ライフサイエンスコーパス: perirhinal

1 with previous reports supporting a role for perirhinal acetylcholine in object information acquisiti

2 This revealed perirhinal activation when the task required the integra

3 her perspective is that both hippocampal and perirhinal activity are predictive of overall memory str

4 disproportionately on recollection, whereas perirhinal activity predicts recognition success when de

5 the underlying mechanisms, we recorded BLA, perirhinal and entorhinal neurons during an appetitive t

6 inal cortex and an anterior stream including perirhinal and lateral entorhinal cortex.

7 Specifically, perirhinal and lateral entorhinal cortices are thought t

8 ial entorhinal cortex in humans, and between perirhinal and parahippocampal cortex as a function of i

9 al lobe (MTL), showing domain specificity in perirhinal and parahippocampal cortices (for object-proc

10 and the medial temporal lobe including both perirhinal and parahippocampal cortices and the posterio

11 g evidence for domain-specificity within the perirhinal and parahippocampal cortices.

12 The perirhinal and postrhinal cortex receives major choliner

13 We further showed that the perirhinal and the lateral entorhinal cortices received

14 ns in the cortex (entorhinal, retrosplenial, perirhinal) and the amygdala could not be reactivated.

15 ar recordings of basolateral amygdala (BLA), perirhinal, and entorhinal activity.

16 cingulate, prelimbic, infralimbic, insular, perirhinal, and entorhinal cortices as well as to CA1, d

17 ral temporal areas including inferotemporal, perirhinal, and entorhinal cortices.

18 o this end, we simultaneously recorded mPFC, perirhinal, and entorhinal neurons during the acquisitio

19 have demonstrated lamina in the entorhinal, perirhinal, and hippocampal cortices.

20 MTL), including the hippocampus, entorhinal, perirhinal, and parahippocampal cortices, forms a functi

21 tralateral side of the piriform, entorhinal, perirhinal, and parietal cortices as compared with the i

22 oning sessions for the piriform, entorhinal, perirhinal, and parietal cortices, and after the 4th ses

23 eminder session in the piriform, entorhinal, perirhinal, and parietal cortices, but not in the subicu

24 would relate early neurodegeneration of the perirhinal/anterolateral entorhinal cortex to impaired f

25 Specifically, perirhinal area 35 extends into the posterior TPC, where

26 ngulate, bed nucleus of stria terminalis and perirhinal area of oxytocin pretreated rats.

27 ns into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal

28 Critically, only the patient with perirhinal atrophy was impaired.

29 In the perirhinal cases, cholinergic projection neurons are dis

30 Compared with the perirhinal cases, the distribution of cholinergic and no

31 eocortex via an enhancement of entorhinal to perirhinal communication.

32 ing, mPFC activity facilitates entorhinal to perirhinal communication.

33 However, the network properties that support perirhinal contributions to memory are unclear.

34 inputs, an organization that likely impacts perirhinal contributions to memory.

35 ents in the parahippocampal gyrus (BA27) and perirhinal cortex (BA36).

36 ludes signals that are largely unique to the perirhinal cortex (i.e., object familiarity), consistent

37 Perirhinal cortex (PER) has a well established role in t

38 Perirhinal cortex (PER) has a well established role in t

39 The perirhinal cortex (PER) is known to process object infor

40 position that is comparable with that of the perirhinal cortex (PER) with regard to the lateral entor

41 The perirhinal cortex (PER), which is critical for associati

42 The hippocampus and the perirhinal cortex (PR) are reciprocally connected both d

43 Pretraining lesions of rat perirhinal cortex (PR) severely impair pavlovian fear co

44 Golgi-impregnated neurons from rat perirhinal cortex (PR) were classified into one of 15 di

45 s activity in "persistent-firing" neurons of perirhinal cortex (PR).

46 the major white matter tracts converging on perirhinal cortex (PrC) and hippocampus (HC) would be di

47 edial temporal lobe (MTL), in particular the perirhinal cortex (PrC) and hippocampus (HC), are best c

48 l clusters evoked by acoustic stimuli in the perirhinal cortex (PRC) and in AC of freely behaving mal

49 merous studies support the importance of the perirhinal cortex (PRC) and parahippocampal cortex (PHC)

50 pal region are functionally divided into the perirhinal cortex (PRC) and the lateral entorhinal corte

51 emporal lobe cortex (MTLC), most notably the perirhinal cortex (PrC) and the parahippocampal cortex (

52 The perirhinal cortex (PRC) composed of areas 35 and 36 form

53 is well established that the hippocampus and perirhinal cortex (PrC) encode associative and item repr

54 with the aim of elucidating the role of the perirhinal cortex (PRC) in recognition memory.

