ライフサイエンスコーパス: synaptogenesis

1 e of impaired synaptic formation/maturation (synaptogenesis).

2 s C. elegans orthologue MIG-10 also supports synaptogenesis.

3 ensable of molecular events occurring during synaptogenesis.

4 diates glutamate receptor trafficking during synaptogenesis.

5 e transcription factor UNC-3 is required for synaptogenesis.

6 he coordination of dendritic morphology with synaptogenesis.

7 survival, axon outgrowth, axon guidance, and synaptogenesis.

8 d electrophysiological maturation, including synaptogenesis.

9 the period of heightened postnatal cortical synaptogenesis.

10 ctural features are important in instructing synaptogenesis.

11 t for axon guidance, dendrite formation, and synaptogenesis.

12 protein and proteoglycan interactions during synaptogenesis.

13 al vs extrasomal) in chemical and electrical synaptogenesis.

14 f afferents and targets during the period of synaptogenesis.

15 toxicity and promoted dendrite branching and synaptogenesis.

16 leads to impairment of neuronal function and synaptogenesis.

17 e metalloproteinases (MT-MMPs) in excitatory synaptogenesis.

18 rentiation, migration, neurite outgrowth and synaptogenesis.

19 ors utilize the Tiam1-Bcr complex to control synaptogenesis.

20 signaling cascades, and promotes excitatory synaptogenesis.

21 nslation of p250GAP, a negative regulator of synaptogenesis.

22 eceptor expression or enhanced glutamatergic synaptogenesis.

23 barrel cortex by sensory deprivation during synaptogenesis.

24 orticospinal pathways, neuronal pruning, and synaptogenesis.

25 to young adult development, coincident with synaptogenesis.

26 comes highly phosphorylated at serine-9 upon synaptogenesis.

27 Conversely, increased Mafb accelerates synaptogenesis.

28 n growth, and terminal axon branching during synaptogenesis.

29 ms that glial cells use to regulate neuronal synaptogenesis.

30 ble if PSD-95 expression is prevented during synaptogenesis.

31 gration and adhesion, neurite outgrowth, and synaptogenesis.

32 r astrocytes, are key regulators of neuronal synaptogenesis.

33 146a, which inhibited neuroligin 1-dependent synaptogenesis.

34 driving synaptic scaffold recruitment during synaptogenesis.

35 s critical for regulation of adhesion during synaptogenesis.

36 developmental functions of astrocytes during synaptogenesis.

37 o-activator 1alpha inhibits spinogenesis and synaptogenesis.

38 Isl1SS subset and inhibits branch growth and synaptogenesis.

39 including cell migration, axon guidance, and synaptogenesis.

40 onal roles in axon guidance and in GABAergic synaptogenesis.

41 hfinding but were downregulated beginning in synaptogenesis.

42 -response profiles for neurite outgrowth and synaptogenesis.

43 s is dependent on neuronal activity prior to synaptogenesis.

44 during postnatal development coinciding with synaptogenesis.

45 ressed on cortical neurons before and during synaptogenesis.

46 igh-throughput and quantitative screening of synaptogenesis.

47 hfinding to dendrite growth and branching to synaptogenesis.

48 , neuronal plasticity, spine maturation, and synaptogenesis.

49 hippocampus and showed increased excitatory synaptogenesis.

50 gest that Ribeye plays an organizing role in synaptogenesis.

51 us NT-3 is necessary for SGN axon growth and synaptogenesis.

52 role in horizontal cell differentiation and synaptogenesis.

53 binding of VCP to NF1, resulting in reduced synaptogenesis.

54 oss-of-function mutant in inducing GABAergic synaptogenesis.

55 d scaffolding molecules necessary for proper synaptogenesis.

56 n that plays a role in synaptic adhesion and synaptogenesis.

57 an unavoidable concomitant of rapid adaptive synaptogenesis.

58 ved in neuritogenesis, dendritic growth, and synaptogenesis.

59 roligins and link astrocyte morphogenesis to synaptogenesis.

60 uding axon guidance, target recognition, and synaptogenesis.

61 xon wiring, such as elongation, pruning, and synaptogenesis.

62 ll differentiation, neuronal innervation and synaptogenesis.

63 development, dendritic spine formation, and synaptogenesis.

64 erate the substrate for specific patterns of synaptogenesis.

65 endrite arborisation, neuronal survival, and synaptogenesis.

