ライフサイエンスコーパス: oxidatively

1 otential (-0.60 V), it will not stress cells oxidatively.

2 The resting state Fe(III) is unreactive oxidatively.

3 ion of LNM by cellular thiols, LNM E1 can be oxidatively activated by cellular reactive oxygen specie

4 isomerase antagonizes the rescue provided by oxidatively active Ero1.

5 o((i)Pr(2)PNMes)(3)Zr(THF) has been shown to oxidatively add CO(2), generating (OC)Co((i)Pr(2)PNMes)(

6 natable chelating aryldiphosphine ligand, to oxidatively add unactivated aryl chlorides at room tempe

7 mediate in nickel-catalyzed cross-couplings, oxidatively adding alkyl electrophiles through a monomet

8 multaneously measured, including products of oxidatively and nitratively damaged DNA (8-hydroxy-2'-de

9 Immunoblot analyses showed that TE is oxidatively and nitrosatively modified by peroxynitrite

10 aviour, and thereby enabled the formation of oxidatively and physically stable lipid nanoparticles.

11 ted state [Ir(ppy)2(dtbbpy)](+)* can be both oxidatively and reductively quenched by Ni4P2 and TEOA,

12 An all-inorganic, oxidatively and thermally stable, homogeneous water oxid

13 ite this structural similarity, HiPIPs react oxidatively at physiological potentials, whereas Fds are

14 Complex 3 is quenched oxidatively by [Co(dmgH)pyCl]2+ (1) with a rate constant

15 functional evidence that Hp protects Hb when oxidatively challenged with H(2)O(2) preserving CD163-me

16 /mL) and, after phenolic removal, cells were oxidatively challenged with H(2)O(2).

17 se enzymes utilize a non-heme iron center to oxidatively cleave a carbon-carbon double bond of a caro

18 xygenases (CCDs) are a class of enzymes that oxidatively cleave carotenoids into apocarotenoids.

19 (II)-Bc was further demonstrated to bind and oxidatively cleave DNA under reduction conditions in the

20 ite and use dioxygen and a reducing agent to oxidatively cleave glycosidic linkages in polysaccharide

21 ally important copper-dependent enzymes that oxidatively cleave polysaccharides.

22 ethers and related ArCH(2)OR substrates are oxidatively cleaved by 4-acetamido-2,2,6,6-tetramethylpi

23 Provitamin A carotenoids are oxidatively cleaved by beta-carotene 15,15'-dioxygenase

24 catalyzed reactions in which diketonates are oxidatively cleaved using O2 as the terminal oxidant.

25 lcohol residue of the coupling product 4 was oxidatively cleaved with sodium periodate in the presenc

26 m Mg-protoporphyrin IX monomethyl ester, Ho1 oxidatively cleaves heme to form biliverdin, and HemF ox

27 charide monooxygenases (PMOs) are capable of oxidatively cleaving chitin, cellulose, and hemicellulos

28 mino-1-hydroxyethylphosphonic acid, which is oxidatively converted by PhnZ to inorganic phosphate and

29 phthoxide derivatives give the corresponding oxidatively coupled bi-2-naphthol products in 68-95% yie

30 derivatives, whereas sinapaldehyde is either oxidatively coupled into S'(8-8)S' and lignin or convert

31 cultures and supported that monolignols are oxidatively coupled not only in the cell wall but also i

32 wever, the [Cu(mu-O)2Pt]+ core is capable of oxidatively coupling 2,4-di-tert-butylphenol and 2,4-di-

33 d-poor, not associated with HDL, extensively oxidatively cross-linked, and functionally impaired.

34 ions in an Aer dimer was assessed in vivo by oxidatively cross-linking serial cysteine substitutions.

35 with t-BuONO to form acyloximes which can be oxidatively cyclized to yield ioxazoles.

36 of ppk mutants to both heat and acid and may oxidatively damage (carbonylate) destabilized MetA.

37 Copper-phenanthroline complexes oxidatively damage and cleave nucleic acids.

38 TH1 cleanses the cellular nucleotide pool of oxidatively damaged 8-oxo-dGTP, preventing mutagenesis b

39 rotease responsible for degrading denatured, oxidatively damaged and certain regulatory proteins in t

40 a coli Nei/Fpg, is involved in the repair of oxidatively damaged bases in mammalian cells.

