ライフサイエンスコーパス: hydrogen peroxide

1 was important for V. cholerae resistance to hydrogen peroxide.

2 tric measurement of the enzymatic by-product hydrogen peroxide.

3 umes oxygen without generating superoxide or hydrogen peroxide.

4 to have a lower limit of detection of 368 nM hydrogen peroxide.

5 ation, reducing the generation of superoxide/hydrogen peroxide.

6 rom E. coli treated with a sublethal dose of hydrogen peroxide.

7 strongly quenched in the presence of aqueous hydrogen peroxide.

8 levels of the toxic reactive oxygen species hydrogen peroxide.

9 radicals through laser-induced photolysis of hydrogen peroxide.

10 observed to oxidize water via elimination of hydrogen peroxide.

11 ormation of the superoxide anion (O2*-) into hydrogen peroxide.

12 rticles to controllably produce bactericidal hydrogen peroxide.

13 ows promise for the in vivo visualization of hydrogen peroxide.

14 prove the specificity of the sensor towards hydrogen peroxide.

15 ch could be normalized by the application of hydrogen peroxide.

16 y with O-phenylenediamine in the presence of hydrogen peroxide.

17 AscH(-) on metastatic disease is mediated by hydrogen peroxide.

18 or ABTS(.-) anion radical in the presence of hydrogen peroxide.

19 e family member, catalyzes the production of hydrogen peroxide.

20 ing continuous on-site production of neutral hydrogen peroxide.

21 ce of oxidative stress, finally convert into hydrogen peroxide.

22 uconolactone and reduces molecular oxygen to hydrogen peroxide.

23 suggested regulated production of apoplastic hydrogen peroxide.

24 d iron ions catalyst for oxygen reduction to hydrogen peroxide.

25 m ethanoic acid and CO(2) upon reaction with hydrogen peroxide (150 mM).

26 Detectability was down to picomoles of hydrogen peroxide (4 pmol for CL and 210 pmol for ampero

27 h induced the formation of callose papillae, hydrogen peroxide accumulation and the Salicylic acid (S

28 chemistry and produce reactive radicals from hydrogen peroxide activation have been extensively studi

29 species produced by Rhizobium and found that hydrogen peroxide added to benign Escherichia coli can c

30 After treatment by RO, the UV/hydrogen peroxide advanced oxidation process, and chlora

31 vel biosensor is used to detect intratumoral hydrogen peroxide, allowing real-time monitoring of resp

32 The use of hydrogen peroxide altered AQP3 and NOTCH1 expression, an

33 e production of harmful byproducts including hydrogen peroxide, ammonia, and reactive aldehydes.

34 llent peroxidease-like catalytic activity in hydrogen peroxide-Amplex red (AR) system (AR is oxidized

35 Hydrogen peroxide and 1,4-dioxane degradations were maxi

36 On the other hand, the reaction of hydrogen peroxide and ammonium thiocyanate followed by o

37 experiments were repeated in the presence of hydrogen peroxide and AMP-PNP, an ATP analog and competi

38 lyze the reduction of superoxide radicals to hydrogen peroxide and are important in the protection ag

39 when embedded peroxidasin was supplied with hydrogen peroxide and bromide.

40 The reactivity of hydrogen peroxide and catalytic hydroiodic acid toward 3

41 Reactive oxygen species - superoxide, hydrogen peroxide and hydroxyl radicals - have long been

42 n a feed-forward mechanism for generation of hydrogen peroxide and induction of metabolic stress thro

43 aused by NAD(+)-depleting genotoxins such as hydrogen peroxide and methylmethane sulfonate.

44 xidant enzyme that can effectively breakdown hydrogen peroxide and minimize the downstream reactive o

45 conversion of superoxide free radicals into hydrogen peroxide and oxygen, is known to be among the s

46 ctive toward specific Prx substrates such as hydrogen peroxide and peroxynitrite.

47 Oxidative stress parameters such as, hydrogen peroxide and reactive substances were significa

48 including thiol depletion and generation of hydrogen peroxide and superoxide, but none of them can f

49 particles move spontaneously in solutions of hydrogen peroxide and that their motions can be rational

50 The reactive oxygen species hydrogen peroxide and the polyunsaturated fatty acid ara

51 d both the TGF-beta1-dependent production of hydrogen peroxide and the presence of myeloperoxidase (M

52 eliminates the influences of indigenous milk hydrogen peroxide and thiocyanate.

