ライフサイエンスコーパス: dentate gyrus

1 emarkably enriched in granule neurons of the dentate gyrus.

2 ber of granule cells and PV interneurons per dentate gyrus.

3 neurogenesis and synaptic plasticity in the dentate gyrus.

4 ion, up to seven laminae were evident in the dentate gyrus.

5 oimmune, and epigenetic changes in the adult dentate gyrus.

6 tions of fear and extinction memories in the dentate gyrus.

7 forant pathway in the molecular layer of the dentate gyrus.

8 y was observed in dendritic zones of CA1 and dentate gyrus.

9 ominent and dynamic source of Shh within the dentate gyrus.

10 or expression in mature granule cells in the dentate gyrus.

11 sed microvascular blood-flow velocity in the dentate gyrus.

12 the proportion of adult-born neurons in the dentate gyrus.

13 ulates adult neurogenesis in the hippocampal dentate gyrus.

14 neurogenesis and synaptic plasticity in the dentate gyrus.

15 n susceptible mice could not be found in the dentate gyrus.

16 affected by PD except for a decrease in the dentate gyrus.

17 cerebellar cortex, insect mushroom body, and dentate gyrus.

18 rogenesis and dendritic spine density in the dentate gyrus.

19 lt lateral ventricle subventricular zone and dentate gyrus.

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

21 d the glutamatergic rMF sprouting within the dentate gyrus.

22 cal layers II-III, IV, and V, as well as the dentate gyrus.

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

24 e of increasing neuronal excitability of the dentate gyrus.

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

26 s in the subventricular zone and hippocampal dentate gyrus.

27 pocampal size and decreased thickness of the dentate gyrus.

28 er and robust morphological sprouting in the dentate gyrus.

29 ng the function of neurogenesis in the adult dentate gyrus.

30 rging that human pattern separation requires dentate gyrus.

31 uption of synaptic transmission in the mouse dentate gyrus.

32 4 weeks led to volume reduction only in the dentate gyrus.

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

34 proliferation and neurogenesis in the adult dentate gyrus.

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

36 tural and functional plasticity of the adult dentate gyrus.

37 the cells and the majority of spines in the dentate gyrus.

38 piriform cortex, 0.24 ug . g(-1) +/- 0.04 in dentate gyrus, 0.17 ug . g(-1) +/- 0.04 in hippocampus)

39 immunoreactive for reelin and project to the dentate gyrus [17, 18].

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

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

42 rties of netfeedback inhibition in the mouse dentate gyrus, a region critically involved in pattern s

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

44 emonstrate that dopamine D1 receptors in the dentate gyrus act as a pivotal mediator of antidepressan

45 y neurons in the dentate hilus that regulate dentate gyrus activity and function.

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

47 d transcriptomic-wide changes in the ventral dentate gyrus after SDS.

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

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

50 heories of hippocampal function suggest that dentate gyrus and CA(2,3) (DG/CA(2,3)) are biased to dif

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

52 Here we find this distributed code in the dentate gyrus and CA1 subregions of the hippocampus.

53 nments may not be recognized as different by dentate gyrus and CA1 without LC input.

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

55 We changed the conductances of simulated dentate gyrus and CA3 hippocampal neurons according to o

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 ions in the synaptic connections between the dentate gyrus and CA3, which are thought to be critical

59 se in neuronal cytoplasmic inclusions in the dentate gyrus and cornu ammonis regions 1 and 2 of patie

60 4 (TLR4) on excitability of the hippocampal dentate gyrus and epileptogenesis after brain injury.

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

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

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

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

65 GABAergic LRNs preferentially innervate the dentate gyrus and the CA3 area of the hippocampus, regio

66 ongly related to microglia activation in the dentate gyrus and the prefrontal cortex.

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

68 4 mRNA, being highest in the olfactory bulb, dentate gyrus, and cerebellum.

69 substructures: the cornu ammonis (CA1-CA4), dentate gyrus, and subiculum.

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

71 In the banded mongoose the dentate gyrus appears to be comprised of up to seven lam

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

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

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

75 h TLE display loss of PV interneurons in the dentate gyrus but questions persist.

