ライフサイエンスコーパス: ethidium

1 he affinity of phencyclidine, proadifen, and ethidium.

2 of Escherichia coli DeltaacrAB to transport ethidium.

3 of the structurally similar but positive dye ethidium.

4 t cationic propidium and monovalent cationic ethidium.

5 ed the translocation of amphiphilic cationic ethidium.

6 yclohexyl]-3,4-piperidine ([(3)H]TCP), [(3)H]ethidium, [(3)H]tetracaine, [(14)C]amobarbital, and 3-(t

7 85-405 nm) from the nonspecific formation of ethidium (480-520 nm).

8 The binding sites of ethidium, a noncompetitive antagonist of the nicotinic a

9 The des-amino ethidium analog exhibits fluorescence quenching upon bin

10 st, covalent attachment of the photoreactive ethidium analog to DNA resulted in marked enhancement of

11 hondrial DNA with DNase and by separation of ethidium and 2-hydroxyethidium using cationic micellar e

12 rug' binding studies show that MepR binds to ethidium and DAPI with comparable affinities (K(d) = 2.6

13 Relative ethidium and DCFH fluorescence intensities in HCRAs expo

14 Increases in ethidium and dihydroethidium levels, markers of one-elec

15 parse the observed binding free energies of ethidium and propidium into five underlying contribution

16 retching to investigate DNA intercalation by ethidium and three ruthenium complexes.

17 of a membrane pore permeable to dyes such as ethidium, and to release of the pro-inflammatory cytokin

18 ergetics, consistent with electrogenic 2H(+)/ethidium(+) antiport.

19 only used for nucleic acid staining, such as ethidium, are familiar examples.

20 strands were constructed containing tethered ethidium as a photooxidant.

21 volves a covalent modification of guanine by ethidium, based upon HPLC analysis of the nucleoside pro

22 (ii) Ethidium binding converts deoxynucleoside sugar puckers

23 metal-like MPC core is partially released by ethidium binding to DNA, as observed by an increase in t

24 tes could be compensated for by the other in ethidium binding.

25 Laser photocleavage experiments revealed two ethidium-binding sites in the substrate R1.1 RNA.

26 binding, commensurate with the proportion of ethidium-bound nucleotides in the complex.

27 The cation of the salt ethidium bromide (3,8-diamino-5-ethyl-6-phenylphenanthri

28 dino-2-phenylindone (an AT-specific binder), ethidium bromide (a nonspecific binder), and chromomycin

29 ransfer takes place between DNA-intercalated ethidium bromide (DNA-EB) and the electrostatically boun

30 ble to remyelinate demyelinated axons inside ethidium bromide (EB) demyelination lesion in adult spin

31 ircular dichroism (CD) spectroscopy, and the ethidium bromide (EB) displacement assay.

32 rbance we measured changes in geometric mean ethidium bromide (EB) fluorescence intensities in subpop

33 rescence resonance energy transfer (FRET) to ethidium bromide (EB) intercalated within double-strande

34 Ethidium bromide (EB) is known to inhibit cleavage of ba

35 ng; energy is transferred from the CCP to an ethidium bromide (EB) molecule intercalated into the dsD

36 a cells depleted of mtDNA via treatment with ethidium bromide (EB) were found to contain reduced stea

37 abeled with fluorescein amidite (FAM-ssDNA), ethidium bromide (EB), and graphene oxide (GO) are emplo

38 r previously by the intraspinal injection of ethidium bromide (EB).

39 complexation with the phenanthridinium drug ethidium bromide (EB).

40 We utilize ethidium bromide (EtBr) as a model intercalator to demon

41 tween genomic DNA and the intercalating drug ethidium bromide (EtBr) have been determined by use of a

42 Zn(2+) complexation inhibited ethidium bromide (EtBr) intercalation and stabilized FdU

43 al effects of binding the intercalating drug ethidium bromide (EtBr) to 160 base pair (bp) fragments

44 vo mtDNA polymerase activity assay utilizing ethidium bromide (EtBr) to deplete mtDNA, showed that po

45 hemichannel activity as evident by enhanced ethidium bromide (EtBr) uptake that could be blocked by

46 ility and a decreased ability to intercalate ethidium bromide (EtBr).

