ライフサイエンスコーパス: redox reaction

1 amine layers were confirmed by the increased redox reaction.

2 of the EDL that abruptly changes due to the redox reaction.

3 e are required to maximize the yield of this redox reaction.

4 a cheap alternative for this intramolecular redox reaction.

5 ies of the compounds on each half of the LDH redox reaction.

6 europium metal, and a melt of imidazole in a redox reaction.

7 surface-bound redox-active moieties on their redox reaction.

8 lattice using a solution disproportionation redox reaction.

9 eaction or a cumulative cationic and anionic redox reaction.

10 ion of quasicrystals under shock without any redox reaction.

11 taining EC product was found to catalyze the redox reaction.

12 the alkynoate partner undergoes an internal redox reaction.

13 Fe(3+) cations are reconstructed without any redox reaction.

14 nd environmental applications exploiting the redox reactions.

15 istic manner, thereby lowering the energy of redox reactions.

16 ly relevant processes that typically involve redox reactions.

17 ecially with regard to biologically mediated redox reactions.

18 promising as improved catalysts for various redox reactions.

19 ial energy production, glycolysis, and other redox reactions.

20 ater interface (MWI), including sorption and redox reactions.

21 d acid production from respiration and other redox reactions.

22 activities for outer-sphere and inner-sphere redox reactions.

23 counter-reaction to accompany polythiophene redox reactions.

24 t with the environment, particularly through redox reactions.

25 is relies heavily on coenzyme F(420) for its redox reactions.

26 ucidate the fundamental aspects of porphyrin redox reactions.

27 and catalyze simple hydrolytic to multistep redox reactions.

28 (MS) is a powerful analytical tool to study redox reactions.

29 es of Miner1 in cellular Fe-S management and redox reactions.

30 tide (NAD) is a classic coenzyme in cellular redox reactions.

31 function in Fe-S cluster shuttling and/or in redox reactions.

32 lorination occurs after completion of flavin redox reactions.

33 ations at Cu2O/Cu interfaces as they undergo redox reactions.

34 intercalation process, inspired by Li2 MnO3 redox reactions.

35 lectronic transition via fast and reversible redox reactions.

36 les, and offer rich active sites for surface redox reactions.

37 allic domains to accept charges and catalyze redox reactions.

38 ore charge in excess of the transition metal redox reactions.

39 e exposed to the electrolyte and involved in redox reactions.

40 insoluble lithium sulfides through multistep redox reactions.

41 ite of the enzyme, includes the pH-dependent redox reactions, accounts for the effect of the proton-m

42 oreductases mediate electron transfer (i.e., redox) reactions across the tree of life and ultimately

43 m the lower diffusion process of ions during redox reaction after prion interaction due to bulk effec

44 ions, e.g. reactions with biomacromolecules, redox reactions, aggregation, and dissolution, may occur

45 Moreover, we show that controlled redox reactions allow for interconversion of these DNA-e

46 o redox-MHD, density gradients caused by the redox reactions also play important roles.

47 rbonyl migration steps via an intramolecular redox reaction and a subsequent beta-elimination step, a

48 tal data for both a simple fast one electron redox reaction and an electron transfer with a following

49 l stability, electronic conduction, vanadium redox reaction and lithium-ion diffusion supported by va

50 es an effective platform for elucidating the redox reaction and oxygen diffusion within transition me

51 , because it alters the driving force of the redox reaction and thus electron transfer kinetics, sign

52 ed organic matter (DOM) affects mercury (Hg) redox reactions and anaerobic microbial methylation in t

53 proteins catalyse a diversity of fundamental redox reactions and are one of the most studied enzyme f

54 erials, in contrast, operate by fast surface redox reactions and are shown to enhance energy storage

55 Coenzymes of cellular redox reactions and cellular energy mediate biochemical

56 a result of density gradients caused by the redox reactions and follow convection flow patterns.

57 ironmental conditions, it can participate in redox reactions and influence the sorption processes at

58 uires external electron acceptors to balance redox reactions and is not fermentative, we find that su

59 denine dinucleotide (NAD(+)) participates in redox reactions and NAD(+)-dependent signaling pathways.

