ライフサイエンスコーパス: nonneuronal

1 These studies identify novel, nonneuronal actions for proNGF and suggest that proNGF r

2 of GLP/G9a leads to derepression of numerous nonneuronal and neuron progenitor genes in adult neurons

3 ified the expression of all the HSV genes in nonneuronal and neuronal cells by RNA-seq analysis.

4 HSV-1) can undergo a productive infection in nonneuronal and neuronal cells such that the genes of th

5 Thus, apoptosis of nonneuronal and neuronal elements accounts for at least

6 uggest what we believe to be a novel form of nonneuronal and neuronal interactions in the mechanisms

7 dization (FISH), which revealed neuronal and nonneuronal aneuploid populations in both the adult mous

8 To determine what cell types, neuronal or nonneuronal, are critical for GABA signaling in palate d

9 ive disorders, the potential contribution of nonneuronal Cdk5-p35 activity has not been explored in t

10 extracellular particles are not involved in nonneuronal cell infections.

11 following incubation with a scrapie-infected nonneuronal cell line or a scrapie brain homogenate.

12 Here, we tested 4 additional human-derived nonneuronal cell lines (cancerous or immortalized) and f

13 ilaments and vimentin filaments expressed in nonneuronal cell lines can lengthen by joining ends in a

14 iCl reduced poly(Q) toxicity in neuronal and nonneuronal cell lines, but this was not associated with

15 neuronal cell lines, was not found in these nonneuronal cell lines.

16 se MEKK did not activate the TPH promoter in nonneuronal cell lines.

17 Some nonneuronal cell nuclei were very strongly immunoreactiv

18 n maximize the contrast between neuronal and nonneuronal cell phenotypes.

19 evious studies suggested a baseline level of nonneuronal cell proliferation in the spinal cord and rh

20 functions as a neuron-specific enhancer and nonneuronal cell repressor.

21 VC is fully grown or regressed, neuronal and nonneuronal cell turnover is regulated by a common mecha

22 E) to regenerate fully both neurosensory and nonneuronal cell types after severe epithelial injury de

23 ters of cells representing both neuronal and nonneuronal cell types and characterized the driving reg

24 The migration of other neuronal and nonneuronal cell types is unaffected in tri mutants.

25 The contributions of diverse nonneuronal cell types to outcome after acute injury, or

26 found that the nuclear architecture in most nonneuronal cell types undergoes progressive and stochas

27 he proprioceptive system, as well as diverse nonneuronal cell types, such as Merkel cells and intesti

28 maged mitochondria induces mitophagy in many nonneuronal cell types.

29 distinct regions, and specific neuronal and nonneuronal cell types.

30 presses neuronal-specific gene expression in nonneuronal cell types.

31 migration and cell spreading of neuronal and nonneuronal cell types.

32 ifications in different types of neuronal or nonneuronal cell types.

33 hen neuroligins or LRRTMs are expressed in a nonneuronal cell, cocultured neurons avidly form heterol

34 (neuronal type) and those undermethylated in nonneuronal cells (glial type), combined with findings o

35 wild-type (wt) virus and IE gene mutants in nonneuronal cells (MRC5) and adult murine trigeminal gan

36 These data suggest that nonneuronal cells (RPE and Muller cells) respond to RD v

37 When placed in culture, nonneuronal cells acquired immunoreactivity for HuD, sug

38 Many types of nonneuronal cells affiliated with hair follicles and blo

39 st that the capacity of RV strains to infect nonneuronal cells and differentially modulate host gene

40 e-mitotic nucleus-centrosome interactions in nonneuronal cells and for apical nuclear migration in ne

41 t understanding of the regulation of Dyn1 in nonneuronal cells and improved algorithms for highly sen

42 ein functions differently in neuronal versus nonneuronal cells and induces lamellipodial protrusions

43 autophagy limits HSV-1 productive growth in nonneuronal cells and is repressed by the Us3 gene produ

44 1 reproduction in a cell-intrinsic manner in nonneuronal cells and is suppressed by multiple, indepen

45 In nonneuronal cells and neural progenitors, REST inhibits

46 establishes productive (lytic) infections in nonneuronal cells and nonproductive (latent) infections

47 cholinergic receptor (alpha7R) expressed by nonneuronal cells and reduce inflammation.

