ライフサイエンスコーパス: dorsal root ganglion neuron

1 single K562 erythroleukemic cell or a single dorsal root ganglion neuron.

2 ncy of kinases in the regulation of NKCC1 in dorsal root ganglion neurons.

3 ogenous micro and alpha2A receptors in mouse dorsal root ganglion neurons.

4 GF-stimulated neurite outgrowth from primary dorsal root ganglion neurons.

5 (TTX)-resistant sodium channels in amphibian dorsal root ganglion neurons.

6 els (VGCCs) in beta arr2+/+ and beta arr2-/- dorsal root ganglion neurons.

7 enase overexpression in peripheral nerve and dorsal root ganglion neurons.

8 responses of the majority of cold-sensitive dorsal root ganglion neurons.

9 f the TTX-resistant, sodium current in mouse dorsal root ganglion neurons.

10 lly evoked action potentials in vitro in rat dorsal root ganglion neurons.

11 e myelinating segments when co-cultured with dorsal root ganglion neurons.

12 ) action potential-induced Ca2+ loads in rat dorsal root ganglion neurons.

13 erentiation in cultures of Schwann cells and dorsal root ganglion neurons.

14 ens was assessed by calcium imaging of mouse dorsal root ganglion neurons.

15 es survival and neurite outgrowth in primary dorsal root ganglion neurons.

16 dings were performed in acutely isolated rat dorsal root ganglion neurons.

17 ing neurite formation in both PC12 cells and dorsal root ganglion neurons.

18 tion potentials and high frequency firing in dorsal root ganglion neurons.

19 n capsaicin-sensitive, but not -insensitive, dorsal root ganglion neurons.

20 esistant Na+ current in small-diameter mouse dorsal root ganglion neurons.

21 ated calcium channels in rat sympathetic and dorsal root ganglion neurons.

22 up-regulates basal P2X3 receptor activity in dorsal root ganglion neurons.

23 d in a significant decrease in the number of dorsal root ganglion neurons.

24 d 45Ca uptake in stably transfected cells or dorsal root ganglion neurons.

25 n CHO cells as well as of endogenous rVR1 in dorsal root ganglion neurons.

26 or-mediated ATP responses in primary sensory dorsal root ganglion neurons.

27 form of GAIP, derived from embryonic chicken dorsal root ganglion neurons.

28 cked native P2X3 and P2X2/3 receptors in rat dorsal root ganglion neurons.

29 ious antigens characteristic of human foetal dorsal root ganglion neurons.

30 a sensory neuronal cell line and primary rat dorsal root ganglion neurons.

31 rat SCs and cocultures of SCs with embryonic dorsal root ganglion neurons.

32 ctional AMPA receptors by a subpopulation of dorsal root ganglion neurons.

33 d stable in oligodendrocytes cocultured with dorsal root ganglion neurons.

34 cally expressing VR1 and primary cultures of dorsal root ganglion neurons.

35 the balance of VD and VI inhibition in chick dorsal root ganglion neurons.

36 rminal domain blocked neurite outgrowth from dorsal root ganglion neurons.

37 n cells and neurite outgrowth from embryonic dorsal root ganglion neurons.

38 cultured either alone or in the presence of dorsal root ganglion neurons.

39 apidly desensitizing ATP-induced currents in dorsal root ganglion neurons.

40 t N-type calcium channels in embryonic chick dorsal root ganglion neurons.

41 necessary to induce growth cone collapse of dorsal root ganglion neurons.

42 the bait to screen a cDNA library from chick dorsal root ganglion neurons.

43 growth cone navigation in vitro, using chick dorsal root ganglion neurons.

44 from neonatal rat hippocampal and adult rat dorsal root ganglion neurons.

45 of ankyrinG to the axonal plasma membrane in dorsal root ganglion neurons.

46 highly potent on native kainate receptors in dorsal root ganglion neurons.

47 potential waveforms in voltage-clamped chick dorsal root ganglion neurons.

48 the localization of the thrombin receptor to dorsal root ganglion neurons.

49 early gene c-jun mRNA and protein in lumbar dorsal root ganglion neurons.

50 d is targeted to nerve terminals of cultured dorsal root ganglion neurons.

51 s not support the survival of sympathetic or dorsal root ganglion neurons.

52 ment of evoked peptide release from isolated dorsal root ganglion neurons.

