ライフサイエンスコーパス: trigeminal neuron

1 adult corneas, whole embryonic corneas, and trigeminal neurons.

2 muli to cause acute or chronic excitation of trigeminal neurons.

3 odontitis upregulates TLR4 expression in the trigeminal neurons.

4 as well as a subset of chemosensitive mouse trigeminal neurons.

5 umably represents activation of second-order trigeminal neurons.

6 teractions between the dental pulp cells and trigeminal neurons.

7 the presence of adenosine A(1) receptors on trigeminal neurons.

8 influence axon growth patterns of embryonic trigeminal neurons.

9 between human HaCaT keratinocytes and mouse trigeminal neurons.

10 (PKC) was determined in acutely dissociated trigeminal neurons.

11 We investigated bursting behavior in rodent trigeminal neurons.

12 ripherally derived survival factor for early trigeminal neurons.

13 essing of nociceptive information by central trigeminal neurons.

14 n of sulfated GAGs canceled their effects on trigeminal neurons.

15 ve (5-HT1) receptors on postsynaptic central trigeminal neurones.

16 lts showed that EP2 and EP3 are expressed in trigeminal neurons (58% and 53% of total neurons, respec

17 and axon degeneration in spontaneously dying trigeminal neurons: although pieces of Wld(S)-expressing

18 In trigeminal neurons and CHO cells, the manipulation of ce

19 deleterious feedback loop in migraine at the trigeminal neurons and provide a general mechanism by wh

20 Postnatally, more trigeminal neurons and types of mystacial pad innervatio

21 is study, we evaluated whether LPS activates trigeminal neurons, and sensitizes TRPV1 responses via T

22 s that LPS is capable of directly activating trigeminal neurons, and sensitizing TRPV1 via a TLR4-med

23 sensor GCaMP3, we show that TRPV1-expressing trigeminal neurons are activated by heat at behaviorally

24 ings are consistent with the hypothesis that trigeminal neurons are capable of detecting pathogenic b

25 visually foraging bird, the majority of duck trigeminal neurons are mechanoreceptors that express the

26 Trigeminal neurons are the major source of cerebrovascul

27 in the axons and cell bodies of adult mouse trigeminal neurons, as well as in the processes and cell

28 F-dependent nodose neurons and NGF-dependent trigeminal neurons at stages during and after the period

29 Knockdown of Piezo2 in duck trigeminal neurons attenuates mechano current with inter

30 demonstration of inhibition of second order trigeminal neurons by direct local application of 5HT1B/

31 trolling the survival and differentiation of trigeminal neurons by regulating expression of each of t

32 nin gene-related peptide (CGRP) release from trigeminal neurons by the serotonergic antimigraine drug

33 YFP fluorescence in wholemounted corneas and trigeminal neuron cultures was determined.

34 mmunohistochemical analyses of human and rat trigeminal neurons demonstrated that a capsaicin-sensiti

35 in defined without NGF whereas BAX-deficient trigeminal neurones died in the absence of NGF.

36 is required for the in vivo survival of many trigeminal neurons during the early stages of target fie

37 In vitro, 22% of cultured trigeminal neurons exhibited YFP neurofluorescence.

38 nal death in the trigeminal ganglion at E14, trigeminal neurons from bcl-2(-/-) embryos initially sur

39 of such cells in zebrafish--Rohon-Beard and trigeminal neurons--have served as models for neural dev

40 , TRPV1, and ASIC3 are often co-expressed in trigeminal neurons, implying the formation of functional

41 Its release from adult rat trigeminal neurons in culture was shown to be markedly i

42 ophysiological recordings from ChR2-positive trigeminal neurons in intact fish revealed that these ce

43 occurs, in part due to molecular changes in trigeminal neurons, including Robo1 downregulation, thus

44 Trigeminal neurons innervating gingivomucosa were identi

45 neurons, and (3) NRM neurons inhibit spinal trigeminal neurons involved in reflex blink circuits.

46 togenesis, the cell count of radial glia and trigeminal neurons is reduced in some mutants of the spa

47 GRP can also be secreted from cell bodies of trigeminal neurons located within the ganglion, the func

48 order to determine whether the mesencephalic trigeminal neurons may receive a direct hypothalamic ore

49 igeminal motoneurons (Mo5) and mesencephalic trigeminal neurons (Me5) are important constituents of t

50 Trigeminal motoneurons (Mo5), mesencephalic trigeminal neurons (Me5), and supratrigeminal (Su5) and

51 ations and burst generation in mesencephalic trigeminal neurons (Mes V).

52 ns in vivo but surprisingly fail to activate trigeminal neuron monocultures.

53 y was used to indicate whether activation of trigeminal neurons occurs in voluntarily diving rats.

54 s deleted established latency in only 10% of trigeminal neurons (P < 0.00001), and these mice were im

55 re were nearly equal proportions of premotor-trigeminal neurons (pre-mV) in the IRt and PCRt.

56 In the present study, we labeled spinal trigeminal neurons projecting to the cochlear nucleus us

57 gradely regulate transcription in developing trigeminal neurons, providing a mechanism of integrating

58 boundary (MHB) domain, the neural crest and trigeminal neurons, raising the possibility that iro1 an

59 raveling toward and contacting mesencephalic trigeminal neurons, some of which were multipolar.

60 Mouse trigeminal neurons survive independently of neurotrophin

61 rring neuronal death at E18, Bcl-2-deficient trigeminal neurons survived with NGF as well as wild-typ

62 2) specifically activates a subpopulation of trigeminal neurons that express TRPA1, a mustard oil- an

63 le-unit recordings were obtained from spinal trigeminal neurons that proved to received convergent in

64 When DPC are cocultured with trigeminal neurons, they promote survival and a specific

65 ontrols the differential gene expressions in trigeminal neurons through both Smad4-independent and Sm

66 We have used cultured trigeminal neurons to demonstrate that sumatriptan can d

67 e chromatin immunoprecipitation in embryonic trigeminal neurons to show that Brn3a is a direct repres

68 We have used primary cultures of trigeminal neurons under conditions simulating migraine

69 At E14 in vivo, the number of trigeminal neurons undergoing apoptosis was significantl

70 dence for NMDA receptor subunits in neonatal trigeminal neurons used in oral-motor circuitry and sugg

71 demonstrated that LPS binds to receptors in trigeminal neurons using competitive binding.

72 When E10 trigeminal neurons were cultured on different substrates

73 Spinal trigeminal neurons were distributed primarily in pars ca

74 By contrast, when trigeminal neurons were seeded onto cryosections of E10

75 and elaborate neurite outgrowth pattern from trigeminal neurons, whereas skin fibroblasts do not prov

76 dy aims to morphometrically characterize rat trigeminal neurons, which express TLR4, and to investiga

77 an excitatory postsynaptic current (EPSC) in trigeminal neurones with a latency of 1.8 +/- 0.1 ms, ji