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1 ive to LH orexin neurons (not dorsomedial or perifornical).
2 cluding bed nucleus of the stria terminalis, perifornical and anterior hypothalamus, periaqueductal g
3 (LH) and medial hypothalamus (MH, including perifornical and dorsomedial areas) were measured after
4 food and abused drugs, whereas those in the perifornical and dorsomedial hypothalamus regulate arous
5 ropeptides orexin A and B are synthesised by perifornical and lateral hypothalamic (LH) neurones and
6 retin-containing cell bodies, located in the perifornical and lateral hypothalamus, were embedded wit
7 5)I]PYY binding in the hypothalamic lateral (perifornical) and dorsal areas, hypothalamic ventromedia
9 The subfornical organ, dorsal hypothalamic, perifornical, and posterior hypothalamic areas were also
10 te intervals, included lateral hypothalamic, perifornical, and retrochiasmatic areas, anterior and po
11 ucleus), hypothalamus (medial preoptic area, perifornical, arcuate, dorsomedial, parasubthalamic, and
12 distinct axonal projections to the anterior perifornical area (APFx) and the paraventricular nucleus
14 the hypothalamus (PVH), lateral hypothalamus/perifornical area (LH/PFA), and anteroventral periventri
15 xclusively in the PeF-LH, which includes the perifornical area (PeF), the lateral hypothalamus (LH),
16 (VLG and IGL); the lateral hypothalamus and perifornical area (VLG); and the retrochiasmatic area (R
17 dial preoptic nucleus, lateral hypothalamus, perifornical area and in the periventricular region at t
19 d to the lateral hypothalamus and contiguous perifornical area but have widespread projections, inclu
20 e median preoptic nucleus and in the rostral perifornical area lateral to the paraventricular nucleus
21 0.3 microgram) from saline injected into the perifornical area of the hypothalamus (PFA), a process t
22 reviously reported CGRP projections from the perifornical area of the hypothalamus to the lateral sep
24 retin (HCRT) neurons are located only in the perifornical area of the lateral hypothalamus and heavil
25 as (hypothalamic paraventricular nucleus and perifornical area) after Arc denervation and their activ
26 ector of tuberal hypothalamus (including the perifornical area) and increased the percentage of Fos-e
27 ), the dorsomedial nucleus (DMN), LH and the perifornical area, but was ineffective in the arcuate nu
28 group of neurons in the lateral hypothalamus/perifornical area, enhances cognitive arousal and also m
29 N) and in orexin (hypocretin) neurons of the perifornical area, two cell groups implicated in the reg
33 p of neurons in the lateral hypothalamic and perifornical areas, a region classically implicated in t
35 in several hypothalamic areas, including the perifornical, dorsomedial, and paraventricular nuclei, a
36 eeding-related targets of vmPFC, the lateral-perifornical hypothalamic area (LH-PeF) and nucleus accu
37 ely caudal to the PVHap/pBNST in the rostral perifornical hypothalamic area (rPFH) provide only minim
38 numerous retrogradely labeled neurons in the perifornical hypothalamic area, few contained melanin-co
39 viz., paraventricular hypothalamic nucleus, perifornical hypothalamic region, A5 catecholamine cell
42 ccRTN neurons respond to stimulation of the perifornical hypothalamus (PeF), a region that regulates
44 ate (NMDA) receptors in the lateral (LH) and perifornical hypothalamus (PFH) are believed to be invol
45 ar nucleus (PVN) of the hypothalamus and the perifornical hypothalamus (PFH) are sites at which micro
46 4, 78, 235 pmol/10 nl) was injected into the perifornical hypothalamus (PFH) of satiated adult male r
47 eating response when microinjected into the perifornical hypothalamus (PFH) or lateral hypothalamus
48 n A and orexin B were microinjected into the perifornical hypothalamus (PFH), lateral hypothalamus (L
49 nd are most effective when injected into the perifornical hypothalamus (PFH), or into the paraventric
50 widespread forebrain regions, including the perifornical hypothalamus (PFH; 30%), ventromedial hypot
51 xin neurons expressing c-Fos in parts of the perifornical hypothalamus and that neural projections or
53 ibition of GABA synthesis in the dorsomedial-perifornical hypothalamus of rats produces anxiety-like
55 tored Hcrt-1 release in the basal forebrain, perifornical hypothalamus, and locus ceruleus (LC) acros
58 ar nuclei, hypothalamic dorsomedial nucleus, perifornical lateral hypothalamic area, and lateral tegm
60 ontal diagonal bands of Broca (VDB and HDB), perifornical lateral hypothalamus (LH), and ventrolatera
61 ptide, melanin-concentrating hormone, in the perifornical lateral hypothalamus in preweanling offspri
64 The hypocretinergic (HCRT) neurons of the perifornical-lateral hypothalamic area (PF-LHA) and sero
68 neuropeptide synthesized exclusively in the perifornical/lateral hypothalamus, is critical for drug
71 ons by the orexin (hypocretin) system in the perifornical/LH area through the lateral vestibular nucl
74 ypocretin-positive neurons were found in the perifornical nucleus and in the dorsal and lateral hypot
75 area, suprachiasmatic nucleus, anterior BST, perifornical nucleus, and periparaventricular nucleus re
76 y innervate orexin neurons in the medial and perifornical parts of the field, but most projections fr
77 animals suggest that neurones located in the perifornical (PF) region of the posterior hypothalamus p
78 pramammillary nucleus, posterior nucleus and perifornical region of the hypothalamus, midline and int
81 wed that neurons in the lateral, dorsal, and perifornical regions of the tuberal and mammillary level
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