ライフサイエンスコーパス: mass spectrometric

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

2 f All Theoretical Fragment Ion Mass Spectra) mass spectrometric acquisitions were performed to obtain

3 Duplicate mass spectrometric analyses and confirmatory next genera

4 ped a targeted approach for the simultaneous mass spectrometric analyses of 16 DNA adducts, which can

5 Radiometric and mass spectrometric analyses of Cs contamination in the e

6 Kinetic and mass spectrometric analyses of human proteins show that

7 Using mass spectrometric analyses of Saccharomyces cerevisiae

8 g different protein substrates and MALDI-TOF mass spectrometric analyses of the generated oligopeptid

9 Mass spectrometric analyses of whole-cell extracts demon

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

11 Biochemical and mass spectrometric analyses showed that the UCR2-catalyt

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

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

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

15 Mass-spectrometric analyses confirmed that conversion is

16 -energy collisional dissociation) multistage mass spectrometric analysis (HCD-MS(n)) and ETD (electro

17 ater labeling combined with sensitive tandem mass spectrometric analysis allowed integrated synthesis

18 ibrinogen for additional investigation using mass spectrometric analysis and electron microscopy.

19 ships between BtAdVs and CAdVs, we conducted mass spectrometric analysis and single-particle cryo-ele

20 Mass spectrometric analysis confirmed that the mutant se

21 Mass spectrometric analysis identified apolipoprotein(a)

22 oinducing peptide (AIP) was responsible, and mass spectrometric analysis identified the S. caprae AIP

23 Mass spectrometric analysis in EC identified five dimeth

24 Mass spectrometric analysis indicates that most of the l

25 Coimmunoprecipitation and mass spectrometric analysis of 293 cells overexpressing

26 vivo classification of human tissue through mass spectrometric analysis of aerosols released during

27 Compared to previous attempts at MALDI-TOF mass spectrometric analysis of barley proteins, the extr

28 unner of automated laboratories dedicated to mass spectrometric analysis of biological samples.

29 Unbiased mass spectrometric analysis of cardiac tissue before and

30 Mass spectrometric analysis of cell extracts identified

31 niques (APPI and APLI) are important for the mass spectrometric analysis of crude oils, given the mai

32 ure, which includes the catalytic water, and mass spectrometric analysis of enzymatic hydrolysis prod

33 fferential scanning calorimetry coupled with mass spectrometric analysis of evolved gases.

34 Hydrogen/deuterium exchange with mass spectrometric analysis of fibrillating glucagon sug

35 Our mass spectrometric analysis of homomeric and heteromeric

36 Mass spectrometric analysis of Ire1 expressed in Escheri

37 Mass spectrometric analysis of LDB1 binding partners in

38 Mass spectrometric analysis of microbial metabolism prov

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

40 toward formation of fluid lipid bilayer, and mass spectrometric analysis of peptides and cytochrome c

41 Finally, using a mass spectrometric analysis of secreted proteins, we dem

42 RNA sequencing and mass spectrometric analysis of SPRIGHTLY-expressing cell

43 Mass spectrometric analysis of the CYP17A1-b5 complexes

44 tion on the digestibility were determined by mass spectrometric analysis of the modified beta-lactogl

45 Mass spectrometric analysis of the phosphoproteome revea

46 tudy, we performed affinity purification and mass spectrometric analysis of the protein microenvironm

47 Raman spectroscopic and mass spectrometric analysis of the reaction solutions re

48 Mass spectrometric analysis of the secretome of P. aerug

49 Mass spectrometric analysis of the starting octasacchari

50 We show the applicability of this setup for mass spectrometric analysis of three common MALDI matric

51 Through mass spectrometric analysis of ubiquitylated proteins af

52 For mixtures, contained-ESI mass spectrometric analysis produces relative ion intens

53 mportant role of GNRs as semiconductors, the mass spectrometric analysis provides a readily available

54 which can subsequently be subjected to rapid mass spectrometric analysis providing insights into the

55 assay and pull-down experiments coupled with mass spectrometric analysis revealed that the cellular p

56 Mass spectrometric analysis revealed that the RxLR seque

57 al trypsinolysis followed by high resolution mass spectrometric analysis reveals that Ub chain branch

58 Mass spectrometric analysis showed that several of these

59 stion of milk proteins by kefir grains, with mass spectrometric analysis showing the release of 609 p

60 of mouse serum in conjunction with targeted mass spectrometric analysis suggested that serum very-lo

