ライフサイエンスコーパス: hippocampal slice

1 cretion by VAMP8 was also observed in murine hippocampal slices.

2 ing electrophysiological field recordings in hippocampal slices.

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

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

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

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

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

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

9 Furthermore, CCNY abolishes LTP in hippocampal slices.

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

11 n injury and enhanced synaptic plasticity in hippocampal slices.

12 Cajal-Retzius cells optogenetically in mouse hippocampal slices.

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

14 ongoing epileptiform activity in mouse acute hippocampal slices.

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

16 ocampal neurons and CA1 pyramidal neurons in hippocampal slices.

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

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

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

20 tional hemichannels in astrocytes from mouse hippocampal slices.

21 d currents in CA1 pyramidal neurons in acute hippocampal slices.

22 hat occur during spreading depression in rat hippocampal slices.

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

24 ivation inhibited Thr-840 phosphorylation in hippocampal slices.

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

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

27 tiation induction in 6-month-old 5xFAD mouse hippocampal slices.

28 ative electrophysiological systems using rat hippocampal slices.

29 pocampal networks in dissociated culture and hippocampal slices.

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

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

32 in and impaired synaptic plasticity in adult hippocampal slices.

33 ng SWRs that occurred spontaneously in mouse hippocampal slices.

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

35 gomer (Abetao)-induced suppression of LTP in hippocampal slices.

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

37 binant noradrenaline transporters and in rat hippocampal slices.

38 arbachol-induced gamma oscillations in mouse hippocampal slices.

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

40 plasticity and synaptic transmission in the hippocampal slices.

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

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

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

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

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

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

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

48 5-HT1A/5-HT7 agonist) reversed mGluR-LTD in hippocampal slices.

49 ein regulation were observed in cultured rat hippocampal slices.

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

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

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

53 the maintenance of LTP in the CA1 region of hippocampal slices.

54 ments on both female and male mouse and rats hippocampal slices.

55 of the functions of this APP domain in acute hippocampal slices.

56 tatory postsynaptic currents (mEPSCs) in rat hippocampal slices.

57 cies, consistently with previous findings in hippocampal slices.

58 dendrites of CA1 pyramidal neurons in mouse hippocampal slices.

59 ently enhances cAMP in neuronal cultures and hippocampal slices.

60 defective LTP in primary neuron cultures and hippocampal slices.

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

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

63 cues presynaptic responses in culture and in hippocampal slices.

64 of CA1 pyramidal neurons in cultured murine hippocampal slices.

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

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

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

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

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

70 r-mediated synaptic currents in heterozygous hippocampal slices also showed a prolonged deactivation

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

72 Electrophysiological recordings from hippocampal slices and activity measurements of glutamic

73 asured using several seizure models in mouse hippocampal slices and acutely induced seizures in rats

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

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

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

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

78 In hippocampal slices and cultured neurons we also observed

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

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

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

82 ed real-time dynamics of GLU and GABA in rat hippocampal slices and observed a significant, nonlinear

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

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

85 ked currents in CA1 pyramidal neurons of rat hippocampal slices, and (iv) recombinant NMDARs expresse

86 l spatial learning in the Barns maze, LTP in hippocampal slices, and expression levels of RyR in the

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

88 injury reduced long-term potentiation in the hippocampal slices, and L-655,708 attenuated this reduct

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

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

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

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

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

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

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

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

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

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

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

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

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

102 Slow periodic activity in the longitudinal hippocampal slice can propagate without chemical synapti

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

104 Astrocytes in hippocampal slices can dynamically regulate synaptic tra

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

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

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

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

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

110 In rat hippocampal slices, cortical synaptoneurosomes, and cult

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

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

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

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

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

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

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

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

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

120 Using organotypic hippocampal slice cultures and primary neuron hippocampa

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

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

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

124 Paraoxon-exposed hippocampal slice cultures exhibited progressive decline

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

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

127 th primary neuronal cultures and organotypic hippocampal slice cultures from wild-type mice.

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

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

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

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

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

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

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

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

136 recordings of pyramidal cells in organotypic hippocampal slice cultures that were generating spontane

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

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

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

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

141 f chronic IFN-gamma exposure on microglia in hippocampal slice cultures, i.e., postnatal parenchyma l

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

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

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

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

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

147 vo in EAE animals and ex vivo in organotypic hippocampal slice cultures.

