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1 ghtly regulated by 25-hydroxycholesterol and geranylgeraniol.
2 97 and augmented by the nonsterol isoprenoid geranylgeraniol.
3 s, which can be chemically complemented with geranylgeraniol.
4 ells was p53-independent and was reversed by geranylgeraniol.
5 and is augmented by the nonsterol isoprenoid geranylgeraniol.
6 d by addition of HMG-CoA, mevalonic acid, or geranylgeraniol.
7 endence of LTP on the non-sterol isoprenoid, geranylgeraniol.
8 olesterol and nonsterol isoprenoids, such as geranylgeraniol.
9 , or the prenylation precursors farnesol and geranylgeraniol.
10 se of the protons of esters of phytol and of geranylgeraniol.
11 ranylated by labelling J774 cells with [(3)H]geranylgeraniol.
12 whereas alendronate activation is blocked by geranylgeraniol.
13 ol, and alendronate effects are prevented by geranylgeraniol.
14 tially by mevalonate and more effectively by geranylgeraniol.
18 vastatin, but not clodronate, are blocked by geranylgeraniol, a precursor of geranylgeranyl diphospha
21 nisomycin, a protein synthesis inhibitor, or geranylgeraniol, an intermediate in the cholesterol bios
22 itavastatin-induced apoptosis was blocked by geranylgeraniol and mevalonate, products of the HMGCR pa
23 tatin effects are prevented by mevalonate or geranylgeraniol, and alendronate effects are prevented b
24 orporation of exogenously provided farnesol, geranylgeraniol, and unnatural analogs of these isopreno
25 e certain sterols, oxysterols, farnesol, and geranylgeraniol, as well as the diphosphate derivatives
28 rporation studies showed that mevalonate and geranylgeraniol, but not farnesol, released the lovastat
30 also supplied with the 20-carbon isoprenoid geranylgeraniol, but not the 15-carbon farnesol, raising
31 adhesion was reversed by co-incubation with geranylgeraniol, but not with farnesol, with concurrent
33 that the oxysterol 25-hydroxycholesterol and geranylgeraniol combine to trigger extraction of reducta
36 lesterol biosynthetic pathway, of which one, geranylgeraniol diphosphate, is required for learning in
38 role of geranylgeranyl isoprenoids GGPP and geranylgeraniol (GGOH) in regulating Abeta production.
39 I as well as combinations of lovastatin with geranylgeraniol (GGOH) or farnesol (FOH) to investigate
40 ch utilizing a combination of lovastatin and geranylgeraniol (GGOH) to potentiate the ability of lova
43 New fluorescent analogues of farnesol and geranylgeraniol have been prepared and then converted to
44 te pathway and that a constant production of geranylgeraniol in a small subset of neurons is required
45 lts identify UBIAD1 as the elusive target of geranylgeraniol in reductase degradation, the inhibition
50 ly related compound, does not substitute for geranylgeraniol nor does another animal model of impaire
51 tent with N-BP inhibition of isoprenylation, geranylgeraniol or farnesol prevented accumulation in S
52 renoids, such as nerolidol, cis-farnesol, or geranylgeraniol, or metabolites in the cholesterol pathw
53 nude mice were maintained on a diet lacking geranylgeraniol, oral pitavastatin caused regression of
54 , when the animal diet was supplemented with geranylgeraniol, pitavastatin failed to prevent tumour g
55 sterification of bacteriochlorophyllide a by geranylgeraniol-PPi during bacteriochlorophyll a biosynt
56 This inhibition is prevented by exogenous geranylgeraniol, probably required for prenylation of GT
57 lyalkenes, including geraniol, farnesol, and geranylgeraniol, providing an efficient and stereoselect
58 led with bacteriochlorophyll esterified with geranylgeraniol, rather than with phytol, implying that
59 AS9-mediated knockout of UBIAD1 relieves the geranylgeraniol requirement for reductase degradation.
61 splacement from reductase in the presence of geranylgeraniol, thereby preventing degradation of reduc
65 farnesyl diphosphate synthase inhibitors or geranylgeraniol transferase I inhibitors, we evaluated c
66 ated activation is blocked by mevalonate and geranylgeraniol whereas alendronate activation is blocke
67 fully by mevalonate and less effectively by geranylgeraniol whereas alendronate effects are blocked
68 f bacteriochlorophyll (BChl) a, phytol, with geranylgeraniol, which possesses three more double bonds
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