ライフサイエンスコーパス: neural progenitor

1 let-7 knock down shortens the cell cycle in neural progenitors.

2 is required for apical nuclear migration in neural progenitors.

3 e differentiation of embryonic stem cells to neural progenitors.

4 n reprogram developing wing discs into brain neural progenitors.

5 of promoting the proliferation of embryonic neural progenitors.

6 rons by knockout of betaII-spectrin in mouse neural progenitors.

7 ients overproduce OLIG2(+) ventral forebrain neural progenitors.

8 embryonic origin and establishment of adult neural progenitors.

9 t, neurons are produced by a diverse pool of neural progenitors.

10 n in mice, by controlling proper division of neural progenitors.

11 g cells, which represent enteric glia and/or neural progenitors.

12 orphogen input to the positional identity of neural progenitors.

13 expression in Drosophila embryonic or larval neural progenitors.

14 ouse embryonic stem cells and differentiated neural progenitors.

15 e used to identify a source of GDNF-targeted neural progenitors.

16 ult stem/progenitor cell, called adult human neural progenitor (AHNP) cells, that we found to be path

17 PEN is dispensable for maintenance of XCI in neural progenitors, although it significantly decreases

18 and D2R signaling on SVZ cell proliferation, neural progenitor and neuronal maturity is differentiall

19 (i) studying their biological role in human neural progenitors and (ii) incorporating TF conditional

20 entricular system and CSF sources (including neural progenitors and choroid plexus).

21 argets in human dorsal and ventral forebrain neural progenitors and excitatory and inhibitory neurons

22 cell types were identified as proliferating neural progenitors and immature neurons, both of which c

23 ZIKV can infect human neural progenitors and impair brain growth.

24 Zika virus (ZIKV) directly infects neural progenitors and impairs their proliferation.

25 intermediate filament expressed strongly in neural progenitors and is thus used widely as a progenit

26 he constitutively active PKM1 isoform, while neural progenitors and medulloblastomas exclusively expr

27 vity, induce ectopic RNA-protein granules in neural progenitors and neurons, and impair translation.

28 of genes in human excitatory and inhibitory neural progenitors and neurons.

29 ine the need for MCT8-dependent TH uptake in neural progenitors and stress the importance of local TH

30 brate neural tube determines the identity of neural progenitors and the function and physiology of th

31 transition of undifferentiated P19 cells to neural progenitors and their ultimate terminal different

32 Neural progenitors are maintained by Notch signalling, w

33 esioned site and (b) in the proliferation of neural progenitors, arguing for a neuroprotective role o

34 dentify impaired differentiation of specific neural progenitors as a common mechanism underlying thes

35 Here we identify a brain-region-specific neural progenitor-based signaling pathway dedicated to r

36 treatment had a pro-proliferative effect on neural progenitors, but neuronal integration occurred on

37 Nestin expression is thus not restricted to neural progenitors, but persists for 2-3 d at lower leve

38 g reduction of self-renewal and expansion of neural progenitors by IE2.

39 ted by fusion of human iPSC-derived cortical neural progenitor cell (iNPC) spheroids, endothelial cel

40 exhibited neurodevelopmental defects due to neural progenitor cell (NPC) apoptosis, which led to red

41 Neural progenitor cell (NPC) culture within three-dimens

42 ing cellular functions of LIS1 in regulating neural progenitor cell (NPC) daughter cell separation.

43 this purpose, we adapted a system to induce neural progenitor cell (NPC) development from mouse embr

44 tested the hypothesis whether disturbance of neural progenitor cell (NPC) differentiation into the ol

45 nction between isogenic wild-type and mutant neural progenitor cell (NPC) lines revealed increased ox

46 ssesses a mitotically active, age-depletable neural progenitor cell (NPC) niche, with unique characte

47 ephaly is associated with disruptions in the neural progenitor cell (NPC) population.

48 cortex development through the regulation of neural progenitor cell (NPC) proliferative and different

49 The mechanisms that determine whether a neural progenitor cell (NPC) reenters the cell cycle or

50 Science, Chavali et al. (2017) identified a neural progenitor cell (NPC)-specific RNA binding protei

51 estions regarding its role as a regulator of neural progenitor cell cycle progression in cerebellar d

52 ected with ZIKV, and propagate virus causing neural progenitor cell death.

