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1 pression were measured using flow cytometry (fluorescence-activated cell sorting).
2 mphoid organs and purified by multiparameter fluorescence activated cell sorting.
3 ression of injected cells after isolation by fluorescence activated cell sorting.
4 ated from the hearts of PG(WT) and PG(TR) by fluorescence activated cell sorting.
5 macrophages by using confocal microscopy and fluorescence activated cell sorting.
6 iciently labeled LAP clones were isolated by fluorescence activated cell sorting.
7 rin-exacerbated respiratory disease by using fluorescence-activated cell sorting.
8 cell injury models using both histology and fluorescence-activated cell sorting.
9 i-67, and cleaved caspase 3 were measured by fluorescence-activated cell sorting.
10 site for genomic editing, can be isolated by fluorescence-activated cell sorting.
11 gammadeltaT cells were purified by fluorescence-activated cell sorting.
12 HSC and CD133 MP levels were analyzed by fluorescence-activated cell sorting.
13 imitations of traditional flow cytometry and fluorescence-activated cell sorting.
14 in calcified arteries by immunostaining and fluorescence-activated cell sorting.
15 ed in the Adult Clinical Trials Group 384 by fluorescence-activated cell sorting.
16 a CD133 and CD39 MP subsets were analyzed by fluorescence-activated cell sorting.
17 ha2 protein expression was measured by using fluorescence-activated cell sorting.
18 OPCs, which could be further purified using fluorescence-activated cell sorting.
19 levels were examined by quantitative PCR in fluorescence-activated cell sorting.
20 d), and B cells (BC4d) were determined using fluorescence-activated cell sorting.
21 ty, allowing the isolation of these cells by fluorescence-activated cell sorting.
22 Transduced cells underwent fluorescence-activated cell sorting.
23 xpression was determined by high-dimensional fluorescence-activated cell sorting.
24 expression of MHC class II/CD80 measured by fluorescence-activated cell sorting.
25 ry molecules (CD80 and CD86) was measured by fluorescence-activated cell sorting.
26 th factor receptor (p75) in conjunction with fluorescence-activated cell sorting.
27 otent cells and committed neural cells using fluorescence-activated cell sorting.
28 ry clones are selected by multiple rounds of fluorescence-activated cell sorting.
29 isolation of the associated subpopulation by fluorescence-activated cell sorting.
30 to the mean fluorescence of GFP measured by fluorescence-activated cell sorting.
31 k of DNA replication, and G2 arrest by using fluorescence-activated cell sorting.
32 D4, Gr1, and Mac1 antibodies and analyzed by fluorescence-activated cell sorting.
33 y directed evolution using yeast display and fluorescence-activated cell sorting.
34 sing combinations of chemokine receptors and fluorescence-activated cell sorting.
35 were labeled with fluorescent antibodies for fluorescence-activated cell sorting.
36 rifying undifferentiated spermatogonia using fluorescence-activated cell sorting.
37 matured by sequential random mutagenesis and fluorescence-activated cell sorting.
38 ic procedure over a period of 16 weeks using fluorescence-activated cell sorting.
39 inergic neurons followed by enrichment using fluorescence-activated cell sorting.
40 nd electron microscopy, lineage tracing, and fluorescence-activated cell sorting.
41 e generated from asynchronous cultures using fluorescence-activated cell sorting.
