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1 by elevations in lung lipid peroxidation and oxidized glutathione.
2 y measures the total GSH pool, including the oxidized glutathione.
3 g can be further promoted by the presence of oxidized glutathione.
4 against either gamma-glutamyl amino acids or oxidized glutathione.
5 rodes (GCE) for the detection of reduced and oxidized glutathione.
6 n assembly required microsomal membranes and oxidized glutathione.
7 P fused to sensor domains to measure H2O2 or oxidized glutathione.
8 nor NOC12, with no effect in the presence of oxidized glutathione.
9 d via treatment of organotypic cultures with oxidized glutathione.
10 nd maintenance of a high ratio of reduced to oxidized glutathione.
11 ncentrations, compared to in the presence of oxidized glutathione.
12  peroxidase, and higher ratios of reduced to oxidized glutathione.
13 edox balance to a higher ratio of reduced to oxidized glutathione.
14 higher concentrations of SAH, adenosine, and oxidized glutathione.
15 related with a decreased ratio of reduced to oxidized glutathione.
16 he production of reactive oxygen species and oxidized glutathione.
17 ontrol, 15.75+/-4.33 micromol/g, P<0.0005; % oxidized glutathione, 4.49+/- 1.87% versus control, 22.8
18           In agreement, the ratio of reduced:oxidized glutathione, a major antioxidant and indicator
19 o our mimetic peptide with its reactivity to oxidized glutathione, a nonspecific substrate.
20  for 24 h) resulted in marked GSH depletion, oxidized glutathione accumulation, hydroxyl radical gene
21                                          The oxidized glutathione-activated TRPC5-like current result
22           Decreasing the ratio of reduced to oxidized glutathione also promoted select disulfide bond
23                Decyl-GS, metolachlor-GS, and oxidized glutathione, although competitive with DNP-GS,
24 3-fold greater steady state concentration of oxidized glutathione and a 3-fold increase in pro-oxidan
25 , and there was an increase in mitochondrial oxidized glutathione and a decrease in mitochondrial red
26           For two reagents with net charges, oxidized glutathione and cystamine, however, the apparen
27 d generation of both reduced glutathione and oxidized glutathione and enhanced production of reactive
28  was refolded in the presence of reduced and oxidized glutathione and further purified by using two i
29 ctase (glr1 delta) accumulate high levels of oxidized glutathione and have a twofold increase in tota
30  was conducted on p21ras S-glutathiolated by oxidized glutathione and identified C118 as the major si
31 lfide bond reduction using dithiothreitol on oxidized glutathione and insulin show reactive-ELDI to b
32                 CT elevated tissue levels of oxidized glutathione and lipid peroxides and elicited sm
33 12 dissociation; however, in the presence of oxidized glutathione and NOC12, FKBP12 dissociation was
34           Oxidative metabolites (glutathione/oxidized glutathione and ophthalmic acid) were similar i
35                    The levels of reduced and oxidized glutathione and pyridine nucleotides in rods we
36 eline levels of tissue AGER1 and glutathione/oxidized glutathione and reduced plasma 8-isoprostanes a
37  indicative of oxidative stress, including % oxidized glutathione and steady-state levels of pro-oxid
38 ted into a denaturant-free buffer containing oxidized glutathione and the nonionic detergent octyl gl
39 nidine HCl, 20% glycerol, 2.5 mM reduced and oxidized glutathione, and 5 mM CaCl2, followed by buffer
40 thione (gamma-L-glutamyl-cysteinyl-glycine), oxidized glutathione, and glutathione S-conjugates.
41 ss in roots, as indicated by accumulation of oxidized glutathione, and induced expression of a gene e
42 s of total glutathione, reduced glutathione, oxidized glutathione, and intracellular reactive oxygen
43 lutathione analog azidophenacyl-glutathione, oxidized glutathione, and the LTD4 antagonist MK571 were
44 tioxidants, measured as reduced glutathione, oxidized glutathione, and their ratio in the blood.
45 n, decreased ratio of reduced glutathione to oxidized glutathione, and up-regulation of superoxide di
46                               High levels of oxidized glutathione are also observed in a trx1 delta,
47 carbonyls, protein methionine sulfoxide, and oxidized glutathione as well as reduced levels of free a
48                                              Oxidized glutathione, as a sole source of cysteine, also
49                      The ratio of reduced to oxidized glutathione, as well as the level of free thiol
50  rather than changes in reduced glutathione, oxidized glutathione, ascorbate and dehydroascorbate con
51 e find that, in contrast, the maintenance of oxidized glutathione at low concentrations is the main f
52  show that restoring the ratio of reduced to oxidized glutathione blocks the glucocorticoid effects o
53 ted in the active site of both enzymes using oxidized glutathione bound to GR as a template.
