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1 ll potential that allows them to self-renew, repopulate a damaged tissue, and then undergo differenti
2 esn't impair their ability to engraft and to repopulate a functional multilineage hematopoietic syste
3  of larvae (e.g., the refugia hypothesis) to repopulate a select subset of the shallow water (<30 m)
4 ertheless, the capacity of cultured cells to repopulate a wounded monolayer is markedly accelerated b
5 ymphopenia-induced peripheral expansion that repopulates a diverse peripheral T cell pool.
6 ic grafts mobilized with NSAIDs had superior repopulating ability and long-term engraftment.
7 to cytoablative stress, and exhibit superior repopulating ability and self-renewal upon serial transp
8  of its rich content of cells with sustained repopulating ability in spite of an apparent deficiency
9 its and progressive decline in hematopoietic repopulating ability of double-knockout (dKO) HSCs.
10 PC numbers but had only minor effects on the repopulating ability of HSCs.
11 ser extent HIF-1alpha, impedes the long-term repopulating ability of human CD34(+) umbilical cord blo
12 g dilution analysis, to assess the long-term repopulating ability of putative murine EpiSC population
13               The self-renewal and long-term repopulating ability of these cells was shown in serial-
14 ipients significantly impaired the long-term repopulating ability of transplanted mouse HSCs shortly
15  region, to maintain hematopoietic stem cell repopulating ability through a miR-675-Igf1r signaling c
16 xpression of which in ESCs confers long-term repopulating ability to ESC-derived HSCs.
17 stem cell (HSC) subtypes with self-renewable repopulating ability, but with different haematopoietic
18              Likely underlying the increased repopulating ability, FOXP3 expressing HSC showed signif
19 rs at the expense of reduced bone marrow HSC repopulating ability, thereby limiting potential therape
20 y for keratinocyte stem cells with long-term repopulating ability.
21 ulating activity, as Foxa3(-/-) HSC fails to repopulate ablated hosts efficiently, implicating for th
22       Aging dramatically reduced HSC in vivo-repopulating activity and lymphoid potential while incre
23 al human hematopoietic cells with short-term repopulating activity cells (STRCs) are needed to facili
24 otype ( approximately 10% HSCs with >6-month repopulating activity in immunodeficient mice) displayed
25 rial replating in vitro and long-term serial repopulating activity in vivo.
26 igration, niche retention, and hematopoietic repopulating activity of hematopoietic stem and progenit
27 activity, its expression is required for the repopulating activity of human HSCs.
28 -state in vivo hematopoiesis or on long-term repopulating activity of Wnt-deficient hematopoietic ste
29 mice to demonstrate that aged ECs impair the repopulating activity of young HSCs and impart a myeloid
30 ar, HSC number, cell cycle status, long-term repopulating activity, and self-renewal capacity were no
31  We validated that Foxa3 is required for HSC repopulating activity, as Foxa3(-/-) HSC fails to repopu
32 ciated with a marked loss of HSCs, long-term repopulating activity, HSC quiescence and common lymphoi
33  cells results in a modest loss of long-term repopulating activity.
34 s short- and long-term in vivo hematopoietic repopulating activity.
35 ll growth and a loss of short- and long-term repopulating activity.
36 enhanced frequency, competence and long-term repopulating activity.
37            The expanded BM showed a distinct repopulating advantage when tested in serial competitive
38 d robust self-renewal capacity and exhibited repopulating advantages over wild-type HSCs.
39                      However, tumors rapidly repopulate after treatment with such compounds.
40 bset of horizontal basal cells (HBCs), which repopulate all microvillar cells and Bowman's glands dur
41 hether E19 fetal hepatocytes can engraft and repopulate an injured adult liver.
42  interactions and of microbial strategies to repopulate and survive in the soil are largely unexplore
43 n microglia were eliminated prior to RSD and repopulated and mice were subjected to acute stress, the
44 ring recovery the injured parenchyma becomes repopulated and repaired by Axin2(+) descendants.
45 of phenotypically corrected HSPCs capable of repopulating and developing proliferation advantage in i
46 receptor antagonism (PLX5622) and allowed to repopulate, and responses to acute stress or immune chal
47 lso impaired in their ability to migrate and repopulate areas subjected to a scratch wound.
48 t affected and the germ cells were gradually repopulated at later developmental stages.
49 -cohort study, we evaluated the phenotype of repopulating B cells and its correlation with donor-spec
50                   The characteristics of the repopulating B cells are currently unknown.
51 s and have been shown able to engraft in and repopulate both animal and human livers.
