ライフサイエンスコーパス: repopulating

1 -portal area of liver lobules after one day, repopulating 25% of the recipient liver by 4 weeks.

2 vitro and show strikingly increased in vivo repopulating abilities after single or sequential bone m

3 In BALB/cByJ (BALB) mice, repopulating abilities decline with age; DR ameliorates

4 6J (B6) and (BALB x B6) F1 hybrid (F1) mice, repopulating abilities increase with age; DR maintains t

5 on of murine HSPCs with short- and long-term repopulating abilities.

6 ic grafts mobilized with NSAIDs had superior repopulating ability and long-term engraftment.

7 rapy approaches aim to take advantage of the repopulating ability and plasticity of multipotent stem

8 to cytoablative stress, and exhibit superior repopulating ability and self-renewal upon serial transp

9 on display decreased frequency and defective repopulating ability as well as decreased lymphoid but i

10 matopoietic cells can be highly enriched for repopulating ability based upon the efflux of the fluore

11 marrow hematopoietic progenitor cell and HSC repopulating ability ex vivo.

12 of its rich content of cells with sustained repopulating ability in spite of an apparent deficiency

13 stem cells (HSCs) had decreased multilineage repopulating ability in vivo compared with WT controls i

14 A precise definition of the repopulating ability is needed to define which HSC subpo

15 its and progressive decline in hematopoietic repopulating ability of double-knockout (dKO) HSCs.

16 empol treatment did not adversely affect the repopulating ability of FA hematopoietic stem cells.

17 ents that regulate engraftment and long-term repopulating ability of hematopoietic stem cells (HSCs)

18 he influence of Flt3 expression on long-term repopulating ability of HSC subpopulations.

19 PC numbers but had only minor effects on the repopulating ability of HSCs.

20 ser extent HIF-1alpha, impedes the long-term repopulating ability of human CD34(+) umbilical cord blo

21 g dilution analysis, to assess the long-term repopulating ability of putative murine EpiSC population

22 The self-renewal and long-term repopulating ability of these cells was shown in serial-

23 ipients significantly impaired the long-term repopulating ability of transplanted mouse HSCs shortly

24 marrow function results from a major loss in repopulating ability per HSC.

25 region, to maintain hematopoietic stem cell repopulating ability through a miR-675-Igf1r signaling c

26 xpression of which in ESCs confers long-term repopulating ability to ESC-derived HSCs.

27 , DR increases or maintains increased marrow repopulating ability with age in the 3 different genotyp

28 n 8-fold reduction in multilineage long-term repopulating ability, a defect not seen in marrow cells

29 olling the balance between proliferation and repopulating ability, a finding of importance in clinica

30 ex differences were noted in HSC competitive repopulating ability, but not HPC numbers, in TIP110(TG)

31 stem cell (HSC) subtypes with self-renewable repopulating ability, but with different haematopoietic

32 Likely underlying the increased repopulating ability, FOXP3 expressing HSC showed signif

33 a p38 MAPK inhibitor significantly increased repopulating ability, supporting an integral role of p38

34 ative signals, can lead to exhaustion of HSC repopulating ability.

35 ions into immunodeficient mice to test their repopulating ability.

36 es in the assays utilized to demonstrate HSC repopulating ability.

37 y for keratinocyte stem cells with long-term repopulating ability.

38 al human hematopoietic cells with short-term repopulating activity cells (STRCs) are needed to facili

39 otype ( approximately 10% HSCs with >6-month repopulating activity in immunodeficient mice) displayed

40 SPCs exhibit testicular repopulating activity in vivo and maintain the ability i

41 rial replating in vitro and long-term serial repopulating activity in vivo.

42 Functionally, the repopulating activity of Fancc(-/-) stem cells from reco

43 ription-5 (STAT5) plays an important role in repopulating activity of hematopoietic stem cells (HSCs)

44 lantations showed no change in the long-term repopulating activity of HSCs from mice exposed to recom

45 activity, its expression is required for the repopulating activity of human HSCs.

46 a microenvironmental defect that reduces the repopulating activity of wild-type HSCs.

