ライフサイエンスコーパス: microtubule cytoskeleton

1 require interaction of the dynamic actin and microtubule cytoskeleton.

2 o the cell surface was mediated by the actin-microtubule cytoskeleton.

3 lin expression to adjust the behavior of the microtubule cytoskeleton.

4 cess involves rebuilding the entire neuronal microtubule cytoskeleton.

5 le hook orientation via interaction with the microtubule cytoskeleton.

6 he other PAR proteins to polarize the oocyte microtubule cytoskeleton.

7 ases, vesicle trafficking, and the actin and microtubule cytoskeleton.

8 s a critical role in the organization of the microtubule cytoskeleton.

9 in regulating the organization of the oocyte microtubule cytoskeleton.

10 ds to marked instability of the radial glial microtubule cytoskeleton.

11 eneoplastic cells may involve changes in the microtubule cytoskeleton.

12 rest, presumably owing to alterations in the microtubule cytoskeleton.

13 rotubules are the signature of the dendritic microtubule cytoskeleton.

14 replace the missing axon by rearranging the microtubule cytoskeleton.

15 ses kinesin motility to maintain a polarized microtubule cytoskeleton.

16 C to promote polarized reorganization of the microtubule cytoskeleton.

17 ery little is known about how they alter the microtubule cytoskeleton.

18 o ensure that the cells entered G1 without a microtubule cytoskeleton.

19 ommunication between the cell cortex and the microtubule cytoskeleton.

20 creased fraction of tubulin to appear in the microtubule cytoskeleton.

21 ealed an association of arginase II with the microtubule cytoskeleton.

22 c reticulum membrane and associates with the microtubule cytoskeleton.

23 g for directed secretion along the polarized microtubule cytoskeleton.

24 t the centrosome and this requires an intact microtubule cytoskeleton.

25 and Dlg1 is required for polarization of the microtubule cytoskeleton.

26 icated in DS and ASDs, as a regulator of the microtubule cytoskeleton.

27 d each involves repolarization of the T-cell microtubule cytoskeleton.

28 ion with the stabilization of the underlying microtubule cytoskeleton.

29 nd manifest disorganization of the root hair microtubule cytoskeleton.

30 and gurken mRNAs and the organization of the microtubule cytoskeleton.

31 SCG10-mediated regulation of the growth cone microtubule cytoskeleton.

32 y natural products to target and perturb the microtubule cytoskeleton.

33 n-mediated signaling and the dynamics of the microtubule cytoskeleton.

34 on of a single flagellum and a subpellicular microtubule cytoskeleton.

35 nt in regulating the complex dynamics of the microtubule cytoskeleton.

36 d RNAs necessary for the polarisation of the microtubule cytoskeleton.

37 and proteins and in the organization of the microtubule cytoskeleton.

38 at G(2)/M with many hallmarks of a defective microtubule cytoskeleton.

39 atory polarity, and centrosomes organize the microtubule cytoskeleton.

40 ated with a local disruption of the synaptic microtubule cytoskeleton.

41 rs as well as the proper organization of the microtubule cytoskeleton.

42 r oocyte markers and the polarisation of the microtubule cytoskeleton.

43 required for normal regulation of the axonal microtubule cytoskeleton.

44 tracellular transport, and regulation of the microtubule cytoskeleton.

45 erexpressed, they associated with the entire microtubule cytoskeleton.

46 ction through the regulation of the synaptic microtubule cytoskeleton.

47 ar processes that are dependent on a dynamic microtubule cytoskeleton.

48 ects specific functional requirements of the microtubule cytoskeleton.

49 gulates the organization and dynamics of the microtubule cytoskeleton.

50 s an important role in the regulation of the microtubule cytoskeleton.

51 y reinforcing their link with the underlying microtubule cytoskeleton.

52 tubulin tyrosination cycle in regulating the microtubule cytoskeleton.

53 llapse of the ER network onto the underlying microtubule cytoskeleton.

54 proteins, and signaling molecules along the microtubule cytoskeleton.

55 at the flows reflect the architecture of the microtubule cytoskeleton.

56 coordinating the remodeling of the actin and microtubule cytoskeleton.

57 dependent on the function of their actin and microtubule cytoskeleton.

58 transport of intracellular cargoes along the microtubule cytoskeleton.

59 correct deployment of the apical complex and microtubule cytoskeleton.

