ライフサイエンスコーパス: glutathione

1 ochondrial antioxidant production (NADPH and glutathione).

2 adenine dinucleotide , glutathione disulfide/glutathione).

3 physiological concentrations of cysteine and glutathione.

4 DHARs) in interactions between ascorbate and glutathione.

5 glutathione reductase, is highly specific to glutathione.

6 his is correlated with the levels of reduced glutathione.

7 ither gamma-glutamyl amino acids or oxidized glutathione.

8 itor MG132 without eliciting any increase in glutathione.

9 umaric acid, acetaldehyde, total and reduced glutathione.

10 polyunsaturated fatty acids, oxylipins, and glutathione.

11 electrochemical sensor for the detection of glutathione.

12 dependent on brain levels of the antioxidant glutathione.

13 in antioxidants including NADPH and reduced glutathione.

14 E) for the detection of reduced and oxidized glutathione.

15 ecies is supported by increased antioxidant; glutathione.

16 g levels of the major biological antioxidant glutathione.

17 de, which is paralleled by a loss of reduced glutathione.

18 ltrasmall gold nanoparticles stabilized with glutathione.

19 thereby depleting the antioxidants NADPH and glutathione.

20 ine and the higher concentrations of reduced glutathione (1.0 and 2.0%) were able to promote a whiter

21 idative stress including reduced taurine and glutathione; (3) inhibition of several developmentally s

22 we find substantial GO-induced oxidation of glutathione, a model intracellular antioxidant, paired w

23 urcumin and decreased the amount of curcumin-glutathione adducts in cells.

24 tural and synthetic compounds and related to glutathione and ascorbate as key endogenous antioxidants

25 oxidative stress by showing an activation of glutathione and ascorbate free radical scavenger systems

26 Glutathione and ascorbate were less effective.

27 damage can be prevented by the antioxidants glutathione and catalase, suggesting that HDM-induced re

28 e protein) levels, oxidative stress markers (glutathione and cystine), and arterial stiffness were ev

29 ed that certain mushroom species are high in glutathione and ergothioneine and should be considered a

30 duced levels of NADPH, deoxynucleotides, and glutathione and increased their sensitivity to radiation

31 lomics analysis demonstrated accumulation of glutathione and its precursor, gamma-glutamylcysteine, a

32 the ability of gallic acid, glycine, reduced glutathione and l-cysteine at 0.1, 0.5, 1.0 and 2.0% lev

33 reductase toward hemithioacetal (product of glutathione and MG), which is most likely caused by S-ni

34 on before and after inhibition of astrocytic glutathione and PgE2 synthesis.

35 hione degradation plays an important role in glutathione and redox homeostasis, and thus it is impera

36 Urate hydroperoxide oxidizes glutathione and sulfur-containing amino acids and is exp

37 Additionally, intracellular glutathione and uncoupling protein 2 (UCP2) gene express

38 ducing conditions (biological thiols such as glutathione) and in human plasma.

39 nucleotides, acetoacetyl-CoA, H2O2, reduced glutathione, and 2-monoacylglycerol were not glucose-res

40 absorbance spectra of the gold nanoparticle, glutathione, and aminosilane complex demonstrated visual

41 es including the choline species, glutamate, glutathione, and GABA.

42 antified by the plasma aminothiols, cystine, glutathione, and their ratio, is associated with mortali

43 led mitochondrial sources of H2O2 as well as glutathione- and thioredoxin-related pathways, with powe

44 s IDH2, thereby regulating the mitochondrial glutathione antioxidant defense system in mice.

45 infection success was also dependent of the glutathione antioxidant system and its main reducing pow

46 Astrocyte synthetic pathways, dependent on glutathione, are involved in cerebrovascular reactivity

47 metabolism, such as lower amounts of Cys and glutathione, as well as a differential composition of gl

48 ives were to determine and compare levels of glutathione, as well as ergothioneine, in different spec

49 olysis product of PL (hPL) was conjugated to glutathione at the C7-C8 olefin, and this complex was bo

50 PC)-deficient mutants (cad1-3) as well as in glutathione biosynthesis (cad2) and PC transport (abcc12

51 ponse and, in combination with inhibition of glutathione biosynthesis, triggers ferroptosis, a non-ap

52 Inhibition of glutathione biosynthesis, which protects cells from reac

53 either in the absence or presence of DOM or glutathione, both of which form strong complexes with Hg

54 ion depends not only on the level of reduced glutathione, but also on the rate of NADPH production, c

55 capability of activated neurons and dynamic glutathione changes during ferroptosis.

