ライフサイエンスコーパス: hippocampal slice

1 Furthermore, CCNY abolishes LTP in hippocampal slices.

2 ged presynaptic [Ca(2+)] transients in mouse hippocampal slices.

3 Cajal-Retzius cells optogenetically in mouse hippocampal slices.

4 erent components of the CA3 network in mouse hippocampal slices.

5 ongoing epileptiform activity in mouse acute hippocampal slices.

6 d post-tetanic potentiation and LTP in mouse hippocampal slices.

7 ocampal neurons and CA1 pyramidal neurons in hippocampal slices.

8 mini of dentate gyrus neurons in adult mouse hippocampal slices.

9 on, but not long-term potentiation, in acute hippocampal slices.

10 dendrites of CA1 pyramidal neurons in mouse hippocampal slices.

11 -access two-photon microscopy in acute mouse hippocampal slices.

12 tional hemichannels in astrocytes from mouse hippocampal slices.

13 ed oligomer-mediated LTP impairment in mouse hippocampal slices.

14 ivation inhibited Thr-840 phosphorylation in hippocampal slices.

15 ed reduction of the sAHP observed ex vivo in hippocampal slices.

16 d long-term potentiation inhibition in mouse hippocampal slices.

17 ative electrophysiological systems using rat hippocampal slices.

18 pocampal networks in dissociated culture and hippocampal slices.

19 ate gyrus granule cells (DGGCs) in adult rat hippocampal slices.

20 lasticity at mossy fiber-CA3 synapses in rat hippocampal slices.

21 in and impaired synaptic plasticity in adult hippocampal slices.

22 ng SWRs that occurred spontaneously in mouse hippocampal slices.

23 locked long-term potentiation (LTP) in acute hippocampal slices.

24 artments in early and later-stage AD mice in hippocampal slices.

25 binant noradrenaline transporters and in rat hippocampal slices.

26 arbachol-induced gamma oscillations in mouse hippocampal slices.

27 y reduces epileptiform bursting in TSC2(+/-) hippocampal slices.

28 plasticity and synaptic transmission in the hippocampal slices.

29 fected cells, primary neuronal cultures, and hippocampal slices.

30 k activity or acute effects on plasticity in hippocampal slices.

31 ion in stratum radiatum of area CA1 in mouse hippocampal slices.

32 zed in cultured cortical neurons or in acute hippocampal slices.

33 ission in the CA1 area compared to wild-type hippocampal slices.

34 ion of inhibitory transmission (iLTD) in rat hippocampal slices.

35 ed NMDA-induced neurotoxicity in acute mouse hippocampal slices.

36 5-HT1A/5-HT7 agonist) reversed mGluR-LTD in hippocampal slices.

37 ein regulation were observed in cultured rat hippocampal slices.

38 ignaling kinases, at spine synapses in adult hippocampal slices.

39 he induction, of BDNF-dependent LTP in acute hippocampal slices.

40 n of gamma oscillations in kainate-activated hippocampal slices.

41 ently enhances cAMP in neuronal cultures and hippocampal slices.

42 We addressed these issues by using mouse hippocampal slices.

43 defective LTP in primary neuron cultures and hippocampal slices.

44 using electrophysiological recordings in rat hippocampal slices.

45 engthening lasting tens of minutes in rodent hippocampal slices.

46 ignalling in CA1 pyramidal cell dendrites in hippocampal slices.

47 and whole-cell recordings in wild-type mouse hippocampal slices.

48 ong-lasting synaptic potentiation (L-LTP) in hippocampal slices.

49 lls in the more physiological environment of hippocampal slices.

50 ry, but not inhibitory, neurotransmission in hippocampal slices.

51 of long-term depression, measured in ex vivo hippocampal slices.

52 cues presynaptic responses in culture and in hippocampal slices.

53 of CA1 pyramidal neurons in cultured murine hippocampal slices.

54 in an in vitro model of seizure activity in hippocampal slices.

55 ost-synaptic potentials (EPSPs) in adult rat hippocampal slices.

56 ing electrophysiological field recordings in hippocampal slices.

57 d pulse facilitation (PPF) in KO and control hippocampal slices.

58 cies, consistently with previous findings in hippocampal slices.

59 min) reduced FMRP levels in wild-type mouse hippocampal slices.

60 ated ERK1/2 are also elevated in Syngap(+/-) hippocampal slices.

61 onists on pyramidal neurons in mouse and rat hippocampal slices.

