ライフサイエンスコーパス: piriform cortex

1 b and in the pyramidal cells of the anterior piriform cortex.

2 ns, and later to layer II/III neurons of the piriform cortex.

3 olinergic modulation of the OB inputs to the piriform cortex.

4 ompared to juvenile rats in both the OFC and piriform cortex.

5 rom several areas, including S1, SR, FM, and piriform cortex.

6 bilateral reversible lesions of the anterior piriform cortex.

7 i.e., the hippocampus, substantia nigra, and piriform cortex.

8 ive input times than neurons in the anterior piriform cortex.

9 (mitral/tufted [MT] cells) projecting to the piriform cortex.

10 undant axo-axonic synapses across the entire piriform cortex.

11 operties of these synapses across the entire piriform cortex.

12 in putative centrifugal cells and posterior piriform cortex.

13 al migration and homologous to the mammalian piriform cortex.

14 ugh phase resetting of delta oscillations in piriform cortex.

15 on of odors more similar to that seen in the piriform cortex.

16 alogous to the representation of odorants in piriform cortex.

17 y bulbs and higher brain regions such as the piriform cortex.

18 he lateral olfactory tract and the posterior piriform cortex.

19 al glutamatergic neurons within normal adult piriform cortex.

20 iate into pyramidal glutamatergic neurons in piriform cortex.

21 n local field potentials within the anterior piriform cortex.

22 integration and analogous to the vertebrate piriform cortex.

23 ctions with both the olfactory bulb (OB) and piriform cortex.

24 temporal cortices, with no changes noted in piriform cortex.

25 anatomical- and theoretical-based models of piriform cortex.

26 f the pseudorabies virus into the rat OB and piriform cortex.

27 y nucleus, the endopiriform nucleus, and the piriform cortex.

28 ating odor response properties of neurons in piriform cortex.

29 istributed ensembles of neurons in the mouse piriform cortex.

30 tion of the intracortical axons in slices of piriform cortex.

31 ck end labeling [TUNEL]) in the rat anterior piriform cortex.

32 /median eminence, paraventricular nuclei and piriform cortex.

33 rs are initially encoded as 'objects' in the piriform cortex.

34 t power gradient originating in the adjacent piriform cortex.

35 sentations of odor identity and intensity in piriform cortex.

36 ctively expressed in different layers of the piriform cortex.

37 presentations of odor objects are encoded in piriform cortex.

38 principal excitatory neuron in the anterior piriform cortex.

39 tral/tufted (MT) cells carrying OB output to piriform cortex.

40 t but not the associational afferents of the piriform cortex.

41 ives rich glutamatergic projections from the piriform cortex.

42 odel of cholinergic modulation in the OB and piriform cortex.

43 olfactory tract (lot) guidepost cells in the piriform cortex.

44 maker circuits in the septal nucleus and the piriform cortex.

45 distributed in the rodent primary olfactory (piriform) cortex.

46 or representations in rat primary olfactory (piriform) cortex.

47 mble activity patterns in primary olfactory (piriform) cortex.

48 d are highly expressed in primary olfactory (piriform) cortex.

49 ity in the mouse primary olfactory (anterior piriform) cortex.

50 essing center for olfactory information, the piriform cortex?

51 m concentration, 0.33 ug . g(-1) +/- 0.04 in piriform cortex, 0.24 ug . g(-1) +/- 0.04 in dentate gyr

52 L labeling in layers I/II of the ipsilateral piriform cortex 24 h after bulbectomy.

53 apse with neurons distributed throughout the piriform cortex [7-10].

54 s involved the dorsal hippocampus (75%), the piriform cortex (87.5%), and the amygdala (25%).

55 The analysis was of piriform cortex, a highly epileptogenic area of cerebral

56 obust interhemispheric asymmetry in anterior piriform cortex activity that emerges during specific st

57 nput from the anterior olfactory nucleus and piriform cortex already by the second week.

58 Pyramidal cells in adult piriform cortex also lack I(h), the mixed Na(+)-K(+) cur

59 Labeled fibers in posterior piriform cortex also were seen after injection into orbi

60 We did not observe these effects in anterior piriform cortex, amygdala or orbitofrontal cortex, indic

61 t of local field potential activity in human piriform cortex, amygdala, and hippocampus.