53 ts and was also detected on the membranes of dorsal root ganglion neurons.

54 BAA receptor-chloride channel complex of rat dorsal root ganglion neurons.

55 imal LVA and HVA Ca2+ conductances in murine dorsal root ganglion neurons.

56 P2Y1 mRNA is concentrated in large-fiber dorsal root ganglion neurons.

57 on-induced intracellular Ca(2+) signaling in dorsal root ganglion neurons.

58 sed TRPV1 activity after TRPA1 activation in dorsal root ganglion neurons.

59 -type (primarily Cav3.2) channels in sensory dorsal root ganglion neurons.

60 of TRPV1 receptor expression to medium sized dorsal root ganglion neurons.

61 ant inhibition of TRPM8 in 48.8% of TRPM8(+) dorsal root ganglion neurons.

62 l imaging of cargo motility in primary mouse dorsal root ganglion neurons.

63 a subpopulation of large-diameter Nav1.8(+) dorsal root ganglion neurons.

64 of the injured central branch of conditioned dorsal root ganglion neurons.

65 used the growth cone collapse assay on chick dorsal root ganglion neurons.

66 stages results in loss of pigment cells and dorsal root ganglion neurons.

67 nvestigate autophagosome dynamics in primary dorsal root ganglion neurons.

68 um, potassium, and calcium channels in mouse dorsal root ganglion neurons.

69 support neurite growth of co-cultured adult dorsal root ganglion neurons.

70 onatal-short splicing isoform of Na(v)1.7 in dorsal root ganglion neurons.

71 pound elicited responses in only a subset of dorsal-root ganglion neurons.

72 ) increased the excitability of neonatal rat dorsal root ganglion neurones.

73 , PKCdelta, and PKC was also observed in the dorsal root ganglion neurons after chronic treatment wit

74 w regions where BPAG1-n was found, including dorsal root ganglion neurons and a small subset of motor

75 receptor that increases cAMP, in a subset of dorsal root ganglion neurons and also within neurons of

76 TRP) family of ion channels, is expressed by dorsal root ganglion neurons and by cells of the inner e

77 bility of single TRPV1 molecules in isolated dorsal root ganglion neurons and cell lines.

78 preferentially expressed in most nociceptive dorsal root ganglion neurons and in sympathetic neurons.

79 ase ion transporter in both cultured primary dorsal root ganglion neurons and injured peripheral nerv

80 for PKCepsilon was found in the majority of dorsal root ganglion neurons and intensely labeled lamin

81 e-collapsing molecule than Nogo-66 for chick dorsal root ganglion neurons and mature cortical neurons

82 nal populations in the chick embryo, sensory dorsal root ganglion neurons and parasympathetic ciliary

83 This was reproduced by exposure of dorsal root ganglion neurons and PC12 cells to cisplatin

84 creases pacemaker currents in large-diameter dorsal root ganglion neurons and results in pacemaker-dr

85 In cocultures of dorsal root ganglion neurons and Schwann cells, collagen

86 t channels enhance resurgent currents within dorsal root ganglion neurons and show by current-clamp t

87 GPR55 is highly expressed in large dorsal root ganglion neurons and, upon activation by var

88 s, we treated myelinating cocultures of DRG (dorsal root ganglion) neurons and Schwann cells with an

89 orn neurons, (2) no effect on MOR-expressing dorsal root ganglion neurons, and (3) no change in basel

90 n prostate cells, PC3 prostate cancer cells, dorsal root ganglion neurons, and hippocampal neurons.

91 solated rat cerebellar Purkinje neurons, rat dorsal root ganglion neurons, and human embryonic kidney

92 emically was present on neurites of cultured dorsal root ganglion neurons, and it was released into t

93 eurons, chemotherapy-induced cytotoxicity of dorsal root ganglion neurons, and retinal ganglion cells

94 similar expression levels in spinal cord and dorsal root ganglion neurons, and that both kinases part

95 is transiently expressed in a wide range of dorsal root ganglion neurons, and that its expression is

96 y desensitizing ATP-gated cation currents in dorsal root ganglion neurons, and that the responses of

97 PV1 current (IC(50) = 0.4 nm) in dissociated dorsal root ganglion neurons, and this IC(50) is approxi

98 lt spinal cord; perikarya and axons of adult dorsal root ganglion neurons; and axons in adult periphe

99 (23-45 degrees C), a subpopulation of small dorsal root ganglion neurons are depolarized by a cation

100 ns is decreased whereas neural crest-derived dorsal root ganglion neurons are increased in number sup

101 ROCKII(-/-) dorsal root ganglion neurons are less sensitive to inhib

102 Kainate receptors in murine dorsal root ganglion neurons are likely to be composed o

103 ll populations is aberrant and crest-derived dorsal root ganglion neurons are misplaced.