56 contained higher levels of ergothioneine and glutathione compared to the first flush, possibly as a r

57 obtained was related to the formation of BSA-glutathione complex.

58 leterious superoxide, the formation of Cu(I)-glutathione complexes might be avoided under normal phys

59 Furthermore, PSP enhanced cellular glutathione concentrations and decreased lipid peroxidat

60 polysulfides were unstable at physiological glutathione concentrations and were reduced with concomi

61 l processes; however, the dynamic changes of glutathione concentrations in living cells remain largel

62 , and greater MRP1-mediated efflux of NO2-OA-glutathione conjugates.

63 n this paper that the stability of the total glutathione content (GSH + GSSG) and GSH in saliva is si

64 Our robust model for the glutathione-Cu(I) equilibrium system sets a firm upper l

65 also reduce Hg bioavailability in swordfish (glutathione, cysteine, homocysteine).

66 of NO2-CLA with low molecular weight thiols (glutathione, cysteine, homocysteine, cysteinylglycine, a

67 d the enzymes and the mechanisms involved in glutathione degradation in detail.

68 Glutathione degradation plays an important role in gluta

69 and catalytic activity of this new enzyme of glutathione degradation, which is involved in continuous

70 nvasive mechanism whereby the secretion of a glutathione-dependent oxidoreductase drives angiogenesis

71 CLIC3 acts as a glutathione-dependent oxidoreductase that reduces TGM2 a

72 n glutaredoxin activity, which catalyzes the glutathione-dependent reduction of DHA.

73 Furthermore, glutathione depletion failed to attenuate the protective

74 reactive oxygen species and the depletion of glutathione depletion in cells.

75 Glutathione depletion, mimicking in vivo conditions expe

76 Unexpectedly, Pml(-/-) embryos survive acute glutathione depletion.

77 cytes; 3) metabolic pathways associated with glutathione detoxification and tryptophan degradation we

78 d only be recapitulated in wild-type mice by glutathione dialysis.

79 the enzymatic mechanism of the reduction of glutathione disulfide (GSSG) by the reduced a domain of

80 omitant formation of glutathione persulfide, glutathione disulfide, and H2S.

81 de phosphate , flavin adenine dinucleotide , glutathione disulfide/glutathione).

82 The redox pair glutathione (GSH) and glutathione disulphide (GSSG) forms the most important r

83 transcripts, we observed impaired levels of glutathione (downstream Nrf2 antioxidant) in TDP-43M337V

84 one probe will enable opportunities to study glutathione dynamics and transportation and expand our u

85 hat can quantitatively monitor the real-time glutathione dynamics in living cells.

86 M7Vs accumulate Zn(2+) in a glutathione-enriched, reduced lumen when cytosolic Zn(2+

87 We found that glutathione enters the ER by facilitated diffusion throu

88 ighest level of 2.0% for glycine and reduced glutathione favored protein extractability and a weaker

89 4 mm and kcat of 225.2 +/- 15 min(-1) toward glutathione for human ChaC1).

90 4 mm and kcat of 15.9 +/- 1.0 min(-1) toward glutathione for human ChaC2; Km of 2.2 +/- 0.4 mm and kc

91 rbon source for pyrimidine biosynthesis, and glutathione for redox balance.

92 consistently competes as a nucleophile with glutathione for the o-quinone of caftaric acid.

93 Both glutathione forms were detected in these complex biologi

94 Consistent with a radical pathway, glutathione fully suppresses catalysis.

95 wine during the first 6months, and the total glutathione gradually declined up to 12months.

96 Additionally, DOM and glutathione greatly decreased Hg sorption by G. sulfurre

97 his process can be triggered by depletion of glutathione (GSH) and accumulation of lipid reactive oxy

98 thiol oxidation kinetics was studied, using glutathione (GSH) and cysteine (CYS) as model systems.

