ライフサイエンスコーパス: cytoskeletal

1 r FOXC1, in addition to FOXC2, in regulating cytoskeletal activity in lymphatic valves.

2 inated cell-cell junctions and multicellular cytoskeletal activity.

3 ed nuclear shape fluctuations in response to cytoskeletal activity.

4 cale and into the mechanisms governing rapid cytoskeletal adaptation to environmental changes.

5 he best studied apicomplexans; however, many cytoskeletal adaptations are broadly conserved and preda

6 ial role played by lamin-chromatin and lamin-cytoskeletal alterations in determining nuclear shape mo

7 iven the role of dysregulated expressions of cytoskeletal and cytoskeleton-regulatory proteins in tum

8 We apply this system to regulate cytoskeletal and enzymatic functions of two non-tagged e

9 TRIM9 and TRIM67 interact with cytoskeletal and exocytic proteins, but the full interac

10 However, they did not enable cytoskeletal and fibroblast polarization; elastomers wit

11 Cell shape is regulated by cell adhesion and cytoskeletal and membrane dynamics.

12 distances, we inferred that duplications in cytoskeletal and membrane-trafficking families were amon

13 ciency in mice downregulates CCN1 and alters cytoskeletal and mitogenic gene expression.

14 lso applied it to light microscopy images of cytoskeletal and nucleoskeletal networks.

15 smic domains and mediating interactions with cytoskeletal and signaling proteins.

16 the nucleus, which, together with long-term cytoskeletal and supracellular rearrangements, protects

17 stinct regulatory mechanisms control F-actin cytoskeletal and/or membrane maintenance in post-organel

18 ) modified expression of host mitochondrial, cytoskeletal, and innate immunity genes.

19 th haemodynamic phenotypes and regulation of cytoskeletal arborization(3,4).

20 in are highly dynamic and dependent on local cytoskeletal architecture in cells in both 2D and 3D env

21 RHO GTPases are key regulators of the cytoskeletal architecture, which impact a broad range of

22 Myofibrils are huge cytoskeletal assemblies embedded in the cytosol of muscl

23 tactin, and the formin mDia2, regulates both cytoskeletal assembly and stability.

24 cal pathways, including (i) glycolysis, (ii) cytoskeletal assembly and/or signaling, and (iii) NF-kap

25 f drugs targeting the motor-clutch system or cytoskeletal assembly.

26 c finger 268 (zif268) and activity regulated cytoskeletal-associated protein (Arc) immediate-early ge

27 idation is via effects on activity-regulated cytoskeletal-associated protein (ARC) in downstream brai

28 The cellular localization and the cytoskeletal association of Scrib and Lgl1 are interdepe

29 Cytoskeletal-bound HYAL2 functions as a key regulator of

30 haracterized internal dynamical processes in cytoskeletal bundles: filament assembly and disassembly,

31 acrophages, associated with a RhoA-dependent cytoskeletal change, an increase in cell motility, and g

32 , our data reveal that maturation-associated cytoskeletal changes alter the biophysical properties of

33 pinocytosis in vitro and in vivo by inducing cytoskeletal changes in macrophages.

34 est that microtubule dynamics coordinate the cytoskeletal changes required for wound repair and the c

35 do not fully account for the rapid platelet cytoskeletal changes that occur in blood flow.

36 organization, a phosphoproteome enriched for cytoskeletal changes, with reduced phosphocofilin and in

37 ls expressing IgLON5 abrogated the indicated cytoskeletal changes.

38 human IECs, we demonstrated that ACD-induced cytoskeletal collapse activated extracellular signal-reg

39 is process, the function of septins, another cytoskeletal component that associates with actin and mi

40 uronal Phactr1/PP1 substrates, which include cytoskeletal components and regulators.

41 d CD44-mediated adhesion, where adhesive and cytoskeletal components are mechanistically coupled by a

42 ontractility, but how it is coupled to other cytoskeletal components is poorly understood.

