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1 chromatography-tandem mass spectrometry with multiple reaction monitoring.
2 e obtained using selected ion monitoring and multiple reaction monitoring.
3 nd the internal standard were analyzed using multiple reaction monitoring.
4 es were selected for quantification applying multiple reaction monitoring.
5 ere used to identify class-specific ions for multiple reaction monitoring.
6 lts were confirmed by targeted analysis with multiple reaction monitoring.
7 Data acquisition under MS/MS was attained by multiple reaction monitoring.
8 counterparts were analyzed by LC-MS/MS using multiple reaction monitoring, a multiplexed form of the
9 and after incubation with the receptor using multiple reaction monitoring allowed a ranking of the li
10 analysis was compared to a targeted, pseudo-multiple reaction monitoring analysis of proteotypic pep
12 containing compounds were pinpointed through multiple-reaction-monitoring analysis, while full-scan i
13 ndem mass spectrometry method, using dynamic multiple reaction monitoring and a 1.8-mum particle size
14 ds involved in the TCA cycle using scheduled multiple reaction monitoring and single ion monitoring m
15 successfully quantified using the method of multiple reaction monitoring and stable isotope dilution
17 was first used as an internal standard in a multiple reaction monitoring assay to measure PICALM con
22 le reaction monitoring kits, but some of the multiple reaction monitoring-based measurements differed
24 ce liquid chromatography (HPLC) multiplexing multiple reaction monitoring cubed (MRM(3)) assay for se
26 pray ionization mass spectrometry coupled to multiple reaction monitoring (ESI-MS/MRM) has been appli
29 -flow LC mass spectrometry (MS) method using multiple reaction monitoring for the application to larg
30 ost comprehensive study so far of the use of multiple reaction monitoring for the quantitation of gly
31 mass spectrometer to perform simultaneously multiple-reaction monitoring for microsomal stability an
32 tion of the major phenolics was performed by multiple reaction monitoring in a triple quadrupole mass
36 l, good agreement was observed between the 2 multiple reaction monitoring kits, but some of the multi
37 ray ionization tandem mass spectrometry with multiple reaction monitoring (LC-ESI-MS/MS-MRM) to simul
38 eversed phase HPLC separation, combined with multiple reaction monitoring mass spectrometric detectio
40 an assay based on liquid chromatography and multiple reaction monitoring mass spectrometry (LC-MRM M
41 in quantification with liquid chromatography-multiple reaction monitoring mass spectrometry (LC-MRM)
43 iquid chromatography/electrospray ionization multiple reaction monitoring mass spectrometry (LC/ESI-M
44 internal standards in liquid chromatography/multiple reaction monitoring mass spectrometry (LC/MRM-M
48 ications were performed on 11 proteins using multiple reaction monitoring mass spectrometry (MRM-MS),
51 high-throughput, and sensitive peptide-based multiple reaction monitoring mass spectrometry assay, al
53 ate markers were verified using quantitative multiple reaction monitoring mass spectrometry in sera o
54 s with PMI or spontaneous MI by quantitative multiple reaction monitoring mass spectrometry or immuno
55 e discovery set were verified using targeted multiple reaction monitoring mass spectrometry quantifie
56 ghly reproducible nano liquid chromatography-multiple reaction monitoring mass spectrometry-based qua
61 ombined chemical modification of lysines and multiple-reaction monitoring mass spectrometry to identi
63 lytically characterized a multiplexed immuno-multiple reaction monitoring-mass spectrometry (immuno-M
65 ultrahigh performance liquid chromatography/multiple-reaction monitoring-mass spectrometry (UPLC-MRM
66 ured simultaneously by liquid chromatography/multiple-reaction monitoring-mass spectrometry in 1090 i
68 iquid chromatography-electrospray ionization/multiple reaction monitoring/mass spectrometry (LC-ESI/M
69 table isotope dilution liquid chromatography-multiple reaction monitoring/mass spectrometry (LC-MRM/M
76 quid chromatography-tandem mass spectrometry-multiple reaction monitoring method to simultaneously qu
79 e differences in the proteomes, we developed multiple reaction monitoring methods for cucumber protei
80 nization-mass spectrometry) operating in the multiple reaction monitoring mode (MRM) with collision-i
85 le loss and permitted quantitation using the multiple reaction monitoring mode of the mass spectromet
86 rometry with electrospray ionization using a multiple reaction monitoring mode to obtain superior sen
87 graphy tandem mass spectrometry method using multiple reaction monitoring mode to separate and quanti
88 d chromatography-tandem mass spectrometry in multiple reaction monitoring mode using isotopically lab
89 ctly analyzed by LC-MS/MS (run of 13 min) in Multiple Reaction Monitoring mode using labeled glutathi
90 nalysis was performed in negative ionization/multiple reaction monitoring mode with five different ti
91 meter operating in positive ion electrospray multiple reaction monitoring mode, with a total run time
99 ajor bioactive compounds was performed using multiple-reaction monitoring mode with continuous polari
101 binding protein from cow's milk coupled with multiple-reaction-monitoring-mode tandem mass spectromet
102 riple quadruple analyser and operated in the multiple reaction monitoring modes on the contaminated s
103 performed by tandem mass spectrometry in the multiple reaction monitoring (MRM) acquisition mode.
