ライフサイエンスコーパス: derived cell

1 ed rat-sized pancreata composed of mouse-PSC-derived cells.

2 ed these parameters in peripheral blood ECFC-derived cells.

3 er cells in cultures of EGFR-expressing TNBC-derived cells.

4 gates cNCCs towards the OFT, composed of SHF-derived cells.

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

6 t-derived hepatocytes, and apparently, donor-derived cells.

7 esenchymal stem cells and human osteosarcoma-derived cells.

8 pe also observed in CEP215-deficient patient-derived cells.

9 ive attenuation of viral replication in tick-derived cells.

10 xosomes were taken up by CD45(+) bone marrow-derived cells.

11 rived from the same tissue and postnatal rat-derived cells.

12 t cells via IL-1beta secreted by bone marrow-derived cells.

13 ting novel therapeutic strategies in patient-derived cells.

14 ome breakage and radials in human FA patient-derived cells.

15 by altered collagen-MMP production in EndMT-derived cells.

16 n the recruitment of circulating bone marrow-derived cells.

17 ogenesis, and recruit protumoral bone marrow-derived cells.

18 ere severely restricted to replicate in tick-derived cells.

19 pendent differences between normal and tumor-derived cells.

20 ctors, was globally decreased in the patient-derived cells.

21 cerebellar ataxia type 10 (SCA10) in patient-derived cells.

22 nd 53 have neuroprotective properties in SMA-derived cells.

23 ive NLRP3 inflammasome activation in myeloid-derived cells.

24 hemical inhibitors in cell lines and patient-derived cells.

25 ing cell growth and inducing death in cancer-derived cells.

26 indicating immune rejection of certain hiPSC-derived cells.

27 blated in adults and replaced by bone marrow-derived cells.

28 es, cell structures constitutive of monocyte-derived cells.

29 ough the induction of tetherin in hepatocyte-derived cells.

30 mportance of Grhl2 activity in trophectoderm-derived cells.

31 oot canal with periodontal and alveolar bone-derived cells.

32 -bound enhancer activity in islet- and liver-derived cells.

33 30 had no myelotoxicity on human bone marrow-derived cells.

34 uding endothelial cells and bone marrow (BM)-derived cells.

35 pproaches in cultured neurons and PD patient-derived cells.

36 iles of cord blood and peripheral blood ECFC-derived cells.

37 matory signaling in endothelial cells and BM-derived cells.

38 ading frame for transduction of human muscle derived cells.

39 n cholesterol in mice lacking miR-146a in BM-derived cells.

40 activation protected model mice and patient-derived cells.

41 to 35% of the liver was repopulated by donor-derived cells.

42 ectly damage ependyma, contained no ependyma-derived cells.

43 ences of actin mutations in affected patient-derived cells.

44 re highly expressed in peripheral blood ECFC-derived cells.

45 ay of the ZSWIM6 mRNA in affected individual-derived cells.

46 educed CD200R surface expression by monocyte-derived cells.

47 the microsymbiont is allowed to enter root (-derived) cells.

48 thelial cells constitute >60%, hematopoietic-derived cells 5% to 10%, and fibroblasts <20% of the non

49 ibiotics, MHC II(+)CD226(-)CD11c(-) monocyte-derived cells accumulated in peritoneal and pleural cavi

50 Furthermore, although monocyte-derived cells acquire key characteristics of the embryon

51 ed, diffusible cofactor together with a skin-derived cell adhesion complex to orchestrate the molecul

52 Administration of cardiosphere-derived cells after reperfusion limits infarct size meas

53 Notably, IRF5 deficiency in non-bone marrow-derived cells also contributes to the increased atherosc

54 Subsequent experiments including patient-derived cells and a mouse model support both a pathogeni

55 Evaluation of GFP expression in organ-derived cells and blood by flow cytometry demonstrated e

56 adout involving interactions between patient-derived cells and cancer drugs.

57 ction via NRF2, OSGIN1, and P53 in human CNS-derived cells and contributes to our understanding of ho

58 cortex were mediated by peripheral-monocyte-derived cells and did not require microglial function in

59 an important cross-talk between bone marrow-derived cells and epithelial secretory Paneth cells.

60 ient to direct differentiation of testicular-derived cells and ESCs to form functional mammary epithe

61 reduces cell death in HD mouse- and patient-derived cells and HD transgenic mouse brains.

