ライフサイエンスコーパス: dorsal root ganglion

1 s of capsaicin-responsive neurons in primate dorsal root ganglion.

2 a the release of substance P in the skin and dorsal root ganglion.

3 eferentially expressed in C fibers in lumbar dorsal root ganglions.

4 ressed in a subset of sensory neurons of the dorsal root ganglion and in cutaneous mechanoreceptors k

5 antly over time, a number of changes, in the dorsal root ganglion and in dorsal horn observed after t

6 NR2B receptor protein expression in both the dorsal root ganglion and spinal dorsal horn ipsilateral

7 mpairs channel slow inactivation within both dorsal root ganglion and superior cervical ganglion neur

8 the peripheral nervous system within sensory dorsal root ganglion and sympathetic ganglion neurons an

9 m channel is preferentially expressed within dorsal root ganglion and sympathetic ganglion neurons an

10 The survival of dorsal root ganglion and sympathetic neurons is promoted

11 be responsible for pathology observed in the dorsal root ganglion and the sensory ganglionopathy docu

12 conditions originate in the periphery, where dorsal root ganglion and trigeminal ganglion neurons fee

13 s: cortical (embryonic rat), embryonic chick dorsal root ganglion, and P-19 (mouse embryonic carcinom

14 Here we developed a dorsal root ganglion axon-oligodendrocyte-hGC co-culture

15 integrin transport and traffic in adult rat dorsal root ganglion axons and PC12 cells.

16 d force apparatus, we demonstrate that chick dorsal root ganglion axons exhibit a tension buffering o

17 al JNK substrate, is lost rapidly from mouse dorsal root ganglion axons following axotomy.

18 siveness of thin fibre afferents not only at dorsal root ganglion, but also at muscle tissue levels.

19 ple host axons when co-cultured with primary dorsal root ganglion cells and formed myelin after trans

20 n the plasma membrane of pancreatic beta and dorsal root ganglion cells and link steroid hormone sign

21 These results may be relevant to dorsal root ganglion cells and to other neurons that coe

22 ficantly suppressed 5-HT-evoked responses in dorsal root ganglion cells from wild-type mice.

23 contrast to its effect on the hair cell and dorsal root ganglion cells in culture; (iv) SLV recyclin

24 Experiments on dorsal root ganglion cells show that, for each of a grou

25 sensory terminals of primary mechanosensory dorsal root ganglion cells, so the presence of such a sy

26 le for the PGE2-induced sensitization of rat dorsal root ganglion cells.

27 tion of lymphoid cell kinase in Schwann cell-dorsal root ganglion cocultures and dorsal root ganglion

28 The administration of NO donors to primary dorsal root ganglion cultures prevents axonal degenerati

29 Treatment of isolated dorsal root ganglion cultures with myocilin stimulates c

30 y of glial cells and reduced spinal cord and dorsal root ganglion cytokine levels without affecting p

31 To determine whether dorsal root ganglion damage was associated with altered

32 y establishment and reactivation using human dorsal root ganglion-derived neuronal HD10.6 cells as an

33 hat CXCL12 and CXCR4 were upregulated in the dorsal root ganglion (DRG) after chronic compression of

34 injury causes down-regulation of MORs in the dorsal root ganglion (DRG) and diminishes the opioid eff

35 most prominent subtypes expressed in the rat dorsal root ganglion (DRG) and dorsal spinal cord.

36 ed and manipulated MrgprA3(+) neurons in the dorsal root ganglion (DRG) and found that they exclusive

37 sensory neuronal preparations, such as whole dorsal root ganglion (DRG) and hindpaw tissues, revealed

38 titutive autophagosome biogenesis in primary dorsal root ganglion (DRG) and hippocampal cultures.

39 KChIP2, KChIP3, DPP6, and DPP10 in adult rat dorsal root ganglion (DRG) and spinal cord by immunohist

40 hannel NaV1.7 is preferentially expressed in dorsal root ganglion (DRG) and sympathetic ganglion neur

41 tion after axotomy was abolished in both the dorsal root ganglion (DRG) and the distal sciatic nerve.

