ライフサイエンスコーパス: multiple reaction monitoring

1 pectrometry (UHPLC-QqQ-MS) operating in MRM (Multiple Reaction Monitoring).

2 chromatography-tandem mass spectrometry with multiple reaction monitoring.

3 e obtained using selected ion monitoring and multiple reaction monitoring.

4 nd the internal standard were analyzed using multiple reaction monitoring.

5 es were selected for quantification applying multiple reaction monitoring.

6 ere used to identify class-specific ions for multiple reaction monitoring.

7 Polar reversed-phase column and MS/MS under multiple reaction monitoring.

8 ential mobility spectrometry with subsequent multiple reaction monitoring.

9 lts were confirmed by targeted analysis with multiple reaction monitoring.

10 Data acquisition under MS/MS was attained by multiple reaction monitoring.

11 h positive and negative modes with scheduled multiple reactions monitoring.

12 counterparts were analyzed by LC-MS/MS using multiple reaction monitoring, a multiplexed form of the

13 We use multiple reaction monitoring acquisition mode (MRM) with

14 omatography with triple-quad MS operating in multiple reaction monitoring acquisition was used, apply

15 and after incubation with the receptor using multiple reaction monitoring allowed a ranking of the li

16 analysis was compared to a targeted, pseudo-multiple reaction monitoring analysis of proteotypic pep

17 of human growth hormone in human urine using multiple reaction monitoring analysis.

18 roteins, where the method involves scheduled multiple-reaction monitoring analysis and the use of syn

19 gh-performance liquid chromatography (UHPLC) multiple-reaction monitoring analysis and were stable un

20 containing compounds were pinpointed through multiple-reaction-monitoring analysis, while full-scan i

21 ndem mass spectrometry method, using dynamic multiple reaction monitoring and a 1.8-mum particle size

22 ds involved in the TCA cycle using scheduled multiple reaction monitoring and single ion monitoring m

23 successfully quantified using the method of multiple reaction monitoring and stable isotope dilution

24 We used multiple-reaction monitoring and liquid chromatography-U

25 ed mass spectrometry (MS) methods [MS1, MRM (multiple reaction monitoring), and DIA].

26 was first used as an internal standard in a multiple reaction monitoring assay to measure PICALM con

27 We report here that multiple reaction monitoring assay using internal standa

28 proteins providing the basis for an LC-MS/MS multiple reaction monitoring assay.

29 ptide/flanking sequence were measured with a multiple reaction monitoring assay.

30 Multiple reaction monitoring assays, calibration curve c

31 tally verified proteotypic peptides used for multiple reaction monitoring assays.

32 le reaction monitoring kits, but some of the multiple reaction monitoring-based measurements differed

33 d in wound healing were further validated by multiple reaction monitoring-based targeted analysis.

34 The multiple reaction monitoring capability of LC-MS/MS was

35 method was optimized by careful selection of multiple reaction monitoring, capture reagents, magnetic

36 prehensive lipidomics automated workflow for multiple reaction monitoring (CLAW-MRM), a platform desi

37 ce liquid chromatography (HPLC) multiplexing multiple reaction monitoring cubed (MRM(3)) assay for se

38 Here, we developed a multiple reaction monitoring cubed (MRM(3)) method coupl

39 Use of a UHPLC-MS/MS multiple reaction monitoring-cubed method improved the s

40 Dynamic multiple reaction monitoring (DMRM) and internal standar

41 ctrometry (UHPLC/QqQ MS) operated in dynamic multiple reaction monitoring (dMRM) mode.

42 etry (UHPLC-QqQ-MS) performed in the dynamic multiple reaction monitoring (dMRM) mode.

43 ividual ribonucleosides by LC-MS via dynamic multiple reaction monitoring (DMRM).

44 mization were then used to develop a dynamic multiple-reaction monitoring (dMRM)-based strategy to si

45 pray ionization mass spectrometry coupled to multiple reaction monitoring (ESI-MS/MRM) has been appli

46 ay ionization-isotope dilution-MS/MS using a multiple reaction monitoring experiment.

