ライフサイエンスコーパス: progenitor cell

1 the differentiation of resident mesenchymal progenitor cells.

2 at CSCs originate from non-malignant stem or progenitor cells.

3 ramming of cord blood hematopoietic stem and progenitor cells.

4 over osteogenic differentiation of skeletal progenitor cells.

5 ISPR interference experiment in human neural progenitor cells.

6 ecrease in mature oligodendrocytes and their progenitor cells.

7 self-renewal and differentiation of stem and progenitor cells.

8 pro-commitment factor in spermatogonial stem/progenitor cells.

9 induced pluripotent stem cell-derived neural progenitor cells.

10 ion, differentiation, and migration of basal progenitor cells.

11 regulating embryonic stem and hematopoietic progenitor cells.

12 mia TF1 cells and primary hematopoietic stem-progenitor cells.

13 M)-derived fibrocytes and a variety of local progenitor cells.

14 y in particular cell types, such as stem and progenitor cells.

15 ulation of heterogeneous, lineage-restricted progenitor cells.

16 self-renewal activity in hematopoietic stem/progenitor cells.

17 ance and function of haematopoietic stem and progenitor cells.

18 proliferation and differentiation of nephron progenitor cells.

19 tems to generate distinct spatial domains of progenitor cells.

20 s in the majority of haematopoietic stem and progenitor cells.

21 essing tumours originating from intermediate progenitor cells.

22 ld be generated by a limited set (<1,000) of progenitor cells.

23 ferentially expressed gene within osteoclast progenitor cells.

24 Aergic specification of the patients' neural progenitor cells.

25 g with increased aneuploidy in hematopoietic progenitor cells.

26 nals regulate the state and fate of stem and progenitor cells.

27 tional capacities of various types of EC and progenitor cells.

28 tachment and differentiation of PC-12 neural progenitor cells.

29 form population compared with adult stem and progenitor cells.

30 tment capacity by seeking to expand stem and progenitor cells.

31 tion, despite lower global levels of 5hmC in progenitor cells.

32 granulocyte and macrophage development from progenitor cells.

33 progeny of a defined population of dividing progenitor cells, a daunting task in the developing cent

34 igenomic profiling of hematopoietic stem and progenitor cells across ontogeny (as explored in this is

35 Consistent with enrichment for stem/progenitor cells, ALDH+ cells have greater WNT signaling

36 Single-cell genotyping of circulating CD34 + progenitor cells allows the reconstruction of MF phyloge

37 e we show that acute responses to alcohol in progenitor cells altered gene expression in their descen

38 results in an aberrant expansion of lymphoid progenitor cells and a high penetrance formation of chro

39 An alternative approach to utilize progenitor cells and circulatory factors and to improve

40 developing cerebral cortex, including neural progenitor cells and developing neurons.

41 ries of mouse embryonic stem cells, neuronal progenitor cells and differentiated neurons and identify

42 gnature and promotes organoid formation from progenitor cells and enhances regeneration following inj

43 , making them distinct from other CML or AML progenitor cells and from normal haematopoietic stem cel

44 nt-naive chronic myeloid leukemia (CML) stem/progenitor cells and identified that miR-185 levels anti

45 on and disease progression that involve stem/progenitor cells and inflammation in a tissue-specific m

46 antage by enhancing self-renewal of stem and progenitor cells and inhibiting their differentiation.

47 nts had an increased number of proliferating progenitor cells and lost quiescent stem cells.

48 redominant mature neutrophils, and decreased progenitor cells and lymphocytes.

49 Splenic erythroid progenitor cells and mesenchymal stromal cells contribut

50 quitous across several cell types, including progenitor cells and migrating neurons but their functio

51 when silencing Mcp1) the release of stem and progenitor cells and of leukocytes from the bone marrow.

52 reased CNTF and BMP4 transcription in neural progenitor cells, and a neutralizing antibody against CN

53 mbers and function of hematopoietic stem and progenitor cells, and frequency of niche cells were not

54 on and bone progenitor cells but also muscle progenitor cells, and it controls musculoskeletal system

55 a major regulator of mammary epithelial stem/progenitor cells, and its activity is dysregulated under

56 cific requirement for Sp2 in neural stem and progenitor cells, and reveal mechanistic differences bet

57 e of the nuclear lamins in adult neural stem/progenitor cells (ANSPCs), underlies age-related alterat

58 gent regulation of the two different adipose progenitor cells (APCs).

