ライフサイエンスコーパス: glossopharyngeal

1 es suggest convergence of chorda tympani and glossopharyngeal afferent axons onto single neurons of t

2 eal (GLX), chorda tympani (CTX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transect

3 It was found that individual neurons in both glossopharyngeal and chorda tympani nerves differed in t

4 ng is associated with terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleu

5 codes generate neurons of the distal facial, glossopharyngeal and vagal ganglia, which convey sensati

6 ed in food detection and localization, while glossopharyngeal and vagal nerve innervated taste buds (

7 entire body including the barbels, while the glossopharyngeal and vagal nerves innervate oropharyngea

8 The morphology of the facial, glossopharyngeal and vagus nerves are abnormal in Spry1-

9 ypoxic and gastric extension events from the glossopharyngeal and vagus nerves, respectively.

10 s in defects in the facial nerve and not the glossopharyngeal and vagus nerves, suggesting that the f

11 vity from two separate autonomic nerves: the glossopharyngeal and vagus nerves.

12 and Carassius auratus, i.e., in their vagal, glossopharyngeal, and facial lobes, providing the first

13 r laryngeal, pharyngeal branch of the vagus, glossopharyngeal, and hypoglossal.

14 ed for the expression of drgx in the facial, glossopharyngeal, and vagal cranial ganglia.

15 The glossopharyngeal, chorda tympani, and greater superficia

16 nters the saccular chamber and in having the glossopharyngeal foramen separated from the metotic fiss

17 For instance, the glossopharyngeal (GL) nerve and neurons receiving its pr

18 de thresholds were measured before and after glossopharyngeal (GLX), chorda tympani (CTX), or combine

19 cal stimulation of the lingual branch of the glossopharyngeal (GP) nerve (which innervates taste buds

20 CT), greater superficial petrosal (GSP), and glossopharyngeal (IX) nerves in the rostral pole of the

21 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves terminate in overlapping pa

22 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were labeled in rats fed a

23 ial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves were visualized concurrentl

24 Chorda tympani (CT) and glossopharyngeal (IXth) nerves relay taste information f

25 the third arch neural crest, and are missing glossopharyngeal motor neurons.

26 ter-tasting compounds were recorded from rat glossopharyngeal (n = 30) and chorda tympani (n = 22) ne

27 o the posterior tongue in the absence of the glossopharyngeal nerve (GL) (CT-PostTongue) or cross-reg

28 The additional section of the glossopharyngeal nerve (GL) flattened the sucrose concen

29 n which the chorda tympani nerve (CT) and/or glossopharyngeal nerve (GL) was transected (Experiment 1

30 The rat glossopharyngeal nerve (GL), which innervates posterior

31 tympani (CTX), bilateral transection of the glossopharyngeal nerve (GLX), or combined neurotomy (DBL

32 reater superficial petrosal nerve (GSP), and glossopharyngeal nerve (IX), three nerves that innervate

33 innervate oral structures, particularly the glossopharyngeal nerve (IX), were observed.

34 nd synaptology of the afferent fibers of the glossopharyngeal nerve (IXN) in the hamster were studied

35 dosage only partially rescued defects in the glossopharyngeal nerve and was not sufficient to rescue

36 rphic characters for gnathostomes (e.g., the glossopharyngeal nerve leaves the braincase via the meto

37 issue is illustrated by the condition of the glossopharyngeal nerve relative to the parachordal plate

38 hyan-like condition), the arrangement of the glossopharyngeal nerve relative to the surrounding struc

39 udy prompted a different hypothesis: Because glossopharyngeal nerve section similarly devastates quin

40 Responses were more depressed in the glossopharyngeal nerve than in the chorda tympani nerve

41 ichthyans are probably derived in having the glossopharyngeal nerve that enters the saccular chamber

42 ncreased neural activity via a branch of the glossopharyngeal nerve to nucleus tractus solitarius; th

43 ral, central, and behavioral consequences of glossopharyngeal nerve transection (GLX), regeneration,

44 Glossopharyngeal nerve transection (GLX), which has no r

45 taste also occurs on the rear of the tongue (glossopharyngeal nerve), but the relationship between te

46 ter compounds, was cross-reinnervated by the glossopharyngeal nerve, even though this nerve typically

47 By contrast, the glossopharyngeal nerve, which is not highly sensitive to

48 the carotid labyrinth were innervated by the glossopharyngeal nerve.

49 er superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood that are expanded a

50 tioning the greater superficial petrosal and glossopharyngeal nerves at postnatal day 15 (P15), P25,

51 a tympani, greater superficial petrosal, and glossopharyngeal nerves have distinct but overlapping te

52 neurotrophin expression in adult taste buds, glossopharyngeal nerves were cut unilaterally.

53 a tympani, greater superficial petrosal, and glossopharyngeal nerves were labeled in adult wild-type

54 ly derived afferent neurons of the vagal and glossopharyngeal nerves) contain TrkA and TrkC, and tran

55 e information is conveyed via the facial and glossopharyngeal nerves, while general mucosal innervati

56 innervation is carried by the trigeminal and glossopharyngeal nerves.

57 and peripheral ganglia of the trigeminal and glossopharyngeal nerves.

58 For glossopharyngeal neurons, some similarity to quinine was

59 d, quinine evoked the greatest response from glossopharyngeal neurons.

60 n the wild-type hindbrain, facial (nVII) and glossopharyngeal (nIX) motor neurons are induced in rhom

61 Neither the glossopharyngeal nor the chorda tympani nerve is necessa

62 ular formation nuclei, the raphe nuclei, the glossopharyngeal nuclei, and the Purkinje cell layer of

63 reticular formation, the raphe nucleus, the glossopharyngeal nuclei, and the Purkinje cell layer of

64 ngue (chorda tympani), the posterior tongue (glossopharyngeal), or palatal taste receptors (greater s

65 Chemoafferent neurones, located in the glossopharyngeal petrosal ganglion, already exhibited de

66 rom two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed responses to all ta

67 m a posterior entry zone in the absence of a glossopharyngeal root in val mutants, but instead course

68 es converge to a posterior entry zone at the glossopharyngeal root.

69 tion > trigeminal section > thermal injury = glossopharyngeal section > greater superficial petrosal

70 rease in area across the pressure range with glossopharyngeal stimulation at any given level.

71 ere concentric with the HG stimulations, but glossopharyngeal stimulation resulted in a greater incre

72 er excitotoxic lesions in the NTS, and vagal-glossopharyngeal terminal sprouting in the NTS may under

73 nervated by all sensory trigeminal rami, the glossopharyngeal/vagal nerve, and cutaneous rami of spin

74 with those on brainstem motor neurons of the glossopharyngeal/vagal nucleus, which have been shown to