47 Due to the higher detection sensitivity, multiple reaction monitoring experiments using a triple

48 The use of multiple reaction monitoring facilitated the selective d

49 esulting platform included LC-MS analysis in multiple reaction monitoring for quantitative analysis o

50 -flow LC mass spectrometry (MS) method using multiple reaction monitoring for the application to larg

51 ost comprehensive study so far of the use of multiple reaction monitoring for the quantitation of gly

52 mass spectrometer to perform simultaneously multiple-reaction monitoring for microsomal stability an

53 y/mass spectrometry targeted assay, based on multiple reaction monitoring, for quantification of N-Hc

54 tion of the major phenolics was performed by multiple reaction monitoring in a triple quadrupole mass

55 e use of dried blood spot (DBS) sampling and multiple reaction monitoring in proteomics.

56 Selected and multiple reaction monitoring involves monitoring a multi

57 Two different commercial multiple reaction monitoring kits and an antibody-based

58 l, good agreement was observed between the 2 multiple reaction monitoring kits, but some of the multi

59 ray ionization tandem mass spectrometry with multiple reaction monitoring (LC-ESI-MS/MS-MRM) to simul

60 rometry (LC-MS/MS) and liquid chromatography-multiple reaction monitoring (LC-MRM) mass spectrometric

61 quid chromatography-tandem mass spectrometry multiple reaction monitoring (LC-MS/MS MRM) assay.

62 y probes together with liquid chromatography-multiple-reaction monitoring (LC-MRM) analysis, we also

63 , relying on scheduled liquid chromatography-multiple-reaction monitoring (LC-MRM) coupled with synth

64 eversed phase HPLC separation, combined with multiple reaction monitoring mass spectrometric detectio

65 The multiple reaction monitoring mass spectrometric method a

66 nocapture-liquid chromatography coupled with multiple reaction monitoring mass spectrometry (LBA-LC-M

67 an assay based on liquid chromatography and multiple reaction monitoring mass spectrometry (LC-MRM M

68 in quantification with liquid chromatography-multiple reaction monitoring mass spectrometry (LC-MRM)

69 Liquid chromatography multiple reaction monitoring mass spectrometry (LC-MRM)

70 iquid chromatography/electrospray ionization multiple reaction monitoring mass spectrometry (LC/ESI-M

71 internal standards in liquid chromatography/multiple reaction monitoring mass spectrometry (LC/MRM-M

72 Here we report quantification using multiple reaction monitoring mass spectrometry (MRM MS)

73 Multiple reaction monitoring mass spectrometry (MRM-MS)

74 Our group developed multiple reaction monitoring mass spectrometry (MRM-MS)

75 All products were analysed by multiple reaction monitoring mass spectrometry (MRM-MS)

76 By multiple reaction monitoring mass spectrometry (MRM-MS)

77 Here, we investigate the potential of Multiple Reaction Monitoring Mass Spectrometry (MRM-MS),

78 ications were performed on 11 proteins using multiple reaction monitoring mass spectrometry (MRM-MS),

79 bin (Mb) and myosin (My) were analyzed using multiple reaction monitoring mass spectrometry (MRM-MS).

80 Stable isotope labeling-multiple reaction monitoring mass spectrometry (SIL/MRM-

81 high-throughput, and sensitive peptide-based multiple reaction monitoring mass spectrometry assay, al

82 We used liquid chromatography-multiple reaction monitoring mass spectrometry for targe

83 ate markers were verified using quantitative multiple reaction monitoring mass spectrometry in sera o

84 r clinical applications, we have adapted the multiple reaction monitoring mass spectrometry method fo

85 s with PMI or spontaneous MI by quantitative multiple reaction monitoring mass spectrometry or immuno

86 e discovery set were verified using targeted multiple reaction monitoring mass spectrometry quantifie

87 ghly reproducible nano liquid chromatography-multiple reaction monitoring mass spectrometry-based qua

88 was detected in virus-infected honey bees by multiple reaction monitoring mass spectrometry.

