ライフサイエンスコーパス: spectrometric

1 on is often blunted due to insufficient mass spectrometric accuracy.

2 Theoretical Fragment Ion Mass Spectra) mass spectrometric acquisitions were performed to obtain a mo

3 Duplicate mass spectrometric analyses and confirmatory next generation

4 Mass-spectrometric analyses confirmed that conversion is perf

5 targeted approach for the simultaneous mass spectrometric analyses of 16 DNA adducts, which can be e

6 Radiometric and mass spectrometric analyses of Cs contamination in the enviro

7 Kinetic and mass spectrometric analyses of human proteins show that Notum

8 ferent protein substrates and MALDI-TOF mass spectrometric analyses of the generated oligopeptides.

9 Mass spectrometric analyses of whole-cell extracts demonstrat

10 isotopic labelling and affinity-capture mass spectrometric analyses on samples obtained from cultures

11 Biochemical and mass spectrometric analyses showed that the UCR2-catalytic do

12 Therefore, we performed quantitative mass spectrometric analyses to define the epitopes formed in

13 e users to perform complex quantitative mass spectrometric analyses with ease.

14 se assay as well as in situ and ex situ mass spectrometric analyses.

15 gy collisional dissociation) multistage mass spectrometric analysis (HCD-MS(n)) and ETD (electron tra

16 labeling combined with sensitive tandem mass spectrometric analysis allowed integrated synthesis rate

17 ogen for additional investigation using mass spectrometric analysis and electron microscopy.

18 between BtAdVs and CAdVs, we conducted mass spectrometric analysis and single-particle cryo-electron

19 Mass spectrometric analysis confirmed that the mutant secrete

20 Mass spectrometric analysis identified apolipoprotein(a) (apo

21 cing peptide (AIP) was responsible, and mass spectrometric analysis identified the S. caprae AIP as a

22 Mass spectrometric analysis indicates that most of the lysine

23 Coimmunoprecipitation and mass spectrometric analysis of 293 cells overexpressing pro-c

24 classification of human tissue through mass spectrometric analysis of aerosols released during elect

25 ), was developed for flame atomic absorption spectrometric analysis of aluminum (Al) and chromium (Cr

26 pared to previous attempts at MALDI-TOF mass spectrometric analysis of barley proteins, the extractio

27 of automated laboratories dedicated to mass spectrometric analysis of biological samples.

28 Unbiased mass spectrometric analysis of cardiac tissue before and </=7

29 Mass spectrometric analysis of cell extracts identified 352 p

30 s (APPI and APLI) are important for the mass spectrometric analysis of crude oils, given the mainly u

31 which includes the catalytic water, and mass spectrometric analysis of enzymatic hydrolysis products

32 ntial scanning calorimetry coupled with mass spectrometric analysis of evolved gases.

33 Hydrogen/deuterium exchange with mass spectrometric analysis of fibrillating glucagon suggeste

34 Our mass spectrometric analysis of homomeric and heteromeric TRPM

35 Mass spectrometric analysis of Ire1 expressed in Escherichia

36 Mass spectrometric analysis of LDB1 binding partners in leuke

37 Mass spectrometric analysis of microbial metabolism provides

38 Affinity purification and subsequent mass-spectrometric analysis of Nedd8-conjugated proteins from

39 of our knowledge using state of the art mass spectrometric analysis of particle and gas-phase composi

40 Finally, using a mass spectrometric analysis of secreted proteins, we demonstr

41 RNA sequencing and mass spectrometric analysis of SPRIGHTLY-expressing cells rev

42 Mass spectrometric analysis of the CYP17A1-b5 complexes ident

43 on the digestibility were determined by mass spectrometric analysis of the modified beta-lactoglobuli

44 we performed affinity purification and mass spectrometric analysis of the protein microenvironment o

45 Raman spectroscopic and mass spectrometric analysis of the reaction solutions reveale

46 Mass spectrometric analysis of the secretome of P. aeruginosa

47 Mass spectrometric analysis of the starting octasaccharide mi

48 how the applicability of this setup for mass spectrometric analysis of three common MALDI matrices, a

