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1 nd of Broca, nucleus basalis of Meynert, bed nucleus of stria terminalis, amygdala, and hippocampus.
2 ll as subcortical structures such as the bed nucleus of stria terminalis and amygdala.
3 of CRF and noradrenaline transmission in bed nucleus of stria terminalis and central amygdala, and do
4 rated in the central amygdaloid nucleus, bed nucleus of stria terminalis and globus pallidus, followe
5     Some of the AR-containing neurons in bed nucleus of stria terminalis and in the dorsal part of th
6 were observed in the anterior cingulate, bed nucleus of stria terminalis and perirhinal area of oxyto
7 cortex, central nucleus of the amygdala, bed nucleus of stria terminalis, and posterior ventral tegme
8 n the magnocellular basal forebrain, the bed nucleus of stria terminalis, and the anterior hypothalam
9 he infundibular stalk; the amygdala; the bed nucleus of stria terminalis; and the paraolfactory gyrus
10 Ps via implanted DBS electrodes from the bed nucleus of stria terminalis (BNST area) in 12 patients (
11 omitantly alter BI and metabolism in the bed nucleus of stria terminalis (BNST) region and that indiv
12  (MPOA-AH), lateral septal nucleus (LS), bed nucleus of stria terminalis (BNST), and periaqueductal g
13 in stress-related regions, including the bed nucleus of stria terminalis (BNST), which is implicated
14 tration decreased bNOS-ir neurons in the bed nucleus of stria terminalis (BNST).
15  in limbic system structures such as the bed nucleus of stria terminalis (BST) and the medial nucleus
16    Fluorogold was iontophoresed into the bed nucleus of stria terminalis (BST), central nucleus of th
17 ns (core and shell), olfactory tubercle, bed nucleus of stria terminalis (BST), medial, central, cort
18  to the extended amygdala (primarily the bed nucleus of stria terminalis; BST), on the whole, the BST
19 ude the olfactory bulb, cerebral cortex, bed nucleus of stria terminalis, hippocampus, habenular nucl
20 ly that VGAT neurons in the amygdala and bed nucleus of stria terminalis inhibit MCH cells.
21  of the extended amygdala, including the bed nucleus of stria terminalis, interstitial nucleus of the
22 benula, central nucleus of the amygdala, bed nucleus of stria terminalis, lateral septum, and spinal
23 taining neurons in forebrain structures (bed nucleus of stria terminalis, medial preoptic area, later
24  the other examined areas, including the bed nucleus of stria terminalis,medial amygdala, and medial
25 in the MPOA, the caudate-putamen and the bed nucleus of stria terminalis of castrates.
26 and paraventricular hypothalamic nuclei, bed nucleus of stria terminalis, paraventricular thalamic nu
27 immunoreactive terminals examined in the bed nucleus of stria terminalis, parvocellular paraventricul
28 ) and the adjacent posterior part of the bed nucleus of stria terminalis (pBNST).
29 he paraventricular nucleus (PVN) and the bed nucleus of stria terminalis, revealed global pattern cha
30  fibers of varying density were noted in bed nucleus of stria terminalis, septal nuclei, nucleus accu
31 n various nuclei in the basal forebrain (bed nucleus of stria terminalis, septum, parastrial nucleus,
32 put from basal forebrain structures, the bed nucleus of stria terminalis, the lateral preoptic area,
33  medial preoptic area (MPOA) and ventral bed nucleus of stria terminalis (VBST) during maternal behav
34 edial preoptic area; ventral part of the bed nucleus of stria terminalis; ventrolateral division of t

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