ライフサイエンスコーパス: precursor cell

1 d adipocytes arise from a common mesenchymal precursor cell.

2 cific marker and nestin, a marker for neural precursor cells.

3 from intracellular stores within neutrophil precursor cells.

4 ps have already transplanted neural stem and precursor cells.

5 be entirely managed by CatS in neutrophilic precursor cells.

6 3 (RIP3)-dependent necroptosis in erythroid precursor cells.

7 fic early expansion of IL-5Ralpha-expressing precursor cells.

8 ension in the apical cell cortex of endoderm precursor cells.

9 proliferation and differentiation of various precursor cells.

10 migration and morphology in embryonic neural precursor cells.

11 n and the expansion of IL-5Ralpha-expressing precursor cells.

12 flammatory serine proteases in hematopoietic precursor cells.

13 in the early specification of chromatophore precursor cells.

14 ntiation of early effector cells into memory precursor cells.

15 cell layer and perturbed the formation of QC precursor cells.

16 tribute to the localization of hematopoietic precursor cells.

17 ogenitors and apical attachment of ependymal precursor cells.

18 cing cells cycle faster than early activated precursor cells.

19 sting the presence of multipotent adipogenic precursor cells.

20 ling maintains and expands subsets of neural precursor cells.

21 and recruitment of resident oligodendroglial precursor cells.

22 s is used as a marker for induced pancreatic precursor cells.

23 perturbing expression of each gene in HGSOC precursor cells.

24 eling the epigenetic landscape of the cancer precursor cells.

25 s into cardiovascular progenitors and neural precursor cells.

26 ted into the chromosomes of egg and/or sperm precursor cells.

27 ymal stem cells, fibroblasts, and adipogenic precursor cells.

28 and innervated myofibers from human myogenic precursor cells.

29 ch haploid gametes are produced from diploid precursor cells.

30 neurons generated are phagocytosed by glial precursor cells.

31 l as in oligodendrocytes and oligodendrocyte precursor cells.

32 ric brain tumour that arises from cerebellar precursor cells.

33 exercise-signalled proliferation of neuronal precursor cells.

34 y subsets of TFs which become inactivated in precursor cells.

35 were detected only at very low levels in few precursor cells.

36 gnature genes, began to be activated in Treg precursor cells.

37 odermal, NK2 homeobox 1-expressing (NKX2-1+) precursor cells.

38 ysis of ERK activity over time in the vulval precursor cells, a well-characterized paradigm of epider

39 Accordingly, loss of CHMP5 in thymocyte precursor cells abolished T cell development, a phenotyp

40 rupting key cell signaling for hematopoietic precursor cell activation and commitment to granulocyte

41 ernational comparison of survival trends for precursor-cell acute lymphoblastic leukaemia (ALL) and a

42 sts and adipocytes are derived from the same precursor cells, adipocyte differentiation may occur at

43 Survival from precursor-cell ALL was very close to that of all lymphoi

44 these data suggest that the transcriptome of precursor cells already contains the genes necessary for

45 g depends on the epigenetic landscape of the precursor cell and is mediated by TETs at the H19 locus.

46 results in a severe reduction of xanthophore precursor cells and a complete depletion of differentiat

47 deficiency of neural-crest-derived skeletal precursor cells and consequently craniofacial anomalies.

48 O) is synthesized by neutrophil and monocyte precursor cells and contributes to host defense by media

49 cells, a host of immune cells, and adipocyte precursor cells and fibroblasts.

50 Somatic gonadal precursor cells and germ cells fail to proliferate fully

51 iosynthesis and cell proliferation in neural precursor cells and in brain tumors.

52 CatC and its proform in human hematopoietic precursor cells and in differentiated mature immune cell

53 brain, Pax6 is expressed in ventricular zone precursor cells and in specific subpopulations of neuron

54 ation, and increased loss of oligodendrocyte precursor cells and mature oligodendrocytes.

55 iptome-wide transformation between astrocyte precursor cells and mature post-mitotic astrocytes.

56 CSF, increased the number of oligodendrocyte precursor cells and promoted remyelination within lesion

57 f such pathways, we exposed mouse osteoblast precursor cells and rat primary mesenchymal stromal cell

58 and Eomes, promoting the expansion of memory precursor cells and their differentiation into functiona

59 re osteoblasts dedifferentiate to osteogenic precursor cells and thus represent an important source o

60 s recapitulated in vitro with fetal neuronal precursor cells and TLR2/6, but not TLR2/1, ligands.

