ライフサイエンスコーパス: neurite outgrowth

1 Fos transcription factor, thereby enhancing neurite outgrowth.

2 homology domain, the central domain affects neurite outgrowth.

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

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

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

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

7 ion reverses sSORLA-dependent enhancement of neurite outgrowth.

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

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

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

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

12 rites, whereas high concentrations inhibited neurite outgrowth.

13 control the cytoskeletal dynamics that power neurite outgrowth.

14 Rho GTPase signaling networks that regulate neurite outgrowth.

15 at promote neuronal cell differentiation and neurite outgrowth.

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

17 ue inhibitors of metalloproteinase-3 reduced neurite outgrowth.

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

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

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

21 n cultures and were accompanied by increased neurite outgrowth.

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

23 Hox activities by promoting subtype-specific neurite outgrowth.

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

25 channel alpha subunits to cell adhesion and neurite outgrowth.

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

27 luR5 and showed that its expression promotes neurite outgrowth.

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

29 and neuronal differentiation, and stimulated neurite outgrowth.

30 effectively inhibits microtubule-sliding and neurite outgrowth.

31 program and binds to important regulators of neurite outgrowth.

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

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

34 ncreases sensitivity to nocodazole following neurite outgrowth.

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

36 rrect neuronal development requires tailored neurite outgrowth.

37 S-PrP promoted PC12 cell neurite outgrowth.

38 the mechanisms essential for Wnt3a-dependent neurite outgrowth.

39 noncanonical signaling that is required for neurite outgrowth.

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

41 eceptor type 1 (CB1) receptors, and impaired neurite outgrowth.

42 f neural stem cell (NSC) differentiation and neurite outgrowth.

43 ion of PAK1 influences the actin dynamics of neurite outgrowth.

44 vide energy and metabolic roles required for neurite outgrowth.

45 rs counteracts MAST2-mediated suppression of neurite outgrowth.

46 t this mutation is associated with increased neurite outgrowth.

47 HTS-amenable phenotypic assay that measured neurite outgrowth.

48 h other and imbalances result in stalling of neurite outgrowth.

49 s can terminate whole cell responses such as neurite outgrowth.

50 ully identified small molecule inhibitors of neurite outgrowth.

51 to analyze the complexity of how they guide neurite outgrowth.

52 uding loss of protein function and decreased neurite outgrowth.

53 r pathways with upregulated genes related to neurite outgrowth.

54 d stromal cell-derived factor 1 and promoted neurite outgrowth.

55 ate on cell adhesion, neuronal migration and neurite outgrowth.

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

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

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

59 heral nerve tissue capable of showing robust neurite outgrowth (~5 mm), myelination of hNs by primary

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

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

62 nglion (DRG) neurons resulted in significant neurite outgrowth after 5 days.

63 ural crest-derived PC-12 cells, and enhanced neurite outgrowth after nerve growth factor stimulation.

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

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

66 ly, these assays detected a 51% reduction in neurite outgrowth and a 60% increase in growth cone area

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

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

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

70 translational stabilization of STMN2 rescued neurite outgrowth and axon regeneration deficits induced

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

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

73 cantly enhanced TGNC survival with extensive neurite outgrowth and branching as evaluated by immunocy

74 ditional phenotypic abnormalities, including neurite outgrowth and branching deficits and impaired el

75 Neurite outgrowth and branching were reduced in AP-4-HSP

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

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

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

79 s engraved with nanoscale grooves to promote neurite outgrowth and cell migration.

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

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

82 Bifenthrin-stimulated neurite outgrowth and CREB phosphorylation were dependen

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

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

85 rough multiple signalling pathways, impaired neurite outgrowth and dominantly inhibited glutamatergic

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

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

88 es from the endoplasmic reticulum to support neurite outgrowth and facilitate axon regrowth after inj

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

90 ignaling on mitochondrial trafficking during neurite outgrowth and find that it enhances their prolif

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

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

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

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

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

96 Slower neurite outgrowth and increased sensitivity to axonal st

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

98 ted from muscle is detrimental to motoneuron neurite outgrowth and maintenance.

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

100 pathy, we first showed that NSI-189 enhances neurite outgrowth and mitochondrial functions in culture

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

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

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

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

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

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

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

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

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

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

111 activates EGFR/ERK/Fos signaling to enhance neurite outgrowth and regeneration.SIGNIFICANCE STATEMEN

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

113 The effects of S-PrP on PC12 cell neurite outgrowth and Schwann cell migration were simila

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

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

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

117 Neurite outgrowth and STAT3 activation in vitro were sev

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

119 vidual cytokines have been shown to modulate neurite outgrowth and synaptic connectivity in cultured

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

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

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

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

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

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

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

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

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

129 e up- or downregulated in neurons to control neurite outgrowth, and establish parallels between micro

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

131 associated Ser/Thr kinase 2 (MAST2) inhibits neurite outgrowth, and its inhibition therefore represen

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

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

134 To address this, we quantified apoptosis, neurite outgrowth, and synapse number in the LUHMES huma

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

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

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

138 self in interphase cells and specifically in neurite outgrowth are unknown.

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

140 nsitivity to metalloproteinase inhibitors in neurite outgrowth assays.