55 The perirhinal cortex (PRc) is essential for visual recognit

56 The perirhinal cortex (PRC) is proposed to both represent hi

57 Although it is well established that the perirhinal cortex (PRC) makes an important contribution

58 s from each sensory stream are integrated in perirhinal cortex (PRc) of the anteromedial temporal lob

59 basis of episodic recollection, whereas the perirhinal cortex (PRc) supports familiarity for individ

60 Specifically, it remains unclear whether perirhinal cortex (PrC) supports item-based familiarity

61 subregions that connect differentially with perirhinal cortex (PRC) vs parahippocampal cortex (PHC)

62 elated fMRI to address the role of the human perirhinal cortex (PRC), and its interactions with the h

63 For instance, it has been proposed that perirhinal cortex (PRC), parahippocampal cortex (PHC), a

64 MTL), in particular the hippocampus (HC) and perirhinal cortex (PrC), play domain-sensitive roles in

65 TEd projects primarily to perirhinal cortex (PRC), which in turn projects to later

66 Here, we demonstrate that the perirhinal cortex (PRc), within the MTL, plays a role in

67 nds the contributions of the hippocampus and perirhinal cortex (PrC).

68 The perirhinal cortex (PRh) and basolateral amygdala (BLA) a

69 responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a d

70 responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a t

71 The perirhinal cortex (PRh) is widely accepted as having an

72 ne details; for example, in the locus of the perirhinal cortex activation.

73 Significantly, only perirhinal cortex activity is modulated by meaning varia

74 ern separation-related signals in DG/CA3 and perirhinal cortex and (2) source memory signals in poste

75 ory strength is nonlinear in hippocampus and perirhinal cortex and also distinctly different in those

76 h taste and olfactory cortical areas and the perirhinal cortex and appears to be involved in assessme

77 secondary somatosensory, retrosplenial, and perirhinal cortex and contralateral S1.

78 ial memory are typically associated with the perirhinal cortex and hippocampal formation, respectivel

79 In particular, the effects in entorhinal and perirhinal cortex and hippocampus might be important for

80 by greater across-item pattern similarity in perirhinal cortex and in parahippocampal cortex, but gre

81 hese findings reach beyond simple notions of perirhinal cortex and lateral entorhinal cortex neurons

82 Specifically, perirhinal cortex and lateral entorhinal cortex represen

83 gardless of subsequent memory, we found that perirhinal cortex and parahippocampal cortex exhibited d

84 e left entorhinal cortex, beginning with the perirhinal cortex and shifting through hippocampal subfi

85 vel had higher c-fos activity in the rostral perirhinal cortex and the lateral entorhinal cortex.

86 anatomically conserved locations within the perirhinal cortex and the temporal pole.

87 Thus, perirhinal cortex appeared to integrate timing informati

88 e data indicate that behaviors requiring the perirhinal cortex are disrupted in advanced age, and sug

89 ding the hippocampus, entorhinal cortex, and perirhinal cortex are thought to be part of a unitary sy

90 ort that bilateral, excitoxic lesions of the perirhinal cortex attenuate rats' familiarity-based stim

91 tion and establish a functional homology for perirhinal cortex between species, although we propose t

92 dial temporal lobe, especially involving the perirhinal cortex Brodmann area 36 and entorhinal cortex

93 The discovery that bilateral lesions of the perirhinal cortex can leave configural (structural) lear

94 AD-67 immunohistochemistry, we show that the perirhinal cortex contains GABAergic neurons with long-r

95 al (especially spatial) information, whereas perirhinal cortex contributes to and is necessary for fa

96 perirhinal cortex, only damage to the caudal perirhinal cortex correlated significantly with recognit

97 Finally, activation in the perirhinal cortex correlated with successful associative

98 human lesion studies have demonstrated that perirhinal cortex damage impairs complex object discrimi

99 of the sensitivity of object recognition to perirhinal cortex damage is not the result of standard h

100 The second factor was extent of perirhinal cortex damage.

101 te the object-recognition deficit seen after perirhinal cortex damage.