41 r DNA glycosylases responsible for repairing oxidatively damaged bases in mammalian genomes and the a

42 A glycosylase, NEIL1, specific for repair of oxidatively damaged bases in the genome via the base exc

43 h overlapping substrate ranges for repairing oxidatively damaged bases via the base excision repair (

44 s that suppress oxidative stress or detoxify oxidatively damaged biomolecules, i.e., haptoglobin, glu

45 DNA can be oxidatively damaged by ROS, which may lead to carcinogen

46 Distal dG's are also oxidatively damaged by the peroxyl radicals.

47 RNA molecules of natural sequence that were oxidatively damaged by treatment with hydrogen peroxide

48 Phagocytic removal of aged or oxidatively damaged cells and macromolecules is an indis

49 elective binding of avidin to DNA containing oxidatively damaged deoxyguanosine.

50 Prx1, is associated with the accumulation of oxidatively damaged DNA and a tumor-prone phenotype.

51 bacterial Nei/Fpg, is involved in repairing oxidatively damaged DNA bases.

52 tion of nucleotide selectivity on normal and oxidatively damaged DNA by three single-subunit RNAPs pr

53 We report that the OGG1-initiated repair of oxidatively damaged DNA is a prerequisite for GDP --> GT

54 suggest that neurons can efficiently repair oxidatively damaged DNA, and that both DNA damage and re

55 as well as structurally perturbed DNAs (e.g. oxidatively damaged DNA, UV-irradiated DNA, alkylated DN

56 ed elevated levels of lipid peroxidation and oxidatively damaged DNA.

57 t to NO and H2O2 and is capable of repairing oxidatively damaged Fe-S of iron regulatory protein 1 (I

58 be particularly important for the repair of oxidatively damaged Fe-sulphur clusters of aconitase and

59 from Agrobacterium vitis S4, deaminates two oxidatively damaged forms of adenine: 2-oxoadenine and 8

60 g aging and that a subset of nucleoporins is oxidatively damaged in old cells suggests that the accum

61 that up to 50% of messenger RNAs (mRNA) are oxidatively damaged in the affected area of Alzheimer's

62 Here we report that DJ-1 is oxidatively damaged in the brains of patients with idiop

63 Oxidatively damaged lipid membranes are known to promote

64 nction with prior results demonstrating that oxidatively damaged membranes cause Abeta42 to misfold a

65 ract (RWE) exposure, we have identified nine oxidatively damaged mitochondrial respiratory chain-comp

66 S) increased and the efficiency of repair of oxidatively damaged mtDNA decreased as consequences of e

67 function in the folding process by repairing oxidatively damaged nascent polypeptides and unfolded pr

68 e of O2-sensitive [NiFe] hydrogenases and/or oxidatively damaged protein.

69 back to L-methionine consequently repairing oxidatively damaged proteins and peptides.

70 We find that oxidatively damaged proteins are also localized there, h

71 increased reactive oxygen species levels and oxidatively damaged proteins in the cells as well as imp

72 entially by offsetting the increased load of oxidatively damaged proteins, in this non-human primate

73 ylene reduction) activity and an increase in oxidatively damaged proteins.

74 oxide reductases are key enzymes that repair oxidatively damaged proteins.

75 e (PMSR) is a ubiquitous enzyme that repairs oxidatively damaged proteins.

76 ubunit proteases critical for the removal of oxidatively damaged proteins.

77 Endonuclease VIII (Nei) excises oxidatively damaged pyrimidines from DNA and shares stru

78 xoG), suggesting a possible role in removing oxidatively damaged RNA.

79 Importantly, oxidatively damaged SOD1 aggregates have been observed i

80 phagy therefore normally functions to remove oxidatively damaged Sup35, which accumulates in cells gr

81 udies of this relationship demonstrated that oxidatively damaged synthetic lipid membranes promoted a

82 demonstrate in vitro that nitrogenase can be oxidatively damaged under anoxic conditions and that the

83 The oxidatively damaged, but not the native protein, is a su

84 as well as structurally perturbed DNAs (e.g. oxidatively damaged, UV-irradiated, or alkylated DNA).

