ライフサイエンスコーパス: engraft

1 transplanted subcutaneously alone failed to engraft.

2 All recipients of TN-depleted PBSCs engrafted.

3 enated rewarming (COR) for 90 minutes before engrafting.

4 iver or adult bone marrow (BM) more robustly engrafted adults.

5 e, we studied whether redirected T cells can engraft after adoptive transfer, without prior T-cell de

6 topoietic stem cells and progenitors fail to engraft after transplantation.

7 ma cell lines and patient-derived xenografts engraft and adopt a metastatic program in chick embryos.

8 f TECs, and further show that young TECs can engraft and directly drive the growth of involuted thymu

9 ized different HBV subtypes and were able to engraft and expand in immune-competent HBV transgenic mi

10 As a consequence, donor HSCs failed to engraft and hematopoiesis was suppressed.

11 injection, mesenchymal stem cells (MSCs) may engraft and influence host myocardium.

12 human glial progenitor cells (hGPCs) densely engraft and myelinate the hypomyelinated shiverer mouse.

13 croenvironment for tumor cells to be able to engraft and proliferate at secondary sites.

14 entiate into hematopoietic colonies but also engraft and reconstitute multilineage adult blood.

15 y of its haematopoietic stem cells (HSCs) to engraft and reconstitute the blood and bone marrow of an

16 ly that self-assembled allogeneic constructs engraft and reject similar to allogeneic skin despite th

17 vestigated whether E19 fetal hepatocytes can engraft and repopulate an injured adult liver.

18 1 infection, these coreceptor negative cells engraft and traffic normally, and are protected from inf

19 At day 100, 35 (92%) of 38 patients were engrafted and alive in the cyclophosphamide 50 mg/kg coh

20 These engrafted and expanded human HLCs were permissive to in

21 Seven patients (29%) who were engrafted and living more than 2 years after transplanta

22 cells transplanted into ossicle-bearing mice engrafted and maintained human HSCs in the niche.

23 s into a bone defect microenvironment, FCSCs engrafted and regenerated intramembranous bone.

24 When injected into dystrophic mice, MiPs engrafted and repaired both skeletal and cardiac muscle,

25 The findings indicated that transplanted KC engrafted and survived in recipient livers throughout th

26 se data demonstrate that genome-edited HSPCs engraft, and contribute to multilineage repopulation aft

27 n assays, we show that HSCs emerge, migrate, engraft, and differentiate in the absence of cdh5 expres

28 Importantly, solifenacin treatment of engrafted animals reduced auditory brainstem response in

29 In engrafted aorta, selected peptides containing Arg or Arg

30 l research focused on the ability of MSCs to engraft at sites of tissue injury, increasing evidence s

31 2.1 +/- 0.2%, while control EphB2(low) BMSCs engrafted at 0.3 +/- 0.1% (P<0.01).

32 EC-induced PSC-MPP engrafted at a markedly higher level in NOD/SCID/IL-2 re

33 anted Nalm-6 or Molm-13 human leukemia cells engrafted at a threefold higher rate in adipocyte-rich C

34 The engrafted B-1 cell population expressed a VH-DH-JH compo

35 (-)CD34(+)CD38(lo) stem cell population, and engrafted B-1 cells in humanized mice exhibit an Ig-usag

36 In CD47-deficient syngeneic hosts, engrafted B16 melanomas were 50% more sensitive to irrad

37 livers preconditioned with ischemia did not engraft better than hepatocytes from control livers.

38 able to migrate through the blood stream and engraft bone marrow (BM) niches.

39 rains into which human immune systems can be engrafted can help bridge this gap.

40 ing function, proT2-cells exhibited superior engrafting capacity.

41 ingly, this was completely reversed with SCJ engrafted CCR7(-/-) DCs in all parameters tested.

42 ve hematopoiesis and production of long-term engrafting CD34+ cells, suggesting these ligands are cri

43 Precise control over engrafted cell activity is highly desired, as cells do n

44 Measurements of long-term engrafted cells (up to 32 wk) demonstrated that hdCK3mut

45 l explants demonstrated proliferation of the engrafted cells and ability to generate crypt-like struc

46 at a small number of enzyme-proficient liver-engrafted cells can improve phenotype.

47 Engrafted cells could be localized to the stroma surroun

48 ed control of graft function, and activating engrafted cells drives behavioral changes in transplante

49 and cancer; yet models for direct imaging of engrafted cells has been limited.

