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5 s hysteresis results from the formation of a Donnan potential at high pH which shifts the ionic equil
8 electrolyte concentration consistent with a Donnan potential due to the selective partitioning of io
9 solution-diffusion model taking into account Donnan exclusion and unhindered advection due to imperfe
10 ss, two Donnan effects, osmotic pressure and Donnan equilibrium potentials, are significantly amplifi
11 electrostatic models (Gouy-Chapman-Stern and Donnan-plus-binding) used to compute electrical potentia
13 properties of the hemichannels (also cast as Donnan potentials) will produce either an accumulation o
16 ncentrations determined with the soil column Donnan membrane technique in a range of soils varying in
17 paper (75-mum thickness), a cation-exchange Donnan exclusion membrane (FKL), and a silver-foil worki
19 the transmembrane Cl(-) gradient: (i) fixed 'Donnan' charges inside and outside the cell; (ii) the pr
21 3-8), which is contrary to expectations from Donnan theory and the observed high rejection of salts.
24 quilibrium simultaneously to establish Gibbs-Donnan equilibrium in a polyelectrolyte-directed mineral
25 d solution-diffusion model that incorporates Donnan electrostatic exclusion of ions and unhindered ad
26 xyquinoline allowed sensing through inducing Donnan osmotic pressure and tuning its lattice spacing.
27 lt-polyelectrolyte preferential interaction (Donnan) coefficient (Gamma(u)coul) per polyion charge at
30 acidification, and that an interior-negative Donnan potential is responsible for low endosomal [Cl-]
32 predicted using both WHAM/Model VII and NICA-Donnan speciation models for both traditionally and mild
34 trode and a biocompatible and nonpolarizable Donnan exclusion anion-exchanger membrane reference/coun
35 mplementary approaches: a direct approach of Donnan equilibrium dialysis read out by atomic emission
37 echnical aspects describing the influence of Donnan equilibria on neuronal chloride ion (Cl(-)) distr
39 oncentrations below or above a set value of 'Donnan' charges, and show that at any value of these fix
43 eases in salt concentration, suggesting that Donnan osmotic pressure is negligible above this thresho
48 cellular milieu are negatively charged, the Donnan potential provides an additional driving force fo
49 solutions has two principal components: the Donnan contribution and a contribution due to protein-pr
52 established theoretical models including the Donnan theory and the Poisson-Boltzmann cylindrical cell
54 lysis further indicated that, because of the Donnan equilibrium at cation exchange membrane-anolyte/c
57 y, high solution concentrations suppress the Donnan exclusion effect of the charged RED membranes, se
58 ludes the electrostatic potential due to the Donnan equilibrium, which arises from the semipermeable
59 cation of glucose signal was ascribed to the Donnan exclusion and ensuing Nafion-gated ionic fluxes,
60 hat a MDP of up to -5 mV, in addition to the Donnan potential, may be generated at high workloads, ev
61 e amount of genome packaged by utilizing the Donnan potential (through increases in the capsid radius
65 Theoretical analysis of the relaxation to Donnan equilibrium utilized for such vesicle uptake assa
66 pecies to the protein hydrogel gives rise to Donnan potentials that change the hydrogel volume causin
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