ライフサイエンスコーパス: cell sorting

1 using flow cytometry (fluorescence-activated cell sorting).

2 on in B cell (sub)populations, without prior cell sorting.

3 by using an IL10 cytokine-capture assay and cell sorting.

4 e latter coupled with fluorescence-activated cell sorting.

5 ifferences in intercellular adhesion mediate cell sorting.

6 arpen through differential adhesion-mediated cell sorting.

7 ogenic mesoderm with high efficiency without cell sorting.

8 he previously proposed differential adhesion cell sorting.

9 tory disease by using fluorescence-activated cell sorting.

10 surface receptor expression and enriched by cell sorting.

11 iod of 16 weeks using fluorescence-activated cell sorting.

12 digestion followed by fluorescence-activated cell sorting.

13 by fluorescence in situ hybridization after cell sorting.

14 RNA isolated from CD154(+) cells purified by cell sorting.

15 y quantitative PCR in fluorescence-activated cell sorting.

16 sterior tail bud, contributing to asymmetric cell sorting.

17 HDR edited cells by a factor of two through cell sorting.

18 r histocompatibility complex multimer-guided cell sorting.

19 the requirement for genetic modifications or cell sorting.

20 r immunostaining in situ and flow cytometric cell sorting.

21 ession is a classical mechanism for in vitro cell sorting.

22 nd G2 arrest by using fluorescence-activated cell sorting.

23 odies and analyzed by fluorescence-activated cell sorting.

24 esign resurfaced gp120 antigens for single-B-cell sorting.

25 ing yeast display and fluorescence-activated cell sorting.

26 emokine receptors and fluorescence-activated cell sorting.

27 escent antibodies for fluorescence-activated cell sorting.

28 w cytometry was used for T-cell analysis and cell sorting.

29 ic envelope probes for differential single B cell sorting.

30 ucer Bim enriched for cardiomyocytes without cell sorting.

31 d spermatogonia using fluorescence-activated cell sorting.

32 ls without the introduction of transgenes or cell sorting.

33 urface structures of different cells governs cell sorting.

34 andom mutagenesis and fluorescence-activated cell sorting.

35 cells was assessed by fluorescence-activated cell sorting.

36 igh-speed and high-throughput image-assisted cell sorting.

37 sing only sequencing read alignments without cell sorting.

38 natures associated with HSC activity without cell sorting.

39 individuals by fluorescence-activated single-cell sorting.

40 te mediated by differential E-cadherin based cell sorting.

41 ed by fluorescence- and flow cytometry-based cell sorting.

42 ther variation of surface structures induces cell-sorting.

43 Western blotting; 3) fluorescence-activated cell sorting; 4) immunohistochemistry; 5) immunofluoresc

44 /survival, as well as fluorescence-activated cell sorting according to fluorescent reporter phenotype

45 a sheathless acoustic fluorescence activated cell sorting (aFACS) system by combining elasto-inertial

46 y grouped by means of fluorescence-activated cell sorting allowed additional subclassification based

47 nfocal microscopy and fluorescence-activated cell sorting analyses showed transplanted HSPCs emigrate

48 Microscopy and fluorescence-activated cell sorting analyses suggest that most BAs are mononucl

49 of cell-surface properties as shown by cell-cell sorting analyses.

50 ated by histology and fluorescence-activated cell sorting analyses.

51 ignal was detected by fluorescence-activated cell sorting analysis in the CD90(+) fibroblasts.

52 Fluorescence-activated cell sorting analysis of monolayers and PIs revealed a h

53 man fibroblasts, with fluorescence-activated cell sorting analysis revealing that a small percentage

54 Fluorescence-activated cell sorting analysis was performed on biopsy samples 1

55 By using fluorescence-activated cell sorting analysis, fibrocytes (CD45(+) and collagen

56 e-lapse microscopy or fluorescence-activated cell sorting analysis.

57 were characterized by fluorescence-activated cell sorting analysis.

58 functional as well as fluorescent-activated cell sorting analysis.

59 nostaining, and FACS (fluorescence-activated cell sorting) analysis (CD45(+)CD11b(+)Ly6G(-)CD64(+)F4/

60 used flow cytometric (fluorescence-activated cell sorting) analysis to quantify TCR-Valpha7.2-express

61 ng combined bacterial fluorescence-activated cell sorting and 16S rRNA sequencing.

