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1 LN was confirmed by immunohistochemistry and fluorescence activated cell sorter.
2 were separated from uninfected cells with a 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 e of Flk-1 expression on EPCs as assessed by fluorescence-activated cell sorter.
7 and transformed R. typhi were isolated in a 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 uman CMFs was determined using Western blot, fluorescence-activated cell sorter analysis and confocal
24 induced CCR5 down-modulation as detected by 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 4 expressed on mammalian epithelial cells in fluorescence-activated cell sorter analysis, as well as
86 )CD14(+) cells, determined and phenotyped by fluorescence-activated cell sorter analysis, in the peri
87 ivo analysis of monocytes was performed with fluorescence-activated cell sorter analysis, inflammator
88 permissive to infection, as demonstrated by fluorescence-activated cell sorter analysis, suggesting
89 e and Western blotting, cetuximab binding by fluorescence-activated cell sorter analysis, the number
90 bodies (PRA) were negative before surgery by fluorescence-activated cell sorter analysis, the PRA 3 d
91 n quantitative polymerase chain reaction and fluorescence-activated cell sorter analysis, we found th
92 oying both immunofluorescence microscopy and fluorescence-activated cell sorter analysis, we localize
93 nonuclear cells percentages were measured by fluorescence-activated cell sorter analysis, whereas ser
111 d to sort the MPCs by Hoechst 33342 staining/fluorescence-activated cell-sorter analysis before injec
112 in was undetectable in triple-mutant mice on fluorescence-activated cell-sorter analysis of periphera
114 ed with the photoaffinity linker and used in fluorescence-activated cell sorter and ELISA analyses.
116 ed through analysis of activation markers by fluorescence-activated cell sorter and induction of infl
117 on of pig cells in the blood was assessed by fluorescence-activated cell sorter and polymerase chain
118 P(+) ICC from the jejunum were purified by a fluorescence-activated cell sorter and validated by cell
120 32/30, 27, and 14-kDa isoforms, purified by fluorescence-activated cell sorter, and analyzed in colo
121 Hematopoietic cell chimerism was followed by fluorescence-activated cell sorter, and graft survival w
122 active intracellularly were isolated with a fluorescence-activated cell sorter, and inserts were par
123 We used gene chip, differential display, fluorescence-activated cell sorter, and overexpression a
124 was determined by flow-cytometric analysis (fluorescence-activated cell sorter), apoptosis by DNA fr
125 tured with CD40L-transfected HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic s
126 the development and application of a novel, fluorescence-activated cell sorter based assay that dire
129 on in human cells using a novel nonselective fluorescence-activated cell sorter-based method and disc
131 uch Sin(-) mutant polioviruses, we devised a fluorescence-activated cell sorter-based screen to selec
132 AEC infected with wild-type P. gingivalis by fluorescence-activated cell sorter, but not with noninva
133 tin-3 and MUC2 expression were determined by fluorescence-activated cell sorter (cell surface galecti
134 received a donor heart that was negative by fluorescence-activated cell sorter cross-match on day 64
135 cells at high rates is now commonplace with fluorescence activated cell sorters, development of comp
137 on was studied in nine patients who received fluorescence activated cell sorter (FACS)-sorted autolog
139 various times after the completion of TLI by fluorescence-activated cell sorter (FACS) analysis and e
143 virion particle was fluorescent as judged by fluorescence-activated cell sorter (FACS) analysis of in
144 ytomegalovirus infection was investigated by fluorescence-activated cell sorter (FACS) analysis of th
146 An excellent correlation was found between fluorescence-activated cell sorter (FACS) analysis resul
149 tectable by both fluorescence microscopy and fluorescence-activated cell sorter (FACS) analysis.
150 tor (VEGF) receptors 1 and 2 was measured by fluorescence-activated cell sorter (FACS) analysis.
153 yme-linked immunosorbent assays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analys
154 and week 5 LTC-IC in CD34+ cells selected by fluorescence-activated cell sorter (FACS) from mobilized
156 ic selection for lineage-negative cells, and fluorescence-activated cell sorter (FACS) sorting for Ly
157 hanced green fluorescent protein (GFP) and a fluorescence-activated cell sorter (FACS) to perform gen
158 P) for selection of high producing clones by fluorescence-activated cell sorter (FACS) to reduce scre
159 acellular cytokine production was assayed by fluorescence-activated cell sorter (FACS), and the expan
162 ies to the CoRbs, we employed a differential fluorescence-activated cell sorter (FACS)-based sorting
163 es and reverse transcriptase-PCR analysis of fluorescence-activated cell sorter (FACS)-purified CD4+
165 o had previously been recipients of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)
166 are in agreement with microarray studies on fluorescence-activated cell sorter (FACS)-sorted cells a
167 set localization was determined by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted periphe
170 od polymorphonuclear leukocytes (PMNs) using fluorescence-activated cell-sorter (FACS) analysis.
171 cated by the appearance of subgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the
173 ocols to define EPCs by culture assays or by fluorescence-activated cell sorter in the context of the
174 Experiments involving separation of cells by fluorescence-activated cell sorter indicate that there i
176 thiols, we have developed a Hi-D (11-color) fluorescence-activated cell sorter method in which we co
177 ve demonstrated a disposable microfabricated fluorescence-activated cell sorter (microFACS) for sorti
179 4 antibody (Ab) (242B58) were examined using fluorescence-activated cell sorter, mixed lymphocyte rea
180 sorted into three different populations by a fluorescence-activated cell sorter, placed in culture, a
181 andem mass spectrometry proteome analysis of fluorescence-activated cell sorter-purified beta-cells,
182 cy of cells carrying the gammaHV68 genome in fluorescence-activated cell sorter-purified cell populat
184 orted a cell separation method that uses the fluorescence-activated cell sorter selection of low Hoes
185 with a retroviral cDNA library, selecting by fluorescence-activated cell sorter single cells displayi
187 genes were significantly deregulated between fluorescence-activated cell sorter-sorted clonal B cells
188 uorescence in situ hybridization analysis of fluorescence-activated cell sorter-sorted CTCs also unra
189 chains by mononuclear cells was analyzed by fluorescence-activated cell sorter staining, Western blo
190 ted Gal such that the RBCs bound anti-Gal by fluorescence-activated cell sorter, suggesting that thes
191 e transduced cells were examined in vitro by fluorescence-activated cell sorter, T-cell proliferation
193 F, and M-CSF plus IFN-gamma) was analyzed by fluorescence-activated cell sorter, using one of the fol
194 adherin immunofluorescence, as quantified by fluorescence-activated cell sorter, varied inversely wit
195 cific estrogen-sensitive cell populations, a fluorescence-activated cell sorter was used to detect, s
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