54 or), and high-energy phosphates, reduced and oxidized glutathione (chromatography), and I/R injury we
55 d glycolysis and higher ratios of reduced to oxidized glutathione compared to SAGM.
56  reduced glutathione and increased levels of oxidized glutathione compared with normal CD34(+) cells.
57 rease in the ratio of reduced glutathione to oxidized glutathione consistent with a 1.6-fold increase
58 rease in dihydrofluorescein fluorescence and oxidized glutathione content between 0 and 8 h after rel
59 idative stress response gene expression, and oxidized glutathione content.
60 xidase and isomerase activity of reduced and oxidized glutathione, Cys, Cys-Cys, and reduced and oxid
61 es several nitrogen-containing compounds and oxidized glutathione derivatives.
62        However, neither oxidative damage nor oxidized glutathione differed between forest types.
63              TR/GR-null livers cannot reduce oxidized glutathione disulfide using NADPH but still req
64 ternal reducing agent, or in the presence of oxidized glutathione, DTNB-reactive thiols of the plasma
65                    Hepatic ratios of reduced:oxidized glutathione, established regulators of gluconeo
66 ial cells, and increased reduced glutathione/oxidized glutathione following Cl2 exposure whereas CysL
67 nes with the concomitant oxidation of GSH to oxidized glutathione (GS-SG).
68                          Exposure to Hg also oxidized glutathione (GSH) to glutathione disulfide (GSS
69 n oxidized redox-system, i.e., a low reduced/oxidized glutathione (GSH-GSSG) ratio.
70 ystine (Cys/CySS), intracellular glutathione/oxidized glutathione (GSH/GSSG) and nicotinamide adenine
71 -related decrease in the ratio of reduced to oxidized glutathione (GSH/GSSG) as well as a pro-oxidizi
72  marker profiles, tissue-reduced glutathione/oxidized glutathione (GSH/GSSG) ratio and oxidative dama
73  nucleus, increases the cellular glutathione/oxidized glutathione (GSH/GSSG) ratio through the upregu
74 intracellular glutathione levels and reduced/oxidized glutathione (GSH/GSSG) ratios.
75 creased GSH content, the ratio of reduced to oxidized glutathione (GSH/GSSG), chlorophyll content, ph
76 of oxidative stress, the ratio of reduced to oxidized glutathione (GSH/GSSG), in a well-controlled st
77 obe, in concert with measurements of reduced/oxidized glutathione (GSH/GSSG), to assess cytosolic red
78 rease in the ratio of reduced glutathione-to-oxidized glutathione (GSH/GSSG), which preceded DNA frag
79 tial due to an increased ratio of reduced to oxidized glutathione (GSH/GSSG).
80 a 38.8% reduction in the ratio of reduced-to-oxidized glutathione (GSH: GSSG, P=2.6x10(-)(2)) among N
81 ecrosis factor (TNF)-alpha after 4 hours and oxidized glutathione (GSSG) after 8 hours indicated deve
82  in lung epithelium as well as the amount of oxidized glutathione (GSSG) and 4-hydroxynonenal (4-HNE)
83           Diamide caused a rapid increase in oxidized glutathione (GSSG) and a loss of mitochondrial
84  redox balance between glutathione (GSH) and oxidized glutathione (GSSG) and initiated mitochondrial
85 = 27 microM, Kii = 48 microM with respect to oxidized glutathione (GSSG) and Kis = 144 microM, Kii =
86 ing reduced glutathione (GSH) while reducing oxidized glutathione (GSSG) and malonaldehyde (MDA) leve
87                            Determinations of oxidized glutathione (GSSG) and reduced glutathione (GSH
88 protein thiols) and intracellularly [altered oxidized glutathione (GSSG) and reduced glutathione leve
89     Similar channel inhibition was seen with oxidized glutathione (GSSG) and thiol-modulating reagent
90                                    Import of oxidized glutathione (GSSG) by S. mutans 33402 in 7H9 me
91 ges in endothelial cell glutathione (GSH) or oxidized glutathione (GSSG) can alter neutrophil adhesiv
92                        Glutathione (GSH) and oxidized glutathione (GSSG) control cellular function an
93 , one possible mechanism being inhibition of oxidized glutathione (GSSG) export from the infected hum
94 lfide bonds by thiol/disulfide exchange with oxidized glutathione (GSSG) has been characterized.
95 cubation of (67)Zn(7)-MT-2 with an excess of oxidized glutathione (GSSG) increased metal donation fou
96  reversed translational inhibition caused by oxidized glutathione (GSSG) or heat shock.