48 tion is a common feature during infection of nonneuronal cells and results in a latency-like state in

49 OBPs are expressed by nonneuronal cells and secreted into the fluid bathing ol

50 minocycline can protect neuronal as well as nonneuronal cells and tissues.

51 In the meantime, new strategies point to nonneuronal cells and to system pathology.

52 ophic factors that regulate proliferation of nonneuronal cells are also involved in neurogenesis.

53 While microtubules in nonneuronal cells are depolymerized by cold, Ca(2+), or

54 I argue that until the roles of nonneuronal cells are more fully understood and consider

55 These ret-expressing nonneuronal cells are strikingly analogous to vertebrate

56 SXE1 protein expression is restricted to nonneuronal cells associated with diverse sensory bristl

57 ptic transmission was reconstituted in these nonneuronal cells by coexpressing glutamate receptors wi

58 or inhibiting macroautophagy in neuronal and nonneuronal cells by modulating mammalian target of rapa

59 Astrocytes do not form myelin, but these nonneuronal cells can promote myelination in ways that a

60 These results demonstrate that nonneuronal cells can transmit signals to distant cells

61 Acute dynein inhibition in nonneuronal cells caused an immediate dispersal of diver

62 e of activity levels, with both neuronal and nonneuronal cells contributing to the balance of excitat

63 Thus, although most nonneuronal cells die rapidly with cytosolic cytochrome

64 s demonstrate that +TIP functions known from nonneuronal cells do not necessarily apply to the regula

65 membrane fission GTPase, can be activated in nonneuronal cells downstream of cancer-relevant signalin

66 of an initial population of new neurons and nonneuronal cells entering HVC.

67 Moreover, we show that nonneuronal cells express dramatically higher levels of

68 However, very few nonneuronal cells expressed GFP.

69 In nonneuronal cells expressing Ca(V)2.1 or Ca(V)2.2 channe

70 Previous work has suggested that in nonneuronal cells filopodia dynamics decrease the rate o

71 de axonal transport and spread from axons to nonneuronal cells for HSV-1pUS9KBDM.

72 rgo neural differentiation in vivo, purified nonneuronal cells from St. 29 quail ganglia were transpl

73 rises because high levels of torsinB protect nonneuronal cells from the consequences of torsinA dysfu

74 Modifying BoNT to bind nonneuronal cells has been attempted to extend therapeut

75 Expression of KalSec14-GFP in nonneuronal cells impaired receptor-mediated endocytosis

76 ibes the variety of cholinergic neuronal and nonneuronal cells in a position to modulate gastrointest

77 1 (CB1) is widely distributed in neurons and nonneuronal cells in brain and peripheral organs includi

78 e model systems highlight the involvement of nonneuronal cells in disease progression and provide new

79 eporter transgenic mice and all neuronal and nonneuronal cells in gC reporter transgenic mice were ne

80 Nearly all nonneuronal cells in ICP0 and ICP27 reporter transgenic

81 The function of these channels in nonneuronal cells in mammals remains to be elucidated, t

82 and is induced in a cell-specific manner in nonneuronal cells in response to a variety of extracellu

83 us (HSV) vectors for transgene expression in nonneuronal cells in the absence of toxic viral-gene act

84 d by the release of inflammatory agents from nonneuronal cells in the area of tissue injury or diseas

85 identified neurons and, to a lesser extent, nonneuronal cells in the brain that were infected during

86 data to determine abundances of neuronal and nonneuronal cells in the brain.

87 At St. 29, neurons and nonneuronal cells in the ciliary ganglion expressed the

88 1) activity is detected in both neuronal and nonneuronal cells in the CNS, and excessive PARP-1 activ

89 TOR-dependent signaling between neuronal and nonneuronal cells in the regulation of myelin and identi

90 own to form such an organized factory in the nonneuronal cells in which its assembly has been best st

91 The number of positive nonneuronal cells increased at 11 and 23 dpi and remaine

92 re we report that beta-neurexin expressed in nonneuronal cells induced postsynaptic density (PSD)-95

93 versely, expression of full-length SynCAM in nonneuronal cells induced synapse formation by coculture

94 A second population of adrenergic nonneuronal cells initially localized with cervical symp

95 general mechanism for lysosome dispersal in nonneuronal cells is adapted to drive polarized transpor

96 e or broadly restricts HSV-1 reproduction in nonneuronal cells is unknown.

