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1 SREB2 expression (hippocampal formation and amygdaloid complex).
2 cleus (Me) is a superficial component of the amygdaloid complex.
3 ods used to define subdivisions of the human amygdaloid complex.
4 f sensory information that occurs within the amygdaloid complex.
5 incides with altered volume and shape of the amygdaloid complex.
6 to the lateral nucleus of the macaque monkey amygdaloid complex.
7 ly involved in feedback inhibition in the BL amygdaloid complex.
8 nerable brain regions of the hippocampus and amygdaloid complex.
9 the bed nucleus of the stria terminalis and amygdaloid complex.
10 nd innervate interneurons in the basolateral amygdaloid complex.
11 gdala (CEm), the major output nucleus of the amygdaloid complex.
12 een suggested to play a role in cochlear and amygdaloid complexes.
14 s found in limbic system areas: (1) extended amygdaloid complex, (2) lateral septum, and (3) infralim
15 adult human subjects was used to investigate amygdaloid complex (AC) activity associated with the sto
18 hypothalamus, the lateral hypothalamus (LH), amygdaloid complex (AD) and thalamus (TH), and to a less
19 PH cortices are also interconnected with the amygdaloid complex, although comparatively little is kno
20 f the anterior and posterior portions of the amygdaloid complex and its surrounding cortical regions
21 cingulate bundle connecting the centromedial amygdaloid complex and middle cingulate cortex to the do
23 with bilateral ibotenic acid lesions of the amygdaloid complex and the hippocampus or were sham oper
24 s mediating anxiety responses, including the amygdaloid complex and the paraventricular hypothalamic
25 describe some quantitative parameters of the amygdaloid complex and their main nuclei that could help
26 ta-opioid receptors is also decreased in the amygdaloid complex and ventral putamen of Alzheimer's di
27 dorsolateral prefrontal cortex, centromedial amygdaloid complex, and middle cingulate cortex volumes
29 Projection neurons of the basolateral (BL) amygdaloid complex are regulated by an intrinsic inhibit
30 n animals implicates stress hormones and the amygdaloid complex as key, interacting modulators of mem
31 ily deactivated sites within the basolateral amygdaloid complex (BLA) or central amygdaloid region (C
32 esent study examined whether the basolateral amygdaloid complex (BLA) participates in the expression
36 hological changes in neuronal density in the amygdaloid complex have been associated with various neu
37 Brain areas analyzed were caudate, putamen, amygdaloid complex, hippocampal formation and various ce
38 ateral lesions restricted to the basolateral amygdaloid complex (i.e., not including the Ce) did not
39 Single-unit activity was recorded from the amygdaloid complex in freely moving rats during an infus
40 as well as the critical contribution of the amygdaloid complex in modulation of memory by emotional
41 btained for the basal ganglia and septal and amygdaloid complexes in amphibians (anamniotic tetrapods
42 on of NK(1) receptor immunoreactivity in the amygdaloid complex, induction of NK(1) receptor endocyto
50 080411 genotype by sex was found in the left amygdaloid complex (male risk allele carriers showed les
52 he medial temporal polar cortex, most of the amygdaloid complex, most or all of the entorhinal cortex
53 azabemide to MAO-B was measured in the right amygdaloid complex of 15 major depressive subjects and 1
54 ns by injecting anterograde tracers into the amygdaloid complex of Macaca fascicularis monkeys and ex
56 ine (DA) transporter and D2 receptors in the amygdaloid complex of subjects with major depression ind
57 nd D2/D3 receptors have been observed in the amygdaloid complex of subjects with major depression.
58 euniens and anterior medial thalamic nuclei, amygdaloid complex, piriform cortex and subfornical orga
59 undant nitrergic cells in the basal ganglia, amygdaloid complex, preoptic area, basal hypothalamus, m
61 We conclude from these observations that the amygdaloid complex provides an excitatory input to areas
63 which include the lateral hypothalamic area, amygdaloid complex, septal-ventral striatal areas, and i
64 the components of the basal ganglia and the amygdaloid complex, the alar and basal hypothalamic regi
66 ing magnetic resonance imaging guidance, the amygdaloid complex was lesioned bilaterally in six rhesu
69 x (Brodmann area 11/32) bilaterally, and the amygdaloid complex were affected, but no significant atr
70 tion could be relayed from the cortex to the amygdaloid complex were investigated by using the antero
71 lesions of the hippocampal formation or the amygdaloid complex were tested on concurrent discriminat
72 l, basal, and accessory basal) nuclei of the amygdaloid complex were the source of most connections b
73 shed afferent to the ventral striatum is the amygdaloid complex, which projects throughout the shell
74 e) plus adjacent portions of the basolateral amygdaloid complex (with either the excitotoxin NMDA or