ライフサイエンスコーパス: multiple reaction

1 A methylation, with most CpGs represented in multiple reactions.

2 ly occurring octamers that are able to prime multiple reactions.

3 der reactions, albeit probably composites of multiple reactions.

4 n one simple operation in place of employing multiple reactions.

5 utine preparation of glycan samples involves multiple reaction and cleaning steps at which sample los

6 e high stability of the DNA/AuNPs allows for multiple reactions and conjugations to be performed with

7 However, the multiple reactions and phase changes in the sulfur conve

8 ng and discharging is intricate and involves multiple reactions and processes.

9 also suitable for large-scale mining, since multiple reactions and their kinetic parameters can be s

10 n (97 male patients): 6 were infants, 20 had multiple reactions, and the median age was 8 years (age

11 exhibit cross-reactivity when components of multiple reactions are present in one reaction vessel.

12 HECT-specific ubiquitin interactions driving multiple reactions are repurposed by a major E3 conforma

13 ansfer reactions by efficiently coordinating multiple reactions between spatially distinct active sit

14 esent in all kingdoms of life and performing multiple reactions beyond O2 chemistry.

15 ple is analyzed in distributive fashion over multiple reaction chambers, allows for enumeration of di

16 e testing of material from a single input to multiple reaction chambers, enabling rapid screening.

17 Multiple reaction channels from two different mechanisms

18 it different competition and selectivity for multiple reaction channels with this surface, determined

19 The reaction can thus follow multiple reaction channels, a feature which is expected

20 proteins that can be S-nitrosylated through multiple reaction channels, including anaerobic/oxidativ

21 eatures of folding mechanisms requires using multiple reaction coordinates, although the number is st

22 that (harsh) reagents are used in excess in multiple reaction cycles makes this technique extra dema

23 el was reused as a peroxidation catalyst for multiple reaction cycles without loss of activity, indic

24 tabilized the nanostructured morphology over multiple reaction cycles, whereas limestone lost its ini

25 Thus, the class C-Vps complex directs multiple reactions during the docking and fusion of vesi

26 ime monitoring or physical partitioning into multiple reactions (e.g., digital PCR).

27 pitaxial growth without the need for tedious multiple reactions for generating tunable shell thicknes

28 a new 2D NP catalyst platform for catalyzing multiple reactions in one pot with maximum efficiency.

29 exity of Abeta self-assembly, which involves multiple reaction intermediates related by nonlinear and

30 mple renewable carbon sources by telescoping multiple reactions into a single fermentation step.

31 t function as molecular machines to catalyze multiple reactions is rapidly reshaping our vision of bi

32 led with analysis by stable isotope dilution multiple reaction mass spectrometry has been shown to ha

33 table isotope dilution liquid chromatography-multiple reaction/mass spectrometry method to quantify f

34 the Hammett study reflects a likelihood that multiple reaction mechanisms are involved.

35 study hence provides additional insight into multiple reaction mechanisms underlying PCE reductive de

36 Ceramides were detected in the multiple reaction mode by tandem mass spectrometry in th

37 lene were quantified using GC-QQQ-MS in MRM (multiple reaction mode) mode.

38 Scheduled multiple reaction monitoring "survey scans" were followe

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

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

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

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

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

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

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

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

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

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

49 Multiple reaction monitoring (MRM) assays have proven su

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

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

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

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

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

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

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

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

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

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

60 Multiple reaction monitoring (MRM) mass spectrometry has

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

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

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

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

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

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

67 Multiple Reaction Monitoring (MRM) of the transition pai

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

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

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

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

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

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

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

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

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

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

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

79 Multiple reaction monitoring (MRM) with optimised transi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 Multiple reaction monitoring assays, calibration curve c

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

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

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

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

106 The use of multiple reaction monitoring facilitated the selective d

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

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

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

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

111 Selected and multiple reaction monitoring involves monitoring a multi

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

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

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

115 The multiple reaction monitoring mass spectrometric method a

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

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

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

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

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

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

122 Multiple reaction monitoring mass spectrometry (MRM-MS)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

142 Using multiple reaction monitoring method, we precisely quanti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 A multiple reaction monitoring protocol was then developed

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

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

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

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

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

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

177 Two multiple reaction monitoring transitions arising from th

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

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

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

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

182 +1% formic acid) and measurement by LC-MS/MS multiple reaction monitoring, offering limit of quantifi

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

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

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

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

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

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

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

190 chromatography-tandem mass spectrometry with multiple reaction monitoring.

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

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

193 es were selected for quantification applying multiple reaction monitoring.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

214 Multiple-reaction monitoring of mass spectrometry in pos

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

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

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

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

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

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

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

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

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

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

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

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

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

228 how the individual and collective effects of multiple reaction parameters (noncoordinating solvent an

229 ehensive overview of the various sources and multiple reaction partners of NO, and of the regulation

230 ects, tunneling contributions, the effect of multiple reaction paths on transmission coefficients, an

231 hanisms in the microsomal P450 systems where multiple reaction pathways draw on reducing power held b

232 The likelihood of multiple reaction pathways made it difficult to relate a

233 that the same enzyme reaction can occur via multiple reaction pathways on a reaction landscape.

234 nduced conformational change and presence of multiple reaction pathways.

235 r oxygen-precovered gold surfaces occurs via multiple reaction pathways.

236 of inactivation of RNR by F(2)CTP involving multiple reaction pathways.

237 lt in complex product mixtures that form via multiple reaction pathways.

238 The nano-texture in the CsMPs records multiple reaction-process steps during meltdown in the s

239 The phage enzyme produced multiple reaction products of differing length with all

240 t the products from any class of reaction in multiple reaction sets would have unique differences in

241 ways such that reactants can participate in multiple reactions simultaneously, reproducing the desir

242 reaction networks in which a molecule having multiple reaction sites reacts irreversibly with multipl

243 ity, but this reagent was able to react with multiple reaction sites, producing an unnecessarily comp

244 s of DNA phosphoryl transfer reactions, with multiple reaction steps catalyzed by the same set of act

245 ormation serves as a feed-forward switch for multiple reaction steps in the BCKD metabolic machine.

246 Kinetic experiments reveal that multiple reaction steps require collaboration between Cl

247 ng block, which is reacted further in one or multiple reaction steps to form the PET tracer.

248 Pharmaceutical production typically involves multiple reaction steps with separations between success

249 ction is conferred by the irreversibility of multiple reaction steps.

250 es is reported that circumvents the need for multiple reaction steps.

251 y, these chymotrypsin-like proteases trigger multiple reactions that are detrimental to bacterial sur

252 hin metal-organic frameworks (MOFs) requires multiple reactions to be performed on a MOF crystal with

253 nfrared camera to monitor the temperature of multiple reactions (up to 24 simultaneous reactions) in