ライフサイエンスコーパス: redox-sensitive

1 ajor phosphatase revealed that the enzyme is redox sensitive.

2 re prevented, suggesting that the pathway is redox-sensitive.

3 smooth muscle, have certain members that are redox-sensitive.

4 neither the AP1/Ets regulatory sites nor the redox sensitive (-1607/2G) site in MMP-1 promoter are in

5 We find that the redox-sensitive [2Fe-2S] cluster protein mitoNEET gates

6 substrate-binding domain of FBXL5 contains a redox-sensitive [2Fe-2S] cluster that, upon oxidation, p

7 rombogenicity through angiotensin II-induced redox-sensitive activation of mitogen-activated protein

8 that the DNA replication machinery may have redox-sensitive activities.

9 ent increase in oxidative damage followed by redox-sensitive adaptations in multiple tissues.

10 hypoxia may have an independent influence on redox-sensitive adaptive responses to exercise and exerc

11 sformation may be mediated, in part, through redox-sensitive AKT signal transduction pathways by up-r

12 g the crucial role of these highly conserved redox-sensitive amino acid residues for P-protein activi

13 These interactions are controlled by a redox-sensitive amino acid, cysteine 10 of Pex5, which i

14 By targeting redox-sensitive amino acids in signaling proteins, the N

15 idative stress response that reactivates the redox-sensitive AMPK and activates the redox-sensitive s

16 We find that cluster formation is redox sensitive and can be blocked by the antioxidant Mi

17 or barrier to a cure for AIDS is exquisitely redox sensitive and could be selectively targeted by Trx

18 Furthermore, we showed that UL32 is redox sensitive and identified two highly conserved oxid

19 menon that is generally assumed to be mainly redox sensitive and promoted by anoxic conditions.

20 on also led to oxidative inactivation of the redox-sensitive and ERK-specific phosphatase, DUSP3/VHR,

21 suggest that ubiquitination of lung ENaC is redox-sensitive and may have significant implications fo

22 Zn/Fe(T) (where Fe(T) = Fe(2+) + Fe(3+)) is redox-sensitive and retains a memory of the valence stat

23 We report that the Nedd8 pathway is redox-sensitive and that under oxidizing conditions Nedd

24 Two novel prodrug polymers POEG-b-PSSDas (redox-sensitive) and POEG-b-PCCDas (redox-insensitive),

25 t mTORC2 complex stability and activation is redox sensitive, and further defined a novel role for p2

26 oderm: since the activity of bZIP factors is redox sensitive, and the initial polarization of oral vs

27 Zn(2+)-LpxC, the activity of Fe(2+)-LpxC is redox-sensitive, and a time-dependent decrease in activi

28 Kv1.5 is widely reported to be redox-sensitive, and the channel possesses 6 potentially

29 vide novel insights for targeting endogenous redox-sensitive antioxidant pathways to ameliorate the d

30 , and sequence analyses, we propose that the redox-sensitive APSK evolved after bifurcation of the su

31 Activation of p38 was redox-sensitive as H(2)O(2) caused p38 phosphorylation,

32 anges cellular metabolism and thus activates redox-sensitive as well as oxygen-dependent signal trans

33 Thus, the SMN complex is a redox-sensitive assemblyosome and an ROS target, suggest

34 or TXNIP increases catalytic activity of the redox-sensitive ATG4B cysteine endopeptidase, leading to

35 The interaction is redox sensitive because NADH is more efficient than the

36 Dimerization is also redox sensitive, being completely abolished by the forma

37 By contrast, the redox-sensitive biosensor roGFP2 was rapidly oxidized in

38 This process appears to be redox-sensitive, but the precise signaling mechanism by

39 related ODA light chains LC3 and LC5 and the redox-sensitive Ca2+ -binding subunit of the docking com

40 cal production as measured by Quest MRI, and redox-sensitive calcium dysregulation as measured by man

41 Here we report a redox-sensitive calibration to determine the oxidation s

42 X4-specific NADPH-driven ROS production, and redox-sensitive CaMKII activation.

43 ere we report that TRPM2, a nonselective and redox-sensitive cation channel, inhibited ROS production

