ライフサイエンスコーパス: bone marrow-derived cell

1 bility to bone metastasis was conferred by a bone marrow-derived cell.

2 epend on T or B lymphocytes, but did require bone marrow derived cells.

3 unts and increased proliferative capacity of bone marrow derived cells.

4 s show the involvement of SphK2 expressed in bone marrow-derived cells.

5 ere mediated by structural cells rather than bone marrow-derived cells.

6 est the restorative function of transplanted bone marrow-derived cells.

7 ists such as imiquimod enhance DNA repair in bone marrow-derived cells.

8 ive IRF3 deficiency in liver parenchymal and bone marrow-derived cells.

9 eotide excision repair genes were studied in bone marrow-derived cells.

10 t was due in large part to loss of S100A9 in bone marrow-derived cells.

11 y radioresistant stromal cells as well as by bone marrow-derived cells.

12 ymal stem cell (MSC) dysfunction in isolated bone marrow-derived cells.

13 ure or in wt mice with circulating Cd39 null bone marrow-derived cells.

14 ctive effect of receptors on radiosensitive, bone marrow-derived cells.

15 n was inhibited in mice that lacked PAF-R in bone marrow-derived cells.

16 ting factor (G-CSF) induces proliferation of bone marrow-derived cells.

17 within radioresistant stromal cells and not bone marrow-derived cells.

18 +)F4/80(-) macrophages, and CD11b(-)F4/80(-) bone marrow-derived cells.

19 constructed with TLR4 only on renal cells or bone marrow-derived cells.

20 in resident cells in the skin rather than by bone marrow-derived cells.

21 is not driven by AhR-dependent signals from bone marrow-derived cells.

22 infection, a phenotype that is localized to bone marrow-derived cells.

23 spleen were dependent on MyD88 expression by bone marrow-derived cells.

24 st in part, on p75 TNF receptor expressed in bone marrow-derived cells.

25 umulation, exosomes were taken up by CD45(+) bone marrow-derived cells.

26 surface of the retina and CXCR4 localized in bone marrow-derived cells.

27 nted into irradiated recipient mice to track bone marrow-derived cells.

28 ion-resistant cells via IL-1beta secreted by bone marrow-derived cells.

29 was greater in chimeras with TLR2 present on bone marrow-derived cells.

30 ry response; however, it was required in non-bone marrow-derived cells.

31 t reperfusion is primarily due to effects on bone marrow-derived cells.

32 chemokines in the recruitment of circulating bone marrow-derived cells.

33 ous renal cells rather than incorporation of bone marrow-derived cells.

34 ly lack or selectively express the A(2A)R on bone marrow-derived cells.

35 rboring the male Y chromosome exclusively in bone marrow-derived cells.

36 induced angiogenesis, and recruit protumoral bone marrow-derived cells.

37 en LC were ablated in adults and replaced by bone marrow-derived cells.

38 ver, CD-160130 had no myelotoxicity on human bone marrow-derived cells.

39 tracked with lung parenchymal cells but not bone marrow-derived cells.

40 cept in bone marrow-derived cells or only in bone marrow-derived cells.

41 aracterized by chronic hypoxia and influx of bone marrow-derived cells.

42 ne system and in irradiated mice lacking all bone marrow-derived cells.

43 esponse observed with aging was dependent on bone marrow-derived cells.

44 disease was due to lack of Fas expression on bone marrow-derived cells.

45 ype controls, an effect that was mediated by bone marrow-derived cells.

46 lpha, and IL-1R function was required on non-bone-marrow-derived cells.

47 grastim alone did not lead to engraftment of bone-marrow-derived cells.

