ライフサイエンスコーパス: FACS

1 FACS analyses with anti-TLR4 Ab showed only minimal chan

2 FACS analysis and CD40L binding studies revealed unchang

3 FACS analysis indicated that IL-15Ralpha was expressed b

4 FACS analysis of mouse spleen cells revealed proinflamma

5 FACS analysis revealed a significant increase in blood m

6 FACS analysis revealed that IL-10 production was associa

7 FACS analysis showed that transferrin-mediated targeting

8 FACS analysis was performed on PBMCs and intrahepatic ly

9 FACS analysis was used to determine percentages of Kit a

10 FACS and electron microscopy analyses showed that GKY25

11 FACS had permitted the isolation of tumor-free populatio

12 FACS has high inter-observer variability and subjectivit

13 FACS identified prominent NPS receptor expression in PVN

14 FACS lineage sorting revealed NK cells and CD4(+) T cell

15 FACS on glycophorin A-positive cells showed that approxi

16 FACS sorting from Hoxb7/enhanced green fluorescent prote

17 FACS sorting showed that these CD16(hi) eosinophils were

18 FACS-purified (c-kit)EGFP(+)/(alphaMHC)mCherry(-) (nonca

19 FACS-purified progenitors from APE2-deficient mice diffe

20 FACS-sorted adult human ductal cells clonally expanded a

21 FACS-sorted and enriched KIR2DS2(+) NK cell subpopulatio

22 FACS-sorted CD105(low) cells demonstrated significantly

23 FACS-sorted endothelial cells isolated from regenerating

24 A FACS-based shRNA screen identified several MMS genes as

25 h standard molecular biology equipment and a FACS machine.

26 We also describe a FACS-based method that is used subsequently to obtain hi

27 NA data at the protein level, we developed a FACS-based protocol designed to phenotype live GI eosino

28 We employed a FACS-based screen for Nlrp3-dependent cell death, using

29 We have used a FACS-based genome-wide screening system to identify tran

30 aptamers are then further optimized using a FACS-based directed evolution approach.

31 We used a "FACS-array" approach to identify 18 genes for transmembr

32 Therefore, our integrated acoustofluidic FACS device is demonstrated to achieve two-way cell sort

33 Our acoustofluidic FACS device uses the "microfluidic drifting" technique t

34 Applying detailed serology, advanced FACS analysis, and systems biology, we discovered that a

35 n addition, the use of reporter genes allows FACS-purification and tracking of cells that have had mu

36 tracellular lipids with BODIPY(505/515), and FACS-based isolation of top 0.5% lipid-rich E. gracilis

37 ets were confirmed via lumi-aggregometry and FACS analysis for P-selectin and LAMP-1 exposure.

38 oved multiple displacement amplification and FACS, to obtain genomic sequences and cell size informat

39 were independently enumerated using ARCA and FACS within 24 hours of blood sample collection, and p<0

40 ly FPR1 protein-positive by Western blot and FACS.

41 was determined by RT-PCR, Western blot, and FACS, and enzymatic activity by HPLC.

42 Confocal and FACS analysis confirmed that MF59 and Pam3CSK4 were the

43 PAD4 activity was increased by diabetes, and FACS detection of histone citrullination, together with

44 denced by colony assays, gene expression and FACS analyses, whereas signaling by ALK-5 leads to the o

45 Confocal images and FACS demonstrated a strong association and co-localizati

46 pancreatic islets by immunofluorescence and FACS.

47 Immunohistochemical and FACS analyses revealed that P-Dex was primarily sequeste

48 qRT-PCR, immunohistochemistry, and FACS analysis identified CD11c(+) Langerin+ cells in the

49 B+ and exon 2B- RNAs in freshly isolated and FACS-sorted wild-type melanoblasts and melanocytes and g

50 hromatin state maps, custom microarrays, and FACS purification of the subventricular zone lineage, we

51 ts such as laser-capture microdissection and FACS, Retro-TRAP is a high-throughput methodology that r

52 Immunofluorescence microscopy and FACS analysis were used to determine levels of alphavbet

53 switching to IgE were analyzed by RT-PCR and FACS.

54 f intact mRNA from fixed, permeabilized, and FACS-purified cell populations.