44 These data support a mechanism whereby redox-sensitive CD40-CD40L interactions induce activatio

45 The redox-sensitive character of enriched metals supports em

46 DX-FTR-TRXs pathway allows the regulation of redox-sensitive chloroplast enzymes in response to light

47 tric oxide (NO) synthesis, eNOS requires the redox-sensitive cofactor tetrahydrobiopterin (BH(4)); ho

48 er the speciation, and thus the mobility, of redox-sensitive contaminants including Cr(VI) is of grea

49 " moieties, polyethylene glycol (PEG) units, redox-sensitive cross-linker, and tumor-specific targeti

50 f alternate functional motifs such as 'KGD', redox-sensitive Cys and hydrophobic Trp/Phe residues arg

51 TRPA1 activation was dependent on essential redox-sensitive cysteine and lysine residues within N-te

52 hydrophobic clamp, including insertion of a redox-sensitive cysteine pair, confirms the importance o

53 ole in the phosphorelay signaling, where its redox-sensitive cysteine residue may provide additional

54 the C797S variant, confirming Cys-797 as the redox-sensitive cysteine residue that regulates kinase a

55 eukaryotic protein kinases, is regulated by redox-sensitive cysteine residues in the kinase domain.

56 Modification of the redox-sensitive cysteine residues on Keap1 disrupts the

57 ochemically, confirming that the C-terminal, redox-sensitive cysteine residues reside within the inte

58 ures of the Aurora A kinase domain delineate redox-sensitive cysteine residues that, upon covalent mo

59 fies the affected proteins and defines their redox-sensitive cysteine(s).

60 Within these compartments, redox sensitive cysteines play a crucial role in regulat

61 Proteins regulated through redox-sensitive cysteines have been characterized but sp

62 ANT1 also contains redox-sensitive cysteines that may be targets for modifi

63 Both proteins employ redox-sensitive cysteines, whose oxidation status direct

64 other cellular components through energy- or redox-sensitive cytosolic kinase signalling and transcri

65 try and secondary ion mass spectrometry) and redox-sensitive detrital grains--reveal that the origina

66 te that CopZ has a strong propensity to form redox-sensitive dimers via two conserved cysteine residu

67 (D,L-lactide-co-glycolide) polymeric core by redox-sensitive disulfide bond, while TET was physically

68 pecific interhelical isopeptide bonds as the redox-sensitive disulfide surrogate.

69 so reveals the presence of a solvent-exposed redox-sensitive disulphide bridge, unique among the subt

70 high drug loading efficiency, stability and redox-sensitive drug release profiles.

71 scovered that a colorimetric sensor array of redox sensitive dyes can detect even very low levels of

72 ts and mitochondrial membrane potential- and redox-sensitive dyes are used to define RSV's impact on

73 levels were monitored with the fluorescent, redox-sensitive dyes CM-H2DCFDA and MitoSOX Red.

74 xygen species, as shown by the activation of redox-sensitive dyes.

75 gII-activated sources of ROS, the downstream redox-sensitive effectors, Ang-(1-7)-stimulated increase

76 s an integrated redox "hub" linking upstream redox-sensitive effects of BH4 and glutathione with redo

77 microorganisms can respire compounds of this redox-sensitive element to reap energetic gains.

78 To trace the distribution of redox sensitive elements (e.g., Fe, Mn), Diffusive Equil

79 l iron may control the sorption mechanism of redox sensitive elements on the surface of clay minerals

80 ed the co-occurrence of four health-relevant redox-sensitive elements (U, As, V, and Cr) in 1494 grou

81 This work shows that redox-sensitive elements structurally incorporated withi

82 monstrates a degree of co-occurrence between redox-sensitive elements, which may pose additional risk

83 channels to H2S required the presence of the redox-sensitive extracellular residue H191, which is als

84 hibitory action requires the presence of the redox-sensitive, extracellular region of the channel whi

85 NF-E2-related factor 2 (Nrf2), a redox sensitive factor, provides cellular defenses again

86 e oxygen species (ROS) were detected using a redox-sensitive fluorescent dye, a cytochrome c reductio

87 In this issue, Merksamer et al. exploit a redox-sensitive fluorescent protein to monitor the envir

88 f benzoxazoles is compatible with a range of redox-sensitive functional groups.

