ライフサイエンスコーパス: neuroepithelial

1 thinning, impaired neurogenesis and loss of neuroepithelial adherens junctions.

2 ion, Tbeta4 expression has a large impact on neuroepithelial and macroscopic brain development.

3 which ALT is prevalent, including cancers of neuroepithelial and mesenchymal origin.

4 Our work further implies that neuroepithelial and neural crest cells are particularly

5 ion, the HFD stimulated the proliferation of neuroepithelial and neuronal precursor cells of the embr

6 nd mediolateral gene expression gradients in neuroepithelial and radial glial progenitors (the 'proto

7 ges in conducting airways, and distinguishes neuroepithelial and tracheal-bronchial gland cell lineag

8 cle arrest that underpins the specificity of neuroepithelial apoptosis and neural crest cell hypoplas

9 Neuroepithelial apoptosis diminished the size of the neu

10 is; thus suggesting that it is p53-dependent neuroepithelial apoptosis that is the primary mechanism

11 some TiPSC-OVs maintained their distinctive neuroepithelial appearance and spontaneously formed prim

12 Neuroepithelial attachments at adherens junctions are es

13 elial cells, promotes the enlargement of the neuroepithelial basal end-foot and traps Hh protein, the

14 that is required for its localization to the neuroepithelial basement membrane (BM) to effectively an

15 opore closure, accompanied by suppression of neuroepithelial bending at the median hinge point and ac

16 cretory precursors juxtaposed to presumptive neuroepithelial bodies (NEBs), distinguished by their st

17 We mapped the formation of lung neuroepithelial bodies (NEBs), innervated clusters of ne

18 esulted in considerable depletion of CGRP in neuroepithelial bodies and submucosal nerve plexuses wit

19 these mice manifested an increased number of neuroepithelial bodies but a reduced number of solitary

20 al and central modulation via stimulation of neuroepithelial bodies of the lung.

21 bers that contact pulmonary endocrine cells (neuroepithelial bodies).

22 submucosal glands/intercartilagenous rings, neuroepithelial bodies, and terminal bronchioles/broncho

23 ly proposed airway chemosensory element, the neuroepithelial body (and its immortalized cellular coun

24 )-expressing stem cells that localize to the neuroepithelial body (NEB) and contribute to renewal of

25 other cancer cell lines including breast and neuroepithelial cancer, melanoma, and leukemia cell line

26 Treatment of neuroepithelial cancers remains a daunting clinical chal

27 Neuroepithelial cell (NEC) elongation is essential for p

28 Neuroepithelial cell (NEC) elongation is one of several

29 kinase activity is essential for regulating neuroepithelial cell adhesion, migration and morphogenes

30 ic reticulum stress, caspase activation, and neuroepithelial cell apoptosis (causal events in type 1

31 (K1361R) embryos show a striking increase in neuroepithelial cell apoptosis and a dramatic loss of ph

32 predominantly leads to exencephaly, induces neuroepithelial cell apoptosis and suppresses autophagy

33 How a naive human neuroepithelial cell becomes an electrophysiologically a

34 Endothelial coculture stimulates neuroepithelial cell contact, activating Notch and Hes 1

35 s in oxidative stress-induced DNA damage and neuroepithelial cell death.

36 expressed transcription factors involved in neuroepithelial cell differentiation.

37 Additionally, neuroepithelial cell junctions in the embryonic rat brai

38 event(s) involved in the maintenance of the neuroepithelial cell layer shortly after its formation.

39 erebral cortical precursor cells reside in a neuroepithelial cell layer that regulates their prolifer

40 All cells expressed nestin, an early neuroepithelial cell marker.

41 autonomously within the retina and brain, as neuroepithelial cell morphology and polarity in these ti

42 as key regulatory elements in the control of neuroepithelial cell proliferation and the neuroblast tr

43 Neuroepithelial cell proliferation must be carefully bal

44 helial stem cell phenotype and regulation of neuroepithelial cell proliferation, suggesting that a mu

45 3, MAD2, CDC28 protein kinase (CKS)1 and 2, neuroepithelial cell transforming gene (NET)1, activator

46 We identify neuroepithelial cell transforming gene 1 (Net1) as a dow

47 athological angiogenesis caused by defective neuroepithelial cell-endothelial cell adhesion and imbal

48 basal progenitors (BPs), differentiate from neuroepithelial cells (NCs) with stem cell properties.

