ライフサイエンスコーパス: engraft

1 invasive tumors more likely to successfully engraft.

2 transplanted subcutaneously alone failed to engraft.

3 All recipients of TN-depleted PBSCs engrafted.

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

5 VLA4+NPC-engrafted 4L;C* midbrains showed 35% increased GCase act

6 Here, we rationally engraft a new paratope, i.e., the extended heavy-chain f

7 daptive and natural killer immune cells, can engraft a wide array of human cancers at 37 degrees C, a

8 eas allogeneic hepatocytes were rejected but engrafted after immunosuppression.

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

10 confirmed that injected stem cells robustly engraft and contribute to all lineages.

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

12 ury can recruit BM progenitors of LSECs that engraft and fail to fully differentiate, which creates a

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

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

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

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

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

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

19 CD33 in HSPC doesn't impair their ability to engraft and to repopulate a functional multilineage hema

20 1 infection, these coreceptor negative cells engraft and traffic normally, and are protected from inf

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

22 irradiated mice, in which they successfully engrafted and differentiated into hematopoietic progenit

23 These engrafted and expanded human HLCs were permissive to in

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

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

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

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

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

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

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

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

32 In engrafted aorta, selected peptides containing Arg or Arg

33 trocytes in humanized glial chimeric mice by engrafting astrocytes differentiated from human-induced

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

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

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

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

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

39 red LSECs by BM endothelial progenitors that engraft but fail to fully mature.

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

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

42 or reduced subcutaneous tumor growth in mT3 engrafted Cdh11(+/+) mice when given in combination with

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

44 ent, significantly induced GFP expression in engrafted cells across tissues, reflecting viral reactiv

45 functional reconstitution in the progeny of engrafted cells at 12 months.

46 Engrafted cells could be localized to the stroma surroun

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

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

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

50 olayers, 10-month-old cortical organoids and engrafted cells in the spinal cords of rats.

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

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

53 Engrafted cells were myeloid-restricted and matched the

54 s representation of spatial distributions of engrafted cells, enabling simulation of clinical therapy

55 was positively correlated with the number of engrafted cells.

56 ent regulation of host neuronal circuitry by engrafted cells.

57 permits the dynamic visualization of single engrafted cells.

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

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

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

61 We identified 5 cases of donor-engrafted CH, with 1 case progressing into myelodysplast

62 Engrafted circulating monocytes transmigrated into the p

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

64 due to limited ability of MDS stem cells to engraft current immunodeficient murine hosts.

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

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

67 s required for disseminating tumour cells to engraft distant sites(4-6).

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

69 repertoire in hematochimeric mice, although engrafted edited clones preserve multilineage and self-r

70 d macrophages that develop during injury can engraft efficiently in the pool of resident peripheral n

71 v) and host T(regs), donor T(regs) failed to engraft even with interleukin-2 (IL-2) support.

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

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

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

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

76 ter BC treatment, multiple cell types can be engrafted from fresh or cryopreserved testicular cells,

77 The long-term engrafted glial-restricted progenitors myelinated dysmye

78 blood disorders, although its application in engrafting hematopoietic stem cells (HSCs) remains unexp

79 RNA-sequencing of engrafted hESC-CMs confirmed the increased expression of

80 All 5 patients engrafted; however, 1 patient at day +13 developed hemop

81 Importantly, the engrafted hPSC-derived microglia exhibit dynamic respons

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

83 this aneuploidy peak: rapid expansion of the engrafted HSPC population and bone marrow microenvironme

84 e percentage of multipotent HSPCs within the engrafted HSPC population was significantly decreased co

85 -) immunocompromised zebrafish that robustly engraft human cancer cells for in excess of 28 d.

86 Here we successfully engraft human microglia derived from embryonic stem cell

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

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

89 model of acute synovitis, where transiently engrafted human IFP-MSC induced local SP reduction.

