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 itudes of monosynaptic EPSCs evoked from the dorsal root and puff NMDAR currents in spinal dorsal hor

5 RPA1-expressing mouse sensory neurons of the dorsal root and trigeminal ganglia.

6 urrent in the primary sensory neurons of the dorsal root and trigeminal ganglia.

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

8 r leukocyte infiltrates, was observed in the dorsal root, autonomic, and enteric ganglia.

9 rmed longitudinal DCI in rats that underwent dorsal root axotomy triggering Wallerian degeneration of

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

11 improves axonal regeneration in vivo after a dorsal root crush in adult female rats.

12 After a dorsal root crush injury, centrally-projecting sensory a

13 n monkeys that following a combined cervical dorsal root/dorsal column lesion (DRL/DCL), both motor a

14 r a dorsal column lesion (DCL) or a combined dorsal root/dorsal column lesion (DRL/DCL), when functio

15 an established deafferentation lesion model (dorsal root/dorsal column) in male monkeys to remove sen

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

17 sensory axons fail to regenerate across the dorsal root entry zone (DREZ) to extend into the spinal

18 sualized the entry of pioneer axons into the dorsal root entry zone (DREZ) with time-lapse imaging in

19 RG neurons failed to extend axons across the dorsal root entry zone after injury, DRG neurons in whic

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

21 ed enhanced regeneration of axons across the dorsal root entry zone into the spinal cord.

22 eer axon breaches the spinal boundary at the dorsal root entry zone.

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

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

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

26 eurons, termed nociceptors, are derived from dorsal root ganglia (DRG) and can undergo changes in mem

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

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

29 al dimorphism in molecular signatures of the dorsal root ganglia (DRG) and spinal cord response, not

30 nels and cyclin-dependent kinase 5 (Cdk5) in dorsal root ganglia (DRG) and spinal dorsal horn.

31 and upregulation of VIP in the corresponding dorsal root ganglia (DRG) and the dorsal horn of the spi

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

33 tes from both PC12 cells and chick embryonic dorsal root ganglia (DRG) bodies, as well as the migrati

34 The dorsal root ganglia (DRG) contain cell bodies of primary

35 The dorsal root ganglia (DRG) contain the somas of first-ord

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

37 Pain was assessed by von Frey assay and dorsal root ganglia (DRG) expression of Calca and Tac1 g

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

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

40 The dorsal root ganglia (DRG) house the primary afferent neu

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

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

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

44 Resident GFAP(+) glia in dorsal root ganglia (DRG) known as satellite glial cells

45 reases PI16 protein levels in fibroblasts in dorsal root ganglia (DRG) meninges and in the epi/perine

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

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

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

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

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 hwann cell-derived exosomes communicate with dorsal root ganglia (DRG) neurons.

53 e demonstrate that incubation of dissociated dorsal root ganglia (DRG) nociceptors with 1 nM BPA incr

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

55 cantly increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE

56 nerative gene expression response in bipolar dorsal root ganglia (DRG) sensory neurons, a regeneratio

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

58 V infection drives pathologic changes in the dorsal root ganglia (DRG) through inflammation, altered

59 pheral nervous system from the autonomic and dorsal root ganglia (DRG) to the axon and any peripheral

60 yclooxygenase-2 (COX-2) is elevated in skin, dorsal root ganglia (DRG), and spinal cord in HbSS-BERK

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

62 uronal cells in primary culture and in mouse dorsal root ganglia (DRG), as determined by the characte

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

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

65 sing a PER2::LUC fusion protein, we isolated dorsal root ganglia (DRG), the primary sensory cell body

66 In dorsal root ganglia (DRG), there is an increase in CGRP(

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

68 Dorsal root ganglia (DRG), which contain the somata of p

69 ll bodies lie predominantly in thoracolumbar dorsal root ganglia (DRG).

70 d latent virus in sensory cell bodies of the dorsal root ganglia (DRG).

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

72 establish lifelong latent infections in the dorsal root ganglia (DRG).

