ライフサイエンスコーパス: subiculum

1 ential connectivity with proximal and distal subiculum.

2 hippocampal outflow regions presubiculum and subiculum.

3 ace between hippocampus and neocortex is the subiculum.

4 ss and gliosis in the hippocampal CA1 and/or subiculum.

5 ry synaptic signaling from CA3 to CA1 to the subiculum.

6 tantia nigra, entorhinal cortex, and ventral subiculum.

7 ed by stimulation of afferent projections to subiculum.

8 d interneurons were exclusive targets in the subiculum.

9 gnificant neuron loss in the hippocampus and subiculum.

10 number of NPY neurons in the hippocampus and subiculum.

11 um border, and higher than 50% in the distal subiculum.

12 n related to the mammalian dentate gyrus and subiculum.

13 cortices, and after the 4th session for the subiculum.

14 hinal, and parietal cortices, but not in the subiculum.

15 neocortex but also in entorhinal cortex and subiculum.

16 the anterogradely labeled fibers within the subiculum.

17 d in the medial geniculate, hippocampus, and subiculum.

18 uced by up to 66% in all three layers of the subiculum.

19 via VGlut2-expressing, bursty neurons in the subiculum.

20 and CA3 subfields, the CA1 subfield, and the subiculum.

21 ined, followed by inactivation of the dorsal subiculum.

22 lesions of the hippocampus that included the subiculum.

23 lar to a type of unit found in the mammalian subiculum.

24 uding the lateral septal nucleus and ventral subiculum.

25 tients suggested specific involvement of the subiculum.

26 nal diversity contributes to function in the subiculum.

27 ts in CA1 always followed events in proximal subiculum.

28 re CA3, possibly in the entorhinal cortex or subiculum.

29 ition areas, ventral hippocampus and ventral subiculum.

30 identified distinct bursting patterns in the subiculum.

31 mma2 were concentrated in sector CA1 and the subiculum.

32 cellular diversity and spatial coding in the subiculum.

33 cornu ammonis (CA1-CA4), dentate gyrus, and subiculum.

34 bfield whose function is poorly known is the subiculum.

35 y expressed isoform of T-channels in the rat subiculum.

36 pyramidal and inhibitory interneurons in the subiculum.

37 a key hippocampal output region, the ventral subiculum.

38 nization as the projections from CA1 and the subiculum.

39 as anomalies in TLE-G were restricted to the subiculum.

40 , while changes in TLE-G were limited to the subiculum.

41 single neurons in hippocampal areas CA1 and subiculum.

42 ampal cornu ammonis 1 to cornu ammonis 3 and subiculum.

43 rom the hippocampus to the neocortex via the subiculum.

44 actions at distal locations, i.e., closer to subiculum.

45 ings in awake mice, we show here that in the subiculum a subset of pyramidal cells is activated, wher

46 nished by excitotoxin lesions of the ventral subiculum, a component of the HF.

47 trinsic neuronal excitability in the ventral subiculum, a hippocampal region that activates dopamine

48 r KCC2 in a subset of pyramidal cells in the subiculum, a key structure generating epileptic activiti

49 all ER-beta-immunoreactive cells within the subiculum, a major output region of the hippocampal form

50 Within this distal portion of the subiculum, a proximodistal gradient of origin maps onto

51 lting novelty signal is conveyed through the subiculum, accumbens, and ventral pallidum to the VTA wh

52 is study we describe how the hippocampus and subiculum act in concert to encode information in a spat

53 was found to begin in CA1 and spread to the subiculum after psychosis onset.

54 ong the proximodistal and radial axes of the subiculum and all identified cells were pyramidal neuron

55 pocampus but exerted only partial effects in subiculum and amygdala.

56 e cut in the apical dendritic region between subiculum and CA1 eliminated afterdischarges in subicula

57 rks demonstrated enhanced involvement of the subiculum and CA1, reflecting a substantial reorganizati

58 al cells and scattered nuclei in the ventral subiculum and CA3 region.

59 Transgenic TTBK1 is highly expressed in subiculum and cortical pyramidal layers, and induces pho

60 d reaches a very large burden, especially in subiculum and deep cortical layers.

61 NAc assemblies, being independent of dorsal subiculum and dispensable for both spatial novelty detec

62 The subiculum and dopamine-enriched midbrain VTA/SN of amphe

63 d that genes differentially expressed in the subiculum and GABAergic interneurons are enriched in the

64 cription of local excitatory circuits of the subiculum and highlights their mechanistic involvement i

65 s in mu-opioid receptor binding occur in the subiculum and hippocampus of Alzheimer's disease brains.

