ライフサイエンスコーパス: dentate gyrus

1 proliferation and neurogenesis in the adult dentate gyrus.

2 isplaced in the outer GCL of the hippocampal dentate gyrus.

3 tural and functional plasticity of the adult dentate gyrus.

4 rtin(+) cells in the subgranular zone of the dentate gyrus.

5 eased adult neurogenesis was observed in the dentate gyrus.

6 ysis of Nestin-GFP-positive RGL cells of the dentate gyrus.

7 of GABAergic interneurons in the hippocampal dentate gyrus.

8 hout the axon/dendrite layers of CA1 and the dentate gyrus.

9 ed slow rhythm with highest amplitude at the dentate gyrus.

10 , both lack a clear homolog of the mammalian dentate gyrus.

11 anisms, and network computation in the adult dentate gyrus.

12 c transmission and network inhibition in the dentate gyrus.

13 rted stress levels and reduced volume in the dentate gyrus.

14 nd the maintenance of sparse activity in the dentate gyrus.

15 ctivity patterns in principal neurons of the dentate gyrus.

16 en in granule neurons of the murine neonatal dentate gyrus.

17 A3, and at P90 the reduction extended to the dentate gyrus.

18 diated, in part, by its aromatization in the dentate gyrus.

19 enitor cells required for development of the dentate gyrus.

20 sion, and an increase in neurogenesis in the dentate gyrus.

21 eurons, especially those in the hilus of the dentate gyrus.

22 t in the lateral perforant path input to the dentate gyrus.

23 milar to the pattern separation shown by the dentate gyrus.

24 naling during development of the hippocampal dentate gyrus.

25 d the glutamatergic rMF sprouting within the dentate gyrus.

26 of neural progenitor pools in the postnatal dentate gyrus.

27 hibition and neurosteroid sensitivity in the dentate gyrus.

28 t from CA3, but no detectable input from the dentate gyrus.

29 ied within and between subregions of CA1 and dentate gyrus.

30 d long-term potentiation specifically in the dentate gyrus.

31 lt lateral ventricle subventricular zone and dentate gyrus.

32 e of increasing neuronal excitability of the dentate gyrus.

33 he COX10 gene, in granule cells of the adult dentate gyrus.

34 s in the subventricular zone and hippocampal dentate gyrus.

35 pocampal size and decreased thickness of the dentate gyrus.

36 er and robust morphological sprouting in the dentate gyrus.

37 rging that human pattern separation requires dentate gyrus.

38 ocampal CA3 area bypassing CA1, CA2, and the dentate gyrus.

39 uption of synaptic transmission in the mouse dentate gyrus.

40 4 weeks led to volume reduction only in the dentate gyrus.

41 nergic terminals (fiber varicosities) in the dentate gyrus.

42 In the dentate gyrus - a key component of spatial memory circui

43 We hypothesized that OSAS would affect the dentate gyrus, a hippocampal subdivision essential to ne

44 tic GABAA receptors in the mouse hippocampus dentate gyrus, a key region associated with epilepsy and

45 RNA sequencing of the ventral dentate gyrus, a mood-regulatory region, identified meta

46 The hippocampal dentate gyrus, a region with ongoing adult neurogenesis,

47 ytes and microglia were also observed in the dentate gyrus across the different stages of tau patholo

48 ogical approaches that Oxtrs in the anterior dentate gyrus (aDG) and anterior CA2/CA3 (aCA2/CA3) of m

49 tors selectively in the granule cells of the dentate gyrus (alpha5DGKO mice).

50 f inhibitory interneurons in the hippocampal dentate gyrus, an important area for seizure propagation

51 d THY-Tau22 mice developed an atrophy of the dentate gyrus and a tau pathology characterized by Gally

52 ongly decreased stimulation-induced EPSPs in dentate gyrus and CA1 (up to 30 and 55%, respectively) v

53 late regions and showed trends toward larger dentate gyrus and CA1 regions of the hippocampus.

