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1 f BrdU impairs the proliferative behavior of neuroepithelial cells.
2 erved in zebrafish lens epithelial cells and neuroepithelial cells.
3 ell polarity in neoplastic transformation of neuroepithelial cells.
4  localization and cell fate determination in neuroepithelial cells.
5 e vertebrate retina develops from a sheet of neuroepithelial cells.
6  forebrain neurectodermal cells to specified neuroepithelial cells.
7 al life are derived from the Nkx6.1+ ventral neuroepithelial cells.
8 oteins on the vitreal endfeet of the retinal neuroepithelial cells.
9 ed in proliferating, undifferentiated retina neuroepithelial cells.
10 nd adherens-junctions within chick and mouse neuroepithelial cells.
11 ehog protein, ptc-2, is expressed by retinal neuroepithelial cells.
12  musashi1) that are expressed in uncommitted neuroepithelial cells.
13 x can regulate survival and proliferation of neuroepithelial cells.
14 orts neurulation by stimulating autophagy in neuroepithelial cells.
15  neuroepithelium affecting morphology of the neuroepithelial cells.
16 o rescue the phenotype of oko meduzy retinal neuroepithelial cells.
17 rn that is consistent with its production by neuroepithelial cells.
18 ty is first detected at embryonic day 8.5 in neuroepithelial cells.
19  protein 2 (Vangl2) gene in as few as 16% of neuroepithelial cells.
20 ations and is most specifically expressed in neuroepithelial cells.
21 alyses highlight the direct CPEC origin from neuroepithelial cells.
22 vered along with rare clusters of persistent neuroepithelial cells.
23 transcriptional program similar to embryonic neuroepithelial cells.
24 P4 to generate dCPECs from human ESC-derived neuroepithelial cells.
25 ng members of the Notch pathway expressed in neuroepithelial cells.
26 rical divisions of polarized radial glial or neuroepithelial cells.
27 re significantly heterogeneous among retinal neuroepithelial cells.
28 h neutral red and appear to be the branchial neuroepithelial cells.
29 ma3d inhibits the proliferation of hindbrain neuroepithelial cells.
30 tid body Type I (glomus) cells and pulmonary neuroepithelial cells.
31  kinase activity is essential for regulating neuroepithelial cell adhesion, migration and morphogenes
32 central nervous system (CNS) is regulated by neuroepithelial cells, although the genes and pathways t
33 ptor, CXCR4, are constitutively expressed on neuroepithelial cells and are believed to be involved in
34 at mediate the transition, we microdissected neuroepithelial cells and compared their transcriptional
35  of activated Yorkie, promotes overgrowth of neuroepithelial cells and delays or blocks their differe
36 rt to a molecular state resembling embryonic neuroepithelial cells and functionally acquire rapid pro
37              In medium that allows growth of neuroepithelial cells and glial progenitors, mutant cell
38 g of postmitotic neurons is mediated through neuroepithelial cells and is necessary for guiding neuro
39 ver, Cited2 was required for the survival of neuroepithelial cells and its absence led to massive apo
40  developing mouse cortex where the expansive neuroepithelial cells and neurogenic radial glial progen
41 e/Afadin, mislocalize in dividing Eph mutant neuroepithelial cells and produce spindle alignment defe
42 tion, DAPLE localizes to apical junctions of neuroepithelial cells and promotes apical cell constrict
43 is driven by neuronal progenitors, including neuroepithelial cells and radial glia.
44 ment, CPECs differentiate from preneurogenic neuroepithelial cells and require bone morphogenetic pro
45                       We first isolate early neuroepithelial cells and show their broad Notch-depende
46 s and is required for apical constriction of neuroepithelial cells and subsequent neural plate bendin
47 rmalities in the cell adhesive properties of neuroepithelial cells and suggest that NMHC-B is essenti
48 involved in transforming epiblast cells into neuroepithelial cells and then into radial glia.
49 migration differentially positions nuclei in neuroepithelial cells and therefore influences selection
50 iating adhesion and signaling events between neuroepithelial cells and vascular endothelial cells.
51 to be expressed along the apical surfaces of neuroepithelial cells and was coexpressed with Shh in th
52  cell populations such as muscle precursors, neuroepithelial cells, and actively proliferating cells.
53 romotes proliferation and differentiation of neuroepithelial cells, and identify Decorin as a novel n
54 ave transiently suppresses Notch activity in neuroepithelial cells, and that inhibition of Notch trig
55 ulation, which underlies constriction of the neuroepithelial cells, and that ultimately drive neural
56 ntegrating NOTCH and SHH signal reception in neuroepithelial cells, and they suggest that loss of GAS
57 ic reticulum stress, caspase activation, and neuroepithelial cell apoptosis (causal events in type 1
58 (K1361R) embryos show a striking increase in neuroepithelial cell apoptosis and a dramatic loss of ph
59  predominantly leads to exencephaly, induces neuroepithelial cell apoptosis and suppresses autophagy
60 n contrast, proliferation of MEKK4-deficient neuroepithelial cells appeared to be largely unaffected.