62 ell-to-cell variability using flow cytometry cell sorting and a microfluidics system for live imaging

63 omato mice by means of fluorescent activated cell sorting and analyzed their miRNAs using NanoStrings

64 ental methods of accomplishing this, such as cell sorting and baiting; however they are time consumin

65 Fluorescence-activated cell sorting and cDNA-microarray analyses revealed that

66 A combination of flow cytometric cell sorting and deep sequencing of the 16S rDNA gene wa

67 ells were assessed by fluorescence-activated cell sorting and degranulation, respectively.

68 rescence-activated cell sorting and magnetic cell sorting and expanded in vitro.

69 tors were purified by fluorescence-activated cell sorting and expression of Fas and Fas-induced apopt

70 Multicolor flow cytometry, cell sorting and growth inhibition assays were employed

71 blood and spleens for fluorescence-activated cell sorting and hearts for 2,3,5-triphenyltetrazolium c

72 By integrating WGA-X with calibrated index-cell sorting and high-throughput genomic sequencing, we

73 n be a label-free alternative to traditional cell sorting and identification.

74 The advent of image-activated cell sorting and imaging-based cell picking has advanced

75 This study utilised cell sorting and immunohistochemistry to identify a phen

76 ach of high-throughput screening, flow-based cell sorting and in vivo transplantation to isolate mark

77 equired for Eph receptor B2 (EphB2)-mediated cell sorting and is conserved among multiple Eph recepto

78 isolated by means of fluorescence-activated cell sorting and magnetic cell sorting and expanded in v

79 icrofluidic devices for applications such as cell sorting and micromixing.

80 cell stable isotope probing, Raman-activated cell sorting and mini-metagenomics.

81 analyzed using index fluorescence-activated cell sorting and parallel targeted transcriptional profi

82 o 20 months in vitro using immunopanning and cell sorting and performed high-depth bulk and single-ce

83 tide library members for each specimen using cell sorting and performing NGS.

84 positively selected using magnetic-activated cell sorting and plated in endothelial-specific growth c

85 In addition, fluorescence-activated cell sorting and polymerase chain reaction analysis reve

86 the lysosome compartment that is amenable to cell sorting and pooled screens.

87 Cell sorting and proliferation assays performed after su

88 The combined fluorescence-activated cell sorting and PROMIDISalpha analyses revealed specifi

89 ion, and intracellular staining coupled with cell sorting and reversal of the cross-links to allow RN

90 tools, combined with fluorescence-activated cell sorting and RNA sequencing, we have separated four

91 y sleep regulators, we combined fluorescence cell sorting and RNA-seq in hcrt:EGFP zebrafish.

92 Through cell sorting and selection according to insulin promoter

93 en the growth of high-throughput sequencing, cell sorting and single cell biology.

94 ic participants, we used allergen-specific T-cell sorting and single-cell gene expression to trace th

95 ing positive selection by magnetic-activated cell sorting and single-cell low-coverage whole-genome s

96 High costs and technical limitations of cell sorting and single-cell techniques currently restri

97 isolated by means of fluorescence-activated cell sorting and studied for Il5 and Il13 mRNA expressio

98 and nano-particles with applications such as cell sorting and studying cell communications.

99 ns were identified using fluorescent-labeled cell sorting and transplantation into immunodeficient NO

100 ions were assessed by fluorescence-activated cell sorting and viral-mediated overexpression in Cre-de

101 Fluorescence activated cell sorting and Western blot were performed in patient-

102 aging, bright-field imaging), cell focusing, cell sorting, and deep learning on a hybrid software-har

103 ct imaging of the accessible genome in situ, cell sorting, and deep sequencing to reveal the identity

104 ptide substrates, bacterial surface-display, cell sorting, and deep sequencing, we have defined the s

105 erase chain reaction, fluorescence-activated cell sorting, and electrophysiological measurements.

106 ies for contamination prevention, rheotactic cell sorting, and microswimmer navigation in complex flo

107 assay, ELISA, UniCAP, fluorescence-activated cell sorting, and PCR.

