ライフサイエンスコーパス: redox state

1 e coordination geometry upon a change in the redox state.

2 protein to function as a sensor of cellular redox state.

3 tial but no changes in the NAD(P)H/NAD(P)(+) redox state.

4 for GSSG, only weakly affected the cytosolic redox state.

5 but differ with respect to the relevant iron redox state.

6 ransfer reactions, leading to the changes in redox state.

7 tors may be involved in sensing the cellular redox state.

8 ss requiring tight control of metabolism and redox state.

9 ates in either the Rh2(II,II) or Rh2(II,III) redox state.

10 h regulates NADP(H) homeostasis and cellular redox state.

11 rriers, which selectively alter the cellular redox state.

12 use the system to quantify the intracellular redox state.

13 direct, compartment-specific manipulation of redox state.

14 nusual additional stabilization of the Cu(I) redox state.

15 xygen species generation and preserving cell redox state.

16 ptic plasticity varies according to cellular redox state.

17 a 4Fe-4S cluster that may sense the cellular redox state.

18 t not by a more reduced cytoplasmic NADH/NAD redox state.

19 states rather than differences arising from redox state.

20 of yeast glycolysis depend on intracellular redox state.

21 stantial effects on tissue energy charge and redox state.

22 their electron-exchange capacities (EEC) and redox states.

23 gh solubility (>1 M) in all battery-relevant redox states.

24 m humic acid samples (1 g HA/L) of different redox states.

25 ed fluorescent probes that can sense general redox states.

26 single-molecule devices by controlling their redox states.

27 e relative ratio of the two different ligand redox states.

28 with substrates and antagonists in different redox states.

29 r knowledge on the diversity of exoplanetary redox states.

30 with spectroscopically determined molecular redox states.

31 olution, volatile compositions and planetary redox states(1-7).

32 he latter to increased hepatic mitochondrial redox state (+167%) and decreased plasma leptin (-45%) a

33 cterized, isostructural series spanning five redox states (2(2+), 2(+), 2, 2(-), 2(2-)) is unique in

34 The two redox states 3(*-) and 3(2-) retain the geared alpha and

35 oxidized Ir particle showed exclusively the redox state (+4), the Ir/IrOx/ATO system exhibited evide

36 , ground-state stabilization, and breadth of redox state accessibility), we prepared three electron-t

37 The redox state across all Cys peptides was shifted toward r

38 They set the cellular energy charge and redox state, act as allosteric regulators, modulate sign

39 nalysis, it is hypothesized that the quinone redox state acts as a feed-forward controller of the CBB

40 m through which changes in the intracellular redox state alter cardiac function.

41 ement of the CBPQT(4+) ring in its different redox states among these three potential recognition sit

42 e a measure of a cell's metabolic energy and redox state, among other processes.

43 2 in the IMS results in a more reduced Mia40 redox state and a delay in oxidative folding and mitocho

44 -energy azo pi* orbitals in the intermediary redox state and additional stabilization of 2 from struc

45 In the present study, changes in arsenic redox state and binding environment in these experiments

46 Mitochondrial dysfunction could alter the redox state and cellular levels of acetyl-CoA, resulting

47 Connections between redox state and complex behavior allow bacteria to link

48 t between experimental quantification of the redox state and device simulation reveals that changes i

49 Quantification of the redox state and EEC of adsorbed NOM is thus crucial for

50 mitochondria, resulting in altered cytosolic redox state and energy deficiency.

51 erse stimuli such as small molecules, light, redox state and gases.

52 isms, which link cytoskeleton remodeling and redox state and impact epithelial plasticity and myofibr

53 However, its contribution to redox state and inflammation in the diabetic heart remai

54 in the ER, maintenance of the ER glutathione redox state and levels likely depends on ER glutathione

55 ron transport is required to ensure adequate redox state and lumen pH.

