ライフサイエンスコーパス: scavenger

1 (Cr) was investigated as a potential uranium scavenger.

2 ing Re ligand structure and adding a ClOx(-) scavenger.

3 ytoprotective effect was abolished by the NO scavenger.

4 ains before and after treatment with an H2O2 scavenger.

5 vo, both of which can be reversed using a MG scavenger.

6 ery low O2 atmosphere, with or without an O2 scavenger.

7 ll-established reactive oxygen species (ROS) scavenger.

8 y NOX inhibitors and reactive oxygen species scavengers.

9 chain components and reactive oxygen species scavengers.

10 es were found to be less potent free radical scavengers.

11 o:LUC2 expression by reactive oxygen species scavengers.

12 exposure compared with identical, untargeted scavengers.

13 greater than commercial, irreversible oxygen scavengers.

14 of mammalian carnivore carrion by vertebrate scavengers.

15 moved back into the terrestrial ecosystem by scavengers.

16 trongly diminished in the presence of the NO scavenger 2-4-carboxyphenyl-4,4,5,5-tetramethylimidazoli

17 superoxide scavenger tempol or the isoketal scavenger 2-hydroxybenzylamine (2-HOBA) normalized blood

18 were inhibited by the nitrogen free radical scavenger 2-phenyl-4,4,5,5,-tetramethylimidazoline-1-oxy

19 Administration of another potent NO scavenger (2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxy

20 by concurrent treatment with the superoxide scavenger 4-hydroxyl-2,2,6,6-tetramethylpiperidine-1-oxy

21 restored by treatment with the peroxynitrite scavenger 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyri

22 , DETA/NO (nitric oxide(NO) donor), PITO (NO scavenger), 8-Br-cGMP (cGMP analog).

23 ed NDMA formation in the presence of radical scavengers (ABTS and trolox) imply that O2 reacted with

24 vengers often act as producers and mammalian scavengers act as scroungers, but we predict that specie

25 Additionally, reactive oxygen species scavenger activity was observed for both compounds.

26 or VEGF receptor 2 and Akt/PKB as well as MG scavenger aminoguanidine and glo1 activation prevented M

27 onin, which is an effective hydroxyl radical scavenger and antioxidant.

28 A hydroxyl radical scavenger and inhibitors of inducible nitric oxide synth

29 d generated by using tBuOH as the OH radical scavenger and measuring its product, formaldehyde.

30 ponents, playing multiple crucial roles as a scavenger and signaling molecule.

31 sed on the basis of experiments with radical scavengers and DMSO-d6 and ESI-MS observations.

32 pic labeling studies, and the use of radical scavengers and electron transfer inhibitors.

33 , and quercetin (QUE) are known free radical scavengers and have shown cardioprotective effects.

34 gree of inhibition by solution-phase radical scavengers and higher rate of reactivity loss from surfa

35 netite + H2O2 one in the presence of radical scavengers and in a natural water matrix, but it induced

36 Experiments with OH scavengers and kinetic model results suggest that organi

37 By combining radical scavengers and kinetic modeling, we have derived quantum

38 c acid-binding polymers can act as molecular scavengers and limit the ability of artificial nucleic a

39 rs may have significant impacts on mammalian scavengers and potentially create trophic cascades.

40 ygen vacancies in the absence of any organic scavengers and precious-metal cocatalysts.

41 s may act as potent superoxide anion radical scavengers and reducing agents.

42 carboline and pinoline) were good OH radical scavengers and their activity was comparable to that of

43 nfluence of NaNO2 and H2O2, hydroxyl radical scavenger, and sunlight was assessed by an experimental-

44 (2) at 0.6 V vs RHE with H2O2 as an electron scavenger, and they show a charge separation efficiency

45 d concerning their active profile as radical scavengers, antimicrobials, estrogen-like activators and

46 However, translation of ROS scavengers (antioxidants) into the clinic has not been s

47 ith water and with/without TEMPO as hydrogen scavenger are studied.