66 ctionally partitioned between neurons within subiculum and hippocampus to uniquely identify trial-spe

67 found in only a few areas, most notably the subiculum and layer V of neocortex.

68 and its subfields, specifically in the right subiculum and left cornu ammonis (CA3).

69 matically reduced GAbeta accumulation in the subiculum and perirhinal cortex, both of which are brain

70 tic methods to demonstrate a role of ventral subiculum and potentially its projections to nucleus acc

71 onosynaptic afferent input from both ventral subiculum and prefrontal cortex, providing an anatomical

72 In other sites, e.g., the subiculum and retrosplenial cortex, there was often less

73 between lateral entorhinal cortex and dorsal subiculum and suggest further that this connection may i

74 mia significantly reduced neuronal damage in subiculum and thalamus and increased the microglial resp

75 ild hypothermia attenuated neuronal death in subiculum and thalamus but not CA1 and, surprisingly, in

76 Here, we show that dorsal subiculum and the circuit, CA1 to dorsal subiculum to me

77 The pattern of dendritic loss in the subiculum and the correlations with NFT densities respec

78 function in two hippocampal subregions--the subiculum and the dentate gyrus--decline normally with a

79 bilateral excitotoxic lesions of the ventral subiculum and the ventral hippocampus.

80 f the cohort, respectively; maximally in the subiculum and ventral pons, but often present elsewhere.

81 Notably, this effect was in the anteromedial subiculum and was not modulated by whether scenes were s

82 hippocampus (CA1, CA2/3, CA4, dentate gyrus, subiculum) and presubiculum layers (PSB1, PSB3) was dete

83 t patterns of afferent input to distal (near subiculum) and proximal (near CA2) zones.

84 tribution of Gad67 in collagen XIX-deficient subiculum, and abnormal levels of gephyrin in collagen X

85 h a thinner cortex in the entorhinal region, subiculum, and adjacent medial temporal lobe subfields.

86 also detected in the hippocampal formation, subiculum, and basolateral amygdala, all of which are im

87 This CA1 output is among others to the subiculum, and both CA1 and subiculum project to the ent

88 us, lateral geniculate body, frontal cortex, subiculum, and cerebellum.

89 ampal formation (hippocampus, dentate gyrus, subiculum, and entorhinal cortex) and amygdala.

90 (presubiculum, parasubiculum, prosubiculum, subiculum, and entorhinal cortex), and anterior fusiform

91 pal formation (dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal cortex).

92 throughout the dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal cortex.

93 ction neurons in the motor cortex, thalamus, subiculum, and hypothalamus.

94 audal levels of the dentate gyrus, CA3, CA1, subiculum, and lateral and medial entorhinal cortices af

95 rtices as well as to CA1, dorsal and ventral subiculum, and parasubiculum of the hippocampus.

96 xpression in the olfactory nuclei, amygdala, subiculum, and some cortical structures, as well as vari

97 Furthermore, removal of the hippocampus, subiculum, and subjacent parahippocampal cortex, added t

98 eoptic area, lateral septal nucleus, ventral subiculum, and supramammillary nucleus, and in brainstem

99 ferentially expressed in neurons of CA1, the subiculum, and the adjacently connected amygdalohippocam

100 n are largely restricted to hippocampus CA1, subiculum, and the amygdalohippocampal area, with a two-

101 pattern completion was observed in CA1, the subiculum, and the entorhinal and parahippocampal cortic

102 of spinophilin mRNA in CA4 (hilus), CA3, the subiculum, and the entorhinal cortex than did the normal

103 lamic regions, the basolateral amgydala, the subiculum, and various cortical regions.

104 ge pyramidal neurons in cortical layer 5 and subiculum are lost.

105 anatomical gradient: neurons in the proximal subiculum are more similar to canonical, sparsely firing

106 s of origin in CA1 and distoproximal axis in subiculum are related to a rostrocaudal axis of terminat

107 Entorhinal projections from CA1 and the subiculum are topographically organized such that a rost

108 The subiculum as a part of the hippocampal formation is the

109 (CA) subfields, dentate gyrus (DG), and the subiculum as well as adjacent medial temporal lobe corti

110 normally receive CA3 outflow such as CA1 and subiculum as well as novel projections beyond the confin

111 from rat brain slices for a projection from subiculum back into area CA1.

