ライフサイエンスコーパス: glutathione peroxidase

1 plexes I, II, III; superoxide dismutase; and glutathione peroxidase).

2 ession of superoxide dismutase isoform 2 and glutathione peroxidase.

3 hione and the phase II detoxification enzyme glutathione peroxidase.

4 of superoxide dismutase (SOD), catalase and glutathione peroxidase.

5 s immediately upstream of ospR and encodes a glutathione peroxidase.

6 bition against glutathione S-transferase and glutathione peroxidase.

7 activating factor acetylhydrolase (PAF), and glutathione peroxidase.

8 drogenase (G6PD), glutathione reductase, and glutathione peroxidase.

9 affected in both catalase and TR but not in glutathione peroxidase.

10 include catalase, superoxide dismutase, and glutathione peroxidase.

11 n down-regulation of thioredoxin, MnSOD, and glutathione peroxidase.

12 tiporter, gamma-glutamylcysteine ligase, and glutathione peroxidase.

13 olesterol, and triglyceride, while increased glutathione peroxidase.

14 ar to that found in mammalian selenocysteine glutathione peroxidases.

15 f manganese superoxide dismutase (MnSOD) and glutathione peroxidase 1 (GPx).

16 ine-induced suppression of the selenoprotein glutathione peroxidase 1 (GPx-1) and endothelial dysfunc

17 Glutathione peroxidase 1 (GPx-1) has been implicated in

18 In animal models, glutathione peroxidase 1 (GPx1) activity is reduced afte

19 Hepatic glutathione peroxidase 1 (GPx1) and selenoprotein S (Sel

20 with (75)Se revealed a loss of the abundant glutathione peroxidase 1 (GPx1) band, whereas other sele

21 Among genes in the GSH family, glutathione peroxidase 1 (GPX1) had the most significant

22 ctor erythroid 2 related factor 2 (Nrf2) and glutathione peroxidase 1 (Gpx1) mRNA in both male and fe

23 , a mitochondrial complex III inhibitor, and glutathione peroxidase 1 (GPX1), a scavenger of hydrogen

24 don 200 (Pro200Leu) of the gene encoding for glutathione peroxidase 1 (GPx1), a selenium-dependent en

25 investigate the impact of overexpression of glutathione peroxidase 1 (GPX1), an intracellular seleno

26 mes superoxide dismutase 2 (SOD2), catalase, glutathione peroxidase 1 (GPX1), and heme oxygenase 1 (H

27 rtion into thioredoxin reductase 1 (TR1) and glutathione peroxidase 1 (GPx1).

28 zymes, including heme oxygenase-1 (HO-1) and glutathione peroxidase 1 (Gpx1).

29 in mice lacking the antioxidant selenoenzyme glutathione peroxidase 1 (GPx1).

30 in reductase 1 concentrations and lymphocyte glutathione peroxidase 1 and 4 activities and concentrat

31 ice but showed higher levels and activity of glutathione peroxidase 1 and methionine-R-sulfoxide redu

32 Human glutathione peroxidase 1 could thereby also be produced,

33 Sec tRNA([Ser]Sec), and consequently reduced glutathione peroxidase 1 expression.

34 ne of the major antioxidant defense enzymes, glutathione peroxidase 1 knockout mice are protected dur

35 C57Bl6 and glutathione peroxidase 1 knockout mice.

36 of hydrogen peroxide in bacterially infected glutathione peroxidase 1 macrophages and that restoring

37 Infected glutathione peroxidase 1 mice showed an early and signif

38 protective effect was suppressed by treating glutathione peroxidase 1 mice with an interleukin-1 rece

39 liver but not stress-related proteins (e.g. glutathione peroxidase 1).

40 2.5-fold) (REV3L, XPMC2H, HNRPUL1, TOR1AIP1, glutathione peroxidase 1, and SCFD2), with CGIs of inter

41 4 did not cause alterations in activities of glutathione peroxidase 1, catalase, Cu/Zn superoxide dis

42 Rdx12 was found to interact with glutathione peroxidase 1, whereas 14-3-3 protein was ide

43 a reactive oxygen species scavenging enzyme glutathione peroxidase 1.