62 is expressed on human and murine bone marrow-derived cells and limits inflammation by suppressing sig

63 or the survival of estrogen-independent MCF7-derived cells and multiple additional estrogen-independe

64 ss of DMF as a therapy for PAH using patient-derived cells and murine models.

65 By contrast, mice lacking ATG5 in monocyte-derived cells and neutrophils (polymorponuclear cells, P

66 iridophore differentiation from neural crest-derived cells and pigment progenitor cells.

67 which is consistent with both MD mesenchyme-derived cells and the purported importance of estrogen r

68 osal repair depended on TNF production by BM-derived cells and TNFR expression by radioresistant IECs

69 ed phenotypically and functionally from lung-derived cells and were crucial for protection against bo

70 re observed, including macrophages, monocyte-derived cells, and dendritic cells that were phenotypica

71 composed of macrophages, monocytes, monocyte-derived cells, and dendritic cells.

72 itro, enhanced substrate turnover in patient-derived cells, and excessive dendritic spine development

73 wn by analyses of the epicardium, epicardial-derived cells, and fate mapping.

74 liferation, migration and invasion of cancer-derived cells, and increases activity of matrix metallop

75 (+) T cells, Ig(+) B cells, CD11b(+) myeloid-derived cells, and major histocompatibility complex (MHC

76 ollectively, our results imply that monocyte-derived cells are critical contributors to psoriasis thr

77 Mammalian-derived cells are cultured on EM substrates, using optim

78 fate mapping wherein microglia and monocyte-derived cells are endogenously labeled with different fl

79 observations support the hypothesis that BM-derived cells are involved in neuroinflammation, and tar

80 The beneficial effects of cardiosphere-derived cells are mediated by the secretion of exosomes

81 directional differentiation because ES cell-derived cells are typically immature with impaired funct

82 etween C1qa(-/-) and WT mice identify non-BM-derived cells as the main local source of C1q that can p

83 Patient-derived cells as well as immortalized cells in which PAR

84 f human induced pluripotent stem cell (iPSC)-derived cells at two differentiation stages on periphera

85 parasites (NF54, 7G8, and 3D7B) and ex vivo-derived cell banks were characterized.

86 one of the first applications for stem cell-derived cells because of the loss of only a single cell

87 al. (2016) show that transplanted human ESC-derived cells biased to produce inhibitory interneurons

88 However, when co-cultured with lymphoid-derived cells, blood-derived CD4 T cells become sensitiz

89 The mobilization of bone marrow-derived cells (BMDC) to distant tissues before the arriv

90 KDR deficiency in murine BM-derived cells (BMDCs) suppressed the differentiation of

91 de (MDP) hydrogel scaffolds with dental pulp-derived cells but were limited in their ability to model

92 mpromised MERS-CoV infection into human lung-derived cells, but had little effect on infection into s

93 Selective stimulation of graft-derived cells by light resulted in excitatory and inhibi

94 ferentiation of adult mesenchymal epicardium-derived cells by modulating the balance between mesenchy

95 omains of DLX3 and GCM1 in human trophoblast-derived cells by performing immunoprecipitation and mamm

96 Monocyte-derived cells called fibrocytes also activate fibroblast

97 Cardiosphere-derived cells (CDCs) confer cardioprotection in acute my

98 eneous tumor; thus, methods to analyze tumor-derived cells circulating in blood should address this d

99 In contrast to solid tumor-derived cells, cMyc and Sp transcriptions are regulated

100 l labeling of zebrafish cranial neural crest-derived cells (CNCCs) to define global gene expression a

101 espread increase in protein turnover in HGPS-derived cells compared to normal cells.

102 HMGB1 silencing in cord blood ECFC-derived cells confirmed its role in regulating vascular

103 ific differences in NEUROD1 binding in islet-derived cells, consistent with evidence that the T2D ris

104 Bone marrow chimeras showed that bone marrow-derived cells contributed to IL-1R-dependent barrier fun

105 MP7 in both bone marrow- and non-bone marrow-derived cells contributes to the development of HFD-indu

106 as unable to express CXCL10 in hematopoietic-derived cells controlled infection more efficiently than

107 data indicate that whereas some bone marrow-derived cells could induce iNKT cell hyporesponsiveness,

108 Our results suggest that hESC-derived cells could provide a potentially safe new sourc

109 presentation over current methods of patient-derived cell culture and xenograft models.

