ライフサイエンスコーパス: DAD

1 DAD is not permanently charged, and the uncharged form e

2 DAD was more frequent in patients who met clinical crite

3 A DAD triggered a spontaneous action potential significant

4 It does not have a DAD domain.

5 le 3-mer sequences: AAA, AAD, ADA, DAA, ADD, DAD, DDA, and DDD.

6 zation (EAD) or delayed afterdepolarization (DAD) or both, is unknown.

7 ons (EADs) and delayed afterdepolarizations (DADs) are voltage oscillations known to cause cardiac ar

8 cytes underlie delayed afterdepolarizations (DADs) that trigger cardiac arrhythmias.

9 2+ release and delayed afterdepolarizations (DADs).

10 quantities were determined by using CAD and DAD detectors.

11 e change from baseline in the ADAS-cog11 and DAD scores (bapineuzumab group minus placebo group) were

12 lay a key role in generating complex EAD and DAD dynamics observed experimentally in cardiac myocytes

13 he effects of Ca-voltage coupling on EAD and DAD dynamics.

14 nd thermodynamics of mDiaN with RhoA.GTP and DAD.

15 onoids has been developed combining MEKC and DAD detection.

16 e monitored and quantified using HPLC-MS and DAD.

17 lowering the regulatory potency of RhoA and DAD on mDiaN.

18 tic suppression of NCX reduces both EADs and DADs.

19 ites increased, integrated Ca transients and DADs became larger and shorter in duration, and the late

20 is model reproduces realistic Ca2+ waves and DADs driven by stochastic Ca2+ release channel (RyR) gat

21 chromatography (LC) coupled to diode array (DAD) and electrospray ionization mass spectrometry (ESI-

22 quid Chromatography (HPLC) with diode array (DAD) and fluorescence (FLD) detection was used to acquir

23 chromatography (HPLC) with photodiode array (DAD), electrochemical (ECD), charged aerosol (CAD), and

24 erization of beta-carotene, characterized by DAD-HPLC, resulted in a 2.5- to 4.8-fold increase in the

25 d combined with diode-array detector (SPE-CE-DAD).

26 Polyphenols were determined by cLC-DAD.

27 ography with photodiode array detection (cLC-DAD) and chemometric tools, was developed to determine p

28 The Hospital Discharge Abstract Database (DAD) was used to identify consecutive adults (>/=18 year

29 and the Disability Assessment for Dementia (DAD, with scores ranging from 0 to 100 and higher scores

30 Unlike DENAQ, DAD acts upstream of retinal ganglion cells, primarily c

31 The use of sequential diode array detection (DAD) and tandem mass spectrometry (MS/MS) allowed direct

32 y (Cap-LC) coupled to diode array detection (DAD) has the potential to estimate mean concentrations o

33 atography (HPLC) with diode-array detection (DAD) was developed.

34 using HPLC coupled to diode array detector (DAD) and electrospray ionization mass spectrometry (ESI-

35 elease in populations of myocytes) determine DAD features in cardiac tissue using a combined experime

36 In screening for DID-DAD disruptors that activate mDia, we identified two mol

37 ing to the DAD of INF2 competes with the DID/DAD interaction, thereby activating actin polymerization

38 as INF2 activators by competing with the DID/DAD interaction.

39 rminal antibody for INF2 that blocks the DID/DAD interaction.

40 , we describe diethylamino-azo-diethylamino (DAD), a third-generation photoswitch that is capable of

41 ing have TRS structures which have different DADs, and pronounced 1 degrees isotope effect on 2 degre

42 l tunneling-ready-states (TRSs) of different DADs were calculated and fitted to the experiments to fi

43 t requires a longer donor-acceptor distance (DAD) in a lighter isotope transfer process.

44 t reactive hydrogen donor-acceptor distance (DAD) is typically ca. 2.7 A, considerably shorter than n

45 requires a shorter donor-acceptor distance (DAD) than that of a lighter isotope.

