ライフサイエンスコーパス: ganglion neuron

1 erythroleukemic cell or a single dorsal root ganglion neuron.

2 ssed by calcium imaging of mouse dorsal root ganglion neurons.

3 action potential firing of superior cervical ganglion neurons.

4 uronal cell line and primary rat dorsal root ganglion neurons.

5 oligodendrocytes cocultured with dorsal root ganglion neurons.

6 expressed in nodose-petrosal and geniculate ganglion neurons.

7 er upon reactivation from latency in sensory ganglion neurons.

8 ther alone or in the presence of dorsal root ganglion neurons.

9 ntracellular Ca(2+) signaling in dorsal root ganglion neurons.

10 ng of sound onset in the postsynaptic spiral ganglion neurons.

11 til after reinnervation by distant gustatory ganglion neurons.

12 latency, consistent with apoptosis of spiral ganglion neurons.

13 tivity after TRPA1 activation in dorsal root ganglion neurons.

14 rily Cav3.2) channels in sensory dorsal root ganglion neurons.

15 ganglion neurons and in almost all myenteric ganglion neurons.

16 innervation of muscle fibers by dorsal root ganglion neurons.

17 eptor expression to medium sized dorsal root ganglion neurons.

18 polymodal and pure mechanosensory trigeminal ganglion neurons.

19 on of TRPM8 in 48.8% of TRPM8(+) dorsal root ganglion neurons.

20 cargo motility in primary mouse dorsal root ganglion neurons.

21 n dorsal root ganglion (DRG) and sympathetic ganglion neurons.

22 tion of large-diameter Nav1.8(+) dorsal root ganglion neurons.

23 ofound effect on excitability of sympathetic ganglion neurons.

24 ed central branch of conditioned dorsal root ganglion neurons.

25 ed responses in only a subset of dorsal-root ganglion neurons.

26 embryonic SAG neurons and adult mouse spiral ganglion neurons.

27 erm synaptic plasticity in superior cervical ganglion neurons.

28 wth cone collapse assay on chick dorsal root ganglion neurons.

29 lts in loss of pigment cells and dorsal root ganglion neurons.

30 utophagosome dynamics in primary dorsal root ganglion neurons.

31 m function of auditory hair cells and spiral ganglion neurons.

32 2, is selective for Na(V) 1.6 in dorsal root ganglion neurons.

33 ng vomeronasal, nasal septal, and Grunenberg ganglion neurons.

34 m, and calcium channels in mouse dorsal root ganglion neurons.

35 ceptive dorsal root ganglion and sympathetic ganglion neurons.

36 rite growth of co-cultured adult dorsal root ganglion neurons.

37 east one respect from that seen with ciliary ganglion neurons.

38 splicing isoform of Na(v)1.7 in dorsal root ganglion neurons.

39 prevent inflammatory responses in trigeminal ganglion neurons.

40 nat2 compound heterozygote superior cervical ganglion neurons.

41 /-) double mutants lose 90-95% of geniculate ganglion neurons.

42 n dorsal root ganglion (DRG) and sympathetic ganglion neurons.

43 ression in approximately one-third of nodose ganglion neurons.

44 turn modulate gene expression in trigeminal ganglion neurons.

45 t of endogenous deltaR in primary trigeminal ganglion neurons.

46 Nav1.6-mediated excitability in dorsal root ganglion neurons.

47 ort single cell RNA sequencing of geniculate ganglion neurons.

48 f the IAN (2-30 d), followed by uninjured V2 ganglion neurons (6-30 d), and then VPM V2 neurons (7-30

49 and PKC was also observed in the dorsal root ganglion neurons after chronic treatment with paclitaxel

50 so resulted in diminished survival of spiral ganglion neurons after hair cell death.