73 pression of alpha6beta4, an nAChR subtype in dorsal root ganglia (DRG).

74 spinal afferent neurons, with cell bodies in dorsal root ganglia (DRG).

75 f GDNF family receptor alpha1 (GFRalpha1) in dorsal root ganglia (DRG).

76 acrophages around injured sensory neurons in dorsal root ganglia (DRG).

77 ed in small-diameter, nociceptive neurons of dorsal root ganglia (DRGs) and is implicated in pain mod

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

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

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

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

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

83 e of Remak bundles, and the transcriptome of dorsal root ganglia (DRGs) provide possible explanations

84 Transcriptome profiling of dorsal root ganglia (DRGs) revealed 138 differentially r

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

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

87 ation within the distal nerve and axotomized dorsal root ganglia (DRGs).

88 TRPC4 is highly expressed in dorsal root ganglia (DRGs).

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

90 omatin; and RNA sequencing were performed in dorsal root ganglia after sciatic nerve or dorsal column

91 , primarily the large sensory neurons of the dorsal root ganglia and cardiomyocytes.

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

93 multicellular spheroids and chick embryonic dorsal root ganglia bodies.

94 y addresses whether epigenetic signatures in dorsal root ganglia discriminate between regenerative an

95 Moreover, neurons extracted from the dorsal root ganglia in animals with intervertebral disc

96 on of the HCAR2 in the sciatic nerve and the dorsal root ganglia in neuropathic mice.

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

98 of axotomy on synaptic transmission between dorsal root ganglia neurons and dorsal horn neurons, we

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

100 cetylcholine receptor (nAChR) is enriched in dorsal root ganglia neurons and is an attractive non-opi

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

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

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

108 After incubation of HEK293 cells and dorsal root ganglia neurons with CS, NE, or trypsin, PAR

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

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

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

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

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

114 .8-Cre-tdTomato mice label 80% of nodose and dorsal root ganglia neurons.

115 Dorsal root ganglia nociceptors protect against STm colo

116 10 transduces neurons in the spinal cord and dorsal root ganglia of immunodeficient mice with higher

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

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

119 Herein, we generate dorsal root ganglia organoids (DRG organoids) by in vitr

120 e of synaptic-like vesicles in navigation of dorsal root ganglia pioneer axons.

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

122 Strikingly, explant of latently infected dorsal root ganglia revealed a decreased and delayed rea

123 Global transcriptional profiling of dorsal root ganglia revealed differential expression, no

124 ons in brain and spinal cord glia as well as dorsal root ganglia satellite glia have been identified

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

126 ysiology and RNA-sequencing was performed on dorsal root ganglia taken from patients with variable pr

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

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

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

130 the receptor PTGER2 (also called EP2) in the dorsal root ganglia to promote visceral hypersensitivity

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

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

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

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

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

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

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

138 the associated inflammatory processes in the dorsal root ganglia, likely by activating stress-respons

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

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

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

142 ly, capsaicin application to the isolated L6 dorsal root ganglia, which produced robust calcium signa

143 % in saline, 50-100 nl) were made into L3-L5 dorsal root ganglia.

144 boring the rs10166942[C] allele in the human dorsal root ganglia.

145 ytoplasm of small to medium sized neurons in dorsal root ganglia.

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

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

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

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

150 midbrain-hindbrain boundary, spinal cord and dorsal root ganglia.

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

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

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

154 tion leads to calcium mobilization in murine dorsal root ganglia.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 Dorsal root ganglion (DRG) sensory neuron subtypes defin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 1.6 is involved in the functional changes of dorsal root ganglion neurons following vincristine treat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

262 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

280 In dorsal root ganglion protein extracts from nSIRT1OE mice

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

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

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

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

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

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

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

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

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

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

291 ented progression of acute poliomyelitis and dorsal root ganglionic inflammation rarely observed in C

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

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

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

295 Transection of the L4 dorsal root or intrathecal infusion of aminobutyrate ami

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

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