61 tudies on CXCR4 expression and regulation in neuroepithelial cells are fundamental for understanding
62 trations ([Ca2+]i) in proliferating cortical neuroepithelial cells are markedly dependent on Ca2+ ent
63                 In the following 10 d, these neuroepithelial cells are specified to OLIG2-expressing
64                                              Neuroepithelial cells are transformed into asymmetricall
65 ches, we show that dystroglycan functions in neuroepithelial cells as an extracellular scaffold to ma
66  of the glass onion phenotype in a subset of neuroepithelial cells as well as its onset following the
67           It was widely localized in retinal neuroepithelial cells at 1 day postfertilization (dpf),
68     These results suggest that the remaining neuroepithelial cells at later stages of animal life are
69 idance molecule netrin-1 was specifically on neuroepithelial cells at the disk surrounding exiting RG
70                                              Neuroepithelial cells at the medial edge of the OOA, sho
71                            How a naive human neuroepithelial cell becomes an electrophysiologically a
72 ed cells, was widespread in undifferentiated neuroepithelial cells, before the initiation of axons.
73  initially detectable when the first retinal neuroepithelial cells began to leave the cell cycle.
74 intrinsic forces generated by alterations in neuroepithelial cell behavior, whereas bending requires
75       In cultures of dissociated neocortical neuroepithelial cells, BMPs increase the number of MAP-2
76 al expression of specific metabolic genes in neuroepithelial cells, but not in neuroblasts, and highl
77                           At cranial levels, neuroepithelial cells can regulate to generate neural cr
78 led to the retraction of the end feet of the neuroepithelial cells, caused an increase in the number
79  PKA-dependent target gene gli-1 in cultured neuroepithelial cells, concomitant with a decrease in DN
80             Endothelial coculture stimulates neuroepithelial cell contact, activating Notch and Hes 1
81 rest cells, with both the ectodermal and the neuroepithelial cells contributing to induced population
82          Alternatively, both neuroblasts and neuroepithelial cells could be capable of dividing asymm
83 gotes also manifest embryonic lethality with neuroepithelial cell death.
84 s in oxidative stress-induced DNA damage and neuroepithelial cell death.
85 inding to its RNA targets, causing premature neuroepithelial cell differentiation and reduced neuroge
86  expressed transcription factors involved in neuroepithelial cell differentiation.
87 hough they divide normally, abl(-/-)arg(-/-) neuroepithelial cells display gross alterations in their
88 , in dissociated cell cultures, some retinal neuroepithelial cells divide asymmetrically and distribu
89           We show that, whereas most retinal neuroepithelial cells divide with their mitotic spindles
90 ited only by the apical daughter cell when a neuroepithelial cell divides vertically.
91 or nonrandomly oriented (i.e., rostrocaudal) neuroepithelial cell division in longitudinal lengthenin
92 is localized to apical adhesive junctions of neuroepithelial cells during neurulation and that Xena k
93 uced swollen/enlarged ER lumens in embryonic neuroepithelial cells during neurulation.
94 is essential for the morphogenic movement of neuroepithelial cells during the formation of the neural
95 athological angiogenesis caused by defective neuroepithelial cell-endothelial cell adhesion and imbal
96                                 We uncovered neuroepithelial cell enriched genes such as Hmga2 and Cc
97     Electron microscopy shows that the dying neuroepithelial cells exhibit the characteristics of apo
98       Following in ovo misexpression of NKL, neuroepithelial cells exit the cell cycle and differenti
99 rolled, in part, by Itgb8, which encodes the neuroepithelial cell-expressed integrin beta8 subunit.
100 hlight the importance of precisely regulated neuroepithelial cell fate for normal brain-CSF biomechan
101                             On the contrary, neuroepithelial cells from all regions of the tectum att
102 ex, sequential transcriptional programs take neuroepithelial cells from proliferating progenitors to
103 et-derived growth factor (PDGF), uncommitted neuroepithelial cells from the developing cortex of embr
104 rreversible retraction of the endfeet of the neuroepithelial cells from the vitreal surface of the re
105  cones traversed or tracked more often along neuroepithelial cells from their natural target area, po
106 on cell neurons and the proliferation of the neuroepithelial cells from which they derive.
107  gene expression between neuroblasts and the neuroepithelial cells from which they derive.
108                                              Neuroepithelial cells further yield successive Notch-dep
109 ion strategy involves symmetrically dividing neuroepithelial cells generating large numbers of asymme
110 he surrounding brain parenchyma, composed of neuroepithelial cells, glia, and neuronal precursors.
