ライフサイエンスコーパス: neural tissue

1 an increase in VEGFR2 within the surrounding neural tissue.

2 Fossil arthropods rarely preserve neural tissue.

3 ition of the amyloid beta-peptide (Abeta) in neural tissue.

4 f extracted myelin lipids and those found in neural tissue.

5 d in the cochlea, not in direct contact with neural tissue.

6 educed proliferation, most strikingly in the neural tissue.

7 a basis for semi-automatic reconstruction of neural tissue.

8 t few have applied these techniques to human neural tissue.

9 f many diseases is the unique involvement of neural tissue.

10 irregularities arise at their interface with neural tissue.

11 nsion and shape and for autonomous CE of the neural tissue.

12 ng of neuronal structure and function within neural tissue.

13 e electrodes that come into contact with the neural tissue.

14 cells could mediate clearance of HSV-1 from neural tissue.

15 extracellular matrix and disperse within the neural tissue.

16 mportant roles in T cells, muscle, bone, and neural tissue.

17 nhibition of BMP results in the formation of neural tissue.

18 ulture" phenomenon and generalize to complex neural tissue.

19 ne cannot alter the normal fate of posterior neural tissue.

20 iophysical and the biochemical properties of neural tissue.

21 microvascular bed that feeds the underlying neural tissue.

22 hotodamage caused by optical imaging in live neural tissue.

23 s for studying the structure and function of neural tissue.

24 that culminates in an exquisitely patterned neural tissue.

25 eased production of ouabain-like factor from neural tissue.

26 enzyme-bound states of intracellular NADH in neural tissue.

27 l deficits caused by compression of adjacent neural tissue.

28 erials are not intrinsically similar to soft neural tissue.

29 iple foci observed at different locations in neural tissue.

30 opposite directions can coexist in the same neural tissue.

31 racellular matrix is an integral part of the neural tissue.

32 ting highly unsaturated fatty acid (HUFA) in neural tissue.

33 mode is required for fossilization of labile neural tissue.

34 ryngeal secretions, cerebrospinal fluid, and neural tissue.

35 ole in both the damage and repair of injured neural tissue.

36 comprehensively map synaptic connections in neural tissue.

37 gical phenomena occurring within a volume of neural tissue.

38 mplementations given the constraints of real neural tissue.

39 der, and (c) surrounding spared but reactive neural tissue.

40 n the adult mouse retina, a disease-relevant neural tissue.

41 Su(Hw) is a repressor of neural genes in non-neural tissues.

42 e broadly distributed in both neural and non-neural tissues.

43 rous proteoglycans found in skin, joints and neural tissues.

44 acity long speculated to reside in mammalian neural tissues.

45 shows IL-1R3 is preferentially expressed in neural tissues.

46 nsferase Vb (GnT-Vb), is highly expressed in neural tissues.

47 essed mainly in the dorsal neuroectoderm and neural tissues.

48 e the development of adjacent neural and non-neural tissues.

49 ndred genes containing long 3' extensions in neural tissues.

50 lating the migration and organization of non-neural tissues.

51 d to vertebrates, as lncRNAs are abundant in neural tissues.

52 modulation of selected cells within complex neural tissues.

53 t fish, accounting for the size reduction of neural tissues.

54 and maintenance of phospholipid membranes in neural tissues.

55 esting that CFI might play a special role in neural tissues.

56 4) Fox-3 expression is restricted to neural tissues.

57 docrine cells as well as other endocrine and neural tissues.

58 uired for clearance of infectious virus from neural tissues.

59 1-enriched proteinaceous inclusions in their neural tissues.

60 heavily expressed in the brain and in human neural tissues.

61 accurately replicate the microenvironment of neural tissues.

62 ion, demonstrating significant enrichment in neural tissues.

63 us tissue by silencing neuronal genes in non-neural tissues.

64 ment by inactivating murine Brca2 throughout neural tissues.

65 ell cycle, apoptosis, and differentiation in neural tissues.

66 domains, ideal for the environments found in neural tissues.

