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1  the subregion approximating the dysgranular gustatory cortex.
2 gation in the functional architecture of the gustatory cortex.
3 ngly similar to those previously observed in gustatory cortex.
4 l PbN and transmits taste information to the gustatory cortex.
5  synaptic properties of the BLA input to the gustatory cortex.
6 s show that bilateral lesions of the insular gustatory cortex (1) fully prevent the suppressive effec
7 al taste reactivity behavior, lesions of the gustatory cortex, a region that has been suggested to be
8 c subjects because the insula is the primary gustatory cortex and has repeatedly been implicated in t
9 irst, we demonstrate that ZIP infusions into gustatory cortex begin interfering with CTA memory 43-45
10 stimulated neurons were found throughout the gustatory cortex, but a "hot spot" was observed in its a
11 et and bitter are represented in the primary gustatory cortex by neurons organized in a spatial map,
12                Here we found that neurons in gustatory cortex can respond either exclusively to tasta
13 ces of discrete states of neural activity in gustatory cortex during taste processing.
14 local microinjection of PKR inhibitor to the gustatory cortex enhanced both positive and negative for
15 activity from neuronal ensembles in primary [gustatory cortex GC)] and secondary gustatory [orbitofro
16 n two sites vital for NaCl taste processing, gustatory cortex (GC) and central amygdala (CeA).
17 neuroimaging experiments have pointed to the gustatory cortex (GC) as one of the areas involved in me
18  signal revealed that neurons in the primary gustatory cortex (GC) can respond to anticipatory cues.
19 by examining the role of neural ensembles in gustatory cortex (GC) during receipt of gustatory stimul
20 hesis, recording single-neuron activity from gustatory cortex (GC) in rats engaged in a two-alternati
21                                      Primary gustatory cortex (GC) is connected (both mono- and polys
22                                          The gustatory cortex (GC) is important for perceiving the in
23                                          The gustatory cortex (GC) is widely regarded for its integra
24 es of indirect evidence suggest that primary gustatory cortex (GC) may be a part of a distributed for
25               Here, we provide evidence that gustatory cortex (GC) may be part of the forebrain circu
26  somatosensory, and olfactory stimuli in the gustatory cortex (GC) of alert rats before and after ass
27 g of taste has focused on either the primary gustatory cortex (GC) or the orbitofrontal cortex (OFC).
28                                  The primary gustatory cortex (GC) receives projections from the baso
29        Taste-related information reaches the gustatory cortex (GC) through two routes: a thalamic and
30  investigated whether neurons in the primary gustatory cortex (GC), a cortical area necessary for tas
31                                              Gustatory cortex (GC), an assemblage of taste-responsive
32        Rostral forebrain structures like the gustatory cortex (GC), bed nucleus of the stria terminal
33 urons in both basolateral amygdala (BLA) and gustatory cortex (GC)-anatomically interconnected nodes
34 n the brainstem and sends projections to the gustatory cortex (GC).
35 out the organization of taste information in gustatory cortex (GC).
36 luences processing of sensory stimuli in the gustatory cortex (GC).
37 cordings made in oral somatosensory (SI) and gustatory cortex (GC).
38 ctivity of single neurons throughout PFC and gustatory cortex (GUS) from two subjects while they perf
39                                  The primary gustatory cortex has been proposed to integrate chemosen
40 tudies investigating taste coding within the gustatory cortex have reported highly segregated, taste-
41 l forebrain structures including the insular gustatory cortex (IC), bed nucleus of the stria terminal
42 in general, electrolytic lesions of insular (gustatory) cortex (IC) were combined with immunostaining
43  (N=8), targeting the conventionally defined gustatory cortex in each hemisphere, and were implanted
44  findings do not rule out involvement of the gustatory cortex in palatability processing, they make e
45 ough multiple neural stations to the primary gustatory cortex in the brain.
46 enic acid lesions to examine the role of the gustatory cortex in the suppression of CS intake induced
47           Besides homeostatic processes, the gustatory cortex, including parts of the insular cortex,
48   In summary, these results suggest that the gustatory cortex is capable of processing multimodal inf
49 among tastes can occur in the absence of the gustatory cortex necessary for taste recognition.
50 scriminated behavioral context, whereas deep gustatory cortex neurons encoded the two conditions iden
51 alysis of multielectrode recordings from the gustatory cortex of alert rats revealed ongoing sequence
52 ulus information in LFPs and spikes from the gustatory cortex of awake rats subjected to tastants and
53 n mammillary bodies, secondary motor cortex, gustatory cortex, prelimbic prefrontal cortex, orbital c
54        Altogether, our results show that the gustatory cortex represents cross-modal stimuli accordin
55                                           In gustatory cortex, single-neuron activity reflects the mu
56 ste responses, and illustrate the ability of gustatory cortex to recapitulate complex behaviours in t
57 d that, on average, approximately 94% of the gustatory cortex was destroyed.
58 g and attention), frontal operculum (primary gustatory cortex) when anticipating palatable food, and
59 mygdala is a taste relay between the primary gustatory cortex, where satiety has no influence on resp
60 cally coupling microelectrode array to rat's gustatory cortex with brain-machine interface (BMI) tech

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