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1 y VR1-positive fibers project to the lateral parabrachial nucleus.
2 n structures such as the locus coeruleus and parabrachial nucleus.
3 dbrain raphe nuclei, periaqueductal gray and parabrachial nucleus.
4 dalar nucleus, retrorubral area, and lateral parabrachial nucleus.
5 pothalamus, periaqueductal gray, and lateral parabrachial nucleus.
6 cleus of the solitary tract, and the lateral parabrachial nucleus.
7 ration provide an input to the region of the parabrachial nucleus.
8 aterodorsal tegmental nucleus (LDT), and the parabrachial nucleus.
9 er-Fuse, intertrigeminal region, and lateral parabrachial nucleus.
10 ect to the nucleus of the solitary tract and parabrachial nucleus.
11 stria terminalis,medial amygdala, and medial parabrachial nucleus.
12 d subparafascicular nucleus, and the lateral parabrachial nucleus.
13  sensory trigeminal nucleus, and the lateral parabrachial nucleus.
14 targets the viscerosensory subregions of the parabrachial nucleus.
15 us nucleus and reversed the asymmetry in the parabrachial nucleus.
16 ad axons that projected to the contralateral parabrachial nucleus.
17 tract (NTS) and with SP, CGRP and MOR in the parabrachial nucleus.
18 the innermost region of the external lateral parabrachial nucleus.
19 antial projection may be relayed through the parabrachial nucleus.
20 teral medulla, A5 area, and internal lateral parabrachial nucleus.
21 ay matter, dorsal raphe nucleus, and lateral parabrachial nucleus.
22 ne (PZ)-project to the wake-promoting medial parabrachial nucleus; (2) PZ neurons express c-Fos after
23 o play a role in appetite suppression is the parabrachial nucleus, a heterogeneous population of neur
24 tial input from glutamatergic neurons in the parabrachial nucleus and adjacent precoeruleus area.
25 whereas CCK-induced neural activation in the parabrachial nucleus and amygdala appeared normal.
26 , ventrolateral periaqueductal gray, lateral parabrachial nucleus and caudal nucleus of the solitary
27 al organ and increased Fos-ir in the lateral parabrachial nucleus and caudal ventrolateral medulla.
28 e activation of neurons localized within the parabrachial nucleus and central amygdala, which constit
29 seen throughout the brain, the region of the parabrachial nucleus and nucleus of the solitary tract (
30 a, and brainstem regions such as the lateral parabrachial nucleus and nucleus of the solitary tract.
31 cal arousal, whereas the projection from the parabrachial nucleus and precoeruleus region, relayed by
32 nnervation of BNST originates in the pontine parabrachial nucleus and targets its anterolateral secto
33 , the A5 area, the ventrolateral part of the parabrachial nucleus and the Kolliker-Fuse nucleus were
34 ke-immunoreactive fibers was detected in the parabrachial nucleus and the NTS, with notable staining
35 s, and reduced spinofugal innervation of the parabrachial nucleus and the periaqueductal gray, import
36 al tegmental nucleus, nucleus pontis oralis, parabrachial nucleus and the white matter in between the
37 ent projections-to the lateral hypothalamus, parabrachial nucleus and ventral tegmental area-each imp
38 us (mPVN), 4.1-times in the external lateral parabrachial nucleus, and 2.6-times in both the inferior
39 eriaqueductal gray, locus coeruleus, lateral parabrachial nucleus, and commissural nucleus tractus so
40 ventral tegmental area, periaqueductal gray, parabrachial nucleus, and dorsal vagal complex.
41 regions including the infralimbic cortex and parabrachial nucleus, and limbic regions including the l
42 ventral tegmental area, periaqueductal gray, parabrachial nucleus, and locus coeruleus.
43 mic area, ventrolateral periaqueductal gray, parabrachial nucleus, and nucleus of the solitary tract)
44 s, dorsomedial hypothalamic nucleus, lateral parabrachial nucleus, and nucleus of the solitary tract.
45  in pons, midbrain (mesencephalic tegmentum, parabrachial nucleus, and periaqueductal gray), hypothal
46 l- and external-lateral subnuclei of lateral parabrachial nucleus, and present intracellularly in the
47 y sensation, receives primary input from the parabrachial nucleus, and projects to the insular cortex
48 rey, the dorsal and linear raphe nuclei, the parabrachial nucleus, and the dorsal vagal complex.
49 emammillary nucleus, ventral tegmental area, parabrachial nucleus, and the dorsal vagal complex.
50 in, including the ventrolateral medulla, the parabrachial nucleus, and the medial geniculate body.
