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1 tin) at the leading edge generates force for cell locomotion.
2 rmation of lamellipodia and filopodia during cell locomotion.
3 etal remodeling, intracellular transport and cell locomotion.
4 ate in modulating actin dynamics to optimize cell locomotion.
5  they fail to release their back ends during cell locomotion.
6  required to maintain cell shape and promote cell locomotion.
7  adhesion turnover, leading to inhibition of cell locomotion.
8 ular processes, including cell spreading and cell locomotion.
9 s of strong cell adhesion, but yet allow for cell locomotion.
10 ating a direct involvement of this enzyme in cell locomotion.
11 ht-directed perturbation techniques to study cell locomotion.
12 and force of membrane extension required for cell locomotion.
13 able of activating pro-MMP-2 and stimulating cell locomotion.
14 ction tail move forward, in the direction of cell locomotion.
15  normal and pathological processes involving cell locomotion.
16 t this aspect of transport is independent of cell locomotion.
17 induced mitogenic signals, cell survival and cell locomotion.
18 eta-gal, whereas AA-Akt blocked VEGF-induced cell locomotion.
19 a gradient of CSF-1 but is not essential for cell locomotion.
20 he contractility of both ends is involved in cell locomotion.
21 ain key aspects of cytokinesis and polarized cell locomotion.
22 ot elicit identical responses with regard to cell locomotion.
23  frame from what could be expected of single cell locomotion.
24 xplore four different minimal mechanisms for cell locomotion: 1), a biophysical model for myosin cont
25  This finding also suggests that directional cell locomotion against resistive forces requires a turg
26 te that the flagellar motors responsible for cell locomotion also play a role, adding or subtracting
27    By recording the position of beads during cell locomotion and after cell removal, we discovered th
28 during coordinated cell movements, including cell locomotion and cell division, we generated a phosph
29 alysis revealed an elevation in the speed of cell locomotion and cell proliferation rate in the conne
30  Cdc42 activity, we show changes in speed of cell locomotion and cell roundness also result from exog
31 ucial for many cellular processes, including cell locomotion and cytokinesis, but are poorly understo
32 tablish and alter cellular morphology during cell locomotion and division.
33                                              Cell locomotion and endocytosis are powered by the rapid
34                                       During cell locomotion and endocytosis, membrane-tethered WASP
35 biophysical processes, developing models for cell locomotion and for drug discovery.
36 n dynamics underlying membrane protrusion in cell locomotion and growth cone chemotaxis.
37 rich structures, likely play a major role in cell locomotion and in mechanical signaling with the sur
38 major cell signaling hub to facilitate tumor cell locomotion and invasion.
39 act with p120 catenin (p120(ctn)) to mediate cell locomotion and proliferation.
40 nizing the cilium, a structure important for cell locomotion and sensing of the surrounding environme
41 lts suggest that the increased plasticity of cell locomotion and the invasiveness of MTLn3 cells resu
42 hput wound closure assay in which individual cell locomotion and wound closure kinetics were quantifi
43  translocation of proteins across membranes, cell locomotion, and catalyzed protein and nucleic acid
44 intracellular transport, organelle dynamics, cell locomotion, and cell division.
45 -1 upregulation and TGF-beta1+EGF-stimulated cell locomotion, as pharmacologic disruption of MEK/p38
46 ous actin (f-actin) are involved in directed cell locomotion, but are poorly understood.
47 motors in living cells are involved in whole-cell locomotion, contractility, developmental shape chan
48                                           As cell locomotion depends on a cell having a polarity, the
49 structures that are crucial for adhesion and cell locomotion during inflammation and metastasis.
50 roperties of biological cells play a role in cell locomotion, embryonic tissue formation, and tumor m
51 , and when exposed to light promptly blocked cell locomotion in a similar manner.
52 n-specific effector T cells had no role in T cell locomotion in the lymph node.
53 und-healing assay, time-lapse recording, and cell locomotion into the lungs of BALB/c nude mice.
54                                   Persistent cell locomotion is a key feature of eukaryotic cells res
55                                  Directional cell locomotion is critical in many physiological proces
56                While the protrusive event of cell locomotion is thought to be driven by actin polymer
57 al asymmetry arises and is maintained during cell locomotion is, however, unclear.
58 gh the N-WASp/Arp2/3 pathway is important in cell locomotion, membrane trafficking, and pathogen infe
59  much the same way the cytoskeleton mediates cell locomotion, mitosis and intracellular vesicular tra
60 but not against alpha1 and alpha2, inhibited cell locomotion on a reconstituted basement membrane in
61 l cell invasive behavior, but not epithelial cell locomotion over the gel surface, is partially regul
62                Instead, in-depth analysis of cell locomotion paths revealed that the distribution of
63                 Thus, metabolic control of T cell locomotion provides new opportunities to interfere
64  within a three-dimensional collagen matrix, cell locomotion results in translocation of the flexible
65 biochemical signals and forces necessary for cell locomotion, suggesting that P2Y(2)Rs may be linked
66 gh microtubules have long been implicated in cell locomotion, the mechanism of their involvement rema
67 mical processes are integrated to accomplish cell locomotion, the same issues, along with certain new
68 lar motility processes ranging from directed cell locomotion to cytokinesis.
69 latory role for cell traction generation and cell locomotion under the physical confinement of the th
70 a that microtubules normally act to restrain cell locomotion was confirmed by treating cells with hig
71 e role of these macromolecular assemblies in cell locomotion, we have determined the 2.6 A resolution
72 ously associated metabolic oscillations with cell locomotion, we hypothesized that patients with abno
73 nt controls invadopodium formation and tumor cell locomotion, we systematically analyzed components o
74 ta1 integrin binding activates RhoA, slowing cell locomotion, whereas laminin-5-alpha3beta1 integrin
75                 To examine the mechanisms of cell locomotion within a three-dimensional (3-D) cell ma

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