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 leus of the diagonal band, and magnocellular preoptic nucleus.
2 gnature of estrogen activation of the medial preoptic nucleus.
3 reased c-Fos expression in the ventrolateral preoptic nucleus.
4 found in many hypothalamic nuclei including preoptic nucleus.
5 Neurons in these areas project to the medial preoptic nucleus.
6 ing the human homologue of the ventrolateral preoptic nucleus.
7 n the ventrolateral preoptic area and median preoptic nucleus.
8 cleus of the stria terminalis and the medial preoptic nucleus.
9 related positively with pTH-ir in the medial preoptic nucleus.
10 g the ventrolateral preoptic area and median preoptic nucleus.
11 n of POMC neurons that project to the medial preoptic nucleus.
12 entrolateral preoptic area and dorsal median preoptic nucleus.
13 RPP-32 immunoreactivity by 92% in the medial preoptic nucleus, 134% in the caudal ventromedial hypoth
15 receptor (MOR) internalization in the medial preoptic nucleus, an important step for full expression
16 ERalphaKO mouse brain regions including the preoptic nucleus and arcuate nucleus of the hypothalamus
17 Ucn III neurons were observed in the median preoptic nucleus and in the rostral perifornical area la
18 ression in the central portion of the medial preoptic nucleus and posterodorsal medial amygdala at PN
19 at at least 30% of the neurons in the median preoptic nucleus and subfornical organ and 14% of the ne
20 a direct input from the osmosensitive median preoptic nucleus and subfornical organ and from the fusi
21 rces of dynorphin input to the magnocellular preoptic nucleus and substantia innominata (MCPO/SI) in
22 the brain areas where in mammals the median preoptic nucleus and the medial amygdala are located.
23 late motivation and reward (i.e., the medial preoptic nucleus and ventral tegmental area) related pos
24 id regulation of OFQ/N and NOP in the medial preoptic nucleus and VMH is consistent with emerging dat
25 jection to the sleep-promoting ventrolateral preoptic nucleus, and a mainly glutamate-thyrotropin-rel
27 eoptic area, medial preoptic nucleus, median preoptic nucleus, and lateral preoptic area, and then it
28 sed in the RVLM, PVH, choroid plexus, median preoptic nucleus, and organosum vasculosum of the lamina
29 he ventromedial preoptic nucleus, the median preoptic nucleus, and the paraventricular hypothalamic n
30 rs included the ventromedial nucleus, medial preoptic nucleus, and ventral premammillary nucleus.
32 Castration reduced PRir in males' medial preoptic nucleus, anteroventral periventricular nucleus,
33 othalamic area, medial preoptic area, median preoptic nucleus, anteroventral periventricular nucleus,
35 athetic pathway appears to target the medial preoptic nucleus as its key nodal point, receiving input
36 in (DAMGO) or endomorphin-1, into the medial preoptic nucleus attenuated lordosis, and their effects
37 fibers in the anteroventral periventricular preoptic nucleus (AVPV) and the central and medial divis
38 r olfactory nucleus, piriform cortex, median preoptic nucleus, basolateral amygdala, hippocampus, med
39 ing neurons were most abundant in the medial preoptic nucleus, bed nucleus of the stria terminalis, a
40 ion; after small lesions of the ventromedial preoptic nucleus, body temperature showed normal circadi
41 A expression was only seen within the median preoptic nucleus but Fos-IR showed little coexpression w
42 uced expression of NOP mRNA in VMH or median preoptic nucleus but reduced expression in the AVPV.
43 ofile, is the homologue of the ventrolateral preoptic nucleus, but physiological data in humans were
47 icular nucleus; reproductive: lateral medial preoptic nucleus; defensive: anterior hypothalamic nucle
48 minantly in the posterior PVN; and 3) medial preoptic nucleus-derived inputs to the PVN are not gluta
49 medial and lateral preoptic areas and medial preoptic nucleus), diencephalon (viz., subincertal nucle
50 rminalis, ventral aspect (INSTv), the medial preoptic nucleus, dorsomedial aspect (MPNdm) and the ven
51 e, whereas, in the medial part of the medial preoptic nucleus, estrogen and progesterone were needed
52 us (rPH), and to a lesser extent, the median preoptic nucleus, exhibited the highest numbers of retro
53 imary somatosensory cortex and magnocellular preoptic nucleus increased on the IL1beta-injected side.