47 -state in vivo hematopoiesis or on long-term repopulating activity of Wnt-deficient hematopoietic ste

48 mice to demonstrate that aged ECs impair the repopulating activity of young HSCs and impart a myeloid

49 old), and Ter119+ (17-fold) peripheral blood repopulating activity than c-Mpl(-/-) BM against wild-ty

50 eficient bone marrow had defective long-term repopulating activity that correlated with increased cel

51 creased endogenous competitive long-term HSC repopulating activity, and permitted efficient and durab

52 ar, HSC number, cell cycle status, long-term repopulating activity, and self-renewal capacity were no

53 We validated that Foxa3 is required for HSC repopulating activity, as Foxa3(-/-) HSC fails to repopu

54 t 1 in 65 000 zebrafish marrow cells contain repopulating activity, consistent with mammalian HSC fre

55 ciated with a marked loss of HSCs, long-term repopulating activity, HSC quiescence and common lymphoi

56 (HSCs) in older mice have decreased per-cell repopulating activity, self-renewal and homing abilities

57 ll growth and a loss of short- and long-term repopulating activity.

58 enhanced frequency, competence and long-term repopulating activity.

59 n 1/100th of the infused cells had long-term repopulating activity.

60 th both short-term and long-term bone marrow repopulating activity.

61 expression of Bmi-1 and enhanced competitive repopulating activity.

62 cells results in a modest loss of long-term repopulating activity.

63 s short- and long-term in vivo hematopoietic repopulating activity.

64 The expanded BM showed a distinct repopulating advantage when tested in serial competitive

65 d robust self-renewal capacity and exhibited repopulating advantages over wild-type HSCs.

66 of phenotypically corrected HSPCs capable of repopulating and developing proliferation advantage in i

67 BM against wild-type competitor in long-term repopulating assays in vivo.

68 mbers in culture, as measured in competitive repopulating assays.

69 -cohort study, we evaluated the phenotype of repopulating B cells and its correlation with donor-spec

70 The characteristics of the repopulating B cells are currently unknown.

71 We show here that repopulating bone marrow cells in certain mouse strains

72 pool, and elevates short-term and long-term repopulating capabilities, leading to the development of

73 elevated Notch signaling and reduced mammary repopulating capability upon transplantation.

74 progenitors, and exhibited reduced long-term repopulating capacity as well as hyper granulocyte-colon

75 Psigma substantially increased long-term HSC-repopulating capacity compared with BM cells from contro

76 t derived xenografts we demonstrate that the repopulating capacity in normal mammary epithelial cells

77 Conversely, young ECs restored the repopulating capacity of aged HSCs but were unable to re

78 quiescence of dormant HSCs and the long-term repopulating capacity of HSC.

79 TPsigma(-) cells substantially increased the repopulating capacity of human HSCs compared with CD34(+

80 ysical and chemical insults compromising the repopulating capacity of the epithelial stem cell compar

81 -derived stem cells demonstrate a diminished repopulating capacity relative to that of purified bone

82 Furthermore, long-term repopulating capacity was also present in a compartment

83 /-) LSK cells had an increased hematopoietic repopulating capacity with an altered cell differentiati

84 ant loss of quiescence and decline in serial repopulating capacity, but no substantial difference in

85 (-/-) HSCs exhibited decreased hematopoietic repopulating capacity, with skewed cell differentiation

86 rly demonstrate the necessity of Shp2 in HSC repopulating capacity.

87 that BCR-ABL(+) cells had long-term in vivo repopulating capacity.

88 , greater competence, and enhanced long-term repopulating capacity.

89 elf-renewal and a severe loss of competitive repopulating capacity.

90 tem cells with enhanced homing and long-term repopulating capacity.

91 lation with severe combined immunodeficiency-repopulating capacity.

92 Attenuation in the extent of acute damage by repopulating cardiomyocytes and vessels decreased signif

93 Extracardiac progenitor cells are capable of repopulating cardiomyocytes at very low levels in the hu

94 Repopulating CD4+ but not CD8+ T cells significantly dim

95 liferation, resulting in increased long-term repopulating cell (LTRC) and competitive repopulating un

96 human SCID (severe combined immunodeficient) repopulating cell (SRC) transduction 3- to 4-fold, resul

97 eased severe combined immunodeficient (SCID)-repopulating cell counts in culture, compared to input a

98 were those in the CD34(-) Flt3R(-) long-term repopulating cell fraction.

99 articularly in the most primitive, long-term repopulating cell population.

100 achieved, neither Notch1 nor Notch2 affected repopulating cell self-renewal.