53 We identified midfetal cortical neural progenitor cell development-more specifically, th

54 oral functional outcome of RAF1 during mouse neural progenitor cell differentiation using an optogene

55 occurs in Down syndrome, is known to affect neural progenitor cell differentiation, while haploinsuf

56 hat complement-derived peptide C3a regulates neural progenitor cell migration and differentiation in

57 26 cells, we identified neural stem cell and neural progenitor cell pools and neurons.

58 critical function in regulation of postnatal neural progenitor cell production in response to Noggin.

59 diate effects of antidepressant treatment on neural progenitor cell proliferation and behavior.

60 l module, confirming that these genes reduce neural progenitor cell proliferation and neurite growth.

61 rmone receptor alpha1 is required for normal neural progenitor cell proliferation in human cerebral c

62 receptor signaling is sufficient to increase neural progenitor cell proliferation in the absence of f

63 ver, the effects of nutrient availability on neural progenitor cell proliferation in vivo are poorly

64 Deletion of HuR does not impair neural progenitor cell proliferation or differentiation,

65 de anion scavenger during IH did not prevent neural progenitor cell proliferation, it mitigated the I

66 rating abnormal neural rosette formation and neural progenitor cell proliferation.

67 The test result with human neural progenitor cell spheroids suggests a remarkable r

68 ration and neurogenesis of adult hippocampal neural progenitor cells (AHNPCs) and in a non-cell auton

69 euronal differentiation of adult hippocampal neural progenitor cells (AHNPCs) following environmental

70 transcellular transmission in differentiated neural progenitor cells (dNPCs) and neuroblastoma SH-SY5

71 ntifying strategies to optimize iPSC-derived neural progenitor cells (hiNPC) for cell transplantation

72 human pluripotent stem cell-derived cortical neural progenitor cells (hNPCs) and found that hippeastr

73 ZIKV efficiently infects human neural progenitor cells (hNPCs) and leads to growth arre

74 Human induced pluripotent stem cell-derived neural progenitor cells (hNPCs) are a promising cell sou

75 Using 3D-differentiated clonal human neural progenitor cells (hNPCs) expressing varying level

76 lateral prefrontal cortex and cortical human neural progenitor cells (hNPCs) was determined using imm

77 KV) infection attenuates the growth of human neural progenitor cells (hNPCs).

78 y in both individual fibroblasts and induced neural progenitor cells (iNPCs).

79 lanted induced pluripotent stem cell-derived neural progenitor cells (iPS-NPCs) could recapitulate an

80 Using induced pluripotent stem cell-derived neural progenitor cells (iPS-NPCs) expressing the novel

81 Neural progenitor cells (NeuPCs) possess a unique nuclea

82 ular endothelial cells (PVEC) crosstalk with neural progenitor cells (NPC) promoting mutual prolifera

83 h a mean age of 90.6 years, Nestin(+)Sox2(+) neural progenitor cells (NPCs) and DCX(+) neuroblasts an

84 sed ZIKV infectivity in both human and mouse neural progenitor cells (NPCs) and led to more severe mi

85 to generate induced pluripotent stem cells, neural progenitor cells (NPCs) and neurons from ASD indi

86 er brain size due to increased cell death in neural progenitor cells (NPCs) and neurons.

87 ion of murine embryonic stem cells (ESCs) to neural progenitor cells (NPCs) and recruits the Mediator

88 othesized that METH impacts HIV infection of neural progenitor cells (NPCs) by a mechanism encompassi

89 Engulfment of synapses and neural progenitor cells (NPCs) by microglia is critical

90 neural differentiation, the HD-iPSC-derived neural progenitor cells (NPCs) demonstrated lower levels

91 Consistently, neural progenitor cells (NPCs) derived from human induce

92 d induced pluripotent stem cells (iPSCs) and neural progenitor cells (NPCs) derived from individuals

93 We had previously determined that neural progenitor cells (NPCs) derived from induced plur

94 Mutations in centrosome genes deplete neural progenitor cells (NPCs) during brain development,

95 The fate of neural progenitor cells (NPCs) during corticogenesis is

96 Grafts of spinal-cord-derived neural progenitor cells (NPCs) enable the robust regener

97 ry behavior and differentiation potential of neural progenitor cells (NPCs) found in the subventricul

98 d how a regenerative program is fulfilled by neural progenitor cells (NPCs) of the spinal cord, we an

99 induced pluripotent stem (iPS) cell-derived neural progenitor cells (NPCs) to repair the FTD-associa