56 provide an indirect measure of the cellular redox state and may be used as an early indicator of the

57 amined for cell cytotoxicity, proliferation, redox state and migration using mouse embryonic fibrobla

58 nfluenced by ecological selection imposed by redox state and mineralogy, possibly due to effects on n

59 hese findings are the first to link cellular redox state and mitochondrial metabolism directly to sle

60 Fe-S) clusters, metal complexes that control redox state and mitochondrial metabolism, have been link

61 al energy production through the NAD(+)/NADH redox state and modulating cellular signaling processes

62 Reduced levels of proteins regulating redox state and neuronal stress markers, as well as incr

63 lain how CP12 integrates responses from both redox state and nicotinamide dinucleotide availability t

64 ROS alter the abundance, thiol redox state and oligomerization of the RCD1 protein in v

65 y and deliver nitric oxide with a controlled redox state and rate is crucial for its pharmaceutical/m

66 1) of Arabidopsis is a sensor of the plant's redox state and regulates transcription of core circadia

67 ic compounds, which hence impact the aquifer redox state and the carbon fate.

68 al deficiency, we analyzed the mitochondrial redox state and the mitochondrial membrane potential in

69 copper and sulfur, notably by changing their redox state and, as a consequence, their ability to bind

70 e coordinated metal ions in their respective redox states and electrical neutrality, as well as relat

71 olic profiles, controlled by their different redox states and expression of Activating Transcription

72 Uranium redox states and speciation in magnetite nanoparticles c

73 s at excessive levels, leading to unbalanced redox states and to potential oxidative stress, which ca

74 Conclusion: (64)Cu-ATSM signal reflects redox state, and altering redox state impacts (64)Cu-ATS

75 activity of TH is modulated by the cellular redox state, and daily rhythms of redox balance in the v

76 lar metabolism, including on the metabolome, redox state, and glucose utilization.

77 a previously unrecognized effect on cardiac redox state, and help to refine the design of impending

78 ative phosphorylation programing, a shift in redox state, and high plasticity for metabolic adaptatio

79 ase is finely regulated by the intracellular redox state, and it is inhibited under stress conditions

80 lated and fine-tuned by the choice of metal, redox state, and ligand(s), (ii) the high directionality

81 he redox potential of a molecule, change its redox state, and thus allow the manipulation of single m

82 ed altered cytoplasmic and mitochondrial pH, redox states, and mitochondrial membrane potential (Delt

83 Rhythmic oscillations in cellular redox state are another universal feature of circadian t

84 nduced changes in immune cell metabolism and redox state are associated with CD4(+) T cell depletion,

85 ations show that changes in the quinone pool redox state are responsible for the apparent inorganic p

86 ibit considerable differences in dynamics of redox states are extracted by statistical machine learni

87 Salinity, pH, and redox states are fundamental properties that characteriz

88 contributions of the three different uranium redox states are quantified with the iterative transform

89 Specifically, homeostatic beta2AR redox states are vital toward agonist-induced cAMP forma

90 NMDAR function was due in part to an altered redox state as bath application of the reducing agent, d

91 io cholerae H-NOX may act as a sensor of the redox state as well as NO.

92 st, ABA and pyrabactin altered the vitamin C redox state at early stages of fruit development and mor

93 ns during ageing, whereas in the cytosol the redox state becomes more oxidizing with age.

94 drogen-bond donor to water539 (W539), the S0 redox state best describes the unusually short O4-OW539

95 ant nitrogen group that spans five different redox states between nitro and amine.

96 associated with restoration of intracellular redox state by Nrf2-related regulation of expression of

97 Correcting the highly oxidized cytosolic NAD-redox state by pyruvate supplementation restored serine

98 hat more subtle changes in the intracellular redox state can act as signals, eliciting responses with

99 a consecutive series of five, six, and seven redox states can be accessed in the resulting SC.7PF6 (0

100 The altered cellular redox state caused by the loss of Pim occurred as a resu

101 altered redox homeostasis and NAD(H) content/redox state control the phenotype of CI mutants and phot

102 nd a functioning D-cluster, involves precise redox-state control, and includes a two-step nickel-bind

103 Yet, how the intracellular redox state controls STING activation is unclear.

104 The large degree of separation between these redox states (DeltaE = 0.51 V, K(C) = 4.17 x 10(8)) allo

105 nize the bc1 complex and bind or unbind in a redox state-dependent manner.