51 alcitonin gene-related peptide (CGRP) in the parabrachial nucleus are critical for relaying pain sign
52 ateral and Kolliker-Fuse subdivisions of the parabrachial nucleus at 6 and 24 hours postinjection and
53 somatic afferents to the VRG via the lateral parabrachial nucleus causes resetting of respiratory rhy
54 f the solitary tract, area postrema, lateral parabrachial nucleus, central lateral nucleus of the amy
55 eas many NPS-positive neurons in the lateral parabrachial nucleus coexpress corticotropin-releasing f
56 up, ventrolateral medulla, central amygdala, parabrachial nucleus, cuneate nucleus, nucleus tractus s
57 lamic nucleus, lateral hypothalamus, lateral parabrachial nucleus, dorsal raphe nucleus, and nucleus
58           Reversible blockade of the lateral parabrachial nucleus eliminated entrainment.
59 ornical organ (SFO) and the external lateral parabrachial nucleus (elPB).
60 tral nucleus of the amygdala (lateral part), parabrachial nucleus (external lateral subnucleus), area
61 tions in the lateral and medial parts of the parabrachial nucleus; far fewer were seen after injectio
62 ed with regard to the forebrain influence on parabrachial nucleus function during CTA acquisition.
63 tegmental field rostral to the obex, and the parabrachial nucleus, had no appreciable effect on the a
64                       Given that the pontine parabrachial nucleus has been implicated in nociceptive
65 dial hypothalamus, lateral hypothalamus, and parabrachial nucleus, identifying these brain regions as
66                 Similar to the corresponding parabrachial nucleus in birds and mammals, the secondary
67 lated polypeptide alpha (calca), a marker of parabrachial nucleus in mammals.
68  in mice by providing GABAergic input to the parabrachial nucleus in the brainstem.
69  bed nuclei of the stria terminalis, and the parabrachial nucleus in the pons.
70 nd dorsal raphe nucleus in the midbrain; and parabrachial nucleus in the pons.
71 lei, locus coeruleus, raphe complex, lateral parabrachial nucleus, inferior olivary complex, vestibul
72 th aversion learning (the lateral and medial parabrachial nucleus, intermediate and caudal nucleus tr
73  nuclei, but some were also found in lateral parabrachial nucleus, intertrigeminal nucleus, principal
74 lpha-hCRH was microinjected into the lateral parabrachial nucleus ipsilateral to the LC recording sit
75                         Hyperactivity of the parabrachial nucleus is also thought to cause starvation
76                                          The parabrachial nucleus is thought to mediate the suppressi
77 detected in: paratrigeminal nucleus, lateral parabrachial nucleus, Kolliker-Fuse nucleus, ventrolater
78 nuclei, nucleus of the posterior commissure, parabrachial nucleus, laterodorsal and pedunculopontine
79 area, lateral habenula, periaqueductal gray, parabrachial nucleus, locus ceruleus, nucleus of the sol
80 h neuropil also, particularly in the lateral parabrachial nucleus, locus coeruleus, lateral septum, d
81 , periaqueductal gray, raphe nuclei, lateral parabrachial nucleus, locus coeruleus, spinal trigeminal
82 us of the solitary tract (rNTS), the lateral parabrachial nucleus (LPB), and the central amygdala (Ce
83 inalis (BST), caudate-putamen (CPu), lateral parabrachial nucleus (LPB), nucleus tractus solitarius (
84 at neurons in the dorsal part of the lateral parabrachial nucleus (LPBd) glutamatergically transmit c
85  solitarius (NTS) projections to the lateral parabrachial nucleus (lPBN) and calcitonin-gene related
86 NMDA) glutamatergic receptors in the lateral parabrachial nucleus (LPBN) are involved in the control
87 y was to investigate the role of the lateral parabrachial nucleus (LPBN) in mediating dorsal PAG modu
88 ergide injected bilaterally into the lateral parabrachial nucleus (LPBN) increases NaCl intake in sev
89 re designed to determine whether the lateral parabrachial nucleus (lPBN) mediates acquisition of cond
90                             Although lateral parabrachial nucleus (lPBN) neurons are implicated in th
91 tion to be mediated by a PVH(MC4R)-->lateral parabrachial nucleus (LPBN) pathway.
92   We also report that neurons in the lateral parabrachial nucleus (LPBN), a brain area that is also i
93 ight the dorsal vagal complex (DVC), lateral parabrachial nucleus (lPBN), and central nucleus of the
94 al ventrolateral medulla (RVLM), and lateral parabrachial nucleus (lPBN); however, EB significantly a
95 somatic afferents, (2) establish whether the parabrachial nucleus mediates entrainment, (3) examine r
96 ar dendritic zone, which included the medial parabrachial nucleus (mPB).