108 e panel of Abs in multicolor flow cytometry, cell sorting, and RNA sequencing we identified and chara

109 l techniques, such as fluorescence-activated cell sorting, and single cell RNA sequencing are expensi

110 bpopulations by using fluorescence-activated cell sorting, and subjected them to next-generation sequ

111 By combining flow cytometry, cell-sorting, and single-cell clonogenic assays, we iden

112 S cells isolated with fluorescence-activated cell sorting, Ano1 expression was 26.5-fold greater in I

113 is a method that uses fluorescence-activated cell sorting, antibiotic tolerance assays, and next gene

114 s the general minimum size for a majority of cell sorting applications.

115 The cell sorting approach also enables the isolation of hapl

116 Here, using a single-cell sorting approach combining tubulin-specific labelli

117 ign and optimization of this Raman-activated cell-sorting approach, illustrate its operation with fou

118 Cell-sorting approaches, to select for correctly pattern

119 cells, we developed a fluorescence-activated cell sorting assay based on fluorescence ubiquitination

120 measured by M1-isoform-fluorescent-activated-cell-sorting assays.

121 ned infarct size, and fluorescence-activated cell sorting assessed cell composition.

122 atic dissociation and fluorescence-activated cell sorting at day 3 following surgery.

123 hniques by translating expert knowledge into cell sorting automation via machine learning algorithms.

124 Using fluorescence-activated cell sorting, B-cell subsets were analyzed.

125 Cell sorting based on the LSC marker GPR56 allowed isola

126 ed a high-throughput, fluorescence-activated cell sorting-based green fluorescent protein-LC3 detecti

127 ing an intersectional fluorescence-activated cell sorting-based strategy, we identified five distinct

128 Our cell sorting-based study of the epidermal cell layer tra

129 ate the mechanisms responsible for classical cell-sorting behaviors, cell intercalation in proliferat

130 ould be isolated with fluorescence-activated cell sorting (BONCAT-FACS) for subsequent genetic analys

131 Cleft-like boundaries represent a type of cell sorting boundary characterized by the presence of a

132 c E-cadherin-based cell-cell adhesion induce cell sorting, but not ECD.

133 Here we demonstrate Raman image-activated cell sorting by directly probing chemically specific int

134 Cell sorting by flow cytometry provided the purest popul

135 Using cell sorting by flow cytometry, we assessed longitudinal

136 nidirectional EphB kinase signaling leads to cell sorting by the Rho kinase-dependent generation of a

137 The system is based on a microfluidic cell sorting chip connected serially to an unanesthetize

138 Fluorescence-activated cell sorting combined with MBs was performed to sort car

139 We used cell sorting combined with RNA sequencing to isolate ste

140 ignalling proteins in Escherichia coli using cell sorting coupled to deep sequencing to analyse large

141 pecific profiling, the technique requires no cell-sorting, cross-linking or antisera, and binding pro

142 A wide range of microfluidic cell-sorting devices has emerged in recent years, based

143 In this study, single cell sorting, DNA sequencing, qPCR and CARD-FISH assays

144 Histological, fluorescence-activated cell sorting, dot blot analysis, and in vitro/ex vivo st

145 However, what drives cell sorting during regeneration of Hydra from cell aggr

146 Fluorescence-activated cell sorting-enriched CD133(-)/EpCAM(-) (double negative

147 ) nickase vector with fluorescence-activated cell sorting enrichment followed by high-throughput geno

148 Cell sorting experiments showed that although healthy hu

149 Fluorescence-activated cell sorting (FACS) allows for rapid enumeration of meta

150 Fluorescence-activated cell sorting (FACS) analysis indicated significant incre

151 n was validated using fluorescence-activated cell sorting (FACS) analysis of inflammatory marker expr

152 tion-PCR (RT-PCR) and fluorescence-activated cell sorting (FACS) analysis were used to investigate ly

153 Fluorescence-activated cell sorting (FACS) and confocal microscopy showed that

154 separate cells using fluorescence activated cell sorting (FACS) and control cellular functions with

155 4(+) T cells and used fluorescence-activated cell sorting (FACS) and fiber-optic array scanning techn

156 We use fluorescence-activated cell sorting (FACS) and genomic sequencing to assign tax

157 Fluorescence-activated cell sorting (FACS) and histopathology studies showed th

158 sorting methods like fluorescence-activated cell sorting (FACS) and magnetic-activated cell sorting

159 ental methods such as Fluorescence Activated Cell Sorting (FACS) and multiplex immunofluorescence.