53 ctivation of cydD renders cells resistant to hydrogen peroxide and to aminoglycoside antibiotics.

54 including singlet oxygen, superoxide anion, hydrogen peroxide, and hydroxyl radicals, to afford supe

55 us propagating the generation of superoxide, hydrogen peroxide, and hydroxyl radicals.

56 icated sunlight, ultraviolet light, ethanol, hydrogen peroxide, and hypochlorite attain 99.9% reducti

57 e species (ROS) quenchers, the generation of hydrogen peroxide, and increased levels of intracellular

58 Life on Earth evolved in the presence of hydrogen peroxide, and other peroxides also emerged befo

59 uch as 2,2,6,6-tetramethylpiperidine-1-oxyl, hydrogen peroxide, and ozone.

60 metal ions, breakdown of radical chains and hydrogen peroxide, and scavenging of reactive oxygen spe

61 lly relevant electrophiles peroxynitrite and hydrogen peroxide, and with the probe monobromobimane, w

62 oxygen species (ROS), such as superoxide and hydrogen peroxide, are mediators of oxidative stress tha

63 as been developed in an aqueous medium using hydrogen peroxide as a benign oxidant and ammonium thioc

64 ia their derived bis(dichloroacetates) using hydrogen peroxide as a mild oxidant that intercepts a tr

65 n high enantiomeric excess (up to 99%) using hydrogen peroxide as oxidant and a Bronsted acid additiv

66 The use of inexpensive tert-butyl hydrogen peroxide as the oxidant to promote the desired

67 acy by using earth-abundant cobalt salts and hydrogen peroxide as the oxidant.

68 n study was performed under electrogenerated hydrogen peroxide at a constant voltage of - 0.6 V vs Hg

69 the effect of modifying okara with alkaline hydrogen peroxide at different H(2)O(2) concentrations a

70 ty in methane oxidation by in situ generated hydrogen peroxide at mild temperature (70 degrees C).

71 contribute to symmetry breaking by producing hydrogen peroxide at the egg's future posterior pole.

72 ignaling, epithelial cells were treated with hydrogen peroxide, biochemical experiments were conducte

73 wth in vitro and provides protection against hydrogen peroxide, bleach, and ciprofloxacin.

74 nning with an acidic copper(II) chloride and hydrogen peroxide bleaching solution.

75 ity to generate superoxide anion radical and hydrogen peroxide by ozone-treated fruit was significant

76 e produced specifically by the generation of hydrogen peroxide by the VL domain of the light chain.

77 e has demonstrated that reactive oxygen (eg, hydrogen peroxide) can activate host cell signaling path

78 roxide radical anion (superoxide dismutase), hydrogen peroxide (catalase), hydroxyl radicals (mannito

79 In the presence of hydrogen peroxide, Cd-MsrB formed reversible intra- and

80 oxidized TMB is linearly associated with the hydrogen peroxide concentration.

81 s including the microfluidic flow system and hydrogen peroxide concentration.

82 ter content, but results in increased needle hydrogen peroxide concentrations and increased expressio

83 The exhaled breath condensate hydrogen peroxide concentrations trended toward higher v

84 Horseradish peroxidase (HRP) and hydrogen peroxide concentrations were directly measured,

85 nd tracking of catechol oxidation byproduct, hydrogen peroxide, confirmed that catechol was oxidized

86 ordancage solution, and the concentration of hydrogen peroxide, copper(II) chloride, and acetic acid

87 ns were highly tolerant to oxidants, such as hydrogen peroxide, cumene hydroperoxide and menadione, c

88 gov website: povidone-iodine, chlorhexidine, hydrogen peroxide, cyclodextrin, Citrox, cetylpyridinium

89 usly added as well as endogenously generated hydrogen peroxide decreases spermathecal contractility b

90 sensory neurons to control the induction of hydrogen peroxide defenses in the organism.

91 to repress expression of catalases and other hydrogen peroxide defenses.

