ライフサイエンスコーパス: hippocampus

1 pendent microarray dataset generated from MS hippocampus.

2 orebrain and gliosis and microgliosis in the hippocampus.

3 the subiculum, the major output area of the hippocampus.

4 pointed to alpha-synuclein pathology in the hippocampus.

5 poral lobe, supplying cortical inputs to the hippocampus.

6 s consistently lateralized the epileptogenic hippocampus.

7 al issue in planning: the role of the dorsal hippocampus.

8 ity via suboptimal adult neurogenesis in the hippocampus.

9 d by theta-burst stimulation in field CA1 of hippocampus.

10 virally overexpressed CREB in CA1 of dorsal hippocampus.

11 precursors and dentate granule cells in the hippocampus.

12 the corpus callosum, lateral ventricles, and hippocampus.

13 dominant-negative CaMKII-alpha (K42M) in the hippocampus.

14 lular levels of acetylcholine in the ventral hippocampus.

15 the generation of theta oscillations in the hippocampus.

16 pinal cord, cerebellum, cerebral cortex, and hippocampus.

17 ility of functional rejuvenation in the aged hippocampus.

18 SMAD-2, -3, and -7; and SMURF-2) in the rat hippocampus.

19 efrontal and parietal cortex, as well as the hippocampus.

20 en when PCP is injected directly into dorsal hippocampus.

21 functional and structural plasticity in the hippocampus.

22 y facilitating long-term potentiation in the hippocampus.

23 torhinal cortex replayed coherently with the hippocampus.

24 ameliorate neurogenesis-defects in the aging hippocampus.

25 rpine induced biphasic changes in pO2 in the hippocampus.

26 tation at the dorsal and ventral ends of the hippocampus.

27 ction of information flow found in the adult hippocampus.

28 the structure and function of neurons in the hippocampus.

29 id produce a volume reduction throughout the hippocampus.

30 ri defined region-of-interest, the bilateral hippocampus.

31 encoding and retrieval of information by the hippocampus.

32 quency coupling between the amygdala and the hippocampus.

33 uron-glia cell-fate switch in the developing hippocampus.

34 that relies on improved neurogenesis in the hippocampus.

35 xpression and autophagosome formation in the hippocampus.

36 y amyloidosis such as the frontal cortex and hippocampus.

37 logies, exhibit negligible expression in the hippocampus.

38 activates nuclear GSK3beta in the cortex and hippocampus.

39 tion of stem cell genes, in the degenerating hippocampus.

40 c phase coupling between piriform cortex and hippocampus.

41 ding of location is thought to depend on the hippocampus.

42 PFC and with glutamatergic signalling in the hippocampus.

43 synaptic plasticity for AKT isoforms in the hippocampus.

44 av 1.6) in area CA1 and dentate gyrus of rat hippocampus.

45 ally interacts with synaptic AMPARs in mouse hippocampus.

46 orrelated with the gray matter volume of the hippocampus.

47 develop after brain injuries that damage the hippocampus.

48 schizophrenia and 196 control subjects) and hippocampus (83 schizophrenia and 187 control subjects).

49 The hippocampus, a brain region subserving roles of spatial

50 The hippocampus, a brain region that is critical for learnin

51 item-specific BOLD activity patterns in the hippocampus, a key structure for representing memories a

52 onal learning; and the white matter near the hippocampus, a structure fundamental for the initial sta

53 ed dentate gyrus granule cell neurons of the hippocampus after a clinically relevant isoflurane anest

54 A decrease in ACSS2 in the hippocampus also leads to defective upregulation of memo

55 d activity in, and connectivity between, the hippocampus, amygdala and ventromedial PFC during condit

56 ouse forebrain (striatum, prefrontal cortex, hippocampus, amygdala, and bed nucleus of the stria term

57 no mood symptoms) was hyperactivation of the hippocampus/amygdala, when controlling for baseline psyc

58 muM in the dentate gyrus (DG) region of the hippocampus and 22.1 +/- 4.9 muM in the cerebral cortex.

59 These neurons project to the hippocampus and are considered to be grid cells represen

60 cells in layer II of the mEC project to the hippocampus and are considered to be space-representing

61 rain, GABAergic neuronal loss in the cortex, hippocampus and basal forebrain and gliosis and microgli

62 eadily detected in the sensory motor cortex, hippocampus and cerebellum of post-mortem brains from HD

63 brain regions (prefrontal cortex, striatum, hippocampus and cerebellum) from 41 schizophrenia patien

64 and mitochondrial swollen morphology in the hippocampus and cerebral cortex.

