ライフサイエンスコーパス: neural progenitor cell

1 as the proliferation and differentiation of neural progenitor cells.

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

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

4 so with differentiation and proliferation of neural progenitor cells.

5 H1 human embryonic stem cells and H1-derived neural progenitor cells.

6 s that influence the cell fates of embryonic neural progenitor cells.

7 for the early activation of the Sox2 gene in neural progenitor cells.

8 s, and is now found to protect the genome of neural progenitor cells.

9 and CRISPR interference experiment in human neural progenitor cells.

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

11 ma-Secretase regulates fate determination of neural progenitor cells.

12 self-renewal and differentiation of diverse neural progenitor cells.

13 n-induced pluripotent stem cell-derived JNCL neural progenitor cells.

14 ts in spindle orientation defects in mitotic neural progenitor cells.

15 on of neuropathology in patient iPSC-derived neural progenitor cells.

16 crease TPP1 activity in patient iPSC-derived neural progenitor cells.

17 duction, indicating a possible early role in neural progenitor cells.

18 derstanding how these cells can act as adult neural progenitor cells.

19 receptors induce long-range calcium waves in neural progenitor cells.

20 th epithelial cells continually recruited as neural progenitor cells.

21 ven genomic loci in embryonic stem cells and neural progenitor cells.

22 in hiPSC-derived neurons but not in matched neural progenitor cells.

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

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

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

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

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

28 ming of proliferation and differentiation of neural progenitor cells.

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

30 man embryonic stem cells and differentiating neural progenitor cells.

31 he function of the miR17-92 cluster in adult neural progenitor cells after experimental stroke.

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

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

34 and neuronal commitment of adult hippocampal neural progenitor cells (AHNPCs).

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

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

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

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

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

40 enerative processes, such as those involving neural progenitor cells and gliosis compared with tumor

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

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

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

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

45 re required to maintain normal production of neural progenitor cells and new mature cholinergic neuro

46 ed pluripotent stem cell-derived NF1 patient neural progenitor cells and Nf1 genetically engineered m

47 nal activity elicits a mitogenic response of neural progenitor cells and OPCs, promotes oligodendroge

48 Neural progenitor cells and the glymphatic system, which

49 ifically, we focus on the use of spinal cord neural progenitor cells and the pipeline starting from p

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

51 gy to conditionally delete alpha-CaMKII from neural progenitor cells and their progeny in adult mice.

52 clones and further differentiated them into neural progenitor cells and then astrocytes.

53 ed LncND (neurodevelopment), is expressed in neural progenitor cells and then declines in neurons.

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

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

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

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

58 eted protein that controls the patterning of neural progenitor cells, and their neuronal and glial pr

59 caused widespread gene expression changes in neural progenitor cells, and together with BAZ1B ChIP-se

60 In the spinal cord, neural progenitor cells are directed to differentiate in

61 Neural progenitor cells are permissive for lytic infecti

62 TRA2B depletion results in apoptosis of the neural progenitor cells as well as disorganization of th

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

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

65 knock-out mice in which Bcl-xL is deleted in neural progenitor cells (Bcl-xL(Emx1-Cre)), we show that

66 proper, resulting in premature depletion of neural progenitor cells beginning at E16.5, which preven

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

68 ription factor Olig2 is expressed in cycling neural progenitor cells but also in terminally different

69 er, it is not yet known whether transplanted neural progenitor cells can migrate, proliferate, and ge

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

71 The conditional knockout (KO) of TFR in neural progenitor cells causes mice to develop progressi

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

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

74 ficantly greater number of nestin-expressing neural progenitor cells compared with control cells.

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

76 RE5::Fzd8 mice showed marked acceleration of neural progenitor cell cycle and increased brain size.

77 ential for neural stem cell self-renewal and neural progenitor cell cycle progression in adult mouse

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

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

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

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

82 gizes with p53 loss and PDGFRA activation in neural progenitor cells derived from human embryonic ste

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

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

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

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

87 In addition, we found that human neural progenitor cells differentiated from induced plur

88 is an important component of the process of neural progenitor cell differentiation during cortical d

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

90 during nervous system development, including neural progenitor cell differentiation, neuronal migrati

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

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

93 a result of defects in the proliferation of neural progenitor cells during development.

94 Nestin, an intermediate filament found in neural progenitor cells during early development and adu

95 epressor Fezf2 for proper differentiation of neural progenitor cells during the development of the Xe

96 Here, human embryonic stem (ES) cell-derived neural progenitor cells, endothelial cells, mesenchymal

97 heir molecular regulation in embryonic mouse neural progenitor cells (eNPCs) has not yet been clarifi

98 tematically profiled transcriptomes of human neural progenitor cells exposed to Asian ZIKV(C), Africa

99 inin coated surface, while the fetal-derived neural progenitor cells (fNPCs) migrated toward the cath

100 found prominent in the ventricular zone and neural progenitor cells from embryonic day 9.5 to postna

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

102 Allele-specific RNA-seq of neural progenitor cells generated from the female ESCs i

103 maturation of pluripotent stem cell-derived neural progenitor cells generates neurons which are char

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

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

106 Human RTT-patient-derived MECP2(R306C) neural progenitor cells had deficits in HDAC3 and FOXO r

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

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

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

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

111 and mosquito cells efficiently infects human neural progenitor cells (hNPCs) derived from induced plu

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

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

114 the production of genetically modified human neural progenitor cells (hNPCs) with familial AD mutatio

115 al differentiation of ReNcell VM (ReN) human neural progenitor cells (hNPCs).

