ライフサイエンスコーパス: ganglion

1 roduced in mice lacking Piezo2 in the nodose ganglion.

2 ted, but had distinct preferences within the ganglion.

3 s the optic lobes toward the supraesophageal ganglion.

4 d to the most medial and anterior 25% of the ganglion.

5 cavity-projecting neurons in the geniculate ganglion.

6 nally, our data identified superior cervical ganglion-10 (SCG10) as an interacting partner of WDR47.

7 lso identifies some other subsets of retinal ganglion and amacrine cell types, along with horizontal

8 DNER, by contrast, is present in ganglion and amacrine cells on P1, also labeling the hor

9 tonin gene-related peptide in the trigeminal ganglion and c-Fos in the trigeminal nucleus caudalis.

10 gnal-to-noise ratio in the dorsal nerve root ganglion and C6 nerve (P < .001) with the multiecho TSE-

11 line, which shows properties of both retinal ganglion and photoreceptor cells.

12 icient to attract leukocytes into the spiral ganglion, and that fractalkine signaling plays a role in

13 nstream motor circuits in the stomatogastric ganglion are well characterized, their anatomical distri

14 regeneration, and we have shown that retinal ganglion cell (RGC) axons regenerate in the lizard Gallo

15 This study explored why lesioned retinal ganglion cell (RGC) axons regenerate successfully in the

16 e mechanisms promoting the growth of retinal ganglion cell (RGC) axons toward visual targets remain l

17 nd CRMP2 was expectedly increased in retinal ganglion cell (RGC) axons upon enhanced GSK3 activity, b

18 elayed from the eye to the brain via retinal ganglion cell (RGC) axons.

19 and is characterized by progressive retinal ganglion cell (RGC) death.

20 restingly, time course and extent of retinal ganglion cell (RGC) degeneration after optic nerve crush

21 Regulated retinal ganglion cell (RGC) differentiation and axonal guidance

22 ressure (IOP) but are protected from retinal ganglion cell (RGC) dysfunction and neuroglial changes t

23 What pathways specify retinal ganglion cell (RGC) fate in the developing retina?

24 dividual somas of neurons within the retinal ganglion cell (RGC) layer can be imaged with a modificat

25 female Nf1-OPG mice exhibit greater retinal ganglion cell (RGC) loss and only females have retinal n

26 en ATP synthesis, and cause specific retinal ganglion cell (RGC) loss.

27 dendritic morphogenesis in a single retinal ganglion cell (RGC) type in mouse called J-RGC.

28 oter resulted in cellular depolarization and ganglion cell action potential firing.

29 The common ganglion cell and inner plexiform layer (GCIPL) and inne

30 anges over time, for example, changes in the ganglion cell and inner plexiform layers, the sites of t

31 ral overexpression of LOTUS enhances retinal ganglion cell axonal regeneration after optic nerve crus

32 thetase/tyrosine hydroxylase expression) and ganglion cell axons via a TrkA receptor (TrkAR)-dependen

33 r plexiform layers, the sites of the retinal ganglion cell bodies and dendrites, respectively.

34 To investigate the relationship between ganglion cell complex (GCC) thickness and photoreceptor

35 Measurement of ganglion cell complex (GCC) thickness may be more sensit

36 iber layer (RNFL) thickness, and the macular ganglion cell complex (GCC) thickness measurements on OC

37 Macular retinal VD, ganglion cell complex (GCC) thickness, and visual field

38 The ganglion cell complex (GCC) was determined by adding the

39 a, central fovea, ganglion cell layer (GCL), ganglion cell complex (GCC), and some sectors of outer n

40 apillary retinal nerve fiber layer (NFL) and ganglion cell complex (GCC).

41 Ganglion cell complex thickness appears to be highly her

42 Ganglion cell complex thickness was not associated with

43 s and ORDs suggests a novel photoreceptor to ganglion cell connection in the mammalian retina.

44 hat link visual field sensitivity to retinal ganglion cell count are discussed.

45 permanent visual dysfunction due to retinal ganglion cell damage in multiple sclerosis and experimen

46 Additionally, ST266 reduced retinal ganglion cell death in vitro.

47 which causes optic nerve damage and retinal ganglion cell death, is the primary risk factor for blin

48 as a key proinflammatory mediator of retinal ganglion cell death.