85 stopped-flow experiments for its ability to oxidatively debrominate 2,4,6-tribromophenol (TBP).

86 inase homolog that catalyzes cleavage of the oxidatively decarboxylated MftA peptide to liberate its

87 ydrogen peroxide via an intermediate that is oxidatively decarboxylated.

88 above 3.5 V (in the presence of Li(2)O(2)), oxidatively decomposing to form Li(2)CO(3).

89 ride monooxygenases (LPMOs) are enzymes that oxidatively deconstruct polysaccharides.

90 (LPMOs) are recently discovered enzymes that oxidatively deconstruct polysaccharides.

91 Complex 2 also is capable of oxidatively deformylating aldehydes, which is a known re

92 However, it is known that PEI will oxidatively degrade at elevated temperatures.

93 re a class of copper-containing enzymes that oxidatively degrade insoluble plant polysaccharides and

94 nes may not mean that all aminopolymers will oxidatively degrade.

95 Exposure to oxidatively degraded MEA increased (p < 0.05) total cell

96 a triazine in which the pyrimidine ring was oxidatively degraded.

97 Catalytic antibodies capable of oxidatively degrading the major psychoactive component o

98 mophenol (TBP) and 2,4,6-trichlorophenol are oxidatively dehalogenated by DHP to form 2,6-dibromo-1,4

99 DHP A is capable of binding and oxidatively dehalogenating some of these compounds.

100 Ethane is oxidatively dehydrogenated with a selectivity up to 95%

101 P450 enzyme from Rhodopseudomonas palustris, oxidatively demethylates 4-methoxybenzoic acid to 4-hydr

102 iron storage and detoxification proteins by oxidatively depositing iron as a hydrous ferric hydroxid

103 lkenyl iminohydantoins may be hydrolyzed and oxidatively deprotected to yield hydantoins and unsatura

104 he incorporation kinetics opposite these two oxidatively derived lesions as well as an abasic site an

105 arbon within the coal structure is easier to oxidatively displace than when pure sp2-carbon structure

106 Mn(III) in solution or at the surface, that oxidatively dissolved the UO2 more rapidly than could th

107 analytes is enabled by newly introducing an oxidatively doped poly(3,4-ethylenedioxythiophene) film

108 face during the deposition step and detected oxidatively during the stripping step.

109 anisotropic gold nanostructures as they are oxidatively etched in a graphene liquid cell with a cont

110 suggest that many bacteria may not generally oxidatively fold proteins, and implicate the bacterial h

111 thiol oxidases initiate a disulfide relay to oxidatively fold secreted proteins.

112 In addition, we oxidatively folded a fully reduced SMB in aqueous soluti

113 the construction of conjugates incorporating oxidatively folded protein domains in their native confo

114 other pro-inflammatory agents, such as sn-2 oxidatively fragmented phospholipids.

115 drolysis of both nontruncated and truncated (oxidatively fragmented) species of oxidized PS species,

116 trometry (FT-ICR MS) indicate the lack of an oxidatively functional tricarboxylic acid (TCA) cycle an

117 ation, pristine carbon nanotubes (PCNTs) and oxidatively functionalized carbon nanotubes (FCNTs) were

118 can be readily realized intramolecularly by oxidatively generated beta-diketone-alpha-gold carbenes

119 Oxidatively generated damage to DNA induced by a pyrenyl

120 chanisms have been considered to account for oxidatively generated DNA damage by TPZ.

121 gen-sensitive drug radical (2) that leads to oxidatively generated DNA damage under hypoxic condition

122 ents existing methods for the measurement of oxidatively generated DNA damage.

123 Unlike some other oxidatively generated DNA lesions, cdG and cdA are repai

124 Oxidatively generated guanine radical cations in DNA can

125 eptides, and then employed as precursors for oxidatively generating reactive N-acyliminium ions.

