ライフサイエンスコーパス: EDTA

1 EDTA binds remaining copper, thereby speeding up sample

2 EDTA can chelate iron and lead.

3 EDTA chelation therapy has been in off-label use for the

4 EDTA increased Fe- and ZnDa% in all NIS-products, but it

5 EDTA reduced the primary end point (death, reinfarction,

6 EDTA removes Zn(2+) to generate apo-p53, which aggregate

7 EDTA root surface etching could enhance DOX availability

8 EDTA root surface etching enhances DOX availability in t

9 EDTA was more effective than ascorbic acid, and Coenzyme

10 EDTA, a powerful chelating agent, did not have any signi

11 EDTA-loaded albumin NPs did not cause the side effects o

12 EDTA-WB and BS specimens were tested with Xpert (targets

13 EDTA-WB specimens (n = 218) were collected from suspecte

14 into 1 ViraStim HIV-1 activation tube and 1 EDTA tube.

15 in 1% v/v methanol (pH 5.5) and 20mmolL(-1) EDTA, 2mmolL(-1) KHP, 40mmolL(-1) (NH4)2CO3 in 1% v/v me

16 Mg(2+), Zn(2+), Cu(2+), K(1+), EDTA and beta-mercaptoethanol resulted in enhanced xylan

17 methods were linear in the range of 0-100mg EDTA equivalents/L.

18 s TaqMan HIV-1 Test v2.0 (CAP/CTM) using 162 EDTA plasma samples collected from patients undergoing H

19 th 0.12% chlorhexidine, 20% citric acid, 24% EDTA/1.5% NaOCl, or sterile saline and assessed surface

20 degradable collagen membrane (COL) after 24% EDTA root surface etching was evaluated.

21 affected roots were etched with neutral 24% EDTA as in group 2.

22 oots etched for 2 minutes with a neutral 24% EDTA gel before grafting of the associated vertical defe

23 ta-TCP after root surface treatment with 24% EDTA may be a suitable method to improve nHA retention i

24 caling and root planing and treated with 24% EDTA, EMD, and/or human blood in six clinically related

25 33 (37%) patients had diabetes mellitus (322 EDTA and 311 placebo).

26 equine clinical treatments N-acetylcysteine, EDTA, and hydrogen peroxide to disrupt in vitro biofilms

27 h disodium ethylene diaminetetraacetic acid (EDTA) that were designed to target calcified elastic lam

28 CK) (10.3%), ethylendiaminetetraacetic acid (EDTA) (8.7%) and pepstatin A (1.2%).

29 ing 50 mmol/L Ethylendiamintetraacetic acid (EDTA) at pH 10 as extractant.

30 s addition of ethylendiamintetraacetic acid (EDTA) reduced the radical formation.

31 study, both ethylenediaminetetraacetic acid (EDTA) and diethylenetriamine pentaacetic acid (DTPA) wer

32 chelators, ethylenediaminetetraacetic acid (EDTA) and ethyleneglycoltetraacetic acid (EGTA), are use

33 racted from ethylenediaminetetraacetic acid (EDTA) anticoagulant-treated blood samples (~500 mul) and

34 id (AA) and Ethylenediaminetetraacetic acid (EDTA) are commonly used to counter act this reaction and

35 ng chelator ethylenediaminetetraacetic acid (EDTA) but decrease it in the absence of EDTA, ruling out

36 from metal-ethylenediaminetetraacetic acid (EDTA) complexes at delta 2.70ppm for Mg(2+) and delta 2.

37 of disodium ethylenediaminetetraacetic acid (EDTA) elevated the level of H2O2 generated in the same i

38 the use of ethylenediaminetetraacetic acid (EDTA) in DMSO exerts superior control over wafer coverag

39 mination of ethylenediaminetetraacetic acid (EDTA) in feed and premix formulations was developed and

40 olutions of ethylenediaminetetraacetic acid (EDTA) in hydrazine for O-glycan release.

41 sing (51)Cr-ethylenediaminetetraacetic acid (EDTA) plasma clearance counting but is time-consuming an

42 ction using ethylenediaminetetraacetic acid (EDTA) producing detergentless microemulsions.

