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1 perate South Atlantic using an original flow cytometric (14)CO2-tracer approach.
2                 Immunohistochemical and flow cytometric analyses demonstrated that prednisolone treat
3                               Moreover, flow cytometric analyses for B-cell markers revealed an MDM2-
4                                         Flow cytometric analyses further confirmed that over-expressi
5                          Our multicolor flow cytometric analyses of human decidual leukocytes detecte
6                                         Flow cytometric analyses of human fibrocytes (CD45(+) and col
7 Virtually digested" WSI enabled quantitative cytometric analyses of individual cells displayed in a v
8                                Notably, flow cytometric analyses of lung CD8(+) T cells revealed a sh
9 zed by immunohistochemistry, along with flow cytometric analyses of lymphocytes for iNOS expression a
10 AFIA versus clodronate-treated mice and flow cytometric analyses of myeloid lineage cells in the bone
11                                         Flow cytometric analyses on dendritic cells (DCs) in vitro an
12   Cell numbers were adequate to perform flow cytometric analyses on T cell lineage, T cell activation
13                                Finally, flow cytometric analyses revealed that IL-15 increases the pr
14                                         Flow cytometric analyses showed significant accumulation of M
15                                         Flow cytometric analyses showed that the susceptibility of EC
16 microglia within tissue sections and by flow cytometric analyses.
17 at various times after immunization for flow cytometric analyses.
18 the traditional sample-by-sample approach in cytometric analysis and highlight the need for scalable
19 7-H4 protein expression was examined by flow cytometric analysis and immunohistochemical staining.
20  and cytokine profiles were assessed by flow cytometric analysis and multiplex assay.
21                                         Flow-cytometric analysis and quantitative real-time polymeras
22 ddress this, we combined multiparameter flow cytometric analysis and T-cell subpopulation sorting wit
23                                         Flow cytometric analysis and Western blots showed that blocki
24                                      By flow cytometric analysis at early times during infection, nei
25                              A parallel flow cytometric analysis confirmed the electrochemical result
26                                         Flow cytometric analysis demonstrated an expanded CD19+ CD5+
27                                         Flow cytometric analysis found elevated renin content in prin
28                                         Flow cytometric analysis indicated GPR18 deficiency more stro
29                                         Flow cytometric analysis indicated that treatment with caper
30 as evidenced by a mammosphere assay and flow cytometric analysis of aldehyde dehydrogenase 1 (ALDH1)
31                                         Flow cytometric analysis of basophil responses implied labeli
32 ts with AAV and 19 healthy controls for flow cytometric analysis of CD4+ T cell populations.
33 utational algorithms have been developed for cytometric analysis of cells and proteins in subcellular
34                                         Flow cytometric analysis of cells from rectal biopsy specimen
35  cell cycle and apoptosis studies using flow cytometric analysis of cellular DNA content.
36                                         Flow cytometric analysis of CNS-infiltrating mononuclear cell
37                                 Ex vivo flow-cytometric analysis of DENV-specific CD4(+) T cells reve
38  in lymphocytes were quantified through flow cytometric analysis of H2AX phosphorylation (gamma-H2AX)
39                                   Using flow cytometric analysis of harvested MKs, we show that while
40     Fluidigm BioMark and multiparameter flow cytometric analysis of HIV-specific cytolytic CD4+ T cel
41 chain-reaction (qPCR) assay, as well as flow-cytometric analysis of IgG antibody responses against tw
42                                         Flow cytometric analysis of Il17a(-/-)Apoe(-/-) and Il17ra(-/
43 or vehicle, tumour load was measured by flow cytometric analysis of infiltrated spleens, and subclona
44                                         Flow cytometric analysis of ischemic muscles at day 2 reveale
45                                         Flow cytometric analysis of lung cells revealed that the numb
46                                         Flow cytometric analysis of lung tissue from H2 R-deficient a
47                                         Flow cytometric analysis of lymphocytes in the blood, lymph n
48                                         Flow cytometric analysis of microglial cells obtained from in
49                                         Flow cytometric analysis of MOLT-4 cells treated with EERB sh
50                                         Flow cytometric analysis of multiple organs, including the ki
51                                         Flow cytometric analysis of mutant Lkt-treated PMNs revealed
52 rimental allergen challenge model, with flow cytometric analysis of nasal curettage samples, to asses
53                                         Flow cytometric analysis of NPs (n = 9) showed that 5.1% +/-
54                                         Flow cytometric analysis of peripheral blood B cells of 30 MC
55 thy subjects were included for 11-color flow cytometric analysis of peripheral blood for IgG4-express
56                                   Here, flow cytometric analysis of peripheral blood mononuclear cell
57 nced pan-lymphopenia as demonstrated by flow cytometric analysis of peripheral blood.