55 e epithelia can be isolated by pipetting and FACS sorting into a population of corneal epithelial-lik

56 Ultrastructural, proteomic and FACS analyses of Atg16L-positive vesicles reveal that 30

57 on laser microdissected tubular segments and FACS-sorted renal immune cells and identified the S3 pro

58 nversion via three consecutive targeting and FACS events.

59 ippocampal neurons as indicated by TUNEL and FACS analysis.

60 e plasminogen activator receptor (uPAR), and FACS analysis with antibody directed against the C termi

61 ross-presentation and CD137 activation-based FACS to enrich for polyclonal CD8+ T effector T cells.

62 rs (hOPCs) directly, we used CD140a/O4-based FACS of human forebrain and microarray to hOPC-specific

63 oides pteronyssinus (Der p) allergen, before FACS phenotyping and co-culture with allogeneic CD4+ T c

64 to our knowledge, of BONCAT-FISH and BONCAT-FACS within an environmental context, we probe the trans

65 fluorescence-activated cell sorting (BONCAT-FACS) for subsequent genetic analyses.

66 nd chaperonin 60 (GroEL) as revealed by both FACS analysis and confocal microscopy imaging.

67 s showed no signs of impaired viability, but FACS revealed significantly reduced TH immunoreactivity

68 By FACS analysis, both the lungs and spleens of BALB Cftr(t

69 nd cell surface LDLR levels were analyzed by FACS.

70 Cs, as detected in Myf5(nLacZ/+) mice and by FACS sorting, and this effect was inhibited by Ang II AT

71 ceptors biophysically, biochemically, and by FACS staining.

72 nescence-associated cell-surface antigens by FACS analysis and a newly developed cell-based ELISA.

73 subpopulations as simultaneously assessed by FACS analysis from peripheral leukocytes.

74 erent pneumococcal serotypes, as assessed by FACS and immunofluorescence analysis.

75 were found to express high levels of CD25 by FACS.

76 of PMA/ionomycin stimulated CD4+ T cells by FACS analysis purified from blood of healthy subjects at

77 uced nonspecific interactions with cells (by FACS).

78 of normal rod-shaped cells were collected by FACS and reincubated.

79 treatment by PV sera, which was confirmed by FACS analysis.

80 These data were corroborated by FACS measurements showing a decrease of CD11b(+)/CD45(hi

81 status in primary cultures was determined by FACS analysis.Affymetrix microarray data indicated that

82 whereas cytokine production was evaluated by FACS.

83 the unique marker CD63var, were examined by FACS and by confocal laser scanning microscopy in cell c

84 , we assessed differential RNA expression by FACS-purified adult astrocytes and, on that basis, evalu

85 o-labeled S. aureus bioparticles followed by FACS analysis.

86 nflammation was quantified histologically by FACS and gene expression analysis.

87 cardiovascular progenitors were isolated by FACS for expression of vascular endothelial growth facto

88 CD44(+)CD24(lo)CD166(+) cells, isolated by FACS from mouse small intestine and colon, expressed hig

89 lR1(+) neural progenitors can be isolated by FACS or magnetic sorting (MAC) which give rise to dopami

90 Putative EpiSC populations were isolated by FACS sorting.

91 , and memory tonsil B cells were isolated by FACS, and their capacities for IL-4 and anti-CD40 signal

92 via high-throughput single-cell isolation by FACS.

93 eloped a protocol for hair cell isolation by FACS.

94 Phosphorylated Stats were measured by FACS before and after stimulation with increasing doses

95 and mitochondrial potential was measured by FACS-based JC1 staining.

96 cellular cytokine production was measured by FACS.

97 detected on resting neutrophil membranes by FACS analysis, and expression levels significantly incre

98 isolation of pure nonactivated microglia by FACS.

99 rized circulating phosphatidylserine+ MPs by FACS.

100 oietic contamination are readily obtained by FACS at P0 and from freshly prepared single-cell suspens

101 of cytokine-producing cells was performed by FACS.

102 limbus and their subsequent purification by FACS.

103 es on regenerating support cells purified by FACS.

104 take as single-stranded T-oligo, as shown by FACS analysis.

105 ei are isolated from specimens and sorted by FACS, cDNA libraries are constructed and RNA-seq is perf

106 d donor buffy coats, and ILCs were sorted by FACS.

107 )/eGFP and smMHC/Cre/eGFP mice and sorted by FACS.