43 e (DFO) and ethylenediaminetetraacetic acid (EDTA) reduced lipid oxidation in emulsions with NaCl, wi

44 d enzymatic ethylenediaminetetraacetic acid (EDTA) sensor based on the inhibition and subsequent acti

45 20mmolL(-1) ethylenediaminetetraacetic acid (EDTA), 2mmolL(-1) potassium hydrogen phthalate (KHP) in

46 ptopril and ethylenediaminetetraacetic acid (EDTA), inhibit the hydrolysis of meropenem in vivo.

47 Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), 1,4,7,10-tetraazacyc

48 Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), diethylenetriaminepe

49 tic ligands ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), iminodiacetic acid (

50 (Res.B) to ethylenediaminetetraacetic acid (EDTA)-demineralized dentin with or without zoledronate-c

51 and HFA in ethylenediaminetetraacetic acid (EDTA)-plasma of patients, the obtained analytical precis

52 , and 5 mM) ethylenediaminetetraacetic acid (EDTA).

53 e of (51)Cr-ethylenediaminetetraacetic acid (EDTA).

54 ts included ethylenediaminetetraacetic acid (EDTA; 10%, pH 7.2), phosphoric acid (37%, pH <1), citric

55 chelators mag-fura-2, nitrilotriacetic acid, EDTA, and EGTA estimate K(D) Ni(II) for the tightest sit

56 Added EDTA or ion exchange resin caused no catalyst poisoning,

57 using HIV-1-positive samples (n = 169 adult EDTA plasma, n = 172 adult DBS, and n = 100 infant DBS)

58 eased in heterocysts and akinetes, and after EDTA treatment.

59 y followed by the placement of DOX-COL after EDTA etching of the exposed root surfaces (DOX-COL + EDT

60 placement of DOX blended with beta-TCP after EDTA etching of the exposed root surfaces (DOX-beta-TCP

61 m beta-tricalcium phosphate (beta-TCP) after EDTA root surface treatment.

62 Chelating agents (EDTA formulations) reduced E. coli CFU but were ineffect

63 hibit colour fading during storage, although EDTA had some inhibitory effects in the early stages of

64 This protocol describes an EDTA-based passaging procedure to be used with chemicall

65 r Ni(2)(+) because of the introduction of an EDTA buffer system in the revised medium.

66 Therapy (TACT) showed clinical benefit of an EDTA-based infusion regimen in patients aged >/=50 years

67 We found an effect of iron (P = 0.009) and EDTA (P = 0.012) for reduced BPb concentrations at endpo

68 2)(+), Ca(2+), Zn(2+), Mg(2+) and Cd(2+) and EDTA showed no significant effect on the enzyme activity

69 as aimed at determining the effect of AA and EDTA on the catechol or galloyl iron binding ability of

70 /ml were tested against six levels of AA and EDTA.

71 buffers containing either Tris, acetate, and EDTA (TAE) or Tris, borate, and EDTA (TBE).

72 concentrations than GSH, ascorbic acid, and EDTA.

73 trypsin inhibitor, leupeptin, antipain, and EDTA could not prevent histatin 5, statherin, or PRP1 de

74 acetate, and EDTA (TAE) or Tris, borate, and EDTA (TBE).

75 We optimized NP size, charge, and EDTA-loading efficiency (150-200 nm, zeta potential of -

76 demonstrate that elastin antibody-coated and EDTA-loaded albumin NPs might be a promising nanoparticl

77 , we showed that elastin antibody-coated and EDTA-loaded albumin NPs targeted the damaged elastic lam

78 er ion as an inhibition reagent for GOx, and EDTA as a regeneration reagent.

79 Food fortification with iron and EDTA additively reduces BPb concentrations.

80 ive was to determine the effects of iron and EDTA, alone and in combination, on blood lead (BPb) conc

81 EDTA-1D-RP-nanoUPLC, 2D-RP/RP-nanoUPLC, and EDTA-2D-RP/RP-nanoUPLC to compare their performance in p

82 calcite (104) surface with a dilute Pb- and EDTA-bearing solution that is slightly undersaturated wi

83 apsid swells when exposed to alkaline pH and EDTA.

84 apsid swells when exposed to alkaline pH and EDTA.

85 beta-mercaptoethanol increased while SDS and EDTA inhibited the xylanase activity of both Xyl1 and Xy

86 rinergic P2 receptor antagonist suramin, and EDTA.

87 n 36 negative specimens, including swabs and EDTA blood from control sheep, goats, and cattle.

