ライフサイエンスコーパス: scavenger

1 d the highest activity as H(2)O(2) and HO(*) scavenger.

2 uction and suppressed by a mitochondrial ROS scavenger.

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

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

5 f)(3) as a Lewis acid and TEMPO as an oxygen scavenger.

6 the presence of Nox2 inhibitor or superoxide scavenger.

7 methyl-1-piperidinyloxy (TEMPO) as a radical scavenger.

8 tly prevented by AAD-2004, a potent H(2)O(2) scavenger.

9 nd natural organic matter as sulfate radical scavengers.

10 ase in carrion in the face of declining apex scavengers.

11 of mammalian carnivore carrion by vertebrate scavengers.

12 moved back into the terrestrial ecosystem by scavengers.

13 he extensive acquisition of carrion by avian scavengers.

14 aqueous phase reactions with RhB and aqueous scavengers.

15 rimentiphilum act as efficient heterotrophic scavengers.

16 negatively with ascorbate, TPC, and with ROS scavengers.

17 t proteins (LEA) and reactive oxygen species scavengers.

18 release of these species by the loss of apex scavengers.

19 ly removed by reaction with the formaldehyde scavenger 1,3-cyclohexanedione, whereas the cyclic amina

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

21 rial smooth muscle cells treated with the NO scavenger 2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl

22 We investigate the impact of the dicarbonyl scavenger, 2-hydroxybenzylamine (2-HOBA) on HDL function

23 of cytotoxic additives (e.g., thiols, oxygen scavengers), a feature superior to traditional PALM prob

24 cysteine (NAC), a strong antioxidant and ROS scavenger, abrogated DRP1-dependent mitochondrial fragme

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

26 n is a valuable resource used by facultative scavengers across the globe.

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

28 In Drosophila, glia and hemocytes provide a scavenger activity within and outside the nervous system

29 aches-normobaric hyperoxia, the free radical scavenger alpha-phenyl-butyl-tert-nitrone (alphaPBN), an

30 Through the assessment of a free radical scavenger and an anti-inflammatory endocannabinoid, we h

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

32 emained stable in the presence of ubiquitous scavengers and did not interfere with the receptor bindi

33 volved, genetically encoded organophosphorus scavengers and for broader functionalities of members of

34 resented herein circumvents the use of water scavengers and perfluorooctane sulfonate (PFOS) ligands.

35 ot/shoot ration, enzymatic activities of ROS scavengers and upregulation of stress-responsive genes.

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

37 l supramolecular catalysts, organophosphorus scavengers, and nanostructured materials.

38 t conventional reactive species sensitizers, scavengers, and quenchers need to be carefully applied t

39 351 kg of carrion per individual per year to scavengers, and this subsidy decreased at higher latitud

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

41 th cobalt and in the presence of an electron scavenger are reported.

42 enger species, including nearly all obligate scavengers, are in a state of rapid decline and there is

43 Scavenger assemblages in highly human-impacted areas sus

44 ataset comprising 43 sites, where vertebrate scavenger assemblages were identified using 2,485 carcas

45 iables related to climatic conditions on the scavenger assemblages.

46 n serve as an important source of energy for scavengers at colonial breeding aggregations, particular

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

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

49 se compounds identified a group of promising scavengers, based on the sulfonyl azide template.

50 BE cells with simvastatin or the cholesterol scavenger beta-methylcyclodextrin also blocked ATP relea

51 ucing cholesterol content with a cholesterol scavenger (beta-methylcyclodextrin) or statin compound (

52 t result of ultrafast hole extraction by the scavenger, but is rather caused by long-lived electron a

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

54 Developed here is a cationic molecular scavenger, by screening cationic dendronized polymers, w

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

56 ounds and ascorbic acid that exhibit radical scavenger capacity and reducing power.

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 ness and diversity in terrestrial vertebrate scavenger (carrion-consuming) assemblages, which provide

60 rthermore, we demonstrated that the H(2)O(2) scavenger catalase mimics the effect of Duox1 deficiency

61 ylcysteine, or engineered to express the ROS scavenger catalase specifically within the mitochondria.

62 g other macroecological processes in shaping scavenger communities.

63 e is known about the implications of altered scavenger community composition on the fate and efficien

64 ecological relevance of this process to the scavenger community is poorly understood.

65 This decapping step is catalyzed by the Scavenger Decapping Enzyme (DcpS), in case the mRNA has

66 rt oligonucleotides, we found that the yeast scavenger decapping enzyme decaps RNA transcripts as lon

67 al and human well-being implications of apex scavenger decline, including carrion removal and disease

68 mice with 5E1 and N-acetylcysteine, as a ROS scavenger, decreased tumor DNA damage, inhibited tumor g

69 is degradation pathway: the addition of a NO scavenger decreases the rate of cytochrome b (6) f and R

70 We conclude that Ngb-H64Q-CCC or other CO scavengers demonstrate potential as antidotes that rever

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

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

73 ment focus on dietary manipulations, ammonia scavenger drugs, and orthotopic liver transplantation.