59 Here, megakaryocyte progenitor cells are genetically engineered to overexpre

60 nts that are functionally important in these progenitor cells are largely unknown.

61 Progenitor cells are mobilized from bone marrow niches i

62 caused by ectopic proliferation of misplaced progenitor cells are relatively rare.

63 ll RNA-seq and lineage-tracing, we find that progenitor cells are the principal targets of ageing, wh

64 Bone marrow-derived hematopoietic stem/progenitor cells are vasculogenic and play an important

65 spleen, thymus, and haematopoietic stem and progenitor cells, as well as in CD8(+)CD28(-) T cells fr

66 The abnormal positioning of retinal progenitor cells at birth and ectopic presence of photor

67 Sox9 was expressed in MTJ, tendon, and bone progenitor cells at E13 and in bone at E16.

68 vo autologous CD34(+) hematopoietic stem and progenitor cell-based lentiviral gene therapy following

69 xis, at least in part, mediates colonic stem/progenitor cell behavior.

70 role played by the Notch pathway in cardiac progenitor cell biology remains to be elucidated.

71 n various cell types, including human neural progenitor cells, blocks ZIKV infection.

72 teogenic differentiation of bone mesenchymal progenitor cells (BMSCs).

73 ining (LR) and non-LR hematopoietic stem and progenitor cells both had indistinguishable localization

74 Human adult basal stem/progenitor cells (BSCs) obtained from chronic rhinosinus

75 Human biliary tree stem/progenitor cells (BTSC) within PBGs were isolated from E

76 ox9 is expressed in not only tendon and bone progenitor cells but also muscle progenitor cells, and i

77 GRP1-ires-EGFP enhances fitness of stem- and progenitor- cells, but only in the context of native hem

78 cells derived from an endogenous adult stem/progenitor cell, called adult human neural progenitor (A

79 Basal/stem and luminal progenitor cells can differentiate in culture to generat

80 Nonetheless, progenitor cells can irreversibly commit to an erythroid

81 ng into cardiomyocytes like proposed cardiac progenitor cells, cardiac SP cells fuse with preexisting

82 s at the base of the primary cilia in neural progenitor cells, causing an atypical non-genetic ciliop

83 s, BM hematopoietic cellularity and stem and progenitor cell clonogenicity in mouse BM.

84 primary efficacy end points and endothelial progenitor cell colony-forming unit mobilization in peri

85 In summary, hypothalamic neural stem/progenitor cells comprise subpopulations with multifacet

86 Induced neuronal progenitor cell conversion can produce a high yield of d

87 which were dominated by normal distal airway progenitor cells, COPD lungs were inundated by three var

88 GZ vascularization, Hif1alpha restrains CGN-progenitor cell-cycle exit.

89 Alveolar Type II progenitor cell density and self-renewal were maintained

90 on's disease (PD) tissue sources: (a) neural progenitor cells derived from an endogenous adult stem/p

91 rs AT1 and Mas-are expressed in vasculogenic progenitor cells derived from humans and rodents.

92 In this study we use cultured neural progenitor cells derived from olfactory neuroepithelium

93 Transcriptomic profiling of cortical neural progenitor cells derived from these hiPSCs identified al

94 We identified midfetal cortical neural progenitor cell development-more specifically, the ventr

95 tation promoted neuronal and oligodendrocyte progenitor cell development.

96 llular protein that promotes oligodendrocyte progenitor cell differentiation and myelination in vitro

97 ng A2B5, an early marker in oligodendrocytes progenitor cell differentiation as well as GalC(+)/O1(+)

98 allows us to investigate alveolar epithelial progenitor cell differentiation in vitro.

99 nctional outcome of RAF1 during mouse neural progenitor cell differentiation using an optogenetic RAF

100 Many tissues are produced by specialized progenitor cells emanating from epithelia via epithelial

101 ses the reparative properties of endothelial progenitor cell (EPC) and their exosomes on myocardial r

102 helial microparticles (EMPs) and endothelial progenitor cells (EPCs) and evaluated, in 24 preselected

103 lth burden originating in epidermal stem and progenitor cells (ESPCs) of the skin and mucosa.

104 expression remained depressed in pancreatic progenitor cells even after correction of the coding mut

105 transcriptomes for radial glia, intermediate progenitor cells, excitatory neurons, and interneurons i

106 Further, iAs-exposed proliferative progenitor cells exhibited NRF2 pathway activation that

107 ditory sensory epithelium-the organ of Corti-progenitor cells exit the cell cycle in a coordinated wa

108 ntifies ILK as a target kinase for improving progenitor cell exosome-based cardiac therapies.

