ライフサイエンスコーパス: neuroepithelium

1 le aligned perpendicular to the plane of the neuroepithelium).

2 dulated by diabetes in the murine developing neuroepithelium.

3 during initial delamination of NCCs from the neuroepithelium.

4 by a striking reorganization of the sensory neuroepithelium.

5 ue to impaired stretching of the surrounding neuroepithelium.

6 s, radially oriented, and spanned the entire neuroepithelium.

7 nsion depend on the contractile state of the neuroepithelium.

8 but its foundation is laid in the primitive neuroepithelium.

9 allow neural crest cells to escape from the neuroepithelium.

10 progenitor production and elongation of the neuroepithelium.

11 1 confined to the apical side of the retinal neuroepithelium.

12 rvation is relatively uniform throughout the neuroepithelium.

13 ng progenitors are found medially within the neuroepithelium.

14 onasal retina, through the remaining retinal neuroepithelium.

15 ate and their progeny fully reconstitute the neuroepithelium.

16 stnatal volumetric growth in the vomeronasal neuroepithelium.

17 of sensory epithelia from the primitive otic neuroepithelium.

18 ished as daughter cells reintegrate into the neuroepithelium.

19 VCAM-1 in the mucosal tip compared with the neuroepithelium.

20 than via peripheral nerves or the olfactory neuroepithelium.

21 KK4) is strongly expressed in the developing neuroepithelium.

22 o structures develop from the same embryonic neuroepithelium.

23 al transition (EMT), and delaminate from the neuroepithelium.

24 ressed in the developing otic capsule and/or neuroepithelium.

25 he nervous system, and to a repellent in the neuroepithelium.

26 ediated cell segregation occurs in the early neuroepithelium.

27 ical progenitors in the dorsal telencephalic neuroepithelium.

28 gulating Olig gene expression in the ventral neuroepithelium.

29 ately responsible for regenerating olfactory neuroepithelium.

30 originate from the ventral, but not dorsal, neuroepithelium.

31 of differentiated neurons from a homogeneous neuroepithelium.

32 but exhibits an enlarged lumen and abnormal neuroepithelium.

33 adjacent non-overlapping domains of ventral neuroepithelium.

34 ied developmental defects in the ventricular neuroepithelium.

35 provide structural support for the auditory neuroepithelium.

36 ssues, including heart muscle, epidermis and neuroepithelium.

37 egation of the neural crest lineage from the neuroepithelium.

38 ing a role in neural patterning in the optic neuroepithelium.

39 to receptor proteins provided by the retinal neuroepithelium.

40 n of +Rho-mediated actin assembly within the neuroepithelium.

41 glia are widespread components of the early neuroepithelium.

42 te the expression of NKX2.1 as they exit the neuroepithelium.

43 3 is expressed predominantly in the immature neuroepithelium.

44 system derives from dorsally located rhombic neuroepithelium.

45 ion and cell proliferation in the developing neuroepithelium.

46 cells and afferent processes in the sensory neuroepithelium.

47 veloping lung, liver, and kidney, as well as neuroepithelium.

48 towards cell cycle controls in the germinal neuroepithelium.

49 s, are required for maintenance of the adult neuroepithelium.

50 each their appropriate entry points into the neuroepithelium.

51 soderm cells, as well as cells from adjacent neuroepithelium.

52 pronounced apical-basal contractions of the neuroepithelium.

53 for planar spindle orientation in the chick neuroepithelium.

54 he germinative zone of the earliest cortical neuroepithelium.

55 the FBM neurons and extrinsically within the neuroepithelium.

56 ral and targeted predominantly the olfactory neuroepithelium.

57 gesting that glia cells communicate with the neuroepithelium.

58 tachment of differentiating neurons from the neuroepithelium.

59 termined by its boundaries with the adjacent neuroepithelium.

60 dherens junctions and disorganization of the neuroepithelium.

61 he detachment of its apical process from the neuroepithelium.

62 are making use of the developing fly retinal neuroepithelium.

63 , they detach from the apical surface of the neuroepithelium.

64 the neural crest, which is derived from the neuroepithelium.

65 nds also on the distribution of fluid in the neuroepithelium.

66 t E9.5, the primitive stem cell stage of the neuroepithelium.

67 anchiopods, and that they also remain in the neuroepithelium.

68 in the maintenance of the neuroblasts in the neuroepithelium.

