ライフサイエンスコーパス: cytoskeleton

1 t involve microtubule networks and the actin cytoskeleton.

2 anical coupling of N-cadherin with the actin cytoskeleton.

3 is important for CAP1 to regulate the actin cytoskeleton.

4 ally involved in the regulation of the actin cytoskeleton.

5 vels lead to an aberrant organization of the cytoskeleton.

6 ilin activation, and remodeling of the actin cytoskeleton.

7 nside the nucleus, and the coupling with the cytoskeleton.

8 tein transmits signals to the podocyte actin cytoskeleton.

9 plishes the same task by hijacking the actin cytoskeleton.

10 ation and ectosome release rely on the actin cytoskeleton.

11 tein that connects the LINC complex with the cytoskeleton.

12 ne proteins, adaptor proteins, and the actin cytoskeleton.

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

14 nt myotubes and effects changes in the actin cytoskeleton.

15 tween the extracellular matrix and the actin cytoskeleton.

16 dependent on the presence of an intact actin cytoskeleton.

17 ction pathway that regulates the growth cone cytoskeleton.

18 ular clutch between N-cadherin and the actin cytoskeleton.

19 cating a pronounced stress stiffening of the cytoskeleton.

20 ns of the "corrals" of the cortical spectrin cytoskeleton.

21 surprisingly little is known about its actin cytoskeleton.

22 maintaining myelin structure and the axonal cytoskeleton.

23 and involves the rearrangement of the actin cytoskeleton.

24 rs, the nuclear shell, and coupling with the cytoskeleton.

25 s involved in the rearrangement of the actin cytoskeleton.

26 mitochondrial repositioning to the cortical cytoskeleton.

27 E) and physically connect the nucleus to the cytoskeleton.

28 ssociated with the disruption of the F-actin cytoskeleton.

29 th Mps2 to couple the telomeres to the actin cytoskeleton.

30 n of the WRC and reorganization of the actin cytoskeleton.

31 een the cell membrane and the cortical actin cytoskeleton.

32 mesoscale polymers central to the eukaryotic cytoskeleton.

33 rises from the membrane's connections to the cytoskeleton.

34 anization and dynamics of the cortical actin cytoskeleton.

35 ated in linking the AJ and TJ complex to the cytoskeleton.

36 in attaching the membrane to the underlying cytoskeleton.

37 ened by an elastic meshwork representing the cytoskeleton.

38 t on an intact microtubule network and actin cytoskeleton.

39 of tubulin dimers are key components of the cytoskeleton.

40 uctures that are associated with the keratin cytoskeleton.

41 isrupt lipid membranes, cell walls and actin cytoskeletons.

42 nteractions that converge on distinct axonal cytoskeletons.

43 The actin cytoskeleton, a dynamic network of actin filaments and a

44 Thus, the membrane and cytoskeleton act in concert in distinct subcellular comp

45 rated that ROP dynamics do not depend on the cytoskeleton, acute depolymerization of the cytoskeleton

46 ave demonstrated how altering the actomyosin cytoskeleton affects phagocytic behavior.

47 lls of Arabidopsis thaliana We show that the cytoskeleton aligns with the long axis of the cells.

48 cells, the question arises whether the plant cytoskeleton also responds to geometrical cues.

49 erve as molecular linkages between the actin cytoskeleton and a diverse collection of receptors, incl

50 nesprin experiences tension generated by the cytoskeleton and acts as a mechanical sensor of cell pac

51 (+17b) forms does not disrupt the junctional cytoskeleton and AJs during the steady-state or calcium-

52 al of the metabolism inhibitors restored the cytoskeleton and CA4P activity.

53 sing forces: cell contraction via actomyosin cytoskeleton and cell expansion via cell-cell adhesion.

54 lar signals that altered organization of the cytoskeleton and cell-extracellular matrix contacts and

55 optically control the dynamics of the actin cytoskeleton and cellular functions that depend on it.

56 portant for allowing rapid remodeling of the cytoskeleton and efficient T cell polarization.

57 gulate cellular patterning by modulating the cytoskeleton and focal adhesion structures(3-5).

58 centrosomes, which organize the microtubule cytoskeleton and form the poles of the mitotic spindle.

59 ses, thereby triggering changes in the actin cytoskeleton and in transcription.