108 cyte populations in the lungs and spleens by FACS and by evaluating CD3-stimulated cytokine secretion

109 editing coupled to a cell selection step by FACS to identify regulators of SQSTM1.

110 fic GFP fusion protein to isolate tetrads by FACS and (ii) molecular barcodes that are read during ge

111 CD133+ FACS-sorted cells cultured in serum-free medium form 3-f

112 Notably, single cell FACS technology was applied to further promote virus pur

113 We proved via </= five-colour FACS that the manipulation of this in vitro model allowe

114 Subsequently, four-colour FACS verified the ability to determine the biochemical e

115 Competitive FACS increased the frequency of hapten-specific scFvs in

116 lay system and a newly developed competitive FACS procedure was employed to select rare hapten-specif

117 ncept, this study demonstrates that coupling FACS with WGA and microarrays is a promising tool to exp

118 be readily detected in 3D organoid cultures, FACS analysis and in vivo tumour models.

119 Current FACS software requires the user to define sorting gates

120 sil B cells were analyzed by flow cytometry (FACS) and cultured with IL-4 and anti-CD40 to induce CSR

121 d monocytes was evaluated by flow cytometry (FACS).

122 sue barrier via multi-colour flow cytometry (FACS).

123 Our findings demonstrate FACS robustly detects perturbations of bacterial cell sh

124 By combining a previously developed FACS-based selection system for functional expression wi

125 r, studies here that couple high-dimensional FACS sorting with large-scale quantitative IgH deep-sequ

126 Here we describe 'enhancer-FACS-seq' (eFS) for highly parallel identification of ac

127 On postmortem examination, FACS-based enumeration of intracranial tumor-infiltratin

128 First, FACS was successfully applied to a D. mccartyi isolate a

129 e submandibular lymph nodes were removed for FACS analysis, and the jaws were analyzed for bone resor

130 nd that anti-AOC3 antibodies can be used for FACS sorting of myofibroblasts obtained by nonenzymatic

131 igh-performance, portable, and user-friendly FACS instrument.

132 -ISL1 antibodies and chromatin extracts from FACS-purified SAN cells demonstrated that ISL1 directly

133 Gene profiling was generated from FACS-purified neurons leading to the identification of n

134 e use of specific and expensive labels (e.g. FACS or MACS).

135 However, FACS analysis indicated phenotypically differing CD11c(+

136 Here we used comprehensive approaches (ie, FACS sorting, quantitative RT-PCR, immunohistochemistry,

137 d by fluorescence-activated cell sorting (IE-FACS).

138 atopoietic cells with high purity through IE-FACS and profile them via aCGH analysis.

139 and fluorescence-activated cell sorting (IE/FACS), a technique previously used for isolating circula

140 In FACS staining experiments, B27 dimer protein and tetrame

141 Combining CD30 to SSEA4 and TRA-1-81 in FACS greatly enhanced specificity and efficiency of hiPS

142 miR-215 expression is depleted in FACS-enriched cancer stem cells compared with unsorted s

143 nflammatory cytokine IL-1beta was greater in FACS-isolated microglia than in brain-invading monocytes

144 col for the isolation of bona fide hiPSCs in FACS-based selection using an optimized combination of c

145 hown to bind this heparin-binding peptide in FACS analysis, and the interaction was shown to be with

146 including GM-CSF, detected by intracellular FACS and ELISA.

147 d dendritic cells (DCs) and freshly isolated FACS-purified ILCs, we demonstrate that IL-23 and IL-1 s

148 Although methods like FACS and FISH-FC can characterize and isolate cells from

149 MDE-FACS allowed the identification of human butyrylcholines

150 The microscale FACS-Chip-LCMS workflow demonstrated high cellular enric

151 Overall the microscale FACS-Chip-LCMS workflow has shown effectiveness in effic

152 strate is cleaved are isolated by multicolor FACS with fluorescently labeled antiepitope tag antibodi

153 ress this, the current study used multicolor FACS of disaggregated tumor to systematically characteri

154 Multiparameter FACS analysis was used to examine relative expression of

155 ng a combination of biochemical, mutational, FACS, and single molecule super-resolution imaging appro

156 Next, FACS-sorted VEGFR2+ cells expressed highest and lowest l

157 estive of a trend in ARMD using ARCA but not FACS.

