ライフサイエンスコーパス: bone marrow-derived

1 is critical for protection from IRI through bone marrow-derived adenosine 2a receptors.

2 assess the safety and efficacy of autologous bone marrow-derived aldehyde dehydrogenase bright (ALDHb

3 Multipotent adult progenitor cells are a bone marrow-derived, allogeneic, cell therapy product th

4 y STING and IFN-alpha/beta signaling in both bone marrow-derived and -resident cells, which coalesce

5 We found that IL-4-stimulated bone marrow-derived and alveolar macrophages from female

6 f IL-4/IL-13 (M2)-responsive genes in murine bone marrow-derived and alveolar macrophages.

7 The combined adjuvant acts via MyD88 in both bone marrow-derived and non-bone marrow-derived radiores

8 phagocytic cells in the mammalian brain, are bone marrow derived, and cross the blood-brain barrier,

9 On the basis that donor bone marrow-derived antigen-presenting cells are elimina

10 of murine bone marrow-derived mast cells and bone marrow-derived basophils (BMBs) at rest, upon an ad

11 that eicosanoid production profiles between bone marrow-derived (BMDM) and peritoneal macrophages di

12 Conversely, adoptive transfer of bone marrow-derived CD11c(+) cells from bleomycin-treate

13 s study, we hypothesize that AREG induced in bone marrow-derived CD11c(+) cells is essential for pulm

14 that induced AREG specifically in recruited bone marrow-derived CD11c(+) cells promoted bleomycin-in

15 Moreover, depletion of bone marrow-derived CD11c(+) cells suppressed both induc

16 are associated with increased lung homing of bone marrow-derived CD34(+) hematopoietic progenitor cel

17 as detected on cardiac Ly6cHI monocytes, and bone marrow-derived Cd36 was essential for both early ph

18 Interestingly, whereas donor T cell- or bone marrow-derived CD70 plays no role in GVHD, host-der

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

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

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

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

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

24 Bone marrow-derived cells have important roles in cancer

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

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

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

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

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

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

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

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

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

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

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

36 icroenvironment, whereas the contribution of bone marrow-derived circulating precursors is rare.

37 Decline in the number of bone marrow-derived circulating progenitor cells (PCs) i

38 Bone marrow-derived circulating progenitor cells are inv

39 Fibrocytes are bone marrow-derived circulating progenitor cells that ha

40 n T cell development, we sort-purified mouse bone marrow-derived common lymphoid progenitor cells, ea

41 L-dependent necroptosis, specifically in the bone marrow-derived compartment, for disease induction u

42 est that commonly used protocols to generate bone marrow-derived cultured dendritic cells yield a het

43 Bone marrow-derived cultured mast cells (BMCMCs) and per

44 Bone marrow-derived cultured MCs served to identify whet

45 We show that murine bone marrow-derived DC (BMDC) maturation induced by LPS,

46 To test this hypothesis, we pretreated bone marrow-derived DC (BMDC) with polyclonal murine or

47 nct subpopulation of cells within the GM-CSF bone marrow-derived DC culture based on their ability to

48 We show that activated bone marrow-derived DC from conditional Rictor(-/-) mice

49 thermore, co-culture experiments showed that bone marrow derived DCs of MKP-2(-/-) mice had impaired

50 Bone marrow-derived DCs (BMDCs) cultured in high glucose

51 Bone marrow-derived DCs (BMDCs) were adoptively transfer

52 on of NF-kappaB, ERK, p38, and CREB in mouse bone marrow-derived DCs compared with single TLR2 activa

53 ring CD4+ T-cells with OX40 L+Jagged(JAG)-1+ bone marrow-derived DCs differentiated with GM-CSF or tr

54 ased ability to take up HDM antigen, whereas bone marrow-derived DCs display enhanced antigen present

55 onocyte-derived DCs and humanized TLR8 mouse bone marrow-derived DCs enabled benchmarking of the TLR8

56 Additionally, bone marrow-derived DCs loaded with OVA were transferred

57 Exposure of bone marrow-derived DCs to Zn in vitro induced a tolerog

58 In this study, we show that, in addition to bone marrow-derived DCs, PGE2 inhibits IL-27 production

59 ere defective for CASP1 activation in murine bone marrow-derived DCs, splenic DCs, and human blood-de

60 represented less mature cells compared with bone marrow-derived DCs.