97 of this precursor pool was transient because nonneuronal cells isolated from St. 38 ganglia failed to

98 nriched at presynaptic terminals, whereas in nonneuronal cells it colocalizes with clathrin and AP2 i

99 10x more neurons and approximately 12x more nonneuronal cells of relatively constant average size.

100 Dlx1 and Dlx2 expression was seen only in nonneuronal cells of the cochleovestibular ganglion and

101 nrelated to adjacent mesenchymal cells or to nonneuronal cells of the ganglion.

102 tive disorders directed at the BBB and other nonneuronal cells of the neurovascular unit.

103 se in protein ubiquitination was observed in nonneuronal cells on Ca2+ entry induced by ionomycin.

104 Whether it also protects nonneuronal cells or tissues is unknown.

105 ns within the cytoplasm of both neuronal and nonneuronal cells overexpressing Parkin.

106 chambers and observed spread of infection to nonneuronal cells plated in a different compartment.

107 at CCR2 mRNA was up-regulated in neurons and nonneuronal cells present in both compressed L4/L5 and i

108 s that are directly transdifferentiated from nonneuronal cells provide a powerful opportunity to exam

109 neuronal cells whereas the growth pattern on nonneuronal cells remained unchanged.

110 tion of satellite cells and other supportive nonneuronal cells resulted in extensive DRG tissue damag

111 Reconstitution of Sema3A receptor in nonneuronal cells revealed that Sema3A further inhibited

112 Most important, nonneuronal cells that do not express mutant SOD1 delay

113 ules to prefibrillar, extracellular Abeta in nonneuronal cells that express transfected tau and in cu

114 ssociated protein found in both neuronal and nonneuronal cells that is thought to be involved in vesi

115 Odontoblasts are nonneuronal cells that possess many of the features of m

116 uronal genes in neural stem cells (NSCs) and nonneuronal cells through its role as a dynamic modular

117 omplex signaling pathway in both neurons and nonneuronal cells to extend the lifespan of Caenorhabdit

118 ting artificial synapses between neurons and nonneuronal cells to investigate the molecular component

119 re, we use live cell imaging of neuronal and nonneuronal cells to show that SOD1 mutants (G85R and G9

120 ulinization and illustrate the importance of nonneuronal cells to the health of the developing brain.

121 visible neurons on a slide, all surrounding nonneuronal cells were harvested and assayed: 21 copies

122 s of beta-galactosidase-positive neurons and nonneuronal cells were similar at 5 dpi.

123 these results suggest that the maturation of nonneuronal cells within the lesion site lead to failed

124 e of spreading from axons to closely apposed nonneuronal cells within the rat optic nerve after intra

125 of the cells were neurons at St. 29; of the nonneuronal cells, a small population expressed glial ma

126 d for novel targets within motor neurons and nonneuronal cells, agents designed for specific amyotrop

127 ung alveolar wall, in ganglionic neurons and nonneuronal cells, and in skin and in lymph nodes.

128 to the CaMKII-activated CLC-3 conductance in nonneuronal cells, and is absent in clc-3(-/-) mice.

129 ty to cytotoxic agents may be generalized to nonneuronal cells, as splenocytes from male and female 1

130 mRNA transcripts are found in NPCs and other nonneuronal cells, but in these cells nPTB protein expre

131 role in silencing neuronal-specific genes in nonneuronal cells, but the molecular mechanisms of its a

132 In nonneuronal cells, CME of the majority of transmembrane

133 cerebral tissue, consisting of neuronal and nonneuronal cells, complicates the comparative analysis

134 Dcx can bind ubiquitously to microtubules in nonneuronal cells, Dcx is highly enriched in the leading

135 Among nonneuronal cells, glial cells lacked NET immunoreactivi

136 In sympathetic neurons, unlike most nonneuronal cells, growth factor withdrawal-induced apop

137 In nonneuronal cells, herpes simplex virus 1 overcomes host

138 ceptors, regulating migration of neurons and nonneuronal cells, including leukocytes, tumor cells, an

139 eptor family members also have been found in nonneuronal cells, including macrophages [4], keratinocy

140 l-adhesion molecules that, when expressed in nonneuronal cells, induce presynaptic differentiation in

141 required to form the ER network, at least in nonneuronal cells, it is logically assumed that defects

142 Although Bst2 prevented MV release from nonneuronal cells, its deletion had no effect on viral p

143 In cultured neurons and nonneuronal cells, Lfc has been shown both to bind to mi

144 ns, mostly derived from work in vitro and in nonneuronal cells, may not necessarily apply to the very

145 ugh Path is broadly expressed in neurons and nonneuronal cells, mutation of path impinges on nutrient

146 When overexpressed in nonneuronal cells, neurexins induce formation of postsyn

147 Compared with nonneuronal cells, neuronal mitophagy is a much slower a

148 In nonneuronal cells, protein kinase D (PKD) has an importa

149 ediate centrifugal transport of lysosomes in nonneuronal cells, specifically drives lysosome transpor

150 ates migration of not only neurons, but also nonneuronal cells, such as leukocytes and cancer cells.

