1 FID CSI (Free Induction Decay Chemical Shift Imaging) se
2 FID is a tagless approach; the target RNAs and the ligan
3 FID was defined as an intimal disruption with contrast m
4 onclusions can be drawn from this study: (
1)
FID assay with 3 and polynucleotides demonstrates the pr
5 (
2)
FID assay and UV thermal denaturation experiments show t
6 (
5)
FID and ITC titration between 3 and an intramolecular DN
7 (
6)
FID assay using 3 and 512 hairpin DNA sequences that var
8 Patients with
acute FID had a higher risk of aorta-related events than those
9 Although
acute FIDs should be treated early and invasively, lesions dev
10 here were 43 patients (40%) who developed
an FID with larger basal maximum aortic diameter and hemato
11 4 discharged patients, 33 (35%) developed
an FID within the first 6 months of follow-up: 19 evolved w
12 (4) CD
and FID titration studies show a DNA binding site size of 10
13 We conclude that FIE
and FID zones generated by BPEs can be exploited to shape an
14 radaic ion enrichment and depletion (FIE
and FID) on electric field gradients.
15 that simultaneously performs microbatch
and FID crystallization methods in a single device.
16 elated with GC analysis using parallel O
and FID detection.
17 of arterioles was significantly reduced
and FID was augmented.
18 f mitochondrial reactive oxygen species,
and FID is unknown.
19 hile chromatographic methods with UV-VIS
and FID detection were used to determine the free amino acid
20 Archived FIDs and newly acquired aquatolide spectra demonstrate t
21 btained by fluorescence displacement
assays (
FID) and isothermal titration calorimetry (ITC), with bi
22 Charybdotoxin 10(-8) mol/L impaired
both FID (15+/-3% versus 75+/-12%, P<0.05) and hyperpolarizat
23 In the hydrocarbon analysis
by FID, paraffins, naphthenes, and aromatics form distinct
24 Chronic FID was not associated with aorta-related events (hazard
25 The
corresponding FIDs may be readily submitted with publications and coll
26 In free induction
decay (
FID) measurements, proton populations were assigned to (
27 of the single quantum free induction
decay (
FID) revealed that signals from buffer and DNDS-treated
28 tative analysis of NMR free induction
decay (
FID) signals.
29 high-resolution 1D NMR free induction
decay (
FID).
30 analyzing the 35Cl NMR free induction
decay (
FID).
31 in ethnic groups (Fijians of Indian
descent [
FID] and Indigenous Fijians [iTaukei]) in Fiji were recr
32 uel oil by using flame ionization
detection (
FID), without any prefractionation.
33 ography (GC) with flame ionisation
detector (
FID).
34 ry (GC-MS) and GC-flame ionization
detector (
FID) analysis.
35 ource rocks using flame ionization
detector (
FID) and sulfur chemiluminescence detector (SCD).
36 o quantify by SFC-flame ionization
detector (
FID) due to incomplete resolution between the saturate/m
37 detector, e.g. a flame ionization
detector (
FID) or an olfactory (sniffing) port.
38 For example, a flame ionization
detector (
FID) produces data that is especially effective for quan
39 h equipped with a flame ionization
detector (
FID) set at 250 degrees C.
40 h equipped with a flame ionization
detector (
FID).
41 y (GC) coupled to flame ionization
detector (
FID).
42 ermal calorimetry), CD (circular
dichroism),
FID (fluorescent intercalator displacement), and UV (ult
43 : a SlipChip-based free interface
diffusion (
FID) method and a SlipChip-based composite method that s
44 Flow-induced
dilation (
FID) is dependent largely on hyperpolarization of vascul
45 Flow-induced
dilation (
FID) was assessed in isolated arterioles from N(G)-nitro
46 of a fluorescent intercalator
displacement (
FID) assay conducted on a series of hairpin deoxyoligonu
47 nding fluorescent intercalator
displacement (
FID) assay for initial assessment of the DNA binding aff
48 ng a fluorescence intercalator
displacement (
FID) assay.
