ライフサイエンスコーパス: granule neuron

1 afferent connectivity of adult-born dentate granule neurons.

2 l neurons Neuro2A and primary rat cerebellar granule neurons.

3 rget of ethanol in the developing cerebellar granule neurons.

4 itor highly expressed by adult dentate gyrus granule neurons.

5 gh levels of Abeta released from neighboring granule neurons.

6 rofiles to reflect maturation of glia versus granule neurons.

7 MOPP cells before the activation of dentate granule neurons.

8 both the LL-NSCs and embryonically produced granule neurons.

9 to a significant reduction in the density of granule neurons.

10 red with granule progenitors and postmitotic granule neurons.

11 he dentate neuroepithelium that give rise to granule neurons.

12 ajor IF protein in the parallel processes of granule neurons.

13 bined with confocal imaging of dentate gyrus granule neurons.

14 o its crucial role in the differentiation of granule neurons.

15 ilure of Purkinje neurons, Bergmann glia and granule neurons.

16 c capacity of NSCs and eventually diminished granule neurons.

17 ey become postmitotic and differentiate into granule neurons.

18 vo coding properties of early- and late-born granule neurons.

19 and NADH is toxic to cultures of cerebellar granule neurons.

20 to inhibit axon growth in primary cerebellar granule neurons.

21 m, Nrg3 was found in both Purkinje cells and granule neurons.

22 ole in the postnatal migration of cerebellar granule neurons.

23 s a physical complex with endogenous SnoN in granule neurons.

24 primary cultures of postnatal rat cerebellar granule neurons.

25 be enriched in the developing rat cerebellar granule neurons.

26 er, essentially all Ascl1 lineage cells were granule neurons.

27 rial dysfunction and apoptosis in cerebellar granule neurons.

28 glutamatergic synapse regulation in dentate granule neurons.

29 f a set of long neuronal genes in cerebellar granule neurons.

30 compared to quiescent stem cells and mature granule neurons.

31 of Nkx2.1(+) NSCs and the generation of deep granule neurons.

32 mpanied by intrinsic hyperexcitability of DG granule neurons.

33 her DG volume and increased number of mature granule neurons.

34 differentiation of their progeny into mature granule neurons.

35 for REST in the timing of the maturation of granule neurons.

36 although a majority of the cells matured to granule neurons, a few cells remained as immature progen

37 M-dependent neurite elongation in cerebellar granule neurons, a pathway previously shown to be disrup

38 ality and massive degeneration of cerebellar granule neurons, a phenotype that is dose dependently su

39 ithdrawal of neuronal activity in cerebellar granule neurons activated GSK3beta in the nucleus, leadi

40 and pharmacological approaches to show that granule neuron activation in the anterior dorsal cerebel

41 pes and blueberries, protects the cerebellar granule neurons against ethanol-induced cell death.

42 We found that JAZ protects cerebellar granule neurons against potassium deprivation-induced de

43 ssed at high levels in migrating, cerebellar granule neurons, along with Astn1, at developmental stag

44 se using HEK-293 cells and murine cerebellar granule neurons, along with bioluminescence, calcium FLI

45 imary cultures of hippocampal and cerebellar granule neurons, an effect abolished by treatment with t

46 ously unidentified progenitor for cerebellar granule neurons and a cell of origin for medulloblastoma

47 companied by massive apoptosis of cerebellar granule neurons and accumulation of an aggregated and we

48 ucial role in FS-induced IEG induction in DG granule neurons and associated behavioral responses.

49 ncomitant KCNK3 surface losses in cerebellar granule neurons and cell lines.

50 es the death of otherwise healthy cerebellar granule neurons and cortical neurons in culture.

51 Knockdown of Znhit3 in cultured mouse granule neurons and ex vivo cerebellar slices indicate t

52 xicity in primary cultures of rat cerebellar granule neurons and in rat pheochromocytoma (PC12) cell.

53 ethod to label pre and postsynaptic sites in granule neurons and observed a stereotypical development

54 unit-containing GABA(A)Rs of both cerebellar granule neurons and thalamic relay neurons of the latera

55 (A)Rs) are a prominent feature of cerebellar granule neurons and thalamic relay neurons.