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

91 Engrafted human T-cell function was documented by reject

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

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

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

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

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

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

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

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

100 ory properties of IFP-MSC, which selectively engraft in areas of active synovitis/IFP fibrosis induci

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

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

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

104 that are derived from only 50 cells robustly engraft in recipient mice without the normal requirement

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

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

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

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

109 ients in response to appropriate stimuli and engraft in the adult mouse brain.

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

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

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

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

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

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

116 entiation capacity in vitro and successfully engraft in vivo.

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

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

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

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

121 Syngeneic hepatocytes engrafted in liver, whereas allogeneic hepatocytes were

122 nce-activated cell sorting from human islets engrafted in mice.

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

124 Donor-origin mutant clones engrafted in recipients and expanded during the first 10

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

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

127 VLA4+NPCs successfully engrafted in the nGD (4L;C*) mouse brain.

128 These EC clones engrafted in the pulmonary arteries.

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

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

131 Day 4 Th17 cells engrafted, induced release of multiple cytokines includi

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

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

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

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

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

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

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

139 Transplanted human BAs engraft into the inter-scapular region of recipient mice

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

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

142 Donor cells engrafted into bones and differentiated into osteoblasts

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

144 Human pancreatic islets engrafted into immunodeficient mice serve as an importan

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

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

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

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

149 Finally, patient-derived xenografts could be engrafted into our model, opening new avenues for develo

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

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

152 ter ocular injury in mice become permanently engrafted into the tissue, establishing a proinflammator

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 ent of human C-peptide indicated that higher engrafted islet mass resulted in higher human C-peptide

156 CR of liver samples was conducted to confirm engrafted islet numbers after PET imaging.

157 ging yielded high resolution images of liver-engrafted islets and also showed significant retention i

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

159 eactive and autoreactive immunity toward the engrafted islets.

160 t developed collapsing glomerulopathy in the engrafted kidney, which was transplanted from a donor wh

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

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 When the engrafted leukemic cells substantially damaged adjacent

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

166 Infection of the engrafted liver is universal and accelerates progression

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

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

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

170 ry methods that can effectively localize and engraft mesenchymal stem cells (MSCs) with high disease-

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

172 Most importantly, none of the engrafted mice exhibited clinical features of GVHD.

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

174 To address whether engrafted miR-210-positive myeloid or lymphoid cells con

175 These engrafted motor neurons not only reinnervated lower hind

176 Using a human HSC engrafted mouse model and a human iNKT TCR gene engineer

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

178 ects accrue from local myocardial effects of engrafted MSCs.

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

180 Gene expression profiling of engrafted murine leukemia identified reprogramming of ce

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

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

183 viding a supply of bone marrow-derived brain-engrafting myeloid cells with donor wild-type CSF1R to r

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

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

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

187 All patients engrafted neutrophils and platelets at expected times af

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

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

190 Human immune system mice were made by engrafting NOD/SCID/IL2Rgammanull (NSG) mice with human

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

192 3A-APC-potentiated neuronal recruitment from engrafted NSCs might offer a new approach to the treatme

193 Overall our results demonstrate that PBMC-engrafted NSG models are rapid, sensitive, and reproduci

194 PBMC-engrafted NSG, NSG-MHC-DKO, and NSG-SGM3 mice were used

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

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

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

198 PRP impaired engrafting of pancreatic CSC's tumours in nude mice and

199 In both SK-N-AS and BE(2)C cell lines, when engrafted on the chorioallantoic membrane of chick embry

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

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

202 with circulating donor red blood cells among engrafted participants.

203 Only one (6%) of the 16 engrafted patients remained transfusion dependent, and 1

204 In the 4 engrafted patients viral infections were cleared within

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

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

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

208 -type background, Epcr expression marked the engrafting population in the BM.

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

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

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

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

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

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

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

216 irradiation, 42.9%, 85.7%, and 100% of mice engrafted, respectively.