66 re, which may arise from abnormal excitatory synaptogenesis.

67 twork essential for neuronal development and synaptogenesis.

68 fferentiation, including dendritogenesis and synaptogenesis.

69 f GABAARs influences their ability to induce synaptogenesis, a co-culture model system incorporating

70 urite outgrowth, dendritic arborization, and synaptogenesis all exhibited bidirectional concentration

71 h exclusive CNS expression, is implicated in synaptogenesis and AMPA receptor recruitment to immature

72 Because LRRK2 expression levels rise during synaptogenesis and are highest in dorsal striatal spiny

73 hich serve as a necessary component for both synaptogenesis and axonal branch formation, directly reg

74 rsor protein (APP) were performed to examine synaptogenesis and axonal injury.

75 in dorsal spinal cord to promote excitatory synaptogenesis and central sensitization that contribute

76 these V1-IN subclasses is determined before synaptogenesis and circuit formation by a process that i

77 activity either enhances or impairs de novo synaptogenesis and circuit integration of neurons, but h

78 or impair glial motility profoundly impacted synaptogenesis and circuit maturation.

79 Here we show that during a period of synaptogenesis and circuit refinement, before hearing on

80 different MECP2dup iPSC lines have increased synaptogenesis and dendritic complexity.

81 other activity-dependent processes, such as synaptogenesis and dendritic growth, remain unaffected d

82 Our study shows how synaptogenesis and distinct, function-defining signaling

83 n of the serotonin 5-HT(7) receptor promotes synaptogenesis and enhances synaptic activity in hippoca

84 postsynaptic CAMs work in concert to control synaptogenesis and establish a general framework for GAB

85 ble adhesive contacts that are important for synaptogenesis and for tuning synaptic transmission.

86 to actively fire action potentials, undergo synaptogenesis and form neural circuits in vitro.

87 determination and migration, axon guidance, synaptogenesis and function, behavioral neurogenetics, a

88 sed numerous genes and proteins critical for synaptogenesis and gap junction formation, concomitant w

89 od after AIE, suggesting aberrant excitatory synaptogenesis and hyperexcitability in memory-related c

90 Here, we show that during mouse synaptogenesis and in human FXS fibroblasts, a dual dysr

91 Our data highlights a role for Shrm4 in synaptogenesis and in maintaining GABABR-mediated inhibi

92 n kinase A (PKA) activity in the SPNs during synaptogenesis and in response to dopamine receptor Drd1

93 orn was associated with increased excitatory synaptogenesis and increased frequency, but not the ampl

94 This arrangement promotes synaptogenesis and is essential for D: -serine-dependent

95 lthough the role of mature BDNF on GABAergic synaptogenesis and maintenance has been well studied, an

96 regulating cortical or subcortical neuronal synaptogenesis and maturation.

97 ptic densities, regulates activity-dependent synaptogenesis and mature synapse number on cortical lay

98 Neurexins and neuroligins play a key role in synaptogenesis and neurexin-neuroligin adhesion is one o

99 We generated mixed neural cultures analyzing synaptogenesis and neuronal activity using a multielectr

100 to the deregulation of gene sets involved in synaptogenesis and neuronal transmission, all implicated

101 hippocampal synaptic deficits, by promoting synaptogenesis and neurotransmission at glutamatergic te

102 e terminals and mediate key events including synaptogenesis and neurotransmission.

103 luRs) play important roles in the control of synaptogenesis and neurotransmitter release, yet their r

104 nal enrichment for transcription regulation, synaptogenesis and other basic intracellular processes.

105 A single injection triggered a rapid synaptogenesis and persistent increase in glutamatergic

106 ity to promote neuronal survival, outgrowth, synaptogenesis and phagocytosis, and induce the death of

107 rate a novel mechanism underlying inhibitory synaptogenesis and provide new insights in understanding

108 c studies show that ketamine rapidly induces synaptogenesis and reverses the synaptic deficits caused

109 crease in spines, suggesting fasting induced synaptogenesis and spinogenesis.

110 lar and molecular mechanisms that coordinate synaptogenesis and synapse elimination are poorly unders

111 neuroligin 1 and neuroligin 3, have roles in synaptogenesis and synaptic maintenance that appear larg

112 utamate receptor that has important roles in synaptogenesis and synaptic plasticity.