101 human severe combined immunodeficient (SCID)-repopulating cells (SRCs) by transplantation into the no

102 demonstrate that the absolute number of SCID-repopulating cells (SRCs) increased by 5.8-fold in hypox

103 both PMF HPCs, short-term and long-term SCID repopulating cells (SRCs), are JAK2V617F(+) and that JAK

104 reatment resulted in a dramatic loss of SCID-repopulating cells (SRCs), treatment with OKT3 or UCHT1

105 to mobilize murine LTR cells and human SCID repopulating cells (SRCs).

106 etic/severe combined immunodeficiency (SCID)-repopulating cells (SRCs).

107 nhanced clonal outputs from human short-term repopulating cells (STRCs) without affecting their engra

108 Tumour-repopulating cells (TRCs) are a self-renewing, tumorigen

109 tem-like cells that repopulate tumors (tumor-repopulating cells (TRCs)).

110 Recently we have shown that tumor-repopulating cells (TRCs), a highly tumorigenic subpopul

111 , including a 17-fold increase in short-term repopulating cells and a net 23-fold ex vivo expansion o

112 D34+ cells produced a greater number of SCID-repopulating cells and established multilineage hematopo

113 al pitfall of antibody-mediated clearance of repopulating cells and is important for any groups worki

114 ene therapy since they efficiently transduce repopulating cells and may be safer than more commonly u

115 These findings demonstrate that BM-repopulating cells and more differentiated progenitor ce

116 Human repopulating cells are thought to express CD34 and lack

117 creasingly used to assay human hematopoietic repopulating cells as well as leukemia-initiating cells.

118 0-fold increase in the frequency of NOD/SCID repopulating cells compared with CD133+Lin- cells, sugge

119 d in long-term culture, initiating cells and repopulating cells compared with controls.

120 in lineage cells represent a major source of repopulating cells for reconstitution of the intraglomer

121 id markers, are expressed on human long-term repopulating cells from cord blood and bone marrow.

122 red lentiviral transduction of hematopoietic repopulating cells from either stem cell factor (SCF)- a

123 the cell-surface phenotype of hematopoietic repopulating cells from murine yolk sac, aorta-gonad-mes

124 ay demonstrates that Bid-deficient long-term repopulating cells give rise to expanded myelomonocytic

125 ng hematopoiesis by giving rise to long-term repopulating cells in recipient mice with an unexpected

126 vectors to transduce long-term hematopoietic repopulating cells in the dog, a clinically relevant lar

127 fficiently transduce and/or expand long-term repopulating cells in vivo are needed for treatment of d

128 e find that the frequency of these long-term repopulating cells is 1 in 35,000 total epidermal cells,

129 ly posttransplant, and 3% to 5% in long-term repopulating cells over 6 months following HSPC transpla

130 CM niche is capable of directing behavior of repopulating cells remains relatively unexplored.

131 the perivascular niche, where proposed tumor-repopulating cells reside.

132 proximately 3.5% to 33% in myeloid long-term repopulating cells resulting in a functional cure.

133 transduction of canine CD34(+) hematopoietic repopulating cells using a very short, 18-hour transduct

134 efficient lentiviral transduction of canine repopulating cells using an overnight transduction proto

135 tailed macaque (Macaca nemestrina) long-term repopulating cells using VSV-G-pseudotyped HIV-based len

136 Furthermore, enhanced generation of NOD/SCID repopulating cells was seen following culture with lower

137 resence of DL yielded enhanced generation of repopulating cells with higher levels of engraftment of

138 in a multilineage increase in gene-modified repopulating cells with marking levels of greater than 9

139 ry, they efficiently transduce hematopoietic repopulating cells, and self-inactivating (SIN) designs

140 to a pronounced increase in the frequency of repopulating cells, as assessed by extreme limiting dilu

141 betic/severe combined immunodeficiency mouse repopulating cells, compared with day 0 CD34(+)CD38(-)li

142 g NOD.Cg-Prkdc(scid) IL2rg(tm1Wjl) /SzJ mice repopulating cells, induced by combination treatment.

143 an be overexpressed in bone marrow long-term repopulating cells, it is incapable of mediating their t

144 need for caution in genetic manipulation of repopulating cells, particularly when the transgene migh

145 Hematopoietic repopulating cells, red blood cells, and T cells have re

146 to the expansion of CD34(+) cells and marrow-repopulating cells, treatment of IM CD34(+) cells result

147 f BIO5192 and plerixafor mobilized long-term repopulating cells, which successfully engraft and expan

148 in vivo expansion of corrected hematopoietic repopulating cells.

