ライフサイエンスコーパス: actin cytoskeleton

1 ys that involve microtubule networks and the actin cytoskeleton.

2 he organization and dynamics of the cortical actin cytoskeleton.

3 important mechanochemical transducer is the actin cytoskeleton.

4 mobilized all the cancer lines by disrupting actin cytoskeleton.

5 It localizes around the centrioles and to actin cytoskeleton.

6 e response, both crucially influenced by the actin cytoskeleton.

7 motors that move, cross-link, and modify the actin cytoskeleton.

8 t remains a poorly characterized part of the actin cytoskeleton.

9 L2 cytoplasmic relocalization to bind to the actin cytoskeleton.

10 eiotic prophase by coupling telomeres to the actin cytoskeleton.

11 clusters can both respond to and control the actin cytoskeleton.

12 interacts with the neuronal microtubule and actin cytoskeleton.

13 ss motile and more adhesive, with an altered actin cytoskeleton.

14 proteins that interact with and organize the actin cytoskeleton.

15 ves specific remodeling of the intracellular actin cytoskeleton.

16 4 substrates or to mediate remodeling of the actin cytoskeleton.

17 ained with Alexa-488-phalloidin to label the actin cytoskeleton.

18 dhesions and display a disorganized cortical actin cytoskeleton.

19 pendent on an intact microtubule network and actin cytoskeleton.

20 ement in the recruitment of the ring canal F-actin cytoskeleton.

21 aggregation dynamics and their link with the actin cytoskeleton.

22 coupling between adherens junctions and the actin cytoskeleton.

23 namin expressions and disorganization of the actin cytoskeleton.

24 enhanced dynamin expressions, and the intact actin cytoskeleton.

25 nertial regime cannot resolve changes to the actin cytoskeleton.

26 ssociated signaling and rearrangement of the actin cytoskeleton.

27 ation occurs through rapid remodeling of the actin cytoskeleton.

28 in that induces actin gelation and regulates actin cytoskeleton.

29 tein, which links the plasma membrane to the actin cytoskeleton.

30 growth factor (EGF) to reduce the binding to actin cytoskeleton.

31 ons and are dependent on a connection to the actin cytoskeleton.

32 ions of cellular processes, changes in the F-actin cytoskeleton.

33 r reinforcement response that stabilizes the actin cytoskeleton.

34 cular switches best known for regulating the actin cytoskeleton.

35 critically impinging on the integrity of the actin cytoskeleton.

36 and initiate Rac-mediated remodeling of the actin cytoskeleton.

37 perties of cells are mainly derived from the actin cytoskeleton.

38 r mechanical coupling of N-cadherin with the actin cytoskeleton.

39 in and is important for CAP1 to regulate the actin cytoskeleton.

40 critically involved in the regulation of the actin cytoskeleton.

41 n, cofilin activation, and remodeling of the actin cytoskeleton.

42 he protein transmits signals to the podocyte actin cytoskeleton.

43 ing between the extracellular matrix and the actin cytoskeleton.

44 accomplishes the same task by hijacking the actin cytoskeleton.

45 c formation and ectosome release rely on the actin cytoskeleton.

46 membrane proteins, adaptor proteins, and the actin cytoskeleton.

47 iation of L1 from ankyrin-G and the spectrin-actin cytoskeleton.

48 nascent myotubes and effects changes in the actin cytoskeleton.

49 on is dependent on the presence of an intact actin cytoskeleton.

50 molecular clutch between N-cadherin and the actin cytoskeleton.

51 , yet surprisingly little is known about its actin cytoskeleton.

52 steps and involves the rearrangement of the actin cytoskeleton.

53 mily is involved in the rearrangement of the actin cytoskeleton.

54 was associated with the disruption of the F-actin cytoskeleton.

55 her with Mps2 to couple the telomeres to the actin cytoskeleton.

56 ulation of the WRC and reorganization of the actin cytoskeleton.

57 n between the cell membrane and the cortical actin cytoskeleton.

58 that disrupt lipid membranes, cell walls and actin cytoskeletons.

59 t: (1) are structurally defined by a dynamic actin cytoskeleton; (2) appose presynaptic dense project

60 The actin cytoskeleton, a dynamic network of actin filaments

61 I signal is mediated by rearrangement of the actin cytoskeleton, a process referred to as dynamic mas

62 is a tightly regulated process that involves actin cytoskeleton, adaptor proteins, and integrin recep

63 he PM adaptor proteins Sla2 and Ent1 and the actin cytoskeleton and (2) hindering recruitment of Rvs1

64 nin, serve as molecular linkages between the actin cytoskeleton and a diverse collection of receptors

65 activity, which causes reorganization of the actin cytoskeleton and actin-associated endomembranes.