49 e found a temporal area with maximum retinal ganglion cell density ( approximately 5,000-7,000 cells/

50 ies with a more pronounced rate of change in ganglion cell density across the retina generally showed

51 of spatial resolution based on peak retinal ganglion cell density and eye size ( approximately 6-12

52 tion of the retina (i.e., changes in retinal ganglion cell density from the retinal periphery to the

53 Retinal ganglion cell density was 33% lower in glaucoma patients

54 Retinal ganglion cell density was estimated at the same test loc

55 rning, including photoreceptor distribution, ganglion cell density, and organization of interneurons.

56 ats have a pronounced streak of high retinal ganglion cell density, whereas those favoring more enclo

57 ates, over 17 morphological types of retinal ganglion cell have been distinguished by their dendritic

58 strated that macular parameters, such as the ganglion cell inner plexiform layer and optic nerve head

59 showed a thinned (<30% of normal thickness) ganglion cell layer (GCL) that colocalized in 7 of 8 eye

60 ant thinning of total macula, central fovea, ganglion cell layer (GCL), ganglion cell complex (GCC),

61 ayer (INL) and a few cell bodies were in the ganglion cell layer (GCL).

62 The thicknesses of the ganglion cell layer (I3 and N6 sectors), inner plexiform

63 r retinal nerve fiber layer (mRNFL), macular ganglion cell layer (mGCL), macular inner plexiform laye

64 a disclosed a strong DNM1L expression in the ganglion cell layer and axons, and comparison between 3-

65 ing cells have their soma exclusively in the ganglion cell layer and include a small proportion of bi

66 Atrophy of the macular ganglion cell layer and inner plexiform layer (GCIPL) wa

67 , specifically, the thickness of the retinal ganglion cell layer and inner plexiform layer (GCL + IPL

68 80%) of the calretinin positive cells in the ganglion cell layer are ganglion cells, and 20% are disp

69 ic cell type(s) expressing calretinin in the ganglion cell layer are yet to be determined.

70 to be expressed in the inner nuclear and the ganglion cell layer of marmoset retina, however, the spe

71 1 protein was predominantly localized to the ganglion cell layer of the retina, the cell type most af

72 M1-like cells typically had somas in the ganglion cell layer, with 23% displaced to the inner nuc

73 the mRNFL, mGCL, and mIPL parameters and the ganglion cell layer-inner plexiform layer (mGCL-IPL) was

74 h a marked increase in amacrine cells in the ganglion cell layer.

75 ones and combined at the bipolar and retinal ganglion cell level, creating parallel color opponent pa

76 ed visual dysfunction, and prevented retinal ganglion cell loss in experimental optic neuritis, with

77 ectropion uvea, retinal gliosis, and retinal ganglion cell loss.

78 e knockout, reduced inflammation and retinal ganglion cell loss.

79 Double labeling with the ganglion cell marker RBPMS demonstrated that the large m

80 nd disinhibitory inputs to a type of retinal ganglion cell maximizes the signal-to-noise ratio power

81 ionship between visual field sensitivity and ganglion cell number are reviewed.

82 a potential role for biplexiform melanopsin ganglion cell ORDs.

83 od photoreceptors and are transmitted to the ganglion cell output of the retina through the primary r

84 optimal models faithfully recapitulated the ganglion cell outputs.

85 nsically-photosensitive (melanopsin) retinal ganglion cell pathways.

86 Using ganglion cell peak density and eye size (29 mm, axial le

87 gle glaucoma with structural macular retinal ganglion cell plus inner plexiform layer (RGC+IPL) loss

88 on cells made up on average 12% of the total ganglion cell population outside of the foveal region an

89 ification, but reliable markers for specific ganglion cell populations are still rare.

90 icant because chemical synapses on a retinal ganglion cell require the probabilistic release of trans

91 ed increased mitochondrial length in retinal ganglion cell soma and axon, but no degeneration.

92 n and the anatomical location of the retinal ganglion cell soma.

93 ocal imaging of genetically targeted retinal ganglion cell sub-populations in the mouse.

94 There are five melanopsin ganglion cell subtypes (M1-M5).

95 the effect this has on reactive remodeling, ganglion cell survival, and visual function after experi

96 fusion and fission, similarly affect retinal ganglion cell survival.

97 h the idea that the proportion of wide-field ganglion cell types increases in peripheral retina.