158 duced CD38(+) hPGCLCs [ approximately 43% of FACS-sorted embryoid body (EB) cells] from primed-state

159 in efficiently preparing limited amounts of FACS enriched cells in an online manner for proteomic LC

160 RNA-Seq analyses of FACS-isolated wild-type and Six2(GFP(+)) CM cells reveal

161 RNA-sequencing (RNA-seq) analyses of FACS-purified cells from ISL1-deficient SANs revealed th

162 Single-cell gene expression analyses of FACS-sorted macrophages revealed that these subpopulatio

163 Global transcriptomic analysis of FACS-isolated adipocytes confirmed the presence of disti

164 RNA-sequencing analysis of FACS-purified Abcc8(-/-) beta-cells confirmed an increas

165 Transcriptome analysis of FACS-purified choroid plexus epithelial cells also predi

166 Analysis of FACS-purified MDSCs recovered from S. aureus biofilms re

167 We used microChIP and qPCR assays of FACS-purified cells to track changes in the epigenetic s

168 this study, we have compared the behavior of FACS-sorted CD56(dim)CD57(-)KIR(-)NKG2A(+) (NKG2A(+)) an

169 Following multiple iterations of FACS, cells and progeny virions were shown to display hi

170 Phenotyping by RT-PCR of FACS-sorted CD45RO(hi) T cells secreting IL-10 in respon

171 16S rDNA pyrotag sequencing of FACS-sorted cells indicated that PUT- and SPD-transformi

172 ) Tregs by showing functional superiority of FACS-purified CD137(+) Tregs in vitro compared with CD13

173 Cellular transfer of FACS-purified MCs from allogeneic donors into recipients

174 Transplantation of FACS-purified cells from each line resulted in DA neuron

175 In this study, FAIRE-seq on FACS-purified midline cells was performed and the midlin

176 The results from the online FACS-Chip-LCMS workflow starting from 5000 enriched cell

177 To assess the performance of the online FACS-Chip-LCMS workflow, 5000 fluorescent labeled cells

178 use and human prostate cells (either bulk or FACS-sorted single luminal and basal cells), metastatic

179 , combining sampling by limiting dilution or FACS, with imaging and high throughput at competitive co

180 ein is done by immunoassays such as ELISA or FACS that are susceptible to the sequence variation and

181 A dual polychromatic FACS-based biomarker-labeling system based on the IL4-eG

182 Here we present FACS studies of peripheral blood mononuclear cells colle

183 fic intracellular immunolabelling protocols, FACS separation of interphase and mitotic cells, includi

184 Here, we describe a rapid FACS purification strategy to simultaneously isolate pri

185 ce and fluorescence activated cell scanning (FACS).

186 Second, FACS enrichment of cells expressing nucleases linked to

187 alyses of fluorescent-activated cell sorted (FACS) DRG neurons confirmed that this 3'-UTR-extended va

188 ata from fluorescence-activated cell sorted (FACS) SCs and macrophages from wild-type and mutant nerv

189 Fluorescence-activated cell sorter (FACS) analyses revealed significantly lower numbers of C

190 Fluorescence-activated cell sorter (FACS) analysis of cell permeability showed the efficienc

191 sured by fluorescence-activated cell sorter (FACS) analysis.

192 SAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show that extended L

193 se (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and inflammation,

194 erential fluorescence-activated cell sorter (FACS)-based sorting strategy using an Env trimer possess

195 scence- and magnetic-activated cell sorting (FACS and MACS, respectively), to more specialized approa

196 Fluorescence-activated cell sorting (FACS) allows for rapid enumeration of metabolically acti

197 Fluorescence-activated cell sorting (FACS) analysis indicated significant increases in number

198 6), and fluorescence-activated cell sorting (FACS) analysis revealed only minimal cross-reactivity wi

199 Fluorescence activated cell sorting (FACS) analysis revealed that re-expression of miR-23b in

200 lot and fluorescence activated cell sorting (FACS) analysis revealed that silencing of Scrib reduced

201 ermore, fluorescence-activated cell sorting (FACS) and confocal microscopy assays demonstrate that st

202 s using fluorescence activated cell sorting (FACS) and control cellular functions with light sensitiv

203 nd used fluorescence-activated cell sorting (FACS) and fiber-optic array scanning technology (FAST) t

