ライフサイエンスコーパス: spectrometry

1 e product by in situ ambient ionization mass spectrometry.

2 be combined with proteomic analysis by mass spectrometry.

3 ance liquid chromatography ion mobility-mass spectrometry.

4 e dilution-multiple-reaction monitoring-mass spectrometry.

5 matrix, followed by Gas Chromatography/Mass Spectrometry.

6 analyzed using drift time ion mobility mass spectrometry.

7 -line with LC, IMS, and high resolution mass spectrometry.

8 urier transform ion cyclotron resonance mass spectrometry.

9 quid chromatography coupled with tandem mass spectrometry.

10 easily be studied using single droplet mass spectrometry.

11 ganic analysis by liquid chromatography/mass spectrometry.

12 graphy isotope-dilution high-resolution mass spectrometry.

13 ty of CM-101 in rats were measured with mass spectrometry.

14 g flow injection analysis with orbitrap mass spectrometry.

15 Stool samples were analyzed by mass spectrometry.

16 enesis, and hydrogen/deuterium exchange-mass spectrometry.

17 s by using liquid chromatography-tandem mass spectrometry.

18 ed based on (2) H labeling using tandem mass spectrometry.

19 everse phase liquid chromatography with mass spectrometry.

20 microextraction and gas chromatography-mass spectrometry.

21 as megalin, by immunoprecipitation and mass spectrometry.

22 nation with electrothermal atomic absorption spectrometry.

23 n/ionization time-of-flight (MALDI-TOF) mass spectrometry.

24 orescence microscopy with validation by mass spectrometry.

25 its determination by flame atomic absorption spectrometry.

26 oteins that adsorbed were identified by mass spectrometry.

27 zymatic assay and liquid chromatography/mass spectrometry.

28 tification of abrin and its isoforms by mass spectrometry.

29 hromatography-quadrupole time-of-flight mass spectrometry.

30 high resolution mass or time-of-flight mass spectrometry.

31 quantified using nuclear magnetic resonance spectrometry.

32 gel electrophoresis were analyzed using mass spectrometry.

33 ults from NMR and liquid chromatography-mass spectrometry.

34 matography-multiple reaction monitoring/mass spectrometry.

35 high-resolution spectro(micro)scopy and mass spectrometry.

36 tification of O-linked glycopeptides by mass spectrometry.

37 control the total ionization charges in mass spectrometry.

38 was detected at m/z 1088 by a MALDI-TOF mass spectrometry.

39 entified interacting proteins by tandem mass spectrometry.

40 liquid chromatography coupled to tandem mass spectrometry.

41 recise data obtained via multicollector mass spectrometry.

42 n/ionization time of flight (MALDI-TOF) mass spectrometry.

43 ction of GDBT were identified by tandem mass spectrometry.

44 ed by gas chromatography time-of-flight mass spectrometry.

45 upled with single- or triple-quadrupole mass spectrometry.

46 tained by graphite furnace atomic absorption spectrometry.

47 troscopy and single droplet paper spray mass spectrometry.

48 hase microextraction/gas chromatography-mass spectrometry.

49 by capillary electrophoresis coupled to mass spectrometry.

50 estriction and by liquid chromatography-mass spectrometry.

51 ssessed with inductively coupled plasma mass spectrometry.

52 urier transform ion cyclotron resonance mass spectrometry (21T FT-ICR MS).

53 urier transform ion cyclotron resonance mass spectrometry (2D FTICR MS or 2D MS) allows direct correl

54 ls, including vacuum UV photoionization mass spectrometry, absorption and action spectroscopy in the

55 Here, we demonstrate that MALDI-TOF mass spectrometry accurately identified all of the test isola

56 Tandem mass spectrometry after digestion with three proteases and se

57 tion with high mass accuracy/resolution mass spectrometry after direct infusion (i.e., shotgun lipido

58 novel methodology based on the use of ED-XRF spectrometry after thin film deposition on special sampl

59 ram amounts of paCOS using quantitative mass spectrometry, allowing one to rapidly analyze the substr

60 The crystal structures and mass spectrometry also show that when these herbicides bind,

61 plementary techniques including aerosol mass spectrometry (AMS), high-resolution nanospray desorption

62 radiocarbon analysis using accelerator mass spectrometry (AMS).

63 tion membranes using ambient ionization mass spectrometry, an attempt has been made to understand the

64 ut not at 20 degrees C, by SDS-page and mass spectrometry analyses as well as electron microscopy ima

65 The EPR measurements and mass spectrometry analyses further reveal that nitric oxide b

66 ns to CP2 based on crystallographic and mass spectrometry analyses results in variants with greater p

67 Yet, high-resolution mass spectrometry analyses reveal a huge chemical diversity i

68 rophoresis and major spots subjected to mass spectrometry analysis and identification.

