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1 y of surface ORAI1 and increasing the plasma membrane ruffling.
2 supports a functional link between SOCE and membrane ruffling.
3 ated Rac3 causes transformation and leads to membrane ruffling.
4 KIalpha in PDGF-stimulated cells resulted in membrane ruffling.
5 ways that stimulate actin reorganization and membrane ruffling.
6 actin dynamics, lamellipodia protrusion, and membrane ruffling.
7 nosomes but, surprisingly, did not eliminate membrane ruffling.
8 t-Leu-Phe to induce actin reorganization and membrane ruffling.
9 itic cells but may be required downstream of membrane ruffling.
10 ession systems, also inhibited GH-stimulated membrane ruffling.
11 The small GTPase Rac mediates membrane ruffling.
12 luencing actin cytoskeletal organization and membrane ruffling.
13 from the cytosol to the plasma membrane, and membrane ruffling.
14 esponse to stimuli (e.g., serum) that induce membrane ruffling.
15 m pathways such as PAK, JNK/SAPK kinases and membrane ruffling.
16 as a dominant negative for another pathway, membrane ruffling.
17 effect on the ability of RasVal-12 to induce membrane ruffling.
18 Shc mutant, has no effect on IGF-I-mediated membrane ruffling.
19 resembles the time course of IGF-I-mediated membrane ruffling.
20 ncident with increases in cell spreading and membrane ruffling.
21 wortmannin and LY294002 blocks IGF-I-induced membrane ruffling.
22 ined actin stress fibers and showed enhanced membrane ruffling.
23 mplex may regulate growth cone extension and membrane ruffling.
24 inct pathway that regulates adhesion-induced membrane ruffling.
25 ab5-dependent pinocytosis and Rac1-dependent membrane ruffling.
26 ffect of Ha-Ras(G12V) on pinocytosis but not membrane ruffling.
27 of PDGF-induced mitogenesis, chemotaxis, and membrane ruffling.
28 5-P3) also produced actin reorganization and membrane ruffling.
29 yphimurium strains are unable to induce this membrane ruffling.
30 d mutant of Ras, V12Ras, in the induction of membrane ruffling.
31 ynthesis, but retained the ability to induce membrane ruffling.
32 lar fluid and solutes through dynamic plasma membrane ruffling.
33 reased pHi and single cell behaviors such as membrane ruffling.
34 ion of KCNQ2/3 channel currents, and loss of membrane ruffling.
35 ttenuating actin polymerization and reducing membrane ruffling.
36 ytoskeletal organization, and reduced plasma membrane ruffling.
37 s of active GTP-bound Rac and EGF-stimulated membrane ruffling.
38 K3 prevents the formation of CrkII-dependent membrane ruffling.
39 enhanced superoxide production and increased membrane ruffling.
40 is most evident in podosomes and regions of membrane ruffling.
41 associated with enhanced cell spreading and membrane ruffling.
42 ells has no additive effect on the amount of membrane ruffling.
43 o promote cell survival, transformation, and membrane ruffling.
44 ion of p50alpha also restored PDGF-dependent membrane ruffling.
45 membrane trafficking, glucose transport, and membrane ruffling.
46 /- p85beta-/-) are defective in PDGF-induced membrane ruffling.
47 gulators of endocytosis, actin dynamics, and membrane ruffling.
48 spholipase D (PLD) homolog, which facilitate membrane ruffling.
49 ium stimulates signaling pathways leading to membrane ruffling, actin cytoskeleton rearrangements, an
50 of PIPKI-alpha causes pronounced defects in membrane ruffling, actin organization, and focal adhesio
51 s a mitogen, cAMP-elevating agents stimulate membrane ruffling, Akt phosphorylation, and p70 ribosoma