48 atory response involved A2BAR signaling from bone marrow-derived cells, A2BARs located on the lung ti

49 CD11b antibodies further inhibited bone marrow-derived cell adhesion and transmigration to

50 t enhance the survival of MyD88(-/-)-derived bone marrow-derived cells after UV B exposure as was obs

51 nic stem cells, neural stem cells, and adult bone-marrow-derived cells all responded by expressing od

52 Notably, IRF5 deficiency in non-bone marrow-derived cells also contributes to the increa

53 Tgfbr2 deficiency in the bone marrow-derived cells also reduced the size of previ

54 indicate that sbb2(a) is expressed in non-B bone marrow-derived cells and acts in trans.

55 Bone marrow-derived cells and chemokines also play a par

56 1 and CXCR4 contribute to the involvement of bone marrow-derived cells and collaborate with VEGF in t

57 udies reveal an important cross-talk between bone marrow-derived cells and epithelial secretory Panet

58 Cellular fusion between bone marrow-derived cells and host hepatocytes has been

59 BMHs emerge from fusion between donor bone marrow-derived cells and host hepatocytes.

60 PPARgamma is expressed in most bone marrow-derived cells and influences their function.

61 tive bacteria requires caspase-1 activity in bone marrow-derived cells and interleukin-1 receptor sig

62 stigate the relative contribution of TLR2 on bone marrow-derived cells and intrinsic renal cells, we

63 as dependent on the expression of MMP-9 from bone marrow-derived cells and is most likely contributed

64 FcgammaRIIB is expressed on human and murine bone marrow-derived cells and limits inflammation by sup

65 annus originate exclusively from circulating bone marrow-derived cells and not from locally resident

66 ents indicated that CD59a expression on both bone marrow-derived cells and peripheral tissues played

67 ans, we found FcRn to be highly expressed in bone marrow-derived cells and professional APCs in diffe

68 ity to PIFS is determined by the genotype of bone marrow-derived cells and requires the expression of

69 ication and quantification of populations of bone marrow-derived cells and support the view that macr

70 on have been used to analyze the turnover of bone marrow-derived cells and to demonstrate the critica

71 sease development, CCL17 acts on CCR4(+) non-bone marrow-derived cells, and 3) for inflammatory pain

72 tissues and osteoclastogenic propensities of bone marrow-derived cells, and augmented bone destructio

73 included increases in leukostasis, influx of bone marrow-derived cells, and capillary closure.

74 Portal fibroblasts, bone marrow-derived cells, and epithelial to mesenchymal

75 otidases of the CD39 family are expressed by bone marrow-derived cells, and purinergic mechanisms mig

76 n the tumor microenvironment, CD11b(+)Gr1(+) bone marrow-derived cells are a predominant source of pr

77 at therapeutic mechanisms underlying various bone marrow-derived cells are due to paracrine effects.

78 Bone marrow-derived cells are known to play important ro

79 Bone marrow-derived cells are recruited to sites of isch

80 We here demonstrate that bone marrow-derived cells are the major source of MMP-9

81 is in irradiated WT mice, demonstrating that bone marrow-derived cells are the ultimate source of all

82 ome from clinical use in horses treated with bone-marrow-derived cells are presented together with th

83 example, portal fibroblasts, fibrocytes, and bone-marrow-derived cells, as well as cells derived from

84 Liver damage was mediated by bone marrow-derived cells because WT mice transplanted w

85 By exchanging bone marrow-derived cells between CD36-expressing and CD

86 the present study was to investigate whether bone marrow-derived cells (BMCs) can be induced to expre

87 Bone marrow-derived cells (BMCs) have been implicated as

88 lative contributions of parenchymal cell and bone marrow-derived cell (BMDC) B7-H1 expression, we gen

89 l versus a recently recognized new candidate bone marrow-derived cell (BMDC).

