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1 anchial placode gives rise to neurons of the nodose ganglia.
2 g anterograde transsynaptic tracing from the nodose ganglia.
3 lament-positive pulmonary sensory neurons in nodose ganglia.
4 d larger currents compared to those from the nodose ganglia.
5 y, uterine nerve cell bodies were labeled in nodose ganglia.
6 arbocyanine perchlorate (DiI) bilaterally to nodose ganglia.
7 ervating the duodenum were recorded from rat nodose ganglia.
8  polymodal Adelta-fibres that arise from the nodose ganglia.
9 hannels in sensory neurons isolated from rat nodose ganglia.
10 nal populations can be identified within the nodose ganglia.
11 fied as PCR products from mRNA prepared from nodose ganglia.
12 glion and Adelta-fibres from the jugular and nodose ganglia.
13 C6-IR cells were also present in sections of nodose ganglia.
14 rvating the intestine were recorded from rat nodose ganglia.
15 R cells and NOS-IR cells were present in the nodose ganglia.
16 ACAP-IR cells and fibers were present in the nodose ganglia.
17 ion may be carried by the circulation to the nodose ganglia.
18 NOS innervation is probably derived from the nodose ganglia.
19 of a putative sodium channel (NaNG) from dog nodose ganglia.
20 ncluding the petrosal, superior cervical and nodose ganglia.
21 CsA) on cardiac sensory neurons (CSN) of the nodose ganglia.
22 ic plexus were retrogradely labeled from the nodose ganglia.
23  gene expression is prevalent in human adult nodose ganglia.
24          A small percentage of the nAChRs in nodose ganglia also contain alpha2 and alpha4 subunits.
25 GCaMP8s to record calcium signal dynamics in nodose ganglia and (2) the neuronal actuator DREADD to d
26 60% of the labeled neurons were found in the nodose ganglia and 40% in the jugular ganglia.
27 ose-excited and glucose-inhibited neurons in nodose ganglia and characterize their glucose-sensing pr
28 mn (T1 to L1), ipsilateral and contralateral nodose ganglia and ipsilateral dorsal root ganglia from
29 2, Bmal1, and Nr1d1 mRNA is expressed in the nodose ganglia and levels oscillated over a 24 h period.
30 ve monosynaptic vagal sensory input from the nodose ganglia and spinal sensory input from the dorsal
31 ors are found in cranial afferent neurons in nodose ganglia and their central terminations within the
32 ound that aortic baroreceptor neurons in the nodose ganglia and their terminals express ASIC2.
33 he integration of luminal information in the nodose ganglia and transmission to vagal integral sites
34 ent neurons whose cell bodies resided in the nodose ganglia and whose receptive fields were located i
35 mall neurons of dorsal root, trigeminal, and nodose ganglia) and localizes to their sensory terminals
36 CR analysis, its expression is restricted to nodose ganglia, and not present in cortex, hippocampus,
37 e dorsal vagal complex of the hindbrain, the nodose ganglia, and the ganglia of the myenteric and sub
38  observed scattered 5-HT1D-IR neurons in the nodose ganglia, and there was sparse terminal immunoreac
39 re given injections of dextran biotin in the nodose ganglia, and, after tracer transport, stomach who
40 findings indicate that the nAChRs in SCG and nodose ganglia are heterogeneous, which suggests that di
41 cluding the petrosal, superior cervical, and nodose ganglia, as well as ganglia in the myenteric plex
42 e in lung C-fibre terminals arising from the nodose ganglia, but failed to evoke action potential dis
43        NOS-IR cells were also present in the nodose ganglia, but only some exhibited CGRP immunoreact
44        The fast-blue-positive neurons in the nodose ganglia, by contrast, were large in diameter (40
45                                           In nodose ganglia, CAP but not alphabeta-m-ATP evoked inwar
46 vagal sensory neurons located in the jugular-nodose ganglia complex (JNC) with identified receptive f
47 that a majority of the nAChRs in the SCG and nodose ganglia contain the alpha3 and beta4 subunits, bu
48  in vagal afferent neurons isolated from rat nodose ganglia demonstrated that 31/118 (26%) neurons we
49                   Cardiac afferents from the nodose ganglia differed from CDRGNs in having smaller ac
50                     There were no changes in nodose ganglia excitability in TNX deficient mice, sugge
51 e show that vagal sensory neurons within the nodose ganglia exhibit distinct real-time neuronal respo
52           Most vagal afferent neurons in rat nodose ganglia express mRNA coding for the NR1 subunit o
53                             VANs, located in nodose ganglia, express receptors for various gut-derive
54                           Both rat and human nodose ganglia expressed OX-R1 as detected by RT-PCR, an
55  previous studies have demonstrated that the nodose ganglia expresses low levels of delta-opioid rece
56  increased neural proliferation within adult nodose ganglia following capsaicin-induced neuronal deat
57 e used large scale two-photon imaging of the nodose ganglia from our ex vivo preparation isolated fro
58 ified in the visceral sensory neurons of the nodose ganglia from rats through immunocytochemical stud
59 Substance P/Neurokinin A positive neurons in nodose ganglia from virus-inoculated guinea pigs at Day
60                  Neurites from explanted E14 nodose ganglia grew selectively toward cocultured E14 di
61                  These results show that rat nodose ganglia have glucose-excited and glucose-inhibite
62 microinjection of AAV vectors into the vagal nodose ganglia in vivo leads to selective, effective and
63 give rise to all major glial subtypes in the nodose ganglia, including Schwann cells, satellite glia,
64 nous GLP-1, we established a novel bilateral nodose ganglia injection technique to deliver a lentivir
65    To examine this hypothesis, rats received nodose ganglia injections of an adeno-associated virus (
66                               Few neurons in nodose ganglia innervate the uterus.
67 on in neurons within dorsal root ganglia and nodose ganglia innervating the heart.