109 As a result, limb progenitor cells experience delayed prometaphase-to-meta

110 Stem and progenitor cell fate transitions constitute key decision

111 tors can differentially determine adult stem/progenitor cell fate.

112 (2020) show that generating a common progenitor cell for posterior spinal cord and muscle ena

113 Transplantation of muscle progenitor cells for treatment of DMD has been widely in

114 maneuvers, which stimulates mobilization of progenitor cells from bone marrow, migration to areas of

115 c changes that distinguish normal epithelial progenitor cells from early-stage lung cancer, facilitat

116 Furthermore, cultured erythroid progenitor cells from MAM-negative individuals show mark

117 Here we generate induced neuronal progenitor cells from PRKN mutant patient fibroblasts wi

118 distinguishes the pathological detachment of progenitor cells from the normal delamination of daughte

119 o define a potential role for this factor in progenitor cell function.

120 n and modulates inflammation and endothelial progenitor cell function.

121 It is still unclear how these progenitor cells generate the more than 50 unique types

122 2%), normal human bronchial epithelial basal progenitor cells (HBECs) divide for over 200 PD without

123 Using 3D-differentiated clonal human neural progenitor cells (hNPCs) expressing varying levels of am

124 lling pathways that are crucial for stem and progenitor cell homeostasis and function, such as the No

125 However, basal stem/progenitor cell homeostasis is still poorly understood.

126 a microenvironment for the growth of hepatic progenitor cells (HPCs) at the periportal area and subse

127 Human progenitor cells (HPCs) support human cytomegalovirus (H

128 pression of uninfected CD34(+) hematopoietic progenitor cells (HPCs) through an increase in TGF-beta

129 that murine HSCs and committed hematopoietic progenitor cells (HPCs) undergo a gradual, rather than p

130 monstrate that in the hematopoietic stem and progenitor cell (HSPC) compartment aneuploid cells have

131 aling is required for hematopoietic stem and progenitor cell (HSPC) development.

132 Hematopoietic stem and progenitor cell (HSPC) formation and lineage differentia

133 leads to a decline in hematopoietic stem and progenitor cell (HSPC) function.

134 Haematopoietic stem and progenitor cell (HSPC) gene therapy has emerged as an ef

135 Mobilization of hematopoietic stem/progenitor cells (HSPC) from the bone marrow (BM) is imp

136 ly stages, tumors recruit hematopoietic stem/progenitor cells (HSPC) from the bone marrow and differe

137 The fate of hematopoietic stem and progenitor cells (HSPC) is tightly regulated by their bo

138 ration of bone marrow hematopoietic stem and progenitor cells (HSPC), but these cells cannot leave th

139 o healthy age-matched hematopoietic stem and progenitor cells (HSPCs) and correlate the proteomes to

140 Definitive hematopoietic stem and progenitor cells (HSPCs) arise from the transdifferentia

141 Hematopoietic stem and progenitor cells (HSPCs) develop in distinct waves at va

142 Haematopoietic stem and progenitor cells (HSPCs) have been the focus of developm

143 regulated activity of hematopoietic stem and progenitor cells (HSPCs) in the bone marrow (BM).

144 Hematopoietic stem and progenitor cells (HSPCs) in the bone marrow are derived

145 opulating activity of hematopoietic stem and progenitor cells (HSPCs) posttransplant.

146 l deletion of EGFR in hematopoietic stem and progenitor cells (HSPCs) significantly decreased DNA-PKc

147 Hematopoietic stem progenitor cells (HSPCs) stimulate revascularization of

148 data demonstrate that hematopoietic stem and progenitor cells (HSPCs) undergo translational reprogram

149 mphoid-dominant human hematopoietic stem and progenitor cells (HSPCs) using clonal tracking in patien

150 ne therapy with human hematopoietic stem and progenitor cells (HSPCs), each gene-corrected cell and i

151 Hematopoietic stem and progenitor cells (HSPCs), first specified from hemogenic

152 29 CD34(+) lineage(-) hematopoietic stem and progenitor cells (HSPCs), single-cell proteomics, genomi

153 TLR) signaling in MDS hematopoietic stem and progenitor cells (HSPCs), the mechanisms responsible for

154 in up to 60% of human hematopoietic stem and progenitor cells (HSPCs), without impairing cell viabili

155 man cDCs from CD34(+) hematopoietic stem and progenitor cells (HSPCs).