61 ed in terminal effector cells than in memory precursor cells and was regulated by antigenic stimulati

62 o and in vivo experiments in oligodendrocyte precursor cells and zebrafish were performed to test our

63 gration, while in normal cerebellar granule (precursor) cells and MB cells not derived from granule p

64 s and arrested maturation of oligodendrocyte precursor cells, and hypomyelination.

65 ural stem cells, astrocytes, oligodendrocyte precursor cells, and microglia, whereas neurons were les

66 ion, attenuates apoptosis of oligodendrocyte precursor cells, and promotes myelination as well as cli

67 the expression of lineage specific genes in precursor cells, and suggests that hematopoietic stress

68 et molecular events that prime Foxp3(-) Treg precursor cells are largely obscure.

69 Oligodendrocyte precursor cells are the primary source of myelinating ol

70 ranslational interest in the use of stem and precursor cells as a therapeutic agent for chronically i

71 Overexpression of RCANs in osteoclast precursor cells attenuated osteoclast differentiation, w

72 differentiation into MSCs and hematopoietic precursor cells, before the X-chromosome inactivation pr

73 in bone marrow diverts dividing osteoblastic precursor cells (bone marrow stromal cells) to a metabol

74 netic resonance imaging (fMRI), and neuronal precursor cells (BrdU+/Nestin+) were detected by immunof

75 s were stochastically expressed in the early precursor cells, but a few, such as Klf1, were detected

76 R2 drives differentiation of oligodendrocyte precursor cells, but not proliferation or survival.

77 ree TET enzymes are expressed in gonadotrope-precursor cells, but Tet1 mRNA levels decrease markedly

78 gene expression in adult human hematopoietic precursor cells, but the underlying mechanisms are uncle

79 d migration of axial and paraxial mesodermal precursor cells by regulating EMT.

80 In contrast to embryonic precursor cells, C cell-derived tumor cells invading the

81 They are produced by large polyploid precursor cells called megakaryocytes.

82 s may represent a mechanism by which myeloid precursor cells carrying the ELANE mutations evade the p

83 These precursor cells commit to apoptosis-like death under the

84 4) plays a key role in regulating adipogenic precursor cell commitment and differentiation.

85 isition of the KIT mutation in an earlier BM precursor cell confers a significantly greater risk for

86 growth factor (PlGF), secreted by erythroid precursor cells, correlate with increased plasma levels

87 tion boosted the generation of photoreceptor precursor cells, crucial in establishing cell therapy st

88 ine proteases, however, was not abolished in precursor cell cultures.

89 In mesenchymal precursor cells, depletion of WTX and TRIM28 resulted in

90 formation drives HO development and that HO precursor cells derive from a mesenchymal lineage as def

91 es also inhibit the proliferation of granule precursor cells derived from the rhombic lip.

92 Oligodendrocyte precursor cells differentiate into mature oligodendrocyt

93 improved ischemic muscle myopathy and muscle precursor cell differentiation and improved muscle regen

94 novel molecules involved in oligodendrocyte precursor cell differentiation and validated CCL19 as a

95 y, exogenous CCL19 abolished oligodendrocyte precursor cell differentiation observed in patients with

96 Thus, defective precursor cell differentiation, a common trait of aggres

97 n the absence of the formative sieve element precursor cell division, metaphloem identity is seemingl

98 rmation of both terminal effector and memory precursor cells during viral infection.

99 l may target common craniofacial and cardiac precursor cells either directly or indirectly by affecti

100 Exosome complex integrity in erythroid precursor cells ensures Kit receptor tyrosine kinase exp

101 embryonic day (E) 3.25, and the EPI and PrE precursor cells eventually segregate to exclusively expr

102 The muscle precursor cells exhibited a nonspecific pattern compared

103 However, the precursor cells exhibited a resistance to BMP4 owing to

104 gulated differentiation process during which precursor cells express in a coordinated fashion the myo

105 Additionally, epithelial taste precursor cells express Shh transiently, and provide a l

106 Here, we show that neural precursor cell expressed developmentally down-regulated

107 ving the E3 ubiquitin ligase Nedd4-2 (neural precursor cell expressed developmentally down-regulated

108 ith the ubiquitin-like protein NEDD8 (NEural precursor cell expressed Developmentally Down-regulated

