ライフサイエンスコーパス: bone marrow-derived

1 e behaviour and the relative contribution of bone marrow-derived ACE10 macrophages, but not microglia

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

3 rtery, intra-arterially delivered autologous bone marrow-derived ALD-401 in patients with disabling m

4 sone blocks interleukin-1 production in both bone marrow-derived and brain resident macrophage popula

5 We tested IL-5-primed mouse bone marrow-derived and human blood-sorted eosinophil ac

6 conditions and cell types, including murine bone marrow-derived and peritoneal macrophages, human mo

7 n protein O-GlcNAcylation in RAW264.7 cells, bone marrow-derived and peritoneal mouse macrophages, as

8 Using this assay, we showed that bone marrow-derived APC drive approximately half of dele

9 ophage function in nBmp2NLS(tm) mutant mice, bone marrow derived (BMD) macrophages and splenic macrop

10 we observed DNA methylation reprogramming in bone marrow-derived (BMD) monocytes as early as 4 days o

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

12 beneficial in ALSP by providing a supply of bone marrow-derived brain-engrafting myeloid cells with

13 Finally, patient bone marrow-derived CD34(+) cells showed markedly impair

14 Studying the differentiation dynamics of bone marrow-derived CD34+ cells into immature B cells in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Bone marrow-derived circulating progenitor cells are inv

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

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

35 triggered mediator release was determined in bone marrow-derived cultured mast cells (MCs) and human

36 Exogenous PGE(2) attenuated bone marrow-derived cultured MC activation through EP2 a

37 Bone marrow-derived DC subset analysis revealed an incap

38 tively transferred SOCS3(-/-) and SOCS3(+/+) bone marrow-derived DCs (BMDCs) on airway inflammation i

39 regulated CCR7 on Y. enterocolitica-infected bone marrow-derived DCs and purified MLN DCs, which may

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

41 In addition, TNFRp55(-/-) bone marrow-derived DCs in a TNFRp55(-/-) MLN microenvir

42 e regulator of DC maturation, C/EBPbeta(-/-) bone marrow-derived DCs matured much faster enabling the

43 Upon contact with mycobacteria, SPPL2a(-/-) bone marrow-derived DCs show enhanced secretion of IL-1b

44 L1 is expressed in mouse kidney, spleen, and bone marrow-derived DCs, and its expression and activity

45 In SPPL2a(-/-) bone marrow-derived DCs, Dectin-1 is redistributed to en

46 sing infected or transfected spleen cells or bone marrow-derived DCs.

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

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

49 way, previously shown to be used in vitro by bone marrow-derived DCs.

50 HDM + DEP exposed bone marrow derived dendritic cells and IL33 pulsed BMDC

51 hermore, the compound was able to 1) inhibit bone marrow-derived dendritic cell-mediated T cell funct

52 In this study, we show that RSV-infected bone marrow-derived dendritic cells (BMDC) as well as pu

53 eta in lipopolysaccharide (LPS)-primed mouse bone marrow-derived dendritic cells (BMDC).

54 d type I interferon (IFN) responses in mouse bone marrow-derived dendritic cells (DCs).

55 licits a broadened immune responses in mouse bone marrow-derived dendritic cells (mBMDCs) and a syner

56 Using peptide-pulsed bone marrow-derived dendritic cells and transfected muri

57 was also a poor stimulator of maturation of bone marrow-derived dendritic cells compared to E. coli

58 y, we show that the allogeneic EV from mouse bone marrow-derived dendritic cells enhances Ag-specific

59 roblasts and prevented activation of primary bone marrow-derived dendritic cells ex vivo.

60 Studies performed with bone marrow-derived dendritic cells from C-type lectin r

61 primary human foreskin fibroblasts or mouse bone marrow-derived dendritic cells infected with the pr

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

63 table within endocytic compartments in mouse bone marrow-derived dendritic cells.

64 y of LamOVA was characterized in vitro using bone marrow-derived dendritic cells.

65 tion on both RAW264.7 macrophages and murine bone marrow-derived dendritic cells; we now show that SL

66 sts that circulating tumour cells (CTCs) and bone marrow-derived disseminated tumour cells (BM-DTCs)

67 tudy aimed to establish the effects of human bone marrow-derived endothelial progenitor cells (hBMEPC

68 smoke exposure increases erythropoietin and bone marrow-derived erythroferrone and leads to expanded

69 Interestingly, IL33 blockade did not affect bone marrow-derived expansion and local infiltration of

70 involves culture on native decellularized 3D bone marrow-derived extracellular matrix (3D-ECM), which

71 , CXCR6 deficiency inhibited accumulation of bone marrow-derived fibroblasts and myofibroblasts in th

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

73 Bone marrow-derived fibrocytes and the monocyte chemoatt

74 th muscle actin-positive myofibroblasts, and bone marrow-derived fibrocytes.