49 Through mass spectrometric analysis of ubiquitylated proteins affinit

50 For mixtures, contained-ESI mass spectrometric analysis produces relative ion intensities

51 ant role of GNRs as semiconductors, the mass spectrometric analysis provides a readily available tool

52 can subsequently be subjected to rapid mass spectrometric analysis providing insights into the skin

53 and pull-down experiments coupled with mass spectrometric analysis revealed that the cellular protei

54 Mass spectrometric analysis revealed that the RxLR sequence o

55 ypsinolysis followed by high resolution mass spectrometric analysis reveals that Ub chain branching c

56 Mass spectrometric analysis showed that several of these seri

57 of milk proteins by kefir grains, with mass spectrometric analysis showing the release of 609 protei

58 ouse serum in conjunction with targeted mass spectrometric analysis suggested that serum very-low-den

59 d with a fragment separation method and mass spectrometric analysis to compare their secondary struct

60 stabilize regiospecificity, and tandem mass spectrometric analysis to identify and quantify regioiso

61 es, enzyme assays, Western blotting and mass spectrometric analysis to monitor and quantify the invol

62 ed workflow from sample preparation for mass spectrometric analysis to visualization of protein-prote

63 om volume-limited samples, each type of mass spectrometric analysis uncovers only a portion of the co

64 Immunoprecipitation assays and mass spectrometric analysis using beta cells verified Lys met

65 Mass spectrometric analysis was performed after cell lysis.

66 Additionally mass spectrometric analysis was performed with the cells afte

67 Amide hydrogen/deuterium exchange with mass spectrometric analysis was used to identify the interact

68 nd chromatographic separation preceding mass spectrometric analysis were optimized, and the resultant

69 our LIMS system, quantitative chemical mass spectrometric analysis with an ablation rate at the subn

70 n, Co-IP, preparation of the sample for mass spectrometric analysis, and data analysis steps, to the

71 Mass spectrometric analysis, ELISA, and immunoblot confirm th

72 Here, using mass spectrometric analysis, it is demonstrated that the C te

73 After sample preparation and mass-spectrometric analysis, peptide intensity ratios between

74 nt capture, co-immunoprecipitation, and mass spectrometric analysis, we identified a subset of HDAC8

75 ed by immunohistochemistry staining and mass spectrometric analysis.

76 sitives are small owing to the use of a mass spectrometric analysis.

77 that occur during sample preparation or mass spectrometric analysis.

78 ng mice and followed by biochemical and mass spectrometric analysis.

79 mics has been significantly advanced by mass spectrometric analysis.

80 stigated by end-group analysis with ESI mass spectrometric analysis.

81 A(Pro(GGG)) and Um in tRNA(Gln(UUG)) by mass spectrometric analysis.

82 nd biofluid electrolytes for quantiatve mass spectrometric analysis.

83 ry low amount of material available for mass spectrometric analysis.

84 of putative reaction intermediates and mass spectrometric analysis.

85 action and liquid chromatography tandem mass spectrometric analysis.

86 the surface of a working electrode for mass spectrometric analysis.

87 oduction of OGs that can be detected by mass spectrometric analysis.

88 thod for peptide fragmentation prior to mass spectrometric analysis.

89 13)C NMR, UV-Vis spectroscopies and via mass spectrometric analysis.

90 ization with online chemical ionization mass spectrometric analysis.

91 ation of glycopeptides and their tandem mass spectrometric analysis.

92 pheric pressure chemical ionization and mass spectrometric analysis.

93 glycoproteins in whole cell lysates for mass spectrometric analysis.

94 ts directly from skin imprints, using a mass spectrometric analytical strategy.

95 A selected ion flow-drift tube mass spectrometric analytical technique, SIFDT-MS, is describ

96 We provide mass spectrometric and biochemical evidence of an association

97 cant improvements to total selectivity (mass spectrometric and chromatographic), peak identification,

98 Mass spectrometric and crystallographic studies of Pt(II) bin

99 Application of gas chromatography with mass spectrometric and human olfactory "sniffer" detectors re

100 Mass spectrometric and immunochemical analyses showed that NT

101 Additionally, mass spectrometric and immunochemical analyses showed that th

102 Mass spectrometric and immunohistochemical studies have shown

103 Combined mass spectrometric and infrared spectroscopic analyses of in

104 of this ion source is demonstrated with mass spectrometric and ion mobility measurements of acetone,

105 ates this splicing factor, we performed mass spectrometric and kinetic experiments.