66 Rho GTPases control both the actin cytoskeleton and adherens junction stability and a

67 nt in mediating the relationship between the actin cytoskeleton and AQP4-OAP and AQP4-tetramers.

68 beta1 syntrophin is a critical regulator of actin cytoskeleton and autophagy in pancreatic acinar ce

69 ced to optically control the dynamics of the actin cytoskeleton and cellular functions that depend on

70 uggest a molecular link between the SM alpha-actin cytoskeleton and classic fibrogenic signaling casc

71 lls with functional ability to rearrange the actin cytoskeleton and engraft successfully.

72 the integrin adhesion complex that links the actin cytoskeleton and extracellular matrix.

73 y regulates AS of numerous components of the actin cytoskeleton and focal adhesion machineries whose

74 Yet, it is unclear how age disrupts the actin cytoskeleton and how this, in turn, promotes morta

75 c GTPases, thereby triggering changes in the actin cytoskeleton and in transcription.

76 coherent HUVECs, RCalphabeta reinforced the actin cytoskeleton and increased cell stiffness, thus fa

77 N/mum by cytochalasin D treatment to disrupt actin cytoskeleton and increased to approximately 79 pN/

78 endent on changes in the organization of the actin cytoskeleton and is associated with functional cha

79 however, the immune signals that impinge on actin cytoskeleton and its response regulators remain la

80 turbations are sensed through changes in the actin cytoskeleton and mechanosensors at focal adhesions

81 ation, which couples Rho-GTPase signaling to actin cytoskeleton and membrane remodeling.

82 dely studied for its role in controlling the actin cytoskeleton and plays a part in several potential

83 btype switching induced dysregulation of the actin cytoskeleton and reduced the expression of hemides

84 AMOT130 associates to the actin cytoskeleton and regulates tight-junction maintena

85 or a TGN golgin and ITSN-1 in linking to the actin cytoskeleton and regulating the balance between a

86 d an ERR-beta agonist is able to remodel the actin cytoskeleton and similarly suppress GBM cell migra

87 at VEGF activates YAP/TAZ via its effects on actin cytoskeleton and that activated YAP/TAZ induce a t

88 PCS through the interaction among AtEH/Pan1, actin cytoskeleton and the EPCS resident protein VAP27-1

89 we establish a link between the state of the actin cytoskeleton and the expression of pancreatic tran

90 ts, enabling mechanical coupling between the actin cytoskeleton and the extracellular matrix.

91 ity correlate with the ultrastructure of the actin cytoskeleton and the organization of the genome, r

92 iversal scaling between nematic order of the actin cytoskeleton and the substrate-to-cell elastic mod

93 ies change the intracellular organization of actin cytoskeleton and therefore a broad range of cellul

94 IACs) bridge the extracellular matrix to the actin cytoskeleton and transduce signals in response to

95 n of Tns1 leading to a reorganization of the actin cytoskeleton, and a reduction of focal adhesions a

96 echanisms of dasatinib-induced injury to the actin cytoskeleton, and atomic force microscopy to quant

97 apes of many eukaryotic cells depends on the actin cytoskeleton, and changes in actin assembly dynami

98 dhesions, changes in the organization of the actin cytoskeleton, and decreased velocity of cell migra

99 ASAP1 affects integrin adhesions, the actin cytoskeleton, and invasion and metastasis of cance

100 in links cell-cell adhesion complexes to the actin cytoskeleton, and mechanical load strengthens its

101 show significant changes in focal adhesions, actin cytoskeleton, and morphology that are not observed

102 expression of nephrin, significant podocyte actin cytoskeleton, and motility changes.

103 ther with a partial de-polymerization of the actin cytoskeleton, and reduced cell responsiveness to g

104 iated kinases (ROCK1 and ROCK2) regulate the actin cytoskeleton, and ROCK1 and ROCK2 protein abundanc

105 pend on the organization and dynamics of the actin cytoskeleton, and the small, monomeric GTPases Rac

106 was a KEAP1-binding protein that maintained actin cytoskeleton architecture and helped KEAP1 to sequ

107 r level, impacting stress fibre dynamics and actin cytoskeleton architecture.

