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1 emistry), and infiltrating cell populations (flow cytometry).
2 ted transitions across discrete states using flow cytometry.
3 ph nodes, and bone marrow were quantified by flow cytometry.
4 ed using fluorogenic probes, microscopy, and flow cytometry.
5 d cell cycle kinetics were measured by using flow cytometry.
6 was completely C3-dependent, as detected by flow cytometry.
7 d healthy control subjects was analyzed with flow cytometry.
8 ha-stimulated HUVECs and quantified by using flow cytometry.
9 ned via Annexin V/Propidium iodide stain and flow cytometry.
10 an previously reported based on conventional flow cytometry.
11 sis-specific tetramer(+)CD4(+) T cells using flow cytometry.
12 se chain reaction, immunohistochemistry, and flow cytometry.
13 kers and phagocytic ability were assessed by flow cytometry.
14 roducing and non-producing cells purified by flow cytometry.
15 ss using antibody-avid polystyrene beads and flow cytometry.
16 exosomes in epithelial cells was assessed by flow cytometry.
17 Engraftment was assessed by flow cytometry.
18 cocultures were analyzed by using ELISA and flow cytometry.
19 ted from a yeast surface display library via flow cytometry.
20 by nanoparticle tracking analysis (NTA) and flow cytometry.
21 dies by surface plasmon resonance as well as flow cytometry.
22 The expression of CCR7 was determined by flow cytometry.
23 munohistochemistry, electron microscopy, and flow cytometry.
24 rRNA gene-based phylogenetic microarrays and flow cytometry.
25 e molecular composition of human synapses by flow cytometry.
26 y quantitative polymerase chain reaction and flow cytometry.
27 using Western blot, electron microscopy and flow cytometry.
28 vated or injured cells and are detectable by flow cytometry.
29 pressing tumors with immunohistochemistry or flow cytometry.
30 ses of T-cell subsets were measured by using flow cytometry.
31 tly labeled ECL1i in vivo were detected with flow cytometry.
32 ivation of microglial cells were measured by flow cytometry.
33 n an HIV-1-inducible reporter T cell line by flow cytometry.
34 Cell images were acquired with imaging flow cytometry.
35 /AO staining, and cell cycle was analyzed by flow cytometry.
36 peripheral blood DCs was quantified by using flow cytometry.
37 ple sclerosis patients using multiparametric flow cytometry.
38 ns and neutrophil apoptosis were analyzed by flow cytometry.
39 factor expression were assessed by means of flow cytometry.
40 in conjunction with confocal microscopy and flow cytometry.
41 Circulating B cells were characterized by flow cytometry.
42 rasite infection of hepatocyte cell lines by flow cytometry.
43 mma-producing CD4+ T cells, were detected by flow cytometry.
44 culating progenitor cells were enumerated by flow cytometry.
45 ver time in a mouse model of infection using flow cytometry.
46 ulations was evaluated by immunostaining and flow cytometry.
47 ted monocytes (CD14+CD16+) was determined by flow cytometry.
48 s) in lung single-cell preparations by using flow cytometry.
49 vation and histamine release was measured by flow cytometry.
50 en binding and presentation were assessed by flow cytometry.
51 tored immune cell surveillance of the CNS by flow cytometry.
52 the 6 populations of cells were isolated by flow cytometry.
53 ion was assessed by immunohistochemistry and flow cytometry.
54 ated by quantitative PCR, immunoblotting and flow cytometry.
55 nd fenestrated) and open aortic repair using flow cytometry.
56 ymphocytes subsets from cultured blood using flow cytometry.
57 t1 phosphorylation levels were determined by flow cytometry.
58 tochemistry, quantitative RT-PCR, ELISA, and flow cytometry.
59 om NP or tonsil, or after ILC2 coculture, by flow cytometry.
60 ll proliferation and cycle were evaluated by flow cytometry.
61 from allergic patients was analyzed by using flow cytometry.
62 system in the kidney relies predominantly on flow cytometry.
63 d assays and from outgrowth assay readout by flow cytometry.
64 sing 2',7'-dichlorofluorescein diacetate and flow cytometry.
65 were performed by using ELISA, ELISpot, and flow cytometry.
66 and HIV-uninfected controls were analyzed by flow cytometry.
67 comes many limitations of fluorescence-based flow cytometry.
68 ral killer (NK) cell number were measured by flow cytometry.
69 ch were minimal residual disease negative by flow cytometry.
70 and lymph nodes were detected dynamically by flow cytometry.
71 d beta2 integrin adhesion molecules by using flow cytometry.
72 olated from spleen and liver for analysis by flow cytometry.
73 are challenging to distinguish with standard flow cytometry.
74 d antibodies against pan-cytokeratin through flow cytometry.