49 this fluorescent intercalator
displacement (
FID) assay.
50 Fluorescent intercalator
displacement (
FID) is a convenient and practical tool for identifying
51 Focal intimal
disruption (
FID) has been described in >20% of type B intramural hem
52 eeping the solution in the neck channels
for FID stable, the plates of the SlipChip were etched with
53 giving an alternative to the widely used
GC (
FID/MS) methodologies.
54 GC-
FID measurements were performed by including ratios to a
55 GC-
FID results proved that galactose was the dominant sugar
56 GC-
FID/MS (after HS-SPME and ultrasonic solvent extraction)
57 A
GC-
FID method based on the ratio between the integrated pea
58 Acetaldehyde (
GC-
FID) and pyruvic acid (Y15 enzymatic autoanalyser) conte
59 ned fewer constituents based on GC-MS and
GC-
FID analyses.
60 The (1)H NMR and
GC-
FID data from different ratios of SIO were adjusted by a
61 Both nanoLC/EI-MS and
GC-
FID methods were validated and similar results were obta
62 tive composition was studied by GC-MS and
GC-
FID.
63 PAEs) in hydroalcoholic food beverages by
GC-
FID (and peak confirmation by GC-IT/MS) has been set up.
64 29/2012, was developed by
GC-
FID analysis of methyl esters of fatty acids, followed b
65 ends of EU origin) were differentiated by
GC-
FID analysis of sterols and esterified sterols followed
66 dspace and liquid extractions followed by
GC-
FID analysis.
67 parts of Artemisia indica was analysed by
GC-
FID and GC-MS.
68 The extracts were analyzed by
GC-
FID and GC-MS.
69 ts and its extracts were characterized by
GC-
FID and HPLC-UV.
70 yl esters of fatty acids were analysed by
GC-
FID and processed through chemometric tools (PCA, TFA, S
71 According to the results obtained by
GC-
FID for products containing prebiotics, the content of F
72 fatty acid profiles were investigated by
GC-
FID revealing high contents of PUFAs and a high omega-3/
73 Extracts were assayed by
GC-
FID, GC-MS, and LC-MS for the identification of 10 prima
74 xtracted solutes were further analyzed by
GC-
FID.
75 secondary oxidation products of sterol by
GC-
FID/MS and oligomers by HPSEC-RI.
76 s was investigated by gas chromatography (
GC-
FID and GC-MS), while quantitation of a heat-sensitive c
77 pherol (HPLC-FD), fatty acid composition (
GC-
FID), including conjugated linoleic acid (CLA) isomeric
78 Compared to conventional
GC-
FID, the signal-to-noise ratio has been increased by a f
79 hromatography-Flame Ionisation Detection (
GC-
FID) and identified by Gas Chromatography-Mass Spectrome
80 tography with flame ionization detection (
GC-
FID) and wavelength scanned-cavity ring down spectroscop
81 tography with flame ionization detection (
GC-
FID) results for these samples.
82 tography with flame-ionization detection (
GC-
FID) was used to determine a CH(4) response for each of
83 hromatography-flame ionisation detection (
GC-
FID).
84 hromatography-flame ionization detection (
GC-
FID).
85 tography with flame ionization detection (
GC-
FID).
86 chromatograph-flame ionisation detector (
GC-
FID) and the peaks were confirmed using gas chromatograp
87 chromatography-flame ionization detector (
GC-
FID) methods with a large linear dynamic range (3 orders
88 h coupled with flame ionisation detector (
GC-
FID).
89 ography with a flame ionization detector (
GC-
FID).
90 romatography - flame ionization detector (
GC-
FID).
91 cco was analysed using quantitative FTIR,
GC-
FID, LC/MS/MS and GC/MS/MS methodologies, and qualitativ
92 chnique and aroma release using headspace
GC-
FID were studied.