47 Currently, ethidium bromide (EthBr) is the cheapest and most used D

48 Uptake of ethidium bromide (i) was faster in Cx43 and Cx43-EGFP th

49 elination in rodent CNS in the X-irradiation/ethidium bromide (X-EB) model.

50 ansfected with hCx31.9-EGFP took up DAPI and ethidium bromide 5-10 times faster than wild-type cardio

51 ed products were visualized by staining with ethidium bromide after electrophoresis in 1.5% agarose.

52 ; staining at the single-molecule level with ethidium bromide after exhaustive deproteinization of ly

53 Unwinding the supercoiled DNA with ethidium bromide also made DNA resistant to AN/L3.

54 The intercalating agents ethidium bromide and 9-aminoacridine enhanced oxopropeny

55 The system uses dye-based detection with ethidium bromide and a single DNA polymerase-based PCR o

56 nalyzed from single islet cells stained with ethidium bromide and acridine orange, apoptosis using a

57 ld decrease in sensitivity to quinolones and ethidium bromide and an increase in the level of norA tr

58 MDR-dependent efflux of ethidium bromide and berberine from S. aureus cells was

59 ical and B-DNA, displacement of intercalated ethidium bromide and facilitate cooperative binding of H

60 the displacement of DNA duplex intercalated ethidium bromide and gel electrophoresis.

61 binds to genomic DNA to a similar extent as ethidium bromide and Hoechst 33258.

62 Fluorescent quenching of ethidium bromide and of rhodamine covalently attached to

63 thod is at least 50-fold more sensitive than ethidium bromide and permits detection of </=0.25 ng dou

64 Decreased accumulation of ethidium bromide and rhodamine 6G in the hns mutant comp

65 o oligonucleotides with model intercalators (ethidium bromide andactinomycin D) and minor groove bind

66 th DNA in electrophoretic mobility shift and ethidium bromide binding assays.

67 Metal ions also weaken ethidium bromide binding to IRE-RNA with no effect on IR

68 ns in the DNA helix as detected by decreased ethidium bromide binding.

69 Low (micromolar) concentrations of ethidium bromide block RNase III[DeltadsRBD] cleavage of

70 from sodium dodecyl sulfate, novobiocin, and ethidium bromide but failed with other known substrates

71 der-surpassing the sensitivity achieved with ethidium bromide by 200-fold.

72 binding (measured as accessibility of DNA to ethidium bromide by electrophoresis and by fluorescence

73 Moreover, ethidium bromide can be readily removed using isoamyl al

74 We show that ethidium bromide can influence DNA self-assembly, decrea

75 e insertion efficiency, and to resistance to ethidium bromide collectively demonstrate that EmrE mono

76 Ethidium bromide depleted both mutant and normal cells o

77 nding affinity of polyamines to DNA using an ethidium bromide displacement assay showed that homologu

78 o screened for DNA binding efficacy using an ethidium bromide displacement assay.

79 e, circular dichroism, linear dichroism, and ethidium bromide displacement assays, which demonstrated

80 formation (by 2-aminopurine fluorescence and ethidium bromide displacement); (ii) metal ions increase

81 showed potent synergistic activity with the ethidium bromide dye in a strain overexpressing the MepA

82 TM4(85-105) sequence inhibits Hsmr-mediated ethidium bromide efflux from bacterial cells.

83 Because ethidium bromide efflux is an energy-dependent process a

84 The procedure developed here using bacterial ethidium bromide efflux pump activity may be a useful co

85 ed field gel electrophoresis (PFGE) and CsCl/ethidium bromide equilibrium centrifugation demonstrates

86 as determined by mitochondrial function and ethidium bromide exclusion, was not inhibited by the bro

87 Gel electrophoresis and ethidium bromide experiments showed that 9a-9c associate

88 /mL culture produced significantly increased ethidium bromide fluorescence compared to nonexposed con

89 Ethidium bromide fluorescence intensities increased upon

90 roxide anion production was measured with an ethidium bromide fluorescence method.