62 n patch clamp in whole cell configuration in hippocampal slices.

63 ogy in dorsal root ganglia (DRG) neurons and hippocampal slices.

64 naptic plasticity and spine numbers in acute hippocampal slices 2-3 weeks later.

65 In hippocampal slices, 24(S)-HC enhances the ability of sub

66 napses is greatly enhanced in cultured mouse hippocampal slices after chronic (60 h) network-activity

67 sicle pool in CA3-CA1 synapses from an acute hippocampal slice and for the characterization of its an

68 Using direct measurements of LTP in acute hippocampal slices and an in vitro LTP model of stimulat

69 with electrophysiological analysis on acute hippocampal slices and ATP assays in purified cell cultu

70 Here, we use acute hippocampal slices and combine two-photon excitation Ca(

71 ptor 2 (GluR2) subunit surface expression in hippocampal slices and cultured hippocampal neurons, an

72 In hippocampal slices and cultured neurons we also observed

73 ase probability inhibitory synapses in mouse hippocampal slices and fits well with the observation th

74 -clamp and current-clamp recordings in acute hippocampal slices and focal applications of irreversibl

75 from post-hoc-identified cells in acute rat hippocampal slices and identified a subpopulation of mol

76 Despite extensive studies in hippocampal slices and incentive from computational theo

77 In hippocampal slices and intact hippocampal preparations f

78 specifically induced during LTP induction in hippocampal slices and its knockdown in the hippocampus

79 Electrophysiological recordings in acute hippocampal slices and primary hippocampal neuronal cult

80 l, a small-molecule Eg5 inhibitor, on LTP in hippocampal slices and synapse loss in neuronal cultures

81 NRG-1 acutely depotentiates LTP in hippocampal slices, and blocking ErbB kinase activity in

82 ical effect of THC was evaluated using acute hippocampal slices, and hippocampal cannabinoid receptor

83 recycling versus degradation for LTD in rat hippocampal slices, and their correlation with receptor

84 n imaging of FM1-43 vesicular release in rat hippocampal slices; and (ii) transgenic mice expressing

85 expression in glutamatergic terminals, when hippocampal slices are incubated with low concentration

86 ency, measured on pyramidal neurons in acute hippocampal slices at 270 DAT, was reduced in epileptic

87 re made with control stimulation in the same hippocampal slices at 5 minutes, 30 minutes, and 2 hours

88 In hippocampal slices, beta(2) signaling decreases cAMP lev

89 term potentiation (LTP) in the CA1 region of hippocampal slices but had no significant effect on LTP

90 d robust electrophysiological effects in rat hippocampal slices, but showed lower efficacy in striatu

91 ylation had no effect on glutamate uptake in hippocampal slices, but simultaneous inhibition of both

92 ileptiform activity has been demonstrated in hippocampal slices, but use in humans will require more

93 l activity, and synaptic plasticity in acute hippocampal slices by combining electrophysiological ext

94 cetylcholine was optogenetically released in hippocampal slices by expressing the excitatory optogene

95 address this issue, we induced SD in murine hippocampal slices by focal KCl microinjection and visua

96 d that facilitation of spontaneous SPW-Rs in hippocampal slices by increasing gap-junction coupling o

97 ane excitability of CA1 pyramidal neurons in hippocampal slices by lowering the spike threshold possi

98 Importantly, in primary neurons and hippocampal slices, CALHM1 activation facilitated the ph

99 We demonstrate that hippocampal slices can be imaged through transparent gra

100 Astrocytes in hippocampal slices can dynamically regulate synaptic tra

101 whole-cell patch-clamp recordings from acute hippocampal slices, (+)-CIQ, the active enantiomer of th

102 t in decreasing water content in OGD-exposed hippocampal slices, compared with mu, delta, and kappa s

103 any as approximately 50% of synapses in some hippocampal slice conditions.

104 n of CA3-CA1 synaptic input-output curves in hippocampal slices confirmed an age-related decrease in

105 As such, experiments in hippocampal slices continue to progress our understandin

106 ockout mice express EtOH-sensitive mIPSCs in hippocampal slices, correlating with upregulated GABAAR

107 In rat hippocampal slices, cortical synaptoneurosomes, and cult

108 beta-amyloidosis by establishing a long-term hippocampal slice culture (HSC) model.

