ライフサイエンスコーパス: FID

1 FID CSI (Free Induction Decay Chemical Shift Imaging) se

2 FID in larger urban areas on islands with invasive preda

3 FID is a tagless approach; the target RNAs and the ligan

4 FID was defined as an intimal disruption with contrast m

5 FID was higher on islands with invasive predators compar

6 onclusions can be drawn from this study: (1) FID assay with 3 and polynucleotides demonstrates the pr

7 (2) FID assay and UV thermal denaturation experiments show t

8 (5) FID and ITC titration between 3 and an intramolecular DN

9 (6) FID assay using 3 and 512 hairpin DNA sequences that var

10 Patients with acute FID had a higher risk of aorta-related events than those

11 Although acute FIDs should be treated early and invasively, lesions dev

12 here were 43 patients (40%) who developed an FID with larger basal maximum aortic diameter and hemato

13 4 discharged patients, 33 (35%) developed an FID within the first 6 months of follow-up: 19 evolved w

14 re analyzed using gas chromatography with an FID detector.

15 The magnitude of the orthogonalized analyte FID is the signal intensity plotted in the chromatogram.

16 (4) CD and FID titration studies show a DNA binding site size of 10

17 We conclude that FIE and FID zones generated by BPEs can be exploited to shape an

18 radaic ion enrichment and depletion (FIE and FID) on electric field gradients.

19 s applied for qualitative identification and FID for quantification, allowed higher flows and slightl

20 that simultaneously performs microbatch and FID crystallization methods in a single device.

21 elated with GC analysis using parallel O and FID detection.

22 of arterioles was significantly reduced and FID was augmented.

23 f mitochondrial reactive oxygen species, and FID is unknown.

24 hile chromatographic methods with UV-VIS and FID detection were used to determine the free amino acid

25 Archived FIDs and newly acquired aquatolide spectra demonstrate t

26 btained by fluorescence displacement assays (FID) and isothermal titration calorimetry (ITC), with bi

27 Our analysis revealed that the average FID score between virtually stained and H&E-stained imag

28 artially migratory birds had greater average FIDs than sedentary birds, suggesting that they were gen

29 ph (TAG) with simultaneous detection by both FID and EIMS.

30 Charybdotoxin 10(-8) mol/L impaired both FID (15+/-3% versus 75+/-12%, P<0.05) and hyperpolarizat

31 In the hydrocarbon analysis by FID, paraffins, naphthenes, and aromatics form distinct

32 Chronic FID was not associated with aorta-related events (hazard

33 ed by Fourier transform of the corresponding FID.

34 The corresponding FIDs may be readily submitted with publications and coll

35 Two (1)H Free induction decay (FID) (A and B) and four (1)H T(2) Car-Purcell-Meiboom-Gi

36 ious GC-MRR studies, a free induction decay (FID) measurement was Fourier transformed to generate eac

37 In free induction decay (FID) measurements, proton populations were assigned to (

38 of the single quantum free induction decay (FID) revealed that signals from buffer and DNDS-treated

39 tative analysis of NMR free induction decay (FID) signals.

40 high-resolution 1D NMR free induction decay (FID).

41 analyzing the 35Cl NMR free induction decay (FID).

42 E analyzes individual free induction decays (FIDs) and dissects them into sub-FIDs that are transform

43 in ethnic groups (Fijians of Indian descent [FID] and Indigenous Fijians [iTaukei]) in Fiji were recr

44 omatography (GC)-flame ionization detection (FID) allowed for source identification.

45 atography (GC) - flame ionization detection (FID), was optimized and validated for high-sensitivity M

46 uel oil by using flame ionization detection (FID), without any prefractionation.

47 lysed by GC with flame ionization detection (FID).

48 ography (GC) with flame ionisation detector (FID).

49 trometry (MS) and flame ionization detector (FID) analysis.

50 ry (GC-MS) and GC-flame ionization detector (FID) analysis.

51 ource rocks using flame ionization detector (FID) and sulfur chemiluminescence detector (SCD).

52 o quantify by SFC-flame ionization detector (FID) due to incomplete resolution between the saturate/m

53 ctors, a modified flame ionization detector (FID) for quantitative carbon detection (Polyarc reactor)

54 detector, e.g. a flame ionization detector (FID) or an olfactory (sniffing) port.