92 on of energy-dissipating ion channels, while hydrogen peroxide distributes oxidative stress to sensit

93 show that O(2) and associated generation of hydrogen peroxide during the regeneration step drive the

94 xhibited reduced browning, superoxide anion, hydrogen peroxide, electrolyte leakage and malondialdehy

95 Hydrogen peroxide emission was modestly higher in the is

96 experiments, supplementation with exogenous hydrogen peroxide enhanced E. coli growth through AppBCX

97 e quantification of adenosine, dopamine, and hydrogen peroxide fluctuations occurring >10 min from th

98 system to measure exhaled breath condensate hydrogen peroxide for monitoring oxidative stress in ast

99 mes that imitate peroxidase, which scavenges hydrogen peroxide for the mitigation of potential cytoto

100 Hydrogen peroxide formation is dramatically suppressed,

101 oli, the nematode's food source, can deplete hydrogen peroxide from the local environment and thereby

102 The hydrogen peroxide generated by XO catalysed oxidation of

103 Hydrogen peroxide generated in the medium contributed to

104 The oxidation agent is hydrogen peroxide generated on the surface of the TiO(2)

105 imary B cells, we focused on the role of the hydrogen peroxide generator Duox1 in stimulated splenic

106 hanced resistance to M. oryzae and increased hydrogen peroxide (H(2) O(2) ) accumulation.

107 burst of reactive oxygen species (ROS), with hydrogen peroxide (H(2) O(2) ) as the most abundant form

108 tion of organic pollutants and production of hydrogen peroxide (H(2) O(2) ) is an attractive two-in-o

109 knowledgements 1209 References 1209 SUMMARY: Hydrogen peroxide (H(2) O(2) ) is produced, via superoxi

110 Hydrogen peroxide (H(2) O(2) ) is ubiquitous in cells an

111 Hydrogen peroxide (H(2) O(2) ) mediates the biology of w

112 ctions of [(cyclam)Fe(II) ](2+) with aqueous hydrogen peroxide (H(2) O(2) ) or a soluble iodosylbenze

113 und photosystem I and higher accumulation of hydrogen peroxide (H(2) O(2) ) under HL conditions.

114 the mutual presence of glutathione (GSH) and hydrogen peroxide (H(2) O(2) ) with high specificity on

115 of the active material, such reactions yield hydrogen peroxide (H(2) O(2) ), a reactive side-product,

116 el containing cetylpridinium chloride (CPC), hydrogen peroxide (H(2) O(2) ), sodium bicarbonate, and

117 se is secured by the excessive production of hydrogen peroxide (H(2) O(2) ), which is stored in micro

118 Here we show that eCO(2) triggers apoplastic hydrogen peroxide (H(2) O(2) )-dependent auxin productio

119 on, we report on the development of a unique hydrogen peroxide (H(2) O(2) )-sensing motif and its cap

120 ial-derived reactive oxygen species, notably hydrogen peroxide (H(2)O(2)) ([H(2)O(2)](mito)).

121 The UV/hydrogen peroxide (H(2)O(2)) advanced oxidation process

122 nulation with release of myeloperoxidase and hydrogen peroxide (H(2)O(2)) and increased expression of

123 Here, microbial membranes were treated with hydrogen peroxide (H(2)O(2)) and sodium hypochlorite (Na

124 Two species, hydrogen peroxide (H(2)O(2)) and the superoxide anion ra

125 Although hydroxyl radical ((*)OH) and hydrogen peroxide (H(2)O(2)) are regarded as major oxida

126 ing biological redox reactions, I identified hydrogen peroxide (H(2)O(2)) as a normal constituent of

127 dy, by use of in vivo imaging, we identified hydrogen peroxide (H(2)O(2)) as a stressor produced in t

128 trocatalytic reduction of dioxygen (O(2)) to hydrogen peroxide (H(2)O(2)) could be an alternative to

129 Also, treatment of hydrogen peroxide (H(2)O(2)) decreased inhibitory p-Drp1

130 We continuously monitored hydrogen peroxide (H(2)O(2)) from household non-bleach s

131 tion of citrate stabilized AgNPs by O(2) and hydrogen peroxide (H(2)O(2)) in the dark and in irradiat