104 ry neurons; however, Rohon-Beard neurons and dorsal root ganglion neurons are not necessarily derived

105 eurons: PC12 (pheochromocytoma 12) cells and dorsal root ganglion neurons are protected from serum st

106 Larger dorsal root ganglion neurons are stained by an antibody

107 In contrast, dorsal root ganglion neurons are stiffer than P-19 and c

108 initively, GABA-induced peak currents in rat dorsal root ganglion neurons are suppressed by alpha-thu

109 s hTRPM8, and rTRPM3, which are expressed in dorsal root ganglion neurons, are insensitive toward apo

110 and biochemical modulation of T-channels in dorsal root ganglion neurons as measured by a large incr

111 t fates: early-migrating crest cells produce dorsal root ganglion neurons as well as glia and pigment

112 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent

113 nkyrinG constructs transfected into cultured dorsal root ganglion neurons, as well as measurements of

114 age-gated K(+) channel robustly expressed in dorsal root ganglion neurons, becomes dysfunctional upon

115 ibits the outgrowth of axons from rat embryo dorsal root ganglion neurons but promotes Schwann cell m

116 However, conditioning dorsal root ganglion neurons by first lesioning their pe

117 f3r gene expression could not be detected in dorsal root ganglion neurons by single-cell RT-PCR.

118 diated local expression of erythropoietin in dorsal root ganglion neurons can protect in vivo as well

119 ropathy-associated forms of MFN2 in cultured dorsal root ganglion neurons, cells preferentially affec

120 that in small PLCdelta4(-/-) TRPM8-positive dorsal root ganglion neurons cold, menthol and WS-12, a

121 n; and (5) electrophysiology recordings from dorsal root ganglion neurons collected during remission

122 tion of the alpha2delta-1 subunit in sensory dorsal root ganglion neurons contributes to the generati

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

124 of differentiated NB2/d1 cells and cultured dorsal root ganglion neurons decreased NF transport into

125 gic inhibitors enhances neurite outgrowth of dorsal root ganglion neurons derived from adult mice or

126 r expression of functional AMPA receptors by dorsal root ganglion neurons despite immunocytochemical

127 iated inhibition of M current in nociceptive dorsal root ganglion neurons did not reduce the efficacy

128 ject minute volumes of dissociated adult rat dorsal root ganglion neurons directly into adult rat CNS

129 Dorsal root ganglion neurons displayed a fall in resting

130 ition, the area profiles of L6-S1, and L1-L2 dorsal root ganglion neurons (DRG), labelled by fast blu

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

132 tion of FGF2-stimulated neurite outgrowth of dorsal root ganglion neurons (DRGN) cultured in the pres

133 e-associated protein 1B (MAP1B) expressed in dorsal root ganglion neurons (DRGNs) and axolemma-enrich

134 that TLRs 3, 7, and 9 are expressed by human dorsal root ganglion neurons (DRGNs) and in cultures of

135 produce myelin when cocultured with purified dorsal root ganglion neurons (DRGNs) in serum-free and s

136 urite outgrowth from three nerve cell types, dorsal root ganglion neurons (DRGNs), cerebellar granule

137 escent protein (GFP) in primary cultured rat dorsal root ganglion neurones (DRGs).

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

139 that control myelination of TrkA-expressing dorsal root ganglion neurons (DRGs).

140 similarly to that observed for cultured rat dorsal root ganglion neurons (DRGs).

141 el, depolarize resting membrane potential of dorsal root ganglion neurons, enhance spontaneous firing

142 including altered ion channel expression in dorsal root ganglion neurons, enhanced dorsal horn gluta

143 In isolated dorsal root ganglion neurons, EP3 receptor activation co

144 duce a substantial increase in the number of dorsal root ganglion neurons evidencing the presence of

145 a significant neurite growth in the cultured dorsal root ganglion neurons exposed to the inhibitory s

146 Dorsal root ganglion neurons express a wide repertoire o

147 Dorsal root ganglion neurons express an array of sodium

148 Here, we show that only 43% of CQ-excited dorsal root ganglion neurons expressed TRPA1; as expecte

149 mazepine normalized the hyperexcitability of dorsal root ganglion neurons expressing S241T.