111                              A population of neuroepithelial cells has recently been shown to migrate
112                    Our results indicate that neuroepithelial cells have all the necessary components
113 splanting cells to new sites emphasizes that neuroepithelial cells have the potential to integrate in
114                                              Neuroepithelial cells in both mutants fail to apically c
115         The architecture of primary cilia on neuroepithelial cells in Pam(-/-) mouse embryos was also
116                                              Neuroepithelial cells in the developing ventricular zone
117 not support the commonly held view that most neuroepithelial cells in the embryonic CNS VZ are stem c
118  in the presumed segmental cues that specify neuroepithelial cells in the hindbrain.
119                                      Whereas neuroepithelial cells in the medial OPC directly convert
120            Most striking, a subpopulation of neuroepithelial cells in the medial telencephalic wall e
121 s (PDGFR alpha) are expressed by a subset of neuroepithelial cells in the ventral half of the embryon
122 g stem cells, which comprise the majority of neuroepithelial cells in the ventricular zone (VZ) of th
123 prominent towards the apical boundary of the neuroepithelial cells in the ventricular zone.
124 ry neurons emerge from proneural clusters of neuroepithelial cells in the zebrafish.
125  Here, we report that apicobasally polarized neuroepithelial cells in Xenopus laevis have a shorter c
126                                              Neuroepithelial cells infected with Toxoplasma type I ex
127           In the developing mammalian brain, neuroepithelial cells interact with blood vessels to reg
128 opment, from a seemingly homogenous sheet of neuroepithelial cells into a complex structure that is t
129 dium and drives the sequential transition of neuroepithelial cells into neuroblasts.
130 l expansion of the Olig1/Olig2 expression in neuroepithelial cells into the Nkx2.2 domain and a conse
131       Production of astrocytes from cultured neuroepithelial cells is hedgehog independent, whereas o
132 ural tube, and forced expression of Foxj1 in neuroepithelial cells is sufficient to increase cilia le
133 ce of focal adhesions in dissociated retinal neuroepithelial cells isolated from St 25 embryos.
134                                Additionally, neuroepithelial cell junctions in the embryonic rat brai
135  event(s) involved in the maintenance of the neuroepithelial cell layer shortly after its formation.
136 erebral cortical precursor cells reside in a neuroepithelial cell layer that regulates their prolifer
137 cular zone instability in tissue cohesion of neuroepithelial cells, leading to a maturational arrest
138  were recorded from cells of an immortalized neuroepithelial cell line named V1.
139 urons, like projection neurons, develop from neuroepithelial cells located near the ventricular layer
140 rsal- and ventral-most regions of the brain, neuroepithelial cells lose their integrity and begin to
141  the basal cytoplasm did not occur and these neuroepithelial cells lost their columnar morphology.
142         All cells expressed nestin, an early neuroepithelial cell marker.
143 ound in cobblestone lissencephalies in which neuroepithelial cells migrate into superficial layers of
144 autonomously within the retina and brain, as neuroepithelial cell morphology and polarity in these ti
145  basal progenitors (BPs), differentiate from neuroepithelial cells (NCs) with stem cell properties.
146                                Subsequently, neuroepithelial cells (NE) convert into neuroblasts (NB)
147                                              Neuroepithelial cell (NEC) elongation is essential for p
148                                              Neuroepithelial cell (NEC) elongation is one of several
149                  In this study, we show that neuroepithelial cells (NECs), including neural crest cel
150 racellular calcium concentration of isolated neuroepithelial cells (NECs), which are putative oxygen
151 F or EGF promotes the proliferation of mouse neuroepithelial cells (NECs).
152 al crest-derived, and the hypoxia-sensitive 'neuroepithelial cells' (NECs) of fish gills, whose embry
153               Adherent cultures of E10.5 rat neuroepithelial cells (NEP cells) from the caudal neural
154 resent in the developing neural tube (E10.5, neuroepithelial cells; NEP) were examined for the expres
155 port that the knockdown of Htt expression in neuroepithelial cells of neocortex results in disturbed
156  determined that NDE1 is highly expressed in neuroepithelial cells of the developing cerebral cortex,
157 t is a major challenge to understand how the neuroepithelial cells of the developing CNS choose betwe
158 sx-2 is initially expressed by proliferating neuroepithelial cells of the presumptive neural retina,
159                                          The neuroepithelial cells of the sharp boundary regions that
160 , phosphacan surrounds the radially oriented neuroepithelial cells of the telencephalon, whereas neur
161 receptor subunits, whereas the ZI cells were neuroepithelial cells or newly postmitotic neurons, expr
162 e capable of dividing asymmetrically, but in neuroepithelial cells other polarity cues might prevent
163 l, human PSCs are first induced to primitive neuroepithelial cells over 10 d, and then patterned to N
164          Within a column (a small cluster of neuroepithelial cells), postmitotic cells appeared first
165 as key regulatory elements in the control of neuroepithelial cell proliferation and the neuroblast tr
166                                              Neuroepithelial cell proliferation must be carefully bal
167 helial stem cell phenotype and regulation of neuroepithelial cell proliferation, suggesting that a mu
168 inantly localizes to the basolateral side of neuroepithelial cells, promotes the enlargement of the n
169 niche is composed of a diverse repertoire of neuroepithelial cells, radial glia (RG), and intermediat
170 y expressed early in embryogenesis, e.g., in neuroepithelial cells, radial glia, germinal matrix cell
171 re, with peak CPEC competency correlating to neuroepithelial cells rather than radial glia.
