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1                   The pleiotropic actions of hydroxymethylglutaryl CoA reductase inhibitors (statins)
2 d that "high-risk" patients are treated with hydroxymethylglutaryl CoA reductase inhibitors to reduce
3 nhibited by both lovastatin, an inhibitor of hydroxymethylglutaryl CoA reductase, and alendronate.
4 e, we evaluated mice lacking mitochondrial 3-hydroxymethylglutaryl CoA synthase (HMGCS2) to determine
5 his enzyme is unique in that it is the first hydroxymethylglutaryl CoA synthase that is insensitive t
6 e, the first characterization of an archaeal hydroxymethylglutaryl CoA synthase.
7    In this study, the comparative effects of hydroxymethylglutaryl-CoA (HMG-CoA) reductase inhibitors
8                                              Hydroxymethylglutaryl-CoA (HMG-CoA) reductase is the pri
9                                        Avian hydroxymethylglutaryl-CoA (HMG-CoA) synthase is inactiva
10  acetoacetyl-CoA, succinyl-CoA, malonyl-CoA, hydroxymethylglutaryl-CoA (HMG-CoA), and acetyl-CoA in I
11 dicate that HMGCLL1 is an extramitochondrial hydroxymethylglutaryl-CoA lyase.
12 REBP binding to three specific target genes: hydroxymethylglutaryl-CoA reductase (Red), fatty acid sy
13 (AMPK), phosphorylates and regulates in vivo hydroxymethylglutaryl-CoA reductase and acetyl-CoA carbo
14 main, we made a fusion protein between yeast hydroxymethylglutaryl-CoA reductase and GFP.
15  protein pathway and increases expression of hydroxymethylglutaryl-CoA reductase and low density lipo
16 ed in the regulated degradation of wild-type hydroxymethylglutaryl-CoA reductase in the ER membrane.
17 or the hepatic uptake of this liver-specific hydroxymethylglutaryl-CoA reductase inhibitor in rat and
18  hamster ovary cell lines with lovastatin (a hydroxymethylglutaryl-CoA reductase inhibitor) and meval
19 sulfate, and thyroid hormone, as well as the hydroxymethylglutaryl-CoA reductase inhibitor, pravastat
20 dence suggests that long term treatment with hydroxymethylglutaryl-CoA reductase inhibitors, or stati
21 ord "surgery" and the MeSH term for statins "hydroxymethylglutaryl-CoA reductase inhibitors." Studies
22 lated degradation consistent with the native hydroxymethylglutaryl-CoA reductase proteins.
23 ion (cytochrome c) or cholesterol synthesis (hydroxymethylglutaryl-CoA reductase).
24 carboxykinase, and type I deiodinase but not hydroxymethylglutaryl-CoA reductase, cytochrome c, and a
25 e stimulated the rapid inactivation of their hydroxymethylglutaryl-CoA reductase, presumably through
26 tein maturation and promoting degradation of hydroxymethylglutaryl-CoA reductase.
27 of gamma-tocotrienol, indicating the role of hydroxymethylglutaryl-CoA reductase.
28 -binding protein-2 and reduced expression of hydroxymethylglutaryl-CoA reductase.
29 ding protein cleavage-activating protein and hydroxymethylglutaryl-CoA reductase.
30 n regulatory factor 1 (IRF-1), mitochondrial hydroxymethylglutaryl-CoA synthase (HMG-CoA synthase), a
31 pecific beta-lactone inhibitor of eukaryotic hydroxymethylglutaryl-CoA synthase (HMGCS).
32  an effective competitive inhibitor of avian hydroxymethylglutaryl-CoA synthase (Ki = 28 microm).
33 nd catalase, and show that these, as well as hydroxymethylglutaryl-CoA synthase and sarcosine dehydro
34 nding cassette transporters ABCA1 and ABCG5, hydroxymethylglutaryl-CoA synthase and the LDL receptor)
35 odular polyketide synthase (PKS) proteins, a hydroxymethylglutaryl-CoA synthase cassette and three fl
36 -methyl and beta-ethyl branches catalyzed by hydroxymethylglutaryl-CoA synthase homologues that utili
37 ency resulted in up-regulation of intestinal hydroxymethylglutaryl-CoA synthase mRNA and an increase
38                                              Hydroxymethylglutaryl-CoA synthase-catalyzed condensatio
39 nzymes that enolize this analog, occurs with hydroxymethylglutaryl-CoA synthase.
