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1 nalyzed by mass spectrometry (MS) and immuno-spin trapping.
2 O nitrone adduct could be detected by immuno-spin trapping.
3 ture was obtained by electron spin resonance spin trapping.
4 ed methyl radical, which was detected by ESR spin trapping.
5 th phorbol 12-myristate 13-acetate using EPR spin trapping.
6 gen consumption, and electron spin resonance spin trapping.
7 e utilizing phenyl-N-tert-butylnitrone (PBN) spin trapping.
8 py and alpha-phenyl-tert-butyl nitrone (PBN) spin trapping.
9 onstrated by electron paramagnetic resonance spin trapping.
10 tion that was trapped and detected using EPR spin trapping.
11 es and determined O(2)* generation using EPR spin trapping.
12 ure, nitrone adducts were detected by immuno-spin trapping.
13 etion, using electron paramagnetic resonance spin trapping.
14 a hydroethidine fluorescence assay, and EPR spin trapping.
15 generation by 37 and 57%, as measured by EPR spin-trapping.
16 f O(2)(.) generation was investigated by EPR spin-trapping.
19 f nanomaterials and proper conditions of the spin trapping agent (such as incubation time) may lead t
25 ylpyrollidine-N-oxide (DMPO) as a superoxide spin-trapping agent a 12-line EPR spectrum characteristi
26 sis that phenyl-N-tert-butylnitrone (PBN), a spin-trapping agent known to cross the blood-brain barri
34 measured by electron paramagnetic resonance spin trapping and eNOS activity, as measured by [14C]arg
35 ich can be detected and visualized by immuno-spin trapping and has the potential to be further charac
39 have important impacts on the rates of both spin trapping and spin-adduct quenching affecting the le
40 approach, which combines the specificity of spin trapping and the sensitivity of antigen-antibody in
43 roughput plate reader-based oximetry and EPR spin trapping as confirmatory assays, it is now eminentl
46 this method is broadly applicable to enable spin trapping-based quantitative determination of free r
47 xidation conditions, results showed that ESR spin trapping can be useful to evaluate the oxidative su
51 n was assayed in isolated synaptosomes using spin trapping electron paramagnetic resonance (EPR) spec
52 mation of the electron donors, TE(O)A(*), by spin trapping electron paramagnetic resonance spectrosco
56 by a DMPO (5,5-dimethyl-1-pyrroline-N-oxide) spin-trapping EPR method at room temperature on a Bruker
57 These estimates, obtained by quantitative spin-trapping EPR, were confirmed by fluorescence techni
63 metry, electron paramagnetic resonance (EPR) spin trapping experiments indicate that iron catalyzed p
67 nitase with superoxide is provided using ESR spin trapping experiments with 5-diethoxyphosphoryl-5-me
70 ) and alpha-phenyl-N-tert-butylnitrone (PBN) spin-trapping experiments aimed to detect methyl radical
74 we performed electron paramagnetic resonance spin-trapping experiments to directly measure and charac
75 lectron paramagnetic resonance spectroscopic spin-trapping experiments using phenyl N-tert-butylnitro
79 ence for alkyl radical formation through EPR spin-trapping experiments, relative kinetics of radical
83 lived radical intermediates were detected by spin-trapping, hydrogen peroxide by an oxidase electrode
84 dentified by electron paramagnetic resonance spin trapping, immunospin trapping, and MS analysis afte
85 magnetic resonance spectroscopy with in vivo spin trapping in an obese rat model, with or without thi
95 approaches to assessment of RS(*) using EPR spin trapping, mass spectrometric, immunological, and HP
98 g activity of the mutant, as measured by the spin trapping method at low H2O2 concentration, is enhan
100 as measured, over storage time, with the EPR spin trapping method under forced ageing conditions.
