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1 during postnatal development coinciding with synaptogenesis.
2 n that plays a role in synaptic adhesion and synaptogenesis.
3 an unavoidable concomitant of rapid adaptive synaptogenesis.
4 ved in neuritogenesis, dendritic growth, and synaptogenesis.
5 roligins and link astrocyte morphogenesis to synaptogenesis.
6 uding axon guidance, target recognition, and synaptogenesis.
7 ria in Fmr1 knockout mice during the peak of synaptogenesis.
8 xon wiring, such as elongation, pruning, and synaptogenesis.
9 ll differentiation, neuronal innervation and synaptogenesis.
10 development, dendritic spine formation, and synaptogenesis.
11 endrite arborisation, neuronal survival, and synaptogenesis.
12 re, which may arise from abnormal excitatory synaptogenesis.
13 twork essential for neuronal development and synaptogenesis.
14 fferentiation, including dendritogenesis and synaptogenesis.
15 ensable of molecular events occurring during synaptogenesis.
16 diates glutamate receptor trafficking during synaptogenesis.
17 e transcription factor UNC-3 is required for synaptogenesis.
18 he coordination of dendritic morphology with synaptogenesis.
19 survival, axon outgrowth, axon guidance, and synaptogenesis.
20 d electrophysiological maturation, including synaptogenesis.
21 the period of heightened postnatal cortical synaptogenesis.
22 ntial for brain development, lamination, and synaptogenesis.
23 ctural features are important in instructing synaptogenesis.
24 protein and proteoglycan interactions during synaptogenesis.
25 al vs extrasomal) in chemical and electrical synaptogenesis.
26 f afferents and targets during the period of synaptogenesis.
27 toxicity and promoted dendrite branching and synaptogenesis.
28 leads to impairment of neuronal function and synaptogenesis.
29 rentiation, migration, neurite outgrowth and synaptogenesis.
30 ors utilize the Tiam1-Bcr complex to control synaptogenesis.
31 signaling cascades, and promotes excitatory synaptogenesis.
32 nslation of p250GAP, a negative regulator of synaptogenesis.
33 barrel cortex by sensory deprivation during synaptogenesis.
34 orticospinal pathways, neuronal pruning, and synaptogenesis.
35 to young adult development, coincident with synaptogenesis.
36 comes highly phosphorylated at serine-9 upon synaptogenesis.
37 Conversely, increased Mafb accelerates synaptogenesis.
38 xpression rescues KCNH2-3.1-induced impaired synaptogenesis.
39 n growth, and terminal axon branching during synaptogenesis.
40 ms that glial cells use to regulate neuronal synaptogenesis.
41 ble if PSD-95 expression is prevented during synaptogenesis.
42 gration and adhesion, neurite outgrowth, and synaptogenesis.
43 r astrocytes, are key regulators of neuronal synaptogenesis.
44 mulation implemented during neurogenesis and synaptogenesis.
45 146a, which inhibited neuroligin 1-dependent synaptogenesis.
46 driving synaptic scaffold recruitment during synaptogenesis.
47 gluing within the extracellular meshwork or synaptogenesis.
48 orming alpha1 subunit and trigger excitatory synaptogenesis.
49 pulations; of these, 88 are followed through synaptogenesis.
50 ed with the end of early critical periods of synaptogenesis.
51 ple neuronal signaling pathways and regulate synaptogenesis.
52 retraction and extension of neurites and/or synaptogenesis.
53 ns on E8-E10 may implicate Sema signaling in synaptogenesis.
54 may underlie a neurosecretory phenotype and synaptogenesis.
55 ivity in the Drosophila visual system during synaptogenesis.
56 ity to adhesion to oriented cell division to synaptogenesis.
57 nstellation of players regulating inhibitory synaptogenesis.
58 rocyte activation, neuronal homeostasis, and synaptogenesis.
59 s C. elegans orthologue MIG-10 also supports synaptogenesis.
60 erate the substrate for specific patterns of synaptogenesis.
61 t for axon guidance, dendrite formation, and synaptogenesis.
62 e metalloproteinases (MT-MMPs) in excitatory synaptogenesis.
63 eceptor expression or enhanced glutamatergic synaptogenesis.
64 f GABAARs influences their ability to induce synaptogenesis, a co-culture model system incorporating
65 forebrain neurons during the period of major synaptogenesis, a critical window for brain development
67 h exclusive CNS expression, is implicated in synaptogenesis and AMPA receptor recruitment to immature
68 Because LRRK2 expression levels rise during synaptogenesis and are highest in dorsal striatal spiny
69 hich serve as a necessary component for both synaptogenesis and axonal branch formation, directly reg
70 in dorsal spinal cord to promote excitatory synaptogenesis and central sensitization that contribute
71 activity either enhances or impairs de novo synaptogenesis and circuit integration of neurons, but h
74 be investigated, as they play a key role in synaptogenesis and corticogenesis during prenatal develo
77 postsynaptic CAMs work in concert to control synaptogenesis and establish a general framework for GAB
78 ble adhesive contacts that are important for synaptogenesis and for tuning synaptic transmission.
