ライフサイエンスコーパス: hippocampal neuron

1 lei of Purkinje cells, striatal neurons, and hippocampal neurons.

2 spines and synaptic deficits in cultured rat hippocampal neurons.

3 roduce the diverse and complex phenotypes of hippocampal neurons.

4 ity and network synchrony of MeCP2-deficient hippocampal neurons.

5 related coding of space and food stimuli in hippocampal neurons.

6 as lower after epileptiform-like activity in hippocampal neurons.

7 confirm experimentally in culture and slice hippocampal neurons.

8 mediated AMPAR synaptic transmission in mice hippocampal neurons.

9 olarization-stimulated NFAT signaling in rat hippocampal neurons.

10 ature polarised localisation in cultured rat hippocampal neurons.

11 5 complex partner at dendritic spines of rat hippocampal neurons.

12 itic arborization and spine morphogenesis in hippocampal neurons.

13 enriched in the nucleus and synapses of the hippocampal neurons.

14 rface expression of the receptor in cultured hippocampal neurons.

15 and enhanced long-term potentiation (LTP) in hippocampal neurons.

16 in PS1/gamma-secretase- and EphA3-deficient hippocampal neurons.

17 icantly decreases synapse numbers in primary hippocampal neurons.

18 roteins in the postsynaptic density (PSD) of hippocampal neurons.

19 cells, and alpha-synuclein aggregates in rat hippocampal neurons.

20 imaging data of CaMKIIa mRNA and protein in hippocampal neurons.

21 r protein complex, in the development of rat hippocampal neurons.

22 physiological properties of mitochondria in hippocampal neurons.

23 tor (GABAAR)-mediated transmission in mature hippocampal neurons.

24 lar stress-gated switch function in cultured hippocampal neurons.

25 s reshaping includes the addition of newborn hippocampal neurons.

26 N1 controls the plasticity of cultured mouse hippocampal neurons.

27 ical player in Rac1 regulation during OGD in hippocampal neurons.

28 stributes in clusters along the dendrites of hippocampal neurons.

29 go in real time within axons or dendrites in hippocampal neurons.

30 down occludes OGD-induced Rac1 activation in hippocampal neurons.

31 against the deleterious impact of AbetaOs on hippocampal neurons.

32 C1 or mTORC2 in cultured mouse glutamatergic hippocampal neurons.

33 yzed image data on filopodia in cultured rat hippocampal neurons.

34 to stimulate PAK phosphorylation in cultured hippocampal neurons.

35 ions interfere with E-T coupling in cultured hippocampal neurons.

36 l RNA granule substrate and for mGluR-LTD in hippocampal neurons.

37 ction resulted in loss of mushroom spines in hippocampal neurons.

38 cular junctions, neuroendocrine cells and in hippocampal neurons.

39 vent AbetaO-induced synapse loss in cultured hippocampal neurons.

40 epropionic acid) receptor internalization in hippocampal neurons.

41 but not excitatory, postsynapses in cultured hippocampal neurons.

42 membrane proteins in the somatic surface of hippocampal neurons.

43 e receptors (NMDARs), or the surface of live hippocampal neurons.

44 and processing of major NRG isoforms in rat hippocampal neurons.

45 ation in synaptic facilitation of excitatory hippocampal neurons.

46 of the mutant tRNA synthetase, NLL-MetRS, to hippocampal neurons.

47 22/23 complex in both HEK293T cells and live hippocampal neurons.

48 otential, exocytosis, and Ca(2+) in cultured hippocampal neurons.

49 ith 40 nm spatial resolution, on primary rat hippocampal neurons.

50 c-Fos induced by depolarization of cultured hippocampal neurons.

51 s toward the leading edge in growth cones of hippocampal neurons.

52 pressed in T-cells, but also in striatal and hippocampal neurons.

53 m signaling or disrupt the survival of young hippocampal neurons.