43 n explore the contributions from the various cytoskeletal components of the axon to show that the rec

44 Septins are increasingly recognized as novel cytoskeletal components, but details on their regulation

45 Two major cytoskeletal components, microtubules and actin filament

46 CMs, YAP interacts with nuclear-envelope and cytoskeletal components, reflecting an altered mechanica

47 erface between the two structurally distinct cytoskeletal components.

48 ll, we unravel the function of a prokaryotic cytoskeletal constituent that is widespread in magnetic

49 n of neural stem cells (NSCs) by suppressing cytoskeletal contractility.

50 tability via Rac1/Rho-mediated regulation of cytoskeletal contractility.

51 The plasma membrane and the underlying cytoskeletal cortex constitute active platforms for a va

52 ate the localization, strength, duration and cytoskeletal coupling of receptor interactions governing

53 Rudhira depletion impairs cytoskeletal cross-talk, MT stability, and hence focal a

54 disc respond to loss of Short stop (Shot), a cytoskeletal crosslinking spectraplakin protein that we

55 at EB1-APC interactions govern bidirectional cytoskeletal crosstalk by coordinating microtubule and a

56 hen its integrity becomes compromised during cytoskeletal damage and stress by reducing For3 levels.

57 c model that is indicative of nucleoskeletal-cytoskeletal decoupling under high load.

58 unc-87 mutation caused cytoskeletal defects in the body wall muscle and somatic

59 Tdrd7-/- lens precedes cataract, suggesting cytoskeletal defects may contribute to Tdrd7-/- cataract

60 f neddylation in developing neurons leads to cytoskeletal defects, altered actin dynamics and neurite

61 analytically and explore the effect of local cytoskeletal density change.

62 leton should be attracted to regions of high cytoskeletal density, while objects that are smaller tha

63 Here, we describe the cytoskeletal determinant CcfM (curvature-inducing coiled

64 es strongly suggest a role for Myo2 in actin cytoskeletal disassembly and turnover in vivo, and that

65 Cytoskeletal disorganizations were observed starting at

66 y immobile, and its motility was enhanced by cytoskeletal disruption.

67 ion of plexins and semaphorins in regulating cytoskeletal dynamics and cell adhesion that predates th

68 s, some of which are known to regulate actin cytoskeletal dynamics and contractility.

69 NCKAP1/NAP1 regulates neuronal cytoskeletal dynamics and is essential for neuronal diff

70 e in keratocytes, it is tightly connected to cytoskeletal dynamics and mechanics.

71 of shear flow sensing, calcium homeostasis, cytoskeletal dynamics and pressure-dependent outflow sug

72 We show that Tao kinase activity regulates cytoskeletal dynamics and sensory channel localization r

73 The control of cytoskeletal dynamics by dedicator of cytokinesis 2 (DOC

74 unique framework to probe cell migration and cytoskeletal dynamics in a standardized manner.

75 between PTEN and WAVE-Arp2/3-regulated actin cytoskeletal dynamics in epithelial morphogenesis.

76 HDAC6 regulates cytoskeletal dynamics to promote tumor cell migration an

77 invasion of filopodia by MTs, orchestrating cytoskeletal dynamics toward axonal growth.

78 ight control of dendritic growth, branching, cytoskeletal dynamics, and ion channel expression to ens

79 of essential cell processes, including actin cytoskeletal dynamics, by coactivating serum response fa

80 We show that Tao kinase regulates cytoskeletal dynamics, controls sensory ion channel loca

81 , these data demonstrate that Dyn2 regulates cytoskeletal dynamics, in part, by interacting with the

82 volved in various cellular processes such as cytoskeletal dynamics, transcription, and cell cycle pro

83 lated to cellular clearance, metabolism, and cytoskeletal dynamics.

84 n in active gel theories that describe actin cytoskeletal dynamics.

