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1 sm, lysine biosynthesis and degradation, and bile acid biosynthesis.
2 ceptor LRH-1 (also known as NR5A2) regulates bile acid biosynthesis.
3 the classical homeostatic control of hepatic bile acid biosynthesis.
4 id clearance and represses genes involved in bile acid biosynthesis.
5 e by which high levels of bile acids repress bile acid biosynthesis.
6 te-limiting enzyme in the neutral pathway of bile acid biosynthesis.
7 effect of the C-36 serpin peptide on hepatic bile acid biosynthesis.
8 eroxisome and that this is a crucial step in bile acid biosynthesis.
9 lation of genes encoding critical enzymes of bile acid biosynthesis.
10 ), which catalyzes the rate-limiting step in bile acid biosynthesis.
11 ession of CYP7A1 and other genes involved in bile acid biosynthesis.
12 es the reduction of key intermediates during bile acid biosynthesis.
13  sparing the expression of genes involved in bile acids biosynthesis.
14 getic effects that contribute to its role in bile acid biosynthesis: 1) it has the ability to activat
15 r basal levels in PRH dramatically increased bile acid biosynthesis (586% +/- 82%, P < 0.001) but did
16 A1) plays an important role in regulation of bile acid biosynthesis and cholesterol homeostasis.
17  PGC-1alpha is a key activator of CYP7A1 and bile acid biosynthesis and is likely responsible for the
18 (AKR1D1) and AKR1C enzymes are essential for bile acid biosynthesis and steroid hormone metabolism.
19                    Consequences of defective bile acid biosynthesis and transport have been clarified
20 a novel mechanism for feedback repression of bile acid biosynthesis and underscores the vital role of
21 tivates CYP7A1 gene expression and increases bile acid biosynthesis as well.
22 e small heterodimer partner (SHP) suppresses bile acid biosynthesis by heterodimerizing with FTF.
23 hysiological pathway, feedback inhibition of bile acid biosynthesis, by differentially targeting SHP
24 ibits transcription of CYP7A1, a key gene in bile acid biosynthesis, by recruiting histone deacetylas
25 fine a potentially treatable inborn error of bile acid biosynthesis caused by ACOX2 deficiency.
26 To determine whether the primary products of bile acid biosynthesis, cholic acid and chenodeoxycholic
27 nd in Abcd3-/- mice, there was evidence of a bile acid biosynthesis defect.
28 ed increased expression of genes involved in bile acid biosynthesis, efflux transport, and reduced ex
29 iting step in the classic pathway of hepatic bile acid biosynthesis from cholesterol.
30 ediated suppression of the expression of two bile acid biosynthesis genes resulted in a 3-fold lower
31                  However, the role of FTF in bile acid biosynthesis has been studied only in tissue c
32 teroid hydroxylases and modulates sterol and bile acid biosynthesis in vivo.
33 of genes involved in cholesterol and primary bile acid biosynthesis including Cyp7a1.
34 a key hepatic activator of genes involved in bile acid biosynthesis including the cholesterol 7-alpha
35 le products, a dramatic increase was seen in bile acid biosynthesis intermediates (27- and 7,27-hydro
36                       The classic pathway of bile acid biosynthesis is downregulated in PEX2(-/-) mic
37 rd regulation of the rate limiting enzyme in bile acid biosynthesis is provided by oxysterols through
38                                              Bile acid biosynthesis is regulated by both feed-forward
39 dy, the induction of an alternate pathway of bile acid biosynthesis is shown to underlie this unusual
40                                              Bile acid biosynthesis is subjected to feedback regulati
41 te-limiting enzyme in the neutral pathway of bile acid biosynthesis, is feedback-inhibited at the tra
42 1, which catalyzes the rate-limiting step in bile acid biosynthesis, is strongly suppressed.
43 n of hepatic transporters and alterations of bile acid biosynthesis may contribute to development of
44 ial cholesterol transport protein, increases bile acid biosynthesis more than 5-fold via the acidic p
45 els, and CYP7A1, the rate-limiting enzyme in bile acid biosynthesis (p<0.05).
46 zyme that commits cholesterol to the neutral bile acid biosynthesis pathway and is highly regulated.
47            Two key regulatory enzymes in the bile acid biosynthesis pathway are cholesterol 7alpha-hy
48 lesterol 7 alpha-hydroxylase (CYP7A1) of the bile acid biosynthesis pathway is suppressed by bile aci
49 he side chain of C27 steroids in the hepatic bile acid biosynthesis pathway, which begins with 7alpha
50 7a1, the rate-limiting enzyme in the classic bile acid biosynthesis pathway.
51 sic" (neutral) or the "alternative" (acidic) bile acid biosynthesis pathways.
52 specific deletion of SIRT1 increased hepatic bile acid biosynthesis, reduced hepatic accumulation of
53 ogenase (AKR1C4) plays a significant role in bile acid biosynthesis, steroid hormone metabolism, and
54  and eicosanoids; cholesterol metabolism and bile-acid biosynthesis; steroid synthesis and metabolism
55 nisms underlying PXR-mediated suppression of bile acid biosynthesis, we examined the functional cross
56 pha-hydroxylase, the rate-limiting enzyme of bile acid biosynthesis, were constructed by targeted dis

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