49 Subsequently, neuroepithelial cells (NE) convert into neuroblasts (NB)

50 In this study, we show that neuroepithelial cells (NECs), including neural crest cel

51 racellular calcium concentration of isolated neuroepithelial cells (NECs), which are putative oxygen

52 F or EGF promotes the proliferation of mouse neuroepithelial cells (NECs).

53 at mediate the transition, we microdissected neuroepithelial cells and compared their transcriptional

54 of activated Yorkie, promotes overgrowth of neuroepithelial cells and delays or blocks their differe

55 rt to a molecular state resembling embryonic neuroepithelial cells and functionally acquire rapid pro

56 In medium that allows growth of neuroepithelial cells and glial progenitors, mutant cell

57 g of postmitotic neurons is mediated through neuroepithelial cells and is necessary for guiding neuro

58 ver, Cited2 was required for the survival of neuroepithelial cells and its absence led to massive apo

59 developing mouse cortex where the expansive neuroepithelial cells and neurogenic radial glial progen

60 e/Afadin, mislocalize in dividing Eph mutant neuroepithelial cells and produce spindle alignment defe

61 tion, DAPLE localizes to apical junctions of neuroepithelial cells and promotes apical cell constrict

62 is driven by neuronal progenitors, including neuroepithelial cells and radial glia.

63 ment, CPECs differentiate from preneurogenic neuroepithelial cells and require bone morphogenetic pro

64 We first isolate early neuroepithelial cells and show their broad Notch-depende

65 s and is required for apical constriction of neuroepithelial cells and subsequent neural plate bendin

66 migration differentially positions nuclei in neuroepithelial cells and therefore influences selection

67 iating adhesion and signaling events between neuroepithelial cells and vascular endothelial cells.

68 to be expressed along the apical surfaces of neuroepithelial cells and was coexpressed with Shh in th

69 n contrast, proliferation of MEKK4-deficient neuroepithelial cells appeared to be largely unaffected.

70 trations ([Ca2+]i) in proliferating cortical neuroepithelial cells are markedly dependent on Ca2+ ent

71 In the following 10 d, these neuroepithelial cells are specified to OLIG2-expressing

72 Neuroepithelial cells are transformed into asymmetricall

73 ches, we show that dystroglycan functions in neuroepithelial cells as an extracellular scaffold to ma

74 It was widely localized in retinal neuroepithelial cells at 1 day postfertilization (dpf),

75 These results suggest that the remaining neuroepithelial cells at later stages of animal life are

76 Neuroepithelial cells at the medial edge of the OOA, sho

77 We show that, whereas most retinal neuroepithelial cells divide with their mitotic spindles

78 is localized to apical adhesive junctions of neuroepithelial cells during neurulation and that Xena k

79 uced swollen/enlarged ER lumens in embryonic neuroepithelial cells during neurulation.

80 ex, sequential transcriptional programs take neuroepithelial cells from proliferating progenitors to

81 rreversible retraction of the endfeet of the neuroepithelial cells from the vitreal surface of the re

82 gene expression between neuroblasts and the neuroepithelial cells from which they derive.

83 Neuroepithelial cells further yield successive Notch-dep

84 ion strategy involves symmetrically dividing neuroepithelial cells generating large numbers of asymme

85 Our results indicate that neuroepithelial cells have all the necessary components

86 Neuroepithelial cells in both mutants fail to apically c

87 The architecture of primary cilia on neuroepithelial cells in Pam(-/-) mouse embryos was also

88 not support the commonly held view that most neuroepithelial cells in the embryonic CNS VZ are stem c

89 Whereas neuroepithelial cells in the medial OPC directly convert

90 g stem cells, which comprise the majority of neuroepithelial cells in the ventricular zone (VZ) of th

91 Here, we report that apicobasally polarized neuroepithelial cells in Xenopus laevis have a shorter c

92 Neuroepithelial cells infected with Toxoplasma type I ex

93 opment, from a seemingly homogenous sheet of neuroepithelial cells into a complex structure that is t

94 dium and drives the sequential transition of neuroepithelial cells into neuroblasts.

95 l expansion of the Olig1/Olig2 expression in neuroepithelial cells into the Nkx2.2 domain and a conse

96 Production of astrocytes from cultured neuroepithelial cells is hedgehog independent, whereas o

97 ural tube, and forced expression of Foxj1 in neuroepithelial cells is sufficient to increase cilia le

98 ce of focal adhesions in dissociated retinal neuroepithelial cells isolated from St 25 embryos.