69 the neural precursor population of the early neuroepithelium.

70 roperties before their delamination from the neuroepithelium.

71 cial ectoderm and the adjacent telencephalic neuroepithelium.

72 distinguish these cells from the rest of the neuroepithelium.

73 identity, during differentiation of hESCs to neuroepithelium, a neuroectoderm-specific subset of pois

74 chment and generation of motility within the neuroepithelium, a process that has been poorly understo

75 indles oriented parallel to the plane of the neuroepithelium, a substantial minority divides with the

76 henotype is already expressed in the retinal neuroepithelium affecting morphology of the neuroepithel

77 Here we show that the repair of neuroepithelium after lesioning is accompanied by an acu

78 ackscatter microscopy to label the forebrain neuroepithelium and a modified retroviral lineage librar

79 progenitor cells derived from human cortical neuroepithelium and assessed its effects on the cellular

80 ural crest cells that emerge from the dorsal neuroepithelium and coalesce into segmental streams that

81 maintenance of Shh expression in the ventral neuroepithelium and differences in dorsal tissue respons

82 ium and the presence of hematomas within the neuroepithelium and disruption of the basement membrane

83 unication between two developing organs, the neuroepithelium and embryonic blood vessels.

84 rate asymmetric cell division and vertebrate neuroepithelium and epithelial progenitor differentiatio

85 Erm, Pea3, and Er81 in the rostral cortical neuroepithelium and FC regionalization.

86 domyoblasts effaced all but trace amounts of neuroepithelium and generated a distant metastasis entir

87 ignaling in an autocrine manner in the optic neuroepithelium and in a paracrine manner in the lens ec

88 during the development of the telencephalic neuroepithelium and in glioblastoma brain tumor cells.

89 ) is expressed in the mid-dorsal optic tract neuroepithelium and in the axons of developing retinal g

90 vicinity of junctional complexes in retinal neuroepithelium and in the photoreceptor cell layer.

91 ry receptor neurons throughout the olfactory neuroepithelium and in virtually all glomeruli in the ma

92 enous tissue repair by a highly regenerative neuroepithelium and introduce a system to study the mech

93 Pax3, a gene that is expressed in embryonic neuroepithelium and is required for neural tube closure.

94 ulations in the chick to demonstrate that r3 neuroepithelium and its overlying surface ectoderm indep

95 erived from the H-2Kb-tsA58 transgenic mouse neuroepithelium and labelled with [3H]thymidine, were in

96 ior to optic cup formation in both the optic neuroepithelium and lens ectoderm.

97 Placodes form in both the optic neuroepithelium and lens ectoderm.

98 mily, alpha10 (CHRNA10), from both inner-ear neuroepithelium and lymphoid tissue.

99 initially arise in restricted regions of the neuroepithelium and migrate relatively long distances to

100 at disrupts both convergent extension in the neuroepithelium and PCP in the cochlea does not disrupt

101 rtical basement membrane located between the neuroepithelium and pia-meninges.

102 ) embryos is predominantly restricted to the neuroepithelium and remains prominent in neural progenit

103 between apical and basal neurons of the VNO neuroepithelium and rostral versus caudal AOB glomeruli,

104 ion, with major defects in the heart muscle, neuroepithelium and skin epithelium, all of which posses

105 ith antioxidants minimizes cell death in the neuroepithelium and substantially ameliorates or prevent

106 lly restricted to the central nervous system neuroepithelium and temporally controlled with doxycycli

107 tion that forms at the interface between the neuroepithelium and the prospective epidermis of a devel

108 ural fold tips, at the interface between the neuroepithelium and the surface ectoderm, are required f

109 MGE promotes time-dependent survival of this neuroepithelium and the time-dependent specification of

110 neural crest cells are segregated within the neuroepithelium and then delaminate from the neural tube

111 at Notch mutant clones are extruded from the neuroepithelium and undergo premature neurogenesis.

112 is subsequently expressed in the developing neuroepithelium and urogenital ridge.

