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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
47                      Confocal microscopy and fluorescence-activated cell sorting analyses showed tran
48                                              Fluorescence-activated cell sorting analyses were perfor
49                                              Fluorescence-activated cell sorting analyses with anti-p
50                   We used immunostaining and fluorescence-activated cell sorting analyses with in viv
51 g results were corroborated by histology and fluorescence-activated cell sorting analyses.
52                                              Fluorescence activated cell sorting analysis was used to
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
56                                     Finally, fluorescence-activated cell sorting analysis demonstrate
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
59             Immunohistochemical staining and fluorescence-activated cell sorting analysis indicate th
60                   [3H]Thymidine labeling and fluorescence-activated cell sorting analysis indicated t
61 We used a multiparameter approach, including fluorescence-activated cell sorting analysis of cell-sur
62                                     Finally, fluorescence-activated cell sorting analysis of liver CD
63                                              Fluorescence-activated cell sorting analysis of monolaye
64 der protein led to apoptosis, as assessed by fluorescence-activated cell sorting analysis of propidiu
65                                Histology and fluorescence-activated cell sorting analysis of the bone
66                                              Fluorescence-activated cell sorting analysis revealed el
67           In the early posttransplant phase, fluorescence-activated cell sorting analysis revealed pr
68                                              Fluorescence-activated cell sorting analysis revealed re
69    CSCs can be isolated from L2G85 mice, and fluorescence-activated cell sorting analysis showed expr
70                                              Fluorescence-activated cell sorting analysis showed only
71                                              Fluorescence-activated cell sorting analysis suggested t
72                                              Fluorescence-activated cell sorting analysis was perform
73 l viability as a marker of proliferation and fluorescence-activated cell sorting analysis was used to
74 assay) and improved gemcitabine sensitivity (fluorescence-activated cell sorting analysis).
75                           Mass spectrometry, fluorescence-activated cell sorting analysis, and functi
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
78                                     By using fluorescence-activated cell sorting analysis, fibrocytes
79                        Using multi-parameter fluorescence-activated cell sorting analysis, we quantif
80 ed in gastric tissue and peripheral blood by fluorescence-activated cell sorting analysis.
81 xpression of CD86 and CD80 was determined by fluorescence-activated cell sorting analysis.
82 red by using either time-lapse microscopy or fluorescence-activated cell sorting analysis.
83           Immune cells were characterized by fluorescence-activated cell sorting analysis.
84 wed by biodistribution, autoradiography, and fluorescence-activated cell sorting analysis.
85                                              Fluorescence activated cell sorting and immunofluorescen
86                        In this paper, we use fluorescence activated cell sorting and RNA-seq to deter
87    Bone marrow-derived HSCs were purified by fluorescence-activated cell sorting and administered aft
88                                              Fluorescence-activated cell sorting and biochemical anal
89  of microparticles by CACs was determined by fluorescence-activated cell sorting and by fluorescence
90                                              Fluorescence-activated cell sorting and cDNA-microarray
91                                              Fluorescence-activated cell sorting and cell binding ass
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
103             High-viability cells isolated by fluorescence-activated cell sorting and re-suspended in
104 vestigated at the protein and gene levels by fluorescence-activated cell sorting and real-time revers
105          Phenotype analysis was performed by fluorescence-activated cell sorting and real-time revers
106                                              Fluorescence-activated cell sorting and single-cell reve
107              ILC2s were isolated by means of fluorescence-activated cell sorting and studied for Il5
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
111                                      We used fluorescence-activated cell sorting and Western blotting
112             Numerous clones were isolated by fluorescence-activated cell sorting, and affinity matura
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
120                   In IAS cells isolated with fluorescence-activated cell sorting, Ano1 expression was
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
123 l antimicrobial activity was assessed with a fluorescence-activated cell sorting assay.
124 ing quantitative fluorescence analysis using fluorescence-activated cell sorting assay.
125  These 2 patients alone tested positive by a fluorescence-activated cell-sorting assay.
126 d immunosorbent, transfected cell-based, and fluorescence-activated cell-sorting assays.
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
129         Cholinergic neurons were isolated by fluorescence-activated cell sorting based on either tran
130 gion of late embryonic mice were purified by fluorescence-activated cell sorting based on their expre
131 s from normal, RD and HGPS individuals using fluorescence activated cell sorting-based assays.