99 The redox pair glutathione (GSH) and glutathione disulphide (GSSG) form

100 xenograft tumors, MnO2 /DVDMS is reduced by glutathione (GSH) and H2 O2 and reassembled into nanoDVD

101 Bar-Me forms a Michael addition adduct with glutathione (GSH) and inhibits IKKbeta phosphorylation.

102 was verified using dithiothreitol (DTT) and glutathione (GSH) as liberating agents.

103 ed human serum albumin (HSA) pretreated with glutathione (GSH) based on the low pH- and GSH-sensitive

104 specific interaction with tripeptide reduced glutathione (GSH) bioreceptor directly immobilized on th

105 o NADPH and promotes regeneration of reduced glutathione (GSH) by supplying NADPH to glutathione redu

106 al reductants and is especially sensitive to glutathione (GSH) compared to alternative assays.

107 Cys-SSH and its glutathione (GSH) counterpart (GSSH) have been recognize

108 Glutathione (GSH) has so far been considered to facilita

109 -potential amperometric detection of reduced glutathione (GSH) in pH 7.2 phosphate buffer solution (P

110 e presence of high concentrations of reduced glutathione (GSH) inside the cells, thereby facilitating

111 The tripeptide glutathione (GSH) is a crucial intracellular reductant a

112 Reduced glutathione (GSH) is an efficient antioxidant on limitin

113 as a result, maintenance of the antioxidant glutathione (GSH) is essential for their survival and pr

114 We hypothesized that increasing cellular glutathione (GSH) levels would inhibit neuroinflammation

115 superoxide release and reduced mitochondrial glutathione (GSH) levels, although cytosolic GSH remaine

116 is accompanied with higher cytosolic reduced glutathione (GSH) levels.

117 alyzes disulfide bond formation and promotes glutathione (GSH) oxidation to GSSG.

118 h as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH) play crucial roles in maintaining redo

119 ecies (ROS), which trigger the antioxidative glutathione (GSH) response necessary to buffer rising RO

120 s the rate-limiting enzyme for intracellular glutathione (GSH) synthesis.

121 hared function is the conjugation of reduced glutathione (GSH) to endo- and xenobiotics.

122 Cysteine (Cys) and glutathione (GSH) were associated with small increases i

123 igen 2 (NG2) expressed in hepatic pericytes, glutathione (GSH), and malondialdehyde (MDA) concentrati

124 uantification of oxidized (GSSG) and reduced glutathione (GSH), biomarkers of oxidative stress, is de

125 h as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH), play a key role in an extensive range

126 disulfide moiety can directly interact with glutathione (GSH), thereby reducing its intracellular co

127 r cells by producing an antioxidant, reduced glutathione (GSH), through HIF-1-mediated metabolic repr

128 It catalyzes the glutathione (GSH)-dependent dealkylation of alkylcobalam

129 Glutathione (GSH)-induced degradation of self-immolative

130 ased intracellular glutamine, glutamate, and glutathione (GSH).

131 =130 nm) in the presence of the cosubstrate glutathione (GSH).

132 elease of the I(-) ligand in the presence of glutathione (GSH).

133 e oxidation used in the detection of reduced glutathione (GSH).

134 p < 0.0001), thyroxine (T4, p = 0.042), and glutathione (GSH, p = 0.034) concentrations than control

135 to an increased ratio of reduced to oxidized glutathione (GSH/GSSG).

136 DOX release under a redox environment (10mM glutathione, GSH), and demonstrated enhanced cytotoxicit

137 ntioxidants, the sum of oxidized and reduced glutathione (GSSG and GSH) can be measured with essentia

138 concentrations of reduced (GSH) and oxidized glutathione (GSSG), and it enables the calculation of th

139 a by-product of increased levels of oxidized glutathione (GSSG).

140 However, the presence of glutathione had low or no influence on the concentration

141 Suppressed PPP causes compromised glutathione homeostasis and increased oxidative stress,

142 tic studies show that impaired mitochondrial glutathione homeostasis and subsequent mitochondrial dys

143 learance, the pentose phosphate pathway, and glutathione homeostasis.

144 edox poise is tuned by reciprocal control of glutathione import and Ero1 activation.

145 redox state and levels likely depends on ER glutathione import and GSSG export.

146 gh Ero1 reductive activation, which inhibits glutathione import in a negative regulatory loop.

