ライフサイエンスコーパス: nodose ganglia

1 lament-positive pulmonary sensory neurons in nodose ganglia.

2 d larger currents compared to those from the nodose ganglia.

3 arbocyanine perchlorate (DiI) bilaterally to nodose ganglia.

4 ervating the duodenum were recorded from rat nodose ganglia.

5 polymodal Adelta-fibres that arise from the nodose ganglia.

6 hannels in sensory neurons isolated from rat nodose ganglia.

7 nal populations can be identified within the nodose ganglia.

8 fied as PCR products from mRNA prepared from nodose ganglia.

9 glion and Adelta-fibres from the jugular and nodose ganglia.

10 C6-IR cells were also present in sections of nodose ganglia.

11 rvating the intestine were recorded from rat nodose ganglia.

12 R cells and NOS-IR cells were present in the nodose ganglia.

13 ACAP-IR cells and fibers were present in the nodose ganglia.

14 ion may be carried by the circulation to the nodose ganglia.

15 NOS innervation is probably derived from the nodose ganglia.

16 of a putative sodium channel (NaNG) from dog nodose ganglia.

17 ncluding the petrosal, superior cervical and nodose ganglia.

18 CsA) on cardiac sensory neurons (CSN) of the nodose ganglia.

19 ic plexus were retrogradely labeled from the nodose ganglia.

20 gene expression is prevalent in human adult nodose ganglia.

21 A small percentage of the nAChRs in nodose ganglia also contain alpha2 and alpha4 subunits.

22 60% of the labeled neurons were found in the nodose ganglia and 40% in the jugular ganglia.

23 ose-excited and glucose-inhibited neurons in nodose ganglia and characterize their glucose-sensing pr

24 mn (T1 to L1), ipsilateral and contralateral nodose ganglia and ipsilateral dorsal root ganglia from

25 2, Bmal1, and Nr1d1 mRNA is expressed in the nodose ganglia and levels oscillated over a 24 h period.

26 ors are found in cranial afferent neurons in nodose ganglia and their central terminations within the

27 ound that aortic baroreceptor neurons in the nodose ganglia and their terminals express ASIC2.

28 ent neurons whose cell bodies resided in the nodose ganglia and whose receptive fields were located i

29 mall neurons of dorsal root, trigeminal, and nodose ganglia) and localizes to their sensory terminals

30 CR analysis, its expression is restricted to nodose ganglia, and not present in cortex, hippocampus,

31 e dorsal vagal complex of the hindbrain, the nodose ganglia, and the ganglia of the myenteric and sub

32 observed scattered 5-HT1D-IR neurons in the nodose ganglia, and there was sparse terminal immunoreac

33 re given injections of dextran biotin in the nodose ganglia, and, after tracer transport, stomach who

34 findings indicate that the nAChRs in SCG and nodose ganglia are heterogeneous, which suggests that di

35 cluding the petrosal, superior cervical, and nodose ganglia, as well as ganglia in the myenteric plex

36 e in lung C-fibre terminals arising from the nodose ganglia, but failed to evoke action potential dis

37 NOS-IR cells were also present in the nodose ganglia, but only some exhibited CGRP immunoreact

38 The fast-blue-positive neurons in the nodose ganglia, by contrast, were large in diameter (40

39 In nodose ganglia, CAP but not alphabeta-m-ATP evoked inwar

40 vagal sensory neurons located in the jugular-nodose ganglia complex (JNC) with identified receptive f

41 that a majority of the nAChRs in the SCG and nodose ganglia contain the alpha3 and beta4 subunits, bu

42 in vagal afferent neurons isolated from rat nodose ganglia demonstrated that 31/118 (26%) neurons we

43 Cardiac afferents from the nodose ganglia differed from CDRGNs in having smaller ac

44 Most vagal afferent neurons in rat nodose ganglia express mRNA coding for the NR1 subunit o

45 Both rat and human nodose ganglia expressed OX-R1 as detected by RT-PCR, an

46 increased neural proliferation within adult nodose ganglia following capsaicin-induced neuronal deat