102 ections, the density of PHAL(+) axons in the perirhinal cortex decreased steeply with rostrocaudal di

103 There was no evidence that lesions of the perirhinal cortex disrupted the ability to learn the con

104 perception of places and paths, whereas the perirhinal cortex does so for objects and the contents o

105 obtained directly from human hippocampus and perirhinal cortex during a recognition paradigm and appl

106 receptor antagonist scopolamine into the rat perirhinal cortex during different stages (encoding, sto

107 cillations in the amygdala, hippocampus, and perirhinal cortex during this next-day memory test indic

108 the left posterior inferior frontal and left perirhinal cortex for words and objects, respectively, a

109 Tracing studies have revealed that the perirhinal cortex forms strong reciprocal connections wi

110 Bilateral lesions of the perirhinal cortex fully spared the capacity to make feat

111 d points to a need to refine those models of perirhinal cortex function that emphasize its role in re

112 ological study of age-related impairments in perirhinal cortex function.

113 ories and add more weight to the role of the perirhinal cortex in associative encoding of objects.

114 The role of the perirhinal cortex in discriminative eyeblink conditionin

115 providing novel evidence for the role of the perirhinal cortex in episodic intra-item encoding.

116 These findings suggest a key role for the perirhinal cortex in representing and processing object-

117 results demonstrate a specific role for the perirhinal cortex in visual perception and establish a f

118 100 Hz theta burst)-dependent LTP in the rat perirhinal cortex in vitro.

119 ractions between GluR2 and AP2 blocks LTD in perirhinal cortex in vitro.

120 e identified regions in both hippocampus and perirhinal cortex in which activity varied as a function

121 gion for crossmodal perceptual features, and perirhinal cortex integrating these features into higher

122 by providing converging evidence that human perirhinal cortex is also critically involved in process

123 The perirhinal cortex is critical for novelty detection, and

124 Synaptic plasticity in perirhinal cortex is essential for recognition memory.

125 The findings suggest that the perirhinal cortex is important for memory and not for pe

126 Previously it has been suggested that the perirhinal cortex is part of a pathway processing object

127 Our findings suggest that the perirhinal cortex is required for rats to encode familia

128 ated synaptic transmission (EPSC(KA) LTD) in perirhinal cortex layer II/III neurons that is distinct

129 In contrast, rats with perirhinal cortex lesions failed to benefit from increas

130 The effects of perirhinal cortex lesions in rats on spatial memory migh

131 ir differential exploration times, rats with perirhinal cortex lesions showed very poor discriminatio

132 The same rats with perirhinal cortex lesions were also unimpaired on a test

133 Rats with perirhinal cortex lesions were sequentially trained in a

134 ehavior has been observed in young rats with perirhinal cortex lesions.

135 is known to be sensitive to hippocampal and perirhinal cortex lesions.

136 nificant correlation was found between total perirhinal cortex loss and degree of recognition impairm

137 n supports the idea that the hippocampus and perirhinal cortex may be critical for the processing of

138 riments thus suggest that alterations in the perirhinal cortex may be responsible for reducing aged a

139 evidence to suggest that the hippocampus and perirhinal cortex may mediate processes beyond long-term

140 ocampal lesion studies and evidence that the perirhinal cortex may support object memory.

141 imental changes in the prefrontal cortex and perirhinal cortex occurred before metabolic syndrome or

142 We found that neurons in the perirhinal cortex of rats generate sustained firing patt

143 Local administration into perirhinal cortex of the nitric oxide synthase inhibitor

144 lity or interneuron loss was observed in the perirhinal cortex of these aged, memory-impaired monkeys

145 we tested the effects of DPFE infusions into perirhinal cortex on meth-seeking under two different te

146 eolus vulgaris-leucoagglutinin (PHAL) in the perirhinal cortex or adjacent temporal neocortex.

