ライフサイエンスコーパス: hippocampal neuron

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

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

3 axon, and not the dendrites, in cultured rat hippocampal neurons.

4 brain activity to govern the addition of new hippocampal neurons.

5 from the surfaces of dendritic processes in hippocampal neurons.

6 omodulatory effects of serotonin in cultured hippocampal neurons.

7 ices elicited weak postsynaptic responses in hippocampal neurons.

8 ion and neuronal polarity in cultured rodent hippocampal neurons.

9 alize organization of synaptic subdomains in hippocampal neurons.

10 s reshaping includes the addition of newborn hippocampal neurons.

11 ced potentiation of synaptic transmission in hippocampal neurons.

12 currents and led to neuronal apoptosis in KO hippocampal neurons.

13 gulates NR2B transport into the dendrites of hippocampal neurons.

14 rkin's role at glutamatergic synapses of rat hippocampal neurons.

15 tor of Shank3 activation and dynamics in rat hippocampal neurons.

16 N1 controls the plasticity of cultured mouse hippocampal neurons.

17 a signaling and dendritic spines in cultured hippocampal neurons.

18 on abrogates the Wnt-5a-dependent pathway in hippocampal neurons.

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

20 tomography in unstimulated, dissociated rat hippocampal neurons.

21 stributes in clusters along the dendrites of hippocampal neurons.

22 vement and positioning in Sprague Dawley rat hippocampal neurons.

23 similar to endogenous Kv1.2 glycosylation in hippocampal neurons.

24 ) release toward axonal specification of rat hippocampal neurons.

25 plasticity and synapse loss in cortical and hippocampal neurons.

26 es, leading to increased firing rates in rat hippocampal neurons.

27 accumulation in HEK293 cells and rat primary hippocampal neurons.

28 by the overexpression of SIRT6 in HT22 mouse hippocampal neurons.

29 levels of ROS required for axonal growth of hippocampal neurons.

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

31 l-surface Nav1.6 within the soma of cultured hippocampal neurons.

32 crease in dendritic spine density in primary hippocampal neurons.

33 inhibits PrP(Sc)-induced synaptotoxicity in hippocampal neurons.

34 ochemical analyses were performed on primary hippocampal neurons.

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

36 e morphology of dendritic spines of cultured hippocampal neurons.

37 1-P (S1P) upregulates glutamate secretion in hippocampal neurons.

38 stsynaptic currents (sIPSCs) in cultured rat hippocampal neurons.

39 GHSR1a:DRD1:Galphaq heteromeric complexes in hippocampal neurons.

40 eurite number both in PC12 cells and primary hippocampal neurons.

41 hannels for reducing the excitability of CA1 hippocampal neurons.

42 against the deleterious impact of AbetaOs on hippocampal neurons.

43 by alters synaptic activity, specifically in hippocampal neurons.

44 nnel complexes and may influence function of hippocampal neurons.

45 showed clear extracellular labeling of live hippocampal neurons.

46 BA) values and increased spiking of cultured hippocampal neurons.

47 xonal outgrowth in manipulated mouse primary hippocampal neurons.

48 activity (MUA) of dissociated primary mouse hippocampal neurons.

49 ted living PC12 cells as well as in cultured hippocampal neurons.

50 ion memory task and morphological changes of hippocampal neurons.

51 th, which may be critical for development of hippocampal neurons.

52 manipulated its expression in cerebellar and hippocampal neurons.

53 o elicit a downstream response only in ApoE4 hippocampal neurons.

54 synaptic currents (mEPSCs) in cultured mouse hippocampal neurons.

55 ve L1 mosaicism at genomic loci expressed in hippocampal neurons.

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

57 to stimulate PAK phosphorylation in cultured hippocampal neurons.

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

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

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

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

62 cular junctions, neuroendocrine cells and in hippocampal neurons.

63 physiological properties of mitochondria in hippocampal neurons.

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

65 epropionic acid) receptor internalization in hippocampal neurons.

66 but not excitatory, postsynapses in cultured hippocampal neurons.

67 membrane proteins in the somatic surface of hippocampal neurons.