99 urons, like projection neurons, develop from neuroepithelial cells located near the ventricular layer

100 ound in cobblestone lissencephalies in which neuroepithelial cells migrate into superficial layers of

101 port that the knockdown of Htt expression in neuroepithelial cells of neocortex results in disturbed

102 determined that NDE1 is highly expressed in neuroepithelial cells of the developing cerebral cortex,

103 t is a major challenge to understand how the neuroepithelial cells of the developing CNS choose betwe

104 l, human PSCs are first induced to primitive neuroepithelial cells over 10 d, and then patterned to N

105 re, with peak CPEC competency correlating to neuroepithelial cells rather than radial glia.

106 NA and protein was specifically expressed in neuroepithelial cells surrounding retinal axons at the o

107 lian taste buds are comprised of specialized neuroepithelial cells that act as sensors for molecules

108 aste buds are aggregates of 50-100 polarized neuroepithelial cells that detect nutrients and other co

109 c spindle alignment in Drosophila optic lobe neuroepithelial cells through aPKC activity-dependent my

110 The ability of neuroepithelial cells to generate a diverse array of neu

111 This permits the underlying neuroepithelial cells to invade the spinal canal and obs

112 ur studies establish that the progression of neuroepithelial cells to neuroblasts is regulated by Not

113 period that ends as they differentiate from neuroepithelial cells to neuronogenic radial glia.

114 l stem cells (NSCs) undergo transitions from neuroepithelial cells to radial glial cells (RGCs), and

115 ion is highly reminiscent of the switch from neuroepithelial cells to radial glial cells in the devel

116 at Notch signalling augments the response of neuroepithelial cells to Shh, leading to the induction o

117 or Cx43 in which Cx43 acts through non-crest neuroepithelial cells to suppress cellular delamination

118 olecular biology techniques in both cultured neuroepithelial cells treated with a GCN5 inhibitor and

119 Neuroepithelial cells undergo a cell cycle arrest before

120 Cocultures of hES cell-derived neuroepithelial cells with exogenous astrocytes signific

121 man stem cells are first differentiated into neuroepithelial cells with or without exogenous patterni

122 ivo, yet because RGCs develop from polarized neuroepithelial cells within a polarized environment, di

123 al crest-derived, and the hypoxia-sensitive 'neuroepithelial cells' (NECs) of fish gills, whose embry

124 central nervous system (CNS) is regulated by neuroepithelial cells, although the genes and pathways t

125 romotes proliferation and differentiation of neuroepithelial cells, and identify Decorin as a novel n

126 ave transiently suppresses Notch activity in neuroepithelial cells, and that inhibition of Notch trig

127 ulation, which underlies constriction of the neuroepithelial cells, and that ultimately drive neural

128 al expression of specific metabolic genes in neuroepithelial cells, but not in neuroblasts, and highl

129 he surrounding brain parenchyma, composed of neuroepithelial cells, glia, and neuronal precursors.

130 inantly localizes to the basolateral side of neuroepithelial cells, promotes the enlargement of the n

131 niche is composed of a diverse repertoire of neuroepithelial cells, radial glia (RG), and intermediat

132 serve nuclear movements in zebrafish retinal neuroepithelial cells, we show that, except for brief ap

133 Neuroblasts originate from neuroepithelial cells, which are polarized along the api

134 expanding cores of undifferentiated mitotic neuroepithelial cells, which can be tumorigenic.

135 eks, hESCs are induced to differentiate into neuroepithelial cells, which form neural tube-like roset

136 The Drosophila optic lobe develops from neuroepithelial cells, which function as symmetrically d

137 P4 to generate dCPECs from human ESC-derived neuroepithelial cells.

138 ng members of the Notch pathway expressed in neuroepithelial cells.

139 rical divisions of polarized radial glial or neuroepithelial cells.

140 f BrdU impairs the proliferative behavior of neuroepithelial cells.

141 re significantly heterogeneous among retinal neuroepithelial cells.

142 forebrain neurectodermal cells to specified neuroepithelial cells.

143 h neutral red and appear to be the branchial neuroepithelial cells.

144 ma3d inhibits the proliferation of hindbrain neuroepithelial cells.

145 tid body Type I (glomus) cells and pulmonary neuroepithelial cells.

146 ell polarity in neoplastic transformation of neuroepithelial cells.

147 localization and cell fate determination in neuroepithelial cells.

148 e vertebrate retina develops from a sheet of neuroepithelial cells.

149 al life are derived from the Nkx6.1+ ventral neuroepithelial cells.

150 nd adherens-junctions within chick and mouse neuroepithelial cells.