42 ncreases in osmolality excite isolated mouse dorsal root ganglion (DRG) and trigeminal ganglion (TG)

43 Here we study mouse dorsal root ganglion (DRG) axons and show that their ext

44 port that stimulated membrane enlargement in dorsal root ganglion (DRG) axons is triggered by intra-a

45 tigate mRNA expression in colonic tissue and dorsal root ganglion (DRG) cells isolated from 3- and 24

46 It is well established that dorsal root ganglion (DRG) cells synthesize prostaglandi

47 at a dose of 100 mpk PO due to insufficient dorsal root ganglion (DRG) exposure attributed to poor m

48 ge-diameter (>30 mum) sensory neurons of the dorsal root ganglion (DRG) express distinct combinations

49 Transcriptome analyses of rodent whole dorsal root ganglion (DRG) have revealed sex differences

50 IL-6 in skin and phosphorylation of ERKs in dorsal root ganglion (DRG) in a dose-dependent manner.

51 pression and functional role of Panx1 in the dorsal root ganglion (DRG) in the development of chronic

52 ion of HIV infection and is characterized by dorsal root ganglion (DRG) inflammation and intraepiderm

53 The T-junction of sensory neurons in the dorsal root ganglion (DRG) is a potential impediment to

54 gated potassium channel subunit Kcna2 in the dorsal root ganglion (DRG) is critical for DRG neuronal

55 Several recent papers have described a human dorsal root ganglion (DRG) neuron culture model and huma

56 nsgenic mice lacking Merkel cells had normal dorsal root ganglion (DRG) neuron numbers, but fewer DRG

57 EGABA and kinetics into acutely dissociated dorsal root ganglion (DRG) neuron somata.

58 hondrial trafficking plays a central role in dorsal root ganglion (DRG) neuronal cell survival and ne

59 that STOML1 is expressed in at least 50% of dorsal root ganglion (DRG) neurones.

60 nduced spontaneous pain and axonal injury of dorsal root ganglion (DRG) neurons and inhibited CCI-evo

61 um channel that is specifically expressed in dorsal root ganglion (DRG) neurons and peripheral nerve

62 ubcellular distribution of mammalian PATs in dorsal root ganglion (DRG) neurons and, strikingly, foun

63 satellite glial cells (SGCs) surrounding the dorsal root ganglion (DRG) neurons appears to play a rol

64 P1 shows remarkably decreased RNA binding in dorsal root ganglion (DRG) neurons compared with wild-ty

65 Our study shows that dorsal root ganglion (DRG) neurons contain at least two

66 fast-inactivating Kv3.4 potassium current in dorsal root ganglion (DRG) neurons contributes to the hy

67 voltage-gated sodium channels (VGSC) on the dorsal root ganglion (DRG) neurons controlling electrica

68 In dorsal root ganglion (DRG) neurons cultured from rats pr

69 We demonstrate that monkey and human dorsal root ganglion (DRG) neurons do not express apprec

70 v5 are expressed by developing TrkA-positive dorsal root ganglion (DRG) neurons during the period of

71 Nociceptive dorsal root ganglion (DRG) neurons express tetrodotoxin-

72 s axon growth from neurons; adult miR-155 KO dorsal root ganglion (DRG) neurons extend 44% longer neu

73 en implicated in the hyperexcitable state of dorsal root ganglion (DRG) neurons following direct inju

74 arization-evoked Ca2+ transient is larger in dorsal root ganglion (DRG) neurons from tumor-bearing mi

75 Dorsal root ganglion (DRG) neurons from wild-type or fat

76 e firing frequency and spontaneous firing of dorsal root ganglion (DRG) neurons have recently been id

77 ng Na(V)1.7 mutation, which is known to make dorsal root ganglion (DRG) neurons hyperexcitable, but d

78 tion mutations of sodium channel NaV1.7 make dorsal root ganglion (DRG) neurons hyperexcitable.

79 These variants render dorsal root ganglion (DRG) neurons hyperexcitable.

80 e find that chemogenetic activation of adult dorsal root ganglion (DRG) neurons improves axon growth

81 GKIalpha) that regulates axon bifurcation of dorsal root ganglion (DRG) neurons in the spinal cord.

82 We show that dorsal root ganglion (DRG) neurons in transgenic mice ex

83 gnitude and properties by voltage clamp from dorsal root ganglion (DRG) neurons in vivo, after classi

84 -expression network analysis, we categorized dorsal root ganglion (DRG) neurons into different subtyp

85 hat the activity of TRPM3 expressed in mouse dorsal root ganglion (DRG) neurons is inhibited by agoni

86 tion of G(alphaq)-coupled receptors in mouse dorsal root ganglion (DRG) neurons isolated from both se

87 nduced current with activation of ASIC(3) in dorsal root ganglion (DRG) neurons of control rats and r

88 es putative mechanosensitive channels in the dorsal root ganglion (DRG) neurons of these afferents.