65 ulation protects against brain injury in the hippocampus and corpus callosum in rats with vascular de

66 D1 leads to paralysis, along with widespread hippocampus and cortex neurodegeneration, and learning a

67 IL-1beta was increased in both the hippocampus and cortex of mice injected with 4T07 or 4T1

68 AR subunit, which is highly expressed in the hippocampus and cortex throughout development.

69 derived neurotropic factor (BDNF) levels in hippocampus and cortex were detected with immunoblotting

70 synapses connecting pyramidal neurons of the hippocampus and cortex with fast-spiking parvalbumin (PV

71 ssion revealed parallel up-regulation in the hippocampus and cortex, sustained in the hippocampus in

72 autoactivation (pT286) of CaMKIIalpha in the hippocampus and cortex.

73 Brains were examined for morphology of hippocampus and cortex.

74 to increased adult cell proliferation in the hippocampus and enhanced pattern separation ability.

75 rine 1303 (S1303) in the PVN, but not in the hippocampus and frontal cortex, was significantly higher

76 Place cells in the hippocampus and grid cells in the medial entorhinal cort

77 ial activity patterns characteristic for the hippocampus and implicated in memory consolidation and r

78 human cord plasma treatment revitalizes the hippocampus and improves cognitive function in aged mice

79 y unknown role of Cav1.2 channels within the hippocampus and in D1 receptor-expressing cells in extin

80 t that theta-slow gamma coupling between the hippocampus and medial prefrontal cortex (mPFC) is augme

81 We found that neural patterns in the hippocampus and medial prefrontal cortex represented the

82 eous recordings from multiple neurons in the hippocampus and neocortex of rats with chronic temporal

83 ave focused on GABAergic interneurons in the hippocampus and neocortex, particularly fast-spiking par

84 The hippocampus and orbitofrontal cortex (OFC) both make imp

85 ng-range functional connectivity between the hippocampus and other forebrain structures is enabled by

86 uld be associated with reduced volume of the hippocampus and other limbic and paralimbic areas.

87 Observations about the dialog between the hippocampus and prefrontal cortex provide new insights i

88 and perforation (CLP), and serum and brain (hippocampus and prefrontal cortex) samples were obtained

89 In addition to the hippocampus and prefrontal cortex, mice subjected to ELS

90 isms, we recorded neural activity in the rat hippocampus and prefrontal cortex, structures critical f

91 temporal context, a process dependent on the hippocampus and prefrontal cortex.

92 ippocampus and RN parallels that between the hippocampus and prefrontal cortex.

93 minimizing the adverse effects of SE in the hippocampus and preventing SE-induced cognitive and memo

94 ta-dependent functional coupling between the hippocampus and RN parallels that between the hippocampu

95 This contrasted to transient firing in hippocampus and sensory neocortex.

96 a negative association of TSPO levels in the hippocampus and striatum with alcohol dependence severit

97 of hippocampal suppression; rather, both the hippocampus and the amygdala were targeted by a top-down

98 found coordinated reactivations between the hippocampus and the BLA during non-REM sleep following t

99 processing distinct information, such as the hippocampus and the neocortex, share common cellular com

100 insula, and reduced connectivity between the hippocampus and the salience network.

101 icularly within regions of the amygdala, the hippocampus and the ventral hypothalamus.

102 ular, and transcriptomic characterization of hippocampus and two regions cortex in 107 aged donors (m

103 In dorsal hippocampus and ventral hippocampus (VHIPP), lithium-res

104 and greater functional connectivity between hippocampus and ventrolateral prefrontal cortex (vlPFC).

105 both in distant brain regions (striatum and hippocampus) and within the same brain region (striatum)

106 al cortex, insula, globus pallidus, putamen, hippocampus, and amygdala) and homeostatic (hypothalamus

107 prefrontal cortex (PFC), nucleus accumbens, hippocampus, and amygdala.

108 cortex (vmPFC), posteromedial cortex (PMC), hippocampus, and amygdala.

109 ing (thalamus, insula, orbitofrontal cortex, hippocampus, and anterior cingulate cortex).