149 contained normal multilineage hematopoietic repopulating cells.

150 fficient at transducing rhesus hematopoietic repopulating cells.

151 types in vitro, and (5) transplantable liver-repopulating cells.

152 atopoietic stem cell numbers or expansion of repopulating cells.

153 lizumab-treated subjects also contained SCID-repopulating cells.

154 transduction of multipotential hematopoietic repopulating cells.

155 nstrating that they contain bone marrow (BM)-repopulating cells.

156 d committed progenitors as well as primitive repopulating cells.

157 ained multilineage increase in gene-modified repopulating cells.

158 action contain both short-term and long-term repopulating cells.

159 ing cells, and both long-term and short-term repopulating cells.

160 t identifies both murine and human long-term repopulating cells.

161 ve advantage of corrected FA-A hematopoietic repopulating cells.

162 n stable myeloid-B-T multilineage, long-term repopulating clones.

163 mouse, opening a door to the possibility of repopulating damaged sensory epithelia in humans.

164 Here we create heart constructs by repopulating decellularized mouse hearts with human indu

165 ngineering of humanized intestinal grafts by repopulating decellularized rat intestinal matrix with h

166 injured epithelia promotes BMP7 signaling in repopulating, dedifferentiated epithelia.

167 KLF7, and loss of CDKN1A does not rescue the repopulating defect.

168 ound thrombocytopenia and a severe stem cell-repopulating defect.

169 Notably, in the absence of p16INK4a, HSC repopulating defects and apoptosis were mitigated, impro

170 re-HSCs capable of developing into long-term repopulating definitive HSCs.

171 an undergo reprogramming to become long-term repopulating epidermal progenitors following wounding.

172 spensable for the maintenance of established repopulating epidermal stem cells and for the differenti

173 tial (DPsim(hi)) were enriched for long-term repopulating EpiSCs versus unfractionated cells (3.9- an

174 ing dilution transplantation and competitive repopulating experiments demonstrated a dramatic reducti

175 Competitive repopulating experiments show that SCF(+)DLK(+) cells su

176 a novel purification of HSCs with long-term repopulating function and may be considered an alternati

177 5ab(-/-) bone marrow (BM) cells showed equal repopulating function either competitively or noncompeti

178 types (CD34+CD38-) and demonstrated enhanced repopulating function in recipients of serial, secondary

179 ells, a phenotype previously associated with repopulating function.

180 gh ALDH activity further purified cells with repopulating function.

181 However, its application to long-term repopulating haematopoietic stem cells (HSCs) has remain

182 ffect the homing and the number of long-term repopulating haematopoietic stem cells, haematopoietic s

183 The first adult-repopulating hematopoietic stem cells (HSCs) emerge in t

184 support the ex vivo expansion of short-term repopulating hematopoietic stem cells (HSCs), the ex viv

185 ic progenitor cells (HPCs) at the expense of repopulating hematopoietic stem cells (HSCs).

186 ent of CD34(+) cells that contains long-term repopulating hematopoietic stem cells (HSCs).

187 Multipotent long-term repopulating hematopoietic stem cells (LT-HSCs) can self

188 Retention of long-term repopulating hematopoietic stem cells (LT-HSCs) in the b

189 or, is differentially expressed in long-term repopulating hematopoietic stem cells (LTR-HSC).

190 ele resulted in a 50% reduction in long-term repopulating hematopoietic stem cells (LTR-HSCs).

191 scription factors that can amplify long-term repopulating hematopoietic stem cells in a controlled wa

192 en reported to identify functional long-term repopulating hematopoietic stem cells, and has been dete

193 tion of the edited CD34+ cells are long-term repopulating hematopoietic stem cells, demonstrating the

194 he maintenance of immunophenotypic long-term repopulating hematopoietic stem cells, suggesting that a

195 rial transplantation, hallmarks of long-term repopulating hematopoietic stem cells.

196 d colonizes the liver by E10.5, before adult-repopulating hematopoietic stem cells.

197 bility of AMD3100 to mobilize true long-term repopulating hematopoietic stem cells.

198 A delay in functional maturity of repopulating HLA-specific B cells, and in particular tho

199 ying the relative frequencies of hundreds of repopulating HPSC clones in a nonhuman primate.

