ライフサイエンスコーパス: precursor cell

1 rs, evidently the recent progeny of a single precursor cell.

2 stnatal nature of the hematopoietic stem and precursor cell.

3 ication syndrome in patient-derived neuronal precursor cells.

4 signaling that helps to shape nearby tendon precursor cells.

5 bute to preserve the endothelial identity of precursor cells.

6 s seen in highly purified PAR1 KO osteoclast precursor cells.

7 e marks in progenitor-like cells than memory precursor cells.

8 s transiently induced in cultured osteoclast precursor cells.

9 e CD4SP thymocytes, which also contain T reg precursor cells.

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

11 from intracellular stores within neutrophil precursor cells.

12 mature oligodendrocytes and oligodendrocyte precursor cells.

13 l as in oligodendrocytes and oligodendrocyte precursor cells.

14 ric brain tumour that arises from cerebellar precursor cells.

15 exercise-signalled proliferation of neuronal precursor cells.

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

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

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

19 and IDEC models generated from primary human precursor cells.

20 anges in gene expression in lateral skeletal precursor cells.

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

22 ps have already transplanted neural stem and precursor cells.

23 be entirely managed by CatS in neutrophilic precursor cells.

24 3 (RIP3)-dependent necroptosis in erythroid precursor cells.

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

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

27 proliferation and differentiation of various precursor cells.

28 kinetochores and its enrichment in germline precursor cells.

29 0 as an important factor in mammary stem and precursor cells.

30 tions, repair Schwann cells, and mesenchymal precursor cells.

31 in murine Samd14-Enh(-/-) primary erythroid precursor cells.

32 lineage programming and maturation of thymic precursor cells.

33 t differentiation of bone marrow mesenchymal precursor cells.

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

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

36 In the anchor cell/ventral uterine precursor cell (AC/VU) fate decision during C. elegans g

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

38 onment can activate microglia, reduce neural precursor cell activity and impair cognition in mice.

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

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

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

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

43 e cells: the stronger checkpoint in germline precursor cells also depends on PCH-2.

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

45 TCF-1 in early-fate-bifurcation-driving Tex precursor cells and also identify PD-1 as a protector of

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

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

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

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

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

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

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

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

54 hiPSCs, neural precursor cells, and cortical neurons derived from six h

55 beta-catenin pathway in the lateral skeletal precursor cells, and does not influence the Sema3d pathw

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

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

58 (Hi) effectors while fostering KLRG1(Lo) Tex precursor cells, and PD-1 stabilized this TCF-1(+) Tex p

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

60 roliferation and differentiation of myogenic precursor cells, and these actions concertedly inhibit m

61 PCH-2 is enriched in germline precursor cells, and this enrichment relies on conserved

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

63 on and found that SVZ endogenous neural stem/precursor cells are recruited during the remyelination p

64 dy of the efficacy and safety of mesenchymal precursor cells as immunotherapy in patients with advanc

65 ion of skin-derived REDD1 knockout adipocyte precursor cells as indicated by higher lipid accumulatio

66 ellular process expansion by oligodendrocyte precursor cells as well as expression and cellular local

67 stabilization of myelin and oligodendrocyte precursor cells associated with increased nuclear transl

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

69 e CD8(+) T cells became distinct from memory precursor cells before the peak of the T cell response.

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

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

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

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

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

75 an branching trigger oligodendrogenesis from precursor cells by inhibiting platelet-derived growth fa

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

77 Bone marrow mesenchymal precursor cells can differentiate into adipocytes or ost

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

79 nd a highly heterogeneous ILC1, ILC3, and NK precursor cell cluster.

80 it inhibits the effect of BMP2/4 on adipose precursor cell commitment/differentiation.

81 e, intramyocardial injections of mesenchymal precursor cells, compared with injections of a cryoprote

82 ulturing with astrocytes and oligodendrocyte precursor cells (complex culture).

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

84 in sulfate proteoglycan (CSPG) 4 type neural precursor cells (CSPG4Es) were purified from human plasm

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

86 Expression of H3.3K4M in lineage-specific precursor cells depletes H3K4 methylation and impairs ad

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

88 in SBMA mice, and crucially in motor neuron precursor cells derived from SBMA patient stem cells, su

89 d in endodermal organogenesis and pancreatic precursor cell differentiation and development.

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

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

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

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

94 s, it subsequently increases oligodendrocyte precursor cell differentiation, oligodendrocyte generati

95 ranscriptional profile of cycling epithelial precursor cells; distinct from LGR5-expressing cells.

96 d impairing the differentiation of microglia precursor cells during postnatal development.

97 Neural precursor cell dysfunction and white matter dysfunction

98 acteristic vacuoles in myeloid and erythroid precursor cells, dysplastic bone marrow, neutrophilic cu

99 The contribution of endogenous neural precursor cells (eNPCs) located in the subventricular zo

100 e focused our attention on endogenous neural precursor cells (eNPCs) located within the subventricula

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

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

103 lioma, neural stem cells and oligodendrocyte precursor cells, exhibited a high glioma frequency.

