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1 by different regions of the nucleus tractus solitarii.
2 lateral areas of the caudal nucleus tractus solitarii.
3 ntrolateral medulla, and the nucleus tractus solitarii.
5 region to the cardiovascular nucleus tractus solitarii and evaluated the confluence of tracing from t
6 o visceral relay nuclei: the nucleus tractus solitarii and pontine parabrachial complex, and perivent
7 nucleus raphe obscurus, the nucleus tractus solitarii, and the regions of the retrofacial nucleus, n
8 in the area postrema and the nucleus tractus solitarii, believed to be involved in terminal emetic pa
10 mmissural subdivision of the nucleus tractus solitarii (cNTS) using in vivo microdialysis during acti
11 rones within the commissural nucleus tractus solitarii (commNTS) with glycine (40 nmol/80 nl) or with
13 ularis dorsalis, commissural nucleus tractus solitarii, lateral medulla, A5 area, and internal latera
14 ommissural subnucleus of the nucleus tractus solitarii, lateral medulla, medial facial nucleus, A5 ar
15 usions of lidocaine into the nucleus tractus solitarii (NTS) and by propranolol infused into the baso
17 o twenty-two neurones in the nucleus tractus solitarii (NTS) and ventral respiratory group (VRG).
18 of adenosine release in the nucleus tractus solitarii (NTS) and ventrolateral medulla (VLM) during a
19 ateral medulla (VLM) and the nucleus tractus solitarii (NTS) are implicated in the control of a varie
20 e glutamate receptors in the nucleus tractus solitarii (NTS) are necessary for the baroreceptor refle
21 s exogenously applied to the nucleus tractus solitarii (NTS) depressed the baroreceptor cardiac refle
22 rainstem and from within the nucleus tractus solitarii (NTS) during the defence response evoked by hy
23 ignalling is critical in the nucleus tractus solitarii (nTS) for cardiorespiratory homeostasis and in
24 (caudal C1 area) or into the nucleus tractus solitarii (NTS) greatly attenuated the baroreflex and si
25 al aspect of the commissural nucleus tractus solitarii (NTS) in mediating the peripheral chemorecepto
26 d fibers in subnuclei of the nucleus tractus solitarii (NTS) in the squirrel monkey, Saimuri sciureus
27 e recorded simultaneously in nucleus tractus solitarii (NTS) including the dorsal respiratory group (
28 Electrical stimulation of nucleus tractus solitarii (NTS) induced excitatory postsynaptic currents
29 the fourth ventricle or the nucleus tractus solitarii (NTS) inhibits food intake and weight gain.
35 fferent neurotransmission in nucleus tractus solitarii (NTS) neurons, which affect respiratory and au
37 catecholamine neurons in the nucleus tractus solitarii (NTS) of rat, attenuates arterial baroreflexes
38 hat nitric oxide (NO) in the nucleus tractus solitarii (NTS) participates in modulating cardiovascula
39 edial aspects of commissural nucleus tractus solitarii (NTS) received input from cardiopulmonary C fi
40 se, we hypothesized that the Nucleus Tractus Solitarii (NTS) region of the medulla oblongata, to whic
41 hibitory transmission in the nucleus tractus solitarii (NTS) remain unclear, even though this could b
42 noradrenergic relay from the nucleus tractus solitarii (NTS) to corticotropin releasing hormone neuro
43 of direct pathways from the nucleus tractus solitarii (NTS) to the olfactory tubercle and the midlin
44 f L-S-nitrosocysteine in the nucleus tractus solitarii (NTS) were compared and contrasted with those
45 Vestibular afferents to the nucleus tractus solitarii (NTS) were identified for the first time in th
46 Hd) staining patterns in the nucleus tractus solitarii (NTS) were spatially related to terminal sites
47 , we examined LTD in the rat nucleus tractus solitarii (NTS), a brainstem nucleus that relays homeost
48 present on astrocytes in the nucleus tractus solitarii (nTS), an important nucleus in cardiorespirato
49 tors excites neurones in the nucleus tractus solitarii (NTS), but discharge patterns evoked by physio
50 amino acids (EAAs) into the nucleus tractus solitarii (nTS), in a region located immediately rostral
51 ly in the caudal zone of the nucleus tractus solitarii (NTS), mainly within the commissural subnucleu
52 al nucleus, cuneate nucleus, nucleus tractus solitarii (NTS), paraventricular nucleus of the hypothal
53 -fibre-activated neurones in nucleus tractus solitarii (NTS), phrenic nerve activity, tracheal pressu
54 the CNS, particularly in the nucleus tractus solitarii (NTS), the first central site for synaptic con
55 expression increased in the nucleus tractus solitarii (nTS), whereas it decreased in the hypoglossal
63 tegmentum/substantia nigra, nucleus tractus solitarii, nucleus accumbens, thalamus/subthalamus, pari
64 xydopamine or vitamin C into nucleus tractus solitarii of the rat and evaluated the cardiopulmonary c
67 ntrast, all three regions of nucleus tractus solitarii projected to the nucleus ambiguus and dorsal m
68 and caudal to cardiovascular nucleus tractus solitarii sent projections through the pons medial to th
69 mal and central subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, and infer
70 citatory currents (eEPSCs) evoked by tractus solitarii stimulation (TS-eEPSC) of second-order neurons
71 esis that the cardiovascular nucleus tractus solitarii, the site of termination of arterial barorecep
72 cing from the cardiovascular nucleus tractus solitarii to pontine preganglionic neurons labeled retro
73 eurons in the cardiovascular nucleus tractus solitarii to pontine preganglionic parasympathetic neuro
74 cing from the cardiovascular nucleus tractus solitarii to preganglionic parasympathetic neurons in th
75 e exception these cells responded to tractus solitarii (TS) stimulation with a monophasic excitatory
77 ses its neural output to the nucleus tractus solitarii with a subsequent activation of several reflex
78 ateral medulla (CVL) and the nucleus tractus solitarii with immunocytochemical identification of C1 a
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