69 Mass spectrometry analysis demonstrated that cytoplasmic LANA

70 Furthermore, mass spectrometry analysis indicated Lys-72 as an acetylation

71 the seed followed by gas chromatography-mass spectrometry analysis of polar metabolites also revealed

72 Liquid chromatography-tandem mass spectrometry analysis revealed marked differences betwee

73 Immunoprecipitation followed by mass spectrometry analysis showed that several N-terminally t

74 Using mass spectrometry analysis, we found that VLVs contained vira

75 ies, mass analysis, and high-resolution mass spectrometry analysis.

76 as was observed by electrophoresis and mass spectrometry analysis.

77 using high-resolution Fourier-transform mass spectrometry and a novel algorithm of quantitative pathw

78 f the interaction that is measured with mass spectrometry and because it is compatible with laborator

79 les were analyzed using high-resolution mass spectrometry and electron-capture detection to identify

80 Here the authors show that native mass spectrometry and high resolution electron microscopy can

81 NA demethylases, along with advances in mass spectrometry and high-throughput sequencing techniques,

82 aptenation by AX has been approached by mass spectrometry and immunoaffinity techniques.

83 We applied high-resolution mass spectrometry and mass-defect filtering to four PAH-conta

84 intact proteins are analyzed by tandem mass spectrometry and proteoforms, which are defined forms of

85 zed using gas chromatography coupled to mass spectrometry and spectroscopic techniques such as infrar

86 inductively coupled plasma optical emission spectrometry and the digestion efficiency was evaluated

87 subjected to inductively coupled plasma mass spectrometry and transmission electron microscopy for qu

88 ganese using inductively coupled plasma mass spectrometry, and assessed neurodevelopment using the Ba

89 bsorption (near-edge) spectroscopy, ESI mass spectrometry, and DFT methods.

90 ence difference gel electrophoresis and mass spectrometry, and further verified by Western blotting u

91 using fluorescence spectroscopy, native mass spectrometry, and molecular dynamics simulations.

92 organic analysis by gas chromatography/mass spectrometry, and nonvolatile organic analysis by liquid

93 ytometry or cytometry by time-of-flight mass spectrometry, and such tests could be performed after bl

94 (1)H NMR spectroscopy, IR spectroscopy, mass spectrometry, and X-ray crystallography.

95 , followed by quadrupole time-of-flight mass spectrometry (APCI-qTOF-MS), operated in full scan negat

96 Using mass spectrometry approaches, we identified 16 VTPs of the Cy

97 Ultrahigh-resolution mass spectrometry, as well as optical measurements revealed t

98 ilable liquid chromatography and tandem mass spectrometry assay; follicle-stimulating hormone levels

99 Targeted mass spectrometry assays for protein quantitation monitor pep

100 n epi-marks that cannot be detected via mass spectrometry based methods for quantifying the abundance

101 y, we attempted to validate a MALDI-ToF mass spectrometry-based assay for the antifungal susceptibili

102 We demonstrate the utility of mass spectrometry-based global exposure metabolomics combined

103 Mass spectrometry-based imaging indicated a differential loca

104 n alkylating resin-assisted capture and mass spectrometry-based label-free strategy for studying the

105 re analyzed using liquid chromatography-mass spectrometry-based metabolomics.

106 Using mass spectrometry-based phosphoproteomics, we have identified

107 Mass spectrometry-based protein analysis has become an import

108 of an OFFGEL electrophoresis and tandem mass spectrometry-based proteomic approach with a DNA-based m

109 Mass spectrometry-based proteomic profiling was performed on

110 Perspective, we discuss developments in mass-spectrometry-based proteomic technology over the past de

111 hat single time point pulse-chase SILAC mass spectrometry-based proteomics (pSILAC MS) is a sensitive

112 ung metastasis, we applied quantitative mass spectrometry-based proteomics and identified 392 breast

113 Mass spectrometry-based targeted proteomics (e.g., selected r

114 of inorganic clusters relies heavily on mass spectrometry because of, in most cases, their poor respo

115 Carbon fiber ionization mass spectrometry (CFI-MS), which uses a carbon fiber bundle

116 hydrogen-deuterium exchange coupled to mass spectrometry, combined with in vitro and in vivo mutagen

117 Direct phosphorylation assay and mass spectrometry confirm that PKM2 phosphorylates SNAP-23 at

118 mitrella patens Immunoblot analysis and mass spectrometry confirmed enrichment of PpCesA5.

