ライフサイエンスコーパス: cytoskeleton

1 , when in contact with a support such as the cytoskeleton.

2 er mitochondrial trafficking to the cortical cytoskeleton.

3 bitors (GDI), known regulators of RhoGTPases/cytoskeleton.

4 echanical force as well as disruption of the cytoskeleton.

5 patterns via coupling to the activity of the cytoskeleton.

6 forcement response that stabilizes the actin cytoskeleton.

7 nd signaling molecules along the microtubule cytoskeleton.

8 ions (TJ), and the perijunctional actomyosin cytoskeleton.

9 sis are driven by the actomyosin contractile cytoskeleton.

10 ns and differential co-localisation with the cytoskeleton.

11 between extracellular ligands and the actin cytoskeleton.

12 ation, morphology, and dynamics of the actin cytoskeleton.

13 bility to quantify key features of the actin cytoskeleton.

14 component of the outer hair cells' cortical cytoskeleton.

15 envelope to critical regulators of the actin cytoskeleton.

16 s, lipid kinases, phosphatases and the actin cytoskeleton.

17 tural and regulatory components of the actin cytoskeleton.

18 a, within 62 +/- 5 nm, mediated by the actin cytoskeleton.

19 s in non-VSM identified changes in the actin cytoskeleton.

20 ankyrin repeat domain to microtubules of the cytoskeleton.

21 ould establish long-range order in the actin cytoskeleton.

22 en implicated in the regulation of the actin cytoskeleton.

23 nase, which is a critical regulator of actin cytoskeleton.

24 the extracellular matrix, cell adhesion and cytoskeleton.

25 f hereditary diseases affecting the red cell cytoskeleton.

26 raction of the dynamic actin and microtubule cytoskeleton.

27 of cellular enzymes and modification of the cytoskeleton.

28 lity to rearrange the architecture of the MT cytoskeleton.

29 switches best known for regulating the actin cytoskeleton.

30 e latter caused by forces from chromatin and cytoskeleton.

31 and the pulling force applied from the cell cytoskeleton.

32 n claudins, ZO scaffolding proteins, and the cytoskeleton.

33 ally impinging on the integrity of the actin cytoskeleton.

34 nitiate Rac-mediated remodeling of the actin cytoskeleton.

35 s of cells are mainly derived from the actin cytoskeleton.

36 ganization of the actin and microtubule (MT) cytoskeletons.

37 cal roles in controlling the organization of cytoskeletons.

38 lopodia, suggesting that tau links these two cytoskeletons.

39 luorescently labeled motor proteins on these cytoskeletons.

40 al is mediated by rearrangement of the actin cytoskeleton, a process referred to as dynamic mass redi

41 ether exertion of tensile force by the actin cytoskeleton across the integrin-ligand complex is also

42 eness by application of tensile force by the cytoskeleton, across ligand-integrin-adaptor complexes.

43 vasion foci, facilitating the recruitment of cytoskeleton adaptor proteins to mediate pathogen uptake

44 its cytoplasmic domain for binding to actin cytoskeleton adaptors.

45 nical connection between the nucleus and the cytoskeleton, allowing forces exerted through focal adhe

46 that active diffusion is driven by the actin cytoskeleton, although it is also enhanced by the flow.

47 neural progenitors through regulation of the cytoskeleton and cell cycle.

48 d in plant hormone, defense, cell signaling, cytoskeleton and cell wall metabolism in a susceptible r

49 n two highly active systems inside the cell: cytoskeleton and chromatin.

50 membrane, at least partially defined by the cytoskeleton and clathrin-coated pits, in which receptor

51 itical to developing a physical model of the cytoskeleton and designing biomimetic active materials.

52 itiates pathological alteration of the actin cytoskeleton and downstream neurotoxicity.

53 ns (FAs) regulate force transfer between the cytoskeleton and ECM-integrin complexes.

54 th functional ability to rearrange the actin cytoskeleton and engraft successfully.

