ライフサイエンスコーパス: subiculum

1 pyramidal and inhibitory interneurons in the subiculum.

2 ed by stimulation of afferent projections to subiculum.

3 d interneurons were exclusive targets in the subiculum.

4 a key hippocampal output region, the ventral subiculum.

5 gnificant neuron loss in the hippocampus and subiculum.

6 number of NPY neurons in the hippocampus and subiculum.

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

8 n related to the mammalian dentate gyrus and subiculum.

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

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

11 neocortex but also in entorhinal cortex and subiculum.

12 the anterogradely labeled fibers within the subiculum.

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

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

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

16 lesions of the hippocampus that included the subiculum.

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

18 uding the lateral septal nucleus and ventral subiculum.

19 tients suggested specific involvement of the subiculum.

20 ts in CA1 always followed events in proximal subiculum.

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

22 ition areas, ventral hippocampus and ventral subiculum.

23 ion from lateral entorhinal cortex to dorsal subiculum.

24 p to the cell layers of the presubiculum and subiculum.

25 stricted to only one hippocampal region, the subiculum.

26 somatosensory and auditory cortices, and the subiculum.

27 of the dentate gyrus, in areas CA1-CA3, and subiculum.

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

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

30 single neurons in hippocampal areas CA1 and subiculum.

31 bfield whose function is poorly known is the subiculum.

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

33 rom the hippocampus to the neocortex via the subiculum.

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

35 ential connectivity with proximal and distal subiculum.

36 hippocampal outflow regions presubiculum and subiculum.

37 ace between hippocampus and neocortex is the subiculum.

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

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

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

41 tantia nigra, entorhinal cortex, and ventral subiculum.

42 (1.5 vs. 4.5), CA2 hippocampus (0 vs. 3.5), subiculum (0 vs. 4), and cerebellar Purkinje cell layer

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

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

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

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

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

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

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

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

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

52 euronal, neocortical subplate, endopiriform, subiculum; alpha7-discrete, all neocortical layers, hipp

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

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

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

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

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

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

59 was particularly evident in the hippocampus, subiculum and entorhinal and piriform cortices.

60 The extent of dendritic trees in the subiculum and fusiform gyrus was examined by Sholl analy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 eral septum, medial nucleus of the amygdala, subiculum, and amygdalohippocampal area, and then, proje

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

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

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

84 urofibrillary changes in sectors CA1 to CA4, subiculum, and dentate gyrus of 16 subjects with Alzheim

85 envelope in neurons within the hippocampus, subiculum, and entorhinal cortex as well as frontal, tem

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

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

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

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

90 the dentate gyrus, hippocampal fields CA1-3, subiculum, and lateral septal area were significantly co

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

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

93 ted to the lateral entorhinal cortex, dorsal subiculum, and subfield CA1 and mainly targeted the baso

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

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

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

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

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

99 ound consistently for the volume of CA1, the subiculum, and the entorhinal cortex.

100 c regions, including the frontal cortex, the subiculum, and the medial thalamic nuclei.

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

102 equivalent portions of the dentate gyrus and subiculum; and (4) neurogliaform interneurons (n = 2) ch

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

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

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

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

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

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

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

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

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

112 10% near the CA1-CA2 border, 24% at the CA1-subiculum border, and higher than 50% in the distal subi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 granule cells and pyramidal cells in CA1 and subiculum compared to hilus neurons.

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

133 stratum lacunosum-moleculare of CA1 and the subiculum, contrasting with barely detectable activity i

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

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

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

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

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

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

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

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

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

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

144 the anterior cingulate cortex, hippocampus, subiculum, entorhinal cortex, amygdala, mammillary bodie

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

146 Despite similarities between regions, subiculum fields decreased in size whereas hippocampal f

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

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

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

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

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

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

153 as administration into the dorsal or ventral subiculum had no effect.

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

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

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

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

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

159 abolite to transmitter, were elevated in the subiculum, hippocampus, nucleus accumbens, and medial am

160 g serotonergic and noradrenergic activity in subiculum, hippocampus, nucleus accumbens, medial amygda

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

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

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

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

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

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

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

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

169 In particular, the ventral subiculum inhibits hypothalamic-pituitary-adrenal axis (

170 1 (i.e., near CA2) as well as a strip in the subiculum; injections into areas TF, TL, 35, or Pro labe

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 Subiculum is the primary output area of the hippocampus

177 In the CA1 and subiculum, it takes 3.4 and 5.4 years, respectively, for

178 eral and medial entorhinal cortices, ventral subiculum, lateral and basolateral nuclei, and amygdalos

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 ominantly in the anterior olfactory nucleus, subiculum, layer V pyramidal neurons from the cerebral c

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

183 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(-

184 duced responses intermediate to those in the subiculum-lesioned and control rats.

185 The subiculum lesions blocked the fall in pAVP and enhanced

186 yclin B1 were identified in the hippocampus, subiculum, locus coeruleus, and dorsal raphe nuclei, but

187 ppocampus proper, the dentate gyrus, and the subiculum) made by an ischemic procedure, radio frequenc

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

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

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

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

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

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

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

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

196 1-region pyramidal neurons onto burst-firing subiculum neurons, presynaptic in vivo knockout of beta-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 of the molecular layer of the dentate gyrus, subiculum proper and presubiculum was indistinguishable

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

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

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

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

234 refrontal cortex and the hippocampal CA1 and subiculum regions.

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

236 Only subiculum remained spontaneously active.

237 4.3% reductions in the left presubiculum and subiculum, respectively.

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

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

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

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

242 nt in frontal cortex (layers 4-6), posterior subiculum, several thalamic regions, and the interpedunc

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

244 Cells in the hippocampus and subiculum signal spatial location in fundamentally diffe

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

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

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

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

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

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

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

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

253 higher terminal labeling was observed in the subiculum than in CA1 and was particularly prominent in

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

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

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

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

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

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

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

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

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

263 Subiculum, the primary efferent pathway of hippocampus,

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

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

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

267 excitatory and inhibitory elements from the subiculum to CA1.

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

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

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

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

272 Rather, lower subiculum volumes and glutamine concentrations correlate

273 Smaller subiculum volumes were related to poorer verbal memory i

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

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

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

277 Ventral subiculum (vSUB) lesions enhance corticosterone response

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

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

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

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

282 The ventral subiculum was activated during retrieval shortly after l

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

284 total number of neurons in CA1, CA4, and the subiculum was correlated significantly with both the dur

285 Eph-A5-expressing neurons isolated from the subiculum was inhibited by ephrin-A5.

286 The subiculum was the major source of hippocampal projection

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

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

289 ion, the stratum oriens of CA1, CA3, and the subiculum were densely innervated by SP-containing axon

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

291 sal bank, wheras those projecting to CA1 and subiculum were found in superfical layers (mostly layer

292 Cortical neurons and the subiculum were labeled in animals not administered the a

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

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

295 ppocampus proper, the dentate gyrus, and the subiculum) were impaired on two tasks of recognition mem

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

297 culum, parasubiculum, entorhinal cortex, and subiculum, whereas the CA3 field and the dentate gyrus h

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

299 stratum pyramidale of the CA1 subregion and subiculum, while the weakest labeling was observed in th

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