104 th proteins as an internal standard prior to multiple reaction monitoring (MRM) analysis enables pref
105 ry (MS/MS), selected ion recording (SIR) and multiple reaction monitoring (MRM) and identified as met
106 ted polyphenol standards were examined using Multiple Reaction Monitoring (MRM) as the acquisition mo
107 ence strain (CAN97-83) was used to develop a multiple reaction monitoring (MRM) assay that employed s
108 In the present study, we have developed a multiple reaction monitoring (MRM) assay to measure UCH-
111 s a highly selective and sensitive method of multiple reaction monitoring (MRM) by mass spectrometry.
112 dividual laboratories have demonstrated that multiple reaction monitoring (MRM) coupled with isotope
114 im to provide a foundation for designing QqQ multiple reaction monitoring (MRM) experiments for each
120 d (4) detection with electrospray ionization multiple reaction monitoring (MRM) mass spectrometry (MS
124 ion about the species present and to build a multiple reaction monitoring (MRM) method with the MS/MS
125 e method development was performed to create multiple reaction monitoring (MRM) methods for a wide ra
129 ing a cell-penetrating peptide biosensor and multiple reaction monitoring (MRM) on a triple quadrupol
130 s observed during liquid chromatography (LC) multiple reaction monitoring (MRM) quantification method
134 s rely on library searches, known masses, or multiple reaction monitoring (MRM) transitions and are t
135 ed compounds are measured within 4 min using multiple reaction monitoring (MRM) transitions selective
136 cies were compared using their corresponding multiple reaction monitoring (MRM) transitions, and nega
138 ple-quadrupole mass spectrometry method with multiple reaction monitoring (MRM) was employed to measu
139 nization (APCI) in the positive ion mode and multiple reaction monitoring (MRM) were used for LC-MS/M
141 tion in stored milk powder was quantified by multiple reaction monitoring (MRM), a mass spectrometry-
142 used to maximize instrument sensitivity, and multiple reaction monitoring (MRM), in the tandem mass s
143 proteomics approach employing the method of multiple reaction monitoring (MRM), we precisely and qua
144 g ion suppression and permitting predictable multiple reaction monitoring (MRM)-based quantitation wi
146 ion or endosome trafficking to the lysosome, multiple reaction monitoring (MRM)/mass spectrometry (MS
147 ed, cICAT-labeled, and used both to optimize multiple reactions monitoring (MRM) analysis and to conf
148 ILAC-compatible kinome library for scheduled multiple-reaction monitoring (MRM) analysis and adopted
149 and quantitation of the surrogate peptide by multiple-reaction monitoring (MRM) mass spectrometry.
151 raphy-tandem mass spectrometry (LC-MS/MS) by multiple-reaction monitoring (MRM) on a triple quadrupol
153 and mannose-6-phosphate was achieved by UPLC/multiple-reaction monitoring (MRM)-MS, with analytical a
155 /MS) methods: precursor-ion and neutral-loss multiple-reaction-monitoring (MRM), and high-resolution
156 nd 2HPFOA, we optimized a mass-spectrometric multiple-reaction-monitoring (MS/MS) technique and then
158 pectrometry (MS); liquid chromatography (LC)-multiple reaction monitoring-MS; and ultra-high-performa
160 de, we developed an LC-ESI-MS/MS method with multiple reaction monitoring of primary and confirmatory
161 developed a new MS-based strategy, based on multiple reaction monitoring of stable isotope-labeled p
162 n electrospray-tandem mass spectrometry with multiple reaction monitoring of the diagnostic fragment
164 +1% formic acid) and measurement by LC-MS/MS multiple reaction monitoring, offering limit of quantifi
165 gradient reverse-phase HPLC and detected by multiple reaction monitoring on a triple-quadrupole mass
167 ass spectrometric detection was performed by multiple reaction monitoring over a 31-min run time.
173 derivatization with methylamine followed by multiple reaction monitoring scans in a Q-trap mass spec
176 tive assays using scheduled, high resolution multiple reaction monitoring (sMRM-HR), also referred to
177 the extracted ion chromatograms and selected multiple-reaction monitoring spectra of three peptides (
178 By absolute quantification of abundance with multiple reaction monitoring, stoichiometric ratios of m
179 r an additional 104 signaling nodes with the multiple reaction monitoring strategy, an 88% increase i
180 dent acquisition experiment which combined a multiple reaction monitoring survey with dependent enhan
182 was performed with high dynamic range using multiple reaction monitoring that provided new insights
183 phically resolving target peptides and using multiple reaction monitoring to enhance MS sensitivity,
185 nalysis, the method simultaneously monitored multiple reaction monitoring transitions in negative ESI
186 A particular uMS method, ultrathroughput multiple reaction monitoring (uMRM), is reported for one
187 of a few selected AccQ*Tag amino acids with multiple reaction monitoring, varied from 29 to 39 V, wh
188 ctrometry analysis, the targeted approach of multiple-reaction monitoring was used to quantitate the
189 ical ionization in the positive ion mode and multiple reaction monitoring were used for LC-MS/MS.
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