54 s synaptic plasticity in dendritic spines of hippocampal neurons.

55 uronal isoform of human BIN1 in cultured rat hippocampal neurons.

56 r RQ profoundly impacts protein functions in hippocampal neurons.

57 ly inhibited glutamatergic synaptogenesis in hippocampal neurons.

58 nts and increases action potential firing in hippocampal neurons.

59 ctivity in developing and mature cultures of hippocampal neurons.

60 ate neurotoxicity in primary cultures of rat hippocampal neurons.

61 of TrkB-BDNF-signaling endosomes in primary hippocampal neurons.

62 in which SIRT3 is selectively depleted from hippocampal neurons.

63 of SVPs, controlling presynaptic strength in hippocampal neurons.

64 Furthermore, in hippocampal neurons 12 facilitated phasic and tonic GABA

65 ional sci-ATAC-seq preparation from cultured hippocampal neurons (899 high-quality cells, 43,532 mean

66 cute and/or latent HSV-1 infection in mature hippocampal neurons, a region of the brain severely impa

67 In this study, we find that in hippocampal neurons, Abeta acutely induces tubulin postt

68 Silencing CYLD in hippocampal neurons abolishes NMDA-induced chemical long

69 ductances of simulated dentate gyrus and CA3 hippocampal neurons according to our measurements to der

70 activation and enhanced the addition of new hippocampal neurons accumulatively.

71 We present evidence that, in hippocampal neurons, activation of the Sonic hedgehog (S

72 MARCKS stimulates neuritogenesis of primary hippocampal neurons after addition to the culture.

73 er showed that knockdown of MeCP2 in primary hippocampal neurons also resulted in reduced network int

74 since GABA current density was unaffected in hippocampal neurons, although mutant receptors exhibited

75 In hippocampal neuron and microglia co-cultures, synapse el

76 otentials in single trials from cultured rat hippocampal neurons and can be used in concert with gree

77 at the cellular level and most prominent in hippocampal neurons and cerebellar Purkinje cells.

78 ces anterograde axonal trafficking of APP in hippocampal neurons and dampens secretion of the inflamm

79 ippocampal IEDs transiently change firing of hippocampal neurons and disrupted selectively the retrie

80 iously published data from dissociated mouse hippocampal neurons and dissociated rat cortical neurons

81 or appropriate morphogenesis of cortical and hippocampal neurons and fidelitous responses to the axon

82 trates for zebrafish single cell RGCs, mouse hippocampal neurons and goldfish, zebrafish and chick re

83 tory en passant boutons in axons of cultured hippocampal neurons and in hippocampal slices expressing

84 promote the production of Ephexin5 in mature hippocampal neurons and in mice expressing human amyloid

85 RAPL1) regulates dendrite morphology of mice hippocampal neurons and induced pluripotent stem cell-de

86 (VGCCs), and can also be observed in primary hippocampal neurons and Jurkat T cells.

87 CC interactions were modulated by Tau in rat hippocampal neurons and mouse brain.

88 , we established transwell cocultures of rat hippocampal neurons and MSCs.

89 duce distinct effects on the excitability of hippocampal neurons and networks.

90 holipid anchored GFP in the cell membrane of hippocampal neurons and obtain the size and energy of hi

91 ffered as homogenous substrates, neurites of hippocampal neurons and of zebrafish single cell RGCs we

92 nti-NL1 antibodies reduced AbetaO binding to hippocampal neurons and prevented AbetaO-induced neurona

93 ic calcium signals along dendritic arbors of hippocampal neurons and relate this to measures of synap

94 ates dense core vesicle transport in primary hippocampal neurons and rescues integrin trafficking in

95 projections from cell bodies of primary rat hippocampal neurons and sequencing total RNA, we found a

96 itro experiments where CASPR2-IgG binding to hippocampal neurons and to CASPR2-transfected HEK cells

97 with evoked release, both in PC12 cells and hippocampal neurons and was abolished upon charge neutra

98 nsufficient nuclear calcium signaling in CA1 hippocampal neurons and, consequently, reduced expressio

99 ite outgrowth (PC-12 cells and primary mouse hippocampal neurons) and the formation of orientated neu

100 (NPs) for labeling the entire axon tract of hippocampal neurons, and an external magnetic field grad

101 demonstrated infection in cortical neurons, hippocampal neurons, and glial and endothelial cells.

