ライフサイエンスコーパス: cell sorting

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

2 arpen through differential adhesion-mediated cell sorting.

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

4 odies and analyzed by fluorescence-activated cell sorting.

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

6 ing yeast display and fluorescence-activated cell sorting.

7 emokine receptors and fluorescence-activated cell sorting.

8 escent antibodies for fluorescence-activated cell sorting.

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

10 ic envelope probes for differential single B cell sorting.

11 ucer Bim enriched for cardiomyocytes without cell sorting.

12 d spermatogonia using fluorescence-activated cell sorting.

13 ls without the introduction of transgenes or cell sorting.

14 urface structures of different cells governs cell sorting.

15 andom mutagenesis and fluorescence-activated cell sorting.

16 -nucleotide polymorphism arrays after plasma cell sorting.

17 d by enrichment using fluorescence-activated cell sorting.

18 surface receptor expression and enriched by cell sorting.

19 lineage tracing, and fluorescence-activated cell sorting.

20 ronous cultures using fluorescence-activated cell sorting.

21 ogenic mesoderm with high efficiency without cell sorting.

22 n tree representation that can be applied to cell sorting.

23 ng both histology and fluorescence-activated cell sorting.

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

25 se 3 were measured by fluorescence-activated cell sorting.

26 g, can be isolated by fluorescence-activated cell sorting.

27 ells were purified by fluorescence-activated cell sorting.

28 vels were analyzed by fluorescence-activated cell sorting.

29 al flow cytometry and fluorescence-activated cell sorting.

30 by immunostaining and fluorescence-activated cell sorting.

31 l Trials Group 384 by fluorescence-activated cell sorting.

32 otaxis, contact-inhibition of locomotion and cell sorting.

33 ied by multiparameter fluorescence activated cell sorting.

34 sets were analyzed by fluorescence-activated cell sorting.

35 ls after isolation by fluorescence activated cell sorting.

36 d by laser microdissection, cell culture, or cell sorting.

37 was measured by using fluorescence-activated cell sorting.

38 fractions isolated by fluorescence-assisted cell sorting.

39 he previously proposed differential adhesion cell sorting.

40 by fluorescence in situ hybridization after cell sorting.

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

42 y quantitative PCR in fluorescence-activated cell sorting.

43 sterior tail bud, contributing to asymmetric cell sorting.

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

45 r histocompatibility complex multimer-guided cell sorting.

46 the requirement for genetic modifications or cell sorting.

47 r immunostaining in situ and flow cytometric cell sorting.

48 tory disease by using fluorescence-activated cell sorting.

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

50 ther variation of surface structures induces cell-sorting.

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

52 ested additionally by fluorescence-activated cell sorting, a live transfected cell-based assay.

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

54 lle in blood cells, we hypothesized that (i) cell sorting across microporous barriers is regulated by

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

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

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

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

59 ligands was tested by fluorescence-activated cell sorting analysis and by radioligand assay using (18

60 7) were quantified by fluorescence-activated cell sorting analysis and enzyme-linked immunosorbent as

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

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

63 Histology and fluorescence-activated cell sorting analysis of the bone marrow of DSS mice rev

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

65 Fluorescence activated cell sorting analysis was used to determine the phenotyp

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

67 Using multi-parameter fluorescence-activated cell sorting analysis, we quantified the cumulative freq

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

69 were characterized by fluorescence-activated cell sorting analysis.

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

71 autoradiography, and fluorescence-activated cell sorting analysis.

72 Here, we used flow-cytometry-based bacterial cell sorting and 16S sequencing to characterize taxa-spe

73 HSCs were purified by fluorescence-activated cell sorting and administered after hepatectomy.

74 is a frequently used method when it comes to cell sorting and analysis.

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

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

77 Fluorescence-activated cell sorting and cell binding assays for NMO-IgG are the

78 lin stimulation, using fluorescence-assisted cell sorting and cell surface biotinylation.

