ライフサイエンスコーパス: cultured hippocampal neuron

1 T1-R283W to stimulate PAK phosphorylation in cultured hippocampal neurons.

2 ibitory, but not excitatory, postsynapses in cultured hippocampal neurons.

3 o regulate synapse structure and function in cultured hippocampal neurons.

4 -protein signaling in silencing induction in cultured hippocampal neurons.

5 A interference (RNAi) to knockdown AMPARs in cultured hippocampal neurons.

6 the neuromodulatory effects of serotonin in cultured hippocampal neurons.

7 erol modulated Abeta-induced Tau cleavage in cultured hippocampal neurons.

8 ase machinery in neurosecretory cells and in cultured hippocampal neurons.

9 ed by blockade of AMPA receptors (AMPARs) in cultured hippocampal neurons.

10 ate Wnt-5a signaling and dendritic spines in cultured hippocampal neurons.

11 exocytic fusion at the axon and dendrite of cultured hippocampal neurons.

12 ion induced predominant proBDNF secretion in cultured hippocampal neurons.

13 arize the initiation and turning of axons in cultured hippocampal neurons.

14 and the phosphorylation of IRS-1 and tau in cultured hippocampal neurons.

15 ynthase or CAPON) in dendritic patterning of cultured hippocampal neurons.

16 mulated above 25 Hz in both HEK293 cells and cultured hippocampal neurons.

17 O enhance GABAergic synaptic transmission in cultured hippocampal neurons.

18 generation of a toxic 17 kDa tau fragment in cultured hippocampal neurons.

19 receptors (AMPARs) on the plasma membrane of cultured hippocampal neurons.

20 ephrin-B1-induced growth cone withdrawal in cultured hippocampal neurons.

21 id pathology and in Abeta42 oligomer-treated cultured hippocampal neurons.

22 duced occupancy of the promoter by BHLHB2 in cultured hippocampal neurons.

23 minal peptides increase synaptic activity in cultured hippocampal neurons.

24 alyze cell-surface Nav1.6 within the soma of cultured hippocampal neurons.

25 obile FM1-43-labeled vesicles in synapses of cultured hippocampal neurons.

26 uces the density of presynaptic terminals in cultured hippocampal neurons.

27 -state accumulation during axon outgrowth in cultured hippocampal neurons.

28 1b for the morphology of dendritic spines of cultured hippocampal neurons.

29 presynaptic and postsynaptic compartments in cultured hippocampal neurons.

30 ough which BDNF increases synapse density in cultured hippocampal neurons.

31 y of glutamatergic and GABAergic synapses in cultured hippocampal neurons.

32 this Kv2.1 clustering in both HEK cells and cultured hippocampal neurons.

33 lphaCaMKII 5' and 3' untranslated regions in cultured hippocampal neurons.

34 rtical and hippocampal brain sections and in cultured hippocampal neurons.

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

36 AMPAR surface insertion was also observed in cultured hippocampal neurons.

37 in vivo, and brief glutamate stimulation of cultured hippocampal neurons.

38 t in E(GABA) values and increased spiking of cultured hippocampal neurons.

39 activation of presynaptic silent synapses in cultured hippocampal neurons.

40 ntegrins are involved in spine remodeling in cultured hippocampal neurons.

41 s alpha1-chimaerin to the plasma membrane of cultured hippocampal neurons.

42 hRs by expressing epitope-tagged subunits in cultured hippocampal neurons.

43 ney 293 cells stably expressing CB(1) and in cultured hippocampal neurons.

44 re used to disrupt SNARE protein function in cultured hippocampal neurons.

45 elayed the maturation of dendritic spines in cultured hippocampal neurons.

46 ls and on native non-L-type Ca2+ currents of cultured hippocampal neurons.

47 t SNARE-mediated neurotransmitter release in cultured hippocampal neurons.

48 fferentiated living PC12 cells as well as in cultured hippocampal neurons.

49 d the generation of a 17 kDa tau fragment in cultured hippocampal neurons.

50 element-binding protein (pCREB) signaling in cultured hippocampal neurons.

51 tes the growth and branching of dendrites in cultured hippocampal neurons.

52 e loss of AMPA receptors from the surface of cultured hippocampal neurons.

53 c cytochrome c after NMDA overstimulation in cultured hippocampal neurons.

54 MKII is essential for synaptic plasticity in cultured hippocampal neurons.

55 reen fluorescent protein-tagged synapsins in cultured hippocampal neurons.