51 of these pathways in the survival of spiral ganglion neurons after noise exposure and during aging s

52 ural precursor cells and later in the spiral ganglion neurons along with Neurog1 and NeuroD1, we used

53 TRPV1-expressing airway-specific jugular ganglion neurons also express S1PR3 mRNA.

54 uppressed M-current in rat superior cervical ganglion neurons, an effect negated by overexpression of

55 odium current, in small-diameter dorsal root ganglion neurons, an effect that was attenuated by a PI3

56 on occurs in approximately 26% of trigeminal ganglion neurons and 30% of corneal afferent neurons.

57 t increases cAMP, in a subset of dorsal root ganglion neurons and also within neurons of the spinal c

58 for specification of Islet-expressing motor ganglion neurons and atrial siphon muscles.

59 hat alpha2delta3 mRNA is expressed in spiral ganglion neurons and auditory brainstem nuclei and that

60 blished RNA-sequencing dataset of geniculate ganglion neurons and by in situ hybridization, we demons

61 ngle TRPV1 molecules in isolated dorsal root ganglion neurons and cell lines.

62 lucocorticoids in age-related loss of spiral ganglion neurons and extensive studies in the central ne

63 CSE was present in all submucosal ganglion neurons and in almost all myenteric ganglion ne

64 sporter in both cultured primary dorsal root ganglion neurons and injured peripheral nerve.

65 lon was found in the majority of dorsal root ganglion neurons and intensely labeled laminae I and II

66 Na(V)1.7 is highly expressed in dorsal root ganglion neurons and is obligatory for nociceptive signa

67 molecule than Nogo-66 for chick dorsal root ganglion neurons and mature cortical neurons.

68 mice completely ablates MORs in dorsal root ganglion neurons and reduces the MOR expression level in

69 nhance resurgent currents within dorsal root ganglion neurons and show by current-clamp that R185H re

70 ssion is completely deleted from dorsal root ganglion neurons and substantially reduced in the spinal

71 mechanoreceptive and nociceptive trigeminal ganglion neurons and the visual sensory retinal ganglion

72 sensory dorsal root ganglion and sympathetic ganglion neurons and their small diameter peripheral axo

73 within dorsal root ganglion and sympathetic ganglion neurons and their small-diameter peripheral axo

74 Cavalpha2delta1 up-regulation in trigeminal ganglion neurons and Vc/C2.

75 ral transduction of inner hair cells, spiral ganglion neurons and vestibular hair cells.

76 -S Na+ current density in medium dorsal root ganglion neurons and, importantly, mechanical allodynia

77 ocytes, cultured hippocampal and dorsal root ganglion neurons, and brain slices.

78 ells, PC3 prostate cancer cells, dorsal root ganglion neurons, and hippocampal neurons.

79 1A in axons of primary rat superior cervical ganglion neurons, and overexpression or disruption of KI

80 els in mammalian cardiomyocytes, dorsal root ganglion neurons, and pancreatic beta cells.

81 gene-related peptide (CGRP) from dorsal root ganglion neurons, and reduced inflammation in a mouse mo

82 h dorsal root ganglion and superior cervical ganglion neurons, and renders dorsal root ganglion neuro

83 otherapy-induced cytotoxicity of dorsal root ganglion neurons, and retinal ganglion cells (RGCs) in r

84 somatosensory neurons, spiral and vestibular ganglion neurons, and retinal ganglion cells.

85 tly expressed in a wide range of dorsal root ganglion neurons, and that its expression is gradually r

86 plasticity in transfected superior cervical ganglion neurons, and these regulatory effects are preve

87 (IC(50) = 0.4 nm) in dissociated dorsal root ganglion neurons, and this IC(50) is approximately 500 t

88 Furthermore, spiral ganglion neurons are absent in cochleae from Sox2(Lcc/Lc

89 ner hair cells, auditory synapses and spiral ganglion neurons are all present after noise exposure in

90 m the epibranchial placodes, whereas jugular ganglion neurons are derived from the neural crest.