47 ified in the visceral sensory neurons of the nodose ganglia from rats through immunocytochemical stud

48 Substance P/Neurokinin A positive neurons in nodose ganglia from virus-inoculated guinea pigs at Day

49 Neurites from explanted E14 nodose ganglia grew selectively toward cocultured E14 di

50 These results show that rat nodose ganglia have glucose-excited and glucose-inhibite

51 microinjection of AAV vectors into the vagal nodose ganglia in vivo leads to selective, effective and

52 nous GLP-1, we established a novel bilateral nodose ganglia injection technique to deliver a lentivir

53 etween CCK and serotonin at the level of the nodose ganglia may explain the robust postprandial pancr

54 Two groups of nodose ganglia neurones were identified: group A neurone

55 mp recordings were performed on isolated rat nodose ganglia neurons.

56 innervated the bladder and colon in both the nodose ganglia (NG) and L6/S1 and L1/L2 dorsal root gang

57 pinal cord potassium channel) contributes to nodose ganglia (NG) malfunction, disrupting gastrointest

58 ed by allergic inflammation were examined in nodose ganglia (NG) removed from guinea pigs immunized t

59 t in a majority of vagal afferent neurons of nodose ganglia (NG), immunoreactivity for other NMDA rec

60 ly in both the dorsal root ganglia (DRG) and nodose ganglia (NG).

61 the 5-HT3A subunit in superior cervical and nodose ganglia (NG).

62 carbocyanine methanesulfonate (DiI) into the nodose ganglia of animals with prior supranodose de-effe

63 of Fos-immunoreactive neuronal nuclei in the nodose ganglia of LETO rats, but not in the nodose gangl

64 anscripts encoding DCC were expressed in the nodose ganglia of mice from E12 to adulthood but were de

65 nodose ganglia of LETO rats, but not in the nodose ganglia of OLETF rats.

66 ation of GLP-1R mRNA expression in the vagal nodose ganglia of OP rats.

67 m agglutinin-horseradish peroxidase into the nodose ganglia of rats that had received unilateral vent

68 urons in primary neuronal cell cultures from nodose ganglia of rats.

69 on of TRPV1-expressing pulmonary neurones in nodose ganglia of sensitized rats; this increase in TRPV

70 ceptor alpha and beta (LXRalpha/beta) in the nodose ganglia of the vagus nerve.

71 ishes a latent infection in sensory ganglia (nodose ganglia) of the tenth cranial nerve.

72 transcripts and protein were detected in the nodose ganglia, OT signaling might also affect extrinsic

73 immunoreactive neurons in the trigeminal and nodose ganglia over this period of development.

74 ivo gene silencing of PI3K and Erk1/2 in the nodose ganglia prevented ghrelin inhibition of leptin- o

75 gular ganglia) and placode-derived neurones (nodose ganglia) project C-fibres in the vagus, and that

76 ve afferent neurones with cell bodies in the nodose ganglia projected to the rostral trachea and lary

77 superior cervical, and 12 of 36 and 1 of 36 nodose ganglia, respectively.

78 the superior cervical ganglia (SCG), sensory nodose ganglia, stellate ganglia, and pelvic ganglia.

79 The nodose ganglia, the stomach, the first 8 cm of duodenum,

80 t Lipofectamine transfection of cultured rat nodose ganglia to determine the effect of these molecule

81 Na(V)1.7 gene expression in nodose ganglia was effectively and selectively reduced w

82 OX-R1 and -R2 expression by rat and human nodose ganglia was examined by reverse-transcriptase pol

83 Nodose ganglia were collected from 8-week-old female C57

84 The nodose ganglia were labeled starting 4 days PI, suggesti

85 Rat aortic baroreceptor neurones in the nodose ganglia were labelled in vivo by applying a fluor

86 MDA subunits expressed in the left and right nodose ganglia were not significantly different.

87 After at least 1 week, the nodose ganglia were removed and the neurons were culture

88 ely from the NA, neurons of the DmnX and the nodose ganglia were surveyed for DiI labeling.