93 traction-GC-MS (HS-SPME-GC-MS), headspace-
GC-
FID (HS-GC-FID) and stir bar sorptive extraction-GC-MS (
94 gerprints (obtained from an off-line HPLC-
GC-
FID system) for the quantification of extra virgin olive
95 -MS (HS-SPME-GC-MS), headspace-GC-FID (HS-
GC-
FID) and stir bar sorptive extraction-GC-MS (SBSE-GC-MS)
96 The limits of detection (LOD) in
GC-
FID vary between 1.21 and 2.51pgmuL(-1) (RSD11.1) wherea
97 An analytical strategy that incorporates
GC-
FID/O, GC x GC-FID, and MDGC-MS/O analyses with cumulati
98 rifluoride in methanol, and injected into
GC-
FID system.
99 methanol methylation, and injection into
GC-
FID system.
100 fatty acid profiles of muscle and liver (
GC-
FID analysis).
101 bined use of two chromatographic methods (
GC-
FID and HPLC-RID) for the quantification of carbohydrate
102 qualitatively and quantitatively by GC-MS/
GC-
FID results.
103 pounds of the extracts (analysed by GC-MS/
GC-
FID) were C13 and C9 norisoprenoids.
104 sory perception through GCxGC/TOFMS, QDA,
GC-
FID, GC/MS, and GC-O.
105 The proposed sHSS-
GC-
FID method was successfully applied for analysis of 93 s
106 impurities in dietary supplements by sHSS-
GC-
FID technique.
107 crosyringe and directly injected into the
GC-
FID system.
108 The HS-Trap
GC-
FID method was optimized for the parameters: thermostatt
109 f fatty acids (FAMEs) were analysed using
GC-
FID.
110 ghiP) were separated and quantified using
GC-
FID.
111 d-pressed lemon oils were analyzed, using
GC-
FID/MS and FT-MIR, while the non-volatile residues were
112 ous distillation-extraction combined with
GC-
FID, GC-MS, aroma extract dilution analysis, and odour a
113 d liquid-liquid extraction, combined with
GC-
FID, GC-MS, aroma extract dilution analysis, and odour a
114 ere achieved by coupling sol-gel CME with
GC-
FID.
115 strategy that incorporates GC-FID/O, GC x
GC-
FID, and MDGC-MS/O analyses with cumulative solid phase
116 tion of the essential oil was analysed by
GC/
FID and GC/MS.
117 tion-resolved" flame ionization detector (
GC/
FID) or a detector with separation capability.
118 atography with flame ionization detector (
GC/
FID).
119 atography with flame ionisation detector (
GC/
FID).
120 matography/flame ionisation detection (Py-
GC/
FID), pyrolysis-gas chromatography/mass spectrometry (Py
121 lemental compositions (C, H, N, O, S), Py-
GC/
FID, Py-GC/MS and SEM imaging reveal extensive degradati
122 these changes were traced with a standard
GC/
FID set-up, accompanied by sensory panellists.
123 (30) of culinary sage were assessed using
GC/
FID/MS analysis of the hydrodistilled EO (pharmacopoeial
124 nsional GC-flame ionisation detection (
GCxGC-
FID) using a polar/non-polar phase combination for the G
125 raphy with flame ionisation detection (
GCxGC-
FID) was employed to evaluate the effect of SPME fractio
126 (1)
H FID became steeper in all samples during storage, but no
127 tational molecular mobility indicators ((1)
H FID, (1)H T2) during storage.
128 ut fluorescent intercalator displacement (
HT-
FID) assay developed by Boger et al. and a high-resoluti
129 id, and carnauba wax were determined by
HTGC-
FID/MS detection, and the research was focussed mainly o
130 methyl ester 10(-4) mol/L modestly
impaired FID of arterioles from patients without coronary artery
131 -catalase, rotenone, and Mito-TEMPO
impaired FID in healthy adipose arterioles pretreated with cerami
132 ndothelium-derived hyperpolarizing factor
in FID of the human coronary microcirculation.