67 d persistence of elevated levels of virus in neural tissues.

68 erior region without posteriorizing anterior neural tissues.

69 chromatin remodeling was expressed mainly in neural tissues.

70 t, NPR-A gene expression was undetectable in neural tissues.

71 state-of-the-art approaches for bioprinting neural tissues.

72 atification patterns in the retina and other neural tissues.

73 n have long-term deleterious consequences to neural tissues.

74 dissemination by carrying the virus into the neural tissues.

75 ias for circRNA upregulation during aging in neural tissues.

76 oteins in the generation and organization of neural tissues.

77 attern of expression, with highest levels in neural tissues.

78 ssion of the neuronal ankyrin isoform in non-neural tissues.

79 with its reproducible performance in various neural tissues.

80 n in transcriptomic and proteomic studies of neural tissues.

81 region prevents UBE3A-ATS expression in non-neural tissues.

82 via shortening reaction times and saving on neural tissue [8-16].

83 Due to the limited regenerative ability of neural tissue, a diverse set of biochemical and biophysi

84 Signals from neural tissue act on endothelial cells to stimulate bloo

85 ted its role in the regenerative response of neural tissue after ischemic injury using the mice defic

86 lls can differentiate into blood vessels and neural tissue after transplantation to the subcutis of n

87 of irreversible electroporation (IRE) on the neural tissues after ablation in the epidural space of t

88 Conclusion Gadolinium deposition in neural tissues after GBCA administration occurs in the a

89 I to suppress innate immune responses in non-neural tissues against Pseudomonas aeruginosa in Caenorh

90 ylation was defective in Nbs1(DeltaB/DeltaB) neural tissue, although apoptosis occurred normally.

91 nt SOD1 is known to accumulate in the IMS of neural tissue and cause mitochondrial dysfunction.

92 The ectoderm gives rise to both neural tissue and epidermis.

93 e screened for factors enriched in posterior neural tissue and identify spalt-like 4 (sall4), which i

94 rs the molecular and cellular composition of neural tissue and leads to glial scarring, which inhibit

95 r, the relationship between the integrity of neural tissue and neural function has not been previousl

96 UAS/Gal4 system to deplete CFI proteins from neural tissue and observe that in this condition, multip

97 estin-cre mice showed extensive gammaH2AX in neural tissue and p53 deficiency restored brain histolog

98 ion transmitted, and thus, the properties of neural tissue and principles of its organization into ci

99 ntral axis, as well as with expanded cranial neural tissue and reduced cranial surface ectoderm culmi

100 strocytes play essential roles in preserving neural tissue and restricting inflammation after moderat

101 ulating neural activity, the regeneration of neural tissue and the delivery of bioactive molecules fo

102 en receptor, in goldfish (Carassius auratus) neural tissue and used reverse-transcription polymerase

103 esized that rs688 modulates LDLR splicing in neural tissues and associates with AD.

104 ' UTR sequences are selectively expressed in neural tissues and contain putative recognition motifs f

105 nces the kinetics of reovirus replication in neural tissues and highlight a functional role for sialy

106 expressed in endothelium, genes expressed in neural tissues and housekeeping genes.

107 anscript and protein in the mouse retina and neural tissues and is associated with visual dysfunction

108 ttenuated baseline phosphorylation of Erk in neural tissues and led to growth retardation.

109 derived transcript and SMN protein levels in neural tissues and muscle, which were associated with an

110 cient form of IDE expressed in brain and non-neural tissues and recommend novel regions of the IDE ge

111 s compared with lipids characteristic of non-neural tissues and show further acceleration of change i

112 The mechanical mismatch between soft neural tissues and stiff neural implants hinders the lon

113 stula and gastrula stages and is enriched in neural tissues and the pronephros during later embryogen

114 what are the requirements for Shroom3 in non-neural tissues and what factors control Shroom3 transcri

115 CSPP1 is broadly expressed in neural tissue, and its encoded protein localizes to the

116 t by specifically formulating the bioink for neural tissues, and by spatially patterning cell types a

117 rocessed in transfected HEK 293 cells and in neural tissues, and its ectodomain is exposed and accumu

118 sly assumed, independently of mesodermal and neural tissues, and that Pax7 has a crucial function dur

119 , the mechanisms underlying the formation of neural tissue architectures during development of the ce

120 During early development, the Otx2-positive neural tissues are patterned anterior-posteriorly to for

121 ch is distinguished by bilateral necrosis of neural tissue around the ventricles and a sequela of neu

122 never infiltrate it and instead displace the neural tissue as they grow.