89 Expression of the redox-sensitive gap junctional protein Cx43 (Connexin 43

90 thelial cells resulting in the inhibition of redox-sensitive genes.

91 to evaluate in vivo RBC redox status using a redox sensitive GFP (roGFP2) sensor under control of a b

92 by a redox-based topology assay (ReTA) with redox-sensitive GFP and confirmed by a protease protecti

93 Two-photon imaging of redox-sensitive GFP corroborated the finding that mitoch

94 geted viral gene transfer vectors expressing redox-sensitive GFP fused to sensor domains to measure H

95 Taken together, the use of redox-sensitive GFP inside Salmonella significantly adva

96 Redox-sensitive GFP revealed that gsh2 seedlings maintai

97 Furthermore, by targeting the redox-sensitive GFP sensor to various subcellular locali

98 itoPark mice), at the same time expressing a redox-sensitive GFP targeted to the mitochondrial matrix

99 n this study, we describe a system that uses redox-sensitive GFP to nondisruptively measure real-time

100 uence the redox status of cells, we utilized redox sensitive GFP2 (roGFP2) to determine the redox sta

101 2)) augments cellular ROS as detected by the redox-sensitive green fluorescent protein (roGFP) but do

102 We tested the utility of redox-sensitive green fluorescent protein (roGFP)-based

103 orff-perfused hearts based on the use of the redox-sensitive green fluorescent protein 2, coupled to

104 iol redox status by mitochondrially targeted redox-sensitive green fluorescent protein and measuremen

105 g of the hepatic GSH redox potential using a redox-sensitive green fluorescent protein biosensor show

106 specific oxidation of mitochondria-targeted redox-sensitive green fluorescent protein probe.

107 ings were corroborated by measurements using redox-sensitive green fluorescent protein, another prote

108 ) cytosolic oxidation (e.g. oxidation of the redox-sensitive Green fluorescent protein2 probe), (3) a

109 from the development of genetically encoded redox-sensitive green fluorescent proteins (roGFPs), whi

110 Using redox-sensitive green fluorescent proteins targeted to t

111 suggest that 6-TGNP can also react with the redox-sensitive GXXXCGK(S/T)C and GXXXXGK(S/T)C motif of

112 rn reacts with the Cys(20) side chain of the redox-sensitive GXXXCGK(S/T)C motif of RhoC to produce a

113 rm a disulfide adduct between 6-TGTP and the redox-sensitive GXXXXGK(S/T)C motif of Rac1.

114 Loss of NRF2 decreased the expression of the redox-sensitive histone deacetylase, HDAC4, resulting in

115 We also found that Cys-463 is redox-sensitive; in its reduced form, interaction with g

116 nder gene mutations in MDSs license a common redox-sensitive inflammasome circuit, which suggests new

117 Under such periodic changes many redox-sensitive inorganic contaminants undergo speciatio

118 A cysteine-null mutant FKBP12.6 retained redox-sensitive interaction with RyR2, suggesting that t

119 ive, and the channel possesses 6 potentially redox-sensitive intracellular cysteines.

120 inhibiting maturation processes dependent on redox-sensitive JNK and Wnt pathways.

121 In addition, HO-2 is a redox-sensitive K/Ca(2)-associated protein, and BVR is a

122 rious DNA duplex substrates and identified a redox-sensitive Ku-DNA interaction.

123 situ equilibrium redox titrations and thiol redox-sensitive labeling studies showed that the gamma s

124 involvement of the Trx1 inhibitor Txnip as a redox-sensitive ligand of NLRP3 as previously proposed.

125 llular compartments, influence the status of redox-sensitive macromolecules, and protect against oxid

126 ion of their potential for use in assembling redox-sensitive magnetic resonance imaging contrast agen

127 s and MCP1 release by endothelial cells in a redox sensitive manner via NFkappaB activation.

128 es intracellular CD40L and MCP1 release in a redox sensitive manner.