50 The number of engrafted cells in GTN-treated mice was significantly hi

51 o the livers, resulting in a larger bolus of engrafted cells in the host livers under quiescent condi

52 rom human embryonic stem cells and show that engrafted cells replenish depleted precursor numbers, ge

53 Expression of hdCK3mut allowed engrafted cells to be visualized within recipient bone m

54 Engrafted cells were myeloid-restricted and matched the

55 was positively correlated with the number of engrafted cells.

56 ent regulation of host neuronal circuitry by engrafted cells.

57 ation, and that this loss can be reversed by engrafting cells back into an intact CNS environment.

58 ally enhances marking frequency in long-term engrafting cells in mice.

59 the identification of rare subpopulations of engrafting cells in xenotransplantation assays.

60 ive CMs at 3 months post injection indicated engrafted CMs proliferated in the host heart.

61 cell (BMSC) subsets with enhanced ability to engraft/contribute to the resident intestinal cellular p

62 Some engrafted CSCs also formed vascular structures and expre

63 d onto infarcted, immune tolerant rat hearts engrafted, displayed both host and graft-derived vascula

64 week post-infarct immune tolerant rat hearts engrafted, displayed evidence for host vascular coupling

65 r effect of AlloSCT is due to the ability of engrafting donor derived lymphocyte populations to eradi

66 lating cells (STRCs) without affecting their engrafting efficiency.

67 dered by inadequate stem cell number or poor engrafting efficiency.

68 Although all mutant lines engraft fluorescently labeled normal and malignant cells

69 AHNPs engraft following ex vivo expansion and transplantation

70 e islet seeding, the scaffold was allowed to engraft for 28 days to allow the tissue response to damp

71 HSCs engraft for long-term blood cell production and could pr

72 m909 CAR T cells mediated the regression of engrafted FRbeta(+) THP1 AML in vivo.

73 ); proT2, CD34(+)CD7(+)CD5(+)) showed thymus engrafting function, proT2-cells exhibited superior engr

74 Neonatally engrafted hiPSC OPCs robustly myelinated the brains of m

75 AGM AKT-ECs specified into long-term, adult-engrafting HSCs, establishing that a vascular niche is s

76 ransgenic mice and immunodeficient mice with engrafted human CD34(+) cells that HSPCs transduced in t

77 in a NOD/SCID/IL2Rgamma(-/-) mouse model of engrafted human chronic myelogenous leukemia, we now dem

78 The engrafted human glia were gap-junction-coupled to host a

79 ecies-selective properties of human glia, we engrafted human glial progenitor cells (GPCs) into neona

80 isms underlying the remaining defects in the engrafted human immune system and are generating "next g

81 We engrafted human pancreatic islets of Langerhans into the

82 w adjunct approaches to accelerate repair by engrafted human progenitors.

83 elial progenitor cell (EPC) recruitment into engrafted human synovium that was injected intragraft wi

84 eveloped mice with humanized white matter by engrafting human glial progenitor cells (GPCs) into neon

85 By engrafting human HSCs transduced with the oncogene combi

86 Four to 8 weeks later, these engrafted IK were transplanted across a minor histocompa

87 a greater capacity to form spheroids and to engraft immune-deficient mice than did ROR1-negative (RO

88 agocytic myeloid cells in vitro and can also engraft immunodeficient mice, generating myeloerythoid a

89 ultipotent hematopoietic progenitors able to engraft immunodeficient mice.

90 duced IgE-dependent gut inflammation in PBMC-engrafted immunodeficient mice.

91 liver tumor spots, and tumor burden in BLCL-engrafted immunodeficient NOD-SCID/Il2rg(-/-) mice.

92 ly than CD166(-) cells to the bone marrow of engrafted immunodeficient NSG mice.

93 the elimination of AML stem cells capable of engrafting immunodeficient mice by chemotherapeutic agen

94 lished human HD glial chimeras by neonatally engrafting immunodeficient mice with mutant huntingtin (

95 results in their apoptosis and inability to engraft, implicating HIF-1alpha or HIF-2alpha as therape

96 characteristics and have been shown able to engraft in and repopulate both animal and human livers.

97 We find that naive hPSCs robustly engraft in both pig and cattle pre-implantation blastocy

98 (LSCs) that are defined by their ability to engraft in immunodeficient mice.

99 edict CBU potency, defined as the ability to engraft in patients by day 42 posttransplant.

100 H3.3(K27M)-tumor cells serially engraft in recipient mice, and preliminary drug screenin

101 human bone and heart progenitors that could engraft in respective in vivo models.