106 short-circuit is effectively prevented by a redox-state-dependent organization of water molecules wi

107 Discoveries of redox-state-dependent protein kinase S-glutathionylation

108 Deranged cardiac metabolism and abnormal redox state during cardiac diseases foment arrhythmogeni

109 activation and changes in the intracellular redox state during mitosis and provide insights into how

110 osits of the Yangtze Sea to assess the ocean redox state during the Early Cambrian metazoan radiation

111 ctive molecules exhibiting either two stable redox states (e.g., ferrocene and quinones) or more than

112 rocene and quinones) or more than two stable redox states (e.g., metalloporphyrins, polyoxometalates,

113 Flux appeared to be regulated by redox state, energy charge, and metabolite concentration

114 nt increase in the heart and liver cytosolic redox state, estimated from the [lactate]:[pyruvate] rat

115 endent activation/inhibition and active site redox states for various conditions.

116 Changes in redox state have been shown to influence or trigger chro

117 Different redox states have a profound effect on domain orientatio

118 The Ir(III,III), Ir(IV,IV) and Ir(IV,V) redox states have been computationally studied both with

119 t of residues around heme a changes with the redox state, hence suggesting that the H channel could p

120 SM signal reflects redox state, and altering redox state impacts (64)Cu-ATSM metabolism.

121 lly encoded in vivo sensors reporting on the redox state in an organelle-specific manner, we show in

122 Therefore, the role of apoplastic redox state in controlling aphid infestation was explore

123 relationship between (64)Cu-ATSM signal and redox state in human cervical and colon cancer cells.

124 but its role in the regulation of myocardial redox state in humans is unknown.

125 NAD(+) and NADH contents and the NAD(+)/NADH redox state in intact human brain.

126 mediate of cytochrome c oxidase is the first redox state in its catalytic cycle, where proton transfe

127 ed protocol to image and monitor NAD(+)/NADH redox state in living cells and in vivo using a highly r

128 tween Th2 polarization and alteration of the redox state in LP-BM5 infection is presented.

129 iphasic effect on the mitochondrial NADH/NAD redox state in mouse hepatocytes.

130 tudying the intracellular NAD metabolism and redox state in normal and diseased human brain or other

131 a shift towards a more reduced protein thiol redox state in old hearts.

132 differential roles of NOXs in modulating the redox state in response to different shear stresses, whi

133 salt stress tolerance by regulating the GSH redox state in rice.

134 enabled by (i) its ability to stabilize this redox state in solution and (ii) the production and secr

135 ence of taurocholate, as compared with their redox state in the absence of taurocholate.

136 were due to differences in slice health, the redox state in the auditory cortex was assessed by measu

137 ge, into the cellular NAD concentrations and redox state in the brains of healthy volunteers.

138 mediated by epigenetic re-programming of the redox state in the CB chemosensory reflex pathway.

139 Likewise, the redox state in the cytosol and the ER change in an oppos

140 plastoquinone (PQ) pool into a more reduced redox state in the dark caused an enhanced LHCII phospho

141 p-ocean oxygenation.The evolution of oceanic redox state in the past is poorly known.

142 he bonding in solid CP 3 involves noninteger redox states in a resonance hybrid repeat unit best form

143 As the distribution of protonation and redox states in a system is associated with the pH and r

144 s opportunities for evaluating intracellular redox states in biochemical investigations.

145 pic investigations on purified SH in various redox states in combination with density functional theo

146 nd electrochemically reversible one electron redox states in organic media, but in water, the fourth

147 us to obtain real-time live cell imaging of redox states in TfR1-mediated endocytosis, attesting a r

148 Redox states in the auditory cortex of young and aged an

149 ntercellular microenvironment, including the redox state, in regulating antiviral innate immune respo

150 encode enzymes that help to control cellular redox state, including members of the sod3 and nqo1 gene

151 disease stage, all of which affect the thiol redox state, including tHcy.