60 rity in the organisation of the actin-myosin cytoskeleton and is postulated to reflect directional te

61 gh the internal stress within the actomyosin cytoskeleton and its coupling with local rigidity sensin

62 to synergic modifications of the endothelial cytoskeleton and junctional remodeling.

63 complex and coordinated remodelling of their cytoskeleton and membranes.

64 ment of the relationship between the ciliary cytoskeleton and microtubule-based transport in cilia.

65 cally, severases can amplify the microtubule cytoskeleton and not just destroy it.

66 AMOT130 associates to the actin cytoskeleton and regulates tight-junction maintenance an

67 r properties are conferred by changes in the cytoskeleton and represent a new facet of PCP function.

68 ablish a link between the state of the actin cytoskeleton and the expression of pancreatic transcript

69 DG), a key component in the link between the cytoskeleton and the extracellular matrix (ECM).

70 he transmembrane protein linkage between the cytoskeleton and the extracellular matrix in skeletal mu

71 he transmembrane protein linkage between the cytoskeleton and the extracellular matrix in skeletal mu

72 that cells establish between the actomyosin cytoskeleton and the extracellular matrix via integrins

73 abling mechanical coupling between the actin cytoskeleton and the extracellular matrix.

74 rrelate with the ultrastructure of the actin cytoskeleton and the organization of the genome, respect

75 n also provide a structural link between the cytoskeleton and the plasma membranes that maintain cell

76 he generation of intracellular forces by the cytoskeleton and their transmission to an extracellular

77 iates both rigidification of the erythrocyte cytoskeleton and trafficking of the adhesin and key viru

78 Rho GTPases are central regulators of the cytoskeleton and, in humans, are controlled by 145 multi

79 atins and to mediate organization of keratin cytoskeletons and desmosomes.

80 ns1 leading to a reorganization of the actin cytoskeleton, and a reduction of focal adhesions and mic

81 as proteins involved with cell adhesion, the cytoskeleton, and apoptosis, were increased.

82 namic assembly of microtubules, remodels the cytoskeleton, and enhances the acetylation of beta-caten

83 s set of molecules, including myelin, axonal cytoskeleton, and ion channel antigens, in individual pa

84 ks cell-cell adhesion complexes to the actin cytoskeleton, and mechanical load strengthens its bindin

85 ssion of nephrin, significant podocyte actin cytoskeleton, and motility changes.

86 a feedback mechanism between the cell cycle, cytoskeleton, and ROP.

87 larly-polarized-light-dependent force on the cytoskeleton, and that the light-induced periodic mechan

88 n the organization and dynamics of the actin cytoskeleton, and the small, monomeric GTPases Rac and R

89 otic cells, the interactions between GTPase, cytoskeletons, and molecular motors initiate spontaneous

90 KEAP1-binding protein that maintained actin cytoskeleton architecture and helped KEAP1 to sequester

91 teractions that bridge the nucleoskeleton to cytoskeleton are poorly understood in the cardiomyocyte,

92 Cytoskeletons are self-organized networks based on polym

93 These cups are formed by the actin cytoskeleton around signaling patches of Ras, Rac and th

94 tor ribbon synaptic structure depends on the cytoskeleton arrangement, both at the active zone-relate

95 echanical models commonly describe the actin cytoskeleton as a contractile isotropic incompressible m

96 The MreB actin-like cytoskeleton assembles into dynamic polymers that coordi

97 eated is essential for understanding how the cytoskeleton assembles.

98 Activity-regulated cytoskeleton-associated protein (Arc) was identified as

99 trophic factor (Bdnf) and activity-regulated cytoskeleton-associated protein (Arc).

100 transitions in the RPE by targeting Ezrin, a cytoskeleton-associated protein essential for the regula

101 ynergistic decrease of actin and microtubule cytoskeleton-associated proteins in both control and LIV

102 ic and cell biological studies, we suggest a cytoskeleton-based mechanism likely underpins these obse

103 induce mitotic arrest through a microtubule cytoskeleton-based mechanism.

104 Remarkably, impairments in cytoskeleton-based protein-transport systems often under

105 tracellular environment, we observe that the cytoskeleton becomes fluid-like.