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

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

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

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

108 In tsA201, NEDD (neural precursor cell expressed developmentally downregulated p

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

110 achment of the ubiquitin-like protein neural precursor cell expressed, developmentally down-regulated

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

112 Nestin-positive enteric neural precursor cells expressed TLR2 and TLR4.

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

114 n by an E3 ubiquitin ligase, NEDD4-1 (neural precursor cell-expressed developmentally down-regulated

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

116 by mature hematopoietic cells, and erythroid precursor cell expression of Gdf11 has been implicated i

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

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

119 Megakaryocytes (MKs), the precursor cells for platelets, migrate from the endostea

120 ticular tissue allows storage of early sperm precursor cells for use in generating new individuals vi

121 pared to neural crest cells, the presumptive precursors cells for neuroblastoma, by using genome-wide

122 e does not alter erythropoiesis or erythroid precursor cell frequency under normal conditions or duri

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

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

125 cular chondrocytes and prevents chondrogenic precursor cells from repairing cartilage lesions, leadin

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

127 Adipocyte precursor cells generate lipid-filled mature adipocytes

128 Mesenchymal precursor cells have a unique multimodal mechanism of ac

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

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

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

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

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

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

135 sic property of fetal hematopoietic stem and precursor cells (HSPCs) caused by high expression of the

136 Moreover, hematopoietic stem/precursor cells (HSPCs) doubly deficient for Tet2 and Dn

137 Finally, the deletion of Pagr1 in Myf5(+) precursor cells impairs brown adipose tissue and muscle

138 tion by deletion of Olig2 in oligodendrocyte precursor cells impairs spatial memory in young mice, wh

139 After division of a precursor cell in the zebrafish's lateral line, the daug

140 l12-creER(+) BMSCs transform into osteoblast precursor cells in a manner mediated by canonical Wnt si

141 Clinical Events With Allogeneic Mesenchymal Precursor Cells in Advanced Heart Failure) is an ongoing

142 and enhances chondrogenic differentiation of precursor cells in an inflammatory environment may provi

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

144 n the fastest evolving cell fate among vulva precursor cells in Caenorhabditis nematodes, that of P3.

145 old nanocrystal treatment of oligodendrocyte precursor cells in culture resulted in oligodendrocyte m

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

147 s the function of a population of melanocyte precursor cells in hair and vibrissal follicles that exp

148 ers, epigenetic dysregulation in tissue stem/precursor cells in numerous examples of childhood cancer

149 decisions and the existence of committed TRM precursor cells in the circulatory TEFF compartment.

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

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

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

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

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

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

156 share transcriptional regulators with memory precursor cells, including T cell-specific transcription

157 ects on myelination, loss of oligodendrocyte precursor cells, increased apoptosis in the CNS, and imp

158 -response characteristics in oligodendrocyte precursor cells, indicating their participation in the e

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

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

161 P-1 drove differentiation of oligodendrocyte precursor cells into mature oligodendrocytes in vitro.

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

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

164 Finally, the stronger checkpoint in germline precursor cells is regulated by CMT-1, the ortholog of p

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

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

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

168 t uncontrolled YAP1/TAZ activity in neuronal precursor cells leads to ependymoma-like tumours in mice

169 Osteoblast precursor cell line (MC3T3-E1) and primary murine osteob

170 n of the ST2 bone marrow-derived mesenchymal precursor cell line into adipocytes.

171 LL cell line, SEM, and an immortal erythroid precursor cell line, HUDEP-2, to allow for acute depleti

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

173 TMEM106B-deficient Oli-neu oligodendroglial precursor cell line.

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

175 r neutralizing antibodies promotes erythroid precursor cell maturation and red blood cell formation i

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

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

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

179 the enzymatic SET domain in lineage-specific precursor cells mimics H3.3K4M expression, destabilizes

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

181 of primary neuroblastoma tumors, neuroblast precursor cells, neuroblastoma cell lines and various ce

182 ation and differentiation of oligodendrocyte precursor cells (NG2(+) cells) in a decorin-mediated neu

183 and corresponding iPSC studies showed neural precursor cell (NPC) proliferation abnormalities and red

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

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

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

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

188 (ZIKV) causes microcephaly by killing neural precursor cells (NPCs) and other brain cells.

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

190 A subclass of neural stem and precursor cells (NPCs) expresses VLA4 (integrin alpha4be

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

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

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

194 hippocampus of adult mice, quiescent neural precursor cells (NPCs) maintain the highest ROS levels (

195 macological stimulation of endogenous neural precursor cells (NPCs) may promote cognitive recovery an

196 ewal, early neuronal differentiation, neural precursor cells (NPCs), assembled rosettes, and differen

197 on of cortical cells by phagocytosing neural precursor cells (NPCs), but how microglia interact with

198 r findings support the concept that tumor or precursor cells of BLS-type DLBCL are attracted by chemo

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

200 ubsequent developmental stages and comprises precursor cells of the embryo proper and yolk sac(1).