88 glycans released by hydrazine with anhydrous EDTA or disodium salt dihydrate EDTA show high yields of

89 ecretion, defense against detergents such as EDTA and bile salts, and resistance to antimicrobial pep

90 ith environmentally relevant ligands such as EDTA, citrate, and malate provided a bridge between spec

91 Iron chelators, such as EDTA, desferrioxamine, and deferiprone, were found to ca

92 y 5 times) when a sacrificial donor, such as EDTA, is introduced into the system.

93 I) from fairly strong Cu(II) ligands such as EDTA.

94 evidenced by resistance to reversal by both EDTA and thermal treatments.

95 cleaving reagent, iron bromoacetamidobenzyl-EDTA (FeBABE).

96 in conjugated with iron bromoacetamidobenzyl-EDTA, and in vitro transcription.

97 h TFIIB-FeBABE [TFIIB-p-bromoacetamidobenzyl-EDTA-iron(III)] derivatives showed that the TFIIB core d

98 alpha-casein and ss-casein were analyzed by EDTA-1D-RP-nanoUPLC, 2D-RP/RP-nanoUPLC, and EDTA-2D-RP/R

99 Conditioning by EDTA, phosphoric acid, and citric acid exposed growth fa

100 lymer blocks could be readily dissociated by EDTA to afford the unshelled P3HT nanofiber networks, an

101 detected in dentine matrix extracts drawn by EDTA, phosphoric acid, and citric acid from powdered den

102 apidly upon removal of Mg(2+) ions (i.e., by EDTA).

103 loproteases in in vitro aging experiments by EDTA resulted in an approximately 3-fold increase in the

104 with C5b-9, a process that was inhibited by EDTA, in the absence of factor B, and by purinergic P2 r

105 Cs are reduced in a dose-dependent manner by EDTA.

106 All-cause mortality was reduced by EDTA chelation (10% versus 16%; hazard ratio, 0.57; 95%

107 Binding to CHO-CR1 was reduced by EDTA, whereas MgEGTA only reduced the binding of opsoniz

108 e reverse order, i.e., Cd(2+) is removed (by EDTA) first from the beta-domain followed by Cd(2+) remo

109 calcium (KD~2 pM), which can be reversed by EDTA allowing controlled "capture and release" of the sp

110 contrast, depleting Ca from fruit tissue by EDTA or low pH, increased soluble pectin release and spl

111 -bovine serum albumin-gold nanoparticles (Cd-EDTA-BSA-AuNP) conjugate deposited on the conjugation pa

112 ited on the conjugation pad strip and the Cd-EDTA complex formed in the analysis sample for the same

113 ited on the conjugation pad strip and the Cd-EDTA complex formed in the analysis sample for the same

114 tion in drinking and tap waters using the Cd-EDTA-BSA-AuNP conjugate as signal producer tool is intro

115 h the decreasing in concentrations of the Cd-EDTA-BSA-AuNP conjugate deposited in the conjugation str

116 based on competitive reaction between the Cd-EDTA-BSA-AuNP conjugate deposited on the conjugation pad

117 e 2A81G5 monoclonal antibody, specific to Cd-EDTA but not Cd(2+) free, which is immobilized onto the

118 G5 monoclonal antibody (mAb), specific to Cd-EDTA but not Cd(2+) free, which is immobilized onto the

119 rabinoxylan in presence of calcium chelating EDTA, which would indicate that Xyn30D-CBM35 might estab

120 Metal ion chelating resin, or the chelators EDTA and desferrioxamine decreased monatin and indole lo

121 At 21 days, DOX-COL + EDTA group showed 5.3 mug/mL value.

122 hing of the exposed root surfaces (DOX-COL + EDTA).

123 DOX-COL + EDTA-treated group retained more DOX during the periods

124 and oil-soluble antioxidants in combination (EDTA and vitamin E acetate) was less effective than usin

125 d severe growth defects in medium containing EDTA and were rescued by supplementation with zinc.