55 teracts with RhopH1, RhopH3, the erythrocyte cytoskeleton and exported proteins involved in host cell

56 profilin 1, leading to a thickened cortical cytoskeleton and hence sustained integrin activation by

57 nesin-dependent mechanism controlling the MT cytoskeleton and identify loss of Glu-MTs and RNA misloc

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

59 er, the immune signals that impinge on actin cytoskeleton and its response regulators remain largely

60 Cytoskeleton and ligand-bound integrins orient in the sa

61 We isolate the changes in the cytoskeleton and membrane and show that reduction in the

62 We further determined the roles of cytoskeleton and membrane lipids in DRG neuron mechanics

63 Rac1/Cofilin to effect changes in the actin cytoskeleton and neuron/synapse structure.

64 e properties involve altered dynamics of the cytoskeleton and one of its major structural components

65 Actin polymerizes to form part of the cytoskeleton and organize polar growth in all eukaryotic

66 tially identify factors connecting the actin cytoskeleton and peroxisome proliferation.

67 rulence effectors that hijack the host actin cytoskeleton and phosphoinositide signaling to drive pat

68 phosphoproteomics indicated that EGRs target cytoskeleton and plasma membrane-associated proteins.

69 tudied for its role in controlling the actin cytoskeleton and plays a part in several potentially onc

70 Pfn1) is an important regulator of the actin cytoskeleton and plays a vital role in many actin-based

71 switching induced dysregulation of the actin cytoskeleton and reduced the expression of hemidesmosoma

72 pecific Srf deletion leads to impaired actin cytoskeleton and report the existence of finger-like act

73 Cell migration and its dependence on the cytoskeleton and signaling machines have been studied ex

74 interact with nephrin and regulate podocyte cytoskeleton and slit diaphragm dynamics, MAGI2 mutation

75 anical constraints act as cues to orient the cytoskeleton and tension during ventral furrow formation

76 F activates YAP/TAZ via its effects on actin cytoskeleton and that activated YAP/TAZ induce a transcr

77 ested that CD43 is strongly connected to the cytoskeleton and that its interaction with ICAM-1 mainly

78 uscle atrophy induced by fasting, the desmin cytoskeleton and the attached Z-band-bound thin filament

79 rther integration of cellular junctions, the cytoskeleton and the formation of apical-basal polarity.

80 ns, changes in the organization of the actin cytoskeleton, and decreased velocity of cell migration.

81 n transmembrane receptors (TR) and the actin cytoskeleton are crucial for regulating many cytoskeleto

82 signaling and dynamic reorganization of the cytoskeleton are essential processes for the coordinatio

83 ty and dynamic properties of the microtubule cytoskeleton are indispensable for the development of th

84 r axons, and that alphaII spectrin-dependent cytoskeletons are also required for assembly of nodes of

85 Cytoskeletons are cell structural proteins that closely

86 characteristics such as gene expression and cytoskeleton, are promising label-free biomarkers for st

87 ssibly very sensitive assessment of the cell cytoskeleton as a possible tool for medical diagnosis.

88 We model the cytoskeleton as a random geometric graph, with nodes cor

89 acological interventions that altered the MT cytoskeleton as a whole, presented no consistent role.

90 tire mammal red blood cell lipid bilayer and cytoskeleton as modeled by multiple millions of mesoscop

91 tive to pharmacological perturbations of the cytoskeleton as well as differences in the mechanotype o

92 st, MUC1 seems to be weakly connected to the cytoskeleton, as its interactions with ICAM-1 are mainly

93 Activity-regulated cytoskeleton-associated protein (Arc) is an immediate ea

94 other RNA sequences, and heptavalent protein cytoskeleton-associated protein 5 (CKAP5, an alternative

95 GAS2L3 is a recently identified cytoskeleton-associated protein that interacts with acti

96 , as a crucial linker between kAE1 and actin cytoskeleton-associated proteins in polarized cells.

97 array of cold-stable microtubules, and actin cytoskeleton asymmetrical contraction participate in con

98 hesized that RRV might induce changes in the cytoskeleton at both early and late stages of infection.

99 ze with cortactin (CTTN), a regulator of the cytoskeleton at membrane ruffling areas.

100 ners with betaIV spectrin to form a periodic cytoskeleton at the AIS.

101 eptin-dependent reorientation of the F-actin cytoskeleton at the base of the infection cell, which or

102 requires the reorganization of the cortical cytoskeleton at the leading edge of cells and extracellu

103 dicating that IRS-2 requires the microtubule cytoskeleton at the level of downstream effector activat

104 xtracellular signals, and regulate the actin cytoskeleton at the tube apex to drive tip growth.