132              We exploited a high-throughput, fluorescence-activated cell sorting-based green fluoresc
133              Here we describe and validate a fluorescence-activated cell sorting-based protocol that
134                                Our two-color fluorescence-activated cell sorting-based screen provide
135 , high-throughput and quantitative two-color fluorescence-activated cell sorting-based screening stra
136                      Using an intersectional fluorescence-activated cell sorting-based strategy, we i
137                                      Using a fluorescence-activated cell sorting-based strategy, we o
138  BONCAT-labeled cells could be isolated with fluorescence-activated cell sorting (BONCAT-FACS) for su
139                                              Fluorescence-activated cell-sorting, cell-based, and enz
140                                   Multicolor fluorescence-activated cell sorting could isolate distin
141 tological and biochemical analyses following fluorescence-activated cell sorting demonstrate a positi
142                                              Fluorescence-activated cell sorting-enriched CD133(-)/Ep
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
145                                              Fluorescence activated cell sorting (FACS) analysis reve
146                             Western blot and fluorescence activated cell sorting (FACS) analysis reve
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
150                 High throughput screening by fluorescence activated cell sorting (FACS) is a common t
151 he embryo to define cell type and includes a fluorescence activated cell sorting (FACS) procedure tha
152          SmoM2 expressing cells, purified by fluorescence activated cell sorting (FACS) via the genet
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
157                                   RT-qPCR on Fluorescence Activated Cell Sorting (FACS)-sorted tnfa(+
158 SC chimeras were tetraploid as determined by fluorescence activated cell sorting (FACS).
159                                              Fluorescence-activated cell sorting (FACS) allows for ra
160                                              Fluorescence-activated cell sorting (FACS) analysis indi
161                                              Fluorescence-activated cell sorting (FACS) analysis indi
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
164                                 Furthermore, fluorescence-activated cell sorting (FACS) and confocal
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
168                                              Fluorescence-activated cell sorting (FACS) and histopath
169                              This allows for fluorescence-activated cell sorting (FACS) and single-ce
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
172                                              Fluorescence-activated cell sorting (FACS) confirmed tha
173            Nonmitotic cells were assessed by fluorescence-activated cell sorting (FACS) coupled with
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
189                                  We then use fluorescence-activated cell sorting (FACS) to individual
190 cle, Maurice et al. (2013) report the use of fluorescence-activated cell sorting (FACS) to perform a
191                                      We used fluorescence-activated cell sorting (FACS) to purify str
192                                  We employed fluorescence-activated cell sorting (FACS) to sort for c
193          Cells were isolated and purified by fluorescence-activated cell sorting (FACS) using endogen
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
201                              Upon EGFP-based fluorescence-activated cell sorting (FACS), the E/sox2:E
202       To study this question, we developed a fluorescence-activated cell sorting (FACS)- based assay
203 east cancer, we developed a highly sensitive fluorescence-activated cell sorting (FACS)-based assay,
204           Using a fluorescent reporter and a fluorescence-activated cell sorting (FACS)-based transpo
205 s, we performed gene expression profiling of fluorescence-activated cell sorting (FACS)-purified muri
206                                              Fluorescence-activated cell sorting (FACS)-purified Tbx1
207 ), while cytokine production was assessed by fluorescence-activated cell sorting (FACS).
208  Fluorescent yeast cells were selected using fluorescence-activated cell sorting (FACS).
209 g optical imaging, immunohistochemistry, and fluorescence-activated cell sorting (FACS).
210 munosorbent assay (ELISA) and multiparameter fluorescence-activated cell sorting (FACS).
211 sed single cell transcriptional analysis and fluorescence-activated cell sorting (FACS).
212 e breeding of live oil-rich E. gracilis with fluorescence-activated cell sorting (FACS).
213 ine incorporation, and cell size assessed by fluorescence-activated cell sorting (FACS).
214 ate MuSCs from limb muscles of adult mice by fluorescence-activated cell sorting (FACS).
215 ng histological analysis, real-time PCR, and fluorescence-activated cell sorting (FACS).
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
228                                              Fluorescence-activated cell sorting from the skins of tr
229 rt-Seq that combines saturating mutagenesis, fluorescence-activated cell sorting, high-throughput seq
230 od via immunomagnetic enrichment followed by fluorescence-activated cell sorting (IE-FACS).
231 thod involving immunomagnetic enrichment and fluorescence-activated cell sorting (IE/FACS), a techniq
232                                              Fluorescence-activated cell sorting, immunofluorescence,
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
235                                  Indeed, the fluorescence-activated cell sorting-isolated EpCAM(+) HC
236                 Here we describe live animal fluorescence-activated cell sorting (laFACS), a protocol
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
239 and they were isolated from each other using fluorescence-activated cell sorting methods.