217 Erythroid progeny of edited engrafting SCD HSCs express therapeutic levels of HbF an

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

219 Engrafted splenic B-1 cells exhibited a mature phenotype

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

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

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

223 o efficacy of (212)Pb-daratumumab, mice were engrafted subcutaneously with 5 x 10(6) RPMI8226 cells.

224 o efficacy of (212)Pb-Daratumumab, mice were engrafted subcutaneously with 5.106 RPMI8226 cells.

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

226 lity to rearrange the actin cytoskeleton and engraft successfully.

227 ted and on which proteins of interest can be engrafted thanks to widely used genetic tagging strategi

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

229 data indicate that peripheral monocytes can engraft the meninges after an inflammatory challenge, im

230 e infiltrated by inflammatory monocytes that engrafted the meningeal niche and remained in situ for m

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

232 nterfere with the observation and imaging of engrafted tissues.

233 Importantly, engrafted tumors displayed the heterogenous sensitivity

234 Engrafted tumors stably coexpress optical reporters for

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

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

237 -corrected SCD HSPCs retained the ability to engraft when transplanted into non-obese diabetic (NOD)-

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

239 cantly improved behavioral disease outcomes, engrafted widely into capillaries of the gray/white matt

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

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

242 cells was confirmed in immunodeficient mice engrafted with a human AML cell line expressing DeltaNPM

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

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

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

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

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

248 ing apoptosis and improving survival of mice engrafted with AML expressing mtRUNX1.

249 eukemia burden and improved survival of mice engrafted with BETi-P/R sAML cells or patient-derived AM

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

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

252 In vivo biodistribution studies in mice engrafted with breast tumors showed a distinct accumulat

253 humanized, an immune-deficient recipient is engrafted with cells, tissues, or organoids.

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 ly increased survival of mice intracranially engrafted with DIPG cells.

257 All patients engrafted with donor cells.

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

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

260 In mice engrafted with HER2-positive breast cancer tumors, coinj

261 All alloconstructs successfully engrafted with histologic evidence of neovascularization

262 ritis patients into immunodeficient NSG mice engrafted with human arteries.

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

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

265 era) Il2rgamma(tm1hera) (SRG) rat models, co-engrafted with human full-thickness fetal skin, autologo

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 Non-obese diabetic-scid IL2rgammanull mice engrafted with human hematopoietic stem cells (hu-SRC-SC

270 human peripheral blood mononuclear cells or engrafted with human hematopoietic stem cells [human imm

271 Humanized mice engrafted with human hematopoietic stem cells and develo

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

273 Fah (-/-), Rag2 (-/-), and Il2ry (-/-) mice engrafted with human hepatocytes (hFRG mice) and rhesus

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

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

276 Immunodeficient mice engrafted with human peripheral blood mononuclear cells

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

278 d that NOD/SCID/gamma(C) (-/-) c-kit(+) mice engrafted with human tissues 1 day after birth (designat

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

280 natal immune compromised mice after they are engrafted with human umbilical cord blood stem cells.

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

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

283 murine transplant models and humanized mice engrafted with LV-modified HSCs show high levels of LV e

284 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

285 Multiple mice engrafted with MLL-r ALL remained disease free for more

286 ild-type RUNX1 and improved survival of mice engrafted with mtRUNX1-expressing AML.

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

288 and mast cell-deficient Kit(W-sh/W-sh) mice engrafted with NHERF1(+/-) mast cells.

289 miR-155) in human lymphoma cell lines, mice engrafted with patient-derived xenografts (PDXs), and DL

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

291 lung inflammation, immunodeficient mice were engrafted with PBMCs from these allergic donors plus the

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

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

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

295 Mice engrafted with primate tissue make two important plasmod

296 xicity in the humanized NOD/SCID mouse model engrafted with red blood cells from G6PD deficient donor

297 c CAR T cells infused in Nod scid gamma mice engrafted with the human melanoma WM115 cell line have s

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

299 C-deficient Kit(W-sh/W-sh) mice systemically engrafted with WT and CRF(2)(-/-) BMMCs demonstrated the

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