147 ntitative GSH and GSSG biosensors to monitor glutathione import into the ER of yeast cells.

148 Increased ER glutathione import triggers H2O2-dependent Bip oxidation

149 the physiological and pathological roles of glutathione in living cells.

150 nd efficacy in the presence of thiols (e.g., glutathione in mM concentrations).

151 for its vasodilator activity on the level of glutathione in the brain.

152 yclotransferases, as an enzyme that degrades glutathione in the cytosol of mammalian cells.

153 Reduced level of ROS and higher levels of glutathione in VMW were further confirmed.

154 maintain the main intracellular antioxidant, glutathione, in its reduced state.

155 reactivity, and that preserved synthesis of glutathione is essential for the full development of thi

156 n continuous but basal turnover of cytosolic glutathione, is proposed.

157 tral augmentation index (P=0.015), and lower glutathione level (P=0.003), indicative of increased oxi

158 athione transferase genes and elevated total glutathione level were normalized by KD.

159 In addition, glutathione level, thioltransferase activity, m-calpain

160 n species-inducing diethyl maleate increased glutathione levels and (18)F-FASu uptake, whereas gene k

161 enal BH4 levels were closely correlated with glutathione levels and inversely correlated with cardiac

162 metry and function, cardiac histomorphology, glutathione levels and protein levels of cathepsin K and

163 We show that, when glutathione levels are reduced, astrocyte calcium-evoked

164 ebrovascular reactivity to CO2 Reductions in glutathione levels in aging, stroke, or schizophrenia co

165 of nestling frigatebirds, and (ii) that high glutathione levels in red blood cells are associated wit

166 etry based high-throughput quantification of glutathione levels in single cells.

167 UPR-dependent Ero1 induction, and cytosolic glutathione levels increase.

168 eine and sulforaphane, which act to increase glutathione levels through complementary mechanisms.

169 Glutathione levels varied >20-fold (0.11-2.41mg/gdw) wit

170 Additionally, glutathione levels were decreased in Fabry mouse tissues

171 results in NRF2 activation, normalization of glutathione levels, and prevention of PPK in female Krt1

172 roduction, decreased GPx activity, decreased glutathione levels, increased inducible nitric oxide syn

173 athione peroxidase (GPx) activity, decreased glutathione levels, increased inducible nitric oxide syn

174 levels, decreased glycolytic flux, Nrf-2 and glutathione levels, ultimately resulting in caspase-3 ac

175 hermore, these results suggest that depleted glutathione levels, which occur in aging and stroke, wil

176 esponse element Nrf-2, resulting in depleted glutathione levels.

177 th sex-specific fluctuations in footpad skin glutathione levels.

178 f manganese superoxide dismutase and reduced glutathione levels.

179 tion, cystine uptake, and incorporation into glutathione, linking growth factor receptor signaling wi

180 ined for oxidative stress parameters such as glutathione, lipid peroxidation, and calcium levels alon

181 metabolites associated with skeletal muscle glutathione/Met/Cys metabolism (2-hydroxybutanoic acid,

182 ith lipid peroxidation and downregulation of glutathione metabolism proteins, features that are typic

183 Changes in proteins and metabolites of glutathione metabolism were indicative of increased oxid

184 acid metabolism, TCA cycle, gluconeogenesis, glutathione metabolism, pantothenate and CoA biosynthesi

185 represent an altered gamma-glutamyl cycle of glutathione metabolism.

186 eta-oxidation of fatty acids; alterations in glutathione metabolism; and increased serum metabolites

187 We discerned specific changes in glutathione metabolites that uncovered novel facets of M

188 r thiol reactivity with biological proteins (glutathione) of wastewater samples.

189 A stimulatory effect on catalase and glutathione oxidase activities induced by MCs was found

190 cat2), the dhar1 dhar2 combination decreased glutathione oxidation and inhibited cat2-triggered induc

191 acea) genotypes using ABTS, deoxyribose, and glutathione oxidation assays, as well as, SH-SY5Y cells

192 lutathione oxidation, and (3) DHAR-dependent glutathione oxidation influences redox-driven salicylic

193 ntracellular hydrogen peroxide metabolism to glutathione oxidation, and (3) DHAR-dependent glutathion

194 KO heart, protein oxidation and a decreased glutathione/oxidized glutathione ratio were observed, bu

195 In addition, higher glutathione/oxidized glutathione ratios suggested that m

196 Moreover, the ROS scavenger glutathione partially rescued the effects of Coq2-RNAi.

197 mine metabolism, at least in part due to the glutathione pathway, an efficient cellular buffering sys

198 t for fast in solution detection methods for glutathione peptides that have experienced heat stress.