112 ggesting a specific role of 5-HTTLPR for the subiculum, BDNF Val66Met for CA4/dentate gyrus, and COMT

113 iming of the dPAG can modulate plasticity of subiculum-BLA synapses, providing additional evidence th

114 ones (such as lateral entorhinal cortex, CA1/subiculum border and outer molecular layer of dentate) w

115 10% near the CA1-CA2 border, 24% at the CA1-subiculum border, and higher than 50% in the distal subi

116 dal neurons, particularly neurons at the CA1-subiculum border.

117 ornu ammonis [CA] fields 1, 2, and 3 and the subiculum), but, in contrast, target the parahippocampal

118 parietal cortex, ventral tegmental area, and subiculum, but increased cytochrome oxidase activity in

119 t of long-term potentiation (LTP) in the CA1-subiculum, but not in the CA3-CA1 pathway.

120 t of long-term potentiation (LTP) in the CA1-subiculum, but not in the CA3-CA1 pathway.

121 d effects in retrosplenial complex and (pre-)subiculum, but not the thalamus.

122 enerating high frequency burst firing in the subiculum, but the exact nature of these currents remain

123 e selectively from PV neurons of the ventral subiculum by injecting a viral vector expressing tetanus

124 region (including both entorhinal cortex and subiculum) by examining the impact of bilateral NMDA-ind

125 a localized effect along the dentate gyrus, subiculum, CA1 and fissure.

126 t perirhinal cortex, parahippocampal cortex, subiculum, CA1, and CA2/CA3/dentate gyrus (CA2/3/DG) enc

127 We conclude that a subiculum--CA1 circuit supports afterdischarges in both

128 Disruption of this subiculum--CA1 circuit with a radially oriented knife cu

129 Spontaneous activity in isolated subiculum--CA1 slices was produced by bathing slices in

130 a pathologies were primarily detected in the subiculum/CA1 region, which was therefore the focus of a

131 These results indicate that the output of subiculum can be strongly and bidirectionally regulated

132 re distributed spatial representation in the subiculum carries, on average, more information about sp

133 oss of NAAGergic neurons was observed in the subiculum characterized by 71.82% and 77.53% reduction i

134 Intra-ventral subiculum CNO enhanced reversal learning in the same man

135 s, cornu ammonis regions 1, 2 and 4, and the subiculum compared to patients with normal cognition.

136 Our data suggest that the subiculum-containing detour loop is dedicated to meet th

137 Here, human hippocampal subfield (subiculum, cornu ammonis 1-3, and dentate gyrus) targets

138 A specific defect in the subiculum could have widespread effects throughout neuro

139 with the strongest expression in the IC and subiculum, could be targets for treating amygdala-relate

140 s of lidocaine (100 microg) into the ventral subiculum decreased cocaine- or cue-induced reinstatemen

141 The ventral hippocampus and ventral subiculum displayed the earliest seizure activity.

142 om the CA2/CA1 border (proximal) through the subiculum (distal), with more bursting observed at dista

143 VTCs are concentrated in subiculum, distal to CA1.

144 s between the hippocampal subregions CA1 and subiculum do not correspond to abrupt changes in electro

145 NMDA (0, 0.4 or 0.8 microg) into the dorsal subiculum (DS), region CA1, the ventral subiculum (VS),

146 investigated the role of single cells in the subiculum during ripples and found that, dependent on th

147 n has been evidenced in the piriform cortex, subiculum, entorhinal and perirhinal cortices, and parie

148 d in hippocampus parahippocampal structures: subiculum, entorhinal cortex and perirhinal cortex, sept

149 recorded from the hippocampal CA3 subfield, subiculum, entorhinal cortex, and dentate gyrus to quant

150 ound that theta rhythms generated in the rat subiculum flowed backward to actively modulate spike tim

151 electrolytic or sham lesions of the ventral subiculum followed by discriminative avoidance condition

152 n contrast, connectivity of PRC and PHC with subiculum followed not only a proximal-distal but also a

153 tudied the importance of the hippocampus and subiculum for anterograde and retrograde memory in the r

154 responses suggests that the input to dorsal subiculum from any one part of lateral entorhinal cortex

155 Postmortem studies of the subiculum from subjects with schizophrenia have detected

156 erns of axonal arborization, we suggest that subiculum has at least a crude columnar and laminar arch

157 The subiculum has been suggested to be involved in the initi

158 activity of local excitatory circuits of the subiculum has been suggested to be involved in the initi

159 rward projection from hippocampal CA1 to the subiculum has been very well established, accumulating e

160 l place cells, whereas neurons in the distal subiculum have higher firing rates and more distributed

161 ncrease in Abeta accumulation in GDX mice in subiculum, hippocampus, and amygdala.