100 ity of uCPP 3D-printed scaffolds loaded with neural progenitor cells (NPCs) to support axon regenerat

101 Neural progenitor cells (NPCs) undergo rapid proliferati

102 We quantified neural progenitor cells (NPCs), GNs, glia, and DG volume

103 rains and organoids due to the disruption of neural progenitor cells (NPCs), including outer radial g

104 educes spread and output of ZIKV in infected neural progenitor cells (NPCs), the major cells infected

105 n the collective dynamics of cultured murine neural progenitor cells (NPCs), which are multipotent st

106 roliferation and impaired differentiation of neural progenitor cells (NPCs), which resemble neurodeve

107 In neural progenitor cells (NPCs), Ybx1 controls self-renew

108 DNA damage repair essential to proliferating neural progenitor cells (NPCs).

109 iously shown impaired proliferation of SPG11 neural progenitor cells (NPCs).

110 down and RNA-sequencing experiments of human neural progenitor cells (NPCs).

111 e/primed pluripotency to multipotent primary neural progenitor cells (NPCs).

112 strict ZIKV infection in clinically relevant neural progenitor cells (NPCs).

113 emory formation and are highly enriched with neural progenitor cells (NPCs).

114 DISC1 interactomes within iPSC-derived human neural progenitor cells and astrocytes are able to provi

115 interactions involving DISC1 in iPSC-derived neural progenitor cells and astrocytes.

116 injured brain and are critical for altering neural progenitor cells and brain repair.

117 Patient-derived disease models including neural progenitor cells and cerebral organoids showed th

118 of the developing cerebral cortex, including neural progenitor cells and developing neurons.

119 markers in young neurons derived from human neural progenitor cells and human induced pluripotent st

120 tes that an increase in the proliferation of neural progenitor cells and hyper-expansion of cortical

121 ex in wild-type and bi-allelic mutant ACTL6B neural progenitor cells and neurons revealed increased g

122 l schizophrenia (SZ) hiPSC-derived cohort of neural progenitor cells and neurons.

123 Neural progenitor cells and the glymphatic system, which

124 ome in regulating the mechanical features of neural progenitor cells and the size and configuration o

125 Neural progenitor cells are permissive for lytic infecti

126 ition, the DISC1 interactome in iPSC-derived neural progenitor cells associates in a connected networ

127 zed four distinct types of Tc-foxQ2 positive neural progenitor cells based on differential co-express

128 IPSC-derived neural progenitor cells carrying the risk allele of the

129 how differential migration patterns in human neural progenitor cells compared to those of chimpanzees

130 d depression-like behaviors, suggesting that neural progenitor cells contribute to the effects of BMP

131 Parkinson's disease (PD) tissue sources: (a) neural progenitor cells derived from an endogenous adult

132 Orthotopic engraftment of the neural progenitor cells derived from hiPSCs that have be

133 an counteract DISC1 deficiencies observed in neural progenitor cells derived from induced pluripotent

134 In this study we use cultured neural progenitor cells derived from olfactory neuroepit

135 Transcriptomic profiling of cortical neural progenitor cells derived from these hiPSCs identi

136 IE2-transduced neural progenitor cells gave rise to neurospheres with a

137 Knl1 deletion, segregation errors in mitotic neural progenitor cells give rise to DNA damage on the m

138 Zika virus (ZIKV) targets neural progenitor cells in the brain, attenuates cell pr

139 he placenta, and endothelial, microglial and neural progenitor cells in the fetal brain.

140 ncreased the number of proliferating Sox2(+) neural progenitor cells in the subgranular zone yet redu

141 uce and control directional axon growth from neural progenitor cells in vitro and host axons in a rat

142 ll markers and Notch target genes in primary neural progenitor cells in vitro Consistent with this, i

143 ctors (SOX10, OLIG2, NKX6.2) in iPSC-derived neural progenitor cells is sufficient to rapidly generat

144 cly available dataset of Zika virus-infected neural progenitor cells is used to illustrate AIDD's cap

145 Clone formation capacity of neural progenitor cells isolated from the db/db mice is

146 e been explored, we focus here on the use of neural progenitor cells obtained or derived from differe

147 al that in the embryo, disc1 is expressed in neural progenitor cells of the hypothalamus, a conserved

148 settings, such as in vitro HCMV infection of neural progenitor cells or in vivo murine CMV infection

149 ZIKV causes productive replication, infects neural progenitor cells over mature neurons, decreases b

150 tion after 72 hours, preferentially infected neural progenitor cells over mature neurons, reduced bot

151 t early light-induced OptoRAF1 activation in neural progenitor cells promotes cell proliferation and

152 gree of hypermethylation in undifferentiated neural progenitor cells than in mature astrocytes.