102 e the nanoscale distribution of Fyn in mouse hippocampal neurons, and manipulated the expression of T

103 a1c(KO) mice exhibit elevated death of young hippocampal neurons, and that treatment with the neuropr

104 high-cholesterol diet, cholesterol levels in hippocampal neurons are increased.

105 ned brain sections, dendritic arbors of male hippocampal neurons are more complex than females.

106 Our findings present key evidence that the hippocampal neurons are not merely mapping the static en

107 endocrine and neuropeptidergic signaling in hippocampal neurons as a novel substrate of importance i

108 We recorded from hippocampal neurons as male Long-Evans rats performed 6

109 of dendrite branching points in CA1 and CA2 hippocampal neurons associated to hippocampal cognitive

110 otein, in the dendrites and soma of cultured hippocampal neurons at different developmental stages, a

111 In rat hippocampal neurons, ATP production by either glycolysis

112 of acquired epilepsy, we show that principal hippocampal neurons become intrinsically hyperexcitable.

113 Wnt5a expression in hippocampal neurons begins postnatally, and its deletion

114 ssed in both excitatory and inhibitory mouse hippocampal neurons (both sexes), its chronic stimulatio

115 These decreases were greater in lower-firing hippocampal neurons but also higher-firing frontal corti

116 n of Pyk2 reduces dendritic spine density of hippocampal neurons by a kinase-dependent mechanism.

117 f the modulation of the individual firing of hippocampal neurons by an IED predicted the extent of re

118 ences to increase the addition of adult-born hippocampal neurons by increasing the firing of active D

119 NA isolated specifically from Ctcf CKO mouse hippocampal neurons by ribosomal affinity purification i

120 Fo ATP synthase function in primary cultured hippocampal neurons by using non-lethal oligomycin A tre

121 In hippocampal neurons, calcium ion (Ca2+) flux through N-m

122 ansmission at glutamatergic synapses between hippocampal neurons cause enlargement of the dendritic s

123 S-SCAM knockdown in cultured hippocampal neurons caused a drastic loss of both pre- a

124 BAI1 loss from mouse or rat hippocampal neurons causes dendritic hypertrophy, wherea

125 included a smaller cortical lesion, reduced hippocampal neuron cell death, and decreased NOX2- and N

126 viral-mediated selective IL-1R1 deletion in hippocampal neurons confirmed that IL-1 receptor in the

127 found that most presynapses of cortical and hippocampal neurons contain only Munc13-1, whereas appro

128 ality of trajectory-dependent information in hippocampal neurons correlated with task performance.

129 us release events in synapses formed between hippocampal neurons cultured from rats of both sexes.

130 ese changes, we recorded from pairs of mouse hippocampal neurons cultured in a two-neuron microcircui

131 ed by decreased dendritic complexity in male hippocampal neurons cultured in phenol red-free media or

132 uction, we treated mixed-sex embryonic mouse hippocampal neuron cultures with the iron chelator defer

133 In dissociated rat hippocampal neuron cultures, we used fluorescent Zn(2+)

134 Mature dendritic spines on CA1 pyramidal hippocampal neurons decreased 4 days after the precipita

135 mologous to human CRMP4 (S541Y), in cultured hippocampal neurons derived from Crmp4-knockout (KO) mic

136 cal for assembly of stalled polysomes in rat hippocampal neurons derived from embryos of either sex.