162 te cortex, amygdala, parahippocampal cortex, subiculum, hippocampus, hypothalamus, medial caudate nuc

163 ngles (NFTs), and Abeta plaque burden in the subiculum in AD and elderly controls.

164 The role of the ventral subiculum in cocaine- or cue-induced cocaine-seeking beh

165 o cognition, and a unique role for the human subiculum in discrimination of complex scenes from diffe

166 , neuronal loss was attenuated by 44% in the subiculum in mice 4 months of age and 18% in layer V of

167 Spikes were found in the subiculum in the aged human brain but only infrequently;

168 targeted spines whereas the thalamus and the subiculum, in addition to spines, targeted proximal and

169 In addition, ventral subiculum inactivation prevented OFC neurons from integr

170 Our findings on synaptic plasticity in the subiculum indicate that regular firing and bursting cell

171 nections and guide future studies on how the subiculum interacts with CA1 to regulate hippocampal cir

172 The cellular morphology in the subiculum is immature at this age, reaching maturity by

173 that communication between CA3, CA1 and the subiculum is not exclusively unidirectional or excitator

174 Our findings suggest that the subiculum is specialized to compress sparse hippocampal

175 rneurons (mostly basket cells) in sector CA1/subiculum is sufficient to induce hyperexcitability and

176 The subiculum is the major output structure of the hippocamp

177 stream structures.SIGNIFICANCE STATEMENT The subiculum is the major output structure of the hippocamp

178 Subiculum is the primary output area of the hippocampus

179 ricular hypothalamus, habenula, hippocampus, subiculum, lateral septal nucleus, anterior cingulate co

180 and inferior colliculi, islands of Calleja, subiculum, lateral septum, lateral and dorsomedial hypot

181 Patients with schizophrenia had smaller subiculum (left, p = .035; right, p = .031) and right pr

182 p = 1.4 x 10(-5); right, p = 2.3 x 10(-6)), subiculum (left, p = 3.7 x 10(-6); right, p = 2.8 x 10(-

183 r, despite this substantial compression, the subiculum maintains finer scale temporal properties that

184 al hypothalamus, dorsal hippocampus, ventral subiculum, medial prefrontal cortex or amygdala in cocai

185 These studies suggest that modulation of subiculum neuron excitability by adenosine is mediated v

186 Efferents of the CA1-projecting subiculum neurons also target the perirhinal cortex, an

187 a multi-path environment, a subpopulation of subiculum neurons robustly encoded the axis of travel.

188 ch to restrict expression of KORD in ventral subiculum neurons that project to nucleus accumbens shel

189 versibly inhibited action potentials (AP) in subiculum neurons that were evoked by stimulation of the

190 and echolocation via two kinds of remapping: subiculum neurons turned on or off, while CA1 neurons sh

191 ral amygdala preferentially innervates spiny subiculum neurons, presumed pyramidal projection neurons

192 1-region pyramidal neurons onto burst-firing subiculum neurons, presynaptic in vivo knockout of beta-

193 t by depolarizing current injection steps in subiculum neurons, suggesting a presynaptic mechanism of

194 post synaptic currents (EPSCs) recorded from subiculum neurons.

195 disynaptic "ESA" (entorhinal cortex-ventral subiculum-nucleus accumbens) pathway is responsible for

196 In contrast, in the subiculum, numerous cells exhibited strong hybridization

197 between contra- and ipsilateral sides in the subiculum of conditioned animals.

198 ling this description in recordings from the subiculum of freely moving rats.

199 l and entorhinal cortices and to the ventral subiculum of hippocampus.

200 perirhinal, and retrosplenial cortices; CA1/subiculum of hippocampus; claustrum, tania tecta, latera

201 antero-dorsal thalamic nucleus and the post-subiculum of mice by comparing their activity in various

202 The basolateral amygdala and the ventral subiculum of the hippocampal formation are two of the ma

203 is effect depends on activity in the ventral subiculum of the hippocampus (vSub).