52 Rac1 effector binding loop shown to abolish membrane ruffling also abolishes interaction with POR1.
53 d -independent growth assays, cell cycle and membrane ruffling analyses showed that Akt exerts estrog
55 hat schwannoma-derived Schwann cells exhibit membrane ruffling and aberrant cell spreading when plate
59 oteins Rho and Rac have a regulatory role in membrane ruffling and activated Rho has been shown to st
63 that MARCKS and PKC regulate actin-dependent membrane ruffling and cell adhesion, perhaps via a PIP2-
65 221F fails to induce JNK and PAK activation, membrane ruffling and cell migration, suggesting that it
66 ed to function downstream of Arf6 to control membrane ruffling and cell migration, this pathway has n
67 tly, inhibition of Hsp90 activity suppressed membrane ruffling and cell migration, while expression o
69 mediates attachment-induced JNK activation, membrane ruffling and cell motility in a Rac-dependent m
72 ependent of Rac1 activation, actin-dependent membrane ruffling and cell spreading are Rac1-dependent
74 This mmLDL activates macrophages inducing membrane ruffling and cell spreading, activation of ERK1
75 anism by which Neisseria gonorrhoeae elicits membrane ruffling and cellular invasion of the cervical
76 ed actin remodeling manifested by peripheral membrane ruffling and circular dorsal ruffles (CDRs).
77 onococcal PLD may be necessary to potentiate membrane ruffling and clustering of gonococci on the cer
78 s engaged with extracellular matrix, whereas membrane ruffling and decreased actin stress fibers indu
80 s in the actin-binding domain cause aberrant membrane ruffling and defective actin stress fibre forma
81 ed cytoskeletal rearrangements manifested by membrane ruffling and disruption of intercellular juncti
83 ress fibers and exhibit clear differences in membrane ruffling and filopodial extension when stained
85 ed PAK1 have been reported to either promote membrane ruffling and focal adhesion assembly or cause f
89 eta but not Nckalpha blocks Rac1-L62-induced membrane ruffling and formation of lamellipodia, suggest
90 ment caused shape changes in the cells, with membrane ruffling and formation/retraction of thin actin
92 V), an activated Ras mutant, stimulated both membrane ruffling and horseradish peroxidase uptake.
93 erexpression of MAYP decreased CSF-1-induced membrane ruffling and increased filopodia formation, mot
95 arrangements encompass increased Rac-induced membrane ruffling and lamellipodia, Cdc42-initiated filo
96 cretion system (T3SS), leading to pronounced membrane ruffling and macropinocytic uptake of attached
97 ity is initially manifested by inhibition of membrane ruffling and macropinocytosis in infected macro
103 mulation of two distinct insulin bioeffects, membrane ruffling and mitogenesis, in 3T3-L1 adipocytes
104 -assisted laser inactivation) blocked plasma-membrane ruffling and motility of Fos-transformed fibrob
106 triking morphological alterations, including membrane ruffling and numerous pseudopodial protrusions,
107 d areas 5-7-fold greater than NHSC, aberrant membrane ruffling and numerous, frequently disorganized
108 sion under these conditions causes extensive membrane ruffling and overrides the block in membrane fu
110 coupled events, our study demonstrates that membrane ruffling and pinocytosis are regulated by disti
111 h lacking a functional SH2 domain, inhibited membrane ruffling and pinocytosis induced by GH and PDGF
112 g three Rac-dependent readouts: induction of membrane ruffling and pinocytosis, stimulation of cell m
114 AYP is a negative regulator of CSF-1-induced membrane ruffling and positively regulates formation of
116 to wounding was characterized by (1) plasma membrane ruffling and protrusion into the wound, (2) lam
118 monella typhimurium into host cells requires membrane ruffling and rearrangement of the actin cytoske
119 Rac allele was able to rescue the defect in membrane ruffling and restore the localization of a fluo
122 ts estrogen-like activity on cell growth and membrane ruffling and that a selective ErbB2 inhibitor,
123 aldesmon may be a key protein that modulates membrane ruffling and that this may involve changes in c
124 cation to the membrane, which in turn causes membrane ruffling and the formation of cellular protrusi
125 Our experiments show that activation of membrane ruffling and transcriptional activation of c-ju
126 to the transcription factor c-Jun and cause membrane ruffling and transformation, indicating that sw
128 infected cells with 2-10 muM P27 caused cell membrane ruffling and uptake of virus and polymerized fo
129 ine, and filamentous actin filament into the membrane rufflings and uropods of human neutrophils.
