ライフサイエンスコーパス: dorsal root

1 Within the dorsal root (a site remote from injury) we noted a redis

2 spinal cord slice preparation with attached dorsal roots also demonstrated that CFA inflammation red

3 the sympathetic trunk or Remak fibers of the dorsal roots, although, in those structures, they wrappe

4 channel expressed in sensory neurons of the dorsal root and trigeminal ganglia.

5 Expressed in somatosensory neurons of the dorsal root and trigeminal ganglion, the transient recep

6 Both NECAB1/2 are transported into dorsal roots and peripheral nerves.

7 In the dorsal roots and proximal peripheral nerves of mice and

8 Dorsal root avulsion results in permanent impairment of

9 ote recovery of sensorimotor functions after dorsal root avulsion, and that these effects are mediate

10 gdorferi antigen was detected in the DRG and dorsal roots by immunofluorescence staining and confocal

11 la zoster virus (VZV) establishes latency in dorsal root, cranial nerve, and enteric ganglia and can

12 regeneration in adult rat spinal cord after dorsal root crush and adeno-associated virus transgene e

13 f sensory axons into the spinal cord after a dorsal root crush as well as substantial axon regrowth i

14 ensory axons to the brainstem after brachial dorsal root crush in adult rats.

15 Section of the repaired dorsal roots distal to the transplant completely abolish

16 ed its efficacy in enhancing regeneration of dorsal root (DR) axons, whose regenerative capacity is p

17 ion channel that is expressed in a subset of dorsal root (DRG) and trigeminal ganglia sensory neurons

18 glia regenerated through the tenascin-C-rich dorsal root entry zone into the dorsal column up to C1 l

19 Light micrographs of the dorsal root entry zone show the peripheral nervous syste

20 n the spinal electrodes were placed over the dorsal root entry zone.

21 Sensory nerves emanating from the dorsal root extensively innervate the surfaces of mammal

22 mal and distal peripheral nerve segments and dorsal roots from mice and pigtail monkeys (Macaca nemes

23 e protease inhibitor, was upregulated in the dorsal root ganglia (DRG) after nerve injury, which was

24 cleared from plasma but all persisted in the dorsal root ganglia (DRG) and sciatic nerve (SN) for up

25 hese effects correlated with degeneration in dorsal root ganglia (DRG) and sciatic nerve and abundanc

26 To define which dorsal root ganglia (DRG) are activated by BAT SNS stimu

27 Peripheral sensory neurons in the dorsal root ganglia (DRG) are the initial transducers of

28 g the C133W SPT mutant, we found that mutant dorsal root ganglia (DRG) during growth in vitro exhibit

29 ransducing peripheral sensory neurons of the dorsal root ganglia (DRG) express kainate receptors (KAR

30 N-nitrosourea (ENU)-induced mutation affects dorsal root ganglia (DRG) formation in ouchless mutant z

31 he cell bodies of primary nociceptors within dorsal root ganglia (DRG) has been found to make major c

32 mber of TRPV1(+) neurons is increased in the dorsal root ganglia (DRG) in paclitaxel-treated rats and

33 spartate receptors (NMDARs) expressed in the dorsal root ganglia (DRG) in the inflammatory sensitizat

34 ed in primary afferent neurons isolated from dorsal root ganglia (DRG) innervating the lower gastroin

35 Delivering gene constructs into the dorsal root ganglia (DRG) is a powerful but challenging

36 Traffic of activated monocytes into the dorsal root ganglia (DRG) is critical for pathology in H

37 We have previously shown that dorsal root ganglia (DRG) neurons activate the mammalian

38 itro and in patch-clamp electrophysiology in dorsal root ganglia (DRG) neurons and hippocampal slices

39 ECE-1 are expressed and colocalize in murine dorsal root ganglia (DRG) neurons and human skin nerves.

40 h lipid kinases generate PIP2 in nociceptive dorsal root ganglia (DRG) neurons and if these kinases r

41 Using recombinant systems, mouse-cultured dorsal root ganglia (DRG) neurons and in vivo experiment

42 acutely dissociated small diameter (<27 mum) dorsal root ganglia (DRG) neurons and on miniature (m)EP

43 rvous system revealed that Schwann cells and dorsal root ganglia (DRG) neurons developed abnormally i

44 r in which gain-of-function mutations render dorsal root ganglia (DRG) neurons hyperexcitable.

