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1 ined by monitoring the fluorescence of 2',7'-dichlorofluorescein.
2 xpression, as measured by oxidation of 2',7'-dichlorofluorescein.
3 ere determined by measuring the oxidation of dichlorofluorescein.
4 erted by the C60 aerosols as measured by the dichlorofluorescein acellular assay but not by the uric
5   Fluorescence intensity of the probes 2',7'-dichlorofluorescein and C11-BODIPY increased more rapidl
6                     Measured K(m) values for dichlorofluorescein and difluorofluorescein cephalospori
7  mo of age when killed) using histochemical (dichlorofluorescein and dihydroethidine) and bioluminesc
8 n of dichlorodihydrofluorescein diacetate to dichlorofluorescein and hydroethidium to ethidium, was i
9 tes were monitored by cis-parinaric acid and dichlorofluorescein assays, respectively.
10 and study of five new analogues of the 2',7'-dichlorofluorescein-based Zn(2+) sensor Zinpyr-1 (ZP1).
11   The oxidation of the fluorescent dye 2',7'-dichlorofluorescein (DCF) by horseradish peroxidase was
12 s shown by: reduction of ONOO(-)-induced 2,7-dichlorofluorescein (DCF) fluorescence in synaptosomes;
13 ar reactive oxygen species was examined with dichlorofluorescein (DCF) fluorescence.
14 tron transfer) sensors on the basis of 2',7'-dichlorofluorescein (DCF) fluorophore conjugated with tw
15 onditions while fluorescence imaging of 2, 7-dichlorofluorescein (DCF) was used to assess ROS generat
16 f DCFH to a green fluorescent product, 2',7'-dichlorofluorescein (DCF), required the uptake of extrac
17 piny neurons using fluorescence imaging with dichlorofluorescein (DCF).
18 tion of dichlorodihydrofluorescein (DCFH) to dichlorofluorescein (DCF).
19 red the generation of hydrogen peroxide with dichlorofluorescein (DCF).
20 barbituric acid [TBA]-reacting material, and dichlorofluorescein [DCF]), and 4) cortisol, growth horm
21 uorescence of oxidized dihydroethidium and a dichlorofluorescein derivative.
22  polyurethane) containing a lipophilic 2',7'-dichlorofluorescein derivative.
23 e exposed to the dye 5-(and 6)-carboxy-2',7'-dichlorofluorescein diacetate (CDCFDA).
24 epatoma cell line (HepG2) were quantified by dichlorofluorescein diacetate (DCF-DA) dye assay, wherea
25 eactive oxygen species (ROS) with the use of dichlorofluorescein diacetate (DCFDA), dihydroethidium,
26  was measured by calcein AM assay, and 2',7'-dichlorofluorescein diacetate (DCFH-DA) was used to dete
27 al cultures and fecal microbiota using 2',7'-dichlorofluorescein diacetate and flow cytometry.
28 g the H2O2-sensitive fluorescent probe 2',7'-dichlorofluorescein diacetate and flow cytometry.
29 tive species content was assayed using 2',7'-dichlorofluorescein diacetate dye, inducible nitric oxid
30 Likewise, the alphaAR-stimulated increase in dichlorofluorescein diacetate fluorescence was abolished
31 (2)-induced ROS formation, assessed from 2,7-dichlorofluorescein diacetate fluorescence.
32 r reactive oxygen species were measured with dichlorofluorescein diacetate fluorescence.
33  measured by the oxidant sensitive dye 2',7'-dichlorofluorescein diacetate in murine macrophage J774.
34     ROS levels were quantitated by the 2',7'-dichlorofluorescein diacetate method.
35 e oxygen species (ROS; mitosox red and 2',7'-dichlorofluorescein diacetate), NADPH, NADP(+) and ATP c
36                                        Using dichlorofluorescein diacetate, a detector of endogenous
37 ) were detected using the fluorescent probes dichlorofluorescein diacetate, dihydrorhodamine 123, and
38 his finding, we used 5-(and-6)-carboxy-2',7'-dichlorofluorescein diacetate, succinimidyl ester "mixed
39          Using the ROS-sensitive probe 2',7'-dichlorofluorescein diacetate, we found that antisense s
40 ygen species (ROS) were measured using 2',7'-dichlorofluorescein diacetate.
41 en species (ROS) were determined using 2',7'-dichlorofluorescein diacetate.
42 cuole-specific dye, 5-(and -6)-carboxy 2',7'-dichlorofluorescein diacetate.
43 ng a H2O2-sensitive fluorescent probe, 2',7'-dichlorofluorescein diacetate.
44 ndicated by the oxidation of preloaded 2',7'-dichlorofluorescein diacetate.
45 and immunostaining), oxidative stress (2',7'-dichlorofluorescein-diacetate and Amplex Red analysis),
46 s and acyl group size are optimized in 2',7'-dichlorofluorescein diisobutyrate.
47                  H2O2-mediated intracellular dichlorofluorescein fluorescence and apoptosis were enha
48 d H(2)O(2)- and lipid peroxide-induced 2',7'-dichlorofluorescein fluorescence and protein oxidation.
49  binding activities, and DNA synthesis using dichlorofluorescein fluorescence by flow cytometry and s
50  intact lung demonstrated that the increased dichlorofluorescein fluorescence in these models of ROS
51  reactive oxygen species (ROS) generation by dichlorofluorescein fluorescence of hepatocytes.
52 duced neurotoxicity and also demonstrated no dichlorofluorescein fluorescence or increased lipid pero
53 n of reactive oxidants as evident from 2',7'-dichlorofluorescein fluorescence studies.
54  chemiluminescence), hydrogen peroxide H2O2 (dichlorofluorescein fluorescence), and expression and ac
55  *NO inhibited the TfR-mediated iron uptake, dichlorofluorescein fluorescence, and apoptosis in H2O2-
56 n was inferred from the relative increase in dichlorofluorescein fluorescence, and the degree of lipi
57 ive stress by assays for lipid peroxidation, dichlorofluorescein fluorescence, and tyrosine nitration
58 mitochondrial ROS generation, as measured by dichlorofluorescein fluorescence, which we have termed m
59                   Ethidium bromide and 2',7'-dichlorofluorescein, fluorescent products of the membran
60             ROS production was determined by dichlorofluorescein imaging.
61  the Mrp2 substrate 5-(and-6)-carboxy-2', 7'-dichlorofluorescein in IPLs from PB-treated rats after a
62 orescence associated with oxidation of 2',7'-dichlorofluorescein, indicating increased levels of intr
63  species, as measured by the fluorescence of dichlorofluorescein-loaded cells, and this was blocked b
64                                 Furthermore, dichlorofluorescein measurements indicated that there wa
65  polymorphonuclear-leukocytes, as assayed by dichlorofluorescein (P < 0.05).
66 triggered when the liberated indicator 2',7'-dichlorofluorescein reacts with the polymeric coating ma
67 eled with the gap junction tracer, dicarboxy-dichlorofluorescein, revealed extensive dye transfer to
68                         A transient burst of dichlorofluorescein (sensitive to H2O2 oxidation that wa
69           Here, we report an analog of 2',7'-dichlorofluorescein that can be used as a fluorescent se
70 sible by observing the fluorescence of 2',7'-dichlorofluorescein-the intracellular, oxidized form of
71              Using fluorescence imaging with dichlorofluorescein to visualize intracellular H2O2, we
72 uction of ROS, measured in cells loaded with dichlorofluorescein, were compatible with a role for ROS