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1  magnocellular preoptic area, and substantia innominata).
2 the medial preoptic area, and the substantia innominata.
3 l area, medial preoptic area, and substantia innominata.
4 tic area, medial septal area, and substantia innominata.
5 um, the internal capsule, and the substantia innominata.
6 nocellular preoptic area, and the substantia innominata.
7 s dense projections to the caudal substantia innominata, a distinct caudal dorsolateral region of the
8 heaviest inputs are to the caudal substantia innominata and adjacent central amygdalar nucleus, retro
9 leus, formed a continuum with the substantia innominata and bed nucleus of the stria terminalis, supp
10  to the nucleus accumbens, caudal substantia innominata and central amygdalar nucleus, thalamic parav
11 the nucleus accumbens through the substantia innominata and fundus of the striatum.
12 d lateral SNC (caudal half of the substantia innominata and globus pallidus).
13 ng the caudal globus pallidus and substantia innominata and moderate input from the horizontal limb o
14 ively associated with V(T) in the substantia innominata and several cortical regions of interest incl
15 nd in a narrow band bordering the substantia innominata and the globus pallidus.
16 ral pallidum and anterior half of substantia innominata), and lateral SNC (caudal half of the substan
17  associated nucleus accumbens and substantia innominata); and behavioral state control (supramammilla
18 iagonal band of Broca, within the substantia innominata, and in a narrow band bordering the substanti
19 rum, tania tecta, lateral septum, substantia innominata, and medial and lateral preoptic nuclei of th
20 the nucleus of the diagonal band, substantia innominata, and preoptic region), entopeduncular nucleus
21 m, the diagonal band complex, the substantia innominata, and the amygdala of both animals.
22 rd prediction (nucleus accumbens, substantia innominata, and ventral tegmental area), ingestive behav
23 endopiriform nucleus, dorsal BST, substantia innominata, and, most prominently the amygdala--primaril
24 ala, and basal nucleus of Meynert/substantia innominata; and sent efferents to the pons, superior col
25 al band nuclei, the sublenticular substantia innominata, bed nucleus of the stria terminalis, ventral
26 entral pallidum, globus pallidus, substantia innominata, globus pallidus, and internal capsule, where
27 territory of the human brain, the substantia innominata, have been identified.
28 strum, nucleus accumbens, septum, substantia innominata, lateral preoptic area, and diagonal band nuc
29 sconnection of the accumbens, FS, substantia innominata/magnocellular preoptic nucleus (SI/MA), and b
30 agnocellular preoptic nucleus and substantia innominata (MCPO/SI) in mice and determined the effects
31 ain nucleus basalis and posterior substantia innominata (NBM/SI(p)) comprise the major source of chol
32 cleus basalis magnocellularis and substantia innominata (NBM/SI) attenuate operant suppression induce
33 cleus basalis magnocellularis and substantia innominata (NBM/SI) may be important in mediating aversi
34  the globus pallidus, whereas the substantia innominata neurons bore similarities to isodendritic neu
35                       Subtypes of substantia innominata neurons could not be distinguished based on a
36                                   Substantia innominata neurons had lower spontaneous firing rates, m
37 mb of the diagonal band (HDB) and substantia innominata/nucleus basalis (SI/NB) following ovariectomy
38 rgic neurons in the contralateral substantia innominata/nucleus basalis (SI/nBM) failed to show the e
39 nucleus (CEA) and the cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) is i
40 onnected CeA from the cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) on p
41 rgic neurons in the sublenticular substantia innominata/nucleus basalis magnocellularis (SI/nBM), as
42 agonal band of Broca (MS) and the substantia innominata/nucleus basalis of Meynert (SI).
43 ), the cholinergic neurons of the substantia innominata/nucleus basalis region, and their innervation
44 hat electrical stimulation of the substantia innominata of the basal forebrain phase shifts the circa
45 o the area of the nucleus basalis/substantia innominata of the basal forebrain.
46 erconnected nucleus accumbens and substantia innominata), orofacial motor control (retrorubral area),
47 ; lateral habenula; zona incerta; substantia innominata; posterior thalamic nuclei; ventral tegmental
48 d that cholinergic neurons of the substantia innominata receive significantly higher numbers of adren
49 rgic and GABAergic neurons of the substantia innominata (SI) and magnocellular preoptic area, but the
50 d comparing loss of the midbrain, substantia innominata (SI), temporoparietal cortex and hippocampus
51 sions activated the sublenticular substantia innominata (SI), where signal increases were observed to
52 dial preoptic area (MPOA) and the substantia innominata (SI).
53 nal and waist region projected to substantia innominata (SI).
54 eus, to the nucleus accumbens and substantia innominata, to hypothalamic parts of the behavior contro
55  nucleus of the stria terminalis, substantia innominata, various thalamic and hypothalamic nuclei, pe
56 omotor system (nucleus accumbens, substantia innominata, ventral tegmental area, and retrorubral area
57 nse projection from the IL to the substantia innominata-ventral pallidum (SI/VP), an area that proces
58 inals in the ventral pallidum and substantia innominata were found to establish synaptic specializati
59 urons in the ventral pallidum and substantia innominata were recorded extracellularly, labeled juxtac