ライフサイエンスコーパス: progenitor cell

1 ch clone consists of the progeny of a single progenitor cell.

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

3 present in downstream myeloid and erythroid progenitor cells.

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

5 but not from the differentiation of putative progenitor cells.

6 marily of neurons with some glial and neural progenitor cells.

7 d differentiating populations of the nephron progenitor cells.

8 icles, suggesting a new source of adipogenic progenitor cells.

9 opment occurs through the differentiation of progenitor cells.

10 AML cells compared with normal hematopoietic progenitor cells.

11 of cardiac progenitor cells and endothelial progenitor cells.

12 ty against normal mobilized peripheral blood progenitor cells.

13 omponent specifically produced by epithelial progenitor cells.

14 s conserved between mouse and human stem and progenitor cells.

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

16 in the differentiation of myeloid-erythroid progenitor cells.

17 give rise to HCCs and iCCAs with markers of progenitor cells.

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

19 l adhesion complex in hematopoietic stem and progenitor cells.

20 h muscle cell differentiation of mesenchymal progenitor cells.

21 ions, where SOX9 is also expressed by neural progenitor cells.

22 xpress proteins typically seen in neuroglial progenitor cells.

23 the murine Pten gene in neonatal neural stem/progenitor cells.

24 enotype was caused by an increase of PDX1(+) progenitor cells.

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

26 ion of oligodendrocytes from oligodendrocyte progenitor cells.

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

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

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

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

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

32 n is thwarted and trigger the appearance of "progenitor" cells.

33 d 82.9%), respectively, 2) connective tissue progenitor cells, 3) platelet-derived growth factor rece

34 In conclusion, progenitor cell activation differs between PSC and PBC a

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

36 ular reaction (DR) as the results of hepatic progenitor cell activation.

37 ng to dissect signaling pathways that govern progenitor cell activity in homeostasis and disease.

38 tic bone marrow cells from 6 patients with B-progenitor cell acute lymphoblastic leukemia, we demonst

39 rs, Sca1 and CD34 (adventitial sca1-positive progenitor cells [AdvSca1]), have the potential to diffe

40 Alternatively, progenitor cells also give rise to HCCs and iCCAs with m

41 f 65 patients who received multipotent adult progenitor cells and 61 patients who received placebo.

42 ly assigned (67 to receive multipotent adult progenitor cells and 62 to receive placebo) in groups 2

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

44 link between therapeutic hematopoietic stem/progenitor cells and cerebral protection in stroke.

45 d a reduced expansion of lymphohematopoietic progenitor cells and defects of thymic epithelial progen

46 ll populations yielding a mixture of cardiac progenitor cells and endothelial progenitor cells.

47 duced injury, likely involving resident stem/progenitor cells and epithelial-mesenchymal transitions.

48 ted in the interstitium derived from nephron progenitor cells and expressed E-cadherin as well as vim

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

50 t an increase in the proliferation of neural progenitor cells and hyper-expansion of cortical surface

51 longated basal processes of the radial glial progenitor cells and impairment of postmitotic neuronal

52 ume but does stabilize levels of endothelial progenitor cells and improve microvascular function, whi

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

54 ice exhibit a massive reduction in endocrine progenitor cells and progeny hormone-producing cells, in

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

56 polyposis, little is known about stem cells/progenitor cells and their ability.

57 re, we investigated the presence of resident progenitor cells and their regenerative potential in a r

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

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

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

61 in myeloid priming of hematopoietic stem and progenitor cells, and its indispensable requirement for

62 d B-lymphocyte development and hematopoietic progenitor cells, and lymphoid organ hypoplasia.

63 very of both long-term repopulating HSCs and progenitor cells, and systemic administration of Dkk1 to

64 igration of parietal epithelial cells (PECs)/progenitor cells, and that the angiotensin (ang) II/ang

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

66 n the RPE and suppression by Sox2 in retinal progenitor cells are necessary for the differential grow

67 icacy signals from clinical trials, for stem/progenitor cell-based interventions for retinal disease.

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

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

70 anced self-renewal of hematopoietic stem and progenitor cells but the mechanisms behind this phenotyp

71 CHD7 is expressed in neural stem and progenitor cells, but its role in neurogenesis during br

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

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

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

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

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

77 ithin the bone marrow hematopoietic stem and progenitor cell compartments in patients with MDS-RS.