45 axons.SIGNIFICANCE STATEMENT Small-diameter dorsal root ganglia (DRG) neurons mediating nociception

46 Nociceptors are a subpopulation of dorsal root ganglia (DRG) neurons that detect noxious st

47 nels were examined in guinea-pig dissociated dorsal root ganglia (DRG) neurons using calcium imaging

48 performed on isolated naive and injured rat dorsal root ganglia (DRG) neurons, and the analgesic eff

49 hyperexcitability and spontaneous firing of dorsal root ganglia (DRG) neurons, whole-cell patch clam

50 acutely dissociated small diameter (<27 mum) dorsal root ganglia (DRG) neurons.

51 rat SCI model depends upon hyperactivity in dorsal root ganglia (DRG) neurons.

52 neuron populations, including cerebellar and dorsal root ganglia (DRG) neurons.

53 rtantly, the trivalent vaccine protected the dorsal root ganglia (DRG) of 32/33 (97%) mice between da

54 e central nervous system, spinal nerves, and dorsal root ganglia (DRG) of rhesus macaques that were i

55 n with rAAV8 would result in transduction of dorsal root ganglia (DRG) or trigeminal ganglia (TG), re

56 verning the maintenance and proliferation of dorsal root ganglia (DRG) progenitors are largely unknow

57 However, proliferation within the dorsal root ganglia (DRG) remains to be characterized.

58 ion of non-coding microRNAs (miRs) occurs in dorsal root ganglia (DRG) sensory neurons.

59 used the up-regulation of Ran and RanGAP1 in dorsal root ganglia (DRG) under basal conditions and dur

60 L4-L5 and L6-S2 dorsal root ganglia (DRG) were collected and compared be

61 the nodose ganglia (NG) and L6/S1 and L1/L2 dorsal root ganglia (DRG) were quantified.

62 from the sciatic nerve (SN), the lumbar 4/5 dorsal root ganglia (DRG), and the trigeminal ganglia (T

63 In mice dorsal root ganglia (DRG), some neurons express calciton

64 g COX-2, EP2, EP4) in endometriosis lesions, dorsal root ganglia (DRG), spinal cord, thalamus and for

65 urons, including some sensory neurons of the dorsal root ganglia (DRG), suggesting an extranuclear ro

66 spinal afferents is well known to reside in dorsal root ganglia (DRG), the morphology and location o

67 nt increased the number of T cells in lumbar dorsal root ganglia (DRG), where CD8(+) T cells were the

68 of cultured primary afferent neurons of the dorsal root ganglia (DRG).

69 rategy in vitro and in vivo, specifically to dorsal root ganglia (DRG).

70 eral cortex of the femur and the ipsilateral dorsal root ganglia (DRG).

71 n and inflammatory cells infiltration in the dorsal root ganglia (DRG).

72 with neuropathic and/or inflammatory pain in dorsal root ganglia (DRGs) and spinal cord both during t

73 tes nerve injury and inflammatory markers in dorsal root ganglia (DRGs) and spinal cord up to 2 wk af

74 induced regulation of NECAB1/NECAB2 in mouse dorsal root ganglia (DRGs) and spinal cord.

75 , starting with gene expression profiling of dorsal root ganglia (DRGs) combined with multi-level bio

76 Rapidly adapting (RA) mechanoreceptors in dorsal root ganglia (DRGs) express Ret and the co-recept

77 d range of optical stimulation parameters on dorsal root ganglia (DRGs) expressing channelrhodopsin 2

78 and sensitization responses to capsaicin in dorsal root ganglia (DRGs) following application of supe

79 ty on the regeneration of different types of dorsal root ganglia (DRGs) neurons after sciatic nerve i

80 -EpOME (9,10-epoxy-12Z-octadecenoic acid) in dorsal root ganglia (DRGs) of paclitaxel-treated mice as

81 pes, and its gene expression is increased in dorsal root ganglia (DRGs) of paclitaxel-treated rats.

82 l afferent neurons, whose cell bodies lie in dorsal root ganglia (DRGs).

83 stimulated axonal growth from chicken or rat dorsal root ganglia (DRGs).

84 e surgical procedure for extraction of human dorsal root ganglia (hDRG) and the necessary modificatio

85 from the 4th lumbar (L4) and 5th lumbar (L5) dorsal root ganglia after L5 spinal nerve ligation (SNL)

86 so commonly develop in other cranial nerves, dorsal root ganglia and peripheral nerves.