48 pports the use of mitochondrion-targeted ROS scavengers as potential adjuvant therapies during severe

49 tion of endogenous coagonists with enzymatic scavengers as well as pharmacological inhibition of endo

50 The treatment of roots with the ROS scavenger ascorbate and the NADPH oxidase inhibitor diph

51 Infusion of tiron, a superoxide scavenger, attenuated the exaggerated pressor reflex and

52 However, some observations of scavengers avoiding feeding on carnivore carrion suggest

53 Administrating the H2S scavenger bismuth mitigates A. parvulum-induced colitis

54 ater susceptibility to treatment with an ROS scavenger but did not result in greater sensitivity to i

55 crucial intracellular reductant and radical scavenger, but it may also coordinate the soft Cu(I) cat

56 concentration, and the presence of an (*)OH scavenger can be important.

57 Scavenger capacity in both DPPH and CAA assays, assessed

58 e been employed to evaluate the free radical scavenger capacity of carotenoid molecules are tabulated

59 ic oxide, superoxide anion, hydroxyl radical scavenger capacity) and cellular antioxidants (sulfhydry

60 cell death was investigated by using several scavengers combined with a partition system.

61 re, targeting mitochondria with free radical scavengers conferred superior protection against aminogl

62 vates miRNA degradation independently of its scavenger decapping activity in the cytoplasmic compartm

63 Large avian scavengers depend on carcasses which are more likely ava

64 s, absence vs presence of a hydroxyl radical scavenger (dimethyl sulfoxide, DMSO), and different pH v

65 and genes for reactive oxygen species (ROS) scavengers, DNA replication and repair, and protein chap

66 ATP-induced nociceptive behaviors, while ROS scavengers dose-dependently attenuated the secondary res

67 treatment with lactulose and the two ammonia scavenger drugs sodium benzoate and phenylacetate.

68 alkane analogues relative to natural radical scavenger (e.g., carbonate) concentrations.

69 ger, mitochondria-targeted hydrogen peroxide scavenger ebselen, reduced Sirt3 S-glutathionylation, di

70 Although vertebrate scavenger efficiency and species composition is likely i

71 usceptibility to hydrolysis by the decapping scavenger enzyme (DcpS) and, when incorporated into RNA,

72 is a potent inhibitor of the mRNA decapping scavenger enzyme (DcpS), but the mechanism whereby DcpS

73 hydrophobic organic pollutant, aldrin.1 ROS scavenger experiments indicated that 1O2 played a signif

74 Instead, scavenger experiments indicated that aqueous electrons a

75 s proposal remains controversial because ROS scavengers fail to retard mitophagy.

76 , an effect that was reversed by the ONOO(-) scavenger, FeTPPS [5,10,15,20-tetrakis-(4-sulfonatopheny

77 Jarosite can be an important scavenger for arsenic (As) and antimony (Sb) in acid min

78 dritic cells (DCs), are the central cellular scavenger for circulating particle-associated antigens i

79 unaffected by pretreatment with the TrkB-Fc scavenger for extracellular BDNF or TrkB antagonism, but

80 sion of oxygen through tissues and acts as a scavenger for nitric oxide or other ROS.

81 eosinophilic asthma and impaired macrophage scavenger function and susceptibility to recurrent infec

82 fied a novel pathway involving P2X7 receptor scavenger function expressed on ocular immune cells as a

83 of GSKIP on beta-catenin is explained by its scavenger function; it recruits the kinases away from th

84 the presence of the less potent free radical scavengers gallic and caffeic acids.

85 Moreover, the ROS scavenger glutathione partially rescued the effects of C

86 Oxidation was inhibited by the STAR scavenger GSH and by the heme ligand CO.

87 ol-catalase (PEG-catalase; hydrogen peroxide scavenger) had no effect.

88 Free radical scavengers have failed to improve patient outcomes, prom

89 We further demonstrate that the heme scavenger hemopexin protects reticulo-endothelial macrop

90 r stress was inhibited by the singlet oxygen scavenger histidine and was accompanied by vacuolar coll

91 ath could be inhibited by the singlet oxygen scavenger histidine in treatments with AO but not with R

92 (apolipoprotein L1) and the hemoglobin (Hb) scavenger Hpr (haptoglobin-related protein).