113 iminating alpha2delta4 in mice abolishes rod synaptogenesis and synaptic transmission to rod ON-bipol

114 opment of neural circuits through regulating synaptogenesis and that SRPX2 is a synaptogenic factor t

115 tamate receptor GluR1, resulting in abnormal synaptogenesis and transmission in the developing SPNs.

116 These populations selectively contribute to synaptogenesis and tumor pathophysiology, providing a bl

117 Neuroligins are proposed to organize synaptogenesis and/or synaptic transmission, but no syst

118 y infiltrated the neuropil coordinately with synaptogenesis, and astrocyte ablation reduced synapse n

119 at postnatal day (P)14, a period of intense synaptogenesis, and at P28, when synapses mature.

120 es such as glutamate uptake and promotion of synaptogenesis, and become mature astrocytes by forming

121 pathways, including neuropeptide signaling, synaptogenesis, and cell adhesion.

122 ranslation is required for axon guidance and synaptogenesis, and dysregulation of this process contri

123 ostsynaptic scaffolds are recruited to drive synaptogenesis, and Mgat1 mutants exhibit loss of both c

124 gical processes including brain development, synaptogenesis, and myelination.

125 e CNS, where they mediate neurite outgrowth, synaptogenesis, and neuronal survival.

126 regulating dendritic and axonal development, synaptogenesis, and neuronal survival.

127 lamination of adult retinal neurons, impairs synaptogenesis, and reduces cone photoreceptor survival.

128 e activated calcium channels, is involved in synaptogenesis, and regulates dendritic morphology.

129 or complex/hybrid N-glycans in morphological synaptogenesis, and strengthened functional synapse diff

130 c NR2B over NR2A controls spine motility and synaptogenesis, and suggest a structural role for the in

131 ifferentiation, dendritic and axonal growth, synaptogenesis, and synaptic pruning, all of which can b

132 s, such as axonal outgrowth and pathfinding, synaptogenesis, and the maturation of ion channel and re

133 tin in target cells plays a critical role in synaptogenesis, and this can be exploited by pathogens t

134 ical axons relaying sensory information, (3) synaptogenesis; and (4) development of functional connec

135 The biochemical pathways that underlie synaptogenesis are complex and incompletely understood.

136 the detailed mechanisms by which PKC induces synaptogenesis are not fully understood.

137 e molecular pathways required for electrical synaptogenesis are not well understood, and whether they

138 ctin regulatory proteins important for early synaptogenesis are poorly defined.

139 chanisms driving MN activity at the onset of synaptogenesis are still poorly understood.

140 plays a crucial role during axonogenesis and synaptogenesis as well as in synaptic transmission and p

141 o understanding of the general principles of synaptogenesis as well as of neuromuscular disorders.

142 ncreased cell proliferation, vascularity and synaptogenesis, as well as reduced apoptosis in the hema

143 cite an example from preliminary studies of synaptogenesis at the calyx of Held, a large nerve termi

144 SS neurons display reduced branch growth and synaptogenesis at the hindbrain-spinal cord junction.

145 However, early CH synaptogenesis before protocalyx formation was not alter

146 This elevated neurotransmission enhances synaptogenesis between BCs and RGCs, without altering th

147 This study provides novel insights into synaptogenesis between central neurons revealing both di

148 as a synapse-enriched protein that promotes synaptogenesis between mammalian cortical neurons.

149 hat these populations differentially support synaptogenesis between neurons.

150 cal neuron cultures, suggesting an effect on synaptogenesis beyond neuromuscular junctions.

151 iods of neurogenesis and migration, up until synaptogenesis, both nitric oxide (NO) and its downstrea

152 mplicated in the control of neurogenesis and synaptogenesis but its potential roles in intervening pr

153 Many molecules regulate synaptogenesis, but intracellular signaling pathways req

154 mily, has been shown to have a clear role in synaptogenesis, but its roles in other tissues have not

155 Netrin-1 promotes branching and synaptogenesis, but the mechanism by which Netrin-1 stim

156 atory motion of the filopodia is crucial for synaptogenesis, but the underlying mechanisms are poorly

157 ribute to many neuronal functions, including synaptogenesis, but their role in the development of syn

158 These results indicate that PKC promotes synaptogenesis by activating PSD-95 phosphorylation dire

159 lasmin proteolysis impairs parallel fiber-PN synaptogenesis by blocking brain-derived neurotrophic fa

160 for neural defects, we were able to increase synaptogenesis by blocking interleukin-6 levels.

