ライフサイエンスコーパス: neurite outgrowth

1 ly with GRIN (G protein-regulated inducer of neurite outgrowth).

2 e regulator GCN1, inducing GCN1 turnover and neurite outgrowth.

3 n cultures and were accompanied by increased neurite outgrowth.

4 oteins as well as growth cone morphology and neurite outgrowth.

5 Hox activities by promoting subtype-specific neurite outgrowth.

6 pproximately 100 pM) ART levels required for neurite outgrowth.

7 channel alpha subunits to cell adhesion and neurite outgrowth.

8 MAPK/ERK via muscarinic receptors to promote neurite outgrowth.

9 luR5 and showed that its expression promotes neurite outgrowth.

10 of these cells and their ability to promote neurite outgrowth.

11 and neuronal differentiation, and stimulated neurite outgrowth.

12 homology domain, the central domain affects neurite outgrowth.

13 lation of MT dynamics, axonal transport, and neurite outgrowth.

14 BDNF to overcome MAG-dependent inhibition of neurite outgrowth.

15 or reduced the effects of ZIP12 knockdown on neurite outgrowth.

16 ncreases sensitivity to nocodazole following neurite outgrowth.

17 protein (TiVAMP)/VAMP-7 vesicles at sites of neurite outgrowth.

18 o2(-/-) neurons from adult mice have stunted neurite outgrowth.

19 the mechanisms essential for Wnt3a-dependent neurite outgrowth.

20 noncanonical signaling that is required for neurite outgrowth.

21 y enhances H-Ras(G/V) stimulatory effects on neurite outgrowth.

22 c factor that promotes neuronal survival and neurite outgrowth.

23 4, 12(S)-, and 15(S)- HETE did not stimulate neurite outgrowth.

24 mpaired neuronal growth factor (NGF)-induced neurite outgrowth.

25 e activity in terms of both neuron birth and neurite outgrowth.

26 gative cross-talk in Akt phosphorylation and neurite outgrowth.

27 endocytosis are required for CHL1-dependent neurite outgrowth.

28 ne-tethered APP intracellular domain-induced neurite outgrowth.

29 of cells with longer neurites by stimulating neurite outgrowth.

30 ibodies leads to alterations in L1-dependent neurite outgrowth.

31 2 cells inhibits nerve growth factor-induced neurite outgrowth.

32 not devices to determine whether BAK affects neurite outgrowth.

33 ronal migration, axon guidance pathways, and neurite outgrowth.

34 in IL-17 (1 ng/ml) significantly potentiated neurite outgrowth.

35 ffective as intact fibronectin in supporting neurite outgrowth.

36 ose homolog of L1 (CHL1) that is involved in neurite outgrowth.

37 y during embryonic development that promotes neurite outgrowth.

38 the endosomes and gene expression (VGF) and neurite outgrowth.

39 terol levels in neurons, known to facilitate neurite outgrowth.

40 ls inhibit nerve growth factor (NGF)-induced neurite outgrowth.

41 ls and a mechanism of depolarization-induced neurite outgrowth.

42 e actin-bundling protein DRR1, which impedes neurite outgrowth.

43 roles in brain development, plasticity, and neurite outgrowth.

44 cy of late target genes and enhanced Map2(+) neurite outgrowth.

45 s in endosome positioning and fission and in neurite outgrowth.

46 rites, whereas high concentrations inhibited neurite outgrowth.

47 control the cytoskeletal dynamics that power neurite outgrowth.

48 Rho GTPase signaling networks that regulate neurite outgrowth.

49 at promote neuronal cell differentiation and neurite outgrowth.

50 tethered to the PM, is sufficient to inhibit neurite outgrowth.

51 ue inhibitors of metalloproteinase-3 reduced neurite outgrowth.

52 GAP-43 expression, Akt phosphorylation, and neurite outgrowth.

53 ated BNIP-H mutation fails to target ACL for neurite outgrowth.