54 ranule and pyramidal cell neurons within the dentate gyrus and CA1 subfields of the hippocampus exhib

55 ion computations ascribed to the hippocampal dentate gyrus and CA3 fields.

56 ociation of years lived in poverty with left dentate gyrus and CA3 hippocampal subfields and left amy

57 f GAD67-cells in caudate-kindled rats in the dentate gyrus and CA3 hippocampal subfields.

58 we report dysfunctional connectivity between dentate gyrus and CA3 networks in the transchromosomic T

59 cated pattern separation computations in the dentate gyrus and CA3 subregions of the hippocampus as a

60 We performed RNA sequencing analyses of the dentate gyrus and entorhinal cortex from each line and f

61 It is suggested that the dentate gyrus and hilar region in the hippocampus perfor

62 f the main cortical afferent pathways to the dentate gyrus and hippocampus are established by birth.

63 ChAT-ir fibers were seen throughout the dentate gyrus and hippocampus, in the mediodorsal, later

64 nlarged brains with an elongated hippocampal dentate gyrus and increased numbers of newborn neurons.

65 Adult neurogenesis persists in the rodent dentate gyrus and is stimulated by chronic treatment wit

66 AMPAR-mediated synaptic transmission in the dentate gyrus and long-term potentiation in the CA1 regi

67 ia-like neural stem cells in the adult mouse dentate gyrus and made the surprising discovery that pro

68 with preclinical models suggesting that the dentate gyrus and mPFC are especially vulnerable to stre

69 ffects of fluoxetine on proliferation in the dentate gyrus and on depressive behavior.

70 a thus support a sparse coding scheme in the dentate gyrus and provide a possible link between struct

71 eurogenesis in the granule cell layer of the dentate gyrus and rescues hippocampal memory defects in

72 gions of the vertebrate brain, including the dentate gyrus and rostral migratory stream in mammals, a

73 cantly reduced in the cortex, but not in the dentate gyrus and the amygdala.

74 Young adults' whole hippocampal, dentate gyrus, and CA3 hippocampal subfields as well as

75 namely, granule cells and mossy cells of the dentate gyrus, and pyramidal cells of areas CA3, CA2, an

76 Finally, we showed that adult dentate gyrus appears similar to immature CA1, demonstra

77 d incorporation of adult-born neurons in the dentate gyrus are critical for spatial learning and memo

78 Adult-born neurons in the hippocampal dentate gyrus are important for flexibly using memories,

79 Discharges of neurons in CA1 and dentate gyrus are modulated by both HRR and theta.

80 RK2 alone does not impair development of the dentate gyrus as animals expressing only ERK1 developed

81 ions in local inhibitory function within the dentate gyrus at time points where sparse activation was

82 her, chronic aromatase inhibition within the dentate gyrus blocked the protective effects of testoste

83 born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integra

84 a critical role of the Ptchd1 protein in the dentate gyrus, but indicate that it is not required for

85 n- and somatostatin-positive interneurons in dentate gyrus, but no change in density of calretinin in

86 clude the basolateral amygdaloid nucleus and dentate gyrus, but the septohippocampal nucleus, lateral

87 s, alpha1 and alpha3 were accentuated in the dentate gyrus, CA1 region, and subiculum, whereas alpha5

88 Genetic lesions of EC and hippocampal dentate gyrus, CA3 and CA1 regions have revealed their d

89 n types in the rodent hippocampal formation (dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal

90 lities and impaired short-term plasticity at dentate gyrus-CA3 excitatory synapses culminate in impai

91 These results highlight the vulnerability of dentate gyrus-CA3 networks to aberrant human chromosome

92 Conversely, hippocampal dentate gyrus/CA3 demonstrated signals consistent with r

93 pe mice, knocking down neuronal BRCA1 in the dentate gyrus caused increased DNA double-strand breaks,

94 ours in mice by optogenetically reactivating dentate gyrus cells that were previously active during a

95 cs and patch-clamp recordings, we found that dentate gyrus cells, long believed to not project to CA2

96 ride regulation was sufficient to elicit the dentate gyrus circuit collapse evident during epilepsy d

97 thin the local circuit generates the massive dentate gyrus circuit hyperactivation evident in animals

98 Mossy cells in the hilus of the dentate gyrus constitute a major excitatory principal ce

99 neurons in the adult subgranular zone of the dentate gyrus contributes to learning.