153 ta from GBM stem-like cells, astrocytes, and neural progenitor cells that are sensitive or resistant

154 glial progenitor cells (RGPs) are the major neural progenitor cells that generate neurons and glia i

155 Addition of neural progenitor cells to the co-culture resulted in th

156 We then selectively ablated dividing neural progenitor cells using a 7-day continuous infusio

157 nuclear YAP1 (nlsYAP5SA) in ventricular zone neural progenitor cells using conditionally-induced NEX/

158 whether CHD7 promotes gene transcription in neural progenitor cells via changes in chromatin accessi

159 RAMA elements in neural progenitor cells were biallelically accessible in

160 model of spinal cord injury, in which human neural progenitor cells were transplanted at the site of

161 mouse embryogenesis drives proliferation of neural progenitor cells within the ventricular zone and

162 tly increased CNTF and BMP4 transcription in neural progenitor cells, and a neutralizing antibody aga

163 mesoscale structure in embryonic stem cells, neural progenitor cells, and cortical neurons.

164 NA levels of Sox1 and Nestin, the markers of neural progenitor cells, and decreased the count of Sox1

165 vival, proliferation, and differentiation of neural progenitor cells, and suggest a basis for its fun

166 hesis in various cell types, including human neural progenitor cells, blocks ZIKV infection.

167 proteins at the base of the primary cilia in neural progenitor cells, causing an atypical non-genetic

168 velopment in a cell type-specific manner: In neural progenitor cells, GPR56 regulates cortical lamina

169 n was examined in neurons derived from human neural progenitor cells, human induced pluripotent stem

170 n (H3K4me2) in EPO treated and control fetal neural progenitor cells, identifying 1,150 differentiall

171 In gliomagenic neural progenitor cells, IDH1(R132H) expression increase

172 Thus, it targets neural progenitor cells, leading to a more severe spectr

173 add to recent evidence in embryonic stem and neural progenitor cells, suggesting a model whereby deve

174 ll survival-based cDNA expression screens in neural progenitor cells, we identify a genetic variant o

175 ablishing the proper expression signature of neural progenitor cells, while catalytic inactivation of

176 ming of proliferation and differentiation of neural progenitor cells.

177 functions upstream to control Hh response of neural progenitor cells.

178 man embryonic stem cells and differentiating neural progenitor cells.

179 as the proliferation and differentiation of neural progenitor cells.

180 ted primarily of neurons with some glial and neural progenitor cells.

181 nic regions, where SOX9 is also expressed by neural progenitor cells.

182 so with differentiation and proliferation of neural progenitor cells.

183 and CRISPR interference experiment in human neural progenitor cells.

184 ies of induced pluripotent stem cell-derived neural progenitor cells.

185 for attachment and differentiation of PC-12 neural progenitor cells.

186 ess GABAergic specification of the patients' neural progenitor cells.

187 ultiple cell types, including astrocytes and neural progenitor cells.

188 iption factors required for the formation of neural progenitor cells.

189 mbryonic brain are stochastic, varying among neural progenitor cells.

190 re phenotypically normal, differentiation to neural progenitors cells (NPCs) was severely impaired.

191 e subjected to neonatal stroke and postnatal neural progenitor cultures, and we analyzed Olig1 expres

192 iR-199 or miR-214 expression in iPSC-derived neural progenitors deficient in MeCP2 restored AKT and E

193 16, and mouse embryonic stem cells and their neural progenitor derivatives.

194 ker genes, distinguishing five major groups: neural progenitors, differentiated neurons, glia, undiff

195 n embryonic stem cells and maintained during neural progenitor differentiation.

196 r-derived cells showing either a spectrum of neural progenitor-differentiation states or glial and st

197 ord for the generation of P1, P2/pMN, and P2 neural progenitor domains.

198 ion into Hopx(+) quiescent radial glial-like neural progenitors during an early postnatal period.

199 hannels are key regulators of the biology of neural progenitors during development and in adult neuro

200 me stability that allows proper expansion of neural progenitors during development.