147 ion of short- and long-range inputs from the perirhinal cortex or temporal neocortex with perirhinal

148 anterior hippocampus, entorhinal cortex, and perirhinal cortex over the 30 s retention interval, with

149 s share common features, suggesting that the perirhinal cortex participates in perceptual discriminat

150 The perirhinal cortex plays a critical role in memory format

151 The perirhinal cortex plays a critical role in recognition a

152 The results suggest that the perirhinal cortex plays a role in discriminative eyeblin

153 Whereas the perirhinal cortex plays an essential role in familiarity

154 n contrast, activity in both hippocampus and perirhinal cortex positively correlated with the subsequ

155 induced pattern effects in orbitofrontal and perirhinal cortex predicted the magnitude of categorical

156 demonstrate that the level of engagement of perirhinal cortex predicts later memory for individual i

157 Projections to the perirhinal cortex primarily targeted the superficial lay

158 The perirhinal cortex processes aspects of recognition memor

159 Importantly, lesions of the perirhinal cortex produce similar deficits and also lead

160 Viral transduction of this peptide in perirhinal cortex produced striking deficits in visual r

161 The rostral portion of the perirhinal cortex receives strong projections from the m

162 Perirhinal cortex removal reduced the contribution of on

163 The reduced inhibition in the perirhinal cortex reported here could contribute to this

164 nhuman primates, and humans suggest that the perirhinal cortex represents information about objects f

165 Infusion of DPFE into perirhinal cortex restored novel object recognition in l

166 s been implicated in spatial memory, whereas perirhinal cortex seems critical for object memory.

167 Lesions of the perirhinal cortex severely impaired acquisition of simul

168 Parahippocampal and perirhinal cortex showed different pattern information p

169 m one item presentation to the next, whereas perirhinal cortex signaled the conjunction of items and

170 Anatomically, the perirhinal cortex sits at the boundary between the media

171 Furthermore, there was a deficit of LTD in perirhinal cortex slices from virally transduced, recogn

172 chniques to provide strong evidence that the perirhinal cortex subserves perception and suggests that

173 supports recollection and that the adjacent perirhinal cortex supports familiarity.

174 Specifically, it has been suggested that the perirhinal cortex supports the perceptual abilities need

175 these two retrograde signalling cascades in perirhinal cortex synaptic plasticity and in visual reco

176 ll have to extend beyond the hippocampus and perirhinal cortex to incorporate a wider network of cort

177 ne transfer to these postsynaptic neurons in perirhinal cortex used a His tag antibody, as the peptid

178 ccelerated function and that activity in the perirhinal cortex was associated with a statistically di

179 iments, rats with excitotoxic lesions of the perirhinal cortex were found to be indistinguishable fro

180 dy highlights the critical importance of the perirhinal cortex within the temporal lobe for recogniti

181 ee MTL areas (hippocampus and entorhinal and perirhinal cortex) and visual area TE as monkeys perform

182 nation of the object recognition system (the perirhinal cortex) performs this critical function.

183 on that consolidated the sound-light memory (perirhinal cortex) was inhibited during formation of the

184 In perirhinal cortex, a lasting decrement in neuronal respo

185 and facilitates long-term depression in the perirhinal cortex, a neural correlate of object recognit

186 tions implemented across the hippocampus and perirhinal cortex, allowing formal rejection of a single

187 n contrast, medial temporal lobe structures (perirhinal cortex, amygdala, hippocampus) and anterior i

188 iggered a switch in mechanisms of LTD in rat perirhinal cortex, an area critical for visual recogniti

189 projecting subiculum neurons also target the perirhinal cortex, an area strongly implicated in object

190 levels of the ventral temporal neocortex or perirhinal cortex, and electron microscopic observations

191 Brain activity in the hippocampal region, perirhinal cortex, and parahippocampal cortex was associ

192 as for visual object representation, such as perirhinal cortex, and reward-guided learning, such as t

193 the entorhinal cortex, the hippocampus, the perirhinal cortex, and rostral parahippocampal cortex.

194 ced GAbeta accumulation in the subiculum and perirhinal cortex, both of which are brain regions requi

195 eciprocally connected to parahippocampal and perirhinal cortex, but evidence for functional subregion

196 study: Patients with lesions, including the perirhinal cortex, but not patients with damage restrict

197 ures other than the hippocampus, perhaps the perirhinal cortex, can support face recognition memory i

198 A signal in the anterior MTL, including perirhinal cortex, indicated the successful retrieval of

199 Within the perirhinal cortex, only damage to the caudal perirhinal

200 t, activity in a different group of regions (perirhinal cortex, parahippocampal cortex, and inferior

201 fore and after this exposure, and found that perirhinal cortex, parahippocampal cortex, subiculum, CA

202 ns of the left hippocampus, and in bilateral perirhinal cortex, predicted subsequent accuracy on the

203 structures: subiculum, entorhinal cortex and perirhinal cortex, septum, and olfactory system in the i

204 the alERC as an extension of the neighboring perirhinal cortex, supporting object memory.