44 Several selenoproteins, including glutathione peroxidases 1 and 3, SelR, and SelT, were no

45 We have found that suppression of glutathione peroxidase-1 (GPx-1) in human microvascular

46 Glutathione peroxidase-1 (GPx-1) is a crucial antioxidan

47 Glutathione peroxidase-1 (GPx-1) is a selenocysteine-con

48 d mice overexpressing the antioxidant enzyme glutathione peroxidase-1 (Gpx1) are protected from exper

49 tical redox axis with the antioxidant enzyme glutathione peroxidase-1 (GPX1) at its hub and identify

50 e identified a role for the network hub gene glutathione peroxidase-1 (GPX1) in pathological remodeli

51 Glutathione peroxidase-1 (GPX1) represents the first ide

52 of the most abundant hepatic selenoprotein, glutathione peroxidase-1 (Gpx1), to 15% of the selenium-

53 nt genes than chow-fed young mice, including glutathione peroxidase-1 and -4, catalase, superoxide di

54 Levels of glutathione peroxidase-1 and catalase, however, were not

55 n the medium Se group the expression of lung glutathione peroxidase-1 and liver selenoprotein P were

56 Transgenic expression of the glutathione peroxidase-1 antioxidant enzyme (GPX1) in db

57 l of hexokinase-2, hormone sensitive lipase, glutathione peroxidase-1, and myosin heavy chain IIa in

58 of antioxidants, superoxide dismutase 1 and glutathione peroxidase-1, were significantly upregulated

59 ere, we studied how the H2O2-reducing enzyme glutathione peroxidase 2 (GPx2) regulates H2O2 stress an

60 ntioxidant and prooxidant enzymes, including glutathione peroxidase 2 and 3 (GPx2 and GPx3), peroxire

61 ntioxidant mechanism that uses mitochondrial glutathione peroxidase 2.

62 human and mouse Grx2 was lower than that of glutathione peroxidases (2.5 and 0.8x10(4) s(-1) M(-1),

63 oxidase-1 (GPx-1), gastrointestinal specific glutathione peroxidase-2 (GPx-2), thioredoxin reductase-

64 We report a glutathione peroxidase 3 (AaGPx3) involved in the comple

65 Expression of glutathione peroxidase 3 (GPx3) is down-regulated in a v

66 Plasma Se, SePP, and glutathione peroxidase 3 (GPx3) levels increased with su

67 the reactive oxygen species (ROS) scavenger glutathione peroxidase 3 (GPx3) positively correlates wi

68 this report, we found that the expression of glutathione peroxidase 3 (GPx3) was widely inactivated i

69 ein 1 (HIVEP1), von Willebrand factor (VWF), glutathione peroxidase 3 (GPX3), and platelet-derived gr

70 r the optimal activity of the selenoproteins glutathione peroxidase 3 (GPx3; <86.9 ng mL(-1)) and iod

71 Glutathione peroxidase 3 is a selenium-dependent enzyme

72 reas antioxidant proteins, paraoxonase 2 and glutathione peroxidase 3, were down-regulated in the eye

73 Glutathione peroxidase-3 (GPx-3) is a selenocysteine-con

74 The other extracellular selenoprotein, glutathione peroxidase-3 (Gpx3), has not been shown to t

75 Glutathione peroxidase 4 (GPX4) and arachidonic acid 15-

76 educed levels of superoxide dismutase (Sod), glutathione peroxidase 4 (Gpx4) and peroxiredoxin 3 (Prd

77 The expression of glutathione peroxidase 4 (GPX4) in H295R cells, however,

78 The selenium-dependent glutathione peroxidase 4 (GPX4) inhibits ferroptosis, co

79 The enzyme glutathione peroxidase 4 (GPX4) is a central regulator o

80 The antioxidant enzyme glutathione peroxidase 4 (Gpx4) is a key regulator of ox

81 The selenoenzyme glutathione peroxidase 4 (Gpx4) is a major scavenger of

82 Glutathione peroxidase 4 (Gpx4) is an essential antioxid

83 The selenoenzyme glutathione peroxidase 4 (Gpx4) is an intracellular anti

84 Glutathione peroxidase 4 (GPX4) is essential for cell me

85 hat cellular redox homeostasis maintained by glutathione peroxidase 4 (GPX4) is required for STING ac

86 Glutathione peroxidase 4 (Gpx4) is uniquely involved in

87 te-specific knockout mice lacking either the glutathione peroxidase 4 (GPx4) or thioredoxin reductase

88 glutathione-dependent lipid hydroperoxidase glutathione peroxidase 4 (GPX4) prevents ferroptosis by

89 Glutathione peroxidase 4 (GPX4) protects against lipid p

90 Glutathione peroxidase 4 (GPX4) uses glutathione to prot

91 andscape, and can be exploited by inhibiting glutathione peroxidase 4 (GPX4) with small-molecules.

