ライフサイエンスコーパス: actin cytoskeleton

1 bond could establish long-range order in the actin cytoskeleton.

2 ave been implicated in the regulation of the actin cytoskeleton.

3 ine kinase, which is a critical regulator of actin cytoskeleton.

4 ation are generated by a dynamic filamentous actin cytoskeleton.

5 o activate integrins and to link them to the actin cytoskeleton.

6 uding cytokines and proteins involved in the actin cytoskeleton.

7 suggested to be strongly associated with the actin cytoskeleton.

8 tly link the cadherin.catenin complex to the actin cytoskeleton.

9 -MMP and its ability to bind the subcortical actin cytoskeleton.

10 in and was inhibited by stabilization of the actin cytoskeleton.

11 roteins with diverse roles in remodeling the actin cytoskeleton.

12 a and this phenomenon is orchestrated by the actin cytoskeleton.

13 cular switches best known for regulating the actin cytoskeleton.

14 ts and engulfed them by remodelling of their actin cytoskeleton.

15 rized growth even in complete absence of the actin cytoskeleton.

16 tion and dynamics that mirrored those of the actin cytoskeleton.

17 tins, Cdc42, Borgs, and restructuring of the actin cytoskeleton.

18 , and rho/rac signaling, which regulates the actin cytoskeleton.

19 nd reinforcement of an initially low-tension actin cytoskeleton.

20 r reinforcement response that stabilizes the actin cytoskeleton.

21 coordination of cell-cell junctions and the actin cytoskeleton.

22 signaling confer plasticity to the podocyte actin cytoskeleton.

23 s depend on the proper organization of their actin cytoskeleton.

24 e RhoA GTPase, a well-known modulator of the actin cytoskeleton.

25 se infection requires subversion of the host actin cytoskeleton.

26 d mechanically induced reorganization of the actin cytoskeleton.

27 heir size and density are constrained by the actin cytoskeleton.

28 between the cadherin.catenin complex and the actin cytoskeleton.

29 he connectivity of adhesion receptors to the actin cytoskeleton.

30 interplay between membrane receptors and the actin cytoskeleton.

31 e Diaph3 (aka mDia2) is a major regulator of actin cytoskeleton.

32 spine synapses is determined in part by the actin cytoskeleton.

33 and MYO7B, which link protocadherins to the actin cytoskeleton.

34 raction between the FHDC1 FH2 domain and the actin cytoskeleton.

35 -dependent apoptosis and disruption of the F-actin cytoskeleton.

36 critically impinging on the integrity of the actin cytoskeleton.

37 , which physically links this complex to the actin cytoskeleton.

38 enerating membrane protrusions driven by the actin cytoskeleton.

39 d a more contracted phenotype and an altered actin cytoskeleton.

40 h mechanical and dynamical properties of the actin cytoskeleton.

41 l degeneration due to a dysregulation of the actin cytoskeleton.

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

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

44 mbrane between extracellular ligands and the actin cytoskeleton.

45 rganization, morphology, and dynamics of the actin cytoskeleton.

46 he inability to quantify key features of the actin cytoskeleton.

47 clear envelope to critical regulators of the actin cytoskeleton.

48 roteins, lipid kinases, phosphatases and the actin cytoskeleton.

49 structural and regulatory components of the actin cytoskeleton.

50 RPalpha, within 62 +/- 5 nm, mediated by the actin cytoskeleton.

51 indings in non-VSM identified changes in the actin cytoskeleton.

52 irectional challenges created by the complex actin cytoskeleton, a network of actin filaments and act

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

54 The actin cytoskeleton--a complex, nonequilibrium network co

55 Wnt/beta-catenin induced alterations to the actin cytoskeleton, acquisition of a migratory phenotype

56 or whether exertion of tensile force by the actin cytoskeleton across the integrin-ligand complex is

57 tes in its cytoplasmic domain for binding to actin cytoskeleton adaptors.

58 ns that RhoA and formin switch force-induced actin cytoskeleton alignment and that either K113E or E1

59 find that active diffusion is driven by the actin cytoskeleton, although it is also enhanced by the

60 by schizophrenia susceptibility loci is the actin cytoskeleton, an organelle necessary for synaptic

61 ce of Srf in controlling the organization of actin cytoskeleton and actin-based protrusions for myobl

62 a decrease in its affinity for the spectrin/actin cytoskeleton and causing global membrane destabili

63 thway that coordinates reorganization of the actin cytoskeleton and cell migration.