106 Mass spectrometric and mutational analyses reveal that K133 o

107 and a low-P sandy soil by combining advanced spectrometric and spectroscopic techniques to introduce

108 Light-scattering, mass spectrometric, and nuclear magnetic resonance characteri

109 However, many mass spectrometric applications benefit from protein ions tha

110 native strategy to the well-established mass spectrometric approach and thus effectively adds to the

111 Our high-resolution mass spectrometric approach can unambiguously differentiate b

112 eport the development of a quantitative mass spectrometric approach combined with microfluidic techno

113 Notably, a mass spectrometric approach showed that ARH3-deficient mouse

114 We present a mass spectrometric approach to characterize and monitor the i

115 targeted, liquid chromatography-coupled mass spectrometric approach.

116 Herein, we highlight mass spectrometric approaches commonly applied to identify in

117 etic, biochemical, and highly sensitive mass spectrometric approaches, we identified an alternative m

118 eps as required for traditional protein mass spectrometric approaches.

119 ovel interaction partner of JLP through mass spectrometric approaches.

120 describe a high-throughput, label-free mass spectrometric assay to characterize acyltransferase enzy

121 is is the case with iPLAbeta as well, a mass spectrometric assay was employed to determine the rate o

122 Herein, the first chiral dopant-based mass spectrometric assay, with its foundation rooted in the C

123 using either flow cytometry or a novel mass spectrometric assay.

124 Furthermore, both spectrometric assays (total phenolic content and radical

125 ance using liquid chromatography-tandem mass spectrometric assays of serum and timed urine samples in

126 mechanistic studies including those of mass spectrometric back reaction screening experiments, which

127 Here, we provide mass spectrometric-based evidence to show that metallodrug in

128 Here, we report chromatographic and mass spectrometric behavior of 904 authentic standards collec

129 Mass spectrometric characterisation identified novel MUPs in

130 ng an anti-IL-4/IL-13 bispecific IgG, a mass spectrometric characterization method was developed usin

131 is known to severely interfere with the mass-spectrometric characterization of analyte molecules.

132 Mass spectrometric characterization of McrA from the methanog

133 revolutionary technology that couples a mass spectrometric-cleavable chemical cross-linker with high-

134 e been observed and characterized under mass spectrometric conditions.

135 ruct, proteomic sample preparation, and mass spectrometric data acquisition and analysis.

136 Mass spectrometric data and information quality were based on

137 aviolet visible (PDA) UV-Vis spectra, ESI-MS spectrometric data and spiking experiments with authenti

138 hromatographic and ultrahigh resolution mass spectrometric data are concerned.

139 Acquired mass spectrometric data argues against formation of oligomers

140 iently searching liquid chromatographic/mass spectrometric data for unknown compounds has been develo

141 sible OpenMS software implements common mass spectrometric data processing tasks through a well-defin

142 ols and ready-made workflows for common mass spectrometric data processing tasks, which enable users

143 ly available for untargeted analysis of mass spectrometric data sets, it does not always identify met

144 oteomic sample takes 1 d, acquiring the mass spectrometric data takes 2-5 d and analysis of the data

145 We report crystallographic and mass spectrometric data that reveal that pironetin forms a co

146 However, mass spectrometric data typically contain large amounts of mi

147 Mass spectrometric data was processed using the laboratory-bu

148 olydispersity index determined from the mass spectrometric data were in line with both the label valu

149 gy, the original liquid chromatographic/mass spectrometric data were not available to compare with th

150 liquid chromatographic high-resolution mass spectrometric data.

151 ing approaches is the complexity of the mass spectrometric data.

152 ucial for the routine interpretation of mass spectrometric data.

153 : (1) validate the comparability of two mass spectrometric datasets and (2) accurately calculate the

154 onation with inductively coupled plasma mass spectrometric detection (AF(4)-ICP-MS) was applied for q

155 gas chromatography with time-of-flight mass spectrometric detection (GC x GC-TOFMS).