126 chloride solution, to quantitatively convert EDTA species in the samples into the Fe(III)-EDTA comple

127 nd results for GFR from chromium-51 ((51)Cr) EDTA excretion measurements ((51)Cr-EDTA GFR) from white

128 ween (68)Ga-EDTA GFR ((68)Ga-GFR) and (51)Cr-EDTA GFR ((51)Cr-GFR), using serial plasma sampling and

129 (51)Cr-EDTA GFR was compared with the estimated GFR (eGFR) from

130 ((51)Cr) EDTA excretion measurements ((51)Cr-EDTA GFR) from white patients >/= 18 years of age with h

131 (68)Ga-EDTA and (51)Cr-EDTA were injected concurrently in 31 patients.

132 mately 3 times the renal clearance of (51)Cr-EDTA.

133 erular filtration rate (GFR), assessed by Cr-EDTA clearance at pre-transplant evaluation, were retros

134 of inulin (n=488) and plasma clearance of Cr-EDTA (n=337).

135 tion technique and by renal extraction of Cr-EDTA, respectively.

136 integration of photocatalytic reaction of Cu-EDTA and one-dimensional (1D) ultralong and ultrathin Ti

137 ances the environmental sustainability of Cu-EDTA treatment via TiO2 photocatalysis.

138 In this light-initiated system, Cu-EDTA was oxidized by TiO2 thus releasing Cu(2+) which wa

139 he method is demonstrated using six cysteine-EDTA-Cu(2+) mutants of the 56-residue B1 immunoglobulin-

140 ecies (inorganically complexed or cysteine-, EDTA-, or NOM-bound) and solid-bound Hg(II) (carboxyl-/t

141 1.30 mm compared with open-flap debridement, EDTA, or placebo, but no significant difference compared

142 , we investigate the impact of citrate, DFB, EDTA, and NTA on biogenic UO(2) reoxidation with ferrihy

143 d not prevent the activation of FAK, nor did EDTA-mediated inactivation of the integrin.

144 for accelerated stored SOSDEs with different EDTA concentrations.

145 th anhydrous EDTA or disodium salt dihydrate EDTA show high yields of the native O-glycans compared w

146 a 500-mL chelation solution (3 g of disodium EDTA, 7 g of ascorbate, B vitamins, electrolytes, procai

147 Chelation therapy with disodium EDTA has been used for more than 50 years to treat ather

148 intravenous chelation regimen with disodium EDTA, compared with placebo, modestly reduced the risk o

149 ially available structural analogues of DMA: EDTA, TmDTA, and CyDTA.

150 In the absence of DMRB, EDTA facilitated reductive solubilization of 89% (withou

151 sine Equivalent Chelating Capacity) or EECC (EDTA Equivalent Chelating Capacity) indice according to

152 The resulting concentration of eluted EDTA was 10- to 200-fold higher than that originally pre

153 Ethylenediaminetetraacetate (EDTA) is currently the most abundant organic pollutant d

154 Ethylenediaminetetraacetate (EDTA) suppressed the Cu effect.

155 chelating agent ethylenediaminetetraacetate (EDTA) selectively chelated with the interfering metal io

156 ate (AQDS), and ethylenediaminetetraacetate (EDTA).

157 tion in situ by ethylenediaminetetraacetate (EDTA) and high performance liquid chromatography hyphena

158 External EDTA and copper ions can be used to reversibly switch ca

159 n vivo hydroxyl radical footprinting with Fe-EDTA was developed, and, together with results from a cy

160 r FeNa-ethylenediaminetetraacetic acid (FeNa-EDTA) were applied to hard red winter (HRW) and hard whi

161 These were Chelex-100 for EDTA and CyDTA, Amberlite CG50 for TmDTA and Amberlite I

162 = 3) and +0.30 +/- 0.07 (1sigma, n = 4) for EDTA, TmDTA, CyDTA, and DMA, respectively.

163 ine complexes and approximately 250 days for EDTA-bound Hg(II).

164 TA, 3.3 mug/dL (95% CI: 3.1, 3.5 mug/dL) for EDTA, and 3.7 mug/dL (95% CI: 3.5, 3.9 mug/dL) for place

165 of -22.89--31.72 mV, loading efficiency for EDTA~20%) for in vivo targeting in rats.