60 ee radicals that may play a role in observed redox reactions and ROS generation.

61 ducting black SnO2-x , which homogenizes the redox reactions and stabilizes fine, fracture-resistant

62 ed mechanistic support for proposed cysteine redox reactions and suggested novel redox mechanisms, in

63 ation influences both the rate of cytochrome redox reactions and the balance between the reduced and

64 her layered compounds can be intercalated by redox reactions and then converted chemically to suspens

65 hree orthogonal stimuli (metal coordination, redox reaction, and guest binding) is reported.

66 this approach for the parallel addressing of redox reactions, and report the construction of a DNA mi

67 eliminateion of nitric oxide (NO) via facile redox reactions, and the elimination dynamics was evalua

68 Protein motions control the rates of heme redox reactions, and these effects are amplified at low

69 ution Cu(y)Fe(1-y)F(2), reversible Cu and Fe redox reactions are achieved with surprisingly small hys

70 Although the redox reactions are critical for efficient mitochondrial

71 These redox reactions are mediated by the DNA strand and invol

72 ic reagents and discrete alcohol-to-carbonyl redox reactions are not required.

73 Redox reactions are proposed that explicitly couple the

74 related to immunity and reduction-oxidation (redox) reactions are up-regulated in Ae. aegypti infecte

75 Transition metal atoms often participate in redox reactions as catalytic sites, where ligand groups

76 ated with surface or near-surface reversible redox reactions, as observed with RuO2.xH2O in an acidic

77 thodes for lithium batteries store charge in redox reactions associated with the transition metal cat

78 The observed surface-confined redox reaction at both CNT and N-CNT electrodes is from

79 Redox reaction at the molecule/Ag interface is identifie

80 rylamide) (GN) polymers were synthesized via redox reactions at 20-50 degrees C.

81 le electrons in PMMA that can participate in redox reactions at a rather negative potential.

82 e DNA base pairs provides a means to promote redox reactions at a remote site and potentially to effe

83 an electron from other substrates to mediate redox reactions at ambient temperature with high atom ef

84 ely efficient electrocatalysts (catalysts of redox reactions at electrodes).

85 Redox reactions at iron mineral surfaces play an importa

86 The improvement mostly stems from robust redox reactions at nitrogen-associated defects that tran

87 and donate electrons in many biogeochemical redox reactions at oxic/anoxic interfaces.

88 dynamic electrochemistry investigations into redox reactions at the solid/gas interface, free of any

89 nitored by the change in current of the AgNF redox reaction before and after hybridization using cycl

90 The reversible non-volatile redox reaction between metal and metal oxide may provide

91 Transhydrogenase couples the redox reaction between NADH and NADP+ to proton transloc

92 ll membrane using the energy released by the redox reaction between NADH and ubiquinone.

93 The method was based on a redox reaction between the I3(-) and SO3(2-) ions, after

94 xidation of Si is subsequently governed by a redox reaction between the ions and Si.

95 ctor, and explain the results in view of the redox reaction between the polymer, water and oxygen in

96 radical was examined as the analogue of the redox reaction between the PSII tyrosyl radical and the

97 ed gold electrode, which is modulated by the redox reaction between uric acid and hexacyanoferrate io

98 Interfacial redox reactions between adsorbed Mn(II) and solid-phase

99 Redox reactions between CeO2 NPs and Fe2+ lead to the fo

100 No evidence was found for redox reactions between Fe(II) and As(V) or As(III), or

101 es and between microbes and molecules, local redox reactions between molecules, and hydrolysis.

