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1 to a significant reduction in the density of granule neurons.
2 red with granule progenitors and postmitotic granule neurons.
3 he dentate neuroepithelium that give rise to granule neurons.
4 ajor IF protein in the parallel processes of granule neurons.
5 bined with confocal imaging of dentate gyrus granule neurons.
6 o its crucial role in the differentiation of granule neurons.
7 ilure of Purkinje neurons, Bergmann glia and granule neurons.
8 c capacity of NSCs and eventually diminished granule neurons.
9 ey become postmitotic and differentiate into granule neurons.
10 and NADH is toxic to cultures of cerebellar granule neurons.
11 to inhibit axon growth in primary cerebellar granule neurons.
12 ole in the postnatal migration of cerebellar granule neurons.
13 s a physical complex with endogenous SnoN in granule neurons.
14 primary cultures of postnatal rat cerebellar granule neurons.
15 of Nkx2.1(+) NSCs and the generation of deep granule neurons.
16 be enriched in the developing rat cerebellar granule neurons.
17 er, essentially all Ascl1 lineage cells were granule neurons.
18 rial dysfunction and apoptosis in cerebellar granule neurons.
19 receptor in transfected cells and cerebellar granule neurons.
20 mpanied by intrinsic hyperexcitability of DG granule neurons.
21 does attenuate MAG inhibition of cerebellar granule neurons.
22 ha(6)r), including ZIC2, a unique marker for granule neurons.
23 del using primary cultures of rat cerebellar granule neurons.
24 ciated with an age-dependent loss of dentate granule neurons.
25 mycin and chloroquine on cultured cerebellar granule neurons.
26 cerebellar nuclei, in addition to cerebellar granule neurons.
27 her DG volume and increased number of mature granule neurons.
28 f a set of long neuronal genes in cerebellar granule neurons.
29 differentiation of their progeny into mature granule neurons.
30 for REST in the timing of the maturation of granule neurons.
31 afferent connectivity of adult-born dentate granule neurons.
32 l neurons Neuro2A and primary rat cerebellar granule neurons.
33 compared to quiescent stem cells and mature granule neurons.
34 rget of ethanol in the developing cerebellar granule neurons.
35 itor highly expressed by adult dentate gyrus granule neurons.
36 gh levels of Abeta released from neighboring granule neurons.
37 rofiles to reflect maturation of glia versus granule neurons.
38 MOPP cells before the activation of dentate granule neurons.
39 both the LL-NSCs and embryonically produced granule neurons.
40 although a majority of the cells matured to granule neurons, a few cells remained as immature progen
41 M-dependent neurite elongation in cerebellar granule neurons, a pathway previously shown to be disrup
42 ality and massive degeneration of cerebellar granule neurons, a phenotype that is dose dependently su
43 ithdrawal of neuronal activity in cerebellar granule neurons activated GSK3beta in the nucleus, leadi
44 the alpha6beta2delta receptor modulates the granule neuron activity as well as potential mechanisms
47 ssed at high levels in migrating, cerebellar granule neurons, along with Astn1, at developmental stag
48 imary cultures of hippocampal and cerebellar granule neurons, an effect abolished by treatment with t
49 ously unidentified progenitor for cerebellar granule neurons and a cell of origin for medulloblastoma
50 companied by massive apoptosis of cerebellar granule neurons and accumulation of an aggregated and we
51 ucial role in FS-induced IEG induction in DG granule neurons and associated behavioral responses.
55 ow that beta-catenin is expressed in newborn granule neurons and in neural progenitor cells in the hi
56 xicity in primary cultures of rat cerebellar granule neurons and in rat pheochromocytoma (PC12) cell.
57 ethod to label pre and postsynaptic sites in granule neurons and observed a stereotypical development
58 unit-containing GABA(A)Rs of both cerebellar granule neurons and thalamic relay neurons of the latera
61 Smarc proteins influence the development of granule neurons and whether this population may serve as
62 st neuronal lineage of the telencephalon, DG granule neurons, and in the development of the stem cell
65 ARP expression, while those in dentate gyrus granule neurons are not, indicating that variable TARP/A
67 tion, and survival of hippocampal adult-born granule neurons are unaffected in the APP bigenic mice,
69 ively increased in CA1 pyramidal and dentate granule neurons, as well as in microglia in mice that de
70 rol mice, reflecting decreased production of granule neurons at the peak period of DG neurogenesis.