54 n kinase (MAPK) signaling pathway to augment neurite outgrowth.

55 e) and Grin1 (G protein regulated inducer of neurite outgrowth 1).

56 Neurite outgrowth, a canonical CRMP2 function, was moder

57 olated sympathetic neurons lacking Egr3 have neurite outgrowth abnormalities when treated with NGF an

58 dentify potentially essential groups for the neurite outgrowth activity.

59 and this pathway plays a significant role in neurite outgrowth, activity-dependent plasticity, and co

60 effects of simvastatin on axonal injury and neurite outgrowth after experimental TBI and explored th

61 In addition, exosomal miR-124-3p promoted neurite outgrowth after scratch injury, characterized by

62 DN1 fused to a fluorescent protein inhibited neurite outgrowth, an effect that was mimicked by shRNA

63 ng neurons, ectopic Nrf2 expression inhibits neurite outgrowth and aborization, and electrophysiologi

64 strate a role for KLF16 in regulation of RGC neurite outgrowth and as a methylation-sensitive transcr

65 he JNK inhibitor suppressed Netrin-1-induced neurite outgrowth and axon attraction.

66 amellipod formation in fibroblasts and drive neurite outgrowth and axon guidance in neurons.

67 nown function, and STMN3, a gene involved in neurite outgrowth and axonal and dendritic branching.

68 Physiological levels of ROS support neurite outgrowth and axonal specification, but the mech

69 ess numerous neurogenic markers, and mediate neurite outgrowth and axonal targeting.

70 nce the cytoskeleton as LRRK2 mutants reduce neurite outgrowth and cause an accumulation of hyperphos

71 of polySia on trigeminal neurites inhibited neurite outgrowth and caused axon defasciculation, but d

72 TNN is involved in neurite outgrowth and cell migration in hippocampal expl

73 Nogo-A is a membrane protein that inhibits neurite outgrowth and cell migration in the central nerv

74 the transmembrane protein, Nogo-A, inhibits neurite outgrowth and cell spreading in neurons and Nogo

75 utgrowth, while HMGN5 overexpression induces neurite outgrowth and chromatin decompaction; these effe

76 Bifenthrin-stimulated neurite outgrowth and CREB phosphorylation were dependen

77 ide first evidence that DDX3 is required for neurite outgrowth and dendritic spine formation in vitro

78 KA-Rac1 signaling and thereby contributes to neurite outgrowth and dendritic spine formation.

79 When overexpressed, KLF16 inhibits RGC neurite outgrowth and enhances RGC growth cone collapse

80 understanding the role of KLFs in regulating neurite outgrowth and Eph receptor expression will be vi

81 d neuronal migration and maturation (reduced neurite outgrowth and fewer synapses) in 3D layered hydr

82 that altered MeCP2 levels result in aberrant neurite outgrowth and glutamatergic synapse formation.

83 itical region 1 protein modulates both basal neurite outgrowth and growth cone turning.

84 APP expression is required for exuberant neurite outgrowth and hippocampal axonal sprouting obser

85 from p73 knockout mice showed a reduction in neurite outgrowth and in nerve growth factor-mediated ne

86 -mediated generation of L1-80 is involved in neurite outgrowth and in stimulation of migration of cul

87 ing an approximately 3.5-fold improvement in neurite outgrowth and increased action potential firing

88 His257Arg TrpRS also inhibited neurite outgrowth and led to neurite degeneration in the

89 initial viability as wild type, with proper neurite outgrowth and marker expression.

90 sensory ganglia, which include promotion of neurite outgrowth and modulation of glutamate release at

91 ein kinase A (PKA) controls major aspects of neurite outgrowth and morphogenesis and plays an essenti

92 ibits neuregulin release and reduces ex vivo neurite outgrowth and myelination of trigeminal ganglion

93 tein kinase receptor TrkA is known to induce neurite outgrowth and neural cell differentiation.