113 The cyclase was cloned from the neuroepithelium and was found to be identical in structu

114 e most caudomedial edge of the telencephalic neuroepithelium) and found that these mice faithfully re

115 p as retinal tissue, polarity of the retinal neuroepithelium, and confinement of cell divisions to th

116 re-intercalation of daughter cells into the neuroepithelium, and results in ectopic neural progenito

117 oglial cells were visualized penetrating the neuroepithelium; and 3) CX3CR1 and CCR2 distinguished in

118 prechordal (rostral) and epichordal (caudal) neuroepithelium, anteroposterior encroachment of alar lu

119 Cell fates in the optic neuroepithelium are determined by the combinational acti

120 defects that originate exclusively from the neuroepithelium as a result of the simultaneous loss of

121 BLBP is expressed in the rat neuroepithelium as early as E12.5 when there is little o

122 otes Wnt8c expression, which persists in the neuroepithelium as FGF signalling declines.

123 y placode/epidermal ectoderm, and underlying neuroepithelium, as well as the emerging mandibular and

124 it reduced cell proliferation in the rostral neuroepithelium at 10 somites, followed by increased cel

125 sent in well outlined regions of the ventral neuroepithelium at 5 GW, several weeks before oligodendr

126 tructures of the amygdala originate from the neuroepithelium at both sides of the pallial-subpallial

127 is expressed ubiquitously in the ventricular neuroepithelium at embryonic day 10.5 (E10.5) but displa

128 retina, Ush2a mRNA expression appears in the neuroepithelium at embryonic day 17.

129 lay short and stubby cilia on the developing neuroepithelium at embryonic day 9.5 (E9.5).

130 expressed diffusely throughout the cortical neuroepithelium at embryonic days 16 and 17 in the rat,

131 eduction in MKK4 activity in MEKK4-deficient neuroepithelium at sites of neural tube closure.

132 oliferating neuronal progenitor cells of the neuroepithelium, becomes down-regulated during neuronal

133 vergent extension in both axial mesoderm and neuroepithelium, before the onset of neurulation.

134 und that these inductions are limited to the neuroepithelium between the ZLI and the forebrain-midbra

135 The rhombic lip is a discrete strip of neuroepithelium bordering the roofplate of the fourth ve

136 y delete Lhx2 in posteroventral hypothalamic neuroepithelium, both embryonically and postnatally.

137 lusters of cells (proneural clusters) in the neuroepithelium but expression becomes restricted to the

138 ral ganglionic eminence and frontal cortical neuroepithelium but not medial or caudal ganglionic emin

139 pons (RP), enabling rapid innervation of the neuroepithelium by differentiated noradrenergic neurons

140 nin protein forms a honeycomb pattern in the neuroepithelium by labeling the cell periphery in a typi

141 euron progenitor (pMN) domain of the ventral neuroepithelium by the ventral midline signal Sonic hedg

142 bly shortened body axis, convoluted anterior neuroepithelium, caudal dysgenesis, and failure of chori

143 sulted in distinct signals in the developing neuroepithelium, cerebellum, heart, lung, liver, teeth,

144 of neurons that are highly dispersed in the neuroepithelium, consistently coexpress either G alpha(i

145 The olfactory neuroepithelium contained a Ca(2+) binding protein, neur

146 ly proliferative cells even in the primitive neuroepithelium, demonstrating heterogeneity in cell pot

147 ural tube, a markedly increased abundance of neuroepithelium-derived cells outside of the neural tube

148 lacking itgbeta8 from cells derived from the neuroepithelium did not show signs of hemorrhage.

149 ression begins at the time that cells in the neuroepithelium differentiate into neuroblasts.

150 pathway in nasal mucosae-respiratory tracts-neuroepithelium environment in the protection against mi

151 subsequently also found in the rat olfactory neuroepithelium, especially at the apical junctional bel

152 invasion and migration of blood vessels into neuroepithelium, establishment of BBB properties, and ex

153 epithelium are capable of reconstituting the neuroepithelium even after severe damage.

154 The ventricular neuroepithelium exhibited focalized increase of cell pro

155 ogenitor cells dissociated from rat cortical neuroepithelium express muscarinic acetylcholine recepto

156 SCN is derived from a distinct region of the neuroepithelium expressing a combination of developmenta

157 Radial glial progenitors span the neuroepithelium, extending long basal processes to form

158 tion of hair cells into rows during cochlear neuroepithelium extension.

159 nesis, OAZ is highly expressed at the dorsal neuroepithelium flanking the roof plate.

