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1 protein is necessary for TGF-beta1-dependent cell motility.
2 ressing PI3KC2beta activation and its driven cell motility.
3 nces epithelial characteristics and inhibits cell motility.
4 eak calcium fluxes and detectable changes in cell motility.
5 formation of adherens junctions, and reduced cell motility.
6 ial-mesenchymal transition factors and colon cell motility.
7  cellular functions as diverse as memory and cell motility.
8 423) signaling pathway, thus increased tumor cell motility.
9 nd increases membrane protrusion and overall cell motility.
10 red for the ability of GAR22beta to modulate cell motility.
11 eterminant of actin assembly and actin-based cell motility.
12  required for generating locomotive force in cell motility.
13 mellipodia are common features of eukaryotic cell motility.
14 cation of factors that influence Rac1-driven cell motility.
15  migration potential index (CMPI) to measure cell motility.
16 or properly localizing adhesion sites during cell motility.
17 pies for cancer resulting in enhanced tumour cell motility.
18 tween the centrosome and nucleus and reduced cell motility.
19 ich are essential for flagellar assembly and cell motility.
20 at specifically targets RhoA for controlling cell motility.
21 it as an actin-independent form of mammalian cell motility.
22 embryonic development, tissue formation, and cell motility.
23  cell-ECM adhesion, and triggers ECM-induced cell motility.
24 nhibitory effects on chemoattractant-induced cell motility.
25 increased islet infiltration and increased T cell motility.
26 spatiotemporal control of cell spreading and cell motility.
27 ions ranging from cell-cell communication to cell motility.
28 signal transduction that ultimately controls cell motility.
29  the contribution of integrin trafficking to cell motility.
30 r genes involved in the control of malignant cell motility.
31 l cell volume dynamics, thereby facilitating cell motility.
32 over of focal adhesion complexes, and random cell motility.
33 in that plays essential roles in directional cell motility.
34  each parameter relates to the others and to cell motility.
35 affold proteins involved in phagocytosis and cell motility.
36 sponses such as FA dynamics, which determine cell motility.
37 uction and cytoskeletal pathways that govern cell motility.
38                High STAT signalling promotes cell motility.
39 and their timely disassembly is required for cell motility.
40  including cell survival, proliferation, and cell motility.
41 cal exosome function that promotes efficient cell motility.
42 te the F-actin cytoskeleton to support tumor cell motility.
43 components and acting as traction points for cell motility.
44 nd indomethacin abrogated STIM1-mediated CRC cell motility.
45 logical processes associated with collective cell motility.
46  in the ciliate Tetrahymena resulted in slow cell motility.
47  Additionally, it acts as a key component of cell motility.
48 s a potential novel regulator of lung cancer cell motility.
49 ng Rac activation, filopodium formation, and cell motility.
50  drive cancer aggressivity through increased cell motility.
51 hrough effects on muscle differentiation and cell motility.
52 s, reduced cell proliferation, and increased cell motility.
53 ition nor EGF stimulation have any effect on cell motility.
54 changes in epithelial cell-cell adhesion and cell motility.
55 gulates Rac1 transcription to increase tumor cell motility.
56 renal epithelial cells, regulates epithelial cell motility.
57  PAR2 to synergize with TGF-beta1 to promote cell motility.
58 ng edge of cells and play important roles in cell motility.
59 n gel contraction assays were used to assess cell motility.
60 mbly, disturbed cell polarity, and increased cell motility.
61 esting that they may cooperate to facilitate cell motility.
62 focal adhesion traction and, thereby, cancer cell motility.
63 ution to the cortical cytoskeleton and tumor cell motility.
64 lar reversals and leads to severe defects in cell motility.
65 tective role in prostate cancer by impairing cell motility.
66 ay critical roles in the initiation of tumor cell motility.
67 tead was modulated by CB2 agonists to reduce cell motility.