89 argeted mass-spectrometry proteomic analysis-multiple reaction monitoring mass spectrometry.

90 isotopically labeled internal standards, and multiple reaction monitoring mass spectrometry.

91 ior to targeted protein quantification using multiple reaction monitoring mass spectrometry.

92 ombined chemical modification of lysines and multiple-reaction monitoring mass spectrometry to identi

93 period in the Bruneck Study (N = 688) using multiple-reaction monitoring mass spectrometry.

94 Herein, we introduce an ADE-multiple reaction monitoring-mass spectrometry (ADE-MRM-

95 lytically characterized a multiplexed immuno-multiple reaction monitoring-mass spectrometry (immuno-M

96 A liquid chromatography-multiple reaction monitoring-mass spectrometry (LC-MRM-M

97 titatively analyzed by liquid chromatography-multiple reaction monitoring-mass spectrometry (LC/MRM-M

98 ultrahigh-performance liquid chromatography-multiple reaction monitoring-mass spectrometry (UHPLC-MR

99 Stable isotope labeling with multiple reaction monitoring-mass spectrometry demonstra

100 Here, we developed a liquid chromatography/multiple reaction monitoring-mass spectrometry MYDGF ass

101 ultrahigh performance liquid chromatography/multiple-reaction monitoring-mass spectrometry (UPLC-MRM

102 Among 420 target proteins quantified by multiple-reaction monitoring-mass spectrometry assays of

103 ured simultaneously by liquid chromatography/multiple-reaction monitoring-mass spectrometry in 1090 i

104 iquid-chromatography-stable-isotope dilution-multiple-reaction monitoring-mass spectrometry.

105 iquid chromatography-electrospray ionization/multiple reaction monitoring/mass spectrometry (LC-ESI/M

106 table isotope dilution liquid chromatography-multiple reaction monitoring/mass spectrometry (LC-MRM/M

107 ultrahigh-performance liquid chromatography-multiple reaction monitoring/mass spectrometry assay to

108 iquid chromatography-electrospray ionization/multiple reaction monitoring/mass spectrometry.

109 s were performed using liquid chromatography-multiple reaction monitoring/mass spectrometry.

110 These peptides were used to develop a multiple reaction monitoring method (MRM) to detect the

111 We unveil a Multiple Reaction Monitoring method (Scout-MRM) where th

112 We developed a multiple reaction monitoring method based on analyzing c

113 as further quantified using a developed HPLC-multiple reaction monitoring method for HeLa digests wit

114 We have now developed a multiple reaction monitoring method to quantify the biol

115 In parallel, we also developed a targeted multiple reaction monitoring method to quantify the rela

116 quid chromatography-tandem mass spectrometry-multiple reaction monitoring method to simultaneously qu

117 Using multiple reaction monitoring method, we precisely quanti

118 cted masses of the OPD BCKA products using a multiple reaction monitoring method.

119 e differences in the proteomes, we developed multiple reaction monitoring methods for cucumber protei

120 nization-mass spectrometry) operating in the multiple reaction monitoring mode (MRM) with collision-i

121 cted by UV/ESI-MS in the negative ionisation multiple reaction monitoring mode (MRM).

122 ndem mass spectrometry (LC-DAD-ESI-MS/MS) in multiple reaction monitoring mode (MRM).

123 sterilised pate, was analysed by a triggered multiple reaction monitoring mode experiment and triple

124 Separate positive and negative polarity multiple reaction monitoring mode injections were requir

125 and tandem mass spectrometry (MS/MS) in the multiple reaction monitoring mode is described here.