156 gas chromatography with time-of-flight mass spectrometric detection (GC(3)/TOFMS) is described.

157 gas chromatography with time-of-flight mass spectrometric detection (GCxGC/TOFMS) proved to be appro

158 oupled with electrospray ionization and mass spectrometric detection (HPLC/ESI/MS), was employed for

159 with a gas chromatography coupled to a mass spectrometric detection (HS-SPME-GC-MS) as well as heads

160 n in rice using ion chromatography with mass spectrometric detection (IC-ICP-MS), covering the main r

161 r coupled to inductively coupled plasma mass spectrometric detection (ICP-MS).

162 diode array and electrospray ionisation mass spectrometric detection (LC/PDA/ESI-MS).

163 with the multiplex capabilities of ToF mass spectrometric detection allows for the visualization of

164 high resolution time of flight (HR-ToF) mass spectrometric detection and a high throughput acetylchol

165 -labeling technique in combination with mass spectrometric detection and determined the in vivo kinet

166 ar beam (CMB) instruments with rotating mass spectrometric detection and time-of-flight analysis, esp

167 ysis coupled to gas chromatography with mass-spectrometric detection in selected ion monitoring mode

168 concentrations in their brains using a mass spectrometric detection method developed for this purpos

169 for the high-throughput separation and mass spectrometric detection of biomolecules on the milliseco

170 t a peptide binding method coupled with mass spectrometric detection of bound peptide can quantify mA

171 We report a new method for the mass spectrometric detection of fleeting reaction intermediat

172 stigated as an ionization technique for mass spectrometric detection of the compounds in ambient orga

173 ytes with excellent chromatographic and mass spectrometric detection properties.

174 elected reaction monitoring (SRM) based mass spectrometric detection to quantify a positron emission

175 ) between electrochemical oxidation and mass spectrometric detection, enabled by an integrated electr

176 ted, using liquid chromatography-tandem mass spectrometric detection, in order to accurately determin

177 al composition distribution (CCD), with mass spectrometric detection, is described.

178 n ionization time-of-flight (MALDI-TOF) mass spectrometric detection-are attractive analytical approa

179 le benefits when combined with accurate mass spectrometric detection.

180 liquid chromatography (UPLC), both with mass spectrometric detection.

181 samples followed by flame atomic absorption spectrometric detection.

182 l flow injection system was designed for the spectrometric determination of the analyte (=344nm).

183 enging analytes for chromatographic and mass spectrometric determination, particularly the quantitati

184 sodium or proton pump, with noncovalent mass-spectrometric, electrophysiological, and flash photolysi

185 plex was also confirmed by electrospray mass spectrometric (ESI MS) experiments.

186 (-) hampers the electrospray ionization mass spectrometric (ESI-MS) analysis.

187 a signature mass spectrum during tandem mass spectrometric events.

188 Genetic, pharmacological and mass spectrometric evidence in vivo as well as in vitro confi

189 *-), has been investigated in detail by mass spectrometric experiments and quantum chemical calculati

190 reactors, and the broad scope of tandem mass spectrometric experiments applicable to mass-selected io

191 et1 and Eu(3+) subset2 were assigned by mass spectrometric experiments.

192 any of the 4 same foods.A total of 249 mass spectrometric features showed a positive dose-dependent

193 Here, we describe an enzymatic/mass spectrometric fingerprinting method to analyze the FA of

194 Applicability of the obtained mass spectrometric fingerprints for food authentication was e

195 We provide gas chromatographic/mass spectrometric, fluorescence microscopic and radiolabeled

196 r predicted hidden states, we use rapid mass spectrometric footprinting and confirm our models' predi

197 gas phase using two differential tandem mass-spectrometric fragmentation methods, such as collision-i

198 ts were subjected to gas chromatography-mass spectrometric (GC-MS) analysis.

199 A gas chromatography-mass spectrometric (GC-MS) method was utilized for the separa

200 ) method, coupled to gas chromatography/mass spectrometric (GC/MS) analysis, was developed for the an

201 channel them into a gas chromatography/mass spectrometric (GC/MS) system for analysis.