75 n levels of common endothelial markers using flow cytometry, 3 subpopulations of endothelial cells co
77 specific effector T cells were analyzed with flow cytometry after polyclonal and pathogen-specific st
78 novel use of single cell resolution imaging flow cytometry allowed the visualization and quantificat
82 D We performed whole blood transcriptome and flow cytometry analyses on a total of 70 critically inju
86 ocess of tissue homogenization necessary for flow cytometry analysis introduces bias and results in t
87 Confocal microscopy of kidney sections and flow cytometry analysis of glomerular cells from magneti
88 validated 24 hours after removal of GNPs by flow cytometry analysis of mitochondrial depolarisation.
91 ing endothelial microvesicles, identified by flow cytometry analysis, and significantly more microves
92 . cruzi infection by confocal microscopy and flow cytometry analysis, showing a high expression in ma
93 rough confocal laser scanning microscopy and flow cytometry analysis, we demonstrated that protein/li
97 l types and mediators was performed by using flow cytometry and a multiplex assay with bronchoalveola
99 r cells from liver and blood were studied by flow cytometry and analyzed for responses to cytokine an
113 terize reprogrammed iCPCs by immunostaining, flow cytometry and gene expression; differentiate iCPCs
118 ion of differentiated cells is performed via flow cytometry and immunostaining to assess quantitative
119 ric solid tumor cells was tested in vitro by flow cytometry and in vivo by PET/CT imaging and dosimet
124 ge of this dual-functionality probe for both flow cytometry and mass cytometry in a mimetic cell mixt
126 logical and histological studies, as well as flow cytometry and measurements of proinflammatory media
130 eacted with mouse bone marrow neutrophils by flow cytometry and on spleen sections by immunohistochem
132 We enumerated small phytoplankton using flow cytometry and qPCR assays for phylogenetically dist
135 nd gene expression patterns were measured by flow cytometry and quantitative polymerase chain reactio
136 ional activity of MRP1 were determined using flow cytometry and SECM, and our findings show that thes
138 evice has been evaluated in combination with flow cytometry and turned out to be around 25% (cells en
139 iched CD1d(hi) CD5(+) B cells were sorted by flow cytometry and were adoptively transferred to recipi
140 der hemodynamic flow conditions coupled with flow cytometry and Western blot analysis to elucidate th
141 cement in TIC marker expression (examined by flow cytometry) and improved tumorsphere formation effic
142 s of inflammation and sepsis, intracellular (flow cytometry) and secreted cytokines (Luminex), were a
144 Phenotype of immune cells was analyzed by flow cytometry, and cytokines by enzyme-linked immunosor
145 T cell allogeneic responses were measured by flow cytometry, and diapedesis was assessed using transw
147 rofiled antigen-responsive cells in PBMCs by flow cytometry, and examined cells in whole blood obtain
149 pheral blood lymphocyte populations by using flow cytometry, and histologic and ultrastructural analy
150 ections and flat mounts, CD11b-based retinal flow cytometry, and qRT-PCR analysis of key microglia ma
152 lyzed by ELISA or intracellular staining and flow cytometry, and the expression of muscarinic and nic
153 Enzyme-linked immunosorbent assay (ELISA), flow cytometry, and Western blot are common bioanalytica
154 rter protein fusions are evaluated in ELISA, flow cytometry, and Western blot experiments and compare
155 rse transcription polymerase chain reaction, flow cytometry, and Western blotting-in several nonprost
156 poptosis and efferocytosis by morphology and flow cytometry; and GCS efficacy by apoptosis assays and
158 cell signaling, such as the western blot and flow cytometry, are limited in three aspects: 1) The per
159 highlights an alternative approach in using flow cytometry as a sensitive method for detecting ZIKV
162 tly labelled monomeric detection reagents in flow cytometry, as pull-down ligands to selectively enri
164 e of CaValpha2delta1, indicated by two-color flow cytometry assays and confocal imaging, and prevente
165 r miR-145 were used in cell permeability and flow cytometry assays for apoptosis and proliferation.
166 characterized by fluorescence microscopy and flow cytometry assays in BXPC-3 and PANC-1 cells, two pa
169 peripheral blood leucocyte populations using flow cytometry at baseline and after 2 weeks of systemic
170 tiation (CD) proteins used to count cells by flow cytometry, band 3 (CD233), CD71, CD45, and CD41.
171 can be used for both confocal microscopy and flow cytometry based high-throughput quantification of g
172 and Methods A prospective and comprehensive flow cytometry-based immunomonitoring program paralleled
173 acilitate the analysis of LTP, here we use a flow cytometry-based method to track chemically induced
174 MBNL1 locus in HeLa cells and established a flow cytometry-based screening system to identify compou
175 high-throughput neutralization screening and flow cytometry-based sorting of single B cells using HIV
176 of this predicted structure, we developed a flow-cytometry-based assay that measures cytosolic excha
178 ble immunohistochemistry (PCNA-staining) and flow cytometry (BrdU incorporation) revealed that a disc
179 ly offer high fluorescence signal for use in flow cytometry, but also show better performance in mass
181 Ts were quantitatively and qualitatively via flow cytometry characterized ex vivo and after culture w
184 uld increase the concordance between SAB and flow cytometry crossmatch (FCXM) results, thus enabling
185 T cells and dendritic cells were assessed by flow cytometry, cytokines by multiplex enzyme-linked imm
186 ation of the laboratory procedure and of the flow cytometry data analyses, as well as clinical valida
187 ly synthesize low-dimensional projections of flow cytometry data that typically have a high number of
192 ers in the airways were assessed by means of flow cytometry, ELISA, Luminex, and immunohistochemistry
197 culating phenotypic diversity estimates from flow cytometry (FCM) data of minute amounts of sample.
