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1 and might thus help to identify odors in the olfactory cortex.
2 of the adult mouse hippocampus and accessory olfactory cortex.
3 rom piriform cortex, the traditional primary olfactory cortex.
4 ory transmission in pyramidal neurons of rat olfactory cortex.
5 he original engram are preserved in unimodal olfactory cortex.
6 in independent subnetworks of neurons in the olfactory cortex.
7 so present in projections from the OB to the olfactory cortex.
8 ty of odor signals that are delivered to the olfactory cortex.
9 factory neuroepithelium, olfactory bulb, and olfactory cortex.
10 itic inputs with coincidence excitation from olfactory cortex.
11 stantially enhanced in the limbic system and olfactory cortex.
12 ted through the axons of bulb neurons to the olfactory cortex.
13 n adult Rana pipiens induces a projection to olfactory cortex.
14 onjugated to horseradish peroxidase into the olfactory cortex.
15 etween the bilateral OFC and between the OFC-olfactory cortex.
16 al connectivity in higher-order areas beyond olfactory cortex.
17 c connectivity analyses, within and from the olfactory cortex.
18 to determine how odor identity is encoded in olfactory cortex.
19 entral relay before being transferred to the olfactory cortex.
20 te to the olfactory bulb, and migrate to the olfactory cortex.
21 OM cells) contribute to odor coding in mouse olfactory cortex.
22  olfactory epithelium and relays this to the olfactory cortex.
23 ape processing of sensory information in the olfactory cortex.
24 he telencephalic area Dp, the homolog of the olfactory cortex.
25 ry processing occurs at the level of primary olfactory cortex.
26 ells and cortical neurons in slices of mouse olfactory cortex.
27 amic inhibition in space and time within the olfactory cortex.
28 networks formed by the subregions of primary olfactory cortex.
29 en shown to depend on synaptic adaptation in olfactory cortex.
30 s unclear how this map is represented in the olfactory cortex.
31 c mechanisms shaping odor representations in olfactory cortex.
32  and fate decisions to generate neocortex or olfactory cortex.
33 ation in long-term functional changes within olfactory cortex.
34 olfactory bulb, and hence shape signaling to olfactory cortex.
35  result of reduced plasticity in the primary olfactory cortex.
36  to be combined in individual neurons in the olfactory cortex.
37 that odor coding is broad and distributed in olfactory cortex.
38 ates NMDA receptors at primary inputs to the olfactory cortex.
39 ume loss was most severe in the amygdala and olfactory cortex (82-83% of controls), especially the ca
40 ed functional lateralization in both primary olfactory cortex - a region critical for odor memory and
41 ium signals in populations of neurons in the olfactory cortex, a brain region laying approximately 5
42  apoptotic death of pyramidal neurons in rat olfactory cortex after total bulbectomy.
43 ceptor to the olfactory bulb and then to the olfactory cortex, allowing visualization of cortical neu
44 e neuron and volume loss in the amygdala and olfactory cortex, although the patterns and extent of lo
45 dor convergence occurs in posterior piriform olfactory cortex and calls for a reformulation of classi
46 rmality in extrahippocampal divisions of the olfactory cortex and cortical and subcortical structures
47          Here, we used viral injections into olfactory cortex and fluorescent nucleus sorting to enri
48 n the thalamus, receiving strong inputs from olfactory cortex and having reciprocal connections with
49 cortex (PCX) is the largest component of the olfactory cortex and is hypothesized to be the locus of
50 performing sequential developmental roles in olfactory cortex and neocortex.
51  evoke robust fMRI activity in the bilateral olfactory cortex and thalamus and that fMRI response mag
52 t inputs to the hippocampus from the primary olfactory cortex and the general expansion of telencepha
53 gion that in other vertebrates gives rise to olfactory cortex and, when present, to other components
54 erior olfactory nucleus (AON) is part of the olfactory cortex, and its extensive connections to multi
55 sses in the olfactory bulb, olfactory nerve, olfactory cortex, and nervus terminalis located on the a
56 wed significant volume loss in the amygdala, olfactory cortex, and septal region, but others displaye
57                                    Amygdala, olfactory cortex, and septum occasionally displayed earl
58  was identified superficially, dorsal to the olfactory cortex, and was subsequently covered by the Nr
59 were studied in slices of anterior piriform (olfactory) cortex, and Schaffer-commissural synapses wer
60 at are functionally connected to the primary olfactory cortex; and (3) a greater reduction in global
61 her-level association functions derived from olfactory cortex; and human cortical evolution was enhan
62 ergic feedback selectively from the anterior olfactory cortex (AOC) to the OB.