91 In contrast, chick mandibular ganglion neurons are located rostrally to maxillary neur

92 In the cochlea, spiral ganglion neurons are organized in a basal to apical prog

93 In contrast, dorsal root ganglion neurons are stiffer than P-19 and cortical cell

94 d rTRPM3, which are expressed in dorsal root ganglion neurons, are insensitive toward apomorphine tre

95 ical modulation of T-channels in dorsal root ganglion neurons as measured by a large increase in the

96 sensitization of native TRPV1 in dorsal root ganglion neurons as well as of recombinant TRPV1 express

97 g of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and enteric neurons

98 ically distinct from other classes of spiral ganglion neurons because they extend a peripheral axon b

99 +) channel robustly expressed in dorsal root ganglion neurons, becomes dysfunctional upon calcineurin

100 e to a loss of cochlear hair cells or spiral ganglion neurons, both of which normally express Foxo3.

101 use hippocampal slices and superior cervical ganglion neuron boutons (sites of synaptic NE release).

102 ton microscopy to image taste responses from ganglion neurons buried deep at the base of the brain.

103 rs ago to depend on innervation from distant ganglion neurons, but the underlying mechanism has remai

104 However, conditioning dorsal root ganglion neurons by first lesioning their peripheral axo

105 was confirmed in cultured murine sympathetic ganglion neurons by RT-PCR and immunofluorescent stainin

106 ression could not be detected in dorsal root ganglion neurons by single-cell RT-PCR.

107 ll PLCdelta4(-/-) TRPM8-positive dorsal root ganglion neurons cold, menthol and WS-12, a selective TR

108 lectrophysiology recordings from dorsal root ganglion neurons collected during remission showed const

109 We observed that the pelvic ganglion neurons contributed a number of extrinsic fiber

110 alpha2delta-1 subunit in sensory dorsal root ganglion neurons contributes to the generation of chroni

111 lity to seal the reticular lamina and spiral ganglion neuron counts are normal, a key requirement for

112 Correspondingly, dorsal root ganglion neurons cultured in G-CSF failed to respond to

113 fine selectivity in the taste preference of ganglion neurons; demonstrate a strong match between TRC

114 ta were generated in airway-specific primary ganglion neurons, demonstrating that tiotropium inhibite

115 tion of M current in nociceptive dorsal root ganglion neurons did not reduce the efficacy of retigabi

116 We show that these abdominal ganglion neurons directly activate the female-specific p

117 Dorsal root ganglion neurons displayed a fall in resting cytoplasmic

118 lesions and reduced in models of dorsal root ganglion neuron (DRGN) axon regeneration.

119 7, and 9 are expressed by human dorsal root ganglion neurons (DRGNs) and in cultures of primary mous

120 Here we show in adult mice that dorsal root ganglion neurons (DRGs) and CST neurons fail to upregula

121 ze resting membrane potential of dorsal root ganglion neurons, enhance spontaneous firing, and increa

122 ltered ion channel expression in dorsal root ganglion neurons, enhanced dorsal horn glutamate release

123 In isolated dorsal root ganglion neurons, EP3 receptor activation counteracted t

124 Spiral ganglion neurons exhibit spontaneous activity at least b

125 show that only 43% of CQ-excited dorsal root ganglion neurons expressed TRPA1; as expected, the respo

126 malized the hyperexcitability of dorsal root ganglion neurons expressing S241T.

127 In transfected small rat dorsal root ganglion neurons, expression of L1302F and L811P evoked

128 we find that CAST/Ei mouse adult dorsal root ganglion neurons extend axons more on CNS myelin than th

129 instance, in the developing cochlea, spiral ganglion neurons extend their peripheral processes throu

130 y, where dorsal root ganglion and trigeminal ganglion neurons feed pain information into the CNS.

131 c3 and NFATc4 in hippocampal and dorsal root ganglion neurons following electrically evoked elevation

132 (RAE1), is re-expressed in adult dorsal root ganglion neurons following peripheral nerve injury, trig

133 ved in the functional changes of dorsal root ganglion neurons following vincristine treatment and it

134 stant (TTX-R) sodium currents in dorsal root ganglion neurons following vincristine treatment.

135 iments to examine the role of Sox2 in spiral ganglion neuron formation.