110 sgACC], left dorsolateral prefrontal cortex, hippocampus, and basolateral amygdala) to identify imagi

111 positive astrocytes increased in the Tg(CJD) hippocampus, and blocking IL-1 receptor signaling restor

112 y matter volume in the orbitofrontal cortex, hippocampus, and cerebellum; white matter integrity in t

113 elicit fear behaviors include the amygdala, hippocampus, and medial prefrontal cortex.

114 discrete areas of the brain (olfactory bulb, hippocampus, and midbrain) and reduction of the hepatic

115 immediate-early gene Fos in the SCN, dorsal hippocampus, and olfactory bulb.

116 ptic proteins synaptophysin and PSD95 in the hippocampus, and prevented BCCAO-induced loss of total a

117 the frontal cortex, parietotemporal cortex, hippocampus, and thalamus whereas the increase in (18)F-

118 e rescued by reducing PERK expression in the hippocampus, and that reducing PERK expression in the hi

119 Posterior hippocampus appears to support context encoding, a proce

120 he dentate gyrus (DG) to the CA3 area of the hippocampus are distinctive for their prominent short-te

121 Granule cells in the dentate gyrus of the hippocampus are thought to be essential to memory functi

122 from zero except for (18)F-FPSCH when using hippocampus as the reference region.

123 xpressed in neurons of the CA3 region of the hippocampus, as transducing OCN's regulation of hippocam

124 ed as deep as 380 mum in the mouse cortex or hippocampus at a 30-Hz volume rate while discriminating

125 cerebral injection of RAGE antibody into the hippocampus at days 15, 17, and 19 post-CLP reduced Abet

126 We focused on the response of the hippocampus at early (2-weeks) and late (20-week) time p

127 al-mediated deletion of Cav1.2 in the dorsal hippocampus attenuated extinction of cocaine CPP.

128 In parallel, the posterior hippocampus became less involved as schema objects were

129 Notably, reactivation was stronger for the hippocampus-BLA correlation patterns representing the ru

130 ed the expression of PKMzeta in the mPFC and hippocampus but not in the orbitofrontal cortex.

131 paralleled changes in the medial septum and hippocampus, but not in other neural structures.

132 PS and ES similarly induced DeltaFosB in the hippocampus, but only PS significantly increased DeltaFo

133 In vivo imaging of prodromal hippocampus CA1 subfield oxidative stress in models of A

134 d to downstream neurons, suggesting that the hippocampus can generate longer sequences of repeated ac

135 tical and subcortical brain regions (cortex, hippocampus, caudate-putamen, nucleus accumbens, thalamu

136 tic spine and synapse loss in the cortex and hippocampus, concomitant with memory impairment and neur

137 .15), amygdala (d=-0.19), caudate (d=-0.11), hippocampus (d=-0.11), putamen (d=-0.14), and intracrani

138 motor area, left parahippocampal gyrus, and hippocampus; decreased brain activity in right lateral o

139 amics to maintain episodic-like accuracy and hippocampus dependency of remote memory.

140 lexibility of declarative memories, are both hippocampus-dependent and decline in aging.

141 ld affect adult hippocampal neurogenesis and hippocampus-dependent behaviors.

142 ent habit memory, at the expense of flexible hippocampus-dependent cognitive memory.

143 f Infant Development and at age 6.5 y with a hippocampus-dependent delayed-recall task.

144 ng via a target gene, VEGFD, is required for hippocampus-dependent fear memory consolidation and exti

145 ression of Cav-1 in the adult brain prevents hippocampus-dependent learning and memory deficits, rest

146 ht into how the circadian clock can regulate hippocampus-dependent learning by controlling molecular

147 .SIGNIFICANCE STATEMENT The consolidation of hippocampus-dependent memories is causally related to re

148 a causal role for thalamic sleep spindles in hippocampus-dependent memory consolidation, conveyed thr

149 e-induced spindles, improve consolidation of hippocampus-dependent memory during sleep.

150 that mice lacking PRMT8 also exhibit reduced hippocampus-dependent memory.

151 ic suppression of thalamic spindles impaired hippocampus-dependent memory.

152 PCP (5 mg/kg, i.p.) impairs a well learned, hippocampus-dependent place avoidance behavior in rats t

153 l narrowing on threat cues at the expense of hippocampus-dependent processing of the broader context.