42 rase chain reaction; 2) Western blotting; 3) fluorescence-activated cell sorting; 4) immunohistochemi
43 ropositive cases were tested additionally by fluorescence-activated cell sorting, a live transfected
44 ns based on cell growth/survival, as well as fluorescence-activated cell sorting according to fluores
45 s with CVID homogenously grouped by means of fluorescence-activated cell sorting allowed additional s
46 e or intracellular staining and multi-colour fluorescence activated cell sorting alone or in combinat
53 ro specific binding of ligands was tested by fluorescence-activated cell sorting analysis and by radi
54 nt interleukin-17 (IL-17) were quantified by fluorescence-activated cell sorting analysis and enzyme-
55 plant or OVA-B16F10 tumor could be traced by fluorescence-activated cell sorting analysis as effector
57 ding was assessed by cell binding assays and fluorescence-activated cell sorting analysis in a variet
58 fluorescence protein signal was detected by fluorescence-activated cell sorting analysis in the CD90
61 We used a multiparameter approach, including fluorescence-activated cell sorting analysis of cell-sur
64 der protein led to apoptosis, as assessed by fluorescence-activated cell sorting analysis of propidiu
69 CSCs can be isolated from L2G85 mice, and fluorescence-activated cell sorting analysis showed expr
73 l viability as a marker of proliferation and fluorescence-activated cell sorting analysis was used to
76 gammaH2A.X assay, cell cycle progression by fluorescence-activated cell sorting analysis, and PARP-1
77 assays, a nuclear fragmentation assay, using fluorescence-activated cell sorting analysis, and time-l
87 Bone marrow-derived HSCs were purified by fluorescence-activated cell sorting and administered aft
89 of microparticles by CACs was determined by fluorescence-activated cell sorting and by fluorescence
92 m differentiated cultures were purified with fluorescence-activated cell sorting and characterized.
93 nd healthy control subjects were isolated by fluorescence-activated cell sorting and compared for the
94 t day 21, we harvested blood and spleens for fluorescence-activated cell sorting and hearts for 2,3,5
95 wing acute drug exposure using intracellular fluorescence-activated cell sorting and immunoblot analy
96 ubset of primary HSCs was demonstrated using fluorescence-activated cell sorting and immunofluorescen
97 h and without asthma was examined by RT-PCR, fluorescence-activated cell sorting and immunohistochemi
98 l model for beta2AR expression, we performed fluorescence-activated cell sorting and isolated cells t
99 uorescently mark the ZPA or AER, followed by fluorescence-activated cell sorting and low-cell H3K27ac
100 LC2s and TH2 cells were isolated by means of fluorescence-activated cell sorting and magnetic cell so
101 Direct comparisons with cell isolation by fluorescence-activated cell sorting and magnetic-bead-ba
102 , single MEP cells were analyzed using index fluorescence-activated cell sorting and parallel targete
104 vestigated at the protein and gene levels by fluorescence-activated cell sorting and real-time revers
108 ined from healthy control subjects underwent fluorescence-activated cell sorting and then were cocult
109 xp3GFP+ CBir1-Tg Treg cells were isolated by fluorescence-activated cell sorting and transferred into
110 ell type-specific functions were assessed by fluorescence-activated cell sorting and viral-mediated o
113 followed by mass spectrometry, phospho-flow fluorescence-activated cell sorting, and antibody arrays
114 by means of RT-PCR, Western immunoblotting, fluorescence-activated cell sorting, and double-immunofl
115 try, quantitative polymerase chain reaction, fluorescence-activated cell sorting, and electrophysiolo
116 tterns were examined by immunocytochemistry, fluorescence-activated cell sorting, and enzyme-linked i
117 fluorescent labeling, immunohistochemistry, fluorescence-activated cell sorting, and quantitative PC
118 ions, isolated these subpopulations by using fluorescence-activated cell sorting, and subjected them
119 lls from mouse intestine were isolated using fluorescence-activated cell sorting, and transcriptional
121 ersister-FACSeq, which is a method that uses fluorescence-activated cell sorting, antibiotic toleranc
122 nd to be negative, should be retested with a fluorescence-activated cell sorting assay when available
127 loride staining determined infarct size, and fluorescence-activated cell sorting assessed cell compos
