ライフサイエンスコーパス: multiple reaction

1 der reactions, albeit probably composites of multiple reactions.

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

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

4 ring adaptation by their capacity to promote 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 , thereby allowing chip-based integration of multiple reactions and facilitating the minimization of

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

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

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

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

12 Complex behavior emerges as equilibria of multiple reactions are coupled.

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

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

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

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

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

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

19 Multiple reaction channels from two different mechanisms

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

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

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

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

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

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

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

27 esters of natural carboxylic acids, also in multiple reaction cycles.

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

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

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

31 ond enzyme (designated CsGA1ox/ds) performed multiple reactions, including 1beta-oxidation and 9,11-d

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

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

34 A single enzyme active site that catalyzes multiple reactions is a well-established biochemical the

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

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

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

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

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

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

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

42 Scheduled multiple reaction monitoring "survey scans" were followe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 Multiple reaction monitoring (MRM) assays have proven su

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

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

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

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

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

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

66 Multiple reaction monitoring (MRM) is a liquid chromatog

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

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

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

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

71 Multiple reaction monitoring (MRM) mass spectrometry has

72 Multiple reaction monitoring (MRM) mass spectrometry is

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

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

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

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

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

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

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

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

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

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

83 Multiple Reaction Monitoring (MRM) of the transition pai

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

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

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

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

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

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

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

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

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

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

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

95 Multiple reaction monitoring (MRM) with optimised transi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

125 Multiple reaction monitoring assays, calibration curve c

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

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

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

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

130 The use of multiple reaction monitoring facilitated the selective d

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

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

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

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

135 Selected and multiple reaction monitoring involves monitoring a multi

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

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

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

139 The multiple reaction monitoring mass spectrometric method a

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

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

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

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

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

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

146 Multiple reaction monitoring mass spectrometry (MRM-MS)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Using multiple reaction monitoring method, we precisely quanti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

198 A multiple reaction monitoring protocol was then developed

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

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

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

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

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

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

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

206 Two multiple reaction monitoring transitions arising from th

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

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

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

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

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

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

213 +1% formic acid) and measurement by LC-MS/MS multiple reaction monitoring, offering limit of quantifi

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

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

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

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

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

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

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

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

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

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

224 chromatography-tandem mass spectrometry with multiple reaction monitoring.

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

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

227 es were selected for quantification applying multiple reaction monitoring.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

254 Multiple-reaction monitoring of mass spectrometry in pos

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 of these plasticity genes were revealed with multiple reaction norms along the temperature gradient.

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

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

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

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

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

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

276 Multiple reaction pathways, including H/F exchange, diss

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

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

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

280 nduced conformational change and presence of multiple reaction pathways.

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

282 We further predict multiple reactions producing CaO(3) by geologically abun

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

284 ctive chemistry leading to the production of multiple reaction products.

285 aces, with central hub molecules involved in multiple reactions, requires a modification of existing

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

287 Extension to the monitoring of multiple reactions simultaneously is also realized by op

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

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

290 also realized by operating the reactor with multiple reaction slugs at the same time.

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

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

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

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

295 eity that allows KSI to efficiently catalyze multiple reaction steps.

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

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

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

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

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