56 Here, granule neurons and their progenitors represent the most

57 Smarc proteins influence the development of granule neurons and whether this population may serve as

58 st neuronal lineage of the telencephalon, DG granule neurons, and in the development of the stem cell

59 trasted with different targets in cerebellar granule neurons, and was consistent with circadian defec

60 Granule neurons appeared most sensitive to TTA exposure

61 The synaptic changes in CA1 and dentate granule neurons are not observed when synaptic transmiss

62 ARP expression, while those in dentate gyrus granule neurons are not, indicating that variable TARP/A

63 Cerebellar granule neurons are the most abundant neurons in the bra

64 tion, and survival of hippocampal adult-born granule neurons are unaffected in the APP bigenic mice,

65 ecomes expressed on the axons of postmitotic granule neurons as they leave the inner EGL (iEGL).

66 ively increased in CA1 pyramidal and dentate granule neurons, as well as in microglia in mice that de

67 rol mice, reflecting decreased production of granule neurons at the peak period of DG neurogenesis.

68 cessary for late-phase maturation of dentate granule neurons both in DG development and during adult

69 t only for the compensatory replenishment of granule neurons but also for scaling interneuron and ast

70 dentate region, and they, in turn, generate granule neurons, but not other neurons, throughout devel

71 NP, potentiated axon outgrowth in cerebellar granule neurons by activating the sequential tyrosine ph

72 time by the equally early innervations of DG granule neurons by glutamatergic mossy cells.

73 tive stress-induced cell death in cerebellar granule neurons by specific regulation of the mRNA for t

74 In mouse cerebellar slice recordings, WT granule neurons can be induced to fire action potentials

75 7V) and wild-type peptides in rat cerebellar granule neuron (CGN) cultures.

76 -6 DPP6-S to the gamma of native [cerebellar granule neuron (CGN)] and reconstituted Kv4.2 channels.

77 ase (nNOS) can protect developing cerebellar granule neurons (CGN) against alcohol-induced death both

78 ke Modifier (SUMO) pathway in rat cerebellar granule neurons (CGN) and that SUMOylation of NaV1.2 cha

79 e extracellular matrix to control cerebellar granule neurons (CGN) GZ occupancy.

80 nd OGC in primary cultures of rat cerebellar granule neurons (CGNs) and cerebellar astrocytes showed

81 he neuroprotective role of LFG in cerebellar granule neurons (CGNs) and PCs in an organotypic cerebel

82 ynitrite to the damage induced in cerebellar granule neurons (CGNs) by treatment with the NO donor S-

83 activity promotes the survival of cerebellar granule neurons (CGNs) during the postnatal development

84 essibility and gene expression in cerebellar granule neurons (CGNs) of the developing mouse.

85 Here, we show that cerebellar granule neurons (CGNs) or neuroblastoma cells exposed to

86 In cerebellar granule neurons (CGNs) primed to undergo apoptosis by lo

87 induces apoptosis in primary rat cerebellar granule neurons (CGNs) principally via inhibition of Rac

88 re, we demonstrate in primary rat cerebellar granule neurons (CGNs) that oxidative or nitrosative str

89 tes neurite outgrowth of cultured cerebellar granule neurons (CGNs) via homophilic adhesion.

90 ta1 promotes neurite outgrowth in cerebellar granule neurons (CGNs) via homophilic cell adhesion, fyn

91 al root ganglion neurons (DRGNs), cerebellar granule neurons (CGNs), and hippocampal neurons.

92 growth cone formation in cultured cerebellar granule neurons (CGNs), dorsal root ganglions (DRGs) and

93 , and Cdc42, induces apoptosis of cerebellar granule neurons (CGNs).

94 ite formation in developing mouse cerebellar granule neurons (CGNs).

95 uring dendritogenesis in maturing cerebellar granule neurons (CGNs).

96 of target promoters in developing cerebellar granule neurons (CGNs).

97 on and maturation of post-mitotic cerebellar granule neurons (CGNs).

98 that activation of the motor-learning-linked granule neuron circuit reorganizes neuronal chromatin in

99 lian brain.SIGNIFICANCE STATEMENT Cerebellar granule neurons comprise over half the neurons in the br

100 allel fiber axons, both early- and late-born granule neurons convey a functionally diverse sensorimot

101 oporation, we find that early- and late-born granule neurons convey similarly diverse sensorimotor in

102 in vivo profoundly impairs the formation of granule neuron dendrite arbors in the cerebellar cortex.

103 5 knockout mice harbor long, highly branched granule neuron dendrites with impaired dendritic claw di

104 promotes the differentiation of postsynaptic granule neuron dendritic claws in the cerebellar cortex.