91 tocol to quantify PCR products, by measuring ethidium bromide fluorescence of PCR products excised fr

92 Ethidium bromide fluorescence of the product DNA was use

93 measured by lucigenin chemiluminescence and ethidium bromide fluorescence) and impaired endothelium-

94 (measured by lucigenin chemiluminescence and ethidium bromide fluorescence) that was inhibited or red

95 s of A vessels produced O(2)(.-) (shown with ethidium bromide fluorescence).

96 Data from circular dichroism, inhibition of ethidium bromide fluorescence, interstrand cross-linking

97 DNA cross-linking, assayed by ethidium bromide fluorescence, was significantly inhibit

98 polyamines retain their ability to displace ethidium bromide from calf thymus DNA and are rapidly ta

99 grouped depending on whether they displaced ethidium bromide from DNA.

100 ed with Southern blot analysis compared with ethidium bromide gel electrophoresis (EtBr) for all mRNA

101 Ethidium bromide has served as a classic DNA intercalato

102 rsed both tolerance to INH and resistance to ethidium bromide in BCG.

103 p inhibitor reserpine inhibits resistance to ethidium bromide in both wild-type M. smegmatis and the

104 Inclusion of ethidium bromide in the reaction mixture leads to a grea

105 stranded DNA with hybridization detected via ethidium bromide intercalation, further establishing tec

106 Titration of ethidium bromide into the assay decreased activity to a

107 is responsible for drug resistance and that ethidium bromide is a novel substrate for P55.

108 lls were transplanted into the X-irradiation/ethidium bromide lesioned dorsal columns of immunosuppre

109 embrane permeable DNA-associating vital dye, ethidium bromide monoacetate (visible wavelength single

110 cted by staining with either acridine orange/ethidium bromide or annexin-V-fluorescein/propidium iodi

111 ignals that could be reversed by addition of ethidium bromide or by DNA melting, suggesting that flav

112 of the protein association to treatment with ethidium bromide or micrococcal nuclease.

113 ed protein response in wild-type worms using ethidium bromide or paraquat triggered statin resistance

114 Fluorescence-based binding assays that use ethidium bromide or Rev peptide displacement are used to

115 Twisting was controlled using ethidium bromide or SYBR Green I as model intercalators.

116 luorescence derived from the displacement of ethidium bromide or thiazole orange from the DNA of inte

117 Animals received ethidium bromide plus photon irradiation producing discr

118 Films treated with ethidium bromide prompt switching of dsDNA to ssDNA befo

119 transcription-PCR amplification followed by ethidium bromide staining (PCR-ETBr) or nucleic acid hyb

120 The results of gel electrophoresis and ethidium bromide staining of the DNA fingerprints obtain

121 n to orange/yellow shifts on acridine orange/ethidium bromide staining, and cell surface annexin V bi

122 s of total DNA in an agarose gel followed by ethidium bromide staining, and subsequent scanning of th

123 as 100 viable trophozoites as determined by ethidium bromide staining, while no signal was obtained

124 sualized after separation in agarose gels by ethidium bromide staining.

125 sis on 2 % agarose gels, and visualized with ethidium bromide staining.