152 Nlrp3(-/-) macrophages presented a protected redox state, increased maximum and reserve oxygen consum

153 nd elucidation of the mechanisms whereby the redox state influences circadian regulation.

154 ects of cardiac biology including myocardial redox state, intracellular Ca(2+) cycling, the electroph

155 that Cu-ATSM signal is dependent on cellular redox state, irrespective of hypoxia.

156 Here we show that the mantle redox state is central to the chemical composition of at

157 A balanced redox state is critical for proper healing.

158 Because competing redox state is known to drive isotopic fractionation, we

159 r quantifying intracellular NAD contents and redox state is limited to a few in vitro or ex vivo assa

160 )] model cluster in its one-hole (S = (1)/2) redox state is thoroughly characterized.

161 ectronic and geometrical features in various redox states, it is established that, depending on wheth

162 conformational forms in two different flavin redox states; (iv) reactivity of the reduced FMN domain

163 with difficult-to-treat asthma, the cysteine redox state might represent a potential therapeutic targ

164 o yield a thermodynamically constrained four-redox-state model of E3 that simulates pH-dependent acti

165 ing key influence on Earth's climate and the redox state of (sub)surface Earth.

166 Quantification of the redox state of 1098 Cys residues using OxICAT revealed t

167 GAPDH and PRK are coregulated by the redox state of a conditionally disordered protein CP12,

168 icroscopy (SECM) to in situ characterize the redox state of a single cardiomyocyte in terms of the ap

169 These data suggest that the redox state of adipocytes controls the development of ur

170 These data suggest that the redox state of bacteria during infection differs signifi

171 ach presented here allows observation of the redox state of both metal centers, a direct read-out of

172 However, the relationship between the redox state of cardiomyocytes and their mechanical micro

173 ationship between mechanical factors and the redox state of cardiomyocytes.

174 act as oxidants to balance the intracellular redox state of cells in anoxic biofilm subzones.

175 s assessed by measuring 29 cytokines and the redox state of circulating albumin (HNA2), a marker of s

176 asured Kd values are highly dependent on the redox state of CPR.

177 loss of kinase activity suggesting that the redox state of Cys-246 and Cys-266 is a critical determi

178 arging state of tRNA but is regulated by the redox state of cytochrome c.

179 he steady-state level of ROS, as well as the redox state of each compartment, is different at any giv

180 thermore, the derivation of the quantitative redox state of each TM in each color shows that the cont

181 The redox state of Earth's convecting mantle, masked by the

182 Asn378 side chain, that is modulated by the redox state of FAD.

183 Alteration of the redox state of FAD4 or PRXQ through site-directed mutage

184 rature can also be influenced by varying the redox state of ferrocene in the polymer main chain.

185 By switching the redox state of ferrocenyl units - separately or in a coo

186 al mass transfer calculations to predict the redox state of fluids generated during serpentinite dehy

187 tion in S47 cells; this is due to an altered redox state of GAPDH in S47 cells that inhibits its abil

188 roup of heme a3 and, to a lesser degree, the redox state of heme a and protonation state of Glu286.

189 l oxidized the subarc mantle, increasing the redox state of island arc parental melts, and thus igneo

190 imal diversification but also influenced the redox state of island arc rocks, which are building bloc

191 ors the electron transport chain through the redox state of its FAD cofactor.

192 d that the DIDS inhibitor does not alter the redox state of MitoNEET.

193 These results demonstrate that the redox state of noninnocent Z-ligands can be used to cont

194 rolling a tetrazine ligation by changing the redox state of one of the reactants.

195 carboxysomes in the cell correlates with the redox state of photosynthetic electron transport chain.

196 al quenching in the dark, which measures the redox state of Q(A) within PSII without any of the compl

197 chanism, in which the interdependence of the redox state of QA and the binding by HCO3(-) regulates a

198 vicinity of a nuclear repository control the redox state of radionuclides, which in turn has a strong

199 The possibility of tipping points in the redox state of sediments and oceans, which allow large a

200 ma oceans may have profound influence on the redox state of subsequently formed mantles and the overl

201 The redox state of the "remote" metal (Ni) modulates the hyd

202 rce microscopy (AFM) to demonstrate that the redox state of the [4Fe4S] clusters regulates the abilit

203 The reduced redox state of the active-site copper and not the subseq

204 re is no relationship with the stability and redox state of the administered compounds and that, if t

205 pe ratios are a sediment paleo proxy for the redox state of the ancient ocean.

