ライフサイエンスコーパス: somata

1 nhibitory-like synapses on auditory efferent somata.

2 in AVP-labeled somata but not in OC-labeled somata.

3 localization and trafficking within neuronal somata.

4 e terminals at great distances from cellular somata.

5 ciceptive marker, pERK, in pancreas afferent somata.

6 onal plexi around a subpopulation of sensory somata.

7 the delayed PKA activation in sensory neuron somata.

8 synaptic terminals on HMNs, but not in their somata.

9 uished from other ipRGCs by their very large somata.

10 sed to motor neuron dendrites rather than to somata.

11 slow components in small, medium, and large somata.

12 naptic profiles around MNTB principal neuron somata.

13 s targeted and enclosed Kv3.3-immunoreactive somata.

14 he human neuronal transcriptome inclusive of somata.

15 utamate and then examined levels of pCREB in somata.

16 higher than the stiffnesses of dendrites and somata.

17 ot found in vestibular afferent dendrites or somata.

18 nd pCaMKII in neurofilament 200-positive DRG somata.

19 ting in a more uniform distribution over the somata.

20 cits robust vesicular ATP release from their somata.

21 ncreased F-actin concentration in astrocytic somata.

22 n part because male XIIts neurons had larger somata.

23 contacted nearly five times more often than somata.

24 , followed by axon terminals, dendrites, and somata.

25 tal; and perpendicular bipolar or multipolar somata.

26 he first two types were the most frequent on somata.

27 is in presynaptic interneuron axons, but not somata.

28 issociated dorsal root ganglion (DRG) neuron somata.

29 liable synaptic inhibition at principal cell somata.

30 er and of higher amplitude than those in the somata.

31 cell membrane of RON astrocyte processes and somata.

32 ate hippocampal neuron axons, dendrites, and somata.

33 h most occurring in processes rather than in somata.

34 rates, and amplitudes in fine processes and somata.

35 peptide-positive terminals, some innervating somata.

36 increases in astrocyte processes but not in somata.

37 buted both postsynaptically in dendrites and somata (51% of GluR5,6,7 immunoreactive (-ir) profiles)

38 sing immunofluorescence labeling of neuronal somata, a single astrocyte enwraps on average four neuro

39 greater frequency in regions where pericyte somata adjoined the endothelium.

40 ult mice (1) differ from those in astrocytic somata and (2) are modulated by glutamate and ATP.

41 (1) the granule cell layer that contains all somata and (2) the molecular layer that contains the den

42 Approximately 36% of the M2R-labeled somata and 16% of the more numerous M2R-labeled dendrite

43 Punctate expression was found in somata and along the dendritic shaft, but FLNa was not d

44 and inhibit dopamine release, especially at somata and along varicose neurites that emerge from thes

45 same time, synapses disappear from Purkinje somata and appear in great numbers on the dendrites.

46 ong varicose neurites that emerge from these somata and arborize in various levels of the retina.

47 entire juvenile ganglion, which included the somata and arbors of all the neurons.

48 o control mesopontine cholinergic neurons at somata and at divergent projections within distinct midb

49 immunoreactive vesicles also were present in somata and axon terminals with or without CRFr labeling.

50 lation of synaptic efficacy are concurrently somata and axon terminals, with the direction of cortica

51 itecture, e.g., the spatial distributions of somata and axonal projection patterns, probably the resu

52 gous to the ability of degenerating neuronal somata and axons to bind silver ions (argyrophilia - the

53 The action potentials generated in the somata and axons, including axon collaterals, of somatos

54 rnae that shadow retinal ganglion cell (RGC) somata and axons, protoplasmic astrocytes, vascular endo

55 formed earlier, beginning at 10 dpi, on the somata and basal dendrites of new cells in the granule c

56 OR immunoreactivity within TH-immunoreactive somata and dendrites in the LC as well as localized to p

57 s of EAAC1 protein are widely distributed in somata and dendrites of all hippocampal neurons.

58 all four AMPAR subunits were detected in the somata and dendrites of CA3 and CA1 pyramidal cells and

59 iscrete subset of inhibitory synapses on the somata and dendrites of cerebellar Purkinje cells.