52  (+) LT-HSCs while NEO1(-) Hoxb5 (+) LT-HSCs repopulate both LT-HSC fractions.
53 that in healthy allografts, protective ILC3s repopulate by 2-4 weeks postoperatively, but in rejectin
54 increased so that up to 35% of the liver was repopulated by donor-derived cells.
55  of the allograft, fall as the graft becomes repopulated by hematopoietic cells of the NOD2 mutant re
56 nocyte-depleted interfollicular epidermis is repopulated by melanocyte precursors from hair follicle
57 s) are self-renewing in the steady state but repopulated by myeloid precursors after injury.
58 er times, the ablated skin was progressively repopulated by non-recombined Chk1-expressing cells and
59 elevated Notch signaling and reduced mammary repopulating capability upon transplantation.
60 progenitors, and exhibited reduced long-term repopulating capacity as well as hyper granulocyte-colon
61 Psigma substantially increased long-term HSC-repopulating capacity compared with BM cells from contro
62 owever, certain acinar subpopulations have a repopulating capacity during regeneration, raising the h
63 t derived xenografts we demonstrate that the repopulating capacity in normal mammary epithelial cells
64           Conversely, young ECs restored the repopulating capacity of aged HSCs but were unable to re
65 quiescence of dormant HSCs and the long-term repopulating capacity of HSC.
66 TPsigma(-) cells substantially increased the repopulating capacity of human HSCs compared with CD34(+
67 ysical and chemical insults compromising the repopulating capacity of the epithelial stem cell compar
68                       Furthermore, long-term repopulating capacity was also present in a compartment
69 /-) LSK cells had an increased hematopoietic repopulating capacity with an altered cell differentiati
70 ant loss of quiescence and decline in serial repopulating capacity, but no substantial difference in
71 (-/-) HSCs exhibited decreased hematopoietic repopulating capacity, with skewed cell differentiation
72 lation with severe combined immunodeficiency-repopulating capacity.
73 rly demonstrate the necessity of Shp2 in HSC repopulating capacity.
74                                              Repopulating CD4+ but not CD8+ T cells significantly dim
75 were those in the CD34(-) Flt3R(-) long-term repopulating cell fraction.
76 ement membrane vs. non-basement membrane) on repopulating cell phenotype and function has important i
77 articularly in the most primitive, long-term repopulating cell population.
78 reatment resulted in a dramatic loss of SCID-repopulating cells (SRCs), treatment with OKT3 or UCHT1
79 nhanced clonal outputs from human short-term repopulating cells (STRCs) without affecting their engra
80                                       Tumour-repopulating cells (TRCs) are a self-renewing, tumorigen
81                                        Tumor-repopulating cells (TRCs) are cancer stem cell (CSC)-lik
82 tem-like cells that repopulate tumors (tumor-repopulating cells (TRCs)).
83            Recently we have shown that tumor-repopulating cells (TRCs), a highly tumorigenic subpopul
84 , including a 17-fold increase in short-term repopulating cells and a net 23-fold ex vivo expansion o
85 D34+ cells produced a greater number of SCID-repopulating cells and established multilineage hematopo
86 ene therapy since they efficiently transduce repopulating cells and may be safer than more commonly u
87 d in long-term culture, initiating cells and repopulating cells compared with controls.
88 in lineage cells represent a major source of repopulating cells for reconstitution of the intraglomer
89 ction efficiency for long-term hematopoietic repopulating cells in humanized mice and rhesus macaques
90 ng hematopoiesis by giving rise to long-term repopulating cells in recipient mice with an unexpected
91 fficiently transduce and/or expand long-term repopulating cells in vivo are needed for treatment of d
92 ly posttransplant, and 3% to 5% in long-term repopulating cells over 6 months following HSPC transpla
93 CM niche is capable of directing behavior of repopulating cells remains relatively unexplored.
94 proximately 3.5% to 33% in myeloid long-term repopulating cells resulting in a functional cure.
95 to a pronounced increase in the frequency of repopulating cells, as assessed by extreme limiting dilu
96 g NOD.Cg-Prkdc(scid) IL2rg(tm1Wjl) /SzJ mice repopulating cells, induced by combination treatment.
97 action contain both short-term and long-term repopulating cells.
98 ing cells, and both long-term and short-term repopulating cells.
99 t identifies both murine and human long-term repopulating cells.
100 in vivo expansion of corrected hematopoietic repopulating cells.