204 ilizing fluorescence-activated cell sorting (FACS) and high-throughput microscopy to identify L. mono

205 Fluorescence-activated cell sorting (FACS) and histopathology studies showed that the observe

206 ows for fluorescence-activated cell sorting (FACS) and single-cell deposition and thereby eliminates

207 Fluorescence-activated cell sorting (FACS) confirmed that donor- and host-specific levels of

208 gy with fluorescence-activated cell sorting (FACS) demonstrated that micropallet arrays offered enhan

209 fluidic fluorescence activated cell sorting (FACS) device that simultaneously performs on-demand, hig

210 without fluorescence-activated cell sorting (FACS) enrichment of haploid cells.

211 city of fluorescence activated cell sorting (FACS) for multicolor sorting to simultaneously screen fo

212 ines by fluorescence-activated cell sorting (FACS) form spheroids in Matrigel.

213 ated by fluorescence-activated cell sorting (FACS) from B1-EGFP mice, which express enhanced green fl

214 through fluorescence-activated cell sorting (FACS) greatly reduced teratoma-formation potential of he

215 ning by fluorescence activated cell sorting (FACS) is a common task in protein engineering and direct

216 ysis, a fluorescence-activated cell sorting (FACS) method was developed in this study to separate D.

217 tion by fluorescence-activated cell sorting (FACS) of c-kit(+) hematopoietic progenitor cells from mi

218 ed with fluorescence-activated cell sorting (FACS) of millions of aptamers expressed in Escherichia c

219 ants by fluorescence-activated cell sorting (FACS) of pooled mutants stained with the lipid-sensitive

220 ludes a fluorescence activated cell sorting (FACS) procedure that results in no perturbation of trans

221 ates by fluorescence-activated cell sorting (FACS) revealed significant macrophage and neutrophil inf

222 ed with fluorescence-activated cell sorting (FACS) to allow for efficient isolation of cell populatio

223 on, and fluorescence-activated cell sorting (FACS) to analyze intestinal epithelial cells isolated fr

224 ry with fluorescence-activated cell sorting (FACS) to enrich a transposon library for bacterial cells

225 hen use fluorescence-activated cell sorting (FACS) to individually measure the relative affinities of

226 use of fluorescence-activated cell sorting (FACS) to perform a high-throughput analysis of gut micro

227 We used fluorescence-activated cell sorting (FACS) to purify striatal neurons activated during cocain

228 mployed fluorescence-activated cell sorting (FACS) to sort for cells that are recognized by trimer cr

229 fied by fluorescence-activated cell sorting (FACS) using endogenous expression of enhanced green fluo

230 rted by fluorescence-activated cell sorting (FACS), and V(D)J transcripts are amplified by RT-PCR.

231 itional fluorescence activated cell sorting (FACS), are rare cell populations known to be elevated in

232 lity of fluorescence-activated cell sorting (FACS), can detect, quantify, and enrich bacteria with mo

233 grating fluorescence activated cell sorting (FACS), focused ultrasonication, microfluidics, immobiliz

234 ed with fluorescence-activated cell sorting (FACS), so that individual cells, including stem cells, c

235 nsitive fluorescence-activated cell sorting (FACS)-based assay, which allowed us to enumerate metasta

236 r and a fluorescence-activated cell sorting (FACS)-based transposon screen, we find that deletion of

237 ling of fluorescence-activated cell sorting (FACS)-purified murine PCs at various stages of their pos

238 Fluorescence-activated cell sorting (FACS)-purified Tbx18-expressing cells behaved as MSCs in

239 qPCR on Fluorescence Activated Cell Sorting (FACS)-sorted tnfa(+) and tnfa(-) macrophages showed that

240 ssed by fluorescence-activated cell sorting (FACS).

241 mice by fluorescence-activated cell sorting (FACS).

242 CR, and fluorescence-activated cell sorting (FACS).

243 t deficiency by flow-activated cell sorting (FACS).

244 ssed by fluorescence-activated cell sorting (FACS).

245 ained by fluorescent activated cell sorting (FACS).

246 d using fluorescence-activated cell sorting (FACS).

247 ry, and fluorescence-activated cell sorting (FACS).

248 rameter fluorescence-activated cell sorting (FACS).

249 ined by fluorescence activated cell sorting (FACS).