119 ron microscopy, as well as ion mobility-mass spectrometry coupled to infrared (IR) spectroscopy to st

120 The use of mass spectrometry coupled with chemical cross-linking of prot

121 Based on cross-linking-coupled mass spectrometry, crystal structure of the CPSF160-WDR33 sub

122 ldwide, we demonstrate that using SWATH-mass spectrometry data acquisition we can consistently detect

123 data-dependent, high-resolution tandem mass spectrometry (ddHRMS/MS) method capable of detecting all

124 eling with multiple reaction monitoring-mass spectrometry demonstrated that hypoxia and rapamycin tre

125 ry well suited for online coupling with mass spectrometry due to the relatively high volatility and l

126 F) and infant formula (IF) using tandem mass spectrometry (electron transfer dissociation).

127 Recent advances in top-down mass spectrometry enabled identification of intact proteins,

128 urier transform ion cyclotron resonance mass spectrometry (ESI-FTICRMS) and discovers additional subs

129 he proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay and model membranes of defin

130 raphy (LC) with electrospray ionization mass spectrometry (ESI-MS) in native conditions to study the

131 tive-ion electrospray ionization tandem mass spectrometry (ESI-MS/MS) method has been developed for t

132 ar beam vacuum-UV (VUV) photoionization mass spectrometry experiments were performed to understand th

133 ed and combined with flame atomic absorption spectrometry (FAAS) for pre-concentration and indirect d

134 scan field asymmetric waveform ion mobility spectrometry (FAIMS) combined with liquid chromatography

135 Also, mass spectrometry, flow cytometry, and electron microscopy an

136 approach based on liquid chromatography-mass spectrometry for revealing subtle biogeographical trends

137 ration is provided of the use of native mass spectrometry for screening fragments against a protein-D

138 e-pot two-nanoprobe approach coupled to mass spectrometry for simultaneous quantification and post-tr

139 liquid chromatography coupled to tandem mass spectrometry for the detection of blood-derived products

140 S (chromatin affinity purification with mass spectrometry), for the affinity purification of a sequen

141 urier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS) and quantify DOM photochemical

142 urier Transform-Ion Cyclotron Resonance-Mass Spectrometry (FT-ICR-MS), which delivered the molecular

143 urier transform ion cyclotron resonance mass spectrometry (FTICR MS).

144 characterized by Fourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SE

145 romatography-inductively coupled plasma mass spectrometry (GC-ICPMS) measurement conditions are emplo

146 potential of gas chromatography-ion mobility spectrometry (GC-IMS) to differentiate lactic acid bacte

147 Gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-tandem ma

148 ensitive, and robust gas chromatography-mass spectrometry (GC-MS) method for the simultaneous determi

149 Using gas chromatography mass spectrometry (GC-MS), we identified compounds typically

150 and then analyzed by gas chromatography-mass spectrometry (GC-MS).

151 live oil: (i) gas chromatography-tandem mass spectrometry (GC-MS/MS) for GC-amenable pesticides; (ii)

152 Gas cluster ion beam-secondary ion mass spectrometry (GCIB-SIMS) has shown the full potential of

153 Herein, using Gas Chromatography Mass Spectrometry (GCMS), we demonstrate that the major stero

154 Mass spectrometry has become a primary tool for glycan analys

155 Mass spectrometry has become an enabling technology for the i

156 of high-resolution techniques, such as mass spectrometry-has led to enhancements of our knowledge re

157 provided by hydrogen/deuterium exchange mass spectrometry (HDX-MS) in the protein therapeutic field i

158 we show how hydrogen/deuterium-exchange mass spectrometry (HDX-MS) provides detailed insight into the

159 genesis and hydrogen deuterium exchange mass spectrometry (HDX-MS) to identify critical residues for

160 proaches of hydrogen/deuterium exchange mass spectrometry (HDX-MS), fast photochemical oxidation of p

161 ater, complemented by hydrogen exchange mass spectrometry (HDX/MS).