60 is an essential step in the formation of the microtubule cytoskeleton.

61 ciate with the nuclear envelope (NE) and the microtubule cytoskeleton.

62 h associate with membranes and the actin and microtubule cytoskeleton.

63 growth and are independent of the actin and microtubule cytoskeletons.

64 en implicated in regulation of the actin and microtubule cytoskeletons.

65 g maintenance does not require the actin and microtubule cytoskeletons.

66 pendent modulation of the synaptic actin and microtubule cytoskeletons.

67 hanges require the coordination of actin and microtubule cytoskeletons.

68 pupal cells and is mediated by the actin and microtubule cytoskeletons.

69 nd morphogenesis by remodeling the actin and microtubule cytoskeletons.

70 uring meiosis in integrating the F-actin and microtubule cytoskeletons.

71 ace expression required functional actin and microtubule cytoskeletons.

72 cytokinesis, and the regulation of actin and microtubule cytoskeletons.

73 the bud acts as a link between the actin and microtubule cytoskeletons.

74 amics and organization of both the actin and microtubule cytoskeletons.

75 enkorper, respectively, depends on actin and microtubule cytoskeletons.

76 hoA activation, alterations in the actin and microtubule cytoskeleton affecting neuronal morphology,

77 ity at the "wrist" is evident as an impaired microtubule cytoskeleton along the shaft.

78 and the Tea cell-end marker proteins of the microtubule cytoskeleton, along with specific kinesins a

79 larity involves both a reorganization of the microtubule cytoskeleton and a change in tubulin PTMs.

80 nt link between Dnd1, mRNA localization, the microtubule cytoskeleton and axis specification.

81 BMP signaling is also necessary for a normal microtubule cytoskeleton and axonal transport; analysis

82 n hippocampal neurons and then disrupted the microtubule cytoskeleton and caused neuritic degeneratio

83 The centrosome organizes the microtubule cytoskeleton and consists of a pair of centr

84 ive binding sites for both the actin and the microtubule cytoskeleton and could thus mediate crosstal

85 monstrate that disorganization of the T cell microtubule cytoskeleton and defects in hMunc13-4 or Rab

86 couples the membrane fusion machinery to the microtubule cytoskeleton and demonstrate that Munc18-2 a

87 passing the normal requirement for an intact microtubule cytoskeleton and for microtubule-dependent p

88 We also show that the connection between the microtubule cytoskeleton and HIF-1alpha regulation is lo

89 bing and involves disruption to the platelet microtubule cytoskeleton and inflation through fluid ent

90 a mechanistic link between disruption of the microtubule cytoskeleton and inhibition of tumor angioge

91 metric network associated with the polarized microtubule cytoskeleton and is concentrated with transl

92 rotein that interacts with and regulates the microtubule cytoskeleton and is required for neuronal mi

93 The microtubule cytoskeleton and its interacting proteins we

94 presynaptic motoneuron disrupts the synaptic microtubule cytoskeleton and leads to disassembly of the

95 g, which results in local disassembly of the microtubule cytoskeleton and loss of axonal transport in

96 uding disruption of the smooth ER (SER), the microtubule cytoskeleton and mitochondria.

97 As in animal cells, both an intact microtubule cytoskeleton and progression through mitosis

98 ervous system cells sense injury using their microtubule cytoskeleton and respond by dividing to repl

99 arly in the germline for organization of the microtubule cytoskeleton and subsequent oocyte determina

100 ide good evidence that SI signals target the microtubule cytoskeleton and suggest that signal integra

101 Here we show that the microtubule cytoskeleton and the centrosomes follow the

102 sion bodies by a process requiring an intact microtubule cytoskeleton and the cytoplasmic deacetylase

103 a forward genetic screen, we showed that the microtubule cytoskeleton and the JIP3 protein UNC-16 exe

104 In contrast, the microtubule cytoskeleton and the localization of the mic

105 xyloglucan affects both the stability of the microtubule cytoskeleton and the production and patterni

106 h atypical PKC, and that both the acetylated microtubule cytoskeleton and the Vangl2-VAMP1 distributi

107 Both the microtubule cytoskeleton and tubular ER are important fo

108 ere, we examine the interactions between the microtubule cytoskeleton and Wnt/PCP signaling during ze

109 PCP signaling influences the polarity of the microtubule cytoskeleton and, conversely, microtubules a

110 Formin proteins regulate the actin and microtubule cytoskeletons and also control the activity

111 view addresses connections between the actin/microtubule cytoskeletons and organelles in animal cells

112 llular calcium, and intact microfilament and microtubule cytoskeletons and were independent of Rho/Rh

113 (1) They build centrosomes that organize the microtubule cytoskeleton, and (2) they template cilia, m

114 quires sustained calcium influxes, an intact microtubule cytoskeleton, and functional LAT.