161 ndicate that EphBs control axon guidance and synaptogenesis by distinct mechanisms and provide a new

162 inhibitors that improve neuroligin-1-induced synaptogenesis by modulating class-I HDACs.

163 ere is no cell-autonomous regulation of cone synaptogenesis by neurotransmission.

164 n of some BC neighbors resulted in increased synaptogenesis by the remaining axons in a transmission-

165 With a fixed number of neurons, adaptive synaptogenesis can control the speed of synaptic develop

166 tified three conceptually distinct routes to synaptogenesis: cell-cell contact mediated by adhesion p

167 ued the morphological neuronal phenotype and synaptogenesis defects from ASD neuronal co-cultures.

168 The phosphomimetic fully rescues these synaptogenesis defects, whereas the dephosphomimetic pro

169 o the first developmental milestones such as synaptogenesis, dendrite formation, and maturation of in

170 This synaptogenesis depended on TCR variable domains, the kin

171 mutants revealed that APP potently promotes synaptogenesis depending on copper binding to the GFLD.

172 NMDAR inhibition by Pb(2+) during synaptogenesis disrupts downstream trans-synaptic signal

173 that whereas dNedd4S promotes neuromuscular synaptogenesis, dNedd4Lo inhibits it and impairs larval

174 and offers a system for the future study of synaptogenesis during adult retinal regeneration.

175 We investigated the role of NR2 subunits in synaptogenesis during the period in which expression and

176 receptor tyrosine kinases mediate excitatory synaptogenesis early during development, and then later

177 Remarkably, TrkC-IgG reduced axon growth and synaptogenesis even in the presence of BDNF, indicating

178 ctivity-dependent, unidirectional control of synaptogenesis exerted by the dominant input.

179 opose that dysregulation of such specific MN synaptogenesis genes, compounded by many additional tran

180 al factors including regional differences in synaptogenesis, glucose metabolism, and myelination acro

181 synapses has been shown, a specific role in synaptogenesis has not been described.

182 rcellular signaling, but the requirements in synaptogenesis have not been well tested.

183 ly promotes neurogenesis, neuritogenesis and synaptogenesis; however, the underlying molecular mechan

184 mechanisms that are relevant to depression: synaptogenesis, immunomodulation and regulation of glyco

185 DAT-containing filopodia may be involved in synaptogenesis in developing DA neurons.

186 expression of DISC1 suppresses glutamatergic synaptogenesis in developing neuromuscular junctions.

187 show that mouse Sema5A negatively regulates synaptogenesis in early, developmentally born, hippocamp

188 state, results in a selective enhancement of synaptogenesis in gamma-aminobutyric acidergic interneur

189 neural hearing loss and prevented the normal synaptogenesis in inner hair cells (IHCs) in the newly i

190 ansiently coexpressed with FMRP during early synaptogenesis in layer- and region-specific pyramidal n

191 Spontaneous activity is thought to regulate synaptogenesis in many parts of the developing nervous s

192 n GPCR that is required for spinogenesis and synaptogenesis in mice and rats.

193 f motoneuron developmental cell death and of synaptogenesis in mouse embryo (E13.5).

194 ethyl-D-aspartate antagonist that stimulates synaptogenesis in prefrontal cortex (PFC).

195 n postnatal development indicated a delay in synaptogenesis in Slitrk6-deficient animals.

196 is characterized by extensive glutamatergic synaptogenesis in striatal spiny projection neurons (SPN

197 ction with immunohistochemistry, to quantify synaptogenesis in the auditory cortex of normal hearing

198 (SRPX2) gene encodes a protein that promotes synaptogenesis in the cerebral cortex.

199 pathways regulating mRNA translation during synaptogenesis in the genesis of neurodevelopmental diso

200 for the development of neuronal pathways and synaptogenesis in the hypothalamus.

201 easurements of neural cell proliferation and synaptogenesis in the ICH border zone.

202 olamine increases glutamate transmission and synaptogenesis in the medial prefrontal cortex (mPFC).

203 mammalian target of rapamycin and increased synaptogenesis in the prefrontal cortex are crucial in m

204 I is modified by O-GlcNAc during hippocampal synaptogenesis in the rat.

205 hevin and SPARC, as regulators of excitatory synaptogenesis in vitro and in vivo.

206 l three is necessary for abnormally elevated synaptogenesis in vivo.