162 n-deuterium exchange (HDX) coupled with mass spectrometry (HDXMS) is a rapid and effective method for

163 nteraction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) for polar pesticides, and; (i

164 atography-diode array detection- tandem mass spectrometry (HPLC-DAD-MS/MS) identified 29 phenolics be

165 erformance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method with multiple reaction

166 source graphite furnace molecular absorption spectrometry (HR-CS GF MAS) via molecular absorption of

167 have developed a novel high-resolution mass spectrometry (HRMS) based approach for analyzing large-m

168 lytical methods such as high-resolution mass spectrometry (HRMS) can help to characterize chemical co

169 ectron spray ionization high resolution mass spectrometry (hydrophilic fraction) and fluorescence spe

170 were measured using inductively coupled mass spectrometry (ICP-MS) and high-resolution ICP-MS, respec

171 scopy (EDX), inductively coupled plasma mass spectrometry (ICP-MS), amino acid analysis, and spectros

172 uantified by Inductively Coupled Plasma Mass Spectrometry (ICP-MS), single-particle-ICP-MS (sp-ICP-MS

173 etermined by inductively coupled plasma mass spectrometry (ICPMS).

174 Immunoprecipitation-mass spectrometry identified ribosome-binding protein 1 (RRBP

175 nalysis by liquid chromatography tandem mass spectrometry identified this compound as prostaglandin (

176 w for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strategy to distin

177 easurements resulting from ion mobility-mass spectrometry (IM-MS) experiments provide a promising ort

178 NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM-MS), AFM, and TEM.

179 n, and cryosectioned in preparation for mass spectrometry imaging (MSI).

180 liquid chromatography-fluorescence, and mass spectrometry imaging approaches to profile and visualize

181 Mass spectrometry imaging was applied to compare NIMS sensiti

182 ix-assisted laser desorption ionization mass spectrometry imaging, we identified a number of lipids t

183 Direct analysis by mass spectrometry (imaging) has become increasingly deployed

184 easured using gas chromatography-tandem mass spectrometry in 80 children aged 15-71 months.

185 ollowed by liquid chromatography-tandem mass spectrometry, in order to detect biomarkers useful for i

186 ydrogen/deuterium exchange monitored by mass spectrometry indicated that a loss of 4-5 kJ/mol/protome

187 es in analytical separation techniques, mass spectrometry instrumentation, and data processing platfo

188 Using various low- and high-resolution mass spectrometry instruments with several collision energies

189 ade and Remsima were examined by native mass spectrometry, ion mobility, and quantitative peptide map

190 these measurements, i.e., isotope ratio mass spectrometry (IRMS), with very encouraging results.

191 Electrospray ionization mass spectrometry is used extensively to measure the equilibr

192 Aerosol mass spectrometry is used to investigate how the ozone (O3) c

193 wn ultraviolet photodissociation (UVPD) mass spectrometry is used to track snapshots of conformationa

194 ser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS).

195 ionization ion mobility time-of-flight mass spectrometry (LAESI-IMS-TOF-MS) was used for the analysi

196 combined with liquid chromatography and mass spectrometry (LC-FAIMS-MS) is shown to enhance peak capa

197 d chromatography high resolution tandem mass spectrometry (LC-HRMS/MS).

198 pic patterns from liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-MS (GC-MS) d

199 ISPE) followed by liquid chromatography-mass spectrometry (LC-MS) for biomarker determination using P

200 development of a liquid chromatography-mass spectrometry (LC-MS) method to separate and quantify R-

201 In spite of the liquid chromatography-mass spectrometry (LC-MS)-based detection of BPDE-N(2)-dG in

202 Untargeted liquid-chromatography-mass spectrometry (LC-MS)-based metabolomics analysis of huma

203 Liquid chromatography tandem mass spectrometry (LC-MS/MS) has proven to be a powerful anal

204 Sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) screening for 23 classes of PFAS

205 -SPME) and liquid chromatography tandem mass spectrometry (LC-MS/MS) was used for collection, identif

206 GC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were used to quantify volatile a

207 ntified by liquid chromatography-tandem mass spectrometry (LC-MS/MS) within the hydrolysates.

208 olites via liquid chromatography-tandem mass spectrometry (LC-MS/MS), (13)C6-metabolites were radioca

209 lyzed with liquid chromatography-tandem mass spectrometry (LC-MS/MS).

210 oupled with radioactivity detection and mass spectrometry (LC-RAD/MS).

211 d high-resolution liquid chromatography-mass spectrometry (LC/MS) techniques to investigate the role

212 ed through liquid chromatography/tandem mass spectrometry (LC/MS-MS).

213 ize a combination of gas chromatography-mass spectrometry, liquid chromatography-fluorescence, and ma

214 erformance liquid chromatography tandem mass spectrometry (MAE-SPE-UHPLC-MS/MS).