198 njugates toward GAGs binding was examined by flow cytometry, fluorescence microscopy, and gel electro
199 examined mature human skin-derived MCs using flow cytometry for expression of antigen-presenting mole
200 lar (LG) MK pool (defined by side scatter on flow cytometry) gives rise to a mature high granular (HG
202 e platelets to agonists in vitro assessed by flow cytometry (high-responder donors) are cleared more
203 llows: BAT-CD63 upregulation was assessed by flow cytometry; HR-released histamine was quantified by
204 cardiac-specific heterozygous Bin1 deletion, flow cytometry identified 47% less cBIN1-MPs in plasma,
207 helial to mesenchymal transition (EMT) using flow cytometry, immunofluorescence, and quantitative rev
208 asibility is demonstrated by validation with flow cytometry, immunohistochemistry and single-cell RNA
210 5 + FOXP3 + CD127dim/-) were evaluated using flow cytometry in 32 patients with cGvHD treated by ECP
212 unts were assessed by immunofluorescence and flow cytometry in T and B cells isolated from human PBMC
213 osinophils were identified by microscopy and flow cytometry in the lungs and paratracheal lymph nodes
220 y, the differential presence of DPP4 allowed flow cytometry-mediated isolation of senescent cells usi
223 d SW480 cell survival, which was detected by flow cytometry, MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-di
224 Our immunohistochemical data, combined with flow cytometry (N = 5) which identified a small number o
229 itu hybridization (in situ hybridization and flow cytometry) of primary lymphocytes from patients wit
232 1 clinical trials, and quantified by 4-color flow cytometry or allele-specific oligonucleotide real-t
234 imens were analyzed by means of conventional flow cytometry or cytometry by time-of-flight mass spect
235 plication of MRD assessment techniques, like flow cytometry or polymerase chain reaction-based method
239 scription-quantitative PCR, microarrays, and flow cytometry, or indirectly, by the presence of oncoge
243 hway, and kinetics of albumin trafficking by flow cytometry, quantitative confocal microscopy, and an
245 Atomic force microscopy, high-resolution flow cytometry, real-time quantitative RT-PCR, and mass
246 oE, and healthy controls, were analyzed with flow cytometry regarding levels of CD23, CD44, CD54, CRT
248 oimaging, super-resolution microscopies, and flow cytometry reveal almost 100-fold more efficient co-
249 racterization of circulating monocytes using flow cytometry revealed increased chemokine receptor exp
257 supplement technology to the microscopy and flow cytometry, the microfluidic deformability sensor wo
262 esent the development of rapid methods using flow cytometry to characterize several aspects of the ph
264 healthy children (n=20) using multiparameter flow cytometry to detect markers of T cell maturation, e
266 sion tomography imaging, gamma counting, and flow cytometry to evaluate the biodistribution, nanomedi
267 emia, we used high-resolution microscopy and flow cytometry to highlight the heterogeneity of drug ac
272 use overexpression studies, mutagenesis, and flow cytometry to show that ICAP1 contains a functional
273 as assessed by detection of virus antigen by flow cytometry together with various hematopoietic cell
274 were analyzed for immune cell composition by flow cytometry, Toll-like receptor (TLR) expression by q
275 sion line and a T-DNA insertion mutant using flow cytometry, transactivation and electrophoretic mobi
276 -induced polyfunctional cellular activity by flow cytometry, transcriptional profiling, epigenetic, a
278 tory T (Treg)-cell induction was assessed by flow cytometry using a transgenic T-cell transfer model.
279 nying evidence from immunohistochemistry and flow cytometry using antibodies with conformationally se
280 approximately 300 proteins by multiparameter flow cytometry using multiple aneuploid model systems su
281 The high-dimensionality of data generated by flow cytometry usually makes it difficult to visualize.
282 -DQ-gluten tetramer-based assay, we combined flow-cytometry variables in a multiple regression model
293 aging by confocal microscopy and analysis by flow cytometry, we synthesized derivatives of Taxol link
295 , ELISA, western blot, mass spectrometry and flow cytometry were used to screen for autoantibodies, i
297 eads to loss of gene expression as judged by flow cytometry, Western blot or immunofluorescence.
298 idney tissue, VTEA replicated the results of flow cytometry while providing detailed analysis of the
299 f allergic patients were quantified by using flow cytometry with QuantiBRITE beads and compared with
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