172                                     Germinal neuroepithelial cells retained specific 3[H]prazosin bin
173  tension of delaminating NCC and neighboring neuroepithelial cells, revealed that round NCC are extru
174                                 Furthermore, neuroepithelial cell shape and architecture were disrupt
175 ce versa, establishing an important role for neuroepithelial cell shape in human brain expansion.
176                               Mice harboring neuroepithelial cell-specific Trim71 deletion or CH-spec
177 clude withdrawal from mitosis by multipotent neuroepithelial cells, specification to particular cell
178  is localized to the basal cortex of mitotic neuroepithelial cells, suggesting that c-NUMB regulates
179 ore than 20-fold in cultured E10.5 hindbrain neuroepithelial cells, suggesting that PACAP activates p
180 NA and protein was specifically expressed in neuroepithelial cells surrounding retinal axons at the o
181 lian taste buds are comprised of specialized neuroepithelial cells that act as sensors for molecules
182 aste buds are aggregates of 50-100 polarized neuroepithelial cells that detect nutrients and other co
183                     In the absence of Nurr1, neuroepithelial cells that give rise to dopaminergic neu
184                               Vangl2-deleted neuroepithelial cells themselves continue to apically co
185 c spindle alignment in Drosophila optic lobe neuroepithelial cells through aPKC activity-dependent my
186 axons, radial glia, spinal axonal tracts and neuroepithelial cells through associations with heparan
187                               The ability of neuroepithelial cells to generate a diverse array of neu
188  intrinsic change in the potential of spinal neuroepithelial cells to generate neurons.
189                  This permits the underlying neuroepithelial cells to invade the spinal canal and obs
190 anscriptional cascade of PC development from neuroepithelial cells to mature PCs.
191 ur studies establish that the progression of neuroepithelial cells to neuroblasts is regulated by Not
192  period that ends as they differentiate from neuroepithelial cells to neuronogenic radial glia.
193  that affect the transition of proliferating neuroepithelial cells to postmitotic retinal cells.
194 l stem cells (NSCs) undergo transitions from neuroepithelial cells to radial glial cells (RGCs), and
195 ion is highly reminiscent of the switch from neuroepithelial cells to radial glial cells in the devel
196 sruption of the pial basal lamina caused the neuroepithelial cells to retract their pial end feet and
197 at Notch signalling augments the response of neuroepithelial cells to Shh, leading to the induction o
198 or Cx43 in which Cx43 acts through non-crest neuroepithelial cells to suppress cellular delamination
199 t the retinal basal lamina, by anchoring the neuroepithelial cells to the pial surface of the retina,
200  to the brain, providing an anchoring of the neuroepithelial cells to the pial surface, and allowing
201  3, MAD2, CDC28 protein kinase (CKS)1 and 2, neuroepithelial cell transforming gene (NET)1, activator
202                                  We identify neuroepithelial cell transforming gene 1 (Net1) as a dow
203                                          The neuroepithelial cell transforming gene 1 (Net1) is a gua
204 olecular biology techniques in both cultured neuroepithelial cells treated with a GCN5 inhibitor and
205 ring phase 1, the cell differentiates from a neuroepithelial cell type and extends an axon out of the
206                                              Neuroepithelial cells undergo a cell cycle arrest before
207 serve nuclear movements in zebrafish retinal neuroepithelial cells, we show that, except for brief ap
208                                              Neuroepithelial cells were labelled via their ventricula
209                   Neuroblasts originate from neuroepithelial cells, which are polarized along the api
210  expanding cores of undifferentiated mitotic neuroepithelial cells, which can be tumorigenic.
211 eks, hESCs are induced to differentiate into neuroepithelial cells, which form neural tube-like roset
212      The Drosophila optic lobe develops from neuroepithelial cells, which function as symmetrically d
213               Cocultures of hES cell-derived neuroepithelial cells with exogenous astrocytes signific
214 man stem cells are first differentiated into neuroepithelial cells with or without exogenous patterni
215 ivo, yet because RGCs develop from polarized neuroepithelial cells within a polarized environment, di

 
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