136 current (I(AHV)) in nociceptive dorsal root ganglion neurons from 7-day-old rats.

137 Trigeminal ganglion neurons from adult female Sprague Dawley rats w

138 In this study, dissociated dorsal-root ganglion neurons from mice were exposed to various pharm

139 avior and activation of cultured dorsal root ganglion neurons from mice.

140 Cultured adult dorsal root ganglion neurons from nSIRT1OE mice, maintained at high

141 1 and Pirt, and that dissociated dorsal root ganglion neurons from Pirt knock-out mice have an appare

142 on endogenous TRPA1 in cultured dorsal root ganglion neurons from rats and in the enterochromaffin m

143 p recordings of small and medium dorsal root ganglion neurons from vincristine-treated animals reveal

144 ied ATP in fura-2 loaded isolated geniculate ganglion neurons from wild-type and P2X3 knockout mice.

145 capacity when compared to adult dorsal root ganglion neurons from wild-type mice.

146 This finding advances our knowledge of how ganglion neurons generate uncharacteristic electrical im

147 the VZV immediate-early 63 (IE63) protein in ganglion neurons has been described, but there are signi

148 Type I spiral ganglion neurons have a unique role relative to other se

149 ects of the Del-L955 mutation on dorsal root ganglion neuron hyperexcitability with those produced by

150 al ganglion neurons, and renders dorsal root ganglion neurons hyperexcitable and superior cervical ga

151 m channel Na(V)1.7, which render dorsal root ganglion neurons hyperexcitable, are present in a substa

152 ort, isoform of Na(v)1.7 renders dorsal root ganglion neurons hyperexcitable, reducing the current th

153 ; each of the mutations rendered dorsal root ganglion neurons hyperexcitable.

154 current-clamp that R185H renders dorsal root ganglion neurons hyperexcitable.

155 neurons hyperexcitable and superior cervical ganglion neurons hypoexcitable.

156 ouring enterocytes through P2Y(2) and nodose ganglion neurones in co-cultures through P2X(2/3)-recept

157 ed neurite elongation in isolated trigeminal ganglion neurons in a dose-dependent manner.

158 Disorganized central projections of spiral ganglion neurons in a Wnt/PCP pathway mutant, Prickle1,

159 ic vesicles along axons of mouse dorsal root ganglion neurons in culture promotes myelin induction by

160 ic autapses established by superior cervical ganglion neurons in culture show that presynaptic termin

161 ors (nAChRs) on the surface of chick ciliary ganglion neurons in culture.

162 RNA to gain entry into adult rat dorsal root ganglion neurons in culture.

163 s readily detected in a subset of trigeminal ganglion neurons in latently infected calves but not in

164 eletion-induced axon regeneration of retinal ganglion neurons in the adult CNS is attenuated upon Tet

165 the spontaneous activity of IHCs and spiral ganglion neurons in the developing cochlea and prevents

166 Here, we show that sensory and ganglion neurons in the ectodermal epithelium of the mod

167 ting that these features characterize spiral ganglion neurons in the fully developed ear.

168 ed URX and RIP neurons, two pairs of lateral ganglion neurons in the head, and the unpaired PQR and P

169 find that treatment of adult rat dorsal root ganglion neurons in vitro with LRP1 agonists (the recept

170 functional and can myelinate rat dorsal root ganglion neurons in vitro, and form myelin in Shiverer m

171 omatostatin-like immunoreactivity in ciliary ganglion neurons in vivo and in vitro, controls PSS2 exp

172 etic depolarization of GABAergic dorsal root ganglion neurons in vivo reduced acute and chronic perip

173 ation at postsynaptic sites in avian ciliary ganglion neurons in vivo.

174 oes not depend on the age of the dorsal root ganglion neurons in which the mutant is expressed.