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

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

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

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

120 We choose V2 neural progenitor cells in developing zebrafish embryo a

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

122 ay critical for the onset and maintenance of neural progenitor cells in the embryonic and adult nervo

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

124 y cellular excess, including accumulation of neural progenitor cells in the periventricular, hippocam

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

126 Proliferation of neural progenitor cells in the subventricular zone leads

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

128 regulates differentiation and maturation of neural progenitor cells in vitro by orchestrating both c

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

130 ZIKV infects neural progenitor cells in vitro, though its effects on

131 ta was sufficient to rescue the phenotype of neural progenitor cells in vitro.

132 aR1 on the apical surface of mouse embryonic neural progenitor cells in vivo and on human embryonic s

133 limbic and cortical areas, which also harbor neural progenitor cells, in comparison with the trigemin

134 e show that growth factor depletion in human neural progenitor cells induces ROS production in mitoch

135 neurospheres formed by stem cells and mouse neural progenitor cells injected intravitreally in mice

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

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

138 Intermediate neural progenitor cells (INPs) need to avoid differentia

139 mising strategy to induce differentiation of neural progenitor cells into functional neurons.

140 forelimb function after grafting multipotent neural progenitor cells into sites of SCI.

141 The attrition of neural progenitor cells involves p53-dependent cell deat

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

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

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

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

146 Here we show that in neural progenitor cells isolated from the adult mouse hi

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

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

149 A in a single nucleus, isolated from a mouse neural progenitor cell line and from dissected hippocamp

150 influencing PAR and S1PR signals in resident neural progenitor cells, may be potent modulators of bot

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

152 ss molecular convergence, we generated human neural progenitor cell models of 9q34 deletion syndrome,

153 Neural progenitor cells (NeuPCs) possess a unique nuclea

154 We previously reported that GC-mediated neural progenitor cell (NPC) apoptosis may be responsibl

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

156 ogenesis and define the relationship between neural progenitor cell (NPC) behavior and vessel growth.

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

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

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

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

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

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

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

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

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

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

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

168 ks the transition from aerobic glycolysis in neural progenitor cells (NPC) to neuronal oxidative phos

169 ferentiated from Olig2-negative hESC-derived neural progenitor cells (NPC-Astros), particularly in th

170 of FTY720 treatment on the biology of mouse neural progenitor cells (NPCs) after transplantation in

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

172 We determined that miR-19 is enriched in neural progenitor cells (NPCs) and downregulated during

173 It has been established that ZIKV disrupts neural progenitor cells (NPCs) and leads to embryonic mi

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

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

176 in neural development, we analyzed purified neural progenitor cells (NPCs) and neurons from developi

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

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

179 of neurogenesis, the number of proliferating neural progenitor cells (NPCs) and the number of young,

180 opment, tight regulation of the expansion of neural progenitor cells (NPCs) and their differentiation

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

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

183 nscriptional networks that CHD8 regulates in neural progenitor cells (NPCs) by reducing its expressio

184 evelopmental disorders using patient-derived neural progenitor cells (NPCs) can be facilitated by 3D

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

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

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

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

189 between self-renewal and differentiation of neural progenitor cells (NPCs) dictates neurogenesis and

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

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

192 at neural stem cells (NSCs) and intermediate neural progenitor cells (NPCs) employ a zinc-finger tran

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

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

195 r-4) expressing central nervous system (CNS) neural progenitor cells (NPCs) from both BD patients com

196 Neural progenitor cells (NPCs) have distinct proliferati

197 Neural progenitor cells (NPCs) have regenerative capabil

198 We also show that MLV infection of neural progenitor cells (NPCs) in culture did not affect

199 ted from nestin(+) subventricular zone (SVZ) neural progenitor cells (NPCs) in normal adult mice.

