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1 imicked by the gap junction inhibitor 18beta-glycyrrhetinic acid (1 microM) with a similar time cours
2 nuated by the gap junction inhibitor 18alpha-glycyrrhetinic acid (18alpha-GA; 50 microM), and a synth
3               A conspicuous effect of 18beta-glycyrrhetinic acid (18beta-GA) and carbenoxolone, which
4 n genes, and gap junction uncouplers, 18beta-glycyrrhetinic acid (18beta-GA) and octanol blocked Ca(2
5 gative of -70 mV and was inhibited by 18beta-glycyrrhetinic acid (20 mum).
6 propagate is reduced dramatically by 18alpha-glycyrrhetinic acid, a blocker of gap junctions.
7 sfer was elicited by treatment with 18-alpha-glycyrrhetinic acid (AGA).
8         Inhibition of GJC utilizing 18-alpha-glycyrrhetinic acid (AGRA) blocks the maturation of pre-
9                              We used 18alpha-glycyrrhetinic acid (alphaGA) to block gap junction cond
10 Proliferation assays showed that addition of glycyrrhetinic acid (an 11 beta-HSD2 inhibitor) resulted
11 ects of 11beta-HSD2 were abrogated by 18beta-glycyrrhetinic acid, an 11beta-HSD inhibitor, and in cel
12                   Permeation is inhibited by glycyrrhetinic acid, an agent that also increases interc
13  junction and hemichannel inhibitors 18 beta-glycyrrhetinic acid and carbenoxolone, even in cells wit
14 uncouplers (1-octanol, carbenoxolone, 18beta-glycyrrhetinic acid and connexin mimetic peptide) elimin
15 treated with the gap junction blocker 18beta-glycyrrhetinic acid before freezing, the intercellular i
16 he effect of the gap junction blocker 18beta-glycyrrhetinic acid (betaGA) on the differentiation of p
17 nic hearts with a gap junction blocker, beta-glycyrrhetinic acid (BGA).
18                                       18beta-Glycyrrhetinic acid blocked the high K(+)-hyperpolarizat
19 onal communication, like heptanol and 18beta-glycyrrhetinic acid, blocked not only gap junctional com
20 ing gap junctional hemichannels with 18alpha-glycyrrhetinic acid, blocking ATP receptors with pyridox
21 lycyrrhizin (GL), and its metabolite, 18beta-glycyrrhetinic acid (GA), in a hepatocyte model of chole
22 hymol, parthenolide, andrographolide, 18beta-glycyrrhetinic acid, lupeol, ursolic acid and beta-sitos
23 ion, a connexin mimetic peptide and 18-alpha-glycyrrhetinic acid, markedly reduced the secretion of I
24 ocytes with the 11beta-HSD2 inhibitor 18beta-glycyrrhetinic acid mimicked the effect of exogenous adm
25                                              Glycyrrhetinic acid monoglucuronide (GAMG) is a great va
26         A combination of Ba(2)(+) and 18beta-glycyrrhetinic acid near completely blocked the ACh-hype
27                 Hemichannel blockers, 18beta-glycyrrhetinic acid or La3+, blocked depolarization-indu
28 he gap junction blockers octanol and 18alpha-glycyrrhetinic acid, or the A kinase inhibitor Rp diaste
29 y gap-junctional blockers, oleamide and beta-glycyrrhetinic acid, or were reversed by returning extra
30 ax) = 50.4 +/- 6.5 %) and 100 microM 18alpha-glycyrrhetinic acid (pD(2) = 6.04 +/- 0.14; R(max) = 40.
31    The putative gap junction blocker 18 beta-glycyrrhetinic acid suppressed the ACh-induced responses
32 alog of the naturally occurring triterpenoid glycyrrhetinic acid, which contains a 2-cyano substituen
33 slices, the gap junctional blocker, 18 alpha-glycyrrhetinic acid, whilst not preventing the full-blow
34 anol, heptanol, flufenamic acid, and 18alpha-glycyrrhetinic acid) with affinities close to those repo

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