102 chanism of quenching, which occurred through redox reactions between the 11-MUA-Au NDs and the Fe(II)

103 s, but minor secondary products from coupled redox reactions between the products and reactants are a

104 n(II) often coexists with Mn(IV) oxides, and redox reactions between the two (e.g., comproportionatio

105 to the rates and extents of complexation and redox reactions between these important and complex envi

106 This study shows that redox reactions between U(VI) and mackinawite may occur

107 fficient charge separation and decoupling of redox reactions, bio-inspired artificial systems typical

108 n structure, O(2) release kinetics, and PSII redox reactions both within and outside the oxygen-evolv

109 They could include measuring not only redox reactions but also dissolution/precipitation react

110 lfulvenes increases the reversibility of the redox reactions, but does not appear to further stabiliz

111 ffer sustainable alternatives to traditional redox reactions, but strategies are needed to enhance th

112 mportant role in heterogeneous catalysis and redox reactions, but their buried nature makes them diff

113 SEED quantitatively maps the local redox reaction by scanning a laser on the array of enzym

114 resent in these complexes can participate in redox reactions by toggling between different oxidation

115 Under laminar flow conditions, a redox reaction can be driven on the upstream generator e

116 The occurrence of a redox reaction can be rationalized by comparing the redo

117 These redox reactions can affect the toxicity of CeO2 NPs by i

118 l as a mechanism for regulating DNA binding, redox reactions can control replication by modulating th

119 range of parameter values suggests that the redox reactions can increase desorption of BER enzymes n

120 We tested the hypothesis that Y122OH redox reactions cause structural changes in the diferric

121 he observed electroactivity is from FAD, the redox reaction center of GOx.

122 e strategies involving thiols and associated redox reactions; comparisons to a model diatom, Thalassi

123 nd F radicals produced by this unprecedented redox reaction could be exploited as electrodes, light-e

124 Our results suggest that, during the redox reaction, Cys43 in a luminal loop of human VKOR fo

125 For redox reactions, deuterium tracing can provide additiona

126 an important role in cancer cells mediating redox reactions, DNA replication, and telomere maintenan

127 in operando spectromicroscopy to verify that redox reactions drive the resistance change.

128 functions in coagulation, inflammation, and redox reactions due to their unique protein cargo.

129 d formation has typically been attributed to redox reactions during precipitation from fluids or magm

130 cal STM, we suggest that the single-molecule redox reaction dynamics at the hemin-Ag interface is pri

131 We have probed single-molecule redox reaction dynamics of hemin (chloride) adsorbed on

132 trigger an intense interest in catalysis of redox reactions-electrochemical and photochemical-partic

133 table set of core genes coding for the major redox reactions essential for life and biogeochemical cy

134 In liquid cell TEM/STEM redox reaction experiments, the hydrated electrons e(-)a

135 piration and photosynthesis based on quinone redox reactions face a danger of wasteful energy dissipa

136 f the binding sites thereby facilitating the redox reaction for the detection of capsaicin.

137 A kinetic model based on recognized key redox reactions for these two species further indicated

138 uranium (U(IV)) through enzymatic or abiotic redox reactions has the potential to alter U mobility in

139 can be broken and oxygen loss and/or oxygen redox reactions have been proposed to explain the phenom

140 Intramolecular redox reaction: heating N-alkyl, N-allyl-, and N-benzyl-

141 In the vascular system, redox reactions help regulate key physiologic responses

142 a stepwise combination of disproportionation redox reactions, hydrazine reduction, or carbonyl decomp

143 l analytical tool for studying mechanisms of redox reactions, identification of products and intermed

144 ion of dihydroorotate to orotate in the only redox reaction in pyrimidine biosynthesis.

145 The overall rate of the redox reaction in the micromodel required a three-domain

146 se activity, which catalyzes thiol disulfide redox reactions in a variety of substrate proteins.

147 wild-type PsbO from spinach facilitate PSII redox reactions in a very similar manner, and nonspecifi

148 ics-based electrochemical current imaging of redox reactions in aqueous droplets with diameters varyi

149 ive molecules, which catalyse a multitude of redox reactions in biological systems.

150 ubiquinone designed to reversibly report on redox reactions in biological systems.

151 ocesses that ultimately form the backbone of redox reactions in both anaerobic and aerobic respiratio

152 s utilized by numerous enzymes that catalyze redox reactions in carbon, nitrogen, and sulfur metaboli

153 onds has potential for tuning multi-electron redox reactions in emerging energy-storage applications,

154 llenging for biological hydride transfer and redox reactions in general.