151 oteins on the vitreal endfeet of the retinal neuroepithelial cells.

152 ed in proliferating, undifferentiated retina neuroepithelial cells.

153 ehog protein, ptc-2, is expressed by retinal neuroepithelial cells.

154 orts neurulation by stimulating autophagy in neuroepithelial cells.

155 erved in zebrafish lens epithelial cells and neuroepithelial cells.

156 vered along with rare clusters of persistent neuroepithelial cells.

157 transcriptional program similar to embryonic neuroepithelial cells.

158 resent in the developing neural tube (E10.5, neuroepithelial cells; NEP) were examined for the expres

159 cells acquire apicobasal polarity and adopt neuroepithelial character prior to other regions of the

160 d early depletion of adenylyl cyclase III in neuroepithelial cilia, implicating deficient pathway rep

161 This neuroepithelial circuit can serve as both a sensory cond

162 This neuroepithelial circuit was reconstituted in vitro by co

163 Classic sensory systems rely on neuroepithelial circuits to convert stimuli into signals

164 Treatment of dissociated mouse cortical neuroepithelial cluster cell cultures with the NO syntha

165 Regular dissociation of the neuroepithelial clusters in suspension, and in the prese

166 rchestrates the differential growth of optic neuroepithelial compartments during vertebrate eye devel

167 The optic neuroepithelial continuum of vertebrate eye develops int

168 Cell expulsion through neuroepithelial contraction represents a mechanism for r

169 the lumen of the nasal cavity than are their neuroepithelial counterparts, therefore having quicker a

170 These findings identify neuroepithelial cross-talk as a potential novel target i

171 of the ECM in the development of complex 3D neuroepithelial cysts that recapitulate key steps in ear

172 This suggests that the neuroepithelial default state is IPC-like, whereas OPC i

173 aring loss and vestibular dysfunction due to neuroepithelial defects in the inner ear.

174 aring loss and vestibular dysfunction due to neuroepithelial defects in the inner ear.

175 se cortical progenitors, we found that early neuroepithelial deletion of ciliary Arl13b led to a reve

176 growth factor A (VEGF) isoforms during early neuroepithelial development in the mammalian central ner

177 ch pathway, known to be involved in cochlear neuroepithelial development.

178 The process of neuroepithelial differentiation from human pluripotent s

179 pothesized that hypomethylation of Pax3 upon neuroepithelial differentiation may be inhibited by hype

180 egulators, including E2f1 and CyclinD, delay neuroepithelial differentiation, and Fat-Hippo signaling

181 ctrum of neural tube defects associated with neuroepithelial disorganization and enhanced progenitor

182 ns intrathalamica (ZLI), a transverse linear neuroepithelial domain in the alar plate of the dienceph

183 genetic manipulations, we found that one IPC neuroepithelial domain progressively transformed into mi

184 scription factor MITF plays central roles in neuroepithelial domain specification and differentiation

185 , the Pax proteins start being detectable in neuroepithelial domains.

186 sic fibroblast growth factor), activated the neuroepithelial enhancer of the nestin gene, and gave ri

187 We found neuroepithelial expression of the genes during prenatal

188 to their correct location before they adopt neuroepithelial fate.

189 xpression of Tbeta4 led to the production of neuroepithelial folds resembling gyri and sulci, which a

190 s characterization of Fat-Hippo signaling in neuroepithelial growth and differentiation also provides

191 d pressure during development, we found that neuroepithelial growth depends on not only chemical morp

192 d in the progression of stem cells along the neuroepithelial-->radial glia-->astrocyte lineage.

193 permanent hearing loss through apoptosis of neuroepithelial hair cells and afferent neurons of the c

194 ce ectoderm shows a shift from epithelial to neuroepithelial identity (with ectopic expression of N-c

195 SC colonies at 3% O(2), where they acquire a neuroepithelial identity over a period of 2 weeks.

196 d-B) caused the transformation of OPC to IPC neuroepithelial identity.

197 Olfactory neuroepithelial injury included loss of olfactory neuron

198 However, after experimentally induced neuroepithelial injury, ckPCs are activated such that th

199 one, disrupted cell adhesion and compromised neuroepithelial integrity.

200 Our study uncovers early mesenchymal-neuroepithelial interactions that have long-range effect

201 ed in restricted dorsoventral domains of the neuroepithelial layer at early developmental stages (E2.

202 The membrane fraction of the neuroepithelial layer of the rat exhibited Ca(2+)-depend

203 ated and transmitted during the folding of a neuroepithelial layer.