123 applicability to in vivo calcium imaging of neural tissue, as well as other smooth muscle tissue.

124 mated technologies to probe the structure of neural tissue at nanometer resolution and use them to ge

125 M) has become an essential tool for studying neural tissue at resolutions below 10 nm x 10 nm x 10 nm

126 ound in oligodendroglioma samples and normal neural tissue but also in a wide spectrum of malignant c

127 for inhibition of Fgf signalling in inducing neural tissue but it is not sufficient to maintain neura

128 te SH2B1(TgKO) mice expressing SH2B1 only in neural tissue but not in other tissues.

129 requires protein O-mannosylation activity in neural tissue but not the meninges.

130 ion, which we show not only marks definitive neural tissue, but also tissue that is not yet committed

131 is involved in cancer, vascular defects, and neural tissue, but is largely unexplored in immune syste

132 th SMN2 transcript as well as SMN protein in neural tissue, but only minimally in peripheral tissue.

133 rP(C)) is widely expressed in neural and non-neural tissues, but its function is unknown.

134 xpression of GPIalpha btx in surrounding non-neural tissues, but not in neurons, does not prevent cel

135 (miRNAs) are highly expressed in vertebrate neural tissues, but the contribution of specific miRNAs

136 rs of oxidative death in both neural and non-neural tissues, but their precise mechanism of action re

137 ons and/or use of cellular grafts to protect neural tissue by local delivery of growth or trophic fac

138 SYN1 gene transcription is suppressed in non-neural tissues by the RE1-silencing transcription factor

139 ioside GM3, a glycosophingolipid enriched in neural tissue, by adding sialic acid to lactosylceramide

140 The ways neural tissue can be stimulated to evoke artificial sens

141 Deafferentation of neural tissue can result in cell death, morphological ch

142 expressed in endocrine, neuroendocrine, and neural tissues, can be accurately quantified by RIA, and

143 spite of progressive extracellular edema in neural tissue, capillary endothelial cell tight junction

144 ound that ectopic expression of Gdf11 in the neural tissue causes a rostral displacement of Hoxc prot

145 ting enzyme-2 (ECE-2), which is expressed in neural tissues, cleaves 'big endothelin' to produce the

146 tral cells induces the production of ectopic neural tissue considerably outside the neural field.

147 for human islet isolations contained bovine neural tissue contaminants.

148 several known restorative actions on damaged neural tissue, could play a role.

149 We measured gene expression patterns for 24 neural tissues covering the mouse central nervous system

150 e nervous system and doublesex specified non-neural tissues culminated with claims that fruitless was

151 ission electron microscopy (ssTEM) images of neural tissue currently requires many hours of manual tr

152 This early signal of neural tissue damage may be important in setting up seco

153 nal diseases, results in vasogenic edema and neural tissue damage, causing vision loss.

154 present great promise regarding treatment of neural tissue damage, such as spinal cord injury (SCI).

155 ity, and free-radical release, contribute to neural tissue damage.

156 4 increases SMN expression in neonatal mouse neural tissues, delays motor neuron loss at PND11 and am

157 Cells in the developing neural tissue demonstrate an exquisite balance between p

158 No detectable neural tissue deposition or MR imaging signal was observ

159 we have characterized glial precursors from neural tissue derived from early embryonic ages.

160 ed expression of these two IG20-SVs in human neural tissues derived from cerebral cortex, hippocampus

161 cts for studying the earliest steps of human neural tissue development and the pathogenesis of brain

162 euronal differentiation, and interruption of neural tissue development.