126 (18)F]Fluorodeoxy thymidine-1 (PC-FLT-1), an oxidatively immolative positron emission tomography (PET

127 In contrast, the oxidatively impaired E18D mutant behaves as an inactive

128 conclude that a combined perturbation of the oxidatively-impaired NO -cGMP signaling pathway is a bet

129 s donors of Fe(II) to ISC scaffold proteins, oxidatively inactivated [3Fe-4S](+) aconitase, and ferro

130 ociated with an increase in the abundance of oxidatively inactivated protein-tyrosine phosphatases.

131 n turn, promoted IL-4 receptor activation by oxidatively inactivating PTP1B that physically associate

132 This communication describes oxidatively induced Ar-CF(3) bond-forming reductive elim

133 ional design of first generation systems for oxidatively induced Aryl-CF(3) bond-forming reductive el

134 f four carboxymethylated DNA lesions and two oxidatively induced bulky DNA lesions including (5'S) di

135 This communication describes studies of oxidatively induced C-C bond-forming reductive eliminati

136 possibly both Ni(III) and Ni(IV) species, in oxidatively induced C-heteroatom bond formation reaction

137 III) species in cross-coupling reactions and oxidatively induced C-heteroatom bond formation reaction

138 1 and 4 days after irradiation, we monitored oxidatively induced clustered DNA lesions (OCDL), DNA do

139 first step of base excision repair (BER) of oxidatively induced DNA damage.

140 In humans, the oxidatively induced DNA lesion 8-hydroxyguanine (8-oxoG)

141 The oxidatively induced DNA lesions 2,6-diamino-4-hydroxy-5-

142 most studies on the role of CSB in repair of oxidatively induced DNA lesions have focused on 7,8-dihy

143 hat BRCA1 plays a role in cellular repair of oxidatively induced DNA lesions.

144 ly, the results provide strong evidence that oxidatively induced DSBs arise in HC as well as euchroma

145 le describes the high-yielding and selective oxidatively induced formation of ethane from mono-methyl

146 This communication describes a series of oxidatively induced intramolecular arene C-H activation

147 ) measured by gamma-H2AX focus formation and oxidatively induced non-DSB clustered DNA lesions (OCDLs

148 a nickelaoxetane demonstrated protonolysis, oxidatively induced reductive elimination, deoxygenation

149 c addition of nitromethane anion followed by oxidatively induced reductive elimination.

150 ogen = Cl or Br) of diverse alpha-olefins by oxidatively intercepting Mizoroki-Heck intermediates.

151 Among the first peptides to be oxidatively labeled after temperature-induced triggering

152 tion of the seco-ester in the presence of an oxidatively labile dithiane, a highly refined protecting

153 In particular, alkenes with oxidatively labile functional groups, such as alcohols,

154 is a chronic inflammatory process driven by oxidatively modified (atherogenic) lipoproteins, chemoki

155 rosine (quantitative immunofluorescence), an oxidatively modified amino acid and marker of oxidative

156 roxidase/glutathione antioxidant system, and oxidatively modified amino acids were measured in subjec

157 Of these, the SOD1 pI 6.0 isoform is oxidatively modified by carbonylation, and the pI 5.0 is

158 of hypertension, we determined that proteins oxidatively modified by highly reactive gamma-ketoaldehy

159 Finally, D1:(130)E and D2:(246)M are oxidatively modified by O2(*-) formed by the reduction o

160 ed reactive oxygen species production, which oxidatively modified cysteinyl thiols in the eNOS-activa

161 spectroscopy, we have identified a number of oxidatively modified D1 and D2 residues.

162 ctive probe (ARP) quantitatively reacts with oxidatively modified depurinated/depyrimidinated (abasic

163 Identification of the oxidatively modified DNA base OG to guide BER activity i

164 8-Oxoguanine, one of the oxidatively modified DNA bases, is a typical biomarker o

165 ulated due to disease and/or aging result in oxidatively modified DNA, carbohydrates, proteins, and l

166 The levels of lipid peroxide, oxidatively modified DNA, electron transport complex III

167 assess the possibility that Artemis acts on oxidatively modified double strand break termini, its ac

168 in hepatic I/R injury, the proteins that are oxidatively modified during I/R damage are poorly charac

169 duction and suggest a role in the removal of oxidatively modified fatty acids from membranes.