101 ve advantage of corrected FA-A hematopoietic repopulating cells.
102 the basal compartment, which harbors mammary repopulating cells.
103 in DNA-bound insulator proteins that rapidly repopulate chromatin as the bodies disassemble upon retu
104 ity, and rat CLiPs were shown to extensively repopulate chronically injured liver tissue.
105 n stable myeloid-B-T multilineage, long-term repopulating clones.
106                    Delivery of stem cells to repopulate damaged cardiac tissue may be an attractive a
107                                              Repopulated DCLK1-overexpressing primary human hepatocyt
108                                The organoids repopulated decellularized liver discs and formed liver-
109                           Finally, PiPS-SMCs repopulated decellularized vessel grafts and ultimately
110           Here we create heart constructs by repopulating decellularized mouse hearts with human indu
111 ngineering of humanized intestinal grafts by repopulating decellularized rat intestinal matrix with h
112 KLF7, and loss of CDKN1A does not rescue the repopulating defect.
113 re-HSCs capable of developing into long-term repopulating definitive HSCs.
114 nal stem/progenitor-like cells, were able to repopulate different nephron portions of renal extracell
115 d that Ly49G2(high) single-positive NK cells repopulated, displayed an activated phenotype, and were
116 viduals upon which natural selection acts to repopulate ecosystems with offspring, the proposed mater
117 ration, across all species, breeding females repopulate ecosystems with offspring.
118 inking the rates with which breeding females repopulated ecosystems, to the stability of ecosystems.
119 cytes to new neurons that innervate into and repopulate endogenous neural circuits.
120 proliferative Lgr5(-) cells that are able to repopulate entire glands, including the base, upon deple
121 tial (DPsim(hi)) were enriched for long-term repopulating EpiSCs versus unfractionated cells (3.9- an
122 ing dilution transplantation and competitive repopulating experiments demonstrated a dramatic reducti
123 ellularized human liver cubic scaffolds were repopulated for up to 21 days using human cell lines hep
124 ing therapy and show very limited ability to repopulate from donor bone marrow.
125 s) and establish that P-SSCs are a long-term repopulating, functionally distinct SSC subset responsib
126        However, its application to long-term repopulating haematopoietic stem cells (HSCs) has remain
127 ffect the homing and the number of long-term repopulating haematopoietic stem cells, haematopoietic s
128 ger age and persistence of higher VCN in the repopulating hematopoietic cells are associated with bet
129                              The first adult-repopulating hematopoietic stem cells (HSCs) emerge in t
130 ic progenitor cells (HPCs) at the expense of repopulating hematopoietic stem cells (HSCs).
131 ent of CD34(+) cells that contains long-term repopulating hematopoietic stem cells (HSCs).
132                        Multipotent long-term repopulating hematopoietic stem cells (LT-HSCs) can self
133                       Retention of long-term repopulating hematopoietic stem cells (LT-HSCs) in the b
134 scription factors that can amplify long-term repopulating hematopoietic stem cells in a controlled wa
135 en reported to identify functional long-term repopulating hematopoietic stem cells, and has been dete
136 tion of the edited CD34+ cells are long-term repopulating hematopoietic stem cells, demonstrating the
137 he maintenance of immunophenotypic long-term repopulating hematopoietic stem cells, suggesting that a
138 rial transplantation, hallmarks of long-term repopulating hematopoietic stem cells.
139  75% of cells in a highly enriched long-term repopulating HSC (LT-HSC) pool (Lin(-)Sca1(+)c-Kit(hi)CD
140  In contrast, long-term, but not short-term, repopulating HSC engraftment was impaired significantly,
141 opic miR-193b expression restricts long-term repopulating HSC expansion and blood reconstitution.
142 xpanded 3-fold and maintained this long-term repopulating HSC phenotype.
143                           However, long-term repopulating HSCs (LT-HSCs) persist when Runx1 is condit
144 ined for a population enriched for long-term repopulating HSCs (LT-HSCs) versus their more differenti
145 lays a critical role in preserving long-term repopulating HSCs (LT-HSCs).
146 rogeny, including closely related short-term repopulating HSCs (ST-HSCs) and fully differentiated lym
147 bient oxygen decreases recovery of long-term repopulating HSCs and increases progenitor cells, a phen
148 l cells results in a deficiency of long-term repopulating HSCs and intra-aortic cluster cells.