200 75% of cells in a highly enriched long-term repopulating HSC (LT-HSC) pool (Lin(-)Sca1(+)c-Kit(hi)CD

201 In contrast, long-term, but not short-term, repopulating HSC engraftment was impaired significantly,

202 opic miR-193b expression restricts long-term repopulating HSC expansion and blood reconstitution.

203 rophin caused a marked increase in long-term repopulating HSC numbers in culture, as measured in comp

204 xpanded 3-fold and maintained this long-term repopulating HSC phenotype.

205 IFN-gamma is sufficient to promote long-term repopulating HSC proliferation in vivo; furthermore, HSC

206 However, long-term repopulating HSCs (LT-HSCs) persist when Runx1 is condit

207 ined for a population enriched for long-term repopulating HSCs (LT-HSCs) versus their more differenti

208 sis and detected Id1 expression in long-term repopulating HSCs (LT-HSCs).

209 lays a critical role in preserving long-term repopulating HSCs (LT-HSCs).

210 rogeny, including closely related short-term repopulating HSCs (ST-HSCs) and fully differentiated lym

211 Similar to freshly isolated HSCs, repopulating HSCs after culture were positive for the st

212 bient oxygen decreases recovery of long-term repopulating HSCs and increases progenitor cells, a phen

213 l cells results in a deficiency of long-term repopulating HSCs and intra-aortic cluster cells.

214 tro increased the recovery of both long-term repopulating HSCs and progenitor cells, and systemic adm

215 ermediate blood progenitors but of long-term repopulating HSCs as well.

216 A clonal analysis of repopulating HSCs demonstrates that lymphoid-biased HSCs

217 ession and is required to generate long-term repopulating HSCs in the AGM.

218 HSC cycling and reduces functional long-term repopulating HSCs in the bone marrow.

219 ant and increased the frequency of long-term repopulating HSCs present in murine bone marrow after li

220 n, that an increased proportion of long-term repopulating HSCs proliferate during M. avium infection,

221 Long-term repopulating HSCs reside in several, perhaps overlapping

222 Thus, the full repertoire of repopulating HSCs was covered.

223 nitor cells, although selection of long-term repopulating HSCs was not seen.

224 t NPM promotes the self-renewal of long term repopulating HSCs while attenuated their commitment to m

225 self-renewal, the highest being on long-term repopulating HSCs, and decreases with differentiation, w

226 ls (HSCs), the ex vivo survival of long-term repopulating HSCs, and the prolonged in vivo expansion o

227 egress of murine HSPCs, including long-term repopulating HSCs, over mature leukocytes.

228 progenitor cells (MPPs) as well as long-term repopulating HSCs, while delaying myeloid differentiatio

229 ecreased ability to support the expansion of repopulating HSCs.

230 ecreased ability to support the expansion of repopulating HSCs.

231 antation confirmed transduction of long-term repopulating HSCs.

232 a net 23-fold ex vivo expansion of long-term repopulating HSCs.

233 - KSL fraction, which is highly enriched for repopulating HSCs.

234 sulted in an approximate 8-fold expansion of repopulating HSCs.

235 ts an approximately 20-fold net expansion of repopulating human cord blood HSCs, a number potentially

236 SDS scaffolds were toxic to repopulating human mesenchymal stem cells (hMSC).

237 of CML cells, as well as their efficiency in repopulating immunodeficient mice, both in the presence

238 alysis aimed at revealing their identity and repopulating in vivo capacity.

239 CAM(+) cells are true progenitors capable of repopulating injured rat liver.

240 Interestingly, repopulating irradiated control mice with bone marrow de

241 staining revealed approximately 5% to 10% of repopulating liver cells expressing human alpha1-antitry

242 ession on large vessel endothelial cells and repopulating LSECs.

243 Long-term repopulating (LT) hematopoietic stem cells (HSCs) are th

244 AMD3100 also mobilized murine long-term repopulating (LTR) cells that engrafted primary and seco

245 for the maintenance of established long-term repopulating (LTR) HSCs in the adult.

246 es expansion of multipotent cells capable of repopulating lymphoid and megakaryocyte lineages, which

247 in a transplantable, premalignant, long-term repopulating, MDS-initiating cell.

248 Using a long-term repopulating model, they demonstrate that epidermal stem

249 Extracardiac progenitor cells are capable of repopulating most major cell types in the heart, but the

250 , dendritic cells, and monocytes/macrophages repopulating mouse tissues.