102 s was associated with the capacity to stably engraft in secondary recipients.

103 ysfunctional HSCs, which do not successfully engraft in secondary recipients.

104 ouse colon organoids and human CRC organoids engraft in the distal colon and metastasize to the liver

105 Because few intravenously administered MSCs engraft in the myocardium, studies have mainly utilized

106 other hematologic disorders do not robustly engraft in these conventional models.

107 rogenitor cells (HSC/Ps) fail to effectively engraft in transplantation experiments, exhibiting norma

108 or cells while maintaining their capacity to engraft in vivo into humanized mice.

109 ntial in vitro and were the only fraction to engraft in vivo, although at low levels, following propa

110 argeting and can form nephron organoids that engraft in vivo, functionally couple to the host's circu

111 uced pluripotent stem cells (iPSCs) that can engraft in vivo.

112 entiation capacity in vitro and successfully engraft in vivo.

113 city of these human cells to physiologically engraft in xenotransplantation assays.

114 c adenocarcinoma specimens were successfully engrafted in 15 (60%) of 25 attempts.

115 ALDH(+) CSC from patients (n = 6) engrafted in hESCT within 4 to 12 weeks whereas none eng

116 tion of human hematopoietic progenitor cells engrafted in immune deficient mice (huNSG) results in vi

117 Genome-edited HSPCs also engrafted in immune-deficient mice long-term, confirming

118 differentiated state in stroma coculture and engrafted in immunodeficient mice.

119 Pre-clinical studies on ACC tumors engrafted in mice showed efficacy and low toxicity of AZ

120 ells and inhibited their tumorigenicity when engrafted in nude mice.

121 d in hESCT within 4 to 12 weeks whereas none engrafted in the flank.

122 t 7 d post-transplant, the EphB2(high) BMSCs engrafted in the ISC region at levels of 2.1 +/- 0.2%, w

123 ifferentiated from hESCs and hiPSCs could be engrafted in the liver parenchyma of immune-deficient tr

124 nted adult KC were successfully targeted and engrafted in the liver with retention of innate immune a

125 nt but not on the function of islets already engrafted in the liver.

126 le with human foetal epicardial explants and engrafted in the subepicardial space in vivo.

127 rogenitors that can be expanded in vitro and engrafted in vivo.

128 CNS-infiltrating cells, with multiple clones engrafting in both the CNS and periphery.

129 s are responsible for the production of DRs, engrafting in the recipient liver and localizing to the

130 Human CD82(+) muscle cells robustly engraft into a mouse model of muscular dystrophy.

131 bone marrow-derived circulating EPCs do not engraft into blood vessels, but that such circulating ce

132 d with light-inducible NPs containing RA can engraft into bone marrow in vivo in the proximity of oth

133 PSCs) with a myogenic propensity are able to engraft into both cardiac and skeletal muscles.

134 last ability to cross the vessel wall and to engraft into damaged myofibres through the modulation of

135 re colony-forming-cell potential and durably engraft into immune-deficient mice after primary and sec

136 freshly isolated hBTSCs were equally able to engraft into immunocompromised mice yielding cells with

137 Transplanted generic ECs engraft into regenerating tissues and acquire features o

138 we document that human MiPs can successfully engraft into the skeletal muscle and hearts of dystrophi

139 The iPLCs were successfully engrafted into a damaged airway, highlighting this signi

140 e show that SDF-1alpha-expressing COS1 cells engrafted into a regeneration-incompetent digit amputati

141 Donor cells engrafted into bones and differentiated into osteoblasts

142 splantation assays in which donor cells were engrafted into host mdx limb muscle.

143 r inflammation was induced in human arteries engrafted into immunodeficient mice that were reconstitu

144 - and CB-iPSC-derived VPs reliably homed and engrafted into injured retinal capillaries, with incorpo

145 del of TNBC in which Eo771/MUC1-C cells were engrafted into MUC1 transgenic mice, we showed that targ

146 a mouse model in which human glial cells are engrafted into neonatal mice that are both immunodeficie

147 Importantly, when engrafted into nude mice, decitabine(R) and PKC412(R) ha

148 on channel channelrhodopsin-2, which we then engrafted into partially denervated branches of the scia

149 NPCs engrafted into spinal cords of JHMV-infected mice exhibi

150 l of liver failure, the rat liver stem cells engrafted into the host liver where they differentiated

151 When normal hematopoietic cells are engrafted into the model, only discrete areas of the BM

152 nes and tested their capacity for homing and engrafting into murine retina in an ischemia-reperfusion

153 disease phenotype to normal mice, since mice engrafted intrastriatally with mHTT hGPCs exhibit worse

154 e first hematopoietic stem cells (HSCs) that engraft irradiated adult mice arise in the aorta-gonad-m

155 These data indicate that engrafted islet beta-cell mass is markedly improved with

156 To determine whether CIT07 improves engrafted islet beta-cell mass, our center measured beta

157 ent as assessed by the long-term function of engrafted islets.