105 ability phenotype displayed in dentate gyrus granule neurons derived from patients with bipolar disor

106 hypoplasia in mice, due to the impairment of granule neuron differentiation, induction of apoptosis a

107 n and thus activation of genes essential for granule neuron differentiation.

108 In electron micrographs, degenerating granule neurons displayed a unique morphology characteri

109 erating neuronal precursors of glutamatergic granule neurons exhibit significant tangential migration

110 Wnt7a(-/-) dentate granule neurons exhibited dramatically impaired dendriti

111 profile for Arc transcription in hippocampal granule neurons following behavior that is not observed

112 to GSK3beta inhibition protected cerebellar granule neurons from either GSK3beta activation- or neur

113 sing these developmental cues to generate DG granule neurons from human pluripotent stem cells.

114 eurons derived from adult mice or cerebellar granule neurons from postnatal rodents cultured on CNS i

115 R, and GIRK channel subunits, and cerebellar granule neurons from RGS6(-/-) mice showed a significant

116 and on GluA2-containing AMPARs in cerebellar granule neurons from stargazer mice transfected with TAR

117 mutant TBP aggregates in primary cerebellar granule neurons from transgenic SCA17 mice.

118 induced by neuronal activity and as dentate granule neurons functionally integrate in the developing

119 artment interactions to orchestrate distinct granule neuron gene expression modules.

120 Newborn granule neurons generated from neural progenitor cells (

121 We found that cerebellar granule neuron germinal zone exit is regulated by protea

122 hypothesize that it may be related to fewer granule neurons (GN) in the dentate gyrus (DG), a defect

123 In this process, granule neurons (GNs) migrate along Bergmann glia (BG),

124 tivation kinetics of the I(SA) in cerebellar granule neurons has voltage dependence that is remarkabl

125 extual fear and intrinsic excitability of DG granule neurons, implying that enhancing or dampening DG

126 vel stimulus, SINEs are activated in dentate granule neurons in a time course that is similar to that

127 cohesin in anterior dorsal cerebellar vermis granule neurons in adult mice disrupts enhancer-promoter

128 rant pathway (MOPP) cells innervated newborn granule neurons in adult mouse brain.

129 e GPCRs were overexpressed in rat cerebellar granule neurons in culture, the transfected neurons exhi

130 during apoptosis in rat and mouse cerebellar granule neurons in culture.

131 ocess, generating all prenatal and postnatal granule neurons in defined spatiotemporal order.

132 ed dendrites during maturation of cerebellar granule neurons in dissociated cultures and in cerebella

133 interneurons, switch their fate and generate granule neurons in mice.

134 (TAPs) resulted in generation of fewer YFP+ granule neurons in Notch1 iKO mice.

135 Reduced excitability of dentate granule neurons in response to strong depolarizing stimu

136 early genes c-fos and arc in new and mature granule neurons in sedentary mice, it has no such effect

137 For example, cerebellar granule neurons in staggerer and lurcher mutant mice ini

138 Death of cerebellar granule neurons in Tg(DeltaCR) mice is not accompanied b

139 birth, specification, and differentiation of granule neurons in the adult hippocampus.

140 d strikingly triggers excessive migration of granule neurons in the cerebellar cortex.

141 ential stage in the lineage from NSCs to new granule neurons in the dentate gyrus.

142 ce, which show delayed neuronal migration of granule neurons in the developing cerebellum in addition

143 ects, and persistence of ectopic clusters of granule neurons in the external granule layer.

144 Granule neurons in the hippocampal dentate gyrus (DG) re

145 d increased complexity of newly born dentate granule neurons in the hippocampus of Ts65Dn mice.

146 neurons in the olfactory bulb, pyramidal and granule neurons in the hippocampus, and pyramidal cells

147 in primary neurons and impairs migration of granule neurons in the rat cerebellar cortex in vivo.

148 luntary and forced locomotion, whereas other granule neurons in the same region respond similarly to

149 methylation landscape of adult mouse dentate granule neurons in vivo before and after synchronous neu

150 essibility landscapes of adult mouse dentate granule neurons in vivo before and after synchronous neu

151 cohesin preferentially to gene enhancers in granule neurons in vivo.

152 y of dendritic spines in hippocampal dentate granule neurons in vivo.