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
242                       The procedure involves fluorescence-activated cell sorting of a library, deep s
243     Four rounds of quantitative screening by fluorescence-activated cell sorting of an error-prone li
244                                              Fluorescence-activated cell sorting of CD24 high versus
245                             Here, we applied fluorescence-activated cell sorting of green fluorescent
246 ng IL-17A-producing cells were identified by fluorescence-activated cell sorting of myeloid versus ly
247                                              Fluorescence-activated cell sorting of nuclei from infec
248 entially methylated loci was performed after fluorescence-activated cell sorting of oligodendrocyte a
249                                         Upon fluorescence-activated cell sorting, only Prominin-1/Nes
250 s) were isolated as side population cells by fluorescence-activated cell sorting or isolated by clona
251                         DCs were purified by fluorescence-activated cell sorting or with immunomagnet
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
254                                              Fluorescence-activated cell sorting purification of huma
255 n a small subpopulation of CD133+ cells, and fluorescence-activated cell sorting-purified CD133+ PrEC
256             The in vitro characterization of fluorescence-activated cell sorting-purified cells is co
257            Using gradient centrifugation and fluorescence-activated cell sorting, rat G cells were pr
258  of NKG2D and its ligands were determined by fluorescence-activated cell sorting, real-time polymeras
259            RH-positive parasites sorted with fluorescence-activated cell sorting resumed growth at 10
260                                  Analysis by fluorescence-activated cell sorting revealed that hookwo
261                                              Fluorescence-activated cell sorting revealed that type I
262                                              Fluorescence-activated cell sorting, RNA sequencing, qua
263 rpin RNA depletion, cDNA overexpression, and fluorescence-activated cell sorting selection.
264                                              Fluorescence-activated cell sorting showed significantly
265           These results were corroborated by fluorescence activated cell sorting showing a 48% yield
266 thermore, gene expression analysis comparing fluorescence-activated cell sorting-sorted cancer SP cel
267           We show by confocal microscopy and fluorescence-activated cell sorting that amino acids 50
268                             We have found by fluorescence-activated cell sorting that increased AC133
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
273                                      We used fluorescence-activated cell sorting to identify circulat
274 were screened in a high-throughput manner by fluorescence-activated cell sorting to identify clones w
275                                      We used fluorescence-activated cell sorting to identify precurso
276                                      We used fluorescence-activated cell sorting to isolate a pure po
277                  The library was screened by fluorescence-activated cell sorting to isolate binders t
278 display, enzyme-mediated bioconjugation, and fluorescence-activated cell sorting to isolate cells exp
279                           We used multicolor fluorescence-activated cell sorting to isolate different
280                                      We used fluorescence-activated cell sorting to isolate each cell
281                                      We used fluorescence-activated cell sorting to isolate EGFP(+) c
282                Using CD140a/PDGFRalpha-based fluorescence-activated cell sorting to isolate fetal OPC
283 e(X) antigen can be used in conjunction with fluorescence-activated cell sorting to isolate neurosphe
284                                      We used fluorescence-activated cell sorting to isolate reinstate
285 ombination with flow cytometric analysis and fluorescence-activated cell sorting to isolate responses
286                                      We used fluorescence-activated cell sorting to measure hepatic l
287                                      We used fluorescence-activated cell sorting to purify these popu
288                              The method uses fluorescence-activated cell sorting to screen randomly m
289 chain reaction (qPCR), or immunoblot assays; fluorescence-activated cell sorting was performed to ide
290                                After 2 days, fluorescence-activated cell sorting was used to enrich f
291                                              Fluorescence-activated cell sorting was used to isolate
292                                              Fluorescence-activated cell sorting was used to study th
293                                        Using fluorescence-activated cell sorting we further show that
294                                  Next, using fluorescence-activated cell sorting, we compared gene ex
295                                 By employing fluorescence-activated cell sorting, we have generated g
296                                        Using fluorescence-activated cell sorting, we identified alveo
297                                           By fluorescence-activated cell sorting, we isolated JG cell
298            CD45(low)CD271+ cells isolated by fluorescence-activated cell sorting were enumerated and
299                           ELISA and antibody fluorescence-activated cell sorting were used to examine
300  a novel approach that combines the power of fluorescence-activated cell sorting with barcode microar

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