201 nes to control the proliferative capacity of neural progenitors, ensuring the generation of correct n

202 In health, microglia influence neural progenitor fate decisions, astrocyte activation,

203 In the zebrafish spinal cord, neural progenitors form stereotypic patterns despite noi

204 mbryonic, early postnatal, and adult dentate neural progenitors further reveal common molecular and e

205 Thus neural progenitor grafts can form functional synaptic su

206 elayed OptoRAF1 activation in differentiated neural progenitor had little effect on glia marker expre

207 Here, we investigate how neural progenitors halt cell division in response to nut

208 x2 homeodomain transcription factor promotes neural progenitor identity in the lateral ganglionic emi

209 oliferation and symmetric division of apical neural progenitors in human and mouse models.

210 absence of BubR1 decreases the proportion of neural progenitors in mitosis, specifically in metaphase

211 d the migratory behaviour of early olfactory neural progenitors in neurog1 mutant embryos.

212 rol the proliferation and differentiation of neural progenitors in the adult hippocampal dentate gyru

213 PlexinC1 is selectively expressed in early neural progenitors in the adult mouse DG and mediates th

214 a malignant pediatric tumor that arises from neural progenitors in the cerebellum.

215 The presence and identity of neural progenitors in the enteric nervous system (ENS) o

216 day 11.5 give rise to proliferative Hopx(+) neural progenitors in the primitive dentate region, and

217 altered, 2) the population of proliferating neural progenitors in the SVZ was reduced, whereas the p

218 Depletion of Zfp609 or Nipbl from cortical neural progenitors in vivo is detrimental to neuronal mi

219 The Blbp-Cre driver that targets embryonic neural progenitors induced tumors exhibiting a large-cel

220 opulation of transit-amplifying intermediate neural progenitors (INP) similar to that found in the de

221 multiple transiently amplifying intermediate neural progenitors (INPs) from a single neural stem cell

222 the developmental potential of intermediate neural progenitors (INPs) generated by asymmetrically di

223 During larval stages, intermediate neural progenitors (INPs) serially express Dichaete (D),

224 euroblasts generate a series of intermediate neural progenitors (INPs) that each produce 4-6 GMCs and

225 n of doublecortin-positive adult hippocampal neural progenitors into functionally mature neurons.

226 ndicate that MCT8-dependent TH uptake in the neural progenitors is essential for early events in cort

227 induced pluripotent stem cells to forebrain neural progenitors is markedly reduced, but mutant proge

228 that the major effect of BubR1 deficiency on neural progenitors is to impair the mitotic checkpoint.

229 fective proliferation and differentiation of neural progenitors is unlikely the single underlying cau

230 Neural progenitors lacking Lgl1 had decreased N-cadherin

231 Temporal patterning of neural progenitors leads to the sequential production of

232 cortex is populated by neurons derived from neural progenitors located throughout the embryonic tele

233 unofluorescence for established neuronal and neural progenitor marker proteins and compared the resul

234 xpressed higher levels of key ectodermal and neural progenitor markers and lower levels of markers fo

235 ed self-organization of neuruloids harboring neural progenitors, neural crest, sensory placode and ep

236 tterning mechanisms discovered in Drosophila neural progenitors (neuroblasts) involve progenitor-intr

237 ion and migration patterns of the adult-born neural progenitor (NP) lineages in detail.

238 n human pluripotent stem cell (hPSC)-derived neural progenitors (NPs) using a genome-wide CRISPR-Cas9

239 buprofen-treated mice that display increased neural progenitor numbers (Ki67 positive) in the subvent

240 Here, we show that proliferating cortical neural progenitors of human embryonic brains highly expr

241 ansitory and transcriptionally distinct from neural progenitors of post-embryonic stages.

242 vivo RNAi vector-based knockdown of MCT8 in neural progenitors of the chicken optic tectum, a layere

243 In the neural progenitors of the developing central nervous sys

244 urther show that MSI1 is highly expressed in neural progenitors of the human embryonic brain and is m

245 GSX2 is highly expressed in neural progenitors of the lateral and median ganglionic

246 rly, 5hmC is enriched in neurons compared to neural progenitors of the ventricular zone in the mouse

247 at the microRNA (miRNA) let-7 accumulates in neural progenitors over time throughout the developing C

248 g to increased cell death, which reduces the neural progenitor pool and severely disrupts brain devel

249 an important role in neural development and neural progenitor pool maintenance.