153 FOXO proteins in hippocampal and cerebellar granule neurons, including in the rat cerebellar cortex

154 ivity in Schwann cells but not in cerebellar granule neurons, indicating a specific sensitivity of th

155 We report that in cultured cerebellar granule neurons induced to die by low potassium treatmen

156 odomain, and promoted survival of cerebellar granule neurons induced to undergo apoptosis.

157 lopment of cortical projections: although DG granule neuron input originating from the entorhinal cor

158 atally generated wild-type and Pten knockout granule neurons integrating into the dentate gyrus using

159 l withdrawal-induced apoptosis in cerebellar granule neurons is associated with aberrant cell cycle a

160 During development, dentate granule neurons lacking Klf-9 show delayed maturation as

161 Embryonic hippocampal and adult-born dentate granule neurons lacking Trim9 exhibit several morphologi

162 erent phenotypes: 1) folded (C- or V-shaped) granule neuron layer, concave toward the hilus and delim

163 sing progenitors (NEPs) are committed to the granule neuron lineage.

164 dicating that, among the subset of activated granule neurons, locomotion (44%-56%) and facial air puf

165 treme cerebellar atrophy due to almost total granule neuron loss.

166 In cultured cerebellar granule neurons, low neuronal activity triggers the intr

167 a novel transcriptional regulator of dentate granule neuron maturation, Kruppel-like factor 9 (Klf-9)

168 ighest in the cerebellum and increased after granule neuron maturation.

169 population with layering aberrations, severe granule neuron migration defects, and persistence of ect

170 pment, associated with an earlier failure in granule neuron migration in the cerebellum, reduced neur

171 to regulate branching in primary neurons and granule neuron migration in vivo.

172 Bergmann fiber scaffold formation, impaired granule neuron migration, and upset Purkinje cell matura

173 Granule neuron number tended toward a reduction in anter

174 ver, GABARs expressed on hippocampal dentate granule neurons of epileptic animals are modified such t

175 containing alpha6 and delta subunits in the granule neurons of the cerebellum.

176 ent in the cortex, subiculum, parasubiculum, granule neurons of the dentate gyrus, and some brainstem

177 ression appears to be remarkably enriched in granule neurons of the dentate gyrus.

178 zation of sensorimotor information in vermal granule neurons of the developing mammalian brain.SIGNIF

179 We find that Smad2 is expressed in primary granule neurons of the developing rat cerebellar cortex.

180 t of the chromatin remodeling enzyme Chd4 in granule neurons of the mouse cerebellum increases access

181 irthdate" or birthdate and knock-out Pten in granule neurons of the murine neonatal dentate gyrus.

182 t axon branching and self-contact in primary granule neurons of the rat cerebellar cortex.

183 SHH tumours closely resembled granule neurons of varying differentiation states that c

184 t necessary for TMT-induced death of dentate granule neurons or local activation of microglia; howeve

185 It is generally believed that cerebellar granule neurons originate exclusively from granule neuro

186 eads to the formation of ectopic branches in granule neuron parallel fiber axons in the cerebellar co

187 rat pups profoundly impairs the formation of granule neuron parallel fiber axons in the rat cerebella

188 Chd4 profoundly impairs the establishment of granule neuron parallel fiber/Purkinje cell synapses in

189 ction in stress-activated dentate gyrus (DG) granule neurons play a crucial role in these behavioral

190 n the control of proliferation of cerebellar granule neuron precursor cells (GCPs), located in the ex

191 lum, with approximately 25% originating from granule neuron precursor cells (GNPCs) after aberrant ac

192 dgehog (Shh) stimulates the proliferation of granule neuron precursor cells (GNPs) by activating the

193 to Shh stimulation in NIH3T3 and cerebellar granule neuron precursor cells in a p53-independent mann

194 Further, Vav1 activity regulated granule neuron precursor germinal zone exit and migratio

195 erebellum due to a significant inhibition of granule neuron precursor proliferation.

196 ing development, proliferation of cerebellar granule neuron precursors (CGNP), candidate cells-of-ori

197 We further show that cerebellar granule neuron precursors (CGNP), which are believed to

198 hh)-induced neuroproliferation in cerebellar granule neuron precursors (CGNP).

199 ase Huwe1 has been inactivated in cerebellar granule neuron precursors (CGNPs) and radial glia.