130 reatment with GGTIs led to the inhibition of membrane-ruffling and transforming activities of both ac
131 SHEP1 unable to promote Cas-Crk association, membrane ruffling, and cell migration toward epidermal g
132 Gas6 stimulated lamellipodial extension, membrane ruffling, and chemotaxis of immortalized NLT Gn
133 was rapid, involved extensive cholangiocyte membrane ruffling, and culminated in parasite penetratio
134 d GLUT4 translocation, growth factor-induced membrane ruffling, and DNA synthesis, indicating that Pt
137 is required for growth hormone (GH)-induced membrane ruffling, and increases mitogenesis stimulated
138 olocalization with cortical actin filaments, membrane ruffling, and lamellipodia formation, compared
140 o1c promoted G-actin accumulation and plasma membrane ruffling, and Myo1c knockdown confirmed its con
141 FO showed hepatocyte autophagosomes, nuclear membrane ruffling, and porphyrin-containing vacuoles wit
142 otilities, including surveillance movements, membrane ruffling, and process extension or retraction.
143 eas Rac regulates lamellipodia formation and membrane ruffling, and RhoA regulates the formation of s
144 vated by MLCK at the cell periphery controls membrane ruffling, and that the spatial regulation of ML
145 threonine kinase, to induce lamellipodia and membrane ruffling, and to activate the c-Jun NH2-termina
146 mice failed to become polarized, to undergo membrane ruffling, and to migrate in response to chemoki
147 k results in localized actin polymerization, membrane ruffling, and, ultimately, pathogen entry.
149 e is provided that actin-myosin assembly and membrane ruffling are regulated by distinct signaling pa
150 abnormal proliferation, cell morphology, and membrane ruffling are suppressed by the TRQQKRP motif de
152 In fibroblasts PAK1 localizes to areas of membrane ruffling, as well as to amiloride-sensitive pin
153 d MLC phosphorylation and blocked peripheral membrane ruffling, as well as turnover of focal adhesion
154 Knockdown of RalA or Sec5 results in reduced membrane ruffling at sites of attachment and impairs bac
157 ccumulation of the PI(4,5)P(2) biosensor and membrane ruffling at the opposite side of the cells.
158 activated Ras(V12) mutant induces prominent membrane ruffling, branching morphogenesis on three-dime
159 d and platelet-derived growth factor-induced membrane ruffling but not Bradykinin-induced filopodia f
161 ealed that the DN construct had no effect on membrane ruffling, but dramatically inhibited stress fib
163 POR1, a Rac1-interacting protein involved in membrane ruffling, but not with the dominant-negative mu
164 take by 36%, GLUT4 translocation by 35%, and membrane ruffling by 50%, all of which are phosphatidyli
166 ed versions of POR1 inhibit the induction of membrane ruffling by an activated mutant of Rac1, V12Rac
167 rowth factors stimulate actin remodeling and membrane ruffling by integration of signaling pathways t
168 tor (PDGF)-induced chemotaxis was to promote membrane ruffling by regulating phosphatidylinositol 3,4
169 role of STIM1 and ORAI1 in the promotion of membrane ruffling by showing that phospho-STIM1 localize
170 ation during ruffling, and the inhibition of membrane ruffling by the Ca(2+)-channel inhibitor SKF963
171 sulted in distinct linear or circular/dorsal membrane ruffling, c-Abl-null cells demonstrated dramati
174 ator of diverse cellular functions including membrane ruffling, cell cycle progression, and transform
176 cell spreading, lamellipodia formation, and membrane ruffling, cell morphologies generated by active
177 R), which also induces actin reorganization, membrane ruffling, cell spreading, polarization, and mig
178 t of PI3K, local PI(3,4,5)P(3) synthesis and membrane ruffling could be induced, with corresponding l
179 s typical of FCepsilonRI signaling including membrane ruffling, cytoskeletal rearrangements, and, in
181 little effect on the rate and morphology of membrane ruffling, demonstrating that early production o
182 e, we suggest a role of N-WASP in regulating membrane ruffling downstream of phosphatidylinositol 4,5
185 changes in actin-dependent processes such as membrane ruffling, filopodial protrusion, and cell motil
187 a striking increase in spontaneous motility, membrane ruffling, formation of long actin extensions (f
189 nduced actin cytoskeleton reorganization and membrane ruffling in 3T3-L1 fibroblasts and Rat1 cells t
192 and Rhotekin leads to loss of Rho-dependent membrane ruffling in response to epidermal growth factor
194 T4 translocation, c-fos expression, and cell membrane ruffling in single-cell microinjection assay.
195 of the constitutively active RacV12 induces membrane ruffling, increases PI4KIIbeta translocation to
196 , we show that SCH 51344 specifically blocks membrane ruffling induced by activated forms of H-RAS, K
197 ve mutants of SH2-Bbeta are shown to inhibit membrane ruffling induced by constitutively active Rac.