154 Rat hippocampus-dependent spatial memory was evaluated on po

155 nervation of newly born neurons in the adult hippocampus develops concurrently, and excitatory input

156 spatial cognitive behavior and suggest that hippocampus discharge coordination is crucial to spatial

157 erated immature neurons (NGIs) in the dorsal hippocampus (dNGIs) of adult mice and regulate both the

158 dings reveal a critical role of CRTC1 in the hippocampus during associative memory, and provide evide

159 or is related to functional responses in the hippocampus during encoding has not been studied directl

160 ales showed stronger cFos activity in dorsal hippocampus during memory retrieval and context generali

161 al response in the subiculum subfield of the hippocampus during scene, but not face or object, discri

162 However, intra-hippocampus EEG recordings during virtual navigation in

163 evidence of 7-9 Hz rhythmicity in raw intra-hippocampus EEG traces during real as well as virtual mo

164 TATEMENT The dorsal and ventral parts of the hippocampus encode spatial information at very different

165 verexpression of Cav-1 in the adult and aged hippocampus enhances functional MLRs with corresponding

166 kinase (PERK) expression or activity in the hippocampus enhances neuronal excitability and cognitive

167 Stimulation of the mouse hippocampus evoked spiking activity that was readily dis

168 f neurons versus astroglia in the developing hippocampus.Finally, we confirm that Lhx2 binds a highly

169 ect the proinflammatory cytokine IL-6 in the hippocampus, followed up by alterations in the mRNA and

170 ted whether DNA methylation is altered in MS hippocampus following demyelination.

171 require rapid synaptic plasticity within the hippocampus for their formation and are gradually consol

172 e used direct recordings in the amygdala and hippocampus from human epilepsy patients to examine osci

173 l metabolism across regions of the amygdala, hippocampus, frontal cortex, and hypothalamus.

174 itro and migration of their progenies in the hippocampus granular layer in vivo.

175 TBI penumbra and hippocampus had higher cellular proliferation.

176 Although the hippocampus has provided the gateway for understanding s

177 The hippocampus has the largest number of differentially exp

178 modeling of AMPAR-NMDAR interactions in the hippocampus, highlights the translational value of this

179 from the PFC and limbic regions, such as the hippocampus (HP).

180 roarray analysis of mRNA from Ctcf CKO mouse hippocampus identified increased transcription of inflam

181 her, these results suggest that nBMP2 in the hippocampus impacts memory formation.

182 stantial overexpression of CaMK2N2 in dorsal hippocampus impairs LTM formation, but not LTM maintenan

183 n, suggesting that interneurons local to the hippocampus implement control over intrusive thoughts.

184 s in subregions of the caudate, putamen, and hippocampus in 22q-dup relative to 22q-del carriers.

185 the hippocampus and cortex, sustained in the hippocampus in association with novelty but in the corte

186 essential to elicit the participation of the hippocampus in avoidance memory reconsolidation, which i

187 ational" accounts suggest a key role for the hippocampus in complex scene perception.

188 missural inputs to the CA1 area of the mouse hippocampus in cultured slices, acute slices and in vivo

189 Chronic stress produces volume loss in the hippocampus in humans and atrophy of CA3 pyramidal cells

190 xcitability in the aged CA3 subregion of the hippocampus in rats, monkeys, and humans.

191 Volume deficits of the hippocampus in schizophrenia have been consistently repo

192 ) (via a synapsin promoter, SynCav1), in the hippocampus in vivo in adult (6-month-old) and aged (20-

193 Overexpression of CK1epsilon in the mouse hippocampus increased tau phosphorylation and impaired s

194 At 28 d, saline-treated rats showed hippocampus-independent retrieval and lack of discrimina

195 a coordinate system that, together with the hippocampus, informs an individual of its location relat

196 However, dorsal hippocampus inputs to LS showed enhanced neuronal activa

197 The contextual information encoded in the hippocampus is conveyed to the mPFC and amygdala for con

198 The hippocampus is critical for episodic memory, and synapti

199 The hippocampus is critical for producing stable representat

200 The hippocampus is critical for the formation and use of epi

201 r, the location and function of TRPV1 in the hippocampus is debated.

202 As the ventral hippocampus is integral to neurocircuitry that mediates

203 ry avoidance task in rats, we found that the hippocampus is involved in memory reconsolidation only w

204 Present results indicate that the hippocampus is necessary to respond in an appropriately

205 However, the hippocampus is not a uniform structure and consists of s

206 g GABAergic interneurons into the developing hippocampus is slowed in Pafah1b1(+/-) mice.