200 Cerebellar granule neuron precursors (CGNPs) depend on signaling by

201 volves extensive proliferation of cerebellar granule neuron precursors (CGNPs) induced by Sonic Hedge

202 Postnatal proliferation of cerebellar granule neuron precursors (CGNPs), proposed cells of ori

203 rapid peri-natal proliferation of cerebellar granule neuron precursors (CGNPs), proposed cells-of-ori

204 Cerebellar granule neuron precursors (CGNPs), proposed cells-of-ori

205 In primary cerebellar granule neuron precursors (CGNPs), proposed Shh-associat

206 signaling in proliferating mouse cerebellar granule neuron precursors (CGNPs).

207 , which normally stimulates proliferation of granule neuron precursors (GNP) during cerebellar develo

208 Despite an extended proliferation of granule neuron precursors (GNP) in the postnatal externa

209 development, Shh spurs the proliferation of granule neuron precursors (GNP), the precursor cells of

210 the uncontrolled proliferation of cerebellar granule neuron precursors (GNP).

211 Granule neuron precursors (GNPs) are the most actively p

212 In addition, granule neuron precursors (GNPs) are thought to represen

213 Cerebellar granule neuron precursors (GNPs) can give rise to medull

214 that SMB55 cells, and the primary cerebellar granule neuron precursors (GNPs) from which they derive,

215 h) regulates the proliferation of cerebellar granule neuron precursors (GNPs) in part via expression

216 r granule neurons originate exclusively from granule neuron precursors (GNPs) in the external germina

217 nd that cerebellar ectopia were derived from granule neuron precursors (GNPs) that had migrated inwar

218 ocytes) were trans-differentiated from tumor granule neuron precursors (GNPs), which normally never d

219 ate from abnormally proliferating cerebellar granule neuron precursors (GNPs).

220 um: multipotent neural stem cells (NSCs) and granule neuron precursors (GNPs).

221 remature down-regulation of proliferation of granule neuron precursors and precocious maturation of B

222 is highly enriched at the primary cilium of granule neuron precursors and suppresses Shh signaling b

223 nds to block the proliferation of cerebellar granule neuron precursors expressing an oncogenic form o

224 derepressed, whereas Brg-deleted cerebellar granule neuron precursors failed to respond to Shh to in

225 methasone (Dex) impairs the proliferation of granule neuron precursors in the cerebellum, which are t

226 The first role is to amplify the number of granule neuron precursors in the external granular layer

227 ebellar germinal zones, including cerebellar granule neuron precursors in the external granule layer.

228 y found that the proliferation of cerebellar granule neuron precursors is significantly reduced in Np

229 of N-Myc or cyclin D1 in primary cerebellar granule neuron precursors isolated from Ink4c(-/-), p53(

230 ing activity and suppresses proliferation of granule neuron precursors.

231 In cerebellar granule neurons primed to undergo apoptosis, FoxG1 expre

232 Stimulation of granule neuron progenitor (GNP) proliferation is a centr

233 duction is due to decreased radial glial and granule neuron progenitor cell proliferation.

234 Disorganized chromatin limits Purkinje and granule neuron progenitor expansion, resulting in abnorm

235 or the regulated proliferation of cerebellar granule neuron progenitors (CGNP) and for the growth of

236 lasia, decreased proliferation of cerebellar granule neuron progenitors (CGNP), and Purkinje (PC) neu

237 in lineage-committed Ptch1 (+/-) cerebellar granule neuron progenitors (CGNPs) accelerated tumorigen

238 yos, as well as in vitro cultured cerebellum granule neuron progenitors (CGNPs) and SmoM2-driven medu

239 gside differentiation to regulate cerebellar granule neuron progenitors (CGNPs) and to prevent medull

240 Cerebellar granule neuron progenitors (CGNPs) express Aspm when mai

241 Atr deletion in cerebellar granule neuron progenitors (CGNPs) induced proliferation

242 quires regulated proliferation of cerebellar granule neuron progenitors (CGNPs).

243 ription program that drives proliferation of granule neuron progenitors (GNP) within the external ger

244 ion and induce differentiation of cerebellar granule neuron progenitors (GNPs) and primary GNP-like m

245 c-Myc (Myc) or MycN overexpression in granule neuron progenitors (GNPs) induces Group 3 (G3) o

246 nd functional target screening in cerebellar granule neuron progenitors (GNPs) reveal that Zeb1 inhib

247 ome are thought to originate from cerebellar granule neuron progenitors (GNPs) that fail to undergo n

248 signaling causes increased proliferation of granule neuron progenitors (GNPs), and predisposes these

249 coordinated spatiotemporal interplay between granule neuron progenitors (GNPs), Purkinje neurons, and

250 liferation and differentiation of cerebellar granule neuron progenitors (GNPs).