199 d was evaluated to visually detect denatured glutathione peptides, utilizing gold nanoparticle aggreg

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

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

202 The antioxidant glutathione peroxidase (GPx) and inflammation biomarkers

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

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

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

206 Human glutathione peroxidase 1 could thereby also be produced,

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

208 C57Bl6 and glutathione peroxidase 1 knockout mice.

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

210 Infected glutathione peroxidase 1 mice showed an early and signif

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

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

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

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

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

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

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

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

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

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

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

222 equence for sulfide oxidation being: H2S --> glutathione persulfide --> sulfite --> sulfate, than wit

223 stable in the reducing intracellular milieu, glutathione persulfide could serve as a persulfide donor

224 d were reduced with concomitant formation of glutathione persulfide, glutathione disulfide, and H2S.

225 the direction of thiosulfate to sulfite and glutathione persulfide; sulfur transfer in the reverse d

226 tty acid metabolism, and the biosynthesis of glutathione, phospholipids, NADPH, and coenzyme Q10.

227 Glutathione plays many important roles in biological pro

228 een oxidatively prestressed by depleting the glutathione pool by buthionine sulfoximine treatment.

229 little effect on phenotype or ascorbate and glutathione pools in standard conditions.

230 nylation of endogenous substrates, depleting glutathione pools, an activity that DmGST may lack.

231 We previously showed that the glutathione precursor, N-acetylcysteine (NAC), prevented

232 Although NAC is thought to be a glutathione precursor, NAC protected primary astrocytes

233 lementing primary wild-type hepatocytes with glutathione precursors improves cell survival following

234 ) release from the vesicles, whereas reduced glutathione prevents TRPM7-dependent cytosolic Zn(2+) in

235 We envision that this new glutathione probe will enable opportunities to study glu

236 decreased hemoglobin digestion, and enhanced glutathione production.

237 Cysteine, homocysteine, glutathione, quercetin, albumin and tannic reduce bioava

238 dw) and were highly correlated with those of glutathione (r=0.62, P<0.001).

239 kinetic analysis of ndSQR is consistent with glutathione rather than sulfite being the predominant ac

240 idation and a decreased glutathione/oxidized glutathione ratio were observed, but the opposite was fo

241 In addition, higher glutathione/oxidized glutathione ratios suggested that microprobed cells exhi

242 ation of cellular redox status in particular glutathione redox balance.

243 Consistent with this, intracellular glutathione redox capacity was decreased and UCP2 gene e

244 xhibit increased oxidative stress, decreased glutathione redox capacity, and highly active mitochondr

245 s and nutrient transporters, together with a glutathione redox moiety, which is likely to act as the

246 be reduced in the ER, maintenance of the ER glutathione redox state and levels likely depends on ER

247 oxidation, and calcium levels along with the glutathione reductase and thioltransferase enzyme activi

248 nificantly higher levels of malondialdehyde, glutathione reductase enzyme activity, and calcium level

249 igh sensitivity of mature gametocytes to the glutathione reductase inhibitor and redox cycler drug me

250 uced glutathione (GSH) by supplying NADPH to glutathione reductase or thioredoxin reductase.

251 nolic content, ascorbic acid and the enzymes glutathione reductase, catalase, ascorbate peroxidase an

252 ygenase-1, NAD(P)H dehydrogenase, quinone 1, glutathione reductase, glutamate-cysteine ligase catalyt

253 The enzyme, glutathione reductase, is highly specific to glutathione

254 including catalase, glutathione synthetase, glutathione reductase, NADPH-cytochrome P450 reductase,

255 drogenase and reoxidation to N(tz) ADP(+) by glutathione reductase.