149 tro increased the recovery of both long-term repopulating HSCs and progenitor cells, and systemic adm
150 d promotes in vitro propagation of long-term repopulating HSCs by preventing differentiation.
151 ession and is required to generate long-term repopulating HSCs in the AGM.
152 HSC cycling and reduces functional long-term repopulating HSCs in the bone marrow.
153                                    Long-term repopulating HSCs reside in several, perhaps overlapping
154 udies showed that the expansion of long-term repopulating HSCs was accompanied by synchronized expans
155 rtantly, upon macrophage depletion, no adult-repopulating HSCs were detected, thus implicating a role
156 lantation assays demonstrated that long-term repopulating HSCs were highly enriched within the gata2a
157  egress of murine HSPCs, including long-term repopulating HSCs, over mature leukocytes.
158 a net 23-fold ex vivo expansion of long-term repopulating HSCs.
159 ture that characterizes functional long-term repopulating HSCs.
160 that the estimated minimum number of active, repopulating HSPCs (which ranged from 2000 to 50 000) wa
161 entiation and myofilament formation from the repopulated human multipotential cardiovascular progenit
162                  SDS scaffolds were toxic to repopulating human mesenchymal stem cells (hMSC).
163 malization of CD1d expression exclusively in repopulated immature B cells.
164 reases the ability of the cells to long-term repopulate immunodeficient mice compared with equivalent
165 of CML cells, as well as their efficiency in repopulating immunodeficient mice, both in the presence
166 hitosan/gelatin composite, could transiently repopulate immunologically compromised mice skin to rega
167                       Gram-negative bacteria repopulated in the smokers faster than in the non-smoker
168 ate that distinct stem/progenitor cell pools repopulate injured tissue depending on the extent of the
169 rs remain TNF sensitive in vitro and fail to repopulate irradiated mice.
170                               Interestingly, repopulating irradiated control mice with bone marrow de
171                              WT HSC normally repopulated Itpkb(-/-) hosts, indicating an HSC-intrinsi
172 gesting a model wherein a parasite reservoir repopulates itself indefinitely, whereas some progeny ar
173 ensively after transplantation and therefore repopulate large parts of the recipient's hematopoietic
174       These factors in turn reprogrammed the repopulating liver macrophage enhancer landscape to conv
175 zed transcriptomic and epigenetic changes in repopulating liver macrophages following acute Kupffer c
176 ution returned to normal in 2 weeks, but the repopulated livers were unable to fully respond to drug-
177  in vitro, and markedly eliminated long-term repopulating LSCs and infiltrating blast cells, conferri
178                                    Long-term repopulating (LT) hematopoietic stem cells (HSCs) are th
179  the GFP sorted cells failed to give rise to repopulated mammary glands in de-epithelialized recipien
180 tion prevented the behavioral decline in the repopulated mice, and it supported behavioral recovery i
181                           Following TBI, the repopulated microglia displayed a ramified morphology si
182 was elevated, both in all brain cells and in repopulated microglia.
183              The beneficial effects of these repopulating microglia are critically dependent on inter
184 uman fibroblast-derived hepatocytes that can repopulate mouse livers.
185 +) ISCs dramatically proliferate to clonally repopulate multiple contiguous crypts and villi.
186                Currently, the possibility to repopulate naturally obtained scaffolds with cells of di
187 served numbers of long-term HSCs, yet cannot repopulate nor sustain itself after transplantation agai
188 gical mobilization, resulting in a chimeric, repopulated organ.
189 ith intact subunits in sucrose gradients and repopulate polysomes after a short starvation-induced tr
190 y less capable than more naive phenotypes of repopulating postdepletion, providing a potential mechan
191              By contrast, the clonogenic and repopulating potential of normal hematopoietic stem and
192 macological inhibition of EZH2 decreases the repopulating potential of p53 mutant HSPCs.
193 had a severely reduced competitive long-term repopulating potential.
194 ny of these CB CD34+ cells lose their marrow-repopulating potential.
195  irradiated recipients, and enhanced in vivo repopulating potential.
196 ng to aggressive lymphomas with an increased repopulating potential.
197 f-2alpha-deficient HSCs and their ability to repopulate primary recipients, indicating that Hif-1alph
198 ain large numbers of mouse mitochondria that repopulate recipient mouse cells along with the injected
199 M niche has a role in modulating response of repopulating recipient cells toward AR-BP scaffolds for
200  via an unexpected proliferative response to repopulate residual tumours between chemotherapy cycles,
201 PDGFR-beta(+) MSCs, including the ability to repopulate secondary grafts.
202 base edits could be produced in multilineage-repopulating self-renewing human HSCs with high frequenc
203  HuHF MelSCs that can potentially be used to repopulate skin for pigmentation.
204 rsor cells proliferate and mature adipocytes repopulate skin wounds following inflammation and in par
205 t allow lingering immunosuppressive cells to repopulate small pockets of residual disease quickly.