126 ma COLO 16 cells were chronically exposed to ethidium bromide to inhibit mitochondrial DNA synthesis

127 Further studies using acridine orange and ethidium bromide to measure apoptosis revealed that mdr1

128 Binding ethidium bromide to one of these RNA fragments, which wo

129 Strikingly, both ethidium bromide transport and normal cell surface prope

130 educed mitochondrial DNA (mtDNA) contents by ethidium bromide treatment or myocytes treated with know

131 Reduction of mtDNA content in DRHEp2 by ethidium bromide treatment reduced the resistance.

132 everal mtDNA forms after severe depletion by ethidium bromide treatment showed that replication and m

133 Ethidium bromide uptake assays revealed increased envelo

134 urrent, and, when expressed in HEK293 cells, ethidium bromide uptake was only approximately 5% that o

135 nfrequent or brief opening could account for ethidium bromide uptake.

136 lity of pgs1Delta to grow in the presence of ethidium bromide was due to defective cell wall integrit

137 Ethidium bromide was used as the intercalating dye for l

138 g a DNA-targeting intercalating agent (i.e., ethidium bromide) resulted in a marked shift of the clea

139 ramphenicol), transcription and replication (ethidium bromide), and function (rotenone, rhodamine 6G)

140 after cell staining with acridine orange and ethidium bromide).

141 Of the 6 compounds that did not displace ethidium bromide, 2 also inhibited B-ZIP binding to DNA

142 More importantly, cytosine arabinoside, ethidium bromide, 5-azacytidine and aspirin all signific

143 oparticles capped with DNA intercalated with ethidium bromide, a fluorescent molecule.

144 aternary ammonium on an aromatic ring (e.g., ethidium bromide, acriflavine hydrochloride, 2-N-methyle

145 ase in resistance to hydrophilic quinolones, ethidium bromide, and cetrimide and also to sparfloxacin

146 rmeable to Lucifer yellow, Alexa Fluor(350), ethidium bromide, and DAPI, which have valences of -2, -

147 cobacterium smegmatis is more susceptible to ethidium bromide, and drug resistance is restored by the

148 rculosis iniA in BCG conferred resistance to ethidium bromide, and the deletion of iniA in M. tubercu

149 the use of simple DNA intercalators, such as ethidium bromide, as tools to facilitate the error-free

150 Unlike ethidium bromide, both eilatin and the eilatin-containin

151 hat DXR and other DNA intercalators, such as ethidium bromide, can rapidly intercalate into mtDNA wit

152 In addition to hypersensitivity to ethidium bromide, cells that lack the lprG-Rv1410c opero

153 contrast, other DNA-binding agents, such as ethidium bromide, distamycin, and doxorubicin, inhibit t

154 drugs including echinomycin, actinomycin-D, ethidium bromide, Hoechst 33342, and cis-C1 were subject

155 rophoresis in agarose gels and staining with ethidium bromide, produced DNA fragments in the 4.0- to

156 Further, acridine orange, ethidium bromide, propidium iodide and DAPI staining dem

157 erine and palmatine and the DNA intercalator ethidium bromide, revealed a change in the absorbance an

158 aphy, SYBR Gold stain is more sensitive than ethidium bromide, SYBR Green I stain, and SYBR Green II

159 proteins during recovery from treatment with ethidium bromide, when mtDNA replication is stimulated i

160 Ethidium bromide, which binds reversibly to DNA via inte

161 optosis was determined by DNA fragmentation, ethidium bromide-acridine orange nuclear stain and TdT-m

162 PI viability was examined with ethidium bromide-acridine orange, and apoptosis was exam

163 An insertion mutant of the ethidium bromide-induced all7631 did not show any signif

164 lt rat sciatic nerves into X-irradiation and ethidium bromide-induced demyelinated dorsal column lesi

165 e investigated the effect of previous focal, ethidium bromide-induced demyelination of brain stem whi

166 x and 543-nm excitation for the detection of ethidium bromide-labeled nucleic acids (i.e., RNA).

167 ed fluorescence (LIF) was employed to detect ethidium bromide-labeled RNA molecules under native cond

168 nes were confirmed as Salmonella specific on ethidium bromide-stained agarose gels by Southern hybrid

169 by BrdU uptake and cell counts of calcein AM/ethidium bromide-stained cells.