40 f acetyl-CoA, acetoacetyl-CoA, succinyl-CoA, hydroxymethylglutaryl-CoA, and malonyl-CoA confirmed tha
41 iNOS expression, and NF-kappaB activation by hydroxymethylglutaryl-CoA, mevalonate, and farnesyl pyro
42 ration of (E)-3-methylglutaconyl-CoA to (3S)-hydroxymethylglutaryl-CoA.
43 oid biosynthesis, is catalyzed by the enzyme hydroxymethylglutaryl-CoAreductase (HMGR).
44 domized trials, calcium channel blockers and hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inh
45                                              Hydroxymethylglutaryl coenzyme A reductase (HMGCoAR) is
46        Mevalonate depletion by inhibition of hydroxymethylglutaryl coenzyme A reductase impairs post-
47 his study aimed to investigate the impact of hydroxymethylglutaryl coenzyme A reductase inhibitor (st
48 nse of C-reactive protein to initiation of a hydroxymethylglutaryl coenzyme A reductase inhibitor (st
49                                              Hydroxymethylglutaryl coenzyme A reductase inhibitors (s
50                       Long-term therapy with hydroxymethylglutaryl coenzyme A reductase inhibitors (s
51  We sought to determine whether therapy with hydroxymethylglutaryl coenzyme A reductase inhibitors (s
52 f the most recent clinical trials with the 3-hydroxymethylglutaryl coenzyme A reductase inhibitors (s
53         Clinical trials suggest that hepatic hydroxymethylglutaryl coenzyme A reductase inhibitors ma
54                                              Hydroxymethylglutaryl coenzyme A reductase inhibitors re
55 , including cholesterol metabolic processes, hydroxymethylglutaryl-coenzyme A (CoA) reductase activit
56 sterol pathways, I found that mRNA levels of hydroxymethylglutaryl-coenzyme A (HMG-CoA) synthase, squ
57  (FPP), which are lipids downstream from the hydroxymethylglutaryl-coenzyme A block, were also examin
58 ylase [At1g03090 and At4g34030] and putative hydroxymethylglutaryl-coenzyme A lyase [At2g26800]) base
59 the computational annotation of At2g26800 as hydroxymethylglutaryl-coenzyme A lyase.
60 of previously reported methods for screening hydroxymethylglutaryl-coenzyme A reductase (HMGR) inhibi
61                                Inhibitors of hydroxymethylglutaryl-coenzyme A reductase (statins) inc
62                                              Hydroxymethylglutaryl-coenzyme A reductase degradation o
63 nate, indicating a direct effect of vascular hydroxymethylglutaryl-coenzyme A reductase inhibition.
64    Pretreatment of Jurkat T-cells with the 3-hydroxymethylglutaryl-coenzyme A reductase inhibitor, lo
65       In earlier studies of the influence of hydroxymethylglutaryl-coenzyme A reductase inhibitors (a
66 sterol regulatory element-binding protein 1, hydroxymethylglutaryl-coenzyme A reductase, and apolipop
67           We also observed lower activity of hydroxymethylglutaryl-coenzyme A reductase, the key enzy
68 he degradation of the yeast Hmg2p isozyme of hydroxymethylglutaryl-coenzyme A reductase.
69 ame deletion mutants confirmed the role of a hydroxymethylglutaryl-coenzyme A synthase cassette, thre
70                                              Hydroxymethylglutaryl (HMG) CoA reductase inhibitors (st
71 l1L) is an adaptor protein for the E3 ligase hydroxymethylglutaryl reductase degradation protein 1 (H
72 lean proof for the reversible dehydration of hydroxymethylglutaryl-S-PksL via incorporation of 2H or

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