56 ocalizes with the NMDA receptor at spines of cultured hippocampal neurons.

57 etastin increased [Ca2+]i in a population of cultured hippocampal neurons.

58 wo kinds of GABAA receptors are expressed on cultured hippocampal neurons.

59 ippocampus, increases dendritic branching in cultured hippocampal neurons.

60 demonstrated by three independent assays in cultured hippocampal neurons.

61 ell surface to intracellular compartments in cultured hippocampal neurons.

62 ty of calpain to cleave the NMDA receptor in cultured hippocampal neurons.

63 channel molecules to the initial segment of cultured hippocampal neurons.

64 ASIC1 was not gated by synaptic activity in cultured hippocampal neurons.

65 agonist-induced internalization of GluRs in cultured hippocampal neurons.

66 beta-actin mRNA localization in dendrites of cultured hippocampal neurons.

67 ation-induced changes in cytosolic Ca(2+) in cultured hippocampal neurons.

68 ites lacking postsynaptic specializations in cultured hippocampal neurons.

69 -5-methylisoxazole-4-propionate receptors in cultured hippocampal neurons.

70 and downregulates synaptic AMPAR function in cultured hippocampal neurons.

71 ustering of GABA(A) receptors (GABA(A)Rs) in cultured hippocampal neurons.

72 afficking and activation of TrpC channels in cultured hippocampal neurons.

73 ed role in regulating synaptic plasticity in cultured hippocampal neurons.

74 essed in Xenopus oocytes, HEK 293 cells, and cultured hippocampal neurons.

75 e distribution of channels into dendrites of cultured hippocampal neurons.

76 particle tracking of individual GABA(A)Rs in cultured hippocampal neurons.

77 state also exists for native Kv2.1 found in cultured hippocampal neurons.

78 inhibited physiological IRS-1pTyr in mature cultured hippocampal neurons.

79 urrent (mIPSC) amplitudes and GABA levels in cultured hippocampal neurons.

80 subdomains adjacent to activated synapses in cultured hippocampal neurons.

81 excitatory postsynaptic currents (EPSCs) in cultured hippocampal neurons.

82 s undergoing dendrite-selective transport in cultured hippocampal neurons.

83 , and prevent AbetaO-induced synapse loss in cultured hippocampal neurons.

84 zing factor for axon/dendrite development in cultured hippocampal neurons.

85 fficient endocytosis of synaptic vesicles in cultured hippocampal neurons.

86 d the response of pH(i) to depolarization in cultured hippocampal neurons.

87 creases dendrite number when knocked down in cultured hippocampal neurons.

88 In cultured hippocampal neurons 7-8 days in vitro (DIV7-8),

89 In cultured hippocampal neurons, a high ProN/N-cad ratio do

90 Our detailed time-lapse analyses of cultured hippocampal neurons, a widely used model system

91 rotrusions and at dendritic branch points in cultured hippocampal neurons--a distribution reminiscent

92 nal genetic approach to remove both genes in cultured hippocampal neurons after synapses are establis

93 Here, we report that in cultured hippocampal neurons, alpha-amino-3-hydroxy-5-me

94 In cultured hippocampal neurons, although the two splice va

95 surface expression in hippocampal slices and cultured hippocampal neurons, an effect mimicked by LP-2

96 ry postsynaptic currents (mIPSCs) in primary cultured hippocampal neurons, an effect opposite to that

97 But our work reveals, in cultured hippocampal neurons and a heterologous expressi

98 in non-neuronal cells, and increased in both cultured hippocampal neurons and brain tissue from Fbxo2

99 ial steps for PFF formation, PFF addition to cultured hippocampal neurons and confirmation of aggrega

100 EPSCs were recorded from cultured hippocampal neurons and DSE evoked by a 15 s de

101 at the axon initial segment of AnkG-depleted cultured hippocampal neurons and fails to recruit neurof

102 study, we performed whole-cell recordings of cultured hippocampal neurons and found that NMDAR activa

103 e determined its subcellular localization in cultured hippocampal neurons and HEK 293T cells.

104 GFP-tagged alpha1A subunit were expressed in cultured hippocampal neurons and HEK cells to understand

105 is phosphorylation reduced axon formation in cultured hippocampal neurons and impaired polarization o

106 DNF downregulated the proteasome activity in cultured hippocampal neurons and in hippocampal synapton

107 thin synapses at key developmental stages in cultured hippocampal neurons and in hippocampus in vivo.