126 le loss and permitted quantitation using the multiple reaction monitoring mode of the mass spectromet

127 rometry with electrospray ionization using a multiple reaction monitoring mode to obtain superior sen

128 graphy tandem mass spectrometry method using multiple reaction monitoring mode to separate and quanti

129 d chromatography-tandem mass spectrometry in multiple reaction monitoring mode using isotopically lab

130 ctly analyzed by LC-MS/MS (run of 13 min) in Multiple Reaction Monitoring mode using labeled glutathi

131 S/MS system with electrospray ionization and multiple reaction monitoring mode was used, after a bina

132 nalysis was performed in negative ionization/multiple reaction monitoring mode with five different ti

133 Quantification was conducted in the multiple reaction monitoring mode with two specific tran

134 meter operating in positive ion electrospray multiple reaction monitoring mode, with a total run time

135 y-tandem mass spectrometry (LC-MS/MS) in the multiple reaction monitoring mode.

136 tion of unique product ions when analyzed in multiple reaction monitoring mode.

137 spectrometry (LC-ESI-MS/MS) in the positive multiple reaction monitoring mode.

138 quadrupole mass spectrometer operated in the multiple reaction monitoring mode.

139 wed by tandem mass spectrometry detection in multiple reaction monitoring mode.

140 zation-tandem mass spectrometry in scheduled multiple reaction monitoring mode.

141 th a triple quadrupole analyser operating in Multiple Reaction Monitoring mode.

142 obtained with GC-triple-quadrupole method in multiple reaction monitoring mode.

143 pe-coded dimethyl labeling with LC-QqQ MS in multiple reaction monitoring mode.

144 simultaneously quantified by LC-MS/MS in the multiple reaction-monitoring mode.

145 HPLC-tandem mass spectrometry (LC/MS/MS) in multiple reaction-monitoring mode.

146 ajor bioactive compounds was performed using multiple-reaction monitoring mode with continuous polari

147 ionization mass spectrometer in positive-ion multiple-reaction-monitoring mode.

148 binding protein from cow's milk coupled with multiple-reaction-monitoring-mode tandem mass spectromet

149 riple quadruple analyser and operated in the multiple reaction monitoring modes on the contaminated s

150 trometry data acquired in either selected or multiple reaction monitoring modes.

151 ILIC) with Zeno trap-enabled high-resolution multiple reaction monitoring (MRM(HR)).

152 inert surface coating of column hardware and multiple reaction monitoring (MRM) acquisition fully cov

153 performed by tandem mass spectrometry in the multiple reaction monitoring (MRM) acquisition mode.

154 analyses was comparable to triple quadrupole multiple reaction monitoring (MRM) analyses at up to 5 o

155 In multiple reaction monitoring (MRM) analyses, however, th

156 th proteins as an internal standard prior to multiple reaction monitoring (MRM) analysis enables pref

157 LTPs allergens were further determined with multiple reaction monitoring (MRM) analysis.

158 ry (MS/MS), selected ion recording (SIR) and multiple reaction monitoring (MRM) and identified as met

159 f proteotypic peptides with MS [e.g., immuno-multiple reaction monitoring (MRM) and immuno-matrix-ass

160 s study, we show a rapid (<1 min) and robust multiple reaction monitoring (MRM) approach for the trac

161 Here we take a multiple reaction monitoring (MRM) approach to different

162 ted polyphenol standards were examined using Multiple Reaction Monitoring (MRM) as the acquisition mo

163 ence strain (CAN97-83) was used to develop a multiple reaction monitoring (MRM) assay that employed s

164 In the present study, we have developed a multiple reaction monitoring (MRM) assay to measure UCH-

165 In addition, we tested hundreds of multiple reaction monitoring (MRM) assays for isotope ra

166 Multiple reaction monitoring (MRM) assays have proven su

167 ntification using Spectrum Mill software and multiple reaction monitoring (MRM) based confirmation of

168 s a highly selective and sensitive method of multiple reaction monitoring (MRM) by mass spectrometry.

169 Multiple reaction monitoring (MRM) confirmed role of cat

170 dividual laboratories have demonstrated that multiple reaction monitoring (MRM) coupled with isotope

171 s of peak picking and quality assessment for multiple reaction monitoring (MRM) data demands signific

172 on-induced dissociation (CID) efficiency for multiple reaction monitoring (MRM) detection.