89 mate transporter 3-lineage (Vglut3(lineage)) dorsal root ganglion (DRG) neurons play an important rol

90 uronal cell line (NG108-15) and with primary dorsal root ganglion (DRG) neurons resulted in significa

91 cell patch-clamp recordings from dissociated dorsal root ganglion (DRG) neurons revealed enhanced tet

92 rophysiological characterization of isolated dorsal root ganglion (DRG) neurons revealed that RPRFami

93 Calcium-imaging studies on dissociated dorsal root ganglion (DRG) neurons revealed the peptide'

94 We identified the subpopulation of dorsal root ganglion (DRG) neurons that are activated by

95 Nociceptors are a particular subtype of dorsal root ganglion (DRG) neurons that detect noxious s

96 t IgG-IC directly excited a subpopulation of dorsal root ganglion (DRG) neurons through the neuronal

97 ciatic nerve allows the central processes of dorsal root ganglion (DRG) neurons to spontaneously rege

98 4-well format axon degeneration assay in rat dorsal root ganglion (DRG) neurons using a trophic facto

99 native background K(+) conductance of mouse dorsal root ganglion (DRG) neurons was examined by the w

100 Depolarization-induced calcium influx in dorsal root ganglion (DRG) neurons was inhibited by both

101 sly reported that sustained ASIC currents in dorsal root ganglion (DRG) neurons were enhanced by natu

102 Porcine lumbosacral dorsal root ganglion (DRG) neurons were neurochemically

103 hat voltage-gated sodium channels (VGSCs) in dorsal root ganglion (DRG) neurons were sensitized in a

104 that reduction of GRK2 or increased EPAC1 in dorsal root ganglion (DRG) neurons would promote the tra

105 uring the development and differentiation of dorsal root ganglion (DRG) neurons, and on adult DRG neu

106 ts were performed on small-diameter (<30 um) dorsal root ganglion (DRG) neurons, cultured from fentan

107 When fentanyl (0.5 nm) was applied to dorsal root ganglion (DRG) neurons, cultured from opioid

108 In rat dorsal root ganglion (DRG) neurons, exposure to E-2 in a

109 thereby producing hyperexcitability of small dorsal root ganglion (DRG) neurons, which include nocice

110 ury induces changes in gene transcription in dorsal root ganglion (DRG) neurons, which may contribute

111 genes more proximately to promote latency in dorsal root ganglion (DRG) neurons.

112 m involved in regulation of TRPM8 in sensory dorsal root ganglion (DRG) neurons.

113 potential (TRP) channel V1 (TRPV1)-positive dorsal root ganglion (DRG) neurons.

114 s significantly reinforced in Pirt-deficient dorsal root ganglion (DRG) neurons.

115 pid inward currents and action potentials in dorsal root ganglion (DRG) neurons.

116 ked Ca(2+) transient in putative nociceptive dorsal root ganglion (DRG) neurons.

117 rade Rab7-vesicles within axons of rat E15.5 dorsal root ganglion (DRG) neurons.

118 racterized in cocultures of OECs and primary dorsal root ganglion (DRG) neurons.

119 hanism of TRPV1-ANO1 channel coupling in rat dorsal root ganglion (DRG) neurons.

120 rease of ATF-3 and TRPV1 immunoreactivity in dorsal root ganglion (DRG) neurons.

121 tally regulated and governs axonal growth in dorsal root ganglion (DRG) neurons.

122 ent and resurgent currents in large-diameter dorsal root ganglion (DRG) neurons.

123 ignals induced by PregS and CIM0216 in mouse dorsal root ganglion (DRG) neurons.

124 vels of Tet3 and 5-hydroxylmethylcytosine in dorsal root ganglion (DRG) neurons.

125 with microglia BV-2 cells exposed to G-CSF, dorsal root ganglion (DRG) nociceptors become hyperexcit

126 melanoma and normal neural tissues including dorsal root ganglion (DRG) produce PD-L1 that can potent

127 Dorsal root ganglion (DRG) sensory neuron subtypes defin

128 ort functional expression of SHANK3 in mouse dorsal root ganglion (DRG) sensory neurons and spinal co

129 analyze the detailed molecular signatures of dorsal root ganglion (DRG) sensory neurons.

130 ge-gated sodium channels (Navs) expressed in dorsal root ganglion (DRG) sensory neurons.

