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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.
11 iet or control diet plus cholic acid (1%) or ursodeoxycholic acid (1%) for 10 days.
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
15                           Taurine-conjugated ursodeoxycholic acid, a hydrophilic bile acid, similarly
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
20          Of note, both ursocholanic acid and ursodeoxycholic acid also rescued mitochondrial function
21 acid, radioactivity was detected in both the ursodeoxycholic acid and chenodeoxycholic acid fractions
22 ntial forms of therapy, including the use of ursodeoxycholic acid and cholecystokinin.
23 alysis in 168 patients with PSC treated with ursodeoxycholic acid and followed up from November 2004
24 changes in the pharmacokinetic parameters of ursodeoxycholic acid and its conjugates.
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
28                                              Ursodeoxycholic acid and S-adenosyl-L-methionine are the
29                                              Ursodeoxycholic acid and S-adenosylmethionine are anti-f
30                           The combination of ursodeoxycholic acid and simvastatin for the resolution
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
35                           Corticosteroids or ursodeoxycholic acid are treatment options for patients
36                  To evaluate the efficacy of ursodeoxycholic acid as adjunctive therapy in type 1 aut
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
39                                    Ursodiol (ursodeoxycholic acid) benefits patients with primary bil
40 d by restoring biliary secretion with 24-nor-ursodeoxycholic acid but were significantly reduced by o
41                                       Use of ursodeoxycholic acid can improve alkaline phosphatase an
42                             We conclude that ursodeoxycholic acid can improve certain laboratory test
43                                    Moreover, ursodeoxycholic acid can reduce apoptosis by minimizing
44                                              Ursodeoxycholic acid caused a dose-dependent decrease in
45 , sitosterol, cholic acid, deoxycholic acid, ursodeoxycholic acid, cholestyramine, bile fistula, lova
46                                 In contrast, ursodeoxycholic acid did not exhibit any of these effect
47              Bile acids deoxycholic acid and ursodeoxycholic acid differentially regulate human beta-
48 holic acid, the specific activity of biliary ursodeoxycholic acid exceeded the specific activity of c
49  a multicenter randomized trial of high dose ursodeoxycholic acid for PSC.
50      Maternal management is symptomatic with ursodeoxycholic acid; for the fetus, however, this is a
51  important, because effective treatment with ursodeoxycholic acid has been shown to halt disease prog
52                                              Ursodeoxycholic acid has the potency to suppress eosinop
53 was confirmed for both ursocholanic acid and ursodeoxycholic acid in a Parkin-deficient neuronal mode
54               Initial results from high-dose ursodeoxycholic acid in halting disease progression, how
55 periority of 24-norursodeoxycholic acid over ursodeoxycholic acid in reducing histological disease pr
56                                     However, ursodeoxycholic acid increased activity 84% (P < .05) an
57  experiments provide the first evidence that ursodeoxycholic acid is effective for preventing adenoma
58                                              Ursodeoxycholic acid may have a role as a colorectal and
59                       Oral administration of ursodeoxycholic acid may improve bile flow and reduce ga
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
62               The chemoprevention effects of ursodeoxycholic acid on colorectal dysplasia await furth
63 ng the effects of deoxycholic acid (DCA) and ursodeoxycholic acid on the expression and release of Hb
64 ) occurred as commonly in patients receiving ursodeoxycholic acid or placebo.
65 id (deoxycholic acid, chenodeoxycholic acid, ursodeoxycholic acid, or glycochenodeoxycholic acid) in
66                         Despite therapy with ursodeoxycholic acid, prednisone, and then tacrolimus, h
67                                              Ursodeoxycholic acid prevents eosinophilic degranulation
68                                              Ursodeoxycholic acid remains the most studied medical tr
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
73                                              Ursodeoxycholic acid strongly promoted interleukin (IL)-
74 ewed interest in developing therapies beyond ursodeoxycholic acid that are aimed at both slowing dise
75                             The formation of ursodeoxycholic acid, the 7 beta-hydroxy epimer of cheno
76                                              Ursodeoxycholic acid, the standard first-line treatment
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
79  cirrhosis who had an inadequate response to ursodeoxycholic acid therapy.