75 bolished in wild-type mice transplanted with bone marrow derived from Cx(3)cr1cre(ERT2)Vegf(flox/flox

76 oduction, PI3Kdelta kinase-dead mutant donor bone marrow-derived GC B cells still supported BO cGVHD

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

78 Early thymic progenitors (ETPs) are bone marrow-derived hematopoietic stem cells that remain

79 Bone marrow-derived hematopoietic stem/progenitor cells

80 the continuous colonization of the thymus by bone-marrow-derived hematopoietic progenitors that migra

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

82 notypically primitive CD34(+) cord blood and bone-marrow-derived HSPCs.

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

84 Here, we establish that bone marrow-derived IL1beta stimulates breast cancer cel

85 xperiments indicated that cibinetide lowered bone-marrow-derived-immature-dendritic cell maturation a

86 a causal role of the miR-106b~25 cluster in bone marrow-derived leukocytes in mediating stress resil

87 rmore, either genetic depletion of P2X7Rs in bone-marrow derived leukocytes or pharmacological block

88 Importantly, intranasal transfer of bone marrow-derived M-MDSCs from mice able to produce IL

89 have used a novel platform that integrates a bone marrow-derived macrophage and live H. pylori co-cul

90 Bone marrow-derived macrophage cultures from the Notch2(

91 ent livers enhanced macrophage activation in bone marrow-derived macrophage cultures.

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

93 Our in vitro data suggest that bone marrow-derived macrophage-conditioned media induces

94 Further investigation revealed that bone marrow derived macrophages (BMDM) from the Muc-1(KO

95 Bone marrow derived macrophages isolated from WT or Notc

96 onal impact of GH on macrophage programming, bone marrow derived macrophages were treated with GH or

97 vo cytokine secretion by peritoneal cells or bone marrow derived macrophages.

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

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

100 In this study, we found that murine bone marrow-derived macrophages (BMDMs) and a human leuk

101 Bone marrow-derived macrophages (BMDMs) are recruited to

102 onse to LPS challenge, MEK2-deficient murine bone marrow-derived macrophages (BMDMs) exhibited lower

103 ate that LPS/IFNgamma polarization decreased bone marrow-derived macrophages (BMDMs) formation of pro

104 We found that bone marrow-derived macrophages (BMDMs) from BTK-deficie

105 Bone marrow-derived macrophages (BMDMs) from I/LnJ mice

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

107 Mirn23a (-/-) bone marrow-derived macrophages (BMDMs) have an attenuat

108 otes NLRP3 inflammasome activation in murine bone marrow-derived macrophages (BMDMs) infected with Gr

109 Bone marrow-derived macrophages (BMDMs) isolated from RO

110 We report that Galpha(i2) in murine bone marrow-derived macrophages (BMDMs) regulates IL-1be

111 Mechanistic studies using bone marrow-derived macrophages (BMDMs) showed that LPS

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

113 veral inflammasome-activating signals in the bone marrow-derived macrophages (BMDMs).

114 Using bone marrow-derived macrophages (BMM s) and CD4(+) T cel

115 In vitro priming of bone marrow-derived macrophages (BMM s) with IL-4 or TSG

116 nsistent with the in vivo data, infection of bone marrow-derived macrophages (BMM) with lethal Ehrlic

117 ates HuR expression in cardiac- and cultured bone marrow-derived macrophages (BMMO) and stimulates Hu

118 response to L. monocytogenes, P2X5-deficient bone marrow-derived macrophages (BMMs) exhibit defective

119 ogenesis was greatly enhanced in cultures of bone marrow-derived macrophages (BMMs) from Notch2(tm1.1

120 racellular concentrations of R. australis in bone marrow-derived macrophages (BMMs) of TLR4(-/-) and

121 entration of R. australis in Atg5(flox/flox) bone marrow-derived macrophages (BMMs) than in Atg5(flox

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

123 ne marrow-derived macrophages or VEGFR1(+/-) bone marrow-derived macrophages (M1-like phenotype), we

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

125 ome and Ingenuity Pathway Analysis of murine bone marrow-derived macrophages after exposure to this v

126 nscriptome analysis of mouse lymph nodes and bone marrow-derived macrophages after incubation with ac

127 Using bone marrow-derived macrophages and a murine model of pe

128 MV treatment of bone marrow-derived macrophages and bone marrow progenit

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

130 Bone marrow-derived macrophages and dendritic cells, lam

131 t cytokine that prompts the proliferation of bone marrow-derived macrophages and granulocytes.

