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1  12, 14, and 15 between perfluorodecalin and n-octanol.
2 obtained by cocrystallizing antiamoebin with n-octanol.
3 hatidylcholine (POPC) bilayer interfaces and n-octanol.
4 que because it is a simpler model to explain n-octanol actions on the GABAA receptor.
5 multiple sites to exert multiple actions, or n-octanol acts as a partial agonist to manifest these ac
6              Two models were used to explain n-octanol agonistic and potentiating actions on the alph
7 ns on the alpha1beta2gamma2S GABAA receptor: n-octanol binds to multiple sites to exert multiple acti
8     The measured partition coefficient in an n-octanol/buffer system of AMPO was similar to those of
9                                          The n-octanol effects on the gamma-aminobutyric acid type A
10 ces of phosphatidylcholine bilayers and into n-octanol, have been determined by W. C. Wimley, S. H. W
11                            Coapplications of n-octanol increased peak currents evoked by 3 microM GAB
12       Conversely, the membrane intercalator, n-octanol, increased cholesterol oxidation, transfer, an
13                                 In addition, n-octanol modulated GABA-induced currents in a concentra
14 avior of sensitizer release in n-butanol and n-octanol occurs at an optimal temperature of 20 degrees
15     One-minute preapplication of 1000 microM n-octanol slightly potentiated 3 microM GABA-induced cur
16 ne systems and finally the diisobutylamine + n-octanol system was selected to enhance the carbonation
17             Ethanol decreased the potency of n-octanol to inhibit ACh currents, possibly resulting fr
18 drophobic side-chains is larger than that of n-octanol to water transfer free energies.
19 ee energies of transferring side-chains from n-octanol to water, indicates that the magnitude of prot
20 ot observed when the peptide is dissolved in n-octanol, trifluoroethanol or sodium dodecyl sulfate mi
21                                              n-Octanol was also capable of evoking a small current wi
22 ations and no potentiation was observed when n-octanol was coapplied with 1000 microM GABA.
23 ting point, vapour pressure at 20 degrees C, n-octanol-water partition coefficient and solubility in
24 in tern eggs varied inversely with log10KOW (n-octanol-water partition coefficient), shifting egg con
25  positively correlated with their respective n-octanol-water partition coefficients (R(2) = 0.65).
26 tential of the chalcogenopyrylium dye or the n-octanol/water partition coefficient, log P.
27 kyl and alkyl carboxylates between water and n-octanol were determined as a measure of their lipophil

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