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1 from the vMALDI-LIT, which should facilitate selected reaction monitoring.
2 a triple-quadrupole mass spectrometer using selected reaction monitoring.
3 in with identification and quantification by selected reaction monitoring.
4 ers formed in BEAS-2B cells was obtained via selected reaction monitoring.
5 y LC/tandem mass spectrometric analyses with selected reaction monitoring.
6 dentification and quantitation were based on selected reaction monitoring.
7 and tandem mass spectrometric detection with selected reaction monitoring.
8 and tandem mass spectrometric detection with selected reaction monitoring.
9 metry using synthetic internal standards and selected reaction monitoring.
10 obtained with data-dependent acquisition or selected reaction monitoring.
11 different mass spectrometry technique called selected reaction monitoring.
12 d quantification of the residues using GC-MS selected reaction monitoring.
13 dified proteins after proteolysis by using a selected reaction monitoring analysis in a tandem mass s
14 arge-switch high mass accuracy LC-MS/MS with selected reaction monitoring and product ion accurate ma
19 o be sufficiently reproducible for scheduled selected reaction monitoring assays to be performed on d
22 of the five compounds in less than 30 s, and selected reaction monitoring detection from low nano- to
23 were demonstrated in positive ion mode using selected reaction monitoring detection of rhodamine dyes
27 ctrospray ionization mass spectrometry (with selected reaction monitoring) enabled the analysis of th
28 pproach using electron transfer dissociation-selected reaction monitoring (ETD-SRM) was developed to
29 fic CID reaction pathways can offer value to selected reaction monitoring experiments (SRM) as it may
31 m cholesterol esters (NL 368.5) and specific selected reaction monitoring for DAG molecular species,
32 hy-tandem mass spectrometry method utilizing selected reaction monitoring for measuring the absolute
33 using a 5.0 min preconcentration period with selected reaction monitoring for tamoxifen (m/z 372 -->
38 itivity enhancement in liquid chromatography selected reaction monitoring (LC-SRM) analyses of low-ab
39 Here, we present a liquid chromatography-selected reaction monitoring (LC-SRM) approach that we d
40 iquid chromatography/mass spectrometry using selected reaction monitoring (LC/SRM-MS) holds great pro
41 f the long-gradient separations coupled with selected reaction monitoring (LG-SRM) for targeted prote
42 enzodiazepines isolated from human urine via selected reaction monitoring liquid chromatography/mass
43 1.2 min using a positive ion turbo-ionspray selected reaction monitoring liquid chromatography/mass
44 eversed phase HPLC separation, combined with selected reaction monitoring mass spectrometric detectio
45 ctrophoresis for selected ion monitoring and selected reaction monitoring mass spectrometric detectio
48 hty-eight novel quantitative assays based on selected reaction monitoring mass spectrometry were deve
49 periments were then validated using targeted Selected Reaction Monitoring mass spectrometry with a tr
50 The proteomic findings were confirmed using selected reaction monitoring mass spectrometry, validati
52 trospray ionization-tandem mass spectrometry-selected reaction monitoring method for the combined ana
54 the use of targeted quantitative proteomics (selected reaction monitoring methods) and in vitro recom
56 trometry (nanoLC-NSI/MS/MS) under the highly selected reaction monitoring mode and using a triple qua
57 triple quadrupole linear ion trap using the selected reaction monitoring mode for quantification as
58 Mass spectral data were recorded in either selected reaction monitoring mode or in full scan ion tr
59 ay ionization mass spectrometry operating in selected reaction monitoring mode to determine the absol
61 atmospheric pressure chemical ionization in selected reaction monitoring mode with deuterium-labeled
62 idation products using the compound-specific selected reaction monitoring mode, which allows the char
75 ppaB/RelA, TG) triplets were validated by LC-selected reaction monitoring-MS and the results of STAT1
76 onducted without sample derivatization using selected reaction monitoring of mass transitions that ar
79 ts can be measured by mass spectrometry with selected reaction monitoring or selected ion monitoring
80 geted proteomics experiments performed using selected reaction monitoring, parallel reaction monitori
82 in electron ionisation with highly specific selected reaction monitoring, quantification being perfo
83 L-1alpha-stimulated cartilage, confirmed the selected reaction monitoring results indicating compleme
86 is demonstrated for CS disaccharides, and a selected reaction monitoring scheme is used to quantify
87 o develop a targeted proteomics method using selected reaction monitoring (SRM) aimed at quantitative
89 tandem mass spectrometry (LC-ESI MS/MS) with selected reaction monitoring (SRM) and quantitation by h
90 ccurate peptide losses to be determined in a Selected Reaction Monitoring (SRM) assay, thus, enabling
92 oaches using both high-resolution (HRMS) and selected reaction monitoring (SRM) based mass spectromet
93 cs approach based on mass spectrometric (MS) selected reaction monitoring (SRM) detection was exploit
96 andem mass spectrometer using time-triggered selected reaction monitoring (SRM) in positive electrosp
98 eting histone acetylation and methylation by selected reaction monitoring (SRM) is one of the current
99 F1-2, IBP2-7, ALS, KLK6-7, ISK5, and PLF4 by selected reaction monitoring (SRM) liquid chromatography
102 s on the high sensitivity and specificity of selected reaction monitoring (SRM) mass spectrometry, ma
104 e and complex tryptic peptide matrices using selected reaction monitoring (SRM) mass spectrometry.
105 s cerevisiae by coupling a SILAC approach to selected reaction monitoring (SRM) mass spectrometry.
106 le quadrupole mass spectrometer operating in selected reaction monitoring (SRM) mode for sample quant
109 ation of the corresponding steroid esters in selected reaction monitoring (SRM) mode, for the first t
113 m normal and mutant alleles were detected by selected reaction monitoring (SRM) of their product ions
116 from gel-based approaches to the upcoming LC-selected reaction monitoring (SRM) technique which combi
117 sitivity was reduced by interferences in the selected reaction monitoring (SRM) transition of the sig
118 d quantitation, which is based on predefined selected reaction monitoring (SRM) transitions for selec
120 ile quantitative analysis is performed using selected reaction monitoring (SRM) using a triple quadru
126 nt selection and multiplexing) for sensitive selected reaction monitoring (SRM)-based targeted protei
134 hromatography (LC)/mass spectrometry (MS) in selected-reactions-monitoring (SRM) mode provides a powe
135 pectrometry-based targeted proteomics (e.g., selected reaction monitoring, SRM) is emerging as an att
138 a workflow for targeted mass spectrometry by selected reaction monitoring that permits quantitative a
139 rt a novel approach using (18)O labeling and selected reaction monitoring to detect carbapenemase act
140 vivo, we used tandem mass spectrometry with selected reaction monitoring to quantify the regiospecif
144 andem mass spectrometry method that utilizes selected reaction monitoring was used to measure the abs
145 noprecipitation, and targeted proteomics via selected reaction monitoring, we show that the gene enco
146 polar metabolomics profiling platform using selected reaction monitoring with a 5500 QTRAP hybrid tr
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