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 repress neuronal gene transcription in both nonneuronal and neuronal cell lines.

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

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

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

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

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

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

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

11 extracellular particles are not involved in nonneuronal cell infections.

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

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

14 xpression experiments with both neuronal and nonneuronal cell lines showed that the LTE locus has an

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

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

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

18 se two promoters occurs in both neuronal and nonneuronal cell lines.

19 While Sema3A binding to NP-1 does not alter nonneuronal cell morphology, Sema3A interaction with NP-

20 Some nonneuronal cell nuclei were very strongly immunoreactiv

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

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

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

24 dissociated and separated into neuronal and nonneuronal cell suspensions by differential filtration.

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

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

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

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

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

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

31 y differentiate to a variety of neuronal and nonneuronal cell types.

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

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

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

35 maged mitochondria induces mitophagy in many nonneuronal cell types.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 Nonneuronal cells engineered to express neuroligins indu

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

67 However, very few nonneuronal cells expressed GFP.

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

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

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

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

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

73 rces generated by the outgrowth of axons and nonneuronal cells from the proximal stump and the constr

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 Viral proteins were detected in neurons and nonneuronal cells in acutely infected ganglia, but were

78 1 (CB1) is widely distributed in neurons and nonneuronal cells in brain and peripheral organs includi

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

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

81 Nearly all nonneuronal cells in ICP0 and ICP27 reporter transgenic

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

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

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

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

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

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

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

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

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

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

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

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

97 10x more neurons and approximately 12x more nonneuronal cells of relatively constant average size.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 Neurons were separated from nonneuronal cells to investigate their inherent cell dea

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

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

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

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

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

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

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

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

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

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

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

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

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

131 In nonneuronal cells, CME of the majority of transmembrane

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

133 Among nonneuronal cells, glial cells lacked NET immunoreactivi

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

135 In nonneuronal cells, herpes simplex virus 1 overcomes host

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

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

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

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

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

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

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

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

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

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

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

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

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

149 In nonneuronal cells, the cell surface protein dystroglycan

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

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

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

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

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

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

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

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

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

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

160 esponsive to classic autophagy inducers than nonneuronal cells.

161 as the synaptogenic signal produced by these nonneuronal cells.

162 likely functions as an antiviral protein in nonneuronal cells.

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

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

165 dimethylation to suppress neuronal genes in nonneuronal cells.

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

167 e intense USF immunostaining in neurons than nonneuronal cells.

168 n differentially in vesicular trafficking in nonneuronal cells.

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

170 contact between axons and GluR4-transfected nonneuronal cells.

171 easily activated than has been observed with nonneuronal cells.

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

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

174 hibiting the expression of neuronal genes in nonneuronal cells.

175 ngs validate therapeutic approaches aimed at nonneuronal cells.

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

177 mage response that aids viral replication in nonneuronal cells.

178 enhanced in neuronal cells as compared with nonneuronal cells.

179 IPs are known MT polymerization promoters in nonneuronal cells.

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

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

182 nctional activity of nPTB in neuronal versus nonneuronal cells.

183 equire damage from mutant SOD1 acting within nonneuronal cells.

184 to regulate membrane traffic in neuronal and nonneuronal cells.

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

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

187 , 2, or 7 is required for HSV replication in nonneuronal cells.

188 nfection does not spread from these infected nonneuronal cells.

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

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

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

192 cle arrest and neurogenic differentiation in nonneuronal cells.

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

194 ce, RSLE, which is absent in L1 expressed in nonneuronal cells.

195 central nervous system differs from that in nonneuronal cells.

196 or mRNA levels were restricted to ganglionic nonneuronal cells.

197 isoforms found in melanocytes and many other nonneuronal cells.

198 stantially more prevalent in neurons than in nonneuronal cells.

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

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

201 sion during clathrin-mediated endocytosis in nonneuronal cells.

202 mediated signaling in the nervous system and nonneuronal cells.

203 and a converse relationship is observed for nonneuronal cells.

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

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

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

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

208 ding the neocortex, these were identified as nonneuronal cells; evidence for newly generated neurons

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

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

211 Nonneuronal cholinergic signaling is also involved in im

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

213 toreceptor differentiation but also promotes nonneuronal cone cell specification in early Drosophila

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

215 lice donor and acceptor, was observed in the nonneuronal Cos-1 cell line.

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

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

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

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

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

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

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

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

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

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

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

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

228 Neuronal and nonneuronal isoforms of the InsP3R1 differ by alternativ

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

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

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

232 flux in cultured primary neurons, but not in nonneuronal LRP-containing cells in the same culture.

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

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

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

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

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

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

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

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

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

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

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

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

245 in a range of cell types, including those of nonneuronal origin.

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

247 Nonneuronal pathology in neocortex (activated astroglia

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

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

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

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

252 SEMCAP-2 is a closely related nonneuronal protein.

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

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

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

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

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

258 mportant regulatory function in neuronal and nonneuronal secretory cells.

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

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

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

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

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

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

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

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

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

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

269 kinase) that specifically phosphorylates the nonneuronal t-SNARE SNAP-23 in vivo.

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

271 r of neuron-specific gene expression in both nonneuronal tissue and developing neurons.

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

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

274 bunit are widely distributed in neuronal and nonneuronal tissue.

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

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

277 ded polyglutamine domain in the brain and in nonneuronal tissues in patients with HD.

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

283 eurons actively suppress immune responses of nonneuronal tissues.

284 repressor that decreases gene expression in nonneuronal tissues.

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

286 cellular types, including both neuronal and nonneuronal tissues.

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

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

289 ered gene regulation in neuronal compared to nonneuronal tissues.

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

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

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

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

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

295 124a expression, allowing the persistence of nonneuronal transcripts.

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

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

298 However, nonneuronal uptake limited relative differences between

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

300 ts may be in part through a Y1alpha and/or a nonneuronal Y2 receptor, which were cloned from both the