98 ay compensates for losses incurred by the ON ganglion cell, and improves the processing of positive c

99 nerve fiber layer (RNFL) and macular retinal ganglion cell-inner plexiform layer (GCIPL) change over

100 Minimum rim width (MRW), ganglion cell-inner plexiform layer thickness (GC-IPLT),

101 ar study population (ETDRS </=35) had normal ganglion cell-inner plexiform layer thickness and normal

102 relations were found between CS at 6 cpd and ganglion cell/inner plexiform layer thickness at inferot

103 Retinal direction-selective ganglion cells (DSGCs) have the remarkable ability to en

104 direction preferences of direction-sensitive ganglion cells (DSGCs) in flattened mouse retinas in vit

105 urst amacrine cells onto direction-selective ganglion cells (DSGCs).

106 the functional output of direction-selective ganglion cells (DSGCs).

107 Ganglion cells (GCs) are fundamental to retinal neural c

108 The intrinsically photosensitive M1 retinal ganglion cells (ipRGC) initiate non-image-forming light-

109 ound in intrinsically photosensitive retinal ganglion cells (ipRGCs) [11-19].

110 ed that intrinsically photosensitive retinal ganglion cells (ipRGCs) are critical for this refinement

111 Intrinsically photosensitive retinal ganglion cells (ipRGCs) combine direct photosensitivity

112 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment melanop

113 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigment mela

114 Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate the pupillary light refl

115 small subset of intrinsically photosensitive ganglion cells (ipRGCs) of the mammalian retina.

116 retina, intrinsically photosensitive retinal ganglion cells (ipRGCs), has had a revolutionary impact

117 We asked how ON-OFF direction-selective ganglion cells (ooDSGCs) in mouse retina acquire their b

118 naling secondary to axonal damage in retinal ganglion cells (RGCs) and other neurons.

119 Precise connectivity between retinal ganglion cells (RGCs) and thalamocortical (TC) relay neu

120 Retinal ganglion cells (RGCs) are frequently divided into functi

121 Retinal ganglion cells (RGCs) are tasked with transmitting all l

122 Retinal ganglion cells (RGCs) are the sole projecting neurons of

123 the retina, where distinct types of retinal ganglion cells (RGCs) are tuned to specific visual featu

124 nges in transected axons of purified retinal ganglion cells (RGCs) from wild-type and Wld(S) rat reti

125 e interaction between astrocytes and retinal ganglion cells (RGCs) in the eye to characterize a secre

126 Loss of retinal ganglion cells (RGCs) is a key pathological process in T

127 In retinal ganglion cells (RGCs) of blind rd1 mice, photoswitch-cha

128 e TBK1 labelling was detected in the retinal ganglion cells (RGCs) of Tg-TBK1 mice than in wild-type

129 ABSTRACT: How retinal ganglion cells (RGCs) process and integrate synaptic, me

130 Retinal ganglion cells (RGCs) receive convergent input from bipo

131 her mammals, the majority of injured retinal ganglion cells (RGCs) survive with relatively high spont

132 Here we identify a subset of retinal ganglion cells (RGCs) that controls mouse looming-evoked

133 rods and cones of the retina, but on retinal ganglion cells (RGCs) that detect the ambient light leve

134 rcuit is comprised of projections of retinal ganglion cells (RGCs) to ipsilateral and contralateral t

135 origin to its 1.2 million axons, the retinal ganglion cells (RGCs), are particularly vulnerable to ne

136 Ret is initially expressed in retinal ganglion cells (RGCs), followed by horizontal cells (HCs

137 inals then drive the output neurons, retinal ganglion cells (RGCs), following light increments and de

138 pathies are associated with death of retinal ganglion cells (RGCs), neurons that project their axons

139 Retinal ganglion cells (RGCs), the neurons that connect the eyes

140 y of light-driven responses in mouse retinal ganglion cells (RGCs).

141 ye to the brain by distinct types of retinal ganglion cells (RGCs).

142 ing disease characterized by loss of retinal ganglion cells (RGCs).

143 axon growth in CNS neurons including retinal ganglion cells (RGCs).

144 pathies, is characterized by loss of retinal ganglion cells (RGCs).

145 ins 72 (HSP72) induction behavior in retinal ganglion cells (RGCs-5) to provide a possible solution f

146 IK-1, TASK-3, TRAAK, and TREK-2) and retinal ganglion cells (TASK-1, TREK-1, TWIK-1, TWIK-2 and TWIK-

147 impaired the removal of dead labeled retinal ganglion cells after optic nerve crush, but remarkable h

148 ur injections also transduced 10% of spiral ganglion cells and a much larger fraction of their satel

149 n 8 degrees of the central field) to retinal ganglion cells and associated central visual field (VF)

150 ured the topographic distribution of retinal ganglion cells and determined the spatial resolution of

151 Using maximum density of total ganglion cells and eye size (35 mm, axial length), we es

152 cordings from synaptically connected retinal ganglion cells and LGN neurons and measured the influenc

153 n of essentially the same markers of retinal ganglion cells and neuronal cells as seen in 661W cells.

