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1 limit of normal (ULN) despite treatment with ursodeoxycholic acid.
2 maining 17% of bile acids were identified as ursodeoxycholic acid.
3 re commonly in the 21 patients randomized to ursodeoxycholic acid.
4 c acid > cholic acid > hyodeoxycholic acid > ursodeoxycholic acid.
5 apidly triggered by a diet supplemented with ursodeoxycholic acid.
6 r in patients with an inadequate response to ursodeoxycholic acid.
7 ry cirrhosis who had inadequate responses to ursodeoxycholic acid.
8 adequate response to first-line therapy with ursodeoxycholic acid.
9 All patients were treated with ursodeoxycholic acid.
10 be attributable to liver transplantation or ursodeoxycholic acid.
12 e, or incomplete response were randomized to ursodeoxycholic acid (13-15 mg/kg daily) or placebo for
13 lic acid (3alpha-OH, 7alpha-OH, 12alpha-OH), ursodeoxycholic acid (3alpha-OH, 7beta-OH), and lithocho
14 colonic mucosal tissue in vitro In contrast, ursodeoxycholic acid (50-200 microM) inhibited both basa
16 4-Phenyl butyric acid and taurine-conjugated ursodeoxycholic acid alleviated ER stress in cells and w
17 mittance and following treatment with either ursodeoxycholic acid alone (10 mg/kg thrice daily, n = 1
18 lus ursodeoxycholic acid was not superior to ursodeoxycholic acid alone for the prevention or occlusi
19 hemical response occurred under therapy with ursodeoxycholic acid, alone or in combination with immun
21 acid, radioactivity was detected in both the ursodeoxycholic acid and chenodeoxycholic acid fractions
23 alysis in 168 patients with PSC treated with ursodeoxycholic acid and followed up from November 2004
25 activity calculation, and the routine use of ursodeoxycholic acid and low-dose steroids (modified pro
26 were similar before and after treatment with ursodeoxycholic acid and no different than after placebo
27 e drugs that antagonize BS toxicity, such as ursodeoxycholic acid and nor-ursodeoxycholic acid, may b
31 might be reduced by early enteral feedings, ursodeoxycholic acid, and cholecystokinin-octapeptide.
32 its were corrected by oral administration of ursodeoxycholic acid, and the addition of an oral proton
33 compound ursolic acid and the licensed drug ursodeoxycholic acid are chemically closely related to u
34 results indicate that substantial amounts of ursodeoxycholic acid are formed in patients treated with
37 acid as a naturally occurring compound, and ursodeoxycholic acid as an already licensed drug as prom
38 r, phenylbutyric acid and taurine-conjugated ursodeoxycholic acid attenuated HNE-induced leukocyte ro
40 d by restoring biliary secretion with 24-nor-ursodeoxycholic acid but were significantly reduced by o
45 , sitosterol, cholic acid, deoxycholic acid, ursodeoxycholic acid, cholestyramine, bile fistula, lova
48 holic acid, the specific activity of biliary ursodeoxycholic acid exceeded the specific activity of c
51 important, because effective treatment with ursodeoxycholic acid has been shown to halt disease prog
53 was confirmed for both ursocholanic acid and ursodeoxycholic acid in a Parkin-deficient neuronal mode
55 periority of 24-norursodeoxycholic acid over ursodeoxycholic acid in reducing histological disease pr
57 experiments provide the first evidence that ursodeoxycholic acid is effective for preventing adenoma
60 of multiple cholesterol stone formation, and ursodeoxycholic acid may partially halt the formation of
61 xicity, such as ursodeoxycholic acid and nor-ursodeoxycholic acid, may be effective at all disease st
63 ng the effects of deoxycholic acid (DCA) and ursodeoxycholic acid on the expression and release of Hb
65 id (deoxycholic acid, chenodeoxycholic acid, ursodeoxycholic acid, or glycochenodeoxycholic acid) in
69 C, which is unrelated to disease severity or ursodeoxycholic acid response, is significant and comple
70 el insights into the mechanisms of action of ursodeoxycholic acid should advance our understanding of
71 ears following biopsy, including response to ursodeoxycholic acid, show identical changes to patients
72 ies, showed identical treatment responses to ursodeoxycholic acid, similar rates and types of nonhepa
74 ewed interest in developing therapies beyond ursodeoxycholic acid that are aimed at both slowing dise
77 dults with PBC and an inadequate response to ursodeoxycholic acid therapy (i.e., alkaline phosphatase
78 The precise role of weight reduction and ursodeoxycholic acid therapy in the favorable alteration
83 18:0/18:1), PS(14:1/14:0), dihydroxyacetone, ursodeoxycholic acid, tryptophan, L-valine, cycloserine,
84 assigned to ceftriaxone also received 300 mg ursodeoxycholic acid twice daily and those assigned to p
86 d, double-blind, placebo-controlled trial of ursodeoxycholic acid (UDCA) (10-12 mg/kg/d) taken as a s
89 uate the safety and estimate the efficacy of ursodeoxycholic acid (UDCA) and clofibrate in the treatm
91 patients with AMA-negative PBC treated with ursodeoxycholic acid (UDCA) and/or liver transplantation
92 igation (BDL) in mice and how treatment with ursodeoxycholic acid (UDCA) and/or S-adenosylmethionine
94 acid (DCA), chenodeoxycholic acid (CDCA) or ursodeoxycholic acid (UDCA) caused sustained MAPK activa
95 s are inconclusive regarding the efficacy of ursodeoxycholic acid (UDCA) for treating primary scleros
101 d-line treatment for PBC in combination with ursodeoxycholic acid (UDCA) in adults with an inadequate
102 more, we investigated the mechanism by which ursodeoxycholic acid (UDCA) inhibits LXR-induced lipogen
116 This study sought to assess the effects of ursodeoxycholic acid (UDCA) on endothelial function and
117 d a meta-analysis to evaluate the effects of ursodeoxycholic acid (UDCA) on pruritus, liver test resu
123 rmine the influence of IBD and the effect of ursodeoxycholic acid (UDCA) therapy on the course of the
124 ed that feeding the cytoprotective bile acid ursodeoxycholic acid (UDCA) to rats resulted in signific
129 e of them were treated in the follow up with ursodeoxycholic acid (UDCA), eight received during a tri
130 diagnosis reports, response to therapy with ursodeoxycholic acid (UDCA), laboratory results, and sym
132 frequently progresses despite treatment with ursodeoxycholic acid (UDCA), the only approved therapy.
133 eutic option available for these patients is ursodeoxycholic acid (UDCA), which slows the progression
141 ecifically, our approach involves the use of ursodeoxycholic acid (Urso) due to its ability to decrea
142 Sulindac was tested in combination with ursodeoxycholic acid (ursodiol), a naturally occurring 7
144 f 1 kg), and the finding that ofloxacin plus ursodeoxycholic acid was not superior to ursodeoxycholic
147 NF-kappaB, an effect that was attenuated by ursodeoxycholic acid, whereas an NF-kappaB inhibitor, BM
149 Moreover, the hepatoprotective bile acid ursodeoxycholic acid, which reverses hydrophobic bile ac
150 ed drug in primary sclerosing cholangitis is ursodeoxycholic acid, which, despite a range of potentia
151 properties of hydrophilic bile acids such as ursodeoxycholic acid, with the distinct ability to speci
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