110 Remarkably, reverse-genetics-derived cell culture-adapted PEDVAVCT12 harboring unclea

111 s (ASOs) increases SMN expression in patient-derived cells, cultured neurons, and the mouse central n

112 In primary human somatotroph adenoma-derived cell cultures, STAT3 suppression with the specif

113 n mice challenged with syngeneic tumorsphere-derived cells delayed established subcutaneous tumor gro

114 Patient-derived cells demonstrated an extended FA phenotype, whi

115 In this regard, monocyte-derived cells, depleted by CLs, internalized S. pneumoni

116 as showed that Mif expression in bone marrow-derived cells did not affect fibrosis and inflammation a

117 Moreover, patient-derived cells display a developmental phenotype: young p

118 loss of Hsp72 or Nek6 function in noncancer-derived cells disturbs neither spindle formation nor mit

119 s Axl but that Axl deficiency in bone marrow-derived cells does not affect lesion size, cellularity,

120 nt and not replaced by monocytes or adult BM-derived cells during infection, but were locally maintai

121 Shh also inhibited enteric neural crest-derived cell (ENCC) proliferation, promoted neuronal dif

122 Epicardium-derived cells (EPDCs) contribute cardiovascular cell typ

123 These unidentified SMC-derived cells exhibit phenotypes of other cell lineages,

124 ar level, Sparc-null and healthy-aged tendon-derived cells exhibited a more contracted phenotype and

125 In contrast, CD4(+)YFP(+)GFP(-) T cell-derived cells expanded rapidly and upregulated IL-10 exp

126 that human peripheral and intestinal myeloid-derived cells express laccase domain-containing 1 (LACC1

127 All myeloid-derived cells expressed C5aR2, although with different i

128 le-containing hepatocytes declined and donor-derived cells expressed human AAT protein.

129 njury-induced neointima did not contain VSMC-derived cells expressing a different fluorescent reporte

130 ommon in atherosclerotic lesions, with EndMT-derived cells expressing a range of fibroblast-specific

131 of this role of ES to regulate neural crest-derived cell fate and differentiation in vivo, knockdown

132 ntrinsic difference between normal and tumor-derived cells for the activities of IFI16 and HSV-1 ICP0

133 oeba (genotype T4) or stimulated with amoeba-derived cell-free conditioned medium.

134 Donor-derived cell-free DNA (dd-cfDNA) is a noninvasive test o

135 roportions and the tissue-of-origin of tumor-derived cell-free DNA in a blood sample using genome-wid

136 Also at the PanIN2 stage, pancreas acinar-derived cells frequently invade along sensory neurons in

137 in Rickettsia montanensis infection of tick-derived cells from a natural host, Dermacentor variabili

138 ury to allow distinction of extrarenal or BM-derived cells from intrinsic renal cells.

139 isolated two distinct populations of muscle-derived cells from skeletal muscle: (i) a rapidly adheri

140 E542K and p.E545A) were identified in lesion-derived cells from the other four patients, also by dire

141 In contrast, VSMC-derived cells generating the neointima after vascular in

142 The therapeutic effects of iPSC-derived cells have been investigated in many preclinical

143 Bone marrow-derived cells have important roles in cancer development

144 it is not clear if these induced pluripotent-derived cells have the same reparative capacity as physi

145 Human umbilical tissue-derived cells (hUTCs) were previously shown to have prot

146 reen for LATS2-interacting proteins in liver-derived cells identified the transcription factor SREBP2

147 Bioengineering organs, by growing patient-derived cells in biomaterial scaffolds in the presence o

148 Finally, we identify similar neural-crest derived cells in both the avian and non-human primate sp

149 eracts specifically with a subset of myeloid-derived cells in human blood, whereas CV1 binds all myel

150 on of adipocytes from bone marrow progenitor-derived cells in mice challenges this paradigm and indic

151 for constitutive Nlrp3 activation in myeloid derived cells in mice deficient in IL-17 or TNF.

152 ic macrophage-, dendritic cell-, or monocyte-derived cells in tissues driven by recurrent mutations a

153 The role of mesenchymal-derived cells in TSC tumorigenesis was investigated thro

154 n of macrophage, dendritic cell, or monocyte-derived cells in various tissues and organs of children

155 anized through the activation of bone marrow-derived cells in various tissues.