106 tin-binding proteins that modulate the actin cytoskeleton both directly, via F-actin bundling, and in

107 pushing and pulling activities of the actin cytoskeleton, but migration directionality is largely co

108 depend on forces applied by the T cell actin cytoskeleton, but until recently, the underlying mechani

109 late the dynamics and functions of the actin cytoskeleton by forming long chains along the two strand

110 ule that regulates the dynamics of the actin cytoskeleton by transmitting signals from the plasma mem

111 Upon disruption of the actin cytoskeleton by treatment of the cells with latrunculin

112 plasma membrane and an intermediate filament cytoskeleton called the inner-membrane complex (IMC).

113 This work reveals how the actin cytoskeleton can be harnessed to overcome energetic barr

114 The actin cytoskeleton can regulate neurotransmitter receptors and

115 ein MreB at the inner membrane into a sturdy cytoskeleton capable of transforming spherical liposomes

116 To understand how the cytoskeleton caters to these different demands, this rev

117 edgehog signaling, pointing to a key role in cytoskeleton-cilia interdependency.

118 mbly of the linker of the nucleoskeleton and cytoskeleton complex, a heteroprotein complex composed o

119 such as the linker of the nucleoskeleton and cytoskeleton complex, are formed by heterotypic interact

120 nent of a plant Linker of Nucleoskeleton and Cytoskeleton complex, associates with F-actin and is, al

121 protein of the linker of nucleoskeleton and cytoskeleton complex.

122 that RePRP interacts with the highly ordered cytoskeleton components actin and tubulin both in vivo a

123 ng makers for odontoblastic differentiation, cytoskeleton components and growth factors.

124 ll number, with local disorganization of the cytoskeleton components F-actin and pMLC2.

125 le proteins, endo- and exocytosis cofactors, cytoskeleton components, and trafficking proteins.

126 the molecular-motor-driven motion of the MT cytoskeleton confined between plasma membrane and nucleu

127 The actin cytoskeleton consists of structurally and biochemically

128 aggregates were also associated with severe cytoskeleton damage, rapid internalization inside the ne

129 multiple cell lines with varying degrees of cytoskeleton disruption and during the EMT.

130 DC, cellular components other than the actin cytoskeleton dominate the response.

131 The actin cytoskeleton drives cell motility and is essential for n

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

133 Using latrunculin A to depolymerize the cytoskeleton during endocrine induction, we developed a

134 of MTs by motors and the load acting on this cytoskeleton during growth.

135 cell polarity (PCP) proteins, which regulate cytoskeleton dynamics and appear necessary for some axon

136 The RhoA/ROCK-mediated actin cytoskeleton dynamics have been implicated in adipogenes

137 ical network of activators and repressors of cytoskeleton dynamics have been invoked to explain these

138 LF1 protein, with affected genes involved in cytoskeleton dynamics, membrane dynamics, RNA processing

139 e experimentally observed features of the MT cytoskeleton dynamics.

140 aminin-1 and fibronectin, suggesting altered cytoskeleton dynamics.

141 or pore formation, pore characteristics, and cytoskeleton effects were studied.

142 ty to anchor the highly elastic and tough IF cytoskeleton endowed vertebrates with robust tissues cap

143 The septin cytoskeleton exhibits a number of critical cellular func

144 Microtubule cytoskeleton exists in various biochemical forms in diff

145 e physiological tethering to the surrounding cytoskeleton, extracellular matrix and cells, and tissue

146 airs MYH7-mediated, AMPK-dependent sarcomere-cytoskeleton filament interactions and plasma membrane a

147 der mechanism, regulating the highly ordered cytoskeleton for development of "short-but-heavy" roots

148 SARS-CoV-2 reorganizes the host cytoskeleton for efficient cell entry and controls host

149 ombined, our results suggest that the septin cytoskeleton forms a diffusive barrier around nascent po

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

151 repositioning due to an interplay between MT cytoskeleton geometry and motor forces and confirms the

152 though it is well known that the microtubule cytoskeleton has a central role in establishing neuronal

153 Although the actomyosin cytoskeleton has been implicated in clathrin-mediated en

154 inflamed and fibrotic tissues; however, the cytoskeleton has not been adequately explored as a thera

155 the assembly and maintenance of apicomplexan cytoskeletons, illuminating how they template and orient

156 derlie the distinctive development of the MT cytoskeleton in axons and dendrites: the cross-linking l

157 hese data draw a link between NMDARs and the cytoskeleton in brain endothelial cells that regulates B

158 little is known about the role of the septin cytoskeleton in inflammation.