137 rved an overexpression of KCNC1 and KCNC2 in hippocampal neurons derived from lithium responders.

138 ns in the amygdala and lateral hypothalamus, hippocampal neurons discriminated between tastes predomi

139 ting reinstatement, a separate population of hippocampal neurons distinguishes different scene cues (

140 Following CCI injury, hippocampal neurons downregulated d-serine levels, while

141 known as KDR or FLK1) are expressed in mouse hippocampal neurons during development, with VEGFR2 loca

142 6 proteins that were altered in synthesis in hippocampal neurons during spatial memory formation.

143 nd cause degeneration of dendrites on murine hippocampal neurons, effects that entirely dependent on

144 ZipACR expressed in cultured mouse hippocampal neurons enabled precise photoinhibition of i

145 vity in the hippocampus but it's unclear how hippocampal neurons encode movement state.

146 asting morphological changes in cortical and hippocampal neurons even during a sedentary period of ra

147 In isolated primary hippocampal neurons ex vivo, extracellular acetate induc

148 Consistent with this hypothesis, hippocampal neurons exhibited increases in intrinsic exc

149 In cultured rat hippocampal neurons, exogenously expressed Nir2 did not

150 -clamp physiology in conditional null mutant hippocampal neurons expressing Cre and either wildtype,

151 e scrutinized cryo-electron tomograms of rat hippocampal neurons for the occurrence and spatial distr

152 of alphaSyn pathology in cultured excitatory hippocampal neurons from both sexes of mice.

153 role in the postsynaptic development of rat hippocampal neurons from both sexes.

154 ression at the AIS of cultured rat embryonic hippocampal neurons from both sexes.

155 herence of calcium transients from DIV 12-15 hippocampal neurons from GCaMP6s mice after applying var

156 In primary cultures of hippocampal neurons from knockouts, NMDA had no neurotox

157 Consequently, in hippocampal neurons from male and female FMRP KO mice, w

158 K293 cells and from NMDA receptors native to hippocampal neurons from male and female rats, we record

159 Hippocampal neurons from Mecp2 knockout (KO) mice do not

160 proteolytic processing of Nrxns in cultured hippocampal neurons from mice and rats of both sexes.

161 Hippocampal neurons from mice lacking PRMT8 have no dete

162 ontrol RIM and Munc13-1 activity in cultured hippocampal neurons from mice of either sex and compared

163 uence underlying the life-long generation of hippocampal neurons from quiescent neural stem cells (NS

164 of individual synaptic vesicles in cultured hippocampal neurons from rats of both sexes with advance

165 Acutely dissociated hippocampal neurons from Scn8a(N1768D/+) mice showed inc

166 Principal hippocampal neurons from such epileptic animals display

167 that isoflurane disrupts the development of hippocampal neurons generated in the early postnatal per

168 In primary hippocampal neurons, germline NR1 autoantibodies strongl

169 ine, structural remodeling of prefrontal and hippocampal neurons has been proposed as critical.

170 and memory loss, whereas their cortical and hippocampal neurons have lower rate of neuritogenesis in

171 an OGD-induced increase in Rac1 activity in hippocampal neurons; however, the identity of an antagon

172 ed potassium (SK)-channel dysfunction causes hippocampal neuron hyperexcitability in the FXS mouse mo

173 genetic conditional ablation of Hdac1 in CA1 hippocampal neurons (i.e., Camk2a-cre;Hdac1(fl/fl)), we

174 get-differentiated subpopulations of ventral hippocampal neurons identify a circuit by which fear may

175 lammation with LPS increases excitability in hippocampal neurons in a sex- and age-dependent manner t

176 interleukin-33 (IL-33) is expressed by adult hippocampal neurons in an experience-dependent manner an

177 e for a mitochondrial protein deacetylase in hippocampal neurons in behavioral and GABAergic synaptic

178 ial cells in renal failure, and cortical and hippocampal neurons in brain trauma.