79 determination and migration, axon guidance, synaptogenesis and function, behavioral neurogenetics, a
80 n open field, and showed reduced activity of synaptogenesis and glutamate regulators in hippocampus.
81 od after AIE, suggesting aberrant excitatory synaptogenesis and hyperexcitability in memory-related c
84 n kinase A (PKA) activity in the SPNs during synaptogenesis and in response to dopamine receptor Drd1
85 orn was associated with increased excitatory synaptogenesis and increased frequency, but not the ampl
87 lthough the role of mature BDNF on GABAergic synaptogenesis and maintenance has been well studied, an
89 correlated with a decrease in Nrxn-mediated synaptogenesis and miniature event frequency in excitato
90 Neurexins and neuroligins play a key role in synaptogenesis and neurexin-neuroligin adhesion is one o
94 We generated mixed neural cultures analyzing synaptogenesis and neuronal activity using a multielectr
95 ction was found to be crucial for excitatory synaptogenesis and neuronal sensitisation which in turn
96 to the deregulation of gene sets involved in synaptogenesis and neuronal transmission, all implicated
97 hippocampal synaptic deficits, by promoting synaptogenesis and neurotransmission at glutamatergic te
98 luRs) play important roles in the control of synaptogenesis and neurotransmitter release, yet their r
99 nal enrichment for transcription regulation, synaptogenesis and other basic intracellular processes.
101 ity to promote neuronal survival, outgrowth, synaptogenesis and phagocytosis, and induce the death of
102 er highlights the impact of alphaSyn PFFs on synaptogenesis and physiological function, which may be
103 etory trafficking contributes to LTP-induced synaptogenesis and primes the new spines for future plas
104 rate a novel mechanism underlying inhibitory synaptogenesis and provide new insights in understanding
105 uration and neurite outgrowth, disruption of synaptogenesis and reduced neural network functioning.
107 They recycle neurotransmitters, stimulate synaptogenesis and synaptic neurotransmission, form part
109 Thus, SPARCL1 selectively boosts excitatory synaptogenesis and synaptic transmission by a novel mech
110 ctively boosts excitatory but not inhibitory synaptogenesis and synaptic transmission by a novel mech
111 iminating alpha2delta4 in mice abolishes rod synaptogenesis and synaptic transmission to rod ON-bipol
112 opment of neural circuits through regulating synaptogenesis and that SRPX2 is a synaptogenic factor t
113 en training regimens during neurogenesis and synaptogenesis and the resulting plastic responses has b
114 alphaSyn fibrils impaired the initiation of synaptogenesis and their physiological functions, thereb
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
118 y infiltrated the neuropil coordinately with synaptogenesis, and astrocyte ablation reduced synapse n
120 extension, impaired dendritic branching and synaptogenesis, and caused rapid cell death during cereb
121 f BBSome function negatively impacts retinal synaptogenesis, and causes horizontal cell defects in a
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
127 , restored rates of protein synthesis during synaptogenesis, and normalized the key phenotypic featur
128 lamination of adult retinal neurons, impairs synaptogenesis, and reduces cone photoreceptor survival.
129 e activated calcium channels, is involved in synaptogenesis, and regulates dendritic morphology.
130 role of PTX3 in promoting the first wave of synaptogenesis, and show that interplay of TSP1 and PTX3
131 or complex/hybrid N-glycans in morphological synaptogenesis, and strengthened functional synapse diff
133 ifferentiation, dendritic and axonal growth, synaptogenesis, and synaptic pruning, all of which can b
134 in neuronal proliferation, differentiation, synaptogenesis, and synchronized firing, whereas exosome
136 s, such as axonal outgrowth and pathfinding, synaptogenesis, and the maturation of ion channel and re
137 tin in target cells plays a critical role in synaptogenesis, and this can be exploited by pathogens t
138 ical axons relaying sensory information, (3) synaptogenesis; and (4) development of functional connec
141 e molecular pathways required for electrical synaptogenesis are not well understood, and whether they
142 olecular mechanisms that underlie excitatory synaptogenesis are only partially resolved, in part beca
145 plays a crucial role during axonogenesis and synaptogenesis as well as in synaptic transmission and p
146 mote the glutamatergic neurotransmission and synaptogenesis, as well as strongly enhance neuronal net
147 cite an example from preliminary studies of synaptogenesis at the calyx of Held, a large nerve termi
148 egulation in expression of genes involved in synaptogenesis, axonogenesis and neuroprotection suggest
150 This study provides novel insights into synaptogenesis between central neurons revealing both di
151 ln1) and postsynaptic receptor GluD2 mediate synaptogenesis between granule cells and Purkinje cells
155 iods of neurogenesis and migration, up until synaptogenesis, both nitric oxide (NO) and its downstrea
156 has alternative roles in development such as synaptogenesis, boundary formation, and vasculogenesis.
