ライフサイエンスコーパス: neural progenitor cell

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

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

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

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

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

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

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

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

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

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

11 th epithelial cells continually recruited as neural progenitor cells.

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

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

14 n and premature differentiation of embryonic neural progenitor cells.

15 iption factor expressed in adult hippocampal neural progenitor cells.

16 s an important component of FGF signaling in neural progenitor cells.

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

18 large lineages by transient amplification of neural progenitor cells.

19 ential transducers of PS1 signaling in adult neural progenitor cells.

20 ge plane orientation regulates the output of neural progenitor cells.

21 the developmental potential is restricted in neural progenitor cells.

22 so with differentiation and proliferation of neural progenitor cells.

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

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

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

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

27 h interferes with maturation and survival of neural progenitors cells.

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

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

30 ential of stem/progenitor cells, adult human neural progenitor cells ("AHNPs") isolated from idiopath

31 Thus, we postulate that human neural progenitor cells aid recovery after stroke throug

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

33 Neural progenitor cells and capillaries, detected on hip

34 RhoA-deficient embryos exhibit expansion of neural progenitor cells and exencephaly-like protrusions

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

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

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

38 mouse Lin41 (mLin41) is highly expressed in neural progenitor cells and its expression declines duri

39 Defects in spindle orientation in neural progenitor cells and migration of neurons probabl

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

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

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

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

44 e mechanism of Shh-induced transformation of neural progenitor cells and suggest that induction of Sn

45 undergo somatic retrotransposition in human neural progenitor cells and that an increase in human-sp

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

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

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

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

50 ns generated in vitro from adult hippocampal neural progenitor cells and, in parallel, a decrease in

51 x2, a transcription factor expressed in many neural progenitor cells, and directly by an interaction

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

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

54 sion profile enriched for genes expressed in neural progenitor cells, and this was associated with in

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

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

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

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

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

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

61 n glioblastoma, gliosis, non-tumor brain and neural progenitor cells by SDS-PAGE, immunoblot, mass sp

62 hese findings show that transplanted enteric neural progenitor cells can generate functional enteric

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

64 the Sleeping Beauty transposon in cerebellar neural progenitor cells caused widespread dissemination

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

66 as and expression of activated RAS or RAF in neural progenitor cells combined with either AKT activat

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

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

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

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

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

72 we manipulated the expression of ZNF804A in neural progenitor cells derived from human cortical neur

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

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

75 Strikingly, Tsc1-null neural progenitor cells develop into highly enlarged gia

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

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

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

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

80 d a potential target for the manipulation of neural progenitor cell differentiation.

81 Loss of RhoA in neural progenitor cells disrupts adherens junctions and

82 lution results primarily from an increase in neural progenitor cell divisions in its two principal ge

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

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

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

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

87 lusion that GT-tMRI can noninvasively reveal neural progenitor cells during vascularization.

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

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

90 Furthermore, RhoA-deficient neural progenitor cells exhibit accelerated proliferatio

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

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

93 uch cell typing is inadequate for preserving neural progenitor cells for any meaningful stem cell the

94 nt of the transcription programs required in neural progenitor cells for the proper specification of

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

96 dentifying and isolating distinct classes of neural progenitor cells from the central nervous system.

97 cluster plays an important role in mediating neural progenitor cell function and that the Shh signali

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

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

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

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

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

103 SOD1(G93A) rats were injected with human neural progenitor cells (hNPCs) bracketing the phrenic m

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

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

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

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

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

109 of hESCs, such as neural fate specification, neural progenitor cell identity maintenance, and the tra

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

111 han during differentiation, and expressed in neural progenitor cells, immature and matured neurons an

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

113 tion of neural stem-like cells but not early neural progenitor cells in the adult hippocampus.

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

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

116 n both the chick and mouse and restricted to neural progenitor cells in the ganglionic eminence that

117 ogenitor cells-one of the best-characterized neural progenitor cells in the mammalian brain.

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

119 Proliferation of neural progenitor cells in the subventricular zone leads

120 report that mosaic induction of Tsc1 loss in neural progenitor cells in Tsc1(cc) Nestin-rtTA(+) TetOp

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

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

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

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

125 increased proliferation of rodent and human neural progenitor cells in vitro.

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

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

128 However, our mechanistic studies of neural progenitor cells indicate mLin41 is not required

129 Ectopic expression of Atf5 in neural progenitor cells induces expression of multiple O

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

131 Here we show that neural progenitor cells infected with lentiviral vectors

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

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

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

135 genesis by inhibiting the differentiation of neural progenitor cells into neurons.

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

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

138 erentiation, suggesting that PS1 function in neural progenitor cells is gamma-secretase-dependent.