93 icantly inhibited in the presence of radical scavengers (humic acid, carbonate), in complex aquatic m

94 c complex, [Ni(TMC)](+), is deployed as a CO scavenger in order to inhibit the deactivation of [Ni(cy

95 important function of sialic acids as a ROS scavenger in skeletal muscles, expanding our understandi

96 ess interactions between mammalian and avian scavengers in one of the most diverse scavenging guilds

97 adical generated and the presence of radical scavengers in solution.

98 rent density and the concentrations of HO(*) scavengers in the source water.

99 tructure-with both generalized predators and scavengers included in the most frequently found groups.

100 Evidence for the [Ni(TMC)](+) acting as a CO scavenger includes the observation of [Ni(TMC)(CO)](+) b

101 Reactions with various electron scavengers including H(+), NO2(-), NO3(-) and H2O2 show

102 Addition of the CO scavenger is shown to dramatically increase the catalyti

103 Their activity as hydroxyl radical (OH) scavengers is reported here by using three different met

104 , a well-known reactive oxygen species (ROS) scavenger, is co-treated with ETO, it inhibits an ETO-in

105 -beta-cyclodextrin (HPbetaCD), a cholesterol scavenger, is currently undergoing Phase 2b/3 clinical t

106 sted to serve as a proton buffer and radical scavenger, its physiological function remains mysterious

107 reased resistance afforded by the superoxide scavenger manganese, and inactivation of aconitase.

108 st that ongoing population declines in avian scavengers may have significant impacts on mammalian sca

109 Therapeutic supplementation of Hb scavengers may restore vascular NO signaling and attenua

110 pertension with a mitochondria-targeted H2O2 scavenger, mitochondria-targeted hydrogen peroxide scave

111 reconditioned during EVLP using the ROS/RNS scavenger Mn(III)-tetrakis (4-benzoic acid) porphyrin ch

112 The DCPS protein is the scavenger mRNA decapping enzyme which functions in the l

113 The H2O2 scavenger N,N(1)-dimethylthiourea reversed the MeJA-indu

114 pathway activated and the application of ROS scavenger N-acetyl cysteine (NAC) completely blocked the

115 Addition of the ROS scavenger N-acetyl cysteine prevented p62 accumulation i

116 erotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of inte

117 Pretreatment with the ROS scavenger N-acetyl-L-cysteine, the ERK1/2 inhibitor UO12

118 ontrast, although treatment with the radical scavenger N-tert-butyl-a-phenylnitrone (PBN) also reduce

119 al horn neurons, an effect eliminated by ROS scavenger N-tert-butyl-alpha-phenylnitrone (PBN) and P2X

120 lso, using the reactive oxygen species (ROS) scavengers N-acetyl cysteine and Mito-TEMPO, we determin

121 The ROS scavenger, N-acetyl-cysteine, blocks both the mixture-in

122 Coexpression of Gbetagamma-specific scavengers-namely, the carboxyl terminus of the G protei

123 ognized as an effective reductant and oxygen scavenger, nanoparticulate FeS was evaluated for its rol

124 Herein, we demonstrate that nucleic acid scavengers (NASs) can limit pathological inflammation an

125 own therian to invade a durophagous predator-scavenger niche.

126 sodium iodide, with the sodium serving as a scavenger of bromide and iodide serving as a nucleophile

127 s suggesting that the protein functions as a scavenger of cytotoxic aldehydes produced by metabolism

128 available through the diet, is an effective scavenger of each of the aforementioned reactive species

129 the alkyl hydroperoxide reductase, a primary scavenger of endogenous hydrogen peroxide was also ident

130 n monocytes incubated with apyrase, a potent scavenger of extracellular ATP.