97 0 micromol/L) and cysteinyl-glycine, but not oxidized glutathione (GSSG) or OTC, blunted the LPS-indu
98               Exposure of the Na,K-ATPase to oxidized glutathione (GSSG) resulted in an increase in t
99 ), an enzyme that catalyzes the reduction of oxidized glutathione (GSSG) to GSH in the presence of be
100 idative stress cells show an increase in the oxidized glutathione (GSSG) to reduced glutathione (GSH)
101 pathic hearts show an increased recycling of oxidized glutathione (GSSG) to reduced glutathione (GSH)
102  responses for reduced glutathione (GSH) and oxidized glutathione (GSSG) were linear over more than f
103 ular levels of reduced glutathione (GSH) and oxidized glutathione (GSSG) were measured by HPLC.
104            During chilling stress, levels of oxidized glutathione (GSSG) were significantly higher in
105 sicular entry has come from the formation of oxidized glutathione (GSSG) within the interior of the v
106 l and channel activity with those induced by oxidized glutathione (GSSG), a cytosolic product of oxid
107 mine the concentrations of reduced (GSH) and oxidized glutathione (GSSG), and it enables the calculat
108 dehyde (MDA), H(2)O(2), electrolyte leakage, oxidized glutathione (GSSG), and total glutathione (GT),
109 re assayed for reduced glutathione (GSH) and oxidized glutathione (GSSG), by the sensitive enzymatic
110                                         GSH, oxidized glutathione (GSSG), cysteine, GSH efflux, DNA s
111 f glucose, sorbitol, fructose, myo-inositol, oxidized glutathione (GSSG), glycolytic intermediates, m
112 nstrated that high ROS levels, via increased oxidized glutathione (GSSG), induce isoform-specific S-g
113           Increasing the flux of O-2 yielded oxidized glutathione (GSSG), peaking when the flux of NO
114 eumoniae-exposed mice had elevated levels of oxidized glutathione (GSSG), resulting in a dramatic cha
115 lfhydryl group, S-hexylglutathione (SHG) and oxidized glutathione (GSSG), were inactive per se but at
116 ress because they had significantly elevated oxidized glutathione (GSSG).
117 PC), and to react with entrapped GSH to form oxidized glutathione (GSSG).
118  also as a by-product of increased levels of oxidized glutathione (GSSG).
119 ion (thiolation) promoted by the presence of oxidized glutathione (GSSG).
120 ase activity could be fully reactivated with oxidized glutathione (GSSG).
121 tathione (GSx) within 8 h, without change in oxidized glutathione (GSSG); no effect was seen in pure
122 n value for the [reduced glutathione (GSH)]/[oxidized glutathione (GSSG)] ratio was significantly dec
123 facing conformations (with and without bound oxidized glutathione [GSSG]), together with closed and o
124                                              Oxidized glutathione(GSSG) was a much less effective inh
125 neously gets converted to the oxidized form (oxidized glutathione, GSSG).
126                                              Oxidized glutathione, (GSSG) has also been found to inhi
127 these peaks arose from Ni(II) coordinated to oxidized glutathione, histidine, aspartate, and ATP.
128 utathione in the liver and lowered levels of oxidized glutathione in both liver and blood.
129  levels and an increased ratio of reduced-to-oxidized glutathione in mitochondria.
130 ) and could therefore be oxidized rapidly by oxidized glutathione in the cytosol.
131 hiols and the relative levels of reduced and oxidized glutathione in the ER to control Ero1p activity
132 equently the equilibrium between reduced and oxidized glutathione in the lumen of these compartments.
133 tion in GLR1 drastically increases levels of oxidized glutathione in these two subcellular compartmen
134  lower redox ratio of reduced glutathione to oxidized glutathione) in children with autism.
135 eous increases in the levels of cysteine and oxidized glutathione, in addition to reduced glutathione
136 SSG redox ratio was decreased and percentage oxidized glutathione increased in both cytosol and mitoc
137 ge glutathione levels or ratio of reduced to oxidized glutathione (indicative of oxidative stress) in
138 fide couple of reduced glutathione (GSH) and oxidized glutathione is a key regulator of major transcr
139 e, in protection against chlorine compounds, oxidized glutathione is almost as effective as reduced g
140 ta provides in vivo evidence suggesting that oxidized glutathione is present in the E. coli periplasm
141 ed glutathione as is its drug transport, and oxidized glutathione, itself a substrate for transport,
142                                Intracellular oxidized glutathione leads to TRPC5 activation via TRPC5
143  lung lavage fluid, and increased (P < 0.05) oxidized glutathione levels in the lung lavage fluid.