55 For example, a flame ionization detector (FID) produces data that is especially effective for quan

56 h equipped with a flame ionization detector (FID) set at 250 degrees C.

57 matography (GC) - flame ionization detector (FID) was used for determining MOH in olive oils (OOs) an

58 S response with a flame ionization detector (FID), a near-universal detector for organics, to quantif

59 e obtained with a flame ionization detector (FID).

60 meter (qMS) and a flame ionization detector (FID).

61 h equipped with a flame ionization detector (FID).

62 y (GC) coupled to flame ionization detector (FID).

63 ermal calorimetry), CD (circular dichroism), FID (fluorescent intercalator displacement), and UV (ult

64 nd at different temperatures using different FID processing parameters showed no resolved splitting o

65 : a SlipChip-based free interface diffusion (FID) method and a SlipChip-based composite method that s

66 Flow-induced dilation (FID) is dependent largely on hyperpolarization of vascul

67 Flow-induced dilation (FID) was assessed in isolated arterioles from N(G)-nitro

68 of a fluorescent intercalator displacement (FID) assay conducted on a series of hairpin deoxyoligonu

69 nding fluorescent intercalator displacement (FID) assay for initial assessment of the DNA binding aff

70 ng a fluorescence intercalator displacement (FID) assay.

71 this fluorescent intercalator displacement (FID) assay.

72 Fluorescent intercalator displacement (FID) is a convenient and practical tool for identifying

73 Focal intimal disruption (FID) has been described in >20% of type B intramural hem

74 n ideal synthetic quality metric called Dist-FID.

75 Two metrics, Frechet Inception Distance (FID) and Kernel Inception Distance (KID), were used to q

76 n Score (IS) and Frechet Inception Distance (FID), computed on diffusion- and generative adversarial

77 n Score (IS) and Frechet Inception Distance (FID).

78 e measurement of Flight Initiation Distance (FID) and categorization of the type of flight response b

79 , reaction time, flight-initiation distance (FID), vulture remaining index, and latency to return.

80 ehaviour (e.g., flight initiation distance - FID) change depending on whether invasive predators are

81 Each FID yields a single intensity value after Gram-Schmidt o

82 urban and non-urban populations of finches, FID was lower in urban finch populations, but only above

83 eeping the solution in the neck channels for FID stable, the plates of the SlipChip were etched with

84 First, analyte-free FIDs are used to construct a basis set representing the

85 proposed here to extract peak intensity from FID using the Gram-Schmidt vector orthogonalization meth

86 A single out-line HPLC-GC (FID) analytical method is applied to acquire the chromat

87 giving an alternative to the widely used GC (FID/MS) methodologies.

88 echniques for quantification (HPLC-ELSD, GC- FID).

89 GC-FID measurements were performed by including ratios to a

90 GC-FID results proved that galactose was the dominant sugar

91 GC-FID/MS (after HS-SPME and ultrasonic solvent extraction)

92 GC-FID/MS analysis was performed with two different extract

93 y-step approach to easily adapt and use a GC-FID as an olfactometer, as well as a detailed descriptio

94 y-step approach to easily adapt and use a GC-FID as an olfactometer, as well as a detailed descriptio

95 A GC-FID method based on the ratio between the integrated pea

96 Acetaldehyde (GC-FID) and pyruvic acid (Y15 enzymatic autoanalyser) conte

97 as analysed after treatment using Agilent GC-FID.

98 ned fewer constituents based on GC-MS and GC-FID analyses.

99 0 min trapping time followed by GC-MS and GC-FID analysis identified 23 and 30 common VOCs from the p

100 The (1)H NMR and GC-FID data from different ratios of SIO were adjusted by a

101 Both nanoLC/EI-MS and GC-FID methods were validated and similar results were obta

102 Using field trials and GC-FID oil analysis we characterized plant materials from a

103 e analyses were carried out using NMR and GC-FID techniques.

104 tive composition was studied by GC-MS and GC-FID.

105 with mass spectrometry (UPLC-QTOF-MSE and GC-FID/MS).

106 characterized via UPLC-ESI-QTOF-MS(E) and GC-FID/MS.