58                                         Flow-cytometric analysis of primary human NK cells as well as
59                                   Using flow cytometric analysis of resected adenomatous parathyroid
60 livary flow measurement, histologic and flow cytometric analysis of salivary glands, and serum antinu
61                                 We used flow cytometric analysis of sinonasal mucosal tissues of 29 C
62                                         Flow cytometric analysis of splenocytes from infected mice re
63                              Similarly, flow cytometric analysis of stromal cells revealed a signific
64                                         Flow cytometric analysis of SUSD3-knockdown cells revealed bl
65                                         Flow cytometric analysis of synaptosome preparations was used
66 pheral blood samples were processed for flow cytometric analysis of T-cell populations.
67                                         Flow cytometric analysis of tetramer-reactive B cell subsets
68                                         Flow cytometric analysis of the cell cycle demonstrated an in
69                                         Flow cytometric analysis of the ocular infiltrate in WT mice
70                                         Flow cytometric analysis of tumor-infiltrated macrophages sho
71                                         Flow cytometric analysis on the collected samples found that
72                                         Flow cytometric analysis revealed 3 distinct neutrophil popul
73                                         Flow cytometric analysis revealed 97.9%+/-1.5% and 94.3%+/-5.
74                                         Flow cytometric analysis revealed a significant reduction of
75                                         Flow-cytometric analysis revealed increased numbers of regula
76                                         Flow cytometric analysis revealed significant enrichment for
77                                         Flow cytometric analysis revealed significant reduction of fr
78                                         Flow cytometric analysis revealed that a sizable sub-populati
79                                         Flow cytometric analysis revealed that the percentage of PD-1
80                                         Flow cytometric analysis revealed that upregulation of CD95 e
81                                         Flow cytometric analysis reveals the presence of a higher con
82                                         Flow cytometric analysis showed a 41.7% increase in the mean
83                                         Flow cytometric analysis showed aFP treatment elicited an inc
84                                         Flow cytometric analysis showed alterations in tumor-infiltra
85                                         Flow cytometric analysis showed impairment of erythroid diffe
86                                         Flow cytometric analysis showed that CD1a(+) cells in NPs mig
87 is decreased plaque macrophage content, flow cytometric analysis showed that the numbers of circulati
88                            Edu-labelled flow cytometric analysis showed that the percentage of the Ed
89                                         Flow cytometric analysis showed the increase in IFN-gamma cor
90                                         Flow cytometric analysis shows that both the location and act
91                                   Finally, a cytometric analysis shows that the TREM1 rs6910730(G) al
92                      B cell ELISpot and flow cytometric analysis suggest that short-term fostamatinib
93                                         Flow cytometric analysis suggested that Ifitm3(-/-) macrophag
94                                 Ex vivo flow cytometric analysis supported a direct effect of myeloma
95 l in vitro affinity selections based on flow cytometric analysis that allows fine quantitative discri
96                           Here, through flow cytometric analysis the small-molecule macrocycle cyclot
97 ssue explants and optimized a method of flow cytometric analysis to directly quantify infection rates
98                                         Flow cytometric analysis was used to investigate the origin o
99                                         Flow cytometric analysis was used to monitor immune cell freq
100                                By using flow cytometric analysis, enzyme and receptor inhibitors, and
101 onfirmed by fluorescence microscopy and flow-cytometric analysis, whereas cell cycle effects are only
102 ral blood mononuclear cell samples with flow cytometric analysis.
103 ication of single platelet depletion by flow cytometric analysis.
104 mmunoblotting, immunocytochemistry, and flow cytometric analysis.
