ライフサイエンスコーパス: dorsal root ganglia

1 % in saline, 50-100 nl) were made into L3-L5 dorsal root ganglia.

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

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

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

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

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

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

8 subclasses of peripheral neurons from mouse dorsal root ganglia.

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

10 expressed in nociceptive sensory neurons of dorsal root ganglia.

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

12 C activity is found associated with TRPV1 in dorsal root ganglia.

13 00 years ago, VZV was carried along in their dorsal root ganglia.

14 mRNA and protein expression was detected in dorsal root ganglia.

15 nal segments in cocultures with neurons from dorsal root ganglia.

16 ently infected neurons in trigeminal but not dorsal root ganglia.

17 prevalent in distal sural nerves compared to dorsal root ganglia.

18 tained the lowest mean HSV-2 DNA load in the dorsal root ganglia.

19 essed in cardiac sensory neurons in thoracic dorsal root ganglia.

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

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

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

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

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

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

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

27 e neurons from cultures of dissociated mouse dorsal-root ganglia.

28 resent in mouse and human sensory neurons of dorsal root ganglia, a substantial number of peripheral

29 haracteristic lysosomal storage pathology in dorsal root ganglia affecting neurons, satellite cells (

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

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

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

33 sections showed intense Na(V)1.8 labeling in dorsal root ganglia and intracardiac ganglia and only mo

34 d genes that is primarily expressed in human dorsal root ganglia and mast cells.

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

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

37 lar aberrations are apparent in prephenotype dorsal root ganglia and primary sensory neurons from dt

38 Olfm1 is coexpressed with NgR1 in dorsal root ganglia and retinal ganglion cells in embryo

39 to severe degenerative pathologic changes in dorsal root ganglia and sciatic nerve.

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

41 was detected in peptidergic neurons of mouse dorsal root ganglia and spinal cord that transmit itch a

42 -derived neurotrophic factor in the thoracic dorsal root ganglia and spinal cord, and down-regulated

43 olog of Cbln2 and examined its expression in dorsal root ganglia and spinal cord.

44 to two functionally discrete structures, the dorsal root ganglia and sympathetic ganglia (SGs), are u

45 ith alterations in the central compartments (dorsal root ganglia and the spinal cord) and symptomatic

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

47 cluding locus ceruleus, retina, hippocampus, dorsal root ganglia, and adrenal chromaffin cells.

48 s tested, including spleen, paw skin, lumbar dorsal root ganglia, and lumbar spinal cord, postinfecti

49 TRPA1 in dermal sensory nerve fibers, their dorsal root ganglia, and mast cells.

50 a isoform is neuroprotective in hippocampal, dorsal root ganglia, and retinal neurons, but its proper

51 (Axolotl) the correct number and spacing of dorsal root ganglia are regenerated.

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

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

54 essures up to 65 +/- 30 Pa for 10 min, while dorsal root ganglia axons can resist to pressures up to

55 We found that dorsal root ganglia axons have a 20% lower elastic modul

56 Application of CSPGs to postnatal rat dorsal root ganglia axons results in an increase in the

57 multicellular spheroids and chick embryonic dorsal root ganglia bodies.

58 eir associated small-diameter neurons in the dorsal root ganglia (both IB4- and TrkA-positive), expre

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

60 TRPv1 protein expression in dorsal root ganglia, but not skeletal muscle, was signif

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

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

63 C)) acted as an enhancer in hypothalamic and dorsal root ganglia cells and responded to MAPK activati

64 ignificantly more active in hypothalamic and dorsal root ganglia cells but, significantly, and in con

65 cation transporter 2 (OCT2) is expressed on dorsal root ganglia cells within the nervous system wher

66 nction on specification and morphogenesis of dorsal root ganglia, craniofacial skeleton and melanopho

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

68 rdiac outflow tract septation and thymic and dorsal root ganglia development.