46 d to the SMRT deacetylase activation domain (DAD), which mediates HDAC3 binding and activation, and H

47 ed for the Diaphanous autoinhibitory domain (DAD), which is C-terminal to the formin homology 2 domai

48 C-terminal diaphanous-autoregulatory domain (DAD) and the C terminus (CT) of formins have also been s

49 hrough its diaphanous autoregulatory domain (DAD) that resembles a Wiskott-Aldrich syndrome protein h

50 C-terminal Diaphanous-autoregulatory domain (DAD).

51 s of polymers based on donor-acceptor-donor (DAD) moieties 2,1,3-benzoselenadiazole, 2,1,3-benzothiad

52 ns in BAL CXCR3 ligand concentrations during DAD.

53 failure, increase the probability of extreme DADs by multiple orders of magnitude.

54 First, DAD and FLD chromatographic-fingerprint datasets were se

55 orescent and diode array detectors (HPLC-FLD/DAD) and confirmed by gas chromatography coupled with ma

56 e-sink factors in cardiac tissue to generate DADs of sufficient amplitude to trigger action potential

57 nd the rate of DADs were unaltered; however, DADs had lower amplitude in hetKO.

58 HPLC-DAD analysis detects a total of 10 polyphenolic compound

59 HPLC-DAD analysis of the samples revealed lumichrome (4.7-10.

60 HPLC-DAD provided suitable linearity, precision and accuracy.

61 HPLC-DAD provided suitable linearity, precision and accuracy.

62 HPLC-DAD was employed to evaluate the extraction parameters,

63 HPLC-DAD-ESI-MS(n) analyses allowed the identification of six

64 HPLC-DAD/ESI-MS(n) measurements in the fruits' peel and pulp

65 ility to transform the p-coumaric acid (HPLC-DAD).

66 In addition, HPLC-DAD was adequate for determining the three foremost para

67 on of the ISO 3632 (2011) method and an HPLC-DAD method for safranal quantity determination in saffro

68 To evaluate stilbene concentration, an HPLC-DAD method was validated.

69 and were quantitatively evaluated in an HPLC-DAD-based metabolomics study.

70 An HPLC-DAD-ESI-MS method was developed to investigate the distr

71 An HPLC-DAD-MS method is described to analyze textile dyes in di

72 In the present investigation, an HPLC-DAD/ESI-MS method for the complete analysis of tannins a

73 Chromatographic analysis (HPLC-DAD/ESI-MS) of blue maize extracts showed the presence o

74 amples were characterized by CIELAB and HPLC-DAD analyses.

75 ition by spectrophotometric methods and HPLC-DAD analysis and the in vitro antioxidant activity of di

76 a combination of spectrophotometric and HPLC-DAD methods was used to analyse the phenolic composition

77 yphenol compounds (Folin Ciocalteau and HPLC-DAD), total flavonoids (reaction with AlCl3) and antioxi

78 yl-leucine (HHL), as model peptide, and HPLC-DAD, as analytical method.

79 nolics (measured by Folin Ciocalteu and HPLC-DAD-ESI/MS(n)) at harvest and during storage for 21days

80 erformed by means of HPLC-ESI-HR-MS and HPLC-DAD.

81 were analysed by spectrophotometry and HPLC-DAD.

82 safranal content obtained by UV-vis and HPLC-DAD.

83 ualities, conventional analyses such as HPLC-DAD or LC-MS lose valuable information on metabolite loc

84 ) and a Port wine (PR), was analysed by HPLC-DAD after purification by solid phase extraction (SPE).

85 ere quantitated in regular intervals by HPLC-DAD analyses.

86 Ascorbic acid was monitored by HPLC-DAD and colour intensity by spectrophotometric measureme

87 Aqueous supernatants were analyzed by HPLC-DAD and extractable anthocyanin contents were obtained.

88 benthamiana by analyzing carotenoids by HPLC-DAD and the volatile products by GC/MS.