129 ubiquitin-mediated degradation by Keap1 in a redox-sensitive manner through modifications of distinct

130 e 15-Lox1-15(S)-HETE axis activates EGFR via redox-sensitive manner, which in turn mediates Src-Jak2-

131 hat enzymatic activity can be regulated in a redox-sensitive manner.

132 PK pathways, which in turn are controlled by redox-sensitive MAPK phosphatases (MKPs).

133 s of F. tularensis prevent the activation of redox-sensitive MAPK signaling components, NF-kappaB sig

134 MPs reduced NO release and increased ROS and redox-sensitive marker expression.

135 tive stress induced microglia activation and redox-sensitive matrix metalloproteinase 9 (MMP9) stimul

136 tivity, thereby raising the possibility that redox-sensitive mechanisms underlie amino acid-dependent

137 up on this possibility and found TRX to be a redox-sensitive mediator of TCA cycle flux.

138 rapamycin (TOR) revealed that it contains a redox-sensitive membrane anchor in its C terminus.

139 ry direct evidence of crystallization from a redox-sensitive metallic liquid phase in the deep mantle

140 ns of Hg and lesser amounts of As, and other redox sensitive metals to groundwater and surface water.

141 record expansion of the oceanic inventory of redox-sensitive metals and the growth of the marine sulp

142 Mn is one of the most abundant redox-sensitive metals on earth.

143 s with low affinity for organic matter, some redox-sensitive metals, and some metals with exceptional

144 agation of the reaction front is retarded by redox-sensitive mineral dissolution reactions and carbon

145 ic determinants of 2-OG levels, we uncover a redox sensitive mitochondrial lipoylation pathway, depen

146 CHCHD4, which is the central component of a redox-sensitive mitochondrial intermembrane space import

147 e to oxidative stress and identified a novel redox-sensitive mitochondrial TXNIP-Trx2-ASK1 signaling

148 oxidative stress, our studies focused on the redox-sensitive mitogen-activated protein kinase kinase

149 The small heat-shock protein HSP27 is a redox-sensitive molecular chaperone that is expressed th

150 es a previously undefined mechanism by which redox-sensitive molecules signal via apoptotic pathways

151 The redox-sensitive MOPC absorbances ( approximately 465-630

152 ocal inhibition of Rho GTPase activity via a redox-sensitive motif.

153 le Mn coordination complex with utility as a redox-sensitive MR probe.

154 d C-7 compounds were identified as promising redox-sensitive MRI contrast agents.

155 t the TSC complex plays an important role in redox-sensitive mTORC1 regulation and argues for the act

156 HMGB1 is a ubiquitous redox-sensitive multifunctional protein that serves as b

157 alters the abundance and oxidation state of redox-sensitive multiple proteins and that these changes

158 Here, we synthesized a redox-sensitive nano-micelle formed by hyaluronic acid (

159 We will then provide a synopsis of the redox-sensitive NF-B and PGC-1alpha signalling pathways

160 mediated production of ROS and activation of redox-sensitive NF-kappaB were PKCdelta dependent, sugge

161 hly regulated defense systems, including the redox sensitive Nrf2-Keap1 signaling pathway involved in

162 uclear factor-kappaB p65, a component of the redox-sensitive nuclear transcription factor nuclear fac

163 rved in typical 2-Cys Prxs, TpAhpC undergoes redox-sensitive oligomer formation.

164 Using a transgenic mouse expressing a redox-sensitive optical probe targeted to the mitochondr

165 One candidate is the redox-sensitive oxidoreductase TMX1 that is enriched on

166 ever, the geochemical behavior of this toxic redox-sensitive oxyanion in anoxic environments is poorl

167 unx2 in diabetes mellitus is regulated via a redox-sensitive pathway that involves a direct interacti

168 s induced by air pollution are activation of redox-sensitive pathways and a role for antioxidants in

169 and adipose tissue/adipocytes and focused on redox-sensitive pathways, Rho kinase activity, and prote

170 oth NO and ROS modulate inflammation through redox-sensitive pathways.

171 l major classes promoted accumulation of the redox-sensitive phenazine pyocyanin (PYO).