61 oupled with a fragment separation method and mass spectrometric analysis to compare their secondary s

62 on to stabilize regiospecificity, and tandem mass spectrometric analysis to identify and quantify reg

63 sources, enzyme assays, Western blotting and mass spectrometric analysis to monitor and quantify the

64 )-based workflow from sample preparation for mass spectrometric analysis to visualization of protein-

65 es from volume-limited samples, each type of mass spectrometric analysis uncovers only a portion of t

66 Immunoprecipitation assays and mass spectrometric analysis using beta cells verified Ly

67 Mass spectrometric analysis was performed after cell lys

68 Additionally mass spectrometric analysis was performed with the cells

69 Amide hydrogen/deuterium exchange with mass spectrometric analysis was used to identify the int

70 tes and chromatographic separation preceding mass spectrometric analysis were optimized, and the resu

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

72 A proteomic (two-dimensional PAGE with mass spectrometric analysis) comparison between the Delt

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

74 Mass spectrometric analysis, ELISA, and immunoblot confi

75 Here, using mass spectrometric analysis, it is demonstrated that the

76 ovalent capture, co-immunoprecipitation, and mass spectrometric analysis, we identified a subset of H

77 blished by immunohistochemistry staining and mass spectrometric analysis.

78 se positives are small owing to the use of a mass spectrometric analysis.

79 ions that occur during sample preparation or mass spectrometric analysis.

80 f aging mice and followed by biochemical and mass spectrometric analysis.

81 ipidomics has been significantly advanced by mass spectrometric analysis.

82 investigated by end-group analysis with ESI mass spectrometric analysis.

83 n tRNA(Pro(GGG)) and Um in tRNA(Gln(UUG)) by mass spectrometric analysis.

84 kground biofluid electrolytes for quantiatve mass spectrometric analysis.

85 he very low amount of material available for mass spectrometric analysis.

86 ation of putative reaction intermediates and mass spectrometric analysis.

87 extraction and liquid chromatography tandem mass spectrometric analysis.

88 from the surface of a working electrode for mass spectrometric analysis.

89 vo production of OGs that can be detected by mass spectrometric analysis.

90 ew method for peptide fragmentation prior to mass spectrometric analysis.

91 MR, (13)C NMR, UV-Vis spectroscopies and via mass spectrometric analysis.

92 latilization with online chemical ionization mass spectrometric analysis.

93 ethylation of glycopeptides and their tandem mass spectrometric analysis.

94 atmospheric pressure chemical ionization and mass spectrometric analysis.

95 from glycoproteins in whole cell lysates for mass spectrometric analysis.

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

97 Top-down mass-spectrometric analysis shows that the main binding

98 After sample preparation and mass-spectrometric analysis, peptide intensity ratios be

99 atients directly from skin imprints, using a mass spectrometric analytical strategy.

100 A selected ion flow-drift tube mass spectrometric analytical technique, SIFDT-MS, is de

101 We provide mass spectrometric and biochemical evidence of an associ

102 gnificant improvements to total selectivity (mass spectrometric and chromatographic), peak identifica

103 Mass spectrometric and crystallographic studies of Pt(II

104 Application of gas chromatography with mass spectrometric and human olfactory "sniffer" detecto

105 Mass spectrometric and immunochemical analyses showed th

106 Additionally, mass spectrometric and immunochemical analyses showed th

107 Mass spectrometric and immunohistochemical studies have

108 Combined mass spectrometric and infrared spectroscopic analyses o

109 lity of this ion source is demonstrated with mass spectrometric and ion mobility measurements of acet

110 horylates this splicing factor, we performed mass spectrometric and kinetic experiments.

111 Mass spectrometric and mutational analyses reveal that K

112 Light-scattering, mass spectrometric, and nuclear magnetic resonance chara

113 However, many mass spectrometric applications benefit from protein ion

114 alternative strategy to the well-established mass spectrometric approach and thus effectively adds to

115 Our high-resolution mass spectrometric approach can unambiguously differenti

116 we report the development of a quantitative mass spectrometric approach combined with microfluidic t

117 Notably, a mass spectrometric approach showed that ARH3-deficient m

118 We present a mass spectrometric approach to characterize and monitor

119 an untargeted, liquid chromatography-coupled mass spectrometric approach.

120 Herein, we highlight mass spectrometric approaches commonly applied to identi

121 g genetic, biochemical, and highly sensitive mass spectrometric approaches, we identified an alternat

122 on steps as required for traditional protein mass spectrometric approaches.