132 Hydrogen peroxide (H(2)O(2)) is a major reactive oxygen

133 Hydrogen peroxide (H(2)O(2)) is a reactive oxygen specie

134 The reaction with hydrogen peroxide (H(2)O(2)) is considered to be the mai

135 us low-level supply or in situ generation of hydrogen peroxide (H(2)O(2)) is essential for the stabil

136 l radical ((*)OH) generated by photolysis of hydrogen peroxide (H(2)O(2)) is most commonly used, the

137 timately reproduction.SIGNIFICANCE STATEMENT Hydrogen peroxide (H(2)O(2)) is often studied in a patho

138 U.S.A, 116, 19294-19298 (2019)] that hydrogen peroxide (H(2)O(2)) is spontaneously produced i

139 Hydrogen peroxide (H(2)O(2)) is used as the default phot

140 s a DeltamumT mutant is no more sensitive to hydrogen peroxide (H(2)O(2)) killing than wild-type A. b

141 Mechanistically, excessive hydrogen peroxide (H(2)O(2)) originated from monoamine o

142 renal water reabsorption, and AQP3-mediated hydrogen peroxide (H(2)O(2)) permeability can enhance cy

143 Hydrogen peroxide (H(2)O(2)) plays an important role phy

144 Streptococcus parasanguinis, a hydrogen peroxide (H(2)O(2)) producing oral commensal, h

145 igher mitochondrial respiratory capacity and hydrogen peroxide (H(2)O(2)) production than aSAT (p < 0

146 n type-II pathways resulting in promotion of hydrogen peroxide (H(2)O(2)) production.

147 Hydrogen peroxide (H(2)O(2)) quantification in biomedici

148 enzyme family with functions that range from hydrogen peroxide (H(2)O(2)) reduction to post-translati

149 d excellent electrocatalytic activity toward hydrogen peroxide (H(2)O(2)) reduction.

150 not required for aerobic respiration but for hydrogen peroxide (H(2)O(2)) respiration using cytochrom

151 ferric reducing antioxidant power (FRAP) and hydrogen peroxide (H(2)O(2)) scavenging assays, showed t

152 i) ferric ions (Fe(3+)) reducing power; (iv) hydrogen peroxide (H(2)O(2)) scavenging.

153 ase in skeletal muscle oxidative stress, the hydrogen peroxide (H(2)O(2)) specific, genetically-encod

154 Hydrogen peroxide (H(2)O(2)) synthesis generally require

155 QP3) is a transporter of water, glycerol and hydrogen peroxide (H(2)O(2)) that is expressed in variou

156 Here, we used hydrogen peroxide (H(2)O(2)) to induce oxidative stress

157 ve DNA damage induced by exogenously applied hydrogen peroxide (H(2)O(2)) upregulates PD-L1 expressio

158 n small scale electrocatalytic production of hydrogen peroxide (H(2)O(2)) using a rotating ring-disk

159 s of aqueous oxidation of dissolved SO(2) by hydrogen peroxide (H(2)O(2)) using pH-buffered, submicro

160 Epithelial production of hydrogen peroxide (H(2)O(2)) was analyzed in murine colo

161 dismutation of virus-mediated generation of hydrogen peroxide (H(2)O(2)) we developed a model of int

162 at 27 of them, mainly polyphenols, generated hydrogen peroxide (H(2)O(2)) when added to Dulbecco's mo

163 ucose, oxidised glucose to gluconic acid and hydrogen peroxide (H(2)O(2)) while the chitin-AcOH decom

164 enzyme-like behavior for the degradation of hydrogen peroxide (H(2)O(2)) with a K(m) of about 13 mM

165 l in response to peroxynitrite (ONOO(-)) and hydrogen peroxide (H(2)O(2)) with photoacoustic signal i

166 and function in HeLa cells after exposure to hydrogen peroxide (H(2)O(2)), a reagent commonly used to

167 Once activated, the reactive species hydrogen peroxide (H(2)O(2)), hypochlorous acid, and sin

168 al oxygen reduction towards 2e(-) pathway to hydrogen peroxide (H(2)O(2)), instead of the traditional

169 C is also activated, which in turn elevates hydrogen peroxide (H(2)O(2)), likely by stimulating nico

170 After reacting with hydrogen peroxide (H(2)O(2)), sickle-cell hemoglobin (Hb

171 present in honey: sugars, gluconic acid, and hydrogen peroxide (H(2)O(2)), which result from the enzy

172 he Pbp1 methionine residues are sensitive to hydrogen peroxide (H(2)O(2))-mediated oxidation in vitro

173 stem implemented on the paper was based on a hydrogen peroxide (H(2)O(2))-rhodamine b (RhoB)-cobalt m

174 ght after being exposed to a strong oxidant, hydrogen peroxide (H(2)O(2)).