160 As the neuroepithelium folds during corticostriatal sulcus form

161 l is retracted cleanly from the lumen of the neuroepithelium, followed by movement of the cell body o

162 Failure of this migration during neuroepithelium formation leads to ectopic determination

163 that are specifically expressed in zones of neuroepithelium from which oligodendrocyte precursors em

164 ei are scattered continuously throughout the neuroepithelium, from anteroventral to posteromedial.

165 x gene Lhx2, which is expressed in the optic neuroepithelium, fulfils such a role.

166 In the olfactory neuroepithelium, globose basal cells (GBCs) are consider

167 Newborn mice lacking itgbeta8 from the neuroepithelium had hemorrhages in the cortex, ganglioni

168 Targeted deletion of itgbeta8 from the neuroepithelium, however, resulted in bilateral hemorrha

169 The rhombic lip (RL) is the neuroepithelium immediately adjacent to the roof plate o

170 al abnormalities associated with the retinal neuroepithelium in albino mice, is consistent with other

171 .5 transgene expression is restricted to the neuroepithelium in dorsal retina, and by E14.5 only imma

172 Analyses of the neuroepithelium in MEKK4-deficient embryos showed massiv

173 between the apical and basal surfaces of the neuroepithelium in phase with their cell cycle, a proces

174 yolk sac and in periventricular cells of the neuroepithelium in the brain.

175 Pyramidal cells are derived from the neuroepithelium in the cortical ventricular zone, and us

176 junctions and causes disorganization of the neuroepithelium in the developing nervous system.

177 opment revealed that the anterior cerebellar neuroepithelium in the early embryonic cerebellum was ex

178 e initially expressed in distinct domains of neuroepithelium in young embryos.

179 ot disrupt Dvl2 membrane distribution in the neuroepithelium, in contrast to its drastic effect on Dv

180 previously unrecognized role for mesenchyme-neuroepithelium interactions in the mid-hindbrain during

181 ment of the cerebral cortex from a primitive neuroepithelium into a complex laminar structure underly

182 ate retina develops from an undifferentiated neuroepithelium into an organized and laminated structur

183 Differentiation of the pluripotent neuroepithelium into neurons and glia is accomplished by

184 ing nervous system: subdivision of the early neuroepithelium into precursors with distinct molecular

185 Transplantation of BrdU-labeled MGE or LGE neuroepithelium into the basal telencephalon of unlabele

186 demonstrate that bipotentiality of the optic neuroepithelium is associated with the initial coexpress

187 support the view that the bipotential optic neuroepithelium is characterized by overlapping gene exp

188 Expression of Nkx6.1 in the remaining neuroepithelium is closely associated with, and regulate

189 the mid-hindbrain boundary (MHB) within the neuroepithelium is dependent on the interface of Otx2 an

190 Deficiency of apical retinal neuroepithelium is indicated by altered localization of

191 Cilia outgrowth in cells of the neuroepithelium is initiated but the axonemes are severe

192 ural progenitors in the developing mammalian neuroepithelium is marked by cadherin-based adherens jun

193 Finally, cytoskeletal polarity within the neuroepithelium is perturbed in mutant embryos.

194 nal cord and that proper organization of the neuroepithelium is required for appropriate left-right m

195 Detachment of newborn neurons from the neuroepithelium is required for correct neuronal archite

196 expression within the ventral telencephalic neuroepithelium is specifically lost in the BF-1(-/-) mu

197 Since the contractile state of the neuroepithelium is tightly regulated by non-muscle myosi

198 Limbal epithelium, which, like the neuroepithelium, is ectodermally derived, participates i

199 lso develops a progressive denudation of the neuroepithelium, leading to periventricular nodule forma

200 Fate-mapping analysis after olfactory neuroepithelium lesioning shows that HBCs are competent

201 agenesis, replacement of the ventral RPE by neuroepithelium-like tissue, and ectopic expression of o

202 ate both neuronal and non-neuronal olfactory neuroepithelium lineages.

203 , is essentially a small island of olfactory neuroepithelium located bilaterally at the ventral base

204 examine their distinct dynamics in olfactory neuroepithelium maintenance and regeneration.

205 During brain morphogenesis, the neuroepithelium must fold in specific regions to delinea

206 escence and the distribution of fluid in the neuroepithelium, namely subretinal fluid or posterior re

207 The telencephalic neuroepithelium (NE) of mammalian brain has an apical-ba

208 sal cells (HBCs) function as adult olfactory neuroepithelium neural stem cells and examine their dist

209 established from cultures of adult olfactory neuroepithelium obtained from patients and cadavers as d

210 We evaluated the olfactory neuroepithelium (OE) and brain regional responses to a n

211 stnatal rat OB cells and embryonic olfactory neuroepithelium (OE) slice explants.