109 mosomes 1, 4, 15, and 18, and Nedd4l (neural precursor cell expressed developmentally downregulated g

110 f neddylation, that conjugates Nedd8 (neural precursor cell expressed developmentally downregulated)

111 onarily conserved 8-kD protein NEDD8 (NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWN-REGULATED

112 onjugating either ubiquitin or Nedd8 (Neural precursor cell expressed, developmentally down-regulated

113 on is the conjugation of the molecule neural precursor cell expressed, developmentally down-regulated

114 In this study, we identified NEDD4 (neural precursor cell expressed, developmentally downregulated

115 ne microarray analysis, we discovered neural precursor cell expressed, developmentally downregulated

116 ubiquitin-related modifier) or NEDD8 (neural precursor cell expressed, developmentally downregulated

117 Neural precursor cell expressed, developmentally downregulated-

118 biquitin protein ligase) and NEDD4-1 (Neural precursor cell-expressed developmentally down regulated

119 eracts with the E3 ubiquitin ligase neuronal precursor cell-expressed developmentally down-regulated

120 Neuronal precursor cell-expressed developmentally down-regulated

121 (CSN5), an isopeptidase that removes neural precursor cell-expressed, developmentally down-regulated

122 erived growth factor BB (PDGF BB) and neural precursor-cell-expressed developmentally down-regulated

123 Precursor cells expressing TCRs within a certain low-aff

124 thens the proliferative activity of neuronal precursor cells, facilitates the neuronal migration towa

125 n of terminal-effector cell fates and memory-precursor cell fates, respectively.

126 scription of regulatory catalogues of normal precursor cells for different ovarian cancer subtypes, a

127 emature and expanded differentiation of lens precursor cells forming the lens vesicle, implicating Sn

128 ible methods for manufacturing photoreceptor precursor cells from adult skin in a non-profit cGMP env

129 associated with SCN/AML may protect myeloid precursor cells from apoptosis induced by the NE mutants

130 ns of subcutaneous injection of human muscle precursor cells from the rectus abdominis muscle into nu

131 Sarcomas, and the mesenchymal precursor cells from which they arise, express chondroit

132 f proliferative pathways and oligodendrocyte precursor cell gene expression profile in CIC mutant gli

133 Adipocyte precursor cells generate lipid-filled mature adipocytes

134 Because renin-positive precursor cells give rise to mesangial cells during neph

135 he neural stem cells (NSCs), including glial precursor cells (GPCs), of Alzheimer's disease (AD) are

136 otent stem cell (iPSC)-derived photoreceptor precursor cells have the potential to restore vision to

137 nsformation and adoptive transfer of primary precursor cells (hepatoblasts).

138 Transplantation of human muscle precursor cells (hMPCs) is envisioned for the treatment

139 Studies in hippocampal neuronal precursor cells (HNPCs) demonstrate that IGF-1 stimulate

140 a procedure for differentiating human neural precursor cells (hNPCs) in vitro, followed by isolation

141 -RUNX1 expression in hematopoetic stem cells/precursor cells (HSC/PC) and postnatal infections for hu

142 tion in NIH3T3 and cerebellar granule neuron precursor cells in a p53-independent manner.

143 ses mitochondrial thermogenesis in adipocyte precursor cells in a tissue-autonomous manner.

144 , explaining the random culling (atresia) of precursor cells in bilaterians.

145 s to follow Notch receptors in sensory organ precursor cells in Drosophila.

146 ocodazole- and cytochalasin-D-treated neural precursor cells in large-fiber topography, but was not c

147 The activity of neural precursor cells in the adult hippocampus is regulated by

148 ces cell death and differentiation of neural precursor cells in the developing fetus.

149 identity is first specified from totipotent precursor cells in the embryo.

150 igated the evolutionary origin of SVZ neural precursor cells in the prenatal cerebral cortex by testi

151 odents has shown that Tbr2-expressing neural precursor cells in the SVZ produce excitatory neurons fo

152 tains a consistent population size of neural precursor cells in the ventricular zone, both in the hea

153 stimulate differentiation of oligodendrocyte precursor cells in vitro, in animal models, and in human

154 so seen in isolated SmoA1 cerebellar granule precursor cells in vitro, indicating that the effect of

155 able for the survival of early telencephalic precursor cells, in which any one of three FGFRs (FGFR1,

156 Transplantation of healthy photoreceptor precursor cells into diseased murine eyes leads to the p

157 r formation during differentiation of muscle precursor cells into engineered muscle tissue as a poten

158 on factor is required for differentiation of precursor cells into mature osteoblasts.