107 PAEs) in hydroalcoholic food beverages by GC-FID (and peak confirmation by GC-IT/MS) has been set up.

108 29/2012, was developed by GC-FID analysis of methyl esters of fatty acids, followed b

109 ends of EU origin) were differentiated by GC-FID analysis of sterols and esterified sterols followed

110 greement (75-125%) with those obtained by GC-FID analysis, demonstrating the accuracy of the develope

111 dspace and liquid extractions followed by GC-FID analysis.

112 The extracts were analyzed by GC-FID and GC-MS.

113 parts of Artemisia indica was analysed by GC-FID and GC-MS.

114 According to essential oils analysis by GC-FID and GC/MS, the major constituents were alpha-pinene,

115 ts and its extracts were characterized by GC-FID and HPLC-UV.

116 antioxidant capacity were investigated by GC-FID and ORAC method, respectively.

117 yl esters of fatty acids were analysed by GC-FID and processed through chemometric tools (PCA, TFA, S

118 According to the results obtained by GC-FID for products containing prebiotics, the content of F

119 fatty acid profiles were investigated by GC-FID revealing high contents of PUFAs and a high omega-3/

120 According to the results obtained by GC-FID, B-bourbonene, B-gurjunene, B-elemene and cedrenol w

121 According to the results obtained by GC-FID, beta-bourbonene, beta-gurjunene, beta-elemene and c

122 Extracts were assayed by GC-FID, GC-MS, and LC-MS for the identification of 10 prima

123 Based on the results of sugar analysis by GC-FID, glycosidic linkage by GC-MS, NMR spectroscopy, and

124 Based on the results of sugar analysis by GC-FID, glycosidic linkage by GC-MS, NMR spectroscopy, and

125 The spirits were characterized by GC-FID, HS-SPME GC-MS, and sensory analysis by trained pane

126 microextraction (HS-SPME) and analysed by GC-FID.

127 xtracted solutes were further analyzed by GC-FID.

128 Fatty acid profiling was conducted by GC-FID.

129 l particle silica gel SPE and analyzed by GC-FID.

130 secondary oxidation products of sterol by GC-FID/MS and oligomers by HPSEC-RI.

131 Fatty acids (FA) were analyzed by GC-FID; tocopherols, sterols, squalene, and phenolics compo

132 nzene and Xylenes) by gas chromatoghaphy (GC-FID), and trace elements by inductively coupled plasma o

133 s was investigated by gas chromatography (GC-FID and GC-MS), while quantitation of a heat-sensitive c

134 pherol (HPLC-FD), fatty acid composition (GC-FID), including conjugated linoleic acid (CLA) isomeric

135 Compared to conventional GC-FID, the signal-to-noise ratio has been increased by a f

136 hromatography-flame ionisation detection (GC-FID) analysis revealed that mutations in two subunits of

137 hromatography-Flame Ionisation Detection (GC-FID) and identified by Gas Chromatography-Mass Spectrome

138 hromatography-Flame Ionization Detection (GC-FID) and in dynamic conditions by Proton Transfer Reacti

139 tography with flame ionization detection (GC-FID) and phosphorus-31 nuclear magnetic resonance ((31)P

140 tography with flame ionization detection (GC-FID) and wavelength scanned-cavity ring down spectroscop

141 tography with flame ionization detection (GC-FID) results for these samples.

142 tography with flame-ionization detection (GC-FID) was used to determine a CH(4) response for each of

143 hy coupled to flame ionization detection (GC-FID), using this instrumental technique as an alternativ

144 hromatography-flame ionisation detection (GC-FID).

145 hromatography-flame ionization detection (GC-FID).

146 tography with flame ionization detection (GC-FID).

147 hromatography-flame ionization detection (GC-FID).

148 tography with flame ionization detection (GC-FID).

149 coupled with flame ionisation detection (GC-FID).

150 chromatograph-flame ionisation detector (GC-FID) and the peaks were confirmed using gas chromatograp

151 chromatography-flame ionization detector (GC-FID) methods with a large linear dynamic range (3 orders

152 ography with a flame ionization detector (GC-FID) were performed.

153 romatography - flame ionization detector (GC-FID).

154 hromatographic-flame ionization detector (GC-FID).

155 h coupled with flame ionisation detector (GC-FID).

