ライフサイエンスコーパス: progenitor

1 nsity-dependent methylation in the placental progenitor.

2 ymal transition (EMT) from NMP to mesodermal progenitor.

3 ing-directed (CASD) reprogramming to cardiac progenitors.

4 ollowing differentiation from post-embryonic progenitors.

5 ive signal in primary bone marrow-derived GM progenitors.

6 ifferentiated stem cells and more restricted progenitors.

7 ber and proportion of bone marrow B-lymphoid progenitors.

8 regulators in embryonic and adult urothelial progenitors.

9 etes the protein GON4-like (GON4L) in B cell progenitors.

10 ot receive MFSD2A-overexpressing endothelial progenitors.

11 riginates from region-specific myoepithelial progenitors.

12 ve CD25(+) GITR(+) Foxp3(-) thymic Treg cell progenitors.

13 ntiated acinar cells to proliferative ductal progenitors.

14 and Fgf function additively to generate dHb progenitors.

15 specified sets of cells derived from common progenitors.

16 s from the transformation of immature T-cell progenitors.

17 genitors originate from Eya1-expressing otic progenitors.

18 , which represent enteric glia and/or neural progenitors.

19 an give rise to myeloid and lymphoid lineage progenitors.

20 ggests that neovessels form from endothelial progenitors able to assemble the intimal layers.

21 Reductions in progenitor activity were not observed when cells were di

22 to influence the generation of hematopoietic progenitors, although the pathways underlying this proce

23 software program quantitatively assesses the progenitor and committed states in single-cell RNA-seq d

24 een proliferation and quiescence of myogenic progenitor and stem cells is tightly regulated to ensure

25 r SHH in promoting proliferation of these RP progenitors and for differentiation of pituitary cell ty

26 expression level is high in undifferentiated progenitors and gradually declines during differentiatio

27 Mouse BM progenitors and human mesenchymal stem cells (MSCs) appe

28 ZIKV can infect human neural progenitors and impair brain growth.

29 rlapped an enhancer active in common myeloid progenitors and influenced its activity.

30 titutively active PKM1 isoform, while neural progenitors and medulloblastomas exclusively expressed t

31 expression, mitotic progression in neuronal progenitors and post-mitotic neuronal survival.

32 ethylated regions occur at sites inactive in progenitors and reflect the de novo acquisition of AML-s

33 to initiate SMCs reprogramming into vascular progenitors and that members of the Notch signalling pat

34 types each originate from Nkx2-1(+) foregut progenitors and the minimal pathways claimed to regulate

35 The expression of Tcf4 commenced in progenitors and was further upregulated in pDCs, correla

36 ced self-renewal, expansion of hematopoietic progenitors, and myeloid differentiation bias.

37 that cells in the CE domain are multipotent progenitors, and suggesting that an asymmetric division

38 In vivo, myeloid cells and their progenitors are an important site of HCMV latency, and o

39 While some progenitors are bona fide multipotent and contribute pro

40 We show that Hdac8-deficient hematopoietic progenitors are compromised in colony-forming cell seria

41 ant embryos, proliferating rx3+ hypothalamic progenitors are not maintained normally and neuronal dif

42 , the differentiation state of individual BC progenitors at mitosis is not arbitrary but matches the

43 e we identify a brain-region-specific neural progenitor-based signaling pathway dedicated to regulati

44 or and beta1 integrin expression profiles of progenitors between the first and second trimesters sugg

45 is not only required in the early pancreatic progenitors, but has additional essential activities wit

46 n and differentiation of the follicular cell progenitors, but is downregulated after birth.

47 erties of photoreceptors in early vertebrate progenitors by comparing lamprey to other vertebrates.

48 g B cell programming of multipotent lymphoid progenitors by restricting chromatin accessibility at B

49 We show that hES-derived striatal progenitors can be transplanted in animal models and can

50 mportant regulator of hematopoietic stem and progenitor cell (HSPC) biology.

51 ure of the CD34(+)CD38(-) hematopoietic stem/progenitor cell (HSPC) compartment and interrogated domi

52 Neural progenitor cell (NPC) culture within three-dimensional (

53 e mechanisms that determine whether a neural progenitor cell (NPC) reenters the cell cycle or exits a

54 er features of hepatocyte fate characterized progenitor cell activation in PBC versus PSC.