90 Studies in animal models have shown that bone marrow-derived cells (BMDC) could be involved in th

91 However, migration of bone marrow-derived cells (BMDC) into the CNS is a margi

92 Recent findings suggest that bone marrow-derived cells (BMDC) may contribute to tissu

93 nsplantation or organ allograft suggest that bone marrow-derived cells (BMDC) may differentiate into

94 The mobilization of bone marrow-derived cells (BMDC) to distant tissues befo

95 owth might be promoted by the recruitment of bone marrow-derived cells (BMDC), which include endothel

96 so the recruitment of tumor growth-promoting bone marrow-derived cells (BMDC).

97 he accumulation of transplanted adult GFP(+) bone-marrow-derived cells (BMDC) in the substantia nigra

98 After myocardial infarction (MI), bone marrow-derived cells (BMDCs) are found within the m

99 Exogenous bone marrow-derived cells (BMDCs) are promising therapeu

100 However, selective inactivation of A2ARs in bone marrow-derived cells (BMDCs) by transplanting bone

101 radiated and bone marrow transplanted mice, bone marrow-derived cells (BMDCs) fuse with Purkinje neu

102 Transplanted adult bone marrow-derived cells (BMDCs) have been shown to ado

103 odel that irradiation induces recruitment of bone marrow-derived cells (BMDCs) into the tumors, resto

104 Analysis of developmental plasticity of bone marrow-derived cells (BMDCs) is complicated by the

105 regarding the effects of transplantation of bone marrow-derived cells (BMDCs) on the severity of dia

106 Bone marrow-derived cells (BMDCs) participate in the gro

107 Increasing evidence suggests that myeloid bone marrow-derived cells (BMDCs) play a critical role i

108 -derived angiogenic cells (BMDACs) and other bone marrow-derived cells (BMDCs) play important roles i

109 ogenesis is performed by beta(3) integrin on bone marrow-derived cells (BMDCs) recruited to sites of

110 Cell fusion is one mechanism by which bone marrow-derived cells (BMDCs) take on the gene expre

111 Injury induces the recruitment of bone marrow-derived cells (BMDCs) that contribute to the

112 diabetes induces the appearance of abnormal bone marrow-derived cells (BMDCs) that fuse with neurons

113 ry tumors facilitate metastasis by directing bone marrow-derived cells (BMDCs) to colonize the lungs

114 as been shown to enhance the contribution of bone marrow-derived cells (BMDCs) to regenerating skelet

115 oxide synthase (iNOS) on the recruitment of bone marrow-derived cells (BMDCs) to the CBLB after acou

116 The contribution of bone marrow-derived cells (BMDCs) to tumour neovasculari

117 d a chimeric mouse model in which A(2A)Rs on bone marrow-derived cells (BMDCs) were selectively inact

118 by complex interactions between vascular and bone marrow-derived cells (BMDCs), and neurofibromin reg

119 To determine the contribution of bone marrow-derived cells (BMDCs), we exposed tumor-bear

120 However, bone marrow-derived cells (BMDCs), which are frequently

121 o thought to mobilize into blood circulation bone marrow-derived cells (BMDCs), which may subsequentl

122 y pro-angiogenic pathways and recruitment of bone marrow-derived cells (BMDCs).

123 ontrol progenitor recruitment is mediated by bone marrow-derived cells, but is not cell autonomous.

124 Either systemic depletion of all bone marrow-derived cells (by irradiation) or local depl

125 aken together, these data suggest that young bone marrow-derived cells can alleviate renal aging in o

126 Subpopulations of bone marrow-derived cells can be induced to assume a num

127 MMP-14 from bone marrow-derived cells can influence the collagen con

128 Adult bone marrow-derived cells can participate in muscle rege

129 l of DMD, have demonstrated that circulating bone marrow-derived cells can participate in skeletal mu

130 ng MOs/MPs or selective targeting of CCR2 in bone marrow-derived cells caused delayed clinical deteri

131 chimeras in which CD80/86- or CD40-deficient bone marrow-derived cells coexist with wild-type (WT) ce

132 isease, which demonstrates that PD-L1 on non-bone marrow-derived cells confers the protective effect.