156 ography with a flame ionization detector (GC-FID).

157 erent meat products and optimizing a fast GC-FID (flame ionization detector) run.

158 smethylation procedure followed by a fast GC-FID run.

159 cco was analysed using quantitative FTIR, GC-FID, LC/MS/MS and GC/MS/MS methodologies, and qualitativ

160 On the other hand, GC-FID analysis detected acrylamide in only these three mod

161 chnique and aroma release using headspace GC-FID were studied.

162 traction-GC-MS (HS-SPME-GC-MS), headspace-GC-FID (HS-GC-FID) and stir bar sorptive extraction-GC-MS (

163 Reverse phase-HPLC, GC-FID and rapid resolution-LC/tandem mass spectrometry wer

164 gerprints (obtained from an off-line HPLC-GC-FID system) for the quantification of extra virgin olive

165 -MS (HS-SPME-GC-MS), headspace-GC-FID (HS-GC-FID) and stir bar sorptive extraction-GC-MS (SBSE-GC-MS)

166 column/dual flame ionization detector (HS-GC-FID/FID), a technique routinely used in forensic toxicol

167 The limits of detection (LOD) in GC-FID vary between 1.21 and 2.51pgmuL(-1) (RSD11.1) wherea

168 An analytical strategy that incorporates GC-FID/O, GC x GC-FID, and MDGC-MS/O analyses with cumulati

169 methanol methylation, and injection into GC-FID system.

170 rifluoride in methanol, and injected into GC-FID system.

171 fatty acid profiles of muscle and liver (GC-FID analysis).

172 bined use of two chromatographic methods (GC-FID and HPLC-RID) for the quantification of carbohydrate

173 traits and analytical techniques (GC-MS, GC-FID, HPLC, and spectrophotometry).

174 qualitatively and quantitatively by GC-MS/GC-FID results.

175 pounds of the extracts (analysed by GC-MS/GC-FID) were C13 and C9 norisoprenoids.

176 phic platforms (GC x GC/TOFMS, GC-O-OSME, GC-FID and GC/MS).

177 sory perception through GCxGC/TOFMS, QDA, GC-FID, GC/MS, and GC-O.

178 The proposed sHSS-GC-FID method was successfully applied for analysis of 93 s

179 impurities in dietary supplements by sHSS-GC-FID technique.

180 In this work a SPE/GC-FID method, incorporating the use of a 1-g silica cartri

181 , dry extract) and analytical techniques (GC-FID, GC-MS, HPLC-DAD).

182 in the GC-MS profiles, 9 volatiles in the GC-FID profiles and 29 phenolic compounds in the HPLC-DAD/M

183 crosyringe and directly injected into the GC-FID system.

184 al fatty acids and soluble sugars through GC-FID and HPLC-RI, respectively, as well as the mineral pr

185 The HS-Trap GC-FID method was optimized for the parameters: thermostatt

186 analysis, with the latter two found using GC-FID analysis as well.

187 , and determined the lipid profiles using GC-FID, 13C NMR and 31P NMR spectroscopy.

188 nols and flavan-3-ols) was analyzed using GC-FID, LC-DAD and LC-MS methods, whereas the volatile comp

189 ghiP) were separated and quantified using GC-FID.

190 f fatty acids (FAMEs) were analysed using GC-FID.

191 d-pressed lemon oils were analyzed, using GC-FID/MS and FT-MIR, while the non-volatile residues were

192 Acids and sugars were analyzed with GC-FID and volatiles with HS-SPME-GC-MS and GC-O.

193 ous distillation-extraction combined with GC-FID, GC-MS, aroma extract dilution analysis, and odour a

194 d liquid-liquid extraction, combined with GC-FID, GC-MS, aroma extract dilution analysis, and odour a

195 after the fermentation were analyzed with GC-FID, HPLC-DAD, and HPLC-MS.

196 ese wines through GC-O-OSME together with GC-FID, MS resulted in the designation of 19 degrees Brix a

197 ere achieved by coupling sol-gel CME with GC-FID.

198 strategy that incorporates GC-FID/O, GC x GC-FID, and MDGC-MS/O analyses with cumulative solid phase

199 injecting the vapor phase collected in a GC/FID.