64 palladin in regulating the plasticity of the actin cytoskeleton and cellular force generation in resp

65 cal actomyosin cortex, involving a polarized actin cytoskeleton and centrally positioned myosin, with

66 We show that elasticity depends on the actin cytoskeleton and conclude by discussing how these

67 ractions between CD1d cytosolic tail and the actin cytoskeleton and correlates with enhanced iNKT cel

68 ith K2 siRNA showed disorganization of their actin cytoskeleton and decreased spreading.

69 wn of OSGEP or TP53RK induced defects in the actin cytoskeleton and decreased the migration rate of h

70 rin initiates pathological alteration of the actin cytoskeleton and downstream neurotoxicity.

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

72 rized growth at cell tips by controlling the actin cytoskeleton and exocytosis [2-4].

73 such as paxillin and Hic-5 are important for actin cytoskeleton and focal adhesion remodelling and co

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

75 n that links the extracellular matrix to the actin cytoskeleton and is stimulated by periostin.

76 itionally, we found that displacement of the actin cytoskeleton and its continued association with Fc

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

78 e conclude that spatial constraints, via the actin cytoskeleton and LINC complex, mediate nuclear cha

79 of the receptor, and cellular factors (e.g. actin cytoskeleton and lipid rafts) influence the assemb

80 cellular processes such as regulation of the actin cytoskeleton and maintenance of endoplasmic reticu

81 nated by reciprocal interactions between the actin cytoskeleton and mechanical forces.

82 ections between the extracellular matrix and actin cytoskeleton and mediate phenotypic responses via

83 This leads to changes in the actin cytoskeleton and membrane dynamics, which in turn

84 lar matrix (ECM) via its connection with the actin cytoskeleton and membrane integrins.

85 (Daam1), has been proposed to regulate cell actin cytoskeleton and microtubule (MT) reorganization f

86 ion of Rac1/Cofilin to effect changes in the actin cytoskeleton and neuron/synapse structure.

87 nd motility, rely on rapid remodeling of the actin cytoskeleton and on actin filament severing by the

88 R expression altered the organization of the actin cytoskeleton and PDZ-binding proteins in both HEK2

89 potentially identify factors connecting the actin cytoskeleton and peroxisome proliferation.

90 cts virulence effectors that hijack the host actin cytoskeleton and phosphoinositide signaling to dri

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

92 in 1 (Pfn1) is an important regulator of the actin cytoskeleton and plays a vital role in many actin-

93 BOI1 and BOI2 are paralogs important for the actin cytoskeleton and polar growth.

94 er relies on the spatial organization of the actin cytoskeleton and proper positioning/assembly of in

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

96 t SC-specific Srf deletion leads to impaired actin cytoskeleton and report the existence of finger-li

97 This migration is facilitated by the actin cytoskeleton and Rho-associated coiled-coil kinase

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

99 tology of these 491 proteins singled out the actin cytoskeleton and the actin polymerization factor,

100 ct the extracellular matrix (ECM) with the F-actin cytoskeleton and transduce mechanical forces gener

101 catenin depletion disrupts the intracellular actin cytoskeleton, and by using total internal reflecta

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

103 n required NMDA receptor activity, a dynamic actin cytoskeleton, and the transacting RNA-binding prot

104 ed that the organization and dynamics of the actin cytoskeleton are controlled by a large array of ac

105 Dynamic rearrangements of the actin cytoskeleton are crucial for cell shape and migrat

106 between transmembrane receptors (TR) and the actin cytoskeleton are crucial for regulating many cytos

107 The effects of Kv3.3 on the actin cytoskeleton are mediated by the binding of the cy

108 1 induces changes in the organization of the actin cytoskeleton as part of its virulence function in

109 sential for the integrity of the subcortical actin cytoskeleton as well as for TCR-driven WASp activa

110 uch as cell-cell contact, cell polarity, and actin cytoskeleton, as well as a wide range of signals,

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

112 that links membrane proteins to the spectrin-actin cytoskeleton, associates with VE-cadherin and inhi

113 of an array of cold-stable microtubules, and actin cytoskeleton asymmetrical contraction participate

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

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

116 se effectors that control key aspects of the actin cytoskeleton, but their role in proliferation and

117 oordination between the microtubule (MT) and actin cytoskeletons, but the mechanisms underlying this

118 e uncovered a new layer of regulation of the actin cytoskeleton by a member of a conserved protein fa

119 4A counteracts EGF-induced rearrangements of actin cytoskeleton by dephosphorylating eplin at two kno

120 align, they undergo rapid remodeling of the actin cytoskeleton by local activation of the small GTPa

121 are involved in bridging the membrane to the actin cytoskeleton by membrane protein phosphorylation,

122 nsights into the regulatory mechanism of the actin cytoskeleton by NHERF1.

