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1 pathetic neurons by different regions of the nucleus tractus solitarii.
2 y, mostly in the lateral areas of the caudal nucleus tractus solitarii.
3 al and caudal ventrolateral medulla, and the nucleus tractus solitarii.
4 erents and glutamatergic transmission in the nucleus tractus solitarii abolished rimonabant-induced h
5 at same pontine region to the cardiovascular nucleus tractus solitarii and evaluated the confluence o
6 vely localized to visceral relay nuclei: the nucleus tractus solitarii and pontine parabrachial compl
7 ins three structures: the area postrema, the nucleus tractus solitarii, and the dorsal motor nucleus
8 neurones in the nucleus raphe obscurus, the nucleus tractus solitarii, and the regions of the retrof
9 ty of receptors in the area postrema and the nucleus tractus solitarii, believed to be involved in te
10 ats, selective inhibition of the commissural nucleus tractus solitarii (cNTS) significantly reduced t
11 ered from the commissural subdivision of the nucleus tractus solitarii (cNTS) using in vivo microdial
12 nhibition of neurones within the commissural nucleus tractus solitarii (commNTS) with glycine (40 nmo
14 Interleukin (IL)-1beta microinjected in the nucleus tractus solitarii increases fR and the predictab
15 subnucleus reticularis dorsalis, commissural nucleus tractus solitarii, lateral medulla, A5 area, and
16 aris dorsalis, commissural subnucleus of the nucleus tractus solitarii, lateral medulla, medial facia
18 e blocked by infusions of lidocaine into the nucleus tractus solitarii (NTS) and by propranolol infus
19 ivity of nuclei comprising the DVC, i.e. the nucleus tractus solitarii (NTS) and the dorsal motor nuc
20 ultaneously up to twenty-two neurones in the nucleus tractus solitarii (NTS) and ventral respiratory
21 The time course of adenosine release in the nucleus tractus solitarii (NTS) and ventrolateral medull
22 s of the ventrolateral medulla (VLM) and the nucleus tractus solitarii (NTS) are implicated in the co
24 te that GLP-1-producing (PPG) neurons in the nucleus tractus solitarii (NTS) are the predominant sour
26 oxide (NO) donors exogenously applied to the nucleus tractus solitarii (NTS) depressed the barorecept
27 surface of the brainstem and from within the nucleus tractus solitarii (NTS) during the defence respo
28 Glutamatergic signalling is critical in the nucleus tractus solitarii (nTS) for cardiorespiratory ho
29 cytokine Interleukin-1beta (IL-1beta) in the nucleus tractus solitarii (nTS) from ALI but not sham ra
30 vel of the obex (caudal C1 area) or into the nucleus tractus solitarii (NTS) greatly attenuated the b
31 within the caudal aspect of the commissural nucleus tractus solitarii (NTS) in mediating the periphe
32 ining neurons and fibers in subnuclei of the nucleus tractus solitarii (NTS) in the squirrel monkey,
33 ary neurones were recorded simultaneously in nucleus tractus solitarii (NTS) including the dorsal res
35 ion of leptin to the fourth ventricle or the nucleus tractus solitarii (NTS) inhibits food intake and
42 local circuitry activated by vagal input to nucleus tractus solitarii (NTS) neurones in immature rat
43 depresses the afferent neurotransmission in nucleus tractus solitarii (NTS) neurons, which affect re
45 BH-SAP) damages catecholamine neurons in the nucleus tractus solitarii (NTS) of rat, attenuates arter
46 have suggested that nitric oxide (NO) in the nucleus tractus solitarii (NTS) participates in modulati
47 urones in caudomedial aspects of commissural nucleus tractus solitarii (NTS) received input from card
48 for this response, we hypothesized that the Nucleus Tractus Solitarii (NTS) region of the medulla ob
49 lation of the inhibitory transmission in the nucleus tractus solitarii (NTS) remain unclear, even tho
50 beta acts via a noradrenergic relay from the nucleus tractus solitarii (NTS) to corticotropin releasi
51 behavior by way of direct pathways from the nucleus tractus solitarii (NTS) to the olfactory tubercl
52 microinjection of L-S-nitrosocysteine in the nucleus tractus solitarii (NTS) were compared and contra
54 diaphorase (NADPHd) staining patterns in the nucleus tractus solitarii (NTS) were spatially related t
55 In this study, we examined LTD in the rat nucleus tractus solitarii (NTS), a brainstem nucleus tha
56 it is first integrated within the brainstem nucleus tractus solitarii (nTS), a critical contributor
57 er 2 (EAAT2) is present on astrocytes in the nucleus tractus solitarii (nTS), an important nucleus in
58 iac mechanoreceptors excites neurones in the nucleus tractus solitarii (NTS), but discharge patterns
59 ns of excitatory amino acids (EAAs) into the nucleus tractus solitarii (nTS), in a region located imm
60 minate bilaterally in the caudal zone of the nucleus tractus solitarii (NTS), mainly within the commi
61 dala, parabrachial nucleus, cuneate nucleus, nucleus tractus solitarii (NTS), paraventricular nucleus
62 ivity of vagal C-fibre-activated neurones in nucleus tractus solitarii (NTS), phrenic nerve activity,
63 pherally and in the CNS, particularly in the nucleus tractus solitarii (NTS), the first central site
64 stnatal age, NR1 expression increased in the nucleus tractus solitarii (nTS), whereas it decreased in
73 GF21 in the baroreflex afferent pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).
74 t in the ventral tegmentum/substantia nigra, nucleus tractus solitarii, nucleus accumbens, thalamus/s
75 injected 6-hydroxydopamine or vitamin C into nucleus tractus solitarii of the rat and evaluated the c
79 teral, rostral, and caudal to cardiovascular nucleus tractus solitarii sent projections through the p
80 stral, subpostremal and central subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus cau
81 test the hypothesis that the cardiovascular nucleus tractus solitarii, the site of termination of ar
82 onfluence of tracing from the cardiovascular nucleus tractus solitarii to pontine preganglionic neuro
83 c pathway from neurons in the cardiovascular nucleus tractus solitarii to pontine preganglionic paras
84 anterograde tracing from the cardiovascular nucleus tractus solitarii to preganglionic parasympathet
85 erficial and deep dorsal horn project to the nucleus tractus solitarii via two distinct pathways.
86 sor which increases its neural output to the nucleus tractus solitarii with a subsequent activation o
87 e caudal ventrolateral medulla (CVL) and the nucleus tractus solitarii with immunocytochemical identi