131 Pretreatment of cells with catalase, a scavenger of H2O2, or DUOX1 down-regulation by siRNA abr

132 e glutathione peroxidase 4 (Gpx4) is a major scavenger of phospholipid hydroperoxides.

133 A simple and highly efficient catalytic scavenger of poisonous organophosphorus compounds, based

134 f human serum albumin, which is the dominant scavenger of reactive electrophiles in serum.

135 Albumin is a potent scavenger of reactive oxygen species (ROS).

136 y vultures (Cathartes aura) were the primary scavengers of arboreal carrion, suggesting such resource

137 beta-Carbolines were scavengers of OH in the three assays and in the presence

138 nd hence the lifestyle of these organisms as scavengers of proteinaceous compounds from surrounding m

139 gamma-Tocopherol is effective scavengers of reactive nitrogen species and prevents DNA

140 Scavengers of reactive oxygen species and peroxynitrite

141 ochondrial transition permeability pore, and scavengers of reactive oxygen species did not attenuate

142 ydrophilic carbon clusters (PEG-HCCs), known scavengers of the ROS superoxide (O2(*-)) and hydroxyl r

143 Within scavenging communities, avian scavengers often act as producers and mammalian scavenge

144 queous O2, and studied the impact of radical scavengers on NDMA formation.

145 Consistent with this, addition of a ROS scavenger or anaerobic culture conditions also worked to

146 A reactive oxygen species scavenger or, even more effectively, clinically approved

147 s with catalase (an extracellular superoxide scavenger) or NSC 23766 (a Rac GTPase inhibitor) complet

148 ession of stromal ascorbate peroxidase (H2O2 scavenger) or treatment with DCMU (photosynthesis inhibi

149 other species are free-living microbivores, scavengers, or predators of insects or other nematodes.

150 resent an important resource to invertebrate scavengers, particularly in landscapes with efficient ve

151 whereas the in vivo use of the peroxynitrite scavenger phenylboronic acid, a novel synthetic molecule

152 ulfonatophenyl)porphyrin] or a peroxynitrite scavenger (phenylboronic acid) had markedly less Tlr4 re

153 s additive acts as an oxidant or as a halide scavenger promoting Pd-catalyst turnover.

154 mpartmentalization of Hb by erythrocytes and scavenger protein complexes is an archetypical mechanism

155 tissue distribution of cell-free Hb and its scavenger protein complexes.

156 tion of an archetypical function by which Hb scavenger proteins could preserve NO signaling during he

157 Mammals synthesize the scavenger proteins haptoglobin and hemopexin, which bind

158 , gefitinib treatment in the presence of ROS scavenger provided a partial rescue of mitochondrial abe

159 mechanisms were also explored through use of scavenger reagents.

160 ophagy, augmented phagocytosis, and enhanced scavenger receptor (macrophage receptor with collagenous

161 For transgenic mice generation, the human scavenger receptor (SR-A) promoter/enhancer was used to

162 le EGF-like domains 10 (Megf10) is a class F scavenger receptor (SR-F3) expressed on astrocytes and m

163 express, together with Vgamma4 and CCR6, the scavenger receptor 2 and are mainly restricted to innate

164 gnificantly increased the expression of SRA (scavenger receptor A), modified low-density lipoprotein

165 anti-Marco-neutralizing Abs and the class A scavenger receptor antagonist polyinosinic acid inhibite

166 oprotein lipase and hepatic uptake of HDL by scavenger receptor B-I are the driving forces of HDL-cho

167 s due to a splice donor site mutation in the scavenger receptor B1 (SCARB1; also known as SR-B1) gene

168 81, while HEPC98 primarily blocks binding to scavenger receptor B1 and heparan sulfate.

169 Scavenger receptor BI (SR-BI) is the major receptor for

170 ells and live or dead Listeria monocytogenes scavenger receptor BI (SR-BI), an anti-atherogenic lipid

171 nct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR-BI), respectively, to infect h

172 CV entry by lipid transfer receptors such as scavenger receptor BI (SR-BI).

173 igation and puncture; using adrenal-specific scavenger receptor BI mice as an inducible corticosteroi

174 Using scavenger receptor BI mice as the first relative adrenal

175 vival in cecal ligation and puncture-treated scavenger receptor BI mice but causes more septic death

176 Scavenger receptor BI null and adrenal-specific scavenge

177 venger receptor BI null and adrenal-specific scavenger receptor BI null mice.

