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1                        The densest target of subfornical axons is the anterior tip of the third ventr
2     Recently, ATII-responsive neurons in the subfornical organ (SFO) and aldosterone-sensitive neuron
3 emide-treated rats showed Fos-IR in both the subfornical organ (SFO) and around the organum vasculosu
4                                          The subfornical organ (SFO) and the area postrema (AP), two
5  the mesencephalic trigeminal nucleus (meV), subfornical organ (SFO) and the external lateral parabra
6 sculosum of the lamina terminalis (OVLT) and subfornical organ (SFO) became infected.
7                                          The subfornical organ (SFO) has been suggested to be importa
8 ted that angiotensinergic stimulation in the subfornical organ (SFO) has effects on the anterior thir
9    Here we reveal an unexpected role for the subfornical organ (SFO) in the anticipatory regulation o
10                                          The subfornical organ (SFO) is a circumventricular organ rec
11                                          The subfornical organ (SFO) is a forebrain structure that co
12                                          The subfornical organ (SFO) of the brain has long been consi
13 of angiotensin Type 1 (AT1) receptors in the subfornical organ (SFO) on this effect.
14 lamic nucleus (PVH), peri-subfornical organ, subfornical organ (SFO) or hippocampus (dentate gyrus an
15 tions in O2*- production specifically in the subfornical organ (SFO), a brain region lying outside th
16  This study examined the hypothesis that the subfornical organ (SFO), a circumventricular organ with
17 gical abnormalities in the circumventricular subfornical organ (SFO), a region outside the blood-brai
18 c paraventricular and supraoptic nuclei, the subfornical organ (SFO), and the organum vasculosum of t
19 anum vasculosum lamina terminalis (OVLT) and subfornical organ (SFO), are potential sites that could
20 lis, including organum vasculosum (OVLT) and subfornical organ (SFO), as well as in the magnocellular
21 V3V), paraventricular hypothalamus (PVN) and subfornical organ (SFO), but unchanged in anterior pitui
22                  Renin induced Fos-ir in the subfornical organ (SFO), median preoptic (MnPO), supraop
23 thors examined the effects of lesions of the subfornical organ (SFO), median preoptic nucleus (MnPO),
24  hypertension, free radical signaling in the subfornical organ (SFO), one of the forebrain circumvent
25 d along the lamina terminalis (LT) (i.e. the subfornical organ (SFO), organum vasculosum (OV) and the
26  Fos-positive cells than control rats in the subfornical organ (SFO), organum vasculosum lamina termi
27 cell nuclei than vehicle-treated rats in the subfornical organ (SFO), organum vasculosum lamina termi
28  nucleus (SON), median preoptic area (MePO), subfornical organ (SFO), organum vasculosum of the lamin
29 alis (OVLT), medial preoptic nucleus (MNPO), subfornical organ (SFO), supraoptic (SON) and paraventri
30 tified in the paraventricular nucleus (PVN), subfornical organ (SFO), supraoptic nucleus (SON), nucle
31 mic ANGII mediates stress responding via the subfornical organ (SFO), we first found that the timing
32 dian preoptic nucleus (MnPO), but not in the subfornical organ (SFO).
33 munoreactivity was markedly increased in the subfornical organ (SFO).
34 ut did not influence c-fos expression in the subfornical organ (SFO).
35 ts with intact brains or with lesions of the subfornical organ (SFO).
36 paraventricular (PVN) nuclei, but not in the subfornical organ (SFO).