163 Mice ablated for NMII-B in neural tissues die between postnatal day 12 and 22 witho

164 ld-type Gfr gene restored the HRP epitope in neural tissues, directly demonstrating that the Gfr muta

165 in human brain, synapses, retina, and other neural tissues, displays beneficial actions in neuronal

166 Xenopus Wnt11-R is expressed in neural tissue, dorsal mesenchyme derived from the dermat

167 agonists emanating from the organiser induce neural tissue dorsally.

168 We present example data sets from mammalian neural tissue, Drosophila brain, and Chlamydomonas reinh

169 of this gene is predominately restricted to neural tissue during embryogenesis and is expressed in a

170 main protein that is expressed in developing neural tissues during mouse embryogenesis.

171 hots of neural activity in a large volume of neural tissue, e.g., a complete mouse brain, by circumve

172 In contrast to other neural tissues, eliminating beta-catenin did not signifi

173 of hMSCs and hence, would be beneficial for neural tissue engineering scaffolds.

174 ctive scaffolds or supporting substrates for neural tissue engineering.

175 e diverse facets of the challenging field of neural tissue engineering.

176 C differentiation and are thus important for neural tissue engineering.

177 didate genes are preferentially expressed in neural tissue, especially during the prenatal period, an

178 luding a reduction in the amount of anterior neural tissue, especially in the telencephalic, optic an

179 eralfold higher than in other neural and non-neural tissues examined, consistent with the requirement

180 How can neural tissue exhibit both type I and type II excitabili

181 nitor cell from the 8-cell embryo formed the neural tissue fated clone through divisions to the 32-ce

182 dysregulated expression of chemokines in the neural tissues, favors development of CNS autoimmune dis

183 erface between the blood circulation and the neural tissue features unique characteristics that are e

184 ll death and the progressive degeneration of neural tissue following traumatic brain injury (TBI) hav

185 onent of a long-term immune cell presence in neural tissues following genital HSV-1 infection and pla

186 phobic fluorescent dye are retained in local neural tissue for up to 5 days and that PgP can efficien

187 Neural tissue formation is induced by growth factors tha

188 th genes were cell-autonomously required for neural tissue formation, as defined by the pan-neural ma

189 procedure to use a GMP-manufactured, bovine neural tissue-free collagenase blend.

190 Ectopic Sox3 caused induction of neural tissue from a very early stage of cell specificat

191 gies to attenuate neuroinflammation, protect neural tissue from collateral injury, and enhance endoge

192 1 or Nbs1 hypomorphic mutations, we analyzed neural tissue from Mre11(ATLD1/ATLD1) and Nbs1(DeltaB/De

193 patients with temporal lobe epilepsy and in neural tissues from animal models of epilepsy.

194 conducted in three brain regions and two non-neural tissues from humans, chimpanzees, macaque monkeys

195 tral nervous system (CNS) barriers partition neural tissues from the blood, providing a homeostatic e

196 of all other cells tested, including retina, neural tissue, glial cells, and a cancer cell line.

197 We find that neural tissue has marked non-ohmic and frequency-filteri

198 The extracellular ionic environment in neural tissue has the capacity to influence, and be infl

199 ar behaviors underlying CE in the epithelial neural tissue, have not been identified.

200 mutants reveals that Pikfyve is critical in neural tissues, heart, lung, kidney, thymus, and spleen.

201 When acting on neural tissue, however, testosterone can be metabolized

202 DAC11 and neural cells in vitro, we examined neural tissue in a previously uncharacterised Hdac11 kno

203 that can potentially access large volumes of neural tissue in a single treatment is intra-arterial (I

204 ression of NKCC1 results in the formation of neural tissue in ectodermal explants.

205 Rat SH2B1beta was specifically expressed in neural tissue in SH2B1-transgenic (SH2B1(Tg)) mice.

206 Here we use the structural context of the neural tissue in which dendritic trees exist to drive th

207 long-term repression of target genes in non-neural tissues in adult zebrafish.