105 cally examine the factors that contribute to cytoskeleton-based regulation of motor protein motility,

106 e to the sudden breakdown of the erythrocyte cytoskeleton, before permeabilization and eventual ruptu

107 Cytoskeleton-binding agents, that alter the architecture

108 irection as retrograde actin flow with their cytoskeleton-binding beta-subunits tilted by applied for

109 s demonstrate the importance of the spectrin cytoskeleton both at the AIS and throughout the nervous

110 ation between the microtubule (MT) and actin cytoskeletons, but the mechanisms underlying this MT-act

111 vered a new layer of regulation of the actin cytoskeleton by a member of a conserved protein family t

112 three-dimensional tomographic images of the cytoskeleton by a segmentation algorithm.

113 nteracts EGF-induced rearrangements of actin cytoskeleton by dephosphorylating eplin at two known ext

114 , they undergo rapid remodeling of the actin cytoskeleton by local activation of the small GTPase Rac

115 sed CD147 as a tumor marker and regulator of cytoskeleton, cell growth, stress response, or immune ce

116 at day+2, we found significant metabolic and cytoskeleton changes in target organ ECs in gene array a

117 Actin was thought to be the sole cytoskeleton compartment presented in dendritic spines,

118 nown as the linker of the nucleoskeleton and cytoskeleton complex.

119 ier.SIGNIFICANCE STATEMENT A periodic axonal cytoskeleton consisting of actin and spectrin has been p

120 e findings suggest that microdomains and the cytoskeleton constrain AtHIR1 dynamics, promote AtHIR1 o

121 crotubules reveal that an intact microtubule cytoskeleton contributes to IRS-2- but not IRS-1-mediate

122 Miller studies how the cytoskeleton controls cellular shape change.

123 el mechanism that, through modulation of the cytoskeleton, controls Notch activation at the T cell:AP

124 cover universal features underlying membrane-cytoskeleton coordination during cytokinesis.

125 Unlike traditional cytoskeletons, CrvA localizes to the periplasm and thus

126 cytoskeleton are crucial for regulating many cytoskeleton-dependent cellular processes such as cell s

127 ing as tracks for transport, the microtubule cytoskeleton directs intracellular trafficking by regula

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

129 on by YopO that would clarify its effects on cytoskeleton disruption.

130 an essential connector between receptor and cytoskeleton during chemotaxis.

131 Depolymerizing the actin cytoskeleton during cytokinesis also does not affect the

132 or NET2A in signal transduction to the actin cytoskeleton during fertilization.

133 lexes are regulated to connect nuclei to the cytoskeleton during nuclear migration is unknown.

134 c1/CDC42 GTPases, in the regulation of actin cytoskeleton dynamics and cell-cell adhesion.

135 a transcriptional program to further control cytoskeleton dynamics and thus establish a feedforward l

136 obust compensatory mechanisms that safeguard cytoskeleton dynamics at the synapse.

137 rotein essential for the regulation of actin cytoskeleton dynamics in diverse biological processes.

138 Actin cytoskeleton dynamics play vital roles in most forms of

139 ociated protein that functions in regulating cytoskeleton dynamics, especially in neurons.

140 tant roles in several neuronal functions, as cytoskeleton dynamics, injured neurons regeneration, syn

141 beta-spectrin interferes with spectrin-actin cytoskeleton dynamics, leading to a loss of a cytoskelet

142 revealed that membrane microdomains and the cytoskeleton, especially microtubules, restrict the late

143 he dominant role of integrins in controlling cytoskeleton, focal adhesion, actomyosin contraction, an

144 demonstrate the broad importance of spectrin cytoskeletons for nervous system function and developmen

145 n the live-cell plasma membrane and in actin cytoskeleton-free, cell-derived giant plasma membrane ve

146 me biosynthesis, and mTORC2, which regulates cytoskeleton functions.

147 way through these macromolecules which actin-cytoskeleton-generated tensile force takes when applied

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

149 term analysis revealed that wound healing-, cytoskeleton-, immune system-, stress response-, phospho

150 udy how ATP-driven activities and actomyosin cytoskeleton impact basal membrane fluctuations in adher

151 rs to be an important modulator of the actin cytoskeleton, implicating maintenance of muscular functi

152 wards understanding the diverse roles of the cytoskeleton in autophagy.

153 We show that the actin cytoskeleton in both growing and elongated hypocotyl cel

154 sham revealed a relation to mitochondria and cytoskeleton in both species.