207 pathway modulating structural and functional synaptogenesis, including the GPI-anchored heparan sulfa

208 regeneration is delayed or absent, blue-cone synaptogenesis increases and ectopic synapses are made w

209 Blue cone synaptogenesis increases in mutants lacking ultraviolet

210 Further, TGF-beta1-induced synaptogenesis involves neuronal activity and secretion

211 iants supports the hypothesis that perturbed synaptogenesis is at the heart of autism.

212 Although the role of Netrin in synaptogenesis is conserved throughout evolution, the me

213 nexplored question is whether the process of synaptogenesis is coordinated with the adoption of speci

214 edly impaired, consistent with the idea that synaptogenesis is dependent on dendritic translation/rel

215 Synaptogenesis is driven by bidirectional trans-synaptic

216 we also found that Ntf3's effect on cochlear synaptogenesis is highly localized.

217 ectively, our results suggest that lateralis synaptogenesis is intrinsically nonselective and that in

218 hich these instructive roles play out during synaptogenesis is not well understood.

219 sm of developmental plasticity wherein rapid synaptogenesis is promoted by the coordinated actions of

220 st that a main role of SYD-2/Liprin-alpha in synaptogenesis is to regulate the polymerization of DPs.

221 We propose that Np65, by regulating IHC synaptogenesis, is critical for auditory function in mam

222 del of synapse development, such as adaptive synaptogenesis, it is possible to study such overproduct

223 ns display abnormal neurogenesis and reduced synaptogenesis leading to functional defects in neuronal

224 During synaptogenesis, macromolecular protein complexes assembl

225 sms, regulates postnatal PN dendritogenesis, synaptogenesis, mitochondrial structure and function, an

226 s lost as a result of Pb(2+) exposure during synaptogenesis, namely Synaptophysin (Syn) and Synaptobr

227 NMDA receptors (NMDARs) are critical to synaptogenesis, neural circuitry and higher cognitive fu

228 Elucidating the mechanisms that coordinate synaptogenesis, neuronal activation, and neurotransmitte

229 anisms controlling neural circuit formation, synaptogenesis, neuronal polarity, and dendritic arboriz

230 During in vitro synaptogenesis, NF-kappaB enhances dendritic spine and e

231 In contrast, EphB-mediated synaptogenesis occurred normally when the kinase activit

232 We found that synaptogenesis occurs synchronously across cortical area

233 In area CA1 of the mature hippocampus, synaptogenesis occurs within 30 minutes after the induct

234 nges in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a longe

235 pic mechanism by which one afferent controls synaptogenesis of another afferent, but not vice versa.

236 by Foxp2 in neonatal mouse striatum controls synaptogenesis of corticostriatal inputs and vocalizatio

237 nvestigated the developmental time course of synaptogenesis of FS cell in mouse visual cortex.

238 ng SGN axon growth in the organ of Corti and synaptogenesis on IHCs.

239 etries in the patterns of axon extension and synaptogenesis on the same axis.

240 ses nor whether OSNs retain the capacity for synaptogenesis once mature, is known.

241 hat whereas both profilins are needed during synaptogenesis, only PFN2a is crucial for adult spine pl

242 neurotransmission does not prevent GABAergic synaptogenesis onto RBC axons.

243 whether spontaneous activity itself promotes synaptogenesis or plays a purely permissive role remains

244 but is not required for ribbon organization, synaptogenesis, or synaptic transmission.

245 ing and identify the vesicular transport and synaptogenesis pathways as the major targets of the fear

246 In macaque monkeys, cortical synaptogenesis peaks during early infancy and developmen

247 Importantly, the synaptogenesis phenotype can be rescued by a treatment a

248 In particular, zyx-1 mutant synaptogenesis phenotypes were suppressed by disrupting

249 Synaptogenesis plays a central role in associative learn

250 unilateral brain damage results in aberrant synaptogenesis, potentially of transcallosal projections

251 Although synaptogenesis predominates in the early stages and prun

252 nt synapses in D1-type neurons, likely via a synaptogenesis process, whereas morphine induced silent

253 n of glutamate transmission and induction of synaptogenesis, providing novel targets for a new genera

254 endogenous Mind the gap (MTG) lectin, a key synaptogenesis regulator.

255 role in shutting down expression of specific synaptogenesis-related genes in the cerebellum, resultin

256 s been characterized, the molecular steps of synaptogenesis remain largely unknown.