207 The hippocampus is the main locus of episodic memory formati

208 Long-term potentiation (LTP) in the rat hippocampus is the most extensively studied cellular mod

209 The hippocampus is the only known brain region where physiol

210 spatial navigation and episodic memory, the hippocampus is thought to play a critical role in disamb

211 This finding, which was selective to the hippocampus, is not predicted by standard theoretical ac

212 wn that the volume of CA1, a subfield of the hippocampus, is selectively reduced in the early stages

213 requires coordinated neural activity in the hippocampus, medial prefrontal cortex (mPFC), and amygda

214 This network comprises the hippocampus, medial prefrontal cortex, and left angular

215 ore network of neural regions, including the hippocampus, medial prefrontal cortex, and left angular

216 entiation (LTP), consistent with deficits in hippocampus-mediated behaviors.

217 This pattern was specific to the hippocampus, most pronounced in the gamma band, and not

218 lapping and distinct cell populations in the hippocampus, neocortex, and cerebellum during developmen

219 We focus on the hippocampus neuronal cell death, as well as the potentia

220 e small and precise at the dorsal end of the hippocampus, neurons at the ventral end have comparative

221 ingle neurons from the prefrontal cortex and hippocampus of 15 normal individuals (aged 4 months to 8

222 ein and activity increased in the cortex and hippocampus of Cdh1 cKO mice.

223 Pyramidal neurons from the hippocampus of Celsr3 knockout mice exhibit loss of appr

224 LFP)-related currents during seizures in the hippocampus of chronically implanted freely moving rats.

225 cell mediated capillary constrictions in the hippocampus of epileptic mice than in that of normal mic

226 A new study recording from the hippocampus of flying bats has revealed populations of n

227 de, CDAGRKQKC (DAG), that accumulates in the hippocampus of hAPP-J20 mice at different ages.

228 Our results suggest that the hippocampus of Hp 1-1 carriers may be more vulnerable to

229 This evidence was validated in the hippocampus of humans who died following status epilepti

230 the status of autophagosome formation in the hippocampus of immature rats with SE.

231 Although alterations in the cortex and hippocampus of MIA offspring have been described, less e

232 N1 by knocking-down its expression in dorsal hippocampus of mice.

233 of PERK expression in the CA1 region of the hippocampus of middle-aged male mice using a viral vecto

234 us, and that reducing PERK expression in the hippocampus of middle-aged mice enhances hippocampal-dep

235 pG sites (loci 2) of Bdnf promoter IV in the hippocampus of PSD mice.

236 ed in the dorsolateral prefrontal cortex and hippocampus of untreated patients with first-episode psy

237 ll reduction in D1 and 5-HT2A binding in the hippocampus of zQ175 compared with WT animals.

238 Discussions of the hippocampus often focus on place cells, but many neurons

239 C3 deacetylase activity in either the dorsal hippocampus or basal nucleus of the amygdala enhanced co

240 aminar organization of dendrites such as the hippocampus or cerebellum.

241 Theta oscillations in the hippocampus orchestrate such timing as demonstrated by a

242 llocentric mechanism potentially tied to the hippocampus, others postulate that disoriented navigator

243 ent was observed in the cortex (P = 0.0014), hippocampus (P = 0.0005), and thalamus (P < 0.0001).

244 han WT mice in the thalamus (P = 0.0004) and hippocampus (P = 0.0332).

245 tures (nucleus accumbens, amygdala, caudate, hippocampus, pallidum, putamen, thalamus, and lateral ve

246 Six GM regions including the right hippocampus/parahippocampus, right orbitofrontal gyrus,

247 However, the structure of the hippocampus possesses dorsal and ventral subregions, eac

248 en showed higher activation during stress in hippocampus, precuneus, superior temporal gyrus (STG) an

249 in adult neural stem/progenitor cells in the hippocampus prevents the developmental maturation of wor

250 sular, cingulate, and piriform cortices) and hippocampus proper.

251 dge about bilateral amygdala, accumbens, and hippocampus reductions in ADHD.