92 ibition of the ferroptosis-inhibiting enzyme glutathione peroxidase 4 (GPX4)(10).

93 e phospholipid hydroperoxide-reducing enzyme glutathione peroxidase 4 (GPX4)(3,4) and radical-trappin

94 Small molecules that inhibit glutathione peroxidase 4 (GPX4), a phospholipid peroxida

95 Glutathione peroxidase 4 (GPX4), an antioxidant defense

96 membranes unless the lipid hydroperoxidase, glutathione peroxidase 4 (GPX4), reduces these toxic lip

97 orm of cell death triggered by inhibition of glutathione peroxidase 4 (GPX4), which catalyzes the red

98 This inhibition was mediated by glutathione peroxidase 4 (GPx4), which preferentially de

99 f glutathione metabolism pathways, including glutathione peroxidase 4 (GPX4), which protected cells f

100 f intracellular antioxidant enzymes, such as glutathione peroxidase 4 (GPX4).

101 that ferroptosis is primarily controlled by glutathione peroxidase 4 (GPX4).

102 ion of selenoproteins, including antioxidant glutathione peroxidase 4 (GPX4).

103 inhibiting the phospholipid hydroperoxidase glutathione peroxidase 4 (GPX4).

104 ted necrosis that is critically dependent on glutathione peroxidase 4 (GPX4).

105 elevated levels of the mitochondrial form of glutathione peroxidase 4 and was fully dependent on the

106 naturally occurring selenoprotein homolog of glutathione peroxidase 4 in fowlpox virus.

107 mine, an anticancer drug, as an inhibitor of glutathione peroxidase 4 lipid repair activity, which wa

108 Intratumoral glutathione peroxidase 4 overexpression or acyl-CoA synt

109 In addition, glutathione peroxidase 4 was found to be a Rdx12 redox t

110 strated by decreased expression of catalase, glutathione peroxidase 4, and glutathione synthetase gen

111 including thioredoxin reductases 1 and 3 and glutathione peroxidase 4, were expressed in normal or re

112 ace of Sec was commonly observed in GPx1 and glutathione peroxidase 4.

113 s the lipid hydroperoxide-detoxifying enzyme glutathione peroxidase 4.

114 3a2 inhibition was synthetically lethal with glutathione peroxidase-4 (GPX4) inhibition; GPX4 inhibit

115 iated with reduced levels of glutathione and glutathione peroxidase-4 (Gpx4), along with increased fr

116 ptosis but not in that induced by inhibiting glutathione peroxidase-4 (GPX4), the most downstream com

117 Glutathione peroxidase-4 (GPx4), which specifically meta

118 antly down-regulating the antioxidant enzyme glutathione peroxidase-4.

119 05; copper/zinc superoxide dismutaseP< 0.05; glutathione peroxidase 4P< 0.01] and increased lipoxygen

120 ysteine insertion sequences (SECIS) of human glutathione peroxidase (58 nt) and thioredoxin reductase

121 ton's disease, we identify the age-regulated glutathione peroxidase 6 (Gpx6) gene as a modulator of m

122 Here, we provide evidence that glutathione peroxidase 8 (GPX8), a poorly characterized

123 The glutathione peroxidases, a family of selenocysteine-cont

124 improved superoxide dismutase, catalase and glutathione peroxidase activities in H2O2 treated CCD an

125 Changes in platelet glutathione peroxidase activity and in plasma selenium a

126 d decreases in glutathione concentration and glutathione peroxidase activity and increased glutathion

127 oxidative parameters in the brain, enhanced glutathione peroxidase activity as well as reduced nitri

128 Platelet glutathione peroxidase activity did not change significa

129 ium cyanide but had no effect on catalase or glutathione peroxidase activity in the presence of kaini

130 worsening, CuZnSOD overexpression increased glutathione peroxidase activity in the presence of sodiu

131 proximately 22 kDa and has little detectable glutathione peroxidase activity in vitro.