170 M2.5 increased 7-ketocholesterol (7-KCh), an oxidatively modified form of cholesterol, in plasma inte

171 It has been shown that oxidatively modified forms of proteins accumulate during

172 It has been shown that oxidatively modified forms of proteins accumulate during

173 We suggest that oxidatively modified free fatty acids and lyso-PS specie

174 merous studies have reported the presence of oxidatively modified high-density lipoprotein (OxHDL) wi

175 aken to examine whether a T cell response to oxidatively modified IgG contributes to the inflammation

176 e circulating T cells that are responsive to oxidatively modified IgG, a possible pathogenic mechanis

177 , elongation factor Tu, was found to be more oxidatively modified in norleucine-substituted cells, co

178 eviously that apolipoprotein A-I (apoA-I) is oxidatively modified in the artery wall at tyrosine 166

179 d member of the HSP70 family, in response to oxidatively modified LDL (oxLDL) and immune complexes pr

180 in aortae from hyperlipidemic mice and that oxidatively modified LDL (oxLDL) induces activation of m

181 e role of low density lipoproteins (LDL) and oxidatively modified LDL (oxmLDL) in the expression and

182 amily guanine nucleotide exchange factors by oxidatively modified LDL in macrophages.

183 generally more circulating glycated LDL than oxidatively modified LDL.

184 vestigators to study the role of atherogenic oxidatively modified lipids (oxylipids).

185 tivity is lost following cell treatment with oxidatively modified low density lipoprotein and IFN-gam

186 iates the recognition and internalization of oxidatively modified low density lipoprotein by vascular

187 Oxidatively modified low density lipoproteins, central t

188 Exposure to oxidatively modified low-density lipoprotein enhanced th

189 lipids (oxPLs) that are typically present in oxidatively modified low-density lipoprotein.

190 itrosative stress markers, and activities of oxidatively modified mitochondrial proteins were measure

191 suggest that apoptotic cell death generates oxidatively modified moieties, which can induce autoimmu

192 macrophage phenotypic changes in response to oxidatively modified molecules are not known.

193 n isotherms, we show that the presence of an oxidatively modified phosphatidylcholine, 1-palmitoyl-2-

194 he conformation of calmodulin (CaM) bound to oxidatively modified plasma-membrane Ca(2+)-ATPase (PMCA

195 also report the binding affinity of CaM with oxidatively modified PMCA (K(d) = 9.8 +/- 2.0 nM), indic

196 reported loss in CaM-stimulated activity for oxidatively modified PMCA is not a result of reduced CaM

197 trast, proteolysis was partially blocked for oxidatively modified PMCA, even in the presence of ATP.

198 ease and subsequent decrease in the level of oxidatively modified protein.

199 mammalian cells are enriched 3.3-15-fold for oxidatively modified proteins and that failure to execut

200 rite scavenger metalloporphyrin (MnTMPyP) on oxidatively modified proteins and their functions.

201 s in which accumulation of ubiquitinated and oxidatively modified proteins has an etiologic role.

202 n proteins in EAD with previously identified oxidatively modified proteins in MCI and late-stage AD.

203 The results showed that levels of oxidatively modified proteins increased with age, not on

204 re is now consensus that the accumulation of oxidatively modified proteins is cytotoxic and causally

205 This study was aimed at investigating the oxidatively modified proteins underlying the mechanism f

206 The identities of the oxidatively modified proteins were determined using mass

207 We hypothesized that identity of these oxidatively modified proteins would lead to greater unde

208 n proteolytic pathway recognizes and removes oxidatively modified proteins, and that failure of this

209 Abeta(1-42) treatment leads to oxidatively modified proteins, consistent with the notio

210 ed in recognition and proteolytic removal of oxidatively modified proteins, which are produced upon c

211 ply, and chaperones were identified as being oxidatively modified proteins.

212 vative with the aldehyde/keto group found in oxidatively modified proteins.

213 in carbonyl immunoreactivity, which reflects oxidatively modified proteins.