131 AP7) during collateral branch development of dorsal root ganglion (DRG) sensory neurons.

132 Pharmacological studies in rodent dorsal root ganglion (DRG) show their analgesic effect i

133 and the potential target ion channels in rat dorsal root ganglion (DRG) slices.

134 Primary sensory afferents of the dorsal root ganglion (DRG) that innervate the skin detec

135 ta) might act directly on nociceptors in the dorsal root ganglion (DRG) to cause pain sensitization.

136 neurons infected in vivo was examined using dorsal root ganglion (DRG) xenografts maintained in mice

137 dent outgrowth and traction forces from PNS (dorsal root ganglion (DRG)) and CNS (hippocampal) neuron

138 set of nonpeptidergic nociceptors within the dorsal root ganglion (DRG), and knockdown of Kv4.3 selec

139 etermine the protein levels of P2X(3) in the dorsal root ganglion (DRG), and the whole cell patch cla

140 ceptive neurons in the adjacent uninjured L4 dorsal root ganglion (DRG), as revealed by both in vivo

141 reduction in K(+) channel expression in the dorsal root ganglion (DRG), but little is known about th

142 In neurons isolated from mouse dorsal root ganglion (DRG), native TRPM3 channels were i

143 icular pain model, local inflammation of the dorsal root ganglion (DRG), we observed marked increases

144 in nociceptor (pain-sensing) neurons of the dorsal root ganglion (DRG), where they transmit the larg

145 agi-1 are largely unknown, but we found that dorsal root ganglion (DRG)-specific knockdown of Magi-1

146 of heterogeneous expression of ASIC3 in the dorsal root ganglion (DRG).

147 200 in large-diameter A-fiber neurons in the dorsal root ganglion (DRG).

148 Kcna2, in first-order sensory neurons of rat dorsal root ganglion (DRG).

149 80% reduction in the sensory neurons of the dorsal root ganglion (DRG).

150 l V1 expressed in the nociceptive neurons of dorsal root ganglion (DRG).

151 vivo forepaw muscles/median and ulnar nerves/dorsal root ganglion (DRG)/spinal cord (SC) recording pr

152 n in capsaicin-sensitive nociceptors using a dorsal root ganglion (DRG)/spinal cord neuron co-culture

153 ar CFA injection and in the ipsilateral L4/5 dorsal root ganglions (DRGs) 1 and 3 days after CFA inje

154 ly by small-sized primary sensory neurons in dorsal root ganglions (DRGs) that coexpress the itch sig

155 efficacy could be correlated with the mouse dorsal root ganglion exposure and Na(V)1.7 potency assoc

156 Coculture of cancer cells with dorsal root ganglion extracts revealed that Schwann cell

157 ann cell-dorsal root ganglion cocultures and dorsal root ganglions from Lck(-/-) mice show a reductio

158 ongation of actin-based filopodia from mouse dorsal root ganglion growth cones.

159 at the Ascl1 promoter, isolated from murine dorsal root ganglion (hypermethylated) and striated cell

160 permeant cAMP analog, 8-bromo cAMP, into the dorsal root ganglion induced mechanical hyperalgesia and

161 analysis (TCA), we focused on large-diameter dorsal-root ganglion (L-DRG) neurons with myelinated axo

162 that signals emanating from within the mouse dorsal root ganglion mediated partly by early-born neuro

163 imulated oligodendrocytes was validated in a dorsal root ganglion microfluidics chamber platform.

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

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

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

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

168 adapting, mechanically activated currents in dorsal root ganglion neuronal cultures are absent in Pie

169 voltage-gated sodium channel Nav1.7 underlie dorsal root ganglion neuronal hyperexcitability and pain

170 We therefore established a robust dorsal root ganglion neuronal model that mirrors key cel

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

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

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

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

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

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

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

178 nnel isoform Na(V)1.7 is highly expressed in dorsal root ganglion neurons and is obligatory for nocic

179 illin(Cre/+) mice completely ablates MORs in dorsal root ganglion neurons and reduces the MOR express

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

181 ch MOR expression is completely deleted from dorsal root ganglion neurons and substantially reduced i

182 to alter TTX-S Na+ current density in medium dorsal root ganglion neurons and, importantly, mechanica

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

184 s reduces desensitization of native TRPV1 in dorsal root ganglion neurons as well as of recombinant T

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

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

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

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

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

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

191 Dorsal root ganglion neurons displayed a fall in resting

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

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

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

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

196 cid Early 1 (RAE1), is re-expressed in adult dorsal root ganglion neurons following peripheral nerve