144 between study groups were observed in either oxidized glutathione levels or redox index (P > 0.05, F
145 young human alphaL-crystallin fractions with oxidized glutathione, levels of PSSG were determined by
146 -10 mM) in phosphate buffer (pH 7.4) yielded oxidized glutathione, nitrite, nitrous oxide, and ammoni
147                                  Relative to oxidized glutathione, NOV-002 was an equivalent substrat
148 other oxidants such as hydrogen peroxide and oxidized glutathione on the oxidation of this protein in
149  M, one to two orders of magnitude less than oxidized glutathione or any other glutathione derivative
150 xymethylated bovine serum albumin, RCM-BSA), oxidized glutathione or Hg2+.
151      Treatment of A. thaliana seedlings with oxidized glutathione or paraquat induces APS reductase a
152 ccurs through thiol-disulphide exchange with oxidized glutathione or reaction of oxidant-induced prot
153 on to all GS conjugates and not simulated by oxidized glutathione or reduced glutathione.
154  activity against other disulphides, such as oxidized glutathione or thioredoxin.
155  after incubation with the oxidants diamide, oxidized glutathione, or hydrogen peroxide or with nitri
156 centrations of homocysteine (P < 0.0001) and oxidized glutathione (P < 0.0001) than did controls.
157 r glutathione, which reduces the Cys-SeOH of oxidized glutathione peroxidase, was able to reduce the
158 rotein oxidation and a decreased glutathione/oxidized glutathione ratio were observed, but the opposi
159 ated in HKCs, while arginine and glutathione/oxidized glutathione ratio were reduced.
160 tive stress, and a lower reduced glutathione/oxidized glutathione ratio.
161  lipid peroxidation, or a low glutathione to oxidized glutathione ratio.
162 ironment as indicated by improved reduced to oxidized glutathione ratio.
163 s was evidenced by a decrease in the reduced oxidized/glutathione ratio, imbalance of cellular antiox
164 decreased cellular NADPH/NADP(+) and reduced/oxidized glutathione ratios (GSH/GSSG) and increased cel
165              In addition, higher glutathione/oxidized glutathione ratios suggested that microprobed c
166 s, smt15-1 cells had an increased reduced-to-oxidized glutathione redox ratio throughout the cell cyc
167 es that of cysteine, whereas the spectrum of oxidized glutathione resembles that of cystine.
168 wed that incubation of alpha-crystallin with oxidized glutathione results in significant loss of its
169                                        Using oxidized glutathione S-transferase as a model substrate,
170 ice had less pulmonary neutrophil influx and oxidized glutathione than wild-type littermates at 7 day
171                                              Oxidized glutathione, the drug-glutathione S-conjugate D
172 t was competitively inhibited by reduced and oxidized glutathione, the glutathione conjugates S-(p-az
173 city, the drug glutathione conjugate APA-SG, oxidized glutathione, the LTD4 antagonist MK571, arsenat
174 yme inhibitor diphenylene iodonium (DPI) and oxidized glutathione, the preferred electron acceptor of
175 ve stress in GBM cells, an effect blocked by oxidized glutathione, thioredoxin, and redox enzyme over
176 n the hematopoietic niche, Ifi30 can recycle oxidized glutathione to allow HSPCs to dampen their leve
177     It also has a major role in transporting oxidized glutathione to help maintain redox balance and
178 ione, formed by disulfide rearrangement with oxidized glutathione to inhibit and stabilize the enzyme
179 on; reduced Trx reacts nonenzymatically with oxidized glutathione to maintain a high glutathione/glut
180 ne reductase (GR) catalyzes the reduction of oxidized glutathione to reduced glutathione.
181         Plasma concentrations of reduced and oxidized glutathione, vitamin B-6, homocysteine, cystein
182 tress markers, such as lipid peroxidation or oxidized glutathione, we uncovered a unique profile of l
183                 However, the K(m) values for oxidized glutathione were 9muM for GGT1 and 43muM for GG
184 ELF and the concentration of glutathione and oxidized glutathione were determined.
185                              Renal levels of oxidized glutathione were significantly higher in cy/+ t
186 t noted and the levels of total, reduced and oxidized glutathione were similar in transgene (+) and (
187 isulfide bond when s-COMT was incubated with oxidized glutathione, whereas cysteines 69, 95, 157, and
188 ably, alterations in the ratio of reduced to oxidized glutathione, which is the primary determinant o
189 s, as evidenced by the decrease in levels of oxidized glutathione with reference to reduced glutathio

 
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