139 ocytes, suggesting that multipotentiality of neural progenitor cells is not affected by reduced level

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

141 How self-renewal versus differentiation of neural progenitor cells is temporally controlled during

142 proliferation and self-renewing capacity of neural progenitor cells isolated from Pak4 knockout brai

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

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

145 use model, recombination and loss of Tsc1 in neural progenitor cells leads to brain enlargement, hype

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

147 in41 acts as a temporal regulator to promote neural progenitor cell maintenance, not via the regulati

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

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

150 igate this further, we modeled PMSE in mouse neural progenitor cells (mNPCs) in vitro and in developi

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

152 Neural progenitor cells (NeuPCs) possess a unique nuclea

153 Neural progenitor cells, neurons, and glia of the normal

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

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

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

157 Signaling through GABA(A) receptors controls neural progenitor cell (NPC) development in vitro and is

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

159 ed for pharmacological approaches to enhance neural progenitor cell (NPC) function particularly in ne

160 s adult hippocampal neurogenesis by altering neural progenitor cell (NPC) proliferation and survival;

161 rse neurological side effects due to reduced neural progenitor cell (NPC) proliferation.

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

163 ions in the mouse model is the fetal brain's neural progenitor cell (NPC)-rich subventricular zone.

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

165 Recent success using neural progenitor cells (NPC) in models of adult neurode

166 Transplantation of neural progenitor cells (NPC) is a promising therapeutic

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

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

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

170 ive disorder (MDD), antidepressants increase neural progenitor cells (NPCs) and capillaries in the hu

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

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

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

174 Mature neurons (MNs), neural progenitor cells (NPCs) and neuroblastoma cells (

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 cells, iPS-derived neural stem cells (NSCs), neural progenitor cells (NPCs) and neurons suggests that

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

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

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

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

182 ta-catenin pathway promotes proliferation of neural progenitor cells (NPCs) at early stages and induc

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

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

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

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

187 Neural progenitor cells (NPCs) can repair damaged myelin

188 subventricular zone (SVZ), S phase entry of neural progenitor cells (NPCs) correlates with a local i

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

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

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

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

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

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

195 lipid that can induce pleomorphic effects in neural progenitor cells (NPCs) from the cerebral cortex,

196 of TNF-alpha on cell fate decision in human neural progenitor cells (NPCs) has rarely been studied.

197 Neural progenitor cells (NPCs) have distinct proliferati

198 Neural progenitor cells (NPCs) have regenerative capabil

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

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

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

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

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

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

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

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

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

208 cyte antigen receptor, is expressed in adult neural progenitor cells (NPCs) of the dentate gyrus.

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

210 discrete areas of the adult mammalian brain, neural progenitor cells (NPCs) produce fewer new neurons

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

212 Neural progenitor cells (NPCs) residing in the subgranul

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

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

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

216 We found mouse neural progenitor cells (NPCs) to have a secretory prote

217 secrete CXCL12, enhancing the recruitment of neural progenitor cells (NPCs) to lesion sites via long-

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

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

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

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

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

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

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

225 neuronal differentiation and self-renewal of neural progenitor cells (NPCs), supported the survival o

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

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

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

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

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

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

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

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

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

235 1-6), several of which are enriched in fetal neural progenitor cells (NPCs).

236 ely, in proliferation and differentiation of neural progenitor cells (NPCs).

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

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

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

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

241 uently accompanied by an overall decrease in neural progenitor cell number at later time points.

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

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

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

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

246 cent microscopy, we demonstrated that living neural progenitor cells (PC-12.1), as well as the cells

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

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

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

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

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

252 4 plays a critical role in the regulation of neural progenitor cell proliferation and in establishing

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

254 Neural progenitor cell proliferation was determined by u

255 annabinoid type 1 receptors (CB(1)R) promote neural progenitor cell proliferation, and in the liver t

256 d a key regulator in controlling hippocampal neural progenitor cell proliferation, and reversed the i

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

258 ed regional specificity in the properties of neural progenitor cells, revealed by the function of a m

259 , and sensitivity to oxidative stress in rat neural progenitor cells (rNPCs).

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

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

262 Conditional mutant mice lacking SRF in neural progenitor cells (Srf-Nestin-cKO) exhibit strikin

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

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

265 nhances the generation of neurons in a human neural progenitor cell system in vitro and also the gene

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

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

268 both developmental and adult-born cohorts of neural progenitor cells that contribute to the pool of a

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

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

271 with expression of EphB2 in nestin-positive neural progenitor cells that migrate medially from the l

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

273 cell-surface markers currently available for neural progenitor cells, this provides an invaluable too

274 In either uninfected GBM cells or neural progenitor cells, thought to be the GBM precursor

275 ll diversification depends on the ability of neural progenitor cells to divide asymmetrically to gene

276 vestigated the ability of transplanted human neural progenitor cells to enhance this structural plast

277 from the expression of TRF2 in proliferating neural progenitor cells to expression of a unique short

278 for timing the spatiotemporal transition of neural progenitor cells to neurons.

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

280 r results show the first evidence that human neural progenitor cell treatment can significantly incre

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

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

283 Reduction of PS1 expression in neural progenitor cells was accompanied by a decrease in

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

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

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

287 RAMA elements in neural progenitor cells were biallelically accessible in

288 Neural progenitor cells were labeled with fluorescent pr

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

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

291 by secreted FGFs stimulates proliferation of neural progenitor cells, whereas direct integrative nucl

292 s to identify the asymmetric determinants in neural progenitor cells, which could be tumor suppressor

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

294 uclear translocation and mitotic division of neural progenitor cells, while the role of DCX in cortic

295 bgranular zone of the dentate gyrus contains neural progenitor cells with self-renewal and multilinea

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

297 Neural progenitor cells within the developing thalamus a

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.