コーパス検索結果 (１語後でソート)
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1 No ATP release was observed in the posterior hypothalamus.
2 discovered hypocretin system located in the posterior hypothalamus.
3 ion, and for neuronal differentiation in the posterior hypothalamus.
4 c axons that originate from perikarya in the posterior hypothalamus.
5 rsomedial nucleus, lateral hypothalamus, and posterior hypothalamus.
6 from the lateral septum, preoptic area, and posterior hypothalamus.
7 +/- 1.4 x 10(-6) ml x g(-1) x ml(-1) at the posterior hypothalamus.
8 the hypothalamus, originating mainly in the posterior hypothalamus.
9 ammillary and retromammillary regions of the posterior hypothalamus.
10 udal to the optic chiasm to the level of the posterior hypothalamus.
11 halamus, whereas SP mRNA predominated in the posterior hypothalamus.
12 , the ventrolateral arcuate nucleus, and the posterior hypothalamus.
13 ly larger lesions involving the anterior and posterior hypothalamus.
14 at the level of the mammillary bodies in the posterior hypothalamus.
15 ives input from histaminergic neurons in the posterior hypothalamus.
16 onomo predicted a wake-promoting area in the posterior hypothalamus and a sleep-promoting region in t
17 significant activation of the contralateral posterior hypothalamus and contralateral ventral midbrai
18 these neurons are widespread throughout the posterior hypothalamus and project to multiple targets i
19 ke immunoreactivity were present in both the posterior hypothalamus and the nucleus of the solitary t
21 function (preoptic nuclei), autonomic tone (posterior hypothalamus), and behavioral/homeostatic inte
22 nd of the canonical pathway expressed in the posterior hypothalamus, and that both Wnt8b and Lef1 act
23 ine D1- and D2-like receptor activity in the posterior hypothalamus/anterior ventral tegmental area (
24 3390 (1-4 mug total bilateral dose) into the posterior hypothalamus/anterior VTA differentially eleva
25 tivity to D1-like receptor antagonism in the posterior hypothalamus/anterior VTA may partly mediate t
26 mug total bilateral dose) injected into the posterior hypothalamus/anterior VTA significantly elevat
28 mammillary nucleus and adjacent parts of the posterior hypothalamus completely rescued the sleepiness
29 into the medial amygdala, nucleus accumbens, posterior hypothalamus, dorsal raphe, and ventral tegmen
30 ajor arousal-promoting system located in the posterior hypothalamus, has never been examined in head
32 confirm the hypothesized involvement of the posterior hypothalamus in the pathophysiology of HH and
33 lei were found in the retrosplenial area the posterior hypothalamus including the supramammillary nuc
34 so identified LHb outputs to the lateral and posterior hypothalamus, median raphe, dorsal raphe, and
37 cleus (MnPO), anterior hypothalamus (AH) and posterior hypothalamus (PH) using a standard ABC immunoc
38 as well as higher expression of GAD67 in the posterior hypothalamus (PH), compared with HSR monkeys.
39 a terminalis, paraventricular nucleus (PVN), posterior hypothalamus, precommissural nucleus, deep mes
40 cated in the perifornical (PF) region of the posterior hypothalamus promote wakefulness and suppress
42 ives input from histaminergic neurons in the posterior hypothalamus that are active during the day.
43 ontal areas primarily labeled neurons in the posterior hypothalamus that were equally distributed in
44 thalamus, and arousal systems located in the posterior hypothalamus, the basal forebrain and the brai
45 uclei, the dorsal and lateral regions of the posterior hypothalamus, the central gray, the cerebellum
47 M2-like immunoreactivity were present in the posterior hypothalamus, whereas those expressing EM1-lik
48 reoptic region, lateral, paraventricular and posterior hypothalamus, zona incerta, periaqueductal gra
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