89 molecular weight phenolic compounds by HPLC-DAD showed a significant (p<0.05) content increase of th

90 Compositional analysis by HPLC-DAD showed that the distribution of phenolic compounds i

91 A method for 18 phenolic monomers by HPLC-DAD was developed, validated, and applied to samples.

92 flavonols concentrations determined by HPLC-DAD were studied during drying.

93 The contents of flavonoids (by HPLC-DAD) and proanthocyanidins (n-butanol/HCl assay), reduci

94 o oxidative disappearance (monitored by HPLC-DAD) and that of the mixtures to retain their antioxidan

95 sation with n-butanol/HCl, flavonols by HPLC-DAD, reducing capacity by ferric ion reducing antioxidan

96 ogenic acid contents were determined by HPLC-DAD, total anthocyanin content by pH-differential spectr

97 yx of ripe fruits) were investigated by HPLC-DAD-APCI-MS(n).

98 ated for their quantitative profiles by HPLC-DAD-ESI-MS analyses.

99 were found only in PS as identified by HPLC-DAD-ESI-MS(n).

100 fferent phenolics were characterised by HPLC-DAD-ESI-MS-MS and UPLC-HR-QTOF-MS-MS.

101 k currant in Finland were identified by HPLC-DAD-ESI-MS/MS.

102 es and 4 betacyanins were identified by HPLC-DAD-ESI/MS(n), 23 and 15 new compounds being described i

103 papaya L.) (LP), were characterized by HPLC-DAD-ESI/MS(n), the antioxidant capacity was evaluated by

104 the phenolic compounds were analyzed by HPLC-DAD-ESI/MS, and the antioxidant activity was evaluated u

105 a spuria were tentatively identified by HPLC-DAD-ESI/MS.

106 Analyses were performed by HPLC-DAD-ESI/MS.

107 repared as infusions, were evaluated by HPLC-DAD-ESI/MS.

108 ides, were identified and quantified by HPLC-DAD-MS analysis.

109 of them were tentatively identified by HPLC-DAD-MS and are xanthophylls present under an esterified

110 - and beta-carotene, were quantified by HPLC-DAD-MS in fourteen genotypes of wheat, barley and tritor

111 enoid profile of different genotypes by HPLC-DAD-MS(n).

112 potato provenances were investigated by HPLC-DAD-MS(n).

113 ntioxidant metabolites were measured by HPLC-DAD-MS/MS in mature fruits and their biological activiti

114 observation of anthocyanins profile by HPLC-DAD-MS/MS was conducted.

115 from the banana pulp were determined by HPLC-DAD-MS/MS, and the colour of the banana skin was determi

116 analyzed five commercial olive oils by HPLC-DAD-TOF/MS to evaluate their lignan content and detected

117 in fresh hypanthium were determined by HPLC-DAD.

118 tion of 41 commercial chocolates was by HPLC-DAD.

119 ed with 1 mL methanol and determined by HPLC-DAD.

120 followed spectrophotometrically and by HPLC-DAD.

121 quercetin, were identified from EEAP by HPLC-DAD.

122 xtraction conditions were determined by HPLC-DAD.

123 PCs were then further quantified by HPLC-DAD.

124 nd 2 methylxanthines were quantified by HPLC-DAD.

125 vis according to ISO 3632 (2011) and by HPLC-DAD.

126 -anthocyanins adducts, were analyzed by HPLC-DAD/ESI-MS.

127 n basolateral media at 1, 3 and 18 h by HPLC-DAD/MS.

128 Changes on phenolic composition (HPLC-DAD-MS), copigmentation/polymerisation (spectrophotometr

129 omatography with diode-array detection (HPLC-DAD).

130 omatography with diode-array detection (HPLC-DAD).

131 d chromatography-diode array detection (HPLC-DAD).

132 raphy coupled to diode array detection (HPLC-DAD).

133 phy, coupled to a diode array detector (HPLC-DAD) and a mass spectrometer (UPLC-MS), was used to comp

134 coupled with photodiode array detector (HPLC-DAD), respectively.