68 acellular signaling intermediates engulfment cell motility 1 (ELMO1) and Rac1, as ABCA1 induction was
69                               Engulfment and cell motility 1/dedicator of cytokinesis 180 (Elmo1/Dock
70 T4aP are more widespread and are involved in cell motility(3), DNA transfer(4), host predation(5) and
71  -40 +/- 4%), which ended up to reduction in cell motility (-46 +/- 5%) with inhibition of p-SRC.
72 rease in the persistence of lamellipodia and cell motility, a phenotype consistent with cortactin- an
73 el takes into account the main mechanisms of cell motility - acto-myosin dynamics, as well as substra
74 M2s have well established essential roles in cell motility, adhesion, and cytokinesis and less well d
75     However, the role of these proteins in T-cell motility, adhesion, and in vivo trafficking remains
76  leading to PDL1-mediated suppression of TFH cell motility, alteration of TFH cell differentiation, r
77 r the small Rho GTPase Rac1, a key player in cell motility and adhesion, we explored the vimentin-VAV
78 ted serine-threonine kinase (PAK1) regulates cell motility and adhesion.
79 ng via c-Met is known to promote endothelial cell motility and angiogenesis.
80  the peptide reveals specific alterations in cell motility and cell morphology indicating that the MG
81 ing pathways involved in cell proliferation, cell motility and cell polarity.
82 ching epithelial end buds, where it enhances cell motility and cell-cell adhesion dynamics.
83    sh-RNA-mediated knockdown of CBL enhanced cell motility and colony formation in NSCLC cells, and t
84  in a wound-healing in vitro assay, impaired cell motility and cytokinesis.
85 ition of ILK signaling, which is involved in cell motility and cytoskeletal reorganization, resulted
86 ay stronger E-cadherin localization, reduced cell motility and decreased dynamics of transient cell s
87                            We found that TRM cell motility and dendrite formation required an intact
88 tumor cells corresponding to increased tumor cell motility and dissemination.
89 d sporulation (spo0A, sigE, sigma-70, bofA), cell motility and division (ftsA, ftsK, ftsY, ftsH, ftsE
90  expression of these genes promotes melanoma cell motility and early steps in metastasis.
91 e of lactate in control of proinflammatory T cell motility and effector functions, our findings provi
92 ed actin networks at the leading edge during cell motility and endo/exocytosis, whereas the WASH comp
93 acrophage CSF-1R pTyr-721 signaling promotes cell motility and enhancement of tumor cell invasion in
94 ibited cell proliferation, colony formation, cell motility and expression of beta-catenin, Snail, Slu
95 on did not impact cell viability but reduced cell motility and extracellular matrix invasion, as well
96         Our results further demonstrate that cell motility and focal adhesion turnover require intera
97 reexpression in GAR22beta(-/-) cells reduced cell motility and focal adhesion turnover.
98      Finally, sublethal doses of CSE reduced cell motility and gel contraction, whereas STE had less
99  with a speed determined by the interplay of cell motility and growth, a well-known characteristic of
100 ction on them causes adhesion maturation for cell motility and growth.
101 ese results, we propose that deficiencies in cell motility and guidance contribute to most of the for
102 lagellar assembly, but they are required for cell motility and hence infection.
103  ST-mediated microtubule destabilization and cell motility and implicate the cellular phosphatase cat
104                 This also induced PC3 cancer cell motility and increased colony size in 2D cultures.
105 echanisms of how PRL regulates breast cancer cell motility and invasion are not fully understood.
106 oratory identified PTPN23 as a suppressor of cell motility and invasion in mammary epithelial and bre
107  initiates a signaling circuit essential for cell motility and invasion of metastatic melanoma.
108 he appropriation of primordial mechanisms of cell motility and invasion, and the influence of multipl
109 een shown to be involved in modulating tumor cell motility and invasion, cancer stem cell viability a
110  suggest that LRIG1 may oppose breast cancer cell motility and invasion, cellular processes that are
111 uld regulate mTORC2-dependent bladder cancer cell motility and invasion.
112 clonogenic colony formation, and the loss of cell motility and invasion.