151 obustly palmitoylated Gp130 in cotransfected nonneuronal cells, supporting the possibility that Gp130

152 In nonneuronal cells, the cell surface protein dystroglycan

153 While frequently studied in nonneuronal cells, the functions of cortactin in neurona

154 at, with 86 billion neurons and just as many nonneuronal cells, the human brain is a scaled-up primat

155 ole of KIBRA in several diverse processes in nonneuronal cells, the molecular function of KIBRA in ne

156 In nonneuronal cells, the tyrosine kinase FAK is a major re

157 ng that HSV DNA has been found to persist in nonneuronal cells, these results fuel speculation that H

158 Both in synaptosomes and in nonneuronal cells, this decrease was blocked by FK506 (a

159 plicated in clathrin-mediated endocytosis in nonneuronal cells, though little is known about its func

160 intenance of new HVC neurons, as well as new nonneuronal cells, was higher at the onset of breeding c

161 ate any Ca(2+) current in either neuronal or nonneuronal cells, we nevertheless tested whether a fatt

162 ribbon synapses, syntaxin 3 is also found in nonneuronal cells, where it has been implicated in the t

163 V-1 DNA were detected in approximately 5,200 nonneuronal cells, while nine VZV genomes were detected

164 een shown to play a role in VZV infection of nonneuronal cells, with distinct consequences for infect

165 lpha-Syn further enhance CME in neuronal and nonneuronal cells.

166 ch regulates early and late events in CME in nonneuronal cells.

167 inding of the REST/NRSF repressor complex in nonneuronal cells.

168 as an enhancer in neurons and a silencer in nonneuronal cells.

169 mbrane abnormalities in Tor1a(DeltaE/DeltaE) nonneuronal cells.

170 esponsive to classic autophagy inducers than nonneuronal cells.

171 as the synaptogenic signal produced by these nonneuronal cells.

172 e glucose-dependent upregulation of VDUP1 in nonneuronal cells.

173 epression of some neuronal-specific genes in nonneuronal cells.

174 dimethylation to suppress neuronal genes in nonneuronal cells.

175 cking properties of the wild-type protein in nonneuronal cells.

176 e intense USF immunostaining in neurons than nonneuronal cells.

177 n differentially in vesicular trafficking in nonneuronal cells.

178 epressor of alternative pre-mRNA splicing in nonneuronal cells.

179 contact between axons and GluR4-transfected nonneuronal cells.

180 easily activated than has been observed with nonneuronal cells.

181 e and paracrine hormone in a wide variety of nonneuronal cells.

182 ronal precursor cells (NPC), glia, and other nonneuronal cells.

183 hibiting the expression of neuronal genes in nonneuronal cells.

184 ngs validate therapeutic approaches aimed at nonneuronal cells.

185 enomes were detected in approximately 14,200 nonneuronal cells.

186 mage response that aids viral replication in nonneuronal cells.

187 enhanced in neuronal cells as compared with nonneuronal cells.

188 eurabin-I, promotes filopodia in neurons and nonneuronal cells.

189 ethylase G9a to silence NRSF target genes in nonneuronal cells.

190 nctional activity of nPTB in neuronal versus nonneuronal cells.

191 equire damage from mutant SOD1 acting within nonneuronal cells.

192 to regulate membrane traffic in neuronal and nonneuronal cells.

193 nt of the endocytic machinery in neurons and nonneuronal cells.

194 olocalizes with F-actin in both neuronal and nonneuronal cells.

195 , 2, or 7 is required for HSV replication in nonneuronal cells.

196 nfection does not spread from these infected nonneuronal cells.

197 ected neuronal cells, but not in transfected nonneuronal cells.

198 s to neurons by blocking their expression in nonneuronal cells.

199 cle arrest and neurogenic differentiation in nonneuronal cells.