60 elationship of NA axon varicosities with the somata and dendrites of identified gastric preautonomic

61 f nitrergic interneurons already apposed the somata and dendrites of SMI-32 labeled neurons even at t

62 p recordings from layer V pyramidal neuronal somata and dendrites of the adult rat lateral EC to inve

63 cular cues, structurally permissive neuronal somata and dendrites remain unmyelinated.

64 revealed NOX2 immunolabeling in postsynaptic somata and dendrites that also expressed the NMDA recept

65 enhanced synchronized Ca(2+) oscillations in somata and dendrites that were blocked by ryanodine.

66 MOC somata and dendrites were innervated by three different

67 microscopy, pDOR-ir primarily was located in somata and dendrites, associated with endomembranes, or

68 and Ric-3 and alpha7 subunits were found in somata and dendrites, but not axons, of inhibitory inter

69 SCN neurons mainly expressed VPAC2R in their somata and dendrites, not axons.

70 beta-ir was most frequently in TH-containing somata and dendrites, particularly on endoplasmic reticu

71 ately one-third of the labeled profiles were somata and dendrites, some of which showed overlapping s

72 us firing generates tonic Ca signals in both somata and dendrites, which drop during 500 ms, 100 Hz t

73 trocytic processes that intercalate neuronal somata and dendrites.

74 a robust fluorescent signal was detected in somata and dendrites.

75 odulate LC activity by their localization to somata and dendrites.

76 d in dendritic processes showed that, of the somata and dendritic processes exhibiting GPR177, 32% co

77 synaptic vesicles in excitatory synapses on somata and dendritic processes of multipolar GABAergic i

78 Somata and dendritic processes that contained both GPR17

79 t evidence that IL-17 can act on sympathetic somata and distal neurites to enhance neurite outgrowth,

80 oreactivity did not entirely cover astrocyte somata and exhibited clusters at processes.

81 ells in primates, are characterized by large somata and extensive basilar dendrites.

82 Dscam, exhibiting an aberrant clustering of somata and fasciculation of dendrites.

83 Furthermore, alpha-MSH and AgRP-ir somata and fibers are pronounced at 5 days post fertiliz

84 it of 2 microm for the diameters of neuronal somata and found average volumes of 6.5 mum(3) for lamin

85 triggers the communication between neuronal somata and glial cells.

86 l distribution of GPR177 and MOR in striatal somata and in dendritic processes showed that, of the so

87 n neurons increases Ca(V) channel density in somata and in presynaptic terminals.

88 ile gephyrin puncta are enriched on neuronal somata and in the medial neuropil.

89 Stage I neurons had small somata and lacked dendrites.

90 o form heterotypic GJs with oligodendrocytic somata and lamellae.

91 smic tubulovesicular endomembrane systems in somata and large dendrites, but was more often located a

92 rally, in lamina V and had relatively larger somata and more extensive dendritic trees.

93 d with age in rTg4510 brain, particularly in somata and neurites containing Alz50-positive tau aggreg

94 sed in the hippocampal dentate gyrus neurons somata and neuropil and hippocampus proper (CA3, CA1) of

95 shment and maintenance in adulthood of small somata and neuropil staining within regions of rostral t

96 etected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients

97 ylcholine receptors (nAChRs) located at both somata and presynaptic elements.

98 are distributed predominantly at motoneuron somata and primary dendrites.

99 ctive axonal extension and misorientation of somata and processes of inhibitory neurons in the dentat

100 ent spontaneous calcium signals in astrocyte somata and processes that conventional GCaMP2 failed to

101 immunostaining pattern, and labeling of cell somata and processes was observed only occasionally.

102 taining was also observed in horizontal cell somata and processes.

103 functional SK channels are expressed in the somata and proximal dendrites of adult rat CA1 pyramidal

104 Kv2.1 subunits were clustered and located on somata and proximal dendrites of all pyramidal cells.

105 abundant number of GABAergic synapses on the somata and proximal dendrites of CA1 pyramidal cells of

106 Kv2.1 and Kv2.2(long) are colocalized in the somata and proximal dendrites of cortical pyramidal neur

107 e the perineuronal nets (PNs) which surround somata and proximal dendrites of distinct neuron types.