150 In transfected small rat dorsal root ganglion neurons, expression of L1302F and L

151 pic screen, we find that CAST/Ei mouse adult dorsal root ganglion neurons extend axons more on CNS my

152 Two days PI, dorsal root ganglion neurons (first-order sympathetic af

153 l nitric oxide synthase (nNOS) is induced in dorsal root ganglion neurons following axotomy in young

154 tion of NFATc3 and NFATc4 in hippocampal and dorsal root ganglion neurons following electrically evok

155 ence that voluntary exercise can prime adult dorsal root ganglion neurons for increased axonal regene

156 A-type K(+) current (I(AHV)) in nociceptive dorsal root ganglion neurons from 7-day-old rats.

157 was investigated in vitro by using cultured dorsal root ganglion neurons from adult rat.

158 m photoactivated axonal segments in cultured dorsal root ganglion neurons from DLS/LeJ and dl20J dilu

159 ratching behavior and activation of cultured dorsal root ganglion neurons from mice.

160 tch-clamp studies were performed on cultured dorsal root ganglion neurons from Mrgprd(-/-) and Mrgprd

161 between TRPV1 and Pirt, and that dissociated dorsal root ganglion neurons from Pirt knock-out mice ha

162 ne also acts on endogenous TRPA1 in cultured dorsal root ganglion neurons from rats and in the entero

163 viously well characterized in small diameter dorsal root ganglion neurons from various species.

164 In this study, dissociated dorsal-root ganglion neurons from mice were exposed to v

165 es in single growth cones of embryonic chick dorsal root ganglion neurons grown in culture.

166 petrosal ganglion (PG), nodose ganglion, and dorsal root ganglion neurons grown in the presence or ab

167 n of the effects of the Del-L955 mutation on dorsal root ganglion neuron hyperexcitability with those

168 erior cervical ganglion neurons, and renders dorsal root ganglion neurons hyperexcitable and superior

169 ons in sodium channel Na(V)1.7, which render dorsal root ganglion neurons hyperexcitable, are present

170 neonatal-short, isoform of Na(v)1.7 renders dorsal root ganglion neurons hyperexcitable, reducing th

171 ant channels; each of the mutations rendered dorsal root ganglion neurons hyperexcitable.

172 and show by current-clamp that R185H renders dorsal root ganglion neurons hyperexcitable.

173 ng and neural-crest-derived cells, including dorsal root ganglion neurons, hypophysis, and the choroi

174 ade from the somata of ipsilateral L6 and S1 dorsal root ganglion neurones in anaesthetised untreated

175 ene-related peptide (CGRP) from cultured rat dorsal root ganglion neurons in a cannabinoid receptor-

176 We used time-lapse imaging of adult dorsal root ganglion neurons in an in vitro model of the

177 from synaptic vesicles along axons of mouse dorsal root ganglion neurons in culture promotes myelin

178 tudies using electrical stimulation of mouse dorsal root ganglion neurons in culture show that the te

179 -clamp recordings from small-medium diameter dorsal root ganglion neurons in culture, (+/-)-epibatidi

180 Using primary dorsal root ganglion neurons in culture, here we show an

181 , enables siRNA to gain entry into adult rat dorsal root ganglion neurons in culture.

182 nt neurotrophin-responsive subpopulations of dorsal root ganglion neurons in dystonia musculorum (dt)

183 a(v)1.3, Na(v)1.6, Na(v)1.8, and Na(v)1.9 in dorsal root ganglion neurons in experimental diabetes an

184 cules related to spinal laminar targeting of dorsal root ganglion neurons in mice, we have characteri

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

186 odium channel mRNA and protein expression in dorsal root ganglion neurons in rats with streptozotocin

187 Na(v)1.8 immunoreactivity was reduced in L6 dorsal root ganglion neurons in the antisense-treated ra

188 nism of transgene-mediated GABA release from dorsal root ganglion neurons in vitro and in vivo.

189 Dorsal root ganglion neurons in vitro express a number o

190 We now find that treatment of adult rat dorsal root ganglion neurons in vitro with LRP1 agonists

191 sed and released erythropoietin from primary dorsal root ganglion neurons in vitro, and following sub

192 calcium in suramin-induced neurotoxicity in dorsal root ganglion neurons in vitro.

