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1 he mitochondrial activity is associated with sterol 27-hydroxylase, a cytochrome P450 (CYP27A1); howe
2 ylase activity decreased 68% (P < 0.01), but sterol 27-hydroxylase activity increased 66% (P < 0.05)
8 increased hepatic cholesterol and stimulated sterol 27-hydroxylase and alternative bile acid synthesi
9 including cholesterol 7alpha-hydroxylase and sterol-27-hydroxylase, and the oxysterol nuclear recepto
10 liver, suggesting that LPS may down-regulate sterol 27-hydroxylase by decreasing the binding of HNF-1
12 thway of bile acid synthesis is initiated by sterol 27-hydroxylase (CYP27) with subsequent 7alpha-hyd
15 cholesterol 7alpha-hydroxylase (Cyp7a1) and sterol 27-hydroxylase (Cyp27a1) double knockout (DKO) mi
16 -limiting step in the classical pathway, and sterol 27-hydroxylase (CYP27A1) initiates the hydroxylat
18 binding cassette transporter A1 (ABCA1), and sterol 27-hydroxylase decreased during progression from
19 A cDNA library prepared from hepatic mRNA of sterol 27-hydroxylase-deficient mice was screened with a
20 rol 7alpha-hydroxylase, and alternative, via sterol 27-hydroxylase) in New Zealand white rabbits fed
25 rosis factor and interleukin (IL)-1 decrease sterol 27-hydroxylase mRNA levels by 48 and 80%, respect
26 oreover, LPS progressively decreases hepatic sterol 27-hydroxylase mRNA levels by 75% compared with c
28 esterol 7 alpha-hydroxylase (C7 alpha H) and sterol 27-hydroxylase (S27H) and rates of bile acid synt
29 ecular mechanisms of LPS-induced decrease in sterol 27-hydroxylase show that LPS markedly decreases m
30 hepatic cholesterol 7 alpha-hydroxylase and sterol 27-hydroxylase that control bile acid synthesis i
31 1) is a ubiquitously expressed mitochondrial sterol 27-hydroxylase that plays an important role in th
32 that LPS markedly decreases the activity of sterol 27-hydroxylase, the rate-limiting enzyme in the a