251 dulloblastomas that originate from unipotent granule neuron progenitors in the brain.

252 Genetic inactivation of Chd7 in cerebellar granule neuron progenitors leads to cerebellar hypoplasi

253 lum, MyoD was expressed in the proliferating granule neuron progenitors that are thought to be precur

254 Nestin but not Math1, a marker of committed granule neuron progenitors.

255 xperience increased firing of active dentate granule neurons rapidly and robustly.

256 that inhibition of Tiam1 function in dentate granule neurons reduces synaptic AMPA receptor function

257 wake behaving male and female mice to record granule neuron responses to diverse sensorimotor cues ta

258 contrast to core precerebellar populations, granule neuron responses were relatively heterogeneous,

259 sociated glycoprotein addition to cerebellar granule neurons resulted in a reduction in the associati

260 t that gene-profiling analyses in cerebellar granule neurons reveal that the large majority of genes

261 onjugating enzyme UBC13 in rodent cerebellar granule neurons robustly increases the number of paralle

262 This work demonstrates that granule neurons secrete FGF9 to control formation of the

263 However, little is known about granule neuron signaling at the population scale during

264 glutamatergic synapse regulation in dentate granule neurons.SIGNIFICANCE STATEMENT Several lines of

265 In behavior analyses, granule neuron-specific knockout of RNF8 or UBC13 impair

266 n and find that, although the birth order of granule neurons specifies the positioning of their paral

267 hereas membrane depolarization in cerebellar granule neurons stimulated endogenous proNT-3 secretion,

268 es indicate that ZNHIT3 is indispensable for granule neuron survival and migration, consistent with t

269 messenger RNAs from synchronously developing granule neurons (Sync-TRAP) showed that conditional knoc

270 rotein as an entry point into the cerebellar granule neuron system in combination with super-resoluti

271 slocation of FOXO1 in primary rat cerebellar granule neurons that are deprived of neuronal activity.

272 Strikingly, we identify populations of granule neurons that differentially encode voluntary and

273 A subpopulation of granule neurons that innervated the CA3 region expressed

274 itory niche factor from local mature dentate granule neurons that regulates multiple phases of adult

275 Strikingly, we also uncover populations of granule neurons that respond differentially to voluntary

276 aining NMDA receptors (NMDARs) in cerebellar granule neurons, that when expressed on the surface, pro

277 In mouse cerebellar granule neurons the effects of neuregulin-1 (type I) are

278 Igfbp5 down-regulation occurred in granule neurons through a non-cell-autonomous mechanism

279 behavior to record transgenically identified granule neurons throughout a cerebellar population.

280 ells (NSCs) generate new hippocampal dentate granule neurons throughout adulthood.

281 behaving mice revealed hyperresponsivity of granule neurons to sensorimotor stimuli upon Chd4 knocko

282 tial firing, by studying cultured cerebellar granule neurons treated with siRNA targeted against Scn4

283 find a requirement for MST1 in cell death of granule neurons upon withdrawal of growth factors and ne

284 ulation of glutamatergic synapses in dentate granule neurons using a combination of molecular, electr

285 aptic vesicle cycling in cultured cerebellar granule neurons.Using FM dyes to label the pool of recyc

286 calcium imaging with birth date labeling of granule neurons via in vivo electroporation, we find tha

287 ore, Cdk5 gene deletion specifically from DG granule neurons via viral-mediated gene transfer also re

288 s revealed that intrinsic excitability of DG granule neurons was enhanced by adiponectin deficiency a

289 Using cultures of cerebellar granule neurons, we show that expression of TLE1 is redu

290 ously studied the phenotype of dentate gyrus granule neurons, we turned our attention to studying the

291 aled that approximately half (54%) of vermal granule neurons were activated during these recordings.

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 ating E2 enzyme (UBC13) in rodent cerebellar granule neurons, which greatly increases the parallel fi

297 strategy, tested on rat neonatal cerebellar granule neurons, which involves a 48-hour preconditionin

298 y coupling in vivo Ca(2+) imaging of dentate granule neurons with a novel, unrestrained virtual reali

299 In addition, cerebellar granule neurons with an RNAi-mediated knockdown in POSH

300 lines produced strong labeling in cerebellar granule neurons, with additional expression in the corte