100 sy to test which pathological changes in the dentate gyrus correlate with seizure frequency and help

101 We identified distinct layers in the dentate gyrus corresponding to the granule cell layer an

102 nhibition of adult neurogenesis in the mouse dentate gyrus decreases hippocampal network activation a

103 n-immunoreactive axons were exuberant in the dentate gyrus despite loss of immunopositive hilar neuro

104 The dentate gyrus (DG) and area CA3 of the hippocampus have

105 The hippocampal dentate gyrus (DG) and CA3 are known to contribute to th

106 ies have provided indirect evidence that the dentate gyrus (DG) and CA3 hippocampal subregions suppor

107 at mossy fiber (mf) connections between the dentate gyrus (DG) and CA3 neurons in vivo are still elu

108 tatin-expressing-interneurons (SOMIs) in the dentate gyrus (DG) control formation of granule cell (GC

109 y culture, neurons of the CA1 region and the dentate gyrus (DG) express high Np65 levels, whereas exp

110 nd radial glia-like cells in the hippocampal dentate gyrus (DG) granular cell layer.

111 Moreover, we investigated the dentate gyrus (DG) granule cell reactivity and synaptic

112 rly gene (IEG) induction in stress-activated dentate gyrus (DG) granule neurons play a crucial role i

113 ower GluN1 protein levels selectively in the dentate gyrus (DG) in vitro.

114 the cornu ammonis (CA) subfields CA1-4, the dentate gyrus (DG) including a granule cell layer (GCL)

115 CK) inhibitory interneurons of the mammalian dentate gyrus (DG) initiate the therapeutic response to

116 Here we show that PV-PIIs in rat and mouse dentate gyrus (DG) integrate their intrinsic activity ov

117 Adult neurogenesis in the dentate gyrus (DG) is strongly influenced by drug-taking

118 The hippocampal dentate gyrus (DG) is thought to be responsible for proc

119 Dentate gyrus (DG) is widely thought to provide a teachi

120 We recently reported that hippocampal dentate gyrus (DG) neurons differentiated from induced p

121 acid) content in reactive astrocytes in the dentate gyrus (DG) of a mouse model for AD (5xFAD) that

122 Neurogenesis in the dentate gyrus (DG) of the adult hippocampus is a process

123 Infusions of adiponectin into the dentate gyrus (DG) of the hippocampus in fear-conditione

124 ) a population of cells in either the dorsal dentate gyrus (DG) of the hippocampus or the basolateral

125 nd DISC1 influence adult neurogenesis in the dentate gyrus (DG) of the hippocampus, we hypothesized t

126 Cs resulted in fewer adult-born cells in the dentate gyrus (DG) overall, reducing populations across

127 spite abundant evidence that the hippocampal dentate gyrus (DG) plays a critical role in memory, it r

128 Granule neurons in the hippocampal dentate gyrus (DG) receive their primary inputs from the

129 brain varied between 6.6 +/- 0.7 muM in the dentate gyrus (DG) region of the hippocampus and 22.1 +/

130 d S1 cortex, decreased NLGN2 mRNA in CA1 and dentate gyrus (DG) regions of the hippocampus, and incre

131 ll proliferation and survival in the ventral dentate gyrus (DG) subgranular zone of Ghsr-null mice th

132 re indicative of a disrupted function of the dentate gyrus (DG) subregion of the brain, and they impr

133 The dentate gyrus (DG) subregion of the hippocampus is widel

134 Synapses from the dentate gyrus (DG) to the CA3 area of the hippocampus ar

135 The dentate gyrus (DG), a part of the hippocampal formation,

136 s in the hippocampus and particularly in the dentate gyrus (DG), a region of active neurogenesis and