108 Occasional synapses on GABAergic somata and proximal dendrites were also observed in the

109 gnificantly fewer synaptic contacts on their somata and proximal dendrites, and those contacts were s

110 whose axon terminals surround principal cell somata and proximal dendrites, have a privileged and inf

111 t cells innervate hundreds of pyramidal cell somata and proximal dendrites.

112 ber and function of synapses on motor neuron somata and proximal dendrites.

113 in-expressing basket interneurons innervated somata and proximal pyramidal cell dendrites, whereas ni

114 tive (-IR) horizontal cells had small, round somata and robust, bulbous dendritic endings, whereas ca

115 The NPY-GFP+ neurons displayed small somata and short dendrites embedded in a cloud of highly

116 Stage II neurons had larger somata and short dendrites.

117 tently activates MAPK in both sensory neuron somata and synaptic neuropil.

118 luR4, NR1, PSD-95, and PSD-93), that TH cell somata and tapering neurites are also immunopositive for

119 nt Ca(2+) signalling is well established for somata and terminals of mammalian spinal motor neurons,

120 govern the spatial arrangement of astrocyte somata and territory overlap in ferret visual cortex usi

121 onstrate the exchange of TDP-43 between cell somata and the presence of TDP-43 oligomers in microvesi

122 In the central bee brain, the IC somata and their dendritic region, we observed an age-de

123 he presence of functional SK channels in the somata and their role in controlling the intrinsic firin

124 dly, single-caged IP3 led to less release in somata and was ineffective in dendrites and spines.

125 bunit mRNAs were virtually restricted to the somata and were absent from the dendrites of granule cel

126 ed dPNs had diameters larger than 70% of CoG somata and were restricted to the most medial and anteri

127 ls are among the simplest neurons, with tiny somata and, on average, just four dendrites.

128 PNMT-ir) axons were detected among orexin-ir somata, and close appositions between PNMT-ir axonal var

129 both primary afferent terminals and isolated somata, and markedly attenuated mechanical behavioral hy

130 ession also varied in the neuropil, neuronal somata, and/or cellular processes in the subregions.

131 ng from the main dendrite or new growth from somata, appear at a high frequency in some aging neurons

132 rminals, as the ultrastructure of motoneuron somata appeared to be normal at the stages when synaptic

133 of projection and local interneurons, whose somata are in the lateral soma cluster (LC) and medial s

134 o be confined within the area in which their somata are located.

135 vious studies showing that motor neuron cell somata are markedly more vulnerable to axotomy in neonat

136 Ipsilateral pRS neuron somata are on average larger than contralateral.

137 The compartments for axon and somata are separated by a physical partition that has a

138 ng a wide amplitude range, and display large somata as well as membrane protrusions.

139 shape; they are infrequent and found on the somata as well as the dendrites.

140 Retrograde tracing revealed that somata associated with different axonal projection pathw

141 The lack of PDF-like-immunoreactive somata associated with the onychophoran optic ganglion c

142 i with increased size of neuronal nuclei and somata, ataxia, and premature death.

143 two-photon calcium imaging of CA1 place cell somata, axons and dendrites in mice navigating a virtual

144 found no change in the number of Muller cell somata between mice strains, indicating no cell prolifer

145 esV nucleus is restricted to mostly pairs of somata between which electrical transmission is supporte

146 ncreased nuclear NK3R density in AVP-labeled somata but not in OC-labeled somata.

147 ression of P2X4 receptors on AgRP-NPY neuron somata, but instead, we found clear evidence for functio

148 ansmembrane potentials in CA3 pyramidal cell somata by 0.18 mV per V m(-1) applied.

149 We visualize PV- and mAChR-immunoreactive somata by dual-immunofluorescence confocal microscopy an

150 within a small group of neurons having their somata clustered.

151 in small proliferation zones within neuronal somata clusters in the olfactory deutocerebrum of adult

152 rmore, neuroprotection of corticospinal cell somata coincided with increased axonal sprouting in the

153 Pericyte somata covered only 7% of the total capillary length in

154 reased capillary diameter by 21% at pericyte somata, decreased capillary block by 25% and increased p

155 vity is associated with the membranes of the somata, dendrites and axons of cholinergic neurons in th

156 in the vestibular nuclei and was detected in somata, dendrites and synaptic terminals.

157 ll populations where it could be detected in somata, dendrites and synaptic terminals.