108 Changes in the actin cytoskeleton are a primary mechanism mediating the

109 These cups are formed by the actin cytoskeleton around signaling patches of Ras, Rac

110 hat DPDG1s and DPDG2s developed disorganized actin cytoskeleton as a consequence of disrupted APOL1-m

111 cell mechanical models commonly describe the actin cytoskeleton as a contractile isotropic incompress

112 geting the mechanoresponsive proteins of the actin cytoskeleton as a new strategy to improve the surv

113 ves a massive reorganization of membrane and actin cytoskeleton as well as an important intracellular

114 The actin cytoskeleton assembles into diverse load-bearing n

115 of small GTP-binding proteins that regulate actin cytoskeleton assembly and cellular contractility.

116 VE regulatory complexes (WRC), which control actin cytoskeleton assembly.

117 idency, as a crucial linker between kAE1 and actin cytoskeleton-associated proteins in polarized cell

118 ZNF185 is an actin-cytoskeleton-associated Lin-l 1, Isl-1 and Mec-3 (

119 and for septin-dependent remodeling of the F-actin cytoskeleton at the appressorium pore.

120 ires septin-dependent reorientation of the F-actin cytoskeleton at the base of the infection cell, wh

121 couples the cadherin-catenin complex to the actin cytoskeleton at the intercalated disk (ICD), a uni

122 e to extracellular signals, and regulate the actin cytoskeleton at the tube apex to drive tip growth.

123 of alpha(IIb)beta(3) may be mediated by the actin cytoskeleton, because surface-bound fibrinogen is

124 findings show that through remodeling of the actin cytoskeleton, beta-AR-mediated stress hormone sign

125 of actin-binding proteins that modulate the actin cytoskeleton both directly, via F-actin bundling,

126 The domains form independent of the actin cytoskeleton, but acto-myosin contractility induce

127 ven by pushing and pulling activities of the actin cytoskeleton, but migration directionality is larg

128 have been described to depend mostly on the actin cytoskeleton, but the rapid transport of fully pol

129 aling depend on forces applied by the T cell actin cytoskeleton, but until recently, the underlying m

130 s regulate the dynamics and functions of the actin cytoskeleton by forming long chains along the two

131 nals from the podocyte slit diaphragm to the Actin cytoskeleton by recruiting proteins that can inter

132 molecule that regulates the dynamics of the actin cytoskeleton by transmitting signals from the plas

133 Upon disruption of the actin cytoskeleton by treatment of the cells with latrun

134 This work reveals how the actin cytoskeleton can be harnessed to overcome energeti

135 The actin cytoskeleton can regulate neurotransmitter recepto

136 ylation, to discern a mechanism by which the actin-cytoskeleton can be released in FSGS.

137 The actin cytoskeleton consists of structurally and biochemi

138 seen in typical fibroblasts yields excessive actin cytoskeleton, decreases nuclear volume and reduces

139 r, has been recently implicated in myofibril actin cytoskeleton differentiation, and the myopathies i

140 d by xDC, cellular components other than the actin cytoskeleton dominate the response.

141 The actin cytoskeleton drives cell motility and is essential

142 The actin cytoskeleton drives many essential biological proc

143 We used actin cytoskeleton drugs to modify the traffic dynamics.

144 of Rac1/CDC42 GTPases, in the regulation of actin cytoskeleton dynamics and cell-cell adhesion.

145 Here we show that regulators of actin cytoskeleton dynamics can bidirectionally determin

146 In conclusion, ROCK2 activity-mediated actin cytoskeleton dynamics contribute to the inhibition

147 The RhoA/ROCK-mediated actin cytoskeleton dynamics have been implicated in adip

148 nd reveals that they might play roles in the actin cytoskeleton dynamics in cochlear hair cells, and

149 rmin protein essential for the regulation of actin cytoskeleton dynamics in diverse biological proces

150 tin filaments (F-actin) and that ExoY alters actin cytoskeleton dynamics in vitro, via an unknown mec

151 ansduction pathways and in the regulation of actin cytoskeleton dynamics, including numerous guanine

152 SCA5 beta-spectrin interferes with spectrin-actin cytoskeleton dynamics, leading to a loss of a cyto

153 human lymphocytes is involved in controlling actin cytoskeleton dynamics, restraining PI3K/AKT signal

154 nd pulmonary edema through the modulation of actin cytoskeleton dynamics.