154 idbrain, converging projections from retinal ganglion cells and neurons in visual cortex must be alig

155 The progressive death of retinal ganglion cells and resulting visual deficits are hallmar

156 ise 3.5% (12,300) of the total population of ganglion cells and show a similar distribution pattern w

157 Directional responses in retinal ganglion cells are generated in large part by direction-

158 Melanopsin-expressing retinal ganglion cells are intrinsically photosensitive cells th

159 Alpha ganglion cells comprise 3.5% (12,300) of the total popul

160 s, we showed that, in rats, axons of retinal ganglion cells converge on hypothalamic neurons that pro

161 In the third, up to 91 ganglion cells converged from both eyes, revealing a bin

162 nputs from the melanopsin-containing retinal ganglion cells encode spatial information and therefore

163 KEY POINTS: A subpopulation of retinal ganglion cells expresses the neuropeptide vasopressin.

164 A small population of retinal ganglion cells expresses the photopigment melanopsin and

165 was recently discovered that some melanopsin ganglion cells extend dendrites into the outer retina.

166 cannabis could alter the function of retinal ganglion cells in humans.

167 tral neurotransmission, studying the retinal ganglion cells in individuals who regularly use cannabis

168 Our results show that three types of thorny ganglion cells in marmoset retina can be identified with

169 that, contrary to standard models, specific ganglion cells in mouse retina are suppressed after a ra

170 in transmission of action potentials by the ganglion cells in regular cannabis users, which could su

171 died the morphology and diversity of retinal ganglion cells in Steller's sculpin Myoxocephalus stelle

172 e, we identified calretinin positive retinal ganglion cells in the common marmoset Callithrix jacchus

173 We recorded from OFF delta retinal ganglion cells in the guinea pig retina and monitored sy

174 bers of a functional pair of sustained alpha ganglion cells in the mouse retina.

175 Melanopsin-containing ganglion cells in the retina represent, at least in part

176 ated optic nerves as well as loss of retinal ganglion cells indicated optic atrophy.

177 changes of the optic nerve head and retinal ganglion cells is the hallmark of glaucoma diagnosis.

178 The calretinin positive ganglion cells made up on average 12% of the total gangl

179 Ganglion cells of a single type thus do not code for one

180 In the first, 1-5 ganglion cells of mostly the same type converged from on

181 We estimated a total of 243,000 ganglion cells of which 3.4% (8,300) comprise alpha cell

182 These retinal ganglion cells project predominately to our biological c

183 brain is the primary region to which retinal ganglion cells project their axons in the chick.

184 extensive work has revealed how the retinal ganglion cells respond to extracellular electrical stimu

185 Experiments on dorsal root ganglion cells show that, for each of a group of interfa

186 ow that a homogeneous population of fast OFF ganglion cells simultaneously encodes two radically diff

187 xpressed certain markers specific to retinal ganglion cells such as Rbpms, Brn3b (Pou4f2), Brn3c (Pou

188 sking requires melanopsin-expressing retinal ganglion cells that detect blue light and project to the

189 d transsynaptic tracing to label the retinal ganglion cells that provide input to individual principa

190 en shown to restore the responses of retinal ganglion cells to light in mouse models of retinal degen

191 orm microcircuits with bipolar, amacrine and ganglion cells to process visual information in the inne

192 ressing intrinsically photosensitive retinal ganglion cells upon illumination.

193 etinin-positive amacrine cells and a loss of ganglion cells was detected.

194 Two types of melanopsin-expressing ganglion cells were distinguished based on their dendrit

195 most central and amacrine cells and retinal ganglion cells were on the outside.

196 ive-response (PhNR; originating from retinal ganglion cells) and i-wave components were extracted fro

197 4) were either narrow thorny or broad thorny ganglion cells, 14 cells were displaced amacrine cells.

198 and HA immunoreactivity (FMRFamide: 4 optic ganglion cells, 4-5 hair cells; HA: 3 optic ganglion cel

199 ganglion cells, 4-5 hair cells; HA: 3 optic ganglion cells, 8 hair cells).

200 ositive cells in the ganglion cell layer are ganglion cells, and 20% are displaced amacrine cells.