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

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

70 hat inactivation or depletion of Rab5 in rat hippocampal neurons abrogates the somatodendritic polari

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

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

73 dose-dependent inhibitory effect of 5-HT on hippocampal neuron activities, indicating the effectiven

74 ery of this novel form of temporal coding in hippocampal neurons advances our fundamental understandi

75 Syt10 is required for NPAS4 to protect hippocampal neurons against excitotoxic cell death.

76 Here, we show that in rat hippocampal neurons although spontaneous and evoked glut

77 and in vivo in the cytoplasm of mature human hippocampal neurons and activated microglia, but is abse

78 r examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for an

79 A receptor (sst2A) is localized on principal hippocampal neurons and displays anticonvulsant properti

80 ture sequencing (RC-seq) on individual human hippocampal neurons and glia, as well as cortical neuron

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

82 es in a genetically homogenous population of hippocampal neurons and illustrate the profound effects

83 T1C deficiency disrupted spine maturation in hippocampal neurons and impaired spatial learning, but t

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 5 was produced by primary cultures of murine hippocampal neurons and microglia, as well as by the mur

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

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

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

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

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

92 pensable coreceptor for p75(NTR) and TrkB in hippocampal neurons and suggest SORCS2 as the link betwe

93 alyzed RIM-BP-deficient synapses in cultured hippocampal neurons and the calyx of Held.

94 Studies in cultured hippocampal neurons and the COS-7 cell line demonstrate

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

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

97 cifically internalized into rat cortical and hippocampal neurons, and cleaves Synaptosomal-Associated

98 , astrocytosis, a reduction in the number of hippocampal neurons, and reduced staining of TAR-DNA bin

99 GABAA receptors of cerebellar granule cells, hippocampal neurons, and thalamic relay neurons, 4-PIOL

100 PrP(C) co-localizes with NCAM in mouse hippocampal neurons, and this interaction is mainly medi

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

102 nships of glycine-evoked currents in primary hippocampal neurons are inwardly rectifying upon desensi

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

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

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

106 Using primary cultures of rat hippocampal neurons as a quantitative model of polarized

107 not KLC, is essential for axon elongation in hippocampal neurons as well as axon regeneration in sens

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

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

110 In rat hippocampal neurons, ATP production by either glycolysis

111 Cholinergic fibers innervate hippocampal neuron axons, dendrites, and somata.

112 d in the distal region of axons in polarized hippocampal neurons before any stimulation and does not

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

114 GluT4 is also expressed in some hippocampal neurons, but its functional role in the brai

115 ternal brain activities govern the firing of hippocampal neurons, but which specific firing patterns

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

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

118 ual exocytic events of NMDA receptors in rat hippocampal neurons by total internal reflection fluores

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

120 the current study, we explored whether human hippocampal neurons can also demonstrate the ability to

121 While considerable research indicates hippocampal neurons can represent sequences of locations

122 We found that in cultured cGKII KO hippocampal neurons, cGKII-dependent phosphorylation of

123 We found that hippocampal neurons code for the temporal context of ite

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

125 Ievoked in Xenopus oocytes, HEK293 cells and hippocampal neurons; correctly predicts the dose-depende

126 Finally, in cultured autaptic hippocampal neurons, CRIP1a overexpression attenuated bo

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

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

129 diminished miR-188-5p expression in primary hippocampal neuron cultures and that miR-188-5p rescued

130 athways, we combined FRET imaging of cAMP in hippocampal neuron cultures with spatial mechanistic mod

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

132 mp2b reduced dendritic branching of cultured hippocampal neurons, decreased excitatory synapse densit

133 Studies in dissociated rat hippocampal neurons demonstrated the enhancement of dend

134 restored by coculturing them with normal rat hippocampal neurons, demonstrating a critical role for s

135 Here live imaging of Drosophila and hippocampal neuron dense-core vesicles (DCVs) containing

136 bule organization in primary cultures of rat hippocampal neurons, dentate granule cells in mouse orga

137 Accordingly, in mouse hippocampal neurons, depletion of DOCK10 or expression o

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

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

140 reintroduced the mutant into cultured mouse hippocampal neurons devoid of all synapsins.

141 Here, using hippocampal neurons (DIV 15-20) cultured in microfluidic

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

143 particle tracking time-course experiments on hippocampal neurons during AIS development.

144 nderstanding of the subthreshold behavior of hippocampal neurons during these events remains incomple

145 d dendritic outgrowth and spine formation of hippocampal neurons, echoing neuronal deficits underling

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

147 ly, knockdown of Tet or inhibition of BER in hippocampal neurons elevated excitatory glutamatergic sy

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

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

150 ivation of Shh receptors in the dendrites of hippocampal neurons engages a trans-neuronal signaling p

151 appetite through which ghrelin signaling in hippocampal neurons engages LHA orexin signaling.