156 RNA delivery to human hematopoietic stem and progenitor cells (HSPCs).

157 differentiates into haematopoietic stem and progenitor cells (HSPCs).

158 ency in monocytes and hematopoietic stem and progenitor cells (HSPCs).

159 le Cdx2 expression in hematopoietic stem and progenitor cells (HSPCs).

160 ce the engraftment efficacy of hUCB HSCs and progenitor cells (HSPCs).

161 ts from dysfunctional hematopoietic stem and progenitor cells (HSPCs).

162 C/Gal-10 in human cord blood-derived CD34(+) progenitor cells impairs eosinophil granulogenesis.

163 regulates differentiation of gastric cardia progenitor cells in a mouse model of BE.

164 The basal keratinocyte progenitor cells in cultured epithelial autografts (CEAs

165 h is highly activated in intestinal stem and progenitor cells in geriatric mice.

166 f vasoprotective axis in bone marrow-derived progenitor cells in health and disease.

167 y clears SCs and rejuvenates tissue stem and progenitor cells in naturally aged mice without causing

168 he door to the pharmacological activation of progenitor cells in situ.

169 1 receptor type 1) on hematopoietic stem and progenitor cells in the bone marrow and stimulates granu

170 in(-)Sca-1(+)c-Kit(+) hematopoietic stem and progenitor cells in the bone marrow and the production o

171 Dental mesenchymal progenitor cells in the dental follicle lie at the heart

172 along the ventricles accumulates millions of progenitor cells in the developing brain.

173 of the proliferative capability of the crypt progenitor cells in vivo, lack of crypt base columnar st

174 y establishes genetic tools to ablate tendon progenitor cells in zebrafish larvae, finding that larva

175 (NF-kappaB) (pL2.Lgr5.p65fl/fl), in Lgr5(+) (progenitor) cells in L2-IL1B mice (which overexpress int

176 th individual fibroblasts and induced neural progenitor cells (iNPCs).

177 s required for the differentiation of dermal progenitor cells into a myofibroblast/CAF phenotype and

178 rmal proliferation of hematopoietic stem and progenitor cells is critical for development of new appr

179 e metabolic control of the state and fate of progenitor cells is in its infancy.

180 ilable dataset of Zika virus-infected neural progenitor cells is used to illustrate AIDD's capabiliti

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

182 in 2D cultures of a human bladder epithelial progenitor cell line in a dose-dependent manner, achievi

183 hich both pathways are activated in stem and progenitor cells, LSCs expanded under chemotherapy-induc

184 We show that basal stem/progenitor cell maintenance is regulated by a balance be

185 Multipotent Adult Progenitor Cells (MAPC((R)) ) possess potent immunomodul

186 hat OLFM4 is co-expressed with multiple stem/progenitor cell marker genes in prostate epithelial cell

187 mmatory environment promotes oligodendrocyte progenitor cells maturation and myelin regeneration acro

188 neuronal cells derived from isolated stem or progenitor cells may provide insight into maturation in

189 r mechanisms that control epicardium-derived progenitor cell migration, and the functional contributi

190 The PREMIER trial (Plaque Regression and Progenitor Cell Mobilization With Intensive Lipid Elimin

191 Using Kasumi-3 cells as a myeloid progenitor cell model endogenously expressing MHC class

192 how cell-extrinsic forces impact mesenchymal progenitor cell (MPC) fate.

193 rols proliferation of multipotent pancreatic progenitor cells (MPCs) and their segregation into bipot

194 he lung mediated by pathological mesenchymal progenitor cells (MPCs) that manifest autonomous fibroge

195 By contrast, multipotent progenitor cells (MPPs) show greater variation in distan

196 Bone marrow (BM) mesenchymal stem and progenitor cells (MSPCs) are a critical constituent of t

197 e demonstrate that lung mesenchymal vascular progenitor cells (MVPC) modulate adaptive angiogenesis v

198 During brain development, progenitor cells need to balanceproliferation and differ

199 lular functions of LIS1 in regulating neural progenitor cell (NPC) daughter cell separation.