175 We find that FMRP knockdown in dorsal root ganglion neurons increases Ca(V) channel density in soma

176 ASIC currents in both groups of dorsal root ganglion neurons, independent of mu opioid receptor stim

177 was also demonstrated in native dorsal root ganglion neurons indicating that heterodimerization may

178 was immunolocalized predominantly to spiral ganglion neurons, indicating that DFNB86 deafness might

179 l-regulated kinase expression in dorsal root ganglion neurons, induced by co-cultured MRMT-1 carcinom

180 ctivity in the Dsx(F)-up-regulated abdominal ganglion neurons inhibits female receptivity, indicating

181 d increased Trpm3 mRNA levels in dorsal root ganglion neurons innervating the inflamed paw, and augme

182 Prph((-/-)) mice lacked type II spiral ganglion neuron innervation of the outer hair cells, whe

183 The increase of Gata3 in auditory ganglion neurons is accompanied by decreased expression

184 s action potential generation in dorsal root ganglion neurons is associated with radicular/neuropathi

185 ver, if the peripheral branch of dorsal root ganglion neurons is lesioned before lesioning the centra

186 hin the type I and type II classes of spiral ganglion neurons is necessary to appreciate their functi

187 ss-desensitization was absent in dorsal root ganglion neurons lacking beta-arrestin 2.

188 Accordingly, mouse dorsal root ganglion neurons lacking TRPV1 only responded to protons

189 Next, we genetically identified the taste ganglion neurons mediating each of the five basic taste

190 When expressed in dorsal root ganglion neurons, mutant p.Arg222His channels increase e

191 in the position of postmigratory dorsal root ganglion neurons, neural crest derivatives for which mig

192 Unlike dorsal root ganglion neurons, Nf1 heterozygous (Nf1+/-) hippocampal

193 nd Ca(2+) imaging experiments on dorsal root ganglion neurons, NGF- and IL-6-induced increases in exc

194 apoptosis in the stria vascularis and spiral ganglion neurons of the inner ear, and progressive E2F1-

195 mechanosensitive channels in the dorsal root ganglion neurons of these afferents.

196 Approximately 45% of dorsal root ganglion neurons of transgenic mice were EGFP-positive (

197 oanatomically recognizable mapping of spiral ganglion neurons onto distinct locations in the cochlea

198 n, genetically deleting GluN1 in dorsal root ganglion neurons or alpha2delta-1 genetic KO similarly a

199 rat endocrine GH(3) cells, mouse dorsal root ganglion neurons or cardiac myocytes, and recombinant hu

200 cannot be explained by a loss of geniculate ganglion neurons or degeneration of central axons.

201 ent pathology among supporting cells, spiral ganglion neurons, or cells of the cochlear lateral wall.

202 In the cochlea, spiral ganglion neurons play a critical role in hearing as they

203 These results suggest that spiral ganglion neurons possess electrophysiological mechanisms

204 ects of the cochlea are innervated by spiral ganglion neurons, presumably under the tropic influence

205 Type II spiral ganglion neurons provide afferent innervation to outer h

206 )1.8 and Slack K(Na) channels in dorsal root ganglion neurons regulating excitability and pain.

207 ommissural neurons, motoneurons, dorsal root ganglion neurons, retinal ganglion cells, and callosal p

208 Similar analyses of dorsal root ganglion neurons revealed a salutary effect of pioglitaz

209 ntaneous activity in dissociated dorsal root ganglion neurons, reversed hypersensitivity of hindlimb

210 hat, in the turtle, mandibular and maxillary ganglion neuron rostrocaudal segregation and trigeminal

211 nd G protein modulation in superior cervical ganglion neurones (SCGNs).

