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1 human insular cortex, which contains primary gustatory cortex.
2 synaptic properties of the BLA input to the gustatory cortex.
3 the subregion approximating the dysgranular gustatory cortex.
4 gation in the functional architecture of the gustatory cortex.
5 ngly similar to those previously observed in gustatory cortex.
6 l PbN and transmits taste information to the gustatory cortex.
7 aste-specific and non-taste responses in the gustatory cortex.
8 onditioning-active neuronal ensembles within gustatory cortex.
9 n associated with the depicted foods, within gustatory cortex.
10 s show that bilateral lesions of the insular gustatory cortex (1) fully prevent the suppressive effec
11 al taste reactivity behavior, lesions of the gustatory cortex, a region that has been suggested to be
12 c subjects because the insula is the primary gustatory cortex and has repeatedly been implicated in t
13 monstrate that chemoselective neurons in the gustatory cortex are broadly responsive to intraoral che
14 electrophysiological studies identified the gustatory cortex as a site of convergent olfactory and g
15 irst, we demonstrate that ZIP infusions into gustatory cortex begin interfering with CTA memory 43-45
16 stimulated neurons were found throughout the gustatory cortex, but a "hot spot" was observed in its a
17 et and bitter are represented in the primary gustatory cortex by neurons organized in a spatial map,
19 oS(2) memtransistors construct an electronic-gustatory-cortex comprising a hunger neuron, appetite ne
21 local microinjection of PKR inhibitor to the gustatory cortex enhanced both positive and negative for
23 activity from neuronal ensembles in primary [gustatory cortex GC)] and secondary gustatory [orbitofro
26 neuroimaging experiments have pointed to the gustatory cortex (GC) as one of the areas involved in me
27 signal revealed that neurons in the primary gustatory cortex (GC) can respond to anticipatory cues.
29 by examining the role of neural ensembles in gustatory cortex (GC) during receipt of gustatory stimul
30 This study examines how neurons in the mouse gustatory cortex (GC) encode taste information when gust
31 hesis, recording single-neuron activity from gustatory cortex (GC) in rats engaged in a two-alternati
33 ive experimental evidence indicates that the gustatory cortex (GC) is engaged in taste perception, pa
38 es of indirect evidence suggest that primary gustatory cortex (GC) may be a part of a distributed for
40 ties, whether and how response properties of gustatory cortex (GC) neurons change as a function of th
41 somatosensory, and olfactory stimuli in the gustatory cortex (GC) of alert rats before and after ass
42 g of taste has focused on either the primary gustatory cortex (GC) or the orbitofrontal cortex (OFC).
47 om the primary taste thalamus to the primary gustatory cortex (GC) shows distinct properties compared
50 investigated whether neurons in the primary gustatory cortex (GC), a cortical area necessary for tas
55 plored the neural correlates of taste in the gustatory cortex (GC), less is known about its role in e
56 ing that relies on Hebbian mechanisms within gustatory cortex (GC), to show that animals conditioned
57 urons in both basolateral amygdala (BLA) and gustatory cortex (GC)-anatomically interconnected nodes
65 ctivity of single neurons throughout PFC and gustatory cortex (GUS) from two subjects while they perf
67 on of the insular cortex (IC), the so-called gustatory cortex, has a well-established role in the rep
68 tudies investigating taste coding within the gustatory cortex have reported highly segregated, taste-
69 to multimodal chemosensory processing by the gustatory cortex, highlighting the distinct representati
70 l forebrain structures including the insular gustatory cortex (IC), bed nucleus of the stria terminal
71 in general, electrolytic lesions of insular (gustatory) cortex (IC) were combined with immunostaining
72 (N=8), targeting the conventionally defined gustatory cortex in each hemisphere, and were implanted
73 taste types is a defining feature of primary gustatory cortex in other animals, their identification
74 findings do not rule out involvement of the gustatory cortex in palatability processing, they make e
78 enic acid lesions to examine the role of the gustatory cortex in the suppression of CS intake induced
80 In summary, these results suggest that the gustatory cortex is capable of processing multimodal inf
82 e aversion learning by continuously tracking gustatory cortex neuronal taste responses in alert male
83 scriminated behavioral context, whereas deep gustatory cortex neurons encoded the two conditions iden
84 alysis of multielectrode recordings from the gustatory cortex of alert rats revealed ongoing sequence
86 ulus information in LFPs and spikes from the gustatory cortex of awake rats subjected to tastants and
87 his, we recorded single-unit activity in the gustatory cortex of behaving female rats during the intr
88 n mammillary bodies, secondary motor cortex, gustatory cortex, prelimbic prefrontal cortex, orbital c
90 demonstrate that inactivation of the insular gustatory cortex selectively impairs expression of retro
92 ustatory signals interact nonlinearly in the gustatory cortex to enhance the identity coding of both
93 ste responses, and illustrate the ability of gustatory cortex to recapitulate complex behaviours in t
96 g and attention), frontal operculum (primary gustatory cortex) when anticipating palatable food, and
97 mygdala is a taste relay between the primary gustatory cortex, where satiety has no influence on resp
98 cally coupling microelectrode array to rat's gustatory cortex with brain-machine interface (BMI) tech