155 ive mice to study the role of the actomyosin cytoskeleton in driving the remodeling of membranes of l

156 s homolog, R-Ras, stabilizes the microtubule cytoskeleton in endothelial cells leading to endothelial

157 Given the prominence of the cytoskeleton in growth cone collapse, we assessed the re

158 Furthermore, organization of the actin cytoskeleton in growth plate chondrocytes was disrupted.

159 und that induction of cell stress alters the cytoskeleton in IECs via changes in the actin-binding pr

160 al particles, and rearrangement of the actin cytoskeleton in infected cells.

161 to a mislocalization of AIM1 from the actin cytoskeleton in invasive cancers, advanced prostate canc

162 assessed the involvement of the microtubule cytoskeleton in IRS-dependent signaling.

163 l has tested the requirement of the spectrin cytoskeleton in maintenance of axon integrity.

164 dence highlights the importance of the actin cytoskeleton in modulating inflammatory responses.

165 current understanding of the function of the cytoskeleton in podocytes and the associated implication

166 AIM1 strongly associates with the actin cytoskeleton in prostate epithelial cells in normal tiss

167 s are universal tools for studying the actin cytoskeleton in single cells in culture, tissues, and mu

168 VASP family member EVL to assemble the actin cytoskeleton in the apical cortex and in protruding lame

169 These data demonstrate a role for the axon cytoskeleton in the assembly of a critical neuronal doma

170 ends on spatial control of dynamics of actin cytoskeleton in the foot processes.

171 s to accomplish directional transport on the cytoskeleton in vivo.

172 To assess the influence of AMPK on the actin cytoskeleton in VSM of resistance arteries with regard t

173 show that the elastic response of our model cytoskeleton, in which the spectrin polymers are treated

174 site to another, involves remodeling of the cytoskeleton including altered microtubule dynamics.

175 the entropic elasticity of the RBC spectrin cytoskeleton, including domain unfolding/refolding.

176 l epithelial barrier, including keratinocyte cytoskeleton, intercellular junctions, and cell adhesion

177 binding partners and PTMs that divide the MT cytoskeleton into functionally distinct subsets.

178 diseases because disruption of the spectrin cytoskeleton is a common molecular pathology.

179 The actin cytoskeleton is a complex network controlled by a vast a

180 The actin cytoskeleton is a critical regulator of cytoplasmic arch

181 -dependent excess stabilization of the actin cytoskeleton is a key phosphorylation-dependent mediator

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

183 pectrum antiviral drugs.IMPORTANCE The actin cytoskeleton is a structure that gives the cell shape an

184 The actin cytoskeleton is an attractive target for bacterial toxin

185 The actin cytoskeleton is an essential intracellular filamentous s

186 The fission yeast actin cytoskeleton is an ideal, simplified system to investiga

187 The regulation of nuclear state by the cytoskeleton is an important part of cellular function.

188 Regulation of the actin cytoskeleton is crucial for normal development and funct

189 chorage of this axoglial complex to the axon cytoskeleton is essential for efficient CNS node formati

190 The actin cytoskeleton is essential for many fundamental biologica

191 new evidences that MoVrp1 involved in actin cytoskeleton is important for growth, morphogenesis, cel

192 A dynamic actin cytoskeleton is necessary for viral entry, intracellular

193 hes to show that reorganisation of the actin cytoskeleton is required for dark-induced stomatal closu

194 binding protein and that a functioning actin cytoskeleton is required for NaCl-induced peroxisome div

195 ests that the presence of an intact cortical cytoskeleton is required for zinc-induced cis multimeriz

196 Here we test the hypothesis that the actin cytoskeleton is the primary barrier to transcellular tun

197 protein known primarily for its role in the cytoskeleton, is routinely found to be associated with m

198 ordination between the actin and microtubule cytoskeletons, leading to motor neuron degeneration.

199 in A/C form the LInker of Nucleoskeleton-and-Cytoskeleton (LINC) bridging complex at the nuclear enve

200 members of the linker of nucleoskeleton and cytoskeleton (LINC) complex, may interact with incoming

201 lly mediated by linker of nucleoskeleton and cytoskeleton (LINC) complexes connecting the nucleus to

202 n biological membranes, many factors such as cytoskeleton, lipid composition, crowding, and molecular

203 s, such as cytoplasmic vesicles or the actin cytoskeleton, markedly alters Gag subcellular distributi

204 howed some degree of colocalization with the cytoskeleton marker beta-tubulin.

