ライフサイエンスコーパス: nodose ganglion

1 are reproduced in mice lacking Piezo2 in the nodose ganglion.

2 denum by GFP-positive neurons located in the nodose ganglion.

3 rs are exclusively A-fibres arising from 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 m currents are similarly distributed between nodose ganglion A-fibres and C-fibres innervating the lu

12 Those fibres derived from the nodose ganglion adapted rapidly, whereas those derived f

13 for recording of isometric tension while the nodose ganglion and attached vagus nerve were pulled int

14 ylrhodamine and biotin was injected into the nodose ganglion and used to label the terminal arbors of

15 urons, in developing petrosal ganglion (PG), nodose ganglion, and dorsal root ganglion neurons grown

16 hin-4 (NT-4) to perikarya in the ipsilateral nodose ganglion, and transganglionically transported [12

17 injection of horseradish peroxidase into the nodose ganglion anterogradely labelled axonal boutons we

18 Neurons of the nodose ganglion are derived from the epibranchial placod

19 trast, embryonic day 15 superior cervical or nodose ganglion axons grew heavily into the same age hea

20 three findings: 1) the presence of NADPHd in nodose ganglion cells with morphological features of fir

21 chnique, we identified cultured adult rabbit nodose ganglion cells with slow AHPs in current-clamp mo

22 acutely dissociated vagal afferent neurones (nodose ganglion cells) of the ferret to investigate the

23 acutely dissociated vagal afferent neurones (nodose ganglion cells) of the ferret to investigate the

24 vation of guinea pig airway-specific primary nodose ganglion cells.

25 The nodose ganglion contained the somata of mainly fast-cond

26 om these results we concluded that the vagal nodose ganglion contains neurones that may possess only

27 , no such changes were observed in the vagal nodose ganglion, demonstrating that the effect of high o

28 ot affect the adaptation of rapidly adapting nodose ganglion-derived nerve endings in response to mec

29 The electrophysiological adaptation of nodose ganglion-derived neurones following prolonged sup

30 nucleus of the solitary tract, the target of nodose ganglion-derived visceral afferents.

31 Dorsal root ganglion and nodose ganglion expressed all isoforms except for CA IX.

32 nating from neurogenic placodes, such as the nodose ganglion, failed to express EGFP, suggesting that

33 otinylated dextran amine (BDA) into the left nodose ganglion in rats.

34 Vagal afferents were labeled by nodose ganglion injections of wheat germ agglutinin-hors

35 Animals received nodose ganglion injections of wheat germ agglutinin-hors

36 roxidase (0.5-1.0 mul) was injected into the nodose ganglion ipsilateral to the vagotomized side.

37 Nodose ganglion neurones (NGNs) become less excitable fo

38 tch-clamp recording from acutely dissociated nodose ganglion neurones (NGNs) we have examined the ion

39 e in properties between P2X2/3 receptors and nodose ganglion neurones further supports the conclusion

40 Here we show that OEA directly excited nodose ganglion neurones, the cell bodies of vagal affer

41 ndles and patch clamp recordings of isolated nodose ganglion neurons (NGNs).

42 ganglion neurons, and that the responses of nodose ganglion neurons to ATP show altered kinetics and

43 ilar age-related changes in the responses of nodose ganglion neurons to BDNF were observed in culture

44 n a subpopulation of vagal afferent neurons (nodose ganglion neurons), the pattern of impulse activit

45 Unlike nodose ganglion neurons, both retinal ganglion cells (RG

46 which have only 45% of the normal number of nodose ganglion neurons, exhibit selective losses of the

47 Adult inferior vagal ganglion neurons (nodose ganglion neurons, NGNs) were acutely isolated 4-6

48 GFP expression in approximately one-third of nodose ganglion neurons.

49 ion in the sustained ATP-induced currents in nodose ganglion neurons.

50 toxin B (CT-B) from NTS-X to NADPHd-positive nodose ganglion neurons; and 3) striking reductions of N

51 root ganglion (DRG) and approximately 50% of nodose ganglion neurons] to evoke a depolarizing inward

52 In the nodose ganglion, NF-immunoreactive neurones accounted fo

53 ncreatic inflammation, we studied pancreatic nodose ganglion (NG) and dorsal root ganglion (DRG) sens

54 d currents in dorsal root ganglion (DRG) and nodose ganglion (NG) neurons that innervate the stomach

55 e expressed in vagal afferent neurons in the nodose ganglion (NG), we also systematically compared MC

56 pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).

57 g MTII injection into the NTS ipsilateral to nodose ganglion removal was significantly attenuated, wh

58 Finally, unilateral nodose ganglion removal, resulting in degeneration of va

59 ed synapsin I phosphorylation ipsilateral to nodose ganglion removal.

60 Nodose ganglion sensory neurones exert a significant ref

61 placode marker Pax2 and form neurons in the nodose ganglion that express the epibranchial neuron mar

62 etramethylrhodamine dextran (TMR-D) into the nodose ganglion to label vagal aortic afferents (at 3 an

63 tract that could be anterogradely labeled by nodose ganglion tracer injections was quantitatively ass

64 tracing of vagal afferents arising from the nodose ganglion was achieved with biotinylated dextran a

65 he retrograde transport of [125I]NT-3 to the nodose ganglion was reduced by NT-3 and by NGF, and the

66 main bronchi with the right vagus nerve and nodose ganglion were isolated from guinea-pigs passively

67 nocortin-4 receptor (MC4R) expression in the nodose ganglion, where the cell bodies of vagal sensory

68 TrkA and TrkC and the absence of TrkB in the nodose ganglion, whereas the profile for NT-4 suggests a

69 d 24 months of age were injected in the left nodose ganglion with 3 microl of either 4% wheat germ ag