155 probe and studied the thermodynamics of its redox reactions in heterogeneous iron systems, namely go

156 gands to facilitate solid-state ligand-based redox reactions in nonporous coordination solids, giving

157 The unusual redox reactions in PSII often lead to damage, degradatio

158 spectrometer is extremely powerful to study redox reactions in real time and identify unstable react

159 fide (DMTS) as a model compound to study its redox reactions in rechargeable lithium batteries.

160 Fast, reversible redox reactions in solids at low temperatures without th

161 ng oxidoreductases and potentially catalyzed redox reactions in the Archean oceans.

162 patic artery of rats selectively deregulated redox reactions in tumor tissues by increasing levels of

163 iratory chain, oxidative stress response, or redox reactions in various metabolic pathways.

164 TO) where ITO undergoes reduction-oxidation (redox) reaction in the presence of electrolyte in most s

165 rticles (NPs), a better understanding of the redox reaction-induced surface property changes of CeO2

166 This redox reaction inhibits the MEF2C-PGC1alpha transcriptio

167 ancillary ligand design, (2) employing mild redox reactions instead of harsh photochemical methods t

168 The redox reactions involve reduction of FeO and SiO2 to Fe

169 The intramolecular redox reaction involves a hydride transfer that occurs b

170 The O redox reaction involves the formation of localized hole

171 otentials clarify some misconceptions in the redox reactions involving Abeta and provide new insight

172 Understanding the extent and kinetics of redox reactions involving Fe-bearing clay minerals has b

173 Here we investigate the rate equation of redox reactions involving reduction by e(-)aq generated

174 rectification is due to the SAM, and not to redox reactions involving the Ga2O3 film, and confirms t

175 Redox reactions involving these two thiol groups sensiti

176 enetically encoded sensors that function via redox reactions involving thiol and disulfide groups.

177 nce spectra provide evidence that the Y122OH redox reaction is associated with a frequency change to

178 A redox reaction is conducted on a polymer film on a rotat

179 This redox reaction is deactivated in water, as the reducing

180 two oxidations of the overall four-electron redox reaction is directly associated with this in situ

181 tability of iron-bound organic carbon in the redox reaction is limited.

182 fluctuation dynamics of the single-molecule redox reaction is measured under no external electric po

183 uinone, and the free energy released by this redox reaction is used to create an electrochemical grad

184 n complex I at which energy generated by the redox reaction is used to initiate proton translocation.

185 donors, the formal potential of the quinone redox reactions is tuned into the potential region in wh

186 e.g., the input of energy to drive critical redox reactions, is a defining feature of syntrophy.

187 al conductance switching allows the study of redox reaction kinetics and thermodynamics at single mol

188 in Fe(III) bioreduction, we investigated the redox reaction kinetics of reduced flavin mononucleotide

189 lectrical connection is required to activate redox reactions, large arrays of electrodes can be contr

190 omplex, [Ni(Me4[12]aneN4)(CO)]PF6, effects a redox reaction leading to the diselenido dinickel(II) co

191 All of the compounds underwent irreversible redox reactions, leading to unstable electrogenerated ra

192 A redox reaction mechanism has also been established, wher

193 Through a fundamental understanding of the redox reaction mechanism in Li2 MnO3 , Na(Li1/3 Mn2/3 )O

194 attribute this phenomenon to the particular redox-reaction mechanism of HRP that involves two separa

195 Yan et al. now identify a thiol-redox reaction mediated by the membrane protein GDE2 and

196 n be extracted from biomass directly and its redox reaction mimics the bio-electrochemical process of

197 A redox reaction model was proposed based on the pH depend

198 This role differs from the redox reactions normally catalyzed by short chain dehydr

199 Using the anionic redox reaction (O(2-) /O(-) ), this Mn-oxide is predicte

200 ydrogen bubbles generated by the spontaneous redox reaction occurring at the inner Zn surface.

201 is powered by self-electrophoresis caused by redox reactions occurring on the two different metal seg

202 stream collector electrode where the reverse redox reaction occurs.

203 metric effect of accumulated Fe(III) against redox reaction of a suitable probe.