132 rden was dramatically reduced in both murine bone marrow-derived macrophages and hamsters, in associa

133 cluded IL-12, TNF-alpha, and IL-6 in primary bone marrow-derived macrophages and LPS-induced IL-12/18

134 In vitro, bone marrow-derived macrophages and lymphoid endothelial

135 l changes were shown to be similar in murine bone marrow-derived macrophages and TAMs isolated from m

136 Using Tmem203 knockout bone marrow-derived macrophages and transient knockdown

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

138 id compartments, causes long-term changes in bone marrow-derived macrophages by suppressing interleuk

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

140 Similar to human cells, bone marrow-derived macrophages from A20-deficient mice

141 In tissue culture models, MaR1 treatment of bone marrow-derived macrophages from aged mice protected

142 as chemotaxis in response to LPS and C5a in bone marrow-derived macrophages from BVR (fl/fl) and Lys

143 rom Cyp46a1(-/-) mice as well as retinal and bone marrow-derived macrophages from Cyp27a1(-/-) and Cy

144 parison, gene expression was investigated in bone marrow-derived macrophages from Cyp46a1(-/-) mice a

145 This response was lost in bone marrow-derived macrophages from mice deficient in A

146 ur findings in cultured macrophages, primary bone marrow-derived macrophages from MPV17(-/-) mice, a

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

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

149 rd M2 macrophage activation was confirmed in bone marrow-derived macrophages from Slc7a2(-/-) mice.

150 city and inflammatory cytokine production of bone marrow-derived macrophages from TLR2(-/-) mice.

151 the expression and significance of GLUT6 in bone marrow-derived macrophages from wild-type and GLUT6

152 Using bone marrow-derived macrophages from WT and RIP2-KO mice

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

154 we report that IFN-beta signaling in murine bone marrow-derived macrophages has a cell-intrinsic pro

155 uce mTOR signalling in the microglia but not bone marrow-derived macrophages in both in vitro and in

156 arly, FENDRR overexpression in primary mouse bone marrow-derived macrophages increased mRNA expressio

157 lso confirmed enhanced osteoclastogenesis by bone marrow-derived macrophages isolated from the Kdm3C

158 le, if any, iRhom2 was detectable in mEFs or bone marrow-derived macrophages lacking ADAM17, suggesti

159 expression and cytokine production in mouse bone marrow-derived macrophages of different genotypes:

160 h MEK1/2 inhibitor U0126 or genetically with bone marrow-derived macrophages or DCs from Tpl2(-/-) mi

161 Mfrn1 (-/-)/Mfrn2 (-/-) bone marrow-derived macrophages or skin fibroblasts in v

162 d adoptive transfer of VEGF(165)b-expressing bone marrow-derived macrophages or VEGFR1(+/-) bone marr

163 n of MST1 in mouse embryonic fibroblasts and bone marrow-derived macrophages potentiated the TNFalpha

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 Silencing of NM23-M1 in mouse bone marrow-derived macrophages resulted in decreased ph

168 Bone marrow-derived macrophages secreted IL1B and IL18,

169 Co-culture with VDR-activated bone marrow-derived macrophages suppresses UPR target ge

170 ility group B1, stimulated Kupffer cells and bone marrow-derived macrophages to produce cytokines by

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

172 r found that TMAO induces M1 polarization of bone marrow-derived macrophages via the nucleotide-bindi

173 Furthermore, the secretome of MaR1-treated bone marrow-derived macrophages was identified as osteoi

174 Murine bone marrow-derived macrophages were derived into mature

175 Coculture of bone marrow-derived macrophages with ERCs from DKO mouse

176 RNA sequencing (RNASeq) analysis showed that bone marrow-derived macrophages with IRE1alpha deletion

177 Co-culture of bone marrow-derived macrophages with organotypic tumour

178 e protocol that details several in vitro (in bone marrow-derived macrophages) and in vivo (in mice) s

179 In mouse bone marrow-derived macrophages, heme induced HO-1, lipi

180 In a range of cell lines (murine bone marrow-derived macrophages, human monocytic THP-1 c

181 itional measurement of TNF-alpha shedding on bone marrow-derived macrophages, meprin beta/ADAM protea

182 g pathways are delayed in P2-deficient mouse bone marrow-derived macrophages, mouse embryonic fibrobl

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

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

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

186 odels, and in vitro on endothelial cells and bone marrow-derived macrophages.

187 response could be recapitulated in vitro in bone marrow-derived macrophages.