155 e some Tcf21-dependent effects, related with actin cytoskeleton dysregulation and apoptosis.

156 ts demonstrate PHIP's role in regulating the actin cytoskeleton, focal adhesion dynamics, and tumor c

157 on, cells exhibited rapid disassembly of the actin cytoskeleton, followed by shedding of plasma membr

158 Here the retrograde flow of the actin cytoskeleton follows the texture of the substrate,

159 N16 and RAB11FIP3 (involved in regulation of actin cytoskeleton) for prevalent HF with reduced ejecti

160 ZO-1 interacts with the actin cytoskeleton, gap, and adherens junction proteins

161 e pathway through these macromolecules which actin-cytoskeleton-generated tensile force takes when ap

162 The actin cytoskeleton generates forces on membranes for a w

163 ty are largely mediated by regulation of the actin cytoskeleton; however, the underlying mechanisms r

164 appears to be an important modulator of the actin cytoskeleton, implicating maintenance of muscular

165 ng viral particles, and rearrangement of the actin cytoskeleton in infected cells.

166 whose members preferentially localize to the actin cytoskeleton in mechanically stimulated cells thro

167 ng evidence highlights the importance of the actin cytoskeleton in modulating inflammatory responses.

168 er investigate the role of [Ca(2+) ] and the actin cytoskeleton in podocytes, we used a double fluore

169 AIM1 strongly associates with the actin cytoskeleton in prostate epithelial cells in norma

170 DeActs are universal tools for studying the actin cytoskeleton in single cells in culture, tissues,

171 e Ena/VASP family member EVL to assemble the actin cytoskeleton in the apical cortex and in protrudin

172 rgan of Corti and much lower expression of F-actin cytoskeleton in the cochlea compared with wild-typ

173 Although the properties of the actin cytoskeleton in the cytoplasm are well characteriz

174 ics, in this work, we probed the role of the actin cytoskeleton in the dynamics, ligand binding, and

175 adhesions to result in the reorganization of actin cytoskeleton in the entire cell.

176 er depends on spatial control of dynamics of actin cytoskeleton in the foot processes.

177 To assess the influence of AMPK on the actin cytoskeleton in VSM of resistance arteries with re

178 ayers in the coordination between the MT and actin cytoskeletons in growth cones (GCs) during axon gu

179 lation of fibroblasts induces changes in the actin cytoskeleton including stress fiber (SF) reinforce

180 KD cells have intrinsic abnormalities in the actin cytoskeleton, including mislocalization of the TJ

181 The actin cytoskeleton is a complex network controlled by a

182 The actin cytoskeleton is a critical regulator of cytoplasmi

183 The actin cytoskeleton is a dynamic array of filaments that

184 lation-dependent excess stabilization of the actin cytoskeleton is a key phosphorylation-dependent me

185 Regulated reorganization of the actin cytoskeleton is a prerequisite for proper platelet

186 The dynamic rearrangement of the actin cytoskeleton is an essential component of many mec

187 Dynamic regulation of the actin cytoskeleton is an essential feature of cell motil

188 The fission yeast actin cytoskeleton is an ideal, simplified system to inv

189 The rapid remodeling of actin cytoskeleton is associated with spine enlargement

190 Reorganization of the actin cytoskeleton is crucial for cellular processes, in

191 Regulation of the actin cytoskeleton is crucial for normal development and

192 The actin cytoskeleton is essential for many fundamental bio

193 NIFICANCE STATEMENT Proper regulation of the actin cytoskeleton is essential for the structural stabi

194 A dynamic actin cytoskeleton is necessary for viral entry, intrace

195 The actin cytoskeleton is of profound importance to cell sha

196 The actin cytoskeleton is regulated by many proteins includi

197 re flattened under load and lose volume; the actin cytoskeleton is reorganized, with myosin II recrui

198 The actin cytoskeleton is required for cell expansion and im

199 pproaches to show that reorganisation of the actin cytoskeleton is required for dark-induced stomatal

200 Key to the function of the actin cytoskeleton is the mechanisms that control its as

201 Here we test the hypothesis that the actin cytoskeleton is the primary barrier to transcellul

202 Actin cytoskeleton is well-known for providing structura

203 mily of small GTPases and a regulator of the actin cytoskeleton, is critical for the normal developme

204 uces nephrotoxicity through altered podocyte actin cytoskeleton, leading to injurious cellular biomec

205 Here, we demonstrate that myosin XI and the actin cytoskeleton mediate CSC delivery to the PM by coo

206 link between membrane-integral PRKs and the actin cytoskeleton, mediated through interactions betwee

207 Actin cytoskeleton-mediated FA growth and maturation thu

208 The actin cytoskeleton mediates mechanical coupling between

209 coupling of alpha(M)beta(2) integrin to the actin cytoskeleton mediates phagocytosis.