113            Adhesion turnover is critical for cell motility and invasion.
114 d a program of gene expression that promoted cell motility and invasion.
115 get of rapamycin (mTOR), and increased tumor cell motility and invasion.
116  important factor for Src-mediated increased cell motility and invasion.
117 reases malignant phenotype potential such as cell motility and invasive growth of melanoma cells.
118 wth and tumor growth in mice, and suppressed cell motility and invasiveness both in vitro and in vivo
119 idine (5-AzaC) potently blocks the increased cell motility and invasiveness induced by Src activation
120 xogenous expression suppressed the increased cell motility and invasiveness phenotypes when Src was a
121 bserved that hypoxic gradients guide sarcoma cell motility and matrix remodeling through hypoxia-indu
122                                              Cell motility and migration requires the reorganization
123 lar matrix interactions, cell morphogenesis, cell motility and migration.
124  CD56 in developmental synapse structure, NK cell motility and NK cell development.
125 tress fiber formation to promote endothelial cell motility and permeability.
126 P) pathway, which has been shown to regulate cell motility and polarity in the pulmonary vasculature.
127  restraining RAS and PI3-kinase promotion of cell motility and potentially tumour metastasis.
128 eraction with PI3-Kinase p110alpha decreases cell motility and prevents activation of Rac GTPase.
129 unction for ErbB3 in enhancing breast cancer cell motility and sensitization of the P-Rex1/Rac1 pathw
130 eraction impaired EMT and the acquisition of cell motility and stemness.
131 tors of integrin-beta3 signaling that affect cell motility and survival, observed during GN in wild-t
132 sically slow NMIIB dynamics, thus increasing cell motility and traction and enabling chemotaxis.
133 EF28 or p190RhoGEF) promotes colon carcinoma cell motility and tumor progression via interaction with
134                           RAS also regulates cell motility and tumour invasiveness, but the role of d
135 ibited significant selectivity in inhibiting cell motility and tumourigenesis of ccRCC cells with VHL
136  crucial for many cellular functions such as cell motility and wound healing, as well as other proces
137 reased LKB1 expression, inhibited individual cell-motility and abrogated the stem-like phenotype of b
138 reduces tumor cell proliferation, suppresses cell motility, and abolishes metastatic dissemination in
139  including Snail and Twist expression, tumor cell motility, and anoikis resistance.
140 active lipid that limits PI3KC2beta-governed cell motility, and ceramide is proposed to serve as a me
141  function, as a regulator of FA dynamics and cell motility, and demonstrate that it facilitates the i
142 c networks of cell proliferation, apoptosis, cell motility, and DNA damage.
143 a play critical roles in fluid clearance and cell motility, and dysfunction commonly results in the p
144 x has been used to model matrix contraction, cell motility, and general fibroblast biology.
145 h a higher percentage of CSCs, higher cancer-cell motility, and higher resistance to chemotherapeutic
146 otein superfamily of molecules important for cell motility, and implicated in cancer progression.
147 e that has been implicated in cell adhesion, cell motility, and matrix breakdown, for example, during
148 ling on podocyte shape, actin rearrangement, cell motility, and nephrin endocytosis.
149 A-associated functions, such as cytokinesis, cell motility, and organelle trafficking, are dependent
150 ons strongly interfered with bleb formation, cell motility, and the ability of the cells to reach the
151 ally, miR-203 suppressed cell proliferation, cell motility, and the angiogenesis-inducing capacity of
152 d is involved in transcriptional regulation, cell motility, and trans-Golgi transport.
153 ergistic directional forces generated during cell motility are essential for adaptive T-cell immunity
154 ncers and has recently been linked to cancer cell motility as a context-dependent regulator of multip
155          As islet infiltration progressed, T cell motility became Ag independent, with a loss of T ce
156 f light, or how photoreceptors affect single-cell motility behavior.