156 posure on the migratory capacity of monocyte-derived cells in vitro and in vivo.

157 lization is revealed to be dominant in tumor-derived cells in which ICP0 is nonfunctional.

158 The number of Troy-derived cells increases after folic acid-induced injury.

159 e-stranded locked nucleic acids into patient-derived cells increases FXN protein expression to levels

160 All cholesterol-depleted neuron-derived cells, independent of the method of reduction, e

161 th study cohorts, intracapillary bone marrow-derived cells, indicative of leukostasis, were only obse

162 In addition, patient specific iPSC-derived cells induce minimal or no immune response in vi

163 Integration of stem cell-derived cells into native cellular environment remains a

164 mediated by glomerulus-infiltrating myeloid-derived cells is a key pathogenic event in lupus nephrit

165 -dependent infiltration of mouse bone marrow-derived cells is abundant in demyelinating areas, but th

166 pression in both endothelial and bone marrow-derived cells is essential for arteriogenesis in respons

167 unogenicity of autologous human iPSC (hiPSC)-derived cells is not well understood.

168 on the viability and fusion of a trophoblast-derived cell line (BeWo).

169 nt cytokine secretion from a Sezary syndrome-derived cell line and patient isolates.

170 ansfect the retinal pigment epithelium (RPE)-derived cell line ARPE-19, and human primary RPE (hRPE)

171 CD34+ cells, respectively), and in a patient-derived cell line expressing TEL-AML1 (REH).

172 A patient-derived cell line revealed reduced levels of endogenous

173 ere, we examine in mouse and in a mouse limb-derived cell line the dynamic events that activate and r

174 We used an AML-derived cell line to determine whether TSC2 restitution

175 ut a proteomic analysis of a B cell lymphoma-derived cell line, BJAB, that requires UBQLN1 for surviv

176 -based knockdown of GNPAT in the human liver-derived cell line, HepG2/C3A.

177 biaxial stretch injuries (BSI) on a neuronal derived cell line, HT22 cells, were assessed in an in vi

178 y or sufficient for loss of IFI16 in a tumor-derived cell line.

179 atin state at enhancers specific to endoderm-derived cell lineages in gut tube intermediates.

180 ato reporter strain to identify neural crest-derived cell lineages including the peripheral autonomic

181 r, inefficient replication in several mucosa-derived cell lines and airway epithelial cultures sugges

182 Here, we used derived cell lines and cells from patients to investigat

183 ncreases YAP1 expression and activity in CRC-derived cell lines and in mouse models.

184 ytotoxicity by OSU-T315 is noted in both CLL-derived cell lines and primary CLL cells relative to nor

185 investigate the role of Nrf2 in PEL and PEL-derived cell lines and show that KSHV latency induces Nr

186 Autophagy-deficient tumor-derived cell lines are respiration-impaired and starvati

187 ly permissive infection was common in cancer-derived cell lines but was also a feature of nontransfor

188 olorectal cancer cell line DLD1 and two DLD1-derived cell lines carrying single-chromosome aneuploidi

189 Here we compare genomic data from 65 kidney-derived cell lines from the Cancer Cell Line Encyclopedi

190 Tumor-derived cell lines have served as vital models to advanc

191 essing the effect of 130 drugs on 639 cancer-derived cell lines in order to identify novel interactio

192 ance of utilizing low-passage-number patient-derived cell lines in studying CA to more faithfully rec

193 The utility of tumor-derived cell lines is dependent on their ability to reca

194 Ovarian tumor-derived cell lines MKP-Liver and MKP-Lung cells reproduc

195 Liver-derived cell lines producing full-length HBV and HBsAg p

196 rray expression analysis using tumor and OSE-derived cell lines reveal a 121 gene signature associate

197 Characterization of TRNT1 in patient-derived cell lines revealed reduced but detectable TRNT1

198 -seq and gene expression analyses of patient-derived cell lines revealed that H3K9me3 mediates differ

199 a paired genome-wide siRNA screen in patient-derived cell lines reveals that WABS cells do not tolera

200 We created two Ovcar8-derived cell lines that differed only in their TWIST1 ex

201 orage-independent growth in multiple patient-derived cell lines, and tumorigenesis in a xenograft mod

202 duced growth inhibition of a number of tumor derived cell lines, demonstrating the potential of tanky

203 When these analyses were extended to renal-derived cell lines, quantitative RT-PCR did not detect A

204 Correspondingly, in GCB-derived cell lines, the IRE1 promoter carried increased

205 Through cell-based assays on several human-derived cell lines, we show that VCC is unlikely to util

206 Using patient-derived cell lines, we show that zebrafish larvae xenotr

207 ed with mis-localization of TIP60 in patient-derived cell lines.

