ライフサイエンスコーパス: progenitor

1 ngs can be translated to human DCs and their progenitors.

2 able, likely due to low frequency of mutated progenitors.

3 dynamically marks a range of dental and bone progenitors.

4 stogenesis from Fndc5-transgenic bone marrow progenitors.

5 Notch1 is expressed by and active in TEC progenitors.

6 ematopoietic colony-forming units and T cell progenitors.

7 rcuit of autoregulation operating in nephron progenitors.

8 y and lack silenced chromatin like embryonic progenitors.

9 programs the development of ILC2s from their progenitors.

10 11b + and CD11b- cells, and in hematopoietic progenitors.

11 e fate of LTi progenitors versus non-LTi ILC progenitors.

12 in dexamethasone-treated PB and CB erythroid progenitors.

13 ected by increased maturation of erythrocyte progenitors.

14 rogramming of Muller glia into proliferating progenitors.

15 erive from multiple sources of hematopoietic progenitors.

16 ubunit of the E1 for neddylation in cortical progenitors.

17 ciated with impaired TEAD4 expression in CTB progenitors.

18 that eNePs are the earliest human neutrophil progenitors.

19 equires maintenance and expansion of myeloid progenitors.

20 and CD18, respectively, as markers of these progenitors.

21 was also detected in neonatal BAT and brown progenitors.

22 -beta in the development of ILC2s from their progenitors.

23 population of peritoneal basophil-mast cell progenitors.

24 PLV-LMCs do not derive from skeletal muscle progenitors.

25 essed preferentially and highly on erythroid progenitors.

26 ential for the differentiation of blood cell progenitors.

27 In progenitors, 5hmC did not correlate with gene transcript

28 ferentiation of RGs into apical intermediate progenitors, a more restricted progenitor type lacking a

29 Conditional deletion of Hdac3 within myeloid progenitors accelerates healing of cortical bone defects

30 Bone-marrow-derived progenitors actively engage DNA repair but also imprint

31 est that LumP and PrU cells have multipotent progenitor activity in organoid formation and tissue rec

32 e mice enhanced mammary epithelial cell stem/progenitor activity, elevated expression of estrogen rec

33 ee of which (L2/L3/L4) emerged from a common progenitor after the loss of the MmpS6/MmpL6-encoding Mt

34 m/progenitor cell, called adult human neural progenitor (AHNP) cells, that we found to be pathologica

35 eity within GMPs, it is unclear if committed progenitors already exist among these progenitors and ho

36 Repeated injection of HoxB8 progenitors also allowed us to maintain stable circulati

37 expression (marker of labyrinth trophoblast progenitors), altered maternal blood space, decreased fe

38 Importantly, the abnormal myeloid progenitors (AMPs), a leukemia-initiating cell populatio

39 tified 25 candidate cell types that included progenitor and differentiating states with computational

40 ly specified primary human airway epithelial progenitor and smooth muscle cells.

41 eletal myogenesis and the transition between progenitor and stem cell states are unclear.

42 lar system and CSF sources (including neural progenitors and choroid plexus).

43 imple design principle of organ growth where progenitors and differentiated cells expand in harmony w

44 lidation defined the transcriptomes of naive progenitors and erythroid-, megakaryocyte-, and leukocyt

45 mitted progenitors already exist among these progenitors and how they may behave differently during i

46 ot clear what promotes transition of ISCs to progenitors and how this fate decision is established.

47 The roles that neuronal and glial progenitors and mature cells play in CNS angiogenesis an

48 expression and accessible chromatin between progenitors and MG, primarily in neurogenic genes.

49 ll-autonomous effect of MyHC-emb on myogenic progenitors and myoblasts is mediated by the fibroblast

50 es in human excitatory and inhibitory neural progenitors and neurons.

51 hat driver genes are often expressed in both progenitors and postmitotic cells.

52 neage bias, increased generation of lymphoid progenitors and rebalanced HSC lineage output in transpl

53 ional activity and accumulation of erythroid progenitors and that it may do so in an AhR-dependent fa

54 of pDCs from bone marrow dendritic cell (DC) progenitors and their maintenance is driven by the trans

55 in bone marrow and spleen became multipotent progenitors and, occasionally, some HSCs gave rise to me

56 controlling the level of Shh activity in pMN progenitors, and also regulates the allocation of oligod

57 id-, megakaryocyte-, and leukocyte-committed progenitors, and we identified CD44, CD326, ICAM2/CD9, a

58 lary ECs and respective resident endothelial progenitors appear to be at the origin of CCM lesions.