198 an insulin receptor (HIRc-B), SHIP inhibited membrane ruffling induced by insulin and IGF-I by 76 +/-
199 contrast, there was no significant change in membrane ruffling induced by PMA in the cells expressing
203 lone A cells inhibited alpha6beta4-dependent membrane ruffling, lamellae formation, and migration.
204 mber of the Rho-family GTPases that promotes membrane ruffling, leading edge extension, and cell spre
205 co-opt the host actin cytoskeleton to induce membrane ruffling, leading to the uptake of the bacteriu
206 ll as cell polarity, lamellipodial assembly, membrane ruffling, macropinocytosis, and collective cell
207 amma receptor- mediated phagocytosis and for membrane ruffling mediated by structurally distinct rece
208 SV12, where V12 indicates valine-12) induces membrane ruffling, mitogen-activated protein (MAP) kinas
211 ion, ghrelin led to actin polymerization and membrane ruffling on cells, with the specific co-localiz
214 differ from Rac1 in its ability to stimulate membrane ruffling or to interact with SmgGDS and IQGAP1-
215 ce of granule swelling and fusion, increased membrane ruffling, or exocytosis upon Ag challenge.
216 a on Ser(2152) is required for Pak1-mediated membrane ruffling, our results suggest a novel role for
217 y is dispensable for GBP2 recruitment and PV membrane ruffling; parasites can replicate, egress and s
218 H 51344 inhibits a critical component of the membrane ruffling pathway downstream from RAC and sugges
219 ersely, increasing cytosolic Ca(2+) enhances membrane ruffling, PI3K activity, and F-actin accumulati
220 ased pHi in single cells can drive localized membrane ruffling responses within seconds and increased
221 Kit-mediated filamentous actin assembly and membrane ruffling, secretory enhancement and adhesion to
222 ation stimulated by bradykinin and in dorsal membrane ruffling stimulated by PDGF, whereas the Cdc42G
223 acts as a dominant negative mutant, blocked membrane ruffling, suggesting that PIPKIalpha and PIP2 p
224 he Raji-S1 cells but does inhibit the active membrane ruffling that is necessary for cell polarizatio
225 ing that ARF6 regulates a pathway leading to membrane ruffling that occurs after the activation and m
231 nduces actin cytoskeleton rearrangements and membrane ruffling to gain access into nonphagocytic cell
232 ase Rac1, established its ability to promote membrane ruffling, transformation, and activation of c-j
233 for their roles in actin rearrangements and membrane ruffling, translocated effectors also affect ho
234 Both PS and anti-PSR antibodies stimulated membrane ruffling, vesicle formation, and "bystander" up
236 Ha-Ras(G12V)-stimulated pinocytosis but not membrane ruffling was abolished by either wortmannin or
237 or-induced cytoskeletal rearrangement, i.e., membrane ruffling, was significantly inhibited (78 +/- 1
238 n and platelet-derived growth factor-induced membrane ruffling, we investigated whether NIH 3T3 cells
239 tial adhesion to fibronectin also stimulates membrane ruffling; we show that this ruffling is indepen
240 domain induce formation of lamellipodia and membrane ruffling, when transiently expressed in fibrobl
241 RhoGAP is rapidly translocated to regions of membrane ruffling, where it colocalizes with polymerized
243 broblasts induced lamellipodia formation and membrane ruffling, which was unrelated to the substrate
244 r purine doses caused process retraction and membrane ruffling, which were blocked by joint applicati
245 actin polymerization-dependent spreading and membrane ruffling while Rac1-independent BCR capping rem
246 asion-deficient mutant (achieved by inducing membrane ruffling with epidermal growth factor) induced
247 ector, resulted in a dramatic stimulation of membrane ruffling without affecting the uptake of horser