206          Both ALDH1(br) and ALDH1(low) cells repopulated stem cell heterogeneity, formed spheroids, a
207 erentiate into the less primitive short-term repopulating stem cells (ST-HSCs), which themselves prod
208 plexes preferentially expressed in long-term repopulating stem cells, is essential for adult hemopoie
209 6 weeks and efficient targeting of long-term repopulating stem cells.
210 y is associated with long-lasting effects on repopulated T cells and subsequent increased rates of in
211 veral studies have analyzed the phenotype of repopulated T-lymphocytes following alemtuzumab inductio
212 tor-transduced progenitor cells were able to repopulate the B-cell compartment with a normal distribu
213                        The dormant cells can repopulate the biofilms following alleviation of antibio
214 plant, HSPCs need to expand substantially to repopulate the BM and replenish the peripheral blood cel
215 se progenitors can migrate out of the lungs, repopulate the bone marrow, completely reconstitute bloo
216 i; PAR(2) mobilization and de novo synthesis repopulate the cell surface with intact receptors and su
217              Given that peripheral monocytes repopulate the central nervous system after CSF1R inhibi
218 ed depletion rapidly enter the cell cycle to repopulate the cortex with altered spatial distribution.
219 buffering it to a level such that Zn(2+) can repopulate the defective binding site, but how it accomp
220 e proliferate, migrate, and differentiate to repopulate the depigmented epidermis.
221                 Limbal epithelial stem cells repopulate the donor site as early as 1 year after limbu
222 g each hair cycle, exhibit self-renewal, and repopulate the DS and the DP with new cells.
223 estigated whether cells of renin lineage can repopulate the glomerulus after podocyte injury and serv
224 f reconstitution and the types of cells that repopulate the host.
225              Thus, nonlethally injured cells repopulate the kidney epithelium after injury in the abs
226 epatic stem/progenitor cells can effectively repopulate the liver with advanced fibrosis/cirrhosis.
227 planted in vivo into wild-type stroma, fully repopulate the mammary gland fat pad, undergo unperturbe
228  myeloid cells with donor wild-type CSF1R to repopulate the microglial niche.
229 urther, we demonstrate that the B cells that repopulate the MZ in aged bumble mice were distinct from
230 are killed by viruses, circulating monocytes repopulate the open niche.
231   In chronic infection, HIV-1 escape mutants repopulate the plasma, and V3 and CD4bs nAbs emerge that
232 tic cell transplantation (HCT) is applied to repopulate the recipient myeloid compartment, including
233 o resume normal proliferation and eventually repopulate the sample.
234  endothelial cell progenitor cells (BM SPCs) repopulate the sinusoid as liver sinusoidal endothelial
235 ith reduced capacity to repair myofibers and repopulate the stem cell reservoir in vivo following tra
236 urst following IR and an impaired ability to repopulate the thymus after IR.
237 n may allow them to survive chemotherapy and repopulate the tumor after exposure to chemotherapeutics
238 with the exclusive ability to self-renew and repopulate the tumor and have been reported to be less s
239 t reservoir of mutant cells that can expand, repopulate the tumor, and result in the rapid emergence
240 specialized niches, which resist therapy and repopulate the tumour.
241 acity to undergo periclinal cell division to repopulate the vascular stem cell pool.
242                  Transplanted stellate cells repopulated the damaged rat liver by contributing to the
243  rescued as newly generated immature neurons repopulated the granule cell layer upon termination of t
244 grated in the ECM scaffold and spontaneously repopulated the lining of decellularized vessels.
245 rred in a hematopoietic stem cell (HSC) that repopulated the myeloid but not the lymphoid lineage.
246 oke patients without tPA treatment gradually repopulated the numbers of circulating regulatory T cell
247 ctive B cells that had escaped depletion and repopulated the periphery through homeostatic expansion.
248 thritis symptoms rapidly returned as B cells repopulated the repertoire.
249 ours after injection of dimethylnitrosamine, repopulated the sinusoid as LSECs and reduced liver inju
250  temozolomide, pre-GEPCOT cells survived and repopulated the SVZ.