133 an studies has advanced our knowledge of how bone marrow derived cells contribute to neoangiogenesis.

134 Stimulatory IgG receptors (FcgammaRs) on bone marrow-derived cells contribute to the pathogenesis

135 In this study, we investigated whether bone marrow-derived cells contribute to the renewal of a

136 l FIZZ1 expression, whereas STAT6 present in bone marrow-derived cells contributed to airway eosinoph

137 However, LTalpha-deficient bone marrow-derived cells contributed to CP formed in CD

138 Bone marrow chimeras showed that bone marrow-derived cells contributed to IL-1R-dependent

139 found that LMP7 in both bone marrow- and non-bone marrow-derived cells contributes to the development

140 Stellate cells, portal myofibroblasts, and bone marrow derived cells converge in a complex interact

141 the JCI, Koh and colleagues assessed whether bone marrow-derived cells could alter their fate under c

142 erefore, our data indicate that whereas some bone marrow-derived cells could induce iNKT cell hypores

143 otein-tagged mouse CD63 expressed in primary bone marrow-derived cell cultures.

144 mice with fluorescent green protein-labeled, bone marrow-derived cells demonstrated conclusively the

145 arrow chimeras showed that Mif expression in bone marrow-derived cells did not affect fibrosis and in

146 IL-1R deficiency in bone marrow-derived cells did not affect the inflammator

147 Selective ablation of PAR-2 from bone marrow-derived cells did not prevent matriptase-dri

148 Our results suggest that bone marrow-derived cells differentiated into smooth mus

149 heterogeneous population of tissue-resident bone marrow-derived cells; distinct MC subpopulations ar

150 contrast, Lin and coworkers found that some bone marrow-derived cells do appear to incorporate into

151 Thus, our data indicate that bone marrow-derived cells do not make a significant cont

152 mice express Axl but that Axl deficiency in bone marrow-derived cells does not affect lesion size, c

153 Moreover, we show that bone marrow-derived cells drive this process.

154 Gstm1 deletion in the parenchyma, and not in bone marrow-derived cells, drives renal inflammation.

155 Moreover, transplantation of ADFP-null bone marrow-derived cells effectively attenuated atheros

156 These cell types include skeletal myoblasts, bone-marrow derived cells, endothelial progenitors, and

157 ession of protective MHC class II alleles in bone marrow-derived cells establishes robust self-tolera

158 Furthermore, in vitro these bone marrow-derived cells exhibit - as do pancreatic bet

159 G-CSF+FL therapy mobilized bone marrow-derived cells exhibiting increased expressio

160 this context, dermal/stromal fibroblasts and bone marrow-derived cells expressed increased levels of

161 ANKL, and with a reduction in the numbers of bone-marrow-derived cells expressing the markers CD11b a

162 Bone-marrow-derived cells facilitate tumour angiogenesis

163 n-1 in both retina-resident immune cells and bone marrow-derived cells for beta(1, 3)-glucan-elicited

164 However, transplantation of bone marrow-derived cells from hepcidin-deficient mice (

165 cells after UV B exposure as was observed in bone marrow-derived cells from MyD88(+/+) mice.

166 This was dependent on MyD88, as bone marrow-derived cells from MyD88(-/-) mice did not i

167 Bones and bone marrow-derived cells from PAR1 KO and wild-type (WT

168 as been a call to establish proof that these bone marrow-derived cells function appropriately in thei

169 This unique plasticity makes bone marrow-derived cells good candidates for cell thera

170 Deficiency of AT(1a) receptors in bone marrow-derived cells had no effect on Ang II-induce

171 n of hybrids between cancer cells and normal bone marrow-derived cells have been advocated as tumor p

172 Bone marrow-derived cells have been shown to take on fun

173 Lyn knockout mice repopulated with wild-type bone marrow-derived cells have higher vascular permeabil

174 Bone marrow-derived cells have important roles in cancer

175 on the potential of genetic manipulation of bone marrow-derived cells in an attempt to further enhan

176 of pathological roles of various subsets of bone marrow-derived cells in atherosclerosis may lead to

177 the contribution of PPARalpha expression by bone marrow-derived cells in atherosclerosis, male and f

178 ngs provide novel insights about the role of bone marrow-derived cells in ischemic preconditioning an

179 explore the role of endogenous cells versus bone marrow-derived cells in mediating tubule repair.