200 urpose, we adapted a system to induce neural progenitor cell (NPC) development from mouse embryonic s

201 a mitotically active, age-depletable neural progenitor cell (NPC) niche, with unique characteristics

202 dothelial cells (PVEC) crosstalk with neural progenitor cells (NPC) promoting mutual proliferation, f

203 Consistently, neural progenitor cells (NPCs) derived from human induced pluri

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

205 Grafts of spinal-cord-derived neural progenitor cells (NPCs) enable the robust regeneration o

206 vior and differentiation potential of neural progenitor cells (NPCs) found in the subventricular zone

207 SIX2 (SIX homeobox 2)-positive nephron progenitor cells (NPCs) give rise to all epithelial cell

208 Nephron progenitor cells (NPCs) give rise to all segments of fun

209 IMPA1-deficient neuronal progenitor cells (NPCs) revealed substantial deficits in

210 In neural progenitor cells (NPCs), Ybx1 controls self-renewal and

211 age repair essential to proliferating neural progenitor cells (NPCs).

212 d RNA-sequencing experiments of human neural progenitor cells (NPCs).

213 including the transition of neural stem and progenitor cells (NSCs) from proliferative to differenti

214 Altered neural stem/progenitor cell (NSPC) activity and neurodevelopmental d

215 Neural stem/progenitor cell (NSPC) grafts can integrate into sites o

216 s, in cultured primary mouse neural stem and progenitor cells (NSPCs).

217 ntiviral injection can efficiently transduce progenitor cells of the adult mammary gland and use that

218 mbal melanocytes with limbal epithelial stem/progenitor cells on fibrin hydrogels pre-incubated with

219 By marking progenitor cells, one can observe their subsequent locat

220 and receptors that regulate oligodendrocyte progenitor cell (OPC) and oligodendrocyte formation and

221 srupting Fth iron storage in oligodendrocyte progenitor cells (OPCs) after demyelination.

222 OL progenitor cells (OPCs) are not specified into distinct

223 tion, and differentiation of oligodendrocyte progenitor cells (OPCs).

224 nt/beta-catenin signaling in oligodendrocyte progenitor cells (OPCs).

225 a reduction in proliferating oligodendrocyte progenitor cells (OPCs).

226 e progression or survival in iPSCs and glial progenitor cells or astrocyte differentiation.

227 s, we identified neural stem cell and neural progenitor cell pools and neurons.

228 t carcinogenesis, with a focus on effects on progenitor cell pools in the mammary gland.

229 and, which can affect cell fate decisions in progenitor cell pools.

230 Exogenous dual delivery of progenitor cell population and therapeutic growth factor

231 entifies Dist-Luminal-C cells as the luminal progenitor cell population in invagination tips and sugg

232 ions, notably within the spermatogonial stem/progenitor cell population in postnatal testis.

233 bout the influence of RBPs on the biology of progenitor cell populations in other lineages.

234 Identifying resident or donor stem/progenitor cell populations is crucial for augmenting th

235 At the onset of periodontal development, progenitor cell populations such as dental follicle cell

236 distinct functionality of these mesenchymal progenitor cell populations that regulate tooth eruption

237 d regulates proper cell fates of mesenchymal progenitor cell populations.

238 nsgenic mouse expressing H3.3K27M in diverse progenitor cell populations.

239 gth but is a result of a failure to maintain progenitor cell populations.

240 We report that mouse hypothalamic stem/progenitor cells produce multiple pancreatic, gastrointe

241 phosphamide treatment, mostly KRT14(+) basal progenitor cells proliferated in response to injury, pea

242 ses neurogenesis and reduces oligodendrocyte progenitor cell proliferation (OPC) in the developing SV

243 elays epithelial invagination, and decreases progenitor cell proliferation and dental epithelium cell

244 g pathway, which controls organ size through progenitor cell proliferation and differentiation, is dy

245 nd acts as a novel mediator in prostate stem/progenitor cell proliferation and differentiation.

246 cal ventricular zones provide a platform for progenitor cell proliferation and migration.

247 e, confirming that these genes reduce neural progenitor cell proliferation and neurite growth.

248 Deletion of HuR does not impair neural progenitor cell proliferation or differentiation, but it

249 How salamanders accomplish progenitor cell proliferation while faithfully maintaini

250 Myogenesis includes sequential stages of progenitor cell proliferation, myogenic commitment and d

251 abnormal neural rosette formation and neural progenitor cell proliferation.

252 ns, is produced by basal cells and restrains progenitor cell proliferation.

253 esorbing osteoclasts to orchestrate balanced progenitor cell recruitment and activation.

254 effects on the function of colonic stem and progenitor cells remain largely unexplored.