37 he median preoptic nucleus (MnPO) and/or the subfornical organ (SFO); are required for the developmen
38 e neurons in the median preoptic nucleus and subfornical organ and 14% of the neurons in the fusiform
39 reases AT(1) binding in brain areas outside (subfornical organ and area postrema) and inside (paraven
40 f circulating origin has ready access to the subfornical organ and area postrema, where it can bind t
41 he osmosensitive median preoptic nucleus and subfornical organ and from the fusiform nucleus of the b
42 , including regions of the brain such as the subfornical organ and hypothalamus, could potentially us
43  vasculosum of the lamina terminalis and the subfornical organ and increased Fos-ir in the lateral pa
44 general categories: humeral sensory-related (subfornical organ and median preoptic nucleus, involved
45                                          The subfornical organ and organum vasculosum lamina terminal
46 ng binding of angiotensin II (ANG II) at the subfornical organ and organum vasculosum of the lamina t
47 (1) receptor expression was increased in the subfornical organ and periventricular nucleus of the hyp
48  binding and mRNA expression not only in the subfornical organ and the median eminence, situated outs
49  Stimulation of glutamatergic neurons in the subfornical organ drives drinking behavior, but the brai
50       We show that optogenetic activation of subfornical organ excitatory neurons, marked by the expr
51 data suggest that ACE2 overexpression in the subfornical organ impairs Ang II-mediated pressor and dr
52  appetite of angiotensin II generated in the subfornical organ in the brain.
53                We show that thirst-promoting subfornical organ neurons are negatively reinforcing and
54  CO2-evoked neuronal firing in patch-clamped subfornical organ neurons was dependent on acid sensor T
55 ntrast, activation of a second population of subfornical organ neurons, marked by expression of the v
56 etically separable neural populations in the subfornical organ that trigger or suppress thirst.
57  to AT(1) receptors in the pituitary and the subfornical organ was measured following estrogen treatm
58 leus (MnPO) receives afferent input from the subfornical organ, a circumventricular organ that has be
59 ayer of the olfactory bulb, medial habenula, subfornical organ, and area postrema.
60 nucleus of the thalamus, supraoptic nucleus, subfornical organ, and paraventricular hypothalamic nucl
61 eral septum, nucleus of the stria terminals, subfornical organ, and periaqueductal gray.
62 paraventricular nucleus of the hypothalamus, subfornical organ, and the area postrema.
63 g Fluorogold in the median preoptic nucleus, subfornical organ, and the fusiform nucleus were all sig
64 rojections from the median preoptic nucleus, subfornical organ, and the fusiform nucleus.
65 ventricular nucleus of the hypothalamus, the subfornical organ, and the organum vasculosum of the lam
66 t, Y1-R mRNA expression was also seen in the subfornical organ, anterior hypothalamic area, dorsal hy
67                                          The subfornical organ, dorsal hypothalamic, perifornical, an
68 tarius, and circumventricular organs such as subfornical organ, median eminence, and area postrema.
69 ventricular organs including choroid plexus, subfornical organ, median eminence, and area postrema.
70  The most intensely labeled CVOs include the subfornical organ, median eminence, area postrema and ch
71                     These areas included the subfornical organ, median preoptic nucleus, organum vasc
72 ular regions), rostral forebrain structures (subfornical organ, organum vasculosum of the lamina term
73 oughout the CNS, including areas such as the subfornical organ, pineal gland, neurohypophysis, and hy
74 ventricular hypothalamic nucleus (PVH), peri-subfornical organ, subfornical organ (SFO) or hippocampu
75  are much more extensive than those from the subfornical organ, suggesting that the MnPO/OVLT serves
76     In the CVOs, DEPTOR was expressed in the subfornical organ, the median eminence, and the area pos
77 ject detectably to Barrington's nucleus, the subfornical organ, the median preoptic and parastrial nu
78 ay structures such as the area postrema, the subfornical organ, the paraventricular hypothalamic nucl
79 ateral septum, the medial preoptic area, the subfornical organ, the paraventricular thalamus, the sub
80 ns that contain neuronal elements, i.e., the subfornical organ, the vascular organ of the lamina term
81                                 Furthermore, subfornical organ-targeted ACE2 overexpression dramatica
82 ctivity (with a peak at 7 days) in the mouse subfornical organ.
83 hypothalamic paraventricular nucleus and the subfornical organ.
84 proinflammatory cytokine IL-1beta within the subfornical organ.
85 strocytes, but was present in neurons in the subfornical organ.
86 lei, amygdaloid complex, piriform cortex and subfornical organ.
87 in the ventromedial hypothalamic nucleus and subfornical organ.
88 id and mineral homeostasis, most notably the subfornical organ.

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