208 Some family members are also enriched in neural tissues in both vertebrates and invertebrates.

209 crophages do not damage and may even protect neural tissues in EAN.

210 ion of BMP signaling is sufficient to induce neural tissues in vivo remains controversial.

211 ers of nonepithelial tissues (mesenchyme and neural tissue) in both primary and immortalized squamous

212 l tetramers are prevalent in lymphocytes and neural tissues, in which octamers are abundant but hexam

213 Here we report that both melanoma and normal neural tissues including dorsal root ganglion (DRG) prod

214 Biophysical stimulation of neural tissue induced demyelination and Schwann cell pro

215 The first neural tissue induced is anterior and subsequent neural

216 during embryonic development induces ectopic neural tissue, inhibits eye formation, and perturbs the

217 d for three or more hours differentiate into neural tissue instead of adopting their normal epidermal

218 that gene therapy should be directed to the neural tissue instead of the meninges.

219 hways responsible for subdivision of midline neural tissue into hypothalamic and floorplate domains a

220 This study reveals the location of FAAH in neural tissue involved in peripheral nociceptive transmi

221 Delayed revascularization of ischemic neural tissue is a major impediment to preservation of f

222 hat the amount of pathological aggregates in neural tissue is exceedingly low, precluding examination

223 The propagation of activity in neural tissue is generally associated with synaptic tran

224 The delivery of therapeutics to neural tissue is greatly hindered by the blood brain bar

225 al tissue induced is anterior and subsequent neural tissue is posteriorized to form the midbrain, hin

226 We investigated how glutamate in a neural tissue is protected from catabolism.

227 chanism by which agrin exerts its effects in neural tissue is unknown.

228 humans, but the role of PtdIns(3,5)P2 in non-neural tissues is poorly understood.

229 iest step in this process - the induction of neural tissue - is intimately linked to patterning of th

230 As an embryo gastrulates or makes neural tissue it shortens across the dorso-ventral axis

231 localized in cytoplasmic puncta in zebrafish neural tissue, it is on the plasma membrane in mib1 muta

232 ng and histopathologic examination showed no neural tissue lesions within the spinal cord; however, f

233 two-photon imaging, we show that neurons and neural tissue maintain basal stores of loosely bound cop

234 hough these cell lines were not derived from neural tissue, many neurobiologically relevant genes wer

235 temporal spectra nor processed by registered neural tissue maps.

236 ctive action of perisynaptic CSPGs in mature neural tissue may account for the therapeutic effects of

237 However, genes with essential roles in non-neural tissues may be missed in traditional loss-of-func

238 We review a range of bioprinted neural tissue models and discuss how they can be used to

239 uch as axon guidance, synapse formation, and neural tissue morphogenesis.

240 t signaling is able to posteriorize anterior neural tissues, neural crest induction by Wnts has been

241 eural plate during neurula stages and in the neural tissue of adult frogs.

242 Microarrays of neural tissue of animal models of the disease showed dec

243 ple functions in the development of anterior neural tissue of vertebrate embryos.

244 t performs these functions in epithelial and neural tissues of both insects and mammals, as well as i

245 s involved in the regulation of apoptosis in neural tissues of both WKY and SHRSP rats.

246 In contrast, although virus titers in neural tissues of p55-/- N13 mice were elevated to level

247 To determine whether gadolinium deposits in neural tissues of patients with intracranial abnormaliti

248 f the brain and spinal cord without damaging neural tissues or triggering foreign body reactions.

249 xpression of OLIG2 is normally restricted to neural tissues, overexpression of OLIG2 has been shown i

250 Due to limited access to human neural tissue, pathogenetic studies have, so far, mostly

251 hanical properties of the LC (PC2) or of the neural tissue (PC4), rotation of the peripapillary scler

252 In neural tissue, PCDH-gamma, together with PCDH-alpha, for

253 e connective tissue (laminar) and prelaminar neural tissue (prelaminar) components of optic nerve hea

254 studies have shown that during development, neural tissues produce mRNAs with particularly long 3'UT

255 avage site within the hevin sequence for the neural tissue proteinase ADAMTS4.