109 Like PSD-95, activity blockade in a rat hippocampal slice culture increases SynDIG1 palmitoylati

110 uced tau hyperphosphorylation in organotypic hippocampal slice cultures (OHSC) and applied marker-ind

111 g from ROS and RNS production in organotypic hippocampal slice cultures (OHSC), as well as its potent

112 ellular fluid collected from rat organotypic hippocampal slice cultures (OHSCs) by electroosmotic flo

113 We have tested this by examining organotypic hippocampal slice cultures (OHSCs) exposed to oxygen glu

114 oA in the extracellular space of organotypic hippocampal slice cultures (OHSCs).

115 tensiometric Ca(2+) indicator in organotypic hippocampal slice cultures (one- and two-photon) and the

116 (i.e. post-treatment protocol in organotypic hippocampal slice cultures and cortical neurons) can be

117 Using organotypic hippocampal slice cultures and primary neuron hippocampa

118 function, we used sparse transfection of rat hippocampal slice cultures and whole-cell recordings in

119 Expression of CRISPR/Cas9 in hippocampal slice cultures completely eliminated NMDA re

120 se deprivation-induced injury in organotypic hippocampal slice cultures confirmed that calpains were

121 in AMPAR ischaemic plasticity in organotypic hippocampal slice cultures exposed to oxygen glucose dep

122 egulated, in cortical neuron and organotypic hippocampal slice cultures from rat, either by the previ

123 PAK3, or inhibition of PAK3 function in rat hippocampal slice cultures interfere with activity-media

124 ltures of primary hippocampal neurons and in hippocampal slice cultures is similarly enhanced by PCB-

125 To this end, we infected hippocampal slice cultures of different rat strains with

126 The effects were confirmed in vitro by using hippocampal slice cultures of female mice.

127 We imaged organotypic hippocampal slice cultures of rat, in which astrocytes m

128 ntate granule cells in organotypic entorhino-hippocampal slice cultures of Thy1-GFP mice.

129 In entorhino-hippocampal slice cultures prepared from SP-deficient mi

130 By analyzing CA1 pyramidal neurons in mutant hippocampal slice cultures that are essentially devoid o

131 orded from CA3 pyramidal neuron pairs in rat hippocampal slice cultures to characterize synaptic and

132 biolistically transfected astrocytes in rat hippocampal slice cultures to facilitate fluorescent con

133 g activity of hundreds of neurons in cortico-hippocampal slice cultures using a high-density 512-elec

134 bolic responses to traumatic brain injury in hippocampal slice cultures, and observed marked upregula

135 microglia-neuron interactions in organotypic hippocampal slice cultures, i.e., postnatal cortical tis

136 via RyR- and miR132-dependent mechanisms in hippocampal slice cultures.

137 del of rMS using mouse organotypic entorhino-hippocampal slice cultures.

138 using rapid high-pressure freezing (HPF) of hippocampal slice cultures.

139 tive NMDAR antagonist, D-APV, in organotypic hippocampal slice cultures.

140 ere also produced in ex vivo optic nerve and hippocampal slice cultures.

141 on compared to single agents in immature rat hippocampal slice cultures.

142 nockdown of PYK2 blocks LTD, but not LTP, in hippocampal slice cultures.

143 beta aggregation and deposition in long-term hippocampal slice cultures.

144 y synapses over prolonged periods of time in hippocampal slice cultures.

145 In isolated hippocampal slices, decaying long-term potentiation can

146 We find that hippocampal slices, either prepared from rats following

147 Whole-cell hippocampal slice electrophysiological recordings and mo

148 ional assay (EC50, 36 nM) and carbachol in a hippocampal slice electrophysiology assay (EC50, 165 nM)

149 n of MS-DBB glutamatergic fiber terminals in hippocampal slices elicited weak postsynaptic responses

150 voflurane-induced preconditioning in the rat hippocampal slice enhances the hypoxic hyperpolarization

151 addition, acute treatment of an organotypic hippocampal slice epilepsy model with Sema4D reveals tha

152 inant or synthetic Aeta-alpha was applied on hippocampal slices ex vivo, long-term potentiation was l

153 naptic currents in both cultured neurons and hippocampal slices exposed to E2, while their frequency

154 strocytic lactate was also observed in acute hippocampal slices exposed to NH4(+) and in the somatose

155 y upregulates synaptic NMDAR currents in rat hippocampal slices, facilitating induction of long-term

156 In biolistically transduced hippocampal slices, fluorescently tagged GLT-1 puncta ov

157 In acutely prepared hippocampal slices, frequency and amplitude of mEPSCs an

158 ced dendritic spine expansion is impaired in hippocampal slices from 15- and 21-d-old synaptopodin-de

159 ayed for restoration of synaptic function in hippocampal slices from AD-transgenic mice, reversal of

160 U0409551 directly enhances NMDAR function in hippocampal slices from adult male SR-/- mice.

161 affer collateral/commissural fibers in acute hippocampal slices from adult mice transduced with the g

162 ptic responses of mature and immature GCs in hippocampal slices from adult mice.