123 s a novel interaction partner of JLP through mass spectrometric approaches.

124 ts in an ultrasensitive enzyme-linked immune mass spectrometric assay (ELIMSA).

125 nd we describe a high-throughput, label-free mass spectrometric assay to characterize acyltransferase

126 er this is the case with iPLAbeta as well, a mass spectrometric assay was employed to determine the r

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

128 pared using either flow cytometry or a novel mass spectrometric assay.

129 clearance using liquid chromatography-tandem mass spectrometric assays of serum and timed urine sampl

130 ental mechanistic studies including those of mass spectrometric back reaction screening experiments,

131 Here, we provide mass spectrometric-based evidence to show that metallodr

132 Here, we report chromatographic and mass spectrometric behavior of 904 authentic standards c

133 Mass spectrometric characterisation identified novel MUP

134 Using an anti-IL-4/IL-13 bispecific IgG, a mass spectrometric characterization method was developed

135 Mass spectrometric characterization of McrA from the met

136 trix is known to severely interfere with the mass-spectrometric characterization of analyte molecules

137 ), a revolutionary technology that couples a mass spectrometric-cleavable chemical cross-linker with

138 s have been observed and characterized under mass spectrometric conditions.

139 construct, proteomic sample preparation, and mass spectrometric data acquisition and analysis.

140 Mass spectrometric data and information quality were bas

141 gas chromatographic and ultrahigh resolution mass spectrometric data are concerned.

142 Acquired mass spectrometric data argues against formation of olig

143 efficiently searching liquid chromatographic/mass spectrometric data for unknown compounds has been d

144 extensible OpenMS software implements common mass spectrometric data processing tasks through a well-

145 85 tools and ready-made workflows for common mass spectrometric data processing tasks, which enable u

146 freely available for untargeted analysis of mass spectrometric data sets, it does not always identif

147 ed proteomic sample takes 1 d, acquiring the mass spectrometric data takes 2-5 d and analysis of the

148 We report crystallographic and mass spectrometric data that reveal that pironetin forms

149 However, mass spectrometric data typically contain large amounts

150 Mass spectrometric data was processed using the laborato

151 and polydispersity index determined from the mass spectrometric data were in line with both the label

152 lmology, the original liquid chromatographic/mass spectrometric data were not available to compare wi

153 es in liquid chromatographic high-resolution mass spectrometric data.

154 -linking approaches is the complexity of the mass spectrometric data.

155 is crucial for the routine interpretation of mass spectrometric data.

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

157 ractionation with inductively coupled plasma mass spectrometric detection (AF(4)-ICP-MS) was applied

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

159 (3D) gas chromatography with time-of-flight mass spectrometric detection (GC(3)/TOFMS) is described.

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

161 hy, coupled with electrospray ionization and mass spectrometric detection (HPLC/ESI/MS), was employed

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

163 iation in rice using ion chromatography with mass spectrometric detection (IC-ICP-MS), covering the m

164 ulizer coupled to inductively coupled plasma mass spectrometric detection (ICP-MS).

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

166 bined with the multiplex capabilities of ToF mass spectrometric detection allows for the visualizatio

167 llel high resolution time of flight (HR-ToF) mass spectrometric detection and a high throughput acety

168 otope-labeling technique in combination with mass spectrometric detection and determined the in vivo

169 lecular beam (CMB) instruments with rotating mass spectrometric detection and time-of-flight analysis

170 ng LK concentrations in their brains using a mass spectrometric detection method developed for this p

171 llows for the high-throughput separation and mass spectrometric detection of biomolecules on the mill

172 e that a peptide binding method coupled with mass spectrometric detection of bound peptide can quanti

173 We report a new method for the mass spectrometric detection of fleeting reaction interm

174 investigated as an ionization technique for mass spectrometric detection of the compounds in ambient

175 analytes with excellent chromatographic and mass spectrometric detection properties.

176 and selected reaction monitoring (SRM) based mass spectrometric detection to quantify a positron emis

177 4.5 s) between electrochemical oxidation and mass spectrometric detection, enabled by an integrated e

178 alidated, using liquid chromatography-tandem mass spectrometric detection, in order to accurately det

179 hemical composition distribution (CCD), with mass spectrometric detection, is described.

