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1 an effect particularly evident in the dorsal basolateral nucleus.
2  dorsolateral lateral nucleus, and posterior basolateral nucleus.
3 s and that Te2, but not Te3, projects to the basolateral nucleus.
4 ucleus and the adjacent part of the anterior basolateral nucleus.
5                                       In the basolateral nucleus 72% of somatostatin (SOM), 73% of pa
6                           Projections to the basolateral nucleus arose from superfical layers (mostly
7 e lesions of the central nucleus (CE) or the basolateral nucleus (BA) of the amygdala in rats followe
8 ase in the number of neurons and glia in the basolateral nucleus between adolescence and adulthood; a
9 is expressed in the BLA, particularly in the basolateral nucleus (BL), in male and female rodents.
10 raining lesions of the basal nuclei [BM plus basolateral nucleus (BL)] abolish conditioned fear respo
11 es excitatory and inhibitory inputs from the basolateral nucleus (BLA) and serotonin receptor subtype
12 carinic receptors (M2Rs) in the rat anterior basolateral nucleus (BLa) is critical for the consolidat
13                       The amygdalar anterior basolateral nucleus (BLa) plays a vital role in emotiona
14 tron microscopic examination of the anterior basolateral nucleus (BLa) revealed that 5-HT+ axon termi
15 ynaptic transmission in projections from the basolateral nucleus (BLA) to the CeL, while inhibitory t
16  terminals onto pyramidal neurons in the rat basolateral nucleus (BLa).
17 analyzed in the posterior subdivision of the basolateral nucleus (BLp), which is densely innervated b
18  sensitization of noradrenergic receptors on basolateral nucleus efferents has wide-ranging implicati
19 to mediate distinct incentive processes: the basolateral nucleus encodes emotional events with refere
20 n neurons in the anterior subdivision of the basolateral nucleus exhibited low levels of CCK immunore
21                                   PNs in the basolateral nucleus, identified in vitro by their distin
22 number of glia, as well as the volume of the basolateral nucleus, increases between adulthood and old
23 terminals in the anterior subdivision of the basolateral nucleus innervated interneurons that were ei
24                In addition, aging of the rat basolateral nucleus is accompanied by significant increa
25    We have previously shown that activity in basolateral nucleus of amygdala (ABL) responds to unexpe
26 l cortices; to nucleus accumbens; and to the basolateral nucleus of amygdala.
27 es of norepinephrine were collected from the basolateral nucleus of male Sprague-Dawley rats.
28    One of the main subcortical inputs to the basolateral nucleus of the amygdala (BL) originates from
29                                          The basolateral nucleus of the amygdala (BL) receives LA inp
30 orted that these effects depend on an intact basolateral nucleus of the amygdala (BLA) and efferents
31 nd spine density of pyramidal neurons in the basolateral nucleus of the amygdala (BLA) and increased
32                                          The basolateral nucleus of the amygdala (BLA) and medial pre
33                                          The basolateral nucleus of the amygdala (BLA) and prelimbic
34                                          The basolateral nucleus of the amygdala (BLA) and the orbito
35 nal-regulated kinase (ERK) activation in the basolateral nucleus of the amygdala (BLA) and was necess
36  nucleus of the solitary tract; NTS) and the basolateral nucleus of the amygdala (BLA) are active ear
37           The orbitofrontal cortex (OFC) and basolateral nucleus of the amygdala (BLA) are important
38 tage-gated calcium channels (L-VGCCs) in the basolateral nucleus of the amygdala (BLA) are necessary
39 ed that bilateral excitotoxic lesions of the basolateral nucleus of the amygdala (BLA) block the enha
40 atergic inputs onto pyramidal neurons in the basolateral nucleus of the amygdala (BLA) contribute to
41                                          The basolateral nucleus of the amygdala (BLA) has been impli
42 y portion of the insular cortex (GC) and the basolateral nucleus of the amygdala (BLA) however, its s
43       Stimulating mu opioid receptors in the basolateral nucleus of the amygdala (BLA) in anesthetize
44 in releasing factor (CRF), injected into the basolateral nucleus of the amygdala (BLA) in male Wistar
45 y of pharmaco-behavioral data implicates the basolateral nucleus of the amygdala (BLA) in the facilit
46                                          The basolateral nucleus of the amygdala (BLA) modulates memo
47 ntagonist) administered bilaterally into the basolateral nucleus of the amygdala (BLA) of male Spragu
48 cally attenuating the activity of either the basolateral nucleus of the amygdala (BLA) or the ventral
49 ed whether blocking of NMDA receptors in the basolateral nucleus of the amygdala (BLA) prevents new f
50 ated administration of NPY directly into the basolateral nucleus of the amygdala (BLA) produces selec
51 tween the orbitofrontal cortex (OFC) and the basolateral nucleus of the amygdala (BLA) provide a crit
52                                          The basolateral nucleus of the amygdala (BLA) receives dense
53                    Individual neurons in the basolateral nucleus of the amygdala (BLA) responded to b
54                         Projections from the basolateral nucleus of the amygdala (BLA) to the cortex
55 ynaptic connectivity of the pathway from the basolateral nucleus of the amygdala (BLA) to the medial
56 e central nucleus of the amygdala (CeA), the basolateral nucleus of the amygdala (BlA), or the bed nu
57 smission in projections from the mPFC to the basolateral nucleus of the amygdala (BLA), whereas inhib
58 (BFc) neurons send a dense projection to the basolateral nucleus of the amygdala (BLA).