157            Actin filaments have key roles in cell motility but are generally claimed to be passive in
158 nt, which both correlated significantly with cell motility but not bulk matrix stiffness within the r
159 ) is crucial for mucus granule secretion and cell motility, but little is known concerning its functi
160 g the balance between cell proliferation and cell motility, but the regulators of this process are la
161 d structure from bacterial flagella-to drive cell motility, but the structural basis of this function
162 ns, the purinergic A2b receptor can regulate cell motility, but the underlying mechanism remains unkn
163 r functions such as environmental sensing or cell motility, but they also grab for particles and with
164  Messenger RNA localization is important for cell motility by local protein translation.
165 nd open the possibility that CRMP-1 controls cell motility by modulating Arp2/3 activation.
166 motes directionally persistent and effective cell motility by reinforcing otherwise transient polariz
167 otes matrix metalloproteinase-2 activity and cell motility by ROS-activated c-Jun N-terminal kinase p
168 ment of numerous cellular processes, such as cell motility, cell division and endocytosis.
169 n many diverse cellular processes, including cell motility, cell division, intracellular transport, a
170 or, such as cell morphology, cell mechanics, cell motility, cell signaling, all of which can potentia
171 tyrosine kinases in developmental processes, cell motility, cell trafficking/adhesion, and cancer, no
172 lls related to Wnt signaling, including high cell motility, cell-cycle progression, and the overexpre
173 ssion, whereas increased tissue rigidity and cell motility/contractility help mediate tumour progress
174                                              Cell motility depends on factors such as nutrient concen
175                                              Cell motility depends on tight coordination between the
176 s identified enrichment of genes involved in cell motility, differentiation, DNA binding, response to
177                                              Cell motility, division, and structural integrity depend
178 ion also increased and sustained endothelial cell motility, driving cells to become tip cells.
179 g protein whose normal function is to enable cell motility during development of tissues and organs o
180 y which an upregulated cadherin can generate cell motility during EMT.
181 s with integrin complexes and is involved in cell motility during interphase.
182 erve as a multi-step mechanism to coordinate cell motility during migration.
183 a quantitative reference model for fin-field cell motility during vertebrate fin bud initiation and s
184 simulations that incorporate accurate immune cell motility dynamics.
185 cular manipulations and drug applications on cell motility, effects of alterations in subcellular act
186 s essential for biological functions such as cell motility, embryonic development, and muscle contrac
187 s, Persistent Random Walk, we found that the cell motility estimates among six cell lines used in thi
188 te behaviors, we show that no differences in cell motility exist among cell types and that sorting dy
189 I1, which together with other EVI1-dependent cell motility factors such as RHOJ regulated breast carc
190 plicative histones, ribosomal biogenesis and cell motility functions.
191 r Fgf24 levels disrupts the normal fin-field cell motility gradient and results in anteriorly biased
192 y H2O2 that contribute to actin dynamics and cell motility have not been characterized.
193       Notably, both light and H2O2 enhance T-cell motility in a Lck-dependent manner.
194 might be particularly important for neuronal cell motility in a soft or poorly adhesive matrix enviro
195 ights into the mechanisms controlling immune cell motility in complex tissue environments.
196                                              Cell motility in higher organisms (eukaryotes) is crucia
197  Here, we provide a precise description of T cell motility in lymph nodes and a computational model t
198          Directed migration is essential for cell motility in many processes, including development a
199            The computer-assisted analysis of cell motility in mixed suspensions showed that the swimm
200  which has recently been reported to control cell motility in monocytes, alongside reduced VLA-4 expr
201 ctions of PLK1 as a key regulator of EMT and cell motility in normal prostate epithelium and prostate
202 amily of five related proteins that modulate cell motility in response to extracellular signals.
203 ng of the ECM leads to both cell cycling and cell motility in serum-stimulated primary mouse dermal f
204 utes to contractility of striated muscle and cell motility in several contexts.
205 ongation of the embryonic axis by regulating cell motility in the presomitic mesoderm and by controll
206                                            T cell motility in tissues resembles a random or Levy walk
207 ty, we show that spontaneous pauses during T cell motility in vitro and in vivo coincide with episode
208 umor-secreted cytokine that stimulates tumor cell motility in vitro and metastasis in vivo.