94 urotrophin in promoting both SAG directional neurite outgrowth and neuronal survival and is expressed

95 L1-induced neurite outgrowth and neuronal survival are reduced in M

96 c and heterophilic interactions and enhances neurite outgrowth and neuronal survival homophilically,

97 lding a transmembrane fragment that promotes neurite outgrowth and neuronal survival in cell culture.

98 The L1 cell adhesion molecule promotes neurite outgrowth and neuronal survival in homophilic an

99 ory systems and promotes mouse and chick SAG neurite outgrowth and neuronal survival, demonstrating k

100 These data indicate that C3 reduces neurite outgrowth and neuronal viability in vitro and re

101 sure to bifenthrin commencing 2 DIV-enhanced neurite outgrowth and persistently increased SCO frequen

102 simvastatin reduces axonal injury, enhances neurite outgrowth and promotes neurological functional r

103 Patient-derived MSNs displayed enhanced neurite outgrowth and ramification, whereas synaptic den

104 administration induces a selective effect on neurite outgrowth and regeneration of myelinated fibers

105 bfamily of glutamate receptors that modulate neurite outgrowth and regulate glutamate release at the

106 brane dynamics-based cellular events such as neurite outgrowth and spine formation in vitro.

107 of downstream signaling cascades, impacting neurite outgrowth and spine formation.

108 and local translation of mRNAs important for neurite outgrowth and stabilization, thus contributing t

109 Neurite outgrowth and STAT3 activation in vitro were sev

110 findings indicate that Reg-1alpha regulates neurite outgrowth and suggest that this effect is mediat

111 network formation by directly affecting both neurite outgrowth and synapse development.

112 amily of cell adhesion molecules involved in neurite outgrowth and synapse formation.

113 F804A in processes such as neural migration, neurite outgrowth and synapse formation.

114 fficking, neuronal maturation and migration, neurite outgrowth and synaptic density and plasticity, a

115 ts cell mitosis, differentiation, migration, neurite outgrowth and synaptogenesis.

116 ectional concentration-response profiles for neurite outgrowth and synaptogenesis.

117 that Dvl2/3 phosphorylation correlated with neurite outgrowth and that casein kinase 1delta, one of

118 dl has distinct effects on cell survival and neurite outgrowth and that increasing the expression of

119 l action of SynIII on axon specification and neurite outgrowth and that the expression of a functiona

120 adverse effects on cell survival and reduced neurite outgrowth and the number of newly generated neur

121 the stiffness of neurons changes both during neurite outgrowth and upon disruption of microtubules of

122 ng the role of the FRMD7 gene in controlling neurite outgrowth, and albinism, in which recent models

123 in subunit o, G protein regulated-inducer of neurite outgrowth, and CDC42 signaling within T cells.

124 ally important, promoting axonal elongation, neurite outgrowth, and dendritic branching.

125 ability to attenuate cell adhesion, promote neurite outgrowth, and enhance cell migration as has bee

126 thetic somata and distal neurites to enhance neurite outgrowth, and identify a novel potential role f

127 actors associated with neuronal survival and neurite outgrowth, and increased LRP1B and G protein-cou

128 generation by stimulating synapse formation, neurite outgrowth, and neuronal survival.

129 ases the effect of recombinant Reg-1alpha on neurite outgrowth, and Reg-1alpha is not effective when

130 morphine inhibited neuronal differentiation, neurite outgrowth, and survival of adult mouse hippocamp

131 involved in neuronal migration and adhesion, neurite outgrowth, and synaptogenesis.

132 ulate with the formation of focal adhesions, neurite outgrowth, and the morphology of neuroblastoma.

133 of control astrocytes with neurons enhances neurite outgrowth, and this is reduced with SREBP2 knock

134 functional proteins with roles in autophagy, neurite outgrowth, and vesicle transport.

135 strates of APP-binding peptide alone sustain neurite outgrowth; APP dosage controls GC adhesion to la

136 inhibition of adhesion, cell spreading, and neurite outgrowth, as well as for RhoA activation.