108 tection of synaptic and action potentials in cultured hippocampal neurons and intact leech ganglia.

109 ively localized to the axonal growth cone of cultured hippocampal neurons and is required for specifi

110 d PICK1 coimmunoprecipitate from extracts of cultured hippocampal neurons and P4 cortices, and immuno

111 L1 were used to force cluster the protein on cultured hippocampal neurons and PC12 cells, which were

112 d myc in the C terminus was expressed in rat cultured hippocampal neurons and PC12 cells.

113 e impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memor

114 n became up-regulated during polarization of cultured hippocampal neurons and remained at high levels

115 We then use paired recordings from cultured hippocampal neurons and show that GABAergic tra

116 pendent dendritic outgrowth and branching in cultured hippocampal neurons and slices is mediated thro

117 Cultured hippocampal neurons and synaptoneurosomes deriv

118 2, and analyzed RIM-BP-deficient synapses in cultured hippocampal neurons and the calyx of Held.

119 Studies in cultured hippocampal neurons and the COS-7 cell line dem

120 Vezatin knock-down in cultured hippocampal neurons and Vezatin conditional kno

121 interacts with PSD-95 in dendritic spines of cultured hippocampal neurons, and as a GTPase-activating

122 glyceraldehyde-3-phosphate dehydrogenase in cultured hippocampal neurons, and directly compare their

123 actin is concentrated in dendritic spines of cultured hippocampal neurons, and the N-terminal half of

124 Based on lysotracker red imaging in cultured hippocampal neurons, antipsychotic drugs (APDs)

125 current methods of gene delivery for primary cultured hippocampal neurons are limited by toxicity, tr

126 Cultured hippocampal neurons are transfected with PAGFP-

127 observed that DHT rapidly activates CREB in cultured hippocampal neurons, as evidenced by CREB phosp

128 apping protein, in the dendrites and soma of cultured hippocampal neurons at different developmental

129 the same striking patterns of attachment to cultured hippocampal neurons, binding on dendrite surfac

130 morlin stimulated microtubule disassembly in cultured hippocampal neurons but had no significant effe

131 DNF translated from long 3' UTR Bdnf mRNA in cultured hippocampal neurons, but not from short 3' UTR

132 (R1) protein (ICP10 PK) blocks apoptosis in cultured hippocampal neurons by activating the extracell

133 kers for synaptic function and plasticity in cultured hippocampal neurons by NaPB-treated astroglial

134 Knockdown of PSD-93 in cultured hippocampal neurons by RNA interference disrupt

135 ion of the EphB receptor tyrosine kinases in cultured hippocampal neurons by their ephrinB ligands in

136 of GRIP1 by small interfering RNA (siRNA) in cultured hippocampal neurons caused a loss of dendrites,

137 c activation of mu-opioid receptors (MOR) in cultured hippocampal neurons causes two forms of synapti

138 Immunofluorescent staining of cultured hippocampal neurons confirmed the synaptic loca

139 ols, respectively, when expressed in primary cultured hippocampal neurons, consistent with previous s

140 The spiking frequency of cultured hippocampal neurons correlated with the level o

141 rsible fragmentation of the Golgi complex in cultured hippocampal neurons cultured in hyperexcitable

142 enhanced GABAergic synaptic transmission in cultured hippocampal neurons (days-in-vitro 10-14) prepa

143 genous Chmp2b reduced dendritic branching of cultured hippocampal neurons, decreased excitatory synap

144 ng pathways involved in axon formation using cultured hippocampal neurons demonstrates a role for Ca(

145 ive of synaptic homeostasis were observed in cultured hippocampal neurons derived from alpha(1A) (-/-

146 ich is homologous to human CRMP4 (S541Y), in cultured hippocampal neurons derived from Crmp4-knockout

147 and spontaneous neurotransmitter release in cultured hippocampal neurons derived from PS1 knock-out

148 lutamate release at presynaptic terminals of cultured hippocampal neurons detected with the vesicle t

149 r together as double or triple KDs (TKDs) in cultured hippocampal neurons, did not decrease synapse n

150 In cultured hippocampal neurons, dominant-negative mutants

151 on is increased in dendritic spines of mouse cultured hippocampal neurons during LTP.