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

70 infection or shortly after virus reached the dorsal root ganglia, disease severity was significantly

71 infectious gE2-del virus was recovered from dorsal root ganglia (DRG) after multiple routes of inocu

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

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

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

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

76 pes simplex virus 1 (HSV-1) and HSV-2 DNA in dorsal root ganglia (DRG) and spinal cord (SC) were quan

77 icular cartilage and synovium, as well as in dorsal root ganglia (DRG) and spinal cord from a rat mod

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

79 a glutamate receptor and transporters in the dorsal root ganglia (DRG) and spinal cord.

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

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

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

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

84 itry, in particular spinal cord targeting of dorsal root ganglia (DRG) axons and differentiation of n

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

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

87 Dorsal root ganglia (DRG) contain somatosensory neurons

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

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

90 We used dorsal root ganglia (DRG) explants and Drosophila larval

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

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

93 Here we used the ZW-X mouse line to analyze dorsal root ganglia (DRG) for intraganglionic connection

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

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

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

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

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

99 Changes in dorsal root ganglia (DRG) included macrophage infiltrati

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

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

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

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

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

105 The sensory neurons of the dorsal root ganglia (DRG) must project accurately to the

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

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

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

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

110 hydrolyze extracellular AMP to adenosine in dorsal root ganglia (DRG) neurons and in the dorsal spin

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

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

113 Dorsal root ganglia (DRG) neurons are known to express n

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

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

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

117 he enhanced excitability of colon projecting dorsal root ganglia (DRG) neurons observed in diabetes i

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

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

120 receptor activation was investigated in rat dorsal root ganglia (DRG) neurons using whole cell patch

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

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

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

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

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

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

127 om developing growth cones (GCs) of isolated dorsal root ganglia (DRG) neurons.

128 tential vanilloid-1 (TRPV1)-expressing mouse dorsal root ganglia (DRG) neurons.

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

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

131 isoform, Nes-S, was identified in neurons of dorsal root ganglia (DRG) of adult rats.

132 cells (BMDCs) that fuse with neurons in the dorsal root ganglia (DRG) of mice, leading to diabetic n

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

134 urrent study investigated MC4R expression in dorsal root ganglia (DRG) of the MC4R-GFP reporter mouse

135 (B(1)) and GABA(B(2)) mRNA, in the L4 and L5 dorsal root ganglia (DRG) of the rat in the absence of i

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

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

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

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

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

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

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

143 We found that in rat dorsal root ganglia (DRG) TMEM16C was expressed mainly i

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

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

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

147 Dorsal root ganglia (DRG) were examined for histological

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

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

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

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

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

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

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

155 in acutely and latently infected guinea pig dorsal root ganglia (DRG), suggesting that this region i

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

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

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

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

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

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

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

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

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

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

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

167 ncluding the sensory neurons and glia of the dorsal root ganglia (DRG).

168 sensory neurons from rat trigeminal (TG) and dorsal root ganglia (DRG).

169 s and concomitant changes in the innervating dorsal root ganglia (DRG).

170 s, including sensory neurons and glia of the dorsal root ganglia (DRG).

171 (2+) influx in cultured primary neurons from dorsal root ganglia (DRG).

172 NaV1.8 mRNA in the injured nerve but not in dorsal root ganglia (DRG).

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

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

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

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

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

178 anglia neurons--trigeminal ganglia (Vg), and dorsal root ganglia (DRG): C(2), C(5), T(5), L(5)--were

179 oth peripheral and central neuronal tissues (dorsal root ganglia [DRG], spinal cord, and brain), wher

180 d in peripheral somatosensory neurons of the dorsal root ganglia (DRGs) and have been implicated in i

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

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

183 ressed by specific subsets of neurons in the dorsal root ganglia (DRGs) and spinal cord starting shor

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

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

186 ced nociception, 5,6-EET levels increased in dorsal root ganglia (DRGs) and the dorsal spinal cord, a

187 Neurons in the mouse dorsal root ganglia (DRGs) are composed of a variety of

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

189 diated depletion of overall GAP-43 mRNA from dorsal root ganglia (DRGs) decreased the length of axons

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

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

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

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

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

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

196 here was a 33% neuronal loss in the lumbar 5 dorsal root ganglia (DRGs) of the db(-)/db(-) mouse vers

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

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

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

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

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

202 types of nociceptors have been described in dorsal root ganglia (DRGs).

