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1 le intracytoplasmic fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester and brom
2 amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and siz
3 lood mononuclear cell suppression assays and carboxyfluorescein diacetate succinimidyl ester assays w
4 ADOR antagonists or agonists were tested in carboxyfluorescein diacetate succinimidyl ester assays.
5 roliferating responder cells was assessed in carboxyfluorescein diacetate succinimidyl ester-based as
6 valuated using 3H-thymidine (3H-TdR) uptake, carboxyfluorescein diacetate, succinimidyl ester (CFDA-S
8 than the wild type strain, as determined by carboxyfluorescein diacetate succinimidyl ester (CFSE) l
9 l CD34(+) cells were labeled with 5-(and 6-)-carboxyfluorescein diacetate succinimidyl ester (CFSE) t
11 tected by flow cytometry after labeling with carboxyfluorescein diacetate succinimidyl ester (CFSE),
12 hogenesis, we examined migratory profiles of carboxyfluorescein diacetate succinimidyl ester (CFSE)-l
14 taneous injection of alum adjuvant including carboxyfluorescein diacetate succinimidyl ester (CFSE).
15 hly isolated NK cells labeled with 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester (CFSE)
18 collagenase perfusion and labeled using 5(6)-carboxyfluorescein diacetate succinimidyl-ester (CMFSE).
19 assessed by proliferation (thymidine uptake, carboxyfluorescein diacetate succinimidyl ester dye dilu
20 s of cell division using the fluorescent dye carboxyfluorescein diacetate succinimidyl ester indicate
21 The pretreated Lewis(BN) lymphocytes were carboxyfluorescein diacetate succinimidyl ester labeled
22 n vivo were assessed by adoptive transfer of carboxyfluorescein diacetate succinimidyl ester-labeled
24 the proliferation of adoptively transferred carboxyfluorescein diacetate succinimidyl ester-labeled
25 adhesion was measured by the retention of 5-carboxyfluorescein diacetate succinimidyl ester-labeled
27 ation of donor CD8+ T-cells in recipients of carboxyfluorescein diacetate succinimidyl ester-labeled
29 o recruit adoptively transferred 5- (and -6)-carboxyfluorescein diacetate succinimidyl ester-labeled
31 r to T cell-deficient host mice by injecting carboxyfluorescein diacetate succinimidyl ester-labeled
33 Carboxyfluorescein diacetate, succinimidyl ester-labeled
34 ation was visualized by adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester-labeled
36 -bromo-2'-deoxyuridine)- and CFSE [5-(and 6)-carboxyfluorescein diacetate succinimidyl ester]-labeled
37 lococcus enterotoxin B was determined by the carboxyfluorescein diacetate succinimidyl ester measurem
38 The proliferation capacities of carboxyfluorescein diacetate succinimidyl ester-positive
39 responses were studied by thymidine uptake, carboxyfluorescein diacetate succinimidyl ester staining
40 acellular fluorescent marker CFSE (5-(and-6)-carboxyfluorescein diacetate succinimidyl ester) to trac
41 FITC-based membrane-binding dye, 5-(and -6)-carboxyfluorescein diacetate succinimidyl ester, to allo
42 CD4-cell proliferation, the fluorescein dye carboxyfluorescein diacetate succinimidyl ester was used
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