85 ation, a modification with a major impact on cytoskeletal dynamics.

86 immune dysfunction in MKL1 deficiency, with cytoskeletal dysfunction and defective extravasation of

87 NTNAP4/Neurexin-IV (Nrx-IV) and the membrane cytoskeletal effector Adducin/Hu-li tai shao (Hts) as pr

88 nock-out mouse model and determined that the cytoskeletal effector FMNL1 is selectively required for

89 Little is known about the specific role of cytoskeletal effectors that mediate mechanical forces an

90 a negative feedback loop among RhoA and its cytoskeletal effectors to inhibit contractility.

91 hese with the retraction of the membrane and cytoskeletal elements impacted by calcium signaling.

92 d with enlarged compartments and filamentous cytoskeletal elements in the CIH group was less than the

93 endosomal-lysosomal and autophagy pathways, cytoskeletal elements, AD-related genes, ionotropic and

94 ate filaments, the strongest and most stable cytoskeletal elements, are not known to directly partici

95 , docked at precisely spaced intervals along cytoskeletal elements, promoted phase partitioning of ca

96 omposed of secretory organelles and specific cytoskeletal elements.

97 Cytoskeletal events and signalling pathways potentially

98 arious systems including bacterial colonies, cytoskeletal extracts, or shaken granular media.

99 rate protrusion, has similar width range and cytoskeletal features but makes contact with the substra

100 ecludes simple diffusion through the mesh of cytoskeletal fibers.

101 nanoparticles are entangled with the cells' cytoskeletal fibres.

102 ial force directions, thus stabilizing those cytoskeletal filament architectures that result in shear

103 Thus, our multiscale modeling correlates cytoskeletal filament size with conformational changes i

104 of taking several consecutive steps along a cytoskeletal filament.

105 Bundles of cytoskeletal filaments and molecular motors generate mot

106 The architecture and connectivity of cytoskeletal filaments change in response to mechanical

107 ns are small beta-helical proteins that form cytoskeletal filaments in a range of bacteria.

108 cts that depends on the local density of the cytoskeletal filaments on which motors operate.

109 cell nucleus can be moved or reorganized by cytoskeletal filaments under various conditions (for exa

110 eins kinesin and myosin and their associated cytoskeletal filaments, we review recent work aiming for

111 es and co-assemble into hetero-oligomers and cytoskeletal filaments.

112 ranging from metabolism to the nucleation of cytoskeletal filaments.

113 f root hairs, including the rearrangement of cytoskeletal filaments.

114 molecular clutch, which couples integrins to cytoskeletal forces to drive particle engulfment.

115 We uncover an unexpected versatility in cytoskeletal form that may prompt a significant developm

116 ulate monomeric G-protein function and alter cytoskeletal function.

117 C), a protein with both tumor suppressor and cytoskeletal functions, concentrates at the microtubule-

118 , transcription, mitochondrial activity, and cytoskeletal functions.

119 oblasts exhibit reduced DNA damage, enhanced cytoskeletal gene expression, and actomyosin contractili

120 hanced expression of ECM, focal adhesion and cytoskeletal genes and suppression of many adipocyte pro

121 Transcripts from 58 of 106 cytoskeletal genes studied increased or decreased more t

122 cardiac muscle developmental/contractile and cytoskeletal genes, highlighting key regulation processe

123 ly overlaps with UNC-87 in maintaining actin cytoskeletal integrity in vivo and has both common and d

124 Objective: Here, we sought to determine how cytoskeletal interactions with the LINC complex regulate

125 on force transmission through the essential cytoskeletal linker talin.