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

77 prominently expressed on the neurons of the dentate gyrus, but its role in mediating behavioral resp

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

79 resentations for overlapping memories in the dentate gyrus/CA(2,3) and subiculum subfields of the hip

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

81 strongest effects on the CA3 region and the dentate gyrus (CA3-DG) of the hippocampus, alongside ass

82 00 distinct neuron type pairs throughout the dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal

83 The dentate gyrus-CA3 circuit of the hippocampus is continuo

84 etical models and the known functions of the dentate gyrus-CA3 circuit, acute or chronic manipulation

85 dorsolateral septum (DLS) as a relay of the dentate gyrus-CA3 circuit.

86 projecting pyramidal cells, but not putative dentate gyrus/CA3-projecting stellate cells, represented

87 granule cells, the projection neurons of the dentate gyrus, can exhibit both pattern separation and i

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

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

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

91 contextual fear memory engrams in the mouse dentate gyrus contain functionally distinct neuronal ens

92 nt developed more neuronal inclusions in the dentate gyrus, cornu ammonis regions 1, 2 and 4, and the

93 more neuronal cytoplasmic inclusions in the dentate gyrus, cornu ammonis regions 1-4 and entorhinal

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

95 ocampal subfield CA3 (but less pronounced in dentate gyrus) correlated with this form of mnemonic pat

96 on of D1R-expressing cells within the dorsal dentate gyrus (dDG), but not the dorsal CA1 (dCA1).

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

98 NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellu

99 r perturbation expressed only in hippocampal dentate gyrus (DG) and assessed its association with hip

100 r representations for unexpected items, with dentate gyrus (DG) and CA3 being more sensitive to expec

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

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

103 n processes instantiated upstream within the dentate gyrus (DG) and CA3 subregions.

104 ; they innervated interneurons mostly in the dentate gyrus (DG) and CA3.

105 The dentate gyrus (DG) and proximal CA3 (pCA3) regions have

106 tion of computational circuits involving the dentate gyrus (DG) and proximal CA3.

107 heta-band short range communications between dentate gyrus (DG) and the Ammon's horn (CA1) within the

108 Mossy cells (MCs) of the dentate gyrus (DG) are a major group of excitatory hilar

109 on.SIGNIFICANCE STATEMENT Mossy cells in the dentate gyrus (DG) are an integral component of the DG/p

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

111 The dentate gyrus (DG) controls information flow into the hi

112 g advantage of the fact that the hippocampal dentate gyrus (DG) gives rise to newborn DGCs throughout

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

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

115 The dentate gyrus (DG) has a key role in hippocampal memory

116 Within the mammalian hippocampus, the dentate gyrus (DG) has the unique characteristic of exhi

117 oung adult-born granule cells (abGCs) in the dentate gyrus (DG) have a profound impact on cognition a

118 ferent regions and layers of the hippocampus dentate gyrus (DG) in an electric stimulation rodent mod

119 The reorganization of the dentate gyrus (DG) in TLE may create pathological conduc

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

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

122 The hippocampal dentate gyrus (DG) is a unique brain region maintaining

123 emory impairments.SIGNIFICANCE STATEMENT The dentate gyrus (DG) is important for learning, memory, pa

124 on from the supramammillary nucleus (SuM) to dentate gyrus (DG) is needed for contextual memory, soci

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

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

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

128 Adult hippocampal dentate gyrus (DG) neural stem cells (NSCs) continuously

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

130 rylated tau in GABAergic interneurons in the dentate gyrus (DG) of AD patients and mice.

131 Neuronal hyperactivity was found in the dentate gyrus (DG) of leuprolide-treated females, but no

132 imuli.SIGNIFICANCE STATEMENT The hippocampal dentate gyrus (DG) of rodents generates newborn dentate

133 ells (DGCs) are generated in the hippocampal dentate gyrus (DG) of rodents through a process called a

134 roblasts and neuronal differentiation in the dentate gyrus (DG) of the hippocampus and significantly

135 Sparse populations of neurons in the dentate gyrus (DG) of the hippocampus are causally impli

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

137 he animal analog of ECT, neurogenesis in the dentate gyrus (DG) of the hippocampus is observed.

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

139 sis in the subventricular zone (SVZ) and the dentate gyrus (DG) of the hippocampus, whereas the impla

140 Dentate gyrus (DG) of the mammalian hippocampus gives ri

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

142 Theoretical work suggests that the dentate gyrus (DG) performs this role for memory process

143 DD) and suicide risk and potentially affects dentate gyrus (DG) plasticity.

144 The dentate gyrus (DG) plays a central role in the process o

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

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

147 elopment, in particular with assembly of the dentate gyrus (DG) region of the hippocampus.