179 ond messengers and kinases and used them, in hippocampal neurons in culture and intact brain slices,

180 mate receptors of the AMPA and NMDA types in hippocampal neurons in culture induces changes in the ne

181 ses the clustering of Cav1.2 in dendrites of hippocampal neurons in culture.

182 in the hippocampus, we recorded from single hippocampal neurons in macaque monkeys navigating a virt

183 amined the spatial coding characteristics of hippocampal neurons in mice and rats navigating in diffe

184 this possibility, we recorded the firing of hippocampal neurons in mice navigating virtual reality e

185 o monitor NKA transport activity in male rat hippocampal neurons in situ We report that this activity

186 from the cytosol/dendrites to the nucleus of hippocampal neurons in the mouse brain.

187 ampus and contribute to hyperexcitability of hippocampal neurons in this model of SCN8A encephalopath

188 econstruct effective networks of primary rat hippocampal neurons in vitro.

189 The resultant structural alterations in hippocampal neurons in vivo are associated with improvem

190 Notably, while rodent hippocampal neurons, including populations in subfield C

191 HP2(D61G) in excitatory, but not inhibitory, hippocampal neurons increased ERK signaling and impaired

192 ression and functional output, as HRD1 KD in hippocampal neurons increased Tomo-1 protein level and d

193 onstrated that shRNA knockdown of PACSIN1 in hippocampal neurons increases KCC2 expression and hyperp

194 ur results reveal that inducing autophagy in hippocampal neurons is a necessary mechanism to enhance

195 m concentration ([Ca2+]i) in cultured preCGG hippocampal neurons is chronically elevated, 3-fold comp

196 ronal store-operated calcium entry (nSOC) in hippocampal neurons is regulated by STIM2 protein.

197 utophagy, we find that inducing autophagy in hippocampal neurons is required to form novel memory by

198 precursors (SVPs) to en passant synapses in hippocampal neurons is specified by an interplay between

199 In post-mitotic cultured hippocampal neurons, knockdown of mis12 increased the fi

200 Furthermore, hippocampal neurons lacking APP family exhibit hyperexci

201 Hippocampal neurons lacking both NgR1 and LilrB2 exhibit

202 requency epileptiform discharges in cultured hippocampal neurons leads to caspase-dependent cleavage

203 Treatment also decreased hippocampal neuron loss and rescued cognitive deficits.

204 ective ablation of PTP1B in neurons prevents hippocampal neuron loss and spatial memory deficits in a

205 rf72 alleles exacerbated cognitive deficits, hippocampal neuron loss, glial activation and accumulati

206 In cultured hippocampal neurons, Lphn2 maintained synapse numbers vi

207 Augmenting survival of young hippocampal neurons may thus provide an effective therap

208 ross the axonal arborization of cultured rat hippocampal neurons (mixed male and female).

209 vs. AE3(-/-) mice show that AE3 (present in hippocampal neurons, not astrocytes; mediates HCO3(-) ef

210 re, but new data from Chen-Engerer et al. in hippocampal neurons now challenge this idea and indicate

211 sed in a cell line derived from PrP knockout hippocampal neurons, NpL2.

212 n and is able to restore their deficiency in hippocampal neurons obtained from PS1-M146V-KI AD mouse

213 e, a significant overexpression of A(2A)R in hippocampal neurons of aged humans, which is aggravated

214 We show that in cultured rat hippocampal neurons of both sexes, TRIM46 levels steadil

215 Our results show that, in mouse hippocampal neurons of either sex, presynaptic autophagy

216 Electrophysiological recordings from hippocampal neurons of KCTD knock-out mice are consisten

217 We found that, in hippocampal neurons of male mice, the BAD-BAX-caspase-3

218 orms of tau, as well as LAMP1 and p62 in the hippocampal neurons of tauopathy mice.

219 sparse expression was observed in excitatory hippocampal neurons of the CA1- or CA3-region.