63 egration of sensory information in mammalian olfactory cortex are unclear.
64 nizes electrical activity in human piriform (olfactory) cortex, as well as in limbic-related brain ar
65      By contrast, the prevailing view in the olfactory cortex, based on the reconstruction of dozens
66  for reward prediction does not occur within olfactory cortex, but rather in circuits involving the o
67 interneurons before being transmitted to the olfactory cortex by mitral and tufted (M/T) cells.
68 inting to a potential mechanism by which the olfactory cortex can actively and dynamically gate senso
69 f this much larger dataset revealed that the olfactory cortex connectivity is spatially structured.
70 mus and that fMRI response magnitudes in the olfactory cortex differ across odors.
71  information processing may occur within the olfactory cortex, direct electrophysiological evidence f
72  the septum, dorsomedial thalamus, amygdala, olfactory cortex, dorsal and ventral hippocampus, substa
73  amplitude of high-frequency oscillations in olfactory cortex during correct trials.
74  for the entrainment of slow oscillations in olfactory cortex during ketamine-xylazine anesthesia.
75 evidence of sensory-specific reactivation of olfactory cortex during remembering.
76 These results suggest that SWS replay in the olfactory cortex enhances memory consolidation, and that
77         Progenitors did not generate ectopic olfactory cortex following Lhx2 deletion at E11.5.
78 ncluding six-layer neocortex and three-layer olfactory cortex, generated by telencephalic progenitors
79 calretinin (CR) were found in the neocortex, olfactory cortex, hippocampus, and amygdala, these neuro
80 noreactivity were observed in the neocortex, olfactory cortex, hippocampus, and amygdala.
81 c operations across the serial stages of the olfactory cortex-hippocampus network.
82                                           In olfactory cortex, however, pyramidal cells receive direc
83 ed by reinforced population responses in two olfactory cortex hubs and communicated to other brain re
84      Here we identify a specific area of the olfactory cortex in mice that induces stress hormone res
85 recently identified a region of the piriform olfactory cortex in rats that responds to both taste and
86  that is enriched in hippocampus and primary olfactory cortex in the adult mouse brain.
87  process the signal and then relay it to the olfactory cortex in the brain.
88        Here, we will discuss the role of the olfactory cortex in the recognition, separation and comp
89 es revealed a stereotyped sensory map in the olfactory cortex in which signals from a particular rece
90 ct to the head is associated with changes in olfactory cortex, including decreased gray matter densit
91                                 In the mouse olfactory cortex, individual odorants are represented by
92                                           In olfactory cortex, inhibition regulates activity-dependen
93 means clustering to parcellate human primary olfactory cortex into clusters based on whole-brain func
94                  How this map is linked with olfactory cortex is unknown.
95 our space have not yet been described in the olfactory cortex, it remains unclear how odour relations
96 ory bulb; it may be due to plasticity within olfactory cortex itself.
97             We found that neural activity in olfactory cortex largely reflects sensory coding, with v
98 puncta in the dorsolateral prominence of the olfactory cortex may have relevance to the functional or
99  non-topographic projections to and from the olfactory cortex may suggest a flat, non-hierarchical or
100 tiating predictie information; the piriform (olfactory) cortex meanwhile clusters similar and co-occu
101  that "global" inhibition within the primary olfactory cortex might accomplish a similar end.
102  of a greater experimental tractability, the olfactory cortex might prove to be instrumental in uncov
103 uronal types in the hippocampus, cerebellum, olfactory cortex, neocortex, and elsewhere express from
104 ears of coevolution alongside the neocortex, olfactory cortex neurons retain molecular signatures of
105  of either spherical or rodlike shape in the olfactory cortex, nucleus isthmi, and hypothalamus.
106 hesized to help bind information together in olfactory cortex (OC).
107 allial portions of the FB, equivalent to the olfactory cortex of amniote vertebrates, whereas social
108 recorded from small groups of neurons in the olfactory cortex of awake rats while they consumed taste
109 e we show that blockade of mGluRs within the olfactory cortex of awake, behaving rats diminishes habi
110 ions of as few as 300 neurons in the primary olfactory cortex of mice suffices for associative learni
111 eruli to third-order neurons (neurons in the olfactory cortex of vertebrates or Kenyon cells in the m
112 tions of gamma oscillations in the piriform (olfactory) cortex of awake mice to understand their depe
113 lectrical activity of neurons in the primary olfactory cortex on a rapid (<1 s) timescale but leaves
114 ed in KO compared with WT mice in either the olfactory cortex or hippocampus.