178 ion of unesterified fatty acid (FA) with the scavenger receptor CD36 has been actively researched, wi

179 The scavenger receptor CD36 is a critical factor initiating

180 We show that preformed scavenger receptor CD36 is redistributed to the cell mem

181 pidemic conditions is enhanced when platelet scavenger receptor CD36 recognizes oxidized lipids in ox

182 Antibody to the scavenger receptor CD36 reduced the internalization of S

183 Recently, we have identified scavenger receptor class A member I (SR-AI) as a recepto

184 LDL receptor (LDLR), the very LDLR, and the scavenger receptor class B member 1 in hepatocytes; knoc

185 as SDC1, as well as LDLR, very LDLR, and the scavenger receptor class B member 1, which promote HCV e

186 SR-B1 (scavenger receptor class B type 1), encoded by the gene

187 l nine variants showed reduced dependence on scavenger receptor class B type I (SR-BI) for infection.

188 Lentiviral short hairpin RNA knockdown of scavenger receptor class B type I (SR-BI) in vitro and S

189 was critically dependent on the presence of scavenger receptor class B type I and ATP Binding Casset

190 05.12 +/- 1.13 nm) conjugated to recombinant scavenger receptor class B, member 2 (SCARB2) protein wi

191 )-cholesteryl ester (CE) uptake, mediated by scavenger receptor class B, type 1 (SR-B1).

192 In enterocytes, scavenger receptor class B, type 1 (SR-B1, encoded by SC

193 escribe for the first time the expression of scavenger receptor class F, member 1 (SCARF-1) on hepati

194 The scavenger receptor cluster of differentiation (CD)36 pro

195 Furthermore, the substitution of CD163 scavenger receptor cysteine-rich (SRCR) domain 5 with a

196 Surprisingly, Loxl3 N-terminal scavenger receptor cysteine-rich (SRCR) repeats, rather

197 ssed on gammadelta T cells and belong to the scavenger receptor cysteine-rich (SRCR) superfamily.

198 nerating a 65-kDa form lacking the first two scavenger receptor cysteine-rich domains.

199 array containing 13 members, are part of the scavenger receptor cysteine-rich family.

200 clearance mechanism that requires the glial scavenger receptor Draper and downstream phagocytic engu

201 CD163 is a scavenger receptor expressed on innate immune cell popul

202 mokine receptor CXCR7 (ACKR3) functions as a scavenger receptor for chemokine CXCL12, a molecule that

203 valuable model for investigating the role of scavenger receptor function and the immune system in the

204 rium Lactococcus lactis confers adherence to scavenger receptor gp340, human vaginal epithelium, and

205 CD36 is a scavenger receptor involved in fatty acid metabolism, in

206 The class A scavenger receptor known as MARCO (macrophage receptor w

207 ar matrix and its endocytic clearance by the scavenger receptor low density lipoprotein receptor-rela

208 The scavenger receptor LOX-1 found in endothelial cells bind

209 The scavenger receptor macrophage receptor with collagenous

210 One of the receptors expressed by MZM is scavenger receptor macrophage receptor with collagenous

211 agocytosis have been reported, including the scavenger receptor MARCO and integrin alpha3beta1.

212 proaches revealed selective induction of the scavenger receptor MARCO, which was required for enhance

213 l MPhi (SPM) that expressed CD138(+) and the scavenger receptor Marco.

214 r advanced glycation endproducts (RAGE) is a scavenger receptor of the Ig family that binds damage-as

215 athway in fibrogenesis in which a macrophage scavenger receptor protects against organ fibrosis by re

216 hanism that may be shared by SR-BI and CD36, scavenger receptor proteins highly homologous to LIMP-2.