80   Patients maintained their existing dose of ursodeoxycholic acid throughout the study.
81                                              Ursodeoxycholic acid-treated DCs have less capacity than
82                                              Ursodeoxycholic acid treatment of OVA-sensitized mice pr
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
85                                              Ursodeoxycholic acid (UDC) and hyocholic acid (HC) feedi
86 d, double-blind, placebo-controlled trial of ursodeoxycholic acid (UDCA) (10-12 mg/kg/d) taken as a s
87                 Intriguingly, treatment with ursodeoxycholic acid (UDCA) ameliorates eosinophilia as
88                       Oral administration of ursodeoxycholic acid (UDCA) and cholesterol causes bile
89 uate the safety and estimate the efficacy of ursodeoxycholic acid (UDCA) and clofibrate in the treatm
90                                We identified ursodeoxycholic acid (UDCA) and deoxycholic acid (DCA) a
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
93                                              Ursodeoxycholic acid (UDCA) can protect hepatocytes from
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
96                                              Ursodeoxycholic acid (UDCA) has been shown in small, ope
97                                              Ursodeoxycholic acid (UDCA) has been shown to be a safe
98                                              Ursodeoxycholic acid (UDCA) has been suggested to be of
99                                              Ursodeoxycholic acid (UDCA) has shown effectiveness as a
100                                              Ursodeoxycholic acid (UDCA) improves liver function in p
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
103                                              Ursodeoxycholic acid (UDCA) is a beneficial medical ther
104                                              Ursodeoxycholic acid (UDCA) is a safe and effective medi
105                                              Ursodeoxycholic acid (UDCA) is a safe and effective medi
106                                              Ursodeoxycholic acid (UDCA) is a safe and effective trea
107                                              Ursodeoxycholic acid (UDCA) is no longer recommended for
108                                              Ursodeoxycholic acid (UDCA) is the only approved treatme
109                                              Ursodeoxycholic acid (UDCA) is the only approved treatme
110                    Despite limited benefits, ursodeoxycholic acid (UDCA) is the only Food and Drug Ad
111                                              Ursodeoxycholic acid (UDCA) is the only known beneficial
112                                              Ursodeoxycholic acid (UDCA) is used for the treatment of
113                                              Ursodeoxycholic acid (UDCA) is used to treat primary bil
114                                              Ursodeoxycholic acid (UDCA) is widely used for cholangio
115                            Standard doses of ursodeoxycholic acid (UDCA) lead to improvements in bioc
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
118                                              Ursodeoxycholic acid (UDCA) or S-adenosylmethionine (SAM
119                      We have also shown that ursodeoxycholic acid (UDCA) prevented AOM-induced colon
120                                              Ursodeoxycholic acid (UDCA) prevents the formation of ga
121                    The hydrophilic bile salt ursodeoxycholic acid (UDCA) protects against the membran
122                                              Ursodeoxycholic acid (UDCA) protects cells from the apop
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
125                  High-dose (28-30 mg/kg/day) ursodeoxycholic acid (UDCA) treatment improves serum liv
126  GF mdr2(-/-) mice and abrogated in vitro by ursodeoxycholic acid (UDCA) treatment.
127 d, double-blind, placebo-controlled trial of ursodeoxycholic acid (UDCA) versus placebo.
128 ), and effects of treatment with 4-PB and/or ursodeoxycholic acid (UDCA) were assessed.
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
131                                              Ursodeoxycholic acid (UDCA), methotrexate, and colchicin
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
134                  The biochemical response to ursodeoxycholic acid (UDCA)--so-called "treatment respon
135 nthesis and steady-state pharmacokinetics of ursodeoxycholic acid (UDCA).
136 ntional treatment with the natural bile acid ursodeoxycholic acid (UDCA).
137 stasis of pregnancy (ICP) and treatment with ursodeoxycholic acid (UDCA).
138 nged substantially with the introduoction of ursodeoxycholic acid (UDCA).
139 irrhosis (PBC) and an incomplete response to ursodeoxycholic acid (UDCA).
140 d in AC and was prevented by the hydrophilic ursodeoxycholic acid (UDCA).
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
143 ar 50 mg/day, or seladelpar 200 mg/day while ursodeoxycholic acid was continued.
144 f 1 kg), and the finding that ofloxacin plus ursodeoxycholic acid was not superior to ursodeoxycholic
145                                          The ursodeoxycholic acid was synthesized from chenodeoxychol
146    Treatment responses to corticosteroids or ursodeoxycholic acid were poor.
147  NF-kappaB, an effect that was attenuated by ursodeoxycholic acid, whereas an NF-kappaB inhibitor, BM
148                                              Ursodeoxycholic acid, which in vivo is converted to its
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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