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1 denum by GFP-positive neurons located in the nodose ganglion.
2 rs are exclusively A-fibres arising from the nodose ganglion.
3 are reproduced in mice lacking Piezo2 in the nodose ganglion.
4 strema, nucleus tractus solitarius (NTS) and nodose ganglion.
5 strema, nucleus tractus solitarius (NTS) and nodose ganglion.
6 from the medulla oblongata, spinal cord, and nodose ganglion.
7 trols) was injected with WGA-HRP in the left nodose ganglion.
8 horseradish peroxidase (WGA-HRP) in the left nodose ganglion.
9 l after the main period of cell death in the nodose ganglion.
10 gglutinin-horseradish peroxidase in the left nodose ganglion.
11  array (MEA) inserted into the left or right nodose ganglion.
12 an increase in c-Fos positive neurons in the nodose ganglion.
13 m currents are similarly distributed between nodose ganglion A-fibres and C-fibres innervating the lu
14                Those fibres derived from the nodose ganglion adapted rapidly, whereas those derived f
15 for recording of isometric tension while the nodose ganglion and attached vagus nerve were pulled int
16 ylrhodamine and biotin was injected into the nodose ganglion and used to label the terminal arbors of
17 2X2(+) neurons were found exclusively in the nodose ganglion and were activated by alphabetamATP and
18 psin reporter expression in the vagus nerve, nodose ganglion, and brainstem.
19 urons, in developing petrosal ganglion (PG), nodose ganglion, and dorsal root ganglion neurons grown
20 hin-4 (NT-4) to perikarya in the ipsilateral nodose ganglion, and transganglionically transported [12
21 injection of horseradish peroxidase into the nodose ganglion anterogradely labelled axonal boutons we
22                               Neurons of the nodose ganglion are derived from the epibranchial placod
23 trast, embryonic day 15 superior cervical or nodose ganglion axons grew heavily into the same age hea
24 three findings: 1) the presence of NADPHd in nodose ganglion cells with morphological features of fir
25 chnique, we identified cultured adult rabbit nodose ganglion cells with slow AHPs in current-clamp mo
26 acutely dissociated vagal afferent neurones (nodose ganglion cells) of the ferret to investigate the
27 acutely dissociated vagal afferent neurones (nodose ganglion cells) of the ferret to investigate the
28 vation of guinea pig airway-specific primary nodose ganglion cells.
29                                          The nodose ganglion contained the somata of mainly fast-cond
30 om these results we concluded that the vagal nodose ganglion contains neurones that may possess only
31 , no such changes were observed in the vagal nodose ganglion, demonstrating that the effect of high o
32 ot affect the adaptation of rapidly adapting nodose ganglion-derived nerve endings in response to mec
33       The electrophysiological adaptation of nodose ganglion-derived neurones following prolonged sup
34 nucleus of the solitary tract, the target of nodose ganglion-derived visceral afferents.
35                     Dorsal root ganglion and nodose ganglion expressed all isoforms except for CA IX.
36 nating from neurogenic placodes, such as the nodose ganglion, failed to express EGFP, suggesting that
37 otinylated dextran amine (BDA) into the left nodose ganglion in rats.
38              Vagal afferents were labeled by nodose ganglion injections of wheat germ agglutinin-hors
39                             Animals received nodose ganglion injections of wheat germ agglutinin-hors
40 roxidase (0.5-1.0 mul) was injected into the nodose ganglion ipsilateral to the vagotomized side.
41                                              Nodose ganglion neurones (NGNs) become less excitable fo
42 tch-clamp recording from acutely dissociated nodose ganglion neurones (NGNs) we have examined the ion
43 e in properties between P2X2/3 receptors and nodose ganglion neurones further supports the conclusion
44  neighbouring enterocytes through P2Y(2) and nodose ganglion neurones in co-cultures through P2X(2/3)
45                                     Cultured nodose ganglion neurones showed no changes in response t
46       Here we show that OEA directly excited nodose ganglion neurones, the cell bodies of vagal affer
47 ndles and patch clamp recordings of isolated nodose ganglion neurons (NGNs).
48 to selectively transduce stomach-innervating nodose ganglion neurons and express the excitatory DREAD
49  ganglion neurons, and that the responses of nodose ganglion neurons to ATP show altered kinetics and
50 ilar age-related changes in the responses of nodose ganglion neurons to BDNF were observed in culture
51 n a subpopulation of vagal afferent neurons (nodose ganglion neurons), the pattern of impulse activit
52                                       Unlike nodose ganglion neurons, both retinal ganglion cells (RG
53  which have only 45% of the normal number of nodose ganglion neurons, exhibit selective losses of the
54       Adult inferior vagal ganglion neurons (nodose ganglion neurons, NGNs) were acutely isolated 4-6
55 GFP expression in approximately one-third of nodose ganglion neurons.
56 ion in the sustained ATP-induced currents in nodose ganglion neurons.
57 toxin B (CT-B) from NTS-X to NADPHd-positive nodose ganglion neurons; and 3) striking reductions of N
58 root ganglion (DRG) and approximately 50% of nodose ganglion neurons] to evoke a depolarizing inward
59                                       In the nodose ganglion, NF-immunoreactive neurones accounted fo
60 ncreatic inflammation, we studied pancreatic nodose ganglion (NG) and dorsal root ganglion (DRG) sens
61 o autonomic ganglia of the neck, namely, the nodose ganglion (NG) and the superior cervical ganglion
62 d currents in dorsal root ganglion (DRG) and nodose ganglion (NG) neurons that innervate the stomach
63 e expressed in vagal afferent neurons in the nodose ganglion (NG), we also systematically compared MC
64 pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).
65 erwent right cervical vagotomy caudal to the nodose ganglion, or sham surgery.
66 g MTII injection into the NTS ipsilateral to nodose ganglion removal was significantly attenuated, wh
67                          Finally, unilateral nodose ganglion removal, resulting in degeneration of va
68 ed synapsin I phosphorylation ipsilateral to nodose ganglion removal.
69                                              Nodose ganglion sensory neurones exert a significant ref
70  placode marker Pax2 and form neurons in the nodose ganglion that express the epibranchial neuron mar
71 etramethylrhodamine dextran (TMR-D) into the nodose ganglion to label vagal aortic afferents (at 3 an
72 tract that could be anterogradely labeled by nodose ganglion tracer injections was quantitatively ass
73 crest-derived cells in, and surrounding, the nodose ganglion transiently expressed Phox2b, a master r
74  tracing of vagal afferents arising from the nodose ganglion was achieved with biotinylated dextran a
75 he retrograde transport of [125I]NT-3 to the nodose ganglion was reduced by NT-3 and by NGF, and the
76  main bronchi with the right vagus nerve and nodose ganglion were isolated from guinea-pigs passively
77 nocortin-4 receptor (MC4R) expression in the nodose ganglion, where the cell bodies of vagal sensory
78 TrkA and TrkC and the absence of TrkB in the nodose ganglion, whereas the profile for NT-4 suggests a
79 d 24 months of age were injected in the left nodose ganglion with 3 microl of either 4% wheat germ ag