197 1.6 is involved in the functional changes of dorsal root ganglion neurons following vincristine treat

198 -S) and resistant (TTX-R) sodium currents in dorsal root ganglion neurons following vincristine treat

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

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

201 Cultured adult dorsal root ganglion neurons from nSIRT1OE mice, maintai

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

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

204 voltage-clamp recordings of small and medium dorsal root ganglion neurons from vincristine-treated an

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

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

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

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

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

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

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

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

213 rocytes are functional and can myelinate rat dorsal root ganglion neurons in vitro, and form myelin i

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

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

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

217 We detected increased Trpm3 mRNA levels in dorsal root ganglion neurons innervating the inflamed pa

218 t spontaneous action potential generation in dorsal root ganglion neurons is associated with radicula

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

220 es putative mechanosensitive channels in the dorsal root ganglion neurons of these afferents.

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

222 In addition, genetically deleting GluN1 in dorsal root ganglion neurons or alpha2delta-1 genetic KO

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

224 affolds Na(V)1.8 and Slack K(Na) channels in dorsal root ganglion neurons regulating excitability and

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

226 mouse and human by a subpopulation of TRPV1+ dorsal root ganglion neurons specialized in detecting pa

227 .2/Kv7.3 heteromers and native M currents in dorsal root ganglion neurons suggest the following concl

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

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

230 onstellation pharmacology to investigate rat dorsal root ganglion neurons using two models of periphe

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

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

233 Retrograde labelling of bladder-projecting dorsal root ganglion neurons was used to investigate exp

234 A significant proportion (18-19%) of dorsal root ganglion neurons were double labelled by dye

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

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

237 We observed a significant number of dorsal root ganglion neurons with dichotomized afferents

238 -resistant sodium current, in small-diameter dorsal root ganglion neurons, an effect that was attenua

239 in cardiomyocytes, cultured hippocampal and dorsal root ganglion neurons, and brain slices.

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

241 Ca(V)2 channels in mammalian cardiomyocytes, dorsal root ganglion neurons, and pancreatic beta cells.

242 calcitonin gene-related peptide (CGRP) from dorsal root ganglion neurons, and reduced inflammation i

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

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

245 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

265 sites alters Nav1.6-mediated excitability in dorsal root ganglion neurons.

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

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

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

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

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

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

272 wn increased innervation of muscle fibers by dorsal root ganglion neurons.

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

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

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

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

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

278 nvestigate autophagosome dynamics in primary dorsal root ganglion neurons.

279 on toxin, Cn2, is selective for Na(V) 1.6 in dorsal root ganglion neurons.

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

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

282 The sensitization of dorsal root ganglion nociceptors in BDL rats was associa

283 currents recorded from small neurons in the dorsal root ganglion of normal rats are potentiated by e

284 lymer, following inflammatory exposures in a dorsal root ganglion organotypic coculture system.

285 ore variable across cultures than in primary dorsal root ganglion, particularly for genes related to

286 Intracellular recordings from ex vivo dorsal root ganglion preparations revealed that Kv9.1 kn

287 y processes characterized by spinal cord and dorsal root ganglion production of proinflammatory cytok

288 In dorsal root ganglion protein extracts from nSIRT1OE mice

289 fer elevated intracellular calcium levels in dorsal root ganglion pruriceptors, and (iii) injection o

290 ly ( approximately 71%) expressed in Nppb(+) dorsal root ganglion pruriceptors.

291 SIRT2 accumulated in the nuclei of dorsal root ganglion sensory neurons and prevented neuro

292 P that binds and regulates multiple mRNAs in dorsal root ganglion sensory neurons and thereby promote

293 ated virus (AAV) has been shown to transduce dorsal root ganglion sensory neurons following direct in

294 r microtubule-associated protein 7 (MAP7) in dorsal root ganglion sensory neurons.

295 ta from an in vitro preparation of small rat dorsal root ganglion somata showing a reduction in the m

296 ptor found on select immune, epithelial, and dorsal root ganglion/spinal cord neuronal cells.

297 In the dorsal root ganglion, subpopulations of cells express co

298 peripheral immune cell infiltration into the dorsal root ganglion, suggesting that adaptive immune re

299 We show here that synaptic contacts from dorsal root ganglions to a small number of dorsal column

300 Noting the prevalence of Slo2.2 in dorsal root ganglion, we find that KO of Slo2.2, but not