135 aphy coupled to a diode array detector (HPLC-DAD).

136 array and mass spectrometry detectors (HPLC-DAD-MS(n)), and on the antioxidant activity evaluated by

137 is study, a simple, rapid and efficient HPLC-DAD-APCI(+)-MS method was developed and applied to ident

138 chemical composition of leaf employing HPLC-DAD.

139 on its formation were studied employing HPLC-DAD.

140 Results from HPLC-DAD analysis clearly showed that native structures of ph

141 chromatography coupled with DAD and MS (HPLC-DAD-MS).

142 anol and analyzed with UPLC-DAD-ESI-MS, HPLC-DAD, and NMR.

143 he aim of this work was to set up a new HPLC-DAD method for simultaneously analysing 14 polyphenolic

144 he work was to confirm applicability of HPLC-DAD method for analysis of total content of vitamin C (T

145 a validated chromatographic procedure (HPLC-DAD) after a preliminary drying step and an opportune ex

146 ir degradation compounds were regularly HPLC-DAD-analyzed.

147 furfural compounds were examined by RP-HPLC-DAD in 20 commercial milk-based powdered infant formula

148 CA down to 0.2%, w/w was achieved by RP-HPLC-DAD using aqueous acetonitrile elution solvent (pH=2.8).

149 matography-Diode Array Detection (IP-RP-HPLC-DAD).

150 and ellagic acids were identified by RP-HPLC-DAD, also coupled to off-line matrix assisted laser deso

151 RP-HPLC-DAD-FLU separation enabled us to identify 20 derivatives

152 array detector and a mass spectrometer (HPLC-DAD-ESI/MS).

153 spray time-of-flight mass spectrometry (HPLC-DAD-ESI-TOF/MS) of the diverse persimmon juices produced

154 ctrospray ionisation mass spectrometry (HPLC-DAD-ESI/MS(n)) and antioxidant potential.

155 ionization/ion trap mass spectrometry (HPLC-DAD-ESI/MS(n)).

156 -array detection and mass spectrometry (HPLC-DAD-MS), were chlorogenic acid, isoorientin and swertiaj

157 ray detection-tandem mass spectrometry (HPLC-DAD-MS/MS) analytical approach was developed for retinoi

158 ay detection- tandem mass spectrometry (HPLC-DAD-MS/MS) identified 29 phenolics belonging to phenolic

159 In the present study HPLC-DAD-ESI/MS(2) was used to investigate the compounds cont

160 In this study HPLC-DAD-MS/MS was applied for the identification of compound

161 asonic solvent extraction) and targeted HPLC-DAD were applied.

162 The HPLC-DAD analysis demonstrated that, lycopene was obtained in

163 The HPLC-DAD assay showed the presence of mostly tannins and flav

164 The HPLC-DAD method revealed that, out of 13BPs, only six are sel

165 rocedure, validation parameters for the HPLC-DAD-MS(n) based characterisation and quantitation method

166 The HPLC-DAD-MS/MS method was applied to freshly extracted canola

167 The HPLC-DAD/ESI-MS profiles allowed the tentative identification

168 Therefore, HPLC-DAD might be preferable to UV-vis for determining the sa

169 extraction mediated by LGH-15 prior to HPLC-DAD allows the determination of 14 phenols in onion, oli

170 ion-microextraction (USAEME) coupled to HPLC-DAD has been developed to identify and quantify several

171 der field conditions were studied using HPLC-DAD after QuEChERS extraction.

172 ds were identified and quantified using HPLC-DAD and among them, malvidin-3-glucoside and its derivat

173 tion and quantification were done using HPLC-DAD and LC-MS/MS.

174 ajor constituents were elucidated using HPLC-DAD and UHPLC-HRMS/MS (hybrid IT-Orbital trap spectromet

175 sation of vitamin D3 were studied using HPLC-DAD and UHPLC-MS/MS.