163 o mGlu5 receptor activation were abnormal in hippocampal slices from AS mice compared with wild-type

164 etanic stimulation (TS) in the CA1 region of hippocampal slices from both nulliparous female and male

165 In contrast, in hippocampal slices from calpain-1 knock-out (KO) mice, a

166 spine resolution in pyramidal neurons in rat hippocampal slices from either sex.

167 Cells transcribing P2rx7 in hippocampal slices from epileptic mice displayed enhance

168 To test those possibilities in hippocampal slices from epileptic pilocarpine-treated ra

169 Moreover, treating hippocampal slices from fmr1 KO mice with Kv4 channel bl

170 We examined this issue using hippocampal slices from guinea pigs and mice.

171 ts, we recorded whole-cell currents in acute hippocampal slices from hAPP mice with and without tau.

172 ced oscillatory activity generated in CA3 of hippocampal slices from heterozygous GAD67-GFP (Deltaneo

173 Hippocampal slices from juvenile and adult GluN3A KO mic

174 Using acute hippocampal slices from mice of either sex with genetic

175 Here we show in acute hippocampal slices from mice that endogenous NPY, releas

176 on glutamatergic neurons in neocortical and hippocampal slices from neonatal mouse pups in vitro, bu

177 d local field potentials and single cells in hippocampal slices from normal rats.

178 n during whole-cell patch clamp recording in hippocampal slices from pilocarpine-treated rats.

179 function and calcium homeostasis using acute hippocampal slices from PS conditional knockout mice and

180 absence of NMDAR activation, we examined in hippocampal slices from rats and mice, an NMDAR-independ

181 Ex vivo preparations of hippocampal slices from rats that have been subjected to

182 In hippocampal slices from rats treated with nicotine for 1

183 alyzed NMDA-dependent synaptic plasticity in hippocampal slices from Tg(CJD) mice, which model a gene

184 erm potentiation (LTP), in the CA1 region of hippocampal slices from this mouse, is impared at Tg2576

185 ostsynaptic potentials (IPSPs) between acute hippocampal slices from Ts65Dn mice and diploid (2N) wil

186 peptide, reduces glutamate release in acute hippocampal slices from wild-type but not APP deficient

187 induced by theta burst stimulation (TBS) in hippocampal slices from wild-type mice was associated wi

188 In cornu ammonis area 1 hippocampal slices from wild-type mice, TBB impairs neur

189 associated with phosphorylated PAK in adult hippocampal slices from wild-type, but not Fmr1-KO, mice

190 minority of O/A interneurons in MLA-treated hippocampal slices from WT animals and alpha7(-/-) mice,

191 Here, using hippocampal slices from young adult male rats and mice,

192 -clamp recording and biochemical analyses in hippocampal slices from young adult rats, we show that E

193 itors cycloheximide and emetine to acute rat hippocampal slices have no effect on total KCC2 protein

194 In hippocampal slices, IGF-II promotes IGF-II receptor-depe

195 ictal-like activity induced by incubation of hippocampal slices in an Mg(2+)-free solution led to a f

196 that GluN2C expression is increased in acute hippocampal slices in response to ischemia.

197 l and anatomical techniques applied to mouse hippocampal slices in vitro to directly address this que

198 he dentate gyrus (DG) or CA1 region of mouse hippocampal slices in vitro.

199 pplied these neuropeptides directly to human hippocampal slices in vitro.

200 d paired patch-clamp recordings in acute rat hippocampal slices, in combination with post hoc identif

201 hanol locally increases 3alpha,5alpha-THP in hippocampal slices, in the absence of adrenal influence.

202 ry/inhibitory imbalance observed in SynII(-) hippocampal slices indirectly, not by correcting the def

203 e, we report that neuronal depolarization in hippocampal slices induces a calcium and protein phospha

204 easing O-GlcNAcylation in Sprague Dawley rat hippocampal slices induces an NMDA receptor and protein

205 potentiation (LTP) in the CA1 region of the hippocampal slice is not altered in Dyt1 DeltaGAG hetero

206 Electrophysiology studies showed that hippocampal slices isolated from these mice are more sus

207 ed short-term synaptic plasticity in a mouse hippocampal slice model can be reduced by LEI105.

