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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 d quantification of the residues using GC-MS selected reaction monitoring.
10 collagen content, myofibroblast numbers, and selected reaction monitoring.
11 metry using synthetic internal standards and selected reaction monitoring.
12 obtained with data-dependent acquisition or selected reaction monitoring.
13 different mass spectrometry technique called selected reaction monitoring.
14 dified proteins after proteolysis by using a selected reaction monitoring analysis in a tandem mass s
17 ngII-regulated proteins was quantified using selected reaction monitoring and normalized by urine cre
18 arge-switch high mass accuracy LC-MS/MS with selected reaction monitoring and product ion accurate ma
20 liable and high-throughput mass spectrometry-selected reaction monitoring assay that targets 48 key p
24 o be sufficiently reproducible for scheduled selected reaction monitoring assays to be performed on d
27 ed to sphingolipid and glycerophosphocholine selected reaction monitoring datasets, we demonstrate ov
28 of the five compounds in less than 30 s, and selected reaction monitoring detection from low nano- to
29 were demonstrated in positive ion mode using selected reaction monitoring detection of rhodamine dyes
33 ctrospray ionization mass spectrometry (with selected reaction monitoring) enabled the analysis of th
34 pproach using electron transfer dissociation-selected reaction monitoring (ETD-SRM) was developed to
35 fic CID reaction pathways can offer value to selected reaction monitoring experiments (SRM) as it may
37 m cholesterol esters (NL 368.5) and specific selected reaction monitoring for DAG molecular species,
38 hy-tandem mass spectrometry method utilizing selected reaction monitoring for measuring the absolute
39 using a 5.0 min preconcentration period with selected reaction monitoring for tamoxifen (m/z 372 -->
44 itivity enhancement in liquid chromatography selected reaction monitoring (LC-SRM) analyses of low-ab
45 Here, we present a liquid chromatography-selected reaction monitoring (LC-SRM) approach that we d
46 iquid chromatography/mass spectrometry using selected reaction monitoring (LC/SRM-MS) holds great pro
47 f the long-gradient separations coupled with selected reaction monitoring (LG-SRM) for targeted prote
49 enzodiazepines isolated from human urine via selected reaction monitoring liquid chromatography/mass
50 1.2 min using a positive ion turbo-ionspray selected reaction monitoring liquid chromatography/mass
51 eversed phase HPLC separation, combined with selected reaction monitoring mass spectrometric detectio
52 ctrophoresis for selected ion monitoring and selected reaction monitoring mass spectrometric detectio
53 ultra high performance liquid chromatography-selected reaction monitoring mass spectrometry (UHPLC-SR
56 hty-eight novel quantitative assays based on selected reaction monitoring mass spectrometry were deve
57 periments were then validated using targeted Selected Reaction Monitoring mass spectrometry with a tr
58 The proteomic findings were confirmed using selected reaction monitoring mass spectrometry, validati
61 trospray ionization-tandem mass spectrometry-selected reaction monitoring method for the combined ana
64 the use of targeted quantitative proteomics (selected reaction monitoring methods) and in vitro recom
66 trometry (nanoLC-NSI/MS/MS) under the highly selected reaction monitoring mode and using a triple qua
67 triple quadrupole linear ion trap using the selected reaction monitoring mode for quantification as
68 Mass spectral data were recorded in either selected reaction monitoring mode or in full scan ion tr
69 ay ionization mass spectrometry operating in selected reaction monitoring mode to determine the absol
71 atmospheric pressure chemical ionization in selected reaction monitoring mode with deuterium-labeled
72 idation products using the compound-specific selected reaction monitoring mode, which allows the char
85 icro-LC-(T-uLC) with narrow-window-isolation selected-reaction monitoring MS(NWI-SRM) for ultra-sensi
86 ppaB/RelA, TG) triplets were validated by LC-selected reaction monitoring-MS and the results of STAT1
87 onducted without sample derivatization using selected reaction monitoring of mass transitions that ar
90 ts can be measured by mass spectrometry with selected reaction monitoring or selected ion monitoring
91 geted proteomics experiments performed using selected reaction monitoring, parallel reaction monitori
93 in electron ionisation with highly specific selected reaction monitoring, quantification being perfo
94 L-1alpha-stimulated cartilage, confirmed the selected reaction monitoring results indicating compleme
97 is demonstrated for CS disaccharides, and a selected reaction monitoring scheme is used to quantify
98 o develop a targeted proteomics method using selected reaction monitoring (SRM) aimed at quantitative
100 tandem mass spectrometry (LC-ESI MS/MS) with selected reaction monitoring (SRM) and quantitation by h
101 ccurate peptide losses to be determined in a Selected Reaction Monitoring (SRM) assay, thus, enabling
103 oaches using both high-resolution (HRMS) and selected reaction monitoring (SRM) based mass spectromet
104 cs approach based on mass spectrometric (MS) selected reaction monitoring (SRM) detection was exploit
107 t, a highly specific, sensitive method using Selected Reaction Monitoring (SRM) in positive electrosp
108 andem mass spectrometer using time-triggered selected reaction monitoring (SRM) in positive electrosp
110 eting histone acetylation and methylation by selected reaction monitoring (SRM) is one of the current
111 F1-2, IBP2-7, ALS, KLK6-7, ISK5, and PLF4 by selected reaction monitoring (SRM) liquid chromatography
114 s on the high sensitivity and specificity of selected reaction monitoring (SRM) mass spectrometry, ma
116 e and complex tryptic peptide matrices using selected reaction monitoring (SRM) mass spectrometry.
117 s cerevisiae by coupling a SILAC approach to selected reaction monitoring (SRM) mass spectrometry.
118 le quadrupole mass spectrometer operating in selected reaction monitoring (SRM) mode for sample quant
121 ation of the corresponding steroid esters in selected reaction monitoring (SRM) mode, for the first t
126 m normal and mutant alleles were detected by selected reaction monitoring (SRM) of their product ions
128 tandem mass spectrometer (MS/MS) operated in selected reaction monitoring (SRM) or multiple reaction
130 from gel-based approaches to the upcoming LC-selected reaction monitoring (SRM) technique which combi
131 here multiple iterations of the same, single selected reaction monitoring (SRM) transition are collec
132 sitivity was reduced by interferences in the selected reaction monitoring (SRM) transition of the sig
133 d quantitation, which is based on predefined selected reaction monitoring (SRM) transitions for selec
135 ile quantitative analysis is performed using selected reaction monitoring (SRM) using a triple quadru
137 3 cells, which were analyzed over a range of selected reaction monitoring (SRM), data-independent acq
143 nt selection and multiplexing) for sensitive selected reaction monitoring (SRM)-based targeted protei
151 hromatography (LC)/mass spectrometry (MS) in selected-reactions-monitoring (SRM) mode provides a powe
152 pectrometry-based targeted proteomics (e.g., selected reaction monitoring, SRM) is emerging as an att
155 a workflow for targeted mass spectrometry by selected reaction monitoring that permits quantitative a
156 rt a novel approach using (18)O labeling and selected reaction monitoring to detect carbapenemase act
158 vivo, we used tandem mass spectrometry with selected reaction monitoring to quantify the regiospecif
162 andem mass spectrometry method that utilizes selected reaction monitoring was used to measure the abs
163 noprecipitation, and targeted proteomics via selected reaction monitoring, we show that the gene enco
164 polar metabolomics profiling platform using selected reaction monitoring with a 5500 QTRAP hybrid tr