205 uman memory: whether the hippocampus and the perirhinal cortex, two key components of the medial temp

206 rocess critical for the expression of LTD in perirhinal cortex, underlies visual recognition memory.

207 In synapses in the perirhinal cortex, we have directly compared the Ca(2+)

208 ns bilaterally in hippocampus, as well as in perirhinal cortex, where activity during learning increa

209 ted match and mismatch signals in the monkey perirhinal cortex, where match signals were selective fo

210 ject location memory, but was reduced in the perirhinal cortex, which corresponds to impaired long-te

211 ted intrinsic functional connectivity of the perirhinal cortex, which is typically the first brain re

212 nterior medial temporal lobes, including the perirhinal cortex, which serve to integrate complex obje

213 c information is uniquely represented in the perirhinal cortex, which was also increasingly engaged f

214 e medial temporal lobe (MTL)--in particular, perirhinal cortex--support not just memory but certain k

215 not eCB-dependent signalling is important in perirhinal cortex-dependent visual recognition memory.

216 studies suggest that at least one component-perirhinal cortex-might also contribute to perceptual pr

217 l topography at a fine-grained level in left perirhinal cortex.

218 arity effect for words was localized to left perirhinal cortex.

219 rade signalling mechanisms in LTD and LTP in perirhinal cortex.

220 model the projection from rat postrhinal to perirhinal cortex.

221 s been suggested between parahippocampal and perirhinal cortex.

222 ciation with large MTL lesions that included perirhinal cortex.

223 in basal ganglia and parietal, temporal, and perirhinal cortex.

224 s in the contribution of the hippocampus and perirhinal cortex.

225 in basal ganglia and parietal, temporal, and perirhinal cortex.

226 uated the responses of neurons in high-level perirhinal cortex.

227 er brain regions such as the hippocampus and perirhinal cortex.

228 presented configural stimuli depends on the perirhinal cortex.

229 d with a reduction in neural activity in the perirhinal cortex.

230 l of HD to assess synaptic plasticity in the perirhinal cortex.

231 amine receptors visualized in layer I of the perirhinal cortex.

232 cognitive tasks requiring the prefrontal and perirhinal cortex.

233 IL-1beta in the basolateral amygdala or the perirhinal cortex.

234 of behavioral impairments in young rats with perirhinal cortical lesions.

235 ort that lower firing rates observed in aged perirhinal cortical principal cells are associated with

236 pocampus and surrounding parahippocampal and perirhinal cortices during the retrieval of episodic mem

237 e piriform cortex, subiculum, entorhinal and perirhinal cortices, and parietal and occipital cortices

238 nterior medial temporal lobe (entorhinal and perirhinal cortices, anterior hippocampus, and amygdala)

239 rhinal (a homolog of the LEC in rodents) and perirhinal cortices, but not in the posteromedial entorh

240 ivity in the LEC is shaped by input from the perirhinal cortices, hippocampus, and amygdala, and thus

241 articularly pronounced in the entorhinal and perirhinal cortices, where it could be observed in one o

242 asubiculum) as well as in the entorhinal and perirhinal cortices.

243 D emphasise the role of the temporopolar and perirhinal cortices.

244 n in localized regions of the entorhinal and perirhinal cortices.

245 e ATL, namely, A13 with the temporopolar and perirhinal cortices.

246 For example, animals and humans with perirhinal damage are unable to distinguish familiar fro

247 ent studies indicating that the formation of perirhinal-dependent memories requires activation of mus

248 In the standard cue relapse test, perirhinal DPFE infusions did not alter meth-seeking in

249 etween a novel cue and meth-conditioned cue, perirhinal DPFE infusions shifted the pattern of respond

250 project to distant brain areas, such as the perirhinal, entorhinal, and endopiriform cortices.