59 reases extracellular glutamate levels in the basolateral nucleus of the amygdala (BLA).
60 h an activation of beta-adrenoceptors in the basolateral nucleus of the amygdala (BLA).
61 ry cortex (GC) receives projections from the basolateral nucleus of the amygdala (BLA).
62            PCDH10 is highly expressed in the basolateral nucleus of the amygdala (BLA).
63 d in the developing brain, especially in the basolateral nucleus of the amygdala (BLA).
64  the medial prefrontal cortex (mPFC) and the basolateral nucleus of the amygdala (BLN).
65 grams) was bilaterally administered into the basolateral nucleus of the amygdala and evoked clear-cut
66 l and medial-dorsal thalamic nuclei, and the basolateral nucleus of the amygdala before training.
67 planted with bilateral cannulae aimed at the basolateral nucleus of the amygdala complex and infused
68                                      The rat basolateral nucleus of the amygdala continues to develop
69                                The posterior basolateral nucleus of the amygdala is known to mediate
70 ion of post-synaptic 5-HT1A receptors in the basolateral nucleus of the amygdala may produce anxiogen
71 ons between the orbitofrontal cortex and the basolateral nucleus of the amygdala may provide a critic
72  stereotaxically placed within the posterior basolateral nucleus of the amygdala of rats at successiv
73 ents examining the effects of lesions of the basolateral nucleus of the amygdala on the glucocorticoi
74                                          The basolateral nucleus of the amygdala receives an extremel
75 BA receptor agonist muscimol centered in the basolateral nucleus of the amygdala was given to inactiv
76  Phaseolus vulgaris leucoagglutinin into the basolateral nucleus of the amygdala), with the dendritic
77 %) and alpha1 transcript levels (63%) in the basolateral nucleus of the amygdala, and [(3)H]Ro 15-178
78 region of the hippocampus, as well as in the basolateral nucleus of the amygdala, than did ovariectom
79            We examine the involvement of the basolateral nucleus of the amygdala, the central nucleus
80  sites in the CA1 region of the hippocampus, basolateral nucleus of the amygdala, ventral tegmental a
81 ed the ratio of gamma2L/S transcripts in the basolateral nucleus of the amygdala.
82  transduction mechanisms, potentially in the basolateral nucleus of the amygdala.
83 , in area CA1 of the hippocampus, and in the basolateral nucleus of the amygdala.
84 elective vulnerability of neurons within the basolateral nucleus of the amygdala.
85  acid (1S,3R-ACPD) were characterized in the basolateral nucleus of the amygdala.
86 f fear neurons and extinction neurons in the basolateral nucleus of the basal amygdala (BA(L)) has be
87 d that at least 85-95% of the neurons in the basolateral nucleus projecting to the prefrontal cortex
88 abeled fibers originating from the posterior basolateral nucleus shows a sharp curvilinear increase w
89 6 amygdala neurons, located primarily in the basolateral nucleus that responded linearly to the value
90 % of aspartate-immunoreactive neurons in the basolateral nucleus were also glutamate positive and tha
91 hough a few in the anteroventral part of the basolateral nucleus were associated with larger pyramida
92     Less dense labelling was observed in the basolateral nucleus, where it was possible to clearly vi
93 versive learning is mediated by the amygdala basolateral nucleus whereas performance, in this case of
94 heavily innervated the intrinsic paralaminar basolateral nucleus, which is associated with plasticity
95  was widely and uniformly distributed in the basolateral nucleus, with both pyramidal and non-pyramid