effects of infusions of the NO donors sodium

18 n response to cholate and diosgenin, but the choleretic effects of these two steroids are mediated by

19 Choleretic effects of VIP were examined using isolated p

20 t canalicular membrane, both E(2)17G and the choleretic estradiol-3-beta-D-glucuronide (E(2)3G) inhib

21 rgo cholehepatic shunting should be powerful choleretics in humans.

22 well as that of taurocholate administered in choleretic or trace radiolabel amounts (around 60%, P <

23 Earlier work showed that TUDC exerts its choleretic properties in the perfused rat liver in an al

24 cholylglycylamF has hepatocyte transport and choleretic properties most closely resembling those of a

25 c biotransformation, transport kinetics, and choleretic properties were defined in rat and hamster bi

26 Upon exposure of couplets to a choleretic stimulus (i.e. dibutyryl cAMP), aquaporin 8 r

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