74 While administration of a superoxide anion scavenger during IH did not prevent neural progenitor ce

75 We provide two models of scavenger dynamics to demonstrate that the mesoscavenger

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

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

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

79 Instead, scavenger experiments indicated that aqueous electrons a

80 nts, deuterium labeling studies, and radical scavenger experiments.

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

82 high-molecular weight biologically relevant scavengers failing to strip the metal from the peptide.

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

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

85 In addition, the reactive oxygen species scavenger glutathione (GSH) was upregulated in chRCC due

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

87 We hypothesized that the MGO scavenger glyoxalase 1 (GLO1) reverses bone marrow-deriv

88 tant to understand how the reduction of this scavenger guild influences the fate of carrion resources

89 ecause ectopic expression of catalase, a ROS scavenger, halted the in vitro-induced differentiation.

90 ue to conflicts with humans, many vertebrate scavengers have experienced population declines due to d

91 anced after removal of the nitric oxide (NO) scavenger hemoglobin.

92 steine rich protein is involved as a radical scavenger in several pathological conditions associated

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

94 surements, we also exploit species-selective scavengers in electron paramagnetic resonance spectrosco

95 ystem functions and the services provided by scavengers in human-dominated landscapes in the Anthropo

96 The efficiency of these scavengers in in vitro and in vivo experiments was demon

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

98 Consumption probabilities of both scavengers in relation to habitat covariates suggested c

99 an the reaction with the target compound and scavengers in the aqueous phase, underscoring the signif

100 lable fallen nestlings that were consumed by scavengers in the Everglades of Florida, USA.

101 affected by the presence of hydroxyl radical scavengers, indicating the likely involvement of nitroge

102 Common ROS scavengers inhibited the oxidation of bisphenol A (BPA),

103 We previously showed that the amyloid scavenger, insulin-degrading enzyme (IDE), generates T40

104 We expect the development of H(2) S scavengers is an alternative approach to address this pr

105 ondrially enriched electron and free radical scavengers JP4-039 and XJB-5-131 improved RC function an

106 tyl-l-cysteine (NAC), an oxygen free radical scavenger, led to a reduction in the FoxO1 inhibition-in

107 ons for the proposed use of mackinawite as a scavenger material for uranium in groundwater systems ar

108 deplete N-terminal and internal peptides by scavenger materials.

109 o elevated temperature and abundant obligate scavengers, may reduce the severity of the infectious ou

110 (picoseconds) in the presence of an electron scavenger, minimizing recombination.

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

112 or the mitochondrial reactive oxygen species scavenger MitoTEMPO.

113 Macrophages act as scavengers, modulating the immune response against patho

114 tion conditions on the activity of the yeast scavenger mRNA decapping enzyme DcpS and examined decapp

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

116 d by the NOX inhibitor VAS2870 or by the ROS scavenger N-acetyl cysteine (NAC).

117 be rescued by treatment of cells with a ROS scavenger N-acetyl cysteine or protease inhibitors.

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

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

120 cynin, and the reactive oxygen species (ROS) scavenger N-acetylcysteine, suggesting that ROS contribu

121 e effects were mitigated by the free radical scavenger N-acetylcysteine, which also reverted phagocyt

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

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

124 antly, treatment with an oxygen free radical scavenger, N-acetyl-l-cysteine (NAC), attenuated the Fox

125 The oxygen radical scavenger, N-acetylcysteine (NAC), attenuates the chemot

126 lls were pre-treated with the oxygen radical scavenger, N-acetylcysteine, the NKA inhibitory activity

127 -donating capacity of the hole (or electron) scavengers needs to be high enough to allow for the extr

128 ions of mesoscavengers, those less-efficient scavengers occupying mid-trophic levels, is improving; y

129 The effect on cancer development of a potent scavenger of dicarbonyl electrophiles, 5-ethyl-2-hydroxy

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

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

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

133 Supplementation of N-acetylcysteine (NAC), a scavenger of reactive oxygen species (ROS), diminished t

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

135 Furthermore, EBS is an excellent scavenger of reactive oxygen species.

136 ed form of glutathione (GSH), but also is an scavenger of soft electrophiles such as ACR.

137 the F. alocis SOR protein is a key enzymatic scavenger of superoxide radicals and protects the bacter

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

139 Since chemical sensors and scavengers of H(2) S share the same criteria, we constru

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

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

142 Exposure to scavengers of reactive oxygen species, such as glutathio

143 Scavengers of superoxide radical anion (superoxide dismu

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

145 owledge investigating the role of vertebrate scavengers on ecosystem services provided through carrio

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

147 TD of ovBNST neurons was prevented by a BDNF scavenger or in the presence of TrkB inhibitors, indicat

148 that favor O(3) (i.e., addition of an (*)OH scavenger) or (*)OH (i.e., pH 11) were investigated.