123 f actin binding proteins that reorganize the actin cytoskeleton by promoting polymerization, stabiliz

124 Regulation of CPG2 binding to the actin cytoskeleton by protein kinase A directly impacts

125 y overexpression of the related ADF4 and the actin cytoskeleton destabilizers, cytochalasin D and lat

126 ecreased its expression levels, resulting in actin cytoskeleton disassembly.

127 elucidate the molecular mechanism underlying actin cytoskeleton disorganization by NHERF1, a combined

128 Phosphorylated HspB1 is recruited to the actin cytoskeleton, displaying prominent accumulation on

129 The actin cytoskeleton drives many essential processes in vi

130 esponsible for anchoring basal bodies to the actin cytoskeleton during ciliogenesis as well as in mat

131 Depolymerizing the actin cytoskeleton during cytokinesis also does not affe

132 extracellular matrix, the membrane, and the actin cytoskeleton during egg elongation.

133 role for NET2A in signal transduction to the actin cytoskeleton during fertilization.

134 ping protein transduces ROS signaling to the actin cytoskeleton during innate immunity.

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

136 erent synaptic input and requires changes in actin cytoskeleton dynamics and protein synthesis.

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

138 Actin cytoskeleton dynamics play vital roles in most for

139 ssing platelet activity, where it alters the actin cytoskeleton dynamics, and downregulation of WDR1

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

141 promoting pulmonary edema via regulation of actin cytoskeleton dynamics.

142 -beta1-induced paracellular permeability and actin cytoskeleton dynamics.

143 wn to control cell growth and proliferation, actin-cytoskeleton dynamics, and mTOR signaling.

144 function experiments reveal that polymerized actin cytoskeleton (F-actin) in HeLa cells is disorganiz

145 f the chemokine-activated alpha4beta1 to the actin cytoskeleton favors integrin immobilization, which

146 APs) in the live-cell plasma membrane and in actin cytoskeleton-free, cell-derived giant plasma membr

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

148 By linking the Golgi to the actin cytoskeleton, GOLPH3 promotes reorientation of the

149 The actin cytoskeleton has a direct impact on the control of

150 In recent years, the actin cytoskeleton has been demonstrated to play a key r

151 hysiologic role of dynamin in regulating the actin cytoskeleton has been linked to the maintenance of

152 The cortical actin cytoskeleton has been shown to be critical for the

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

154 We show that the actin cytoskeleton in both growing and elongated hypocot

155 s and karyorrhexis as well as changes to the actin cytoskeleton in CLas-exposed midgut cells.

156 A role for the F-actin cytoskeleton in CME is well established, and recen

157 Here, we discuss the role of the actin cytoskeleton in controlling receptor compartmental

158 apid reorganization and stabilization of the actin cytoskeleton in dendritic spines enables cellular

159 Cdc42 have a central role in regulating the actin cytoskeleton in dendritic spines, thereby exerting

160 5 reduced cell survival and destabilized the actin cytoskeleton in differentiated human podocytes.

161 Furthermore, organization of the actin cytoskeleton in growth plate chondrocytes was disr

162 protein synthesis and reorganization of the actin cytoskeleton in hippocampal dendritic spines durin

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

164 dition to a mislocalization of AIM1 from the actin cytoskeleton in invasive cancers, advanced prostat

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

166 Therefore, defects in the regulation of the actin cytoskeleton in neurons have been implicated in ne

167 at it could link post-Golgi traffic with the actin cytoskeleton in plants.

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

169 runculin to investigate participation of the actin cytoskeleton in regulating functional interactions

170 cell imaging, we investigate the role of the actin cytoskeleton in regulating mitochondrial fission a

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

172 ent and to induce fast reorganization of the actin cytoskeleton in synaptic plasticity.

173 ame signaling pathway that links TCRs to the actin cytoskeleton in TCR-driven actin assembly.