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

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

80 robust NEUROG3 expression within a subset of progenitor cells control the size of the endocrine popul

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

82 mouse heart tube are hypoxic, while cardiac progenitor cells (CPCs) expressing islet 1 (ISL1) in the

83 Cardiac progenitor cells (CPCs) have been shown to promote cardi

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

85 engthening of the G1 phase of the pancreatic progenitor cell cycle is essential for proper induction

86 During progression through the progenitor cell cycle, NEUROG3 phosphorylation is driven

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

88 R/Cas9 mutagenesis in hematopoietic stem and progenitor cells demonstrated that it is necessary for a

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

90 teract DISC1 deficiencies observed in neural progenitor cells derived from induced pluripotent stem c

91 understanding of how hematopoietic stem and progenitor cells develop from precursors, how progenitor

92 r 28 days of in vitro culture, hiPSC-derived progenitor cells differentiate into a monolayer of polar

93 Treg directly promoted oligodendrocyte progenitor cell differentiation and myelination in vitro

94 strict Yap/Taz activities to promote nephron progenitor cell differentiation in the mammalian kidney.

95 n, myofibroblast activation, stem and tissue progenitor cell differentiation, and angiogenesis.

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

97 nitor cells and defects of thymic epithelial progenitor cell differentiation.

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

99 ithin these loci were modest, Hdac3(Delta/-) progenitor cells displayed global changes in chromatin s

100 llular transmission in differentiated neural progenitor cells (dNPCs) and neuroblastoma SH-SY5Y (dSY5

101 letion of Tgfbr2 in myogenic or chondrogenic progenitor cells does not manifest in midline defects.

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

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

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

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

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

107 Circulating endothelial progenitor cells (EPCs) were quantified at baseline and

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

109 nchymal cells can regulate epithelial KIT(+) progenitor cell expansion during murine salivary gland o

110 ta-catenin-mediated intestinal stem cell and progenitor cell expansion in CD patients, human cells, a

111 e alters splicing and reverts haematopoietic progenitor cell expansion induced by mutant U2AF1 expres

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

113 ng mice that express KrasG12D in multipotent progenitor cells (Flt3Cre+ KrasG12D mice).

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

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

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

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

118 During embryonic development, fields of progenitor cells form complex structures through dynamic

119 e oculis (So) orchestrate the progression of progenitor cells from asynchronous cell division to G1 a

120 clinically to harvest hematopoietic stem or progenitor cells from bone marrow and to sensitize cance

121 propose that generation of resident vascular progenitor cells from differentiated SMCs is a normal ph

122 s nerve repair by preventing oligodendrocyte progenitor cells from differentiating into myelinating o

123 factor receptor alpha (PDGFRalpha) positive progenitor cells from fetal bovine skeletal muscle and i

124 re system to expand peripheral blood CD34(+) progenitor cells from patients with DBA and differentiat

125 conversion produces haematopoietic stem and progenitor cells from pluripotent stem cells and holds p

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

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

128 IE2-transduced neural progenitor cells gave rise to neurospheres with a lower

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

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

131 nces progenitor cell release and may promote progenitor cell homing to ischemic calf muscle.

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

133 in maintaining normal hematopoietic stem and progenitor cell (HSC/P) functions.

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

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

136 mechanisms regulating hematopoietic stem and progenitor cell (HSPC) fate choices remain ill-defined.

137 enerated from CD34(+) hematopoietic stem and progenitor cells (HSPC-NK cells) in in vitro and in vivo

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

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

140 Hematopoietic stem and progenitor cells (HSPCs) are vulnerable to endogenous da

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

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

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

144 Mobilization of hematopoietic stem and progenitor cells (HSPCs) from the bone marrow (BM) into

145 tion and migration of hematopoietic stem and progenitor cells (HSPCs) in the bone marrow (BM) microen

146 ng enzyme METTL3 in human hematopoietic stem/progenitor cells (HSPCs) promotes cell differentiation,

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

148 d blood CD34(+) human hematopoietic stem and progenitor cells (HSPCs), the cells of origin for myeloi

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

150 an cord blood-derived hematopoietic stem and progenitor cells (HSPCs).

151 , is overexpressed in MDS hematopoietic stem/progenitor cells (HSPCs).