115  discriminable fMRI activity patterns in the olfactory cortex or thalamus using two different multiva
116 ent with oxytocin's function in the anterior olfactory cortex, particularly in social cue processing,
117           Here, we asked whether the primary olfactory cortex (piriform cortex [PC]) encodes odor inf
118 In the olfactory system, activity in primary olfactory cortex (piriform cortex) is thought to determi
119 nformation is communicated to, and from, the olfactory cortex (piriform cortex, PC) are not known.
120                The representation of odor in olfactory cortex (piriform) is distributive and unstruct
121                        We speculate that the olfactory cortex plays a key role in tuning the readout
122 at AmPir, a small area comprising <5% of the olfactory cortex, plays a key part in the hormonal compo
123 gen level-dependent (BOLD) signal at primary olfactory cortex (POC) was weaker in AD than in HC subje
124  probe this attentional mechanism in primary olfactory cortex (POC).
125 .05) and spinophilin (SPH) (p < 0.05) in the olfactory cortex, post synaptic density-95 (PSD-95) (p <
126 hitecture, physiology, and plasticity of the olfactory cortex, principally the piriform cortex, will
127 nsiently increased the drive of the anterior olfactory cortex projecting to olfactory bulb interneuro
128 we selectively express channelrhodopsin-2 in olfactory cortex pyramidal cells and show that cortical
129                                              Olfactory cortex pyramidal cells integrate sensory input
130 postnatal time window at sensory synapses of olfactory cortex pyramidal cells.
131 to generate three-layer cortex, phenocopying olfactory cortex rather than lateral neocortex.
132 fact that multiple structures of the primary olfactory cortex receive projections from the olfactory
133 lly organized retinal projection in the frog olfactory cortex revealed that the temporal retina is th
134 lectrophoresis of DNA purified from lesioned olfactory cortex showed a ladder pattern of fragmentatio
135 by olfactory bulb afferents to the piriform (olfactory) cortex significantly contributes to adaptatio
136 e analysis of paired whole-cell recording in olfactory cortex slices.
137                        This coupling between olfactory cortex slow oscillations and respiration may r
138 y perceived or not, depending on whether the olfactory cortex succeeds in activating the endopiriform
139 g evidence for slow- and fast-wave states in olfactory cortex that appear to gate the inflow of infor
140 ime window and is a feature intrinsic to the olfactory cortex that can be explained by the integratio
141 eferences of principal neurons in the OB and olfactory cortex that innervate granule cells (GCs) may
142                       In vivo, activation of olfactory cortex that only weakly affects spontaneous M/
143  bulb (OB) receives top-down inputs from the olfactory cortex that produce direct excitation and feed
144 tatory inputs mostly from the regions of the olfactory cortex that project back to the OB.
145 ribe a novel seizure pattern peculiar of the olfactory cortex that resembles focal seizures with low-
146 eveals a sequence of ictogenic events in the olfactory cortex that were never described before in oth
147  found nostril-specific responses in primary olfactory cortex that were predictive of the accuracy of
148 ncrease dynamic functional connectivity from olfactory cortex to cerebral areas processing multisenso
149 h reinforces the top-down influence from the olfactory cortex to early stages of olfactory informatio
150 papers analyze the features of feedback from olfactory cortex to olfactory bulb.
151                                          The olfactory cortex uses taste and smell to create new info
152 e probed the excitatory network in the mouse olfactory cortex using variance analysis of paired whole
153 information is then transmitted to piriform (olfactory) cortex, via axons of olfactory bulb mitral an
154 to provide evidence of apoptosis; neurons in olfactory cortex were counted by stereology.
155 y tubercle is also the region of the primary olfactory cortex where participants with chronic olfacto
156 ibuted subnetworks are weak or absent in the olfactory cortex, whereas a hierarchical excitatory topo
157  all of the pallial amygdala but also to the olfactory cortex, which hitherto was considered to arise
158                                       In the olfactory cortex, which lacks an obvious columnar struct
159 heterogeneous functional connectivity in the olfactory cortex with a resolution surpassing substantia
160 t cell bodies, were studied in rat piriform (olfactory) cortex with antisera to gamma-aminobutyric ac

 
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