204 e produced during the larval period from two neuroepithelial layers called the outer and inner optic

205 mode of axogenesis and dendritogenesis from neuroepithelial-like processes may act to preserve neigh

206 mark for the production of similar long-term neuroepithelial-like stem cells (lt-NES) from pluripoten

207 bouton (B) afferents distinguished by their neuroepithelial locations into BT units near the torus a

208 m cell markers Thy-1, c-kit, and CD34 or the neuroepithelial marker neural cell adhesion molecule 1.

209 r glia partially dedifferentiate, re-express neuroepithelial markers and re-enter the cell cycle.

210 ent with ethanol induction of cell cycle and neuroepithelial maturation in the absence of apoptosis.

211 onal knockout of the small GTPase Cdc42 from neuroepithelial (NE) and radial glial (RG) cells in the

212 re we find that cell cycle dynamics of human neuroepithelial (NE) cells differ from radial glial (RG)

213 Pluripotent stem cells are induced to form neuroepithelial (NE) cells that form neural tube-like ro

214 igoneuronal precursors, neuronal precursors, neuroepithelial/neural crest precursors, or astrocyte pr

215 Neuroepithelial organization is first apparent at the ma

216 Here we show that proper neuroepithelial organization maintained by RhoA GTPase i

217 The early neuroepithelial organization of the eye field requires L

218 of NSCs, a property tightly linked to their neuroepithelial origin, appear to be the key determinant

219 Differences in neuroepithelial patterning and neurogenesis modes contri

220 l that alphaE-catenin is highly expressed in neuroepithelial precursor cells in the developing cortic

221 have enlarged lateral ventricles lined with neuroepithelial precursor cells, reflecting an expansion

222 n the lateral ganglionic eminence (LGE), the neuroepithelial precursor of the neostriatum.

223 By E15, expansion of the neuroepithelial precursor pool is complete and any decre

224 nic subcortical telencephalon where distinct neuroepithelial precursors generate defined interneuron

225 ll subset of OPCs arise from common olig2(+) neuroepithelial precursors in rhombomeres r5 and r6, but

226 de that (1) Fgfr3 marks astrocytes and their neuroepithelial precursors in the developing CNS and (2)

227 (mTERT) prevented telomere collapse and the neuroepithelial precursors produced continued to divide,

228 les are derived from proliferative pcdh19(+) neuroepithelial precursors.

229 ormal neuronal differentiation, with loss of neuroepithelial progenitor cell phenotype in the subvent

230 During retinal development, neuroepithelial progenitor cells divide in either a symm

231 n at early developmental stages when retinal neuroepithelial progenitor cells predominate, we sought

232 are the only glial cell type produced by the neuroepithelial progenitor cells that generate the verte

233 network and signaling processes in polarized neuroepithelial progenitor cells.

234 addition at the pallial edge from a discrete neuroepithelial progenitor pool of the posterior telence

235 e and cell-cell interactions of radial glial neuroepithelial progenitors by the Lis1-Nde1 complex is

236 nascent cell-cell adhesion clusters between neuroepithelial progenitors contribute to define orienta

237 ons differentiated, more dorsally positioned neuroepithelial progenitors descended to the pMN domain

238 Understanding how ventral neuroepithelial progenitors differentiate into MSNs is c

239 r heighten the potential for using olfactory neuroepithelial progenitors for future autologous cell r

240 The transition of dividing neuroepithelial progenitors to differentiated neurons an

241 are positioned within the apical membrane of neuroepithelial progenitors, we hypothesized that loss o

242 ulates the integrity and cytoarchitecture of neuroepithelial progenitors.

243 retina are generated from common pool(s) of neuroepithelial progenitors.

244 s as well as N-CAM-positive, nestin-positive neuroepithelial progenitors.

245 factor receptor (EGFR) activation to promote neuroepithelial proliferation and neuroblast formation.

246 n of actin-associated processes in directing neuroepithelial proliferation.

247 roglial characteristics but retain important neuroepithelial properties.

248 each olfactory lamella but scattered in the neuroepithelial region.

249 loss of Lgl1 in mice results in formation of neuroepithelial rosette-like structures, similar to the

250 ndbrain develops as a series of well-defined neuroepithelial segments or rhombomeres.

251 eodomain proteins-Vax1 and Vax2-control this neuroepithelial segregation.