132 way modulation; however, treatment to reduce glutathione peroxidase activity increased 5-LO metabolit

133 However, glutathione peroxidase activity was an order of magnitud

134 elenium-deficient human subjects showed that glutathione peroxidase activity was optimized before sel

135 Sepp1 and selenium concentrations as well as glutathione peroxidase activity were determined in the t

136 ted genes in the small intestine, intestinal glutathione peroxidase activity, secreted Relm-beta prot

137 Indeed, a recombinant SelH shows significant glutathione peroxidase activity.

138 Oxidative stress was assayed by measuring glutathione peroxidase activity.

139 idase and a 2-fold increase in mitochondrial glutathione peroxidase activity.

140 ntioxidants in fa/fa rats and also decreased glutathione peroxidase activity.

141 chondrial manganese superoxide dismutase and glutathione peroxidase and a 2-fold increase in mitochon

142 with higher activity of antioxidant enzymes (glutathione peroxidase and catalase).

143 nction as mimetics of the antioxidant enzyme glutathione peroxidase and catalyze the reduction of hyd

144 PB also down-regulated glutathione peroxidase and glutathione reductase, which

145 ncreased the activities of hepatic catalase, glutathione peroxidase and glutathione S transferase com

146 iet improved superoxide dismutase, catalase, glutathione peroxidase and GR activities and eNOS, iNOS

147 ene expression of a cadre of cytosolic (e.g. glutathione peroxidase and heat shock proteins) and mito

148 Cu,Zn superoxide dismutase or intracellular glutathione peroxidase and non-transgenic mice were expo

149 ne-S-transferase, phospholipid hydroperoxide glutathione peroxidase and peroxidase were significantly

150 ed dual roles in EC barrier function through glutathione peroxidase and phospholipase A(2) activity.

151 edoxin 6 (Prdx6), a bifunctional enzyme with glutathione peroxidase and phospholipase A2 (PLA(2)) act

152 Glutathione peroxidase and Sepp1Delta240-361 accounted f

153 ectopic expression of ROS-scavenging enzymes glutathione peroxidase and superoxide dismutase effectiv

154 The activities of catalase, glutathione peroxidase and superoxide dismutase were sig

155 met assay), activity of detoxifying enzymes (glutathione peroxidase and superoxide dismutase) in eryt

156 intake is needed to maximize the activity of glutathione peroxidases and other selenoproteins.

157 re affected by this H2O2 including catalase, glutathione peroxidase, and 4 alpha-carbinolamine dehydr

158 id-reactive substances (TBARS), glutathione, glutathione peroxidase, and 6-hydroxy-2,5,7,8-tetramethy

159 in and mRNA expression, as well as catalase, glutathione peroxidase, and glutathione reductase tissue

160 constitutively higher glutathione reductase, glutathione peroxidase, and higher ratios of reduced to

161 de [MDA]) and antioxidant enzymes (catalase, glutathione peroxidase, and superoxide dismutase).

162 tathione) and enzymatic antioxidant markers (Glutathione peroxidase, and superoxide dismutase).

163 ditionally, the activities of peroxidase and glutathione peroxidase, and the peroxiredoxin abundance

164 in breast cancer cells, such as catalase and glutathione peroxidase, and to inactivate tumor suppress

165 es such as superoxide dismutases, catalases, glutathione-peroxidases, and peroxiredoxins.

166 N-induced catalase, superoxide dismutase and glutathione peroxidase antioxidant enzyme activities but

167 ralizing enzyme of many organisms, and their glutathione peroxidases are in the phospholipid class wi

168 and lipid peroxidation assays, we identified glutathione peroxidase as a candidate for reducing PPD.

169 al, and GPXs, APX, and MSRA2 genes (encoding glutathione peroxidase, ascorbate peroxidase, and methio

170 nd between H and L mice in liver (except for Glutathione Peroxidase), brain or mammary glands.