148 The CA3 and dentate gyrus (DG) regions of the hippocampus are consid

149 Neural stem cells (NSCs) in the dentate gyrus (DG) reside in a specialized local niche t

150 their proliferation in the adult hippocampus dentate gyrus (DG) subgranular zone.

151 affer collateral synapses and perforant path-dentate gyrus (DG) synapses of the hippocampus.

152 attern separation processes supported by the dentate gyrus (DG) to prevent interference from overlapp

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

154 Acute neuronal activation of the dentate gyrus (DG) using cFos immunohistochemistry was m

155 rant path (PP) to the molecular layer of the dentate gyrus (DG) where information is filtered and con

156 Dentate gyrus (DG), a "gate" that controls information f

157 ocused on the hippocampus and especially the dentate gyrus (DG), a vulnerable brain region and one of

158 s and impaired GABAergic transmission in the dentate gyrus (DG), accompanied by schizophrenia-like be

159 (MCs), a major cell type in the hilus of the dentate gyrus (DG), are unique in providing extensive lo

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

161 ch of the three major hippocampal subfields, dentate gyrus (DG), CA3, and CA1, has a unique function

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

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

164 ltered inputs from the entorhinal cortex and dentate gyrus (DG), the proximal CA3 region of aged rats

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

166 nts of adult neurogenesis in the hippocampal dentate gyrus (DG), while the effects of antidepressants

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

168 ncement, but whether, and to what extent can dentate gyrus (DG)-resident neural stem cells drive rege

169 s, and aberrant mossy fiber sprouting in the dentate gyrus (DG).

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

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

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

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

174 ks between behavior and transcription in the dentate gyrus (DG).

175 n the function of neurons in the hippocampal dentate gyrus (DG).

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

177 ically profile the granule cell layer of the dentate gyrus (DG-GCL) in human hippocampus and contrast

178 Neuroblasts within the aged dentate gyrus display a senescence-associated secretory

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

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

181 Within the dentate gyrus evidence for adult hippocampal neurogenesi

182 del of temporal lobe epilepsy, the epileptic dentate gyrus excessively recruits granule cells in beha

183 The dentate gyrus expressed synaptic function and neurogenes

184 (2020) report that human tau accumulation in dentate gyrus GABAergic interneurons disrupts AHN and st

185 We further demonstrate that in dentate gyrus GCs these conductance correlations are lik

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

187 We recorded populations of dentate gyrus granule cells (DG GCs) and lateral entorhi

188 we characterized threshold K(+) currents in dentate gyrus granule cells (DGGCs) and CA1 pyramidal ce

189 in-positive (DCX(+)) ABGCs as well as DCX(-) dentate gyrus granule cells 2 weeks after a stroke or sh

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

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

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

193 d a hyperexcitability phenotype displayed in dentate gyrus granule neurons derived from patients with

194 Having previously studied the phenotype of dentate gyrus granule neurons, we turned our attention t

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

196 ignificantly associated with smaller CA3 and dentate gyrus hippocampal subfield volumes but not with

197 This region, comprised of the dentate gyrus, hippocampus proper, subiculum, presubicul

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

199 cognitive functions and neurogenesis (e.g., dentate gyrus, hypothalamus, olfactory areas, cerebellum

200 pus, a widely accepted model posits that the dentate gyrus improves learning and memory by enhancing

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

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

203 nized interneuron firing between the CA1 and dentate gyrus in epileptic mice.

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

205 we simultaneously recorded from the CA1 and dentate gyrus in pilocarpine-treated epileptic mice with

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

207 al and incorporation of neurons in the adult dentate gyrus increases after chronic stress and suggest

208 gest that stimulation of D1 receptors in the dentate gyrus is a potential adjunctive approach to impr

209 hypothesized that adult neurogenesis in the dentate gyrus is an ongoing process that maintains norma

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

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

212 ing to test the hypothesis that aging of the dentate gyrus is linked to impaired beacon discriminatio

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

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

215 AV-Cre mediated ablation of Shh in the adult dentate gyrus led to a marked degeneration of MCs.

216 In addition, ablation of Shh in the adult dentate gyrus led to increased neural precursor cell pro

217 ls and differentiated these into hippocampal dentate gyrus-like neurons and astrocytes.

218 ower motor neurons, iPSC-derived hippocampal dentate gyrus-like neurons and primary astrocytes.

