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

1 tubulin tyrosination cycle in regulating the microtubule cytoskeleton.

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

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

4 coordinating the remodeling of the actin and microtubule cytoskeleton.

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

6 transport of intracellular cargoes along the microtubule cytoskeleton.

7 correct deployment of the apical complex and microtubule cytoskeleton.

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

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

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

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

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

13 cess involves rebuilding the entire neuronal microtubule cytoskeleton.

14 le hook orientation via interaction with the microtubule cytoskeleton.

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

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

17 in regulating the organization of the oocyte microtubule cytoskeleton.

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

19 le is to provide a point of anchoring to the microtubule cytoskeleton.

20 eneoplastic cells may involve changes in the microtubule cytoskeleton.

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

22 rotubules are the signature of the dendritic microtubule cytoskeleton.

23 replace the missing axon by rearranging the microtubule cytoskeleton.

24 ses kinesin motility to maintain a polarized microtubule cytoskeleton.

25 C to promote polarized reorganization of the microtubule cytoskeleton.

26 our knowledge, role in the regulation of the microtubule cytoskeleton.

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

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

29 ommunication between the cell cortex and the microtubule cytoskeleton.

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

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

32 c reticulum membrane and associates with the microtubule cytoskeleton.

33 g for directed secretion along the polarized microtubule cytoskeleton.

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

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

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

37 ion with the stabilization of the underlying microtubule cytoskeleton.

38 nd manifest disorganization of the root hair microtubule cytoskeleton.

39 st alpha-tubulin, which exhibit a simplified microtubule cytoskeleton.

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

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

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

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

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

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

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

47 the interaction between mitochondria and the microtubule cytoskeleton.

48 require interaction of the dynamic actin and microtubule cytoskeleton.

49 proteins, and signaling molecules along the microtubule cytoskeleton.

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

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

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

53 atory polarity, and centrosomes organize the microtubule cytoskeleton.

54 tracellular transport, and regulation of the microtubule cytoskeleton.

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

56 ects specific functional requirements of the microtubule cytoskeleton.

57 gulates the organization and dynamics of the microtubule cytoskeleton.

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

59 y reinforcing their link with the underlying microtubule cytoskeleton.

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

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

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

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

64 pendent modulation of the synaptic actin and microtubule cytoskeletons.

65 hanges require the coordination of actin and microtubule cytoskeletons.

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

67 nd morphogenesis by remodeling the actin and microtubule cytoskeletons.

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

69 ace expression required functional actin and microtubule cytoskeletons.

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

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

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

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

74 We now show that microtubule cytoskeleton alteration and decreased acetyl

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

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

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

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

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

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

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

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

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

84 the core of centrosomes, which organize the microtubule cytoskeleton and form the poles of the mitot

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

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

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

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

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

90 The microtubule cytoskeleton and its interacting proteins we

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

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

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

94 Paradoxically, severases can amplify the microtubule cytoskeleton and not just destroy it.

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

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

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

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

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

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

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

102 Both the microtubule cytoskeleton and tubular ER are important fo

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

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

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

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

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

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

109 ng the spatial organization of the actin and microtubule cytoskeleton, and biasing the directionality

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

111 Actin and microtubule cytoskeletons appear to significantly regula

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 ndicated a synergistic decrease of actin and microtubule cytoskeleton-associated proteins in both con

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

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

129 f tubulin to induce mitotic arrest through a microtubule cytoskeleton-based mechanism.

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

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

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

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

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

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

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

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

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

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

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

141 These results indicate that microtubule cytoskeleton contributes to the pathogenesis

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

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

144 ryotes, the organization and function of the microtubule cytoskeleton depend on the allocation of dif

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

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

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

148 Disruption of the microtubule cytoskeleton disturbed vesicular transport o

149 e imaging to show a novel arrangement of the microtubule cytoskeleton during apical constriction: med

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

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

152 Polarization of the microtubule cytoskeleton during early oogenesis is requi

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

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

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

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

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

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

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

160 Microtubule cytoskeleton exists in various biochemical f

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

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

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

164 Although it is well known that the microtubule cytoskeleton has a central role in establish

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

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

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

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

169 The microtubule cytoskeleton has proven to be an effective t

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

171 Disruption of the microtubule cytoskeleton impairs tumor angiogenesis by i

172 2 modulates the organization and dynamics of microtubule cytoskeleton in a Ca(2+)-independent manner

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

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

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

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

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

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

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

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

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

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

183 th and transverse patterning of the cortical microtubule cytoskeleton in hypocotyl cells.

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

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

186 , spatiotemporally precise modulation of the microtubule cytoskeleton in living cells, and promise ne

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

188 -115) is a ubiquitous MAP that organizes the microtubule cytoskeleton in mitosis and neuronal branchi

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

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

191 help to adjust the shape and function of the microtubule cytoskeleton in space and time.

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

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

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

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

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

197 Previous work implicated the microtubule cytoskeleton in the maintenance of epidermal

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

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

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

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

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

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

204 activity might be expected to break down the microtubule cytoskeleton, inhibiting these enzymes in vi

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

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

207 Dividing cells reorganize their microtubule cytoskeleton into a bipolar spindle, which m

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 We find that the microtubule cytoskeleton is a major contributor to epith

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

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

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

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

218 The microtubule cytoskeleton is critical for muscle cell dif

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

220 The microtubule cytoskeleton is involved in regulation of ce

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

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

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

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

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

226 An intact microtubule cytoskeleton is required for insulin-stimula

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

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

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

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

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

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

233 differential expression of genes involved in microtubules, cytoskeleton linkages, and motor activity.

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

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

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

237 The luminal tether Climp63 and microtubule cytoskeleton modulate their nanoscale dynami

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

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

240 f centrosomes, which organize the interphase microtubule cytoskeleton of most animal cells and form t

241 The microtubule cytoskeleton of pancreatic islet beta-cells

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

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

246 to centrosome disorganization and disrupted 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 First the microtubule cytoskeleton plays an important role in the

250 The microtubule cytoskeleton plays critically important role

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

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

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

254 The actin and microtubule cytoskeletons regulate cell shape across phy

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

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

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

258 inhibitors are prime reagents for studies in microtubule cytoskeleton research, being applicable acro

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

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

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

262 Each time a cell divides, the microtubule cytoskeleton self-organizes into the metapha

263 The microtubule cytoskeleton serves as a dynamic structural

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

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

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

267 The microtubule cytoskeleton supports diverse cellular morph

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

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

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

271 Giardia has a complex microtubule cytoskeleton that includes eight flagella an

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

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

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

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

276 The cortical microtubule cytoskeleton thus may provide a platform to

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

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

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

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

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

282 ed role of APC2 in integrating the actin and microtubule cytoskeletons to mediate cellular morphologi

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

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

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

286 The remodeling of the microtubule cytoskeleton underlies dynamic cellular proc

287 mber of essential pathways converge upon the microtubule cytoskeleton, understanding how cells utiliz

288 Stabilization of microtubule cytoskeleton using Paclitaxel improved intra

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

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

291 F-actin and microtubule cytoskeletons were examined by fluorescence

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

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