201 urons, dorsal root ganglion neurons, retinal ganglion cells, and callosal projection neurons during a

202 Cell targets were ganglion cells, bipolar cells, Muller cells, and photore

203 receptors, bipolar cells, amacrine cells and ganglion cells, but have not been conclusively identifie

204 receptors, bipolar cells, amacrine cells and ganglion cells, but they have not been identified in hor

205 ther important cell classes, such as retinal ganglion cells, have proven much more challenging to ima

206 While we focused our efforts on the retinal ganglion cells, our transcriptomes of developing chick c

207 Unlike DENAQ, DAD acts upstream of retinal ganglion cells, primarily conferring light sensitivity t

208 of ephrin-A3 (Efna3) in a subset of retinal ganglion cells, quantitatively altering the retinal EFNA

209 difference is reflected in the responses of ganglion cells, the output cells of the retina.

210 particularly preserving survival of retinal ganglion cells.

211 through retinal photoreceptor, bipolar, and ganglion cells.

212 imally shaped the responses of foveal midget ganglion cells.

213 with a large soma were identified as parasol ganglion cells.

214 sensitivity of foveal and peripheral midget ganglion cells.

215 tely after axonal injury in purified retinal ganglion cells.

216 odulate the excitatory signal of bipolar and ganglion cells.

217 , along with close to half of the vestibular ganglion cells.

218 s from the output neurons of the retina, the ganglion cells.

219 nverging inputs from similarly tuned retinal ganglion cells.

220 nts, we estimated a total of 353,000 retinal ganglion cells.

221 The vertebrate ciliary ganglion (CG) is a relay station in the parasympathetic

222 The mouse geniculate ganglion contains chemosensory neurons innervating lingu

223 the labeled DPANs in dissociated trigeminal ganglion cultures using calcium microfluorometry, and we

224 Neurons of the cochleovestibular ganglion (CVG) transmit hearing and balance information

225 raphic organization and magnitude of retinal ganglion density reflect the specific ecological needs t

226 of the solitary tract, the target of nodose ganglion-derived visceral afferents.

227 omatosensory neurons (58%) in the geniculate ganglion did not.

228 nd CXCR4 were upregulated in the dorsal root ganglion (DRG) after chronic compression of DRG (CCD), a

229 f 100 mpk PO due to insufficient dorsal root ganglion (DRG) exposure attributed to poor membrane perm

230 fficking plays a central role in dorsal root ganglion (DRG) neuronal cell survival and neurotransmiss

231 ating Kv3.4 potassium current in dorsal root ganglion (DRG) neurons contributes to the hyperexcitabil

232 vity of TRPM3 expressed in mouse dorsal root ganglion (DRG) neurons is inhibited by agonists of the G

233 cal characterization of isolated dorsal root ganglion (DRG) neurons revealed that RPRFamide increases

234 tors are a particular subtype of dorsal root ganglion (DRG) neurons that detect noxious stimuli and e

235 changes in gene transcription in dorsal root ganglion (DRG) neurons, which may contribute to nerve in

236 ed by PregS and CIM0216 in mouse dorsal root ganglion (DRG) neurons.

237 and 5-hydroxylmethylcytosine in dorsal root ganglion (DRG) neurons.

238 lia BV-2 cells exposed to G-CSF, dorsal root ganglion (DRG) nociceptors become hyperexcitable.

239 normal neural tissues including dorsal root ganglion (DRG) produce PD-L1 that can potently inhibit a

240 collateral branch development of dorsal root ganglion (DRG) sensory neurons.

241 ptidergic nociceptors within the dorsal root ganglion (DRG), and knockdown of Kv4.3 selectively induc

242 model, local inflammation of the dorsal root ganglion (DRG), we observed marked increases in mechanic

243 or (pain-sensing) neurons of the dorsal root ganglion (DRG), where they transmit the large outward co

244 ed in the nociceptive neurons of dorsal root ganglion (DRG).

245 By imaging Aplysia's pedal ganglion during fictive locomotion, here we show that it

246 f chemosensory neurons within the geniculate ganglion (GG).

247 rojecting to the labrum, brain, and thoracic ganglion have received less attention.

248 1 promoter, isolated from murine dorsal root ganglion (hypermethylated) and striated cells (hypomethy

249 indicate that the innervation of the ciliary ganglion is more complex than previously thought, and th

250 o co-culture neural stem cell-derived spiral ganglion-like neurons (ScNs) and mouse auditory cochlear

251 Left stellate ganglion (LSG) hyperactivity promotes ischemia induced v

252 godendrocytes was validated in a dorsal root ganglion microfluidics chamber platform.