209 we analyze rat C6 and patient-derived glioma cell motility in vitro using micropatterned linear track
210 omes were employed and confirmed to suppress cell motility in vitro.
211  identified a crucial effect of SHP2 on TNBC cell motility in vivo.
212 ominent increases in [Ca(2+) ]i and promotes cell motility in wound healing and transwell migration a
213 ctions such as cell division, apoptosis, and cell motility, including motility of protease-inhibited
214 en independently implicated as regulators of cell motility, including pore size, crosslink density, s
215 se inhibitor, thereby inhibiting endothelial cell motility, independently of pore function.
216 Our modeling method indicated that decreased cell motility inside the aggregates, a biased walk towar
217 regulating many cellular functions including cell motility, intercellular and intracellular signaling
218 sin motor proteins that drive cell division, cell motility, intracellular trafficking and ciliary fun
219 of the PI3K-AKT pathway in the regulation of cell motility, invasion and metastasis.
220 P to be a novel regulator in prostate cancer cell motility, invasion, and castration-resistant growth
221  novel gene that positively regulates cancer cell motility, invasion, and metastasis through distinct
222 d functions in integrin signaling to promote cell motility, invasion, proliferation, and survival.
223 tion of v-Src kinase, resulting in increased cell motility, invasiveness, and tumorigenicity and prov
224 ch as the epithelial-mesenchymal transition, cell motility, invasiveness, angiogenesis, and metastasi
225                           The acquisition of cell motility is an early step in melanoma metastasis.
226          The control over the acquisition of cell motility is central for a variety of biological pro
227 ts cytoplasmic domain, but the activation of cell motility is disrupted.
228                                  Mesenchymal cell motility is driven by polarized actin polymerizatio
229 sodium lactate-mediated inhibition of CD4+ T cell motility is due to an interference with glycolysis
230                                  Directional cell motility is essential for normal development and ph
231                  This selective control of T cell motility is mediated via subtype-specific transport
232                         To work effectively, cell motility is regulated by a complex network of signa
233                                              Cell motility is required for diverse biological process
234           We propose that vimentin's role in cell motility is to govern the alignment of traction str
235 uitment of follower cells but not for leader cell motility itself, which instead utilizes focal adhes
236 tigations showed that MCPIP1 regulated ccRCC cell motility, lung metastasis, and mesenchymal phenotyp
237                              Such unexpected cell motility may reflect a novel mechanism by which spe
238                      This dose also enhanced cell motility mediated by 100 microM-H2O2, while higher
239 al mechanistic studies, we found that cancer cell motility mediated by the actin-related protein 2/3
240 ologue of mammalian mediator of ErbB2-driven cell motility, MEMO-1, as a protein that inhibits BLI-3/
241  extracellular signals to regulate malignant cell motility, metastasis, and cell-cycle progression, b
242 nd archival tumors positively correlate with cell motility, metastatic potential, and grade, includin
243                 PKDs have a critical role in cell motility, migration and invasion of cancer cells.
244 normal colorectal epithelial cells increased cell motility, migration and invasion, which were associ
245 on factor activity results in a reduction in cell motility, migration, and chemotaxis, all of which a
246 ary for understanding how vinculin regulates cell motility, migration, and wound healing, and for und
247 cer metastasis, and regulatory mechanisms of cell motility need to be uncovered for developing novel
248 ceptor tyrosine kinase to control fibroblast cell motility, neuronal dendrite morphogenesis and stabi
249 s quantified by chemotaxis assays and single-cell motility observations.
250                  While ZAK depletion reduced cell motility of HeLa and HCT116 cells, its overexpressi
251 of cell-substrate adhesion and the resulting cell motility on the substrate.
252    Our results suggest that Rac1 and related cell motility pathways might be associated with plasma a
253 es regulate diverse cellular events, such as cell motility, polarity, and vesicle traffic.
