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