257 nisms coordinating excitatory and inhibitory synaptogenesis remain unknown.

258 These three aspects of synaptogenesis require activation of a variety of intera

259 Synaptogenesis requires orchestrated communication betwe

260 Synaptogenesis requires orchestrated intercellular commu

261 ay matter following preadolescence overtakes synaptogenesis, resulting in a more efficient, adult-lik

262 etween SMA motoneurons and astrocytes impair synaptogenesis seen in SMA pathology, possibly due to th

263 neurodevelopment of excitatory postsynaptic synaptogenesis, setting the stage for neuronal interconn

264 d with increased glutamate transmission, and synaptogenesis, similar to N-methyl-D-aspartate receptor

265 nt at postsynaptic specializations is key in synaptogenesis, since this step confers functionality to

266 condition that survive long enough to permit synaptogenesis studies.

267 clear how this switch affects the process of synaptogenesis, synapse maturation, and synapse stabiliz

268 ch supports the positive role of lecithin in synaptogenesis, synaptic development and maturation.

269 pecific microRNA and plays a pivotal role in synaptogenesis, synaptic plasticity and structural remod

270 glutamate receptor (NMDAR) is essential for synaptogenesis, synaptic plasticity, and higher cognitiv

271 eceptors (NMDARs) have a fundamental role in synaptogenesis, synaptic plasticity, and learning and me

272 on through the modulation of neuritogenesis, synaptogenesis, synaptic plasticity, and memory consolid

273 and function, including neuronal migration, synaptogenesis, synaptic plasticity, and myelination.

274 pecifically, the adaptive algorithm includes synaptogenesis, synaptic shedding, and bi-directional sy

275 sion, with enrichment of genes important for synaptogenesis, synaptic transmission, photoreceptor mor

276 WF), neurogenesis (BrdU TUJ1, DCX and NeuN), synaptogenesis (synaptophysin) and apoptosis (TUNEL).

277 he functional relations of key regulators of synaptogenesis that contribute to both typical cortical

278 ndicate that BAI1 plays an important role in synaptogenesis that is mechanistically distinct from its

279 r of cell-type specific features of auditory synaptogenesis that offers a new entry point for treatin

280 mmune response signaling, axon guidance, and synaptogenesis that significantly influenced DMN modulat

281 gnaling in astrocytes and promote excitatory synaptogenesis, thereby increasing seizure susceptibilit

282 OSN synaptogenesis, therefore, provides a sustained potentia

283 ynaptic adhesion molecules, are important in synaptogenesis through a well-characterized trans-synapt

284 late morphology, intrinsic excitability, and synaptogenesis to form neural circuits.

285 ced arborization is accompanied by increased synaptogenesis to maintain synapse number.

286 are hyperactive due to increased excitatory synaptogenesis using electrophysiology, calcium imaging,

287 ase C (PKC) promotes synaptic maturation and synaptogenesis via activation of synaptic growth factors

288 sensitization modulates spine formation and synaptogenesis via CREB-mediated miR132 upregulation, wh

289 expression required for dendritogenesis and synaptogenesis via delayed occupancy of target promoters

290 urotrophic factor (NTF)-dependent excitatory synaptogenesis, via two proteolytic fragments generated

291 Consistent with this notion, PLM synaptogenesis was independent of alpha-actinin and ENA-

292 To examine its role in mediating synaptogenesis, we deleted afadin (mllt1), using a condi

293 ting GluN2 subunits in single neurons during synaptogenesis, we find that both GluN2B and GluN2A supp

294 e capable of promoting neuronal survival and synaptogenesis when co-cultured with iPSC-derived neuron

295 y parvalbumin-expressing interneurons during synaptogenesis, whereas Adamts4 mRNA is exclusively gene

296 n target of rapamycin complex 1 (mTORC1) and synaptogenesis, which have been implicated in the rapid

297 sory neuron hyperexcitability and excitatory synaptogenesis, which together lead to central sensitiza

298 pinal cord resulted in abnormal motor neuron synaptogenesis, which was not rescued by immigration of

299 RGFP968, were most effective at stimulating synaptogenesis, while the selective HDAC3 inhibitor, RGF

300 ponds to the period of process outgrowth and synaptogenesis, with robust expression in hippocampal an

301 arisons confirmed massive cell death, before synaptogenesis, within 1-4 DIV upon loss of t-SNAREs (sy