204 FC), basolateral amygdala (BLA), and ventral subiculum of the hippocampus (vSub).

205 nsular, and entorhinal cortices, the ventral subiculum of the hippocampus, dorsal tenia tecta, claust

206 l cortex (mPFC) and ventral (but not dorsal) subiculum of the hippocampus.

207 nterneurons in pre-limbic cortex and ventral subiculum of the hippocampus.

208 alamus, basolateral amygdala and the ventral subiculum of the hippocampus.

209 cGMP, is preferentially expressed in CA1 and subiculum of the VHIPP.

210 lbumin (PV) neurons has been observed in the subiculum of TLE patients and in animal models of TLE.

211 al prefrontal cortex, and dorsal and ventral subiculum on acquisition of a lever-pressing task for fo

212 on of connections from CA3 to CA1 and CA1 to subiculum, our results indicate that bursting neurons ar

213 more prominent inhibitory role than ventral subiculum over stress-induced HPA endpoints.

214 ain, expression was prominent in the cortex, subiculum, parasubiculum, granule neurons of the dentate

215 t long-term potentiation (LTP) in the CA1 to subiculum pathway is lower by 34%, (P<0.0001) in brain s

216 vely, these results suggest that the ventral subiculum plays an important role in cocaine-seeking beh

217 Here, we recorded HFOs in slices of the subiculum prepared from human hippocampal tissue resecte

218 Other input structures include the subiculum, presubiculum, and anterior thalamus.

219 ections from the macaque monkey hippocampus, subiculum, presubiculum, and parasubiculum to the entorh

220 an hippocampal formation (DG, CA1, CA2, CA3, subiculum, presubiculum, and parasubiculum) as well as i

221 the CA1 field of the hippocampus and in the subiculum, presubiculum, and parasubiculum.

222 formation, including the entorhinal cortex, subiculum, presubiculum, and parasubiculum.

223 F subfields DG, CA3, CA2, CA1, prosubiculum, subiculum, presubiculum, and parasubiculum.

224 ed of the dentate gyrus, hippocampus proper, subiculum, presubiculum, parasubiculum and the entorhina

225 nnervation of the hippocampus as well as the subiculum, presubiculum, parasubiculum, the medial and l

226 hippocampus, pyramidal cells in CA1 and the subiculum process sensory and motor cues to form a cogni

227 Hippocampal lesions that included the subiculum produced marked anterograde amnesia and a 1-30

228 ng others to the subiculum, and both CA1 and subiculum project to the entorhinal cortex to close the

229 e adult data, in that distal portions of the subiculum project to the medial entorhinal cortex, where

230 Inhibiting dorsal subiculum projections to the anterior thalamic nuclei pr

231 ollowed by separate inhibition of the dorsal subiculum projections to the anterior thalamic nuclei.

232 icit revealed the key contribution of dorsal subiculum projections to the anteromedial and anterovent

233 rbital cortex, anterior cingulate cortex and subiculum) provide only minimal protection.

234 in the hippocampal formation, the dorsal pre-subiculum (PrSd), before and after eye opening in pre-we

235 ing evidence that the classical CA3, CA1 and subiculum pyramidal cell types all exhibit prominent and

236 gions affected by AD, in particular the left subiculum (r = 0.38, P = .005) and the left entorhinal v

237 The subiculum receives direct inputs from area CA1 of the hi

238 refrontal cortex and the hippocampal CA1 and subiculum regions.

239 tal cortex, ventral hippocampus, and ventral subiculum, regions involved in the regulation of sensori

240 Only subiculum remained spontaneously active.

241 Furthermore, memory reactivation and subiculum representation predicted faster and more accur

242 d CA(1) Furthermore, memory reactivation and subiculum representation predicted success when inferrin

243 ng overlapping pair encoding, DG/CA(2,3) and subiculum representations for indirectly related images

244 lateral geniculate body, frontal cortex, and subiculum, respectively.

245 4.3% reductions in the left presubiculum and subiculum, respectively.

246 The subiculum (SB) is the principal target of the axons of t

247 Neurons in the subiculum (Sb; close to the deep EC layers) also contain

248 the ventrolateral septum, the anteroventral subiculum, several preoptic nuclei, the anterior bed nuc

249 Activity in the subiculum showed the same temporal decline, but primaril

250 T8-immunopositive deposits were found in the subiculum, stratum oriens of hippocampal field CA1, and

251 ayer (ML) that continuously crosses adjacent subiculum (Sub) and CA fields.