59 Adipocyte progenitors (APs) express platelet-derived growth factor

60 These beige fat progenitors are marked by PDGFRalpha, Sca1, and CD81 and

61 mes from embryonic day (E)7.5, when endoderm progenitors are specified, to E10.5 liver, when liver pa

62 In the absence of FAO, the progenitors are unable to differentiate and exhibit alte

63 We show that early neurogenic progenitors arise from asymmetric divisions.

64 cally defined culture system for distal lung progenitors as organoids derived from single adult human

65 In contrast, hPSC-derived HOXA(+) CD34(+) progenitors, as well as human cord blood CD34(+) cells,

66 sis (Arabidopsis thaliana) and their diploid progenitors, as well as one natural tetraploid and its s

67 Development of progenitor B cells (ProB cells) into precursor B cells (

68 self-renewal or differentiation of cortical progenitor behaviors in vivo, a variable we have termed

69 s (MPCs) and their segregation into bipotent progenitors (BPs) and unipotent pro-acinar cells (PACs).

70 (genome composition DDSS), and its putative progenitors, Brachypodium distachyon (DD) and Brachypodi

71 g tendon, whether neighboring tissues harbor progenitors capable of mediating regeneration.

72 Both LC-like and DC offspring from this progenitor carried the BRAF mutation, confirming their c

73 f human ACT products, we identified a memory-progenitor CD39-negative stem-like phenotype (CD39(-)CD6

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 Hematopoietic stem progenitor cells (HSPCs) stimulate revascularization of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Here, megakaryocyte progenitor cells are genetically engineered to overexpre

127 Progenitor cells are mobilized from bone marrow niches i

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

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

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

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

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

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

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

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

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

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

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

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

140 1 receptor type 1) on hematopoietic stem and progenitor cells in the bone marrow and stimulates granu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 form population compared with adult stem and progenitor cells.

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

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

172 granulocyte and macrophage development from progenitor cells.

173 over osteogenic differentiation of skeletal progenitor cells.

174 regulating embryonic stem and hematopoietic progenitor cells.

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

176 the differentiation of resident mesenchymal progenitor cells.

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

178 system (MPS) is a family of cells including progenitors, circulating blood monocytes, resident tissu

179 eage population, damage-associated transient progenitors (DATPs), that arises during alveolar regener

180 /differentiation behaviors in mouse cortical progenitor differentiation.

181 We found that neural crest progenitors display elevated expression of DICER, which

182 lin Tuba8, transiently expressed in cortical progenitors, drives differentiation of RGs into apical i

183 ive of their identities as ductular reaction progenitors (DRPs) and TICs.

184 are key regulators of the biology of neural progenitors during development and in adult neurogenic n

185 ontractility also impaired movement of basal progenitors during hair placode morphogenesis and dimini

186 Future studies of these LMC progenitors during maintenance and repair of PLVs, along

187 -stem-cell (HSC)-independent erythro-myeloid progenitors (EMPs) present in the murine yolk sac.

188 gates protrude from the entire length of the progenitor fibril.

189 both neuroepithelium cells and radial glial progenitors follow the same developmental trajectory dur

190 PCs; an initial wave of lymphomyeloid-biased progenitors, followed by precursors of hematopoietic ste

191 fferentiated in vitro from embryonic retinal progenitors for the effects of aging and, independently,

192 encing revealed that epidermal developmental progenitors form a more uniform population compared with

193 In the zebrafish spinal cord, neural progenitors form stereotypic patterns despite noisy morp

194 CD34+c-Kit+Flt3+ progenitors from blood of both high- and low-risk LCH pa

195 se pathways and RTK signaling in bone marrow progenitors from mice with MLL1-rearranged AML.

196 ) is expressed predominantly in granule cell progenitors (GCPs) in the cerebellum, as was shown in Jd

197 ramatic loss of the CNV and reversion to the progenitor genotype and drug susceptibility phenotype.

198 (hPSCs) revealed that HOXA(neg/low) CD34(+) progenitors give rise to NK cells that, similar to murin

199 entiation skewed toward granulocyte-monocyte progenitors (GMP) during joint and intestinal inflammati

200 odomain transcription factor promotes neural progenitor identity in the lateral ganglionic eminence (

201 C26UCA led to developmental arrest of B cell progenitors in bone marrow; poly-reactivity of the VRC26

202 es may promote expansion of abnormal myeloid progenitors in del(5q) MDS, and in rare cases drive the

203 dinate both the proper positioning of B cell progenitors in the bone marrow (BM) microenvironment and

204 caused by epigenetic rewiring of multipotent progenitors in the bone marrow, which overcomes the immu

205 uction requires direct engagement of myeloid progenitors in the bone marrow.

