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1 gonal band, magnocellular preoptic area, and substantia innominata).
2 ptal area, the medial preoptic area, and the substantia innominata.
3 edial septal area, medial preoptic area, and substantia innominata.
4 edial preoptic area, medial septal area, and substantia innominata.
5 tral pallidum, the internal capsule, and the substantia innominata.
6 um, the magnocellular preoptic area, and the substantia innominata.
7 BSTju sends dense projections to the caudal substantia innominata, a distinct caudal dorsolateral re
8 e BST, its heaviest inputs are to the caudal substantia innominata and adjacent central amygdalar nuc
9 medial nucleus, formed a continuum with the substantia innominata and bed nucleus of the stria termi
10 ense inputs to the nucleus accumbens, caudal substantia innominata and central amygdalar nucleus, tha
13 BF, including the caudal globus pallidus and substantia innominata and moderate input from the horizo
15 l SNC (ventral pallidum and anterior half of substantia innominata), and lateral SNC (caudal half of
16 al area and associated nucleus accumbens and substantia innominata); and behavioral state control (su
17 l limb of diagonal band of Broca, within the substantia innominata, and in a narrow band bordering th
18 pus; claustrum, tania tecta, lateral septum, substantia innominata, and medial and lateral preoptic n
19 (including the nucleus of the diagonal band, substantia innominata, and preoptic region), entopeduncu
20 edial septum, the diagonal band complex, the substantia innominata, and the amygdala of both animals.
21 ol and reward prediction (nucleus accumbens, substantia innominata, and ventral tegmental area), inge
22 al septum, endopiriform nucleus, dorsal BST, substantia innominata, and, most prominently the amygdal
23 f the amygdala, and basal nucleus of Meynert/substantia innominata; and sent efferents to the pons, s
24 the diagonal band nuclei, the sublenticular substantia innominata, bed nucleus of the stria terminal
25 d nuclei, ventral pallidum, globus pallidus, substantia innominata, globus pallidus, and internal cap
27 ercle, claustrum, nucleus accumbens, septum, substantia innominata, lateral preoptic area, and diagon
28 atomical disconnection of the accumbens, FS, substantia innominata/magnocellular preoptic nucleus (SI
29 ut to the magnocellular preoptic nucleus and substantia innominata (MCPO/SI) in mice and determined t
30 d to the nucleus basalis magnocellularis and substantia innominata (NBM/SI) attenuate operant suppres
31 s in the nucleus basalis magnocellularis and substantia innominata (NBM/SI) may be important in media
32 neurons in the globus pallidus, whereas the substantia innominata neurons bore similarities to isode
35 rizontal limb of the diagonal band (HDB) and substantia innominata/nucleus basalis (SI/NB) following
36 of cholinergic neurons in the contralateral substantia innominata/nucleus basalis (SI/nBM) failed to
37 s that disconnected CeA from the cholinergic substantia innominata/nucleus basalis magnocellularis (S
38 la central nucleus (CEA) and the cholinergic substantia innominata/nucleus basalis magnocellularis (S
39 the cholinergic neurons in the sublenticular substantia innominata/nucleus basalis magnocellularis (S
40 b of the diagonal band of Broca (MS) and the substantia innominata/nucleus basalis of Meynert (SI).
41 ucleus (CeA), the cholinergic neurons of the substantia innominata/nucleus basalis region, and their
42 monstrate that electrical stimulation of the substantia innominata of the basal forebrain phase shift
44 ng with interconnected nucleus accumbens and substantia innominata), orofacial motor control (retroru
45 ypothalamus; lateral habenula; zona incerta; substantia innominata; posterior thalamic nuclei; ventra
46 is indicated that cholinergic neurons of the substantia innominata receive significantly higher numbe
47 f glutamatergic and GABAergic neurons of the substantia innominata (SI) and magnocellular preoptic ar
48 so performed comparing loss of the midbrain, substantia innominata (SI), temporoparietal cortex and h
49 cial expressions activated the sublenticular substantia innominata (SI), where signal increases were
52 septal nucleus, to the nucleus accumbens and substantia innominata, to hypothalamic parts of the beha
53 septum, bed nucleus of the stria terminalis, substantia innominata, various thalamic and hypothalamic
54 oups: somatomotor system (nucleus accumbens, substantia innominata, ventral tegmental area, and retro
55 naptic terminals in the ventral pallidum and substantia innominata were found to establish synaptic s
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