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1 xpression, as measured by oxidation of 2',7'-dichlorofluorescein.
2 ere determined by measuring the oxidation of dichlorofluorescein.
3 erted by the C60 aerosols as measured by the dichlorofluorescein acellular assay but not by the uric
4 Fluorescence intensity of the probes 2',7'-dichlorofluorescein and C11-BODIPY increased more rapidl
6 mo of age when killed) using histochemical (dichlorofluorescein and dihydroethidine) and bioluminesc
7 n of dichlorodihydrofluorescein diacetate to dichlorofluorescein and hydroethidium to ethidium, was i
9 and study of five new analogues of the 2',7'-dichlorofluorescein-based Zn(2+) sensor Zinpyr-1 (ZP1).
10 The oxidation of the fluorescent dye 2',7'-dichlorofluorescein (DCF) by horseradish peroxidase was
11 s shown by: reduction of ONOO(-)-induced 2,7-dichlorofluorescein (DCF) fluorescence in synaptosomes;
13 tron transfer) sensors on the basis of 2',7'-dichlorofluorescein (DCF) fluorophore conjugated with tw
14 onditions while fluorescence imaging of 2, 7-dichlorofluorescein (DCF) was used to assess ROS generat
15 f DCFH to a green fluorescent product, 2',7'-dichlorofluorescein (DCF), required the uptake of extrac
19 barbituric acid [TBA]-reacting material, and dichlorofluorescein [DCF]), and 4) cortisol, growth horm
23 epatoma cell line (HepG2) were quantified by dichlorofluorescein diacetate (DCF-DA) dye assay, wherea
24 eactive oxygen species (ROS) with the use of dichlorofluorescein diacetate (DCFDA), dihydroethidium,
25 was measured by calcein AM assay, and 2',7'-dichlorofluorescein diacetate (DCFH-DA) was used to dete
28 tive species content was assayed using 2',7'-dichlorofluorescein diacetate dye, inducible nitric oxid
29 Likewise, the alphaAR-stimulated increase in dichlorofluorescein diacetate fluorescence was abolished
32 measured by the oxidant sensitive dye 2',7'-dichlorofluorescein diacetate in murine macrophage J774.
34 e oxygen species (ROS; mitosox red and 2',7'-dichlorofluorescein diacetate), NADPH, NADP(+) and ATP c
36 ) were detected using the fluorescent probes dichlorofluorescein diacetate, dihydrorhodamine 123, and
37 his finding, we used 5-(and-6)-carboxy-2',7'-dichlorofluorescein diacetate, succinimidyl ester "mixed
44 and immunostaining), oxidative stress (2',7'-dichlorofluorescein-diacetate and Amplex Red analysis),
47 d H(2)O(2)- and lipid peroxide-induced 2',7'-dichlorofluorescein fluorescence and protein oxidation.
48 binding activities, and DNA synthesis using dichlorofluorescein fluorescence by flow cytometry and s
49 intact lung demonstrated that the increased dichlorofluorescein fluorescence in these models of ROS
51 duced neurotoxicity and also demonstrated no dichlorofluorescein fluorescence or increased lipid pero
53 chemiluminescence), hydrogen peroxide H2O2 (dichlorofluorescein fluorescence), and expression and ac
54 *NO inhibited the TfR-mediated iron uptake, dichlorofluorescein fluorescence, and apoptosis in H2O2-
55 n was inferred from the relative increase in dichlorofluorescein fluorescence, and the degree of lipi
56 ive stress by assays for lipid peroxidation, dichlorofluorescein fluorescence, and tyrosine nitration
57 mitochondrial ROS generation, as measured by dichlorofluorescein fluorescence, which we have termed m
60 the Mrp2 substrate 5-(and-6)-carboxy-2', 7'-dichlorofluorescein in IPLs from PB-treated rats after a
61 orescence associated with oxidation of 2',7'-dichlorofluorescein, indicating increased levels of intr
62 species, as measured by the fluorescence of dichlorofluorescein-loaded cells, and this was blocked b
65 triggered when the liberated indicator 2',7'-dichlorofluorescein reacts with the polymeric coating ma
66 eled with the gap junction tracer, dicarboxy-dichlorofluorescein, revealed extensive dye transfer to
69 sible by observing the fluorescence of 2',7'-dichlorofluorescein-the intracellular, oxidized form of
71 uction of ROS, measured in cells loaded with dichlorofluorescein, were compatible with a role for ROS
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