101 ction of the G93A mutant, as measured by the spin trapping method, is enhanced relative to that of th
102 his reveals a general problem of the regular spin-trapping method in determining radical formation ki
103 e Fenton reaction, a novel tool based on EPR spin trapping methodology was developed to quantify wine
104 c resonance spectroscopy in conjunction with spin-trapping methodology to directly determine whether
106 pported by quantum chemical calculations and spin trapping methods, led to the identification of a fa
110 that Fe(DTCS)2 and Fe(MGD)2 are efficient at spin trapping NO* but their maximal efficiency may be af
111 In contrast, Fe(MGD)2 was more efficient at spin trapping NO* from the lipopolysaccharide-activated
112 hich appears to have distinct advantages for spin trapping O(2)(*-) compared to the well-studied spin
114 edicted to be the most suitable nitrones for spin trapping of *OH due to the similarity of their ther
115 be the most efficient substitution site for spin trapping of *OH, and their spin adducts are predict
118 enzyme activity of XO, respectively, by EPR spin trapping of O-*(2) using 5-(diethoxyphosphoryl)-5-m
121 metry of the disulfide radical anion and the spin trapping of the primary thiyl radical formed from t
126 ssing need to develop nitrones with improved spin trapping properties and controlled delivery in cell
127 be ideal in molecular tethering for improved spin-trapping properties and could pave the way for impr
129 sides of the nitronyl function improves the spin-trapping properties, with 4-HOOC-PBN-CH(2)OAc and 4
130 shown that detection of free radicals by ESR spin trapping provides useful information on the suscept
131 of a nitropyridine to form a nitrosopyridine spin-trapping reagent and an exquisitely selective terti
134 placement, and electron spin resonance (ESR)-spin trapping showed that superoxide production and gene
140 mutation on the order of 10(8) M(-1) . s(-1) Spin-trapping studies also demonstrated that the rate of
141 -Pyridyl-1-oxide)-N-tert-butylnitrone (POBN)/spin-trapping studies demonstrated that the interaction
143 -NQR suffered a mild loss as measured by EPR spin trapping, suggesting the protective role of S-gluta
144 alidate the application of rapid-scan EPR to spin trapping, superoxide was generated by the reaction
145 u(II)-H(2)O(2) oxidizing system using immuno-spin trapping supplemented with electron paramagnetic re
146 oxide)-N-tert-butyl-nitrone (4-POBN)-ethanol spin-trapping system, the 4-POBN-.CH(CH3)OH spin adduct
147 er, using a 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping system, we were able to demonstrate signif
148 yridyl-1-oxide)-N-tert-butyl-nitrone/ethanol spin-trapping system, we were able to detect HO. formati
149 n situ electron paramagnetic resonance (EPR) spin trapping technique and radical trapping with probe
150 ,5-dimethyl-1-pyrroline N-oxide-based immuno-spin trapping technique to investigate the MPO-triggered
151 onance spectroscopy, in conjunction with the spin trapping technique, we have shown previously that A
154 ith peroxisome proliferators is lacking, the spin-trapping technique and electron spin resonance spec
155 ogen peroxide was investigated using the ESR spin-trapping technique and the nitroso spin traps 3,5-d
157 investigated by the electron spin resonance spin-trapping technique using 5-diethoxyphosphoryl-5-met
158 generation by SCR was measured with the EPR spin-trapping technique using DEPMPO (5-diethoxylphospho
160 by electron paramagnetic resonance using the spin-trapping technique, and by the oxidation of oxymyog
161 cal ((.)CN) that was detected, using the ESR spin-trapping technique, as the 5,5-dimethyl-1-pyrroline
162 )/(*)CN by the electron spin resonance (ESR) spin-trapping technique, can be generated by horseradish
168 efore, using electron paramagnetic resonance spin trapping techniques we measured the dose-dependent
171 By using electron paramagnetic resonance spin-trapping techniques, we monitored NO and .O2- forma
173 hoxyphosphoryl)-5-methyl-1-pyrroline-N-oxide spin trapping to characterize the potential of lucigenin
178 by electron paramagnetic resonance following spin trapping was increased in patients compared with he
179 on of radical production and the kinetics of spin trapping was performed in the presence of a series
180 ere, in situ electron paramagnetic resonance spin trapping was used to compare radicals produced by u
181 lectron spin resonance (ESR) with or without spin trapping, which is not available in most bioresearc
182 mation from hydrogen peroxide as measured by spin trapping with 5, 5'-dimethyl-1-pyrrolline N-oxide (
184 hich was here detected and quantified by ESR spin trapping with 5-diethoxyphosphoryl-5-methyl-1-pyrro
187 tic resonance measurements as well as immuno-spin trapping with antibodies against protein 5,5-dimeth
191 reliability, specificity and sensitivity of spin trapping with heterogeneous immunoassays for the de
192 thylenes) (POE)] was investigated by EPR and spin-trapping with 3,5-dibromo-4-nitrosobenzenesulfonate
193 we demonstrate using electron spin resonance spin-trapping with 5-diethoxyphosphoryl-5-methyl-1-pyrro