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1 ased on reduction of the proteins' molecular molar volume.
2 ites, zeotypes, and mesoporous materials) to molar volume.
3 dditional constraint on the system's partial molar volume.
4 nteraction that exhibits a change in partial molar volume.
5  layer due to the significant changes in the molar volumes.
6  rotor) from which the reversible changes in molar volume (1.2 +/- 0.2 cubic centimeters) and entropy
7                        The change in partial molar volume and enthalpy between the keto and enol form
8                       The changes in partial molar volume and specific molar surface area between the
9 ese measurements the changes in the apparent molar volume and the apparent molar adiabatic compressib
10 h pressure are characterized by low standard molar volume and/or high standard free energy changes up
11                      Here, we report partial molar volumes and activity coefficients of glycerophosph
12     Computed and measured densities, partial molar volumes, and thermal expansion coefficients are al
13 have been further used to calculate apparent molar volume, apparent specific volume, isentropic appar
14 ed were used to compute apparent and partial molar volume, apparent specific volumes, partial molar e
15            The adsorption changes of partial molar volumes are in good agreement with other literatur
16 tion dependence of the thermodynamic partial molar volumes, as well as recent data from neutron diffr
17                  Therefore, standard partial molar volumes at infinite dilution have been calculated
18                             Standard partial molar volumes at infinite-dilution and corresponding vol
19                               The changes in molar volume become more negative as ring number increas
20                                  The partial molar volume change for dissociation was -209 +/- 13 ml/
21                                              Molar volume changes for the I3(-)/I- redox couple and f
22                                 From partial molar volume data, estimates were 25 and 128 mol H2O/mol
23 both specific molar surface area and partial molar volume data.
24                 Comparison of solute partial molar volumes deduced from measurement of solution densi
25 es, and (iii) determine the relative partial molar volume (DeltaV degrees ) and isothermal compressib
26                           Changes in partial molar volumes (DeltaV) and isothermal compressibilities
27 ow range from 13.0 to 27.1 kJ/mol, while the molar volumes extend from 135.9 to 248.8 cm(3)/mol; thus
28 s from Debye-Huckel limiting law of apparent molar volume for acesulfame-K was obtained at given temp
29                                     Apparent molar volumes for monosaccharides, disaccharides, deriva
30 he concomitant changes in molar enthalpy and molar volume, for each PAH on monomeric (2.7 micromol/m2
31  consistent with previous results on partial molar volumes in the liquid-crystal phase.
32 is dissolved in an ionic liquid, its partial molar volume is much smaller than that observed in most
33                             But although its molar volume monotonically decreases with pressure, the
34                      The values for apparent molar volume obtained at given temperatures showed negat
35 increases with the CO2 concentration, with a molar volume of CO2 of about 0.038 L/mol, corresponding
36 fect is explained by a change of the partial molar volume of the insulin variants associated with the
37                                   The higher molar volume of the product can create an impervious she
38        The latter number is greater than the molar volume of the protein.
39                                          The molar volume of the solute correlated only moderately wi
40 on of the molar enthalpy, molar entropy, and molar volume of the stationary phase, all of which depen
41       Unfolding by pressure implies that the molar volume of the unfolded state of a protein is small
42 onships between the enthalpy changes and the molar volumes of the donor cations were found which asym
43          The differences between the partial molar volumes of these peptides in the stationary and mo
44                                      Partial molar volumes of transfer (DeltatV2( degrees )) and visc
45                                  The partial molar volume (PhiV degrees ) indicates hydrophilic inter
46 o 248.8 cm(3)/mol; thus, almost doubling the molar volume results in only a modest energetic destabil
47 monstrate that dissolved water has a partial molar volume (V&cjs1171;H2O) that is independent of the
48  correlation is then found between D(PE) and molar volume, V(m) (A(3)/mol): logD(PE) (m(2)/s) = 0.014
49  apparent molar volumes (V2,varphi), partial molar volumes (V2( degrees )) at infinite-dilution, and
50 des have been studied from measured apparent molar volumes (V2,varphi), partial molar volumes (V2( de
51                    From these data, apparent molar volumes (V2,varphi), viscosity B-coefficients and
52                                      Partial molar volumes, V2( degrees ), and partial molar isentrop
53                                     Apparent molar volumes, V2,varphi, apparent specific volumes, ASV
54 ent molar volume (varphiV), standard partial molar volume (varphiV(0)), the slope (SV( *)), apparent
55             Using experimental data apparent molar volume (varphiV), standard partial molar volume (v
56        The change in the proteins' molecular molar volume was caused by changes in protein folding, a
57  behavior, becoming more native-like (higher molar volume) with increasing denaturant concentration.

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