160 This allows for fluorescence-activated cell sorting (FACS) and single-cell deposition and there

161 Fluorescence-activated cell sorting (FACS) and subsequent microarray analysis o

162 st five weeks without fluorescence-activated cell sorting (FACS) enrichment of haploid cells.

163 rness the capacity of fluorescence activated cell sorting (FACS) for multicolor sorting to simultaneo

164 d the capabilities of fluorescence-activated cell sorting (FACS) from fluorescence intensity profiles

165 roughput screening by fluorescence activated cell sorting (FACS) is a common task in protein engineer

166 e genomic analysis, a fluorescence-activated cell sorting (FACS) method was developed in this study t

167 hils were purified by fluorescence-activated cell sorting (FACS) protocol resulting in >= 99% purity

168 ve cells recovered by fluorescence-activated cell sorting (FACS) reveals that the phylogenetic compos

169 We employed fluorescence-activated cell sorting (FACS) to sort for cells that are recognize

170 ng cell type, we used fluorescence-activated cell sorting (FACS) to sort the glial and vascular cells

171 quantify by combining fluorescence-activated cell sorting (FACS) with annexin V staining.

172 henotypic analysis by fluorescence-activated cell sorting (FACS), a CRISPR-Cas9-mediated approach was

173 single-cell-sorted by fluorescence-activated cell sorting (FACS), and V(D)J transcripts are amplified

174 CR, western blotting, fluorescence-activated cell sorting (FACS), enzyme-linked immunosorbent assay,

175 mlessly combined with fluorescence-activated cell sorting (FACS), so that individual cells, including

176 ed a highly sensitive fluorescence-activated cell sorting (FACS)-based assay, which allowed us to enu

177 escent reporter and a fluorescence-activated cell sorting (FACS)-based transposon screen, we find tha

178 pression profiling of fluorescence-activated cell sorting (FACS)-purified murine PCs at various stage

179 Fluorescence-activated cell sorting (FACS)-purified Tbx18-expressing cells beha

180 RT-qPCR on Fluorescence Activated Cell Sorting (FACS)-sorted tnfa(+) and tnfa(-) macrophag

181 which were sorted by fluorescence activated cell sorting (FACS).

182 loid as determined by fluorescence activated cell sorting (FACS).

183 reporters purified by fluorescence activated cell sorting (FACS).

184 oughput screening via fluorescence-activated cell sorting (FACS).

185 rich E. gracilis with fluorescence-activated cell sorting (FACS).

186 cell size assessed by fluorescence-activated cell sorting (FACS).

187 cles of adult mice by fluorescence-activated cell sorting (FACS).

188 d in combination with fluorescence-activated cell sorting (FACS).

189 , and then isolated by fluorescent activated cell sorting (FACS).

190 and by fluorescence- and magnetic-activated cell sorting (FACS/MACS).

191 ing yeast display and fluorescence-activated cell sorting followed by deep sequencing.

192 e isotope tracing and fluorescence-activated cell sorting followed by liquid chromatography-high-reso

193 ) were isolated using fluorescence activated cell sorting for bulk RNA sequencing (RNA-Seq).

194 s niche and the potential of Raman-activated cell sorting for identifying key players in targeted pro

195 O4(+) OPCs can be isolated by cell sorting for myelination studies, or they can be ter

196 kidney homogenates by fluorescence-activated cell sorting for whole genome microarray analysis.

197 logies, namely metaphase spread analysis and cell sorting, for the identification of haploid human ce

198 ells were isolated by fluorescence-activated cell sorting from disaggregated late blastula- and gastr

199 ve cells suitable for fluorescence-activated cell sorting from human islets engrafted in mice.