200 undant, early regulatory roles during CME in nonneuronal cells.

201 likely functions as an antiviral protein in nonneuronal cells.

202 IPs are known MT polymerization promoters in nonneuronal cells.

203 the intron-exon junction in neurons, but not nonneuronal cells.

204 at are widely expressed in many neuronal and nonneuronal cells.

205 stantially more prevalent in neurons than in nonneuronal cells.

206 of lytic versus latency decision of HSV-1 in nonneuronal cells.

207 ription across the genome in neurons than in nonneuronal cells.

208 ntially methylated (DM) between neuronal and nonneuronal cells.

209 sion during clathrin-mediated endocytosis in nonneuronal cells.

210 mediated signaling in the nervous system and nonneuronal cells.

211 and a converse relationship is observed for nonneuronal cells.

212 fficiently generic that it may be applied to nonneuronal cellular structures.

213 Here, we ectopically expressed CerS2, a nonneuronal CerS producing C22-C24 ceramides, in neurons

214 thetic innervation of organs but also detect nonneuronal cholinergic activity in infections.

215 Nonneuronal cholinergic signaling is also involved in im

216 esting mechanistic models for disassembly of nonneuronal clathrin coats has been limited by the absen

217 and then induces neighboring cells to become nonneuronal cone cells.

218 Moreover, electrical stimulation activates a nonneuronal, Cx40-dependent vasodilator response that sp

219 daptive immune escape" mechanism acting as a nonneuronal determinant of clinical onset of disease.

220 etween groups were validated on neuronal and nonneuronal DNA fractions isolated by fluorescence-assis

221 not distinguish differentiated neurons from nonneuronal ectoderm as it does in many other animals, b

222 of KSHV infection-induced transformation of nonneuronal endothelial cells into cells with neuroendoc

223 Most of them were nonneuronal (endothelial cells and cells in the white ma

224 uce ectopic bft expression in the PNS and in nonneuronal epidermis.

225 efforts to comprehensively map neuronal and nonneuronal epigenomes in hundreds of specimens.

226 were sufficient to relocalize cellugyrin, a nonneuronal form of synaptogyrin, from nonsynaptic regio

227 ubunit rescued the cleft palate phenotype, a nonneuronal GABAergic system is implicated in palate dev

228 We also identified a prominent source of nonneuronal GFRalpha3-IR that is likely to be glial.

229 apoptotic profiles appeared to be primarily nonneuronal in nature, in that they exhibited no immunoh

230 MCF7 predominantly expresses the nonneuronal isoform of L1, as do 16 of 17 other cell lin

231 Neuronal and nonneuronal isoforms of the InsP3R1 differ by alternativ

232 F7 cells with overexpression or knockdown of nonneuronal L1 isoform revealed that L1 expression leads

233 uronal-like morphology to cells of different nonneuronal lineages.

234 or (nAChR) types are abundantly expressed in nonneuronal locations, but their functions remain unknow

235 ding or nonbreeding conditions, neuronal and nonneuronal maintenance were similarly low.

236 se that these glial effects may constitute a nonneuronal mechanism for sedative action of anesthetic

237 containing proteins and, in particular, with nonneuronal members of the Src kinase family.

238 s, indicating unexpected connections between nonneuronal membrane traffic at the Golgi complex execut

239 In a nonneuronal model system, clustering of PSD-95, stargazi

240 for the 2-kb LAT in transiently transfected nonneuronal monkey COS-1 cells, suggesting that the stab

241 or neurons is enhanced by damage incurred by nonneuronal neighboring cells, via an inflammatory respo

242 glia (72% of all cells) than neurons, and a nonneuronal:neuronal ratio of 2.7.

243 transcriptional regulation, in neuronal and nonneuronal nuclei collected from prefrontal cortex (PFC

244 ne for epigenome mapping in the neuronal and nonneuronal nuclei from the postmortem brain.

245 at new neuronal number correlated with a new nonneuronal number within each cohort of new neurons.

246 h neuronal (glutamatergic and GABAergic) and nonneuronal (oligodendrocytes, microglia, astrocytes, an

247 eripheral injury activates both neuronal and nonneuronal or glial components of the peripheral and ce

248 emonstration of a spatial memory system in a nonneuronal organism, supporting the theory that an exte

249 t transfection of cells of both neuronal and nonneuronal origin with LAT-GFP expression vectors, low-

250 cells demonstrated that synaptogyrin or its nonneuronal paralog cellugyrin targets efficiently to sy

251 Nonneuronal pathology in neocortex (activated astroglia

252 uitously expressed proteins that promote the nonneuronal pathway of calcitonin/calcitonin gene-relate

253 y tagged with H3K4me3 in neuronal but not in nonneuronal PFC chromatin.