126 disrupt tensed F-actin binding in vitro and cytoskeletal localization in cells, demonstrating a comm

127 levation of stress-responsive chaperones for cytoskeletal maintenance in post-nuclear degradation len

128 HSPB1 functions in cytoskeletal maintenance, and its reduction in Tdrd7-/-

129 n't change the expression levels of neuronal cytoskeletal marker beta3-tubulin and synaptic marker po

130 We suggest that poor cytoskeletal mechanical features are caused by altered e

131 chemical signaling with membrane tension and cytoskeletal mechanics to show how signaling events are

132 nuclear integrity, protein trafficking, and cytoskeletal-microtubule organization, leading to cell c

133 lysis identified the molecular chaperone and cytoskeletal modulator, HSPB1, among high-priority downr

134 Cytoplasmic dynein is the most complex cytoskeletal motor protein and is responsible for numero

135 The ability of cytoskeletal motors to move unidirectionally along filam

136 y shows that a Cdc42-dependent supracellular cytoskeletal network provides a scaffold integrating loc

137 ynamics and mechanical strength of the actin cytoskeletal network.

138 trafficking vesicular cargo within a dynamic cytoskeletal network.

139 real-time mechanical adaptation of the actin cytoskeletal network.

140 tudy highlights crucial interactions between cytoskeletal networks during cell division.

141 Thus, we show the potential contribution of cytoskeletal networks in the transmission of prion propa

142 Intermediate filament (IF) cytoskeletal networks simultaneously support mechanical

143 erformed computational simulations of active cytoskeletal networks under an external tensile force.

144 th cone morphology require rearrangements of cytoskeletal networks, and changes in microtubules and a

145 curs through the action of molecular motors, cytoskeletal networks, and the nucleus.

146 A new study reveals the role of distinct cytoskeletal networks, both guided by the polarity facto

147 th cone morphology require rearrangements of cytoskeletal networks, but the roles of intermediate fil

148 e development and disassembly of local actin cytoskeletal networks.

149 Microscopy images of cytoskeletal, nucleoskeletal and other structures contai

150 ions in the coupling of the lamin shell with cytoskeletal or chromatin tethers as well as with polyco

151 ROCK inhibition rescued cytoskeletal or junctional integrity changes induced by

152 cular motors are known to be responsible for cytoskeletal ordering and force generation, but their co

153 heir effects on microtubule (MT) and F-actin cytoskeletal organization across the epithelium.

154 lular processes such as signal transduction, cytoskeletal organization and cell polarity, cell prolif

155 t their silencing was accompanied by altered cytoskeletal organization and induction of ciliation, wh

156 hosphorylation of ADF4 by CPK3 governs actin cytoskeletal organization associated with pattern-trigge

157 Furthermore, cytoskeletal organization has to adapt to axons of drama

158 t other cell-surface antibodies, disrupt the cytoskeletal organization in cultured rat hippocampal ne

159 ls their complex structures, with a focus on cytoskeletal organization in free-living cells, ciliates

160 lular geometry contributes to the control of cytoskeletal organization in living plant cells.

161 e NC1-peptide-mediated disruptive effects on cytoskeletal organization in Sertoli cell epithelium and

162 enes and underscore the importance of proper cytoskeletal organization in tissue homeostasis.

163 Effects on cell migration, invasion, and cytoskeletal organization in vitro were tested in high-A

164 A polarized cytoskeletal organization is typical for muscle cells, b

165 oorly understood in the cardiomyocyte, where cytoskeletal organization is unique.

166 e developing human cortex by maintaining the cytoskeletal organization of oRG cells and the radial gl

167 n important role for Tao kinase signaling in cytoskeletal organization to maintain proper dendritic a

168 phages exhibited marked differences in actin cytoskeletal organization, a phosphoproteome enriched fo

169 mediate proximal T cell receptor signaling, cytoskeletal organization, and immune synapse formation.

170 To investigate how cell shape, cytoskeletal organization, and molecular motors cross-ta

171 n ECM stiffness can modulate the morphology, cytoskeletal organization, and subcellular pattern of fo

172 in the regulation of vesicular trafficking, cytoskeletal organization, autophagy, and metabolism.