152 We have previously shown that, in cultured hippocampal neurons, endogenous Pcdh-gammaC5 fo

153 infusion of active CaM-kinase I (CaMKI) into cultured hippocampal neurons enhances miniature EPSC amp

154 Third, glutamate stimulation of cultured hippocampal neurons evoked a rapid (in minutes)

155 ERbeta, DPN, to prevent neurodegeneration in cultured hippocampal neurons exposed to excitotoxic glut

156 mic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh

157 An exposure of cultured hippocampal neurons expressing mitochondrially

158 letely and reversibly blocked by dynasore in cultured hippocampal neurons expressing the fluorescent

159 uorescence and digital imaging microscopy in cultured hippocampal neurons, FMRP and Fmr1 mRNA were lo

160 In cultured hippocampal neurons from a DeltaPIX knock-in mo

161 Recent work with cultured hippocampal neurons from a premutation (Fmr1 CG

162 density and long-term potentiation (LTP) in cultured hippocampal neurons from embryonic rats.

163 rates of Venus-PSD-95 mRNA was increased in cultured hippocampal neurons from Fmr1 KO mice compared

164 Electrophysiological recordings of cultured hippocampal neurons from knock-in mice revealed

165 gamma-secretase cleavage product (A beta) in cultured hippocampal neurons from mdc9(-/-) or wild-type

166 properties of synaptic transmission between cultured hippocampal neurons from MeCP2 knockout and wil

167 es of the proteolytic processing of Nrxns in cultured hippocampal neurons from mice and rats of both

168 ion of amino-terminal ligands, we first used cultured hippocampal neurons from N2A and N2B knock-out

169 esults demonstrate that agmatine can protect cultured hippocampal neurons from NMDA- or glutamate-ind

170 vectors expressing CAT or GPX still protect cultured hippocampal neurons from oxygen/glucose depriva

171 Analysis of cultured hippocampal neurons from quadruple knock-out mi

172 tracking of individual synaptic vesicles in cultured hippocampal neurons from rats of both sexes wit

173 lexes from hippocampal brain homogenates and cultured hippocampal neurons from Sprague Dawley rats.

174 served a specific delay in axon outgrowth in cultured hippocampal neurons from synapsin III knock-out

175 introducing each isoform into glutamatergic cultured hippocampal neurons from synapsin triple knock-

176 nsfecting wild-type synaptotagmin I DNA into cultured hippocampal neurons from synaptotagmin I knock-

177 Whole-cell voltage-clamp recordings of cultured hippocampal neurons from Tau-Mecp2 mice reveal

178 Cultured hippocampal neurons from the Pcdh-gamma triple

179 ective failure of BDNF-dependent survival in cultured hippocampal neurons from the trisomy 16 (Ts16)

180 s for Ca2+ stimulation of adenylyl cyclases, cultured hippocampal neurons from transgenic mice lackin

181 functional analyses in zebrafish embryos and cultured hippocampal neurons from wild-type and Ctnnd2 n

182 In cultured hippocampal neurons, GIT1 is enriched in both p

183 the formation of rods in a maximum of 19% of cultured hippocampal neurons in a time- and concentratio

184 V pools via V-Glut1-pHluorin fluorescence in cultured hippocampal neurons in response to alterations

185 s synapses in rat hippocampus in vivo and in cultured hippocampal neurons in vitro.

186 We conclude that DIDS induces apoptosis in cultured hippocampal neurons, in spite of the fact that

187 lipid rafts exist abundantly in dendrites of cultured hippocampal neurons, in which they are associat

188 nduced enhancement of neurite outgrowth from cultured hippocampal neurons indicating an important fun

189 Abeta42 oligomer treatment of cultured hippocampal neurons induced similar effects, ac

190 thermore, the expression of this fragment in cultured hippocampal neurons induced the formation of nu

191 Overexpression of alpha1-chimerin in cultured hippocampal neurons inhibits formation of new s

192 MiR21 levels in cultured hippocampal neurons inversely correlate with ne

193 otentiation of synaptic transmission between cultured hippocampal neurons is accompanied by an increa

194 ew release sites during potentiation between cultured hippocampal neurons is due to (a) conversion of

195 e show here that NMDAR stimulation of PLC in cultured hippocampal neurons is necessary for AKAP79/150

196 t that phosphorylation of endogenous KCC2 in cultured hippocampal neurons is regulated by PKC-depende

197 Conversely, in cultured hippocampal neurons, knockdown of a Pol1 coacti

198 tudy vesicle dynamics inside the synapses of cultured hippocampal neurons labeled with the fluorescen

199 similar degree of protection is observed in cultured hippocampal neurons lacking caspase-2, which ar

200 roducts was also increased in hippocampi and cultured hippocampal neurons lacking Fbxo2.