115 translational silencing, polarization of the microtubule cytoskeleton, and posterior localization of

116 on is independent of the organisation of the microtubule cytoskeleton, and seems to depend instead on

117 An intact actin and microtubule cytoskeleton appears to be required for the

118 The dynamics of the microtubule cytoskeleton are controlled by microtubule-a

119 ns between membrane-bound organelles and the microtubule cytoskeleton are crucial to establish, maint

120 The integrity and dynamic properties of the microtubule cytoskeleton are indispensable for the devel

121 Both the actin and microtubule cytoskeleton are known to play a role in med

122 Recent studies indicate the actin and microtubule cytoskeletons are a final common target of m

123 ly, our work demonstrates that the actin and microtubule cytoskeletons are coordinated during cytokin

124 codazole, suggesting that both the actin and microtubule cytoskeletons are important for invasion.

125 Tubulins, the protein constituents of the microtubule cytoskeleton, are present in all known eukar

126 Cells assemble a mirror-symmetric microtubule cytoskeleton around the tissue midline, whic

127 dy development requires an intact fusome and microtubule cytoskeleton as it is blocked by mutations i

128 of nuclei, centrosomes, chromosomes, and the microtubule cytoskeleton as well as the particular sensi

129 eads to marked changes in both the actin and microtubule cytoskeleton, as well as a surprising asymme

130 are potential coordinators of the actin and microtubule cytoskeletons, as they can both nucleate act

131 cooperative reorganization of the actin and microtubule cytoskeletons, as well as the turnover of ce

132 p35, which, in turn, modulate the actin and microtubule cytoskeleton assembly and enable newly gener

133 nd ORB proteins are required to organise the microtubule cytoskeleton at stage 9, and to prevent prem

134 sruption, indicating that IRS-2 requires the microtubule cytoskeleton at the level of downstream effe

135 As a consequence, the microtubule cytoskeleton becomes destabilized and cell m

136 is inhibited, with no effect on the actin or microtubule cytoskeleton being observed.

137 cleus to the anterior side along a polarized microtubule cytoskeleton, but this mechanism has not bee

138 coordinates regulation of the actin and the microtubule cytoskeleton by binding and activating the W

139 EB1 is key factor in the organization of the microtubule cytoskeleton by binding to the plus-ends of

140 mutations that contribute to or modulate the microtubule cytoskeleton by causing perturbations of neu

141 eas MCAK promotes rapid restructuring of the microtubule cytoskeleton by making catastrophe a first-o

142 though it has long been appreciated that the microtubule cytoskeleton can be post-translationally mod

143 pendent on Pak activity, suggesting that the microtubule cytoskeleton can be regulated through inacti

144 hese contact lenses also prevented actin and microtubule cytoskeleton changes typically induced by UV

145 ich it maintains a balance between actin and microtubule cytoskeleton components, thereby contributin

146 r disrupt microtubules reveal that an intact microtubule cytoskeleton contributes to IRS-2- but not I

147 icate that upon injury, the integrity of the microtubule cytoskeleton controls cell division in the C

148 morphogenesis to determine how the actin and microtubule cytoskeletons cooperate to pattern the cell

149 tion to serving as tracks for transport, the microtubule cytoskeleton directs intracellular trafficki

150 genesis, when the polarisation of the oocyte microtubule cytoskeleton directs the localisation of bic

151 e of actin assembly, and perturbation of the microtubule cytoskeleton disrupts this zone as well as l

152 Disruption of the microtubule cytoskeleton disturbed vesicular transport o

153 not impair the effects of NGF on the axonal microtubule cytoskeleton during branching.