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

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

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

155 In gliomagenic neural progenitor cells, IDH1(R132H) expression increased the a

156 her Atxn1 or Ube2e2 in primary mouse adipose progenitor cells impaired adipocyte differentiation, sug

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

158 duced the proliferation of adult neural stem/progenitor cells in a cell-autonomous manner in vitro an

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

160 The survival of MRD stem or progenitor cells in the absence of oncogenic kinase sign

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

162 transcriptomes from individual mixed lineage progenitor cells in the chick as these cells offer a win

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

164 small 22q11.2 segments, in adult neural stem/progenitor cells in the hippocampus prevents the develop

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

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

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

168 e growth and self-renewal of alveolar type 2 progenitor cells, including IL-6/Stat3, Bmp, and Fgf sig

169 d differentiation in AML blasts and AML stem/progenitor cells, inhibited cell growth and colony forma

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

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

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

173 research demonstrates also that intermediate progenitor cells (IPCs) are the main target cells for ZI

174 Transcriptome analysis of neural stem and progenitor cells isolated directly from the dentate gyru

175 We demonstrate that nephron progenitor cells lacking Pax2 fail to differentiate into

176 Thus, it targets neural progenitor cells, leading to a more severe spectrum of c

177 tion alters molecular properties of stem and progenitor cells, leading to changes in their shape and

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

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

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

181 NA expression in the bone marrow mesenchymal progenitor cell line ST2, we discover that BMP2 induces

182 The bipotent hepatic progenitor cell line, HepaRG, can be directed to differe

183 omeostasis of skin is sustained by epidermal progenitor cells localized within the basal layer of the

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

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

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

187 ls (which then become HCC cells that express progenitor cell markers), or to transdifferentiate into

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

189 plement-derived peptide C3a regulates neural progenitor cell migration and differentiation in vitro a

190 the IPF lung harbors fibrogenic mesenchymal progenitor cells (MPCs) that serve as a cell of origin f

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

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

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

194 high-efficiency protocol to generate nephron progenitor cells (NPCs) and kidney organoids to facilita

195 erate induced pluripotent stem cells, neural progenitor cells (NPCs) and neurons from ASD individuals

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

197 ed that METH impacts HIV infection of neural progenitor cells (NPCs) by a mechanism encompassing NFka

198 Engulfment of synapses and neural progenitor cells (NPCs) by microglia is critical for the

199 ed pluripotent stem cells (iPSCs) and neural progenitor cells (NPCs) derived from individuals with he

200 The fate of neural progenitor cells (NPCs) during corticogenesis is determi

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

202 d pluripotency to multipotent primary neural progenitor cells (NPCs).

203 ent tissue stem cells, including neural stem/progenitor cells (NSCs).

204 Lsh depleted neural stem/progenitor cells (NSPCs) display reduced growth, increas

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

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

207 In neurospheres prepared from progenitor cells obtained from the subventricular and th

208 We show that DONSON is expressed in progenitor cells of embryonic human brain and other prol

209 show that in the developing skin, epidermal progenitor cells of mice lacking p63 transcription facto

210 in the embryo, disc1 is expressed in neural progenitor cells of the hypothalamus, a conserved region

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

212 ion of genetically wild-type oligodendrocyte progenitor cells, oligodendrocyte differentiation and de

213 that drive the maturation of oligodendrocyte progenitor cells (OPCs) during the remyelination process

214 opmentally, environmental manipulation of OL progenitor cells (OPCs) has profound effects on the esta

215 rentiation and maturation of oligodendrocyte progenitor cells (OPCs) involve the assembly and disasse

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

217 ly demyelinated lesions have oligodendrocyte progenitor cells (OPCs) within their borders.

218 In oligodendrocyte progenitor cells (OPCs), Lrp1 is required for cholestero

219 in perturb the maturation of oligodendrocyte progenitor cells (OPCs), thereby impeding remyelination,

220 impairing differentiation of oligodendrocyte progenitor cells (OPCs).

221 in repair by differentiating oligodendrocyte progenitor cells (OPCs).

222 mmation, and an expansion of oligodendrocyte progenitor cells (OPCs).

223 ation and differentiation of oligodendrocyte progenitor cells (OPCs).

224 vitro by incubation of cultured endothelial progenitor cells or spleen-derived endothelial cells wit

225 Genetic ablation of TrkB in neural stem/progenitor cells, or pharmacologic disruption of ERK sig

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

227 Murine hematopoietic progenitor cells overexpressing MPP1 acquired the abilit

228 generative capacity, assessed as circulating progenitor cell (PC) numbers, is an independent predicto

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

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

231 shift to asymmetric cell divisions impairing progenitor cell pool expansion.