61 hat PGE2 inhibits IL-27 production in murine bone marrow-derived DCs.

62 3) showed lower expression in ES-DCs than in bone marrow-derived DCs.

63 ons resulted in activation and maturation of bone marrow derived dendritic cells (BMDCs) and induced

64 sted the therapeutic advantage of S1pr3(-/-) bone marrow-derived dendritic cell (BMDC) transfers in k

65 11e, 11i and 12b were found to reduce mouse bone marrow-derived dendritic cell (DC) pathogen-associa

66 high)and production of IL-12p40 in MyD88(-/-)bone marrow-derived dendritic cells (BMDCs) compared to

67 ted pro-IL-1beta and pro-IL-18 processing in bone marrow-derived dendritic cells (BMDCs) in response

68 In this article, we show that bone marrow-derived dendritic cells (BMDCs) incubated wi

69 In vitro, bone marrow-derived dendritic cells (BMDCs) stimulated w

70 ivation, promotes migration of both skin and bone marrow-derived dendritic cells (BMDCs), and restrai

71 nes, in J774A.1 macrophage-like cells and in bone marrow-derived dendritic cells (BMDCs).

72 Treatment of TIDC and bone marrow-derived dendritic cells (DC) with IL10 led t

73 OCl on dorsal root ganglia neurons and mouse bone marrow-derived dendritic cells (mBMDCs) were invest

74 ve transfer of Atg5(-/-), but not wild-type, bone marrow-derived dendritic cells augments lung inflam

75 iad3A to TLR4 was increased significantly in bone marrow-derived dendritic cells from wild-type mice,

76 Bone marrow-derived dendritic cells pretreated with vehi

77 ein in B cells, T cells, Ly6C(hi) monocytes, bone marrow-derived dendritic cells, and lung tissue.

78 In bone marrow-derived dendritic cells, IL-33 induces the p

79 w-derived macrophages, but not in Ripk3(-/-) bone marrow-derived dendritic cells, indicating that PGA

80 n a mouse macrophage cell line (J774), mouse bone marrow-derived dendritic cells, mouse neutrophils,

81 for the differentiation and proliferation of bone marrow-derived dendritic cells, potentiates the p65

82 feron-gamma as well as cross-presentation by bone marrow-derived dendritic cells.

83 We evaluated primary bone-marrow-derived Dendritic Cell phenotypes and functi

84 Bone-marrow-derived dendritic cells (BMDCs) were exposed

85 In vitro assays with primary or bone marrow-derived eosinophils were used to determine e

86 k-staining, indulinophilic, beta-granules in bone marrow-derived eosinophils, which were probably imm

87 human peripheral blood eosinophils and mouse bone marrow-derived eosinophils.

88 ), which triggers mobilization and homing of bone marrow-derived EPC (BMD-EPC).

89 sensitive hypertension through regulation of bone marrow-derived fibroblast accumulation and macropha

90 lar matrix protein production and suppressed bone marrow-derived fibroblast accumulation and myofibro

91 a, IL-6 and CD68), decreased accumulation of bone marrow-derived fibroblasts and TGF-beta expression.

92 Bone marrow-derived fibrocytes accumulate in the dermis.

93 functional assessments, we demonstrate that bone marrow-derived G-CSF-responsive cells home to the i

94 ng the lineage-instructive signal in primary bone marrow-derived GM progenitors.

95 e-loaded analogues, causing proliferation of bone marrow-derived GM-progenitors cells.