180 rption ionization time-of-flight (MALDI-TOF) mass spectrometric detection-are attractive analytical a

181 derable benefits when combined with accurate mass spectrometric detection.

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

183 pyrolysis coupled to gas chromatography with mass-spectrometric detection in selected ion monitoring

184 one analytical run for targeted quantitative mass spectrometric determination of metabolites from cen

185 challenging analytes for chromatographic and mass spectrometric determination, particularly the quant

186 iven sodium or proton pump, with noncovalent mass-spectrometric, electrophysiological, and flash phot

187 ) complex was also confirmed by electrospray mass spectrometric (ESI MS) experiments.

188 he DS(-) hampers the electrospray ionization mass spectrometric (ESI-MS) analysis.

189 duce a signature mass spectrum during tandem mass spectrometric events.

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

191 , O2(*-), has been investigated in detail by mass spectrometric experiments and quantum chemical calc

192 flow reactors, and the broad scope of tandem mass spectrometric experiments applicable to mass-select

193 subset1 and Eu(3+) subset2 were assigned by mass spectrometric experiments.

194 ke of any of the 4 same foods.A total of 249 mass spectrometric features showed a positive dose-depen

195 Here, we describe an enzymatic/mass spectrometric fingerprinting method to analyze the

196 Applicability of the obtained mass spectrometric fingerprints for food authentication

197 We provide gas chromatographic/mass spectrometric, fluorescence microscopic and radiola

198 ct our predicted hidden states, we use rapid mass spectrometric footprinting and confirm our models'

199 the gas phase using two differential tandem mass-spectrometric fragmentation methods, such as collis

200 roducts were subjected to gas chromatography-mass spectrometric (GC-MS) analysis.

201 A gas chromatography-mass spectrometric (GC-MS) method was utilized for the s

202 S-BID) method, coupled to gas chromatography/mass spectrometric (GC/MS) analysis, was developed for t

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

204 Here, we combine comprehensive mass spectrometric glycan sequencing and molecular dynam

205 the results of a hydrogen/deuterium exchange mass spectrometric (HDX-MS) investigation of an antibody

206 performance liquid chromatography coupled to mass spectrometric (HPLC-MS/MS) method was developed for

207 C) separation and inductively coupled plasma mass spectrometric (ICP-MS) detection.

208 However, the mass spectrometric identification and characterization o

209 by SDSPAGE followed by in-gel digestion and mass spectrometric identification and characterization.U

210 However, the mass spectrometric identification of cross-linked nuclei

211 h thioredoxin in E. coli cells, allowing for mass spectrometric identification of interacting protein

212 The results demonstrate that mass spectrometric identification of mixtures of chiral

213 tion experiments with cytoskeletal proteins, mass spectrometric identification of MPK6 complexes and

214 ed to explore the utility of this reagent in mass spectrometric identification of specific functional

215 The accuracy of Vitek MS mass spectrometric identifications was assessed for 206

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

217 matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI-MSI) of agarose micro-

218 rent matrix application techniques for MALDI mass spectrometric imaging (MSI) of endogenous metabolit

219 Mass spectrometric imaging (MSI) provides a unique way o

220 Advanced mass spectrometric imaging and surface analysis techniqu

221 Furthermore, we performed mass spectrometric imaging combined with fluorescence in

222 , matrix-free UV-laser desorption/ionization mass spectrometric imaging, and Raman microspectroscopy.

223 Desorption electrospray ionization-mass-spectrometric imaging was used to obtain chemical m

224 cies, classically assigned by using only the mass spectrometric information, were identified as not v

225 e on an engine dynamometer and utilize a new mass-spectrometric instrument to characterize the load d

226 An ionization scheme for fast online mass spectrometric interrogation of levitated droplets i

227 Mass spectrometric investigation indicates the presence

228 ing glycopeptides are very useful for tandem mass spectrometric investigation, the analysis with conv

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

230 digestion followed by liquid chromatographic/mass spectrometric (LC/MS) analysis was used to locate "

231 ve and degraded during sample processing and mass spectrometric measurement.

