ライフサイエンスコーパス: caudalis

1 face (principalis, oralis, interpolaris, and caudalis).

2 rsal horn of the medulla (trigeminal nucleus caudalis).

3 rsal horn of the medulla (trigeminal nucleus caudalis).

4 inal subnucleus interpolaris, and subnucleus caudalis.

5 ls were counted in the trigeminal subnucleus caudalis.

6 d antinociception occurred at the subnucleus caudalis.

7 ganglion and c-Fos in the trigeminal nucleus caudalis.

8 ucleus, trigeminal tract, and dorsal nucleus caudalis.

9 eactivity (Fos-LI) in the trigeminal nucleus caudalis.

10 d to lamina II of the ipsilateral subnucleus caudalis.

11 nd SP-LI increased in ipsilateral subnucleus caudalis.

12 rent profiles in lamina II of rat subnucleus caudalis.

13 terminals within lamina II of the subnucleus caudalis.

14 pression of Fos-LI in the trigeminal nucleus caudalis.

15 tinosa of the spinal trigeminal nucleus pars caudalis.

16 ctivation of cells in the trigeminal nucleus caudalis.

17 rigeminal nucleus subnuclei interpolaris and caudalis.

18 inal cord dorsal horn and trigeminal nucleus caudalis.

19 portion of the ventral lateral nucleus, pars caudalis, (2) the caudal portion of the ventral lateral

20 portion of the ventral lateral nucleus, pars caudalis, (3) the mediodorsal nucleus, (4) the ventral a

21 ta demonstrate that in trigeminal subnucleus caudalis activation of either NK1 or NMDA receptors alon

22 nal ganglia and associated spinal subnucleus caudalis and C1/C2 cervical dorsal spinal cord (Vc/C2).

23 der neurons in the dorsal horn of subnucleus caudalis and cervical C1/C2 spinal cord (Vc/C2, or trige

24 l neurons were distributed primarily in pars caudalis and interpolaris and provided inputs to the coc

25 18% in the transition zone between subnuclei caudalis and interpolaris), and 14% rostral to the obex

26 hese afferents within the trigeminal nucleus caudalis and the spinal cord dorsal horn, 5-HT1D-IR fibe

27 brainstem (i.e., nucleus reticularis pontis caudalis) and the centromedial amygdala as key hubs for

28 al solitary nucleus, periobex dorsal nucleus caudalis), and (3) late Fos-IR at 2-4 weeks (bilateral s

29 bex (22% in C2, 22% in C1, 23% in subnucleus caudalis, and 18% in the transition zone between subnucl

30 tractus solitarii, spinal trigeminal nucleus caudalis, and inferior olivary subnuclei.

31 ostriatal projections arose from VA, VL pars caudalis, and ventral posterior lateral pars oralis nucl

32 These data suggest that the n. trigeminal caudalis blood flow model may be useful in identifying a

33 imulation-induced increases in n. trigeminal caudalis blood flow reflect activation of a large popula

34 sion can be induced in trigeminal subnucleus caudalis by NMDA or neurokinin-1 receptor activation, an

35 protein extravasation model and the nucleus caudalis c-fos expression model.

36 in the trigeminal subnuclei interpolaris and caudalis, C1-2 dorsal horn, and other medullary nuclei.

37 /Vc) transition or the trigeminal subnucleus caudalis-cervical cord (Vc/C1) junction region in the lo

38 al dorsal horn, contralateral dorsal nucleus caudalis, contralateral rostral lateral solitary nucleus

39 ctivity (SP-LI) were evaluated in subnucleus caudalis following induction of sinusitis.

40 ctivating neurones in the trigeminal nucleus caudalis following stimulation of the trigeminovascular

41 lar nucleus (RPPp), the nucleus hypothalamus caudalis (Hc), the nucleus hypothalamus anterioris, the

42 or the magnocellular portion of V subnucleus caudalis in these animals.

43 'protecting' the prospective forebrain from caudalising influences of the organiser, the chick hypob

44 nterpolaris (juvenile tissue) and subnucleus caudalis (juvenile and adult tissue).

45 the ventrolateral nucleus reticularis pontis caudalis labeled neurons in the deep layers of the super

46 ons in superficial laminae of the subnucleus caudalis may be important for the reflex initiation of t

47 mitter patterns within lamina II of the pars caudalis/medullary dorsal horn.