200 Newborn granule neurons generated from neural progenitor cells (NPCs) in the adult hippocampus

201 osis 2 (Nf2; merlin) limits the expansion of neural progenitor cells (NPCs) in the mammalian dorsal t

202 Transplantation of human neural progenitor cells (NPCs) into the brain or spinal

203 Transplants of neural progenitor cells (NPCs) into the injured CNS have

204 Loss of Flna in neural progenitor cells (NPCs) led RGs to undergo change

205 ive prerosette neural stem cells (pNSCs) and neural progenitor cells (NPCs) maintained in chemically

206 Although the signaling elements modulating neural progenitor cells (NPCs) of the adult subventricul

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

208 rapamycin (mTOR) hyperactivity in perinatal neural progenitor cells (NPCs) of tuberous sclerosis com

209 ogical conditions, such as a stroke, trigger neural progenitor cells (NPCs) proliferation and migrati

210 does not significantly alter the pattern of neural progenitor cells (NPCs) specified as neurons at t

211 ons of mouse embryonic stem cells (ESCs) and neural progenitor cells (NPCs) to comprehensively identi

212 nduced pluripotent stem cells and derivative neural progenitor cells (NPCs) to demonstrate that NF1 g

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

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

215 an astrocytes and neurons derived from human neural progenitor cells (NPCs) to yield a fully human BB

216 Neural progenitor cells (NPCs) undergo rapid proliferati

217 mediated by the embryonic expansion of basal neural progenitor cells (NPCs) via deregulation of a bet

218 When hippocampal neural progenitor cells (NPCs) were isolated from TgCRND

219 e expression in embryonic stem cells (ESCs), neural progenitor cells (NPCs), and NPC-derived induced

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

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

222 Neural progenitor cells (NPCs), key players in fetal bra

223 s suggested that ZIKV preferentially targets neural progenitor cells (NPCs), providing an explanation

224 evealed that, in a subset of mouse embryonic neural progenitor cells (NPCs), the cell cycle slows bet

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

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

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

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

229 gestation, the number of 2 types of cortical neural progenitor cells (NPCs)-radial glial cells and in

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

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

232 d the role of proteasomes in self-renewal of neural progenitor cells (NPCs).

233 Cs) can originate upon the transformation of neural progenitor cells (NPCs).

234 luripotent stem cell (iPSC) derived cortical neural progenitor cells (NPCs).

235 PSC-derived neurons is conserved in SZ hiPSC neural progenitor cells (NPCs).

236 ation networks that impose distinct fates in neural progenitor cells (NPCs).

237 exhibit reduced brain size due to decreased neural progenitor cells (NPCs).

238 hybrid mouse embryonic stem cells (ESCs) and neural progenitor cells (NPCs).

239 lesions typically fail to recruit endogenous neural progenitor cells (NPCs).

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

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

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

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

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

245 cell-fate specification of neural stem cells/neural progenitor cells (NSCs/NPCs).

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

247 up-regulated miR17-92 cluster expression in neural progenitor cells of the adult mouse.

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

249 miR17-92 cluster either in cultured ischemic neural progenitor cells or in the subventricular zone (S

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

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

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

253 rchitecture in differentiating primary human neural progenitor cells (phNPCs).

254 s have been identified in the CNS, including neural progenitor cell physiology, astrocyte and microgl

255 26 cells, we identified neural stem cell and neural progenitor cell pools and neurons.

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

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

258 es relevant to circuit assembly by affecting neural progenitor cell proliferation and differentiation

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

260 which in vitro organoid systems recapitulate neural progenitor cell proliferation and neuronal differ

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

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

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

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

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

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

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

268 ese mice allowed us to examine how wild-type neural progenitor cells responded to high levels of Abet

269 netic mechanisms are essential in regulating neural progenitor cell self-renewal, with the chromatin-

270 FR degradation in primary GBM cell lines and neural progenitor cells, sharply reducing the self-renew

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

272 l and epigenomic analysis of six consecutive neural progenitor cell stages derived from a HES5::eGFP

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

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

275 Coincidently, we found a population of neural progenitor cells that are controlled by a complex

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

277 During spinal cord development, ventral neural progenitor cells that express the transcription f

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

279 s are a unique transient epithelial niche of neural progenitor cells that give rise to multiple deriv

280 upporting the recent clinical translation of neural progenitor cell therapy for ALS.

281 development, Nf2 suppresses Yap activity in neural progenitor cells to promote guidepost cell differ

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

283 ls (ESC) and hematopoietic stem cells (HSC), neural progenitor cells, trophoblast stem cells and dist

284 human embryonic stem cells into mesendoderm, neural progenitor cells, trophoblast-like cells, and mes

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

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

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

288 n in vitro-differentiated cardiomyocytes and neural progenitor cells, we identified cardiac enhancers

289 nd negative selection for non-TICs and human neural progenitor cells, we identified TIC aptamers that

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

291 adest H3K4me3 domains as a discovery tool in neural progenitor cells, we identify novel regulators of

292 RAMA elements in neural progenitor cells were biallelically accessible in

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

294 ssion and elevated c-Myc protein in ischemic neural progenitor cells, whereas blockade of the Shh sig

295 data indicate that coe, hesl-3 and sim label neural progenitor cells, which serve to generate new neu

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

297 ion and differentiation of adult hippocampal neural progenitor cells, with in vivo expression of acti

298 ound accumulation of NeuN- and Sox2-positive neural progenitor cells within the subventricular zone (

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

300 nt in zebrafish; knockdown of FURIN in human neural progenitor cells yielded abnormal migration.