158 ucial to ensure the survival and function of engrafted islets.

159 s, but not lymphocytes, from a low number of engrafted JAK2(V617F) SLAM cells.

160 Mast cell-engrafted Kit(W-sh/W-sh) mice infected with P. gingivali

161 However, Ripk1(-/-) progenitors failed to engraft lethally irradiated hosts properly.

162 ogenesis of myeloproliferative neoplasms, we engrafted lethally irradiated recipient mice with bone m

163 now demonstrate the complete elimination of engrafted leukemia after only one course of combined che

164 CLL cells resulted in complete clearance of engrafted leukemia cells.

165 med to the bone marrow in close proximity of engrafted leukemic cells and enhanced survival.

166 When the engrafted leukemic cells substantially damaged adjacent

167 on-treated animals live as long as their non-engrafted littermates.

168 Infection of the engrafted liver is universal and accelerates progression

169 However, glycoengineered hiPS-HSPCs did not engraft long-term, indicating that additional functional

170 Engrafted macrophages produce the cytokine TWEAK (TNF-li

171 nted onto rat hearts, cardiopatches robustly engraft, maintain pre-implantation electrical function,

172 s, the ability for the tumor of a patient to engraft may help identify those patients who will benefi

173 types of genetically MC-deficient mice after engrafting MCs that either do or do not express TNFRSF14

174 rgen-specific gut inflammation in human PBMC-engrafted mice can be avoided by enhancing the numbers o

175 and improves the survival of orthotopically engrafted mice implanted with human PTEN-deficient gliom

176 bone marrow, etc.) analyzed from nearly all engrafted mice.

177 ding the thymus, spleen, and bone marrow, of engrafted mice.

178 These engrafted motor neurons not only reinnervated lower hind

179 However, engrafted MSCs are subjected to acute cell death in the

180 ects accrue from local myocardial effects of engrafted MSCs.

181 early 2000s, investigators have been able to engraft murine recipients with human hematopoietic stem

182 In this study we developed a human PBMC-engrafted murine model of allergen-driven gut inflammati

183 s in culture and maintained their ability to engraft muscle in vivo.

184 Mutant fish engraft muscle, blood stem cells and various cancers.

185 Engrafted muscles displayed large numbers of micro-utrop

186 aematopoietic stem and progenitor cells that engraft myeloid, B and T cells in primary and secondary

187 onic HSCs from E9.5 and E10.5 preferentially engrafted neonates, whereas developmentally mature, defi

188 e brain environment into a favorable one for engrafted neural stem/progenitor cells (NSC/NPCs).

189 READD-dependent stimulation or inhibition of engrafted neurons, revealing D1 receptor-dependent regul

190 ), while also enhancing the content of early engrafting neutrophil and platelet precursors.

191 All patients engrafted neutrophils and platelets at expected times af

192 Modified cells maintained their ability to engraft NOD/SCID/IL2rgamma(null) mice and to produce cel

193 CD26(+) CML LSC engrafted NOD-SCID-IL-2Rgamma(-/-) (NSG) mice with BCR/A

194 Engrafting NOD/SCID/IL-2-Rg (null) mice with human lymph

195 uppressive M2-like phenotype in vitro and in engrafted nonobese diabetic-severe combined immunodefici

196 the survival, maturation, and integration of engrafted NSC/NPCs as a restorative treatment for PD.

197 3A-APC-potentiated neuronal recruitment from engrafted NSCs might offer a new approach to the treatme

198 Here, using human haematopoietic stem cell-engrafted NSG-HLA-DQ8 transgenic mice, we provide direct

199 Intradermal priming of engrafted NSG-SGM3 mice with a chimeric IgE containing h

200 or prognostic AMLs or for samples capable of engrafting NSG mice compared with good risk AMLs or none

201 er microinjection, glomeruli were capable of engrafting on the highly vascularized iris.

202 nced the activity of anti-ErbB2 mAb to treat engrafted or spontaneous tumors as well as lung metastas

203 with circulating donor red blood cells among engrafted participants.