204 e report for the first time the controllable redox reaction of chemically purified ssDNA-HiPco SWNT h

205 The redox reaction of complex I is catalyzed in the hydrophi

206 By cyclic voltammetry, the redox reaction of ferrocenemethanol was shown to take pl

207 s electron transfer rate constant (k(s)) for redox reaction of GOx were found to be 0.48 and 1.12 s(-

208 ectrode is utilized to electrically couple a redox reaction of interest to a complementary fluorogeni

209 ium translocation of individual steps in the redox reaction of Na(+)-NQR.

210 current of 2.60 x 10(-4) mA cm(-2) , a rapid redox reaction of polysulfide, and therefore improved su

211 While the redox reaction of quinones in buffered water is well des

212 veral models being studied for the efficient redox reaction of reactants with silicon through a metal

213 The redox reaction of RFN is a pH-dependent process that req

214 The tunable redox reaction of SWNTs and H2O2 mediated by thiocyanate

215 determine the time-constant connected to the redox reaction of the adsorbed protein assembly.

216 of the tyrosine can occur via a bimolecular redox reaction of the cyclohexadienyl and phenoxyl radic

217 nd show that the frequency dependence of the redox reaction of the protein submonolayer follows as ex

218 dehydrogenase, an enzyme catalyzing the only redox reaction of the pyrimidine biosynthesis pathway, i

219 owed a voltammetric signal due to a one-step redox reaction of the surface-confined myoglobin, in a d

220 using concentrated solar energy mediated by redox reactions of a metal oxide.

221 results definitively demonstrate concurrent redox reactions of both polythiophene and viologen in so

222 report an alternative approach based on the redox reactions of functional groups on the surfaces of

223 sfer significantly as a result of reversible redox reactions of H2Q/Q.

224 The combination of ion intercalation with redox reactions of iodine allows for developing recharge

225 while the porous carbon skeleton facilitates redox reactions of iodine and ion intercalation.

226 The CT mechanism relies on redox reactions of iron-sulfur cofactors that modify the

227 The thermochemical cycle utilizes redox reactions of Mn(II)/Mn(III) oxides.

228 The redox reactions of NO and byproducts such as nitrite can

229 OS) uncoupling and NO consumption induced by redox reactions of NO.

230 dark to light involves marked changes in the redox reactions of photosynthetic electron transport and

231 These redox reactions of polyoxometalates require protons, and

232 precedented microscopic detail regarding the redox reactions of supported oxides, which differs funda

233 Redox reactions of the chromophore methylene blue in aqu

234 roscopy to examine the temperature-dependent redox reactions of the iron-quinone site, using it as a

235 Redox reactions of water at the ESI needle and transport

236 (6) Bubble formation due to redox reactions of water at the high-voltage electrode i

237 is to realize systems capable of catalyzing redox reactions on substrates.

238 ion transport but stops further electrolyte redox reactions on the electrode surface, hence solid el

239 d PsbO subunit is needed to further optimize redox reactions on the PSII oxidizing side.

240 sing nanoscale chemical reactors for surface redox reactions on the subnanometer scale.

241 previous compounds involve a single cationic redox reaction or a cumulative cationic and anionic redo

242 However, the PMMA used for a redox reaction or contacted with Teflon that was deplete

243 o reaction pathways, either by photo-induced redox reaction or hydrolysis reaction, which are respons

244 An optical method of mapping local redox reaction over a monolith electrode using simple la

245 Coenzymes of redox reactions: oxidized/reduced nicotinamide adenine d

246 ex was followed by the two-electron-transfer redox reaction, PdRox:NAD+ + 2e- --> PdRrd:NAD+, when th

247 ow distance dependence associated with these redox reactions permits DNA-mediated signaling over long

248 Microbe-mediated arsenic (As) redox reactions play an important role in the biogeochem

249 n the emerging role of a specific reversible redox reaction, protein methionine oxidation, in vascula

250 The specific redox reaction rate for VO(x) in the Keggin primary stru

251 rent energy of 32.5 kJ/mol, showing that the redox reaction rate is approximately 10(15) times slower

252 howed significant spatial variation in local redox reaction rate that was controlled by the coupled t

253 te that the temperature dependence of native redox reaction rates can be well described by the therma

254 ify the energetics of the cysteine disulfide redox-reaction (reversible potentials for both processes

255 completely mapped the enzymatic sequence of redox reactions starting from the nonadride 5.