205 ; and how organisms with a similar sensitive cytoskeleton may be susceptible to environmental changes

206 ignaling data, suggests that the microtubule cytoskeleton may facilitate access of IRS-2 to downstrea

207 ganization of the outer hair cells' cortical cytoskeleton may have emerged from molecular networks in

208 between membrane-integral PRKs and the actin cytoskeleton, mediated through interactions between PRKs

209 Actin cytoskeleton-mediated FA growth and maturation thus culm

210 ve actin- and microtubule-mediated motility, cytoskeleton-membrane scaffolds and signaling proteins.

211 ding the biochemical phenomena involved with cytoskeleton/membrane attachment.

212 J structure and remodeling of the actomyosin cytoskeleton modify epithelial mechanics.

213 e protein (WASp), which signals to the actin cytoskeleton, modulates autophagy and inflammasome funct

214 genes associated with cell cycle, chromatin, cytoskeleton/motility, immunity, and apoptosis.

215 The actin cytoskeleton network has an important role in plant cell

216 cytoplasm and the relative drag between the cytoskeleton network phase and the water phase also play

217 How effectors reprogram the cytoskeleton network remains unclear.

218 ed after exposure to various drugs affecting cytoskeleton network.

219 nd disease to propose that disruption of the cytoskeleton, nodal architecture, and other components o

220 Our study shows that the actin cytoskeleton of endothelial cells provides both passive

221 presence of mechanisms that finely align the cytoskeleton of the axon with the one of the Schwann cel

222 junctions links the contractile acto-myosin cytoskeletons of adjacent cells, serving as a tension-tr

223 MFs and MTs, were used to study the role of cytoskeleton on PIXV replication.

224 Brownian dynamics simulations of the active cytoskeleton, on metastatic breast cancer cells embedded

225 The modulation exerted by the cytoskeleton onto the nucleus results in changes that ar

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

227 slation reinitiation, but not its effects on cytoskeleton or intracellular trafficking.

228 -isoforms with cellular matrix proteins, the cytoskeleton, or other membrane protein complexes.

229 w that Vps13, like hVps13A, influences actin cytoskeleton organization and binds actin in immunopreci

230 logy Biological Process (GO BP) terms, actin cytoskeleton organization, actin filament-based process,

231 PDAC cells, we defined protein translation, cytoskeleton organization, and cell-cycle regulatory pat

232 evealed a group of molecules associated with cytoskeleton organization, including caldesmon, were dif

233 IP1 contributes to nodal membrane-associated cytoskeleton organization, likely through its interactio

234 Vps13, both in protein trafficking and actin cytoskeleton organization.

235 ds actin, but does not function in the actin cytoskeleton organization.

236 veal a continuous rearward flow of the actin cytoskeleton over slower moving adhesions.

237 ular distribution of peroxisomes through the cytoskeleton-peroxisome connection.

238 rvous system.SIGNIFICANCE STATEMENT Spectrin cytoskeletons play diverse roles in neurons, including a

239 Spectrins form a submembranous cytoskeleton proposed to confer strength and flexibility

240 and identified the network of Rho-recruited cytoskeleton proteins.

241 rate changes in cell morphology, observed as cytoskeleton protrusions-i.e., lamellipodia and filopodi

242 The cytoskeleton regulates podocyte shape, structure, stabil

243 role in promoting the maturation of the axon cytoskeleton, regulating axon trafficking parameters, an

244 ncompass proteins involved in cell adhesion, cytoskeleton regulation and vesicle-mediated transport,

245 miR-142-5p play nonredundant roles in actin cytoskeleton regulation by controlling small GTPase tran

246 substrate, with an unexpected role in actin cytoskeleton regulation via an interaction with the ARP2

247 Although KANK1 is known as a cytoskeleton regulator, its tumorigenic function in MPNS

248 ermin) was initially identified as an actin cytoskeleton-related oligodendroglial protein in the rat

249 molecular composition and structure of these cytoskeletons remain poorly understood.

250 , PI-3-kinase signaling (PIK3R1, VAV1), RHOA/cytoskeleton remodeling (ARHGEF3), RNA splicing (U2AF1),

251 es dysregulation of 64 proteins, involved in cytoskeleton remodeling and in protein synthesis, foldin

252 nd PAK1 as well as regulation of the growth, cytoskeleton remodeling and motility, invasion of PDAC c

253 rotein with critical roles in cell adhesion, cytoskeleton remodeling and nuclear architecture.