200 tion of the essential oil was analysed by GC/FID and GC/MS.

201 tion-resolved" flame ionization detector (GC/FID) or a detector with separation capability.

202 atography with flame ionisation detector (GC/FID).

203 atography with flame ionization detector (GC/FID).

204 Various chromatographic methods (GC/FID, GC/ECD, GC/MS, HPLC/DAD) were used to identify and

205 matography/flame ionisation detection (Py-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py

206 lemental compositions (C, H, N, O, S), Py-GC/FID, Py-GC/MS and SEM imaging reveal extensive degradati

207 graphy-flame ionisation detector (HS-SPME-GC/FID) method was developed for the simultaneous determina

208 these changes were traced with a standard GC/FID set-up, accompanied by sensory panellists.

209 (30) of culinary sage were assessed using GC/FID/MS analysis of the hydrodistilled EO (pharmacopoeial

210 nsional GC-flame ionisation detection (GCxGC-FID) using a polar/non-polar phase combination for the G

211 matography-flame ionisation detection (GCxGC-FID) was developed for the simultaneous extraction, sepa

212 raphy with flame ionisation detection (GCxGC-FID) was employed to evaluate the effect of SPME fractio

213 The DLLME-GCxGC-FID method demonstrated good linearity (10.0-250 mg/L; r

214 pproaches using both synthetically generated FIDs and instrumental data.

215 (1)H FID became steeper in all samples during storage, but no

216 tational molecular mobility indicators ((1)H FID, (1)H T2) during storage.

217 HEART-FID is a multicenter, randomized, double-blind, placebo-

218 eart Failure and Iron Deficiency], and HEART-FID [Randomized Placebocontrolled Trial of Ferric Carbox

219 atment in patients with HF and ID, and HEART-FID trials.

220 R-HF, CONFIRM-HF, AFFIRM-AHF, IRONMAN, HEART-FID and FAIR-HF2), including 7,175 patients.

221 The objective of the HEART-FID trial (Ferric Carboxymaltose in Heart Failure With I

222 The HEART-FID trial used hierarchical end points to better determi

223 The HEART-FID trial will inform clinical practice by clarifying th

224 SpineGAN generated images with higher FID and lower precision scores, but with higher recall a

225 ut fluorescent intercalator displacement (HT-FID) assay developed by Boger et al. and a high-resoluti

226 id, and carnauba wax were determined by HTGC-FID/MS detection, and the research was focussed mainly o

227 methyl ester 10(-4) mol/L modestly impaired FID of arterioles from patients without coronary artery

228 -catalase, rotenone, and Mito-TEMPO impaired FID in healthy adipose arterioles pretreated with cerami

229 There was no significant difference in FID of mesopredatory fishes between the shark model and

230 ndothelium-derived hyperpolarizing factor in FID of the human coronary microcirculation.

231 t which was seen in the greater variation in FID of sedentary bird species.

232 species (sedentary) had greater variation in FID than migratory ones.

233 Catalase inhibited FID (%max dilation; 66+/-8 versus 25+/-7%; P<0.05, n=6),

234 C) using olfactometry (O), flame ionization (FID), and/or mass spectrometry (MS) detection is describ

235 Application of the new IR-FID-CPMG sequence allowed distinction between different

236 effect, but 40 mmol/L KCl attenuated maximal FID.

237 rteriolar tone and the enhanced CYP-mediated FID caused by incubation of vessels with 17beta-E2.

238 ol conditions, prostaglandins (PGs) mediated FID, because indomethacin (INDO) abolished the responses

239 .90 compared to 1.67 for GANs, and a minimum FID score of 69.45 compared to 100.05 for GANs.

240 In this study, a modified FID assay for screening RNA-binding ligands was establis

241 In the chronic phase, most FIDs evolve with slow aortic dilation and without compli

242 s been increased by a factor of 10 with mpGC-FID.

243 ethionyl ester were also elucidated by GC-MS-FID.

244 ed qualitatively and quantitatively by GC-MS/FID.

245 ir fatty acid compositions analyzed by GC-MS/FID.