206 that originate from unipotent granule neuron progenitors in the brain.

207 cits in cell cycle kinetics of proliferating progenitors in the hippocampus.

208 wide range of cell types produced by single progenitors in the neocortex of mice may result from sto

209 er, the proliferative potential of adipocyte progenitors in vivo is unknown (Faust et al., 1976; Faus

210 lymph are increased and act on nearby midgut progenitors inducing Ecdysone-induced-protein-75B (Eip75

211 Hnf4a promotes the differentiation of PT progenitors into mature PT cells by regulating the expre

212 onic raphe nucleus-derived neural stem cells/progenitors into the lesion site of completely transecte

213 controlling the differentiation of committed progenitors into these cell types, however, are incomple

214 reducing proliferative reserve in blood-cell progenitors is causal has important public-health implic

215 found that AXL interacts with hematopoietic progenitor kinase 1 (HPK1) and demonstrate that HPK1 dow

216 -seq on neurons derived from Nestin-positive progenitors labeled by tamoxifen induction at embryonic

217 Moreover, CD34(+)PRLR(+) myeloid progenitors lacked lymphoid developmental potential, but

218 Temporal patterning of neural progenitors leads to the sequential production of divers

219 A possible link between progenitor-like acinar cells and cancer initiators is pr

220 We found PDX1(+)/ALK3(+)/CAII(-) progenitor-like cells in the MPDs of types 1 and 2 diabe

221 e in neurogenesis in both dorsal and ventral progenitor lineages and, if so, whether it regulates com

222 pressed the YAP1 target gene and mesothelial progenitor marker mesothelin, and many mesothelin-positi

223 of mature myeloid cells or their bone marrow progenitors, mediates sustained increased responsiveness

224 We found novel progenitor migrations, timings, dynamic cell-cell intera

225 ls of the mononuclear phagocyte system (MPS; progenitors, monocytes, macrophages, and classical dendr

226 ape the m6A modifications on skin epithelial progenitor mRNAs.

227 a rheostat to control BMP activation in the progenitor niche to determine regenerative outcome in fi

228 migration patterns of the adult-born neural progenitor (NP) lineages in detail.

229 rrow (BM)-resident or circulating myeloid OC progenitors (OCP) expressing the receptor CX(3)CR1.

230 ompounds, the most famous being salicin, the progenitor of aspirin.

231 riticum turgidum ssp. dicoccoides, WEW), the progenitor of both modern tetraploid and hexaploid wheat

232 Thus, we aimed to characterize the progenitors of PLV-LMCs during murine development, towar

233 rs of diverse coronaviruses (CoVs) including progenitors of Severe Acute Respiratory Syndrome (SARS)-

234 from Cre-tdTomato reporter mice specific for progenitors of skeletal myocytes (Pax7(+) and MyoD(+)) a

235 imed to investigate the influence of myeloid progenitors on CD34(+) cell differentiation into CD56(+)

236 Local niches, rather than progenitor origin, or the developmental window during on

237 The major source of airway stem/progenitors other than basal-like cells remains uncertai

238 f hepatocyte markers with no impact on liver progenitors, other endodermal lineages, or vasculature.

239 eading to a depletion of the oligodendrocyte progenitor pool in MS adults.

240 A reduced SHF progenitor pool leads to an underdeveloped right ventric

241 Cre recombinase to indelibly label a defined progenitor population and its progeny.

242 ungs, the density and function of epithelial progenitor populations and the epithelial gene expressio

243 ard identification of innate lymphoid cell 2 progenitor populations.

244 ered by a single population of developmental progenitors presenting a fixed fate imbalance of self-re

245 The progenitor preserves its WNT signaling identity and main

246 cs with genetics, we show that emerging hair progenitors produce both WNTs and WNT inhibitors.