68         Piezo2 in mouse dorsal root, but not nodose ganglia is required to sense gut content, and thi
69 etween CCK and serotonin at the level of the nodose ganglia may explain the robust postprandial pancr
70                                Two groups of nodose ganglia neurones were identified: group A neurone
71 ly in gastric motor and sensory function and nodose ganglia neurones.
72 on of opioid receptors in gastric-projecting nodose ganglia neurons contributes to the reduction in g
73 codone, U-50488, or deltorphin II on gastric nodose ganglia neurons inhibited Ca(2+) currents through
74                                        Thus, nodose ganglia neurons perform real-time encoding of cyt
75      This study demonstrated that in gastric nodose ganglia neurons, agonists targeting all three cla
76 mp recordings were performed on isolated rat nodose ganglia neurons.
77 innervated the bladder and colon in both the nodose ganglia (NG) and L6/S1 and L1/L2 dorsal root gang
78 om thoracolumbar (TL), lumbosacral (LS), and nodose ganglia (NG) in male and female mice.
79 pinal cord potassium channel) contributes to nodose ganglia (NG) malfunction, disrupting gastrointest
80 ed by allergic inflammation were examined in nodose ganglia (NG) removed from guinea pigs immunized t
81 t in a majority of vagal afferent neurons of nodose ganglia (NG), immunoreactivity for other NMDA rec
82 ly in both the dorsal root ganglia (DRG) and nodose ganglia (NG).
83  the 5-HT3A subunit in superior cervical and nodose ganglia (NG).
84 carbocyanine methanesulfonate (DiI) into the nodose ganglia of animals with prior supranodose de-effe
85 of Fos-immunoreactive neuronal nuclei in the nodose ganglia of LETO rats, but not in the nodose gangl
86 anscripts encoding DCC were expressed in the nodose ganglia of mice from E12 to adulthood but were de
87  nodose ganglia of LETO rats, but not in the nodose ganglia of OLETF rats.
88 ation of GLP-1R mRNA expression in the vagal nodose ganglia of OP rats.
89 m agglutinin-horseradish peroxidase into the nodose ganglia of rats that had received unilateral vent
90 urons in primary neuronal cell cultures from nodose ganglia of rats.
91 on of TRPV1-expressing pulmonary neurones in nodose ganglia of sensitized rats; this increase in TRPV
92 ceptor alpha and beta (LXRalpha/beta) in the nodose ganglia of the vagus nerve.
93 ised of the superior (jugular) and inferior (nodose) ganglia of the vagus nerve, receive somatosensor
94 ishes a latent infection in sensory ganglia (nodose ganglia) of the tenth cranial nerve.
95 transcripts and protein were detected in the nodose ganglia, OT signaling might also affect extrinsic
96 immunoreactive neurons in the trigeminal and nodose ganglia over this period of development.
97 ivo gene silencing of PI3K and Erk1/2 in the nodose ganglia prevented ghrelin inhibition of leptin- o
98 gular ganglia) and placode-derived neurones (nodose ganglia) project C-fibres in the vagus, and that
99 ve afferent neurones with cell bodies in the nodose ganglia projected to the rostral trachea and lary
100  superior cervical, and 12 of 36 and 1 of 36 nodose ganglia, respectively.
101 the superior cervical ganglia (SCG), sensory nodose ganglia, stellate ganglia, and pelvic ganglia.
102     Here, we test whether neurons within the nodose ganglia that express angiotensin type-1a receptor
103                                          The nodose ganglia, the stomach, the first 8 cm of duodenum,
104 and spatial transcriptomic analysis of human nodose ganglia tissue identified additional bacterial sp
105 t Lipofectamine transfection of cultured rat nodose ganglia to determine the effect of these molecule
106                  Na(V)1.7 gene expression in nodose ganglia was effectively and selectively reduced w
107    OX-R1 and -R2 expression by rat and human nodose ganglia was examined by reverse-transcriptase pol
108 rade neuronal tracer (DiI) and dye uptake in nodose ganglia was examined.
109                                              Nodose ganglia were collected from 8-week-old female C57
110                                          The nodose ganglia were labeled starting 4 days PI, suggesti
111      Rat aortic baroreceptor neurones in the nodose ganglia were labelled in vivo by applying a fluor
112 MDA subunits expressed in the left and right nodose ganglia were not significantly different.
113                   After at least 1 week, the nodose ganglia were removed and the neurons were culture
114 ely from the NA, neurons of the DmnX and the nodose ganglia were surveyed for DiI labeling.
115 h functionally expressed in dorsal root- and nodose ganglia where they signal through different G pro

 
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