173 im to provide a foundation for designing QqQ multiple reaction monitoring (MRM) experiments for each

174 A combination of multiple reaction monitoring (MRM) fragment ratio normal

175 Selected reaction monitoring and multiple reaction monitoring (MRM) have been a method of

176 Subsequent analysis by ESI-MS/MS with multiple reaction monitoring (MRM) in the presence of de

177 Multiple reaction monitoring (MRM) is a liquid chromatog

178 Multiple reaction monitoring (MRM) is a powerful and pop

179 on Paper Spray Mass Spectrometry (PS-MS) and Multiple Reaction Monitoring (MRM) is described.

180 A rapid multiple reaction monitoring (MRM) mass spectrometric me

181 Data is acquired by MALDI multiple reaction monitoring (MRM) mass spectrometry (MS

182 d (4) detection with electrospray ionization multiple reaction monitoring (MRM) mass spectrometry (MS

183 Multiple reaction monitoring (MRM) mass spectrometry has

184 Multiple reaction monitoring (MRM) mass spectrometry is

185 We have developed a multiple reaction monitoring (MRM) mass spectrometry met

186 In this study multiple reaction monitoring (MRM) mass spectrometry, vi

187 high-resolution mass spectrometry (LC/HRMS); multiple reaction monitoring (MRM) mass spectrometry; an

188 A qualitative LC-QQQ multiple reaction monitoring (MRM) method was developed

189 ion about the species present and to build a multiple reaction monitoring (MRM) method with the MS/MS

190 e method development was performed to create multiple reaction monitoring (MRM) methods for a wide ra

191 The current method progresses upon multiple reaction monitoring (MRM) methods, previously u

192 iguration used and the signal acquisition in multiple reaction monitoring (MRM) mode (both positive a

193 CIT-MS is operationalized using multiple reaction monitoring (MRM) mode and is able to p

194 Multiple reaction monitoring (MRM) mode was used for LC-

195 m mass spectrometry (HPLC-MS/MS) method with multiple reaction monitoring (MRM) mode.

196 ted in selected reaction monitoring (SRM) or multiple reaction monitoring (MRM) modes was developed a

197 To enhance analytical specificity, a Multiple Reaction Monitoring (MRM) MS method was develop

198 Multiple Reaction Monitoring (MRM) of the transition pai

199 ing a cell-penetrating peptide biosensor and multiple reaction monitoring (MRM) on a triple quadrupol

200 ical analysis, and data parsing using custom multiple reaction monitoring (MRM) precursor product ion

201 s observed during liquid chromatography (LC) multiple reaction monitoring (MRM) quantification method

202 Multiple Reaction Monitoring (MRM) remains the gold stan

203 Targeted multiple reaction monitoring (MRM) scanning via triple q

204 Targeted mass spectrometry using multiple reaction monitoring (MRM) showed more impressiv

205 fication at MS1 and MS2 levels comparable to multiple reaction monitoring (MRM) targeted analysis of

206 We used a multiple reaction monitoring (MRM) to detect (13)C, D2-f

207 This protocol employs multiple reaction monitoring (MRM) to search for all put

208 s rely on library searches, known masses, or multiple reaction monitoring (MRM) transitions and are t

209 ed compounds are measured within 4 min using multiple reaction monitoring (MRM) transitions selective

210 cies were compared using their corresponding multiple reaction monitoring (MRM) transitions, and nega

211 Multiple reaction monitoring (MRM) was applied and the s

212 ple-quadrupole mass spectrometry method with multiple reaction monitoring (MRM) was employed to measu

213 nization (APCI) in the positive ion mode and multiple reaction monitoring (MRM) were used for LC-MS/M

214 Multiple reaction monitoring (MRM) with optimised transi

215 tion in stored milk powder was quantified by multiple reaction monitoring (MRM), a mass spectrometry-