133 Catalase
inhibited FID (%max dilation; 66+/-8 versus 25+/-7%; P<0.05, n=6),
134 C) using olfactometry (O), flame
ionization (
FID), and/or mass spectrometry (MS) detection is describ
135 Application of the new
IR-
FID-CPMG sequence allowed distinction between different
136 effect, but 40 mmol/L KCl attenuated
maximal FID.
137 rteriolar tone and the enhanced CYP-
mediated FID caused by incubation of vessels with 17beta-E2.
138 ol conditions, prostaglandins (PGs)
mediated FID, because indomethacin (INDO) abolished the responses
139 In this study, a
modified FID assay for screening RNA-binding ligands was establis
140 In the chronic phase,
most FIDs evolve with slow aortic dilation and without compli
141 s been increased by a factor of 10 with
mpGC-
FID.
142 ethionyl ester were also elucidated by GC-
MS-
FID.
143 ir fatty acid compositions analyzed by GC-
MS/
FID.
144 ed qualitatively and quantitatively by GC-
MS/
FID.
145 ants involved correlating data from the GC-
O/
FID system with GCxGC-time-of-flight mass spectrometry a
146 However, the main advantage
of FID-DECRA was that accurate (<5% error) and precise (2.3
147 Application
of FID-DECRA to 19F NMR data, which contained overlapping s
148 The development
of FID in the acute phase of type B IMH has a poor prognosi
149 ceramide induces a switch in the mediator
of FID from nitric oxide to H2O2.
150 al role in the transition of the mediator
of FID from nitric oxide to mitochondrial-derived H2O2 and
151 The success
of FID is based on the fact that it can be fashioned into a
152 ermined by whether the conditions for FIE
or FID were chosen in the experimental design.
153 or 17-octadecynoic acid 10(-5) mol/L
reduced FID.
154 L but not glibenclamide 10(-6) mol/L
reduced FID.
155 was an independent predictor for the
reduced FID.
156 With FID-DECRA, a single-
sample FID matrix is split into two matrices, allowing quantita
157 conditions for crystallization than
separate FID and microbatch screenings.
158 The FID CSI (Free Induction Decay Chemical Shift Imaging) se
159 The FID SlipChip was designed to screen multiple reagents, e
160 population with the lowest mobility and
the FID population with the highest mobility represent the s
161 on in fluorescence intensity observed in
the FID assay with displacement of the dye molecule from RNA
162 constants and the individual signals in
the FID.
163 evolution delays within the recording of
the FID (free induction decay), not only stretches the recor
164 n times (T1-T2) including acquisition of
the FID signal.
165 h a single exponential function, whereas
the FID signals of untreated control cells were biexponentia
166 The FIDs are available by anonymous ftp at the same location
167 dea that H2O2 is an EDHF that contributes
to FID in HCA from patients with heart disease.
168 sted the hypothesis that H2O2 contributes
to FID in HCA.
169 In subjects without CAD, NO contributes
to FID.
170 hyperpolarization contributes importantly
to FID of human coronary arterioles.
171 ied using in situ FTIR spectroscopy, HPLC-
UV/
FID, and GC-PID and quantified in a yield of (24 +/- 5)
172 Flow-induced
vasodilation (
FID) is a physiological mechanism for regulating coronar
173 With FID-DECRA, a single-sample FID matrix is split into two
174 With FID-GRAM, the Hankel matrix of the sample signal is comp
175 Experimental results for GC x 2GC
with FID and MS for metabolomic analyses of human urine sampl
176 nd composition through GC x GC analysis
with FID, which can be correlated with GC analysis using para
177 This problem does not arise
with FID-DECRA, because comparison with a reference signal is
178 Inaccurate results were obtained
with FID-GRAM when there were differences between the frequen
179 ed patients with type B IMH with and
without FID.
180 k of aorta-related events than those
without FID (hazard ratio: 24.43; 95% confidence interval: 7.65