220 (V)2s using conditional knockout in cultured hippocampal neurons or at the calyx of Held, which aboli

221 Short-term exposure of cultured rat hippocampal neurons or ex vivo human cortical slices to

222 the 27 Kv1-precipitating samples bound live hippocampal neurons or Kv1 extracellular domains, but 16

223 t-mediated repulsion events in primary mouse hippocampal neurons over 9 min at 2 s temporal resolutio

224 ession, which, importantly, impacted several hippocampal neuron plasticity processes.

225 Specifically, ventral hippocampal neurons projecting to the prelimbic cortex,

226 ng, we show that knocking down GluN3A in rat hippocampal neurons promotes the inducible transcription

227 samples were systematically tested for live hippocampal neuron reactivity, IgG precipitation of (125

228 d abundance of ROCK1 in cultured primary rat hippocampal neurons reduced dendritic spine length throu

229 with neocortex.SIGNIFICANCE STATEMENT Rodent hippocampal neurons replay waking events during sharpwav

230 ssential for memory consolidation, mark when hippocampal neurons replay waking firing patterns.

231 tively, stress-dependent IL-1R1 signaling in hippocampal neurons represents a novel mechanism by whic

232 Specifically, cholesterol enrichment of rat hippocampal neurons resulted in enhanced channel activit

233 mics, we determined that CB(1) activation in hippocampal neurons resulted in increased ribosomal prot

234 he cytoskeletal organization in cultured rat hippocampal neurons, resulting in dystrophic neurites an

235 Knockdown of LASP1 in cultured rat hippocampal neurons results in a substantial reduction i

236 ivation of VEGF/VEGFR2 signaling in isolated hippocampal neurons results in increased axon branching.

237 t assays and single molecule imaging in live hippocampal neurons revealed the presence of circulating

238 ysiological activity from large ensembles of hippocampal neurons starting on the first day after eye

239 odels, early-life adversity directly impacts hippocampal neuron structure and connectivity with progr

240 ith clathrin-coated vesicles and synapses of hippocampal neurons, suggesting a crucial role of TBC1D2

241 a specific subset of synapses in CA1-region hippocampal neurons, suggesting that Lphn2 acts as a syn

242 Here, we identified a subset of hippocampal neurons that discriminated between tastes ba

243 We identified a subset of hippocampal neurons that responded to tastes, some of wh

244 Our computational model of BD hippocampal neurons that was based on our measurements r

245 ential for the proper dendritic branching of hippocampal neurons that were cultured in vitro and for

246 red a physiological instability intrinsic to hippocampal neurons that were derived from nonresponder

247 tability that appeared only in CA3 pyramidal hippocampal neurons that were derived from patients with

248 lithium responders) and not in CA3 pyramidal hippocampal neurons that were derived from patients with

249 hese dysregulated in dying and surviving rat hippocampal neurons - that are targeted by ten TBI-alter

250 loss-of-function assays, we show that in rat hippocampal neurons the MPS is an actomyosin network tha

251 When overexpressed in rat hippocampal neurons, the hyperactive BICD2 mutants decre

252 In hippocampal neurons, the overexpression of full-length I

253 lysosomal vesicles to the cytosol in primary hippocampal neurons through the TRPML1 channel.

254 Exposure of primary hippocampal neurons to anti-Drebrin autoantibodies resul

255 pathway may function as a nutrient sensor in hippocampal neurons to couple memory performance to diet

256 baseline alterations caused nonresponder BD hippocampal neurons to drastically shift their excitabil

257 er to deliver precise amounts of reagents to hippocampal neurons to elicit time- and dose-precise res

258 d optogenetics to drive individual mouse CA1 hippocampal neurons to fire in theta frequency bursts to

259 hypothesize that IL-1 acts on this subset of hippocampal neurons to influence cognitive and mood alte

260 erived endocrine signals act on receptors in hippocampal neurons to reduce (leptin, glucagon-like pep

