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1 oduction of oxidants was examined using 2',7'dichlorofluorescin, a dye that forms a fluorescent produ
2 e basis of monitoring the oxidation of 2',7'-dichlorofluorescin by spectrofluorometry, flow cytometry
3 O(-) and that could explain the oxidation of dichlorofluorescin (DCF) by Cu(I),Zn-SOD plus NO.
4 l levels with NACA treatment, as measured by dichlorofluorescin (DCF).
5 ble of oxidizing the fluorescent probe 2',7'-dichlorofluorescin (DCFH) also accumulate intracellularl
6 Single-cell fluorescence microscopy of 2',7'-dichlorofluorescin diacetate (DCF)-loaded cells showed t
7 A myocytes, oxidation of intracellular 2',7'-dichlorofluorescin diacetate (DCFH) dye increased under
8 irectly using confocal microscopy with 2',7'-dichlorofluorescin diacetate (DCFH) or using electron mi
9 onfocal laser scanning microscopy, using 2,7-dichlorofluorescin diacetate (DCFH-DA) as a probe.
10 ss the level of oxidative stress using 2',7'-dichlorofluorescin diacetate (DCFH-DA) fluorescence.
11  oxidation-sensitive fluorescent probe 2',7'-dichlorofluorescin diacetate and laser-scanning confocal
12 n species as measured by a fluorescent 2',7'-dichlorofluorescin diacetate assay, and >85% reduction i
13 nd free radical production determined by the dichlorofluorescin diacetate assay.
14 en species (ROS) (measured as an increase in dichlorofluorescin diacetate fluores-cence) and that sim
15  young rats, as measured by the rates of 2,7-dichlorofluorescin diacetate oxidation.
16 (intracellular oxidative burst activity with dichlorofluorescin diacetate staining) and adhesion (int
17 phosphorylation; the fluorochrome probe 2'7'-dichlorofluorescin diacetate was used to measure cytosol
18 brane-permeable dyes hydroethidine and 2',7'-dichlorofluorescin diacetate, respectively, were used to
19 eroxidation-sensitive fluorescent dye, 2',7'-dichlorofluorescin diacetate, was significantly elevated
20 ion of free radicals was measured with 2',7'-dichlorofluorescin diacetate.
21 lic oxidant levels were measured with 2', 7'-dichlorofluorescin diacetate; emissions of the oxidized
22 on per oxygen consumed, as measured by 2',7'-dichlorofluorescin fluorescence levels, is approximately
23 eneration (reactive oxygen species via 2',7'-dichlorofluorescin oxidation and nitric oxide [NO] via 4
24 rane permeability assessment, and DCF (2',7'-dichlorofluorescin) redox studies.
25 During induction, ROS oxidation of the probe dichlorofluorescin (sensitive to H2O2) increased approxi
26 the fluorescence produced on oxidizing 2',7'-dichlorofluorescin, was significantly lowered in (R)-lip