212 Ca(V) channel activity in superior cervical ganglion neurons (SCGNs).

213 v)1.2/L2 reporter protein in rat dorsal root ganglion neuron-Schwann cell myelinating cocultures, we

214 n particular, we found that fibers of spiral ganglion neurons (SGN) close to the organ of Corti are d

215 t growth factor 8 (FGF8) in mammalian spiral ganglion neurons (SGN) neurite outgrowth has not been ex

216 Optogenetic stimulation of spiral ganglion neurons (SGNs) activated the auditory pathway,

217 ologically distinct classes of type I spiral ganglion neurons (SGNs) are necessary to encode sound in

218 Spiral ganglion neurons (SGNs) are postsynaptic to hair cells a

219 Type II spiral ganglion neurons (SGNs) are small caliber, unmyelinated

220 The mammalian spiral ganglion neurons (SGNs) are specialzed bipolar neurons i

221 pment, primary auditory neurons named spiral ganglion neurons (SGNs) are surrounded by otic mesenchym

222 hieved by functionally diverse type I spiral ganglion neurons (SGNs) at each tonotopic position.

223 have long suggested that survival of spiral ganglion neurons (SGNs) depends on trophic support provi

224 Mammalian cochlear spiral ganglion neurons (SGNs) encode sound with microsecond pr

225 pment of periphery auditory circuits, spiral ganglion neurons (SGNs) extend their neurites to innerva

226 Peripheral axons from auditory spiral ganglion neurons (SGNs) form an elaborate series of radi

227 volves degeneration of hair cells and spiral ganglion neurons (SGNs) from basal to apical cochlea, ma

228 ption of humans, the somata of type I spiral ganglion neurons (SGNs) of most mammalian species are he

229 damages the postsynaptic terminals of spiral ganglion neurons (SGNs) on cochlear inner hair cells (IH

230 Spiral ganglion neurons (SGNs) play a key role in hearing by ra

231 In the auditory system, type I spiral ganglion neurons (SGNs) project their peripheral axons i

232 Spiral ganglion neurons (SGNs) receive input from cochlear hair

233 Spiral ganglion neurons (SGNs) relay acoustic code from cochlea

234 s between inner hair cells (IHCs) and spiral ganglion neurons (SGNs) that carry acoustic information

235 relayed from the ear to the brain via spiral ganglion neurons (SGNs) that receive auditory informatio

236 For sounds of a given frequency, spiral ganglion neurons (SGNs) with different thresholds and dy

237 ributes to the proper organization of spiral ganglion neurons (SGNs) within the Rosenthal's canal and

238 jury can also lead to degeneration of spiral ganglion neurons (SGNs), but this occurs over a period o

239 entary coding by functionally diverse spiral ganglion neurons (SGNs), each changing activity only ove

240 murine cochlea, where two classes of spiral ganglion neurons (SGNs), type I and type II, navigate to

241 diation beam was directed towards the spiral ganglion neurons (SGNs), whereas little responses were s

242 anically to sound waves, and afferent spiral ganglion neurons (SGNs), which respond to glutamate rele

243 in the cochlea, i.e., hair cells and spiral ganglion neurons (SGNs), with a focus on their tonotopic

244 a mini-burst of action potentials in spiral ganglion neurons (SGNs).

245 al auditory fibers (PAFs) and loss of spiral ganglion neurons (SGNs).

246 directly in the sensory epithelium or spiral ganglion neurons (SGNs).

247 sensory hair cells (HCs) and afferent spiral ganglion neurons (SGNs).

248 ndly deaf by electrically stimulating spiral ganglion neurons (SGNs).

249 it auditory information faithfully to spiral ganglion neurons (SGNs).

250 rapid transmission from hair cells to spiral ganglion neurons (SGNs).

251 nsory hair cells and their associated spiral ganglion neurons (SGNs).

252 of action potentials in postsynaptic spiral ganglion neurons (SGNs).

253 and was lacking from the postsynaptic spiral ganglion neurons (SGNs).

254 l properties of the auditory neurons (spiral ganglion neurons, SGNs) stimulated in electrical hearing

255 ick) to the primary auditory neurons (spiral ganglion neurons, SGNs).

256 Quantification of Fzd3 expression in spiral ganglion neurons show a gradient of expression with Fzd3

257 eports that nearly 100% of superior cervical ganglion neurons show phasic class 3 firing.