172 inducing MAPK p38alpha, belong to a group of redox-sensitive phosphatases (protein tyrosine phosphata

173 atic stellate cell (HSC) migration through a redox-sensitive, PI3K-dependent pathway.

174 ries and describe novel mechanisms involving redox-sensitive PKG-1 and Rho kinase.

175 ed hydrogen peroxide, activation of vascular redox-sensitive PKG-1, and downregulation of Rho kinase

176 g flow cytometry, oxidative stress using the redox-sensitive probe dihydroethidium, tissue factor act

177 The fluorescence of the redox-sensitive probe roGFP increased during [Ca(2+)]mt

178 obial denitrification (and potentially other redox-sensitive processes) that could improve water qual

179 s upon IL-4 treatment suggests more than one redox-sensitive protein implicated in this pathway.

180 nd protein interaction "social network" of a redox-sensitive protein in cells with high temporal reso

181 decreased thrombin-induced activation of the redox-sensitive protein kinases (Janus kinase 2, Akt, an

182 We utilized a ratiometric redox-sensitive protein sensor (heat shock protein 33 fl

183 ication of specific cysteine residues within redox-sensitive protein targets, including Cys797 in the

184 DJ-1 is a redox-sensitive protein with multiple roles in cell home

185 These results indicate that NS is a highly redox-sensitive protein.

186 mediated post-translational modifications of redox-sensitive proteins are postulated as a key mechani

187 However, little is known about redox-sensitive proteins in guard cells and how they fun

188 essential E. coli genes encode one-third of redox-sensitive proteins, a finding that might explain t

189 um proteome and identified approximately 300 redox-sensitive proteins.

190 n is largely dependent on the development of redox-sensitive proxies, many of which remain unexplored

191 asuring the oxidation state distribution for redox sensitive radionuclides and other metal ions is ch

192 have a significant impact on the mobility of redox-sensitive radionuclides such as Tc.

193 bsequently, influence the oxidation state of redox-sensitive radionuclides.

194 )Tc-DTPA as noninvasive imaging probes for a redox-sensitive radiotracer and a conservative flow trac

195 METHODS AND We used a novel, redox-sensitive, ratiometric fluorescent protein sensor

196 We present integrated measurements of redox-sensitive ratios of oxidized iron to total iron (F

197 In contrast, redox-sensitive reactions are clearly impacted as seen i

198 ogen cycling, which involves several coupled redox-sensitive reactions.

199 on the development of a genetically encoded redox-sensitive red fluorescent protein (rxRFP).

200 ryonic fibroblast cells, suggesting that the redox-sensitive regulation of mTORC1 occurs independent

201 In this study, we show that the redox-sensitive regulation of mTORC1 occurs via Rheb but

202 y and conserved cysteine provides an unusual redox-sensitive regulation to an enzyme functioning in b

203 conclusion, we identified MKP-1 as a central redox-sensitive regulator of monocyte adhesion and migra

204 gh-mobility group box 1 protein (HMGB1) is a redox-sensitive regulator of the balance between autopha

205 cystathionine beta-synthase (CBS) acts as a redox-sensitive regulator that impairs CBS activity upon

206 difications on Keap1 protein, one of several redox-sensitive regulators of the Nrf2-ARE axis.

207 lar ROS influences the ERK pathway through a redox-sensitive regulatory circuit.

208 demonstrate that caspase-1 and Prdx4 form a redox-sensitive regulatory complex via caspase-1 cystein

209 disulfide proteome, a structural group and a redox-sensitive regulatory group, with the latter having

210 used to quantify site-specific oxidation of redox-sensitive residues of hPHPT1.

211 have tentatively named the protein RsrR for Redox sensitive response Regulator.

212 effect may become critical in volatile-rich, redox sensitive rocks such as carbonate-rich lithologies

213 Cytosol-targeted, redox-sensitive roGFP1 and imaging microscopy showed tha

214 teins in vivo by use of live cell imaging of redox-sensitive S3roGFP.