62 xpressed in the olfactory bulb, hippocampus, piriform cortex, amygdala, hypothalamus, cerebellum, and

63 c-Jun immunoreactivity were observed in the piriform cortex, an area that also showed more positive

64 c suppression of responses from the amygdalo-piriform cortex, an associative temporal cortical struct

65 The three-layered piriform cortex, an integral part of the olfactory syste

66 dy calyx, the insect analog of the mammalian piriform cortex and a center for associative memory.

67 of the basal telencephalon, most notably the piriform cortex and amygdala.

68 le to functionally isolate defined inputs to piriform cortex and assess their potential to activate o

69 cross brain regions, and particularly in the piriform cortex and cortical amygdala.

70 dus within 3 h after KA treatment and in the piriform cortex and hippocampus by 6 h after KA.

71 reased theta-specific phase coupling between piriform cortex and hippocampus.

72 ated by odor-evoked connectivity between the piriform cortex and insula, a region involved in integra

73 us (AON) lies between the olfactory bulb and piriform cortex and is the first bilaterally innervated

74 imaging in the mouse, we show that both the piriform cortex and its sensory inputs from the olfactor

75 d with a direct monosynaptic pathway linking piriform cortex and OFC.

76 Labeled fibers were found in the piriform cortex and olfactory bulb on the side ipsilater

77 , subsets of cells that populate the ventral piriform cortex and olfactory bulb reach these sites by

78 However, the LEC also projects back to the piriform cortex and olfactory bulb.

79 ible changes in odor-evoked fMRI activity in piriform cortex and orbitofrontal cortex (OFC).

80 ed by learning-induced response increases in piriform cortex and orbitofrontal cortex (OFC).

81 nfection from the olfactory bulb (OB) to the piriform cortex and other areas connected to the OB was

82 wever, it did not affect degeneration in the piriform cortex and PLCo indicating that limbic degenera

83 eurons in the somatosensory parietal cortex, piriform cortex and posterolateral cortical amygdaloid n

84 ns that resembled neurogliaform cells of the piriform cortex and provided feedforward inhibition of t

85 phe magnus nucleus, and was decreased in the piriform cortex and septum.

86 e, only C. sociabilis had OTR binding in the piriform cortex and thalamus and V1aR binding in the olf

87 etween the hippocampus and the amygdala, the piriform cortex and thalamus between stress-resistant an

88 idual glomeruli in the olfactory bulb to the piriform cortex and the cortical amygdala.

89 nctional coupling between OFC and olfactory (piriform) cortex and between vmPFC and amygdala revealed

90 related with fMRI activity in midbrain, OFC, piriform cortex, and amygdala.

91 ygdala, cingulate cortex, hippocampus (CA1), piriform cortex, and BNST were lower in OVX+E2 females c

92 e associative network originating within the piriform cortex, and can be reshaped by passive odour ex

93 us at 60 and 120 min following KA and in the piriform cortex, and central nucleus of the amygdala at

94 res were also observed in stratum oriens and piriform cortex, and in cerebellar Purkinje cell areas.

95 l (2-OG), enhanced encoding of food odors in piriform cortex, and shifted food choices toward energy-

96 eurons within hippocampus, central amygdala, piriform cortex, and striatum, brain regions associated

97 d with within-category pattern separation in piriform cortex, and the magnitude of this drug-induced

98 ry areas, the anterior olfactory nucleus and piriform cortex, and the olfactory associated orbital an

99 of the forebrain, including medial amygdala, piriform cortex, and ventrolateral septum, showed low c-

100 ; 4) olfactory-associated structures and the piriform cortex; and 5) sensory and motor trigeminal nuc

101 dal cell connections across the rat anterior piriform cortex (aPC) and found a pronounced gradient of

102 Ensemble activity patterns in anterior piriform cortex (APC) and orbitofrontal cortex (OFC) ref

103 P(+)) cells within the CC, Ctx, and anterior piriform cortex (aPC) and used prelabeling with 5-ethyny

104 Cells in the brain's anterior piriform cortex (APC) are sensitive to IAA deficiency, s

105 Layer 2 principal neurons in the anterior piriform cortex (APC) can be divided into 2 subtypes: se

106 The anterior piriform cortex (APC) has been shown to be an essential

107 NMDA receptor (NMDAR) number in the anterior piriform cortex (aPC) in rat induced by a 10 min pairing

108 he first time that adrenoceptors in anterior piriform cortex (aPC) must be engaged for adult rats to

109 ded neural ensemble activity in the anterior piriform cortex (aPC) of rats performing an odor mixture

110 rivation is in the highly excitable anterior piriform cortex (APC) of the brain.