250 upport a "continuous" model wherein a common neural progenitor population exclusively contributes to

251 The presence of these species-specific neural progenitor populations refines our insight into h

252 egulator PRDM16 is expressed by radial glia, neural progenitors present in both regions; however, its

253 the level and activity of let-7 oscillate as neural progenitors progress through the cell cycle by in

254 hould be intermittent in order to first make neural progenitors proliferate and then, upon discontinu

255 , we evaluated adult neurogenesis, including neural progenitor proliferation and dendrite development

256 sion of mutant DISC1 in astrocytes decreased neural progenitor proliferation and dendrite growth of n

257 UB1B mutation, how BubR1 deficiency disturbs neural progenitor proliferation and neuronal output and

258 he H3K9me2 demethylase PHF2 is essential for neural progenitor proliferation in vitro and for early n

259 ure to rats during the most active period of neural progenitor proliferation induces cytoarchitectura

260 dpoles enter a period of stasis during which neural progenitor proliferation is drastically reduced,

261 he complement activation peptide C5a and the neural progenitor proliferation underpinning formation o

262 These include neural progenitor proliferation, morphogenesis, and neur

263 are the first to identify a role for VGSC in neural progenitor proliferation.

264 ore, compounds 5 and 14 were able to promote neural progenitors proliferation and drive their differe

265 ed with ibuprofen showed increased levels of neural progenitors proliferation and synaptic markers su

266 required for expansion of cerebellar granule neural progenitors, proposed to be cells-of-origin for t

267 s abnormal gene expression in early-stage DS neural progenitors, reduces interneuron production in DS

268 The redox state of the neural progenitors regulates physiological processes suc

269 ersity, but how these cues are integrated in neural progenitors remains unknown.

270 kout offspring show microcephaly and primary neural progenitors require Cep55 and ESCRT for survival

271 und that GOF disrupts mitosis of radial-glia neural progenitors (RGCs), inside-out radial migration o

272 underlying mechanism, demonstrating that LV-neural progenitors secrete a pleiotrophin (PTN)-containi

273 We report that dividing neural progenitors show both aperiodic and periodic HES5

274 aracterization indicates that most embryonic neural progenitor states are transitory and transcriptio

275 eractions enhanced ZIKV replication in human neural progenitor/stem cells.

276 s newly discovered extrinsic cues regulating neural progenitor temporal identity in Drosophila, highl

277 ifferentiate from transcriptionally distinct neural progenitors that are arrayed in discrete domains

278 fferentiation and the proliferative state of neural progenitors through regulation of the cytoskeleto

279 New neurons arise from quiescent adult neural progenitors throughout life in specific regions o

280 n is both dependent on Cre and restricted to neural progenitors, thus circumventing the aforementione

281 ate tumourigenesis by reverting intermediate neural progenitors to a stem cell state.

282 neurosphere-based culture enabled directing neural progenitors to adopt a specific cortical identity

283 demonstrate that nutrient restriction causes neural progenitors to arrest in G2 of the cell cycle wit

284 Tumor cells recruit new neural progenitors to the tumor milieu and facilitate th

285 trajectories reveals that late-stage retinal neural progenitors transcriptionally overlap cell states

286 Neural progenitors (transit amplifying cells and neurobl

287 trocytes generated from regionally specified neural progenitors under the same conditions strongly im

288 Neural progenitors undergo temporal patterning to genera

289 In the developing retina, multipotent neural progenitors undergo unidirectional differentiatio

290 t of p75(NTR) from embryonic day 10 (E10) in neural progenitors using a conditional Nestin-Cre p75(NT

291 ch signalling maintains Hh responsiveness of neural progenitors via a Gli-dependent mechanism in the

292 C5aR1 signaling in neural progenitors was dependent on atypical protein kin

293 acute hyperglycemia, later proliferation of neural progenitors was significantly decreased by chroni

294 filament protein widely used as a marker of neural progenitors, was recently found to be expressed t

295 mediate filament protein highly expressed in neural progenitors, was recently identified in developin

296 nd preferences for three types of endogenous neural progenitors, we provide evidence for the differen

297 Human neural progenitors were more severely affected, especial

298 Neural progenitors were organized in niches in the subep

299 neurogenesis to direct apoptosis in cycling neural progenitors, whereas ATM regulated apoptosis in b

300 human induced pluripotent stem cell-derived neural progenitors, which were subsequently differentiat