159 orally precise modulation of the microtubule cytoskeleton in living cells, and promise new possibilit

160 members preferentially localize to the actin cytoskeleton in mechanically stimulated cells through th

161 omote organelle accumulation at the cortical cytoskeleton in normal mammary epithelial cells.

162 romolecular structures inside liposomes, the cytoskeleton in particular, stands as a central limitati

163 estigate the role of [Ca(2+) ] and the actin cytoskeleton in podocytes, we used a double fluorescent

164 oenvironments, whereas the resistance of the cytoskeleton in response to mechanical cues enables the

165 ial loss of the ability to reorganize the MT cytoskeleton in response to rhizobia, which might rely o

166 n this work, we probed the role of the actin cytoskeleton in the dynamics, ligand binding, and signal

167 es direct polarized growth by regulating the cytoskeleton in time and space and could play similar ro

168 in the coordination between the MT and actin cytoskeletons in growth cones (GCs) during axon guidance

169 ry to the final organization of actin and MT cytoskeletons in single plant cells of Arabidopsis thali

170 of fibroblasts induces changes in the actin cytoskeleton including stress fiber (SF) reinforcement a

171 planar polarization of the hair cell apical cytoskeleton, including the kinocilium and the V-shaped

172 Results show that the presence of the cytoskeleton increases the critical strain of pore forma

173 stigate whether Rac1 depletion disrupted the cytoskeleton-integrin linkage, allowing for cross-model

174 It has structural homology to a cytoskeleton-interacting protein and accumulates at the

175 l therapeutic direction targeting sarcomere- cytoskeleton interactions to induce sarcomere re-organiz

176 The membrane-cytoskeleton interface plays a crucial role in junctiona

177 The actin cytoskeleton is a dynamic array of filaments that underg

178 The dynamic rearrangement of the actin cytoskeleton is an essential component of many mechanotr

179 Remodeling of the intracellular cytoskeleton is critical for cell activation in inflamed

180 w the hydrogel regulates cellular behaviors: cytoskeleton is deformed, cell tentacles are significant

181 ing the initial stages of cell division, the cytoskeleton is extensively reorganized so that a bipola

182 The actin cytoskeleton is of profound importance to cell shape, di

183 ttened under load and lose volume; the actin cytoskeleton is reorganized, with myosin II recruited to

184 The actin cytoskeleton is required for cell expansion and implicat

185 f small GTPases and a regulator of the actin cytoskeleton, is critical for the normal development and

186 kage of paranodal proteins to the underlying cytoskeleton likely contributes to this diffusion barrie

187 ed that Linkers of the Nucleoskeleton to the Cytoskeleton (LINC complexes) are essential for the apic

188 es via the linkers of the nucleoskeleton and cytoskeleton (LINC) complex, which couples the cytoskele

189 ciated with the linker of nucleoskeleton and cytoskeleton (LINC) complex.

190 ton through the Linker of Nucleoskeleton and Cytoskeleton (LINC) complex.

191 amins form Linkers of the Nucleoskeleton and Cytoskeleton (LINC) complexes aligned with actin SFs.

192 Linker of nucleoskeleton and cytoskeleton (LINC) complexes are molecular tethers that

193 Key proteins in the integrin-cytoskeleton linkage are reduced in haemodialysis patien

194 Key proteins in the integrin-cytoskeleton linkage are reduced in MHD patients, sugges

195 xpression of genes involved in microtubules, cytoskeleton linkages, and motor activity.

196 ressibility because the water content of the cytoskeleton may change.

197 These findings suggest the MT cytoskeleton may negatively regulate GSIS by both limiti

198 d nanoclustering of signaling components and cytoskeleton-mediated positive feedback that reinforces

199 t of a complex dynamic interplay between the cytoskeleton, molecular motors, signaling molecules, and

200 for zinc and copper in the modulation of the cytoskeleton morphology in dendrites, a mechanism associ

201 iotemporal evolution of MTOC position and MT cytoskeleton morphology with experimental observations.

202 endoplasmic reticulum (ER) are driven by the cytoskeleton motor machinery as well as the action of ER

203 regulation proteins, glycolytic enzymes, and cytoskeleton/motor proteins, but the core germ plasm pro

204 ls transmitted through the cytoplasmic actin cytoskeleton must be relayed to the nucleus to control g

205 Mechanical instabilities in the active cytoskeleton network and feedback loops in the biochemic

206 and a simplified mechanical model for actin cytoskeleton network competition.