175 lied to construct an enzymatic biosensor for hydrogen peroxide (H(2)O(2)).

176 reased after incubation with the pro-oxidant hydrogen peroxide (H(2)O(2)).

177 n dual-species biofilms via the secretion of hydrogen peroxide (H(2)O(2)).

178 rapeutic effect in cancer cells by producing hydrogen peroxide (H(2)O(2)).

179 major and abundant reactive oxygen species, hydrogen peroxide (H(2)O(2)).

180 and incomplete reduction of oxygen (O(2)) to hydrogen peroxide (H(2)O(2)).

181 ced in the presence of hydroquinone (HQ) and hydrogen peroxide (H(2)O(2)).

182 T3 is a major regulator of mROS, including hydrogen peroxide (H(2)O(2)).

183 olite, is an alpha-ketoacid that reacts with hydrogen peroxide (H(2)O(2)).

184 n, but is also thought to generate cytosolic hydrogen peroxide (H(2)O(2)).

185 ising route toward sustainable production of hydrogen peroxide (H(2)O(2)).

186 wounding stimulates the rapid production of hydrogen peroxide (H(2)O(2)).(1)(,)(2) This then acts as

187 unts of superoxide ([Formula: see text]) and hydrogen peroxide (H(2)O(2)); however, the precise mecha

188 different stresses, subsequently maintaining hydrogen peroxide (H2 O2 ) homeostasis in Arabidopsis.

189 e-1-dependent (NOX1-dependent) production of hydrogen peroxide (H2O2) and 4-hydroxynonenal (4-HNE), w

190 mine (AgNPs-OA) is reported for detection of hydrogen peroxide (H2O2) in wastewater samples.

191 Hydrogen peroxide (H2O2) promotes a range of phenotypes

192 Glucose has been quantified by measuring hydrogen peroxide (H2O2) reduction by chronoamperometry

193 on human intestinal Caco-2 cells exposed to hydrogen peroxide (H2O2)-induced oxidative stress.

194 greatly elevated when cells are treated with hydrogen peroxide (H2O2).

195 highly sensitive and selective detection of hydrogen peroxide (H2O2).

196 g, which was exacerbated upon treatment with hydrogen peroxide (H2O2).

197 herapy (FBIC) was produced with taurolidine, hydrogen peroxide, human serum, potassium iodide and dox

198 We evaluated exhaled breath condensate hydrogen peroxide in 60 patients (ages 20-83; 30 healthy

199 pond to different mycotoxins, menadione, and hydrogen peroxide in a distinguishable manner and with c

200 aluate the sterilization efficacy of gaseous hydrogen peroxide in aseptic filling machines.

201 device to measure exhaled breath condensate hydrogen peroxide in asthma patients and healthy partici

202 sing a catalase control to scavenge residual hydrogen peroxide in calibrant solutions provided analyt

203 ever, in most countries the concentration of hydrogen peroxide in milk is limited or it is even prohi

204 e to describe the method of determination of hydrogen peroxide in milk using high performance liquid

205 uminescence assay and a device for measuring hydrogen peroxide in the exhaled breath condensate of as

206 ng ROS intermediates, we were able to detect hydrogen peroxide in the nucleus through ratiometric ana

207 in system that increase levels of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae

208 s, which can determine dynamic alteration of hydrogen peroxide in tumor, can evaluate the effectivene

209 y catalyze oxygen generation from endogenous hydrogen peroxide in tumors.

210 sted by the finding that elevation of ROS by hydrogen peroxide increased Src phosphorylation, while R

211 is profound sensitivity of telomeres through hydrogen peroxide induced by dysregulated mitochondria r

212 ion and cell cycle progression and inhibited hydrogen peroxide-induced apoptosis.