176 new polymer affinity was studied using HPLC-DAD for different polyphenols using PVPP as a control.

177 ield condition were determined by using HPLC-DAD with QuEChERS method.

178 By using HPLC-DAD, the extraction ability of SPE with the diol phase a

179 2) were tentatively characterized using HPLC-DAD-ESI-MS(n).

180 the berry extracts, were studied using HPLC-DAD-ESI-MS/MS and CUPRAC assays, respectively.

181 components of sumac fruit epicarp using HPLC-DAD-ESI-MS/MS in two different ionisation modes.

182 rom UHPLC and qualitative studies using HPLC-DAD-MS showed that in addition to commonly found phenoli

183 gradation products were monitored using HPLC-DAD-MS(n).

184 exythiazox residues in strawberry using HPLC-DAD.

185 n and detection were accomplished using HPLC-DAD.

186 alivary proteins has been studied using HPLC-DAD.

187 y categories and safranal content using HPLC-DAD.

188 Furthermore, a fully validated HPLC-DAD-CAD method for the quantification of phenolic compou

189 ctroscopic data for this set along with HPLC-DAD analysis of major apocarotenoids assisted identifica

190 ent of phenolic compounds was made with HPLC-DAD.

191 determined using a QuEChERS method with HPLC-DAD.

192 In this work, HPLC-DAD was used for the quantification of major benzoxazino

193 urate HPLC method using HPLC/ESI-MS and HPLC/DAD for simultaneous analysis of iridoids (loganic acid)

194 Comparison of HPLC/ESI-MS and HPLC/DAD indicated that HPLC/ESI-MS is more sensitive, reliab

195 UV/Vis spectrophotometry and HPLC/DAD-ESI/MS were applied to determine, respectively, the

196 this work, UV/Vis spectrophotometry and HPLC/DAD-ESI/MS were applied to determine, respectively, the

197 determined by colorimetric methods and HPLC/DAD.

198 polyphenols and volatile compounds (by HPLC/DAD and GC-MS, respectively) demonstrate that the adsorp

199 s in the mature fruits was performed by HPLC/DAD using weighted linear regression model from 0.05 to

200 A cartridges and subsequent analysis by HPLC/DAD was characterised and applied to the analysis of fru

201 semi-preparative HPLC then analysed by HPLC/DAD/HRMS in both ESI(-) and ESI(+) ionisation mode.

202 omatography with diode array detection (HPLC/DAD) or by gas chromatography with mass spectrometry det

203 ts were separated and analyzed by an RP-HPLC/DAD system.

204 hy coupled to diode array detection (RP-HPLC/DAD) was developed using a fused core pentafluorophenyl

205 n and electron spray-mass spectrometry (HPLC/DAD/ESI-MS) was used to identify the phenolic profile an

206 ion and electrospray-mass spectrometry (HPLC/DAD/ESI-MS); nineteen different phenolic compounds and s

207 imits obtained for ETU and PTU with the HPLC/DAD method were 7 and 16 mug kg(-)(1) in strawberries (f

208 tains a reactive (a) conformer with hydrogen DAD of approximately 3.1 A, approximately van der Waals

209 hindered TRS structure so that the change in DAD due to the change in 1 degrees isotope does not sign

210 nneling-impaired SLO variants show increased DADs and variations in substrate positioning and rigidit

211 INF2-DAD is also predicted to participate in an autoinhibitor

212 Addition of proteins that compete with INF2-DAD for actin binding (profilin or the WH2 from Wiskott-

213 try detection using electrospray ionisation (DAD/ESI-am-MS).

214 whereas all of these factors promoted larger DADs with higher probability of generating triggered act

215 LC-DAD-MS and GC-MS analyses showed major qualitative and q

216 LC-DAD-MS data revealed the presence of pseudohypericin (0.

217 An LC-DAD method was set up and validated and the non-anthocya

218 ations of the plant by ESI-MS, LC-DAD and LC-DAD-ESI-MS.