256 se released from glycogen and used for NADPH/glutathione reduction renders nematodes and human hepato

257 ctively, while we also observed evidence for glutathione-related mechanisms, including metallothionei

258 x), small ubiquitin-related modifier (Sumo), glutathione S-transferase (GST), maltose-binding protein

259 oxidant enzymes (lactoperoxidase, microsomal glutathione S-transferase 2 and 3, glutathione S-transfe

260 astic foci in the liver (increased placental glutathione S-transferase and cytokeratin 8-18 activity;

261 ntrol of a pathogen-inducible promoter, from glutathione S-transferase gene from potato.

262 ese associations are modified by variants in Glutathione S-Transferase genes.

263 Glutathione S-transferase mu 1 (GSTM1) encodes an enzyme

264 icrosomal glutathione S-transferase 2 and 3, glutathione S-transferase peroxidase kappa 1, and glutat

265 Glutathione S-transferase pi 1 (GSTP1) is frequently ove

266 CLICs resemble the omega class of Glutathione S-transferases (GST), yet differ from them i

267 Glutathione S-transferases (GSTs) comprise a diverse fam

268 encoding cytochrome P450 monooxygenases and glutathione S-transferases associated with detoxificatio

269 response genes, such as cytochrome P-450 and glutathione S-transferases, potentially involved in the

270 levels across fuel types were observed for S-glutathione (S-GSH) and S-gamma-glutamylcysteine (S-gamm

271 a proof of concept, a reversible label-free glutathione-S-transferase (GST) biosensor is demonstrate

272 gh polyunsaturated fat liquid diet to female glutathione-S-transferase 4-4 (Gsta4(-/-))/peroxisome pr

273 We find GSSG, S-oxidised glutathione species, and S-nitrosoglutathione as oxidati

274 s vitamin B6 cofactors with the red emitting glutathione stabilized copper nanoclusters (GSH-CuNCs).

275 osing effects of DOM were also observed with glutathione, suggesting that thiols in DOM likely played

276 e latter two being the final products, while glutathione sulphenic acid, glutathione sulphinic acid,

277 products, while glutathione sulphenic acid, glutathione sulphinic acid, and GSSG are rather reaction

278 In one strain, both hly and gshF (encoding a glutathione synthase required for full PrfA activity) we

279 rough increased consumption of glutamate for glutathione synthesis and glutamate secretion by xc(-) a

280 e, oxidative stress associated with impaired glutathione synthesis and nuclear factor erythroid-deriv

281 ln via the blood to the PDTX to fuel Glu and glutathione synthesis while gluconeogenesis occurs in th

282 Because these AAs are involved in glutathione synthesis, we hypothesized they might be rel

283 S) scavenging machinery, including catalase, glutathione synthetase, glutathione reductase, NADPH-cyt

284 l as total antioxidant capacity (TAC), total glutathione (tGSH), and carotenoids in plasma of Baltic

285 on of bioreductants such as ascorbic acid or glutathione, the compound is readily reduced to the corr

286 plays a key role in stabilizing the leaving glutathione thiolate formed.

287 ver of SAM for the synthesis of cysteine and glutathione through transsulfuration.

288 conjugation of electrophilic compounds with glutathione to facilitate their degradation or excretion

289 LanCL1 catalyzes the addition of the Cys of glutathione to protein- or peptide-bound dehydroalanine

290 ated the antioxidant metabolites (ascorbate, glutathione, tocopherols, and polyphenols) and enzymes (

291 have characterized a Drosophila melanogaster glutathione transferase (DmGSTE6) which has activity tow

292 Induction of hepatic glutathione transferase genes and elevated total glutath

293 Glutathione transferase Omega 1 (GSTO1-1) is an atypical

294 Cooking time changed just for reduced glutathione-treated rice, as a result of their weaker pr

295 d reduced (GSH) and oxidized (GSSG) forms of glutathione was assessed by CV studies at physiological

296 Glutathione was denatured using a 70 degrees C water bat

297 ndogenously synthesized or exogenously added glutathione was sufficient to form this modification.

298 se-inactivated C314S mutant with and without glutathione were determined at 1.8, 2.4, and 2.7 A resol

299 physiological concentrations of cysteine and glutathione, while those with longer sulfur chains, Cys-

300 also shared the same specificity for reduced glutathione, with no activity against either gamma-gluta