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1 were separated from uninfected cells with a fluorescence activated cell sorter.
2 LN was confirmed by immunohistochemistry and fluorescence activated cell sorter.
3 smic accumulation of perforin as detected by fluorescence-activated cell sorter.
4 ietic stem cells (LT-HSC) isolated using the fluorescence-activated cell sorter.
5 ch binds terminal N-acetylglucosamine, and a fluorescence-activated cell sorter.
6 and transformed R. typhi were isolated in a fluorescence-activated cell sorter.
7 e of Flk-1 expression on EPCs as assessed by fluorescence-activated cell sorter.
8 separated from fibroblasts with the use of a fluorescence-activated cell sorter.
9 Krt12Cre/+/ROSA(EGFP) mice were examined by fluorescence-activated cell sorter.
10 parately seeded for colony formation using a fluorescence-activated cell sorter.
11 on (SP) cells, that can be isolated with the fluorescence-activated cell sorter.
12 om biopsies of human skeletal muscle using a fluorescence-activated cell sorter along with population
13 ll walls, centrifuged, and suspended in PBS, fluorescence-activated cell sorter analyses revealed the
14 nalization assessments, light microscopy and fluorescence-activated cell sorter analyses were used, r
18 ound to the cell surface, as demonstrated by fluorescence-activated cell-sorter analyses (FACS), and
23 induced CCR5 down-modulation as detected by fluorescence-activated cell sorter analysis and confocal
24 uman CMFs was determined using Western blot, fluorescence-activated cell sorter analysis and confocal
25 t deletion of donor-reactive CD8+ T cells by fluorescence-activated cell sorter analysis and decrease
26 -activated cell sorting and characterized by fluorescence-activated cell sorter analysis and immunocy
27 integrin activation state were determined by fluorescence-activated cell sorter analysis and immunofl
28 est as shown by both biochemical markers and fluorescence-activated cell sorter analysis and signific
29 otential (MMP) using Rhodamine 123 stain and fluorescence-activated cell sorter analysis and subjecti
34 hortly after rickettsial exposure; and (iii) fluorescence-activated cell sorter analysis demonstrates
35 esis, enzyme-linked immunosorbent assay, and fluorescence-activated cell sorter analysis employing a
36 rse transcription-PCR, Western blotting, and fluorescence-activated cell sorter analysis in CD45(+) p
37 ons of ALK4 with the CFC domain of Cripto by fluorescence-activated cell sorter analysis indicate tha
39 with saturation by 100 microM), as shown by fluorescence-activated cell sorter analysis of cells sta
46 tion of bromodeoxyuridine and [3H]thymidine, fluorescence-activated cell sorter analysis of murine le
48 g of DNA ends, DNA fragmentation assays, and fluorescence-activated cell sorter analysis of propidium
49 lls was determined at 48 hours of culture by fluorescence-activated cell sorter analysis of propidium
57 pite alterations in histological appearance, fluorescence-activated cell sorter analysis revealed no
71 at quiescence is induced within 12-24 h, and fluorescence-activated cell sorter analysis suggests tha
76 To explore this hypothesis, we phenotyped by fluorescence-activated cell sorter analysis various huma
78 uperfamily 1A (sTNFRSF1A) were measured, and fluorescence-activated cell sorter analysis was used to
79 re total and apoptotic PMNs as determined by fluorescence-activated cell sorter analysis with Annexin
81 re also examined for cell surface antigen by fluorescence-activated cell sorter analysis with monoclo
82 itochondrial membrane potential (assessed by fluorescence-activated cell sorter analysis) from 15 to
84 taining, transmission electronic microscopy, fluorescence-activated cell sorter analysis, and single-
85 4 expressed on mammalian epithelial cells in fluorescence-activated cell sorter analysis, as well as
87 )CD14(+) cells, determined and phenotyped by fluorescence-activated cell sorter analysis, in the peri
88 ivo analysis of monocytes was performed with fluorescence-activated cell sorter analysis, inflammator
89 permissive to infection, as demonstrated by fluorescence-activated cell sorter analysis, suggesting
90 e and Western blotting, cetuximab binding by fluorescence-activated cell sorter analysis, the number
91 bodies (PRA) were negative before surgery by fluorescence-activated cell sorter analysis, the PRA 3 d
92 n quantitative polymerase chain reaction and fluorescence-activated cell sorter analysis, we found th
93 oying both immunofluorescence microscopy and fluorescence-activated cell sorter analysis, we localize
94 nonuclear cells percentages were measured by fluorescence-activated cell sorter analysis, whereas ser
112 d to sort the MPCs by Hoechst 33342 staining/fluorescence-activated cell-sorter analysis before injec
113 in was undetectable in triple-mutant mice on fluorescence-activated cell-sorter analysis of periphera
115 ed with the photoaffinity linker and used in fluorescence-activated cell sorter and ELISA analyses.
