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

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

5 ion and expression in sensory neurons of the dorsal root ganglion and spinal cord.

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 is preferentially expressed in nocioceptive dorsal root ganglion and sympathetic ganglion neurons.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

25 hVariant 3 is more abundantly expressed in dorsal root ganglion compared with brain and shows basic

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

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

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

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

30 oop L1 reduces Na(v)1.6 current density in a dorsal root ganglion-derived cell line, without changing

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

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

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

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

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

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

37 parts in two major pain-related regions, the dorsal root ganglion (DRG) and spinal cord dorsal horn.

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

39 1.7 which is preferentially expressed within dorsal root ganglion (DRG) and sympathetic ganglion neur

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

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

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

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

44 Ca(2+) imaging in dorsal root ganglion (DRG) cells confirmed LY enhanced C

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 Using live myelinated rat dorsal root ganglion (DRG) cultures, we investigated whe

48 The treatment of myelinating dorsal root ganglion (DRG) explant cultures from neuropa

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

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

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 d texture is the activation of trigeminal or dorsal root ganglion (DRG) mechanosensory neurons, which

56 elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polyly

57 ing sodium channels, thus acutely regulating dorsal root ganglion (DRG) neuron excitability.

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

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

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

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

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

63 the Na(+)/K(+)-ATPase (alpha3) in some large dorsal root ganglion (DRG) neurons and large intrafusal

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

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

66 We used cultured dorsal root ganglion (DRG) neurons as a model of axotomi

67 norepinephrine and sensitizes colon-specific dorsal root ganglion (DRG) neurons by increasing express

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

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

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

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

80 hormones in regulating axonal development of dorsal root ganglion (DRG) neurons in the spinal cord.

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

82 electroporation approach to transfect adult dorsal root ganglion (DRG) neurons in vivo that enables

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

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

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

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

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

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

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

93 luence the electrophysiological responses of dorsal root ganglion (DRG) neurons to mechanical stimula

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

95 Dorsal root ganglion (DRG) neurons transmit sensory info

96 nhanced green fluorescent protein-expressing dorsal root ganglion (DRG) neurons transplanted into the

97 after axonal injury, Nogo-A is increased in dorsal root ganglion (DRG) neurons unable to regenerate

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

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

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

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

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

103 mature rat retinal ganglion cells (RGCs) and dorsal root ganglion (DRG) neurons, and is essential for

104 s in the up-regulation of alpha(2)delta-1 in dorsal root ganglion (DRG) neurons, and there is a conse

105 For KOR(-/-) or KOR-knockdown dorsal root ganglion (DRG) neurons, EGF can no longer ef

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

107 hosphatase (PAP) is expressed in nociceptive dorsal root ganglion (DRG) neurons, functions as an ecto

108 expressed in a subpopulation of nociceptive dorsal root ganglion (DRG) neurons, where it acts as a s

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

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

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

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

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

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

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

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

119 esults in increased NKCC1 phosphorylation in dorsal root ganglion (DRG) neurons.

120 ed potassium (K(Na)) channels in nociceptive dorsal root ganglion (DRG) neurons.

121 l vanilloid type 1 (TRPV1) currents in L6-S2 dorsal root ganglion (DRG) neurons.

122 nels are expressed in the plasma membrane of dorsal root ganglion (DRG) neurons.

123 We characterized KNa channels in adult rat dorsal root ganglion (DRG) neurons.

124 two GsMTx-4-sensitive SACs, are expressed in dorsal root ganglion (DRG) neurons.

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

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

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

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

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

130 studied pancreatic nodose ganglion (NG) and dorsal root ganglion (DRG) sensory neurons (identified b

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

132 pplied to their distal axons, in contrast to dorsal root ganglion (DRG) sensory neurons in which GDNF

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

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

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

136 of BMP signaling, highly expressed in adult dorsal root ganglion (DRG) sensory neurons.

137 otential (TRPV1) receptors, respectively, on dorsal root ganglion (DRG) sensory neurons.

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

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

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

141 of rodent embryonic sensory neurons from the dorsal root ganglion (DRG) to demonstrate the role of cG

142 VZV infection of human dorsal root ganglion (DRG) xenografts in immunodeficient

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

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

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

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

147 Lumbosacral and thoracolumbar dorsal root ganglion (DRG), lumbar sympathetic chain (LS

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

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

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

151 80% reduction in the sensory neurons of the dorsal root ganglion (DRG).

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

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

154 200 in large-diameter A-fiber neurons in the dorsal root ganglion (DRG).

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

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

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

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

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

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

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

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

163 plotted global expression changes in the rat dorsal root ganglion in three peripheral neuropathic pai

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

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

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

167 city, nerve amplitude, and sciatic nerve and dorsal root ganglion morphology at 0.25 x MTD, 0.5 x MTD

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 Dorsal root ganglion neurons displayed a fall in resting

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

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

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

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

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

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

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

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

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

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

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

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

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

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

211 Dorsal root ganglion neurons in vitro express a number o

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

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

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

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

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

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

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

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

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

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

224 .2/Kv7.3 heteromers and native M currents in dorsal root ganglion neurons suggest the following concl

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

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

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

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

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

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

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

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

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

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

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

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

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

238 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 nvestigate autophagosome dynamics in primary dorsal root ganglion neurons.

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

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

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

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

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

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

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

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

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

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

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

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

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

282 apoptosis was observed in the forebrain and dorsal root ganglions of mutant embryos.

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

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

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

286 capsaicin-induced calcium uptake in a mouse dorsal root ganglion primary cell culture assay.

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

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

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

290 Using a nociceptive dorsal root ganglion sensory neuronal cell line, which e

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

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

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

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

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

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

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

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

299 evidence indicates that gene transfer to the dorsal root ganglion using replication-defective herpes

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