252 ecruits the anterior subicular region of the hippocampus, regardless of whether scenes were subsequen

253 comparable neuronal activity is observed in hippocampus region CA3 and the dentate gyrus under both

254 ted with structural differences in vmPFC and hippocampus, regions implicated in emotional processing

255 ervations indicate that BMP signaling in the hippocampus regulates depressive behavior, and that decr

256 uron excitatory activity, electrophysiology, hippocampus-selective behavioral testing, and magnetic r

257 roles of CREB within the dorsal and ventral hippocampus separately in mediating select nicotine with

258 neural networks in vivo and in vitro In the hippocampus, sequential firing of many neurons over peri

259 olumes for multiple cortical regions and the hippocampus showed statistically significant increases a

260 The dlPFC, but not the hippocampus, showed increased activity for altered image

261 cal reporters of PKA activity in acute mouse hippocampus slices, we show that endogenous Galphaq-coup

262 eptor-1 (Crhr1) gene expression, in the left hippocampus specifically, which co-occurred with epigene

263 as9 ribonucleoprotein (RNP) complexes in the hippocampus, striatum and cortex.

264 Reduced forebrain, hippocampus, striatum, amygdala, and cortical volume wer

265 ntorhinal cortex layer II (MECII) and in the hippocampus suggest general and environment-specific map

266 There is increasing evidence that the human hippocampus supports functions beyond just episodic memo

267 Although it is now well established that the hippocampus supports memory encoding [1, 2], little is k

268 by transfecting lentivirus-derived shBDNF in hippocampus suppressed the effect of fluoxetine.

269 PDE11 is an enzyme uniquely enriched in the hippocampus that breaks down cyclic AMP and cyclic GMP.

270 synapses of projection neurons in the murine hippocampus that developed in virtually complete absence

271 are (O-LM) cells are inhibitory cells in the hippocampus that gate information flow, firing while pha

272 In hippocampus, the antidepressant response to ketamine is

273 In the hippocampus, the NFI proteins were expressed during all

274 ally, and along the longitudinal axis of the hippocampus, thereby establishing an associative positiv

275 ptor subfamily 4 (Nr4a) genes Nr4a1-3 in the hippocampus through a mechanism that involves CRTC1 recr

276 activation of direct projections from dorsal hippocampus to prelimbic (PL) cortex and activation of c

277 tation converge on plasticity at one site in hippocampus to prevent encoding of a basic element of co

278 vity prevents interference by "teaching" the hippocampus to retrieve distinct representations of simi

279 he dorsoventral axis, especially from cortex/hippocampus to thalamus/hypothalamus posteriorly.

280 ral axis, especially posteriorly from cortex/hippocampus to thalamus/hypothalamus.

281 ombined with silicon probe recordings in the hippocampus, to identify candidate physiological pattern

282 eta-analysis in other brain regions studied (hippocampus, ventral pallidum and cerebellum), or of the

283 ions, including focal projections to ventral hippocampus, ventrolateral septum, and LHb originated fr

284 hat a CA1 neuronal population in the ventral hippocampus (VH) projects to both the mPFC and amygdala

285 In dorsal hippocampus and ventral hippocampus (VHIPP), lithium-responsive C57BL/6J and 129

286 Increasing BMP signaling in the hippocampus via viral overexpression of BMP4 blocked the

287 Gene expression in the hippocampus was increased after both AE and NMES, with I

288 ded by evidence that HMGB1 infusion into the hippocampus was sufficient to cause anhedonic behavior a

289 using intracranial recordings from the human hippocampus we found more power in the high-frequency ba

290 excitability of afferent connections to the hippocampus, we control the risk of temporal lobe seizur

291 eurogenesis in the dentate gyrus (DG) of the hippocampus, we hypothesized that selective expression o

292 prefrontal cortex (PFC) but not striatum or hippocampus where CK2alpha is also ablated.

293 We subsequently examined the hippocampus, where alpha7 nAChRs are highly expressed, p

294 /KCTD16 hetero-oligomers are abundant in the hippocampus, where they prolong the duration of slow IPS

295 wed that long-term potentiation (LTP) in the hippocampus, which is dependent on intracellular Ca(2+)

296 AD-2/3 and reduced SMAD-7 expression) in the hippocampus, which reduced NSC proliferation because of

297 hat the direct entorhinal cortical inputs to hippocampus, which target the very distal pyramidal neur

298 TBI suppressed long-term potentiation in the hippocampus, which was fully restored with ISRIB treatme

299 duced glial fibrillary acidic protein in the hippocampus, which was impaired in Morris water maze-tra

300 for human alphaS (line M20) injected in the hippocampus with wild-type, H50Q, G51D or A53E alphaS fi