207 in reset, or CaAR-that reorganizes the actin cytoskeleton of mammalian cells in response to calcium i

208 ut their collective function in the dense MT cytoskeleton of neurites remains elusive.

209 The microtubule cytoskeleton of pancreatic islet beta-cells regulates gl

210 oskeleton, which are opposed by the cortical cytoskeleton of the interacting antigen-presenting cell.

211 ll priming involves a tug-of-war between the cytoskeletons of the T cell and the APC, where the actin

212 lecules on one side and connect to the actin cytoskeleton on the other [7].

213 ive, although we do not explicitly model the cytoskeleton or resulting cell morphologies, these resul

214 tion and proliferation (ggnb2, mod5, rergl), cytoskeleton organization (k1C18, mtpn), gonad developme

215 suggest that CPK3 is a missing link between cytoskeleton organization, pattern-triggered immunity an

216 processes related to muscle contraction and cytoskeleton organization.

217 affecting cell motility, cell adhesion, and cytoskeleton organization.

218 atient-derived GBM cells by modulating actin cytoskeleton pathway.

219 se, extracellular matrix, focal adhesion and cytoskeleton pathways.

220 ow the critical role [Ca(2+) ] and the actin cytoskeleton play in podocyte homeostasis.

221 The actin cytoskeleton plays a variety of roles in eukaryotic cell

222 The actin cytoskeleton plays an important role in numerous key bio

223 The microtubule cytoskeleton plays critically important roles in numerou

224 immune pathways, including modulation of the cytoskeleton, production and maturation of cytokines, an

225 on of the long isoform of a single gene, the cytoskeleton protein Ankyrin.

226 gent pathways, including pyrin and the actin cytoskeleton, protein misfolding and cellular stress, NF

227 ation causes a decrease in the expression of cytoskeleton proteins in dendrites and spines.

228 on and evolution of dynein compared to other cytoskeleton proteins such as actin, myosin, and tubulin

229 t were accompanied by increased adhesion and cytoskeleton re-arrangement, indicating the possibility

230 over, CD44 clustering by Gal-9 may influence cytoskeleton rearrangement and coclustering of CD3, whic

231 at reduces nephrin expression, causing actin cytoskeleton rearrangement.

232 Oligodendrocyte myelination depends on actin cytoskeleton rearrangement.

233 ment and regeneration, via Hippo pathway and cytoskeleton regulation.

234 dysregulated expressions of cytoskeletal and cytoskeleton-regulatory proteins in tumor progression, w

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

236 However, the actin cytoskeleton remained intact, suggesting that the traffi

237 res as well as pathway networks that include cytoskeleton remodeling and antigen presentation may con

238 Actin cytoskeleton remodeling in spines is a key element of th

239 w intracellular forces by inducing a drastic cytoskeleton remodeling, in response to signaling molecu

240 y suggest that microRNAs (miR-24-4, miR-21), cytoskeleton remodeling, response to stimuli, and inflam

241 y, involved in the regulation of endothelial cytoskeleton remodeling, was also significantly altered

242 ivating the GTPase RAC1 and modulating actin cytoskeleton remodeling.

243 f cell morphology, cell migration, and actin cytoskeleton remodeling.

244 testis, supporting a role for this kinase in cytoskeleton remodeling.

245 rocesses, including protein quality control, cytoskeleton remodelling and membrane dynamics.

246 cytoskeleton, acute depolymerization of the cytoskeleton removed ROP from the membrane only in recen

247 adjustments of cell shape directed by actin-cytoskeleton reorganization via their respective RhoGEF

248 ed Rac1, a small GTPase widely implicated in cytoskeleton reorganization, cell motility, and metastat

249 1) - was considered to precede auxin-induced cytoskeleton reorganization.