55 ensory-related (subfornical organ and median preoptic nucleus, involved in initiating drinking behavi
56 om hypothalamic regions including the median preoptic nucleus, lateral hypothalamic area, and dorsome
57 in the lateral septal nucleus, ventromedial preoptic nucleus, lateral hypothalamus, perifornical are
58 diol-induced activation of MOR in the medial preoptic nucleus, leading to female sexual receptivity.
59 ng maternal aggression, including the medial preoptic nucleus (likely to represent an important locus
60 in a subset of neurons in the magnocellular preoptic nucleus (MCPO) and the horizontal limb of the d
61 of day or day of estrous cycle in the medial preoptic nucleus, median eminence, ventromedial nucleus,
62 as found in the medial preoptic area, medial preoptic nucleus, median preoptic nucleus, and lateral p
64 SFO), organum vasculosum (OV) and the median preoptic nucleus (MePO)) and in the hypothalamus, have b
65 losum laminae terminalis (OV) and the median preoptic nucleus (MEPO), where most of the somata of the
69 es of projections to the PF/LH is the median preoptic nucleus (MnPN) containing a sleep-active neuron
75 f the third ventricle, containing the median preoptic nucleus (MnPO) and organum vasculosum of the la
76 of the lamina terminalis (OVLT), the median preoptic nucleus (MnPO) and/or the subfornical organ (SF
77 veral lines of evidence implicate the median preoptic nucleus (MnPO) as a downstream site of activati
83 naptic to neurons projecting from the median preoptic nucleus (MnPO) to the dorsomedial hypothalamus.
84 ne whether individual neurones of the median preoptic nucleus (MnPO) with axonal projections to the h
85 leus (PVN), supraoptic nucleus (SON), median preoptic nucleus (MnPO), anterior hypothalamus (AH) and
86 nucleus of the hypothalamus (PVN) and median preoptic nucleus (MnPO), but not in the subfornical orga
87 osum of the lamina terminalis (OVLT), median preoptic nucleus (MNPO), hypothalamic paraventricular nu
88 sions of the subfornical organ (SFO), median preoptic nucleus (MnPO), lateral preoptic area (LPO), or
89 icular nucleus of the thalamus (PVA), median preoptic nucleus (MnPO), periventricular nucleus (Pe), c
90 osum of the lamina terminalis (OVLT), medial preoptic nucleus (MNPO), subfornical organ (SFO), suprao
99 receptor (PR) immunoreactivity in the medial preoptic nucleus (MPN) of the rat brain is due to the in
100 ntral periventricular nucleus (AVPV), medial preoptic nucleus (MPN), arcuate nucleus (ARH), and ventr
101 hat a select subset of neurons in the medial preoptic nucleus (MPN), lateral hypothalamic area (LHA),
102 r levels of V(1a)R binding within the medial preoptic nucleus (MPN), medial preoptic area (MPO), late
103 ir were colocalized in neurons of the medial preoptic nucleus (MPN), the dorsal medial amygdala (dMEA
104 ression induced by dehydration in the median preoptic nucleus (MPN), the supraoptic and paraventricul
105 s of the stria terminalis (BNST), the medial preoptic nucleus (MPN), the ventromedial nucleus (VMN),
108 PV], median preoptic area [MePO], and medial preoptic nucleus [MPN]), at young (3 months), middle-age
109 occupies the central division of the medial preoptic nucleus (MPNc) and consists of a cluster of cel
110 SDN-POA, the central division of the medial preoptic nucleus (MPNc), over the first 13 days postnata
111 e central and medial divisions of the medial preoptic nucleus (MPNc, MPNm, respectively) revealed uni
112 ocalization in the medial part of the medial preoptic nucleus (MPNm), where half of the neurons that
114 andin E synthase-1 (mPGES-1) into the median preoptic nucleus of fever-refractive mPGES-1 knock-out m
115 genetic deletion of the EP3Rs in the median preoptic nucleus of mice resulted in abrogation of the f
117 din E2 (PGE2) to EP3 receptors in the median preoptic nucleus of the hypothalamus, but the origin of
