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 eptor expression to medium sized dorsal root ganglion neurons.

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

4 cargo motility in primary mouse dorsal root ganglion neurons.

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

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

7 ofound effect on excitability of sympathetic ganglion neurons.

8 ed central branch of conditioned dorsal root ganglion neurons.

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

10 embryonic SAG neurons and adult mouse spiral ganglion neurons.

11 t of endogenous deltaR in primary trigeminal ganglion neurons.

12 erm synaptic plasticity in superior cervical ganglion neurons.

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

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

15 utophagosome dynamics in primary dorsal root ganglion neurons.

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

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

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

19 ceptive dorsal root ganglion and sympathetic ganglion neurons.

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

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

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

23 prevent inflammatory responses in trigeminal ganglion neurons.

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

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

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

27 es in the regulation of NKCC1 in dorsal root ganglion neurons.

28 involved in the differentiation of auditory ganglion neurons.

29 o and alpha2A receptors in mouse dorsal root ganglion neurons.

30 ural crest-derived noradrenergic sympathetic ganglion neurons.

31 rdiac cushion, and noradrenergic sympathetic ganglion neurons.

32 se regulation of the CGRP gene in trigeminal ganglion neurons.

33 ularis and was also detectable in the spiral ganglion neurons.

34 ort single cell RNA sequencing of geniculate ganglion neurons.

35 d neurite outgrowth from primary dorsal root ganglion neurons.

36 smission, and output functions of the spiral ganglion neurons.

37 ant sodium channels in amphibian dorsal root ganglion neurons.

38 in beta arr2+/+ and beta arr2-/- dorsal root ganglion neurons.

39 pression in peripheral nerve and dorsal root ganglion neurons.

40 ctivities of the TRPA1 channel in trigeminal ganglion neurons.

41 hese repeats in latently infected trigeminal ganglion neurons.

42 f the majority of cold-sensitive dorsal root ganglion neurons.

43 sistant, sodium current in mouse dorsal root ganglion neurons.

44 ction potentials in vitro in rat dorsal root ganglion neurons.

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

46 action potential firing of superior cervical ganglion neurons.

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

48 oligodendrocytes cocultured with dorsal root ganglion neurons.

49 er upon reactivation from latency in sensory ganglion neurons.

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

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

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

53 latency, consistent with apoptosis of spiral ganglion neurons.

54 tivity after TRPA1 activation in dorsal root ganglion neurons.

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

56 ganglion neurons and in almost all myenteric ganglion neurons.

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

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

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

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

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

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

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

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

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

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

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

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

69 d age-related apoptotic cell death of spiral ganglion neurons and hair cells in the cochlea, and prev

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

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

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

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

74 he second branchial arch generate few facial ganglion neurons and no vestibuloacoustic ganglion neuro

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

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

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

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

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

80 alcium and kinase dependence seen in ciliary ganglion neurons and was absent in hippocampal slices fr

81 R55 is highly expressed in large dorsal root ganglion neurons and, upon activation by various cannabi

82 (2) no effect on MOR-expressing dorsal root ganglion neurons, and (3) no change in baseline tail-fli

83 t is present in afferent calyxes, vestibular ganglion neurons, and both type I and type II HCs.

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

85 1A in axons of primary rat superior cervical ganglion neurons, and overexpression or disruption of KI

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

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

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

89 ession levels in spinal cord and dorsal root ganglion neurons, and that both kinases participate equa

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

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

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

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

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

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

96 nt of the inner ear, auditory and vestibular ganglion neurons are generated in a highly regulated seq

97 that the intrinsic firing features of spiral ganglion neurons are influenced by brain-derived neurotr

98 ROCKII(-/-) dorsal root ganglion neurons are less sensitive to inhibition by Nog

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

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

101 pression in the migraine-relevant trigeminal ganglion neurons are unknown.

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

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

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

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

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

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

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

109 al ganglion neurons and no vestibuloacoustic ganglion neurons, but crest cells in other branchial arc

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

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

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

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

114 expression of erythropoietin in dorsal root ganglion neurons can protect in vivo as well as in vitro

115 ciated forms of MFN2 in cultured dorsal root ganglion neurons, cells preferentially affected in CMT2.