208 Although the hippocampal slice model may not represent the neurons di

209 Using in vitro hippocampal slice models from rats and mice, we performe

210 ntiseizure activity in two acute ex vivo rat hippocampal slice models of epileptiform activity.

211 deleting Pten from neurons in an organotypic hippocampal slice network.

212 In rat hippocampal slices, neuronal activity rapidly decreased

213 -4 weeks) dramatically increased the sAHP in hippocampal slice neurons from young-adult rats.

214 In mouse hippocampal slices, NMDAR EPSCs in a singly activated CA

215 Hippocampal slices obtained 4 d after the induction of i

216 s were absent on GFAP-positive astrocytes in hippocampal slices obtained from GFAP-A7KO offspring fro

217 fer collateral stimulation, were detected in hippocampal slices obtained from Pin1(-/-) mice compared

218 nction and rescues long-term potentiation in hippocampal slices obtained from SR-/- mice.

219 eceptor antagonist (SR144528) or absent from hippocampal slices of CB2 receptor knock-out mice.

220 nd inhibitory synaptic transmission in acute hippocampal slices of Cntnap2(-/-) mice.

221 uced inhibition of long-term potentiation in hippocampal slices of cognitively normal mice.

222 function and recovery upon reoxygenation in hippocampal slices of mice lacking APP (APP(-/-)) or sel

223 kingly, electrophysiological recordings from hippocampal slices of mice lacking PRMT8 reveal multiple

224 rial and synaptic dysfunction in organotypic hippocampal slices of rats.

225 pines inhibited these forms of plasticity in hippocampal slices of rodents.

226 glutamate (mGlu5) receptors was enhanced in hippocampal slices of Ube3A(m-/p+) mice, which model AS.

227 In hippocampal slices, oligomeric Abeta induces eNMDAR-medi

228 or oxygen-glucose deprivation in organotypic hippocampal slices or neurons, p75(NTR) is rapidly induc

229 We demonstrate that hippocampal slices overexpressing PKMzeta show enhanced

230 tual fear memory and to show enhanced LTP in hippocampal slices overexpressing PKMzeta.

231 In hippocampal slices, photolysis of MNI-D-aspartate (4-met

232 nd intracellular recording techniques in the hippocampal slice preparation of immature rats.

233 eptor and subsequent CREB phosphorylation in hippocampal slice preparations and its administration im

234 We used organotypic hippocampal slices prepared from 6-d-old Thy1-YFP mice a

235 Using acute hippocampal slices prepared from adult mice, we report t

236 ion (mGluR-LTD) at CA3-CA1 synapses in acute hippocampal slices prepared from CGG KI mice relative to

237 ntiation (LTP) in experiments using standard hippocampal slice protocols.

238 that early expression of NR2A in organotypic hippocampal slices reduces the number of synapses and th

239 ition of PDE-4 by pharmacologic treatment in hippocampal slices rescues the enhanced mGluR-dependent

240 elective OXTR agonist [Thr(4),Gly(7)]-OXT to hippocampal slices resulted in an acute and lasting pote

241 Electrophysiological recordings of acute hippocampal slices revealed that genetic inactivation of

242 Specifically, our experimental data in mouse hippocampal slices show that acetylcholine biases STDP t

243 tions; and (3) multineuron Ca(2+) imaging in hippocampal slices showed increased spontaneous neuronal

244 AO) in rats and hMCT2 transgenic mice and of hippocampal slices subjected to ASH was assessed, as wel

245 ein levels and in the functional recovery of hippocampal slices subjected to ASH.

246 cation to the postsynaptic fraction in acute hippocampal slices subjected to long-term potentiation.

247 ong-term potentiation in Vav-deficient mouse hippocampal slices, suggesting that Vav-dependent regula

248 Hippocampal slices taken from AT mice exhibited decrease

249 ophysiological study of synaptic function in hippocampal slices taken from Clcn3(-/-) mice before the

250 air recordings were performed in organotypic hippocampal slices taken from genetically modified mice

251 pression (LTD) were significantly reduced in hippocampal slices taken from inflamed animals.