217 We examined whether CD36, a scavenger receptor that recognizes pathogen and modified

218 tein receptor-related protein 1 (LRP-1) is a scavenger receptor that regulates adaptive immunity and

219 transfected cells, we further identified the scavenger receptor type A member I (SR-AI) to be a macro

220 te a cellular pathway whereby membrane-bound scavenger receptor type B-1 (SR-B1) in parent cells beco

221 Scavenger receptor type B-1 (SR-B1), found in lipid raft

222 markers (CD206 (mannose receptor) and CD163 (scavenger receptor)), secretion of IL-10, and TGFbeta an

223 The scavenger receptor, class B type 1 (SR-B1), is a multili

224 es are captured from the blood stream by the scavenger receptor, class B, type I (SR-BI), the so-call

225 CD163, a monocyte- and macrophage-specific scavenger receptor, is shed as soluble CD163 (sCD163) du

226 blocking its interaction with the endocytic scavenger receptor, low-density lipoprotein receptor-rel

227 The scavenger receptor, macrophage receptor with collagenous

228 iver fibrosis to show that deficiency of the scavenger receptor, stabilin-1, exacerbates fibrosis and

229 Studies with scavenger receptor-A1 null mice reveal reduced IL-13 gen

230 te that expression of C-type lectin receptor scavenger receptor-AI (SR-AI) is crucial for promoting M

231 PIP2 on HDL is taken up by target cells in a scavenger receptor-BI-dependent manner.

232 here it can be taken up via the HDL receptor scavenger receptor-BI.

233 This was supported by scavenger receptor-induced local increases in membrane c

234 vated receptor gamma-dependent regulation of scavenger receptor-mediated cholesterol uptake and ABCA1

235 s and is predicted to result in between 7-20 scavenger-receptor cysteine-rich (SRCR) domains within e

236 Although the class A scavenger receptors (SR-As) mediate dsRNA entry, it is u

237 in A-I mimetics are known to bind to class B scavenger receptors (SR-Bs), SR-BI, SR-BII, and CD36, re

238 rium tuberculosis (Mtb) through two types of scavenger receptors (SRs; MARCO and SR-B1), as blockade

239 r peripheral blood cells takes place through scavenger receptors and over time causes disruption in c

240 rsomes, which are internalized by binding to scavenger receptors and subsequently escape the early en

241 The class B scavenger receptors BI (SR-BI) and BII (SR-BII) are high

242 n vitro was dependent on the presence of the scavenger receptors CD36 and MSR1.

243 phages exhibited increased expression of the scavenger receptors CD36 and SCARA1 (encoded by MSR1), w

244 y lipoprotein receptor-1 (LOX-1), one of the scavenger receptors for oxidized low-density lipoprotein

245 ith emerging evidence for the involvement of scavenger receptors in innate immunity, this study addre

246 onic inflammatory liver disease, the role of scavenger receptors in regulating liver inflammation rem

247 ompetitively block oxidized lipid uptake via scavenger receptors on macrophages; second, for sustaine

248 ion receptors could be viewed as a subset of scavenger receptors that are capable of eliciting anti-i

249 Human mesenchymal stem cells (MSCs) express scavenger receptors that internalize lipids, including o

250 cells and macrophages, unlike other typical scavenger receptors that recognize phosphatidylserine on

251 s innate immune responses via complement and scavenger receptors to drive recruitment of and efferocy

252 les from several classes of genes coding for scavenger receptors, beta-carotene oxygenases, and ketol

253 id destruction in the liver via Kupffer cell scavenger receptors, keeping them available for adaptive

254 te preserved absolute expression of the main scavenger receptors, MEGALIN and CUBILIN.

255 nsport (ABCA1, ABCG1 and 27-hydroxylase) and scavenger receptors, responsible for uptake of modified

256 s report, we show that the Stabilin class of scavenger receptors, which were not previously thought t

257 equence, they express a unique repertoire of scavenger receptors.

258 ds, with some receptors being categorized as scavenger receptors.