118 tricular nucleus of the hypothalamus, median preoptic nucleus, organum vasculosum of the lamina termi
119 areas included the subfornical organ, median preoptic nucleus, organum vasculosum of the lamina termi
120 bed nucleus of the stria terminalis, medial preoptic nucleus, paraventricular nucleus, medial amygda
121 nteroventral periventricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprachiasmat
122 f forebrain neurons-one in the posterodorsal preoptic nucleus (PdPN) and one in the lateral part of t
124 l medial amygdala (MeApd), the posterodorsal preoptic nucleus (PdPN), and the medial cell group of th
125 ed with ejaculation, i.e., the posterodorsal preoptic nucleus (PdPN), the lateral part of the postero
126 cur in a variety of mammals, with the medial preoptic nucleus (POM) and the ventromedial hypothalamic
127 for the opioid met-enkephalin in the medial preoptic nucleus (POM) correlates positively with undire
130 We show here that T implants in the medial preoptic nucleus (POM) of castrated male canaries (Serin
133 rogradely labeled from the PVN in the median preoptic nucleus; preoptic and lateral hypothalamic area
134 dial preoptic area and nucleus, ventromedial preoptic nucleus, retrochiasmatic nucleus, paraventricul
135 ens, FS, substantia innominata/magnocellular preoptic nucleus (SI/MA), and bed nucleus of the stria t
136 eurons accumulating Fluorogold in the median preoptic nucleus, subfornical organ, and the fusiform nu
137 t and functional projections from the median preoptic nucleus, subfornical organ, and the fusiform nu
138 s within the AV3V region (the ventral median preoptic nucleus) suppressed water intake following 24 h
140 is, paraventricular hypothalamus, and median preoptic nucleus than did rats fed either mid- or high-N
141 subunit mRNA included the septum, the median preoptic nucleus, the anteroventral periventricular nucl
142 kg), Fos-IR was observed in the ventromedial preoptic nucleus, the median preoptic nucleus, and the p
143 24 hr after estrogen treatment in the medial preoptic nucleus, the principal part of the bed nucleus,
144 -positive cells was identified in the medial preoptic nucleus, the suprachiasmatic nucleus, and the s
145 d cAMP concentrations in the SCN and rostral preoptic nucleus throughout the day in young and middle-
147 trol (subparaventricular zone, ventrolateral preoptic nucleus, tuberomammillary nucleus, supramammill
148 bed nucleus of the stria terminalis, medial preoptic nucleus, ventrolateral portion of the ventromed
149 he visceromotor (infralimbic) cortex, median preoptic nucleus, ventromedial preoptic area, bed nucleu
150 masking, and the sleep-active ventrolateral preoptic nucleus (VLPO) and determined the subsets of me
151 ke-active TMN and sleep-active ventrolateral preoptic nucleus (VLPO) are reciprocally connected, sugg
152 -positive during sleep) in the ventrolateral preoptic nucleus (VLPO) decreases non-rapid eye movement
154 -active neurons located in the ventrolateral preoptic nucleus (VLPO) play a crucial role in the induc
156 at sleep-active neurons in the ventrolateral preoptic nucleus (VLPO) provide a major input to the TMN
158 onent of this circuitry is the ventrolateral preoptic nucleus (VLPO), a hypothalamic region containin
159 ated, at least in part, by the ventrolateral preoptic nucleus (VLPO), a key cell group for producing
160 , we examined afferents to the ventrolateral preoptic nucleus (VLPO), an area critically implicated i
161 e thought to be located in the ventrolateral preoptic nucleus (VLPO), which receives a dense histamin
165 expression in sites such as the ventromedial preoptic nucleus (VMPO) and the hypothalamic paraventric
166 A projection from the BSTp to the medial preoptic nucleus was also weaker in females but was much
167 he stria terminalis (BNST) and to the medial preoptic nucleus, whereas MeA projects to adjacent subnu
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。