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1 ng efforts should incorporate sensitivity to relative permeability.
2 pillary trapping, and at the field-scale via relative permeability.
3  significantly increases their Na(+) to K(+) relative permeability.
4 e effect of gas hydrate saturation change on relative permeability.
5 rnal protons decrease calcium/monovalent ion relative permeability.
6  govern anion-vs.-cation selectivity and the relative permeabilities among anions.
7 ations, but its mutation dramatically alters relative permeabilities among anions.
8 ify the crucial reservoir-scale functions of relative permeability and capillary pressure and their d
9          We then measured the effects on the relative permeability and conductance of the channel to
10 nsistent with increases in the Na(+) to K(+) relative permeability and decreases in electrochemical d
11        A linear correlation between membrane relative permeability and MS2 removal was found.
12 ering quantities of CO(2) residual trapping, relative permeability, and caprock integrity.
13 experiment in which the saturation topology, relative permeability, and tortuosity were kept constant
14  numerical model, due to a decrease in water relative permeability as the pore-space becomes more con
15 the same set of empirical parameters predict relative permeability at all S(h), (ii) includes the eff
16 hydrate-bearing sediments where the proposed relative permeability can account for the evolving hydra
17 polyamines freely permeated TRPV1 (estimated relative permeabilities compared with Na+ were between 3
18 re precluded because of lack of experimental relative permeability data.
19                        Endpoint drainage CO2 relative permeabilities for liquid and supercritical CO2
20 pus oocytes and in HEK293 cells gave similar relative permeabilities for selected anions, suggesting
21 experiments designed to measure CO2 endpoint relative permeability for CO2 displacing brine at in sit
22 -fold higher unitary conductance and greater relative permeability for Na(+) ions, as compared with t
23 olerant HKT1 mutants by a markedly decreased relative permeability for Na+ at high Na+ concentrations
24  phosphate to adenosine appears to shift its relative permeability from channels formed by Cx32 to ch
25                    This study proposes a new relative permeability model for gas hydrate-bearing medi
26 pace CO2 saturation of 0.5, and steady state relative permeabilities of CO2 and water on the order of
27                              We compared the relative permeabilities of five different retinal gap ju
28            Pore radius, estimated by fitting relative permeabilities of organic cations to the Renkin
29 permeability of sodium is decreased, and the relative permeability of calcium and magnesium is increa
30 the receptor (T348K, D352N, D352K) increased relative permeability of chloride ions.
31 cularly applicable for the evaluation of the relative permeability of compounds in a combinatorial li
32 bitors, such as sodium azide, to compare the relative permeability of HDTA conjugates.
33 ns of various ionic composition to determine relative permeability of homomeric rho1 receptors.
34 mbrane and where substitutions influence the relative permeability of the channel to cations and anio
35 T441S) in this region increased the apparent relative permeability of the channel to NH4+.
36                                          The relative permeability of the conductances to I(-) and Cl
37 nel of transgenic mice was influenced by the relative permeability of the mutant AChRs to calcium, on
38                                          The relative permeability of this conductance to anions was
39                   The WT current exhibited a relative permeability P(X)/P(Cl) order of SCN(-) > or =
40 ion (E191D) yielded substantial increases in relative permeability (P(X)/P(Na)).
41  The tail current was carried by K+ and Cs+ (relative permeabilities PCa/PK = 0.22), and was fully bl
42 g 5 mM Ca2+; the values were used to compute relative permeabilities (PNMDG/PNa and PCa/PNa).
43 Li)/P(Cs) by about one-half, and shifted the relative permeability sequence of Cs(+), Rb(+), K(+), an
44                           KCNKO has a common relative permeability series (Eisenman type IV) but cond
45             In the oocyte expression system, relative permeabilities to SCN-, I-, NO3-, Br- and HCO3-
46 ptors containing alpha7 subunits have a high relative permeability to calcium and influence numerous
47                      The receptor has a high relative permeability to calcium and performs a variety
48 ontains the alpha 7 gene product, has a high relative permeability to calcium, and binds alpha-bungar
49 s), because they are widespread, have a high relative permeability to calcium, and regulate numerous
50 tains the alpha7 gene product and has a high relative permeability to calcium.
51 product, because of their abundance and high relative permeability to calcium.
52   There was no significant difference in the relative permeability to INH between these two species.
53 in amplitude to those of WT, but had altered relative permeability to large anions.
54 agonist concentration-dependent increases in relative permeability to large cations and changes in Ca
55           The produced gas reduces the water relative permeability to less than 1% and, therefore, si
56 ion 438 increased, to different extents, the relative permeability to Li(+), K(+), Rb(+), and Cs(+).
57            We now report that this increased relative permeability to NH4+ is sensitive to small chan
58              These channels shared a similar relative permeability to various anions, but the express
59            Therefore, accurate prediction of relative permeability using legacy models (e.g. Brooks-C
60         Also the through-plane water and air relative permeability values and water saturations at di
61                                          The relative permeabilities varied inversely with relative K
62                                              Relative permeabilities were estimated on the basis of t