214 shing characteristic of high specificity for oxidatively modified sn-2 fatty acid residues in phospho

215 lf-quenching probes and exposed to native or oxidatively modified SP-A.

216 In an in vitro elastic fiber assembly model, oxidatively modified TE was unable to form elastic fiber

217 TPases and p21-activated kinase 1 (PAK1) and oxidatively modified the focal contact phosphatase PTP-P

218 ia coli proteins with significantly (30-90%) oxidatively modified thiol groups, which appear to be sp

219 ned to trap chromophore precursor states, is oxidatively modified to generate yellow chromophores tha

220 However, which mitochondrial proteins are oxidatively modified under alcohol-induced oxidative/nit

221 provide in vivo evidence that unbound Hb is oxidatively modified within extravascular compartments c

222 significant proportion of these peptides are oxidatively modified, most commonly through covalent lin

223 Significant accumulation of oxidatively modified, mutagenic DNA lesions (7,8-dihydro

224 munoglobulin M (IgM) natural antibodies bind oxidatively-modified low-density lipoprotein (LDL) and a

225 n this study, we have used this technique to oxidatively modify buried amino acid residues in higher

226 cells in which hydroxyl radicals are used to oxidatively modify proteins.

227 rate for the first time that S-nitrosothiols oxidatively modify PTEN, leading to reversible inhibitio

228 The method has recently been demonstrated to oxidatively modify solvent-accessible sites of proteins

229 synchrotron radiolysis of water was used to oxidatively modify surface residues on PsbP and PsbQ.

230 ); however, in the presence of the bulky and oxidatively more stable tert-butyl alcohol, intramolecul

231 These convert (t1/2 approximately 53 s) to oxidatively N-dealkylated products, producing para-subst

232 uction is increased in tumors that have been oxidatively prestressed by depleting the glutathione poo

233 cts use a P450 enzyme of the CYP4G family to oxidatively produce hydrocarbons from aldehydes.

234 yze the conjugation of toxic xenobiotics and oxidatively produced compounds to reduced glutathione, w

235 show that, similar to Mtb DsbE, Mtb DsbF can oxidatively refold reduced, unfolded hirudin and has a c

236 al mechanistic view of how a methyl group is oxidatively removed from different biological substrates

237 a flavin-dependent histone demethylase that oxidatively removes methyl groups from Lys-4 of histone

238 st, 1 (a Ru(IV)(4)O(4) cluster stabilized by oxidatively resistant [SiW(10)O(32)](8-) ligands); (ii)

239 The oxidatively resistant fluorine substituents allow for th

240 2]10-, comprising a Co4O4 core stabilized by oxidatively resistant polytungstate ligands, is a hydrol

241 ALKBH5 as another mammalian demethylase that oxidatively reverses m(6)A in mRNA in vitro and in vivo.

242 gave good yields of related diols that were oxidatively ring-opened to afford cyclopentane dialdehyd

243 be considered to come up with efficient and oxidatively robust molecular water oxidation catalysts (

244 A new powerful and oxidatively rugged pyrazolate-based water oxidation cata

245 hemoselective, mild, and rapid; however, the oxidatively sensitive nature of the electron-rich aromat

246 repair protein activity associated with such oxidatively sensitive, conformationally plastic/dynamic

247 An oxidatively "sensitive" model emulsion was selected as s

248 When oxidatively stable chelate ligands are bound to the irid

249 Organometallic iridium complexes bearing oxidatively stable chelate ligands are precursors for ef

250 ns are a novel class of readily prepared and oxidatively stable chlorin and bacteriochlorin analogues

251 chlorins are a class of readily prepared and oxidatively stable chlorins.

252 nsfer" (AGET) procedure utilizes a cheap and oxidatively stable copper source (CuSO(4).5H(2)O) and ca

253 It allows using oxidatively stable Cu(II) species that is reduced in sit

254 ve protein emulsifiers for the production of oxidatively stable fish oil-in-water emulsions.

255 alpha/beta hemoglobinopathies and design of oxidatively stable Hb-based oxygen therapeutics.