159 drives the trans-differentiation of central precursor cells into peripheral nervous system-like Schw

160 The cell fate decision of a mesenchymal precursor cell is under the influence of molecular cues

161 Migration of skeletal muscle precursor cells is a key step during limb muscle develop

162 Moreover, proliferation of oligodendrocyte precursor cells is altered by mutant huntingtin both in

163 s impact on brain morphology and neural stem/precursor cells isolated from Hdac11 (KO/KO) mice had co

164 ed in Zfp521-deficient mice, suggesting that precursor cells lacking Zfp521 differentiate preferentia

165 roliferation of hyperplastic sympathoadrenal precursor cells, leading to a reduced latency and increa

166 LARP1 alone in human adult CD34+ bone marrow precursor cells leads to a reduction in 5'TOP mRNAs and

167 med in mouse and human primary hematopoietic precursor cells (Lin- and CD34+ cells, respectively), an

168 ive ASXL1-BAP1 complexes in a haematopoietic precursor cell line results in global erasure of H2AK119

169 We have identified an oligodendrocyte precursor cell line, termed G144, that supports robust l

170 eed the case in the Drosophila sensory organ precursor cell lineage.

171 otent stem cell-derived (iPS-derived) neural precursor cells may represent the ideal autologous cell

172 elets are produced by large bone marrow (BM) precursor cells, megakaryocytes (MKs), which extend cyto

173 Analysis of mouse medulloblastoma and precursor-cell methylation demonstrated a somatic origin

174 postnatal development Sox14/Otx2-expressing precursor cells migrate from the dorsal midbrain to gene

175 X3 and MET activity required for limb muscle precursor cell migration.

176 grammed precursors and establish a hemogenic precursor cell molecular signature.

177 Allogeneic mesenchymal precursor cells (MPCs) injected during left ventricular

178 he differentiation of implanted human muscle precursor cells (MPCs) into mature skeletal muscle.

179 es have demonstrated the induction of neural precursor cells, neurons, cardiomyocytes, and insulin-pr

180 ions of neurons, astrocytes, oligodendrocyte precursor cells, newly formed oligodendrocytes, myelinat

181 NG2-expressing oligodendrocyte precursor cells (NG2 cells) are exposed to various extri

182 signaling to NG2-expressing oligodendrocyte precursor cells (NG2 cells) could be key to rendering my

183 show that ischemic mice treated with neural precursor cell (NPC) transplantation had on neurophysiol

184 he role of olfactory sensory input to neural precursor cell (NPC) turnover in the SVZ but it was not

185 We demonstrate that neural precursor cell (NPC):glioma cell communication underpins

186 n differentiation of individual human neural precursor cells (NPC) into mature neurons are currently

187 m of cellular signaling by which neural stem/precursor cells (NPCs) communicate with the microenviron

188 induced in embryoid bodies (EBs) and neural precursor cells (NPCs) during development.

189 Recent studies have demonstrated that neural precursor cells (NPCs) from the adult subventricular zon

190 t intrathecal transplantation of neural stem/precursor cells (NPCs) in mice with experimental autoimm

191 if L1 mobilization is restricted to neuronal precursor cells (NPCs) in the human brain.

192 roliferation of ventricular zone (VZ) neural precursor cells (NPCs) in vitro.

193 ycogen synthase kinase (GSK) 3beta in neural precursor cells (NPCs) using the glial fibrillary acidic

194 pluripotent stem cells and then to neuronal precursor cells (NPCs).

195 stacks in border cells and peripheral cells, precursor cells of border cells, displayed similar morph

196 the primitive streak differentiate into the precursor cells of major organ systems.

197 with aberrant STAT3 activation in epithelial precursor cells of the glandular stomach, providing a ne

198 ination capacity remains inefficient because precursor cells often fail to generate new oligodendrocy

199 are two distinct subpopulations of quiescent precursor cells, one directly activated by high-KCl depo

200 xcitotoxicity contributes to oligodendrocyte precursor cell (OPC) damage and hypomyelination in both

201 es of Wnt activity determine oligodendrocyte precursor cell (OPC) differentiation and myelination.