152 Intriguingly, hippocampal neurons expressing TERT did not contain hype

153 the time course of synaptic changes in mouse hippocampal neurons following exposure to Abeta42 at pic

154 signaling played a role in the apoptosis of hippocampal neurons following global cerebral ischemia-r

155 rich 7 (PRR7) accumulates in the nucleus of hippocampal neurons following NMDAR activity.

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

157 In hippocampal neurons from BACE1(-/-) mice, loss of M-curr

158 lpain activity in the hippocampus, protected hippocampal neurons from death, preserved cognitive perf

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

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

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

165 aptic short term plasticity were observed in hippocampal neurons from SPL(fl/fl/Nes) mice.

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

167 nal markers were also reduced up to 40%, and hippocampal neurons had smaller dendritic arbors.

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

169 A population of human hippocampal neurons has shown responses to individual co

170 They find that a subset of hippocampal neurons have directional tuning that persist

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

172 (KA) exposure and its absence renders mouse hippocampal neurons highly susceptible to excitotoxic in

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

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

175 Viral expression of PDE4A5 in hippocampal neurons impairs long-term potentiation and a

176 rvival (bromodeoxyuridine) of new adult-born hippocampal neurons in adult male Sprague-Dawley rats.

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

178 lactate dehydrogenase A within cortical and hippocampal neurons in control mice, as well as within a

179 reased dendritic complexity in embryonic rat hippocampal neurons in culture and in vivo.

180 in synapses of the calyx of Held in vivo and hippocampal neurons in culture that combined, but not in

181 , both in HEK-293T cells and in striatal and hippocampal neurons in culture, demonstrates that GHS-R1

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

183 rential Gs/olf coupling in both striatal and hippocampal neurons in culture.

184 We investigated RIM-BP2-deficient murine hippocampal neurons in cultures and slices.

185 Ventral hippocampal neurons in low LG offspring fired action pot

186 gnals, Acharya et al. record the activity of hippocampal neurons in rats running in open two-dimensio

187 ia V-Glut1-pHluorin fluorescence in cultured hippocampal neurons in response to alterations in presyn

188 at 100 Hz in dissociated Sprague Dawley rat hippocampal neurons in single trial recordings.

189 g naturalistic stimulus trains in excitatory hippocampal neurons in the absence of FMRP.

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

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

192 se morphological and localization defects of hippocampal neurons in Trim9(-/-) mice were associated w

193 of Trim9 elevated dendritic arborization of hippocampal neurons in vitro and in vivo Adult-born dent

194 tal stages in embryonic and adult-born mouse hippocampal neurons in vitro and in vivo Embryonic hippo

195 ve mTORC1 alters axon length and polarity of hippocampal neurons in vitro, but the impact of hyperact

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

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

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

199 ependent translation, accompanied by loss of hippocampal neurons, increased anxiety, and impaired cog

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

201 nduced cAMP accumulation in striatal but not hippocampal neurons, indicating the involvement of D1R i

202 Here we show that viral infection of adult hippocampal neurons induces complement-mediated eliminat

203 In cultured rat hippocampal neurons, inhibition of the latter process by

204 entiation (LTP) of synaptic strength between hippocampal neurons is associated with learning and memo

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

206 The polyamine deficit in hippocampal neurons is likely caused by an upregulation

207 E VAMP4 to the somatodendritic domain of rat hippocampal neurons is mediated by recognition of dileuc

208 toxic prion protein-induced degeneration of hippocampal neurons is prevented dose-dependently by int

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

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

211 report that Brg1 deletion in early postnatal hippocampal neurons led to reduced dendritic spine densi

212 Here we report that a distinct population of hippocampal neurons, located in the CA2 subregion, signa

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

214 In cultured hippocampal neurons, Lphn2 maintained synapse numbers vi

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

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

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

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

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

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

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

222 Knockdown of NACHO in cultured hippocampal neurons or knockout of NACHO in mice selecti

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

224 ence of phagocytic microglia without loss of hippocampal neurons or volume.