158 ntracellular Ca2+ concentration ([Ca2+]i) in somata, dendrites, and putative axons of GABAergic neuro

159 ggers focal calcium release in Purkinje cell somata, dendrites, and spines as measured by two-photon

160 activity are evident in the membranes of the somata, dendrites, and spines of pyramidal cells and GAB

161 in-expressing basket interneurons, targeting somata, dendrites, and spines of pyramidal cells, have b

162 re it concentrates in the plasma membrane of somata, dendrites, and spines.

163 es make synaptic contacts with GABAergic PGN somata, dendrites, and spines.

164 inals were symmetrical and contacted spines, somata, dendritic shafts, and occasionally other axonal

165 atergic flocculus target neurons (FTNs) with somata densely surrounded by Purkinje cell terminals pro

166 The proximity of pericyte somata did not predict capillary dilation amplitude.

167 n many parts of the nervous system, neuronal somata display orderly spatial arrangements.

168 -2 and -13a were increasingly present in RGC somata during axonal regrowth.

169 tracellular recordings from rat DRG neuronal somata during stimulation of the dorsal root, we determi

170 n imaging dendrites while recording neuronal somata electrophysiologically.

171 t Nav1.7 was upregulated in small DRG neuron somata, especially those also expressing calcitonin gene

172 These cells had somata exclusively in the INL and monostratified dendrit

173 of age on the survival of motor neuron cell somata following axotomy is well documented, but it rema

174 measured changes in calcium at dendrites and somata, following local perfusion of glutamate.

175 the observation of Brodmann, who found large somata for these neurons in carnivores in general, and f

176 The mean Scholl distance of ACBs from CS somata (for both types 1 and 2 cells) was 66 mum-coincid

177 neurons in microfluidic devices to separate somata from axonal projections in fluidically isolated m

178 endrites and pyramidal-like principal neuron somata from naive rats.

179 in the ventral portion of the ventrolateral somata group and projections along the inner antennocere

180 contrary to the conventional view, neuronal somata have a significant role in cell-cell signaling.

181 lpha4* nAChRs were not found on the neuronal somata; however, nicotine acts via alpha4beta2* nAChRs i

182 of spontaneous Ca(2+) spikes in granule cell somata in a dose-dependent manner.

183 HT1B receptor-containing neuronal puncta and somata in areas of the brain altered by AAS, namely, the

184 strongly label RGC and displaced RGC (dRGC) somata in mouse, rat, guinea pig, rabbit, and monkey ret

185 tion in terminals surrounding pyramidal cell somata in normotopic and heterotopic tish neocortex.

186 In particular, interneurons with somata in strata radiatum (R) and lacunosum-moleculare (

187 ingly, we studied urethral afferent neuronal somata in streptozotocin-induced DM or age-matched vehic

188 o the cerebellar cortex retrogradely labeled somata in the cerebellar nuclei and boutons in the ventr

189 l thalamus, we observed retrogradely labeled somata in the cerebellar nuclei and mossy fiber terminal

190 ral ganglia (CoGs) as well as immunopositive somata in the CoGs and the oesophageal ganglion.

191 ore visible atrophy of their parent neuronal somata in the cuneate nucleus or thalamus.

192 uropil in the commissural ganglia (CoGs), in somata in the esophageal ganglion (OG), in fibers in the

193 Confocal imaging showed that individual somata in the ganglion cell layer bound antibodies again

194 r plexiform layer, in amacrine cells, and in somata in the ganglion cell layer.

195 e outer plexiform layer, amacrine cells, and somata in the ganglion cell layer.

196 NO, soluble guanylate cyclase (sGC), was in somata in the inner and outer nuclear layers and in both

197 maged with diaminofluorescein was present in somata in the inner nuclear layer and in synaptic bouton

198 the cerebellar nuclei, retrogradely labeled somata in the interposed nucleus, and putative collatera

199 1, 3, and 7 DPL, the number of NPY-positive somata in the lesioned cortex was increased significantl

200 es revealed four immunopositive neurons with somata in the pars intercerebralis and arborizations ext

201 er insects, pairs of descending neurons with somata in the pars intercerebralis and ramifications in

202 ncreased in the endoplasmic reticulum of DRG somata, in intracellular vesicular structures within the