252 n alleles affect the polarity of the retinal neuroepithelial sheet and, unexpectedly, both result in

253 c failure of hingepoint formation, defective neuroepithelial sheet-bending, and failure of neural tub

254 Here, we show that hindbrain neuroepithelial stem (hbNES) cells can be derived and ma

255 xpression in primary human hindbrain-derived neuroepithelial stem (hbNES) cells or iPSC-derived NES c

256 ed pluripotent stem (iPS) cell-derived human neuroepithelial stem (NES) cells generated from a Gorlin

257 Here, we evaluated neuroepithelial stem (NES) cells, representative of cere

258 Nestin, a neuroepithelial stem cell marker, was enriched in the OB

259 cal role for elf in the development of a SVZ neuroepithelial stem cell phenotype and regulation of ne

260 control of symmetric division, essential for neuroepithelial stem cell proliferation, is mediated thr

261 the orderly developmental transition from a neuroepithelial stem cell to a functional neuron.

262 conducted gene expression profiling of human neuroepithelial stem cell-derived neurons, stimulated wi

263 , suggesting a sequential differentiation of neuroepithelial stem cells (NEPs) to GRPs to ARPs and th

264 bryonic spinal cord, for example, a group of neuroepithelial stem cells (NSCs) generates motor neuron

265 ntrol of mitotic spindle orientation in both neuroepithelial stem cells and radial glial progenitor c

266 odermal domain that combines slowly dividing neuroepithelial stem cells and rapidly amplifying progen

267 lia of the mouse cerebral cortex emerge from neuroepithelial stem cells around embryonic day 11 and p

268 OPCs develop from the same neuroepithelial stem cells as neurons, can be reprogramm

269 Neuroepithelial stem cells contact CSF-filled ventricles

270 the first demonstration of highly expandable neuroepithelial stem cells derived from the human embryo

271 Mammalian neuroepithelial stem cells divide using a polarized form

272 We found that induction of cortical neuroepithelial stem cells from human ES cells and human

273 ctory loss, caused by a functional switch of neuroepithelial stem cells from regeneration to immune d

274 (RGPC) neurogenesis, but its role earlier in neuroepithelial stem cells is poorly understood.

275 est that, during nervous system development, neuroepithelial stem cells may not only be responsible f

276 deletion and severe apoptosis of the founder neuroepithelial stem cells, accompanied by increased hor

277 sors are sequentially generated in vivo from neuroepithelial stem cells, but do not share a common li

278 t of generation of GRP cells from totipotent neuroepithelial stem cells, of O2A/OPCs from GRP cells a

279 in a cell lineage-specific manner, mainly in neuroepithelial stem cells, radial glia, and astrocytes.

280 Controlled gene deletion of Lis1 in vivo in neuroepithelial stem cells, where cleavage is uniformly

281 a glial-restricted precursor (GRP) cell from neuroepithelial stem cells.

282 demonstrate that RhoA functions to maintain neuroepithelial structures in the developing spinal cord

283 mitotic populations that were present in the neuroepithelial subventricular zone of the developing ne

284 djacent retinal cell divisions at the apical neuroepithelial surface.

285 s in each of these structures in the tongue, neuroepithelial taste cells of the taste bud, and, possi

286 Our data suggest that epithelial cells, neuroepithelial taste cells, or olfactory sensory neuron

287 osensory machinery discovered in specialized neuroepithelial taste receptor cells of the lingual epit

288 fate ectopically and fail to transition from neuroepithelial to cuboidal shape.

289 ary identify Fgf10 as a key regulator of the neuroepithelial to radial glial transition and subsequen

290 Neuroepithelial transforming gene 1 (Net1) is a RhoA gua

291 Neuroepithelial transforming gene 1 (Net1) is a RhoA-sub

292 pithelioma is the second most common primary neuroepithelial tumor of the eye.

293 ration (CNS HGNET-MN1)," and "CNS high-grade neuroepithelial tumor with BCOR alteration (CNS HGNET-BC

294 C alteration (CNS EFT-CIC)," "CNS high-grade neuroepithelial tumor with MN1 alteration (CNS HGNET-MN1

295 The ciliary body epithelial and neuroepithelial tumors (adenoma, adenocarcinoma, and med

296 of the motor cortex in patients with primary neuroepithelial tumors of the central nervous system (CN

297 euroblastic rosettes that resemble primitive neuroepithelial tumors.

298 e diagnoses of low-grade epilepsy associated neuroepithelial tumour (LEAT), vascular malformation, an

299 y from three common causes, dysembryoplastic neuroepithelial tumours (DNTs; eight cases), focal corti

300 erotopia and lissencephaly, dysembryoplastic neuroepithelial tumours, and microdysgenesis.