137 stimulation erased LTP in CA1 but not in the dentate gyrus (DG), although adenosine eliminated potent

138 subfields cornu ammonis 2/3 (CA2/3) and CA4/dentate gyrus (DG), as well as impaired hippocampal micr

139 of neural stem cells (NSCs) in the postnatal dentate gyrus (DG), drastically increased perinatal apop

140 We found that, in the developing dentate gyrus (DG), excitatory drive promotes the somati

141 or, olfaction, and adult neurogenesis in the dentate gyrus (DG), olfactory bulb (OB), and the olfacto

142 neural progenitors in the adult hippocampal dentate gyrus (DG), one of the select regions of the mat

143 dult brain, like the subgranular zone of the dentate gyrus (DG), there is continuous production of ne

144 irical evidence that tonic inhibition in the dentate gyrus (DG), which maintains sparseness of neuron

145 coding mechanism, pattern separation, in the dentate gyrus (DG)-CA3 circuit in resolving interference

146 cal parvalbumin (PV) interneurons within the dentate gyrus (DG).

147 gressive neuron loss and astrogliosis in the dentate gyrus (DG).

148 hippocampal plasticity, particularly in the dentate gyrus (DG).

149 ee of calbindin reduction in the hippocampal dentate gyrus (DG).

150 ions strongly activated granule cells in the dentate gyrus (DG).

151 thickness, and (ii) activity in ERC and the dentate gyrus (DG)/CA3 region.

152 l through the canonical trisynaptic circuit (dentate gyrus [DG] to CA3 to CA1), spontaneous GNA in th

153 ibute to pattern separation functions of the dentate gyrus due to their heightened excitability, wher

154 ress depression-like behaviours and point to dentate gyrus engram cells as potential therapeutic node

155 We also demonstrate that an ablation of dentate gyrus engram cells containing restored spine den

156 m potentiation at perforant path synapses of dentate gyrus engram cells restores both spine density a

157 ve reduction in spine density of hippocampal dentate gyrus engram cells.

158 HRR is most prominent in the dentate gyrus, especially when respiration is slower tha

159 allowed targeted fatty acid analysis of the dentate gyrus granule cell layer and the CA1 pyramidal l

160 bors and dendritic spines in newly generated dentate gyrus granule cell neurons of the hippocampus af

161 to SSRIs, but it is not known whether mature dentate gyrus granule cells (DG GCs) also contribute.

162 aGABAA receptor-mediated tonic inhibition in dentate gyrus granule cells (DGGCs), thereby contributin

163 e identified more than 40 lipid species from dentate gyrus granule cells and CA1 pyramidal neurons of

164 at allows for chronic, functional imaging of dentate gyrus granule cells in awake, behaving mice in a

165 ional' nature implies that burst activity in dentate gyrus granule cells is required for detonation.

166 e normal brain, the sparse activation of the dentate gyrus granule cells maintained by tonic inhibito

167 Experimental data suggest dentate gyrus granule cells play a major role in memory

168 g the activity of its principal neurons, the dentate gyrus granule cells, are missing.

169 citability by modulating tonic inhibition in dentate gyrus granule cells, in a process involving cros

170 reduced the current amplitudes recorded from dentate gyrus granule cells, most likely by targeting pe

171 We synthesize the entire population of dentate gyrus granule cells, the most numerous cell type

172 trophysiological recordings from hippocampal dentate gyrus granule cells, we show that synaptically r

173 y encoded calcium indicators specifically to dentate gyrus granule cells.

174 berrant generation of excitatory synapses in dentate gyrus granule cells.

175 growth, particularly hippocampus, where P21 dentate gyrus granule neurons were decreased 16%, sugges

176 circuit entorhinal cortex layer II (ECII)-->dentate gyrus-->CA3-->CA1 and the monosynaptic circuit E

177 logical mechanisms involving the hippocampal dentate gyrus have been proposed.