171 d immunodetectable endogenous or recombinant glutathione peroxidase but reduced the specific activity

172 as Cu/Zn-superoxide dismutase, catalase, and glutathione peroxidase, but also significantly decreased

173 and restored superoxide dismutase, catalase, glutathione peroxidase, coenzyme Q(10) and ORAC levels i

174 utathione, total antioxidant capacities, and glutathione peroxidase enzymatic activity than did vecto

175 In search for better mimics of the glutathione peroxidase enzymes, pyridoxine-like diseleni

176 ridoxines could also mimic the action of the glutathione peroxidase enzymes.

177 nificantly elevated levels of mRNAs encoding Glutathione Peroxidase enzymes.

178 ects of G418, an aminoglycoside, on cellular glutathione peroxidase expression and function in mammal

179 mechanisms (increased levels of catalase and glutathione peroxidase expression), observed with both P

180 Selenite-induced up-regulation of GPx (glutathione peroxidase) expression-enhanced roGFP2 respo

181 nd catalase activities (FA200), erythrocytes glutathione peroxidase (FB400) and thiobarbituric acid-r

182 enzyme activities related to the GSH usage (glutathione peroxidase, gamma-glutamyl transpeptidase, a

183 Some genes including glucanase, glutathione peroxidase, glutaredoxin, and a profilin wer

184 of malondialdehyde (MDA), and activities of glutathione peroxidase, glutathione reductase and supero

185 nzymatic antioxidants (superoxide dismutase, glutathione peroxidase, glutathione) in human HepG2 cell

186 e this, serum SOD activity and proteins, the glutathione peroxidase/glutathione antioxidant system, a

187 ular oxidants and counteracts suppression of glutathione peroxidase/glutathione reductase (GSH-Px/GSS

188 rowth factor (VEGF), glycolytic enzymes, and glutathione peroxidase (GPX) (P<0.05), and a higher expr

189 pacity (TEAC) levels, and catalase (CAT) and glutathione peroxidase (GPx) activities.

190 Measurements of plasma glutathione peroxidase (GPx) activity and serum selenium

191 Here we consider glutathione peroxidase (GPx) activity as a determinant o

192 ntrol, p<0.1); most likely through enhancing glutathione peroxidase (GPx) activity in liver (4.3-fold

193 variants modify the response of whole-blood glutathione peroxidase (GPx) activity to selenium supple

194 which increased superoxide levels, decreased glutathione peroxidase (GPx) activity, decreased glutath

195 Plasma SEPP1 concentration and glutathione peroxidase (GPX) activity, the latter due la

196 dium and used its selenium to increase their glutathione peroxidase (Gpx) activity.

197 for humans as it plays an important role in glutathione peroxidase (GPx) activity.

198 The antioxidant glutathione peroxidase (GPx) and inflammation biomarkers

199 alase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GPx) and the levels of malondial

200 (GR) by UV spectrophotometry and determined glutathione peroxidase (GPx) expression therein by weste

201 ismutase (SOD) (activity and expression) and glutathione peroxidase (GPx) expression.

202 ynitrite reductase activity of selenoprotein glutathione peroxidase (GPx) has been investigated using

203 10-fold the protein levels of SOD, CAT, and glutathione peroxidase (GPX) in rat primary cortical cul

204 alase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GPX) in vivo.

205 nitric oxide (NO), superoxide dismutase, and glutathione peroxidase (GPX) levels in serum were measur

206 atalase (CAT), reduced glutathione (GSH) and glutathione peroxidase (GPx) levels.

207 Glibenclamide decreased GSH levels and glutathione peroxidase (GPx) of PMNs after exposed to li

208 t during oligodendrocyte maturation, whereas glutathione peroxidase (GPx) was upregulated with a twof

209 oncentration in colostrum follows the order: glutathione peroxidase (GPX) ~ selenoprotein P (SELENOP)

210 line erythrocyte superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) activit

211 oward MDR cells is achieved by inhibition of glutathione peroxidase (GPx), and the mode of inhibition

212 activity of superoxide dismutases (SOD) and glutathione peroxidase (GPx), glutathione (GSH), and cyt

213 superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR)

214 se superoxide dismutase (Mn-SOD), aconitase, glutathione peroxidase (GPx), heat shock protein 70, iso

215 superoxide dismutase (Mn-SOD), catalase, and glutathione peroxidase (GPX), increased accumulation of

216 ing mimetics of the antioxidant selenoenzyme glutathione peroxidase (GPx), via oxidation to the corre

217 yme activity, superoxide dismutase (SOD) and glutathione peroxidase (GPx), vitamin E, lipid peroxidat

218 er that beta-cell-specific overexpression of glutathione peroxidase (GPx)-1 significantly ameliorated

219 s azo-bis-ebselens 7 were poor mimics of the glutathione peroxidase (GPx)-enzymes, nitroebselens 3, 6

220 peroxidase activities of PGHS-2, PGHS-1, and glutathione peroxidase (GPx).