105 e antigen-DR (HLA-DR), and subjected to flow cytometric analysis.
106  from NPs and matched blood samples for flow cytometric analysis.
107 e examined by 7-amino-actinomycin D and flow cytometric analysis.
108  to type 1 alveolar epithelial cells by flow cytometric analysis.
109 ) and increased the S-phase fraction by flow cytometric analysis.
110     Circulating MSCs were quantified by flow cytometric analysis.
111 (HSPCs) were decreased in NHD13 mice by flow cytometric analysis.
112 on therapy underwent a liver biopsy for flow cytometric analysis.
113 ndirect immunofluorescence staining and flow-cytometric analysis.
114                                    Both flow cytometric and antibody-mediated neutralization studies
115                      With histological, flow cytometric and functional analyses, we find that CPCs re
116 ha expression patterns were examined by flow cytometric and immunofluorescence analysis.
117 nly based on single-cell analysis as in flow cytometric and microfluidic cell sorters.
118    Phagocytic uptake was detected using flow cytometric and microscopic techniques.
119             In this study, we developed flow cytometric and T cell enzyme-linked immunosorbent spot (
120                                    Both flow cytometric and transcriptomic analysis indicated stimula
121 Herein we used detailed transcriptomic, flow cytometric, and functional analysis and transcription fa
122 s of lungs were assessed by histologic, flow cytometric, and quantitative PCR analysis.
123 d 25 healthy subjects using an 11-color flow cytometric antibody panel.
124 d 27 healthy subjects using an 11-color flow cytometric antibody panel.
125 lines coupled with RNA interference and flow cytometric approaches, we find that transforming growth
126    In this study, we report a sensitive flow cytometric assay based on magnetic pre-enrichment of CD1
127 it binding of PPS-specific B cells in a flow cytometric assay demonstrating specificity and functiona
128               Here we evaluate a 7-hour flow cytometric assay for assessing Treg function, using supp
129                     We have developed a flow cytometric assay for inflammasome formation, time of fli
130 his study, we used a recently developed flow cytometric assay for the direct ex vivo characterization
131 s volume (MCV) and reticulocytosis; the flow-cytometric assay showed good correlation with the spectr
132 elease assay (IGRA) was combined with a flow cytometric assay that detects induction of CD25(+)CD134(
133                        Using a Click-iT flow cytometric assay to directly measure mitotic protein syn
134                          We developed a flow cytometric assay to profile CD1-restricted T cells ex vi
135                          We developed a flow-cytometric assay to study membrane protein-protein inter
136               A simple, high-throughput flow cytometric assay was developed that uses THP-1 cells and
137               We have used an optimized flow cytometric assay, based on the analysis of unfixed brain
138 he spectrophotomeric assay and the G6PD flow-cytometric assay.
139 ctivation of leukocytes was assessed by flow cytometric assays and by immunofluorescence microscopy.
140                            We then used flow cytometric assays capable of measuring total and Ag-spec
141                                         Flow cytometric assays combined with intra-vital imaging indi
142 ombination of genetic, biochemical, and flow cytometric assays in conjunction with a mathematical mod
143 paramagnetic resonance spectroscopy and flow cytometric assays showed a significant increase in cellu
144                                    Apoptotic cytometric assays showed that pretreatment of CSCs with
145                        This was confirmed by cytometric assays showing that inactive compounds failed
146   Rapid, sensitive, and highly specific flow-cytometric assays were developed for the detection of th
147                          As judged from flow cytometric assays, bacterial killing by GA occurred with
148 ested using the lymphoproliferation and flow cytometric assays.
149 LISA, Luminex, quantitative RT-PCR, and flow cytometric assays.
150                                         Flow cytometric assessment and mathematical modeling of intra
151 d by interferon (IFN)-gamma ELISpot and flow cytometric assessment of directly H-2K reactive cells.
152 t is possible by simple histological or flow cytometric assessments.
153          A single-cell based approach called cytometric bar coding (CyBar) for fast identification of
154 ecay rapidly to pMHC monomers, allowing flow-cytometric-based measurements of monomeric TCR-pMHC diss
155  production by polyp cells was determined by cytometric bead array (CBA) and intracellular cytokine a
156                         We developed a novel cytometric bead array for assessment of antigen-specific
157 4, IL-5, IL-10 and IL-13 were quantified via cytometric bead array in plasma.