258 Recordings from primary sensory trigeminal ganglion neurons show that these neurons exhibit respons

259 Cultured nodose ganglion neurones showed no changes in response to capsa

260 In vivo recordings from postsynaptic spiral ganglion neurons showed a use-dependent reduction in sou

261 n to view the activities of large numbers of ganglion neurons simultaneously analyzes the importance

262 man by a subpopulation of TRPV1+ dorsal root ganglion neurons specialized in detecting painful stimul

263 eromers and native M currents in dorsal root ganglion neurons suggest the following conclusions.

264 the adult mouse cochlea including the spiral ganglion neurons, suggesting changes in expression level

265 on of TMC1 protein in the hair cells, spiral ganglion neurons, supporting cells, and stria ligament i

266 likely to form connections with adult spiral ganglion neurons, supporting that Myc and Notch1 co-acti

267 finitively shows that an identified cerebral ganglion neuron that is a member of a CPG underlying swi

268 erized changes in both hair cells and spiral ganglion neurons that may be relevant for early signs of

269 connectivity between TRCs and their partner ganglion neurons (that is, ensuring that a labelled line

270 In spiral ganglion neurons, the primary afferents in the cochlea,

271 aging in cultured primary murine dorsal root ganglion neurons, the response of neurons after 5-HT app

272 results were obtained with chick sympathetic ganglion neurons, though regulation of receptor mobility

273 TRPV1 is shown in rat and human dorsal root ganglion neurons, TLR4/TRPV1-coexpressing HEK293 cells,

274 ot injury model, transduction of dorsal root ganglion neurons to express kindlin-1 promoted axon rege

275 re we recorded responses in mouse trigeminal ganglion neurons to investigate interactions between the

276 Current-clamp analysis of dorsal root ganglion neurons transfected with G856D mutant channels

277 n of key inflammatory proteins in trigeminal ganglion neurons under basal and inflammatory conditions

278 pharmacology to investigate rat dorsal root ganglion neurons using two models of peripheral nerve in

279 ibits neurite outgrowth in adult dorsal root ganglion neurons, validating Slit2 signaling in primary

280 Previous studies from immature vestibular ganglion neurons (VGNs) identified hyperpolarization-act

281 Vestibular ganglion neurons (VGNs) transmit information along paral

282 tized TRPV1 in mouse nociceptive dorsal root ganglion neurons via HRH1; this effect could be reproduc

283 avior and activation of cultured dorsal root ganglion neurons was dependent on Mrgprs rather than NK-

284 ion of the inner hair cells by type I spiral ganglion neurons was normal.

285 Compartmental culture of trigeminal ganglion neurons was performed in Campenot devices to de

286 Compartmental culture of trigeminal ganglion neurons was performed in Campenot devices to de

287 labelling of bladder-projecting dorsal root ganglion neurons was used to investigate expression of 5

288 Using cultured mouse dorsal root ganglion neurons, we found that myosin II (MII) is requi

289 male and female embryonic mouse dorsal root ganglion neurons, we show that MAP4K4, MINK1, and TNIK a

290 ls expressed in HEK293 cells and dorsal root ganglion neurons were abolished by blocking the S-nitros

291 gnificant proportion (18-19%) of dorsal root ganglion neurons were double labelled by dye tracers inj

292 t types of cutaneous nociceptive dorsal root ganglion neurons were identified as responding to prurit

293 roximately 90% of 5-HT-sensitive dorsal root ganglion neurons were immunoreactive for an antibody to

294 glion neurons and the visual sensory retinal ganglion neurons were resistant to excitability changes

295 neuro-2A cells and primary superior cervical ganglion neurons, where APP is highly expressed, the lac

296 ated activity in inner hair cells and spiral ganglion neurons, which begins at birth and follows a ba

297 phic factor (BDNF), the number of geniculate ganglion neurons, which innervate taste buds, is reduced

298 neurite outgrowth by cocultured dorsal root ganglion neurons, which was prevented by neutralizing BM

299 ble changes in the properties of sympathetic ganglion neurons, while I739V, from patients with severe

300 observed a significant number of dorsal root ganglion neurons with dichotomized afferents innervating