254 ole in various cellular processes, including cell motility, polarity, survival and proliferation.
255 e an important new biological application of cell motility principles.
256           Ceramide treatment also suppressed cell motility promoted by epithelial growth factor, whic
257   Previously we reported that engulfment and cell motility protein 1 (ELMO1) in macrophages mediates
258 ted that polymorphisms in the engulfment and cell motility protein 1 gene (ELMO1) are strongly associ
259 screen in lung cancer cell lines to discover cell motility proteins that show significant changes in
260 ssion analyses showed that regulation of the cell motility receptor RHAMM by the RB/E2F pathway was c
261  made by HGF signalling to pancreatic cancer cell motility remain to be elucidated.
262 y secretory trafficking in the regulation of cell motility remains incompletely understood.
263 ns, the molecular role of vimentin in cancer cell motility remains undefined.
264                                              Cell motility requires the precise coordination of cell
265 ast, sorafenib did not alter MMP activity or cell motility, showing that the changes induced by PLX40
266                                         Rac1 cell motility signaling pathway was associated with plas
267 ed membrane fluidity, resulting in decreased cell motility, stem cell-like properties, and EMT in vit
268                                 Quantitative cell motility studies are necessary for understanding bi
269                            Interpretation of cell motility studies though is often restricted by the
270               Previous studies focusing on T cell motility suggested that the activation of naive T c
271 hysical parameters including number density, cell motility, system size, bulk cell stiffness and stif
272 omputational phase field model of collective cell motility that includes the mechanics of cell shape
273 lipid membranes in endocytosis, trafficking, cell motility, the formation of complex subcellular stru
274 n independently control different aspects of cell motility: the static component controls swimming di
275 ostate cancer cells in vitro, inducing tumor cell motility through a nonproteolytic signal transducti
276 e signaling mechanism by which RSK2 promotes cell motility through leukemia-associated RhoGEF (LARG)-
277 hat H2O2 production contributes to polarized cell motility through localized cofilin inhibition and t
278 evealed a key role for IHF as a repressor of cell motility through the control of FliA sigma factor e
279 lation of cell-cell adhesion is important in cell motility, tissue growth, and for the mechanical int
280 st, we find the lactic acid effect on CD8+ T cell motility to be independent of glycolysis control.
281 nce cell growth, with a moderate increase of cell motility to fibronectin.
282  widely recognized in functions ranging from cell motility to signal transduction.
283 govern many key physiological processes from cell motility to tissue morphogenesis.
284 anging from focal adhesion (FA) dynamics and cell motility to tumour growth, are orchestrated by sign
285 ost important part in metabolism, signaling, cell motility, transport, development, and many other bi
286 lung TIC phenotypes, including tumorspheres, cell motility, tumorigenesis, as well as in vitro and in
287 we present a protocol for the analysis of 3D cell motility using the anisotropic PRW model.
288 of RhoA and Cdc42 GTPases and also regulates cell motility via the modulation of well-known molecules
289 -substrate impedance sensing system, whereas cell motility was assessed using the scratch test and co
290  that links cell mechanics to cell shape and cell motility, we formulate a generalized mechanical inf
291 me monitoring of cytosolic Ca(2+) along with cell motility, we show that spontaneous pauses during T
292 ted with energy metabolism, translation, and cell motility were highly expressed in all four test con
293 reas this would normally physically restrict cell motility, when the particulate network is created u
294 ey role for lateral contractions in amoeboid cell motility, whereas the differences in their traction
295 axis and CIL guides metastatic breast cancer cell motility, whereby cells become progressively insens
296                      Similarly to biological cell motility, which is driven by cytoskeletal component
297                                    Targeting cell motility, which is required for dissemination and m
298 re, ectopic expression of STIM1 promoted CRC cell motility, while depletion of STIM1 with short hairp
299 ic Mena11a expression slows mesenchymal-like cell motility, while isoform-specific depletion of endog
300 ts identified are key regulators that govern cell motility with a high enrichment in focal adhesion a

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