232 deposit upon growth, quantitative elemental mass spectrometric measurements at trace level concentra

233 Mass spectrometric measurements both by electrospray ion

234 Additional mass spectrometric measurements of 20 different organic

235 rties and chemical composition, deduced from mass spectrometric measurements, were providing informat

236 We have established this mass spectrometric method as a dependable, cost-effectiv

237 ted laser desorption/ionization (SALDI)-type mass spectrometric method for analysis and imaging, can

238 A new mass spectrometric method for evaluating metabolite form

239 A rapid multiple reaction monitoring (MRM) mass spectrometric method for the detection and relative

240 y accessible, sensitive, and robust targeted mass spectrometric method selected reaction monitoring,

241 Here, we describe and apply a mass spectrometric method to monitor the association and

242 alidation of a highly accurate and sensitive mass spectrometric method, no trace of BMAA was detected

243 tra performance liquid chromatography-tandem mass spectrometric method.

244 as and liquid chromatographies combined with mass spectrometric methods (gas chromatography/mass spec

245 Modern mass spectrometric methods for quantifying changes in th

246 chemical species in thin tissue sections by mass spectrometric methods has been constrained by the n

247 oth untargeted and targeted isotope-assisted mass spectrometric methods of phosphopeptide quantitatio

248 mponent sample, compared to classical tandem mass spectrometric methods that discard all ions with th

249 Two liquid chromatography-tandem mass spectrometric methods were developed and validated

250 Compared to other mass spectrometric methods, the developed assays require

251 Comprehensive mass spectrometric (MS) analyses were conducted to chara

252 ent separation method, the addition to it of mass spectrometric (MS) analysis, and recent improvement

253 Mass spectrometric (MS) characterization of these molecu

254 -down hydrogen/deuterium exchange (HDX) with mass spectrometric (MS) detection has recently matured t

255 oclonal antibody charge variants with online mass spectrometric (MS) identification.

256 a laborious and time-consuming process, and mass spectrometric (MS) imaging techniques, which show g

257 A highly sensitive mass spectrometric (MS) method was developed and validat

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

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

260 BS can be applied for the concomitant tandem mass spectrometric (MS/MS) analysis of nine pharmaceutic

261 containing 2uPFOA and 2HPFOA, we optimized a mass-spectrometric multiple-reaction-monitoring (MS/MS)

262 We report unexpected mass spectrometric observations of glycosylated human le

263 carryover and improve liquid chromatography-mass spectrometric performance.

264 Mass spectrometric phosphoproteomic measurements further

265 roadly applicable and extendable to multiple mass spectrometric platforms.

266 Mass spectrometric profiling of acylsugars in the S. lyc

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

268 This may be the first mass spectrometric profiling of polyphenol components fr

269 As an alternative, direct mass spectrometric profiling of the mucosal metabolome p

270 We performed a mass spectrometric proteomics characterization of BALF e

271 d by Proton Transfer Reaction Time-of-Flight Mass Spectrometric (PTR-(ToF)MS).

272 id-catalyzed depurination of DNA followed by mass spectrometric quantification of adenine.

273 The mass spectrometric raw data has been deposited in PRIDE

274 a new soft ionization technique that allows mass spectrometric real-time detection of organic compou

275 The mass spectrometric results reveal ample oxidative side r

276 Mass spectrometric results revealed that flocculation in

277 In a mass spectrometric screen to identify PIP3-regulated pro

278 on and increase the analytical throughput of mass spectrometric screening in the routine quality asse

279 e number of structurally similar components, mass spectrometric screens based on high-performance liq

280 cies concentration, and eventually in direct mass spectrometric sensitivity.

281 sed kindlin-3 phosphorylation as detected by mass spectrometric sequencing.

282 itope profiling, computational modeling, and mass-spectrometric sequencing of peptidylarginine deimin

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

284 d stably to HLA-B*18:01, and peptide elution/mass spectrometric studies showed it is naturally presen

285 on Fourier transform ion cyclotron resonance mass spectrometric studies, we determined that water was

286 were validated by photoaffinity labeling and mass spectrometric studies.

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

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

289 il here the development of a soft ionization mass spectrometric technique coupled with preconcentrati

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

291 al composition by using complementary online mass spectrometric techniques in a comprehensive chemica

292 ble with other ambient desorption/ionization mass spectrometric techniques like desorption electrospr

293 d particle-phase products by high-resolution mass spectrometric techniques revealed the formation of

294 ch could easily be implemented in hyphenated mass spectrometric techniques to improve the structural

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

296 rs for both variants by integrating advanced mass spectrometric techniques with available electron mi

297 ing a combination of chemical modifications, mass spectrometric techniques, site-directed mutagenesis

298 udy of the fragmentation behavior using both mass spectrometric techniques.

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

300 of peptides identified in current bottom-up mass spectrometric workflows, although impressive for hi