71 cessary for late-phase maturation of dentate granule neurons both in DG development and during adult
72 t only for the compensatory replenishment of granule neurons but also for scaling interneuron and ast
73 NP, potentiated axon outgrowth in cerebellar granule neurons by activating the sequential tyrosine ph
74 ere immobilized on the surface of cerebellar granule neurons by avidin-mediated cross-linking, and in
76 differentiation of E14 ES cells into mature granule neurons by sequential treatment with secreted fa
77 tive stress-induced cell death in cerebellar granule neurons by specific regulation of the mRNA for t
78 In mouse cerebellar slice recordings, WT granule neurons can be induced to fire action potentials
80 -6 DPP6-S to the gamma of native [cerebellar granule neuron (CGN)] and reconstituted Kv4.2 channels.
81 ase (nNOS) can protect developing cerebellar granule neurons (CGN) against alcohol-induced death both
82 ke Modifier (SUMO) pathway in rat cerebellar granule neurons (CGN) and that SUMOylation of NaV1.2 cha
83 nd OGC in primary cultures of rat cerebellar granule neurons (CGNs) and cerebellar astrocytes showed
84 he neuroprotective role of LFG in cerebellar granule neurons (CGNs) and PCs in an organotypic cerebel
85 ynitrite to the damage induced in cerebellar granule neurons (CGNs) by treatment with the NO donor S-
86 activity promotes the survival of cerebellar granule neurons (CGNs) during the postnatal development
87 y of domoic acid (DomA), by using cerebellar granule neurons (CGNs) from mice lacking the modifier su
91 induces apoptosis in primary rat cerebellar granule neurons (CGNs) principally via inhibition of Rac
92 re, we demonstrate in primary rat cerebellar granule neurons (CGNs) that oxidative or nitrosative str
94 ta1 promotes neurite outgrowth in cerebellar granule neurons (CGNs) via homophilic cell adhesion, fyn
96 growth cone formation in cultured cerebellar granule neurons (CGNs), dorsal root ganglions (DRGs) and
97 2) on the viability of post-natal cerebellar granule neurons (CGNs), the nature of the cell death inv
98 The ability of neurons, such as cerebellar granule neurons (CGNs), to fire action potentials (APs)
105 in vivo profoundly impairs the formation of granule neuron dendrite arbors in the cerebellar cortex.
106 5 knockout mice harbor long, highly branched granule neuron dendrites with impaired dendritic claw di
107 promotes the differentiation of postsynaptic granule neuron dendritic claws in the cerebellar cortex.
108 eal that PIASx drives the differentiation of granule neuron dendritic claws in the cerebellar cortex.
109 (MEF2A) in the morphogenesis of postsynaptic granule neuron dendritic claws in the cerebellar cortex.
110 hypoplasia in mice, due to the impairment of granule neuron differentiation, induction of apoptosis a
112 ting that the cellular physiology of newborn granule neurons differs from that of the existing popula
113 echnique, primary cultures of rat cerebellar granule neurons display a concentration-dependent respon
115 signaling controls the migration of immature granule neurons down the Bergmann glial fibers into the
117 erating neuronal precursors of glutamatergic granule neurons exhibit significant tangential migration
119 s well as cells that appeared to be immature granule neurons expressing PSA-NCAM, calretinin, and Pro
120 profile for Arc transcription in hippocampal granule neurons following behavior that is not observed
121 to GSK3beta inhibition protected cerebellar granule neurons from either GSK3beta activation- or neur
123 eurons derived from adult mice or cerebellar granule neurons from postnatal rodents cultured on CNS i
124 R, and GIRK channel subunits, and cerebellar granule neurons from RGS6(-/-) mice showed a significant
125 and on GluA2-containing AMPARs in cerebellar granule neurons from stargazer mice transfected with TAR
127 induced by neuronal activity and as dentate granule neurons functionally integrate in the developing
128 nditioned medium to induce markers of mature granule neurons (GABAalpha(6)r), including ZIC2, a uniqu
131 hypothesize that it may be related to fewer granule neurons (GN) in the dentate gyrus (DG), a defect
134 tivation kinetics of the I(SA) in cerebellar granule neurons has voltage dependence that is remarkabl
135 extual fear and intrinsic excitability of DG granule neurons, implying that enhancing or dampening DG
137 hours each day, decreases production of new granule neurons in adulthood through a corticosteroid-de
138 e GPCRs were overexpressed in rat cerebellar granule neurons in culture, the transfected neurons exhi
140 ed dendrites during maturation of cerebellar granule neurons in dissociated cultures and in cerebella
144 early genes c-fos and arc in new and mature granule neurons in sedentary mice, it has no such effect
150 ce, which show delayed neuronal migration of granule neurons in the developing cerebellum in addition
154 neurons in the olfactory bulb, pyramidal and granule neurons in the hippocampus, and pyramidal cells
155 in primary neurons and impairs migration of granule neurons in the rat cerebellar cortex in vivo.