170 by visualizing 1.1- to 1.2- kb PAN RNA in an ethidium bromide-stained gel from poly(A)-selected RNA.

171 The ethidium bromide-stained gels are photographed or scanne

172 agarose gel electrophoresis and stained with ethidium bromide.

173 d in increased accumulation of intracellular ethidium bromide.

174 t)DNA by passaging in a low concentration of ethidium bromide.

175 on uridine after eight passages in 50 ng/mL ethidium bromide.

176 nd intercalating ligands: DAPI, Hoechst, and ethidium bromide.

177 gand, and to the classic intercalating agent ethidium bromide.

178 and measured mtDNA after 3-d treatment with ethidium bromide.

179 ethidine in the extracellular environment to ethidium bromide.

180 mycin, bisphenol A, chlorinated phenols, and ethidium bromide.

181 ed by gel electrophoresis in the presence of ethidium bromide.

182 by agarose concentration or the presence of ethidium bromide.

183 et by fluorescence after brief staining with ethidium bromide.

184 demyelinated by the intraspinal injection of ethidium bromide.

185 ly studied MDR substrates, Hoechst 33342 and ethidium bromide.

186 induced upon incubation with erythromycin or ethidium bromide.

187 er rapidly, as revealed after treatment with ethidium bromide.

188 ntibiotics based on the fluorescent molecule ethidium bromide.

189 served fluorescently after labeling DNA with ethidium bromide.

190 thus eliminating the need for staining with ethidium bromide.

191 ophoresis on a 0.8% agarose gel stained with ethidium bromide.

192 DNA fragmentation and ethidium bromide/acridine orange (EB/AO) nuclear stainin

193 ted for apoptosis either by staining with an ethidium bromide/acridine orange mixture (AO/EB) or with

194 emyelinating lesions had been produced using ethidium bromide/X-irradiation.

195 resensitization of Hsmr-expressing cells to ethidium bromide; and was non-hemolytic to human red blo

196 se chain reaction of isolated total RNA from ethidium-bromide-treated and untreated cells.

197 n, as well as the organic monovalent cation, ethidium, but not its divalent analog, propidium.

198 e it is specifically oxidized to fluorescent ethidium by the superoxide anion, whereas mice lacking U

199 its slow intercalation kinetics, relative to ethidium cation not attached to an MPC.

200 otropy (FPA) measurements yield r(t) for DNA/ethidium complexes (1 dye/200 bp) from 0 to 120 ns.

201 Comparison of the apo-Rv3066 and Rv3066-ethidium crystal structures suggests that the conformati

202 Netropsin, ethidium, daunorubicin and actinomycin, ligands with kno

203 Standard intercalators (ethidium, daunorubicin, and actinomycin D) served as con

204 ators with different complexities, including ethidium, daunorubicin, and nogalamycin, have been used

205 of the nucleoside products and studies with ethidium derivatives.

206 propriate for their size range, stained with ethidium, destained, and a quantitative electronic image

207 At 10 microM [(3)H]ethidium diazide, incorporation into the alpha-, beta-,

208 use of a photoactivatible derivative, [(3)H]ethidium diazide.

209 A long-lived transient absorption signal for ethidium dication in poly(dG-dC) confirms that guanine o

210 ngII-infused rabbits that were assessed from ethidium:dihydroethidium was enhanced by addition of CGP

211 occurred, as indicated by abnormal uptake of ethidium dimer into pSC nuclei.