87 lite glia, and no Schwann cell precursors in dorsal root ganglia and peripheral nerves.

88 show that memory CD4 T cells migrate to the dorsal root ganglia and spinal cord in response to infec

89 inhibit mammalian NaV channels expressed in dorsal root ganglia at concentrations up to 100 microM.

90 the vagina and reduced latent viral loads in dorsal root ganglia but induced lower serum neutralizing

91 ta opioid receptor-Ca(2+)channel coupling in dorsal root ganglia desensitized by ARM390 and the rate

92 Dorsal root ganglia Epac1 mRNA levels increase during ne

93 The dorsal root ganglia from the TrkAP782S knock-in mice dis

94 edding of HSV-2 DNA, and latent infection of dorsal root ganglia in guinea pigs.

95 ells, in vitro and is impaired for infecting dorsal root ganglia in mice.

96 by proprioceptive sensory neurons (pSNs) in dorsal root ganglia in mice.

97 Dorsal root ganglia in Zfp36l2 knock-out mice, or wild-t

98 een functional subtypes of sensory neuron in dorsal root ganglia is distorted by Gars mutations, lead

99 ditioning lesion to the peripheral branch of dorsal root ganglia neurons (DRGs).

100 NP)]Ts1, we were able to optically stimulate dorsal root ganglia neurons and generate action potentia

101 model as well as in vitro effects of HOCl on dorsal root ganglia neurons and mouse bone marrow-derive

102 LIF also induced neuronal plasticity in dorsal root ganglia neurons by increasing the number of

103 that in small-diameter, capsaicin-sensitive dorsal root ganglia neurons corresponding to nociceptors

104 impaired response to several pruritogens in dorsal root ganglia neurons excised from NC/Nga mice aft

105 Both human and mouse dorsal root ganglia neurons express IL-31RA, largely in

106 Consistently, GINIP-deficient dorsal root ganglia neurons had lower baclofen-evoked in

107 The number of dorsal root ganglia neurons is not affected by the mutat

108 Transcriptional profiling of IL-31-activated dorsal root ganglia neurons revealed enrichment for gene

109 , the growth cones of primary small-diameter dorsal root ganglia neurons showed abundant IL-31 recept

110 detected both KCNQ2 and KCNQ3 in a subset of dorsal root ganglia neurons that correspond to D-hair Ad

111 s; (iii) suppresses proinflammatory state of dorsal root ganglia neurons to decrease pelvic pain; (iv

112 els, we determined that the treatment of rat dorsal root ganglia neurons with E2 increased mRNA conce

113 d sensory neurons, which account for >40% of dorsal root ganglia neurons, display resistance to rabie

114 previous reports of ASIC3 mRNA expression in dorsal root ganglia neurons, we found that the ASIC3 ant

115 of the electrophysiology dynamics in single dorsal root ganglia neurons.

116 and membrane expression of TRPV1 protein in dorsal root ganglia neurons.

117 nhibits ASIC-like currents in naked mole-rat dorsal root ganglia neurons.

118 inhibited the activity of TRPV1 channels in dorsal root ganglia neurons.

119 myelinating cocultures established from the dorsal root ganglia of embryonic rats.

120 10 transduces neurons in the spinal cord and dorsal root ganglia of immunodeficient mice with higher

121 we isolated neurons with attached SGCs from dorsal root ganglia of mice.

122 ased concentrations in the sciatic nerve and dorsal root ganglia of oxaliplatin treated mice.

123 ncreased activity of the Epac target Rap1 in dorsal root ganglia of WT, but not of Epac1(-/-), mice.

124 gated Na(+), K(+) and Ca(2+) channels in rat dorsal root ganglia or VGSC forms individually expressed

125 After 12 weeks, axons from C6-C7 dorsal root ganglia regenerated through the tenascin-C-r

126 ochemistry was used to detect TRPV4 in human dorsal root ganglia samples (from the National Disease R

127 NCSC-derived human Schwann cells with rodent dorsal root ganglia showed interaction of the Schwann ce

128 ession G-protein-coupled receptors in murine dorsal root ganglia showed that both receptors were amon

129 f thrombospondin-4 (TSP4) in spinal cord and dorsal root ganglia that contributes to neuropathic pain

130 Here, we show in neurons of murine dorsal root ganglia that pro-nociceptive TRPM3 channels,

131 nnel isoforms were natively expressed in rat dorsal root ganglia tissue.