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

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

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

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

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

146 ICM altered neurite outgrowth, but only at concentrations that also

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

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

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

150 The regulation of mitochondrial dynamics in neurite outgrowth by retinoic acid receptor beta signali

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

152 ciently regulated neuronal behavior, such as neurite outgrowths, by conductive hydrogel micropatterns

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

154 cale architecture develops by interaction of neurite outgrowth, cell migration and activity in cultur

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

156 mitochondrial membranes, but caused reduced neurite outgrowth, cell viability, and mitochondrial con

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

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

159 Neurite outgrowth defects of RBM4-depleted neurons were

160 Furthermore, loss of MiDAC results in neurite outgrowth defects that can be rescued by supplem

161 factor associations and could not complement neurite outgrowth defects.

162 sorganization, altered neuron maturation and neurite outgrowth, disruption of synaptogenesis and redu

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

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

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

166 Neurite outgrowth experiments produce an enormous number

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

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

169 tor (NGF) secretion from astrocytes, causing neurite outgrowth from a model neuron cell line.

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

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

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

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

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

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

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

177 S100b stimulates neurite outgrowth from sympathetic neurons in vitro.

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

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

180 oficient at quantifying extensive amounts of neurite outgrowth images with noisy background in microf

181 ulted in microtubule network instability and neurite outgrowth impairment.

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

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

184 Neurite outgrowth in both PNS and CNS neuronal cultures

185 ontotemporal dementia, respectively, reduced neurite outgrowth in cells deficient in ZIP12. Zinc and

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

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

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

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 cells, stimulate their motility, and enhance neurite outgrowth in mouse neuroblastoma Neuro2a cells.

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

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

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 rst confirmed on the basis of maintenance of neurite outgrowth in PC12 cells.

201 dynamics of whole cell responses we studied neurite outgrowth in rat primary cortical neurons in cul

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

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

204 ved peptides targeted to MAST2-PDZ stimulate neurite outgrowth in several neuron types, opening up pr

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

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

207 Neurite outgrowth in the absence of neurotrophic factors

208 nhancement of both synaptic transmission and neurite outgrowth in the marine mollusk Aplysia californ

209 esophageal cancer cells were able to induce neurite outgrowth in the PC12 neuronal cells.

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

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

212 ivery of MT-I/II to adult DRGs also promotes 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 ecessary and sufficient for the induction of neurite outgrowth in vitro and for the survival of retin

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

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 ing its downstream effector, Epac2, enhances neurite outgrowth in vitro, even in the presence of an i

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

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

221 d IV of the electron transport chain reduced neurite outgrowth in ZIP12 deficient cells. Transcriptio

222 roprotection, stem cell differentiation, and neurite outgrowth, independent of enzymatic activity.

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

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

225 It also fails to complement the effect on neurite outgrowth induced by NOVA2 downregulation in vit

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 retion and activity of the myelin-associated neurite outgrowth inhibitor Nogo-A and observed exosomal

229 we demonstrate that genetic deletion of the neurite outgrowth inhibitor Nogo-A or one of its corresp

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

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

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

233 Neurite outgrowth is driven in part by microtubule-slidi

234 Neurite outgrowth is key to the formation of functional

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

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

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

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

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

240 efficacies of these peptides for stimulating neurite outgrowth mirroring their affinities for MAST2-P

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

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

248 In vitro data showed that SC-Exos promoted neurite outgrowth of diabetic DRG neurons and migration

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

250 NogoA inhibits neurite outgrowth of motoneurons (NOM) through interacti

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

252 PK/ERK and PI3K/Akt signaling as well as the neurite outgrowth of PC12 cells.

253 luble agonist (S-220) significantly enhanced neurite outgrowth of postnatal rat cortical neurons and

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

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

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

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

258 ) and microfiber diameter (17-150 um) affect neurite outgrowth (PC-12 cells and primary mouse hippoca

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

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

261 Feature extraction then quantifies dynamic neurite outgrowth phenotypes.

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

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

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

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

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

267 ic data showed association with variation in neurite outgrowth-related genes.

268 The neurite outgrowth response of gp130-deficient neurons to

269 tes undergo neuron-like differentiation with neurite outgrowth, secretory vesicle accumulation, and t

270 stribution of neurons and activity-dependent neurite outgrowth shape long-range interaction, recurren

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

272 fic neddylation of cofilin at K112 regulates neurite outgrowth, suggesting that cofilin neddylation c

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 (the majority being brain specific) disrupts neurite outgrowth, synaptogenesis, and the 'wiring' of t

276 Axon pathfinding, neurite outgrowth, synaptogenesis, neurotransmission, an

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

278 ut not male neurons, the ED peptide enhanced neurite outgrowth that could be suppressed by inhibitors

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

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 PPA at 2 mM decreased neurite outgrowth to (80.70 um +/- 5.5 um) compared to (

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

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

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

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

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

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

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

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

291 Neurite outgrowth was compromised in primary cortical ne

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

293 ounds that promoted both neuroprotection and neurite outgrowth were bioinformatically deconvoluted to

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 ically affected F-actin dynamics and reduced neurite outgrowth, which has been associated with the de

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