208 roved effective against several solid cancer-derived cell lines.

209 is unable to productively infect most cancer-derived cell lines.

210 matopoietic and nonhematopoietic human tumor-derived cell lines.

211 -inactivated human primary NSCLC samples and derived cell lines.

212 c flux in both normal-immortalized and tumor-derived cell lines.

213 but also within individual tumors and tumor-derived cell lines.

214 he loss of IFI16 in several normal and tumor-derived cell lines.

215 mouse and patient tumors as well as in tumor-derived cell lines.

216 undetectable in many commonly studied cancer-derived cell lines.

217 cell division of human or mouse lung cancer-derived cell lines.

218 ocalization in human kidney and human kidney-derived cell lines.

219 n vivo and long-lasting aneuploidy in tumour-derived cell lines.

220 longed growth inhibition in multiple patient-derived cell lines.

221 son of gene expression profiles between iPSC-derived cell lines.

222 0R pathway with MMP12 production by monocyte-derived cells may play a key role in PD progression and

223 rs the accumulation of inflammatory monocyte-derived cells (MCs) in the CNS, leading to improved clin

224 as completely prevented in mice with myeloid-derived cell (MDC)-specific deletion of TNFR1.

225 Cardiosphere-derived cells mediate therapeutic regeneration in patien

226 This includes the use of naturally derived cell membranes, which can bestow nanocarriers wi

227 stigators show that transplanted bone marrow-derived cells migrate to the skin of bone marrow transpl

228 To generate healthy patient-derived cells, mutations might be repaired with new gene

229 ce lacking Jagged1 or Notch2 in neural crest-derived cells (NCCs) of the pharyngeal arches display a

230 During development, embryonic notochord-derived cells (NDCs) are the direct progenitors of cells

231 ated by replacement of PLXNC1 on bone marrow-derived cells or by genetic deletion of Syt7.

232 e, subretinal dose of human umbilical tissue-derived cells (palucorcel [CNTO-2476]) in the eyes of ad

233 We have developed an AAC-11-derived cell-penetrating peptide, herein named RT53, mim

234 )-producing proinflammatory bone marrow (BM)-derived cells (PI-BMDCs) in rodents.

235 Platelets, anucleated megakaryocyte (MK)-derived cells, play a major role in hemostasis and arter

236 ng stable YFP expression in all neural crest-derived cell populations despite loss of Wnt1 expression

237 We find that deficiency of miR-146a in BM-derived cells precipitates defects in hematopoietic stem

238 he miR-193a-3p mimic reduced cord blood ECFC-derived cell proliferation, migration and vascular tubul

239 est that LNGFR(Low+)THY-1(High+) dental pulp-derived cells provide an excellent source of material fo

240 icated that IRAK-M expression by bone marrow-derived cells, rather than structural cells, promoted fi

241 and lose epicardial identity, whereas atrial-derived cells remained 'epithelial-like'.

242 Subsequently, HSC-derived cells replace erythrocytes, granulocytes and mon

243 nding data from purified embryonic stem cell-derived cells representing six sequential stages of hema

244 elective Grhl2 inactivation only in epiblast-derived cells rescued all placental defects but phenocop

245 GnT-III in EOC cell lines and primary tumor-derived cells resulted in an inhibition of Notch signali

246 Depletion of Krt15-derived cells resulted in decreased proliferation, there

247 Importantly, the Runx2 knockdown in bone-derived cells resulted in increased sensitivity to both

248 c labeling of nascent transcripts in patient-derived cells revealed a >3-fold increase (P < 0.05) in

249 aspase-1(KO) specifically within bone marrow-derived cells revealed that monocytes promoted anxiogene

250 Patient-derived cells show increased degradation of IkappaBalpha

251 Patient-derived cells showed engorged lysosomes and a slower aut

252 vity to chronic LPS depends on hematopoietic-derived, cell subset-autonomous TLR4.

253 Drug assays with patient-derived cells such as circulating tumor cells requires m

254 rease the physiologic relevance of human iPS-derived cells, such as cardiomyocytes (iPS-CM).