166 activation tubes were compared to those from EDTA tubes for 7 patients, all patients showed additiona

167 SOSDEs with metal chelator antioxidants e.g. EDTA, than free radical scavenging antioxidants e.g. gal

168 (68)Ga-EDTA and (51)Cr-EDTA were injected concurrently in 31 pa

169 (68)Ga-EDTA can be readily available using an onsite generator,

170 udy aimed to assess agreement between (68)Ga-EDTA GFR ((68)Ga-GFR) and (51)Cr-EDTA GFR ((51)Cr-GFR),

171 The reaction mix contains iron(II) EDTA, sodium ascorbate, hydrogen peroxide and lysozyme.

172 ng EDTA is that it allows to measure Cr(III)-EDTA complex and Cr(VI) simultaneously in an alkaline ex

173 was observed that the formation of a Cr(III)-EDTA complex avoided Cr(III) oxidation for these two ref

174 EDTA species in the samples into the Fe(III)-EDTA complex, and its subsequent detection by Ion-Pair-R

175 (3) provide additional evidence that Pu(III)-EDTA is a more likely mobile form of Pu than Pu(IV)-EDTA

176 n of basophil CD203c in samples collected in EDTA or heparin, stored at 4 degrees C, and analyzed 24

177 ophils was not observed in any conditions in EDTA-treated samples unless exogenous calcium/magnesium

178 mRNA levels of several inflammatory genes in EDTA/DTT when compared to enzymatically released cells.

179 s did not cause the side effects observed in EDTA injection alone, such as decrease in serum calcium

180 When FtsZ was assembled in GMPCPP or in EDTA, the inhibition by SulA was reduced.

181 ere 100% concordant with RealTime results in EDTA plasma samples and in 100 HIV-1-negative adult DBS.

182 sma and its abrogation by heat inactivation, EDTA, and eculizumab.

183 variety of physiologic solutions (including EDTA treated whole blood) and may be rapidly degraded vi

184 ity was assessed on 275 specimens, including EDTA blood, swabs, and tissues from experimentally infec

185 ents with a history of myocardial infarction,EDTA chelation therapy did not have a detectable effect

186 ients with peanut allergy was collected into EDTA or heparin tubes, and samples were stored at 4 degr

187 mixture of ferrous fumarate and sodium iron EDTA (FeFum+NaFeEDTA) in Kenyan infants.Infants (n = 50;

188 a more likely mobile form of Pu than Pu(IV)-EDTA, and (4) provide another example of outer-membrane

189 Additionally, Ca(2+)-, Mg(2+)- and K(+)(EDTA)-ATPase activities were markedly decreased.

190 ofactors (POP5, RPP21, RPP29, RPP30 and L7Ae-EDTA-Fe) revealed specific RNA cleavages, localizing the

191 using different organic complexing ligands, EDTA, and o-phenanthroline.

192 Using the model organic ligands, EDTA and histidine, we show a quantitative correspondenc

193 e resulting amide-linked chelate-lisinopril (EDTA-lisinopril, NTA-lisinopril, DOTA-lisinopril, and GG

194 accelerated stored SOSDEs with high and low EDTA concentrations were found.

195 acid proceeded more rapidly than with 0.5 M EDTA and may offer better preservation of histological a

196 ransducer and to an extra-vesicle messenger (EDTA) is used to control translocation of the transducer

197 Here we describe methidiumpropyl-EDTA sequencing (MPE-seq), a method for the genome-wide

198 oximately 41 mg EDTA, 3) approximately 41 mg EDTA as sodium EDTA (Na2EDTA), or 4) placebo for 28 wk.

199 NaFeEDTA that contained approximately 41 mg EDTA, 3) approximately 41 mg EDTA as sodium EDTA (Na2EDT

200 Addition of 0.1 mM EDTA totally protected the activity of the electrospraye

201 as stable in both 20% mouse serum and 100 mM EDTA, whereas the nickel-conjugated trimers were not sta

202 column was treated with EDTA-Na2 or if 25 mM EDTA-Na2 was added to the sample, was detectable at less

203 NaCl concentrations of approximately 240 mM (EDTA) and 140 mM (EGTA).

204 +/- 0.06 mM), glutathione (1.5 +/- 0.07 mM), EDTA (100 +/- 0.02 mM) and citric acid (186 +/- 0.16 mM)

205 003.2010) to 40 infusions ofa multicomponent EDTA chelation solution or placebo.

206 mM TE/100 g) and chelating activity (252 muM EDTA/100 g).

207 oporous microboxes was developed through Na2 EDTA-assisted ion exchange of CaTiO3 microcubes.