193 adhesion, and promotes neurite extension of dorsal root ganglion neurons in vitro.

194 c or optogenetic depolarization of GABAergic dorsal root ganglion neurons in vivo reduced acute and c

195 ion in the foot, expressed erythropoietin in dorsal root ganglion neurons in vivo.

196 lops as an all-or-none event in cultured rat dorsal root ganglion neurons in which ryanodine receptor

197 activation does not depend on the age of the dorsal root ganglion neurons in which the mutant is expr

198 Selective expression of Na(v)1.7 within dorsal root ganglion neurons including nociceptors (in w

199 We find that FMRP knockdown in dorsal root ganglion neurons increases Ca(V) channel den

200 ed sustained ASIC currents in both groups of dorsal root ganglion neurons, independent of mu opioid r

201 K-2 channels was also demonstrated in native dorsal root ganglion neurons indicating that heterodimer

202 ability of (+)-ACN to inhibit HVA current in dorsal root ganglion neurons, indicating that (+)-ACN ac

203 llular signal-regulated kinase expression in dorsal root ganglion neurons, induced by co-cultured MRM

204 cord injury on the electrical properties of dorsal root ganglion neurones innervating the urinary bl

205 However, if the peripheral branch of dorsal root ganglion neurons is lesioned before lesionin

206 lude that QHGAD67-mediated GABA release from dorsal root ganglion neurons is non-vesicular, independe

207 Small diameter dorsal root ganglion neurons isolated from VR1-null mice

208 In cultured dorsal root ganglion neurons, JYL1421 and KJM429 likewis

209 -alpha2A cross-desensitization was absent in dorsal root ganglion neurons lacking beta-arrestin 2.

210 Accordingly, mouse dorsal root ganglion neurons lacking TRPV1 only responde

211 /or alpha10 expression has been described in dorsal root ganglion neurons, lymphocytes, skin keratino

212 When expressed in dorsal root ganglion neurons, mutant p.Arg222His channel

213 that maintain the position of postmigratory dorsal root ganglion neurons, neural crest derivatives f

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

215 this paper, we report that in PC12 cells and dorsal root ganglion neurons, NGF translocates SphK1 to

216 physiology and Ca(2+) imaging experiments on dorsal root ganglion neurons, NGF- and IL-6-induced incr

217 examined micro-receptor coupling to VDCCs in dorsal root ganglion neurons of delta(+/+), delta(+/-),

218 tors, including mu receptor gene deletion in dorsal root ganglion neurons of mu-/- mice and 18-h incu

219 Approximately 45% of dorsal root ganglion neurons of transgenic mice were EGF

220 Demodulation by opioids was also observed in dorsal root ganglion neurons on the modulation of calciu

221 channels in rat endocrine GH(3) cells, mouse dorsal root ganglion neurons or cardiac myocytes, and re

222 o not cause the death of spinal GABAergic or dorsal root ganglion neurons or of embryonic stem cell-d

223 Bu dramatically down-regulated PKC(alpha) in dorsal root ganglion neurons or the VR1 cell lines, wher

224 In dorsal root ganglion neurons overexpressing RGS3, we fin

225 f alpha7 in the cochlea and in sites such as dorsal root ganglion neurons, peripheral blood lymphocyt

226 otes neurite outgrowth from primary cultured dorsal root ganglion neurons, presumably via homophilic

227 nt PLC protein back into PLC beta3-deficient dorsal root ganglion neurons reduced DAMGO responses to

228 ctance (gK) in cultures of dissociated mouse dorsal root ganglion neurons regardless of the presence

229 accumulation of lamellar inclusion bodies in dorsal root ganglion neurons related to dose of administ

230 CALI of myosin-V in growth cones of chick dorsal root ganglion neurons resulted in rapid filopodia

231 nic spinal commissural neurons, motoneurons, dorsal root ganglion neurons, retinal ganglion cells, an

232 Similar analyses of dorsal root ganglion neurons revealed a salutary effect

233 ppressed spontaneous activity in dissociated dorsal root ganglion neurons, reversed hypersensitivity

234 ng a CD4-Na(v)1.2/L2 reporter protein in rat dorsal root ganglion neuron-Schwann cell myelinating coc