216 lipids including SM and Ceramide (Cer) using Multiple Reaction Monitoring (MRM), as they play a vital

217 used to maximize instrument sensitivity, and multiple reaction monitoring (MRM), in the tandem mass s

218 proteomics approach employing the method of multiple reaction monitoring (MRM), we precisely and qua

219 natured cervid PrP, 19 peptides suitable for multiple reaction monitoring (MRM)-based analysis and sp

220 g ion suppression and permitting predictable multiple reaction monitoring (MRM)-based quantitation wi

221 Multiple reaction monitoring (MRM)-triggered mass spectr

222 solation by 2D-LC, and targeted detection by multiple reaction monitoring (MRM).

223 s (HMOs) in milk samples was developed using multiple reaction monitoring (MRM).

224 ed protein profiling, and lipid analysis via multiple reaction monitoring (MRM).

225 spectrometry (LC-MS/MS) employing scheduled multiple reaction monitoring (MRM).

226 mass spectrometry (LC-MS/MS) workflow, using multiple reaction monitoring (MRM).

227 MS/MS) using both positive and negative-mode multiple reaction monitoring (MRM).

228 ion or endosome trafficking to the lysosome, multiple reaction monitoring (MRM)/mass spectrometry (MS

229 ed, cICAT-labeled, and used both to optimize multiple reactions monitoring (MRM) analysis and to conf

230 ILAC-compatible kinome library for scheduled multiple-reaction monitoring (MRM) analysis and adopted

231 and quantitation of the surrogate peptide by multiple-reaction monitoring (MRM) mass spectrometry.

232 tudy, we applied a high-throughput scheduled multiple-reaction monitoring (MRM) method, along with th

233 rein, we applied a high-throughput scheduled multiple-reaction monitoring (MRM) method, along with th

234 ons enabled quantitation of T and DHT in the multiple-reaction monitoring (MRM) mode.

235 raphy-tandem mass spectrometry (LC-MS/MS) by multiple-reaction monitoring (MRM) on a triple quadrupol

236 set of 234 NGPs was strictly established for multiple-reaction monitoring (MRM) quantification in ser

237 We employed a high-throughput scheduled multiple-reaction monitoring (MRM)-based targeted proteo

238 acyl-phosphate probes, in conjunction with a multiple-reaction monitoring (MRM)-based targeted proteo

239 Herein we established a multiple-reaction monitoring (MRM)-based targeted proteo

240 izing a recently established high-throughput multiple-reaction monitoring (MRM)-based workflow togeth

241 and mannose-6-phosphate was achieved by UPLC/multiple-reaction monitoring (MRM)-MS, with analytical a

242 of Leu-enkephalin in a complex mixture using multiple-reaction monitoring (MRM).

243 mn and quantified by mass spectrometry using multiple-reaction-monitoring (MRM) mode, with a lower li

244 /MS) methods: precursor-ion and neutral-loss multiple-reaction-monitoring (MRM), and high-resolution

245 detect low-abundance oxylipins; however, new multiple-reaction-monitoring (MRM)-based MSI technologie

246 Subsequently, a multiple reaction monitoring MS assay was developed for

247 nd 2HPFOA, we optimized a mass-spectrometric multiple-reaction-monitoring (MS/MS) technique and then

248 r quantification in the saliva samples using multiple reaction monitoring-MS.

249 pectrometry (MS); liquid chromatography (LC)-multiple reaction monitoring-MS; and ultra-high-performa

250 rmance liquid chromatography separation, and multiple reaction monitoring of ceramides.

251 expression pattern was observed via targeted multiple reaction monitoring of EVs from maternal plasma

252 de, we developed an LC-ESI-MS/MS method with multiple reaction monitoring of primary and confirmatory

253 developed a new MS-based strategy, based on multiple reaction monitoring of stable isotope-labeled p

254 h tandem mass spectrometry (UHPLC-MS/MS) for multiple reaction monitoring of target compounds.