210 yndrome protein (WASp), which signals to the actin cytoskeleton, modulates autophagy and inflammasome

211 signals transmitted through the cytoplasmic actin cytoskeleton must be relayed to the nucleus to con

212 ecules and a simplified mechanical model for actin cytoskeleton network competition.

213 The actin cytoskeleton network has an important role in plan

214 Numerous features such as the actin-cytoskeleton network, the glycocalyx network, and

215 Our study shows that the actin cytoskeleton of endothelial cells provides both pa

216 ed actin reset, or CaAR-that reorganizes the actin cytoskeleton of mammalian cells in response to cal

217 opy analyses to visualize the nuclei and the actin cytoskeleton of the gut cells and DNA fragmentatio

218 The adherens junction (AJ) couples the actin cytoskeletons of neighboring cells to allow mechan

219 CM) molecules on one side and connect to the actin cytoskeleton on the other [7].

220 e Ontology Biological Process (GO BP) terms, actin cytoskeleton organization, actin filament-based pr

221 n of patient-derived GBM cells by modulating actin cytoskeleton pathway.

222 ies show the critical role [Ca(2+) ] and the actin cytoskeleton play in podocyte homeostasis.

223 The actin cytoskeleton plays a pivotal role in cell developm

224 The actin cytoskeleton plays a variety of roles in eukaryoti

225 The actin cytoskeleton plays an important role in numerous k

226 The actin cytoskeleton plays multiple critical roles in cell

227 d a rigidity-dependent phenotype whereby the actin cytoskeleton polarized on stiff substrates but not

228 convergent pathways, including pyrin and the actin cytoskeleton, protein misfolding and cellular stre

229 egin near metaphase and are dependent on the actin cytoskeleton rapidly transform the patches into a

230 oop that reduces nephrin expression, causing actin cytoskeleton rearrangement.

231 Oligodendrocyte myelination depends on actin cytoskeleton rearrangement.

232 how that these proteins are also involved in actin cytoskeleton regulated autophagy.

233 sion (FA)-stimulated reorganization of the F-actin cytoskeleton regulates cellular size, shape, and m

234 own as ermin) was initially identified as an actin cytoskeleton-related oligodendroglial protein in t

235 These include proteostasis- and actin cytoskeleton-related proteins but not canonical st

236 these diverse links to the stereocilia dense actin cytoskeleton remain largely unknown.

237 However, the actin cytoskeleton remained intact, suggesting that the

238 CXCR4 activation results in actin cytoskeleton remodeling and PI3K/Akt and Erk signa

239 or of mesenchymal cell adhesion signaling, F-actin cytoskeleton remodeling and single cell migration,

240 Actin cytoskeleton remodeling in spines is a key element

241 dimeric actin-binding proteins that regulate actin cytoskeleton remodeling.

242 eceptor tyrosine kinases that participate in actin cytoskeleton remodeling.

243 by activating the GTPase RAC1 and modulating actin cytoskeleton remodeling.

244 tion of cell morphology, cell migration, and actin cytoskeleton remodeling.

245 ions in cell morphology, cell migration, and actin cytoskeleton remodeling; however, the molecular me

246 The actin cytoskeleton remodels during the first 5 min of in

247 MAF1 protein expression revealed changes in actin cytoskeleton reorganization and altered sensitivit

248 ynamic adjustments of cell shape directed by actin-cytoskeleton reorganization via their respective R

249 The actin cytoskeleton represents a key determinant in maint

250 echanism is not well understood, leaving why actin cytoskeleton responds to topographical features un

251 Short-term actin cytoskeleton response to auxin requires AUX1 and/o

252 Previous studies examined long-term actin cytoskeleton responses to auxin, but plants respon

253 High-resolution electron microscopy of the actin cytoskeleton revealed that stress fibers (SFs) are

254 eletons of the T cell and the APC, where the actin cytoskeleton serves as a mechanical intermediate t