48 dorsal spinal trigeminal complex (Sp5) pars caudalis, near the obex, and the Sp5 pars oralis near th

49 ming of oral tissues from trigeminal nucleus caudalis neurons in female and male wild-type and TRPM8

50 entral intermedius nucleus (Vim) and ventral caudalis nucleus (Vc) of the thalamus, and subthalamic n

51 and a complete absence of barrelettes in the caudalis nucleus.

52 contralateral DCN and pars interpolaris and caudalis of Sp5.

53 s located in the main sensory and subnucleus caudalis of the brainstem and joints, respectively.

54 the superficial aspect of trigeminal nucleus caudalis of the New World owl monkey that is not immunor

55 cellularis lateralis and dorsalis, r. pontis caudalis pars alpha and beta, r. pontis oralis pars medi

56 r targets, to the nucleus reticularis pontis caudalis (PnC), a major component of the ASR circuit, bu

57 rn project to the nucleus reticularis pontis caudalis (PnC), an obligatory relay in the primary acous

58 d 80 ng) into the nucleus reticularis pontis caudalis (PnC), an obligatory synapse in the acoustic st

59 lemniscus (VLL), nucleus reticularis pontis caudalis (PnC), and spinal motoneurons.

60 Kolliker-Fuse nucleus, and pontis centralis caudalis (PoC), in the contralateral pontis centralis or

61 Subnucleus caudalis represented the face in a three-dimensional map

62 N) to the spinal cord and trigeminal nucleus caudalis (Sp5c) has been described.

63 subnuclei interpolaris (SpVi) and subnuclei caudalis (SpVc) and the dorsal column nucleus-based lemn

64 pinal cord and the spinal trigeminal nucleus caudalis (SpVc).

65 ecies, into cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus oralis, an

66 the ipsilateral spinal trigeminal subnucleus caudalis (SVc) and interpolaris (SVi), and the dorsal ra

67 immunoreactivity were the trigeminal nucleus caudalis (TNC) and its caudal extension into the C(1) an

68 were absent from both the trigeminal nucleus caudalis (TNC) and the spinal cord.

69 n female mice) as well as trigeminal nucleus caudalis (TNC) in male and female mice.

70 ecular data show that the trigeminal nucleus caudalis (TNC) is a central structure in headache pathol

71 l dorsal horn from the trigeminal subnucleus caudalis to C2.

72 RVM and PB from the trigeminal interpolaris-caudalis transition zone (Vi/Vc) in male and female rats

73 dorsal portion of the subnuclei interpolaris/caudalis transition zone at the level of the obex was ac

74 lateral Fos-LI was found in the interpolaris-caudalis trigeminal transition zone.

75 iceptive lamina of the trigeminal subnucleus caudalis (TSNC) in the brainstem.

76 s were found predominantly in Vsp subnucleus caudalis (Vc) and in dorsomedial subnucleus oralis.

77 dorsomedial aspect of trigeminal subnucleus caudalis (Vc) evoked by lingual application of carbonate

78 ings were made in the rat trigeminal nucleus caudalis (Vc) from cells with Adelta and C-fibre latency

79 the potential role of sGC in the subnucleus caudalis (Vc) in mediating masseter hypersensitivity und

80 ciceptive responses of trigeminal subnucleus caudalis (Vc) neurons in rats.

81 a, and lamina V of the trigeminal subnucleus caudalis (Vc), exhibited FluoroGold/Fos double staining,

82 of 5-HT3 receptors in the trigeminal nucleus caudalis (Vc), the homolog of the spinal dorsal horn.

83 y region of the spinal trigeminal subnucleus caudalis (Vc), which projects to the PbN.

84 face of the eye to the trigeminal subnucleus caudalis (Vc).

85 roperties similar to those in the subnucleus caudalis (Vc).

86 ventral trigeminal subnucleus interpolaris- caudalis (Vi/Vc) transition or the trigeminal subnucleus

87 igeminal complex, the subnuclei interpolaris/caudalis (Vi/Vc) transition zone and the laminated Vc, o

88 cated a role for the trigeminal interpolaris/caudalis (Vi/Vc) transition zone in response to orofacia

89 ion of the trigeminal subnuclei interpolaris/caudalis (Vi/Vc) transition zone, the percentage of Fos-

90 el of the trigeminal subnucleus interpolaris/caudalis (Vi/Vc) transition zone, there was a selective

91 c, VLo, and the ventral lateral nucleus pars caudalis (VLc), with the density of these projections de

92 eptive fields in subnucleus interpolaris and caudalis were larger than previously mapped receptive fi

93 e perfused, and Vibratome sections from pars caudalis were processed for electron microscopy.

94 rs arriving at the dorsal trigeminal nucleus caudalis, which relays orofacial somatosensory messages