ライフサイエンスコーパス: somata

1 h most occurring in processes rather than in somata.

2 rates, and amplitudes in fine processes and somata.

3 peptide-positive terminals, some innervating somata.

4 increases in astrocyte processes but not in somata.

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

6 localization and trafficking within neuronal somata.

7 e terminals at great distances from cellular somata.

8 ciceptive marker, pERK, in pancreas afferent somata.

9 onal plexi around a subpopulation of sensory somata.

10 orward inhibition in the neighborhood of GoC somata.

11 the delayed PKA activation in sensory neuron somata.

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

13 uished from other ipRGCs by their very large somata.

14 ons that were seen in close proximity to the somata.

15 sed to motor neuron dendrites rather than to somata.

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

17 tensive degeneration of dendrites but not PC somata.

18 naptic profiles around MNTB principal neuron somata.

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

20 utamate and then examined levels of pCREB in somata.

21 ot found in vestibular afferent dendrites or somata.

22 nd pCaMKII in neurofilament 200-positive DRG somata.

23 ting in a more uniform distribution over the somata.

24 cits robust vesicular ATP release from their somata.

25 ncreased F-actin concentration in astrocytic somata.

26 n part because male XIIts neurons had larger somata.

27 al membrane structures in axons and neuronal somata.

28 nhibitory-like synapses on auditory efferent somata.

29 , and giant types based on the size of their somata.

30 he human neuronal transcriptome inclusive of somata.

31 higher than the stiffnesses of dendrites and somata.

32 is in presynaptic interneuron axons, but not somata.

33 issociated dorsal root ganglion (DRG) neuron somata.

34 liable synaptic inhibition at principal cell somata.

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

36 cell membrane of RON astrocyte processes and somata.

37 ate hippocampal neuron axons, dendrites, and somata.

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

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

40 Inactivating POm somata abolished persistent but not initial depolarizati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 ncluding somatic spiking, calcium signals at somata and axons, and striatal dopamine concentrations.

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

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

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

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

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

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

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

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

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

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

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

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

71 trocytic processes that intercalate neuronal somata and dendrites.

72 rotransmitters or neuromodulators from their somata and dendrites.

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

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

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

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

77 Somata and dendritic processes that contained both GPR17

78 Activity in layer 5 pyramidal neuron somata and distal apical trunk dendrites shows surprisin

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 e morphs in the number of galanin-expressing somata and in the distribution of fibers, especially in

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

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 Giant cells had very large irregular somata and long, thick dendrites; their distal dendrites

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 Neurogliaform cells had small somata and numerous short dendrites that formed a dense

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

97 rosslinking by IgG-IC directly activates the somata and peripheral terminals of these neurons to evok

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

99 are distributed predominantly at motoneuron somata and primary dendrites.

100 find that only a small subset of microglial somata and processes exhibited spontaneous calcium trans

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

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

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

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

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

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

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

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

109 immunoreactivity in the BNC was observed in somata and proximal dendrites of nonpyramidal neurons, a

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

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

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

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

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

115 nnervation from the MOC collaterals on their somata and proximal dendrites.

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

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

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

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

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

121 inhibitory plexuses that wrap Purkinje cell somata and terminate as pinceaux at the initial segment

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

123 al-shaped neurons, based on the shape of the somata and the disposition of the dendrites.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 phagocytosing their dendrites while the cell somata are still present.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 n cortex and the relative contributions from somata, dendrites, and axons are often unknown.

160 PV immunoreactivity was found in the labeled somata, dendrites, and axons in all layers and subdivisi

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

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

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

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

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

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

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

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

169 -2 and -13a were increasingly present in RGC somata during axonal regrowth.

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

171 n imaging dendrites while recording neuronal somata electrophysiologically.

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

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

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

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

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

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

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

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

180 All CCK+ somata gave rise to 2-4 dendrites that branched sparingl

181 terminations onto postsynaptic dendrites or somata, giving rise to axo-dendritic and axo-somatic syn

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

183 organization of human DRG neural fibers and somata has not been quantitatively described.

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

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

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

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

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

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

190 pathways that activate and modulate the MOC somata in the brainstem to drive these cochlear effects

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

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

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

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

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

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

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

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

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

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

201 ve (PDF-ir) circadian pacemaker neurons with somata in the lamina (PDFLAs) or somata next to the AME

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

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

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

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

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

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

208 In somata, M2R immunogold particles were often associated w

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

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

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

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

213 eurons with somata in the lamina (PDFLAs) or somata next to the AME (PDFMEs).

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

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

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

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

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

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

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

221 We recorded from rat VGN somata of either sex aged postnatal day (P)9-P21.

222 Although the somata of GABAergic neurons showed little orientation tu

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

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

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

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

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

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

229 Dorsal root ganglia (DRG), which contain the somata of primary sensory neurons, have increasingly bee

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

231 and forming pericellular baskets contacting somata of pyramidal cells.

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

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

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

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

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

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

238 guanylate cyclase (NO-GC), are expressed in somata of T-stellate cells.

239 as observed as perinuclear aggregates in the somata of the frontal cortex of SIV-infected macaques.

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

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

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

243 The somata of the pallidal neurons retrogradely labeled from

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

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

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

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

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

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

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

251 We found that while the density of pial ILA somata only varied slightly, the complexity of ILA proce

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

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

254 Somata positions are not constant but show preferred loc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 nervation and perineural nets around PV cell somata, therefore suggesting that p75NTR expression modu

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

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

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

281 residual tracer coupling of horizontal cell somata was observed.

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

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

284 Labeled somata were also observed within the IC itself.

285 Somata were contacted by cholinergic, adrenergic, nitrer

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

287 rs but no peripheral immunoreactive neuronal somata were detected.

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

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

290 A vast abundance of TH-ir somata were located in the opisthosomal neuromeres, the

291 Neuronal somata were mainly located in a ganglionated plexus arou

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

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

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

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

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

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

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