55 re and intestinal atrophy featuring stem and progenitor cell depletion, a phenotype unexpected from t

56 in Down syndrome, is known to affect neural progenitor cell differentiation, while haploinsufficienc

57 enerative capacity, both LTL and circulating progenitor cell levels are independent and additive pred

58 However, IWP2 increased stem/progenitor cell marker (p63alpha and ABCG2) content and

59 Troy/TNFRSF19 as a segment-committed nephron progenitor cell marker.

60 The cells expressing five of stem/progenitor cell markers are localized in basal layer of

61 ling, differentiation of cells that form the progenitor cell niche, and abnormal proliferation of pro

62 T974 significantly reduced leukemic stem and progenitor cell numbers, reduced regeneration of leukemi

63 epithelial constructs, with maintenance of a progenitor cell phenotype in their (supra)basal layers.

64 In particular, the human progenitor cell population differentiated, matured, and

65 Our data show that Troy marks a renal stem/progenitor cell population in the developing kidney that

66 Herein, we have described a long-lived progenitor cell population in the mouse esophageal epith

67 nce of a long-lived and indispensable Krt15+ progenitor cell population that provides additional pers

68 ched by selection for a CD133(+) endothelial progenitor cell population.

69 ctivity has a strong negative impact on stem/progenitor cell preservation in limbal explant cultures.

70 1 (Mule) controls murine intestinal stem and progenitor cell proliferation by modulating the Wnt path

71 ng taste cell differentiation and taste stem/progenitor cell proliferation.

72 we show that tendon sheath cells harbor stem/progenitor cell properties and contribute to tendon repa

73 hical relationships between various stem and progenitor cell subpopulations driving mammary gland mor

74 hermore, these PA scaffolds support myogenic progenitor cell survival and proliferation and they can

75 Stem/progenitor cell-based interventions have the potential t

76 Stem/progenitor cell-based interventions represent a novel cl

77 We used an ex vivo hematopoietic stem and progenitor cell/EC (HSPC/EC) coculture system as well as

78 BSTRACT: Therapeutic use of c-kit(+) cardiac progenitor cells (CPCs) is being evaluated for regenerat

79 ogical/genetic modification of human cardiac progenitor cells (hCPCs) are necessary interventions to

80 em cell therapy using human c-Kit(+) cardiac progenitor cells (hCPCs) is a promising therapeutic appr

81 d SOX9 expression in human pancreatic ductal progenitor cells (HPNE) and pancreatic ductal cells (HPD

82 ighly expressed in normal hematopoietic stem/progenitor cells (HSPCs) and acute myeloid leukemia (AML

83 al locations specific hematopoietic stem and progenitor cells (HSPCs) are generated de novo.

84 we transplanted human hematopoietic stem and progenitor cells (HSPCs) expressing MLL-AF9 or MLL-Af4 i

85 ent of gene-corrected hematopoietic stem and progenitor cells (HSPCs) from FA patients, either after

86 tic PIGA mutations in hematopoietic stem and progenitor cells (HSPCs) from patients with paroxysmal n

87 of thymopoiesis, from hematopoietic stem and progenitor cells (HSPCs) through to mature T cells.

88 te system, as well as hematopoietic stem and progenitor cells (HSPCs).

89 e expandable and multipotent induced cardiac progenitor cells (iCPCs) from mouse adult fibroblasts us

90 the presence of resident hematopoietic stem/progenitor cells (Lin-/Sca+/c-Kit+; LSK phenotype) in th

91 murine embryonic stem cells (ESCs) to neural progenitor cells (NPCs) and recruits the Mediator subuni

92 d pluripotent stem (iPS) cell-derived neural progenitor cells (NPCs) to repair the FTD-associated N27

93 inal cord include populations of neural stem/progenitor cells (NSPCs) that contribute to the regenera

94 le in developing neurons and oligodendrocyte progenitor cells (OPCs) it induces cellular death.

95 impairing differentiation of oligodendrocyte progenitor cells (OPCs).

96 ferentiation of mouse hematopoietic stem and progenitor cells and also potentiated oncogenic transfor

97 s in young neurons derived from human neural progenitor cells and human induced pluripotent stem cell

98 t mice inhibited the recovery of BM stem and progenitor cells and of complete blood counts following

99 and colony-forming potential of CML stem and progenitor cells and reduced their growth in immunodefic

100 cholangiocyte lineages from embryonic liver progenitor cells and their subsequent maturation to the

101 Bone marrow-derived circulating progenitor cells are involved in tissue repair and regen

102 ur bones are formed from bone marrow myeloid progenitor cells by a complex differentiation process th

103 ferentiation of mouse enteric nervous system progenitor cells by EDN3 requires regulation of Ednrb ex

