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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.
8 ify the crucial reservoir-scale functions of relative permeability and capillary pressure and their d
10 nsistent with increases in the Na(+) to K(+) relative permeability and decreases in electrochemical d
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
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
26 pace CO2 saturation of 0.5, and steady state relative permeabilities of CO2 and water on the order of
29 permeability of sodium is decreased, and the relative permeability of calcium and magnesium is increa
31 cularly applicable for the evaluation of the relative permeability of compounds in a combinatorial li
34 mbrane and where substitutions influence the relative permeability of the channel to cations and anio
37 nel of transgenic mice was influenced by the relative permeability of the mutant AChRs to calcium, on
41 The tail current was carried by K+ and Cs+ (relative permeabilities PCa/PK = 0.22), and was fully bl
43 Li)/P(Cs) by about one-half, and shifted the relative permeability sequence of Cs(+), Rb(+), K(+), an
46 ptors containing alpha7 subunits have a high relative permeability to calcium and influence numerous
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
52 There was no significant difference in the relative permeability to INH between these two species.
54 agonist concentration-dependent increases in relative permeability to large cations and changes in Ca
56 ion 438 increased, to different extents, the relative permeability to Li(+), K(+), Rb(+), and Cs(+).