259 issue macrophages expressing CD163 and CD204 scavenger receptors.

260 l Mito-tempol (a mitochondria-targeted O2(.-)scavenger) reduced mechanical allodynia and decreased pC

261 We used cameras to record scavengers removing carcasses and elapsed time to remova

262 They use this ability to act as cellular scavengers, scanning the vascular surface for potential

263 In addition, we provide advice on scavenger selection, as well as a troubleshooting sectio

264 letion of meiosis I could be restored by ROS scavengers, showing this is the primary trigger for arre

265 To demonstrate its applicability, metal scavengers siderophores were imaged directly from agar c

266 alian scavengers to utilize particular avian scavenger species using preferred food sources similar t

267 This occurred even though the number of scavenger species visiting carcasses and the time needed

268 we further present optimal hydrofluoric-acid scavengers such as Li2SrSiO4, Li2CaSiO4 and CaIn2O4 for

269 O3, LiAl5O8 and ZrP2O7 and hydrofluoric-acid scavengers such as Sc2O3, Li2CaGeO4, LiBO2, Li3NbO4, Mg3

270 rticular importance for a burrowing, benthic scavenger, such as hagfish, which are likely to be expos

271 Studies using hole scavengers suggest that sulfite radicals generated by th

272 decreased in the absence of hydroxyl radical scavengers, suggesting that future research should chara

273 either the cytoplasmic or mitochondrial ROS scavenger superoxide dismutase (SOD) caused a significan

274 verexpression of the reactive oxygen species scavenger superoxide dismutase 1 (SOD1).

275 on of glutathione and ascorbate free radical scavenger systems.

276 Treatment with the superoxide scavenger tempol or the isoketal scavenger 2-hydroxybenz

277 o-treatment with the reactive oxygen species scavenger Tempol prevented FRD-induced apoptosis in WT m

278 he MCA, after incubation with the superoxide scavenger TEMPOL, maximal EDD improved by approximately

279 o-treatment with the reactive oxygen species scavenger Tempol.

280 inhibitor, apocynin, and the nonspecific ROS scavenger, tempol, are shown to reduce oxidative stress

281 364 mug/mL) was a stronger hydrogen peroxide scavenger than gallic acid (EC50 838 mug/mL) and was equ

282 constitute an efficient group of more potent scavengers than quercetin itself, able to deactivate var

283 cioglu introduce vultures, the supreme avian scavengers that now face multiple threats.

284 The most potent free radical scavengers that we tested for in the wine samples were f

285 s of the world's largest terrestrial soaring scavenger, the Andean condor (Vultur gryphus).

286 richia coli lactate dehydrogenase as an NADH scavenger, thereby preventing reversible formaldehyde re

287 In addition to their action as radical scavengers, they act as activators for the intrinsic cel

288 s of ROS on the EPR, we infused a superoxide scavenger, tiron, into the superficial epigastric artery

289 iated as a result of the inefficiency of ROS scavengers to control ROS bursts after high-dose treatme

290 es visiting carcasses and the time needed by scavengers to detect carcasses were similar between both

291 ies-specific cueing will allow for mammalian scavengers to utilize particular avian scavenger species

292 uperoxide dismutase (SOD1), an efficient ROS scavenger, to the site of injury can mitigate SCI-induce

293 als is imagined to react with a paramagnetic scavenger via spin-selective electron transfer.

294 Imidazole, a well-known (1)O2 scavenger, was incorporated in the hydrophobic core of a

295 echanisms and that it is a potent superoxide scavenger, we tested whether cobalamin, a vitamin B12 vi

296 studies with and without oxygen and radical scavengers, we propose that boron-imidates form under th

297 cating that emixustat also acts as a retinal scavenger, which may contribute to its therapeutic effec

298 This finding was supported by the use of ROS scavengers, which reduced CAP-based uptake efficiency.

299 asite transmission leads to the evolution of scavengers with generally low cannibalistic tendencies,

300 lamin) was recently shown to be a superoxide scavenger, with a rate constant similar to superoxide di