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1 hormone (prepro-TRH) mRNA expression in the paraventricular nucleus of the hypothalamus.
2 ior pituitary and in the median eminence and paraventricular nucleus of the hypothalamus.
3 ex, and the parvocellular subdivision of the paraventricular nucleus of the hypothalamus.
4 bed nucleus of the stria terminalis, and the paraventricular nucleus of the hypothalamus.
5 with high levels of oxidative stress in the paraventricular nucleus of the hypothalamus.
6 reased levels of NPY-immunoreactivity in the paraventricular nucleus of the hypothalamus.
7 tegmentum, the periaqueductal gray, and the paraventricular nucleus of the hypothalamus.
8 in the central nervous system, including the paraventricular nucleus of the hypothalamus.
9 gdala, and the parvocellular division of the paraventricular nucleus of the hypothalamus.
10 effect that is dependent upon VDR within the paraventricular nucleus of the hypothalamus.
11 ssion in the brain that was localized to the paraventricular nucleus of the hypothalamus.
12 er, bed nucleus of the stria terminalis, and paraventricular nucleus of the hypothalamus.
13 mpanied by increased oxytocin release in the paraventricular nucleus of the hypothalamus.
14 olved in the development and function of the paraventricular nucleus of the hypothalamus.
15 parvocellular neurosecretory neurons of the paraventricular nucleus of the hypothalamus.
16 d nucleus of the stria terminalis (BNST) and paraventricular nucleus of the hypothalamus.
17 TS and reduction of GLP-1 innervation to the paraventricular nucleus of the hypothalamus.
18 ss responsiveness and transcriptomics of the paraventricular nucleus of the hypothalamus.
19 e stria terminalis, and medial parvocellular paraventricular nucleus of the hypothalamus.
20 -releasing factor (CRF) immunodensity in the paraventricular nucleus of the hypothalamus.
21 ormation and descending connections from the paraventricular nucleus of the hypothalamus.
22 in releasing hormone-positive neurons in the paraventricular nucleus of the hypothalamus.
23 is enriched in CRF-expressing neurons in the paraventricular nucleus of the hypothalamus.
24 reases in the amygdala and no changes in the paraventricular nucleus of the hypothalamus.
25 ton's nucleus, A7, and the dorsal cap of the paraventricular nucleus of the hypothalamus after longer
26 ate cortex, frontal cortex, caudate-putamen, paraventricular nucleus of the hypothalamus, amygdala, a
27 groups A1, A1/C1, C1, C3, and A6 and in the paraventricular nucleus of the hypothalamus and adrenal
29 injection, c-fos appeared exclusively in the paraventricular nucleus of the hypothalamus and central
30 ornical organ and area postrema) and inside (paraventricular nucleus of the hypothalamus and nucleus
31 mmunication in hypertension originating from paraventricular nucleus of the hypothalamus and presenti
32 n releasing factor-containing neurons of the paraventricular nucleus of the hypothalamus and primaril
33 hypothalamus with discrete expression in the paraventricular nucleus of the hypothalamus and supraopt
34 e made to quantify the c-fos response in the paraventricular nucleus of the hypothalamus and the CA1/
35 ing was significantly greater in the AH, the paraventricular nucleus of the hypothalamus and the late
36 sympathoexcitatory brain centres such as the paraventricular nucleus of the hypothalamus and the rost
37 found that PACAP increased CRF levels in the paraventricular nucleus of the hypothalamus and, importa
38 nce or delay in the light cycle, the pineal, paraventricular nucleus of the hypothalamus, and arcuate
39 us tractus solitarius, parabrachial nucleus, paraventricular nucleus of the hypothalamus, and supraop
40 tromedial nucleus; arcuate nucleus; anterior paraventricular nucleus of the hypothalamus; and medial
41 ntified in 11 of 40 brain regions, including paraventricular nucleus of the hypothalamus; anterior an
42 tive axonal projections and terminals in the paraventricular nucleus of the hypothalamus, arcuate nuc
43 e mouse, oxytocin-containing neurones in the paraventricular nucleus of the hypothalamus are activate
45 c and anorexigenic neural projections to the paraventricular nucleus of the hypothalamus at PN 28.