96 ated how age- and tumor-dependent changes to bone marrow-derived hematopoietic cells impact TNBC prog

97 Adoptive transfer of WT bone marrow-derived hematopoietic stem cells reconstitut

98 yte progenitors differentiated in vitro from bone marrow-derived hematopoietic stem cells.

99 f autologous (auto) versus allogeneic (allo) bone marrow-derived hMSCs in NIDCM.

100 safety and efficacy of 2 doses of allogeneic bone marrow-derived human mesenchymal stem cells identic

101 on is completely abrogated in the absence of bone marrow-derived IL-10.

102 ficiently internalized L. monocytogenes With bone marrow-derived in vitro cultures, high multiplicity

103 Bone marrow-derived infiltrating macrophages/monocytes w

104 inguish resident (retinal) from infiltrating bone marrow-derived inflammatory cells and were made dia

105 icantly more toxic than M2pepKLA to primary, bone marrow-derived M2 macrophage, desired selectivity w

106 pro-inflammatory cytokines were increased in bone marrow derived macrophage (BMDM) from PLTP-/-, whil

107 d that treatment of RANKL-stimulated primary bone marrow-derived macrophage (BMDM) cultures with smal

108 otif) ligands 1, 10, and 12, which stimulate bone marrow-derived macrophage recruitment.

109 Bone marrow-derived macrophage were polarized to an M2 p

110 ignificantly higher IL-6 secretion by murine bone marrow derived macrophages (BMDM) compared to cultu

111 ymosan-induced peritonitis, M1- and M2a-like bone marrow derived macrophages, as well as by mesotheli

112 liensis infection of BALB/c (wild-type [WT]) bone marrow derived macrophages.

113 wever expression is increased over 2-fold in bone marrow derived macrophages.

114 lations of wild-type mice with Nrp1-depleted bone marrow-derived macrophages (BMDM) confers resistanc

115 Primary bone marrow-derived macrophages (BMDM) was isolated from

116 n vivo and by isolated resident alveolar and bone marrow-derived macrophages (BMDM).

117 eficient RAW cells and primary PHD2 knockout bone marrow-derived macrophages (BMDM).

118 3 or Pyrin inflammasome activation in murine bone marrow-derived macrophages (BMDMs) as an indicator

119 d NLRP3 was revealed when Nlrc4(S533A/S533A) bone marrow-derived macrophages (BMDMs) expressing phosp

120 Infected Chil1-deficient mice and bone marrow-derived macrophages (BMDMs) from Chil1-defic

121 aB pathway (IKKalpha/beta, NF-kappaB p65) in bone marrow-derived macrophages (BMDMs) from knockout mi

122 Interestingly, IL-4 treatment of bone marrow-derived macrophages (BMDMs) significantly do

123 and adoptive transfer studies revealed that bone marrow-derived macrophages (BMDMs) traffic to the l

124 esser extent at Il1a) reaches high levels in bone marrow-derived macrophages (BMDMs), and the enhance

125 In LPS/ATP-stimulated bone marrow-derived macrophages (BMDMs), CLIC1 or CLIC4

126 nstituted mouse bone marrow neutrophils, and bone marrow-derived macrophages (BMDMs), we showed that

127 or NF-kappaB activation in HEK 293 cells and bone marrow-derived macrophages (BMDMs).

128 RNase L activation and replicates poorly in bone marrow-derived macrophages (BMM), while ns2(H126R)

129 irus replication was attenuated in wild-type bone marrow-derived macrophages (BMMs) and partially res

130 lysis, the bacterial modulation of miRNAs in bone marrow-derived macrophages (BMMs) in which activity

131 Subsequently, rat bone marrow-derived macrophages (BMMs) were cultured in

132 Stimulation of bone marrow-derived macrophages (BMMs) with endotoxin re

133 ligand (RANKL)-induced osteoclastogenesis in bone marrow-derived macrophages (BMMs).

134 appaB reporter system in immortalized murine bone marrow-derived macrophages (iBMDM).