201 Aberrant neurotransmission in cultured hippocampal neurons lacking SV2 was rescued by

202 a thorough analysis of neurotransmission in cultured hippocampal neurons lacking synaptic vesicle pr

203 Introduction of hippocalcin in cultured hippocampal neurons leads to a pronounced I(sAH

204 ed high-frequency epileptiform discharges in cultured hippocampal neurons leads to caspase-dependent

205 at amyloid beta-peptide (Abeta) treatment of cultured hippocampal neurons leads to the inactivation o

206 Here we show that, in cultured hippocampal neurons, lowering [Ca(2+)](e) activ

207 In cultured hippocampal neurons, Lphn2 maintained synapse n

208 , potentiated GABA-activated Cl- currents in cultured hippocampal neurons (< or =1 microm) and direct

209 potential (AP)-mediated network activity in cultured hippocampal neurons maintains eEF2 in a relativ

210 Here, we were able to reproduce in primary cultured hippocampal neurons many of the effects of in v

211 In cultured hippocampal neurons, neurotrophin receptor tyro

212 t both excitatory and inhibitory synapses in cultured hippocampal neurons, newly endocytosed vesicles

213 In cultured hippocampal neurons, nonpalmitoylated ABP-L loc

214 Cultured hippocampal neurons obtained from wild-type, ta

215 Forced expression in cultured hippocampal neurons of two variants, alpha1 or

216 Knockdown of NACHO in cultured hippocampal neurons or knockout of NACHO in mic

217 In cultured hippocampal neurons, overactivation of only ext

218 ity-dependent endocytosis of AMPARs by using cultured hippocampal neurons prepared from knockout (KO)

219 essing chimeric KCC2-KCC4 cDNA constructs in cultured hippocampal neurons prepared from Sprague Dawle

220 In cultured hippocampal neurons, proliferator-activated rec

221 P activities in undifferentiated neurites of cultured hippocampal neurons promote and suppress axon f

222 Light-mediated activation of RO4 in cultured hippocampal neurons reduces neuronal firing wit

223 rdingly, knock-out or knockdown of KCTD12 in cultured hippocampal neurons reduces the magnitude of th

224 ction of the future axon among neurites of a cultured hippocampal neuron requires the activity of gro

225 mic reticulum (ER) to the plasma membrane of cultured hippocampal neurons requires Ca(2+) release fro

226 Cultured hippocampal neurons respond to OGD with a rapid

227 Exogenous application of Narp to cultured hippocampal neurons results in clusters of both

228 at various stages in the differentiation of cultured hippocampal neurons results in substantial loss

229 Indeed, studies in cultured hippocampal neurons reveal that NF-alpha1 treat

230 is of BDNF-induced synaptic strengthening in cultured hippocampal neurons revealed increased expressi

231 Fluorescence microscopy experiments in cultured hippocampal neurons revealed that Arc protein l

232 In cultured hippocampal neurons, septin 11 clusters were fr

233 When expressed in cultured hippocampal neurons, Shank promotes the maturat

234 Cultured hippocampal neurons show proton-gated currents

235 Immunofluorescence of cultured hippocampal neurons showed that 54 +/- 4% of th

236 Immunocytochemistry in epithelial cells and cultured hippocampal neurons showed that endogenous neur

237 Electrophysiological recordings of cultured hippocampal neurons showed that miniature excit

238 Immunofluorescence of cultured hippocampal neurons shows that RNF34 forms clus

239 gomer-induced changes in dendritic spines of cultured hippocampal neurons, sparing mature spine class

240 endent regulation of GIRK channel density in cultured hippocampal neurons that requires activity of N

241 protein-tagged alpha1C subunits expressed in cultured hippocampal neurons, that Ca2+/CaM interaction

242 Here, we show that in cultured hippocampal neurons the surface expression of G

243 In cultured hippocampal neurons, the accumulation of LKB1 a

244 When expressed in cultured hippocampal neurons, the metabotropic glutamate

245 d Fyn are localized together in the axons of cultured hippocampal neurons, the mossy fibers of the hi

246 In cultured hippocampal neurons, the plasma membrane-locali

247 In cultured hippocampal neurons, these proteins are present

248 ly rectifying (GIRK) currents were made from cultured hippocampal neurones to determine the effect of

249 -20-one (C2-NBD 3alpha5alphaP), responses of cultured hippocampal neurons to 10 microM NMDA were pote

250 his study, we assessed the susceptibility of cultured hippocampal neurons to Abeta-dependent 17 kDa t

251 We used cultured hippocampal neurons to analyze the distribution

252 ce RNAs to eliminate Piccolo expression from cultured hippocampal neurons to assess its involvement i

253 timulate undifferentiated minor processes of cultured hippocampal neurons to become axons and whether

254 assessed the effect of the S940A mutation in cultured hippocampal neurons to explore the mechanisms u

255 positive cell numbers induced by exposure of cultured hippocampal neurons to NMDA.