158     Additionally, cytokines were measured by cytometric bead array, and L-ficolin was measured in bro
159 ee supernatants were quantified by using the cytometric bead array, and mRNA expression of transcript
160                                            A cytometric bead array, ELISA, and intracellular cytokine
161 rescein diacetate succinimidyl ester dye and cytometric bead array, formed an in vitro surrogate mark
162 t model, together with immunohistochemistry, cytometric bead array, functional adhesion and migration
163 protein signatures were determined by ELISA, cytometric bead array, or quantitative PCR.
164 n with mitogenic, TLR, and T-cell stimuli by cytometric bead array.
165 on was assessed in supernatants by using the Cytometric Bead Array.
166 evels of CCL11 were measured in plasma using Cytometric Bead Array.
167  cytokines/chemokines were determined with a cytometric bead array.
168           Cytokines in sera were analyzed by cytometric bead array.
169 in-6 and interleukin-10 concentrations using cytometric bead array.
170 ll responses by enzyme-linked immunospot and cytometric bead array.
171 e cell culture was measured with the help of cytometric bead arrays or ELISA assays.
172 n malaria (IL-5 and RANTES) were assessed by cytometric bead assay in April 2008, October 2008, and A
173 asmodium falciparum antigens was assessed by cytometric bead assay or enzyme-linked immunosorbent ass
174 IPAL FINDINGS: MCP-1 protein was measured by cytometric bead assay.
175    We enrolled 27 patients whose median flow cytometric calculated panel reactive antibody (CPRA) was
176 ly, we developed a rapid multiparameter flow cytometric CBU potency assay that enumerates cells expre
177                                         Flow cytometric cell cycle analysis of HUVECs treated with Ss
178                        A combination of flow cytometric cell sorting and deep sequencing of the 16S r
179  ecology was explored through combining flow cytometric cell sorting and molecular techniques to dete
180 ere used for immunostaining in situ and flow cytometric cell sorting.
181                                         Flow cytometric characterization of Ag-specific T cells typic
182  between 1980 and 2013 that include the flow cytometric characterization of leukocyte subsets in the
183 n, we performed detailed functional and mass cytometric cluster analysis of multiple CD8(+) T-cell cl
184 ients with COA were determined by using flow cytometric coexpression of collagen I, CD45, and CD34 or
185                                         Flow cytometric counts revealed that exposure of human macrop
186 p; 76.3% for recipients with a positive flow-cytometric cross-match but a negative cytotoxic cross-ma
187 ay for anti-HLA antibody but a negative flow-cytometric cross-match versus 65.0% for the waiting-list
188 ible and had a negative or low-positive flow cytometric crossmatch (+XM).
189 reened for human antibody binding using flow cytometric crossmatch (FCXM).
190 rossmatch (CDC-XM) and donor cell-based flow cytometric crossmatch (flow-XM) but low level DSA (i.e.,
191  detected by single antigen beads and B flow cytometric crossmatch (XM).
192 t in B4GALNT2 genes were examined using flow cytometric crossmatch assay.
193 alues have been found to correlate with flow cytometric crossmatch results.
194 el was insufficient to cause a positive flow cytometric crossmatch.
195                                         Flow cytometric crossmatching (FXM) is a standard method to a
196 ), was developed and applied to analyze flow cytometric data of bacterial responses to antibiotic exp
197 e 3-dimensional differences between the flow cytometric data of the no-antibiotic treated bacteria an
198                                    When flow cytometric data on mixtures of cell populations are coll
199         The presentation of high-dimensional cytometric data using One-SENSE showed a significant imp
200 uencing or after careful examination of flow cytometric data, as in the reports of lymphocyte-specifi
201 nts and blind multicenter reanalysis of flow cytometric data, resulting in an unprecedented concordan
202 inds of multivariate data sets, such as flow cytometric data, to identify differentially expressed po
203 ng the complexity and information content of cytometric data.