173 unctional terms related to cell division and cytoskeletal organization, which were also enriched for

174 tablished that cell shape can also influence cytoskeletal organization.

175 cular smooth muscle cell stiffness and actin cytoskeletal orientation in response to statin-mediated

176 n remodels total vascular smooth muscle cell cytoskeletal orientation that may additionally participa

177 n force (-40.1%) were lowered and VSMC actin cytoskeletal orientation was reduced (-24.5%) following

178 proteins and regulate cellular stiffness and cytoskeletal orientation, thus impacting the biomechanic

179 proteins and regulate cellular stiffness and cytoskeletal orientation, thus impacting the biomechanic

180 spatial cue to coordinate cell polarity and cytoskeletal oscillation.

181 oss tissues and robust to nucleoskeletal and cytoskeletal perturbations, but it required intact linke

182 system for studying microtubule-independent cytoskeletal phenotypes.

183 ts as a scaffold for signaling complexes and cytoskeletal-plasma membrane interactions.

184 Neurofilaments are abundant space-filling cytoskeletal polymers in axons that are transported alon

185 ling and severing of microtubules, which are cytoskeletal polymers of tubulin subunits.

186 Microtubules are cytoskeletal polymers whose function depends on their pr

187 The actin fold is found in cytoskeletal polymers, chaperones, and various metabolic

188 ultrastructure that is distinct from that of cytoskeletal polymers.

189 the behavior of microtubules (MTs) and other cytoskeletal polymers.

190 that a NUAK2-Hippo signaling axis regulates cytoskeletal processes that govern cell shape during neu

191 The cytoskeletal protein actin polymerizes into filaments th

192 Synapses are enriched in the cytoskeletal protein actin, which determines the shape o

193 ational folding of adjacent domains from the cytoskeletal protein alpha-spectrin using force profile

194 mplicated a role for gamma-adducin (ADD3), a cytoskeletal protein encoded by Add3.

195 otein (MAP) 2 has been perceived as a static cytoskeletal protein enriched in neuronal dendritic shaf

196 eterooligomeric complex required for de novo cytoskeletal protein folding.

197 SPECC1L dosage and function and that SPECC1L cytoskeletal protein functions downstream of IRF6 in pal

198 s in Leishmania mexicana have identified the cytoskeletal protein KHARON as being important for both

199 in-4 (ACTN4)-an important actin crosslinking cytoskeletal protein that provides structural support fo

200 force generators is likely prevented by the cytoskeletal protein titin that connects the thick filam

201 Although neutrophils express the cytoskeletal protein vinculin, they do not form mature f

202 enesis proteins that are linked to a dynamic cytoskeletal protein, either the actin-like MreB or the

203 How then does a non-cytoskeletal protein, SpmX, define and constrain PG synt

204 Sarcomeric (myosin) and cytoskeletal proteins (desmin, tubulin) also underwent 4

205 s are caused by altered expression levels of cytoskeletal proteins and contribute to muscle wasting a

206 Strikingly, cytoskeletal proteins and enzymes involved in energy met

207 All4981 interacts with known cytoskeletal proteins and is indispensable for Anabaena

208 Cytoskeletal proteins and post-translational modificatio

209 protein-protein interaction modules found in cytoskeletal proteins and transcriptional regulators.

210 Metabolic, mitochondrial, sarcomeric, and cytoskeletal proteins are susceptible to 4HNE-adduction

211 Cytoskeletal proteins are well conserved between animal

212 The actin family of cytoskeletal proteins is essential to the physiology of

213 usly, we showed that a hierarchy of spectrin cytoskeletal proteins maintains nodal Na(+) channels (Li

214 The F1-F3 FERM subdomains of cytoskeletal proteins resemble a cloverleaf, but in tali

215 Septins are conserved GTP-binding cytoskeletal proteins that polymerize into filaments by

216 nteractions converge on ankyrin and spectrin cytoskeletal proteins to cluster nodal Na(+) channels du

217 rotective heat shock proteins, disruption of cytoskeletal proteins via histone deacetylases, and the

218 f proteins regulating amino acid metabolism, cytoskeletal proteins, and cellular response to stress.