212 C5aR was also found to be expressed in the neuroepithelium of early human embryos.

213 cted directly into the saccular or utricular neuroepithelium of fascicularis (Macaca fascicularis) or

214 In the neuroepithelium of neurulating embryos, Dvl2 shows DEP d

215 , and the elevated apoptosis observed in the neuroepithelium of the Cited2(-/-) mutants was apparentl

216 Sox2 is expressed highly in the neuroepithelium of the developing CNS and has been shown

217 Wnt7b encode two Wnt ligands produced by the neuroepithelium of the developing CNS coincident with va

218 lar pontine neurons from their origin in the neuroepithelium of the dorsal hindbrain to the ventral m

219 he generation of neural crest cells from the neuroepithelium of the dorsal neural tube.

220 Radial glial cells (RGCs) in the ventricular neuroepithelium of the dorsal telencephalon are the prog

221 n and migration are crucial to transform the neuroepithelium of the embryonic forebrain into the adul

222 The organ of Corti, the auditory neuroepithelium of the inner ear in mammals, consists of

223 Upon morphogenesis, the simple neuroepithelium of the optic vesicle gives rise to four

224 mbryonic surface ectoderm and the underlying neuroepithelium of the optic vesicle.

225 The vertebrate eye develops from the neuroepithelium of the ventral forebrain by the evaginat

226 which has three major components: olfactory neuroepithelium, olfactory bulb, and olfactory cortex.

227 e 1 (LTh-1) redirected TT into the olfactory neuroepithelium (ON/E).

228 In contrast, olfactory neuroepithelium (ONe) located in the nasal passageways h

229 rchitectures such as a multilayered cortical neuroepithelium or an entire optic cup.

230 cursors as a cell culture model of embryonic neuroepithelium or neural crest.

231 o BLM activity was detected in the olfactory neuroepithelium or OSNs.

232 e not significantly altered in the embryonic neuroepithelium or within the postnatal subventricular z

233 letal regulators Rac1 or Cdc42 in the dorsal neuroepithelium, or in the surface ectoderm, we show tha

234 fy the developmental competence of the optic neuroepithelium over time and thereby provide a mechanis

235 o the apical region of the retinal and brain neuroepithelium, partially overlapping the adherens junc

236 nal ganglion cells from the undifferentiated neuroepithelium peripheral to the expanding wave front o

237 Loss of RelA in the regenerating neuroepithelium perturbs the homeostasis between prolife

238 urogenic niches can be viewed as "displaced" neuroepithelium, pockets of cells and local signals that

239 beta8 integrin in the neuroepithelium promotes the activation of extracellular

240 ns of the midbrain and hindbrain ventricular neuroepithelium, raising the possibility that Foxa2 acti

241 ation assays we show that RA activity in the neuroepithelium regulates hindbrain patterning directly

242 ion or the maintenance of neuroblasts in the neuroepithelium represents the ancestral state.

243 results suggest that: (1) the optic vesicle neuroepithelium requires a temporally specific associati

244 of Ilk from embryonic mouse dorsal forebrain neuroepithelium results in severe cortical lamination de

245 FPC function in RGC axons or the optic tract neuroepithelium results in unexpectedly localized pathfi

246 ithelium, and less intense expression in the neuroepithelium, retina, and hindgut.

247 and Fgf17 signaling on the rostral cortical neuroepithelium, revealed by altered expression of Spry1

248 the development of the hemispherical retinal neuroepithelium (RNE), a part of the optic cup.