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

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

151 Lowering of ammonia with the ammonia scavenger ornithine phenylacetate prevented hepatocyte c

152 clusion that it is a powerful oxygen radical scavenger, partially contributed by its molecular catech

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

154 Compared with other dicarbonyl scavengers, pentylpyridoxamine (PPM) most efficaciously

155 To explore whether obligate scavengers persisted by depending on contemporary commun

156 bility prior to hypoxia by increasing the NO-scavenger PHYTOGLOBIN1.

157 ate from the neuroepithelium and provide the scavenger population of the nervous system.

158 The immune scavenger protein DC-SIGN interacts with glycosylated pr

159 mechanisms were also explored through use of scavenger reagents.

160 nd higher plasma levels of the soluble CD163 scavenger receptor (0.84 vs .59 ug/mL, P = .003) than co

161 ugh K63 polyubiquitylation of the macrophage scavenger receptor 1 (MSR1).

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

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

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

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

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

167 We identify scavenger receptor B1 (SR-B1) as an EsxA receptor on air

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

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

170 ation between neutralization sensitivity and scavenger receptor BI dependency during viral entry.

171 This regulation appears tightly linked with scavenger receptor BI dependency, suggesting a role of t

172 ry monocyte subtype and partially via SR-BI (scavenger receptor BI).

173 reactive protein, soluble CD163, and soluble scavenger receptor CD14 were significantly higher during

174 Scavenger receptor CD163 is exclusively expressed on mon

175 as a high binding affinity to the macrophage scavenger receptor CD36 and participates in CD36-mediate

176 and elevated transcript levels for the lipid scavenger receptor CD36 and the nuclear receptor PPARgam

177 Scavenger receptor CD36 contributes significantly to lip

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

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

180 TAMs expressed elevated levels of the scavenger receptor CD36, accumulated lipids, and used fa

181 Fyn kinase, in conjunction with the class B scavenger receptor CD36, regulates the microglial uptake

182 iated ROS production is due to activation of scavenger receptor CD36.

183 n of surface scavenger receptors (i.e. CD36, scavenger receptor class A member 1, triggering receptor

184 marker Ki-67 and the reactive oxygen species scavenger receptor class A member 3.

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

186 O system transferase, coagulation factor XI, scavenger receptor class A5 (SCARA5), and tumor necrosis

187 t genes for its biliary excretion, including scavenger receptor class B member 1 (Scarb1) and ABC sub

188 arsenic exposure, the hepatic expression of scavenger receptor class B member 1 (Scarb1), which is i

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

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

191 Scavenger receptor class B member 2 (SCARB2) is the majo

192 By binding with scavenger receptor class B type 1 (SCARB1), reconstitute

193 herapeutic effect of eHNP-A1-CD15-LDE225 via scavenger receptor class B type 1 (SR-B1) and CD15 on br

194 Here we show in mice that scavenger receptor class B type 1 (SR-B1) in endothelial

195 major HDL-dependent m-RCT pathway via SR-BI (scavenger receptor class B type 1) to the liver, a CETP-

196 ot J6/JFH1(DeltaHVR1/D431G) while decreasing scavenger receptor class B type I coreceptor dependency.

197 s increased envelope breathing and decreased scavenger receptor class B type I HCV coreceptor depende

198 05.12 +/- 1.13 nm) conjugated to recombinant scavenger receptor class B, member 2 (SCARB2) protein wi

199 n (HDL) metabolism is facilitated in part by scavenger receptor class B, type 1 (SR-B1) that mediates

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

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

202 nserved endocytic machinery, composed of the scavenger receptor complex Cubilin/Amnionless and Dab2,

203 Four proteins (Scavenger receptor cysteine rich type 1 protein M130, Fa

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

205 al region, which is composed of 4 repeats of scavenger receptor cysteine-rich (SRCR) domains in LOX-l

206 ple bacterial species involves its conserved Scavenger Receptor Cysteine-Rich (SRCR) domains, localiz

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

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

209 nsmission across synapses requires the glial scavenger receptor Draper and involves a transient visit

210 /CXCR7 range from those of a strictly silent scavenger receptor eventually modulating CXCR4 signaling

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

212 PAN-induced glomerular injury, reducing CD36 scavenger receptor expression and oxidative stress.

213 ry phenotype express high levels of CD163, a scavenger receptor for the hemoglobin-haptoglobin comple

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

215 Increased activity of the multi-ligand scavenger receptor Lectin-like Oxidized LDL Receptor-1 (

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

217 efines tumor-derived IL37 and the macrophage scavenger receptor MARCO as potential therapeutic target

218 eatment by injecting antibodies specific for scavenger receptor MARCO, which is expressed on a specif

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

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

221 complement factor C3, and instead relied on scavenger receptor SR-A6 (MARCO).