111 examines synaptic plasticity in the anterior piriform cortex (aPC) using ex vivo slices from rat pups

112 ction to the ventral portion of the anterior piriform cortex (APC) was substantial, while the dorsal

113 AA (DLAA) concentrations within the anterior piriform cortex (APC), and to a recognition process that

114 f IAA deficiency requires an intact anterior piriform cortex (APC), but does it act alone?

115 specific odorant features, but the anterior piriform cortex (aPCX) and posterior piriform cortex (pP

116 striction, we hypothesized that the anterior piriform cortex (APCx) and the olfactory tubercle (OTu)

117 Anterior piriform cortex (aPCX) neurons rapidly filter repetitive

118 tized and recordings were made from anterior piriform cortex (aPCX).

119 w that spatial ensemble activity patterns in piriform cortex are closely linked to the perceptual mea

120 rceptual codes of odour quality in posterior piriform cortex are degraded in patients with Alzheimer'

121 The orbitofrontal cortex (OFC) and piriform cortex are involved in encoding the predictive

122 rocessing, the projections to the olfactory (piriform) cortex are more diffuse and show characteristi

123 ocation to the physiologically defined "deep piriform cortex" ("area tempestas") from which convulsan

124 sured neural responses in primary olfactory (piriform) cortex as subjects smelled pairs of odorants s

125 hat the diversity in basket cell form in the piriform cortex, as in other areas of the cerebral corte

126 In contrast, in the piriform cortex, as in the majority of cortical regions,

127 KCC3a in the hippocampus, choroid plexus and piriform cortex, as well as KCC4 in the choroid plexus a

128 Primary olfactory (piriform) cortex, as well as anterior hippocampus, was a

129 lly to reach the ventral pallium deep to the piriform cortex at E14.5 in the mouse.

130 patial order in the bulb is discarded in the piriform cortex; axons from individual glomeruli project

131 The largest changes were in the piriform cortex (before: 47.7 +/- 1.4 ms; 18-24 h: 82.3

132 ion-invariant neurons are overrepresented in piriform cortex but not in olfactory bulb mitral and tuf

133 gions, such as the hippocampus, thalamus, or piriform cortex, but not in the cerebellum beginning at

134 dy further explored LEC feedback to anterior piriform cortex by examining how LEC top-down input modu

135 bitrarily chosen subpopulation of neurons in piriform cortex can elicit different behavioral response

136 Steady-state interhemispheric anterior piriform cortex coherence is reduced during the initial

137 reduced microgliosis in the hippocampus and piriform cortex compared with T2(+/+)PS mice.

138 s have unique and redundant functions in the piriform cortex, controlling the timing of differentiati

139 e laminin immunoreactivity is present in the piriform cortex, corpus callosum (myelinated tracts) amy

140 In piriform cortex, CRF1 binding increased in females and d

141 or representations in the primary olfactory (piriform) cortex depend on excitatory sensory afferents

142 njection, the anterior olfactory nucleus and piriform cortex displayed a high alpha-synuclein patholo

143 al stimuli to sensory representations in the piriform cortex during odor-driven social learning.

144 glutamatergic pacemaker circuits within the piriform cortex, each of which can initiate waves of act

145 ons receiving primary olfactory projections (piriform cortex, entorhinal cortex, and amygdala).

146 We now report that OPCs in adult murine piriform cortex express low levels of doublecortin, a ma

147 ted olfactory epithelium and OB, but not the piriform cortex, express similar, sustained circadian rh

148 evated baseline, spontaneous activity in the piriform cortex extends the dynamic range of odor repres

149 e ipsilateral and contralateral OB, AON, and piriform cortex, few studies have examined this circuitr

150 hat extend, largely undiminished, across the piriform cortex, forming a large excitatory network that

151 distributed ensembles of neurons within the piriform cortex, forming cortical representations of odo

152 The piriform cortex had the strongest correlation between th

153 Together these findings suggest that human piriform cortex has access to olfactory content in the t

154 Cholinergic modulation within the piriform cortex has long been proposed to serve importan

155 The olfactory (piriform) cortex has long been hypothesized to encode od

156 To determine whether OPCs in the piriform cortex have inherently different physiological

157 a tecta, and anterior olfactory tubercle and piriform cortex) have cells that express either calbindi

158 n of high-affinity Epb sites was seen in the piriform cortex, hippocampus, caudate/putamen, and cereb

159 In rats and birds, the anterior piriform cortex houses the detector, but its mechanism h

160 ry formed between the olfactory bulb and the piriform cortex in anesthetized mice.