252 complex, including the prosubiculum (ProS), subiculum (Sub), presubiculum, postsubiculum (PoS), and

253 DGH), cornu ammonis fields (CA)2/3, CA1, and subiculum (SUB)].

254 es identified a preferential response in the subiculum subfield of the hippocampus during scene, but

255 ng memories in the dentate gyrus/CA(2,3) and subiculum subfields of the hippocampus, while simultaneo

256 hinner than collaterals that would leave the subiculum, suggesting little or no myelin on local colla

257 ly located neurons in the distal part of the subiculum target the distal portion of the parasubiculum

258 ation was more evident for subfields CA1 and subiculum than for a combined CA2/CA3/dentate gyrus regi

259 this information influences regions like the subiculum that receive input from the hippocampus remain

260 f afferents was also observed in the ventral subiculum, the arcuate nucleus and the ventrolateral sub

261 of intrinsic, glutamatergic afferents of the subiculum, the hippocampus proper, and especially the in

262 he fundus striati, the amygdala, the ventral subiculum, the hypothalamus, midline and intralaminar th

263 cific thalamic and hypothalamic neurons, the subiculum, the lateral parabrachial nucleus, the cuneate

264 However, in the post-subiculum, the main cortical stage of HD signal processi

265 e on excitatory synaptic transmission in the subiculum, the main output area for the hippocampus.

266 valbumin neurons are selectively lost in the subiculum, the major output area of the hippocampus.

267 to the cerebral cortex layers V and VI, the subiculum, the oriens layer of CA1, the medial septum, t

268 proximal-distal axis across the CA1 and the subiculum, the percentages of bursting neurons being 10%

269 Subiculum, the primary efferent pathway of hippocampus,

270 al amygdala to the projection neurons of the subiculum, the spiny pyramidal neurons.

271 iques to characterize Ih in neurons from the subiculum-the major output region of the hippocampal for

272 anatomical and physiological studies on the subiculum to CA1 backprojection, and present recent conc

273 excitatory and inhibitory elements from the subiculum to CA1.

274 primarily sent from pyramidal CA1 layers and subiculum to deep EC layers.

275 sal subiculum and the circuit, CA1 to dorsal subiculum to medial entorhinal cortex layer 5, play a cr

276 significant back-projection pathway from the subiculum to the CA1.

277 We found that an adult-like topography of subiculum-to-parahippocampal projections is present by p

278 r slab, CA3 outputs synchronized CA1 and the subiculum using excitatory mechanisms, as predicted by c

279 ocampal subfield volumes but not with CA1 or subiculum volume.

280 Rather, lower subiculum volumes and glutamine concentrations correlate

281 Smaller subiculum volumes were related to poorer verbal memory i

282 rsal subiculum (DS), region CA1, the ventral subiculum (VS), the rostral entorhinal cortex (ECr) and

283 ctivity, and tested the roles of the ventral subiculum (vSub) and basolateral amygdala in this proces

284 The ventral subiculum (vSub) has been implicated in a wide range of

285 Ventral subiculum (vSUB) lesions enhance corticosterone response

286 The ventral subiculum (vSub) of the hippocampus, in particular, is p

287 system is strongly influenced by the ventral subiculum (vSub) of the hippocampus.

288 o nucleus accumbens (NAc) shell from ventral subiculum (vSub), basolateral amygdala, paraventricular

289 al [prelimbic (PL)] and hippocampal [ventral subiculum (vSUB)] cortical fields.

290 The ventral subiculum was activated during retrieval shortly after l

291 ng healthy elders, signal intensity from the subiculum was correlated selectively with memory perform

292 The subiculum was the major source of hippocampal projection

293 , whereas a region later in the circuit (the subiculum) was active during the recollection of the lea

294 Using retrograde tracer injections in the subiculum, we identified a hippocampal population of ENK

295 rnu ammonis (CA) 2+3, CA4+dentate gyrus, and subiculum were determined with a user-independent segmen

296 lesions of the hippocampus that included the subiculum were made 1, 10, or 30 d after learning to det

297 Full transections between CA1 and subiculum were necessary to functionally isolate the two

298 tuated in the dentate gyrus, CA1 region, and subiculum, whereas alpha5 expression was rather uniform.

299 n boutons from amygdala were larger than the subiculum which, in turn, were larger than the prefronta

300 ward deformation in the medial aspect of the subiculum, with minimal involvement of the Sommer sector