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1 al excitability in projection neurons in the lateral nucleus of the amygdala.
2 ment-binding proteins (CREB) in cells of the lateral nucleus of the amygdala.
3 included bidirectional connections with the lateral nucleus of the amygdala, afferent inputs from th
5 cal layers 5, 6, hippocampal layers CA(2,3), lateral nucleus of the amygdala and in the dorsal raphe
6 zinc-containing neurons, is enriched in the lateral nucleus of the amygdala and in the temporal area
9 out the auditory conditioned stimulus to the lateral nucleus of the amygdala, but not in other condit
10 ting depression of CS-evoked activity in the lateral nucleus of the amygdala, consistent with fear re
11 cluding in the NTS, AP, lateral PBN, central lateral nucleus of the amygdala, dorsal lateral bed nucl
12 trema, lateral parabrachial nucleus, central lateral nucleus of the amygdala, dorsal lateral bed nucl
13 known about the behavioral importance of the lateral nucleus of the amygdala for the storage of impli
14 e report that synapses in projections to the lateral nucleus of the amygdala implicated in auditory f
15 n contrast, FAE increased 5-HTT sites in the lateral nucleus of the amygdala in the adult animal, sug
16 erm potentiation (LTP) can be induced in the lateral nucleus of the amygdala (LA) after stimulation o
18 alized to dendritic shafts and spines in the lateral nucleus of the amygdala (LA) and is postsynaptic
19 that Arc/Arg3.1 protein is regulated in the lateral nucleus of the amygdala (LA) by retrieval of an
20 tion from the posterior thalamus reaches the lateral nucleus of the amygdala (LA) by way of two pathw
21 that transmit auditory CS information to the lateral nucleus of the amygdala (LA) increases auditory-
25 inputs converging on a single neuron in the lateral nucleus of the amygdala (LA) is only modified wh
26 suggests that synaptic plasticity within the lateral nucleus of the amygdala (LA) may be responsible
27 on in the medial geniculate nucleus (MGN) to lateral nucleus of the amygdala (LA) pathway, a key segm
29 , NGFI-A, Zif 268, Krox 24) increases in the lateral nucleus of the amygdala (LA) shortly following c
32 neutral and aversive stimuli converge in the lateral nucleus of the amygdala (LA), in which alteratio
36 anoate (AP7), into either central nucleus or lateral nucleus of the amygdala (LAMG) significantly red
37 cortical and thalamic auditory inputs to the lateral nucleus of the amygdala (LAn) mediate encoding o
39 stimuli enhances activity of neurons in the lateral nucleus of the amygdala (LAT), which is thought
40 ogical recording techniques to show that the lateral nucleus of the amygdala, long thought to be crit
41 ptor glycine site agonist at synapses in the lateral nucleus of the amygdala may depend on the level
44 ptide, as being highly expressed both in the lateral nucleus of the amygdala, the nucleus where assoc
45 lack of TRPC4 potentiation in neurons in the lateral nucleus of the amygdala through two Galphaq/11 p
46 on important for some forms of learning, the lateral nucleus of the amygdala, using in vivo intracell
47 el of emotional learning, is conveyed to the lateral nucleus of the amygdala via two routes: directly
48 rast to c-fos, NGFI-A mRNA expression in the lateral nucleus of the amygdala was greater in the delay
49 potentiation (LTP) in auditory inputs to the lateral nucleus of the amygdala was recently linked to t
50 H-BP containing cells in the basolateral and lateral nucleus of the amygdala were lower in 24-month-o
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