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

175 Recent evidence implicates the actin cytoskeleton in the control of receptor signaling.

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

177 rapid assembly and dynamic remodeling of the actin cytoskeleton in this highly compartmentalized spac

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

179 assemble hemidesmosomes and reorganize their actin cytoskeletons in order to exert traction forces on

180 signals from protein kinase cascades to the actin cytoskeleton, in particular through site-specific

181 A and FK506 restored the distribution of the actin cytoskeleton, increased the expression of synaptop

182 Finally, we show that the disruption of actin cytoskeleton induced by Abeta42 in vitro was inhib

183 at can mechanically link the membrane to the actin cytoskeleton interacts with EphB2 receptors via it

184 e focal adhesions, and reorganization of the actin cytoskeleton into stress fibers.

185 The actin cytoskeleton is a complex network controlled by a

186 The actin cytoskeleton is a critical regulator of cytoplasmi

187 The actin cytoskeleton is a crucial regulator of the intesti

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

189 of TLR9 via the interaction of IRAP with the actin cytoskeleton is a mechanism that prevents hyper-ac

190 We propose that the actin cytoskeleton is a point of integration for recepto

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

192 The actin cytoskeleton is a structural element underlying th

193 road-spectrum antiviral drugs.IMPORTANCE The actin cytoskeleton is a structure that gives the cell sh

194 The actin cytoskeleton is an attractive target for bacterial

195 The actin cytoskeleton is an essential intracellular filamen

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

197 The actin cytoskeleton is composed of a highly dynamic netwo

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

199 ons in cell mechanics are abrogated when the actin cytoskeleton is dismantled.

200 The actin cytoskeleton is essential for many fundamental bio

201 ovided new evidences that MoVrp1 involved in actin cytoskeleton is important for growth, morphogenesi

202 titative image analysis to determine how the actin cytoskeleton is mechanically coupled to the surrou

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

204 The dynamic turnover of the actin cytoskeleton is regulated cooperatively by force a

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

206 actin-binding protein and that a functioning actin cytoskeleton is required for NaCl-induced peroxiso

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

208 Actin cytoskeleton-linked proteins such as talin, vincul

209 acterial and viral pathogens hijack the host actin cytoskeleton machinery to facilitate spread and in

210 y and anti-apoptotic effects, is involved in actin cytoskeleton maintenance and promotes autophagy.

211 locales, such as cytoplasmic vesicles or the actin cytoskeleton, markedly alters Gag subcellular dist

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

213 Actin cytoskeleton-mediated FA growth and maturation thu

214 are mechanosensors through which cells exert actin cytoskeleton-mediated traction forces to sense the

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

216 n of second messengers and the remodeling of actin cytoskeleton necessary for the clustering of lipid

217 The actin cytoskeleton network has an important role in plan

218 assemble and maintain functionally distinct actin cytoskeleton networks with various actin filament

219 for the self-organization of diverse dynamic actin cytoskeleton networks within a common cytoplasm.

220 a molecular motor that powers contraction of actin cytoskeleton networks, recent studies have questio

221 ant did not provoke the rearrangement of the actin cytoskeleton observed after wild-type MCMV infecti

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

223 sion cycle 14A (hCDC14A) associates with the actin cytoskeleton of human cells.

224 cent studies have investigated the dendritic actin cytoskeleton of the cell edge's lamellipodial (LP)

225 ools, we uncovered that perturbations in the actin cytoskeleton or Cdc42 activity minimally affect JU

226 that these dimers exist independently of the actin cytoskeleton or cytoplasmic proteins.

227 es (BCL11B, FOXO1, KIF13B, PAWR, SOX4, SYK), actin cytoskeleton organisation (ACTR3, CDC42BPA, DTNBP1

228 so show that Vps13, like hVps13A, influences actin cytoskeleton organization and binds actin in immun

229 we show that histamine selectively modifies actin cytoskeleton organization induced by TLR4, but not

230 deficient in ACTN1 exhibit changes in their actin cytoskeleton organization, a loss in front-rear po

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

232 9R binds actin, but does not function in the actin cytoskeleton organization.

233 ng of Vps13, both in protein trafficking and actin cytoskeleton organization.

234 not reveal a continuous rearward flow of the actin cytoskeleton over slower moving adhesions.

235 ear RHPN2, a gene involved in organizing the actin cytoskeleton (P = 4.17 x 10(-8)).

236 nvading the peripheral domain only where the actin cytoskeleton permits them to go.