137 l activity at the AT(2) receptor, applying a neurite outgrowth assay in NG108-15 cells.

138 oward their targets, as shown using in vitro neurite outgrowth assays together with time-lapse imagin

139 nsitivity to metalloproteinase inhibitors in neurite outgrowth assays.

140 Heparan sulphate binding is critical to neurite outgrowth, axon formation and synaptic processes

141 Actin polymerization was required for neurite outgrowth, because only low concentrations of ei

142 ts indicate that inhibition of PTEN augments neurite outgrowth beyond that of traditional methods suc

143 ipheral neurons, SRF-DeltaNLS-GFP stimulated neurite outgrowth, branch formation, and growth cone mor

144 nnervation that was correlated with abnormal neurite outgrowth/branching and abnormal cellular distri

145 rmidine blocks myelin-mediated inhibition of neurite outgrowth, but the mechanism underlying this eff

146 ese results indicate that macrophages affect neurite outgrowth by acting at the level of peripheral g

147 that the HC in EN2 indirectly contributed to neurite outgrowth by activating macroglia to produce neu

148 Vaginal smooth muscle cells induced robust neurite outgrowth by cocultured dorsal root ganglion neu

149 ChR2), we identified conditions that enhance neurite outgrowth by three-fold as compared to unstimula

150 g protein activation restores impairments in neurite outgrowth caused by Zn(2+) chelation or ZIP12 kn

151 lular process such as endocytosis, motility, neurite outgrowth, cell proliferation, and apoptosis.

152 D1 and PEDF+DHA induced a 3-fold increase in neurite outgrowth compared with cultures without supplem

153 ACh type 1 receptor (M1R) exhibited enhanced neurite outgrowth, confirming the role of M1R in tonic s

154 ition, introduction of miR-205 prevented the neurite outgrowth defects in the neurons expressing a PD

155 Neurite outgrowth defects of RBM4-depleted neurons were

156 factor associations and could not complement neurite outgrowth defects.

157 PbTx-2 stimulation of neurite outgrowth, dendritic arborization, and synaptoge

158 To measure neurite outgrowth, DRG neurons were given a conditioning

159 It has relevance to our understanding of neurite outgrowth during development and peripheral nerv

160 uits FRMD7 to the plasma membrane to promote neurite outgrowth during development of the oculomotor n

161 ical actions including neuronal survival and neurite outgrowth during development, and after central

162 role in coordinating neuronal migration and neurite outgrowth during neural circuit development.

163 esulted in ectopic expression of NOGO-A, the neurite outgrowth factor that inhibits nerve regeneratio

164 neural adhesion molecule L1, which mediates neurite outgrowth, fasciculation, and pathfinding, is ex

165 Here, we have reported that neurite outgrowth from adult sensory neurons that were m

166 ignaling were required for leptin-stimulated neurite outgrowth from ARH explants in vitro.

167 y, we found that RBM4 was also essential for neurite outgrowth from cortical neurons in vitro.

168 peptide abolished PSA-induced enhancement of neurite outgrowth from cultured hippocampal neurons indi

169 hin receptor TrkA in PC12 cells and increase neurite outgrowth from developing cerebellar granule cel

170 EN2 stimulated significant neurite outgrowth from explants but not from purified RG

171 factor and neurotrophin 3, which stimulated neurite outgrowth from ganglia explants.

172 edding of IgLON family members in regulating neurite outgrowth from mature cortical neurons.

173 r function in transgenic flies and decreased neurite outgrowth from primary cortical neurons, mutant

174 whether FGF8a and FGF8b isoforms affect the neurite outgrowth from SGN cultured in vitro.

175 tocyst-derived factor, which directs initial neurite outgrowth from the statoacoustic ganglion (SAG)

176 ) in mammalian spiral ganglion neurons (SGN) neurite outgrowth has not been examined.

177 nd the neuritogenic activity was assessed by neurite outgrowth image analysis.

178 ulted in microtubule network instability and neurite outgrowth impairment.

