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 LPMOs modify biomass by oxidatively cleaving polysaccharides, thereby enhancing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 Proper repair of oxidatively damaged DNA bases is essential to maintain g

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

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

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

53 nalyses of LIG1 complexes with undamaged and oxidatively damaged DNA unveil that LIG1 employs Mg(2+)-

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 ment in the spin-dependent transport through oxidatively damaged DNA.

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

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

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

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

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

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

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

64 xcises adenines misincorporated opposite the oxidatively damaged lesion, 8-oxo-7,8-dihydroguanine (OG

65 Oxidatively damaged lipid membranes are known to promote

66 ve to iron and pro-oxidants, and accumulated oxidatively damaged lipids because of the reactivity of

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

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

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

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

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

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

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

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

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

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

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

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

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

80 Importantly, oxidatively damaged SOD1 aggregates have been observed i

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

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

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

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

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

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 ve polysaccharide monooxygenases (AA13 PMOs) oxidatively degrade starch and can potentially be used w

95 ting H(2) O(2) as a byproduct, both of which oxidatively degrade thiourea under the reaction conditio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

119 The synthetic utility of tertiary amines to oxidatively generate alpha-amino radicals is well establ

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

121 Oxidatively generated damage to DNA induced by a pyrenyl

122 The resulting oxidatively generated damage to nucleic acids, membrane

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

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

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

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

127 There might be a pattern that oxidatively generated DNA/RNA damage is a weak cancer ri

128 ever, the association between pre-diagnostic oxidatively generated DNA/RNA damage levels and incident

129 readily realized by alpha-oxo gold carbenes oxidatively generated from TBS-terminated alkynes (TBS=t

130 ed on the C(sp(3) )-H insertion chemistry of oxidatively generated gold carbenes.

131 Oxidatively generated guanine radical cations in DNA can

132 This oxidatively-generated damage, likely in combination with

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

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

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

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

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

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

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

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

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

142 This Article demonstrates a mild oxidatively induced C(sp(3))-H activation at a high-vale

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

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

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

146 1 and 4 days after irradiation, we monitored oxidatively induced clustered DNA lesions (OCDL), DNA do

147 , little is known about background levels of oxidatively induced DNA damage in the nematode or how cu

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

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

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

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

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

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

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

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

156 Mechanistic studies suggest an oxidatively induced reductive elimination pathway on rho

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

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

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

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

161 methylene C-H bonds in the presence of more oxidatively labile aromatic functionalities remains a ma

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

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

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

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

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

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

168 d that TNFalpha exposure increased levels of oxidatively modified cysteine(s) of wt OGG1 without impa

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

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

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

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

173 8-Oxoguanine, one of the oxidatively modified DNA bases, is a typical biomarker o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

189 generally more circulating glycated LDL than oxidatively modified LDL.

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

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

192 Oxidatively modified low density lipoproteins, central t

193 Exposure to oxidatively modified low-density lipoprotein enhanced th

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

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

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

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

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

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

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

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

202 Oxidatively modified proteins by IV-FPOP are analyzed by

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

220 exposure, ribo- and deoxyribonucleotides are oxidatively modified.

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

222 Accumulation of oxidatively-modified proteins, due to either increased g

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

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

225 oteins (FPOP), utilizes hydroxyl radicals to oxidatively modify solvent accessible amino acids.

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

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

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

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

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

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

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

233 Flavin monooxygenase RslO9 then oxidatively rearranges the carbon backbone, presumably v

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

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

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

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

238 The oxidatively resistant fluorine substituents allow for th

239 2]10-, comprising a Co4O4 core stabilized by oxidatively resistant polytungstate ligands, is a hydrol

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

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

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

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

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

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

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

247 SEDS microcapsules (SEDS-M) were the most oxidatively stable (total oxidation (Totox): 26.5), foll

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

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

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

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

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

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

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

265 s significant physiological consequences for oxidatively stressed cells.

266 1 acetylation in repair of its substrates in oxidatively stressed cells.

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

268 e mark and OGG1 modulates gene expression 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 We found that oxidatively stressed mitochondria release short mtDNA fr

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

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

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

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

279 rapeutic target in glycolytically dependent, oxidatively stressed tumors.

280 ructures of K63 ubiquitinated ribosomes from oxidatively stressed yeast cells at 3.5-3.2 angstrom res

281 However when oxidatively stressed, control cells exhibited an increas

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

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

284 These transformations allow rapid access to oxidatively transposed cyclopentenones from simple PKR p

285 A facile method to oxidatively trimerize phenols using a catalytic aerobic

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 rolytes have high ionic conductivity but are oxidatively unstable above 4 V, which prevents the use o

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