154 ractions occur between Wnt/PCP signaling and microtubule cytoskeleton during C&E gastrulation movemen

155 Thus a transient specialization of the microtubule cytoskeleton during differentiation of a spe

156 Polarization of the microtubule cytoskeleton during early oogenesis is requi

157 inding protein Shroom3 as a regulator of the microtubule cytoskeleton during epithelial morphogenesis

158 s to interfere with the reorientation of the microtubule cytoskeleton during healing of wounded NIH3T

159 ssociated Futsch to control stability of the microtubule cytoskeleton during nervous system developme

160 ches have implicated genes that regulate the microtubule cytoskeleton during neuronal division, migra

161 The role of the microtubule cytoskeleton during these stomatal movements

162 n coordinating the dynamics of the actin and microtubule cytoskeletons during directional motility of

163 sion and expansion via downstream effects on microtubule cytoskeleton dynamics and auxin signaling, t

164 , ethylene signaling, auxin homeostasis, and microtubule cytoskeleton dynamics.

165 vering events entail focal disruption of the microtubule cytoskeleton, followed by thinning of the di

166 pathic, exhibiting structural defects in the microtubule cytoskeleton, Golgi complex, and mitochondri

167 We demonstrate here that the microtubule cytoskeleton gradually transitions from a ra

168 A role for the microtubule cytoskeleton has also been proposed, but its

169 Although a dynamic microtubule cytoskeleton has been shown to be essential

170 e loss, suppression, or stabilization of the microtubule cytoskeleton has been widely reported to cau

171 n this process, the apparent polarity of the microtubule cytoskeleton has pointed instead to roles fo

172 The microtubule cytoskeleton has proven to be an effective t

173 ization occurs in the absence of a polarized microtubule cytoskeleton, i.e. in grk null mutants, but

174 Disruption of the microtubule cytoskeleton impairs tumor angiogenesis by i

175 2 modulates the organization and dynamics of microtubule cytoskeleton in a Ca(2+)-independent manner

176 drugs or genetic mutations that disrupt the microtubule cytoskeleton in a Saccharomyces cerevisiae m

177 f alpha-tubulin and rsEGFP2 highlighting the microtubule cytoskeleton in all cells.

178 Reduced establishment of the posterior microtubule cytoskeleton in Arp2/3 mutants correlates wi

179 mportance of TON2-mediated regulation of the microtubule cytoskeleton in cell morphogenesis.

180 egulated kinase (ERK) is associated with the microtubule cytoskeleton in cells.

181 otubules and promoted ER alignment along the microtubule cytoskeleton in COS7 cells.

182 Our data provide a link between the microtubule cytoskeleton in embryogenesis and the behavi

183 tion by a Ras homolog, R-Ras, stabilizes the microtubule cytoskeleton in endothelial cells leading to

184 ifferentiation-specific rearrangement of the microtubule cytoskeleton in epidermis, and defines an es

185 pparatus in particular and regulation of the microtubule cytoskeleton in general.

186 portance of tubular ER interactions with the microtubule cytoskeleton in hereditary spastic paraplegi

187 roteins that control the organization of the microtubule cytoskeleton in interphase and mitosis.

188 outcomes, we assessed the involvement of the microtubule cytoskeleton in IRS-dependent signaling.

189 unexpected interdependence of DAPK-1 and the microtubule cytoskeleton in maintenance of epidermal int

190 this study, we investigated the role of the microtubule cytoskeleton in modulating myofibroblast phe

191 ative ultrastructural methods to analyze the microtubule cytoskeleton in myelinated axons in the mid-

192 n Drosophila causes an aberrantly stabilized microtubule cytoskeleton in neurons and defects in synap

193 genic line to determine the structure of the microtubule cytoskeleton in T. gondii.

194 evere alterations in the organization of the microtubule cytoskeleton in the absence of Par6alpha and

195 iation with both the plasma membrane and the microtubule cytoskeleton in the growth cone by live cell

196 egeneration by regulating and organizing the microtubule cytoskeleton in the growth cone.

197 on, reorganization, and stabilization of the microtubule cytoskeleton in the growth cones.

198 s demonstrate the striking difference of the microtubule cytoskeleton in the lamella as compared with

199 quences for the architecture of the cap cell microtubule cytoskeleton in the larval sensilla, even wh

200 ndence of Vangl2, VAMP1, aPKC and the stable microtubule cytoskeleton in the oocyte, shows that mater

201 esting a tight linkage between the actin and microtubule cytoskeleton in these cells.

202 then document defects in both the actin and microtubule cytoskeletons in dia mutant nerve terminals.