179 ed that their presence significantly reduces neurite outgrowth in a 3D in vitro environment.

180 d that KARs modulate neuronal maturation and neurite outgrowth in a bidirectional manner.

181 nduces GSK3beta phosphorylation and inhibits neurite outgrowth in adult dorsal root ganglion neurons,

182 ed impairments of mitochondrial motility and neurite outgrowth in apoE4-expressing neuronal cells.

183 cking BMP signaling prevented leptin-induced neurite outgrowth in ARH explant cultures.

184 Neurite outgrowth in both PNS and CNS neuronal cultures

185 of wild-type, but not mutant, CHC22 blocked neurite outgrowth in cells treated with retinoic acid.

186 ng functionality, but were unable to support neurite outgrowth in cellular and zebrafish models of SM

187 gs identify a novel therapeutic strategy for neurite outgrowth in CNS injury and disease.

188 localized ANT1 and ANT2 regulate L1-mediated neurite outgrowth in conjunction with MMP14.

189 rpenes, trace plant metabolites that enhance neurite outgrowth in cultured neurons.

190 in (kinesin-1) is required for initiation of neurite outgrowth in Drosophila embryonic neurons and th

191 Previously we reported that Wnt3a-dependent neurite outgrowth in Ewing sarcoma family tumor cell lin

192 es and degrades NOGO-A, a major inhibitor of neurite outgrowth in mammalian brain.

193 turnover of NOGO-A, positively impacting on neurite outgrowth in mammalian brain.

194 onstrated the ability of miR-34b to modulate neurite outgrowth in mouse primary hippocampal neuronal

195 Furthermore, knockdown of CHC22 induced neurite outgrowth in neural precursor cells, which was r

196 bute to all-trans-retinoic acid (RA)-induced neurite outgrowth in neuroblastoma Neuro-2a cells throug

197 or 50B11 neurons with PC-3 cells resulted in neurite outgrowth in neuronal cells that was inhibited b

198 ncluding nerve growth factor (NGF), increase neurite outgrowth in part by altering the function and e

199 imetic PLD1 mutant rescued the inhibition of neurite outgrowth in PC12 cells silenced for RSK2, revea

200 roduced as a recombinant protein and induced neurite outgrowth in primary cultures of hippocampal and

201 ulation was associated with an impairment of neurite outgrowth in primary motor neurons.

202 CREST mutations inhibited activity-dependent neurite outgrowth in primary neurons, and CREST associat

203 hosphorylation of Akt and Erk1/2 and impairs neurite outgrowth in response to nerve growth factor (NG

204 may be a widespread mechanism for promoting neurite outgrowth in response to neurotrophic factors.

205 Neurite outgrowth in response to soluble growth factors

206 enhanced the ability of neurons to increase neurite outgrowth in response to the extracellular ligan

207 TrkA-expressing cells, leading to increased neurite outgrowth in sympathetic neurons as a result of

208 mutant was unable to rescue Wnt3a-dependent neurite outgrowth in TC-32 cells following suppression o

209 Neurite outgrowth in the absence of neurotrophic factors

210 t unextinguished actin polymerization drives neurite outgrowth in the presence of actin drugs was not

211 ivery of MT-I/II to adult DRGs also promotes neurite outgrowth in the presence of MAG.

212 e ability of dbcAMP or putrescine to enhance neurite outgrowth in the presence of MAG.

213 We report a novel role for complement C1q in neurite outgrowth in vitro and axon regrowth after SCI.

214 bric to identify a drug that accelerates DRG neurite outgrowth in vitro and optic nerve outgrowth in

215 IL-17-induced neurite outgrowth in vitro appeared to be independent of

216 sing p75 neurotrophin receptor, and enhances neurite outgrowth in vitro Furthermore, we demonstrate t

217 neuronal progenitors significantly increased neurite outgrowth in vitro in a dose- and time-dependent

218 ies was significantly less inhibitory to RGC neurite outgrowth in vitro than was wild-type myelin, in

219 reduced mitochondrial motility, and reduced neurite outgrowth in vitro.