256 The rates and extent of these redox reactions strongly depend on the speciation of the

257 t performance for high-temperature catalytic redox reactions such as water splitting.

258 materials depends on the efficiency of this redox reaction, such that damage can be inhibited by alt

259 t that in photosynthetic organisms, specific redox reactions sustain dark metabolism, with little imp

260 gested the presence of a novel cone-specific redox reaction that generates 11-cis-retinal from 11-cis

261 xide ((*)NO) and nitrite (NO(2)(-))-mediated redox reactions that activate PPARgamma at nanomolar con

262 O, was predicted to occur in the sequence of redox reactions that are coupled to an electron transpor

263 study opens up the possibility of accessing redox reactions that are outside the potential limits se

264 Photoinduced and native redox reactions that contributed to the photobleaching r

265 ticular the LSPR absorption, with reversible redox reactions that do not affect the semiconductor che

266 d chemically in the electrode via reversible redox reactions that involve multiple oxidation states o

267 hloroplasts is controlled by light-dependent redox reactions that target specific enzymes.

268 trahydrofuran (THF) furnishes smoothly, in a redox reaction, the (bisNHC)(Br)Al[Fe(CO)4] complex 3, i

269 acity of this bacterium to perform difficult redox reactions, thereby multiplying its value as a plat

270 gnal by electrically coupling a conventional redox reaction to a fluorogenic reporter reaction on a c

271 ed valence complex, which performs the third redox reaction to give the superoxo/aqua complex.

272 argest estuary.The potential contribution of redox reactions to acidification in coastal waters is un

273 First, it allows the two redox reactions to be carried out with existing chemistr

274 carbon has yet to be coupled with extrinsic redox reactions to develop rechargeable batteries.

275 is, in which solar photons are used to drive redox reactions to produce chemical fuel, is the central

276 mical reaction, such as a disproportionation redox reaction, to generate dilute zerovalent metal atom

277 Dehydration, carbonyl cleavage, and redox reactions turned out to have a large impact on the

278 in the many oxo group functionalizations and redox reactions typically seen with [CrO2]2+, [MoO2]2+ a

279 the role that vitamin K plays in biological redox reactions ubiquitous in key cellular processes, an

280 ry cathode materials have relied on cationic redox reactions until the recent discovery of anionic re

281 reductase (AKR), an enzyme that catalyzes a redox reaction using an NADPH cofactor.

282 When redox reactions were carried out during lactide polymeri

283 antibodies, and DNA, by blocking a solution redox reaction when molecules adsorb and block electrode

284 catalysis by ceria in both hydrogenation and redox reactions where hydrogen is involved.

285 o heteroatom (X)-controlled reversible SC-SC redox reactions whereby the Ge-templated framework reduc

286 allows the 2e(-)/2H(+) quinone/hydroquinone redox reactions while suppressing proton reduction in th

287 We show that the peptide undergoes a redox reaction with copper ions resulting in a disulfide

288 d in copper(I) sulfide (Cu2 S) NCs through a redox reaction with iodine molecules (I2 ), which formed

289 sed that the catalyst undergoes a reversible redox reaction with the substrates to produce a charge t

290 ex is still sufficiently high for a range of redox reactions with cellular species to occur.

291 ch a microbe frozen in ice can metabolize by redox reactions with dissolved small molecules such as C

292 This study investigates the impact of redox reactions with ferrous ions (Fe2+) on the colloida

293 uatic environments, where it participates in redox reactions with surrounding metals, organic compoun

294 terized methylene blue (MB)- and thiol-based redox reactions with the aim of designing an oxygen scav

295 s exhibiting a surface-controlled reversible redox reaction, with a fast heterogeneous electron trans

296 terized are involved in oxidation-reduction (redox) reactions, with the Sec residue located at their

297 rode simultaneously and to examine the local redox reactions within a droplet.

298 Cytochrome b6f catalyzes quinone redox reactions within photosynthetic membranes to gener

299 hate in the mitochondria by participating in redox reactions within the electron transport chain.

300 It is less clear, however, how redox reactions would contribute to acidification.