208 Sterile saline, citric acid, and NaOCl-EDTA may be proposed for use in the treatment of peri-im

209 position using solution (31)P-NMR after NaOH-EDTA extraction.

210 which contained the greatest amount of NaOH-EDTA extractable orthophosphate.

211 h P concentration in FeO strips, Olsen, NaOH-EDTA and water extracts.

212 ey are in complexes with EDTA following NaOH/EDTA extraction.

213 The method was then applied to NaOH/EDTA extracts of a grassland soil, of which paramagnetic

214 ith the operationally defined sorbed and non-EDTA-exchangeable fractions, and relatively little with

215 c Fe and Mn material associated with the non-EDTA-exchangeable fraction, which likely sequesters Pb a

216 cid (EDTA) but decrease it in the absence of EDTA, ruling out uptake by a specific Zn-Cys transporter

217 cetonitrile:water (8:2) with the addition of EDTA and cleaned using solid phase extraction with Hybri

218 Upon addition of EDTA and EGTA, the divalent cations were sequestered fro

219 thod improvement, we present the addition of EDTA during phenol workup.

220 Subsequent addition of EDTA reverses the switching process by extracting the Zn

221 Addition of EDTA to samples prevented de novo acetaldehyde formation

222 affected by the chemical form and amount of EDTA.

223 scribes the intention-to-treat comparison of EDTA chelation vs placebo.

224 /C71V) were modified with an iron complex of EDTA-2-aminoethyl 2-pyridyl disulfide.

225 ions containing such a high concentration of EDTA were found to inhibit Mg(2+)-dependent polymerase c

226 etric titration with known concentrations of EDTA in the thin layer sample was performed.

227 sensors are able to detect concentrations of EDTA that correspond to the amount of Cu(2+) that is use

228 es hindered the straightforward detection of EDTA.

229 The effect of EDTA chelation on the components of the primary end poin

230 he chelating action and dispersing effect of EDTA is critical in growing uniform films.

231 h-funded study of the safety and efficacy of EDTA-based chelation infusions in 1708 post-myocardial i

232 ol transition of the leaving acetyl group of EDTA.

233 Patients received 40 infusions of EDTA chelation or placebo.

234 all samples coated with EMD (irrespective of EDTA) when compared to samples containing human blood.

235 In the presence of EDTA and AQDS, PuO(2).xH(2)O((am)) was completely solubi

236 The presence of EDTA effectively eliminated interference from several me

237 he dockerin module, which in the presence of EDTA resulted in loss of affinity to the cohesin partner

238 d to adsorb surprisingly large quantities of EDTA and EGTA that elute from the resin at NaCl concentr

239 methods by pH adjustment, supplementation of EDTA, and rapid analysis via anion-exchange high-perform

240 strongly dependent on the amount and type of EDTA used and on the concentrations of the major acid-ba

241 -step extraction methods based on the use of EDTA and acetic acid were applied to differently amended

242 of nanoparticles of hydroxyapatite (nHA) on EDTA-treated and non-treated root surfaces in periodonta

243 to survive envelope damage caused by heat or EDTA, but was able to form functional heterocysts.

244 ut there were no positive effects of iron or EDTA on cognitive test scores.

245 revention Project in 20 communities provided EDTA-blood specimens during household surveys.

246 These NPs released EDTA slowly for up to 5 days.

247 The resulting chelate-Rev (EDTA-Rev, DTPA-Rev, NTA-Rev, and DOTA-Rev) conjugates we

248 Results showed EDTA accelerated UO(2) reoxidation the most at an initia

249 EDTA, 3) approximately 41 mg EDTA as sodium EDTA (Na2EDTA), or 4) placebo for 28 wk.

250 re ferrous sulfate (FeSO4) and ferric sodium EDTA (NaFeEDTA).

251 on decreased upon addition of water-soluble (EDTA and ascorbic acid) or oil-soluble (vitamin E acetat

252 reconstitution assay to identify a soluble, EDTA-sensitive activity that resects sliced pre-miRNAs i

253 umvent side effects associated with systemic EDTA chelation therapy.

254 of the exposed root surfaces (DOX-beta-TCP + EDTA).