135 TLR2-induced TNF-alpha production by murine bone marrow-derived macrophages (p < 0.001).

136 also observed by in vitro experiments, using bone marrow-derived macrophages and dendritic cells as r

137 TARM1 expression was also upregulated by bone marrow-derived macrophages and dendritic cells foll

138 A-induced macrophage cell death with primary bone marrow-derived macrophages and high-fat diet-induce

139 Murine bone marrow-derived macrophages and human monocyte-deriv

140 wild-type and T2S mutant bacteria in murine bone marrow-derived macrophages and human U937 cells.

141 s isolated from Anxa2-deficient (Anxa2(-/-)) bone marrow-derived macrophages and lung parenchyma disp

142 In murine bone marrow-derived macrophages and murine embryonic fib

143 In vitro, both the WT bone marrow-derived macrophages and renal mesangial cell

144 in the RAW 264.7 macrophage line and primary bone marrow-derived macrophages but did not affect LXR-d

145 n rates and mROS expression in mock-infected bone marrow-derived macrophages but reduced caspase-depe

146 RP3-dependent interleukin-1beta secretion by bone marrow-derived macrophages by activating nuclear fa

147 Bone marrow-derived macrophages did not release NE in re

148 man monocyte-derived macrophages, and murine bone marrow-derived macrophages following infection with

149 a lower parasite intake, parasite burden in bone marrow-derived macrophages from AnxA1(-/-) mice was

150 LPS-challenged peritoneal and bone marrow-derived macrophages from IkappaBzeta-deficie

151 d M2 macrophage activation were confirmed in bone marrow-derived macrophages from mice with the myelo

152 ng IL-31RA expression on both peritoneal and bone marrow-derived macrophages from mice.

153 Delivery of bone marrow-derived macrophages from miR106b-93-25(-/-)

154 The effects of estrogen are long-lasting; bone marrow-derived macrophages from ovariectomized mice

155 Our previous studies showed that bone marrow-derived macrophages from S100A4(-/-) mice ex

156 Experiments with LPS-activated bone marrow-derived macrophages from wild-type and GILZ

157 n of caspase-1 inhibitors or the infusion of bone marrow-derived macrophages genetically engineered t

158 Bone marrow-derived macrophages incubated with or withou

159 LLO was able to infect and replicate within bone marrow-derived macrophages indistinguishably from t

160 d pro-inflammatory enzymes were monitored in bone marrow-derived macrophages isolated from myeloid ce

161 uced by dsDNA and other microbial ligands in bone marrow-derived macrophages lacking p205 revealed th

162 to measure the mRNA and miRNA expression in bone marrow-derived macrophages over a time-series of 8

163 An expansion of bone marrow-derived macrophages preceded a second phase,

164 CD44(+/+) murine bone marrow-derived macrophages produced higher TNF-alph

165 Ex vivo, TLR9(-/-) bone marrow-derived macrophages produced more A20 than W

166 oxide addition to CB3-infected NOD.Ncf1(m1J) bone marrow-derived macrophages rescued the inflammatory

167 Ex vivo studies using splenocytes and bone marrow-derived macrophages revealed significantly d

168 f IFN-beta expression was also identified in bone marrow-derived macrophages stimulated with B. burgd

169 a production and pyroptosis in primed murine bone marrow-derived macrophages that is mediated by the

170 Correspondingly, mouse bone marrow-derived macrophages that lack either thrombo

171 Mechanistically, in vitro, bone marrow-derived macrophages treated with necrotic bo

172 licited in an analogous fashion using LPS in bone marrow-derived macrophages upon inhibition of caspa

173 Consequently, murine bone marrow-derived macrophages were cocultured with tro

174 In the current study, in vitro treatment of bone marrow-derived macrophages with EDPs induced M1 mac

175 ly active, rescue replication of MHV(Mut) in bone marrow-derived macrophages, and inhibit RNase L-med