161 In recordings from anterior piriform cortex in awake behaving mice, we found that ne

162 ur study suggests a causal role of posterior piriform cortex in differentiating olfactory objects.

163 ative descriptions of the olfactory bulb and piriform cortex in six mammals using stereology techniqu

164 nd olfactory-related oscillations within the piriform cortex in vivo.

165 icited cross-adapting responses in posterior piriform cortex, in accord with the pattern observed in

166 revious reports, these findings suggest that piriform cortex includes multiple subdivisions, which ma

167 In the piriform cortex (including the endopiriform nucleus) of

168 Inactivation of piriform cortex increased odor responsiveness and pairwi

169 In the piriform cortex, individual odorants activate a unique e

170 s including the olfactory nuclei, neocortex, piriform cortex, induseum griseum, hippocampus, thalamus

171 assium changes demonstrates that SLEs in the piriform cortex initiate in the superficial layer 1 lack

172 Pyramidal cells in piriform cortex integrate sensory information from multi

173 Finally, post-training disruption of piriform cortex intracortical association fiber synapses

174 An interesting finding is the absence of the piriform cortex involvement in young male rats and the c

175 or layers I/II and layer III of the anterior piriform cortex ipsilateral and contralateral to the man

176 transsynaptic death of pyramidal neurons in piriform cortex is a nitric oxide-mediated event signale

177 gamma oscillations in the vStr LFP and that piriform cortex is an important driver of gamma-band osc

178 trated that a reduction in plasticity in the piriform cortex is associated with a selective impairmen

179 cells across major cortical subdivisions of piriform cortex is lacking.

180 These observations demonstrate that the piriform cortex is sufficient to elicit learned behavior

181 The olfactory (piriform) cortex is thought to generate odour percepts a

182 d, odor-distinctive patterns of responses in piriform cortex layer 2 principal cells: Approximately 1

183 the peculiar organization of the superficial piriform cortex layers, which are characterized by unmye

184 Both right and left piriform cortex local field potential activities were re

185 ammed spatial relationships may not exist in piriform cortex, making flexible random associations the

186 oligodendrocytes (OLs), whereas those in the piriform cortex may also generate neurons.

187 activity during slow-wave states within the piriform cortex may be shaped by recent olfactory experi

188 learning until mastery, suggesting that each piriform cortex may contribute something unique to odour

189 ssion is seen in anterior olfactory nucleus, piriform cortex, median preoptic nucleus, basolateral am

190 The neural circuits of the piriform cortex mediate field potential oscillations and

191 In temporal piriform cortex, neural responses were evoked by the avC

192 cell fate and later to specify layer II/III piriform cortex neuronal identities.

193 We found that the overall spike rates of piriform cortex neurons (PCNs) were sensitive to the rel

194 Piriform cortex neurons from E14.5 mutant embryos displa

195 n a spatially scattered ensemble of anterior piriform cortex neurons, and the ensemble activity inclu

196 ng how LEC top-down input modulates anterior piriform cortex odor evoked activity in rats.

197 robust odor representations in the anterior piriform cortex of adult rats when odor was associated w

198 However, neurotoxicity in the piriform cortex of immature females treated for 60days a

199 thelium, main olfactory bulb, and olfactory (piriform) cortex of CNGA2 knock-out mice.

200 sensory paleocortex, the primary olfactory (piriform) cortex of mice.

201 might participate in seizure circuitry: the piriform cortex, olfactory tubercle, nucleus accumbens,

202 sensory input in the olfactory bulb through piriform cortex/olfactory bulb synaptic interactions.

203 educes olfactory bulb afferent excitation of piriform cortex, on apoptosis (terminal deoxynucleotidyl

204 tive cell numbers were high in, for example, piriform cortex, paraventricular nucleus, supraoptic nuc

205 tion, the analysis of neural circuits in the piriform cortex (PC) demonstrated the importance of not

206 ng from the association fiber (AF) system in piriform cortex (PC) make axodendritic synapses on granu

207 inhibitory and glutamatergic neurons in the piriform cortex (PC) of mice.