219 were performed with LC-DAD-ESI-MS/MS and LC-DAD-RID was used for the sugar analyses.

220 Matricaria chamomilla L. were studied by LC-DAD and NMR.

221 e acacia, ash and oak wood was studied by LC-DAD-ESI/MS, to identify the phenolic compounds that wood

222 Samples were analysed by LC-DAD-MS/MS and LC-MS.

223 rotannin isomers from EAF was obtained by LC-DAD-QTOFMS, ranging from 374 to 870Da.

224 id-phase microextraction (IT-SPME) to Cap-LC-DAD, the effect of the dilution can be studied as partic

225 uid chromatography-diode array detection (LC-DAD) and liquid-chromatography fluorescence detection (L

226 matography with UV-diode array detection (LC-DAD) for simultaneous determination of the beta-lactam a

227 ulti-residue LC-UV-diode array detection (LC-DAD) method is a powerful and popular alternative for th

228 Chromatography with Diode Array Detector (LC-DAD) and Mass Spectrometry (LC-MS).

229 was applied to LC-DAD, LC-FLD, and fused LC-DAD-FLD data.

230 tural populations of the plant by ESI-MS, LC-DAD and LC-DAD-ESI-MS.

231 ation/identification protocol based on RP-LC-DAD-ESI-MS-MS has been employed for the characterisation

232 RP-LC-DAD-ESI-MS-MS separation/identification protocol has bee

233 rized in cactus pear juice using a single LC-DAD-ESI-MS/MS method.

234 pray ionization tandem mass spectrometry (LC-DAD-ESI-MS/MS) in multiple reaction monitoring mode (MRM

235 pray ionization tandem mass spectrometry (LC-DAD-ESI-MS/MS), whereby the two purine alkaloids were de

236 The LC-DAD and LC-ESI-(HR)MS(n) metabolic profiles showed high

237 ng least-squares (MCR-ALS) was applied to LC-DAD, LC-FLD, and fused LC-DAD-FLD data.

238 ids, and HMF analyses were performed with LC-DAD-ESI-MS/MS and LC-DAD-RID was used for the sugar anal

239 xyloside were separated and identified by LC/DAD/MS and by co-elution with standards.

240 s an inactive (b) conformer with even longer DAD, establishing that stochastic conformational samplin

241 MIFH2 and mDia agonists IMM-01/-02 and mDia2-DAD peptides, which disrupt autoinhibition, to examine t

242 Moreover, DAD was capable of generating ON and OFF visual response

243 y UV-Vis spectroscopy and LC-ESI-(Qq)-TOF-MS-DAD, enabling the identification of some intermediate sp

244 key factors influencing the distribution of DAD amplitude and timing include cytosolic and sarcoplas

245 An episode of DAD was associated with increased risk of CLAD (hazard r

246 sies from 441 recipients with 62 episodes of DAD.

247 Intravitreal injection of DAD restored retinal light responses and light-driven be

248 R) gating and is used to study mechanisms of DAD variability.

249 tients characterized by a high proportion of DAD.

250 l activities of DAAM, we studied the role of DAD-CT regions of Drosophila DAAM in its interaction wit

251 racellular Ca loading, and two mechanisms of DADs are identified, i.e., Ca-wave-dependent and Ca-wave

252 s apply: (1) Although the absolute number of DADs is unaffected, an impaired translation of DADs into

253 aneous Ca(2+) release events and the rate of DADs were unaltered; however, DADs had lower amplitude i

254 Ds is unaffected, an impaired translation of DADs into spontaneous action potentials results from a r

255 duration and the occurrence of EADs promote DADs by increasing intracellular Ca loading, and two mec

256 als that increased intracellular Ca promotes DAD-mediated triggered activity in tissue predominantly

257 ous action potentials results from a reduced DAD amplitude.

258 40-fold, and we show that the WH2-resembling DAD motif is responsible for this increase.