213 n brain microvascular endothelial cells from hydrogen peroxide-induced cell death, as well as preserv

214 nstrated that cyclin C represses a subset of hydrogen peroxide-induced genes under normal conditions

215 yeast mutants supported the conclusion that hydrogen peroxide-induced mutagenesis is not the result

216 Measurements of the frequencies of hydrogen peroxide-induced mutations in proofreading-defe

217 mote angiogenesis and to protect ECs against hydrogen peroxide-induced oxidative stress.

218 efective mutant had increased sensitivity to hydrogen peroxide-induced stress, was inhibited in its a

219 screens based on Ca(2+) imaging, we isolated hydrogen-peroxide-induced Ca(2+) increases (hpca) mutant

220 CM is able to effectively convert endogenous hydrogen peroxide into oxygen and then elevate the produ

221 Hydrogen peroxide is a cosubstrate for the oxidative cle

222 upregulation of genes predicted to detoxify hydrogen peroxide is abolished in an A. baumannii strain

223 In some countries hydrogen peroxide is added to milk as an adulterant for

224 Indirect quantitative evaluation of hydrogen peroxide is carried out according to the amount

225 The rate of reaction of LPMOs with hydrogen peroxide is high, but it is accompanied by rapi

226 -negative bacterium can withstand endogenous hydrogen peroxide is incompletely understood.

227 ators of the bactericidal effects of LTP and hydrogen peroxide is necessary but not sufficient for an

228 This study examines whether an increase in hydrogen peroxide is sustained posttreatment and potenti

229 Since, hydrogen peroxide is the oxidative end product of uric a

230 Hydrogen peroxide is the preeminent chemical weapon that

231 Notably, tert-butyl hydrogen peroxide is used as the sole oxidant for these

232 oxidation of Fe(2+)-PyC3A to Fe(3+)-PyC3A by hydrogen peroxide is very rapid, and we capitalized on t

233 Hydrogen peroxide is widely used for disinfection purpos

234 condary wave of mitochondrial superoxide and hydrogen peroxide lasting for over 48 h after the initia

235 ose who had and showed a trend toward higher hydrogen peroxide levels (mean 172.8 vs 115.9 nM; p = 0.

236 wed that cytoplasmic, but not mitochondrial, hydrogen peroxide levels were reduced in LPS-treated mCA

237 rsors exhibit cytoprotective effects against hydrogen peroxide-mediated toxicity in H9c2 cells and ca

238 These data suggest that dysregulated hydrogen peroxide metabolism is a common mechanism by wh

239 al signaling mechanism in which ROS, such as hydrogen peroxide, modulate AMPAR transport by modifying

240 stress that involves the interaction of one hydrogen peroxide molecule per YME1L monomer with affini

241 roaches, strongly suggest that Duox1-derived hydrogen peroxide negatively regulates proliferative act

242 n showed scavenging capacity for superoxide, hydrogen peroxide, nitric oxide and DPPH (1,1-diphenyl-2

243 Optical emission spectroscopy (OES), whereas hydrogen peroxides, nitrites, nitrates, and pH were meas

244 ts further show that continuous formation of hydrogen peroxide occurs in the presence of Cu(II), SRFA

245 r resulted in the unprecedented detection of hydrogen peroxide on a temporal level not previously see

246 In response to stress induced by hydrogen peroxide or CCCP, parkin degradation also requi

247 re susceptible to the microbicidal effect of hydrogen peroxide or human beta-defensin-3.

248 terosaur Tupandactylus imperator by alkaline hydrogen peroxide oxidation followed by high-performance

249 ple chemiphotobleaching method combines mild hydrogen peroxide oxidation with broad spectrum visible

250 We demonstrate that boronate oxidation by hydrogen peroxide, peroxymonocarbonate, hypochlorite, or

251 Laser-induced hydrogen peroxide photolysis generates hydroxyl radicals

252 Hydrogen peroxide plays a key role in honey antibacteria

253 Moreover, the combination of hydrogen peroxide-producing oral commensal streptococci

254 ntions restored mitochondrial superoxide and hydrogen peroxide production and inactivated HIF (hypoxi

255 uel cells and its selectivity for water over hydrogen peroxide production is important for these tech

256 irectly correlating with marked induction of hydrogen peroxide production.