180 Tumor growth also was affected by bone marrow-derived cells in mice lacking any one or all

181 after 6 mo, there were more FSP-1-expressing bone marrow-derived cells in old-to-old mice compared wi

182 tiation of adipocytes from preadipocytes and bone marrow-derived cells in several species, the relati

183 use bone marrow studies showed that resident bone marrow-derived cells in the cornea can initiate thi

184 te that Wolbachia activates TLR2 on resident bone marrow-derived cells in the corneal stroma to produ

185 predominantly tracked with DAF's absence on bone marrow-derived cells in the graft and required allo

186 Here, we investigated a putative role for bone marrow-derived cells in the induction of epithelial

187 Thus, Ags expressed by the non-bone marrow-derived cells in the liver actively cause CD

188 ein transgenic mice to permit observation of bone marrow-derived cells in the myocardium after acute

189 Whereas the total number of bone marrow-derived cells in the pancreas decreased over

190 ere, we establish that Nf1 heterozygosity of bone marrow-derived cells in the tumor microenvironment

191 Expression of MMP-9 by bone marrow-derived cells in the tumor stroma is also cr

192 s mainly organized through the activation of bone marrow-derived cells in various tissues.

193 Addition of Wnt3A into cultures of bone-marrow-derived cells in combination with TGFbeta1,

194 GFP(+) bone marrow-derived cells included leukocytes and CD45(-

195 tissue repair and by systemically mobilizing bone marrow-derived cells, including a population that c

196 d in a significant increase in the number of bone marrow-derived cells incorporating into the neovasc

197 In both study cohorts, intracapillary bone marrow-derived cells, indicative of leukostasis, we

198 Sema 7a expressing bone marrow-derived cells induce lung fibrosis and alter

199 ic mammary tumor cells resulted in increased bone marrow-derived cell infiltration into the lung in t

200 se findings suggest that MMP-9 released from bone marrow-derived cells influences the progression of

201 latency in the bone marrow, the migration of bone marrow derived cells into the circulation, and intr

202 transplantation models, that engraftment of bone marrow-derived cells into functioning LSECs is rout

203 cardiac function improves after injection of bone marrow-derived cells into infarcted regions in anim

204 Remarkably, the transplantation of wild-type bone marrow-derived cells into irradiated PCD mutant mic

205 CXCR4 antagonists reduced influx of bone marrow-derived cells into ischemic retina and stron

206 Here, infusion of wild-type bone marrow-derived cells into unconditioned, nonirradia

207 These findings indicate that ROCK1 in bone marrow-derived cells is a critical mediator of athe

208 cation, CCR2-dependent infiltration of mouse bone marrow-derived cells is abundant in demyelinating a

209 rafts demonstrate that neovascularization by bone marrow-derived cells is accompanied by the activati

210 studies revealed that PD-L1 expressed on non-bone marrow-derived cells is critical for this resistanc

211 that its expression in both endothelial and bone marrow-derived cells is essential for arteriogenesi

212 ata suggest that activation of the A(2A)R on bone marrow-derived cells is primarily responsible for p

213 We show that a functional TLR4 in bone marrow-derived cells is required for the complete e

214 lity of autocrine stimulation, but influx of bone marrow-derived cells is the major source of increas

215 -) mice were irradiated and repopulated with bone marrow-derived cells isolated from either AT(1a) re

216 DTR-expressing DCs is dominant over control bone marrow-derived cells, leading to small LNs and an o

217 identified that loss of BLT2 expression on a bone marrow-derived cell lineage offers protection again

218 We find that the Gpnmb genotype of bone-marrow derived cell lineages significantly influenc

219 Given that bone marrow-derived cells may differentiate into smooth

220 under conditions of stress is influenced by bone marrow-derived cells may provide important insight

221 Because bone marrow-derived cells mediate many of the effects of

222 tudies suggest that ROCK1 in macrophages and bone marrow-derived cells mediates atherogenesis.