204 nformation contained in a highly dimensional cytometric dataset.
205         We used a stepwise approach for flow cytometric detection and purification of human IgE-expre
206                       These results and flow cytometric detection of CD45 and CD127 suggest the prese
207 EBV-specific T cells were quantified by flow cytometric detection of intracellular interferon-gamma a
208                     We demonstrate that flow cytometric detection of poorly differentiated basal tumo
209 rescein labeled folic acid was used for flow cytometric detection of the expression of functional fol
210 l LT-HSC has been defined as FLT3(-) by flow cytometric detection, we demonstrate that FLT3 is capabl
211 rane assays amenable to high-throughput flow cytometric detection.
212                Modern-era molecular and flow-cytometric diagnostic methods are very sensitive and can
213 F, AMD3100 or ischemia was evaluated by flow cytometric enumeration of circulating Lin(-)Sca-1(+)cKit
214 were harvested at these time points for flow cytometric evaluation of immune cell subtypes and immuno
215 , therapeutic antibodies may complicate flow cytometric evaluation of normal and neoplastic plasma ce
216                       However, both the flow cytometric evaluation of the TCR-Vbeta repertoire on CD4
217 re normal or only slightly reduced, and flow cytometric evaluations of the TCR-Vbeta repertoires of t
218                           We report the flow cytometric (FC) identification and characterization of l
219 reformed DSA detected by single-antigen flow cytometric fluorescent beads (SAFBs).
220 reformed DSA detected by single-antigen flow cytometric fluorescent beads (SAFBs).
221                        We identified by flow cytometric, fluorescent microscopic, immunoblot, and mas
222             Here we sought to develop a flow cytometric gating strategy to reliably identify blood Ig
223     Myeloid cells were characterized in flow cytometric, histologic, and immunohistochemical analyses
224 describe a fluorescence-based multiplex flow-cytometric host cell reactivation assay (FM-HCR) that me
225    Using a fluorescence-based multiplex flow cytometric host cell reactivation assay that provides si
226 eveloped a fluorescence-based multiplex flow-cytometric host cell reactivation assay wherein the acti
227              We describe a protocol for flow cytometric identification of viral reservoirs, based on
228          Multiplexed, phenotypic, intravital cytometric imaging requires novel fluorophore conjugates
229 servations were more deeply analyzed by flow cytometric imaging, confocal imaging, and measurement of
230  T cells were purified and subjected to flow cytometric immune-phenotyping and functional assays.
231 le, rapid, multi-parametric assay using flow cytometric immunofluorescence to reveal interactions amo
232 ate protein-DNA binding is monitored by flow cytometric immunofluorescence, which allows for accurate
233 proliferative, we applied comprehensive flow cytometric immunophenotyping and functional assays of cy
234                                To date, flow cytometric immunophenotyping has not been used to invest
235  CD45 barcoding facilitates accuracy of mass cytometric immunophenotyping studies, thus supporting bi
236 ipts or breakpoints, and multiparameter flow cytometric immunophenotyping.
237 ined single-cell functional assays with flow cytometric index sorting and single-cell gene expression
238            In this article, we report a flow cytometric investigation of B lymphocyte subpopulations
239 tive isolation, complex multi-parameter flow cytometric isolation of phenotypic subsets has facilitat
240                          In conclusion, flow cytometric LPT represents a reliable and useful method f
241                        We established a flow cytometric lymphocyte proliferation test (LPT) for the d
242                                         Flow cytometric membrane integrity staining demonstrated the
243                    The development of a flow-cytometric method allowed us to identify hemophagocytes
244 the infected host, we developed a novel flow cytometric method for measuring lysosome damage.