200 this platform will help expand the basis of cell sorting from mainly protein biomarkers to nucleic a

201 lei were separated by fluorescence-activated cell sorting from postmortem DLPFC of 36 PDS and 26 age-

202 NAb responses, we performed single memory B cell sorting from the peripheral blood of a rhesus macaq

203 s study utilised in vitro functional assays, cell sorting, gene expression and immunohistochemistry t

204 Here we investigate the efficacy of cell sorting, gene expression plasticity, and their comb

205 Although cell sorting has been an anticipated strategy, its appli

206 ted by next-generation sequencing and single-cell sorting, has identified numerous genomic loci that

207 Our methodology utilizes cell sorting, high-throughput sequencing and statistical

208 turating mutagenesis, fluorescence-activated cell sorting, high-throughput sequencing, and mutual inf

209 In silico cell sorting identified macrophages/microglia, CD4(+) T

210 Intelligent image-activated cell sorting (iIACS) is a machine-intelligence technolog

211 terfacial tensions are sufficient to explain cell sorting in aggregates of Hydra cells.

212 owerful tool for high-throughput, size-based cell sorting in diverse biomedical applications.

213 question of the physical mechanisms driving cell sorting in Hydra cell aggregates.

214 analysis from ex vivo fluorescence-activated cell sorting in MDM4-deficient retinal ganglion cells id

215 c(high) monocytes via fluorescence-activated cell sorting in the blood of susceptible and resilient m

216 ful model system for carrying out studies of cell sorting in three dimensions, because of its unique

217 Retinal endothelial cell sorting in wild type C57BL/6 mice was validated by

218 sts were evaluated by fluorescence-activated cell sorting; interleukin 10 (IL-10) and IL-18 and solub

219 Improving microfluidic size-based particle/cell sorting is a challenge to better address the need f

220 d morphogen transport together with directed cell sorting is a potentially favored mechanism to estab

221 oblast protoplasts by fluorescence-activated cell sorting is established, taking advantage of the dis

222 uantitative RT-PCR on flourescence-activated cell sorting-isolated L- and control cells and was enric

223 sample concentration, fluorescence-activated cell sorting, label-free cell/particle separation, and f

224 d cell sorting (FACS) and magnetic-activated cell sorting (MACS) are underreported.

225 nd optimize a protocol of magnetic-activated cell sorting (MACS) to separate them effectively both as

226 sion molecule (EpCAM) via magnetic-activated cell sorting (MACS).

227 terogeneous tumor cell subpopulation using a cell sorting method (sedimentation field flow fractionat

228 otypes, we employed a fluorescence activated cell sorting method to isolate keratinocytes, dendritic

229 They have been isolated by a live-cell sorting method using the germ cell marker DDX4, whi

230 Cell sorting methods are required in numerous healthcare

231 he procedure involves fluorescence-activated cell sorting of a library, deep sequencing of sorted poo

232 titative screening by fluorescence-activated cell sorting of an error-prone library based on fine dis

233 Fluorescence-activated cell sorting of CD24 high versus low cells prospectively

234 Upon fluorescence-activated cell sorting of each neutrophil subset, T-cell prolifera

235 Here, we applied fluorescence-activated cell sorting of green fluorescent protein (GFP)-marked c

236 Cell sorting of medium spiny neurons (MSNs) in indirect

237 i was performed after fluorescence-activated cell sorting of oligodendrocyte and neuronal nuclei.

238 Targeted cell sorting of peripheral blood from operationally tole

239 resents a fast and versatile tool for single-cell sorting of peripheral plasmablasts, streamlining su

240 interacting cells (PIC-seq), which combines cell sorting of physically interacting cells (PICs) with

241 We performed cell sorting of the diagnostic material and assessed the

242 transcriptomics without laborious FACS-based cell sorting or biochemical isolation of the labeled tra

243 d-derived T lymphocytes enriched for CCR9 by cell sorting or culturing with all-trans retinoic acid,

244 -cell suspensions for fluorescence-activated cell sorting or single-cell RNA sequencing analysis.

245 er the cell composition quantification using cell-sorting or single-cell technologies.