259 A RPLC-DAD method for the analysis of eight anthocyanins was de

260 The shorter DAD in D-tunneling, as compared to H-tunneling, could br

261 Moreover, an HDAC3 binding-deficient SMRT DAD mutant coactivated p53 transcriptional activity.

262 ed based on photodiode array UV-vis spectra (DAD), ESI-MS-MS spectrometric data and spiking experimen

263 es C during 240min with UV-Vis spectrometry, DAD-HPLC and TEAC test.

264 a dyad structure (AD) or a triad structure (DAD and ADA) in order to understand the correlations bet

265 o induce diastolic Ca waves and subthreshold DADs.

266 We also demonstrate that DAD-CT makes the FH2 domain more efficient in antagonizi

267 We hypothesized that DAD, the most severe form of acute lung injury, would le

268 ses local filament deformation, allowing the DAD to bind adjacent actin protomers, further disrupting

269 nalizing the absence of organization for the DAD co-oligomer and therefore to draw general rules for

270 We found that the DAD-CT region binds actin in vitro and that its main act

271 and suggest a model where p53 binding to the DAD limits HDAC3 interaction with this coregulator, ther

272 k, we show that actin monomer binding to the DAD of INF2 competes with the DID/DAD interaction, there

273 and HDAC3 could attenuate p53 binding to the DAD region of SMRT.

274 performance liquid chromatography coupled to DAD and electrospray-ionization time-of-flight mass spec

275 performance liquid chromatography coupled to DAD and mass spectrometer detectors was applied to study

276 od was developed for the extraction and UFLC-DAD-ESI-MS analysis of carbonyl compounds (CCs) in oils

277 However, manually processing acquired UHPLC-DAD-HRAM/MS(n) data for flavonoid analysis is very chall

278 sible absorption spectrophotometry and UHPLC-DAD.

279 h determination of phenolic content by UHPLC-DAD-ESI(-)HRMS revealed the presence of 10 phenolics as

280 l analyses of spectral data deduced by UHPLC-DAD-ESI-HRMS and NMR methods.

281 pole Time of Flight mass spectrometry (UHPLC-DAD-ECD-QTOFMS).

282 ate-mass multistage mass spectrometry (UHPLC-DAD-HRAM/MS(n)), have become the tool-of-the-trade for p

283 diode array tandem mass spectrometry (UHPLC-DAD-MS/MS).

284 the standard chromatographic technique UHPLC-DAD (Ultra High Performance Liquid Chromatography with D

285 The results confirmed that the UHPLC-DAD/ESI-am-MS method developed here was convenient and r

286 eteen flavonoids were quantified using UHPLC-DAD MS/MS.

287 One-/two-dimensional NMR and UPLC-DAD-ESI-MS(n) measurements were used to monitor the synt

288 Spectrophotometry and UPLC-DAD-ESI-MS/MS systems were utilized for quantitative ana

289 as recorded using a new fully validated UPLC-DAD method.

290 with aqueous ethanol and analyzed with UPLC-DAD-ESI-MS, HPLC-DAD, and NMR.

291 ol 50% (v/v) was studied by means of HPLC UV-DAD.

292 places liprin-alpha3 allosterically, whereas DAD competes with liprin-alpha3 for a highly overlapping

293 ng phase of the action potential (AP), while DADs are driven by spontaneous calcium (Ca) release duri

294 from wine and analyzed by HPLC combined with DAD and QTOF mass spectrometer.

295 rformance liquid chromatography coupled with DAD and MS (HPLC-DAD-MS).

296 This work outlines HPLC coupled with DAD detection for accurate quantification of patulin (my

297 e obtained, ranging from 10 to 72 mug/g with DAD and 0.01 to 0.23 mug/g with ESI-MS, and the resultin

298 aim a previous gradient RP-HPLC method with DAD detection was modified and validated, according to i

299 lding on this, replacement of Capu-tail with DADs from other formins tunes nucleation activity.

300 Again, replacement of Capu-tail with DADs from other formins tunes the processive association