156 d2 D box enhance axonal growth in cerebellar granule neurons in vitro and in the context of the cereb
157 re closely mimics survival and maturation of granule neurons in vivo and should therefore be adopted
158 methylation landscape of adult mouse dentate granule neurons in vivo before and after synchronous neu
159 essibility landscapes of adult mouse dentate granule neurons in vivo before and after synchronous neu
162 FOXO proteins in hippocampal and cerebellar granule neurons, including in the rat cerebellar cortex
165 lopment of cortical projections: although DG granule neuron input originating from the entorhinal cor
166 l withdrawal-induced apoptosis in cerebellar granule neurons is associated with aberrant cell cycle a
167 onal cell line SH-SY5Y and in rat cerebellar granule neurons is directly sensitive to changes in memb
168 n addition, axonal outgrowth from cerebellar granule neurons is increased on or in CM from ChPF siRNA
170 Embryonic hippocampal and adult-born dentate granule neurons lacking Trim9 exhibit several morphologi
171 erent phenotypes: 1) folded (C- or V-shaped) granule neuron layer, concave toward the hilus and delim
175 a novel transcriptional regulator of dentate granule neuron maturation, Kruppel-like factor 9 (Klf-9)
177 population with layering aberrations, severe granule neuron migration defects, and persistence of ect
178 pment, associated with an earlier failure in granule neuron migration in the cerebellum, reduced neur
180 Bergmann fiber scaffold formation, impaired granule neuron migration, and upset Purkinje cell matura
182 ver, GABARs expressed on hippocampal dentate granule neurons of epileptic animals are modified such t
184 lective inactivation of Pten in post-mitotic granule neurons of the cerebellum and dentate gyrus show
186 ent in the cortex, subiculum, parasubiculum, granule neurons of the dentate gyrus, and some brainstem
187 We find that Smad2 is expressed in primary granule neurons of the developing rat cerebellar cortex.
188 and found relatively low UCHL1 expression in granule neurons of the hippocampus and olfactory bulb, t
189 irthdate" or birthdate and knock-out Pten in granule neurons of the murine neonatal dentate gyrus.
191 t necessary for TMT-induced death of dentate granule neurons or local activation of microglia; howeve
192 It is generally believed that cerebellar granule neurons originate exclusively from granule neuro
193 eads to the formation of ectopic branches in granule neuron parallel fiber axons in the cerebellar co
194 rat pups profoundly impairs the formation of granule neuron parallel fiber axons in the rat cerebella
195 Chd4 profoundly impairs the establishment of granule neuron parallel fiber/Purkinje cell synapses in
196 tial function for SnoN in the development of granule neuron parallel fibers in the cerebellar cortex.
197 ction in stress-activated dentate gyrus (DG) granule neurons play a crucial role in these behavioral
198 n the control of proliferation of cerebellar granule neuron precursor cells (GCPs), located in the ex
199 lum, with approximately 25% originating from granule neuron precursor cells (GNPCs) after aberrant ac
200 dgehog (Shh) stimulates the proliferation of granule neuron precursor cells (GNPs) by activating the
201 to Shh stimulation in NIH3T3 and cerebellar granule neuron precursor cells in a p53-independent mann
204 ing development, proliferation of cerebellar granule neuron precursors (CGNP), candidate cells-of-ori
210 rapid peri-natal proliferation of cerebellar granule neuron precursors (CGNPs), proposed cells-of-ori
214 , which normally stimulates proliferation of granule neuron precursors (GNP) during cerebellar develo
216 development, Shh spurs the proliferation of granule neuron precursors (GNP), the precursor cells of
222 h) regulates the proliferation of cerebellar granule neuron precursors (GNPs) in part via expression
223 r granule neurons originate exclusively from granule neuron precursors (GNPs) in the external germina
224 nd that cerebellar ectopia were derived from granule neuron precursors (GNPs) that had migrated inwar
225 ildhood, is believed to derive from immature granule neuron precursors (GNPs) that normally prolifera
228 remature down-regulation of proliferation of granule neuron precursors and precocious maturation of B
229 is highly enriched at the primary cilium of granule neuron precursors and suppresses Shh signaling b
230 nds to block the proliferation of cerebellar granule neuron precursors expressing an oncogenic form o
231 derepressed, whereas Brg-deleted cerebellar granule neuron precursors failed to respond to Shh to in
232 methasone (Dex) impairs the proliferation of granule neuron precursors in the cerebellum, which are t
233 The first role is to amplify the number of granule neuron precursors in the external granular layer
234 ebellar germinal zones, including cerebellar granule neuron precursors in the external granule layer.
