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 uggesting that FasL activation of Akt/PKB is redox sensitive.

3 ors Ets-1 and c-Jun to the MMP-1 promoter is redox sensitive.

4 Plastidic isoforms were redox sensitive.

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

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

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

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

9 The basis for this mechanism resides in the redox-sensitive active site Cys in PTPs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

26 y reversible by addition of reducing agents (redox sensitive), and independent of both cAMP/protein k

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

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

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

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

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

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

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

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

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

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

37 erythroid 2 p45-related factor 2 (Nrf2) is a redox-sensitive basic leucine zipper transcription facto

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

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

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

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

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

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

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

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

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

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

48 The redox-sensitive character of enriched metals supports em

49 These results support the hypothesis that a redox-sensitive checkpoint regulated the progression of

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

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

52 he CXXC motif of Spx, which is necessary for redox sensitive control of Spx activity in response to o

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

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

55 Identification of one redox-sensitive cysteine (2327) in the native membrane-b

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

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

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

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

60 his approach to the analysis of the free and redox-sensitive cysteine residues of a large membrane pr

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

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

63 Because Ras is known to have redox-sensitive cysteine residues, we tested the hypothe

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

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

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

67 nient method for identifying and quantifying redox-sensitive cysteines in membrane proteins of native

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

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

70 ansition from infection to the expression of redox-sensitive cytokine genes is unknown.

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

72 Translocation of the redox-sensitive delta-isoform of protein kinase C (PKC)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 ve this debate, we use a novel, ratiometric, redox-sensitive fluorescence resonance energy transfer (

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

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

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

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

93 ucial role in this process, although several redox-sensitive genes, proteins and transcription factor

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

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

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

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

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

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

100 Redox-sensitive GFP revealed that gsh2 seedlings maintai

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

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

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

104 GAPDH is a redox-sensitive glycolytic enzyme that also promotes apo

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

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

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

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

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

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

111 Neurons transfected with redox-sensitive green fluorescent protein showed a posit

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

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

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

115 Using redox-sensitive green fluorescent proteins targeted to t

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

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

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

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

120 The data show that roGFP is redox sensitive in plant cells and that this sensor make

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 Here we show that a redox-sensitive mechanism regulates the phosphorylation

141 Taken together, our data support a new redox-sensitive mechanism regulating cTnI phosphorylatio

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

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

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

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

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

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

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

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

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

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

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

153 The redox-sensitive MMP-1 protein expression requires activa

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

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

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

157 The presence of redox-sensitive motifs (cysteine residues, metal co-fact

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

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

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

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

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

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

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

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

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

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

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

169 Our probe design is based on redox-sensitive optical switches, which couple a ketone-

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

171 veal a strategy for limiting expression of a redox-sensitive pathway by using a thiol-based redox swi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 response is the up-regulation of the 32-kDa redox-sensitive protein, heme oxygenase-1.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

218 ases in reductants, such as glutathione, and redox sensitive signaling molecules, such as AP endonucl

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

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

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

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

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

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

225 Numerous redox-sensitive signaling pathways exist in muscle inclu

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

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

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

229 nsight into the potential role of Txnip as a redox-sensitive signaling protein.

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

238 with oxidative stress, Keap1 functions as a redox-sensitive switch and releases Nrf2.

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 Because Nrf2 activation is generally redox-sensitive, the redox insensitivity of this Nrf2-NE

243 116 ppb) O(3) concentrations was examined by redox-sensitive thiol labeling, mass spectrometry, and t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 by regulating the signals that activate the redox-sensitive transcription factor NF-kappaB and cause

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

279 also prevented the LPS-induced activation of redox-sensitive transcription factors such as NF-kappaB

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

281 xygen species which induce the activation of redox-sensitive transcription factors that interact with

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

283 ecipitation assays showed that the prototype redox-sensitive transcription factors, Nrf2, small Maf p

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

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

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

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

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

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

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

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

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

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

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

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

296 ls of endocytic compartments by expressing a redox-sensitive variant of GFP fused to various endocyti

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

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

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

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