104 tor (FGF) signaling promotes self-renewal in progenitor cells by encouraging proliferation and inhibi

105 suggest that Pax2 function maintains nephron progenitor cells by repressing a renal interstitial cell

106 lization of primary mouse hematopoietic stem/progenitor cells compared to analogous gammaretrovirus/l

107 During mammalian embryogenesis, cardiac progenitor cells constituting the second heart field (SH

108 ts of human DF tissues, and these epithelial progenitor cells could be isolated and ex vivo expanded

109 Rev1 hematopoietic stem and progenitor cells displayed compromised proliferation, an

110 ease the viability of hematopoietic stem and progenitor cells during engraftment but also improves tr

111 istinct population of CD146(+) smooth muscle progenitor cells emerges during embryonic development an

112 n that HCMV infection of human hematopoietic progenitor cells engrafted in immune deficient mice (huN

113 wing over time, and their hematopoietic stem/progenitor cells exhibited a long-term competitive trans

114 the first cell fate decision that sets aside progenitor cells for both the new organism and the place

115 inical applications, and skin epidermal stem/progenitor cells for generating such grafts are easy to

116 Prdm16 was required in neural stem/progenitor cells for the expression of Foxj1, a transcri

117 BACKGROUND & AIMS: Neural stem and progenitor cells from the enteric nervous system (ENS) m

118 These features prevented hematopoietic progenitor cells from transmigrating into the developing

119 ation trial of intravenous multipotent adult progenitor cells in 33 centres in the UK and the USA.

120 rther the understanding of the skeletal stem/progenitor cells in adult life.

121 Hematopoietic stem/progenitor cells in the adult mammalian bone marrow ensu

122 D & AIMS: Maintenance and differentiation of progenitor cells in the developing enteric nervous syste

123 presses hepatocyte genes in undifferentiated progenitor cells in vitro and in embryonic mouse livers.

124 ers and Notch target genes in primary neural progenitor cells in vitro Consistent with this, introduc

125 provide insights into how skeletal stem and progenitor cells interact with other cell types to activ

126 followed by intramyocardial delivery of the progenitor cells into neonatal rat hearts, in vivo incub

127 nsplantation of human hematopoietic stem and progenitor cells into SRG-15 mice dramatically improved

128 us transplantation of hematopoietic stem and progenitor cells lentivirally labeled with unique oligon

129 , the further characterization of stem cells/progenitor cells may provide new treatment options for c

130 gest that HDAC1-specific inhibition prevents progenitor cells of the retina from exiting the cell cyc

131 Murine hematopoietic progenitor cells overexpressing MPP1 acquired the abilit

132 ated in developmental assays performed on OL progenitor cells purified from Thap1 null mice.

133 Tendon stem/progenitor cells regulate inflammation in tendon healing

134 Deletion of Hdac3 in cardiac progenitor cells releases genomic regions from the nucle

135 However, markers for most segment-committed progenitor cells remain to be identified.

136 ously unknown population of multipotent stem/progenitor cells that are capable of not only contributi

137 eral mouse models in which hypothalamic stem/progenitor cells that co-express Sox2 and Bmi1 are ablat

138 mice with colitis, transplanted endothelial progenitor cells that overexpressed MFSD2A not only loca

139 a large subset of genes that leads neuronal progenitor cells to distinctive differentiation pathways

140 r the susceptibility of BRCA1(mut/+) luminal progenitor cells to oncogenesis and tissue specificity.

141 prevents the loss of corneal epithelial stem/progenitor cells to replicative senescence and apoptosis

142 tiation is a complex process in which muscle progenitor cells undergo determination and eventually ce

143 The existence of lacrimal gland stem/progenitor cells was proposed in several species, yet th

144 n-deconvolution" logic provides templates of progenitor cells' potentiating effects, and components a

145 creased apoptosis in Sox2(+) neural stem and progenitor cells, and in DCX(+) and Tuj1(+) neurons.

146 critical role of DDT in maintaining HSCs and progenitor cells, and in preventing premature aging.