261 echanisms to determine theta-phase timing of hippocampal neurons to support memory and spatial naviga

262 ging and single nanoparticle tracking in rat hippocampal neurons to unveil the nanoscale topography o

263 Here, we show that APs and EPSPs in mouse hippocampal neurons trigger two spatially segregated and

264 Taken together, the data suggest that in hippocampal neurons, TrkB-signaling endosomes are in fac

265 In hippocampal neurons, two different Munc13s-Munc13-1 and

266 to depolarizing current injections for every hippocampal neuron type from published experiments.

267 us work, the comprehensive knowledge base of hippocampal neuron types Hippocampome.org systematically

268 phorylation of endogenous Nlgn1 in CA1 mouse hippocampal neurons using a photoactivatable tyrosine ki

269 Conversely, overexpressing OGT in mature hippocampal neurons using a viral-mediated approach enha

270 Conversely, chemical stimulation of hippocampal neurons using the epileptogenic agent kainic

271 gged synaptic proteins expressed in cultured hippocampal neurons, using fluorescence recovery after p

272 ion to endosomes is regulated in primary rat hippocampal neurons, using quadruple immunolocalization

273 GD/ischemia contributes to neuronal death in hippocampal neurons via diverse effects on NADPH oxidase

274 fested by impaired long-term potentiation in hippocampal neurons, was also evident in both ipsilatera

275 In primary rat hippocampal neurons, we developed a mitophagy induction

276 itative immunofluorescence in cultured mouse hippocampal neurons, we discovered that the kainate rece

277 the input and output spike trains of single hippocampal neurons, we explored neural codes through wh

278 g lentiviral-mediated shRNA knockdown in rat hippocampal neurons, we find that ZDHHC14 controls palmi

279 In mature hippocampal neurons, we observed rapid translocation of

280 ing synaptic fluorescence probes in cultured hippocampal neurons, we report that trans-synaptic activ

281 ng a molecular replacement approach in mouse hippocampal neurons, we show here that tamalin plays a c

282 ysiological techniques to study cultured rat hippocampal neurons, we show that postsynaptic dysfuncti

283 whether the intrinsic membrane properties in hippocampal neurons were altered as a consequence of ear

284 he EAD-like waveforms of Scn8a(N1768D/+) CA1 hippocampal neurons were blocked by tetrodotoxin, riluzo

285 CA1 hippocampal neurons were exposed to two common insults t

286 working memory and intrinsic excitability of hippocampal neurons were negatively affected by the trea

287 Cultured rat hippocampal neurons were treated with cerebrospinal flui

288 Syt-17 is localized to the Golgi complex in hippocampal neurons, where it coordinates import of vesi

289 ulates in the somatodendritic compartment of hippocampal neurons, where it forms immobile complexes o

290 DCX reduces dendritic complexity of cultured hippocampal neurons, whereas neurons expressing FRY-muta

291 ncreased Cav2.3 translation and R current in hippocampal neurons which is disrupted in FMRP KO mice.

292 ral vector approach in mice, we report novel hippocampal neurons which we refer to as LINCs, as they

293 an imbalance of excitation and inhibition in hippocampal neurons, which affects 'Hebbian' synaptic pl

294 revented homeostatic scaling down in primary hippocampal neurons, which is rescued via charge inversi

295 ed molecular pattern (DAMP) in primary adult hippocampal neurons, while Abeta aggregation is a long-t

296 impact of Cav-1 on structural plasticity of hippocampal neurons with age.

297 By analyzing 24 hippocampal neurons with three distinct single-cell geno

298 ubthreshold theta oscillations of individual hippocampal neurons, with SomArchon showing that the spi

299 educes expression of heteromeric channels in hippocampal neurons without affecting internalization, K

300 ator of NMDA receptor surface trafficking in hippocampal neurons, without altering AMPA receptor traf