219 l as abnormal expression and localization of cytoskeletal proteins, and loss of intracellular nicotin

220 he actin-binding domains (ABDs) of conserved cytoskeletal proteins, including beta-III-spectrin, alph

221 exists in a complex with a variety of actin cytoskeletal proteins, including paxillin and LPP.

222 In the cytoplasm, acetylation of a number of cytoskeletal proteins, including tubulin, cortactin, and

223 mulatory hydrogels and DCs expressing mutant cytoskeletal proteins, we find that increasing stiffness

224 ls suggested dysregulation of sarcomeric and cytoskeletal proteins.

225 , cell signaling, and metabolism, as well as cytoskeletal proteins.

226 ttachment complexes and on interactions with cytoskeletal proteins.

227 on has been related to pathologies, in which cytoskeletal rearrangement and cell migration are altere

228 that Shb interacts with known modulators of cytoskeletal rearrangement and cell mobility, including

229 Cytoskeletal rearrangement is necessary for NK cell lyti

230 s an important control mechanism for NK cell cytoskeletal rearrangement that is differentially regula

231 egulate multiple cellular processes, such as cytoskeletal rearrangement, cell movement, microtubule d

232 rotein Cdc42 by G(s)-coupled GPCRs, inducing cytoskeletal rearrangements and formation of filopodia-l

233 Molecular motors drive cytoskeletal rearrangements to change cell shape.

234 lux causes adherens junction disassembly and cytoskeletal rearrangements to facilitate endothelial ce

235 t, precisely orchestrated nuclear cleavages, cytoskeletal rearrangements, and directed membrane growt

236 cipates in the regulation of cell migration, cytoskeletal rearrangements, and vesicular trafficking i

237 ordination of lipid messenger signaling with cytoskeletal regulation is central to many organelle-spe

238 steps of epithelial TJ biogenesis and actin cytoskeletal regulation.

239 v) regulation of catalytic activity, and (v) cytoskeletal regulation.

240 lar junctions, cell-matrix interactions, and cytoskeletal regulation.

241 The cytoskeletal regulator Phactr1 is a neuronally enriched

242 The actin cytoskeletal regulator Wiskott Aldrich syndrome protein

243 and demonstrated that activity levels of the cytoskeletal regulators Rac1 and RhoA GTPase regulate th

244 k suggests the possibility of more bacterial cytoskeletal regulators to be found in this class.

245 Candidates included cytoskeletal regulators, cytosolic protein transporters,

246 ransport, including calcium transporters and cytoskeletal regulators, that are associated with the RB

247 ulators of myotube guidance that act through cytoskeletal regulatory proteins to pattern the musculos

248 present multimolecular complexes and contain cytoskeletal, regulatory and scaffolding proteins, which

249 Here we report a complementary process of cytoskeletal relaxation that occurs when cortical contra

250 mechanisms that coordinate auxin signaling, cytoskeletal remodeling and cell expansion are poorly un

251 We show cytoskeletal remodeling and changes in expression and ac

252 interaction between TRPV4 and Rac1 leads to cytoskeletal remodeling and intracellular stiffness gene

253 Cdc42 effectors include proteins involved in cytoskeletal remodeling and kinase-dependent transcripti

254 Rac-GTPases are major regulators of cytoskeletal remodeling and their deregulation contribut

255 d with other cellular signaling cascades and cytoskeletal remodeling to support optimal inclusion dev

256 ar forces, which regulate nucleoskeletal and cytoskeletal remodeling, activate signaling pathways, an

257 llular signaling cascades for host invasion, cytoskeletal remodeling, optimal inclusion development,

258 patterning with molecular-level tracking of cytoskeletal remodeling.