157 mplicated in the control of neurogenesis and synaptogenesis but its potential roles in intervening pr
158 cna2d1-4) regulate synaptic transmission and synaptogenesis, but coexpression of multiple alpha2delta
159 rtex coincides with the heightened period of synaptogenesis, but is precipitously downregulated prior
161 atory motion of the filopodia is crucial for synaptogenesis, but the underlying mechanisms are poorly
162 must be concurrent with axon navigation for synaptogenesis, but whether synaptic vesicles are functi
163 These results indicate that PKC promotes synaptogenesis by activating PSD-95 phosphorylation dire
164 ration, axonal outgrowth, axon guidance, and synaptogenesis by activating the GTPase RAC1 and modulat
165 lasmin proteolysis impairs parallel fiber-PN synaptogenesis by blocking brain-derived neurotrophic fa
167 ndicate that EphBs control axon guidance and synaptogenesis by distinct mechanisms and provide a new
169 n-neuronal protein, was reported to increase synaptogenesis by simultaneously binding to presynaptic
170 n of some BC neighbors resulted in increased synaptogenesis by the remaining axons in a transmission-
171 With a fixed number of neurons, adaptive synaptogenesis can control the speed of synaptic develop
172 tified three conceptually distinct routes to synaptogenesis: cell-cell contact mediated by adhesion p
173 ued the morphological neuronal phenotype and synaptogenesis defects from ASD neuronal co-cultures.
175 mutants revealed that APP potently promotes synaptogenesis depending on copper binding to the GFLD.
176 that whereas dNedd4S promotes neuromuscular synaptogenesis, dNedd4Lo inhibits it and impairs larval
180 reveal that pdm3 represses expression of the synaptogenesis gene Msp300 to establish the appropriate
181 opose that dysregulation of such specific MN synaptogenesis genes, compounded by many additional tran
182 al factors including regional differences in synaptogenesis, glucose metabolism, and myelination acro
184 ly promotes neurogenesis, neuritogenesis and synaptogenesis; however, the underlying molecular mechan
185 mechanisms that are relevant to depression: synaptogenesis, immunomodulation and regulation of glyco
186 tory system development and for survival and synaptogenesis in auditory sensory afferent neurons.
187 expression of DISC1 suppresses glutamatergic synaptogenesis in developing neuromuscular junctions.
188 show that mouse Sema5A negatively regulates synaptogenesis in early, developmentally born, hippocamp
189 state, results in a selective enhancement of synaptogenesis in gamma-aminobutyric acidergic interneur
191 neural hearing loss and prevented the normal synaptogenesis in inner hair cells (IHCs) in the newly i
195 is characterized by extensive glutamatergic synaptogenesis in striatal spiny projection neurons (SPN
197 pathways regulating mRNA translation during synaptogenesis in the genesis of neurodevelopmental diso
199 olamine increases glutamate transmission and synaptogenesis in the medial prefrontal cortex (mPFC).
200 mammalian target of rapamycin and increased synaptogenesis in the prefrontal cortex are crucial in m
203 pathway modulating structural and functional synaptogenesis, including the GPI-anchored heparan sulfa
204 regeneration is delayed or absent, blue-cone synaptogenesis increases and ectopic synapses are made w
206 of APP transcription, however, ApoE-induced synaptogenesis involves CREB activation rather than cFos
208 nexplored question is whether the process of synaptogenesis is coordinated with the adoption of speci
212 ectively, our results suggest that lateralis synaptogenesis is intrinsically nonselective and that in
214 sm of developmental plasticity wherein rapid synaptogenesis is promoted by the coordinated actions of
215 st that a main role of SYD-2/Liprin-alpha in synaptogenesis is to regulate the polymerization of DPs.
216 We propose that Np65, by regulating IHC synaptogenesis, is critical for auditory function in mam
217 del of synapse development, such as adaptive synaptogenesis, it is possible to study such overproduct
218 odel of dendrite growth based on competitive synaptogenesis largely recapitulates GluD2 sparse and gl
219 ns display abnormal neurogenesis and reduced synaptogenesis leading to functional defects in neuronal
221 n BDNF/TrkB variants that impair hippocampal synaptogenesis may contribute to a spectrum of neurobeha
223 sms, regulates postnatal PN dendritogenesis, synaptogenesis, mitochondrial structure and function, an
224 Elucidating the mechanisms that coordinate synaptogenesis, neuronal activation, and neurotransmitte
228 nges in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a longe
229 pic mechanism by which one afferent controls synaptogenesis of another afferent, but not vice versa.