178 orm connections with inhibitory cells in the dentate gyrus, hilus, and CA3 regions as they integrate

179 agation pathway of ictal discharges from the dentate gyrus/hilus (DGH) to the medial entorhinal corte

180 ppeared in several AD-related brain regions (dentate gyrus, hippocampal area CA1, piriform and pariet

181 hippocampal subfields including CA1, CA4 and dentate gyrus (HS ILAE Type 1), or predominant cell loss

182 in CA4 and partially affecting also CA3 and dentate gyrus (HS ILAE Type 3, n = 5) showed significant

183 all subfields, whereas TLE-G presented with dentate gyrus hypertrophy, focal increases in T2 intensi

184 ropagation from the entorhinal cortex to the dentate gyrus in 4 weeks.

185 ptic delta-containing GABAA receptors in the dentate gyrus in a mouse perimenstrual-like model of NSW

186 evidence of disrupted microstructure of the dentate gyrus in children with OSAS that may help explai

187 We demonstrate lower mean diffusivity of the dentate gyrus in children with OSAS, which correlates wi

188 s, we demonstrate distinct roles for CA3 and dentate gyrus in human memory and uncover the variegated

189 We recently demonstrated a role for the dentate gyrus in mediating testosterone's protective eff

190 ced aberrant neurogenesis in the hippocampal dentate gyrus in the context of the blood-brain barrier

191 ation of tau and reduced excitability in the dentate gyrus in this mouse model.

192 rphosphorylation of tau was increased in the dentate gyrus in THY-Tau22 mice, the development of neur

193 aloid nucleus, hippocampal CA3 subfield, and dentate gyrus; in contrast, the level is greater in Cape

194 ber of DCX-positive cells in the hippocampal dentate gyrus increased in with G-CSF treatment.

195 risoma-inhibiting interneurons (PIIs) of the dentate gyrus integrate rapidly correlated synaptic inpu

196 These data indicate that the dentate gyrus is a critical node in the temporal lobe se

197 The dentate gyrus is a region subject to intense study in ep

198 We tested the hypothesis that human dentate gyrus is critical for pattern separation, wherea

199 The hippocampal dentate gyrus is critically involved in learning and mem

200 Dentate gyrus is intimately connected to CA3 where, in a

201 The hippocampal dentate gyrus is often viewed as a segregator of upstrea

202 ot suppress ECS-induced proliferation in the dentate gyrus, it blocks dendritic outgrowth of immature

203 7.2 x 10(-6); right, p = 2.3 x 10(-6)), CA4/dentate gyrus (left, p = 1.4 x 10(-5); right, p = 2.3 x

204 gated the cellular phenotypes of hippocampal dentate gyrus-like neurons derived from iPSCs of patient

205 attenuated BDNF release and signaling in the dentate gyrus may account for cognitive and mental defic

206 information processing of cortical inputs in dentate gyrus, may participate in hippocampal-related co

207 verbal learning score correlated with lower dentate gyrus mean diffusivity (r = 0.54, p = 0.004).

208 hildren, as well as potential utility of the dentate gyrus mean diffusivity as an early marker of bra

209 Decreased dentate gyrus mean diffusivity correlated with a higher

210 Path analysis demonstrated that dentate gyrus mean diffusivity mediates the impact of OS

211 stic accuracy of a regression model based on dentate gyrus mean diffusivity reached 85.8% (cross vali

212 e synapse remodeling and neurogenesis in the dentate gyrus, mechanistic studies have revealed both ge

213 llaterals (SC)-CA1 and medial perforant path-dentate gyrus (mPP-DG) synapses in juvenile and adult ra

214 Adult-generated granule cells (GCs) in the dentate gyrus must establish synapses with preexisting n

215 In the central hilus (CH) of the dentate gyrus, Nav 1.1 immunoreactivity was selectively

216 esis and glia in the subventricular zone and dentate gyrus neurogenic niches were evaluated using sin

217 Here we show that CA1, CA3 and dentate gyrus neurons each have unique responses to supp

218 Hsp60 was also increased in the hippocampal dentate gyrus neurons somata and neuropil and hippocampu

219 , we report that deletion of Drosha in adult dentate gyrus NSCs activates oligodendrogenesis and redu

220 perforant path-granule cell synapses in the dentate gyrus of APLP1-deficient mice in vivo.