202 Here, we combine comprehensive mass spectrometric glycan sequencing and molecular dynamics s

203 esults of a hydrogen/deuterium exchange mass spectrometric (HDX-MS) investigation of an antibody-drug

204 rmance liquid chromatography coupled to mass spectrometric (HPLC-MS/MS) method was developed for the

205 paration and inductively coupled plasma mass spectrometric (ICP-MS) detection.

206 However, the mass spectrometric identification and characterization of cro

207 However, the mass spectrometric identification of cross-linked nucleic aci

208 oredoxin in E. coli cells, allowing for mass spectrometric identification of interacting proteins and

209 The results demonstrate that mass spectrometric identification of mixtures of chiral molec

210 experiments with cytoskeletal proteins, mass spectrometric identification of MPK6 complexes and immun

211 explore the utility of this reagent in mass spectrometric identification of specific functionalities

212 A modified isotope dilution mass spectrometric (IDMS) method treating the silicon as the

213 ix-assisted laser desorption/ionization mass spectrometric imaging (MALDI-MSI) of agarose micro-beads

214 matrix application techniques for MALDI mass spectrometric imaging (MSI) of endogenous metabolites fr

215 Mass spectrometric imaging (MSI) provides a unique way of ima

216 Advanced mass spectrometric imaging and surface analysis techniques we

217 Furthermore, we performed mass spectrometric imaging combined with fluorescence in situ

218 Desorption electrospray ionization-mass-spectrometric imaging was used to obtain chemical maps o

219 classically assigned by using only the mass spectrometric information, were identified as not valid

220 an engine dynamometer and utilize a new mass-spectrometric instrument to characterize the load depend

221 An ionization scheme for fast online mass spectrometric interrogation of levitated droplets is pre

222 Mass spectrometric investigation indicates the presence of he

223 lycopeptides are very useful for tandem mass spectrometric investigation, the analysis with conventio

224 Liquid chromatography-tandem mass spectrometric (LC-MS/MS) analysis revealed that the rete

225 tion followed by liquid chromatographic/mass spectrometric (LC/MS) analysis was used to locate "twin"

226 sit upon growth, quantitative elemental mass spectrometric measurements at trace level concentration

227 Mass spectrometric measurements both by electrospray ionizati

228 Additional mass spectrometric measurements of 20 different organic compo

229 petal can be quantitatively characterized by spectrometric measurements with several square-millimetr

230 and chemical composition, deduced from mass spectrometric measurements, were providing information o

231 We have established this mass spectrometric method as a dependable, cost-effective and

232 aser desorption/ionization (SALDI)-type mass spectrometric method for analysis and imaging, can diffe

233 A sorption-spectrometric method for determination of the anionic sy

234 A new mass spectrometric method for evaluating metabolite formation

235 apid multiple reaction monitoring (MRM) mass spectrometric method for the detection and relative quan

236 ry sampling electrothermal atomic absorption spectrometric method is proposed for the determination o

237 essible, sensitive, and robust targeted mass spectrometric method selected reaction monitoring, SRM.

238 We present an absorption spectrometric method using a polytetrafluoroethylene (PT

239 tion of a highly accurate and sensitive mass spectrometric method, no trace of BMAA was detected in t

240 erformance liquid chromatography-tandem mass spectrometric method.

241 loping a near-field, nonresonant, X-band ESR spectrometric method.

242 Spectrometric methodology has been developed to detect d

243 d liquid chromatographies combined with mass spectrometric methods (gas chromatography/mass spectrome

244 While both spectrometric methods are only able measure total carote

245 ical species in thin tissue sections by mass spectrometric methods has been constrained by the need f

246 nt sample, compared to classical tandem mass spectrometric methods that discard all ions with the exc

247 Two liquid chromatography-tandem mass spectrometric methods were developed and validated to de

248 Compared to other mass spectrometric methods, the developed assays require less

249 Comprehensive mass spectrometric (MS) analyses were conducted to characteri

250 eparation method, the addition to it of mass spectrometric (MS) analysis, and recent improvements in

251 Mass spectrometric (MS) characterization of these molecules a

252 al antibody charge variants with online mass spectrometric (MS) identification.