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

80 use of cardiomyocyte-restricted GFP enabled cell sorting and documentation of advanced structural an

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

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

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

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

85 e using intracellular fluorescence-activated cell sorting and immunoblot analyses of BCR-ABL signalin

86 Fluorescence activated cell sorting and immunofluorescence analysis revealed en

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

88 Physical cell separation techniques, such as cell sorting and laser-capture microdissection, can enri

89 A or AER, followed by fluorescence-activated cell sorting and low-cell H3K27ac ChIP-seq, we identifie

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

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

92 s explored through combining flow cytometric cell sorting and molecular techniques to determine the h

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

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

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

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

97 riched in PrE precursors in the ICM prior to cell sorting and prior to overt signs of cell polarisati

98 Cell sorting and proliferation assays performed after su

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

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

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

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

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

104 ll types and was shown here to contribute to cell sorting and survival in migration through constrain

105 collected from fresh surgical specimens via cell sorting and tested for oncogene mutations in a univ

106 ol subjects underwent fluorescence-activated cell sorting and then were cocultured with autologous ac

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

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

109 By combining cell sorting and whole-genome amplification (WGA), we ar

110 n in Arabidopsis (Arabidopsis thaliana) in a cell-sorting and transcriptomic approach to generate a l

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

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

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

114 xenografts proved consistent with A:B-based cell sorting, and intermediate A:B-enhanced tumor growth

115 does not require transgenic modification or cell sorting, and it has been replicated with multiple h

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

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

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

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

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

121 The cell sorting approach also enables the isolation of hapl

122 ld be retested with a fluorescence-activated cell sorting assay when available, particularly in the p

123 tested positive by a fluorescence-activated cell-sorting assay.

124 ected cell-based, and fluorescence-activated cell-sorting assays.

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

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

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

128 of bacterial surface structures can trigger cell sorting based on similar physical principles as in

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

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

131 Using a fluorescence-activated cell sorting-based strategy, we obtained primary Tfh and

132 ily members can account for the differential cell-sorting behavior.

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

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

135 Cell sorting by acoustic waves offers a means to separat

136 CCAST produces an optimal strategy for cell sorting by automating the selection of gating marke

137 et size by cell proliferation and alpha/beta cell sorting by differential activation of transient rec

138 bility that expands the application space of cell sorting by enabling sorting based on cellular infor

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

140 lude single-cell analysis and function-based cell sorting capabilities.

141 ethod was proven by thorough optimization of cell sorting, cell disruption, and PCR conditions.

142 Fluorescence-activated cell-sorting, cell-based, and enzyme-linked immunosorben

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

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

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 Cell-sorting experiments revealed a specific miR-24 enri

150 such as fluorescence- and magnetic-activated cell sorting (FACS and MACS, respectively), to more spec

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

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

153 Fluorescence activated cell sorting (FACS) analysis revealed that re-expression

154 Western blot and fluorescence activated cell sorting (FACS) analysis revealed that silencing of

155 Furthermore, fluorescence-activated cell sorting (FACS) and confocal microscopy assays demon

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

157 4(+) T cells and used fluorescence-activated cell sorting (FACS) and fiber-optic array scanning techn

158 etic screen utilizing fluorescence-activated cell sorting (FACS) and high-throughput microscopy to id

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

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

161 Fluorescence-activated cell sorting (FACS) confirmed that donor- and host-speci

162 this technology with fluorescence-activated cell sorting (FACS) demonstrated that micropallet arrays

163 of an acoustofluidic fluorescence activated cell sorting (FACS) device that simultaneously performs

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

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

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

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

168 better separation by fluorescence-activated cell sorting (FACS) of c-kit(+) hematopoietic progenitor

169 ophores, coupled with fluorescence-activated cell sorting (FACS) of millions of aptamers expressed in

170 high-lipid mutants by fluorescence-activated cell sorting (FACS) of pooled mutants stained with the l

171 l type and includes a fluorescence activated cell sorting (FACS) procedure that results in no perturb

172 ase was combined with fluorescence-activated cell sorting (FACS) to allow for efficient isolation of

173 e chain reaction, and fluorescence-activated cell sorting (FACS) to analyze intestinal epithelial cel

174 d flow cytometry with fluorescence-activated cell sorting (FACS) to enrich a transposon library for b

175 We then use fluorescence-activated cell sorting (FACS) to individually measure the relative

176 13) report the use of fluorescence-activated cell sorting (FACS) to perform a high-throughput analysi

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

178 lated and purified by fluorescence-activated cell sorting (FACS) using endogenous expression of enhan

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

180 rkflow by integrating fluorescence activated cell sorting (FACS), focused ultrasonication, microfluid

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

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

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

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

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

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

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

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

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

190 s, real-time PCR, and fluorescence-activated cell sorting (FACS).