245              In this study we present a flow cytometric method identifying HBEC as CD45 negative, EpC
246  we describe a 2-d, 96-well plate-based flow cytometric method of micronucleus scoring that is simple
247 Vs, we used nanoFACS, a high-resolution flow cytometric method that utilizes light scattering and flu
248 ave developed, validated, and applied a flow cytometric method that will be useful to interrogate the
249                              To date, a flow cytometric method to identify HBEC recovered from lower
250                     Emerging high-resolution cytometric methods have created a pressing need for effi
251                                              Cytometric methods revealed extensive neutrophilic infil
252 ge groups of patients with CHB and used flow cytometric methods to measure production of effector and
253 51 meningioma samples by multiparameter flow cytometric (MFC) immunophenotyping and investigated the
254 motherapy sensitivity by multiparameter flow cytometric minimal residual disease (MFC-MRD) detection
255                                              Cytometric monitoring of microbial community dynamics ca
256                      We compared the BM flow cytometric, morphologic, and cytogenetic features of 28
257   Here we established an assay based on flow cytometric multiparameter assay assessing expression of
258 D38 core gating systems and an 11-color flow cytometric panel were used to determine the frequencies
259 PSFC the fluorescence lifetime is taken as a cytometric parameter to differentiate intracellular even
260 the flexibility of employing a wide range of cytometric parameters for identifying colonies and cells
261  differences between sample and control flow cytometric populations, even in a label-free scheme with
262 table after treatment, correlating with flow cytometric presence or absence of circulating M-PCs.
263  subjects using targeted multiparameter flow cytometric profiling of NK cell phenotypes and functions
264 ent cell barcoding with high-throughput flow cytometric profiling of primary and metastatic colon can
265      Here we show, using transcriptional and cytometric profiling of whole blood collected before vac
266 ografting, and multiplexed phospho-flow (PF) cytometric profiling to study drug response and identify
267 ngle-cell genomic, transcriptional, and mass-cytometric profiling, it remains a challenge to collect
268 erived microparticles by a standardized flow cytometric protocol in 119 patients referred for stress
269 +) regulatory T cells were subjected to flow cytometric quantification and sorting followed by qRT-PC
270 tries, the fixation conditions, and the flow cytometric quantification methods used.
271 y of human cells to HAP was examined by flow cytometric quantification of apoptotic cell death and de
272                                  Phosphoflow cytometric quantification of p70S6K phosphorylation may
273 ce resonance energy transfer (FRET) and flow cytometric quantification.
274                                         Flow cytometric quantitation indicated that GPVI dimers accou
275 s in adhesion receptor expression using flow cytometric quantitation of integrins and l-selectin memb
276 ed, as detected using a high-throughput flow cytometric quantum dot Forster resonance energy transfer
277 expressing P. falciparum antigens and a flow cytometric readout of infection, we are able to robustly
278                              Dual-laser flow cytometric resonance energy transfer (FCET) is a statist
279 uorescent probes were investigated in a flow cytometric screen of ABC transporters.
280 ss-reactive peptide ligand for a duplex flow cytometric screen of FPR1 and FPR2 in color-coded cell l
281 of-principle study, we used comparative flow cytometric screening to identify ICAM-1 as a potential t
282 n alpha-and beta-cells were obtained by flow cytometric sorting after intracellular staining with c-p
283 ere phenotyped and isolated by means of flow cytometric sorting from 18 patients at baseline and 13 p
284 rmal and fibrotic livers via subsequent flow cytometric sorting, thus providing a validated method to
285 ed protocol that eliminated the need of flow cytometric sorting.
286 ls purified by either bead selection or flow cytometric sorting.
287    Using both coimmunoprecipitation and flow-cytometric strategies, we found a bidentate interaction
288                    Here, we developed a flow-cytometric strategy capable of detecting membrane protei
289                                         Flow cytometric studies showed that PGN enhanced the secretio
290                                         Flow cytometric studies using monoclonal antibodies show that
291                                              Cytometric studies utilizing flow cytometry or multi-wel
292 ge segmentation, provides a means to conduct cytometric studies while at the same time preserving cru
293 confirmed in structural, serologic, and flow-cytometric studies.
294 dances and functions of cellular subsets via cytometric studies.
295                                 This in vivo cytometric technique may be useful in a wide range of st
296 the statistical accuracy of traditional flow cytometric techniques to label-free biophysical biomarke
297 ned by fasting blood glucose levels and flow cytometric techniques were used to test for donor-specif
298 chniques, including novel molecular and flow cytometric technologies used for the determination of mi
299                              We review these cytometric technologies, capable of high-content, high-t
300 type of these cells were measured using flow cytometric whole-blood assays.

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