255 The DOX-beta-TCP + EDTA-treated group retained more DOX during the periods

256 At 21 days, the DOX-beta-TCP + EDTA-treated group showed a 194.7 microg/mL value.

257 Six months after therapy, DOX-beta-TCP + EDTA-treated sites showed more significant clinical impr

258 emonstrated in vitro using a low-temperature EDTA-free agarose gel electrophoresis (LTEAGE) procedure

259 allic acid or ethylene diamine tetraacetate (EDTA)] in a sunflower oil salad dressing emulsion (SOSDE

260 und 7A inhibited Fenton reaction better than EDTA, IC50 of 37 vs 54 muM, due to radical scavenging, I

261 AA was found to be more efficient than EDTA in a way that lesser quantity is required for compl

262 Recent research suggests that EDTA chelation may be a well-tolerated and effective tre

263 the predominant proteins extracted from the EDTA-soluble fraction of the OM.

264 ty-nine patients (17% of total; n=115 in the EDTA group and n=174 in the placebo group) withdrew cons

265 ing on the baseline plasma viral load in the EDTA tubes.

266 and reprogramming and how to incorporate the EDTA-based passaging procedure into human induced PSC (i

267 interferences are masked with the use of the EDTA and OVA optimized concentrations, is presented too.

268 e of the complex with the protonation of the EDTA ligand reveals that the free energy barrier in gas

269 leave the RPR at nucleotides proximal to the EDTA-Fe-modified residues.

270 With the EDTA-2D-RP/RP approach, 13 mono-, 6 di-, and 3 triphosph

271 The enzyme was susceptible to EDTA (10mM) with irreversible loss of hydrolytic power.

272 Totally EDTA-demineralized specimens were infiltrated with Res.A

273 erent DNA extraction methods, including Tris-EDTA Method, a modified Cetyltrimethylammonium Bromide (

274 ey protein and casein) and antioxidant type (EDTA, ascorbic acid, catechin, alpha tocopherol, ascorbi

275 Using EDTA-2D-RP/RP-nanoUPLC-MS/MS to examine 500 mug of a hum

276 l bowel (i.e. terminal ileum) biopsies using EDTA/DTT and enzymatic release followed by magnetic bead

277 , was detectable at less than 100 fmol using EDTA-2D-RP/RP-nanoUPLC-MS/MS.

278 Only a few bacteria can degrade it, using EDTA monooxygenase (EmoA) to initiate the degradation.

279 Another benefit of using EDTA is that it allows to measure Cr(III)-EDTA complex a

280 Alternative precleaning setups using EDTA to enhance the removal of free metal or an offline

281 evaluated by testing 207 consecutive venous EDTA WB samples from HIV-1-infected patients attending a

282 e addition of Zn(2+) ions activated, whereas EDTA inhibited, PlcC-derived PLC activity.

283 citric acid increased membrane damage, while EDTA and DTPA had transient effects.

284 With EDTA, Cu levels in the stele were higher than those in t

285 Treatment of dizinc NDM-1 with EDTA results in complete removal of both zinc ions, but

286 on pad that ensures Cd(2+) complexation with EDTA and interference masking through ovalbumin (OVA).

287 tal ions, even if they are in complexes with EDTA following NaOH/EDTA extraction.

288 (hydr)oxide dissolution as demonstrated with EDTA.

289 rked reduction in cardiovascular events with EDTA chelation.

290 lipid oxidation in emulsions with NaCl, with EDTA being more effective.

291 r the dissolution of the core particles with EDTA yields the stimuli-responsive microcapsules that in

292 Flap surgery was performed with EDTA conditioning of the root prior to device implantati

293 sed to TTP plasma that was preincubated with EDTA or heat-inactivated, or to control plasma.

294 It involves treatment of the LC system with EDTA and 2D-RP/RP-nanoUPLC-MS/MS (high pH/low pH) analys

295 The specificity of the assay was tested with EDTA plasma (n = 1,301) and DBS from HIV-negative adults

296 C-MS/MS, even if the column was treated with EDTA-Na2 or if 25 mM EDTA-Na2 was added to the sample, w

297 RealTime test, are FDA cleared for use with EDTA plasma.

298 in peeling, whereas subsequent washing with EDTA abolished this effect, suggesting a role of calcium

299 Pb concentrations at endpoint, but no iron x EDTA interaction.

300 ot in the 1:2 Zn-histidine complex or the Zn-EDTA complexes, is taken up by the organism and reduced