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1 mum, owing mainly to directional movement or simple diffusion.
2 xtended further than might be predicted from simple diffusion.
3 ds of times faster than what is expected for simple diffusion.
4 gesting that recycling pool vesicles move by simple diffusion.
5 es in the IS and that its movement occurs by simple diffusion.
6 sion and increases the proportion exhibiting simple diffusion.
7 esting that nuclear entry does not occur via simple diffusion.
8 obility was not directed but was governed by simple diffusion.
9 cur in a non-targeted fashion as a result of simple diffusion.
10 ggest that anandamide uptake is a process of simple diffusion.
11 tes, cross the intact blood-brain barrier by simple diffusion.
12 n, and from the theoretical distribution for simple diffusion.
13 1, suggesting that import does not occur via simple diffusion.
14 the coexistence of facilitated diffusion and simple diffusion.
15 trations, at rates much faster than that via simple diffusion.
16 barriers, and membrane rafts also occurs by simple diffusion and does not require facilitation by me
17 ly unlike the familiar spreading patterns of simple diffusion, as the kinetics of response are surpri
19 hown to overcome the slow signaling speed of simple diffusion by utilizing diffusive relays, in which
20 ent with IFNgamma spread being governed by a simple diffusion-consumption model and offer insight int
21 l biologically relevant diffusion processes (simple diffusion, continuous-time random walk, caged dif
26 m of the Bicoid profile is consistent with a simple diffusion/degradation model, the observed length
28 l-molecule inhibitors, including delivery by simple diffusion in the growth medium and concentration-
31 Taken together, our results suggest that simple diffusion may account for the nuclear export obse
32 t of endocrine cells is not always through a simple diffusion mechanism as presently thought, but ins
36 and simulation-based inference, we find this simple diffusion model fails to explain the experimental
40 luble recombinant Shh (ShhN)) to support the simple diffusion model of long-range Shh signalling, the
45 h the brain [1], because of the predominant "simple diffusion" model of steroid hormone transport acr
46 3 orders of magnitude less than expected for simple diffusion models, and the binding progress curves
48 ne transport in vitro, most methods focus on simple diffusion of a single analyte across nonbiomimeti
49 Concerning flux across the plasma membrane, simple diffusion of ascorbic acid plays only a small or
50 s can be shaped by mechanisms other than the simple diffusion of RA from a localized posterior source
51 o account for the long-range effects of Shh: simple diffusion of Shh, a relay mechanism in which Shh
53 erns with a mathematical model that combines simple diffusion of the signal with logistic growth of t
55 a localized site, but whether this occurs by simple diffusion or by more elaborate mechanisms is uncl
56 wer in vivo than compared to in vitro, and a simple diffusion process describes the autocorrelation f
58 entrations and/or REE profiles indicative of simple diffusion, signifying minimal alteration, have be
60 ic radius of RNP particles (86 nm) precludes simple diffusion through the mesh of cytoskeletal fibers
61 molecules (<10 kDa) permeate the nucleus by simple diffusion through the pore, but molecules larger
63 .8 nm) is representative of native vWF after simple diffusion to the hydrophobic surface, followed by
64 hough many membrane proteins pass the NPC by simple diffusion, two yeast proteins, ScSrc1/ScHeh1 and
67 , but they are not trapped and can escape by simple diffusion, which may be slow, fast, or directed.
68 uch steeper concentration profiles than does simple diffusion, which may facilitate neutrophil chemot