246 , establishing that protoplast isolation and cell sorting procedures did not greatly alter endogenous

247 Here, we developed a novel cell-sorting protocol that allows the purification to ho

248 lly defined medium; (3) a magnetic-activated cell sorting purification protocol for rapid and effecti

249 We utilized cell sorting quantitative real-time polymerase chain rea

250 and genotypes of the MA-ARB, Raman-activated cell sorting (RACS) was used to sort MA-ARB from human g

251 nd high-throughput biological assays such as cell sorting, rare cell detection, and imaging flow cyto

252 by single-molecule in situ hybridization and cell sorting, rare cells positive for Lgr6 expression in

253 parasites sorted with fluorescence-activated cell sorting resumed growth at 10,000/well whereas RH-ne

254 Cell sorting revealed that the expression of stationary

255 tion assays following fluorescence-activated cell sorting revealed that the high-ROS pollen germinate

256 Fluorescence-activated cell sorting, RNA sequencing, quantitative real-time PCR

257 We developed a cell-sorting scheme to resolve myeloid (My), erythroid (

258 MSC) derived from single clones and live RNA cell sorting showed a direct correlation between DDIT4 a

259 were corroborated by fluorescence activated cell sorting showing a 48% yield of CD31(+)/VE-cadherin(

260 e use of fluorescence labels has enabled new cell-sorting strategies and given new insights into deve

261 a Chinese donor by antigen-specific single B cell sorting, structural and functional studies, and lon

262 Finally, FC cell sorting studies confirm that FC-defined populations

263 llenging for existing fluorescence-activated cell sorting systems.

264 memory T cells using fluorescence-activated cell sorting, TCRbeta sequencing, and RNA-Seq, in reacti

265 s a droplet microfluidic, image-based single-cell sorting technique that is flexible and programmable

266 Using a cell sorting technique, we demonstrate that GFRalpha3 ex

267 ive confocal microscopy, flow cytometry, and cell sorting techniques, we investigated organoid patter

268 Recent advances in cell-sorting techniques and single-cell technologies now

269 devices, and it establishes new insights to cell sorting technology and artificial blood vessel fabr

270 sion that is sorted using magnetic-activated cell sorting technology.

271 tuated sorting are widespread techniques for cell sorting, there is intense research on label-free te

272 The experimental protocol, from cell sorting to a ready-to-sequence library, takes 2-3 d

273 transposon insertion library in tandem with cell sorting to assess genome-wide impact of gene deleti

274 l physiology, we used fluorescence-activated cell sorting to enrich a library of hundreds of Escheric

275 used 16S rRNA gene sequencing and bacterial cell sorting to evaluate gut microbiota composition and

276 led cells isolated by fluorescence-activated cell sorting to generate cell-type-specific transcriptom

277 ay protocol that utilises magnetic activated cell sorting to generate enriched population of RGCs via

278 We used fluorescence-activated cell sorting to isolate reinstatement-activated Fos-posi

279 pure populations of cells as flow cytometry cell sorting to minimize and control for CD4(+) T-cell c

280 light the importance of using flow cytometry cell sorting to minimize contamination by CD4(+) T cells

281 anics in pattern formation, from protein and cell sorting to the generation of tissue shape.

282 holds promise for applications ranging from cell sorting to three-dimensional (3D) printing and tiss

283 For single cells, sorting typically requires 2-4 h and can be perfo

284 ference and makes this pipeline suitable for cell sorting via deep learning.

285 or immunoblot assays; fluorescence-activated cell sorting was performed to identify immune cells.

286 Cell sorting was used to separate chondrocytes based on

287 representation of cellular metabolism after cell sorting, we benchmarked sorted extraction against d

288 Next, using fluorescence-activated cell sorting, we compared gene expression in Fos-positiv

289 Using index and transcriptional single-cell sorting, we comprehensively map all adipose tissue

290 Using transcriptional single-cell sorting, we comprehensively map all immune populati

291 using enrichments and fluorescence-activated cell sorting, we demonstrated successful cultivation of

292 Using multicolor flow cytometry and cell sorting, we observed an accumulation of CD25(high)C

293 Using serial dilutions and flow-based single-cell sorting, we show that viral proteins produced by a

294 ic bead selection methods and flow cytometry cell sorting were compared for their capacity to yield p

295 Cell sorting, whereby a heterogeneous cell mixture organ

296 4.5 embryo digestion, fluorescence-activated cell sorting, whole-genome sequencing and data analysis.

297 CS device is demonstrated to achieve two-way cell sorting with high purity, biocompatibility, and bio

298 ty gradient centrifugation or antibody-based cell sorting with molecular labels of cell viability.

299 ombining chronic demyelination paradigms and cell sorting with RNA sequencing and lipidomics, we find

300 this study, we show that only flow cytometry cell sorting yields a highly pure population of monocyte