203 ss, the movement of trigeminal and facial BM somata is stalled, and their peripheral axons are fewer

204 VGAT varicosities were seen apposed to small somata labeled for glutamate consistent with being presy

205 tes and dendritic spines as well as in a few somata, large dendrites, axons, and axon terminals or mo

206 In somata, M2R immunogold particles were often associated w

207 l slices from epileptic mice also had larger somata, more axon in the molecular layer, and longer den

208 ntral body and a single pair of neurons with somata near the esophageal foramen that gave rise to arb

209 Pathologic forms of tau in neuronal somata, neuropil threads, and plaque-like clusters of ne

210 mber of XIIts neurons and the proportions of somata/neuropil were not sexually dimorphic, the volumes

211 least four prominent SIFamide-immunoreactive somata occur in the pars intercerebralis.

212 ment of gene transcription regulation in the somata of both synaptic partners.

213 its localization and trafficking within the somata of cortical neurons.

214 holography to shape illumination over single somata of cultured neurons.

215 onally, synapses were found on dendrites and somata of deep Layer II principal neurons and Layer III

216 iatal spiny projection neurons than onto the somata of dopaminergic neurons in the SNpc or dorsal str

217 sphorylation was higher in processes than in somata of dopaminergic neurons.

218 to three and one-half times greater onto the somata of dorsal striatal spiny projection neurons than

219 This study provides strong evidence that somata of DRG neurons actively release transmitters and

220 Although the somata of GABAergic neurons showed little orientation tu

221 of efferent neurons originate from neuronal somata of globuli cells covering the hemiellipsoid bodie

222 ing 'Ca(2+) activity in single dendrites and somata of L5 neurons', the final sentence of the second

223 chitecture and the positions of all neuronal somata of multiple cubic millimeter regions of vibrissa

224 siological recordings were obtained from the somata of neurons of the compressed ganglion both in vit

225 currents (ISA s) have been recorded from the somata of nociceptors and spinal lamina II excitatory in

226 positive MSN terminals and the dendrites and somata of other MSNs.

227 lic trigeminal (MesV) nucleus, formed by the somata of primary afferents originating in jaw-closing m

228 n, which shifts from the apical dendrites to somata of pyramidal cells during bursts of sensory input

229 re also found at lower concentrations in the somata of pyramidal neurons as well as other neuron subt

230 and channel density are indeed higher in the somata of rat SNc DA neurons and that this current under

231 s found for the presence of P2XR channels in somata of SCN neurons as P2X2R immunoreactivity colocali

232 The somata of sensory neurons in the distal organ are organi

233 Anatomically, the somata of somatostatin immobility-activated neurons were

234 gn+ interneurons preferentially targeted the somata of SPNs of the so-called 'direct pathway', wherea

235 y prepro-beta-pdh I mRNA was detected in the somata of the lamina ganglionaris (LG) and in the brain.

236 n preoptic nucleus (MEPO), where most of the somata of the neuroendocrine neurons releasing GnRH and

237 aled SCI-induced SA generated in or near the somata of the neurons in vivo.

238 The somata of the pallidal neurons retrogradely labeled from

239 t labeling was in structures surrounding the somata of the principal neurons, suggesting specific loc

240 All NK3-labeled somata of the PVN in control rats showed cytoplasmic but

241 enhanced formation of these clusters on the somata of these neurons.

242 nsistent with previous studies, we found the somata of this L4B subpopulation to reside predominantly

243 With the exception of humans, the somata of type I spiral ganglion neurons (SGNs) of most

244 We found that dendrites, more so than somata, of hippocampal neurons were hyperexcitable in mi

245 long-term potentiation in dendrites, but not somata, of hippocampal neurons.

246 depolarization from regions either close to somata or abundant in dendritic projections.

247 ABAergic boutons were in close apposition to somata or dendrites immunopositive for interneuron cell-

248 ls formed synapses with CaMK+ pyramidal cell somata or large-caliber (proximal) dendrites.

249 No regional differences were found in GAD+ somata, or in norepinephrine transporter or serotonin tr

250 Somata positions are not constant but show preferred loc

251 erved with direct optogenetic control of BLA somata, possibly owing to recruitment of antagonistic do

252 for detecting calcium transients in neuronal somata, processes, and synapses that are triggered by ne

253 ted by interneurons targeting pyramidal cell somata, providing a synaptic substrate for tuning pyrami

254 tion of JHC 1-64-labeled NET in the neuronal somata, proximal extensions and presynaptic boutons.