225 RNA in induced pluripotent stem cell-derived hippocampal neurons originating from lithium-responsive

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

227 In cortical and hippocampal neurons, Pcdh19 was localized along their de

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

229 show that suppressing KCC2 expression in rat hippocampal neurons precludes long-term potentiation of

230 As well, we examined GABAB R currents in hippocampal neurons prepared from GIRK2-trisomic Ts cont

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

232 hs and impaired dendritic spine formation in hippocampal neurons, reflecting the prevalence of ID-ass

233 fering capacity of the cell nucleus in mouse hippocampal neurons regulates neuronal architecture by m

234 es indicates that, to fully understand how a hippocampal neuron represents information, it is vital t

235 tolerance (channel internalization) from rat hippocampal neurons requires protein synthesis, in commo

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

237 egulates dendritic spine formation in rodent hippocampal neurons, resulting in postsynaptic developme

238 ophysiological recording and Ca2+ imaging in hippocampal neurons revealed that the sAHP reduction was

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

240 In developing rat hippocampal neurons, SEPT9 partially colocalizes and com

241 as a novel regulator of embryonic and adult hippocampal neuron shape acquisition and hippocampal-dep

242 Moreover, we find that GluN2C-expressing hippocampal neurons show marked resistance to NMDA-induc

243 Hippocampal neurons show selectivity with respect to vis

244 Quantitative analyses of Golgi-stained hippocampal neurons showed an increase in spine density

245 Moreover, a greater proportion of hippocampal neurons showed selective firing for target i

246 Confocal analysis of rat hippocampal neurons showed that S1P applied at nanomolar

247 synaptic excitatory transmission of primary hippocampal neurons, simultaneously modifying dendritic

248 RAB39B downregulation in mouse hippocampal neurons skews AMPAR composition towards non

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

250 In 1 d in vitro hippocampal neurons, TBB induced a reduction in FGF14 ex

251 l of the subcellular organization of DCVs in hippocampal neurons that are spontaneously active (their

252 N2A or GluN2B elicits an excitatory drive to hippocampal neurons that can be shaped in time to mimic

253 Hippocampal neurons that lack GluA3 were resistant again

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

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

256 In rat hippocampal neurons the kinesin-1 binding domain of APC

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

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

259 rformed whole cell patch clamp recordings of hippocampal neurons to determine the impact of lithium o

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

261 We expressed SEP-TAC-7.3 in dissociated rat hippocampal neurons to examine the lateral mobility, sur

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

263 channel activation mediates the response of hippocampal neurons to hyperglycemia by coupling metabol

264 Here, we have used dissociated rat hippocampal neurons to investigate the pathway for SV pr

265 oncanonical FGF13 binds directly to VGSCs in hippocampal neurons to limit their somatodendritic surfa

266 (+)-induced pHi shifts were used in cultured hippocampal neurons to quantify the rate of KCC2 transpo

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

268 auditory cortex, we found that responses of hippocampal neurons to self-generated sounds were almost

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

270 e, we used subcellular Ca(2+) imaging in rat hippocampal neurons to visualize NMDAR function at indiv

271 We show that cultured hippocampal neurons treated with cytochalasin D or latru

272 on in dendritic spine density in the primary hippocampal neurons treated with oligomeric Abeta1-42 an

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

274 edle arrays, of islets of Langerhans, and of hippocampal neurons under upright optical microscope.

275 dy, we amplified genomic DNA from individual hippocampal neurons using three single-cell DNA amplific

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

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

278 d affinity-purified Tomo-1 from cultured rat hippocampal neurons was ubiquitinated, and the levels of

279 Using dissociated hippocampal neurons we compared properties of cultures g

280 Moreover, by using dissociated hippocampal neurons we show that microbeads loaded with

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

282 Using live-cell imaging in mouse hippocampal neurons, we establish the compartment-specif

283 ays tracking the fate of internalized APP in hippocampal neurons, we found that APP and BACE-1 intera

284 ngle-molecule assays and live imaging in rat hippocampal neurons, we have identified the kinesin-4 KI

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

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

287 f patient antibodies on cultures of live rat hippocampal neurons were determined with immunostaining,

288 ound that dendrites, more so than somata, of hippocampal neurons were hyperexcitable in mice overexpr

289 ongoing fluctuations in brain state, dorsal hippocampal neurons were recorded during spontaneous sei

290 e study of these nitrated oligomers on mouse hippocampal neurons, where an increased NMDAR-dependent

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

292 rowth cones of both neuron-like cells and of hippocampal neurons, where it has the potential to be tr

293 ntially expressed at postsynaptic regions of hippocampal neurons, whereas Kir6.1 was predominant in d

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

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

296 ed GIRK2 currents in GIRK2-trisomic Ts mouse hippocampal neurons, which were normalized in the GIRK2-

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

298 Filling recycling vesicles in hippocampal neurons with HRP and subsequent treatment wi

299 tor- and nuclear calcium-dependent manner in hippocampal neurons within 2-4 h after the induction of

300 opamine receptor-1 (DRD1) are coexpressed in hippocampal neurons, yet ghrelin is undetectable in the