204 Fifteen engrafted patients discontinued immunosuppression medica

205 In the 4 engrafted patients viral infections were cleared within

206 hemoglobin and resolution of hemolysis among engrafted patients were accompanied by stabilization in

207 stem cells yields haematopoietic cells that engraft poorly.

208 CD166(-/-) knockout (KO) LSK cells engrafted poorly in wild-type (WT) recipients and KO bon

209 IFN-gamma-expanded KSL cells engrafted poorly when tested by competitive repopulation

210 We investigated the CNS-engrafting potential of BCP-ALL cells xenotransplanted i

211 -) cells give rise to all blood lineages and engraft primary and secondary immunodeficient mice.

212 vation, of human myelolymphoid HSPCs able to engraft primary and secondary immunodeficient mice.

213 establish persistent replication in vivo, we engrafted primary rhesus macaque hepatocytes into immuno

214 ricular arrhythmias were observed in hESC-CM-engrafted primates.

215 ms could be very prolonged because some CPCs engraft, proliferate, and persist at 1 year.

216 omy (PH), transplanted stem/progenitor cells engrafted, proliferated competitively compared to host h

217 t intravenously injected rhC7 distributed to engrafted RDEB skin, incorporated into its dermal-epider

218 The second trimester cells also engrafted secondary recipients in serial transplantation

219 Engrafted splenic B-1 cells exhibited a mature phenotype

220 emarkably, when transplanted onto nude mice, engrafted SRF-null skin lacked hair but displayed normal

221 In addition, we will discuss the safety of engrafted stem cell-derived OPCs, as well as approaches

222 for determining the fate and persistence of engrafted stem cells.

223 was no predictable relationship between the engrafting subclone and the evolutionary hierarchy of th

224 R-deficient PDAC cells lacked the ability to engraft successfully in immunocompromised mice, but IDH1

225 lity to rearrange the actin cytoskeleton and engraft successfully.

226 In all recipients, islets engrafted successfully as shown by measurable posttransp

227 Importantly, the engrafted TEPs produce T cells capable of in vitro proli

228 cluding the growth of samples that would not engraft the BM of immunodeficient mice.

229 ost-transplantation showed 2 of the 6 clones engrafting the intestine at 4- to 5-fold higher levels (

230 We designed a panel of immunogens engrafting the V1V2 domain into trimeric and pentameric

231 All but 4 patients engrafted, these latter being rescued by a second allogr

232 been hindered by immune system rejection of engrafted tissue.

233 nterfere with the observation and imaging of engrafted tissues.

234 mitochondrial function, stress survival, and engrafted tumor growth.

235 Engrafted tumors stably coexpress optical reporters for

236 cleavage and the ratio of CD133(+) cells in engrafted tumors.

237 t BVF and BRA were preferentially seeded and engrafted upon HSC transplantation.

238 lungs of human CD34+ hematopoietic stem cell engrafted virus-infected NOD.Cg-Prkdc(scid) Il2rg(tm1Wjl

239 Wild-type HSCs could efficiently engraft when transferred to unirradiated, Ash1l-deficien

240 large cohort of patient samples successfully engrafted, which covered all of the important genetic an

241 fibers were observed, showing the fusion of engrafted wild-type myoblasts with muscle fibers; on the

242 prolonged the lifespan of C57BL/KaLwRij mice engrafted with 5TGM1-luc myeloma, an effect comparable t

243 Mouse T cells engrafted with a first-generation CAR failed to develop

244 blished an S. aureus infection model in mice engrafted with a human immune system, compared it with i

245 seventeen patients with MPS-IH successfully engrafted with a median follow-up age of 9.2 years were

246 ist of a tumor antigen-specific Fab molecule engrafted with a peptide neo-epitope, which is bound exc

247 Administration of duvelisib to mice engrafted with a PTCL patient-derived xenograft resulted

248 Short TSLPR CAR treatment of mice engrafted with a TSLPR-expressing ALL cell line induced

249 a decrease in growth kinetics, whereas mice engrafted with Bim knockout tumors showed no reduction i

250 Hypercholesterolemia-prone mice that were engrafted with bone marrow obtained from homozygous or h

251 was significantly improved if the mice were engrafted with bone marrow-derived cultured mast cells f

252 al signs of ocular allergy relative to those engrafted with CD103+ DC.