117 ed through analysis of activation markers by fluorescence-activated cell sorter and induction of infl
118 on of pig cells in the blood was assessed by fluorescence-activated cell sorter and polymerase chain
120 P(+) ICC from the jejunum were purified by a fluorescence-activated cell sorter and validated by cell
122 32/30, 27, and 14-kDa isoforms, purified by fluorescence-activated cell sorter, and analyzed in colo
123 Hematopoietic cell chimerism was followed by fluorescence-activated cell sorter, and graft survival w
124 active intracellularly were isolated with a fluorescence-activated cell sorter, and inserts were par
125 We used gene chip, differential display, fluorescence-activated cell sorter, and overexpression a
126 was determined by flow-cytometric analysis (fluorescence-activated cell sorter), apoptosis by DNA fr
127 tured with CD40L-transfected HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic s
128 the development and application of a novel, fluorescence-activated cell sorter based assay that dire
132 on in human cells using a novel nonselective fluorescence-activated cell sorter-based method and disc
134 uch Sin(-) mutant polioviruses, we devised a fluorescence-activated cell sorter-based screen to selec
135 AEC infected with wild-type P. gingivalis by fluorescence-activated cell sorter, but not with noninva
136 r (FASD) that is analogous to a conventional fluorescence-activated cell sorter, but sorts droplets c
137 tin-3 and MUC2 expression were determined by fluorescence-activated cell sorter (cell surface galecti
138 face proteins used to identify cell types by fluorescence-activated cell sorter.Conclusions: Lung and
139 received a donor heart that was negative by fluorescence-activated cell sorter cross-match on day 64
140 cells at high rates is now commonplace with fluorescence activated cell sorters, development of comp
142 on was studied in nine patients who received fluorescence activated cell sorter (FACS)-sorted autolog
144 various times after the completion of TLI by fluorescence-activated cell sorter (FACS) analysis and e
148 virion particle was fluorescent as judged by fluorescence-activated cell sorter (FACS) analysis of in
149 ytomegalovirus infection was investigated by fluorescence-activated cell sorter (FACS) analysis of th
151 An excellent correlation was found between fluorescence-activated cell sorter (FACS) analysis resul
154 tectable by both fluorescence microscopy and fluorescence-activated cell sorter (FACS) analysis.
155 tor (VEGF) receptors 1 and 2 was measured by fluorescence-activated cell sorter (FACS) analysis.
158 yme-linked immunosorbent assays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analys
159 and week 5 LTC-IC in CD34+ cells selected by fluorescence-activated cell sorter (FACS) from mobilized
160 sorting droplets with commercially available fluorescence-activated cell sorter (FACS) machines, maki
162 ic selection for lineage-negative cells, and fluorescence-activated cell sorter (FACS) sorting for Ly
163 hanced green fluorescent protein (GFP) and a fluorescence-activated cell sorter (FACS) to perform gen
164 P) for selection of high producing clones by fluorescence-activated cell sorter (FACS) to reduce scre
165 acellular cytokine production was assayed by fluorescence-activated cell sorter (FACS), and the expan
166 In vitro evaluation was assessed with a fluorescence-activated cell sorter (FACS), cell adhesion
169 ies to the CoRbs, we employed a differential fluorescence-activated cell sorter (FACS)-based sorting
170 es and reverse transcriptase-PCR analysis of fluorescence-activated cell sorter (FACS)-purified CD4+
172 o had previously been recipients of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)
173 are in agreement with microarray studies on fluorescence-activated cell sorter (FACS)-sorted cells a
174 set localization was determined by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted periphe
177 od polymorphonuclear leukocytes (PMNs) using fluorescence-activated cell-sorter (FACS) analysis.
178 cated by the appearance of subgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the
180 ocols to define EPCs by culture assays or by fluorescence-activated cell sorter in the context of the
181 Experiments involving separation of cells by fluorescence-activated cell sorter indicate that there i
183 thiols, we have developed a Hi-D (11-color) fluorescence-activated cell sorter method in which we co
184 ve demonstrated a disposable microfabricated fluorescence-activated cell sorter (microFACS) for sorti
186 4 antibody (Ab) (242B58) were examined using fluorescence-activated cell sorter, mixed lymphocyte rea
188 sorted into three different populations by a fluorescence-activated cell sorter, placed in culture, a
189 andem mass spectrometry proteome analysis of fluorescence-activated cell sorter-purified beta-cells,
190 cy of cells carrying the gammaHV68 genome in fluorescence-activated cell sorter-purified cell populat
192 orted a cell separation method that uses the fluorescence-activated cell sorter selection of low Hoes
193 with a retroviral cDNA library, selecting by fluorescence-activated cell sorter single cells displayi
195 genes were significantly deregulated between fluorescence-activated cell sorter-sorted clonal B cells
196 uorescence in situ hybridization analysis of fluorescence-activated cell sorter-sorted CTCs also unra
197 chains by mononuclear cells was analyzed by fluorescence-activated cell sorter staining, Western blo
198 ted Gal such that the RBCs bound anti-Gal by fluorescence-activated cell sorter, suggesting that thes
199 e transduced cells were examined in vitro by fluorescence-activated cell sorter, T-cell proliferation
201 rol and COPD lung DC subsets, sorted using a fluorescence-activated cell sorter, to polarize IL-21(+)
202 F, and M-CSF plus IFN-gamma) was analyzed by fluorescence-activated cell sorter, using one of the fol
203 adherin immunofluorescence, as quantified by fluorescence-activated cell sorter, varied inversely wit
204 cific estrogen-sensitive cell populations, a fluorescence-activated cell sorter was used to detect, s