220 o determine the effect of Sema7a exposure on neurite outgrowth in vitro.

221 of aggrecan, brevican, and/or tenascin-R on neurite outgrowth in vitro.

222 terestingly, knockdown of ZNF804A attenuated neurite outgrowth in young neurons, an effect potentiall

223 PbTx-2-exposed neurons showed enhanced neurite outgrowth, increased dendritic arbor complexity,

224 n primary neurons negatively interfered with neurite outgrowth, indicating a causal link between the

225 eby blocks RhoA activation and inhibition of neurite outgrowth induced by myelin-associated inhibitor

226 addition of C3 tripled both myelin-mediated neurite outgrowth inhibition and neuron loss versus myel

227 Neurite outgrowth inhibitor A (Nogo-A) is thought to hav

228 lycoprotein (MAG), a well known inhibitor of neurite outgrowth, inhibits rat SC migration and induces

229 ulation of membrane Cav2.2, the promotion of neurite outgrowth is achieved by dephosphorylation at T5

230 iding is developmentally down-regulated when neurite outgrowth is completed.

231 f approximately 1000 Pa, whereas hippocampal neurite outgrowth is independent of substrate stiffness.

232 Neurite outgrowth is key to the formation of functional

233 CHL1-dependent neurite outgrowth is reduced by inhibitors of lipid raft

234 s; this sliding, like sliding during initial neurite outgrowth, is driven by kinesin-1 and is require

235 lidomide on angiogenesis, teratogenesis, and neurite outgrowth, known detrimental effects of Thalidom

236 r with a key role of microtubule dynamics in neurite outgrowth led to the concept that microtubules d

237 activation, has a role in the control of the neurite outgrowth length in our axon regeneration analys

238 How plexin regulation of neurite outgrowth, lymphoid trafficking, and vascular en

239 The beneficial effects of simvastatin on neurite outgrowth may be mediated through manipulation o

240 We identify a set of stereotypic neurite outgrowth morphodynamic behaviors in a cultured

241 e overexpression of wild-type FRMD7 promotes neurite outgrowth, mutants reduce this effect to differi

242 These nanoliposomes increased neurite outgrowth, network complexity and neural activit

243 cell-cell communication, neuronal migration, neurite outgrowth, neuronal pathfinding, and axonal fasc

244 in the developing nervous system, mediating neurite outgrowth, neuronal polarity, and axon guidance.

245 at disruption of MT dynamics interferes with neurite outgrowth, not by disrupting the net assembly of

246 k cells), Neurotropin augmented insufficient neurite outgrowth observed at suboptimal concentration o

247 H at the plasma membrane mediates L1-induced neurite outgrowth of cerebellar neurons.

248 hat recombinant human IgMs (rHIgM) can guide neurite outgrowth of CNS neurons.

249 sin homolog deleted on chromosome 10) during neurite outgrowth of human embryonic stem cell (hESC)-de

250 the STIM1-Orai pathway effectively abolishes neurite outgrowth of PC-12 cells stimulated by NGF.

251 The effect of CaBP5 on dopamine release and neurite outgrowth of PC12 cells was analyzed using ELISA

252 Simvastatin treatment stimulated the neurite outgrowth of PCNs after OGD, which was attenuate

253 knockdown experiments inhibited NGF-induced neurite outgrowth of rat sensory neurons, while overexpr

254 lation has been reported to be important for neurite outgrowth of sensory neurons; however, the mecha

255 Neurite outgrowth on fibronectin appears to be mediated

256 lpha5 and beta1 integrin sub-units inhibited neurite outgrowth on intact fibronectin.