235 ease MAG inhibition of RGCs, but p75(NTR-/-) dorsal root ganglion neurons show enhanced growth on MAG

236 Dorsal root ganglion neurons showed an increase in neuri

237 .2/Kv7.3 heteromers and native M currents in dorsal root ganglion neurons suggest the following concl

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

239 atin and suramin both result in apoptosis in dorsal root ganglion neurons that may partially explain

240 g calcium imaging in cultured primary murine dorsal root ganglion neurons, the response of neurons af

241 sensitive presynaptic Ca2+ channels in chick dorsal root ganglion neurons through two pathways, one m

242 een TLR4 and TRPV1 is shown in rat and human dorsal root ganglion neurons, TLR4/TRPV1-coexpressing HE

243 potential responses of cultured neonatal rat dorsal root ganglion neurons to capsaicin were examined

244 o, BDNF caused growth cones of NGF-dependent dorsal root ganglion neurons to collapse.

245 at dorsal root injury model, transduction of dorsal root ganglion neurons to express kindlin-1 promot

246 Exposure of PC12 cells and dorsal root ganglion neurons to increased levels of nerv

247 lted in the release of RANTES, which induced dorsal root ganglion neurons to produce tumor necrosis f

248 We have demonstrated that dorsal root ganglion neurons transduced with a recombina

249 Release of GABA from dorsal root ganglion neurons transduced with QHGAD67 was

250 Current-clamp analysis of dorsal root ganglion neurons transfected with G856D muta

251 In cultured mouse dorsal root ganglion neurons, two mechanistically differ

252 crest cells does not result in production of dorsal root ganglion neurons under all conditions sugges

253 receptor coupling to Ca2+ channels in mouse dorsal root ganglion neurons under basal conditions and

254 tion and inhibits neurite outgrowth in adult dorsal root ganglion neurons, validating Slit2 signaling

255 ta anion was genetically altered in cultured dorsal root ganglion neurons via adenoviral vector-media

256 teers, sensitized TRPV1 in mouse nociceptive dorsal root ganglion neurons via HRH1; this effect could

257 produced by gamma-aminobutyric acid in chick dorsal root ganglion neurons, voltage-independent inhibi

258 o block voltage-dependent K+ currents in rat dorsal root ganglion neurones was examined using the pat

259 ratching behavior and activation of cultured dorsal root ganglion neurons was dependent on Mrgprs rat

260 iated suppression of M current native to rat dorsal root ganglion neurons was observed after incubati

261 Release of GABA from transduced dorsal root ganglion neurons was, however, blocked in a

262 , in both acutely dissociated and intact rat dorsal root ganglion neurons, we characterize a novel su

263 Using cultured mouse dorsal root ganglion neurons, we found that myosin II (M

264 In cultures of dorsal root ganglion neurons, we found that Sema3A treat

265 -cell immunoblot assay to study secretion in dorsal root ganglion neurons, we found that the somata u

266 determine whether NGF has a direct effect on dorsal root ganglion neurons, we have begun to investiga

267 tion in both male and female embryonic mouse dorsal root ganglion neurons, we show that MAP4K4, MINK1

268 a(2+) channels expressed in HEK293 cells and dorsal root ganglion neurons were abolished by blocking

269 ge of 1.2, 0.8, 2.1 and 4.4% of the infected dorsal root ganglion neurons were contralateral to the i

270 Growth cones of chick dorsal root ganglion neurons were exposed to well charac

271 two distinct types of cutaneous nociceptive dorsal root ganglion neurons were identified as respondi

272 Approximately 90% of 5-HT-sensitive dorsal root ganglion neurons were immunoreactive for an

273 tage-activated (HVA) calcium channels of rat dorsal root ganglion neurons were studied using the whol

274 those of peripheral nervous system neurons (dorsal root ganglion neurons) were either not enhanced (

275 NKCC1 is highly expressed in dorsal root ganglion neurons, where it is involved in ga

276 y expressed in a small subset of peptidergic dorsal root ganglion neurons, whereas expression of its

277 h-clamp experiments were performed using rat dorsal root ganglion neurons which are endowed with tetr

278 cription contributes to hyperexcitability of dorsal root ganglion neurons, which may produce neuropat

279 duced robust neurite outgrowth by cocultured dorsal root ganglion neurons, which was prevented by neu

280 of about 39 degrees C and is co-expressed in dorsal root ganglion neurons with VR1.