221 rogenitors after bexarotene treatment in the dentate gyrus of APOE3 and APOE4 mice.

222 5) mRNA levels were absent or reduced in the dentate gyrus of BDNF(Met/Met) mice.

223 rneuron-selective calretinin-ir cells in the dentate gyrus of hippocampal-kindled rats, which suggest

224 newly-incorporated DNA were observed in the dentate gyrus of hippocampus at the single cell level.

225 lial density and branching complexity in the dentate gyrus of hippocampus.

226 ed in the dorsolateral prefrontal cortex and dentate gyrus of human postmortem MDD patients.

227 progenitor cells isolated directly from the dentate gyrus of MBD1 mutant (KO) and WT mice showed tha

228 , alpha2, beta2, and gamma2 subunits, in the dentate gyrus of NSW mice.

229 e of a dramatic shift in excitability in the dentate gyrus of Pafah1b1(+/-) mice that may contribute

230 tion in the generation of new neurons in the dentate gyrus of patients with AD and severe neurofibril

231 d neurons significantly declined only in the dentate gyrus of patients with severe tau pathology.

232 on of Ephexin5 expression using shRNA in the dentate gyrus of presymptomatic adolescent hAPP mice was

233 (Nav 1.1, Nav 1.2, Nav 1.6) in area CA1 and dentate gyrus of rat hippocampus.

234 pressed in neural stem cells residing in the dentate gyrus of the adult hippocampus (aNSCs) and MBD1

235 evelopmental stages are recapitulated in the dentate gyrus of the adult hippocampus, where neurons ar

236 unoreactivity and mRNA expression within the dentate gyrus of the dorsal hippocampus (DH).

237 ly, physical EE promoted neurogenesis in the dentate gyrus of the hippocampal formation, but not in t

238 tion into existing neuronal circuitry in the dentate gyrus of the hippocampus and subventricular zone

239 Granule cells in the dentate gyrus of the hippocampus are thought to be essen

240 lished that new neurons are generated in the dentate gyrus of the hippocampus of almost all adult mam

241 ure neurons, and fewer mature neurons in the dentate gyrus of the hippocampus of the mouse brain.

242 retained significantly more new cells in the dentate gyrus of the hippocampus than those trained on t

243 ntrast, knocking down FGF9 expression in the dentate gyrus of the hippocampus using a lentiviral vect

244 hly expressed in the granular neurons in the dentate gyrus of the hippocampus, but it is undetectable

245 STRACT: Exercise signals neurogenesis in the dentate gyrus of the hippocampus.

246 The dentate gyrus of the mammalian hippocampus continuously

247 e status of beta adrenergic signaling in the dentate gyrus of the Ts65Dn mouse model of Down syndrome

248 eight paired helical filaments (PHFs) in the dentate gyrus of wild-type and mutant tau THY-Tau22 mice

249 t inhibitory synapses in hippocampus CA1 and dentate gyrus of young presymptomatic APPPS1 mice (1 to

250 t inhibition of the principal neurons of the dentate gyrus or CA3 via alpha2-containing GABAA recepto

251 infusion did not affect spine density in the dentate gyrus or ventromedial hypothalamus, suggesting s

252 with decreased mean diffusivity of the left dentate gyrus (p = 0.002; false discovery rate corrected

253 in the left hippocampus (cornu ammonis 1-3, dentate gyrus), parahippocampus (presubiculum, parasubic

254 of adrenals in the CA1 pyramidal cell layer, dentate gyrus polymorphic layer, bed nucleus of the stri

255 ain injury can integrate abnormally into the dentate gyrus, potentially mediating temporal lobe epile

256 We also developed a partial "whole-mount" dentate gyrus preparation and observed a dense plexus of

257 Persistent neurogenesis in the dentate gyrus produces immature neurons with high intrin

258 ate from the dentate ventricular zone to the dentate gyrus proper, resulting in premature depletion o