188 C class II expression in ZIP macrophages and bone marrow-derived macrophages.

189 in osteoclast precursors (OCPs) derived from bone marrow-derived macrophages.

190 versus hypoxia serum starvation-VEGFR1(+/-) bone marrow-derived macrophages.

191 uli in human monocytic cell lines and murine bone marrow-derived macrophages.

192 teraction was enhanced by LPS stimulation in bone marrow-derived macrophages.

193 RIM21 upon S Typhimurium infection of murine bone marrow-derived macrophages.

194 ace of lipopolysaccharide-stimulated primary bone marrow-derived macrophages.

195 163 and functionally distinct from classical bone marrow-derived macrophages.

196 to embed Raw264.7 cell line and primary rat bone marrow-derived macrophages.

197 1 phosphorylation and cytokine production in bone marrow-derived macrophages.

198 ating factor)-induced activation of Rac1, in bone marrow-derived macrophages; (b) TRPV4 directly inte

199 Aim2(-/-), Casp1/11(-/-) and Asc(-/-) murine bone-marrow derived macrophages (BMDMs) were infected wi

200 During brain injury or infection, bone-marrow derived macrophages invade neural tissue, ma

201 enterica serovar Typhimurium-infected murine bone-marrow-derived macrophages and thrombin activated h

202 M2 macrophage markers (Mrc1, Arg1, Il10) in bone-marrow-derived macrophages or in SAT from male or f

203 embryonic precursors and become replaced by bone-marrow-derived macrophages over time.

204 Bone marrow derived-macrophages from Fgf2(LMW-/-) mice c

205 cell models indicating TNT functionality in bone marrow derived malignancies and their microenvironm

206 e expression of IL-9 in murine Th9 cells and bone marrow-derived mast cells (BMMC).

207 Primary bone marrow-derived mast cells (BMMCs) and ECs from WT a

208 MC degranulation assays were performed with bone marrow-derived mast cells (BMMCs) derived from wild

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

210 -derived dendritic cells (moDCs), and murine bone marrow-derived mast cells (MC) were stimulated by F

211 We used an ex vivo model of mouse bone marrow-derived mast cells and an IL-33-dependent in

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

213 NF-kappaB transcriptional activity in mouse bone marrow-derived mast cells and cytokine production i

214 re measured after IgE crosslinking in murine bone marrow-derived mast cells and human cord blood-deri

215 We compared bone marrow-derived mast cells from MALT1 knockout (MALT

216 reated IgE cannot access its binding site on bone marrow-derived mast cells, resulting in reduced rel

217 , PGD(2), and thromboxane A(2) production by bone marrow-derived mast cells.

218 rritories are altered only by the arrival of bone marrow-derived MCs during inflammation.

219 ), play a role in the establishment of ET in bone marrow-derived MCs from C57BL/6J mice.

220 ism prevented the development of ET and that bone marrow-derived MCs produce 2-AG in a TLR4-dependent

221 nd the production of MCP 1 (CCL-2) in murine bone marrow-derived MCs.

222 and non-coated Mg plates were cultured with bone marrow derived mesenchymal stem cells (BMSCs) using

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

224 The immunomodulatory effects of bone marrow derived mesenchymal stem cells (MSCs) has be

225 A few fibrocytes-circulating and bone marrow-derived mesenchymal cells-were also detectab

226 pression promoted differentiation of the ST2 bone marrow-derived mesenchymal precursor cell line into

227 ore, the associated morphological changes of bone marrow-derived mesenchymal stem cells (BM-MSC), and

228 /stem cells (CPSC) as a valid alternative to bone marrow-derived mesenchymal stem cells (BMMSC) for c

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

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

231 We defined the phenotypic response of human bone marrow-derived mesenchymal stem cells (hMSCs) to 21

232 nce, and osteo-reparative functions of human bone marrow-derived mesenchymal stem cells (hMSCs) trans

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

234 ed that coculture of chondrocytes (CHs) with bone marrow-derived mesenchymal stem cells (MSCs) improv

235 ounding meniscus or exogenously seeded human bone marrow-derived mesenchymal stem cells (MSCs).

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

237 irects lineage specification of adipose- and bone marrow-derived mesenchymal stem cells.