222 erved yet poorly characterized member of the scavenger receptor superfamily-as a receptor for VEEV.

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

224 s to the receptor for cholesterol-rich HDLs, scavenger receptor type B1 (SCARB1).

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

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

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

228 eceptor that binds CXCL12 and functions as a scavenger receptor, regulating levels of CXCL12 availabl

229 increased the surface expression of the CD36 scavenger receptor, resulting in an increase in phagocyt

230 We show that serum levels of soluble scavenger receptor-A (sSR-A) are increased in patients w

231 es with canonical GPCRs in its function as a scavenger receptor.

232 R-146a mimic oligonucleotide conjugated to a scavenger receptor/Toll-like receptor 9 agonist (C-miR14

233 sociated with enhanced expression of surface scavenger receptors (i.e. CD36, scavenger receptor class

234 Scavenger receptors (SRs) are a large family of cell-sur

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

236 ipocyte glucose uptake and expression of AGE scavenger receptors and Rho signaling mediators, includi

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

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

239 Scavenger receptors clear pathogens, transport lipid, an

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

241 eting is often compromised by recognition by scavenger receptors involved in clearance.

242 ion via direct effects on ECM and by binding scavenger receptors on multiple cell types and signaling

243 Notably, inhibition of hDia1, but not scavenger receptors RAGE or CD36, attenuated AGE-ECM inh

244 stered oligonucleotides can naturally engage scavenger receptors that facilitate cellular transfectio

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

246 h ApoA-I raising agents or blocking relevant scavenger receptors with neutralizing antibodies could,

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

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

249 of genes involved in cholesterol metabolism, scavenger receptors, MERTK, and complement.

250 multiple receptors, including CR3, CRIg, and scavenger receptors, which work synergistically along wi

251 issue macrophages expressing CD163 and CD204 scavenger receptors.

252 n damage via overactivation of innate immune scavenger receptors.

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

254 Our understanding of how apex scavengers regulate populations of mesoscavengers, those

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

256 yet we know little about how extant obligate scavengers responded to this abrupt ecological change.

257 First, we evaluated how scavenger richness (number of species) and diversity (Sh

258 Both scavenger richness and diversity also showed some season

259 ables did not drive latitudinal patterns, as scavenger richness and diversity were not affected by te

260 Vertebrate scavenger richness ranged from species-poor to species r

261 luded in our study was the main predictor of scavenger richness.

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

263 a rapid-response hydrogen reservoir, oxygen scavenger, sensor for power demand, and regulator for hy

264 They serve as peroxide scavengers, sensors, signal transducers, and chaperones,

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

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

267 Many apex scavenger species, including nearly all obligate scaveng

268 acted areas sustained the smallest number of scavenger species, suggesting human activity may be over

269 Remarkably, the addition of hole scavengers such as 4-methylbenzyl alcohol can lead to ~4

270 eriments conducted with an oxidative radical scavenger suggested that plasma-generated radicals do no

271 rmore, myocardial expression of free radical scavenger superoxide dismutase 1 and aldehyde dehydrogen

272 elegans Supporting this model, free radical scavengers suppressed the Rhizobium-induced C. elegans D

273 Melatonin, an endogenous free radical scavenger synthesized by neuronal mitochondria, decrease

274 on of glutathione and ascorbate free radical scavenger systems.

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

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

277 NO synthase inhibitor (L-NAME), a superoxide scavenger (Tempol), and an NADPH oxidase inhibitor (apoc

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

279 ked by mitoTEMPO, a mitochondrial superoxide scavenger that reduced oxidative stress and DNA damage s

280 cular, mammalian mesopredators are efficient scavengers that are often subjected to control, thus, it

281 es protect host cells in vitro by serving as scavengers that can bind multiple toxins, and improve th

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

283 Using hydroxyurea as a radical scavenger, the spin-coupled hidden Cu(II) was observed b

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

285 l density and elevated expression of the ROS scavenger thioredoxin (Trx1) protected NK cells from ROS

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

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

288 al, as we saw a functional response by avian scavengers to increased carrion availability.

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

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

291 suggesting that A. simus was a wide-ranging scavenger utilizing terrestrial and marine carcasses.

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

293 ion, but none of the currently used nitrogen scavengers was superior with regard to long-term neuroco

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 the exclusion of an entire guild of dominant scavengers, we saw little effect on scavenging dynamics

298 nfirm that SCU-102 represents the optimal Tc scavenger with the highest reported clean-up 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