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

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

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

222 Decreased dentate gyrus mean diffusivity correlated with a higher

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

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

225 s of pathway-tracing experiments showing the dentate gyrus mossy fiber projection, and its relationsh

226 20) reveal that post-tetanic potentiation at dentate gyrus mossy fiber synapses is induced by natural

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

228 irm that deficits are specifically linked to dentate gyrus neurogenesis since cyclin D2(-/-) mice als

229 ampus, cerebellum and cortex besides reduced dentate gyrus neurogenesis.

230 ls of the innate immune system reside in the dentate gyrus neurogenic niche of aged brains in humans

231 The computationally simulated BD dentate gyrus neurons had a hyperexcitability phenotype

232 on-touchscreen task and (56)Fe decreased new dentate gyrus neurons relative to Sham.

233 n, similar to what we previously reported in dentate gyrus neurons.

234 ortin immunohistochemistry) cells within the dentate gyrus of adult Egyptian fruit bats from three di

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

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

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

238 Elevated MAALIN in the dentate gyrus of impulsive-aggressive suicides was assoc

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

240 in developing neural cultures and in vivo in dentate gyrus of P4 mouse brain.

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

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

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

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

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

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

247 Adult neurogenesis occurs in the dentate gyrus of the hippocampus during adulthood and co

248 umber of newborn neurons incorporated in the dentate gyrus of the hippocampus during the 10-week post

249 Adult neurogenesis in the dentate gyrus of the hippocampus is highly regulated by

250 anced deposition of perineuronal nets in the dentate gyrus of the hippocampus of AS mice in the absen

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

252 on and the action of antidepressants, in the dentate gyrus of the hippocampus.

253 The dentate gyrus of the mammalian hippocampus continuously

254 ddressed whether mossy fiber inputs from the dentate gyrus onto CA3 principal cells are affected in a

255 Furthermore, deletion of Bdnf in the dentate gyrus, or specifically in LepRb-expressing neuro

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

257 ar delineation in SUVr between groups in the dentate gyrus (p = 0.009).

258 duced with decreased size of the hippocampal dentate gyrus, partial agenesis of the corpus callosum,

259 albumin-expressing interneurons (PVs) in the dentate gyrus provide activity-dependent regulation of a

260 map reset and a familiar map emerged in the dentate gyrus, proximal and distal CA1, and CA3c.

261 ion channel agonist, we studied the role of dentate gyrus PV cells in regulating anxiety-like behavi

262 Activation of the Kv3.1 channel in dentate gyrus PV cells may represent a target for the de

263 e behavior, whereas upregulation of Kv3.1 in dentate gyrus PV cells or acute activation of Kv3.1 usin

264 The activity of dentate gyrus PV cells plays a major role in the behavio

265 enuated capacity of high-frequency firing in dentate gyrus PV cells, and altered short-term plasticit

266 ucidate the function and mechanism of p11 in dentate gyrus PV cells.

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

268 (56)Fe irradiation improved performance on a dentate gyrus-reliant pattern separation task; irradiate

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

270 The dentate gyrus shows a novel phenotype: the infrapyramida

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

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

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

274 rtin-labeled maturing newborn neurons in the dentate gyrus subgranular zone, and a single-Reelin infu

275 of the hippocampal formation (cornu Ammonis, dentate gyrus, subicular complex, and entorhinal cortex)

276 binding in the hippocampus (CA1, CA2/3, CA4, dentate gyrus, subiculum) and presubiculum layers (PSB1,

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

278 al glia-like neural stem cells (RGLs) in the dentate gyrus subregion of the hippocampus give rise to

279 development of glutamatergic perforant path-dentate gyrus synapses, but not in commonly studied in S

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

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

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

283 In the dentate gyrus, the summative effect of these pathologies

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

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

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

287 nockout granule neurons integrating into the dentate gyrus using a variety of methods to examine thei

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

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

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

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

292 between parental education level and CA3 and dentate gyrus volumes; lower parental education level wa

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

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

295 ampus, neurogenesis was nearly absent in the dentate gyrus, which was due to inhibited proliferation

296 ce of NLGN1 decreased neuronal counts in the dentate gyrus, which was not the case in wild-type anima

297 in the CA1 and CA3 fields, the hilus of the dentate gyrus (with sparing of granule cells), and the e

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

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

300 tformin enhanced the recovery of NPCs in the dentate gyrus, with sex-dependent effects on neurogenesi