255 n electrospray-tandem mass spectrometry with multiple reaction monitoring of the diagnostic fragment

256 Multiple-reaction monitoring of mass spectrometry in pos

257 +1% formic acid) and measurement by LC-MS/MS multiple reaction monitoring, offering limit of quantifi

258 gradient reverse-phase HPLC and detected by multiple reaction monitoring on a triple-quadrupole mass

259 tissue extract and quantified by unscheduled multiple reaction monitoring on a TSQ Vantage.

260 ass spectrometric detection was performed by multiple reaction monitoring over a 31-min run time.

261 gration, and multimodal data analysis (e.g., multiple reaction monitoring, precursor ion, and neutral

262 a-independent acquisition (DIA) and parallel/multiple reaction monitoring (PRM/MRM) deliver unrivalle

263 cquired and the speed of analysis of lipids, multiple reaction monitoring profiling (MRM-Profiling) h

264 We performed a quantitative, targeted multiple reaction monitoring proteomic analysis of GB an

265 A multiple reaction monitoring protocol was then developed

266 Mass spectrometry followed by multiple-reaction monitoring provides a unique approach

267 Thirty mass spectrometry-based multiple reaction monitoring quantitative tryptic peptid

268 GC-triple quadrupole mass spectrometer with multiple reaction monitoring, resulting in higher signal

269 eous analysis of 302 drugs using a scheduled multiple reaction monitoring (s-MRM) algorithm.

270 Targeted proteomics by selected/multiple reaction monitoring (S/MRM) or, on a larger sca

271 The experiments have been carried out in Multiple Reaction Monitoring scan mode, in order to obta

272 derivatization with methylamine followed by multiple reaction monitoring scans in a Q-trap mass spec

273 mass spectrometry (APCI-MS/MS) in scheduled multiple reaction monitoring (sMRM) mode.

274 A LC-Q-LIT-MS workflow using scheduled multiple reaction monitoring (sMRM) survey scan, informa

275 tive assays using scheduled, high resolution multiple reaction monitoring (sMRM-HR), also referred to

276 the extracted ion chromatograms and selected multiple-reaction monitoring spectra of three peptides (

277 ted proteomic measurements based on selected/multiple reaction monitoring (SRM/MRM) mass spectrometry

278 ns across multiple samples, such as selected/multiple reaction monitoring (SRM/MRM) or parallel react

279 By absolute quantification of abundance with multiple reaction monitoring, stoichiometric ratios of m

280 r an additional 104 signaling nodes with the multiple reaction monitoring strategy, an 88% increase i

281 dent acquisition experiment which combined a multiple reaction monitoring survey with dependent enhan

282 Scheduled multiple reaction monitoring "survey scans" were followe

283 was performed with high dynamic range using multiple reaction monitoring that provided new insights

284 ion induced dissociation in conjunction with multiple reaction monitoring to achieve group-specific d

285 phically resolving target peptides and using multiple reaction monitoring to enhance MS sensitivity,

286 Two multiple reaction monitoring transitions arising from th

287 nalysis, the method simultaneously monitored multiple reaction monitoring transitions in negative ESI

288 Multiple reaction monitoring transitions were optimized

289 A particular uMS method, ultrathroughput multiple reaction monitoring (uMRM), is reported for one

290 peptides in a standardized method, based on multiple reaction monitoring using a linear ion trap MS,

291 of a few selected AccQ*Tag amino acids with multiple reaction monitoring, varied from 29 to 39 V, wh

292 e and rapid (<2 min per sample) method using multiple reaction monitoring was developed and fully val

293 ctrometry analysis, the targeted approach of multiple-reaction monitoring was used to quantitate the

294 ical ionization in the positive ion mode and multiple reaction monitoring were used for LC-MS/MS.

295 In-line technologies such as multiple reaction monitoring with multistage fragmentati

296 (m/z) of 219.4, while BHA was detected using multiple-reaction monitoring, with a transition from m/z

297 this end, we used DMS in conjunction with a multiple reaction monitoring workflow to assess cannabin