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

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

203 (HERV-W) negatively affects oligodendroglial precursor cell (OPC) differentiation and remyelination v

204 (BZA), as a potent agent of oligodendrocyte precursor cell (OPC) differentiation and remyelination.

205 NS hypomyelination, although oligodendrocyte precursor cell (OPC) numbers are normal.

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

207 ion by negatively regulating oligodendrocyte precursor cell (OPC) proliferation.

208 Oligodendrocyte precursor cell (OPC)-specific TrkB deletion in chemother

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

210 ion in both murine and human oligodendrocyte precursor cells (OPCs) and coculture systems, we find th

211 nal source of human cortical oligodendrocyte precursor cells (OPCs) and define a lineage trajectory.

212 rat Schwann cells (SCs) and oligodendrocyte precursor cells (OPCs) and explored the molecular mechan

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

214 promotes differentiation of oligodendrocyte precursor cells (OPCs) and remyelination in a cross talk

215 Oligodendrocyte precursor cells (OPCs) are abundant in the adult central

216 We report that oligodendrocyte precursor cells (OPCs) contact sprouting endothelial tip

217 During differentiation, oligodendrocyte precursor cells (OPCs) extend a network of processes tha

218 d perivascular clustering of oligodendrocyte precursor cells (OPCs) in certain active MS lesions, rep

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

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

221 f anacardic acid to cultured oligodendrocyte precursor cells (OPCs) rapidly increased expression of m

222 s the inability of recruited oligodendrocyte precursor cells (OPCs) to complete remyelination and to

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

224 at, in injured optic nerves, oligodendrocyte precursor cells (OPCs) undergo transient proliferation b

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

226 itatory neurons and immature oligodendrocyte precursor cells (OPCs), and these contributed almost hal

227 form bona fide synapses with oligodendrocyte precursor cells (OPCs), but the circuit context of these

228 lination, driven by resident oligodendrocyte precursor cells (OPCs), might partially compensate myeli

229 ction, expanding the pool of oligodendrocyte precursor cells (OPCs).

230 ly produce motor neurons and oligodendrocyte precursor cells (OPCs).

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

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

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

234 acetylcholine receptor 1 in oligodendrocyte precursor cells, or promoting oligodendroglial different

235 QC precursor cells originated from the outer layer of stage

236 cells, and PD-1 stabilized this TCF-1(+) Tex precursor cell pool.

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

238 Specifically, an early-life precursor cell population, retained in the mouse cortex

239 ) and differentiated them into photoreceptor precursor cells (PPCs) or retinal organoids (ROs).

240 adult dentate gyrus led to increased neural precursor cell proliferation and their migration into th

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

242 deregulated normal timing for progenitor and precursor cell proliferation following photoreceptor dam

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

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

245 Concomitantly, a medullary precursor cell quiesces, thereby impairing maintenance o

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

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

248 and reversible developmental arrest in which precursor cells remain quiescent and preserve developmen

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

250 f these promoters from their closed state in precursor cells requires function of the spermatocyte-sp

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

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

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

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

255 re wrapped individually by two somatic gonad precursor cells (SGPs).

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

257 by guidance signals towards somatic gonadal precursor cells (SGPs).

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

259 s, by passaging multiple times at the Neural Precursor Cell stage, prior to final differentiation.

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

261 re oligodendrocytes, but not oligodendrocyte precursor cells, suggesting triglial dysfunction mediate

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

263 hibitory for chondrogenic differentiation of precursor cells than conditioned medium from chondrocyte

264 RNA sequencing to identify a beige adipocyte precursor cell that gives rise to thermogenic adipocytes

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

266 (LUHMES) cells are human embryonic neuronal precursor cells that can be maintained as proliferating

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

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

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

270 odulates ferroportin expression on erythroid precursor cells, thereby lowering potentially toxic-free

271 related to its function in mammary stem and precursor cells, this is not the case for its function d

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

273 wer myonuclei and reduced overall numbers of precursor cells throughout postnatal life.

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

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

276 e of neurons originating from enteric neural precursor cells to approximately 10%, compared with appr

277 BMP7 instructs precursor cells to differentiate into LCs that phenotypi

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

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

280 e that fear learning induces oligodendrocyte precursor cells to proliferate and differentiate into my

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

282 exposure of monocytes, which are macrophage precursor cells, to certain stimuli can lead to a hypo-i

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

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

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

286 , regeneration and fibrosis during which HCC precursor cells undergo malignant transformation and lea

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

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

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

290 e initiates patterning of multipotent vulval precursor cells (VPCs) of Caenorhabditis elegans We have

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

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

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

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

295 Numbers of adipocyte precursor cells were lower in REDD1 knockout skin.

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

297 compatible with ectopic Notch activation in precursor cells, where it is normally inactive.

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

299 e 2 results and evaluate whether mesenchymal precursor cells will reduce the rate of nonfatal recurre

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