254 whose function might be critical in various nonneuronal physiologic conditions.

255 ion DNA methylation analysis in neuronal and nonneuronal (primarily glial) nuclei separated from the

256 Thus, the propagation of nonneuronal PrPSc is not pathogenic, but arresting the c

257 Neuronal expression of sid-1 decreased nonneuronal RNAi, suggesting that neurons expressing tra

258 These results point to a unique, nonneuronal role for CDK5 in regulation of Rac1 activity

259 Emerging evidence points to nonneuronal roles for these factors, including the Slit-

260 gual muscles was the shortest among the five nonneuronal routes of inoculation, including another int

261 mportant regulatory function in neuronal and nonneuronal secretory cells.

262 ynapse number can be profoundly regulated by nonneuronal signals, and raise the possibility that glia

263 targeting the catalytic activity of BoNTs to nonneuronal SNARE isoforms.

264 ity of genetically modifying LCs to target a nonneuronal SNARE protein that extends therapeutic poten

265 of a BoNT derivative that cleaves SNAP23, a nonneuronal SNARE protein.

266 more recently by the directed conversion of nonneuronal somatic cells, such as skin fibroblasts, to

267 signaling control the PN between neurons and nonneuronal somatic tissues to achieve balanced tissue e

268 ertile adult males, although females lacking nonneuronal spectrin were sterile.

269 Cyp6a20 is expressed in a subset of nonneuronal support cells associated with pheromone-sens

270 motor neurons, but SOD1 mutant damage within nonneuronal supporting cells reduces motor neuron functi

271 ple cell types, including within neighboring nonneuronal supporting cells, which is crucial to neuron

272 However, prerequisite to develop nonneuronal therapies requires the retargeting the catal

273 est that these signaling pathways may act in nonneuronal tissue to regulate sleep behaviors.

274 leptin, an adipocytokine produced mainly by nonneuronal tissue, has been implicated in the regulatio

275 bunit are widely distributed in neuronal and nonneuronal tissue.

276 The mGluRs are also expressed in nonneuronal tissues and are implicated in a variety of n

277 NS-6 in turn relays the longevity signals to nonneuronal tissues by decreasing the activity of the tr

278 s an assay, a chaperone activity abundant in nonneuronal tissues is now purified and identified to be

279 CACNG4 expression is also observed in nonneuronal tissues undergoing differentiation, specific

280 glutamate receptors have been identified in nonneuronal tissues, including bone, heart, kidney, panc

281 In contrast, nonneuronal tissues, such as kidney, express only syntax

282 e paralogue of TMEM24 primarily expressed in nonneuronal tissues, which correspondingly display a muc

283 ty: basal targets are regulated primarily in nonneuronal tissues, while memory targets are enriched f

284 re the activity of the TRPM channel GTL-2 in nonneuronal tissues.

285 ression of noncanonical UPR genes pqn/abu in nonneuronal tissues.

286 eurons actively suppress immune responses of nonneuronal tissues.

287 repressor that decreases gene expression in nonneuronal tissues.

288 t from the known insulin-mediated pathway in nonneuronal tissues.

289 back loops that operate in many neuronal and nonneuronal tissues.

290 or areas of the brain; it is not detected in nonneuronal tissues.

291 ered gene regulation in neuronal compared to nonneuronal tissues.

292 cellular types, including both neuronal and nonneuronal tissues.

293 lex is required to repress neuronal genes in nonneuronal tissues.

294 neurons, REST leaves miR-124a gene loci, and nonneuronal transcripts are degraded selectively.

295 iR-124a, decreases the levels of hundreds of nonneuronal transcripts, such that its introduction into

296 124a expression, allowing the persistence of nonneuronal transcripts.

297 nal network activity and a novel function of nonneuronal TRPM channels in the fine-tuning of this net

298 In contrast, the nonneuronal ubiquitously expressed 170-kDa isoform of SJ

299 However, nonneuronal uptake limited relative differences between

300 alternative splicing of ELAV target genes in nonneuronal wing disc cells and substitute for ELAV in e