212 (dA)poly(dT) has been investigated using the ethidium displacement assay, isothermal titration calori

213 demonstrate that conversion of a reversible ethidium-DNA complex to an irreversible adduct results i

214 These include ethidium-DNA fluorescence quenching and thermal melting

215 pore formation, as measured by the uptake of ethidium dye, whereas cholesterol loading inhibited this

216 lysis of the fluorescence characteristics of ethidium (E(+)) and 2-OH-E(+) strongly suggests that the

217 Ethidium (E) is a powerful probe of DNA dynamics and DNA

218 fast ET, initiated by excitation of tethered ethidium (E), the intercalated electron acceptor (A); th

219 The same cross-link also impairs ethidium efflux activity by EmrE in Escherichia coli.

220 a previous study, LmrA was shown to mediate ethidium efflux by an ATP-dependent proton-ethidium symp

221 During ethidium efflux, single D142N and D235N replacements res

222 o antibiotic sensitivity, lipid profile, and ethidium efflux.

223 bitors and by determining the proficiency of ethidium efflux.

224 ion repressor, QacR, bound simultaneously to ethidium (Et) and proflavin (Pf).

225 (dppz)(2+), and three organic intercalators, ethidium (Et), thionine (Th), and anthraquinone (AQ).

226 n minutes increases membrane permeability to ethidium (Etd(+)) and Ca(2+) by activating P2X7 receptor

227 ular processes that can oxidize HE probes to ethidium (Etd).

228 Ethidium fluorescence experiments demonstrated that cono

229 NTG treatment increased ethidium fluorescence in rat muscles and urinary F(2)-is

230 Compared to control slices, ethidium fluorescence was 25% higher during HI and 50% h

231 The increases in NADPH oxidase activity and ethidium fluorescence were blocked by either the AT(1) r

232 Using ethidium fluorescence, we demonstrated an increase in su

233 al DNA and (ii) the spectral interference of ethidium fluorescence.

234 rons, the latter evidenced by an increase in ethidium fluorescence.

235 observed by an increase in the intensity of ethidium fluorescence.

236 Hole injection by photoexcited ethidium followed by radical migration to oxidatively su

237 lacement of pre-intercalated and fluorescent ethidium from dsDNA targets (triplex association) and (i

238 ding of transfer RNA to the covalently bound ethidium group.

239 is binding involves the intercalation of the ethidium groups into the tRNA molecule.

240 ate dehydrogenase (G6DP), and calcein AM and ethidium homodimer (calcein AM/EthD-1)] have been adopte

241 analyzed by calcein-acetoxymethyl ester (AM)/ethidium homodimer assay.

242 Using ethidium homodimer cell labeling to evaluate necrosis an

243 eath of all neurons and glia, as detected by ethidium homodimer nuclear staining.

244 death was evaluated with TUNEL staining and ethidium homodimer-1 (EthD) dyes.

245 inally, analyses using the fluorescent probe ethidium homodimer-1 and measurements of release of kera

246 tosis was further confirmed using calcein AM/ethidium homodimer-1 dye and cleavage of poly(ADP-ribose

247 ic injury, and cell death was assessed using ethidium homodimer-1 labeling.

248 in-included slices of rat lungs stained with ethidium homodimer-1 shortly after anesthesia (control)

249 viability was measured using calcein Am and ethidium homodimer-1.

250 ment and common fluorescent dyes (BODIPY and ethidium homodimer-2) to detect both lipoid and DNA cont

251 cetoxymethyl ester (calcein-AM) and 4 microM ethidium homodimer.

252 [bpy = 2,2'-bipyridine] > acridine orange > ethidium, in accordance with measured oxidation potentia

253 of a cross-linker in real time by increased ethidium influx into the cells.