128 were isolated by enzymatic dissociation and fluorescence-activated cell sorting at day 3 following s
130 gion of late embryonic mice were purified by fluorescence-activated cell sorting based on their expre
135 , high-throughput and quantitative two-color fluorescence-activated cell sorting-based screening stra
138 BONCAT-labeled cells could be isolated with fluorescence-activated cell sorting (BONCAT-FACS) for su
141 tological and biochemical analyses following fluorescence-activated cell sorting demonstrate a positi
143 an All-in-One Cas9(D10A) nickase vector with fluorescence-activated cell sorting enrichment followed
144 marrow Meis1 mRNA and significant defects in fluorescence-activated cell sorting-enumerated monocytes
147 me (live cell imaging), separate cells using fluorescence activated cell sorting (FACS) and control c
148 present the development of an acoustofluidic fluorescence activated cell sorting (FACS) device that s
149 In this work, we harness the capacity of fluorescence activated cell sorting (FACS) for multicolo
151 he embryo to define cell type and includes a fluorescence activated cell sorting (FACS) procedure tha
153 hocytes, cell separation is best achieved by fluorescence activated cell sorting (FACS), although mag
154 defined as CD34(+)VEGR2(+) using traditional fluorescence activated cell sorting (FACS), are rare cel
155 nanoLCMS proteomics workflow by integrating fluorescence activated cell sorting (FACS), focused ultr
156 on chromosome 10 (PTEN) was observed both in fluorescence activated cell sorting (FACS)-isolated TICs
162 o 5 months of age, followed by histologic or fluorescence-activated cell sorting (FACS) analysis of m
163 FV-2 showed antibody titers of >1:10(6), and fluorescence-activated cell sorting (FACS) analysis reve
165 tly infected resting CD4(+) T cells and used fluorescence-activated cell sorting (FACS) and fiber-opt
166 n vitro contact cocultures, as determined by fluorescence-activated cell sorting (FACS) and fluoresce
167 fluorescence-based genetic screen utilizing fluorescence-activated cell sorting (FACS) and high-thro
170 om normal mouse intestine using DCAMKL-1 and fluorescence-activated cell sorting (FACS) and subjected
171 sidase under the control of Msx2 promoter by fluorescence-activated cell sorting (FACS) and surveyed
174 A direct comparison of this technology with fluorescence-activated cell sorting (FACS) demonstrated
175 aploid state for at least five weeks without fluorescence-activated cell sorting (FACS) enrichment of
176 ed from 20 patients with HPT and analyzed by fluorescence-activated cell sorting (FACS) for the CD44/
177 e cells isolated from hepatoma cell lines by fluorescence-activated cell sorting (FACS) form spheroid
178 as not detectable in clear cells isolated by fluorescence-activated cell sorting (FACS) from B1-EGFP
179 eparation based on SSEA-5 expression through fluorescence-activated cell sorting (FACS) greatly reduc
180 lectivity based on yeast surface display and fluorescence-activated cell sorting (FACS) is developed
181 In order to facilitate genomic analysis, a fluorescence-activated cell sorting (FACS) method was de
182 This aptamer enables better separation by fluorescence-activated cell sorting (FACS) of c-kit(+) h
183 their binding to fluorophores, coupled with fluorescence-activated cell sorting (FACS) of millions o
184 enables enrichment of high-lipid mutants by fluorescence-activated cell sorting (FACS) of pooled mut
185 Analysis of inflammatory infiltrates by fluorescence-activated cell sorting (FACS) revealed sign
186 scent protein and nuclease was combined with fluorescence-activated cell sorting (FACS) to allow for
187 transcription polymerase chain reaction, and fluorescence-activated cell sorting (FACS) to analyze in
188 ining genes, we employed flow cytometry with fluorescence-activated cell sorting (FACS) to enrich a t
190 cle, Maurice et al. (2013) report the use of fluorescence-activated cell sorting (FACS) to perform a
194 tudying gene expression in cells purified by fluorescence-activated cell sorting (FACS) using intrace
195 ir cells sorted based on GFP expression with fluorescence-activated cell sorting (FACS), and analyzed
196 ative RT-PCR (Q-RT-PCR) of cells isolated by fluorescence-activated cell sorting (FACS), and by immun
197 mory B cells are first single-cell-sorted by fluorescence-activated cell sorting (FACS), and V(D)J tr
198 etry, coupled with the sorting capability of fluorescence-activated cell sorting (FACS), can detect,