97 s of the solitary tract (rNST) to the medial parabrachial nucleus (mPBN) in male Wistar rats using Di
98  that include monoaminergic pathways and the parabrachial nucleus network.
99 ral nucleus of the solitary tract and medial parabrachial nucleus), neuroendocrine system (periventri
100 rvate autonomic control sites, including the parabrachial nucleus, nucleus of solitary tract, and ven
101 tices, paraventricular hypothalamic nucleus, parabrachial nucleus, nucleus of the solitary tract, and
102 f the amygdala, periaqueductal gray, lateral parabrachial nucleus, nucleus of the solitary tract, dor
103  gray, dorsal raphe, ventral tegmental area, parabrachial nucleus, nucleus tractus solitarius, rostra
104 tatory nucleus of catfish, like those of the parabrachial nucleus of birds and mammals, do not posses
105  oxytocin-receptor-expressing neurons in the parabrachial nucleus of mice (Oxtr(PBN) neurons) are key
106 he solitary tract (NTS) and the other in the parabrachial nucleus of the pons (PbN), respectively the
107 1) opioid receptor subtype is present in the parabrachial nucleus of the pons and that these receptor
108 No double labeled perikarya were seen in the parabrachial nucleus or in the amygdaloid nuclei.
109 lar cortex, but not in basolateral amygdala, parabrachial nucleus, or nucleus of the solitary tract.
110 end towards suppression of activation in the parabrachial nucleus (P = 0.0683).
111 ca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricular nucleus of the hyp
112                                          The parabrachial nucleus (PB) is a major relay of noxious an
113                                          The parabrachial nucleus (PB) is known to mediate key respir
114 ract (NTS), ventrolateral medulla (VLM), and parabrachial nucleus (PB) remained.
115  the periaqueductal gray matter (PAG) to the parabrachial nucleus (PB) were studied in the rat follow
116 ea (LHA), the periaqueductal gray (PAG), the parabrachial nucleus (Pb), and the nucleus of the solita
117  the nucleus submedius of the thalamus (Sm), parabrachial nucleus (PB), lateral hypothalamus (LH), or
118 othalamic nuclei, lateral hypothalamic area, parabrachial nucleus (PB), nucleus of the solitary tract
119 ratory chemosensory pathways converge on the parabrachial nucleus (PB), which sends glutamatergic pro
120  to the nucleus tractus solitarius (NTS) and parabrachial nucleus (PB).
121 lutamatergic neurons in the external lateral parabrachial nucleus (PBel) play a critical role in arou
122 d the inner division of the external lateral parabrachial nucleus (PBel).
123                   Interestingly, the lateral parabrachial nucleus (PBL), a critical node in the affec
124  hypothalamus (PVN), and the pontine lateral parabrachial nucleus (PBL; an important component of asc
125  the nucleus of the solitary tract (NTS) and parabrachial nucleus (PBN) after peripheral cholecystoki
126 tergic input to the BNST originates from the parabrachial nucleus (PBN) and consists of asymmetric ax
127 rain areas have been shown to project to the parabrachial nucleus (PBN) and exert inhibitory and exci
128 rvation is due to aberrant activation of the parabrachial nucleus (PBN) and it could be prevented by
129 rior vestibular nucleus (IVN) project to the parabrachial nucleus (PBN) and Kolliker-Fuse (KF) nucleu
130  two major extranuclear targets of rNST, the parabrachial nucleus (PBN) and medullary reticular forma
131                                  The pontine parabrachial nucleus (PBN) and medullary reticular forma
132 ve (CT) afferents, those connecting with the parabrachial nucleus (PBN) and reticular formation (RF),
133             Previous studies showed that the parabrachial nucleus (PBN) contains neurons that are nec
134 eviously reported that lesions of the medial parabrachial nucleus (PBN) enhanced d-fenfluramine (DFEN
135 entered in the gustatory zone of the pontine parabrachial nucleus (PBN) failed to acquire a condition
136       Rats with ibotenic acid lesions of the parabrachial nucleus (PBN) failed to learn a taste avers
137 e "waist" area and external subnuclei of the parabrachial nucleus (PBN) have been implicated in the p
138 es for cannabinoid mechanisms of the pontine parabrachial nucleus (PBN) in modulating intake of presu
139 receives ascending gustatory inputs from the parabrachial nucleus (PbN) in the brainstem and sends pr
140 esions of the gustatory (medial) zone of the parabrachial nucleus (PBN) in the pons eliminate the sal
141  nucleus of the solitary tract (rNST) to the parabrachial nucleus (PBN) in the pons.