251 othelial cells, and these T-cell progenitors repopulated the thymus and differentiated into mature T-
252 pulation selected from a population of cells repopulated the whole original basin of attraction withi
253    A very limited number of HSC clones (<10) repopulated the xenografted thymus, with further restric
254 ly generated and decays to the latter, which repopulates the ground state with tau = 362 ps.
255 lar triplet-state 'reservoir' that thermally repopulates the photoluminescent state of CdSe through e
256       The procedure is aimed at ablating and repopulating the immune repertoire by sequentially mobil
257 disassembling sarcomeres, proliferating, and repopulating the injured area remain unclear.
258 ells remained in the circulation rather than repopulating the mucosa of the small intestine.
259 hlight an ERG-regulated mechanism capable of repopulating the parent tumor through the transient gene
260 ation of functional pulmonary vasculature by repopulating the vascular compartment of decellularized
261 s as the primary source of endothelial cells repopulating the vessel wall following injury.
262 st for extremely long periods of time and to repopulate their own pool size through homeostatic self-
263 seeks to rehabilitate degraded ecosystems by repopulating them with large animals, thereby re-establi
264 bly, microglia have an intrinsic capacity to repopulate themselves after acute ablation.
265                                      We then repopulated this native human cardiac matrix with cardio
266 during embryogenesis and have the ability to repopulate through local proliferation.
267 s in blood after cessation of therapy, which repopulated tissues throughout the body; (b) that multip
268 -) mice in which the peripheral T cells were repopulated to a normal level by syngeneic bone marrow t
269                               Cultured cells repopulated tracheal scaffolds in a heterotopic transpla
270 tant to antiproliferative therapies, able to repopulate tumor bulk, and seed metastasis.
271 arbon flow direction in stem-like cells that repopulate tumors (tumor-repopulating cells (TRCs)).
272  expression enabled prostate cancer cells to repopulate tumors in orthotopic and heterotopic tissues.
273 ance to standard chemotherapeutic agents and repopulate tumours after therapy.
274 ble for maintaining the capacity of HSPCs to repopulate under steady-state conditions, by activating
275 nstrated a dramatic reduction of competitive repopulating units and progressive decline in hematopoie
276 erial transplantation of long-term epidermal repopulating units derived from CD133(+) and CD133(+)Del
277 he potential of hematopoietic progenitors to repopulate upon adoptive transfer or after 5-fluorouraci
278 onditions, Cdk6(-/-) HSCs do not efficiently repopulate upon competitive transplantation, and Cdk6-de
279              We measured at the clonal level repopulating waves, populations' sizes and dynamics, act
280 ng of a decellularized lung scaffold that is repopulated with a patient's own cells could provide des
281 ver/thymus humanized mice, lung implants are repopulated with autologous human hematopoietic cells.
282 nt phenomenon allows for the construct to be repopulated with cells and to be connected to the blood
283 s provides a mechanism by which cells may be repopulated with functioning organelles.
284 G mice backcrossed to the NOD background and repopulated with huHeps and human red blood cells suppor
285                                         Mice repopulated with human hematopoietic cells are a powerfu
286                               Livers of mice repopulated with human hepatocytes (humanized livers) gr
287 re combined immunodeficient mice with livers repopulated with human hepatocytes (humanized livers).
288 plicating and in mice whose livers have been repopulated with human hepatocytes and infected with HBV
289 hat homozygous PIRF mouse livers are readily repopulated with human hepatocytes, and when the murine
290 ) mice and their FRGN littermates were fully repopulated with human hepatocytes.
291  create FRGN mice, whose livers can be fully repopulated with human hepatocytes.
292                However, wild-type recipients repopulated with necdin-null hematopoietic stem/progenit
293 n regions of CD11b-HSVTK transgenic mice are repopulated with new Iba-1-positive cells within 2 wk.
294 the nonobese diabetic (FRGN) background were repopulated with primary human hepatocytes from differen
295     Once in the body, these biomaterials are repopulated with somatic cells of various phenotypes who
296 sing a decellularized deceased donor trachea repopulated with the recipient's respiratory epithelium
297                            Lyn knockout mice repopulated with wild-type bone marrow-derived cells hav
298 that the microglia-depleted brain completely repopulates with new microglia within 1 week of inhibito
299 as in cartilage injured by blunt impact were repopulated within 7-14 days by cells that appeared to m
300 eveals that re-epithelializing keratinocytes repopulate wounds by TGF-beta- and integrin-dependent la

 
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