176 L-1beta secretion was impaired in Pgam5(-/-) bone marrow-derived macrophages, but not in Ripk3(-/-) b

177 rtin messenger RNA and protein expression in bone marrow-derived macrophages, liver, and spleen of mi

178 In SIRT3 knock-out bone marrow-derived macrophages, NLRP3 activation promot

179 We have found that in murine bone marrow-derived macrophages, PGE2 via the cAMP/prote

180 In bone marrow-derived macrophages, protective TLR ligands

181 Like bone marrow-derived macrophages, RNA editing in MG leads

182 Using bone marrow-derived macrophages, we observed that alpha-

183 poorly and induced rapid cell death in mouse bone marrow-derived macrophages.

184 phage cell line RAW264.7, but not in primary bone marrow-derived macrophages.

185 abolished in Toll-like receptor (TLR2)(-/-) bone marrow-derived macrophages.

186 uced mRNA and protein expression of IL-18 in bone marrow-derived macrophages.

187 ta and interleukin 6 messenger RNAs in mouse bone marrow-derived macrophages.

188 potently inhibited Leishmania replication in bone marrow-derived macrophages.

189 uced IL-1beta secretion and NO production in bone marrow-derived macrophages.

190 phage phenotype was absent in peritoneal and bone marrow-derived macrophages.

191 re supported by experiments with Ifitm3(-/-) bone marrow-derived macrophages.

192 optotic cells and are better phagocytes than bone marrow-derived macrophages.

193 man monocyte-derived macrophages, and murine bone marrow-derived macrophages.

194 duced chemokine secretion by neutrophils and bone marrow-derived macrophages.

195 s, but GM-CSF has also been used to generate bone marrow-derived macrophages.

196 inflammasome is attenuated in Nrf2-deficient bone marrow-derived macrophages.

197 elin phagocytosis in vitro by LPS stimulated bone-marrow-derived macrophages from IL-10-null mice fai

198 Treatment of mouse bone-marrow-derived macrophages with lipotoxic hepatocyt

199 Bone marrow-derived mast cell (BMMC) degranulation was a

200 Mice (genetically modified or bone marrow-derived mast cell-reconstituted Sash) were g

201 Bone marrow-derived mast cells (BMMCs) from C57BL/6 wild

202 In this study, we report that, in bone marrow-derived mast cells (BMMCs), gamma-tubulin in

203 Using bone marrow-derived mast cells (BMMCs), we tested the hy

204 Hierarchical clustering demonstrated that bone marrow-derived mast cells and BMBs shared specific

205 arge-scale comparative microarrays of murine bone marrow-derived mast cells and bone marrow-derived b

206 Bone marrow-derived mast cells cultured in TGF-beta1, be

207 ter stimulation with LPS was evaluated using bone marrow-derived mast cells from wild-type and Fyn-de

208 In this study we show that murine bone marrow-derived mast cells rapidly alter their metab

209 CCL7-deficient bone marrow-derived mast cells showed decreased degranul

210 e factor (HIF)-1alpha, which was enhanced in bone marrow-derived mast cells treated with LA.

211 the human FcepsilonRIalpha transgenic mouse bone marrow-derived mast cells via driving internalizati

212 To investigate this, mouse bone marrow-derived mast cells were cultured with or wit

213 IgE and Ag treatment compared with wild-type bone marrow-derived mast cells, but there was no differe

214 In bone marrow-derived mast cells, IgE cross-linking upregu

215 d for genomewide gene expression analysis on bone marrow-derived mast cells.

216 very significant accumulation of T cells and bone marrow-derived matrix-producing cells.

217 the role of this interaction, CD13-deficient bone marrow-derived MCs (BMMCs) were analyzed.

