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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.
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 tron microscopic examination of the anterior basolateral nucleus (BLa) revealed that 5-HT+ axon termi
14 ynaptic transmission in projections from the basolateral nucleus (BLA) to the CeL, while inhibitory t
16 analyzed in the posterior subdivision of the basolateral nucleus (BLp), which is densely innervated b
17 sensitization of noradrenergic receptors on basolateral nucleus efferents has wide-ranging implicati
18 to mediate distinct incentive processes: the basolateral nucleus encodes emotional events with refere
19 n neurons in the anterior subdivision of the basolateral nucleus exhibited low levels of CCK immunore
21 number of glia, as well as the volume of the basolateral nucleus, increases between adulthood and old
22 terminals in the anterior subdivision of the basolateral nucleus innervated interneurons that were ei
24 We have previously shown that activity in basolateral nucleus of amygdala (ABL) responds to unexpe
28 orted that these effects depend on an intact basolateral nucleus of the amygdala (BLA) and efferents
29 nd spine density of pyramidal neurons in the basolateral nucleus of the amygdala (BLA) and increased
33 nal-regulated kinase (ERK) activation in the basolateral nucleus of the amygdala (BLA) and was necess
34 nucleus of the solitary tract; NTS) and the basolateral nucleus of the amygdala (BLA) are active ear
36 tage-gated calcium channels (L-VGCCs) in the basolateral nucleus of the amygdala (BLA) are necessary
37 ed that bilateral excitotoxic lesions of the basolateral nucleus of the amygdala (BLA) block the enha
38 atergic inputs onto pyramidal neurons in the basolateral nucleus of the amygdala (BLA) contribute to
41 in releasing factor (CRF), injected into the basolateral nucleus of the amygdala (BLA) in male Wistar
42 y of pharmaco-behavioral data implicates the basolateral nucleus of the amygdala (BLA) in the facilit
44 ntagonist) administered bilaterally into the basolateral nucleus of the amygdala (BLA) of male Spragu
45 cally attenuating the activity of either the basolateral nucleus of the amygdala (BLA) or the ventral
46 ed whether blocking of NMDA receptors in the basolateral nucleus of the amygdala (BLA) prevents new f
47 ated administration of NPY directly into the basolateral nucleus of the amygdala (BLA) produces selec
48 tween the orbitofrontal cortex (OFC) and the basolateral nucleus of the amygdala (BLA) provide a crit
52 ynaptic connectivity of the pathway from the basolateral nucleus of the amygdala (BLA) to the medial
53 e central nucleus of the amygdala (CeA), the basolateral nucleus of the amygdala (BlA), or the bed nu
54 smission in projections from the mPFC to the basolateral nucleus of the amygdala (BLA), whereas inhib
60 grams) was bilaterally administered into the basolateral nucleus of the amygdala and evoked clear-cut
61 l and medial-dorsal thalamic nuclei, and the basolateral nucleus of the amygdala before training.
62 planted with bilateral cannulae aimed at the basolateral nucleus of the amygdala complex and infused
65 ion of post-synaptic 5-HT1A receptors in the basolateral nucleus of the amygdala may produce anxiogen
66 ons between the orbitofrontal cortex and the basolateral nucleus of the amygdala may provide a critic
67 stereotaxically placed within the posterior basolateral nucleus of the amygdala of rats at successiv
68 ents examining the effects of lesions of the basolateral nucleus of the amygdala on the glucocorticoi
70 BA receptor agonist muscimol centered in the basolateral nucleus of the amygdala was given to inactiv
71 Phaseolus vulgaris leucoagglutinin into the basolateral nucleus of the amygdala), with the dendritic
72 %) and alpha1 transcript levels (63%) in the basolateral nucleus of the amygdala, and [(3)H]Ro 15-178
73 region of the hippocampus, as well as in the basolateral nucleus of the amygdala, than did ovariectom
75 sites in the CA1 region of the hippocampus, basolateral nucleus of the amygdala, ventral tegmental a
81 d that at least 85-95% of the neurons in the basolateral nucleus projecting to the prefrontal cortex
82 abeled fibers originating from the posterior basolateral nucleus shows a sharp curvilinear increase w
83 6 amygdala neurons, located primarily in the basolateral nucleus that responded linearly to the value
84 % of aspartate-immunoreactive neurons in the basolateral nucleus were also glutamate positive and tha
85 hough a few in the anteroventral part of the basolateral nucleus were associated with larger pyramida
86 Less dense labelling was observed in the basolateral nucleus, where it was possible to clearly vi
87 versive learning is mediated by the amygdala basolateral nucleus whereas performance, in this case of
88 was widely and uniformly distributed in the basolateral nucleus, with both pyramidal and non-pyramid
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