191 model of HGprt deficiency by flow-activated cell sorting (FACS).

192 ction was assessed by fluorescence-activated cell sorting (FACS).

193 tive cells obtained by fluorescent activated cell sorting (FACS).

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

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

196 flow-cytometry-based (fluorescence-activated cell sorting; FACS) strategy to detect and quantify pyro

197 f DNA- or chromatin-binding proteins without cell sorting, fixation, or affinity purification.

198 ultracentrifugation, fluorescence-activated cell sorting flow cytometry and real-time reverse transc

199 hate and adenosine triphosphate coupled with cell sorting flow cytometry.

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

201 -specific integration fluorescence-activated cell sorting followed by sequencing (SIF-seq), an unbias

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

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

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

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

206 th retinoid-dependent fluorescence-activated cell sorting from eGFP-expressing rats and transplanted

207 use cells isolated by fluorescence activated cell sorting from human prostate tissue is an essential

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

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

210 Fluorescence-activated cell sorting from the skins of transgenic larvae, follow

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

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

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

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

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

216 st cavity are thought to be instrumental for cell sorting; however, the sequence of events and the me

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

218 gnetic enrichment and fluorescence-activated cell sorting (IE/FACS), a technique previously used for

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

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

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

222 e cell culture and the use of flow cytometry cell sorting in the HTP-derivation of hiPSCs.

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

224 Cell sorting is a central tool in life science research

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

226 Cell sorting is an important screening process in microb

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

228 This novel approach to cell sorting is therefore inexpensive, versatile, and ap

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

230 Even though CCAST is optimized for cell sorting, it can be applied for the identification a

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

232 low cost, and simplicity, this SFE-activated cell sorting method has potential in various application

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

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

235 e present a simple and cost-effective single-cell sorting method using two sequential photopolymeriza

236 We simulate cell sorting, microbial patterning and a bacterial syste

237 th an ochre mutation, fluorescence-activated cell sorting of a library of SUP4oc mutant yeast strains

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

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

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

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

242 ls were identified by fluorescence-activated cell sorting of myeloid versus lymphoid cell populations

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

244 Targeted cell sorting of peripheral blood from operationally tole

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

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

247 Upon fluorescence-activated cell sorting, only Prominin-1/Nestin double-positive cel

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

249 tes in 14 d from multiple hPSC lines without cell sorting or selection.

250 Our approach, PCR-activated cell sorting (PACS), uses TaqMan PCR to detect nucleic a

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

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

253 Fluorescence-activated cell sorting purification of human embryoid body cells d

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

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

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

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

258 te the utility of biotinylated chemokines as cell-sorting reagents.

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

260 Flow cytometry and cell sorting revealed that iNOS is highly expressed in n

261 Cell sorting revealed that the expression of stationary

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

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

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

265 Cell sorting showed that P1 hypomethylation reflects alt

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

267 approach to generate a lateral root-specific cell sorting SKP2B data set that represents the endogeno

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

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

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

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

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

273 population is isolated by magnetic-activated cell sorting technology and purity and cell numbers are

274 We introduce a new cell sorting technology that robustly sorts based on seq

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

276 hat rely on microdissection, cell panning or cell sorting, the TRAP methodology bypasses the need for

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

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

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

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

281 We used fluorescence-activated cell sorting to isolate each cell type for gene expressi

282 d in conjunction with fluorescence-activated cell sorting to isolate neurosphere-forming neural stem

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

284 By using cell sorting to separate silenced and unsilenced cells,

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

286 oninfected Tregs were isolated by flow-based cell-sorting to investigate Treg suppressive capacity an

287 plet digital PCR (ddPCR) and combine it with cell sorting using flow cytometry.

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

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

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

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

292 By employing fluorescence-activated cell sorting, we have generated gene expression profiles

293 Using fluorescence-activated cell sorting, we identified alveolar macrophages as the

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

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

296 Flow cytometry and cell sorting were used to identify, isolate, and quantit

297 Cell sorting, whereby a heterogeneous cell mixture organ

298 ve sorting step in eDAR, which provided fast cell sorting with an improved reproducibility and stabil

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

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