戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
11 nuous from the nucleus accumbens through the substantia innominata and fundus of the striatum.
12 minata), and lateral SNC (caudal half of the substantia innominata and globus pallidus).
13 BF, including the caudal globus pallidus and substantia innominata and moderate input from the horizo
14 e was negatively associated with V(T) in the substantia innominata and several cortical regions of in
15 nominata, and in a narrow band bordering the substantia innominata and the globus pallidus.
16 l SNC (ventral pallidum and anterior half of substantia innominata), and lateral SNC (caudal half of
17 al area and associated nucleus accumbens and substantia innominata); and behavioral state control (su
18 l limb of diagonal band of Broca, within the substantia innominata, and in a narrow band bordering th
19 pus; claustrum, tania tecta, lateral septum, substantia innominata, and medial and lateral preoptic n
20 (including the nucleus of the diagonal band, substantia innominata, and preoptic region), entopeduncu
21 edial septum, the diagonal band complex, the substantia innominata, and the amygdala of both animals.
22 ol and reward prediction (nucleus accumbens, substantia innominata, and ventral tegmental area), inge
23 al septum, endopiriform nucleus, dorsal BST, substantia innominata, and, most prominently the amygdal
24 f the amygdala, and basal nucleus of Meynert/substantia innominata; and sent efferents to the pons, s
25  the diagonal band nuclei, the sublenticular substantia innominata, bed nucleus of the stria terminal
26 d nuclei, ventral pallidum, globus pallidus, substantia innominata, globus pallidus, and internal cap
27  uncharted territory of the human brain, the substantia innominata, have been identified.
28 ercle, claustrum, nucleus accumbens, septum, substantia innominata, lateral preoptic area, and diagon
29 atomical disconnection of the accumbens, FS, substantia innominata/magnocellular preoptic nucleus (SI
30 ut to the magnocellular preoptic nucleus and substantia innominata (MCPO/SI) in mice and determined t
31 asal forebrain nucleus basalis and posterior substantia innominata (NBM/SI(p)) comprise the major sou
32 d to the nucleus basalis magnocellularis and substantia innominata (NBM/SI) attenuate operant suppres
33 s in the nucleus basalis magnocellularis and substantia innominata (NBM/SI) may be important in media
34  neurons in the globus pallidus, whereas the substantia innominata neurons bore similarities to isode
35                                  Subtypes of substantia innominata neurons could not be distinguished
36                                              Substantia innominata neurons had lower spontaneous firi
37 rizontal limb of the diagonal band (HDB) and substantia innominata/nucleus basalis (SI/NB) following
38  of cholinergic neurons in the contralateral substantia innominata/nucleus basalis (SI/nBM) failed to
39 s that disconnected CeA from the cholinergic substantia innominata/nucleus basalis magnocellularis (S
40 la central nucleus (CEA) and the cholinergic substantia innominata/nucleus basalis magnocellularis (S
41 the cholinergic neurons in the sublenticular substantia innominata/nucleus basalis magnocellularis (S
42 b of the diagonal band of Broca (MS) and the substantia innominata/nucleus basalis of Meynert (SI).
43 ucleus (CeA), the cholinergic neurons of the substantia innominata/nucleus basalis region, and their
44 monstrate that electrical stimulation of the substantia innominata of the basal forebrain phase shift
45 infused into the area of the nucleus basalis/substantia innominata of the basal forebrain.
46 ng with interconnected nucleus accumbens and substantia innominata), orofacial motor control (retroru
47 ypothalamus; lateral habenula; zona incerta; substantia innominata; posterior thalamic nuclei; ventra
48 is indicated that cholinergic neurons of the substantia innominata receive significantly higher numbe
49 f glutamatergic and GABAergic neurons of the substantia innominata (SI) and magnocellular preoptic ar
50 so performed comparing loss of the midbrain, substantia innominata (SI), temporoparietal cortex and h
51 cial expressions activated the sublenticular substantia innominata (SI), where signal increases were
52 sing the medial preoptic area (MPOA) and the substantia innominata (SI).
53 h the external and waist region projected to substantia innominata (SI).
54 septal nucleus, to the nucleus accumbens and substantia innominata, to hypothalamic parts of the beha
55 septum, bed nucleus of the stria terminalis, substantia innominata, various thalamic and hypothalamic
56 oups: somatomotor system (nucleus accumbens, substantia innominata, ventral tegmental area, and retro
57 iven the dense projection from the IL to the substantia innominata-ventral pallidum (SI/VP), an area
58 naptic terminals in the ventral pallidum and substantia innominata were found to establish synaptic s
59          Neurons in the ventral pallidum and substantia innominata were recorded extracellularly, lab