235 y found that the proliferation of cerebellar granule neuron precursors is significantly reduced in Np
236 of N-Myc or cyclin D1 in primary cerebellar granule neuron precursors isolated from Ink4c(-/-), p53(
241 Disorganized chromatin limits Purkinje and granule neuron progenitor expansion, resulting in abnorm
242 or the regulated proliferation of cerebellar granule neuron progenitors (CGNP) and for the growth of
243 lasia, decreased proliferation of cerebellar granule neuron progenitors (CGNP), and Purkinje (PC) neu
244 yos, as well as in vitro cultured cerebellum granule neuron progenitors (CGNPs) and SmoM2-driven medu
245 gside differentiation to regulate cerebellar granule neuron progenitors (CGNPs) and to prevent medull
248 ription program that drives proliferation of granule neuron progenitors (GNP) within the external ger
249 ion and induce differentiation of cerebellar granule neuron progenitors (GNPs) and primary GNP-like m
251 nd functional target screening in cerebellar granule neuron progenitors (GNPs) reveal that Zeb1 inhib
252 ome are thought to originate from cerebellar granule neuron progenitors (GNPs) that fail to undergo n
253 l N-Myc deletion limits the proliferation of granule neuron progenitors (GNPs), perturbs foliation, a
254 coordinated spatiotemporal interplay between granule neuron progenitors (GNPs), Purkinje neurons, and
256 Genetic inactivation of Chd7 in cerebellar granule neuron progenitors leads to cerebellar hypoplasi
257 lum, MyoD was expressed in the proliferating granule neuron progenitors that are thought to be precur
260 contrast to core precerebellar populations, granule neuron responses were relatively heterogeneous,
261 sociated glycoprotein addition to cerebellar granule neurons resulted in a reduction in the associati
262 t that gene-profiling analyses in cerebellar granule neurons reveal that the large majority of genes
263 onjugating enzyme UBC13 in rodent cerebellar granule neurons robustly increases the number of paralle
265 the leading process of migrating cerebellar granule neurons senses repulsive Slit molecules by gener
268 rts from our laboratory showed that cultured granule neurons specifically arrest the extension of the
269 hereas membrane depolarization in cerebellar granule neurons stimulated endogenous proNT-3 secretion,
270 es indicate that ZNHIT3 is indispensable for granule neuron survival and migration, consistent with t
271 messenger RNAs from synchronously developing granule neurons (Sync-TRAP) showed that conditional knoc
272 rotein as an entry point into the cerebellar granule neuron system in combination with super-resoluti
273 slocation of FOXO1 in primary rat cerebellar granule neurons that are deprived of neuronal activity.
275 DG were found in close proximity to immature granule neurons that expressed the chemokine SDF-1/CXCL1
277 itory niche factor from local mature dentate granule neurons that regulates multiple phases of adult
278 aining NMDA receptors (NMDARs) in cerebellar granule neurons, that when expressed on the surface, pro
281 behavior to record transgenically identified granule neurons throughout a cerebellar population.
283 responsiveness of CA1 pyramidal and dentate granule neurons to EtOH that we were able to relate to b
284 behaving mice revealed hyperresponsivity of granule neurons to sensorimotor stimuli upon Chd4 knocko
285 tial firing, by studying cultured cerebellar granule neurons treated with siRNA targeted against Scn4
286 find a requirement for MST1 in cell death of granule neurons upon withdrawal of growth factors and ne
287 aptic vesicle cycling in cultured cerebellar granule neurons.Using FM dyes to label the pool of recyc
288 ore, Cdk5 gene deletion specifically from DG granule neurons via viral-mediated gene transfer also re
289 s revealed that intrinsic excitability of DG granule neurons was enhanced by adiponectin deficiency a
292 cularly hippocampus, where P21 dentate gyrus granule neurons were decreased 16%, suggesting abnormal
293 lioside-binding proteins from rat cerebellar granule neurons were identified by quantitative proteomi
294 e report that new neurons, similar to mature granule neurons, were contacted by axosomatic, axodendri
295 es death of otherwise healthy rat cerebellar granule neurons, whereas shRNA-mediated suppression of i
296 strategy, tested on rat neonatal cerebellar granule neurons, which involves a 48-hour preconditionin
297 y coupling in vivo Ca(2+) imaging of dentate granule neurons with a novel, unrestrained virtual reali
298 f age, PDAPP mice also had new dentate gyrus granule neurons with abnormal maturation and fewer dying
300 lines produced strong labeling in cerebellar granule neurons, with additional expression in the corte
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