223 ce, the investigators show that transplanted bone marrow-derived cells migrate to the skin of bone ma

224 Neither adult bone marrow-derived cells nor fetal liver cells from wil

225 We determined that TGF-beta signaling in bone marrow-derived cells, not keratinocytes, regulates

226 These precursors arose from circulating bone marrow-derived cells of monocytic origin.

227 Bone marrow-derived cells of nonmyeloid lineage display

228 e examined the impact of COX-1 deficiency in bone marrow-derived cells on early atherogenesis in the

229 generation de novo of Purkinje neurons from bone marrow-derived cells or by fusion of marrow-derived

230 are ameliorated by replacement of PLXNC1 on bone marrow-derived cells or by genetic deletion of Syt7

231 functional TLR4 in the entire body except in bone marrow-derived cells or only in bone marrow-derived

232 in which up to 5% of myofibers incorporated bone marrow-derived cells over a 16- month period in the

233 he proinflammatory function of JNK1 requires bone marrow-derived cells, particularly mast cells.

234 dynamic and complex pathological process of bone marrow-derived cells playing divergent roles.

235 w transplantation studies showed that Bmx in bone marrow-derived cells plays a critical role in the e

236 In conclusion, a bone marrow-derived cell population is increased in the

237 othelial progenitor cells are a circulating, bone marrow-derived cell population that appears to part

238 Certain bone marrow-derived cell populations, called endothelial

239 , we hypothesized that rat mandible vs. long-bone marrow-derived cells possess different osteogenic p

240 imera studies showed that IRF5 deficiency in bone marrow-derived cells prevents lupus development and

241 tumor-bearing mice to show that host CD13(+) bone marrow-derived cells promote cancer progression via

242 d that absence of p21, either globally or in bone marrow-derived cells, protects against atherosclero

243 CCR2-dependent migration of bone marrow-derived cells provided the driving force for

244 eriments indicated that IRAK-M expression by bone marrow-derived cells, rather than structural cells,

245 Together, these data suggest that: (1) bone marrow-derived cells represent an effective neuropr

246 gnaling by caspase-1(KO) specifically within bone marrow-derived cells revealed that monocytes promot

247 lammation stage of murine wound healing, and bone marrow-derived cells served as a major source of LR

248 ponses seen in C57BL/6 mice was dependent on bone marrow-derived cell-specific expression of tlr4, an

249 ion of MCP-1, which is a chemoattractant for bone marrow-derived cells, specifically MSC.

250 he results indicate that A2AAR activation on bone marrow-derived cells, specifically T or B lymphocyt

251 ytes/macrophages, these actors are joined by bone marrow-derived cells, such as eosinophils and mast

252 termined that sarcomas do not originate from bone marrow-derived cells, such as macrophages, but aris

253 dent upon IL-1R/MyD88 signaling by recruited bone marrow-derived cells, suggesting that resident skin

254 cognate interactions with CD 1 d-expressing bone marrow-derived cells that are both necessary and su

255 Fibrocytes are circulating bone marrow-derived cells that have been implicated in t

256 Here we have isolated E2A-deficient bone marrow-derived cells that have the ability to grow

257 mber of endothelial progenitor cells (EPCs), bone marrow-derived cells that participate in endothelia

258 1(+)CD11b(+) myeloid cells are heterogeneous bone marrow-derived cells that promote inflammation-asso