254 CXCR4 activation results in actin cytoskeleton remodeling and PI3K/Akt and Erk signaling i

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

256 microtubule (MT) dynamics is a key event of cytoskeleton remodeling in the growth cone (GC) during a

257 roteins have been implicated in coordinating cytoskeleton remodeling with lysosome trafficking, the c

258 ronic immune activation, we demonstrate that cytoskeleton remodeling, induced by okadaic acid, restor

259 of phosphoinositide-dependent signaling and cytoskeleton remodeling, which promoted leading-edge for

260 r tyrosine kinases that participate in actin cytoskeleton remodeling.

261 cAMP), BAY60-6583 or Cicaprost induced rapid cytoskeleton remodelling and inhibited proliferation and

262 Our findings also reveal that GOS induces cytoskeleton remodelling in RAW264.7 cells and promotes

263 The actin cytoskeleton remodels during the first 5 min of innate i

264 cells with many uninfected cells, increased cytoskeleton reorganization, and rapid displacement of n

265 e indicates that actin dynamics and membrane-cytoskeleton scaffolds also have essential roles in macr

266 g synthesis to non-PM membranes or the actin cytoskeleton severely reduced net virus particle product

267 showed enrichment in axon guidance and actin cytoskeleton signalling pathways as well as activation o

268 In general, a framework for how the cytoskeleton spatially defines cell-plate formation is l

269 hrocytes, due to impaired actin assembly and cytoskeleton stability.

270 extrinsic JN up-regulated formation of actin cytoskeleton stress fibers, caused redistribution of mor

271 t of tyrosine kinase signaling and the actin cytoskeleton, suggesting selection for avid TCR microclu

272 ation between the basal bodies and the actin cytoskeleton, suggesting that FAK is an important regula

273 ar pathologies converge on disruption of the cytoskeleton, suggesting that this subcellular structure

274 (ARP2/3) complex, which regulates the actin cytoskeleton supporting dendritic spines, produced spine

275 The metazoan actin cytoskeleton supports a wide range of contractile and tr

276 How Shh elicits changes in the growth cone cytoskeleton that drive growth cone turning is unknown.

277 cyte posterior along a polarised microtubule cytoskeleton that grows from non-centrosomal microtubule

278 complexes (linkers of the nucleoskeleton and cytoskeleton) that span the entire NE and mediate nuclea

279 e a common function in stabilizing the actin cytoskeleton, they physically interact in the cytoplasm

280 duce Sertoli cell injury by perturbing actin cytoskeleton through changes in the spatial expression o

281 ively maintained in position by engaging the cytoskeleton through the LINC complex.

282 anscription-independent control of the actin cytoskeleton through the small GTPase RhoA.

283 ssue-level polarization of junctions and the cytoskeleton through unknown mechanisms.

284 patially regulate Rac activity and the actin cytoskeleton to ensure correct epithelial cell shape and

285 connects dynamic reorganization of the actin cytoskeleton to regulation of expression of a wide range

286 YAP to stabilize the anchorage of the actin cytoskeleton to the cell membrane.

287 le of linking mechanical displacement of the cytoskeleton to the opening of the channel.

288 cuss the contributions of organelles and the cytoskeleton to the plant's defense response against mic

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

290 tant similarities in the contribution of the cytoskeleton to these different forms of biomineralisati

291 Epithelial cells in tissues use their actin cytoskeletons to stick together, whereas unattached cell

292 of the cell membrane by disrupting the actin cytoskeleton using cytochalasin D increased the amount o

293 otein kinase A targets at cell adhesions and cytoskeleton: VE-cadherin, p120-catenin, ZO-1, cortactin

294 determined by the organization of the actin cytoskeleton, which is also the main regulator of cell f

295 CDRs involves a drastic rearrangement of the cytoskeleton, which is regulated by the Rho family of GT

296 sculature prior to establishing a deformable cytoskeleton, which is ultimately formed prior to enucle

297 ted axons, alphaII spectrin forms a periodic cytoskeleton with betaIV and betaII spectrin at nodes of

298 n of organelles and the restructuring of the cytoskeleton within eukaryotic cells.

299 e conclude that the spectrin and microtubule cytoskeletons work in combination to protect axons and d

300 e signaling cascades that regulate the actin cytoskeleton, would compromise the structural stability