255 nal epithelium and not restricted to myeloid-derived cells, such as neutrophils.

256 as their adhesion to normal microenvironment-derived cells, suggesting a role in the cross-talk betwe

257 t macrophages, dendritic cells, and monocyte-derived cells that are critical in defense against pneum

258 nd relies heavily on trophoblasts, the fetal-derived cells that comprise the placental barrier.

259 s established during embryogenesis, monocyte-derived cells that develop during adult life and DCs.

260 te using normal, 'para-malignant' and tumour-derived cells that progression to malignant transformati

261 ugh they were functional and composed of rat-derived cells, the resulting pancreata were of mouse siz

262 However, the underlying mechanisms of iPSC-derived cell therapy are still unclear, and limited engr

263 We also identified SVG-A astroglial cell-derived cells to be highly permissive for JUNV infection

264 ace, enabling the clinical potential of hPSC-derived cells to be realized.

265 alpha5 and alphav cooperate on neural crest-derived cells to control the remodelling of the pharynge

266 However, the hepatic functions of these hPSC-derived cells to date are not fully comparable to adult

267 rats were sufficient to redirect testicular derived cells to produce normal mammary epithelial trees

268 advantages and limitations of using patient-derived cells to study or treat epilepsy, as well as cri

269 We investigated the use of iPSCs and iPSC-derived cells to study the impact of genetic variation o

270 rate a significant contribution of nonvenous-derived cells to the dermal lymphatic vasculature.

271 ng the risks associated with direct ES or ES-derived cell transplantation and risk of teratomas.

272 pport further development of autologous iPSC-derived cell transplantation for treatment of PD.

273 otinylatable H3.3 histone variant in CMs and derived cell-type-specific profiles of histone replaceme

274 ctional importance of inflammasomes in blood-derived cell types is well established, it remains poorl

275 genome-scale screens in a wide range of iPSC-derived cell types, dissect developmental pathways, and

276 oncept may be expanded to maturing other PSC-derived cell types, including those containing mutations

277 ormalities in the neural crest and the crest-derived cell types.

278 y be used to reprogram specific neural crest-derived cell types.

279 d to elucidate how the Staphylococcus aureus-derived cell-wall component lipoteichoic acid (LTA) gove

280 MMP12 production by monocyte-derived cells was induced by CSF2 rather than the cycloo

281 g two conditional knockout mouse strains and derived cells, we demonstrate that Brd4 controls cell id

282 of miR-193a-3p mimic treated cord blood ECFC-derived cells, we identified 2 novel miR-193a-3p targets

283 allowing a distinction between dam- and pup-derived cells, we show that foster nursing by an immuniz

284 ferentiation of osteoclasts from bone marrow-derived cells were completely suppressed by knee loading

285 Donor BM-derived cells were present in the lungs of recipient mic

286 Similarly, all lymphoid-derived cells were tdTomato-C3aR(-), except some LP-deri

287 tly, the surviving CD4(+)YFP(+)GFP(+) T cell-derived cells were unresponsive and failed to proliferat

288 ing region 3 sequences from SCID and OS iPSC-derived cells, whereas control iPSCs yielded T-cell prog

289 th human pluripotent stem cell-derived (hPSC-derived) cells, which are currently under investigation

290 derived from bevacizumab-resistant xenograft-derived cells, while recombinant MIF drove M1 polarizati

291 less proliferative and less angiogenic ECFC-derived cells will enhance their vasculo/angiogenic func

292 hat recall-by-genotype studies that use iPSC-derived cells will require cells from at least 20-80 ind

293 ygenase-2 pathway, and treatment of monocyte-derived cells with a CD200R ligand reduced CSF2-induced

294 istent with these findings, human ADPKD cyst-derived cells with heterozygous and homozygous PKD1 muta

295 ically distinct subpopulations of older host-derived cells with self-renewing capacity that are resis

296 l-mediated expansion of glioblastoma patient-derived cells with stem-like properties in vitro and sup

297 mediated maintenance of glioblastoma patient-derived cells with stem-like properties.

298 mmatory cytokines was similar in SLE patient-derived cells, with the exception that IL-10 was slightl

299 g for SMC markers fail to detect >80% of SMC-derived cells within advanced atherosclerotic lesions.

300 lls and their descendants (i.e. Pnmt(+) cell derived cells) within the heart.