208 nic synapses (AASs) in brain slices from the piriform cortex (PC) of mice.

209 n adult rat olfactory bulb (OB) and anterior piriform cortex (PC) were assessed after discrimination

210 For the piriform cortex (PC), results with this technique indica

211 ation of cortical association fibers (AF) in piriform cortex (PC).

212 these mitral/tufted cells in turn project to piriform cortex (PC).

213 ral and granular layers of the OB and in the piriform cortex (PC).

214 ct regions: olfactory bulb (OB) and anterior piriform cortex (PC).

215 and polysynaptically) to primary olfactory (piriform) cortex (PC)-connections that might be hypothes

216 Hyperactive odor-evoked activity in the piriform cortex (PCX) and increased OB-PCX functional co

217 s, we found that 26% of neurons in the mouse piriform cortex (PCX) display modulation in firing to ca

218 The piriform cortex (PCX) is the largest component of the ol

219 s well as local field potentials in the MDT, piriform cortex (PCX), and OFC in rats performing a two-

220 In the piriform cortex (PCx), spatially dispersed sensory input

221 electrophysiological recordings in anterior piriform cortex (PCx), we assessed how cortical neurons

222 nigra (VTA/SN), nucleus accumbens (NAc), and piriform cortex (PFx)-after bilateral olfactory bulbecto

223 rapid elevation of CRH concentrations at the piriform cortex (Pir) and hypothalamic nuclei following

224 ociated with increased Fos expression in the piriform cortex (Pir) neurons projecting to the OFC, but

225 A), dorsomedial striatum (DMS) and olfactory piriform cortex (PIR).

226 ions, a frontal subregion comprising frontal piriform cortex (PirF) and the olfactory tubercle respon

227 eas a temporal subregion comprising temporal piriform cortex (PirT) responded equally across conditio

228 ut the olfactory tubercle (OT) and posterior piriform cortex (pPC) are candidates for decoding reward

229 e-associated astrocytes" (SAAs) in posterior piriform cortex (PPC) are unique by virtue of a direct a

230 ributed ensemble activity in human posterior piriform cortex (PPC) coincides with perceptual ratings

231 resentations of the odor target in posterior piriform cortex (PPC) gave way to poststimulus represent

232 Retrograde tracing from the OB or posterior piriform cortex (PPC) showed that the APC projects to th

233 ons positive for GAD65-EGFP in the posterior piriform cortex (PPC).

234 from single neurons in posterior olfactory (piriform) cortex (pPC) of awake rats while presenting ba

235 nterior piriform cortex (aPCX) and posterior piriform cortex (pPCX) differ markedly in their anatomic

236 on resets the phase of delta oscillations in piriform cortex prior to odor arrival.

237 The piriform cortex provides an ideal system to address this

238 However, piriform cortex pyramidal cells also receive dense intra

239 espread and broadly tuned than excitation in piriform cortex pyramidal cells.

240 enhanced intrinsic neuronal excitability of piriform cortex pyramidal neurons, and in their excitato

241 are primarily located in the in the adjacent piriform cortex rather than in the vStr itself, providin

242 ve suggested a model in which neurons of the piriform cortex receive convergent input from random col

243 n to provide direct evidence that neurons in piriform cortex receive convergent synaptic input from d

244 The olfactory bulb (OB) and piriform cortex receive dense cholinergic projections fr

245 to the olfactory bulb, such that concurrent piriform cortex recordings show no evidence of enhanced

246 d to all odors, whereas activity in anterior piriform cortex reflected sensitivity to odor affect.

247 a while responses immediately downstream, in piriform cortex, remain robust.

248 lt CNS-though rare, neuron production in the piriform cortex remains a possibility.

249 Neurons in piriform cortex, responsive to a given odorant, are not

250 es the composition of synaptic NMDARs in the piriform cortex, resulting in receptors with a higher co

251 ves dorsal olfactory bulb input, whereas the piriform cortex samples the whole olfactory bulb without

252 DCX and PSA-NCAM immunoreactive cells in the piriform cortex, similar to that previously reported in

253 Here we used patch-clamp recordings in rat piriform cortex slices to examine cellular mechanisms th

254 In primary olfactory (piriform) cortex, spatially and temporally dissociable r

255 cus on the hippocampus, somatosensory, paleo/piriform cortex, striatum, and various amygdala nuclei.