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

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

150 Whole-cell hippocampal slice electrophysiological recordings and mo

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

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

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

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

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

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

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

158 axons of cultured hippocampal neurons and in hippocampal slices expressing EB3-EGFP and vGlut1-mCherr

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

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

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

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

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

164 e recorded EPSCs from CA1 pyramidal cells in hippocampal slices from adult rats and used specific inh

165 TBS)-induced long-term potentiation (LTP) in hippocampal slices from AS mice by enhancing SK2 interna

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

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

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

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

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

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

172 olution two-photon microscopy in organotypic hippocampal slices from GAD65-GFP mice of both sexes to

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

174 Hippocampal slices from juvenile and adult GluN3A KO mic

175 contributing to the effects of adenosine in hippocampal slices from male albino rats.

176 into protein-synthesis-dependent late LTP in hippocampal slices from male rats.

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

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

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

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

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

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

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

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

185 e of increased network excitability in acute hippocampal slices from the Mecp2 KO mice.

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

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

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

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

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

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

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

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

194 otentials (fEPSPs) in the CA1 field of mouse hippocampal slices, (iii) NMDAR-mediated miniature excit

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

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

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

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

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

200 n STEP-KO mouse brain, and STEP knockdown in hippocampal slices increases AMPAR-mediated synaptic cur

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

202 Direct application of IL-1beta to ex vivo hippocampal slices induced non-synaptic depolarisation a

203 : "Direct application of IL-1beta to ex vivo hippocampal slices induced non-synaptic depolarisation a

204 : "Direct application of IL-1beta to ex vivo hippocampal slices induced non-synaptic depolarisation a

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

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

207 isodes of sprouted mossy fiber activation in hippocampal slices initiated bursts of recurrent polysyn

208 t slow periodic activity in the longitudinal hippocampal slice is a self-regenerating wave which can

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

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

211 Hippocampal slices lacking Pyk2 are protected from AD-re

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

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

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

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

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

217 In rat hippocampal slices, neuronal activity rapidly decreased

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

219 Hippocampal slices obtained 4 d after the induction of i

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

221 mp recordings and optogenetic stimulation in hippocampal slices obtained from mice of either sex.

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

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

224 cal, and imaging approaches in rat entorhino-hippocampal slices of both sexes.

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

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

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

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

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

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

231 here, we use a GABA 'sniffer' patch in acute hippocampal slices of the rat and document strong depend

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

233 In hippocampal slices, oligomeric Abeta induces eNMDAR-medi

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

235 We demonstrate that hippocampal slices overexpressing PKMzeta show enhanced

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

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

238 In hippocampal slices, picrotoxin-insensitive inhibitory sy

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

240 versed RGFP966-induced enhancement of LTP in hippocampal slice preparations.

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

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

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

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

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

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

247 urther electrophysiological investigation in hippocampal slices revealed significantly reduced long-t

248 Electrophysiological recordings in in vitro hippocampal slices revealed significantly reduced magnit

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

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

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

252 Extracellular recording from hippocampal slices showed no Mg(2+)/NMDA-mediated epilep

253 Electrophysiological recordings on acute hippocampal slices showed that exogenous Amh protein add

254 Extracellular field recordings in hippocampal slices showed that syntaxin-3 cKO did not ex

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

256 Hippocampal slices taken from AT mice exhibited decrease

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

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

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

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

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

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

263 In hippocampal slices, this increase in cleavage products w

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

265 Here we used mouse hippocampal slices to address how PVs signal to newborn

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

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

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

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

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

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

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

273 Using mouse hippocampal slices to study acute oxygen glucose depriva

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

275 Recordings from hippocampal slices treated with endothelial supernatants

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

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

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

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

280 We found that CB(1)-iLTD in acute rat hippocampal slices was associated with protein synthesis

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

282 3 pyramidal neurons on postnatal day 0-6 rat hippocampal slices, we detected robust GlyR activity as

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

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

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

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

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

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

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

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

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

292 When rat hippocampal slices were chronically treated with neuregu

293 Hippocampal slices were cultured and treated with microm

294 In addition, hippocampal slices were prepared 1 week after traumatic

295 In adulthood, hippocampal slices were prepared.

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

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

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

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

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