250 re prime reagents for studies in microtubule cytoskeleton research, being applicable across a range o

251 resolution imaging shows that whereas the MT cytoskeleton resembles a random meshwork in the cells' i

252 Short-term actin cytoskeleton response to auxin requires AUX1 and/or cyto

253 Previous studies examined long-term actin cytoskeleton responses to auxin, but plants respond to a

254 llular pathways, including kinase signaling, cytoskeleton, RNA splicing, DNA repair, and nuclear lami

255 The microtubule cytoskeleton serves as a dynamic structural framework fo

256 s of the T cell and the APC, where the actin cytoskeleton serves as a mechanical intermediate that in

257 eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for or

258 instances mostly focused on DNA damage, the cytoskeleton, SH2-binding phosphotyrosine motifs and mot

259 or pharmacologic stabilization of the septin cytoskeleton significantly inhibited NK cell cytotoxicit

260 s and that conditions favoring a polymerized cytoskeleton strongly inhibited neurogenin 3-induced end

261 proteins involved in regulation of the actin cytoskeleton, such as ARPC2 and WASF1/WAVE1, and presyna

262 In contrast to most other cytoskeleton systems, few MreB-interacting proteins have

263 r force has a profound effect on cell shape, cytoskeleton tension, and cell proliferation through the

264 but also reveals STXBP4 as a player in actin cytoskeleton tension-mediated Hippo pathway regulation.

265 it YAP, a process that is regulated by actin cytoskeleton tension.

266 ratins are the first major components of the cytoskeleton that display prominent cell-to-cell variabi

267 on invadopodia, important extensions of the cytoskeleton that initiate degradation of the basement m

268 shPAB) were characterized by a disorganized cytoskeleton that lacked polarization.

269 ) are essential components of the eukaryotic cytoskeleton that serve as "highways" for intracellular

270 midcell by a dedicated magnetosome-specific cytoskeleton, the "magnetoskeleton." However, how magnet

271 is located in three distinct regions of the cytoskeleton: the base of the flagellum, the subpellicul

272 lular vesicular trafficking and of the actin cytoskeleton, their modifications by bacterial pathogens

273 ns through its effector PAK1 and the tubulin cytoskeleton, thereby enhancing migration and intravasat

274 AVIL regulates the cytoskeleton through modulating F-actin, while mutants d

275 The cortical microtubule cytoskeleton thus may provide a platform to coordinate t

276 to architectural features of the actomyosin cytoskeleton, thus coupling cell metabolism to the mecha

277 lls rely on both signaling modules and actin cytoskeleton to break symmetry and achieve a stable pola

278 by which Dyn2 regulates changes in the actin cytoskeleton to drive cell migration are still unclear.

279 of interacting with Rab11 but might assemble cytoskeleton to facilitate cadherin exocytosis.

280 inal p27 phosphorylation, which disrupts the cytoskeleton to increase cell motility and metastasis.

281 Phagocytes use their actomyosin cytoskeleton to migrate as well as to probe their enviro

282 ding how cytoplasmic signaling modulates the cytoskeleton to produce directed growth cone motility.

283 tand how cytoplasmic signaling modulates the cytoskeleton to produce directed growth cone motility.

284 oupling the intracellular force of the actin cytoskeleton to the environment.

285 toskeleton (LINC) complex, which couples the cytoskeleton to the nuclear lamina and associated chroma

286 ught to regulate force transmission from the cytoskeleton to the nucleus.

287 retion, cell polarity, cell junction, cilia, cytoskeleton, vesicular trafficking, and regulation of b

288 ave revealed many proteins that regulate the cytoskeleton, vesicular transport, and physiology of the

289 This complex is linked to the actin cytoskeleton via a bispecific interaction with an exon 1

290 LIM1) or impeded interactions with the actin cytoskeleton via alpha-actinin (DeltaABD) abrogated migr

291 ical roles in linking membranes to the actin cytoskeleton via direct binding to acidic lipids.

292 inct motifs, and with the cell shape-related cytoskeleton via MreB.

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

294 anslational motion of the cargo in a 3D cell cytoskeleton was obtained.

295 involves forces exerted by the T cell actin cytoskeleton, which are opposed by the cortical cytoskel

296 morphology is determined in part through the cytoskeleton, which connects to the nucleoskeleton throu

297 t of components: small GTPases and the actin cytoskeleton, which implies that the mechanisms downstre

298 athways and can function in the absence of a cytoskeleton, while in keratocytes, it is tightly connec

299 opharmacology targeting the ubiquitous actin cytoskeleton with precision control in the micrometer ra

300 vers certain synaptic proteins via the actin cytoskeleton within the Rab11-related domain of slow rec