259 Excitatory hilar mossy cells (MCs) in the dentate gyrus receive inputs from dentate granule cells

260 umin, somatostatin and neuropeptide Y in the dentate gyrus, reduced aberrant neurogenesis with preser

261 al VitB12, mainly in the cornu ammonis 4 and dentate gyrus region (P= 0.029), which partially mediate

262 ed activity in the cornu ammonis 1 (CA1) and dentate gyrus regions of the hippocampus (P < 0.001, n =

263 The CA1 and dentate gyrus regions of the hippocampus are physically

264 us.SIGNIFICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde sprouting of gr

265 The dentate gyrus serves as a gateway to the hippocampus, fi

266 ctrophysiological and molecular tests in the dentate gyrus showed that subAbeta rats or stressed rats

267 The dentate gyrus shows a novel phenotype: the infrapyramida

268 es 11 to 18 years forecasted diminished left dentate gyrus (simple slope, -14.20; standard error, 5.2

269 udy we investigate the relationships between dentate gyrus structure, hippocampus-dependent cognition

270 ynapses were frequently found in the CA3 and dentate gyrus sub-regions, corresponding to large thorny

271 breakdown in the hippocampus and its CA1 and dentate gyrus subdivisions worsened with mild cognitive

272 ows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure.

273 ed flexibly, and that these neurons regulate dentate gyrus synaptic and spiking responses to neocorti

274 subfield (subiculum, cornu ammonis 1-3, and dentate gyrus) targets of immunomodulation-treated LGI1

275 in hippocampal staining: CB(+) decreased in dentate gyrus (TBI = 2 +/- 0.382, Sham = 4 +/- 0.383, P

276 A second excitatory cell type in the dentate gyrus, the mossy cell, forms an intricate circui

277 n the activation of neural stem cells in the dentate gyrus, their division, and differentiation of th

278 cluding the sprouting of mossy fibers in the dentate gyrus; they establish aberrant recurrent synapse

279 Reduction of fast phasic inhibition in the dentate gyrus through granule cell-selective knock-out o

280 New neurons continue to be generated in the dentate gyrus throughout life, providing this region of

281 ity in CA1 of pre-adolescent rodents, and in dentate gyrus throughout maturity.

282 w and high levels of kainic acid (KA) in the dentate gyrus to assess whether neuronal hyperexcitation

283 d progressive microstructural changes in the dentate gyrus translate to the severity of hippocampal s

284 s observed in hippocampus region CA3 and the dentate gyrus under both conditions.

285 hods to show that EE alters microglia in the dentate gyrus under physiological conditions and robustl

286 ify a role for the astroglial xCT in ventral dentate gyrus (vDG) in stress and antidepressant respons

287 Critically, human dentate gyrus volume decreases with age whereas CA3 volu

288 pattern separation task, we demonstrate that dentate gyrus volume predicts accuracy and response time

289 Further, decreased dentate gyrus volume, and no other subfield volume, medi

290 n of testosterone's aromatization within the dentate gyrus was assessed by local infusion of the arom

291 abelled cells in the subgranular zone of the dentate gyrus was observed.

292 of juxtacellularly recorded cells in CA1 and dentate gyrus were modulated by HRR and theta oscillatio

293 ition and showed increased activation in the dentate gyrus when presented with novel stimuli.

294 Proximal CA3 (near the dentate gyrus), where the recurrent collaterals are the

295 vious observations in the monkey hippocampal dentate gyrus, where MSBs comprised approximately 40% of

296 equency rhythm with largest amplitude in the dentate gyrus, which coupled to respiration-entrained os

297 ith enhanced novelty-induced activity in the dentate gyrus, which may be related to our findings that

298 Adult hippocampal neurogenesis provides the dentate gyrus with heterogeneous populations of granule

299 s of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuro

300 s fibres in the medial entorhinal cortex and dentate gyrus, with no frank noradrenergic cell body los