237 The dynamic regulation of the actin cytoskeleton plays a key role in controlling the s

238 The actin cytoskeleton powers membrane deformation during ma

239 ed to intact epithelia and disruption of the actin cytoskeleton prevented A2BR-induced but not beta2A

240 1d nanoclusters are actively arrested by the actin cytoskeleton, preventing their further coalescence

241 th Lyn in ordered lipid regions and that the actin cytoskeleton regulates this functional interaction

242 3p and miR-142-5p play nonredundant roles in actin cytoskeleton regulation by controlling small GTPas

243 el AKT substrate, with an unexpected role in actin cytoskeleton regulation via an interaction with th

244 e and function by modulating the activity of actin cytoskeleton regulators, that is, Rho GTPases (Rho

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

246 ivation of Rac, leading to disruption of the actin cytoskeleton, release of filamentous actin-bound a

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

248 ration is dependent on adhesion dynamics and actin cytoskeleton remodeling at the leading edge.

249 Actin cytoskeleton remodeling requires the coordinated a

250 esses breast cancer metastasis by regulating actin cytoskeleton remodeling through the control of ECT

251 eceptor tyrosine kinases that participate in actin cytoskeleton remodeling.

252 ogress, a comprehensive understanding of how actin cytoskeleton remodelling supports stable junctions

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

254 ing protein Coronin plays a critical role in actin cytoskeleton reorganization and association with j

255 F3 protein by extracellular stimuli promotes actin cytoskeleton reorganization and facilitates cancer

256 hich in turn activates PKC which induces the actin cytoskeleton reorganization that is required for p

257 ibited RAGE ligand dependent cell signaling, actin cytoskeleton reorganization, cell spreading, and c

258 lular signaling and a bona fide regulator of actin cytoskeleton reorganization.

259 The actin cytoskeleton serves unique structural and supporti

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

261 The actin cytoskeleton shows proximity to vacuoles, and the

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

263 This phenotype is characterized by actin cytoskeleton stiffness, a cell polarization loss a

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

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

266 association between the basal bodies and the actin cytoskeleton, suggesting that FAK is an important

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

268 The actin cytoskeleton supports a vast number of cellular pr

269 The metazoan actin cytoskeleton supports a wide range of contractile

270 ates Rac1, resulting in modifications of the actin cytoskeleton that are essential to maintain cell s

271 ed a novel mechanism for regulating neuronal actin cytoskeleton that explains the specific organizati

272 tacts between the CaMKII dodecamer and the F-actin cytoskeleton that stabilize the initial weak (micr

273 M domain protein that regulates the cortical actin cytoskeleton, the functional significance of this

274 mary static function in stabilization of the actin cytoskeleton, these studies are the first to demon

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

276 to induce Sertoli cell injury by perturbing actin cytoskeleton through changes in the spatial expres

277 VE-cadherin is linked to the actin cytoskeleton through cytoplasmic interactions with

278 t contact adhesions link ECM proteins to the actin cytoskeleton through numerous adaptor and signalin

279 Remodeling of the actin cytoskeleton through the activity of small GTPases

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

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

282 icomponent transmembrane complex linking the actin cytoskeleton to extracellular matrix, is essential

283 cytic machinery is physically coupled to the actin cytoskeleton to facilitate glutamate receptor inte

284 r integrin-mediated cell adhesion, links the actin cytoskeleton to integrin-based cell-extracellular

285 ntially regulate cell-cell junctions and the actin cytoskeleton to mediate invasion in three-dimensio

286 that connects dynamic reorganization of the actin cytoskeleton to regulation of expression of a wide

287 hrough YAP to stabilize the anchorage of the actin cytoskeleton to the cell membrane.

288 plied to integrins propagate from the tensed actin cytoskeleton to the LINC complex and then through

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

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

291 sely, overexpression of KLF15 stabilized the actin cytoskeleton under cell stress in human podocytes.

292 fness of the cell membrane by disrupting the actin cytoskeleton using cytochalasin D increased the am

293 ynamin has been implicated in regulating the actin cytoskeleton via direct dynamin-actin interactions

294 phragm, which is physically connected to the actin cytoskeleton via the transmembrane protein nephrin

295 uple the extracellular matrix to the dynamic actin cytoskeleton, via transmembrane integrins and acti

296 the response to chemoattractants, an intact actin cytoskeleton was essential for reacting to mechani

297 ar pathways, such as vesicle trafficking and actin cytoskeleton, where a regulating role for ATM/ATR

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

299 ding of GFP-tagged CaMKII to tag-RFP-labeled actin cytoskeleton within live cells using total interna

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