254 he MIC data were also confirmed by assays of ethidium influx rates in intact cells, and our results s

255 Ethidium intercalation has been investigated as a means

256 The bound ethidium is found buried within the multidrug-binding si

257 the nAChR, the high-affinity binding site of ethidium is within the lumen of the ion channel and that

258 d MPCs, the energy-transfer quenching of the ethidium ligands by the metal-like MPC core is partially

259 Superoxide production was measured by the ethidium method in cultured neurons treated with oxygen-

260 In this work, a microfluidic platform using ethidium monoazide (EMA) which can only penetrate into d

261 The tiopronin/ethidium MPC binding to DNA was imaged by AFM.

262 Binding of the cationic TMA/ethidium MPC to DNA was efficient and rapid.

263 er N-(2-mercaptopropionyl)glycine (tiopronin/ethidium MPC) or trimethyl(mercaptoundecyl)ammonium (TMA

264 ) or trimethyl(mercaptoundecyl)ammonium (TMA/ethidium MPC).

265 The negatively charged tiopronin/ethidium MPC, in contrast, exhibits slow intercalation k

266 By using the diffusion rates of the dyes ethidium, Nile red, and eosin Y across the outer membran

267 pecific reporter hydroxytriphenylphosphonium ethidium (OH-TPP-E(+)).

268 nce(s) of the 3- and 8-amino substituents of ethidium on the energetic contributions and concomitant

269 ased Cx30-mediated currents with unperturbed ethidium permeability.

270 FBP had no effect on the fluorescence of ethidium produced from superoxide oxidation of hydroethi

271 o three structurally different planar drugs, ethidium, propidium and dequalinium.

272 drugs such as tetraphenylphosphonium (TPP+), ethidium, propidium and dequalinium.

273 for a series of DNA intercalators, including ethidium, propidium, daunorubicin, and adriamycin.

274 The binding of the fluorescent NCIs ethidium, quinacrine, and crystal violet as well as [(3)

275 ic residue with Gly (L83G) also conferred no ethidium resistance phenotype, which supported the concl

276 6, both in the absence and presence of bound ethidium, revealing an asymmetric homodimeric two-domain

277 ith three distinct translocation substrates (ethidium, rhodamine 6G, and tetraphenylphosphonium), as

278 Ala, with five structurally diverse ligands, ethidium, rhodamine 6G, ciprofloxacin, nafcillin, and Ph

279 Additional examination of ethidium shows that it can generate cross-links between

280 The ethidium sites are attached to the nanoparticles as thio

281 The single DNA molecules are ethidium stained, 670 kilobase pair bacteriophage G geno

282 mobility under increasing concentrations of ethidium suggest that the cruciforms undergo a transitio

283 e ethidium efflux by an ATP-dependent proton-ethidium symport reaction in which the carboxylate E314

284 ly, this truncated protein mediates a proton-ethidium symport reaction without the requirement for AT

285 Each nanoparticle bears only one or two ethidium thiolate ligands.

286 -5-mercaptododecyl-6-phenylphenanthridinium (ethidium thiolate).

287 ining residues in the permeation of ions and ethidium through Cx30 hemichannels.

288 oxide-mediated oxidation of hydroethidine to ethidium to dynamically and directly assess the relative

289 changes from enthalpy-driven for the parent ethidium to entropy-driven when both amino groups are re

290 By covalently tethering ethidium to one end of a DNA duplex, we demonstrate the

291 ies, yielding values that ranged from -11.2 (ethidium) to -30 kcal mol(-)(1) (actinomycin D).

292 e mechanistic role of E314 in proton-coupled ethidium transport.

293 displacement of the TFO and replacement with ethidium (triplex dissociation).

294 Dissociation of the ethidium-tRNA complex was monitored as a function of sod

295 potently inhibited ATP-gated Ca2+ influx and ethidium uptake in several leukocyte cell lines (THP-1,

296 adelCcys) restored the current rise time and ethidium uptake to WT levels.

297 of the P2X7 receptor measured by ATP-induced ethidium uptake.

298 to dichlorofluorescein and hydroethidium to ethidium, was inhibited by antisense eNOS oligonucleotid

299 nding of the noncompetitive antagonist [(3)H]ethidium when examined in the presence and absence of ag

300 cyanide m-chlorophenylhydrazone (CCCP), and ethidium, which bind to bacterial MarRs.