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

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

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

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

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

237 ant mice have altered hematopoietic stem and progenitor cell populations in the BM and spleen that ar

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

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

240 1 (Mule) controls murine intestinal stem and progenitor cell proliferation by modulating the Wnt path

241 ve oxygen species, inhibition of neocortical progenitor cell proliferation, induction of premature ne

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

243 vallate papillae, including disruption of TB progenitor-cell proliferation and differentiation.

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

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

246 nce its discovery, the understanding of stem/progenitor cells raised dramatically in the last decade.

247 Hence, targeted activation of TAC-derived progenitor cells, rather than quiescent bulge SCs, for a

248 Tendon stem/progenitor cells regulate inflammation in tendon healing

249 AD, since exercise-induced ischemia enhances progenitor cell release and may promote progenitor cell

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

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

252 However, whether they represent true progenitor cells remains controversial.

253 nature of various putative myocyte-producing progenitor cells remains elusive and undefined across la

254 , but will also advance our understanding of progenitor cell renewal in other cell types/organ system

255 , and abrogated MPP1-dependent hematopoietic progenitor cell replating in methylcellulose.

256 Adult neural stem cells/progenitor cells residing in the basal layer of the olfa

257 , and impaired colonization by hematopoietic progenitor cells, resulting in anemia and embryonic leth

258 These data uncover new mechanisms of retinal progenitor cell (RPC)-to-RGC and human stem cell-to-RGC

259 row (BM)-derived Sinusoidal endothelial cell PROgenitor Cells (sprocs) play a vital role in hepatic r

260 ppel family member KLF7 promotes the corneal progenitor cell state; on many genes, KLF7 antagonized t

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

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

263 to hypermutagenicity in haematopoietic stem/progenitor cells, suggesting a novel TET2 loss-mediated

264 on can fail despite abundant oligodendrocyte progenitor cells, suggesting impairment of oligodendrocy

265 n restored pro-B cell development from Justy progenitor cells, suggesting that GON4L acts at the begi

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

267 Here, we show that Pax6 controls eye progenitor cell survival and proliferation through the a

268 strategy in the Firmicutes phylum wherein a progenitor cell that faces starvation differentiates to

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

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

271 gut endothelium requires MFSD2A; endothelial progenitor cells that overexpress MFSD2A reduce colitis

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

273 ar smooth muscle cells can be traced back to progenitor cells that reside in the wall of the dorsal a

274 otes the expansion of hematopoietic stem and progenitor cells; the development of a synthetic route t

275 to enhance the effectiveness of cardiac stem/progenitor cell therapy for ischemic heart disease.

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

277 eart and the contribution of Sox9(+) hepatic progenitor cells to hepatocytes in the liver.

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

279 Club cells are known to function as regional progenitor cells to repair the bronchiolar epithelium in

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

281 epigenetic regulator of the transition from progenitor cells to terminally differentiated photorecep

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

283 d by steatosis that promotes growth of tumor progenitor cells, underlying the increased risk of liver

284 we also confirmed impaired AM development of progenitor cells using mixed chimera experiments.

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

286 ETATION: Administration of multipotent adult progenitor cells was safe and well tolerated in patients

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

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

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

290 RAMA elements in neural progenitor cells were biallelically accessible in embryo

291 MATERIALS AND Human trophoblast progenitor cells were isolated at 7-14 wk of pregnancy (

292 Neoblast stem cells and progenitor cells were mislocalized in beta1-integrin(RNA

293 Isolated lacrimal gland progenitor cells were tested and characterized by stem c

294 MHC-II significantly increased when CML stem/progenitor cells were treated with the JAK1/2 inhibitor

295 and differentiation of the limbal epithelial progenitor cells when these cells are cultured in two di

296 s proliferative capacity of p63(+) epidermal progenitor cells, while preserving their ability of diff

297 tic pancreas is a potential marker of cancer progenitor cells with an important functional role in PD

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

299 lasts, and in CD34(+) hematopoietic stem and progenitor cells, with increased F-actin in the structur

300 embryogenesis drives proliferation of neural progenitor cells within the ventricular zone and is requ