255 her levels of L-type calcium channels are in somata/proximal dendrites (i.e., 0-26 mum) and distal de

256 Finally, the immunopositive somata ranged in diameter from the smallest to the large

257 on, we show such displacement of cholinergic somata relative to their dendritic stalks and a decline

258 Recording from pyramidal cell somata revealed a similar range of channel conductances,

259 Confocal image analysis of the somata revealed that the normally continuous cortical ba

260 NPY, AGRP, CART, and pomc1a somata showed distribution patterns similar to other tel

261 reparation of small rat dorsal root ganglion somata showing a reduction in the magnitude of tetrodoto

262 Somata sit on the dorsal and lateral surface of the STG

263 ate mainly from excitatory pyramidal neurons somata situated in laminae III and V, the excitatory neu

264 e of both increasing and decreasing neuronal somata size, without adversely affecting survival.

265 outons contacting HSD2-labeled dendrites and somata, suggesting that direct input from the vagus may

266 al injection labeled bilaterally Hcrt-1/Ox-A somata, suggesting that NPS could recruit two distinct n

267 he plasma membrane of ISA -expressing neuron somata supports the existence of Kv4/KChIP/DPPL ternary

268 species were found to consist of around 700 somata, surrounding a central neuropil with 3-5 ventral

269 We report here that TH cell somata, tapering and varicose inner plexiform layer neur

270 ial internal cell layer, had variable-shaped somata that ranged in size from 4-18 microm in diameter

271 most species examined to date or on TH cell somata that release dopamine when exposed to glutamate r

272 and these terminals contacted dendrites and somata that were significantly larger (1.90 +/- 0.30 mum

273 y in other ganglion cells, mostly with large somata, that may constitute one or more additional types

274 number of afferent terminals on motor neuron somata, the amplitude of afferent-evoked synaptic potent

275 rapid movement of PSD-95 from visual neuron somata to synapses.

276 the mean distance of the center of neuronal somata to the closest microvessel was 15 mum.

277 mbrane of Schwann cells adjacent to neuronal somata versus axonal processes.

278 residual tracer coupling of horizontal cell somata was observed.

279 l, presumably inhibitory, synaptic inputs on somata was significantly higher on spiny projection neur

280 individual vesicles transported to neuronal somata, we calculate the projection sites of each neuron

281 Labeled somata were also observed within the IC itself.

282 Horizontal cells formed, and their somata were appropriately aligned, but their neurites di

283 Somata were contacted by cholinergic, adrenergic, nitrer

284 s (group 1), smaller SIFamide-immunoreactive somata were detected in the pars intercerebralis (group

285 rs but no peripheral immunoreactive neuronal somata were detected.

286 t whether alpha3-immunoreactive DRG neuronal somata were exclusively MSAs.

287 As in other mammals, VP-immunoreactive (-ir) somata were found in the paraventricular (PVN) and supra

288 GFRalpha2-immunopositive somata were hypertrophied in NRTN-OE mice.

289 Neuronal somata were mainly located in a ganglionated plexus arou

290 FJB-positive somata were most abundant in the infarct core at 1 DPL,

291 In the superior olivary complex, 5-HT-IR somata were observed in the LSO, another relay to the IC

292 At P10, Muller cell somata were observed in the middle of the INL.

293 The short 3' UTR mRNAs are restricted to somata, whereas the long 3' UTR mRNAs are also localized

294 f matrix metalloproteinase (MMP) at pericyte somata, which was visualized at high resolution in vivo

295 e astrocyte enwraps on average four neuronal somata with an upper limit of eight.

296 We found that neuronal somata with high alpha3 immunointensity were neurofilame

297 require gap junctional coupling of IO neuron somata within 40 microm of one another.

298 e ability of MD to reduce the size of neuron somata within deprived layers of the cat dorsal lateral

299 ccumulation of synaptic vesicles in neuronal somata without altering the distribution of other organe

300 A depolarized the majority of sensory neuron somata, yet produced a net inhibitory effect on the noci