218 After IgE-induced stimulation, bone marrow-derived MCs from Kif5b knockout mice exhibit

219 e recovery of PIRI-CLI by injection of human bone marrow derived mesenchymal stem cells (hBD-MSCs) wi

220 Bone marrow derived mesenchymal stem cells (MSCs) are re

221 issue-engineered tendons differentiated from bone marrow derived mesenchymal stem cells from young (2

222 Bone marrow-derived mesenchymal stem cells (BMSCs) have

223 icant body of evidence has demonstrated that bone marrow-derived mesenchymal stem cells (BMSCs) showe

224 protein to responsive target cells, such as bone marrow-derived mesenchymal stem cells (BMSCs), rema

225 s in the osteogenic differentiation of human bone marrow-derived mesenchymal stem cells (hBMSCs) rema

226 ays employing 3T3-L1 preadipocytes and mouse bone marrow-derived mesenchymal stem cells (mBMSCs) to e

227 overexpressing Msx1 and Msx2 genes in mouse bone marrow-derived mesenchymal stem cells (mBMSCs) to r

228 /scaffold composite graft comprised of human bone marrow-derived mesenchymal stem cells (MSC) combine

229 Bone marrow-derived mesenchymal stem cells (MSC) have be

230 Both bone marrow-derived mesenchymal stem cells (MSCs) and c-

231 acellular vesicles (EVs) secreted from human bone marrow-derived mesenchymal stem cells (MSCs) on SE-

232 enic and adipogenic differentiation of mouse bone marrow-derived mesenchymal stem cells (MSCs).

233 ymal cell populations and the recruitment of bone marrow-derived mesenchymal stem cells and fibrocyte

234 ular viability and activity in primary human bone marrow-derived mesenchymal stem cells and human ost

235 Although bone marrow-derived mesenchymal stem cells have been pre

236 normal omental fibroblasts and adipose- and bone marrow-derived mesenchymal stem cells to obtain can

237 te the chondrogenic differentiation of human bone marrow-derived mesenchymal stem cells was assessed.

238 Treatment of isolated bone marrow-derived mesenchymal stem cells with SR2595 p

239 e marrow stromal cells (BMSCs, also known as bone marrow-derived mesenchymal stem cells) are manufact

240 n blot analysis in the fibrotic liver, human bone marrow-derived mesenchymal stem cells, and human he

241 UC-MSCs in vitro, compared with bone marrow-derived mesenchymal stem cells, displayed a

242 Bone marrow-derived mesenchymal stromal cells (BM-MSCs)

243 nce its down-regulation (DR) in both ex vivo bone marrow-derived mesenchymal stromal cells (MSC) and

244 were then used for the batch transduction of bone marrow-derived mesenchymal stromal cells ex vivo, f

245 howed that deficiency of both nonmyeloid and bone marrow-derived Mif reduced glomerular cell prolifer

246 Specifically, we demonstrate that bone marrow-derived monocytes and macrophages are essent

247 angiogenic growth factor that is produced by bone marrow-derived monocytes and macrophages as part of

248 Bone marrow-derived monocytes and macrophages were the p

249 Sts(-/-) bone marrow-derived monocytes and neutrophils, infected

250 om CX3CR1(+) precursors and postnatally from bone marrow-derived monocytes that colonize the tissue i

251 s after intracoronary infusion of autologous bone marrow-derived mononuclear cells (BMCs) are heterog

252 in vitro, and adoptive transfer of DJ-1(-/-) bone marrow-derived mononuclear cells rescued wild-type

253 an monocyte-derived dendritic cells (moDCs), bone marrow-derived mouse dendritic cells (BMDCs), and m

254 Specifically, we study the early response of bone marrow-derived mouse macrophages and cell line J774

255 ture assay of H. polygyrus bakeri larvae and bone marrow-derived MPhi, we now identify CD11b as the m

256 e response to group B Streptococcus, both in bone marrow-derived MPhis and in mature tissue MPhis, su

257 3 and UNC-93B limit the cytokine response in bone marrow-derived MPhis and microglia, but not in derm

258 OA induced bone marrow derived MSC differentiation towards osteopro

259 erapies (such as hematopoietic stem cells or bone marrow-derived MSC or dendritic cells) for optimiza

260 DC-EV were readily internalized by human bone marrow-derived MSC, without impacting significantly

261 enotypic and functional characteristics with bone marrow-derived MSCs (BM-MSC).