221 evels of intracellular glutathione (GSH) and glutathione peroxidase (GPx).

222 as well as cellular protection genes such as glutathione peroxidase (GPx).

223 ow antioxidant protection by glutathione and glutathione peroxidase (GPX).

224 and H2O2 is converted to H2O by catalase or glutathione peroxidase (GPX).

225 water and oxygen by either catalase (CAT) or glutathione peroxidase (GPX).

226 , non-enzymatic (total thiol) and enzymatic [glutathione peroxidase (GPx)] antioxidant contents and i

227 Cellular glutathione peroxidase (GPx-1), a selenocysteine-contain

228 Plasma glutathione peroxidase (GPx-3) is a selenocysteine-conta

229 Mice deficient in two glutathione peroxidases (GPX), Gpx1 and Gpx2, [Gpx1/2-do

230 m is an essential component of antioxidative glutathione peroxidases (GPx).

231 implicated the selenium-containing cytosolic glutathione peroxidase, GPx-1, as a determinant of cance

232 response to G418, whereas expression of the glutathione peroxidases GPX1 and GPX2 was marginally aff

233 -mediated iron uptake), or transfection with glutathione peroxidase (GPx1) enzyme inhibits intracellu

234 binding sites for TFAP2C, we identified that glutathione peroxidase (GPX1) is regulated by TFAP2C thr

235 ts in a decrease in the activity of cellular glutathione peroxidase (GPx1), an intracellular antioxid

236 Gene delivery of glutathione peroxidase (GPx1), which detoxifies H(2)O(2)

237 Using glutathione peroxidase, Gpx1 and Gpx2, double knockout (

238 calization requires the participation of the glutathione peroxidase Gpx3 and the Yap1-binding protein

239 The glutathione peroxidase GPX3 is the only extracellular me

240 tructural components of the sperm, including glutathione peroxidase GPx4/PHGPx.

241 y on pathways converging on the phospholipid glutathione peroxidase (GPX4), a selenocysteine-containi

242 Among the last group, glutathione peroxidases (GPxs) and peroxiredoxins (Prxs)

243 letion of glutathione causes inactivation of glutathione peroxidases (GPXs) in response to one class

244 Two of these suppressors encode glutathione peroxidases (GPxs), which are conserved anti

245 creased (p<0.05) the activities of catalase, glutathione peroxidase (GSH-Px) and glutathione reductas

246 -hydroxynonenal (HNE) and enzyme activity of glutathione peroxidase (GSH-Px) were analyzed with enzym

247 nhibited by antioxidant enzymes catalase and glutathione peroxidase (H(2)O(2) scavenger), but not by

248 response and detoxification genes, like the glutathione peroxidase homologous gene GPXH/GPX5 and the

249 ivity of catalase, superoxide dismutase, and glutathione peroxidase in atrial tissue of the supplemen

250 essed a mammalian phospholipid hydroperoxide glutathione peroxidase in Escherichia coli from a constr

251 ransgenic cassava overexpressing a cytosolic glutathione peroxidase in storage roots showed delayed P

252 thione reductase inhibition and no effect by glutathione peroxidase inhibition.

253 Preventing H(2)O(2) reduction with the glutathione peroxidase inhibitor, mercaptosuccinate, enh

254 Cellular glutathione peroxidase is a key intracellular antioxidan

255 Here, we found that GPX2, which encodes a glutathione peroxidase, is up-regulated by p63 but not p

256 iminished enzyme activity of the antioxidant glutathione peroxidase, leading to an increase in intrac

257 ) gene encoding a phospholipid hydroperoxide glutathione peroxidase (LePHGPx).

258 The glutathione peroxidase-like activity of 4 was measured i

259 ogen peroxide in the presence of thiophenol (glutathione peroxidase-like activity).