215 Empirically, sustained expression of the redox-sensitive S70pBcl2 prevents oxidative stress-induc

216 ely generating 8-oxo-7,8-dihydroguanine at a redox-sensitive sequence such as GGG.

217 Overall, we characterized a novel, redox-sensitive Sesn2/Pdgfrbeta suppressor pathway that

218 issues throughout the body and activate many redox-sensitive signal transduction and gene expression

219 S, we investigated the effects of 4-OH-E2 on redox-sensitive signal transduction pathways.

220 itoNEET suggest that it may participate in a redox-sensitive signaling and/or in Fe-S cluster transfe

221 nfected macrophages to prevent activation of redox-sensitive signaling components that ultimately res

222 on affects skeletal muscle's performance and redox-sensitive signaling during the inflammatory and re

223 d H2O2 production resulted in disturbance of redox-sensitive signaling including Akt and MAPKs pathwa

224 induced increase in ROS production triggered redox-sensitive signaling mechanism emanating from the c

225 spectrometry-based approach to elucidate the redox-sensitive signaling network (redoxome) mediating t

226 Numerous redox-sensitive signaling pathways exist in muscle inclu

227 cxcl8 gene expression, via the activation of redox-sensitive signaling pathways, and further point ou

228 tentially because of a blunted activation of redox-sensitive signaling pathways.

229 ctive oxygen species, as well as to regulate redox-sensitive signaling pathways.

230 -glutathionylation have fueled discussion of redox-sensitive signaling.

231 This review will highlight two important redox sensitive signalling pathways that contribute to R

232 hem (reactive oxygen species, ROS) stimulate redox-sensitive signalling pathways to modify the cellul

233 duced (i) ROS generation, (ii) activation of redox-sensitive signalling pathways, and (iii) ROS stres

234 sensitivity was mediated by an extracellular redox-sensitive site, which was also highly sensitive to

235 e heads, temperatures, and concentrations of redox-sensitive species, iomeprol and 15 of its transfor

236 n that wound-induced H2O2 is detected by the redox-sensitive Src family kinase (SFK) Lyn within the r

237 s the redox-sensitive AMPK and activates the redox-sensitive stress kinase JNK.

238 This reaction is regulated by redox-sensitive surface thiols, cysteine 55 and 46, whic

239 m, stabilize Rgg conformation, or serve as a redox-sensitive switch.

240 n of specific cysteine residues found within redox-sensitive target proteins.

241 induced by reactive oxygen species (ROS) on redox-sensitive targets such as zinc finger proteins pla

242 116 ppb) O(3) concentrations was examined by redox-sensitive thiol labeling, mass spectrometry, and t

243 oxidant stress, confirming that Cys405 is a redox-sensitive thiol that is necessary for ET(B)-eNOS s

244 Intriguingly, we found redox-sensitive thiols in numerous enzymes composing the

245 also show that the FAD 2'-OH group acts as a redox-sensitive toggle switch that controls PutA-membran

246 e zinc center of Hsp33 appears to act as the redox-sensitive toggle that adjusts the thermostability

247 Given the coupling between redox-sensitive trace element cycles and planktonic prod

248 Here we present iron-speciation, redox-sensitive trace element, and nitrogen isotope data

249 ion is consistent with crustal abundances of redox-sensitive trace elements in saponitic mudstones de

250 xidizing equivalents to mobilize sulfate and redox-sensitive trace metals from land to the oceans whi

251 rant benthic foraminiferal species, peaks in redox-sensitive trace metals, and enhanced (15)N/(14)N r

252 Finally, unlike proxies based on redox-sensitive trace-metal abundances, iron geochemical

253 Here we present sedimentary redox-sensitive trace-metal records from the Antarctic Z

254 lso inhibited the thioredoxin system and the redox sensitive transcription factor NF-kappaB.

255 ed adenosine triphosphate content, and Nrf2 (redox sensitive transcription factor) up-regulation.

