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1 es suggest convergence of chorda tympani and glossopharyngeal afferent axons onto single neurons of t
2         One known pathway involves vagal and glossopharyngeal afferents that project to the nucleus o
3 eal (GLX), chorda tympani (CTX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transect
4 It was found that individual neurons in both glossopharyngeal and chorda tympani nerves differed in t
5 ng is associated with terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleu
6 codes generate neurons of the distal facial, glossopharyngeal and vagal ganglia, which convey sensati
7 ed in food detection and localization, while glossopharyngeal and vagal nerve innervated taste buds (
8 entire body including the barbels, while the glossopharyngeal and vagal nerves innervate oropharyngea
9                The morphology of the facial, glossopharyngeal and vagus nerves are abnormal in Spry1-
10 ypoxic and gastric extension events from the glossopharyngeal and vagus nerves, respectively.
11 s in defects in the facial nerve and not the glossopharyngeal and vagus nerves, suggesting that the f
12 vity from two separate autonomic nerves: the glossopharyngeal and vagus nerves.
13 and Carassius auratus, i.e., in their vagal, glossopharyngeal, and facial lobes, providing the first
14 r laryngeal, pharyngeal branch of the vagus, glossopharyngeal, and hypoglossal.
15 ed for the expression of drgx in the facial, glossopharyngeal, and vagal cranial ganglia.
16                                          The glossopharyngeal, chorda tympani, and greater superficia
17 nters the saccular chamber and in having the glossopharyngeal foramen separated from the metotic fiss
18                            For instance, the glossopharyngeal (GL) nerve and neurons receiving its pr
19 de thresholds were measured before and after glossopharyngeal (GLX), chorda tympani (CTX), or combine
20 cal stimulation of the lingual branch of the glossopharyngeal (GP) nerve (which innervates taste buds
21 CT), greater superficial petrosal (GSP), and glossopharyngeal (IX) nerves in the rostral pole of the
22 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves terminate in overlapping pa
23 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were labeled in rats fed a
24 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were visualized concurrentl
25                      Chorda tympani (CT) and glossopharyngeal (IXth) nerves relay taste information f
26 the third arch neural crest, and are missing glossopharyngeal motor neurons.
27 ter-tasting compounds were recorded from rat glossopharyngeal (n = 30) and chorda tympani (n = 22) ne
28 o the posterior tongue in the absence of the glossopharyngeal nerve (GL) (CT-PostTongue) or cross-reg
29                The additional section of the glossopharyngeal nerve (GL) flattened the sucrose concen
30 n which the chorda tympani nerve (CT) and/or glossopharyngeal nerve (GL) was transected (Experiment 1
31                                      The rat glossopharyngeal nerve (GL), which innervates posterior
32  tympani (CTX), bilateral transection of the glossopharyngeal nerve (GLX), or combined neurotomy (DBL
33 reater superficial petrosal nerve (GSP), and glossopharyngeal nerve (IX), three nerves that innervate
34  innervate oral structures, particularly the glossopharyngeal nerve (IX), were observed.
35 nd synaptology of the afferent fibers of the glossopharyngeal nerve (IXN) in the hamster were studied
36 dosage only partially rescued defects in the glossopharyngeal nerve and was not sufficient to rescue
37 rphic characters for gnathostomes (e.g., the glossopharyngeal nerve leaves the braincase via the meto
38 issue is illustrated by the condition of the glossopharyngeal nerve relative to the parachordal plate
39 hyan-like condition), the arrangement of the glossopharyngeal nerve relative to the surrounding struc
40 udy prompted a different hypothesis: Because glossopharyngeal nerve section similarly devastates quin
41         Responses were more depressed in the glossopharyngeal nerve than in the chorda tympani nerve
42 ichthyans are probably derived in having the glossopharyngeal nerve that enters the saccular chamber
43 ncreased neural activity via a branch of the glossopharyngeal nerve to nucleus tractus solitarius; th
44 ral, central, and behavioral consequences of glossopharyngeal nerve transection (GLX), regeneration,
45                                              Glossopharyngeal nerve transection (GLX), which has no r
46                                    Using the glossopharyngeal nerve transection model, we show that s
47 taste also occurs on the rear of the tongue (glossopharyngeal nerve), but the relationship between te
48 ter compounds, was cross-reinnervated by the glossopharyngeal nerve, even though this nerve typically
49                             By contrast, the glossopharyngeal nerve, which is not highly sensitive to
50 the carotid labyrinth were innervated by the glossopharyngeal nerve.
51 er superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood that are expanded a
52 tioning the greater superficial petrosal and glossopharyngeal nerves at postnatal day 15 (P15), P25,
53 a tympani, greater superficial petrosal, and glossopharyngeal nerves have distinct but overlapping te
54 neurotrophin expression in adult taste buds, glossopharyngeal nerves were cut unilaterally.
55 a tympani, greater superficial petrosal, and glossopharyngeal nerves were labeled in adult wild-type
56 ly derived afferent neurons of the vagal and glossopharyngeal nerves) contain TrkA and TrkC, and tran
57 e information is conveyed via the facial and glossopharyngeal nerves, while general mucosal innervati
58 innervation is carried by the trigeminal and glossopharyngeal nerves.
59 and peripheral ganglia of the trigeminal and glossopharyngeal nerves.
60                                          For glossopharyngeal neurons, some similarity to quinine was
61 d, quinine evoked the greatest response from glossopharyngeal neurons.
62 n the wild-type hindbrain, facial (nVII) and glossopharyngeal (nIX) motor neurons are induced in rhom
63                                  Neither the glossopharyngeal nor the chorda tympani nerve is necessa
64 ular formation nuclei, the raphe nuclei, the glossopharyngeal nuclei, and the Purkinje cell layer of
65  reticular formation, the raphe nucleus, the glossopharyngeal nuclei, and the Purkinje cell layer of
66 ngue (chorda tympani), the posterior tongue (glossopharyngeal), or palatal taste receptors (greater s
67       Chemoafferent neurones, located in the glossopharyngeal petrosal ganglion, already exhibited de
68 rom two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed responses to all ta
69 m a posterior entry zone in the absence of a glossopharyngeal root in val mutants, but instead course
70 es converge to a posterior entry zone at the glossopharyngeal root.
71 tion > trigeminal section > thermal injury = glossopharyngeal section > greater superficial petrosal
72 sed genetic tools that broadly cover a vagal/glossopharyngeal sensory neuron atlas to map, ablate, an
73 ntified a small population of PGE2-detecting glossopharyngeal sensory neurons (petrosal GABRA1 neuron
74 rease in area across the pressure range with glossopharyngeal stimulation at any given level.
75 ere concentric with the HG stimulations, but glossopharyngeal stimulation resulted in a greater incre
76 er excitotoxic lesions in the NTS, and vagal-glossopharyngeal terminal sprouting in the NTS may under
77 nervated by all sensory trigeminal rami, the glossopharyngeal/vagal nerve, and cutaneous rami of spin
78 with those on brainstem motor neurons of the glossopharyngeal/vagal nucleus, which have been shown to
79 CNP events were defined by neuropathy of the glossopharyngeal, vagus, and/or hypoglossal cranial nerv