238 cells in mono-culture and in co-culture with bone marrow-derived mesenchymal stem/stromal cells (BMSC

239 Allogeneic bone marrow-derived mesenchymal stem/stromal cells.

240 In this study, human bone marrow-derived mesenchymal stromal cell (hMSCs) was

241 to evaluate the effect of local injection of bone marrow-derived mesenchymal stromal cells (BM-MSCs)

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

243 t model to test the osteogenic properties of bone marrow-derived mesenchymal stromal cells (MSCs)-see

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

245 sendocardial injection of adult human hMSCs (bone marrow-derived mesenchymal stromal cells) and cKit(

246 Treatment with bone-marrow-derived mesenchymal stromal cells (MSCs) has

247 ood and lungs demonstrated that IL11 acts on bone-marrow-derived mesenchymal stromal cells, which ind

248 A bone marrow-derived MMC9 culture system was used to defi

249 have a limited life span with replacement by bone marrow derived monocytes.

250 iver (Kupffer cells; KCs) macrophages and in bone marrow-derived monocytes (BDMs).

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

252 distinguish between activated microglia and bone marrow-derived monocytes and macrophages in various

253 paracrine-acting protein that is produced by bone marrow-derived monocytes and macrophages to protect

254 Bone marrow-derived monocytes and macrophages were the p

255 phi are programmed locally, independently of bone marrow-derived monocytes during staphylococcal skin

256 ude brain-resident microglia and circulating bone marrow derived-monocytes (BMDMs), are typically gro

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

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

259 Bone marrow-derived MPhis (BMDM) from Slc2a1(M-/-) mice

260 O in bone marrow cells, strongly implicating bone-marrow-derived MPO in the pathogenesis of CKD ather

261 a/CTGF exposure respectively), compared with bone marrow-derived MSC (BM-MSC).

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

263 Herein, we examine the efficacy of a human bone marrow-derived MSC therapy delivered at 3 h or 30 h

264 ges of adipose-derived stem cells (ASCs) and bone marrow-derived MSCs (BMSCs).

265 er 30 minutes, rats were treated with either bone marrow-derived MSCs or a phosphate-buffered saline

266 othelial cells as well as on the capacity of bone marrow-derived MSCs to promote wound healing in vit

267 that restored HSC niche function in cultured bone marrow-derived MSCs.

268 delled the disease by silencing SMS in human bone marrow - derived multipotent stromal cells (MSCs) d

269 ox cues in the regulation and maintenance of bone marrow-derived multipotent stromal cells (BMSCs) th

270 An increasing body of evidence suggests that bone marrow-derived myeloid cells play a critical role i

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

272 stem-native myeloid cells (CNS-myeloids) and bone-marrow-derived myeloid cells (BMDMs) cooperatively

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

274 CIRP for NETosis and PAD4 expression in the bone marrow-derived neutrophils (BMDN) were assessed by

275 Patient bone marrow-derived neutrophils and white blood cells sh

276 Bone marrow-derived neutrophils from ethanol-fed mice sh

277 s neutrophil extracellular trap formation of bone marrow-derived neutrophils.

278 However in mouse bone-marrow-derived neutrophils, where expression of GPR

279 However, in vitro stimulation of murine bone marrow-derived or peritoneal macrophages with IL-33

280 e MGO scavenger glyoxalase 1 (GLO1) reverses bone marrow-derived PC (BMPC) dysfunction through augmen

281 Our findings support that bone marrow-derived, presumably neutrophil, NGAL protect

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

283 sistant multiple myeloma cells as well as on bone marrow-derived primary multiple myeloma cells from

284 y and pharmacology of vasoprotective axis in bone marrow-derived progenitor cells in health and disea

285 lls and thus, are continually replenished by bone marrow-derived progenitors.

286 for human erythroid specification in primary bone-marrow derived progenitors.

287 Bone-marrow-derived progenitors actively engage DNA repa

288 RMs consist of embryo-derived (EMRMs) and bone marrow-derived RMs (BMRMs), but the fate, dynamics,

289 sickle mutation in both peripheral blood and bone marrow-derived SCD HSPCs, a significant reduction i

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

291 cal cord blood stem cells (2; 4%), allogenic bone marrow-derived stem cells (1; 2%), placental stem c

292 ose-derived stem cells (35; 67%), autologous bone marrow-derived stem cells (8; 15%), amniotic stem c

293 lis influences the differentiation of murine bone marrow-derived stem cells (BMSCs) into functional D

294 ty to provide superior angiogenic potency to bone marrow-derived stem cells (BMSCs).

295 onors, myeloablative conditioning (MAC), and bone marrow-derived stem cells.

296 nner and is induced during both immortalized bone marrow derived stromal cell (iBMSC) as well as prim

297 In the context of bone marrow derived stromal cell and adipose derived str

298 As many stromal cell types, including bone marrow-derived stromal cells (BMSCs), display tissu

299 oward peripheral blood mononuclear cells and bone marrow-derived stromal cells.

300 Human blood CD14(+) monocytes are bone marrow-derived white blood cells that sense and res