251 Immunophenotypic analysis showed that repopulating mucosal CD4+ T cells were predominantly of

252 enhanced the rate of formation of short-term repopulating multipotential progenitor cells (MPPs) as w

253 port the expansion of human cells capable of repopulating non-obese diabetic/severe combined immunode

254 t stem cell that gives rise to the long-term repopulating of hematopoietic stem cells, mesenchymal st

255 C is influenced by both short- and long-term repopulating populations and that Flt3 expression may be

256 y less capable than more naive phenotypes of repopulating postdepletion, providing a potential mechan

257 1 regulation of HSC quiescence and long-term repopulating potential and hematopoietic lineage develop

258 Deletion of Slug enhances HSC repopulating potential but not its homing and differenti

259 enance of hematopoietic functions, including repopulating potential by up-regulating Notch-mediated s

260 g deficiency increases HSC proliferation and repopulating potential in vivo after myelosuppression an

261 f the HSC pool and a marked reduction of HSC repopulating potential in vivo.

262 CFU expansion and marrow repopulating potential of cultured Lineage(-)Sca-1(+)CD1

263 By contrast, the clonogenic and repopulating potential of normal hematopoietic stem and

264 r cell cycle greatly impaired the short-term repopulating potential of SKP2 null HSC and their abilit

265 d progressive depletion, defective long-term repopulating potential, and hematopoietic lineage develo

266 adult murine liver that possess potent blood-repopulating potential, approaching that of BM HSCs.

267 irradiated recipients, and enhanced in vivo repopulating potential.

268 bers of cell divisions retained their marrow repopulating potential.

269 isions in vitro while retaining their marrow-repopulating potential.

270 had a severely reduced competitive long-term repopulating potential.

271 ny of these CB CD34+ cells lose their marrow-repopulating potential.

272 uivocally establish the ability of transient repopulating progenitors to initiate myeloid leukemias i

273 p a model system for ex vivo gene therapy by repopulating rat livers with hepatocytes and hepatoblast

274 tem cells as a therapeutic strategy aimed at repopulating regions of bowel, where enteric neurones ar

275 icient mice reflecting recovery of long-term repopulating, self-renewing HSCs.

276 to efficiently mark rhesus macaque long-term repopulating stem and progenitor cells with retroviral v

277 dose, suggesting involvement of a short-term repopulating stem cell or an early myeloid progenitor.

278 erentiate into the less primitive short-term repopulating stem cells (ST-HSCs), which themselves prod

279 oietic progenitor cells (HPCs) and long-term repopulating stem cells from the bone marrow (BM) to the

280 veral months, suggesting that true long-term repopulating stem cells were not permanently deleted.

281 plexes preferentially expressed in long-term repopulating stem cells, is essential for adult hemopoie

282 sistent long-term engraftment of isogenic WT repopulating stem cells.

283 ed myeloerythroid progenitors and functional repopulating stem cells.

284 allow consistent engraftment of isogenic WT repopulating stem cells.

285 ver from bleaching events, the source of the repopulating symbionts is unknown.

286 gorously self-renew, expanding in number and repopulating the host muscle with new satellite cells.

287 The procedure is aimed at ablating and repopulating the immune repertoire by sequentially mobil

288 Recently, it has been suggested that cells repopulating the ischemically injured tubule derive from

289 y, and the residual symbionts began growing, repopulating the light organ.

290 recently described a regulatable system for repopulating the liver of immunodeficient mice (specific

291 least as efficient as mature hepatocytes in repopulating the liver.

292 ells remained in the circulation rather than repopulating the mucosa of the small intestine.

293 s from fetal liver that are fully capable of repopulating the normal adult liver.

294 hlight an ERG-regulated mechanism capable of repopulating the parent tumor through the transient gene

295 ets displayed a specific growth advantage in repopulating the spleen in competitive replacement bone

296 ation of functional pulmonary vasculature by repopulating the vascular compartment of decellularized

297 erm repopulating cell (LTRC) and competitive repopulating unit (CRU) frequency.

298 nstrated a dramatic reduction of competitive repopulating units and progressive decline in hematopoie

299 erial transplantation of long-term epidermal repopulating units derived from CD133(+) and CD133(+)Del

300 We measured at the clonal level repopulating waves, populations' sizes and dynamics, act