256 ositive, we showed that in the motor cortex, piriform cortex, striatum, CA1 region of the hippocampus

257 , known to abolish gamma oscillations in the piriform cortex, strongly reduced vStr gamma power and t

258 the c-Fos protein has been evidenced in the piriform cortex, subiculum, entorhinal and perirhinal co

259 mmunoreactivity were found in the claustrum, piriform cortex (superficial layer), arcuate hypothalami

260 istent with an auto-associative function for piriform cortex supported by recurrent circuitry.

261 nigra, but was increased bilaterally in the piriform cortex, supraoptic nucleus, central nucleus of

262 onic synapse are significantly higher in the piriform cortex than in the neocortex.

263 bulb and sends an associative projection to piriform cortex that has potential roles in the state-de

264 a population of neurons within the anterior piriform cortex that undergo rapid apoptosis following d

265 However, in piriform cortex, the activity of target neurons increase

266 The AC is composed of axons from the piriform cortex, the anterior olfactory nucleus and the

267 idual recognition, particularly the anterior piriform cortex, the CA1 and CA3 regions of anterior dor

268 riched for oxytocin receptors, including the piriform cortex, the left auditory cortex, and CA2 of th

269 a significant projection to OFC arises from piriform cortex, the traditional primary olfactory corte

270 achnoid (> or =3 hours), particularly within piriform cortex; this activity was suppressed by injecti

271 tiple relays in a network extending from the piriform cortex through the hippocampus can be different

272 fMRI data for a node within the ipsilateral piriform cortex to be important for seizure modulation i

273 We introduced channelrhodopsin into the piriform cortex to characterize these intrinsic circuits

274 dendrites and that feedback projections from piriform cortex to olfactory bulb interneurons are a sou

275 stablished major neural pathways linking the piriform cortex to other cortical and subcortical region

276 aired single-unit recordings in rat anterior piriform cortex to test several predictions regarding en

277 heavy, rather selective projection from the piriform cortex to the ventrolateral orbital cortex (VLO

278 orsal (MD) thalamus links primary olfactory (piriform) cortex to olfactory neocortical projection sit

279 revious work showing that pyramidal cells in piriform cortex undergo classical apoptosis within 24 h

280 d by theta burst stimulation in the anterior piriform cortex was normal in KO mice aged < 6 months bu

281 Notably, the projection to piriform cortex was predominantly from ventrolateral orb

282 A nonhabituating response in posterior piriform cortex was tuned to all odors, whereas activity

283 hereas cingulate cortex and to a less extent piriform cortex were affected preferentially by the CIV

284 gs from both the olfactory bulb and anterior piriform cortex were performed in freely breathing ureth

285 DCX and PSA-NCAM immunoreactive cells in the piriform cortex were quantified as measures of plasticit

286 put/output curves for two connections in the piriform cortex were similar to those for the LPP, where

287 Odor representations in anterior piriform cortex were sparser than typical in adult rat a

288 I-III of the parietal cortex and superficial piriform cortex were the most sensitive followed by othe

289 ing channelrhodopsin at multiple loci in the piriform cortex, when paired with reward or shock, elici

290 ory receptors to olfactory bulb, and then to piriform cortex, where ensembles of activated neurons fo

291 tern does not appear to be maintained in the piriform cortex, where stimuli appear to be coded in a d

292 ur results indicate a double dissociation in piriform cortex, whereby posterior regions encode qualit

293 nt mice presented a reduced thickness of the piriform cortex, which affected projection neurons in la

294 enerated in the forebrain, especially in the piriform cortex, which is the main target of the olfacto

295 here is a population of superficial cells in piriform cortex whose survival is tightly regulated by s

296 Such topography has not been observed in the piriform cortex, whose responses to odorants are sparsel

297 ity of the olfactory cortex, principally the piriform cortex, will be described in the context of how

298 ical loop between the olfactory bulb and the piriform cortex, with cortex explaining incoming activit

299 or stimulation enhanced theta power in human piriform cortex, with robust effects at the level of sin

300 o-active neurons that are distributed across piriform cortex without any apparent spatial organizatio