259 of intracellular stiffness and regulation of cytoskeletal remodeling; and (d) TRPV4-Rac1 signaling ax

260 tosis, differentiation and morphogenesis via cytoskeletal remodelling and actomyosin contractility(1-

261 MT)-like regenerative response manifested by cytoskeletal remodelling, junction dissolution, migratio

262 as glucose reabsorption, gluconeogenesis and cytoskeletal remodelling.

263 n formation by single-cells involves complex cytoskeletal remodelling.

264 motility suggest that FASN can mediate actin cytoskeletal remodelling; a process known to be downstre

265 f myelination and axon wrapping by targeting cytoskeletal reorganization and MBP localization to olig

266 line cartilage in vitro via post-contraction cytoskeletal reorganization and structural transformatio

267 e activity-driven expression of proteins and cytoskeletal reorganization at new synapses, requiring p

268 As ELMO1 promotes cytoskeletal reorganization during engulfment, we hypoth

269 Axon guidance cues that stimulate cytoskeletal reorganization within the growth cone direc

270 sociated with inner ear mechanotransduction, cytoskeletal reorganization, myelin development and axon

271 r adaptation is accomplished through dynamic cytoskeletal reorganization.

272 This cytoskeletal scaffold recruits downstream proteins essen

273 These enzymes are spatially controlled by cytoskeletal scaffolding proteins, which both recruit an

274 ombinations of ankyrins, spectrins and other cytoskeletal scaffolding proteins, which cluster ion cha

275 role of the NCKAP1 subunit of the pentameric cytoskeletal SCAR/WAVE complex, a major downstream targe

276 he postnatal lymphatic vasculature and posit cytoskeletal signaling as a therapeutic target in lympha

277 rm, sSORLA, which has been shown to regulate cytoskeletal signaling pathways and cell motility in cel

278 However, the mechanisms that link cytoskeletal signaling to the transcriptional regulatory

279 o control cell viability, cell motility, and cytoskeletal signaling with the high spatial and tempora

280 Importantly, restoring cytoskeletal stability, by actin overexpression, was ben

281 and behaviors including metabolism, growth, cytoskeletal structure and locomotion.

282 nt is directly involved in the regulation of cytoskeletal structure and the maturation of synapses in

283 pts host Rac1 signaling to induce changes in cytoskeletal structure.

284 clusters depend on phosphoinositol pathways, cytoskeletal structures and specific cell-wall component

285 These cytoskeletal structures are able to generate large scale

286 he assembly of actin filaments into distinct cytoskeletal structures plays a critical role in cell ph

287 ccessory binding proteins to different actin cytoskeletal structures through a biophysical feedback l

288 hases in different hosts - rely on elaborate cytoskeletal structures to enable morphogenesis and moti

289 Single-celled protists use elaborate cytoskeletal structures, including arrays of microtubule

290 segregation of multiple flagellum-associated cytoskeletal structures, including the hook complex and

291 roteins that self-assemble into higher order cytoskeletal structures.

292 sidered highly specific for one or the other cytoskeletal system do, in fact, make use of both filame

293 ng between minimally nonlinear signaling and cytoskeletal systems, separately not supporting stable p

294 e that mTOR regulates expression of specific cytoskeletal targets and actin reorganization in oligode

295 n of myelination through regulating specific cytoskeletal targets and cellular process expansion by o

296 nding as a mechanosensing mechanism by which cytoskeletal tension can govern nuclear localization.

297 omotes T-cell synapse symmetry by generating cytoskeletal tension in the plane of the synapse through

298 port initiation rates on the distribution of cytoskeletal tracks and carrier organelles, as well as t

299 s, compatible in magnitude to those found in cytoskeletal transport, can explain the observed magnitu

300 ell activation, WASP is degraded, leading to cytoskeletal unraveling and tension decay, which result