253 progression was significantly slowed in mice engrafted with CD34(+)/CD19(-) or CD34(+)/CD7(-) and CD3

254 T cells engrafted with chimeric AgRs (CAR) are showing exciting

255 , we show that humanized mice, i.e., animals engrafted with components of a human immune system, that

256 All patients engrafted with donor cells.

257 Immunodeficient mice engrafted with either normal or cancerous human cells ar

258 Immunodeficient mice engrafted with functional human cells and tissues, that

259 Treatment of SCID mice engrafted with G6PD-deficient huRBCs with primaquine, an

260 All alloconstructs successfully engrafted with histologic evidence of neovascularization

261 ia burden and increased the survival of mice engrafted with human AML without inducing overt toxicity

262 Immunodeficient mice engrafted with human cells and tissues have provided an

263 ntration of 1 mg/kg to immune-deficient mice engrafted with human CLL cells resulted in complete clea

264 In mice engrafted with human colorectal HT-29 carcinoma cells an

265 e lymphomas when directly injected into mice engrafted with human fetal CD34+ cells and human thymus.

266 type EBOV (Makona variant) infection of mice engrafted with human hematopoietic CD34(+) stem cells (H

267 e current study, we inoculated NSG-SGM3 mice engrafted with human hematopoietic CD34+ stem cells with

268 Immunodeficient mice are now readily engrafted with human hematopoietic cells.

269 Humanized mice engrafted with human hematopoietic stem cells and develo

270 ying a human stem cell factor transgene were engrafted with human hematopoietic stem cells.

271 /-, Rag2-/-, Il2rg-/-, termed the FRG mouse) engrafted with human hepatocytes (FRG huHep).

272 rg(-/-)Sirpa(NOD)Alb-uPA(tg/tg) mice, stably engrafted with human hepatocytes (HUHEP) with or without

273 n hepatocytes in vitro and to humanized mice engrafted with human hepatocytes in vivo but completely

274 Immunodeficient mice engrafted with human HSCs support multidisciplinary tran

275 Here, we describe EVD in mice engrafted with human immune cells (hu-BLT).

276 retransplantation into immunodeficient hosts engrafted with human T cells, panel-reactive antibody--t

277 ull)SCF/GM-CSF/IL3 (NSG-SGM3) strain of mice engrafted with human thymus, liver, and hematopoietic st

278 These mice can also be engrafted with human tissues such as islets, liver, skin

279 iNOS(-/-) mice engrafted with iNOS(+/+) BM exhibited larger infarcts (4

280 olitinib or PU-H71 improved survival of mice engrafted with JAK2V617F-mutant, Tp53-deficient AML, dem

281 Aspergillus fumigatus when mice were heavily engrafted with leukemia cells, had severe chemotherapy-i

282 loss of skeletal muscle mass induced in mice engrafted with Lewis lung carcinoma (LLC) cells or in Ap

283 1-Kit(W/W-v) or C57BL/6J-Kit(W-sh/W-sh) mice engrafted with mast cells that did or did not express VD

284 rdingly, when infused in NSG mice previously engrafted with myeloma, SE cells mediated tumor rejectio

285 ogeneic PBMC and were more severe in animals engrafted with PBMC depleted of CD4(+)CD25(high) cells.

286 ficient NOD/SCID/IL-2Rgamma(null) (NSG) mice engrafted with peripheral blood cells from patients with

287 antly prolongs the survival of NOD/SCID mice engrafted with primary ALL.

288 n vitro and in an orthotopic xenograft model engrafted with primary ALL; in the latter, reduced RAS-m

289 o extended survival of pneumonia in NSG mice engrafted with primary human AML cells.

290 ssful culture of CTCs from the blood of mice engrafted with primary human pancreatic tumors.

291 Mice engrafted with primate tissue make two important plasmod

292 arkedly improved the median survival of mice engrafted with the MCL cells.

293 Mice engrafted with TLR4-deficient hematopoietic cells were p

294 moniae-infected SP-A(-/-)Kit(W-sh/W-sh) mice engrafted with TNF-alpha(-/-) or TNF-R(-/-) MCs have dec

295 unodeficiency/interleukin 2Rgamma(null) mice engrafted with transformed human CD34+ hematopoietic ste

296 s production compared with that seen in mice engrafted with wild-type MCs, whereas burden was unaffec

297 Transplanted BMSCs often fail to engraft within the bone marrow (BM), in part due to the

298 ansplanted cells differentiated into ECs and engrafted within numerous capillaries.

299 Transplanted HSCs engrafted within the bone marrow (BM) of host animals, a

300 The ability of donor cells to engraft without evidence of ongoing HIV-1 infection sugg