255 Intestinal stem and progenitor cells replicate and differentiate in distinct

256 Multipotent retinal progenitor cells (RPCs) generate various cell types in a

257 Deleting Gata3 enhances adult prostate stem/progenitor cells self-renewal capacity in both organoid

258 tic deletion of Dnmt3a and Dnmt3b in nephron progenitor cells (Six2 (Cre) Dnmt3a/3b) and kidney tubul

259 reduced mitochondrial density, and the brown progenitor cells sorted from offspring BAT demonstrated

260 omplex is critical in hematopoietic stem and progenitor cell specification and in the development of

261 The test result with human neural progenitor cell spheroids suggests a remarkable reductio

262 ECs, also called sinusoidal endothelial cell progenitor cells [sprocs]) with diminished repair of inj

263 ssues of origin, including myogenic stem and progenitor cells, stromal cells, and pluripotent stem ce

264 lar marker for the identification of elusive progenitor cell subsets at the earliest stages of T line

265 ses of gene expression while fate mapping of progenitor cells suggests that OHCs and their surroundin

266 rom the expansion of haematopoietic stem and progenitor cells that acquire somatic mutations.

267 mouse stress erythropoiesis use signals and progenitor cells that are distinct from steady-state ery

268 The lateral plate mesoderm (LPM) forms the progenitor cells that constitute the heart and cardiovas

269 enerated from a defined number of ~120 early progenitor cells that expand uniformly with equal growth

270 population of cycling Sox5/6/9+ perichondral progenitor cells that generate new cartilage during adul

271 jection neurons arise from a uniform pool of progenitor cells that lines the ventricles of the forebr

272 The epicardium harbors a population of progenitor cells that undergo epithelial-to-mesenchymal

273 ial magnetic stimulation, intracerebral stem/progenitor cells) that consider precise lesion location

274 to study mammalian regeneration, where stem/progenitor cells (the "blastema") completely regenerate

275 lopment requires the robust proliferation of progenitor cells, the identities of which are establishe

276 face cultures from primary airway basal stem/progenitor cells; this can be replicated using LAE and S

277 MTG16 repress transcription in the earliest progenitor cells to promote exit of ISCs from their nich

278 imers reorganize the epigenomic landscape of progenitor cells to promote neural crest specification.

279 eating these diseases is to utilize stem and progenitor cells to replace neurons in situ, with the ex

280 addition of second heart field (SHF) cardiac progenitor cells to the poles of the heart tube results

281 We also highlight how effective progenitor cell tracing, when combined with recently dev

282 the ventricular radial glia-to-intermediate progenitor cell transition at gestational week 10-as a k

283 vely expressed in trophoblast stem cell-like progenitor cells (TSPCs), and loss of Tead4 in postimpla

284 We then selectively ablated dividing neural progenitor cells using a 7-day continuous infusion of Ar

285 YAP1 (nlsYAP5SA) in ventricular zone neural progenitor cells using conditionally-induced NEX/NeuroD6

286 We detected Sox9 expression in muscle progenitor cells using double-transgenic mice and myobla

287 r CHD7 promotes gene transcription in neural progenitor cells via changes in chromatin accessibility.

288 ival-based cDNA expression screens in neural progenitor cells, we identify a genetic variant of AGS A

289 sequencing to murine hematopoietic stem and progenitor cells, we observed that these mutations disru

290 ETS1 p27 isoform in cord blood hematopoietic progenitor cells, we show that the transcription factor

291 a reservoir site for hematopoietic stem and progenitor cells, which are rapidly exploited as myeloid

292 a subsequent overproduction of intermediate progenitor cells, which leads to the formation of an enl

293 through specific autophagic flux blockade in progenitor cells, which may have potential therapeutic i

294 ining elevated numbers of luminal epithelial progenitor cells, which were surrounded by macrophages.

295 ating capacity and growth of sorted stem and progenitor cells, while AhR activation has the opposite

296 ng the proper expression signature of neural progenitor cells, while catalytic inactivation of DOT1L

297 ting fate-suppressing mechanisms to engineer progenitor cells with multilineage differentiation poten

298 Eto2 null mice and in human CD34+ erythroid progenitor cells with reduced ETO2, loss of ETO2 results

299 and concurrent activation of oligodendrocyte progenitor cells with subsequent remyelination.SIGNIFICA

300 is to associate molecular differences among progenitor cells with their capacity to generate mature