202 delivery method to control oligodendroglial precursor cell (OPC) differentiation through a combinati

203 ing, such as Noggin, promote oligodendrocyte precursor cell (OPC) production after hypoxic-ischemic (

204 mice manifest with decreased oligodendrocyte precursor cell (OPC) proliferation and diminished levels

205 we show that deletion of ciliary IFT80 in OB precursor cells (OPC) in mice results in growth retardat

206 f neural stem cells (NSC) or oligodendrocyte precursor cells (OPC).

207 status, elevated numbers of oligodendrocyte precursor cells (OPCs) and oligodendrocytes, and increas

208 myelination may fail because oligodendrocyte precursor cells (OPCs) do not completely migrate into de

209 tes the ISR in primary mouse oligodendrocyte precursor cells (OPCs) in vitro and that genetically inh

210 ially specified, after which oligodendrocyte precursor cells (OPCs) migrate and proliferate before di

211 vous system and develop from oligodendrocyte precursor cells (OPCs) that must first migrate extensive

212 t a continuum from Pdgfra(+) oligodendrocyte precursor cells (OPCs) to distinct mature oligodendrocyt

213 is known to be expressed in oligodendrocyte precursor cells (OPCs) together with other SoxE factors

214 Human oligodendrocytes precursor cells (OPCs) were stimulated with moderate int

215 ningeal cells, proliferating oligodendrocyte precursor cells (OPCs), and a dense extracellular matrix

216 nd derive from proliferative oligodendrocyte precursor cells (OPCs).

217 mature oligodendrocytes from oligodendrocyte precursor cells (OPCs).

218 Oligodendrocyte precursor cells (OPCs; PDGFRalpha+) produced oligodendro

219 rasure of preexisting chromatin marks in the precursor cell or by de novo assembly.

220 d early on to induce the formation of memory precursor cells or are needed later to sustain memory ce

221 NG2 cells, also known as oligodendrocyte precursor cells or polydendrocytes, which are a resident

222 en proposed to arise either from multipotent precursor cells or pools of heterogeneous, restricted pr

223 QC precursor cells originated from the outer layer of stage

224 eurogenesis are due to an innate decrease in precursor cell performance or to changes in the environm

225 By this way, adult neural precursor cell pool is exhausted and defective neurogene

226 y a unique, endocardially-derived angiogenic precursor cell population for coronary artery formation

227 nsic properties of different oligodendrocyte precursor cell populations affect length?

228 7F expression causes expansion of downstream precursor cell populations, resulting in disease progres

229 subretinal transplantation of photoreceptor precursor cells (PPCs) and retinal progenitor cells (RPC

230 telet-derived growth factor receptor beta(+) precursor cells (preFDCs) that require specific group 3

231 ys a role in regulating hippocampal neuronal precursor cell proliferation following exercise training

232 n in vivo and Tg serum increased mesenchymal precursor cell proliferation in vitro.

233 Conversely, we observed decreased precursor cell proliferation likely due to suppression o

234 ion of ganglioside-mediated oligodendroglial precursor cell proliferation.

235 In the thymus, precursor cells recognize self-glycolipids by virtue of

236 ferase (Gamt) did not affect oligodendrocyte precursor cell recruitment, but resulted in exacerbated

237 Here we show that mouse TRM precursor cells represent a unique CD8(+) T cell subset

238 known as polydendrocytes or oligodendrocyte precursor cells, represent a new entity among glial cell

239 ll populations, but at the expense of losing precursor cells required to maintain a response.

240 n stimulated proliferation of granulopoietic precursor cells, resulting in a marked increase in the r

241 DAOY cells, but not non-transformed granule precursor cells, results in prominent increases in [Ca(2

242 In adult hippocampal neuronal precursor cells, RIT1 controls an Akt-dependent signalin

243 us, WISP2 exerts dual actions in mesenchymal precursor cells; secreted WISP2 activates canonical WNT

244 d parabiotic models, we found that embryonic precursor cells seeded the intestinal mucosa and demonst

245 The observed therapeutic effect of neural precursor cells seems to underlie their capacity to upre

246 ng the fusion of clusters of somatic gonadal precursor cells (SGPs) and their ensheathment of germ ce

247 al germ cells (PGCs) towards somatic gonadal precursor cells (SGPs).

248 dulloblastoma cells not arising from granule precursor cells show neither prominent rises in [Ca(2+)

249 itance, in vitro analysis in oligodendrocyte precursor cells showed that mutant proteins mislocalize.