147 ical secretome of Amnion-derived Multipotent Progenitor cells, contains multiple anti-inflammatory cy

148 postulated pathways include loss of neuronal progenitor cells, damage to the developing vascular syst

149 ultipotent mesenchymal stem cells, committed progenitor cells, fibroblasts, endothelial cells, and im

150 tiation of mouse and human PSCs into cardiac progenitor cells, followed by intramyocardial delivery o

151 xamined in neurons derived from human neural progenitor cells, human induced pluripotent stem cells,

152 me2) in EPO treated and control fetal neural progenitor cells, identifying 1,150 differentially bound

153 enes previously assigned to mesenchymal stem/progenitor cells, including CD146/Mcam, CD44, CD106/Vcam

154 lation of transcriptionally similar stem and progenitor cells, our analysis reveals considerable cell

155 Connective tissue progenitor cells, platelet-derived growth factor recepto

156 recent evidence in embryonic stem and neural progenitor cells, suggesting a model whereby development

157 plicative infection in CD34(+) hematopoietic progenitor cells, we defined classes of low to moderatel

158 on of adult subventricular zone-derived stem/progenitor cells, we describe a sequence of events by wh

159 ree subsets of DCs from single human CD34(+) progenitor cells, we found that specification to the DC

160 short hairpin RNA transduction of erythroid progenitor cells, with global surface proteomic profilin

161 including the cKit(+) hematopoietic stem and progenitor cells.

162 ptional coactivators Yap and Taz, in nephron progenitor cells.

163 or cell niche, and abnormal proliferation of progenitor cells.

164 into a population of corneal epithelial-like progenitor cells.

165 ared with nonmalignant CD34(+) hematopoietic progenitor cells.

166 present in downstream myeloid and erythroid progenitor cells.

167 ising radiation (IR) between neural stem and progenitor cells.

168 omponent specifically produced by epithelial progenitor cells.

169 nied by, the production and rearrangement of progenitor cells.

170 owth is proposed to rely on layer-restricted progenitor cells.

171 d much faster than our understanding of stem/progenitor cells.

172 ion of oligodendrocytes from oligodendrocyte progenitor cells.

173 igh levels of viremia had HBV-infected liver progenitor cells.

174 all known 27 human TRP genes in mesenchymal progenitors cells during white or brown adipogenesis.

175 ring neurogenesis, vertebrate and Drosophila progenitors change over time as they generate a diverse

176 ities to dissect the earliest phases of stem/progenitor clonal (and microenvironment) evolution/diver

177 d the numbers of MPP-derived common lymphoid progenitor (CLP), common myeloid progenitor (CMP), megak

178 on lymphoid progenitor (CLP), common myeloid progenitor (CMP), megakaryocyte-erythroid progenitor (ME

179 stem cells (HSCs) and granulocyte-macrophage progenitors compared with wild-type controls.

180 and normalization of hematopoietic stem and progenitor compartments with emergence of functional mID

181 regulator of IL-7R-STAT signaling in T cell progenitors, contributing to both the quantitative and q

182 During development, endocrine progenitors delaminate, migrate radially and cluster to

183 P1 knock-in premegakaryocyte/erythroid progenitors demonstrate an erythroid-specification bias,

184 gatory subunit of PRC2, embryonic urothelial progenitors demonstrate reduced proliferation with conco

185 expression profile of the ES cell- and adult progenitor-derived, GM-CSF-instructed, nonconventional D

186 RNA expression and splicing, oligodendrocyte progenitor development, and oligodendrocyte morphology a

187 of the stem cells and in the endocrine-cell progenitors differentiating into enteroendocrine cells,

188 normally in vitro, whereas lineage-negative progenitors displayed impaired NK-cell differentiation.

189 y distinct, whereas multipotent and bipotent progenitors do not exhibit different expression profiles

190 n the prophase nucleus of a subset of KIT(+) progenitors during mitosis.

191 shows that nonecotropic replacements in the progenitor ecotropic MLV genome are more extensive than

192 organogenesis from yolk-sac erythro-myeloid progenitors (EMPs) distinct from haematopoietic stem cel

193 s and alphaVbeta3-overexpressing endothelial progenitor EP cells) and the kinase inhibitory activity

194 Early thymic progenitors (ETPs) are endowed with diverse potencies an

195 we demonstrate that SHF ventricular and OFT progenitors exhibit unique sensitivities to a mutation i

196 oxa13 expression that early and late autopod progenitors fated for the wrist and phalanges, respectiv

197 protein Sfrp5 in the mouse identifies common progenitors for the outflow tract (OFT), LV, atrium and

198 bsence of SCF or imatinib treatment prevents progenitors from developing into mast cells in vitro.

199 rast, ectopic expression of NFI-A in myeloid progenitors from NFI-A myeloid cell-deficient mice imped

200 In addition, we show that mast cell progenitors from peripheral blood survive, mature, and p

201 mary cilium maintenance necessary for radial progenitor functions.