142 recordings were made from neurons in the rat parabrachial nucleus (PBN) in three rostro-caudal brain
143                                          The parabrachial nucleus (PBN) is an area of the brain stem
144                                          The parabrachial nucleus (PBN) is located in the rostral dor
145 ctivity (FLI) in several subdivisions of the parabrachial nucleus (PBN) known to be responsive to gus
146 LepRb neurons, which project to and activate parabrachial nucleus (PBN) neurons that control SNS acti
147 aining most of the cells that project to the parabrachial nucleus (PBN) of the pons.
148 ted peptide (CGRP)-expressing neurons in the parabrachial nucleus (PBN) suppress feeding.
149        Hypoglycemia activates neurons of the parabrachial nucleus (PBN) that coexpress leptin recepto
150  the nucleus of solitary tract (NST) and the parabrachial nucleus (PBN) that modulate taste-elicited
151 n gene-related peptide (CGRP) neurons in the parabrachial nucleus (PBN) that transmit anorexic signal
152 ns in the gustatory and visceral zone of the parabrachial nucleus (PBN) to gamma-aminobutyric acid (G
153 evaluated the contributions of the hindbrain parabrachial nucleus (PBN) to systemic Ex4-induced hypop
154 ions, direct delivery of bretazenil into the parabrachial nucleus (PBN), a direct target of AgRP neur
155 mpathetic afferents activates neurons in the parabrachial nucleus (PBN), a region known to play a rol
156 as seen not only in the iNTS but also in the parabrachial nucleus (PBN), and the central nucleus of t
157 area postrema (AP), vestibular nucleus (VN), parabrachial nucleus (PBN), nucleus ambiguus (NA), dorsa
158      The two major components of the pontine parabrachial nucleus (PBN), the medial (gustatory) and l
159 tions from taste responsive sites within the parabrachial nucleus (PBN).
160 tract (NTS), area postrema (AP), and lateral parabrachial nucleus (PBN).
161 aused by hyperactivity of neurons within the parabrachial nucleus (PBN).
162 diate feeding behaviour, such as the lateral parabrachial nucleus (PBN).
163 d Fos-li in the external lateral division of parabrachial nucleus (PBNel) in intact but not in CD rat
164  in brainstem regions, including the lateral parabrachial nucleus, periaqeductal gray, and ventrolate
165 and pontine reticular formation, cerebellum, parabrachial nucleus, periaqueductal gray, thalamus, hyp
166 d double-labeled neurons originated from the parabrachial nucleus, pericoeruleus area, and caudal reg
167 d in brainstem regions including the lateral parabrachial nucleus, peripeduncular area and ventrolate
168 ), ventrolateral periaqueductal gray, dorsal parabrachial nucleus, periventricular and rhomboid nucle
169 r, dorsal and central superior raphe nuclei, parabrachial nucleus, pre-locus coeruleus region, NTS, a
170                   Destruction of the lateral parabrachial nucleus produced a 44 % inhibition of pepto
171 ic neurons of the lateral septum and lateral parabrachial nucleus regulate pancreatic secretion.
172 ral and external lateral subdivisions of the parabrachial nucleus (slPB and elPB, respectively), the
173 amate into the lateral septum or the lateral parabrachial nucleus stimulated vagal pancreatic efferen
174 he outer external lateral subdivision of the parabrachial nucleus that project to the laterocapsular
175    However, the identities of neurons in the parabrachial nucleus that regulate feeding are unknown,
176 dings of significant c-Fos expression in the parabrachial nucleus, the central nucleus of the amygdal
177 ar hypothalamic nuclei, the external lateral parabrachial nucleus, the locus coeruleus, and the nucle
178 ervous system regions, including the lateral parabrachial nucleus, the periaqueductal gray, and lamin
179 cold-induced c-Fos expression in the lateral parabrachial nucleus, thus indicating a site of action w
180           Glutamatergic projections from the parabrachial nucleus to the central amygdala are implica
181 emonstrate that this neural circuit from the parabrachial nucleus to the central nucleus of the amygd
182  Further, cholinergic input from the lateral parabrachial nucleus to the hypothalamus plays a major r
183                     The projections from the parabrachial nucleus to the midline and intralaminar tha
184 tphal nucleus, locus coeruleus (LC), lateral parabrachial nucleus, ventrolateral medulla (VLM) and do
185 c area, bed nucleus of the stria terminalis, parabrachial nucleus, ventrolateral medulla, and nucleus
186               Finally, the waist area of the parabrachial nucleus was densely labeled after CTb injec
187 for parallel processing was reflected in the parabrachial nucleus, where sweetened milk intake result
188 eptum and external subnucleus of the lateral parabrachial nucleus which contained more CRF-ir neurons
189 are synaptically connected to neurons in the parabrachial nucleus, which relays visceral information
190 lateral and external medial subnuclei of the parabrachial nucleus while a significant increase in kap

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