252 of long-term potentiation (LTP) in adult rat hippocampal slices that can account for one temporal seg

253 We show in rat organotypic hippocampal slices that prolonged network silencing indu

254 ssion and also caused synaptic depression in hippocampal slices that was consistent with AMPAR downre

255 we show, using whole-cell recordings in rat hippocampal slices, that group I metabotropic glutamate

256 Herein, we investigated whether in mice hippocampal slices these distinct forms of LTP are speci

257 In hippocampal slices, this increase in cleavage products w

258 we report that brief exposure of adult male hippocampal slices to 1 nM E2 increases the percentage o

259 tage-sensitive dye imaging (VSDi) in ventral hippocampal slices to determine the effects of sazetidin

260 gether with electrophysiology in acute mouse hippocampal slices to dissect the roles of P/Q- and N-ty

261 of tonic GABAA receptor currents in ex vivo hippocampal slices to examine GAT-1 operation under vary

262 geted optogenetic stimulation in acute mouse hippocampal slices to examine how one class of interneur

263 re used chained microRNAs in rat organotypic hippocampal slices to generate a reduced background of e

264 electrophysiologically tagged NMDARs in rat hippocampal slices to identify the molecular determinant

265 e, we used extracellular field recordings in hippocampal slices to investigate adaptations in synapti

266 he CaMKIIalpha promoter in mice and prepared hippocampal slices to produce a model of intrinsic CA1 g

267 oxygenase 1, and 4) immunohistochemistry of hippocampal slices to quantify vital neurons.

268 Using mouse hippocampal slices to study acute oxygen glucose depriva

269 that in rat dentate granule cells in ex vivo hippocampal slices, tonic currents are predominantly gen

270 In wild-type hippocampal slices treated with exogenous amyloid beta p

271 fore, a peptidomimetic furoxan was tested in hippocampal slices treated with oligomeric amyloid-beta

272 In hippocampal slices, treatment with the GABA(B) receptor

273 Application of VU0463271 to mouse hippocampal slices under low-Mg(2+) conditions induced u

274 reased alpha2beta1gamma1 GABAAR pentamers in hippocampal slices using cell-surface cross-linking, fol

275 quantified its buffering capacity in murine hippocampal slices using confocal calcium imaging and th

276 that immunostaining in the CA1 region of rat hippocampal slices was confined to pyramidal neurons.

277 lation of prohibitin in neuronal cultures or hippocampal slices was markedly neuroprotective, whereas

278 3 pyramidal neurons on postnatal day 0-6 rat hippocampal slices, we detected robust GlyR activity as

279 tive dye to image electrical activity in rat hippocampal slices, we explored how long-term potentiati

280 In organotypic rat hippocampal slices, we find that a nonphosphorylatable P

281 -cell confocal microscopy of rat organotypic hippocampal slices, we find that enhancing neuronal acti

282 In hippocampal slices, we found that the GluN2B-selective a

283 using paired whole-cell recordings in rodent hippocampal slices, we report that presynaptic protein s

284 s in young 3xTg-AD and nontransgenic (NonTg) hippocampal slices, we show that increased RyR-evoked ca

285 Using paired recordings in rat hippocampal slices, we show that inhibition in the DG is

286 Here, using mouse organotypic hippocampal slices, we show that the extracellular AMPAR

287 ectrophysiological recordings from acute rat hippocampal slices, we tested the critical BCM predictio

288 ngth of excitatory inputs on PV-INs in acute hippocampal slices were also dependent on Narp and Narp-

289 When rat hippocampal slices were chronically treated with neuregu

290 Hippocampal slices were cultured and treated with microm

291 For the in situ model of ischemia, hippocampal slices were exposed to oxygen glucose depriv

292 atal day 1 to 7 or milk only (Controls), and hippocampal slices were prepared from Control- and CNN-t

293 In adulthood, hippocampal slices were prepared.

294 how that when organotypic cultures of rodent hippocampal slices were treated with a CB2 receptor agon

295 ular field recordings from the CA1 region of hippocampal slices, whereas behavioral techniques were u

296 on and LTP was increased in CaMKIIalpha-HM3D hippocampal slices, whereas slices from CaMKIIalpha-HM4D

297 ork activation (GNA) in the developing mouse hippocampal slices, which is measured macroscopically by

298 Here, we report that treatment of adult rat hippocampal slices with BDNF or with tetraethylammonium

299 Here we report that pretreatment of hippocampal slices with GLP-1(9-36)(amide) prevented imp

300 dress this issue, we probed NA-treated mouse hippocampal slices with pharmacological inhibitors targe