260 Cys36-Cys82 disulfide bond at pH 6.0 in the glutathione peroxidase-like enzyme, oxidant receptor pro

261 O(2) is removed by catalase, peroxiredoxin, glutathione peroxidase-like enzymes and ascorbate peroxi

262 tive stress (superoxide dismutase, catalase, glutathione peroxidase, lipidic and protein peroxidation

263 score, had decreased expression of catalase, glutathione peroxidase, manganese superoxide dismutase,

264 Quantitative data for two phospholipid glutathione peroxidases (MdesPHGPX-1 and MdesPHGPX-2), t

265 In contrast, ebselen (a glutathione peroxidase mimetic and inhibitor of fatty ac

266 onal cells and determined whether ebselen, a glutathione peroxidase-mimetic, protected against MPTP-i

267 Adolescent treatment with the glutathione peroxidase mimic ebselen also reversed behav

268 N-acetyl-L-cysteine (NAC), catalase, and the glutathione peroxidase mimic ebselen.

269 or amino acid hydroperoxides with ebselen, a glutathione peroxidase mimic, were also determined, and

270 essing catalase-, superoxide dismutase-, and glutathione peroxidase-mimicking enzyme properties exhib

271 equence in the 3'-untranslated region of the glutathione peroxidase mRNA, and other translational cof

272 e protein disulfide isomerase, glutaredoxin, glutathione peroxidase, NK-lysin/granulysin, HIV Tat pro

273 Adenoviral overexpression of glutathione peroxidase or cytosolic or mitochondrial cat

274 , such as superoxide dismutase, catalase, or glutathione peroxidase, our results suggest that the TP0

275 roxide dismutase (SOD) mimetic (EUK-134) and glutathione peroxidase overexpression prevented the hypo

276 ession of a novel phospholipid hydroperoxide glutathione peroxidase (PHGPx), which incorporates cyste

277 along with other phospholipid hydroperoxide glutathione peroxidases (PHGPx) from several organisms.

278 dismutase; erythrocyte, platelet, and plasma glutathione peroxidase; platelet and leukocyte cytochrom

279 he preservation of total glutathione levels, glutathione peroxidase protein abundance, and a decrease

280 capsule, SMCP and phospholipid hydroperoxide glutathione peroxidase, provide outstanding examples of

281 Combined treatments increased liver glutathione peroxidase, serum catalase, and colon myelop

282 ytosolic superoxide dismutase (SmCT-SOD) and glutathione peroxidase (SmGPX), and a partial coding seq

283 ivity of the three main antioxidant enzymes: glutathione peroxidase, superoxide dismutase and catalas

284 arameters and antioxidant enzymes, including glutathione peroxidase, superoxide dismutase, and catala

285 ), glutathione S-transferase (GST) and total glutathione peroxidase (t-GPx) were decreased compared w

286 thione S-transferase peroxidase kappa 1, and glutathione peroxidase) than the BN rat, suggesting that

287 eins, one of which is a selenocysteine-based glutathione peroxidase, the first found in insects.

288 In the absence of catalase and glutathione peroxidase, the parasites rely primarily on

289 idants, catalase, phospholipid hydroperoxide glutathione peroxidase, thioredoxin, and glutathione wer

290 cted in either Cu,Zn superoxide dismutase or glutathione peroxidase transgenic mice.

291 rved in either Cu,Zn superoxide dismutase or glutathione peroxidase transgenic mice.

292 oxidant stress by expressing enzymes such as glutathione peroxidase type 1 (GPx-1).

293 ays, including the antiferroptotic mediator, glutathione peroxidase type 4.

294 ductase, tryparedoxin (Tpx), and nonselenium glutathione peroxidase-type enzymes.

295 nuclear (HvGPx42) phospholipid hydroperoxide glutathione peroxidase were isolated from Hydra vulgaris

296 ant strains deficient for peroxiredoxins and glutathione peroxidases were equally sensitive to fatty

297 positive modifications, like an increase in glutathione peroxidase, were detected in muscle (29%) an

298 VC%, respectively), positive associations of glutathione peroxidase with FEV1% and FVC%, and an inver

299 The associations of TBARS and glutathione peroxidase with FVC% in men remained statist

300 isticated fine control of peroxiredoxins and glutathione peroxidases with their backup systems as wel