259 (+) myeloid cells constitute a population of bone marrow-derived cells that promote tumor progression

260 Similarly, the bone-marrow-derived cell that might most effectively eng

261 In conclusion, in bone marrow-derived cells the nuclear receptor Nur77 has

262 In contrast, another bone marrow-derived cell, the T lymphocyte, although cap

263 pression was necessary and sufficient in the bone marrow-derived cells themselves to promote tumor fo

264 Pioneering clinical trials suggest that bone marrow-derived cell therapy enhances neovasculariza

265 One such strategy is the utilization of bone marrow-derived cell therapy.

266 rieties of subsets of immune cells and other bone marrow-derived cells to atherogenesis.

267 he current understanding of contributions of bone marrow-derived cells to atherosclerosis.

268 ent, there was no detectable contribution of bone marrow-derived cells to either skeletal muscle or m

269 parabiosis to introduce fluorescent-labeled bone marrow-derived cells to mice with intestinal tumors

270 across 136,463 resting and stimulated human bone marrow-derived cells to reveal changes in the cis-

271 tagonists effectively prevented targeting of bone marrow-derived cells to the developing retinal vasc

272 To investigate the contribution of bone marrow-derived cells to the formation of tumor vess

273 ling and suppressed the recruitment of these bone marrow-derived cells to the lung.

274 plays a critical role in the recruitment of bone marrow-derived cells to the tumor microenvironment

275 a relative reduction in the contribution of bone marrow-derived cells to tumor stroma.

276 F agonists, which then act on PAF-R-positive bone marrow-derived cells to upregulate IL-10 through CO

277 patic metastasis by enhancing recruitment of bone-marrow-derived cells to the metastatic site.

278 ung cancer cells use caveolin-2 expressed in bone marrow-derived cell types including TAMs to promote

279 fibrosis outside the CNS have identified two bone marrow-derived cell types, fibrocytes and alternati

280 mice with green fluorescent protein-labeled bone marrow-derived cells underwent corneal scrape injur

281 Adoptive transfer of labeled bone marrow-derived cells validated the results in a mur

282 l, we determined that expression of NLRP3 in bone marrow-derived cells was necessary for optimal tumo

283 in vessel size, whereas MyD88 expression by bone marrow-derived cells was obligatory for changes in

284 titis revealed that expression of P2Y(2)R in bone marrow-derived cells was required for liver infiltr

285 ce ANAs, and that lack of H2-O expression in bone marrow-derived cells was sufficient to induce the a

286 aracterizing the composition of infiltrating bone marrow-derived cells, we identified CD11b+/Ly6Cmed/

287 e appearance of these cell types and whether bone marrow-derived cells were capable of acquiring fibr

288 d, approximately 99% of all tumor-associated bone marrow-derived cells were CD45(+) hematopoietic cel

289 and the differentiation of osteoclasts from bone marrow-derived cells were completely suppressed by

290 in the vascular endothelium, indicating that bone marrow-derived cells were not recruited to endothel

291 Immune cells and bone marrow-derived cells were not required for aggressi

292 TLR4 mutant mice transplanted with their own bone marrow-derived cells were protected from hepatic I/

293 In these situations, host bone marrow-derived cells were the key source of the IL-

294 ), VEGFR2(+)/CD34(+), and VEGFR2(+)/CD117(+) bone-marrow derived cells were increased in the peripher

295 ancing airway epithelial remodeling by adult bone marrow-derived cells will be necessary for correcti

296 Historically, SSCs have been defined as bone marrow-derived cells with inconsistent characterist

297 EphA3 is found on mouse bone marrow-derived cells with mesenchymal and myeloid p

298 isite localization of various populations of bone marrow-derived cells with respect to the vasculatur

299 or-antigen presentation to immune T cells by bone-marrow-derived cells within the tumor microenvironm

300 COX-1 deficiency in bone marrow-derived cells worsens early atherosclerosis