250 is with fluorescence-activated cell sorting (FACS).

251 scence- and magnetic-activated cell sorting (FACS/MACS).

252 -based (fluorescence-activated cell sorting; FACS) strategy to detect and quantify pyroptosis in vivo

253 t larval stage (L1) animals using a standard FACS system.

254 /CK(pos)/CD45(neg)/DAPI(pos)) and subsequent FACS sorting.

255 We show that FACS can be used for the precise identification of GFP-e

256 ssion in patients and murine models, and the FACS-based assay gives a highly accurate and quantitativ

257 trospective cohort analysis of data from the FACS (follow-up after colorectal cancer surgery) trial a

258 Subsequent application of the FACS and WGA protocols to two enrichment cultures contai

259 hat allows for the clonal expansion of these FACS-selected progenitors to neural stem cells (NSCs) in

260 HDC expression within these FACS-separated cells was found to coincide with other ma

261 Thus, FACS provides a method to isolate and enrich human sperm

262 t protein (eGFP) and cell surface markers to FACS-isolate DeltaSox2-eGFP(+) GBCs, Neurog1-eGFP(+) GBC

263 otoxic against GBM and K562, and, similar to FACS-sorted or gated KIR2DS2(-) NK cells, significantly

264 sed the objective, anatomically-based tools, FACS and DogFACS (Facial Action Coding Systems), to quan

265 ells, which include genetic lineage tracing, FACS purification, and robust in vitro clonogenic assays

266 ing the arrays and compared to a traditional FACS/Western Blotting-based approach.

267 nic mouse motor neurons isolated by a unique FACS technique.

268 Here we have used FACS with a representative antiplasminogen receptor-indu

269 We therefore used FACS sorting to show that, in mixed neuron glia co-cultu

270 nt cell populations within an organ, we used FACS to dissect GFP-marked cells from Arabidopsis roots

271 Using FACS and RT-PCR, we examined the phenotype of generated

272 Using FACS and transcriptional profiling, we examined the EYFP

273 Using FACS enrichment of cardiac progenitors in RBPJ and RBPJ/

274 Using FACS-isolated populations, we demonstrate that bronchioa

275 estingly, CD34(+)VEGR2(+) EPC analysis using FACS did not produce similar results (p = 0.94).

276 ce of RIF, and bacilli were enumerated using FACS.

277 riants with reduced affinity for c-FMS using FACS.

278 ibodies was concomitantly investigated using FACS analysis, and the results indicated excellent cell

279 ociated Thy1-eYFP neurons are isolated using FACS.

280 In this study, using FACS-based isolation and microarray analysis, we identif

281 ting outcomes and reducing effort when using FACS.

282 rofiling, immunohistochemistry and annexin V FACS staining.

283 m a fusion mixture as single-cell clones via FACS.

284 We demonstrated via FACS that EpCAM is expressed by human spermatogonia but

285 generated LECs, which were then isolated via FACS-sorting with LYVE-1 and PODOPLANIN.

286 sx-9-induced regulation of neurogenesis (via FACS and microarray of SGZ stem and progenitor cells) su

287 with human iPS cell culture and sorting via FACS will be of benefit for researchers performing this

288 We FACS-purified and transcriptionally profiled basal and l

289 n which HCs express GFP driven by Pou4f3, we FACS purified a population of HCs to analyze and compare

290 nhanced binding over the parental clone were FACS-sorted and cloned.

291 reparations of epithelium versus stroma were FACS analyzed for CD11c, CD11b, and CD103 expression.

292 Additionally, when FACS-isolated subpopulations of myeloid cells were trans

293 poxic murine model of PH in combination with FACS to quantify and isolate lung macrophages from two c

294 Combined with FACS, SPARK enabled 51 fold enrichment of PPI-positive o

295 c mice with GFP-expressing HCs, coupled with FACS sorting and tandem mass spectrometry, to define the

296 vitro differentiation system initiated with FACS-sorted adult ductal progenitor-like cells, and (v)

297 rs ( approximately 200) when integrated with FACS.

298 ination of droplet-generating machinery with FACS followed by next-generation sequencing and liquid c

299 (SHP2) domain-specific reporter, paired with FACS and RNA sequencing, we assayed the transcriptome of

300 of monosomy 7 populations was verified with FACS; and patient and donor cells were mixed to test for