132 Instead, HSV-1 spread via the dorsal root ganglia to the autonomic ganglia of the ente

133 ores, and a reduction in latent HSV-2 DNA in dorsal root ganglia to undetectable levels.

134 anscription factor to sensory neurons of the dorsal root ganglia using a gene therapy approach and fo

135 from SNE-injured and contralateral L4 and L5 dorsal root ganglia were cultured in a compartmentalized

136 Lumbosacral dorsal root ganglia were positive for HSV-2 DNA and late

137 r treatment alone when dissociated embryonic dorsal root ganglia were seeded onto inhibitory substrat

138 Neuronal kainate receptors in dorsal root ganglia were sensitive to galectin modulatio

139 ecapitulates the selective death of sensory (dorsal root ganglia) and autonomic neurons observed in F

140 Using embryonic sensory neurons (rat dorsal root ganglia) in a growth cone turning assay, we

141 muscle cells, and neurons in trigeminal and dorsal root ganglia, as detected by light and electron m

142 bpopulation of neurons in the trigeminal and dorsal root ganglia, but was absent in sympathetic neuro

143 ll lines and in nociceptive neurons of mouse dorsal root ganglia, Cat-S and a decapeptide mimicking t

144 A, protein, and histological analysis of the dorsal root ganglia, spinal cord, and cerebellum.

145 neuronal and non-neuronal tissues, including dorsal root ganglia, spinal cord, and keratinocytes.

146 Despite on-target activity in small-diameter dorsal root ganglia, spinal slices, and in a mouse model

147 97%) animals had no evidence of infection of dorsal root ganglia, suggesting that the vaccine may pre

148 In human dorsal root ganglia, TPV4 was expressed by 35% of neuron

149 , and groups of somatosensory neurons in the dorsal root ganglia.

150 eno-associated virus transgene expression in dorsal root ganglia.

151 els were greater than Piezo1 channels in rat dorsal root ganglia.

152 nd reduce levels of phosphorylated VEGFR1 in dorsal root ganglia.

153 nist in BE(2)-C cells, and in trigeminal and dorsal root ganglia.

154 rum/pylorus, enteric neurones, and vagal and dorsal root ganglia.

155 subclasses of peripheral neurons from mouse dorsal root ganglia.

156 g sympathetic, parasympathetic, enteric, and dorsal root ganglia.

157 expressed in nociceptive sensory neurons of dorsal root ganglia.

158 eceptors were among the highest expressed in dorsal root ganglia.

159 fibers in human skin and sensory neurons in dorsal root ganglia.

160 dermal innervation and cell-body loss in the dorsal root ganglia.

161 an immortalized cell line derived from human dorsal root ganglia.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 4-well format axon degeneration assay in rat dorsal root ganglion (DRG) neurons using a trophic facto

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 200 in large-diameter A-fiber neurons in the dorsal root ganglion (DRG).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

253 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

287 d there were no differences in viral load at dorsal root ganglionic (DRG) neurons at day 4 postinfect

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

289 eripheral nerves, but not proximal nerves or dorsal roots, is resistant to tetrodotoxin and that, in

290 , compound action potentials were made, from dorsal roots isolated from rats with or without complete

291 eys (n = 6) received either a unilateral (1) dorsal root lesion (DRL), (2) or a combined DRL/dorsal c

292 lts in axonal regeneration into the SC after dorsal root neurotmesis.

293 ut; they can generate signals in the form of dorsal root reflexes that are transmitted antidromically

294 nts (EPSCs) of dorsal horn neurons evoked by dorsal root stimulation in spinal cord slices from wild-

295 ral root potentials evoked by long and short dorsal root stimulation lengths, to maximize and minimiz

296 nts (EPSCs) of dorsal horn neurons evoked by dorsal root stimulation.

297 Decreasing the time between dorsal-root stimulation, and therefore interepisode inte

298 "natural" locomotor output was evoked using dorsal-root stimulation, ouabain increased burst frequen

299 The SAAs of Adelta- or C-fibers from the L6 dorsal roots were recorded during bladder filling.

300 B2 markedly enhances regeneration of damaged dorsal roots, while evoking little change in intact root