202 ferentiate more efficiently and rapidly than progenitors generated by standard protocols.

203 Flt3Cre+ KrasG12D fetal liver hematopoietic progenitors give rise to a myeloid disease upon transpla

204 progenitor (MEP), and granulocyte-macrophage progenitor (GMP) cells, accompanied by increased cell cy

205 Granulocyte-monocyte progenitors (GMPs) and monocyte-dendritic cell progenito

206 ecular marker for all osteogenic mesenchymal progenitors has not been identified.

207 s retain leukemic stem cells (LSC) and their progenitors in bone marrow and relapse following treatme

208 stimulated the differentiation of remaining progenitors in pulp cultures into functional odontoblast

209 , we report the identification of hair shaft progenitors in the matrix that are differentiated from f

210 these hypotheses, we compared interneuronal progenitors in the medial ganglionic eminences (MGEs), l

211 ich we demonstrate are co-specified with SHF progenitors in the nkx2.5(+) ALPM.

212 Although the importance of neuronal progenitors in vascular development within the CNS is we

213 p-TF2 autonomously repress PV(+) fate in MGE progenitors, in part through directly driving Sox6 expre

214 velopmental potential of intermediate neural progenitors (INPs) generated by asymmetrically dividing

215 hway regulate further differentiation of the progenitors into endothelial lineage.

216 ila neural progenitors (neuroblasts) involve progenitor-intrinsic temporal transcription factor casca

217 cess, resulting in a buildup of intermediate progenitors (IPs) expressing prohemocyte and hemocyte ma

218 Specification of inner ear progenitors is initiated by FGF signalling.

219 Neural progenitors lacking Lgl1 had decreased N-cadherin intern

220 hrosphere (NS) cells, composed by renal stem/progenitor-like cells, were able to repopulate different

221 Furthermore, EVP displayed progenitor-like status with a high proportion of cells i

222 romatin at the nuclear lamina during cardiac progenitor lineage restriction.

223 ogenitors (GMPs) and monocyte-dendritic cell progenitors (MDPs) produce monocytes during homeostasis

224 id progenitor (CMP), megakaryocyte-erythroid progenitor (MEP), and granulocyte-macrophage progenitor

225 numbers of homogeneous midbrain floor plate progenitors (mFPPs) that retain efficient DA neurogenic

226 Mesodermal iPSC-derived progenitors (MiPs) can regenerate both striated muscle t

227 ntly, BCOR knock-down (KD) in normal CD34(+) progenitors modifies their granulocytic and erythroid di

228 following postnatal ablation of granule cell progenitors, Nestin-expressing progenitors, specified du

229 g mechanisms discovered in Drosophila neural progenitors (neuroblasts) involve progenitor-intrinsic t

230 Bipotential neuromesoderm progenitors (NMPs) ensure axial growth of embryos by con

231 network controlling bipotent neuromesodermal progenitors (NMPs) that fuel embryo elongation by genera

232 tinues after gastrulation in neuromesodermal progenitors (NMPs) within the posteriormost embryonic st

233 Aegilops tauschii is the diploid progenitor of the D genome of hexaploid wheat (Triticum

234 r n = 8 genome, which also was the purported progenitor of tribe Arabideae (KAA genome).

235 ates that non-classical monocytes are biased progenitors of alternatively activated macrophages.

236 cial Ca limits vegetative growth in the wild progenitors of both C3 and C4 founder crops.

237 Successful regeneration requires that progenitors of different lineages form the appropriate m

238 helial type 2 cells (AEC2s), the facultative progenitors of lung alveoli, from human PSCs.

239 . 867 million years ago), and thus cannot be progenitors of oxygenic photosynthesis.

240 is due to a cell of origin of bipotent liver progenitors or the plasticity of cellular constituents c

241 These multipotent progenitors originate from Eya1-expressing otic progenit

242 the nuclear periphery rescues myogenesis in progenitors otherwise lacking Hdac3.

243 elicited biased activation of hematopoietic progenitors over mast cells in vitro and in vivo.

244 Individual BMPs promote progenitor patterning or neuronal differentiation by the

245 pulation of cells displaying a hematopoietic progenitor phenotype (CD34(++) CD45(low)) of fetal origi

246 essential for the maintenance of the AdvSca1 progenitor phenotype.

247 ortant role in neural development and neural progenitor pool maintenance.

248 division mode, leading to exhaustion of the progenitor pool.

249 human distal tip epithelium is an analogous progenitor population and tested this by examining morph

250 al essential activities within the endocrine progenitor population.