203 Migrating cells reorganize their actin and microtubule cytoskeletons in response to external cues.

204 d, loss of hDia1 led to perturbations in the microtubule cytoskeleton, including the targeting of mic

205 ore recent advances in understanding how the microtubule cytoskeleton influences mammalian neural ste

206 r mammalian somatic cells, the importance of microtubule cytoskeleton integrity during interphase cel

207 In all eukaryotes, morphogenesis of the microtubule cytoskeleton into a bipolar spindle is requi

208 differentiation, many cells reorganize their microtubule cytoskeleton into noncentrosomal arrays.

209 during this process is the remodeling of the microtubule cytoskeleton, involving disassembly of the c

210 The microtubule cytoskeleton is a dynamic filamentous struct

211 The microtubule cytoskeleton is a highly dynamic network.

212 The microtubule cytoskeleton is a highly dynamic, filamentou

213 ere, we investigated whether the pollen tube microtubule cytoskeleton is a target for the SI signals.

214 dependent forces as it still occurs when the microtubule cytoskeleton is compromised but is blocked w

215 In Alzheimer's disease, the microtubule cytoskeleton is compromised, leading to neur

216 Reorganization of the cortical microtubule cytoskeleton is critical for guard cell func

217 The microtubule cytoskeleton is critical for muscle cell dif

218 iescence entry, the Saccharomyces cerevisiae microtubule cytoskeleton is drastically remodeled.

219 The microtubule cytoskeleton is involved in regulation of ce

220 is have been identified, but the role of the microtubule cytoskeleton is less clear.

221 sis of normal duration, the integrity of the microtubule cytoskeleton is not subject to checkpoint su

222 These arrays are dismantled when the microtubule cytoskeleton is rearranged during mitosis an

223 have identified a novel pathway by which the microtubule cytoskeleton is regulated during sublethal c

224 s transition from interphase to mitosis, the microtubule cytoskeleton is reorganized to form the mito

225 An intact microtubule cytoskeleton is required for insulin-stimula

226 of polymerized tubulin, not dynamics of the microtubule cytoskeleton, is crucial for convergent exte

227 Doublecortin, a component of the microtubule cytoskeleton, is essential in postmitotic ne

228 s, which disrupts organelle transport on the microtubule cytoskeleton, is likely to be the primary di

229 3p localization to cell ends is dependent on microtubule cytoskeleton, its localization to the cell m

230 the closest cortical surface, and the oocyte microtubule cytoskeleton lacks clear axial asymmetry.

231 powerful chemotherapy agents that target the microtubule cytoskeleton, leading to mitotic arrest and

232 nd/or the coordination between the actin and microtubule cytoskeletons, leading to motor neuron degen

233 Disruption of the fibroblast microtubule cytoskeleton leads to an increase in Rho-dep

234 Disruption of the microtubule cytoskeleton leads to failure of apical cons

235 A, or roscovitine resulted in changes in the microtubule cytoskeleton, loss of cellular polarity, and

236 r with the signaling data, suggests that the microtubule cytoskeleton may facilitate access of IRS-2

237 how proteins linking pairing centers and the microtubule cytoskeleton mediate homolog pairing and res

238 Interactions between the actin and microtubule cytoskeletons occur during cell polarization

239 ry of the cell towards the nucleus along the microtubule cytoskeleton of eukaryotic cells.

240 ain the highly curved shapes observed in the microtubule cytoskeleton of living cells.

241 e sole beta-tubulin isoform in the permanent microtubule cytoskeleton of the adult eye and brain.

242 ogenitors, their astroglial progeny, and the microtubule cytoskeleton of these cells in the developin

243 ic paraplegia that involve dependence of the microtubule cytoskeleton on BMP signaling.

244 opose that tea1p has roles in organizing the microtubule cytoskeleton on the tips of microtubules, an

245 o not fill the axonal cytoplasm, disrupt the microtubule cytoskeleton, or affect the transport of syn

246 n, regulating 'water transport process' and 'microtubule cytoskeleton organization'.

247 g from both isoforms intersects in actin and microtubule cytoskeletons, our results suggest that KRas

248 Hence, both actin and microtubule cytoskeletons play important roles in regula

249 The actin and microtubule cytoskeletons play key roles in cell polarit

250 The microtubule cytoskeleton plays an important role in cell

251 First the microtubule cytoskeleton plays an important role in the

252 an retraction and that the disruption of the microtubule cytoskeleton precedes axon pruning.