249 s stem and progenitor cells that support the neuroepithelium's life-long capacity to reconstitute aft

250 gate into the embryo but remain in the outer neuroepithelium, similar to vertebrate neural stem cells

251 n to identify genes enriched in the germinal neuroepithelium, so as to distinguish those expressed in

252 he CNS, with concurrent sparing of olfactory neuroepithelium, strongly suggests that invasion of the

253 glia that extend processes that ensheath the neuroepithelium, suggesting that glia cells communicate

254 e notochord, and diminished in the overlying neuroepithelium, suggesting that sonic hedgehog signalli

255 defects in apical/basal polarity within the neuroepithelium, suggesting that the cfy gene is not cri

256 ear within a region of anterior hypothalamic neuroepithelium that co-expresses mRNA encoding SHH, its

257 expression in the distal tips of the retinal neuroepithelium that form the iris and ciliary body, thu

258 activity of secondary organizers within the neuroepithelium that function by releasing diffusible si

259 over time to produce different neurons; the neuroepithelium that generates neuroblasts is also subdi

260 ombic lip (RL) is an embryonic proliferative neuroepithelium that generates several groups of hindbra

261 ate neuronal progenitors born in the dentate neuroepithelium that give rise to granule neurons.

262 The olfactory epithelium is a sensory neuroepithelium that supports adult neurogenesis and tis

263 aled virtually complete loss of the cochlear neuroepithelium (the organ of Corti) in adult mutant mic

264 pit, multiple discrete regions of underlying neuroepithelium, the mandibular and maxillary arches, in

265 o increase from 9 to 13 h in the neocortical neuroepithelium, the maximum G(1) phase length attainabl

266 yramidal cells are generated in the cortical neuroepithelium: the majority is derived from the gangli

267 vel transgene expression was detected in the neuroepithelium, there was no obvious abnormality in pro

268 ment, Foxg1 directs development of the optic neuroepithelium through transcriptional suppression of W

269 he prevailing model assumes that the dentate neuroepithelium throughout the longitudinal axis of the

270 lts demonstrate the capacity of the cortical neuroepithelium to accommodate different cortical fields

271 ing surface ectoderm and induce the adjacent neuroepithelium to assume the neuroretinal fate.

272 hanisms governing development of the retinal neuroepithelium to be probed in detail.

273 a paracrine signaling pathway that links the neuroepithelium to blood vessels and precisely balances

274 en progenitor cells migrate from the dentate neuroepithelium to establish a germinal zone in the hilu

275 o regulate the timing of the transition from neuroepithelium to neuroblast.

276 lly from the lateral ventricle dentate notch neuroepithelium to populate the tertiary matrix and form

277 cells and newly born granule cells from the neuroepithelium to the dentate gyrus remains intact.

278 Thus, HSV-1 spread from the olfactory neuroepithelium to the TG and reemerged peripherally wit

279 population that travels from the prethalamic neuroepithelium to the ventral lateral geniculate nucleu

280 SPN migrated from the neuroepithelium to the ventrolateral spinal cord and the

281 l migration (prior to E11.5) of SPN from the neuroepithelium to the ventrolateral spinal cord is simi

282 totic SPN undergo primary migration from the neuroepithelium to the ventrolateral spinal cord, and th

283 SPN in the chick first migrate from the neuroepithelium to the ventrolateral spinal cord.

284 progenitors (OLPs) originate in the ventral neuroepithelium under the influence of Sonic hedgehog (S

285 originate from restricted domains of ventral neuroepithelium under the influence of sonic hedgehog pr

286 The olfactory neuroepithelium undergoes continual neurogenesis and, af

287 the new population derives largely from the neuroepithelium ventral and rostral to the ablation.

288 Knowledge of the vomeronasal neuroepithelium (VNNE) microanatomy is disproportionatel

289 on associated with enhanced apoptosis in the neuroepithelium was also observed.

290 ntly, the differentiation of anterior vermis neuroepithelium was shifted rostrally and medially demon

291 A1 is most highly expressed in the embryonic neuroepithelium when the neural progenitors are highly p

292 hila optic lobe originate within a polarised neuroepithelium, where they divide symmetrically.

293 olated from the Fgfr1(Deltaflox) hippocampal neuroepithelium, whereas epidermal growth factor-sensiti

294 FoxD3 was abnormally retained in the dorsal neuroepithelium, whereas Sox10, which is normally requir

295 of terminals across the canalicular sensory neuroepithelium with morphophysiological studies in chin

296 tal process, Foxg1 is expressed in the optic neuroepithelium, with highest levels of expression in th

297 This correlates with an abnormal brain neuroepithelium, with no clear midline and disrupted jun

298 yer cultured hESCs into homogenous primitive neuroepithelium within 1 wk under chemically defined con

299 bular dysfunction due to degeneration of the neuroepithelium within the inner ear.

300 rs undergo dynamic rearrangements within the neuroepithelium, yielding an overall ventral to dorsal m