199 nd their expression levels were confirmed by fluorescence-activated cell sorting (FACS), GFP visualiz
200 fluidic devices are seamlessly combined with fluorescence-activated cell sorting (FACS), so that indi
203 east cancer, we developed a highly sensitive fluorescence-activated cell sorting (FACS)-based assay,
205 s, we performed gene expression profiling of fluorescence-activated cell sorting (FACS)-purified muri
216 ic manner and screened using flow cytometry (fluorescence-activated cell sorting, FACS) for variants
217 and developed a novel flow-cytometry-based (fluorescence-activated cell sorting; FACS) strategy to d
218 ious techniques such as ultracentrifugation, fluorescence-activated cell sorting flow cytometry and r
219 populations using stable isotope tracing and fluorescence-activated cell sorting followed by liquid c
220 Here we describe site-specific integration fluorescence-activated cell sorting followed by sequenci
221 t by either laser capture microdissection or fluorescence-activated cell sorting, followed by microar
222 with non-redundant transposon insertions by fluorescence-activated cell sorting for reduced depositi
223 ons were isolated from kidney homogenates by fluorescence-activated cell sorting for whole genome mic
224 bility to reproducibly use cells isolated by fluorescence activated cell sorting from human prostate
225 ferent populations of cells were isolated by fluorescence-activated cell sorting from disaggregated l
226 re, we purified HSCs with retinoid-dependent fluorescence-activated cell sorting from eGFP-expressing
227 al and non-neuronal nuclei were separated by fluorescence-activated cell sorting from postmortem DLPF
229 rt-Seq that combines saturating mutagenesis, fluorescence-activated cell sorting, high-throughput seq
231 thod involving immunomagnetic enrichment and fluorescence-activated cell sorting (IE/FACS), a techniq
233 e-wide gene expression analysis from ex vivo fluorescence-activated cell sorting in MDM4-deficient re
234 or the isolation of idioblast protoplasts by fluorescence-activated cell sorting is established, taki
237 vation expressly in the transformed cells or fluorescence-activated cell sorting-mediated isolation a
238 ally altering cell phenotypes, we employed a fluorescence activated cell sorting method to isolate ke
240 w-cost, and high-performance microfabricated fluorescence-activated cell sorting (muFACS) technology
241 escent reporter gene with an ochre mutation, fluorescence-activated cell sorting of a library of SUP4
243 Four rounds of quantitative screening by fluorescence-activated cell sorting of an error-prone li
246 ng IL-17A-producing cells were identified by fluorescence-activated cell sorting of myeloid versus ly
248 entially methylated loci was performed after fluorescence-activated cell sorting of oligodendrocyte a
250 s) were isolated as side population cells by fluorescence-activated cell sorting or isolated by clona
252 ively, in RFP-positive Sk-Hep-1 recovered by fluorescence-activated cell sorting (P < 0.04 vs Mu-APT
253 ssion tomography/magnetic resonance imaging, fluorescence-activated cell sorting, polymerase chain re
255 n a small subpopulation of CD133+ cells, and fluorescence-activated cell sorting-purified CD133+ PrEC
258 of NKG2D and its ligands were determined by fluorescence-activated cell sorting, real-time polymeras
266 thermore, gene expression analysis comparing fluorescence-activated cell sorting-sorted cancer SP cel
269 ng directed in vivo angiogenesis assays with fluorescence-activated cell sorting, thereby confirming
270 morphology on bacterial physiology, we used fluorescence-activated cell sorting to enrich a library
271 ne expression from labeled cells isolated by fluorescence-activated cell sorting to generate cell-typ
272 sed them to a starvation stress before using fluorescence-activated cell sorting to identify and isol
274 were screened in a high-throughput manner by fluorescence-activated cell sorting to identify clones w
278 display, enzyme-mediated bioconjugation, and fluorescence-activated cell sorting to isolate cells exp
283 e(X) antigen can be used in conjunction with fluorescence-activated cell sorting to isolate neurosphe
285 ombination with flow cytometric analysis and fluorescence-activated cell sorting to isolate responses
289 chain reaction (qPCR), or immunoblot assays; fluorescence-activated cell sorting was performed to ide
300 a novel approach that combines the power of fluorescence-activated cell sorting with barcode microar
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