250 nes could be differentiated to hematopoietic precursor cells, stage-specific analysis of T cell matur

251 nfected GC Tfh cells may be derived from Tfh precursor cell subsets that become infected in marginal

252 expression of TFs among differentially fated precursor cells suggests additional underlying mechanism

253 mic clone emerged in stepwise fashion from a precursor cell that first contained the phage encoding a

254 by new neurons formed in vivo from dividing precursor cells that are located within myenteric gangli

255 However, a population of distinct precursor cells that give rise to mast cells has remaine

256 nown about the original phenotypes of tissue precursor cells that give rise to plastic-adherent CFU-F

257 ion, and 3) Neurog1(+) /NeuroD1(+) immediate precursor cells that make neurons directly.

258 to be detrimental to the survival of neural precursor cells that surround damaged cortical tissue in

259 normal neural precursor and oligodendroglial precursor cells, the putative cellular origins of high-g

260 proliferation of cultured adult hippocampal precursor cells, their requirement for adult hippocampal

261 nfluenced differentiation of oligodendrocyte precursor cells through a crosstalk with microglial cell

262 e cell positions and to track the progeny of precursor cells through development.

263 quired for the transition from proliferative precursor cell to a more differentiated immature neuron

264 y activation inhibits the differentiation of precursor cells to a neuroendocrine fate.

265 of Ras/MAPK signal in the commitment of the precursor cells to adipose tissues.

266 ion in the embryo and placenta; however, the precursor cells to hemogenic endothelium are not defined

267 fers a poised state to the Foxp3 promoter in precursor cells to make Treg cell lineage commitment res

268 ting the transition of adult oligodendrocyte precursor cells to mature OLs that is essential for myel

269 myogenic differentiation process from muscle precursor cells to mature skeletal muscle tissue in musc

270 that this pathway functions in reproductive precursor cells to primarily target long centromeric hig

271 as is also the asymmetric cell divisions of precursor cells to produce the coupled G-cells and ECL c

272 ously revealed the contribution of nestin(+) precursor cells to the mesenchymal as well as the endoth

273 that Tal1 knockout does not immediately bias precursor cells towards a cardiac fate.

274 n cell division, survival, and commitment of precursor cells towards a myocardial lineage, and overex

275 We here show that neural stem/precursor cell transplantation after ischemic stroke is

276 may be useful in quality control of retinal precursor cell transplantation.

277 d structural properties depending upon their precursor cell type of origin.

278 nded to the conversion of a third osteoclast precursor cell type- dendritic cells.

279 rentiate toward their common adrenal-gonadal precursor cell type.

280 es across the three different ovarian cancer precursor cell types, and evidence of tissue-specific re

281 ulator of osteoclastogenesis from the 3 main precursor cell types: monocytes, macrophages and dendrit

282 Meristemoids, which are stem cell-like precursor cells, undergo asymmetric divisions, generatin

283 intracellular protein, it helps to maintain precursor cells undifferentiated.

284 leaved from both neurons and oligodendrocyte precursor cells via the ADAM10 sheddase.

285 As stem cells are thought to be the tumor precursor cells, visualizing their behavior is crucial f

286 tion in other uterine cells (ventral uterine precursor cells [VUs]) that initially have potential to

287 The number of proliferating neuronal precursor cells was increased with training in VEGF(f/f)

288 Here, specifically targeting adult neural precursor cells, we conditionally express an activated f

289 enes and single-cell cultures of fetal liver precursor cells, we identified the common proximal precu

290 al output in embryonic stem cells and neural precursor cells, we show that the likelihood that genes

291 Here, retinal precursor cells were cultured in a microfluidic chip wit

292 Post-mitotic photoreceptor precursor cells were generated using a stepwise cGMP-com

293 acrophages in LPL(-/-) pups, suggesting that precursor cells were not correctly localized to the alve

294 sistent with the concept that Tbr2(+) neural precursor cells were present in the common ancestor of m

295 ect numbers of WM but not GM oligodendrocyte precursor cells, whereas during astrocytogenesis Ascl1 f

296 rations), to dedifferentiate into hepatocyte precursor cells (which then become HCC cells that expres

297 Taste placodes comprise taste bud precursor cells, which express the secreted factor sonic

298 of CHC22 induced neurite outgrowth in neural precursor cells, which was rescued by stable overexpress

299 colony-forming cells (ECFCs) are endothelial precursor cells with a high proliferative capacity and p

300 nificant increase in proliferation of neural precursor cells without further differentiation into neu