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

204 Dorsal root ganglia Epac1 mRNA levels increase during ne

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

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

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

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

209 ormed gD-2 alone, particularly in protecting dorsal root ganglia in mice and reducing recurrent vagin

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

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

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

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

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

215 er proportion of nociceptors compared to the dorsal root ganglia innervating the rest of the body.

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

217 inant highly Ca(2+)-sensitive PLC isoform in dorsal root ganglia is PLCdelta4.

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

219 se neurons represent a small fraction of the dorsal-root ganglia neuronal population, we were able to

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

221 ation of AC from an AKAP150-TRPV1 complex in dorsal root ganglia neurons abolishes sensitization of T

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

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

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

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

226 lective agonist induced hyperexcitability of dorsal root ganglia neurons and stimulated the release o

227 al manifestations ensue from primary loss of dorsal root ganglia neurons and their associated axons a

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

229 Analysis of co-cultures with rat dorsal root ganglia neurons confirmed that OPCs were mor

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

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

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

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

234 neurons maintains the position of later born dorsal root ganglia neurons in an activity-dependent man

235 t of the trigeminal (V), superior (IX/X), or dorsal root ganglia neurons in which it is expressed, bu

236 Olfm1 inhibited the growth cone collapse of dorsal root ganglia neurons induced by myelin-associated

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

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

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

240 several tissues, and knockdown of Piezo2 in dorsal root ganglia neurons specifically reduced rapidly

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

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

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

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

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

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

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

248 .8-Cre-tdTomato mice label 80% of nodose and dorsal root ganglia neurons.

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

250 ore activated, form of cJun, a JNK target in dorsal root ganglia neurons.

251 of nonpeptidergic nociceptors and myelinated dorsal root ganglia neurons.

252 for temperature and pressure sensitivity in dorsal root ganglia neurons.

253 a(2+) currents in rat T-rich nociceptor-like dorsal root ganglia neurons.

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

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

256 Dorsal root ganglia nociceptors protect against STm colo

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

258 10 transduces neurons in the spinal cord and dorsal root ganglia of immunodeficient mice with higher

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

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

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

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

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

264 ed the EP4 receptor protein in the L4 and L5 dorsal root ganglia over their freely perfused counterpa

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

266 Different types of sensory neurons in the dorsal root ganglia project axons to the spinal cord to

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

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

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

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

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

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

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

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

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

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

277 97%) animals had no evidence of infection of dorsal root ganglia, suggesting that the vaccine may pre

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

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

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

281 xclusively in trigeminal ganglia, and not in dorsal root ganglia, thereby maintaining a role for TRPV

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

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

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

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

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

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

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

289 the TRPV1 expressing neurons in the rostral dorsal root ganglia were more similar to jugular than no

290 on of injury-related genes due to SNI in the dorsal root ganglia were not affected by SDLs.

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

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

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

294 Induction of inflammation within dorsal root ganglia, when combined with other treatments

295 as development progresses in sympathetic and dorsal root ganglia, whereas levels in ciliary ganglia b

296 subset of sensory neurons in the cranial and dorsal root ganglia which does not correspond to any spe

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

298 mns and striking neuronal cell loss from the dorsal root ganglia, which was accompanied by severe mit

299 ed within muscle spindle afferent neurons in dorsal root ganglia with a higher proportion at cervical

300 -regulated K(v)1.1 messenger RNA in thoracic dorsal root ganglia without affecting the expression of