256 d and NH4(+)-induced pHi shifts were used in cultured hippocampal neurons to quantify the rate of KCC

257 ent light-induced membrane depolarization in cultured hippocampal neurons to trigger reliable repetit

258 ng techniques applied to both fixed and live cultured hippocampal neurons to visualize the localizati

259 In single-cultured hippocampal neurons, trains of depolarizations

260 In cultured hippocampal neurons transfected with beta4, per

261 afficking and regulated secretion of BDNF in cultured hippocampal neurons transfected with the met al

262 In PC12 cells and cultured hippocampal neurons, transport activity of GAKI

263 We show that cultured hippocampal neurons treated with cytochalasin D

264 In the cultured hippocampal neurons, treatment with N-methyl-D-

265 o be concentrated in the dendritic shafts of cultured hippocampal neurons under control conditions bu

266 cts of pregabalin on presynaptic function of cultured hippocampal neurons using a powerful technique

267 effects of estradiol on synaptic proteins in cultured hippocampal neurons using immunocytochemistry a

268 rin in regulating synapse function in rodent cultured hippocampal neurons using optical methods and e

269 the stability of synaptic NMDA receptors on cultured hippocampal neurons using the open-channel bloc

270 RNA in differentiated axons and dendrites of cultured hippocampal neurons varying in developmental ma

271 emaphorin 3A-induced growth cone collapse in cultured hippocampal neurons was associated with the par

272 In cultured hippocampal neurons we report that when activit

273 loring dynamic localization of APP/BACE-1 in cultured hippocampal neurons, we found that after synthe

274 expression of stargazin mutant constructs in cultured hippocampal neurons, we identified a novel doma

275 In cultured hippocampal neurons, we observed that rat AKAP1

276 Through a loss-of-function genetic screen in cultured hippocampal neurons, we previously identified t

277 Using synaptic fluorescence probes in cultured hippocampal neurons, we report that trans-synap

278 Using electrophysiology in cultured hippocampal neurons, we show that ketamine and

279 ivity and subdiffraction-limit resolution in cultured hippocampal neurons, we show that two molecules

280 Here, in cultured hippocampal neurons, we used siRNAs against Fmr

281 Mitochondrial populations of resting cultured hippocampal neurons were analyzed.

282 lectin modulation, whereas AMPA receptors in cultured hippocampal neurons were insensitive, which cou

283 Cultured hippocampal neurons were studied since the dend

284 HEK-293 cells or cultured hippocampal neurons were transfected with alpha

285 Cultured hippocampal neurons were used in the present st

286 Morphology and synapses between cultured hippocampal neurons were visualized by confocal

287 red the effects of changes in temperature in cultured hippocampal neurons, where higher average rates

288 hVoS 2.0 performed well in cultured hippocampal neurons, where single action potent

289 lation of IRS-1 (Ser616) and tau (Ser422) in cultured hippocampal neurons, whereas JNK inhibition blo

290 monitoring intracellular calcium [Ca2+]i in cultured hippocampal neurons, which are known to express

291 Here we use optogenetics to stimulate cultured hippocampal neurons with a single stimulus, rap

292 We found that treatment of cultured hippocampal neurons with bFGF heightens express

293 tudy synapse formation by neuroligins, we co-cultured hippocampal neurons with COS cells expressing w

294 Treatment of cultured hippocampal neurons with proneurotrophins induc

295 Knocking down septin 11 in cultured hippocampal neurons with septin 11 small hairpi

296 Treatment of cultured hippocampal neurons with sialidase, which cleav

297 Transfection of cultured hippocampal neurons with stargazin produced two

298 from GABA-B-R1 knock-out mouse brains and in cultured hippocampal neurons with their GABA-B-R1 genes

299 We silenced cultured hippocampal neurons with TTX at 7 days in vitro

300 at serine 31 are colocalized in the axons of cultured hippocampal neurons, with enrichment at the axo