256 lytungstate ligands, is a hydrolytically and oxidatively stable homogeneous water oxidation catalyst

257 Moreover, three new oxidatively stable imidazolidinone catalysts have been d

258 tors and transition metal complexes in their oxidatively stable state (e.g., Cu(II)Br2/ligand) as cat

259 aric acid (STA) soybean oil is a trans-free, oxidatively stable, non-LDL-cholesterol-raising oil that

260 ace of the magnetic elements, rendering them oxidatively stable.

261 providing protective levels of ascorbate in oxidatively stressed algal cells.

262 sera to glaucomatous retinal proteins (or to oxidatively stressed cell culture proteins), thereby sug

263 ted translocation of lipid hydroperoxides in oxidatively stressed cells might enhance cytolethality i

264 as well as total cellular RNA, isolated from oxidatively stressed cells was also pulled down, depende

265 ose deficiency slows nascent chain growth in oxidatively stressed cells, is stimulated by replication

266 s significant physiological consequences for oxidatively stressed cells.

267 odern amino acids tyrosine and tryptophan in oxidatively stressed cells.

268 1 acetylation in repair of its substrates in oxidatively stressed cells.

269 and regulates CTCF-chromatin interactions in oxidatively stressed cells.

270 d for its enhanced mitochondrial activity in oxidatively stressed cells.

271 ndroprotective effects of hyaluronic acid on oxidatively stressed chondrocytes are due to preservatio

272 receptor (AR) in the aging rat liver and in oxidatively stressed hepatoma cells involves exchange of

273 in and in interleukin-1beta, Abeta42, and/or oxidatively stressed human neural (HN) cells in primary

274 rate that ubiquitin conjugates isolated from oxidatively stressed mammalian cells are enriched 3.3-15

275 isms by which this activation takes place in oxidatively stressed neurons are still not fully known.

276 s modulate the aggregation of the protein in oxidatively stressed neurons.

277 K338R/K341R mutant, ectopically expressed in oxidatively stressed OGG1-null mouse embryonic fibroblas

278 e phospholipid cell surface modifications on oxidatively stressed RPE cells.

279 novel mechanisms of complement activation in oxidatively stressed RPE, linking molecular events invol

280 rapeutic target in glycolytically dependent, oxidatively stressed tumors.

281 membranes and (ii) tumor cells that had been oxidatively stressed with the respiratory inhibitor anti

282 However when oxidatively stressed, control cells exhibited an increas

283 In this work, we report an oxidatively terminated Bu3Sn-mediated cyclization of an

284 In contrast to the intact drugs, the oxidatively transformed anthracyclines were substantiall

285 tion than the parent guanine base and can be oxidatively transformed to the genotoxic spiroiminodihyd

286 e lipid bodies (LB) containing electrophilic oxidatively truncated (ox-tr) lipids.

287 d oxygenation generates biologically active, oxidatively truncated lipids in the retina.

288 ugmented hydrophobic mismatch induced by the oxidatively truncated phosphatidylcholine.

289 n from exogenous Edelfosine or the mitotoxic oxidatively truncated phospholipid azelaoyl phosphatidyl

290 3)H]PAF, fluorescent NBD-PAF, or fluorescent oxidatively truncated phospholipid were primarily accumu

291 ed by coinjecting excess unlabeled PAF or an oxidatively truncated phospholipid, and [(3)H]PAF cleara

292 Oxidatively truncated phospholipids are present in ather

293 Circulating oxidatively truncated phospholipids are pro-inflammatory

294 idylcholines, inflammatory and pro-apoptotic oxidatively truncated phospholipids, and platelet-activa

295 atelet-activating factor (PAF) and apoptotic oxidatively truncated phospholipids--are proposed to hav

296 ein (apo)E(-/-) mice with excess circulating oxidatively truncated phospholipids.

297 Bid acting as a co-factor for pro-apoptotic, oxidatively truncated phospholipids.

298 tion motif was defined within oxPC(CD36), an oxidatively truncated sn-2 acyl group with a terminal ga

299 cies possessing a CD36 recognition motif, an oxidatively truncated sn-2 acyl group with a terminal ga

300 CH4 coupling proceeds non-oxidatively with the evolution of H2 on some catalysts,