206 The results presented indicate that the redox state of the apoplast has a profound influence on

207 embled species is actuated upon changing the redox state of the bipyridium units involved in the tect

208 past reports, the catalytically active metal redox state of the catalyst has remained under debate.

209 athways, specifically those sensitive to the redox state of the cell.

210 ips1, but this process is independent of the redox state of the chloroplast.

211 e role of the plastid signal may perform the redox state of the compounds on the acceptor-side of PSI

212 In vitro data show that the redox state of the disulfide bond affects S. aureus biof

213 lectrochemically switched via control of the redox state of the dye.

214 conditions where we are able to control the redox state of the enzyme precisely.

215 the nematode Caenorhabditis elegans that the redox state of the ER is subject to profound changes dur

216 aggregation may be coupled to changes in the redox state of the G93A and A4V mutants upon mild oxidat

217 This effect was caused by an altered redox state of the gamma-subunit under low, but not high

218 llular bioenergetics that was related to the redox state of the iron.

219 m chemical calculations demonstrate that the redox state of the ligands determines the switching stat

220 shell structure for 2, in agreement with the redox state of the ligands.

221 ed the differential roles played by both the redox state of the mNT cluster and dioxygen in cluster t

222 We monitor the redox state of the molecule by tracking its characterist

223 The redox state of the neural progenitors regulates physiolo

224 e are no direct data constraining either the redox state of the ocean or marine biological productivi

225 strated by electrochemically controlling the redox state of the pendent diimide unit of the molecule

226 hanism between intermediate metabolites, the redox state of the plastid and the expression and bindin

227 We discovered that PTOX helps control the redox state of the plastoquinone (PQ) pool in these orga

228 een PSII and PSI, which was sensitive to the redox state of the plastoquinone pool and to the NaCl co

229 ht harvesting complexes II, depending on the redox state of the plastoquinone pool.

230 We further show that the redox state of the PQ pool in etioplasts might control c

231 Our simulations also reveal that the redox state of the quinone pool is the primary determina

232 ween photosynthesis, CO(2) fixation, and the redox state of the quinone pool.

233 NPQ, and the NPQ rate is independent of the redox state of the reaction center.

234 chael reaction whose kinetics depends on the redox state of the redox polymer catalyst, we show that

235 ion of PSI in the mutant correlates with the redox state of the stroma rather than photodamage and th

236 ent with our proposal for an increase in the redox state of the subarc mantle between 800 and 400 Ma

237 result, analytical methods that preserve the redox state of the tissue are urgently needed for refine

238 Altering the redox state of the triiron core resulted in significant

239 could not unequivocally ascertain the final redox state of this residue.

240 tine structures of the Fe(III) and Fe(IV) =O redox states of a B-type DyP.

241 ract superoxide with equal affinity (at both redox states of copper) during diffusion-limited reducti

242 at distinct rates that are dependent on the redox states of FBD.

243 comparing the chemical space of all possible redox states of linear-chain carbon molecules to the cor

244 Obtaining structures of intact redox states of metal centers derived from zero dose X-r

245 challenged by experimentally accessing both redox states of metalloproteins.

246 Although, it is clear that the redox states of proteins involved in plant growth and de

247 F-MS is a suitable separation method for the redox states of Pu, Np, and Fe.

248 roximately 5 ps, which leads to a mixture of redox states of the acceptor ligand.

249 dA to 1.98 A resolution and those of several redox states of the enzyme to different resolutions.

250 (-) ligands of the (2FeH) site for different redox states of the H-cluster.