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

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

118 Cochlear ganglion neurons communicate sound information from coch

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

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

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

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

123 tiated NB2/d1 cells and cultured dorsal root ganglion neurons decreased NF transport into axonal neur

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

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

126 rs enhances neurite outgrowth of dorsal root ganglion neurons derived from adult mice or cerebellar g

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

128 Nicotine application to dissociated ciliary ganglion neurons diminished subsequent GABAA receptor re

129 Dorsal root ganglion neurons displayed a fall in resting cytoplasmic

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

131 7, and 9 are expressed by human dorsal root ganglion neurons (DRGNs) and in cultures of primary mous

132 wth from three nerve cell types, dorsal root ganglion neurons (DRGNs), cerebellar granule neurons (CG

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

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

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

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

137 Spiral ganglion neurons exhibit spontaneous activity at least b

138 t neurite growth in the cultured dorsal root ganglion neurons exposed to the inhibitory substrates.

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

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

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

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

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

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

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

146 Trigeminal ganglion neurons from adult female Sprague Dawley rats w

147 ated axonal segments in cultured dorsal root ganglion neurons from DLS/LeJ and dl20J dilute lethal mi

148 filament array of cultured superior cervical ganglion neurons from DLS/LeJ dilute lethal mice.

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

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

151 udies were performed on cultured dorsal root ganglion neurons from Mrgprd(-/-) and Mrgprd(+/-) mice.

152 1 and Pirt, and that dissociated dorsal root ganglion neurons from Pirt knock-out mice have an appare

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

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

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

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

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

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

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

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

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

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

163 hat this mutation renders DRG and trigeminal ganglion neurons hyperexcitable.

164 rs dorsal root ganglion (DRG) and trigeminal ganglion neurons hyperexcitable.

165 neurons hyperexcitable and superior cervical ganglion neurons hypoexcitable.

166 peptide (CGRP) from cultured rat dorsal root ganglion neurons in a cannabinoid receptor- and TRPV1-in

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

168 used time-lapse imaging of adult dorsal root ganglion neurons in an in vitro model of the glial scar

169 mbers at nicotinic synapses on chick ciliary ganglion neurons in culture execute multiple functions t

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

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

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

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

174 The early degeneration of some cochlear ganglion neurons in knockout mice also indicates an impo

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

176 ion ([Ca2+]i) in a proportion of dorsal root ganglion neurons in primary culture.

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

178 addition, Egr2; Atoh1(CKO) mice lose spiral ganglion neurons in the cochlea and AAN neurons during t

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

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

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

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

183 Dorsal root ganglion neurons in vitro express a number of types of m

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

185 ased erythropoietin from primary dorsal root ganglion neurons in vitro, and following subcutaneous in

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

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

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

189 oot, expressed erythropoietin in dorsal root ganglion neurons in vivo.

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

191 ion of CGRP receptors on cultured trigeminal ganglion neurons increased endogenous CGRP mRNA levels a

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

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

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

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

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

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

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

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

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

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

202 In cultured rat trigeminal ganglion neurons, knockdown of either USF1 or USF2 reduc

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

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

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

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

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

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

209 nd patch clamp recordings of isolated nodose ganglion neurons (NGNs).

210 ro-receptor coupling to VDCCs in dorsal root ganglion neurons of delta(+/+), delta(+/-), and delta(-/

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

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

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

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

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

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

217 These results suggest that spiral ganglion neurons possess electrophysiological mechanisms

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

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

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

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

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

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

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

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

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

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

228 s to a large proportion of rat type I spiral ganglion neurons (SGNs) and their projections to the coc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

255 air cells, the sole afferent input to spiral ganglion neurons (SGNs).

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

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

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

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

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

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

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

263 RPA1 recorded from cell bodies of trigeminal ganglion neurons showed similar behavior with respect to

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

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

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

267 expressed in a population of rat dorsal root ganglion neurons that also responded to ITC.

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

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

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

271 s innervated by only four to five geniculate ganglion neurons; their peripheral fibers do not branch

272 ippocampal interneurons and on chick ciliary ganglion neurons these alpha7-nAChRs are often closely j

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

274 lize the morphologies of individual cochlear ganglion neurons throughout development, from their orig

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

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

277 nglion (DRG) and approximately 50% of nodose ganglion neurons] to evoke a depolarizing inward current

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

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

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

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

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

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

284 ssion of M current native to rat dorsal root ganglion neurons was observed after incubating dissociat

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

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

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

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

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

292 Type II SGNs and vestibular ganglion neurons were unlabeled.

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

294 NKCC1 is highly expressed in dorsal root ganglion neurons, where it is involved in gating sensory

295 in a small subset of peptidergic dorsal root ganglion neurons, whereas expression of its receptor GRP

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

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

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

299 ylinositol linkage (GPIalpha btx) in ciliary ganglion neurons with the retroviral vector RCASBP(A) bl

300 Within this population, cochlear ganglion neurons with type I and type II morphologies ar