247 B cell progenitors progress through sequential and mutually exc

248 MPK activator metformin decreases epithelial progenitor proliferation and increases acid-secreting pa

249 nsic systems, purinergic signaling regulates progenitor proliferation during retinogenesis and regene

250 Intrathymic AAV-transduced progenitors promote a rapid restoration of the thymic ar

251 e marrow-derived macrophages and bone marrow progenitors promoted M2-like macrophage polarization and

252 ological features different from multipotent progenitors, raising the possibility that an intermediat

253 Bcl3, and Id2, which render pDCs and late DC progenitors refractory to physiological stimuli controll

254 which viable interneurons are produced from progenitors remain poorly understood.

255 is in the body, TFR2's function in erythroid progenitors remains controversial.

256 fspring show microcephaly and primary neural progenitors require Cep55 and ESCRT for survival and abs

257 iency of TGF-beta receptor II in bone marrow progenitors results in inefficient development of ILC2s,

258 ession analysis of mirn23a-deficient myeloid progenitors revealed a decrease in TLR and IFN signaling

259 neurons and glia originate from radial glial progenitors (RGs), a type of stem cell typically extendi

260 is executed through a balanced regulation of progenitor self-renewal and differentiation.

261 irect evidence that oncogene-induced loss of progenitor self-renewal is driven by eIF2B5-mediated tra

262 se results reveal that 5' auto-processing of progenitor sgRNAs occurs natively in plants.

263 Further, the resulting neurogenic progenitors show cell biological features different from

264 ancreatic differentiation capacity up to the progenitor stage, but favor somatostatin- and pancreatic

265 raising the possibility that an intermediate progenitor state exists in the retina.

266 differentiation through a paraxial mesoderm progenitor state that generates BAs at high efficiency.

267 em-like to regenerative pulmonary epithelial progenitor states.

268 The indica-type promoter is present in a progenitor subspecies O. nivara and thus was acquired ea

269 l cell divisions of outer radial glial (oRG) progenitors, suggesting cellular functions of LIS1 in re

270 olony-forming activity, c-Kit signaling, and progenitor survival.

271 How pMN progenitors switch from producing motor neurons to OPCs

272 red ejecta mass(3,4) could be explained by a progenitor system that is asymmetric in terms of the ste

273 and induced genes associated with stem-like progenitor T cells.

274 e developing human infant liver, we identify progenitor targeting, delivery efficiencies, and suppres

275 mutation is present in a BM-resident myeloid progenitor that can be mobilized to the blood.

276 Neural stem cells (NSCs) are multipotent progenitors that are responsible for producing all of th

277 give rise to numerous cell types, including progenitors that expressed the prolactin receptor (PRLR)

278 hypothalamus (ARH) are derived from the same progenitors that give rise to ARH neurons.

279 velop in the bone marrow from haematopoietic progenitors that have numerous shared characteristics be

280 KIR genes are densely methylated in NK cell progenitors, there is an implied stage of human NK cell

281 represses muscle differentiation in vascular progenitors, thus restricting these cells to a vascular

282 n protocols and mapped hPSC-derived myogenic progenitors to an embryonic-to-fetal transition period.

283 that induce some early multipotent NKX2-1(+) progenitors to lose lung fate.

284 erning of neurogenesis and the transition of progenitors to neuronal differentiation.

285 e show that ZBED2 can repress the pancreatic progenitor transcriptional program, enhance motility, an

286 ories reveals that late-stage retinal neural progenitors transcriptionally overlap cell states observ

287 intermediate progenitors, a more restricted progenitor type lacking attachment to the basal lamina.

288 The early analysis of progenitors using flow cytometry, immunocytochemistry, a

289 iption factor(s) determining the fate of LTi progenitors versus non-LTi ILC progenitors.

290 we report that the functionality of vascular progenitors (VP) generated from normal and disease-prime

291 nt protein widely used as a marker of neural progenitors, was recently found to be expressed transien

292 filament protein highly expressed in neural progenitors, was recently identified in developing neuro

293 erences for three types of endogenous neural progenitors, we provide evidence for the differential ad

294 CD34(+) thymic progenitors were comprised of a spectrum of specificatio

295 These CD34(+)PRLR(+) myeloid-lineage progenitors were derived from granulocyte monocyte precu

296 Gsx2 interactions are enriched within LGE VZ progenitors, whereas Ascl1-Tcf3 (E-protein) interactions

297 proliferative capacity of human hippocampal progenitors, which may subsequently impact on human cogn

298 h a reduced number of proliferating neuronal progenitors while mutant ugdh zebrafish do not phenocopy

299 relies on the generation of antigen-specific progenitors with stem-like properties.

300 mic coverage of young and old mouse HSCs and progenitors, with broader implications for understanding