253 erprolin homologous protein) complex and the microtubule cytoskeleton promote STIM 1 clustering at si

254 Nocodazole disruption of the microtubule cytoskeleton reduces the insulin-stimulated

255 The actin and microtubule cytoskeletons regulate cell shape across phy

256 ing of signaling molecules and the actin and microtubule cytoskeleton regulates cell shape.

257 novel roles for vertebrate Dchs in actin and microtubule cytoskeleton regulation in the unanticipated

258 ever, the precise organization of the oocyte microtubule cytoskeleton remains an open question.

259 we show that the FTI lonafarnib affects the microtubule cytoskeleton resulting in microtubule bundle

260 this mutant indicates that disruption of the microtubule cytoskeleton results in aberrantly elongated

261 e assembly and organization of the actin and microtubule cytoskeletons, Rho and Cdc42 make several ke

262 ER shaping and network interactions with the microtubule cytoskeleton seem to be the predominant path

263 they traffic to the oocyte along a polarized microtubule cytoskeleton shared by the entire cyst.

264 ing mechanisms; (ii) a negative regulator of microtubule cytoskeleton stability; and (iii) a negative

265 y nocodazole-induced depolymerization of the microtubule cytoskeleton, suggesting that mCCCAP is an i

266 crotubule-nucleating site that regulates the microtubule cytoskeleton temporally and spatially throug

267 iotemporal organization are hallmarks of the microtubule cytoskeleton that allow formation of complex

268 NA to the oocyte posterior along a polarised microtubule cytoskeleton that grows from non-centrosomal

269 ections from the cell surface that contain a microtubule cytoskeleton, the ciliary axoneme, surrounde

270 involve coordinated changes in the actin and microtubule cytoskeletons, this novel function for APC a

271 dynamics and reorganization of the actin and microtubule cytoskeleton through signaling pathways link

272 onstrate spatial asymmetry in the underlying microtubule cytoskeleton throughout the cell division cy

273 teins may have a general role in linking the microtubule cytoskeleton to cortical polarity determinan

274 Fission yeast, which normally rely on the microtubule cytoskeleton to establish their polarity axi

275 olar inclusion bodies that require an intact microtubule cytoskeleton to form.

276 rane trafficking pathways cooperate with the microtubule cytoskeleton to give rise to the primary cil

277 rane proteins and spectrin to the underlying microtubule cytoskeleton to organize and stabilize the p

278 We suggest that septin coupling of the microtubule cytoskeleton to post-Golgi vesicle transport

279 This suggests that MAP7 links Kif5b to the microtubule cytoskeleton to promote nuclear positioning.

280 d spatially regulated communication from the microtubule cytoskeleton to the actin cytoskeleton and t

281 lays a key role in integrating the actin and microtubule cytoskeletons to position centrosomes and mi

282 egrates signaling through both the actin and microtubule cytoskeletons to promote capillary tube asse

283 ape from the endosome, Ad traffics along the microtubule cytoskeleton toward the nucleus.

284 studying how a cell polarizes the actin and microtubule cytoskeletons toward sites of cell growth.

285 f the salivary glands in the fly embryo, the microtubule cytoskeleton undergoes major rearrangements,

286 ll shape changes, possibly by regulating the microtubule cytoskeleton via interactions with APC.

287 roglycan, was altered, and the subsarcolemma microtubule cytoskeleton was disrupted.

288 results were obtained for cells in which the microtubule cytoskeleton was partially diminished by low

289 F-actin and microtubule cytoskeletons were examined by fluorescence

290 the perinuclear region requires a functional microtubule cytoskeleton, whereas clustering of these co

291 l-20 function causes specific defects in the microtubule cytoskeleton, which is the likely molecular

292 te as well as the proper organization of the microtubule cytoskeleton, which together with the fusome

293 istribution after disruption of the cellular microtubule cytoskeleton with high statistical significa

294 were accompanied by a redistribution of the microtubule cytoskeleton with increased numbers of micro

295 d function requires tight integration of the microtubule cytoskeleton with membrane trafficking, and

296 Perturbation of the microtubule cytoskeleton with thiabendazole slowed the t

297 chondria positioning appear dependent on the microtubule cytoskeleton, with kinesin or dynein motors

298 Phr1 is associated with the microtubule cytoskeleton within neurons and selectively

299 associated with disruption of the actin and microtubule cytoskeleton within the yolk cell and defect

300 We conclude that the spectrin and microtubule cytoskeletons work in combination to protect