251 Multiple progenitor populations produce lymphoid and myeloid cell

252 basis for generating distinct cardiovascular progenitor populations that enable the derivation of car

253 During vertebrate heart development, two progenitor populations, first and second heart fields (F

254 ed cell surface markers specific for diverse progenitor populations.

255 3/NuRD protects the multipotency of lymphoid progenitors, preventing B cell-programming transcription

256 ppressive effect of p53 and enhanced ectopic progenitor proliferation after genotoxic injury, thereby

257 ferentiation of new taste bud cells, but not progenitor proliferation, is interrupted in mice treated

258 nd its regulation over genes associated with progenitor proliferation.

259 ned them to categories such as proliferation-progenitor, proliferation-transforming growth factor bet

260 repopulation occurs rapidly from irradiated progenitors rather than via qNSC activation.

261 within the CNS is well recognized, how these progenitors regulate the vasculature outside the CNS rem

262 ion of the Gata1 gene in early hematopoietic progenitors remains to be elucidated.

263 r the expression of every Wnt9b/beta-catenin progenitor renewal target assessed as well as for proper

264 of lineage-committed cells from multipotent progenitors requires the establishment of accessible chr

265 Thus Gli1 marks mesenchymal progenitors responsible for both normal bone formation a

266 nsion of myeloid cells and reduced erythroid progenitors resulting in anemia, with dysregulated expre

267 n murine intermediate mesoderm-derived renal progenitors results in hydronephrosis and failure to dev

268 B lymphopoiesis by acting on early lymphoid progenitors, S100A9 inhibits B lymphopoiesis by acting o

269 rinsic SHM in unmutated portions of VRC-PG04 progenitor sequences.

270 granule cell progenitors, Nestin-expressing progenitors, specified during mid-embryogenesis to produ

271 Unlike oligodendrocyte progenitors, SPNs displayed pronounced resistance to ear

272 several tens of solar masses ejected by the progenitor star at supernova-level energies a few hundre

273 s to lung epithelium rely on passing through progenitor states that have only been described in mouse

274 rate differentiated cells, consistent with a progenitor/stem cell population.

275 rtilage revealed the presence of a divergent progenitor subpopulation characterised by an early senes

276 blast mineralization and enhanced osteoclast-progenitor survival, leading to increased osteoclastogen

277 undant in hematopoietic stem cells and early progenitor T cells, which is in line with a SCID phenoty

278 o generate and isolate human primordial lung progenitors that express NKX2-1 but are initially devoid

279 verse roles in CNS repair, as multipotential progenitors that generate both classes of myelinating ce

280 p skin grafts from mouse and human epidermal progenitors that were engineered by CRISPR-mediated geno

281 ary fungal allergen challenge mobilized ILC2 progenitors to exit the bone marrow.

282 e development requires fusion of mononuclear progenitors to form multinucleated myotubes, a critical

283 fy specific markers of midbrain dopaminergic progenitors to improve their derivation and predict dopa

284 f a region-specific heterogeneity in luminal progenitors to interrogate the differentiation repertoir

285 In vitro differentiation of progenitors transduced with a known Tcra gene in the pre

286 oblasts, which, similar to mouse neocortical progenitors, transiently arrest at prometaphase.

287 Neural progenitors (transit amplifying cells and neuroblasts) b

288 then accurately annotate the extremely large progenitor transposon insertion mutant collections neede

289 hordal mesendoderm and express Fgf10Fgf10(+) progenitors undergo anisotropic growth: those displaced

290 the pre-pro-B cell stage and renders B cell progenitors unresponsive to IL-7.

291 ice in differentiating primary hematopoietic progenitors using image patches from brightfield microsc

292 nts that specify ectodermal cells as placode progenitors using newly identified genes upstream of the

293 ns showed that a lncRNA expressed across all progenitors was required for the myeloid lineage, wherea

294 In studies of human and mouse ENS progenitors, we found activation of the Wnt signaling pa

295 Neural progenitors were organized in niches in the subependymal

296 clonogenic ALDH(+)/CD49f(+)/EpCAM(+) luminal progenitors, which express both basal cell and luminal c

297 lls commonly give rise to transit-amplifying progenitors, whose progeny differentiate into distinct c

298 Stem cells self-renew and produce progenitors with limited proliferative potential.

299 dor (European), Ningyou7 (Chinese) and their progenitors with the Brassica 60 K Illumina Infinium SNP

300 ses, altered transcription appears to be the progenitor, with subsequent post-transcriptional modulat