256 Activation of the redox-sensitive transcription factor NF-E2 related facto

257 essential micronutrient that suppresses the redox-sensitive transcription factor NF-kappaB-dependent

258 Minocycline reduces ubiquitination of the redox-sensitive transcription factor Nrf2 and increases

259 demonstrate that Cu((II))ATSM activates the redox-sensitive transcription factor Nrf2 in human coron

260 unction of minocycline, which stabilizes the redox-sensitive transcription factor Nrf2, thus protecti

261 ion of MIOX induced nuclear translocation of redox-sensitive transcription factor Nrf2, which binds t

262 quent phosphorylation and degradation of the redox-sensitive transcription factor Nrf2.

263 It is unknown whether the redox-sensitive transcription factor nuclear factor eryt

264 Activation of the redox-sensitive transcription factor nuclear factor eryt

265 rythroid 2-related factor 2 (Nrf2/NFE2L2), a redox-sensitive transcription factor plays a critical ro

266 ear erythroid 2-related factor 2 (Nrf2) is a redox-sensitive transcription factor that is the key reg

267 erythroid 2 p45-related factor 2 (Nrf2) is a redox-sensitive transcription factor that regulates expr

268 tor erythroid-2-related factor 2 (Nrf2) is a redox-sensitive transcription factor that regulates the

269 erythroid 2 p45 related factor-2 (Nrf2) is a redox-sensitive transcription factor that up-regulates a

270 ing RNA-treated cells was independent of the redox-sensitive transcription factor, NF-kappaB.

271 ammatory processes as follows: activation of redox-sensitive transcription factors (NFkappaB) and MAP

272 mistry to determine DNA-bound potentials for redox-sensitive transcription factors because such bindi

273 the genome and facilitates the activation of redox-sensitive transcription factors globally in respon

274 In the present study we show that redox-sensitive transcription factors have an essential

275 ytoprotective proteins through activation of redox-sensitive transcription factors is severely attenu

276 active oxygen species-mediated activation of redox-sensitive transcription factors is the hallmark of

277 at DNA-binding sites (response elements) for redox-sensitive transcription factors may also exist in

278 sponses to contraction include activation of redox-sensitive transcription factors such as nuclear fa

279 against oxidative stress are coordinated by redox-sensitive transcription factors that transduce oxi

280 e on muscle ROS generation and activation of redox-sensitive transcription factors.

281 wever, does not seem to be under a classical redox-sensitive transcriptional regulation, being unresp

282 Spx, the redox-sensitive transcriptional regulator and a proteoly

283 tion governing TrfA activity, wherein Spx, a redox-sensitive transcriptional regulator degraded by Cl

284 based on the authigenic accumulation of the redox-sensitive transition element molybdenum in sulphid

285 e of molecular oxygen (P = 3.4 x 10(-8)) and redox-sensitive transition metals and compounds, which i

286 aphy reveals an episode of enrichment of the redox-sensitive transition metals molybdenum and rhenium

287 phosphate oxidase and the activation of the redox-sensitive tyrosine kinase Pyk2 as essential for VE

288 Proline-rich tyrosine kinase 2 (PYK2), a redox-sensitive tyrosine kinase, directly phosphorylates

289 induces oxidation of target cysteines in the redox-sensitive tyrosine phosphatases, LMW-PTP and SHP-2

290 iple levels by Keap1, which targets Nrf2 for redox-sensitive ubiquitin-mediated degradation in the cy

291 This process of redox-sensitive uncoupling of SOD1 from Rac1 was defecti

292 fide isomerase, one of the components of the redox-sensitive unfolded protein response pathway.

293 ified SET1/MLL histone methyltransferases as redox sensitive units of the H3K4-trimethylating complex

294 xes of (232)Th and excess barium, along with redox-sensitive uranium concentrations to examine past v

295 Here, we present a record of redox-sensitive uranium from the central equatorial Paci

296 show, using transgenic mice that expressed a redox-sensitive variant of green fluorescent protein tar

297 rylation at Ser1177 as well as expression of redox-sensitive vascular cell adhesion molecule-1 (VCAM-

298 Because ERK is redox sensitive, we compared the MM cell lines in terms

299 contains an equivalent P-loop Cys, was also redox sensitive, whereas ancestral bacterial FN3K homolo

300 ealed that microvascular K(ATP) channels are redox sensitive, with oxidants increasing their activity