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1 hrome, alpha-smooth muscle actin, IL-33, CD8, and IL-13 and analyzed by flow cytometry.
2  were captured on anti-MHC-class II- or anti-CD63 beads and analyzed by flow cytometry.
3 /-)Tnfr2(-/-) mice along with Il10(-/-) mice (controls) and analyzed by flow cytometry and histology.
4 e exposed to doses of radiation ranging from 2 to 12 Gy and analyzed by flow cytometry.
5 injection; peritoneal lavages were collected after 48 h and analyzed by flow cytometry and ELISA.
6 1-hydroxy-2-methyl-2-buten-4-yl 4-diphosphate [HDMAPP]) and analyzed by flow cytometry to determine Vdelta2T cell phenoty
7 ina propria mononuclear cells and T cells were isolated and analyzed by flow cytometry or cytokine assays.
8                         Mononuclear cells were isolated and analyzed by flow cytometry.
9                                      ILCs were isolated and analyzed by flow cytometry.
10                Circulating CD4(+) T cells were isolated and analyzed by flow cytometry.
11 gous Notch2HCS mice and sex-matched control littermates and analyzed by flow cytometry.
12 en and mesenteric lymph node were collected, processed, and analyzed by flow cytometry.
13        Immune cells were collected from resection sites and analyzed by flow cytometry and in depletion experiments.
14 ranscriptase PCR; leukocytes were isolated, stimulated, and analyzed by flow cytometry and PCR analyses.
15  cells were isolated from mouse and human liver tissues and analyzed by flow cytometry and enzyme-linked ImmunoSpot (ELIS
16  13 lean individuals undergoing cholecystectomy (controls), analyzed by flow cytometry, and cultured; immunophenotypes an
17  identity were analyzed using sphere generation and further analyzed by flow cytometry.
18 nduced by YF-17D and correlated them with immune parameters analyzed by flow cytometry prior to vaccination.
19                                NK cells were phenotypically analyzed by flow cytometry.
20 r Th17- or Th0-polarizing conditions and infected, and then analyzed by flow cytometry.
21 opulation specific for an oxycodone-based hapten (6OXY) was analyzed by flow cytometry paired with Ag-based magnetic enri
22                          Mvarphi and NK cell activation was analyzed by flow cytometry and killing assays, respectively.
23 a, and the expression of surface markers on YFP(+) BMCs was analyzed by flow cytometry.
24                                                    CCR5 was analyzed by flow cytometry in disaggregated lymph node cells
25                               Phenotype of immune cells was analyzed by flow cytometry, and cytokines by enzyme-linked im
26 ctivation of lamina propria dendritic cells and T cells was analyzed by flow cytometry.
27 gens by circulating CD4+ T cells from infected children was analyzed by flow cytometry, and disease severity was defined
28 poptosis was detected by EB/AO staining, and cell cycle was analyzed by flow cytometry.
29                        CD300a expression on eosinophils was analyzed by flow cytometry and evaluated by immuno-fluorescen
30                                          RFP expression was analyzed by flow cytometry and viral culture.
31                    Expression of RANKL protein and mRNA was analyzed by flow cytometry, ELISA, and real-time PCR.
32 tosis of F. nucleatum strains and neutrophil apoptosis were analyzed by flow cytometry.
33                                   Human tonsil B cells were analyzed by flow cytometry (FACS) and cultured with IL-4 and
34                                                  Cells were analyzed by flow cytometry and sorted from species mixtures d
35 fection, phenotype, and cytokine production by T cells were analyzed by flow cytometry or enzyme-linked immunosorbent ass
36                           Resting and stimulated cells were analyzed by flow cytometry, real-time PCR, and by ELISA.
37 , CD4, CD8) and intracellular Foxp3; and labeled cells were analyzed by flow cytometry.
38 ropositive or seronegative and HIV-uninfected controls were analyzed by flow cytometry.
39 itrobenz-2-oxa-1, 3-diazol-4-yl) amino)-2 deoxyglucose were analyzed by flow cytometry on monocyte subpopulations.
40 Leukocytes from ischemic and contralateral hemispheres were analyzed by flow cytometry.
41 lation of CD40, CD80, CD83, CD86, CD58, CCR7 and PD-L1 were analyzed by flow cytometry.
42        Intracellular cytokine levels in BAL leukocytes were analyzed by flow cytometry.
43 and maturation markers on viable MVA-OVA-infected mDCs were analyzed by flow cytometry.
44                                                   MPAs were analyzed by flow cytometry for the 3 monocyte subsets (CD14++
45 cy from patients with COPD and healthy subjects' PBMCs were analyzed by flow cytometry.
46             Treg proportion, number, and proliferation were analyzed by flow cytometry in peripheral blood of patients wi
47                                          Blood samples were analyzed by flow cytometry, endothelial cell colony-forming u
48 age chimerism, clonal deletion, and lymphocyte subsets were analyzed by flow cytometry.
49  during surgical resection and single-cell suspensions were analyzed by flow cytometry.
50            Lung macrophage phenotype and cell turnover were analyzed by flow cytometry and immunohistochemistry.

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