251 and related medial temporal lobe structures (perirhinal, entorhinal, and parahippocampal cortices) im

252 At learning onset, correlated perirhinal-entorhinal firing increased in relation to mP

253 process provided by the model, we uncovered perirhinal-hippocampal desynchronization in the MTL regi

254 Together, these results provide evidence for perirhinal-hippocampal interactions in the selective con

255 mporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the supe

256 injection sites, much more so than following perirhinal injections.

257 r results were obtained with neocortical and perirhinal injections.

258 on, dorsal and ventral auditory, ectorhinal, perirhinal, lateral entorhinal, and anteromedial, poster

259 A perirhinal-lateral entorhinal pathway was more involved

260 Whereas LO, VLO, VO, and MO interact with perirhinal-LEC circuits, the interactions with postrhina

261 Furthermore, the perirhinal lesions did have differential effects in the

262 In contrast, the perirhinal lesions did impair recognition memory.

263 e water maze failed to provide evidence that perirhinal lesions disrupt overall levels of performance

264 results on the habituation experiments, the perirhinal lesions disrupted transfer performance on a c

265 The present study, therefore, compared perirhinal lesions in Sprague-Dawley rats (associated wi

266 This wide range of perirhinal memory signals not only includes signals that

267 ortex is critical for novelty detection, and perirhinal metabotropic glutamate 5 receptors (mGlu5) ar

268 Perirhinal mGlu5 are thus a promising pharmacological ta

269 verall, these results suggest that principal perirhinal neurons are subjected to significantly more i

270 ally stimulating channelrhodopsin-expressing perirhinal neurons at various frequencies while rats loo

271 njection of 17-beta-estradiol, the number of perirhinal neurons double-labeled for ER-beta/GABA was r

272 perirhinal cortex or temporal neocortex with perirhinal neurons in rats.

273 In the normal brain, perirhinal neurons respond to novelty and familiarity by

274 Perirhinal neurons respond to novelty and familiarity by

275 in a specific direction: from entorhinal to perirhinal neurons.

276 Irrespective of the injection site (perirhinal or temporal neocortex) and target nucleus (LA

277 odor category-specific ensemble patterns in perirhinal, orbitofrontal, piriform, and insular cortice

278 poral lobe (MTL)-hippocampus and surrounding perirhinal, parahippocampal, and entorhinal cortical are

279 tudies in human subjects have demonstrated a perirhinal/parahippocampal division, such a division amo

280 n of emergent odor category codes within the perirhinal, piriform, orbitofrontal, and insular cortice

281 ilateral excitotoxic lesions of PRh or PPRh (perirhinal plus postrhinal cortices) in the rat would ca

282 oncholinergic projections from the BF to the perirhinal, postrhinal, and entorhinal cortex by using r

283 parahippocampal region, which comprises the perirhinal, postrhinal, and entorhinal cortices, as well

284 contrast, target the parahippocampal region (perirhinal, postrhinal, lateral and medial entorhinal co

285 to total projection neurons is higher in the perirhinal/postrhinal cases (26-48%) than in the entorhi

286 Pretraining lesions of rat perirhinal (PR) cortex impair fear conditioning to ultra

287 Input from distal cortex (perirhinal (PRH) and lateral entorhinal cortex (LEC)) is

288 CMOR task requires functional integration of perirhinal (PRh) and posterior parietal (PPC) cortices,

289 Recognition of novelty depends upon intact perirhinal (pRh) cortex function, which is compromised b

290 tially progresses through the entorhinal and perirhinal regions before reaching the neocortex.

291 representational similarity analysis of left perirhinal responses, semantic distances between entitie

292 ly labeled (PHAL(+)) axon terminals found at perirhinal sites adjacent to or rostrocaudally distant f

293 known about the functional contributions of perirhinal subregions.

294 ent of both LTD and short-term plasticity at perirhinal synapses.

295 activity increased impulse transmission from perirhinal to entorhinal neurons and that this effect de

296 ly to affect feedforward inhibition from the perirhinal to the entorhinal cortex that gates the flow

297 n to be affected early by tau pathology, the perirhinal-transentorhinal region (area 35) and the ante

298 However, for reasons that remain unclear, perirhinal transfer of neocortical inputs to the entorhi

299 long-range feedforward inhibition regulates perirhinal transfer of neocortical inputs to the entorhi

300 , physiological investigations indicate that perirhinal transmission of neocortical and EC inputs occ