46 is highly expressed in the preoptic area and paraventricular nucleus of the hypothalamus, both region
47 lateral bed nucleus of the stria terminalis, paraventricular nucleus of the hypothalamus, dorsal late
48 hat knockdown of VP and OT production in the paraventricular nucleus of the hypothalamus exerts diver
49 stinct from that of Utx, specifically in the paraventricular nucleus of the hypothalamus (high Uty) a
50 tivate c-fos expression in the hind brain or paraventricular nucleus of the hypothalamus indicating t
51 its from the medial geniculate nuclei to the paraventricular nucleus of the hypothalamus involved in
52 ular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalamus, IPe, arcuat
53 in-releasing hormone (CRH) released from the paraventricular nucleus of the hypothalamus is a major r
54 -releasing factor type 1 receptor within the paraventricular nucleus of the hypothalamus is an import
55 l cortices, taenia tecta, nucleus accumbens, paraventricular nucleus of the hypothalamus, medial nucl
56 d nucleus of the stria terminalis, amygdala, paraventricular nucleus of the hypothalamus, median preo
57 gh level of Fos-like immunoreactivity in the paraventricular nucleus of the hypothalamus over 1.5-3 h
59 ion between the circumventricular organs and paraventricular nucleus of the hypothalamus (PVH) and th
60 monstrate that individual neurons within the paraventricular nucleus of the hypothalamus (PVH) are ca
61 ve absent Crh mRNA and peptide mainly in the paraventricular nucleus of the hypothalamus (PVH) but pr
62 its were identified in subpopulations of the paraventricular nucleus of the hypothalamus (PVH) by dou
66 radiofrequency (RF) lesions were made in the paraventricular nucleus of the hypothalamus (PVH) of mal
67 aporin (SAP), or saline bilaterally into the paraventricular nucleus of the hypothalamus (PVH) or spi
69 e mediation of activational responses of the paraventricular nucleus of the hypothalamus (PVH) provok
71 ed mainly to the hypothalamus, including the paraventricular nucleus of the hypothalamus (PVH), later
72 altered POMC projections to the preautonomic paraventricular nucleus of the hypothalamus (PVH), pancr
73 utonomic nervous system, particularly in the paraventricular nucleus of the hypothalamus (PVH), play
74 ons provide a distinctive innervation of the paraventricular nucleus of the hypothalamus (PVH), with
83 es in the anterior parvicellular part of the paraventricular nucleus of the hypothalamus (PVHap) and
84 gdala (CeA) and, to a smaller extent, in the paraventricular nucleus of the hypothalamus (PVN) (5.2-,
85 xpression of IRS2 and TRPV1 receptors in the paraventricular nucleus of the hypothalamus (PVN) and do
86 cotropin-releasing hormone (CRH) mRNA in the paraventricular nucleus of the hypothalamus (PVN) and in
87 a) produces a functional response within the paraventricular nucleus of the hypothalamus (PVN) and le
88 reduced binding of both radioligands in the paraventricular nucleus of the hypothalamus (PVN) and me
89 tressors and are found within neurons of the paraventricular nucleus of the hypothalamus (PVN) and se
90 te nucleus, nucleus tractus solitarii (NTS), paraventricular nucleus of the hypothalamus (PVN) and su
91 ime, ethanol-induced c-Fos expression in the paraventricular nucleus of the hypothalamus (PVN) and th
94 e stress-related brain nuclei, including the paraventricular nucleus of the hypothalamus (PVN) and th
96 ation of firing activity of neurons from the paraventricular nucleus of the hypothalamus (PVN) by alp
97 and noradrenergic neural projections to the paraventricular nucleus of the hypothalamus (PVN) contri
98 d female rats, nanoinjection of NPY into the paraventricular nucleus of the hypothalamus (PVN) dose-d
99 ERalpha and produce vasopressin (AVP) in the paraventricular nucleus of the hypothalamus (PVN) in new
100 is critical for energy homeostasis, and the paraventricular nucleus of the hypothalamus (PVN) is a k
103 d the Cre/lox system to delete AT1a from the paraventricular nucleus of the hypothalamus (PVN) of mic
104 ction of c-Fos immunoreactivity found in the paraventricular nucleus of the hypothalamus (PVN) of wil
107 ation, a subpopulation of CRH neurons in the paraventricular nucleus of the hypothalamus (PVN) were s
108 e hypocretin neurons project directly to the paraventricular nucleus of the hypothalamus (PVN), and S
109 BST), central nucleus of the amygdala (CEA), paraventricular nucleus of the hypothalamus (PVN), and t
110 e profile of noradrenergic activity with the paraventricular nucleus of the hypothalamus (PVN), and t
111 bed nucleus of the stria terminalis (BNST), paraventricular nucleus of the hypothalamus (PVN), centr
112 tal cortex, striatum, nucleus accumbens, and paraventricular nucleus of the hypothalamus (PVN), in bo
113 ased the number of Fos positive cells in the paraventricular nucleus of the hypothalamus (PVN), nucle
114 and Fos immunoreactivity was measured in the paraventricular nucleus of the hypothalamus (PVN), the p
115 Bilateral nanoinjection of SHU9119 into the paraventricular nucleus of the hypothalamus (PVN), to bl
116 the hindbrain send robust projections to the paraventricular nucleus of the hypothalamus (PVN), which
127 ation of GLP-1 into the arcuate, but not the paraventricular, nucleus of the hypothalamus reduced hep
128 l sympathetic premotor nuclei, including the paraventricular nucleus of the hypothalamus, rostral and
129 dditionally, beta-EP administration into the paraventricular nucleus of the hypothalamus stimulated N
130 ective activation of oxytocin neurons in the paraventricular nucleus of the hypothalamus stimulates i
131 ignificant decrease in AT1 expression in the paraventricular nucleus of the hypothalamus, subfornical
132 served in the nucleus of the solitary tract, paraventricular nucleus of the hypothalamus, supraoptic
133 he number of Fos immunoreactive cells in the paraventricular nucleus of the hypothalamus, supraoptic
134 keting areas: the anterior and posterior LH, paraventricular nucleus of the hypothalamus, thalamus, a
135 g there make appositions onto neurons in the paraventricular nucleus of the hypothalamus that are als
136 6 hours after LPS included the parvocellular paraventricular nucleus of the hypothalamus, the bed nuc
137 leasing hormone (Crh) gene expression in the paraventricular nucleus of the hypothalamus, the central
138 n type-1a receptor-containing neurons of the paraventricular nucleus of the hypothalamus, the goal be
139 nucleus tractus solitarius, locus coeruleus, paraventricular nucleus of the hypothalamus, the interme
140 aoptic nucleus, magnocellular regions of the paraventricular nucleus of the hypothalamus, the subforn
141 ld-restraint in the raphe pallidus (Rpa) and paraventricular nucleus of the hypothalamus was not alte
142 lly activated by GLP-1 administration in the paraventricular nucleus of the hypothalamus, whereas the
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