253 oring cortex glia, and between NBs and their ganglion mother cell daughters.

254 Most brain neuroblasts generate a series of ganglion mother cells (GMCs) that each make two neurons

255 Type II spiral ganglion neurons (SGNs) are small caliber, unmyelinated

256 The mammalian spiral ganglion neurons (SGNs) are specialzed bipolar neurons i

257 jury can also lead to degeneration of spiral ganglion neurons (SGNs), but this occurs over a period o

258 and was lacking from the postsynaptic spiral ganglion neurons (SGNs).

259 connectivity between TRCs and their partner ganglion neurons (that is, ensuring that a labelled line

260 ral transduction of inner hair cells, spiral ganglion neurons and vestibular hair cells.

261 ner hair cells, auditory synapses and spiral ganglion neurons are all present after noise exposure in

262 ression could not be detected in dorsal root ganglion neurons by single-cell RT-PCR.

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

264 avior and activation of cultured dorsal root ganglion neurons from mice.

265 s readily detected in a subset of trigeminal ganglion neurons in latently infected calves but not in

266 eletion-induced axon regeneration of retinal ganglion neurons in the adult CNS is attenuated upon Tet

267 Here, we show that sensory and ganglion neurons in the ectodermal epithelium of the mod

268 etic depolarization of GABAergic dorsal root ganglion neurons in vivo reduced acute and chronic perip

269 avior and activation of cultured dorsal root ganglion neurons was dependent on Mrgprs rather than NK-

270 g of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and enteric neurons

271 +) channel robustly expressed in dorsal root ganglion neurons, becomes dysfunctional upon calcineurin

272 rs ago to depend on innervation from distant ganglion neurons, but the underlying mechanism has remai

273 In transfected small rat dorsal root ganglion neurons, expression of L1302F and L811P evoked

274 ASIC currents in both groups of dorsal root ganglion neurons, independent of mu opioid receptor stim

275 When expressed in dorsal root ganglion neurons, mutant p.Arg222His channels increase e

276 nd Ca(2+) imaging experiments on dorsal root ganglion neurons, NGF- and IL-6-induced increases in exc

277 ommissural neurons, motoneurons, dorsal root ganglion neurons, retinal ganglion cells, and callosal p

278 male and female embryonic mouse dorsal root ganglion neurons, we show that MAP4K4, MINK1, and TNIK a

279 neuro-2A cells and primary superior cervical ganglion neurons, where APP is highly expressed, the lac

280 t of endogenous deltaR in primary trigeminal ganglion neurons.

281 sing single-unit recording in the trigeminal ganglion of anesthetized male rats.

282 wing inflammatory exposures in a dorsal root ganglion organotypic coculture system.

283 across cultures than in primary dorsal root ganglion, particularly for genes related to nervous syst

284 We conclude that 661W is a retinal ganglion precursor-like cell line, which shows propertie

285 Some neurons in the geniculate ganglion project to taste regions in the oral cavity, wh

286 intracellular calcium levels in dorsal root ganglion pruriceptors, and (iii) injection of intraderma

287 mately 71%) expressed in Nppb(+) dorsal root ganglion pruriceptors.

288 glion (TG) and sympathetic superior cervical ganglion (SCG) neurons expressed adrenergic receptors (a

289 e-associated protein 7 (MAP7) in dorsal root ganglion sensory neurons.

290 ccur anywhere along the peripheral autonomic ganglion sites.

291 properties in the crustacean stomatogastric ganglion (STG) of Cancer borealis.

292 s of four neuron types in the stomatogastric ganglion (STG) of the crab Cancer borealis.

293 ctions of the dorsal lobe and in the gnathal ganglion suggest that tyramine receptors are involved in

294 mmune cell infiltration into the dorsal root ganglion, suggesting that adaptive immune responses in n

295 Both sensory trigeminal ganglion (TG) and sympathetic superior cervical ganglion

296 frequently expressed in the same trigeminal ganglion (TG) neuron during reactivation and cooperative

297 ability to genetically manipulate trigeminal ganglion (TG) neurons would be useful in the study of th

298 from the application site to the trigeminal ganglion, the numbers of stained DPANs, and the fluoresc

299 nal activity was recorded from a ventricular ganglion using a microelectrode array, and cardiac elect

300 ional reconstruction of an entire trigeminal ganglion with 2-photon laser scanning fluorescence micro