230 by Foxp2 in neonatal mouse striatum controls synaptogenesis of corticostriatal inputs and vocalizatio
233 hat whereas both profilins are needed during synaptogenesis, only PFN2a is crucial for adult spine pl
238 g to neurogenesis, dendritic development and synaptogenesis organize neural elements into networks kn
239 ing and identify the vesicular transport and synaptogenesis pathways as the major targets of the fear
245 unilateral brain damage results in aberrant synaptogenesis, potentially of transcallosal projections
246 nt synapses in D1-type neurons, likely via a synaptogenesis process, whereas morphine induced silent
247 ns and neuroligins do not themselves mediate synaptogenesis, raising the question of how SPARCL1 enha
248 icits in maturation, surface expression, and synaptogenesis regulated by one amino acid difference wi
250 role in shutting down expression of specific synaptogenesis-related genes in the cerebellum, resultin
256 ay matter following preadolescence overtakes synaptogenesis, resulting in a more efficient, adult-lik
257 etween SMA motoneurons and astrocytes impair synaptogenesis seen in SMA pathology, possibly due to th
258 neurodevelopment of excitatory postsynaptic synaptogenesis, setting the stage for neuronal interconn
259 d with increased glutamate transmission, and synaptogenesis, similar to N-methyl-D-aspartate receptor
261 ch supports the positive role of lecithin in synaptogenesis, synaptic development and maturation.
262 pecific microRNA and plays a pivotal role in synaptogenesis, synaptic plasticity and structural remod
263 glutamate receptor (NMDAR) is essential for synaptogenesis, synaptic plasticity, and higher cognitiv
264 eceptors (NMDARs) have a fundamental role in synaptogenesis, synaptic plasticity, and learning and me
265 on through the modulation of neuritogenesis, synaptogenesis, synaptic plasticity, and memory consolid
266 and function, including neuronal migration, synaptogenesis, synaptic plasticity, and myelination.
267 or understanding the molecular mechanisms of synaptogenesis, synaptic plasticity, and synaptic toxici
268 pecifically, the adaptive algorithm includes synaptogenesis, synaptic shedding, and bi-directional sy
269 ed extracellular matrix proteins in boosting synaptogenesis, synaptic transmission, and synaptic plas
270 sion, with enrichment of genes important for synaptogenesis, synaptic transmission, photoreceptor mor
271 WF), neurogenesis (BrdU TUJ1, DCX and NeuN), synaptogenesis (synaptophysin) and apoptosis (TUNEL).
272 he functional relations of key regulators of synaptogenesis that contribute to both typical cortical
273 ndicate that BAI1 plays an important role in synaptogenesis that is mechanistically distinct from its
274 r of cell-type specific features of auditory synaptogenesis that offers a new entry point for treatin
275 mmune response signaling, axon guidance, and synaptogenesis that significantly influenced DMN modulat
276 e-derived secreted factors are implicated in synaptogenesis, the role of contact-mediated glial-neuro
277 gnaling in astrocytes and promote excitatory synaptogenesis, thereby increasing seizure susceptibilit
281 are hyperactive due to increased excitatory synaptogenesis using electrophysiology, calcium imaging,
282 ase C (PKC) promotes synaptic maturation and synaptogenesis via activation of synaptic growth factors
283 sensitization modulates spine formation and synaptogenesis via CREB-mediated miR132 upregulation, wh
284 expression required for dendritogenesis and synaptogenesis via delayed occupancy of target promoters
285 urotrophic factor (NTF)-dependent excitatory synaptogenesis, via two proteolytic fragments generated
289 ute perturbation of hyaluronan levels during synaptogenesis, we sought to determine how hyaluronan im
290 e capable of promoting neuronal survival and synaptogenesis when co-cultured with iPSC-derived neuron
291 y parvalbumin-expressing interneurons during synaptogenesis, whereas Adamts4 mRNA is exclusively gene
292 s regulate afferent synaptic strength during synaptogenesis, which enables coordinated dampening of t
293 n target of rapamycin complex 1 (mTORC1) and synaptogenesis, which have been implicated in the rapid
294 sory neuron hyperexcitability and excitatory synaptogenesis, which together lead to central sensitiza
295 6 protein is implicated in cell adhesion and synaptogenesis while HAGH protein is related to the oxid
296 RGFP968, were most effective at stimulating synaptogenesis, while the selective HDAC3 inhibitor, RGF
297 synapses with RGCs, preferentially increase synaptogenesis with BCs, and eliminate synapses with wid
298 on neuronal differentiation, migration, and synaptogenesis, with less attention to transcellular int
299 ponds to the period of process outgrowth and synaptogenesis, with robust expression in hippocampal an
300 arisons confirmed massive cell death, before synaptogenesis, within 1-4 DIV upon loss of t-SNAREs (sy