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1 ation and also mediates cell-cell adherence (flocculation).
2 ation, but was not involved in M. aeruginosa flocculation.
3 eins, which results in their aggregation and flocculation.
4 r layer-by-layer assembly or vacuum-assisted flocculation.
5 with surface-adsorbed trastuzumab exhibited flocculation.
6 lacking both CheB1 and CheR1 was delayed in flocculation.
7 particles from secondary- to primary-minimum flocculation.
8 tion in mating, invasion, filamentation, and flocculation.
9 ggregate in the calcium-dependent process of flocculation.
10 th in diploids, haploid invasive growth, and flocculation.
11 ng these cellular functions directly affects flocculation, a cellular differentiation process initiat
12 lution of cooperative behavior by revisiting flocculation, a self-adherence phenotype lacking in most
13 Visual and SEM observations confirmed the flocculation action of the mucilage as visible flocs for
16 FLO1 in the laboratory strain S288C restores flocculation, an altered physiological state, reminiscen
17 addition, we found that Als1p mediates both flocculation and adherence of C. albicans to endothelial
19 highly aggregated Fe(OH)(3), which promotes flocculation and gradual settling of the decomposed cyan
20 eoxidation with chlorine dioxide followed by flocculation and settling have been shown to be effectiv
22 s when predicting diffusive contributions to flocculation and to single collector efficiency in media
23 tic of zinc-deficient cells, suggesting that flocculation and vacuolation serve homeostatic functions
24 istributions during the slow mixing stage in flocculation and, to some extent, their settling charact
29 f the chromophoric DOM (CDOM) was removed by flocculation, approximately 4-5 mg L(-1) total organic c
30 rowth and bud's site selection, clumping and flocculation, as well as increased sensitivity to a wide
35 charge neutralization contributed to kaolin flocculation, but was not involved in M. aeruginosa floc
36 h electrostatic and steric effects, bridging-flocculation can occur in the presence of multivalent ca
38 ferric (Fe(III)) salt was investigated as a flocculation-coagulation system to remove arsenic (As) f
39 binding isotherms, exchange rates, critical flocculation concentrations, and the composition of mixe
41 ow disinfection rates necessitating extended flocculation/contact times to achieve significant log-in
43 diffusion in complex media, aggregation and flocculation, hindered behavior of particles in confined
44 ion of Che1 to the control of chemotaxis and flocculation in A. brasilense remains poorly understood.
46 he addition of NaCl (300-400 mM) only caused flocculation in nanodispersion stabilized by SDS-Tween 8
47 expression and in sequence, suggesting that flocculation in S. cerevisiae is a dynamic, rapidly evol
49 hollow spheres are theorized to form through flocculation, in which the charge-driven aggregation of
54 locculin because of its demonstrated role in flocculation, its structural similarity to other members
55 m were evaluated, including plug dispersion, flocculation kinetics, membrane degradation, and channel
58 PI-stabilized nanoemulsions were unstable to flocculation near the protein isoelectric point (pH 5.0)
59 veral minor components were identified after flocculation (nitrocellulose) or precipitation (sawdust,
62 ncomitant formation of exopolysaccharide and flocculation of heterotroph-methanogen cellular aggregat
63 esses remains unaddressed in coagulation and flocculation of insoluble precipitates (flocs), which pl
64 matter in metal-rich aquatic systems or the flocculation of organic matter in wastewater treatment p
65 observations suggest gelation occurs via the flocculation of semicrystalline colloidal particles, whi
67 multiple excitation wavelengths and similar flocculation or deposition methods in comparative analys
70 surement of target transcript levels and the flocculation phenotype characteristic of Zfs1 deletion.
78 tional water treatment involving coagulation-flocculation-sedimentation may be impeded by vascular pl
80 uble mutants demonstrated that the increased flocculation seen in zfs1Delta mutants is due, at least
82 RF data, as assayed by both the bentonite flocculation test (BFT) and the sheep cell agglutination
84 collisional analysis based on Smoluchowski's flocculation theory was employed to fit the kinetics of
88 ind have properties (e.g. growth inhibition, flocculation, vanadate resistance, stress response) that
96 ction between primary- and secondary-minimum flocculation when the interparticle potential curve refl
97 rated that 9c polyplexes had a low degree of flocculation, whereas 9a and 9b polyplexesd aggregate ra
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