253 borious and time-consuming process, and mass spectrometric (MS) imaging techniques, which show great

254 A highly sensitive mass spectrometric (MS) method was developed and validated to

255 Sensitive and selective mass spectrometric (MS) techniques coupled to ultrahigh perfo

256 Next-generation mass spectrometric (MS) techniques such as SWATH-MS have subs

257 n be applied for the concomitant tandem mass spectrometric (MS/MS) analysis of nine pharmaceuticals i

258 ining 2uPFOA and 2HPFOA, we optimized a mass-spectrometric multiple-reaction-monitoring (MS/MS) techn

259 ity between 5 and 9 wk after injection using spectrometric NaI(Tl) and HPGe detectors, and imaging be

260 We report unexpected mass spectrometric observations of glycosylated human leukocy

261 yover and improve liquid chromatography-mass spectrometric performance.

262 Mass spectrometric phosphoproteomic measurements further iden

263 y applicable and extendable to multiple mass spectrometric platforms.

264 Mass spectrometric profiling of acylsugars in the S. lycopers

265 trometry (REIMS) was used for the rapid mass spectrometric profiling of cancer cell lines.

266 This may be the first mass spectrometric profiling of polyphenol components from cu

267 As an alternative, direct mass spectrometric profiling of the mucosal metabolome provid

268 We performed a mass spectrometric proteomics characterization of BALF exosom

269 Proton Transfer Reaction Time-of-Flight Mass Spectrometric (PTR-(ToF)MS).

270 In addition, the spectrometric quality of the small sensor (size: 6.5mm i

271 talyzed depurination of DNA followed by mass spectrometric quantification of adenine.

272 The mass spectrometric raw data has been deposited in PRIDE (PXD0

273 w soft ionization technique that allows mass spectrometric real-time detection of organic compounds i

274 The mass spectrometric results reveal ample oxidative side reacti

275 In a mass spectrometric screen to identify PIP3-regulated proteins

276 d increase the analytical throughput of mass spectrometric screening in the routine quality assessmen

277 ber of structurally similar components, mass spectrometric screens based on high-performance liquid c

278 concentration, and eventually in direct mass spectrometric sensitivity.

279 profiling, computational modeling, and mass-spectrometric sequencing of peptidylarginine deiminase (

280 indlin-3 phosphorylation as detected by mass spectrometric sequencing.

281 With EP-ESI-MS, the integrated mass spectrometric signals are found to be a monotonic functi

282 ablished through extensive spectroscopic and spectrometric studies (1D, 2D NMR, ESI-MS, and MS/MS).

283 bly to HLA-B*18:01, and peptide elution/mass spectrometric studies showed it is naturally presented b

284 urier transform ion cyclotron resonance mass spectrometric studies, we determined that water was the

285 validated by photoaffinity labeling and mass spectrometric studies.

286 This work deals with the comprehensive spectrometric study of the chlorophyll derivatives prese

287 We developed a portable mass spectrometric system ("miniRuedi") for quantificaton of

288 ed by a newly developed offline aerosol mass spectrometric technique (AMS).

289 re the development of a soft ionization mass spectrometric technique coupled with preconcentration on

290 oligomer growth can be assigned by the mass spectrometric technique.

291 mposition by using complementary online mass spectrometric techniques in a comprehensive chemical cha

292 ith other ambient desorption/ionization mass spectrometric techniques like desorption electrospray io

293 ticle-phase products by high-resolution mass spectrometric techniques revealed the formation of nitro

294 uld easily be implemented in hyphenated mass spectrometric techniques to improve the structural and q

295 We combined a range of mass spectrometric techniques to unravel the location and ext

296 imated for the first time in the kinetic and spectrometric techniques using the certified reference m

297 r both variants by integrating advanced mass spectrometric techniques with available electron microsc

298 combination of chemical modifications, mass spectrometric techniques, site-directed mutagenesis, and

299 tube epithelial cells via a single-run mass spectrometric workflow.

300 eptides identified in current bottom-up mass spectrometric workflows, although impressive for high-th