257 at and mouse neurons is sufficient to induce neurite outgrowth on myelin in vitro and promotes regene

258 Explants were evaluated for neurite outgrowth over 7 days in culture.

259 PTEN inhibition also rescued neurite outgrowth over an inhibitory substrate in vitro.

260 and ERK activation; significantly increases neurite outgrowth (p < 0.01); and overcomes myelin inhib

261 y, both GEF changes are expected to decrease neurite outgrowth, perhaps consistent with their associa

262 activating proteins (GAPs) leads to opposite neurite outgrowth phenotypes.

263 Feature extraction then quantifies dynamic neurite outgrowth phenotypes.

264 om cultured adult rat DRG neurons attenuates neurite outgrowth, pointing to autocrine or paracrine me

265 ctuations in microtubule-based transport and neurite outgrowth, promoting competition between neurite

266 ses of SVZ NPC-secreted factors revealed the neurite outgrowth-promoting factor pleiotrophin, along w

267 ract-lacks transcription factor function and neurite outgrowth properties, causes cell death in cultu

268 [5-HT]) respond with a threefold increase in neurite outgrowth rates.

269 rived reactive oxygen species (ROS) regulate neurite outgrowth, regeneration, and stem cell prolifera

270 The neurite outgrowth response of gp130-deficient neurons to

271 solic proteins involved in axon guidance and neurite outgrowth signaling during neural development.

272 ultured cortical neurons rescued a defect in neurite outgrowth, suggesting a direct role for p53 in r

273 many aspects of brain development, including neurite outgrowth, synapse formation and function, long-

274 hly expressed in the CNS, where they mediate neurite outgrowth, synaptogenesis, and neuronal survival

275 truncated M1 was notably more detrimental to neurite outgrowth than truncated M87, and this was true

276 ty complex class I (MHCI) molecules regulate neurite outgrowth, the establishment and function of cor

277 erentiate normally and adjusts the extent of neurite outgrowth, the number of functional growth cones

278 ARID1B in mouse neuroblastoma cells leads to neurite outgrowth through beta-catenin.

279 have a nontranscriptional role in regulating neurite outgrowth through its membrane association.

280 riggered by neurotrophin-3 remotely inhibits neurite outgrowth through long-range Ca(2+) waves, which

281 s a repellent to promote anteriorly directed neurite outgrowth through the LIN-17/Frizzled receptor,

282 tin-pulp regeneration process by linking the neurite outgrowth to human pulp fibroblast through compl

283 om branch formation and fasciculation during neurite outgrowth to tumor progression and to angiogenes

284 ct neuron number but did promote significant neurite outgrowth to twofold that of control by 48 h, wh

285 d pulp fibroblasts controls the direction of neurite outgrowth toward carious injuries by modulating

286 tionally, we demonstrated that hUTCs support neurite outgrowth under normal culture conditions and in

287 n (1) was identified as a potent enhancer of neurite outgrowth using an in vitro screen.

288 ibit neuronal inflammation and contribute to neurite outgrowth via their transfer into neurons.

289 its neuronal inflammation and contributes to neurite outgrowth via their transfer into neurons.

290 nctional relevance of Dvl phosphorylation in neurite outgrowth was not established.

291 on macrophage accumulation was greater, SCG neurite outgrowth was significantly reduced.

292 model widely used to investigate NGF-induced neurite outgrowth, we found that a few hours of treatmen

293 This derivative also was unable to rescue neurite outgrowth when endogenous Dvl2/3 was suppressed

294 further show that endogenous IMPACT promotes neurite outgrowth whereas GCN2 is a strong inhibitor of

295 ations of KA delayed maturation and enhanced neurite outgrowth, whereas maturation was promoted by hi

296 ld-type AR in PC12 cells results in enhanced neurite outgrowth which is typically followed by rapid n

297 DGL-alpha or DGL-beta expression attenuated neurite outgrowth, which indicates that both isoforms co

298 induces transcriptional changes and impairs neurite outgrowth, while HMGN5 overexpression induces ne

299 mulated the sliding of long microtubules and neurite outgrowth, while its ectopic overexpression in t

300 toma cells expressing PHOX2B led to impaired neurite outgrowth with transcriptional profiles indicati