262 We assessed the effect human bone marrow-derived MSCs have on neonatal porcine islets

263 st the safety of a single dose of allogeneic bone marrow-derived MSCs in patients with moderate-to-se

264 Bone marrow-derived MSCs were harvested and purified fro

265 ental MSCs possess many in vitro features of bone marrow-derived MSCs, including clonogenicity, expre

266 We demonstrate that IL-33 production by bone marrow-derived murine macrophages (bmMFs) requires

267 epatic infection and adoptive transfer of WT bone-marrow-derived Mvarphi conferred protection against

268 thioglycollate-elicited peritoneal Mvarphis, bone marrow-derived Mvarphis and dendritic cells, and RA

269 Bone marrow-derived myeloid cells can accumulate within

270 Ablation of bone marrow-derived myeloid cells exacerbated plaque pat

271 cells promoted strong expression of PD-L1 in bone marrow-derived myeloid cells.

272 ate that lung regeneration is facilitated by bone-marrow-derived myeloid cells that are recruited to

273 ur previous studies demonstrated that murine bone marrow-derived myofibroblasts (BMFs) enhanced tumor

274 ed lipopolysaccharide-mediated activation of bone marrow-derived neutrophils and macrophages in vitro

275 ion in the lungs leads to the recruitment of bone marrow-derived neutrophils, which degranulate azuro

276 -resident subset, distinct from conventional bone-marrow-derived NK.

277 yeloma cells inhibited osteoblastogenesis of bone marrow-derived osteoblast progenitors by suppressin

278 treatment reduced the number and activity of bone marrow-derived osteoclast-like cells in vitro, sugg

279 ), primary murine calvarial osteoblasts, and bone marrow-derived osteoclasts.

280 ich we demonstrate site-specific survival of bone marrow-derived plasma cells and durable antibody re

281 lied on CNS-resident cells, independent from bone-marrow-derived precursors.

282 rable properties for T2 - weighted MRI, with bone marrow-derived primary human mesenchymal stem cells

283 Bone marrow-derived primary macrophages from mice and hu

284 We also collected bone marrow-derived primary macrophages from these mice.

285 We hypothesized that bone marrow-derived proangiogenic progenitor cells that

286 Bone marrow-derived progenitor cells (BMPCs) were isolat

287 sident macrophages that are reconstituted by bone marrow-derived progenitors after a genotoxic insult

288 Murine lung mast cells arise from committed bone marrow-derived progenitors that enter the blood cir

289 ic cells (cDCs) from Flt3L-mobilized primary bone marrow-derived progenitors, suggesting that VCAN pr

290 gal(+) SMC were not derived from circulating bone marrow-derived PW1(+) progenitor cells, confirming

291 ia MyD88 in both bone marrow-derived and non-bone marrow-derived radioresistant cells to induce hemag

292 Chondrogenic differentiation of human bone marrow derived SSCs resulted in significant down-re

293 in the chondrogenic differentiation of human bone marrow derived SSCs.

294 I), bovine serum albumin, and a monolayer of bone marrow-derived stem cells (SCP1).

295 air, including autologous transplantation of bone marrow-derived stem cells in elderly patients.

296 dy, we conducted a DNA methylome analysis of bone marrow-derived stromal cells from myelodysplastic s

297 g the transcriptional activation of CD40L in bone marrow-derived stromal cells.

298 e marrow egress and splenic proliferation of bone marrow-derived suppressor cells, inhibiting the ada

299 o the substitution of original phagocytes by bone marrow-derived surrogates were also examined.

300 2(-/-) mice underwent intranasal transfer of bone marrow-derived wild-type macrophages.