251 rmediate, which is characterized by specific redox states of the metal centers and a distinct protein

252 Several redox states of the octairon cluster are accessible, as

253 Individual redox states of the reductase CntB and the catalytic com

254 e of microsolvation in stabilizing different redox states of Y(D) and facilitating oxidation or media

255 y induce changes in the reduction/oxidation (redox) state of the photosynthetic electron chain that a

256 hat allowed us to monitor alterations in the redox-state of epithelial cells at different stages of m

257 he most simple and basic way of altering the redox-states of organic molecules.

258 EDC), electron accepting capacity (EAC), and redox state) of HS.

259 could be used in the study of the effect of redox states on living systems, and lead to clinical pho

260 The redox state, organic complexation, and phase (dissolved

261 l (2AG), is tightly controlled by the cell's redox state: oxidative signals such as hydrogen peroxide

262 2)GPI exists in two almost equally populated redox states: oxidized, in which all the disulfide bonds

263 Based on the lipoate redox state, PfLipL1 either functions as a canonical lip

264 en different oligomeric states, depending on redox state, pH, posttranslational modifications, and ot

265 ignals derived from perturbations in plastid redox state, plastid gene expression, and tetrapyrrole b

266 transitions of 2-Cys peroxiredoxins such as redox state, post-translational modifications, and pH.

267 edox-active molecules often display multiple redox states, precise control of a molecule's redox pote

268 ly expressing beta2AR, we show that receptor redox state profoundly influences beta2AR orthosteric li

269 henalenyl radical, (Py)Cn(*) exists in three redox states, (Py)Cn(+), (Py)Cn(*), and (Py)Cn(-), in a

270 nhibited respiration and reduced the NAD(P)H redox state, pyridine nucleotide redox states were unaff

271 Cellular redox states regulate the balance between stem cell main

272 change in the energy level alignment of the redox states relative to the Fermi level of the electrod

273 certain specific aspects, like the endosomal redox state, remain less characterized.

274 rich redox chemistry with 7 and 8 observable redox states, respectively.

275 Rescue of the redox state restored responsiveness to TNF-alpha in KRIT

276 it of stoichiometric control over the ligand redox states resulted in synthesis of the reduced framew

277 t with a previously inferred shift in marine redox states, severe perturbations to Earth's climate sy

278 s in organic media, but in water, the fourth redox state shows an unstable nature.

279 rturbations that alter oxygen consumption or redox state support a model in which surfactin-mediated

280 The ligand redox state (TAML(red) or TAML(sq)) determines whether m

281 er reorganization energy and more accessible redox states than the monomeric analogues.

282 ) appear to reflect alterations in the serum redox state that resulted in reduced adduct levels in sm

283 y of this system across three highly reduced redox states that correlate with unusually high Enemark-

284 strate that the catalytic cycle involves two redox states, the three- and five-electron reduced forms

285 t system that serves to balance the cellular redox state through the recycling of photosynthetic NADP

286 However, the mechanisms linking redox state to AF are not well understood.

287 dly altered hepatic mitochondrial fluxes and redox state to promote ketogenesis rather than synthesis

288 ia and changes the mitochondrial NADH/NAD(+) redox state to support ATP production.

289 Transition from a broad range of redox states to a uniformly reducing cytosol facilitates

290 d to be controlled exclusively by the enzyme redox state under physiological conditions.

291 oxide reductase: activity in the 4Cu(I) :1S redox state, use of a second-sphere proton donor, and re

292 We altered redox state using drug strategies and single-gene mutati

293 Not only does PFE allow control of redox states via the electrode potential but also the im

294 ity, Akt activity, and cytosolic NADH/NAD(+) redox state were temporally linked in individual cells a

295 the NAD(P)H redox state, pyridine nucleotide redox states were unaffected by pharmacological or genet

296 hich associates in its bisradical dicationic redox state with the methyl viologen radical cation (MV(

297 ht into the correlation of the intercellular redox state with the regulation of antiviral innate immu

298 lopment of molecules that can switch between redox states with paired and unpaired electrons is impor

299 Furthermore, they have an imbalanced redox state, with downregulation of the antioxidant enzy

300 ping metal turnover, protein association and redox state within these structures.