255 for Gag synthesis to non-PM membranes or the actin cytoskeleton severely reduced net virus particle p

256 taset showed enrichment in axon guidance and actin cytoskeleton signalling pathways as well as activa

257 on of extrinsic JN up-regulated formation of actin cytoskeleton stress fibers, caused redistribution

258 The cell volume, mechanical properties, and actin cytoskeleton structure are tightly connected to ac

259 ding on collagen, associated with an altered actin cytoskeleton structure with less filamentous actin

260 ls of proteins involved in regulation of the actin cytoskeleton, such as ARPC2 and WASF1/WAVE1, and p

261 pendent of tyrosine kinase signaling and the actin cytoskeleton, suggesting selection for avid TCR mi

262 in-2/3 (ARP2/3) complex, which regulates the actin cytoskeleton supporting dendritic spines, produced

263 hway, but also reveals STXBP4 as a player in actin cytoskeleton tension-mediated Hippo pathway regula

264 inhibit YAP, a process that is regulated by actin cytoskeleton tension.

265 a cells associated with alterations to the F-actin cytoskeleton that affected apoptosis.

266 erred to as ring canals; RCs) have a dynamic actin cytoskeleton that drives their expansion to a diam

267 checkpoint controlled by signaling from the actin cytoskeleton that prevents differentiation of a pr

268 tracellular vesicular trafficking and of the actin cytoskeleton, their modifications by bacterial pat

269 xchange regulatory factor-1 complexes to the actin cytoskeleton, thereby averting the rapid internali

270 B share a common function in stabilizing the actin cytoskeleton, they physically interact in the cyto

271 not other progenitor types, by changing the actin cytoskeleton through the activity of the Rho-GTPas

272 the transcription-independent control of the actin cytoskeleton through the small GTPase RhoA.

273 ile cells rely on both signaling modules and actin cytoskeleton to break symmetry and achieve a stabl

274 Generally, viruses use the actin cytoskeleton to control entry and short-range tran

275 nisms by which Dyn2 regulates changes in the actin cytoskeleton to drive cell migration are still unc

276 Polychaetoid and Canoe link Sidekick to the actin cytoskeleton to enable tricellular adherens juncti

277 can spatially regulate Rac activity and the actin cytoskeleton to ensure correct epithelial cell sha

278 s by regulating orchestrated dynamics of the actin cytoskeleton to keep mitotic spindles in syncytial

279 e by coupling the intracellular force of the actin cytoskeleton to the environment.

280 Ezrin and moesin, which link the actin cytoskeleton to the plasma membrane, bind membrane

281 Epithelial cells in tissues use their actin cytoskeletons to stick together, whereas unattache

282 During platelet spreading, the actin cytoskeleton undergoes rapid rearrangement, formin

283 This complex is linked to the actin cytoskeleton via a bispecific interaction with an

284 ons (mLIM1) or impeded interactions with the actin cytoskeleton via alpha-actinin (DeltaABD) abrogate

285 chanical forces by coupling cadherins to the actin cytoskeleton via beta-catenin and the F-actin bind

286 e critical roles in linking membranes to the actin cytoskeleton via direct binding to acidic lipids.

287 muscle through interaction with the cortical actin cytoskeleton via its N-terminal half and with the

288 Many functions in regulating the actin cytoskeleton via RhoA and other pathways have been

289 y in humanized mice that perturbation of the actin cytoskeleton via the lentiviral protein Nef, and n

290 Our model adhesome consists of the actin cytoskeleton-vinculin-talin-integrin-ligand-extrac

291 Actin cytoskeleton was imaged at the same time as an ext

292 By searching for known factors affecting the actin cytoskeleton, we identified Krev interaction trapp

293 (DCs) involves forces exerted by the T cell actin cytoskeleton, which are opposed by the cortical cy

294 mon set of components: small GTPases and the actin cytoskeleton, which implies that the mechanisms do

295 rongly determined by the organization of the actin cytoskeleton, which is also the main regulator of

296 rse, but most members can associate with the actin cytoskeleton with apparent force sensitivity.

297 r photopharmacology targeting the ubiquitous actin cytoskeleton with precision control in the microme

298 t delivers certain synaptic proteins via the actin cytoskeleton within the Rab11-related domain of sl

299 ultiple signaling cascades that regulate the actin cytoskeleton, would compromise the structural stab

300 ce-bearing linkage between integrins and the actin cytoskeleton; yet, direct evidence of tensin's rol