246 ants involved correlating data from the GC-O/FID system with GCxGC-time-of-flight mass spectrometry a

247 However, the main advantage of FID-DECRA was that accurate (<5% error) and precise (2.3

248 Application of FID-DECRA to 19F NMR data, which contained overlapping s

249 The development of FID in the acute phase of type B IMH has a poor prognosi

250 ceramide induces a switch in the mediator of FID from nitric oxide to H2O2.

251 al role in the transition of the mediator of FID from nitric oxide to mitochondrial-derived H2O2 and

252 The signals of FID and EIMS are highly correlated across the chromatogr

253 The success of FID is based on the fact that it can be fashioned into a

254 However, this reduces the number of FIDs and, thus, kinetic data points.

255 ow modulation, coupled with the TOFMS and/or FID to demonstrate compatibility with all typical GC x G

256 ermined by whether the conditions for FIE or FID were chosen in the experimental design.

257 matographic platform (GC x GC) with parallel FID/MS detection was implemented for confirmation and to

258 dators were eradicated ~11 years previously, FID was also higher than on islands with no invasive pre

259 pplied Cadzow denoising on the MCR-processed FIDs, achieving a further increase in the S/N ratio and

260 alibration curves using GC-qMS and GCxGC-qMS/FID document the transfer and adaptation of the original

261 islands with human populations, I quantified FID in urban and non-urban populations of finches.

262 I quantified FID, an antipredator behaviour, in the small ground finc

263 or 17-octadecynoic acid 10(-5) mol/L reduced FID.

264 L but not glibenclamide 10(-6) mol/L reduced FID.

265 was an independent predictor for the reduced FID.

266 t's background noise, and then the remaining FIDs are orthogonalized to this fixed basis set.

267 With FID-DECRA, a single-sample FID matrix is split into two matrices, allowing quantita

268 The entire series of single-scan FIDs spanning the reaction lifetime can be summed to yie

269 conditions for crystallization than separate FID and microbatch screenings.

270 ion decays (FIDs) and dissects them into sub-FIDs that are transformed into pseudo-3D spectra combini

271 asive predators was similar to or lower than FID on islands with no history of invasive predators.

272 The FID CSI (Free Induction Decay Chemical Shift Imaging) se

273 The FID SlipChip was designed to screen multiple reagents, e

274 population with the lowest mobility and the FID population with the highest mobility represent the s

275 ws down to (i) mathematically describing the FID in a tabular format of its component signals and (ii

276 on in fluorescence intensity observed in the FID assay with displacement of the dye molecule from RNA

277 constants and the individual signals in the FID.

278 evolution delays within the recording of the FID (free induction decay), not only stretches the recor

279 n times (T1-T2) including acquisition of the FID signal.

280 mplex data points of the initial part of the FID, without affecting the performance of the untargeted

281 h a single exponential function, whereas the FID signals of untreated control cells were biexponentia

282 The FIDs are available by anonymous ftp at the same location

283 ved by DSC, was better distinguished through FID signals, and correlated to water content through the

284 eum fluid was also performed and compared to FID results: quantitative results obtained for all the a

285 dea that H2O2 is an EDHF that contributes to FID in HCA from patients with heart disease.

286 sted the hypothesis that H2O2 contributes to FID in HCA.

287 In subjects without CAD, NO contributes to FID.

288 hyperpolarization contributes importantly to FID of human coronary arterioles.

289 f EIMS varies on average by ~21% relative to FID for peak-by-peak comparison of oxygenated organic co

290 ied using in situ FTIR spectroscopy, HPLC-UV/FID, and GC-PID and quantified in a yield of (24 +/- 5)

291 Flow-induced vasodilation (FID) is a physiological mechanism for regulating coronar

292 cules into methane before quantification via FID, providing nearly uniform response factors for diver

293 With FID-DECRA, a single-sample FID matrix is split into two

294 With FID-GRAM, the Hankel matrix of the sample signal is comp

295 Experimental results for GC x 2GC with FID and MS for metabolomic analyses of human urine sampl

296 nd composition through GC x GC analysis with FID, which can be correlated with GC analysis using para

297 This problem does not arise with FID-DECRA, because comparison with a reference signal is

298 Inaccurate results were obtained with FID-GRAM when there were differences between the frequen

299 ed patients with type B IMH with and without FID.

300 k of aorta-related events than those without FID (hazard ratio: 24.43; 95% confidence interval: 7.65