256 indirect consequence of posteriorization of neural tissues rather than a direct effect of Wnt signal

257 the molecular cascades through which target neural tissues regulate vessel stabilization and pattern

258 sophila have revealed molecular pathways and neural tissues regulating sleep; however, genes that mai

259 sions to recruit endogenous NPCs and enhance neural tissue repair/regeneration.

260 t a model in which specification of anterior neural tissue requires early FGF-mediated repression of

261 Intriguingly, analysis of T32KO neural tissue revealed a decreased concentration of neur

262 Neural tissue samples dissected from rat brain and the c

263 unfolded protein response was identified in neural tissues (sciatic nerve, spinal cord) of streptozo

264 embrane, a process that requires neurabin (a neural tissue-specific protein).

265 egulation of adenosine-evoked responses by a neural tissue-specific protein, neurabin.

266 changes point to a dynamic modulation of the neural tissue structure upon activation, which remains t

267 GF) receptor TrkA is widely expressed in non-neural tissues suggesting pleiotropic functions outside

268 red to antagonize SHH signaling primarily in neural tissues, suggesting that hedgehog signal transduc

269 CircRNAs are enriched in neural tissues, suggesting that they might have neural f

270 nd reveal extensive movements of the cranial neural tissue that are independent of neural fold zippin

271 mucosa, the organ of smell in the nose, is a neural tissue that regenerates new sensory neurons throu

272 otrophin-3 (NT-3) is highly expressed in non-neural tissues that receive peripheral innervation, we i

273 ing the neuronal phenotype in vertebrate non-neural tissue, the invertebrate homolog is absent, raisi

274 l canal enlargement, cupping, and prelaminar neural tissue thickening.

275 o serous retinal detachment or herniation of neural tissue through the LC defect.

276 y, histology analysis revealed filling-in of neural tissue through the macroporous network and attrac

277 mouse embryo inhibits BMP signaling to allow neural tissue to form as a default fate-in the absence o

278 d either by stimulating or by recording from neural tissue to treat or assist people with sensory, mo

279 genetically normal and unrelated allografted neural tissue transplanted into the brain of affected HD

280 o that tau pathology can manifest in healthy neural tissue transplanted into the brains of patients w

281 n maximizing information storage capacity of neural tissue under resource constraints.

282 Developing neural tissue undergoes a period of neurogenesis followe

283 genes that encode heat shock proteins in non-neural tissues upon exposure to heat.

284 aset (>100,000 spikes) recorded from varying neural tissue (V1 and retina) using different calcium in

285 ons to complete pyritization, revealing that neural tissue was initially preserved as carbonaceous fi

286 arance of infectious HSV type 1 (HSV-1) from neural tissues was also detected.

287 Clearance of infectious virus from neural tissues was not significantly different in perfor

288 neutrophils during murine peritonitis and by neural tissues was separated from natural isomers and su

289 ble transcriptional targets of PGC-1alpha in neural tissue, we conducted a microarray on neuroblastom

290 tein screen with developmental versus mature neural tissues, we identified a group of developmentally

291 Histopathologic characteristics of the neural tissues were assessed and used to select a voltag

292 HSV-1 titers in neural tissues were greatly reduced over time in CD8(+)

293 The prelaminar neural tissues were thickened inferiorly, inferonasally,

294 ensitivity fluorescence microscopy in intact neural tissue, which is hostile to traditional forms of

295 n Opa1 transcript and protein in retinal and neural tissue, which manifests as visual dysfunction in

296 " neurotransmitters allow optical control of neural tissue with high spatial and temporal precision.

297 (CDK5) is expressed at high levels in MM and neural tissues with relatively low expression in other o

298 nical manifestations, we immunostained mouse neural tissues with sera from patients with neuromyotoni

299 larged vascular structures located in benign neural tissues within the cerebellum and spinal cord of

300 ascribed a mechanical role in the support of neural tissues, yet this idea has not been specifically