257 e tested, there were distinct differences in hydrogen peroxide production.

258 the rate of degradation was correlated with hydrogen peroxide production.

259 istribution of oxidative substrates, such as hydrogen peroxide, provide mechanisms to control spatiot

260 it forms a stable dimer under treatment with hydrogen peroxide, recently recognized as a signaling mo

261 from the oxygen reduction reaction (ORR) or hydrogen peroxide reduction on platinum, has been invest

262 de, allowing for the electrocatalysis of the hydrogen peroxide reduction.

263 ethodology as a reliable detection scheme of hydrogen peroxide related enzymatic bioassays for ultras

264 pproach was demonstrated by detection of the hydrogen peroxide released from HeLa cells stimulated wi

265 n that interaction of triphenylphosphine and hydrogen peroxide required about 40 min.

266 and Stb5 are selective for ochratoxin A and hydrogen peroxide, respectively.

267 se system, to test causality for the role of hydrogen peroxide, reversed the P-AscH(-)-induced increa

268 current system through chemiluminescence for hydrogen peroxide sensing.

269 on ability as well as increased motility and hydrogen peroxide sensitivity compared to the wild-type.

270 motility, autoagglutination, quorum sensing, hydrogen peroxide sensitivity, and chicken colonization

271 been made in our understanding of the nature hydrogen peroxide sensors and the role of thiol-dependen

272 ns, unaffected by the presence of oxygen and hydrogen peroxide species, down to concentrations lower

273 ies, which led to a significant reduction in hydrogen peroxide, superoxide anion and malondealdehyde

274 and environmentally friendly tertiary butyl hydrogen peroxide (TBHP)-mediated rearrangement of aryl/

275 nd these patients also trended toward higher hydrogen peroxide than healthy participants (mean 172.8

276 abeled to the secondary antibody and yielded hydrogen peroxide that acted as the measurand and the re

277 coccus pneumoniae generates large amounts of hydrogen peroxide that can accumulate to millimolar conc

278 transient short-term increase in the flux of hydrogen peroxide that is preferentially cytotoxic to ca

279 We observed that in the presence of hydrogen peroxide, the enzyme generates (1)O(2) and that

280 (4) )(3) )SbCl(2) AuCl (1) was oxidized with hydrogen peroxide to afford [((o-(Ph(2) P)C(6) H(4) )(2)

281 roxidase (MPO), a heme protein that converts hydrogen peroxide to hypochlorous acid (HOCl), compared

282 icillamine), nitric oxide, oxidized GSH, and hydrogen peroxide to post-translationally modify and inh

283 can oxidize 3,3,5,5-tetramethylbenzidine by hydrogen peroxide to yield a blue product.

284 Alkaline hydrogen peroxide treatment altered the color, chemical

285 er conditions, such as ionizing radiation or hydrogen peroxide treatment, that generate hydroxyl radi

286 und that fsq enhances cellular resistance to hydrogen peroxide treatment.

287 UV irradiation, oxygen plasma and vaporized hydrogen peroxide treatments, measured with EGA and HPC.

288 l agents (bleomycin, doxorubicin, topotecan, hydrogen peroxide, UV, photosensitized reactions) and fr

289 We evaluated the efficacy of hydrogen peroxide vapor (HPV) to inactivate MS2 and Phi6

290 Low concentration hydrogen peroxide vapor (LCHP; 25 ppm) was effective aga

291 ive and sensitive electrochemical sensing of hydrogen peroxide was carried out at -100 mV vs Ag|AgCl;

292 An increase in intracellular hydrogen peroxide was detected within 3 seconds of inter

293 The recovery of hydrogen peroxide was from 97.8% to 103.8%.

294 mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the cata

295 Intracellular hydrogen peroxide was then measured in response to the i

296 ozone and hydrogen peroxides were found to be responsible for micr

297 duces reactive oxygen species (ROS), such as hydrogen peroxide, which are known modulators of calcium

298 eradish peroxidase, leading to production of hydrogen peroxide, which is measured with an optimized l

299 The released Lap can efficiently generate hydrogen peroxide, which will be further converted into

300 yl oxide produced after the reaction between hydrogen peroxide with triphenylphosphine.