215 er desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) after enzymatic digestion of

216 ed using a unique liquid chromatography-mass spectrometry/mass spectroscopy method quantifying circul

217 Metabolite sampling, followed by mass spectrometry measurements, enabled the preservation of t

218 t amyloid deposition by a novel precise mass spectrometry method at the Washington University School

219 compared to data-dependent acquisition mass spectrometry methods.

220 osidic bond fragmentation during tandem mass spectrometry (MS(2)).

221 ivo sampling and easily interfaced with mass spectrometry (MS) analyzers.

222 Paired use of mass spectrometry (MS) for bacterial identification and autom

223 hods such as liquid chromatography (LC)-mass spectrometry (MS) for the determination of their pharmac

224 Analytical methods based on mass spectrometry (MS) have been successfully applied in biom

225 Mass spectrometry (MS) indicated that OM-MOSP interacts with

226 Mass spectrometry (MS) is an essential part of the cell biolo

227 (Ga-10:1 NOTA-somatropin); (ii) native mass spectrometry (MS) offered in-depth information, a substi

228 tein quantification are based on either mass spectrometry (MS) or on immunochemical techniques, such

229 Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) reports on backbone H-bond fluctuation

230 occurrence of approximately 50 distinct mass spectrometry (MS) signals.

231 muno-biosensing with ambient ionization mass spectrometry (MS) was developed.

232 Despite the ubiquity of mass spectrometry (MS), data processing tools can be surprisi

233 Here, we used a mass spectrometry (MS)-based approach to map the complete gly

234 pes of amino acids, here we used modern mass spectrometry (MS)-based techniques to separate and seque

235 gnetic Resonance (NMR) spectroscopy and mass spectrometry (MS).

236 elated macular degeneration (AMD) using mass spectrometry (MS).

237 of metabolites relies mainly on tandem mass spectrometry (MS/MS) analysis.

238 pray desorption electrospray ionization mass spectrometry (nano-DESI/HRMS), and ultrahigh resolution

239 ng coupled with nanoscale secondary ion mass spectrometry (nanoSIMS) and fluorescence-based biorthogo

240 developed sensitive nanoflow-nanospray mass spectrometry nontargeted profiling technique to identify

241 Targeted mass spectrometry of a surrogate peptide panel is a powerful

242 Tandem mass spectrometry of proteins in immunoprecipitates of mediat

243 Mass spectrometry of stool samples identified novel candidate

244 ith multidimensional gas-chromatography-mass spectrometry-olfactometry improved separating, isolating

245 ahigh-performance liquid chromatography-mass spectrometry over a period of 2 y.Infants (n = 106) were

246 erol measured by this paper-loaded DART mass spectrometry (pDART-MS) is statistically comparable with

247 nalysis of nonplanar samples in ambient mass spectrometry poses a formidable challenge.

248 Data-independent acquisition mass spectrometry promises higher performance in terms of qua

249 y, nanodisc-technology and non-covalent mass spectrometry provides excellent synergies for the analys

250 y-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and scanning electron microscopy

251 n was verified using gas chromatography-mass spectrometry quantification of total fatty acids, and ta

252 troscopy (WDS) and Rutherford backscattering spectrometry (RBS).

253 Diagnostic assessments were blinded to mass spectrometry results.

254 mplexes and hydrogen-deuterium exchange mass spectrometry revealed molecular insights about molecular

255 Affinity enrichment mass spectrometry revealed that the primary ciliogenesis regu

256 In solution, mass spectrometry shows dimers of G.

257 e combine X-ray crystallography, native mass spectrometry, single-channel electrical recording, molec

258 er desorption ionization time-of-flight mass spectrometry, size-exclusion chromatography, circular di

259 gle particle inductively coupled plasma mass-spectrometry (SP-ICP-MS) was used for the first time wit

260 New ultrahigh precision, double-spike mass spectrometry stable Pb isotope data allow clearer discri

261 While previous SWATH-mass spectrometry studies have shown high intra-lab reproduci

262 Mass spectrometry studies of payload release suggested that o

263 Ion mobility and mass spectrometry techniques are coupled with a temperature-c

264 tive to state-of-the-art isotopic ratio mass spectrometry techniques.

265 However, single-cell mass spectrometry technologies have not yet been made compati

266 to high-resolution accurate mass tandem mass spectrometry, the resulting degradation products of chlo

267 highly sensitive chromatography-tandem mass spectrometry.The mean +/- SD 25(OH)D3 concentration for

268 hat uses advanced approaches of NMR and mass spectrometry to analyze the fate of individual atoms fro

269 ed chemical cross-linking combined with mass spectrometry to capture the transient interaction of Psb

270 M is a peptide mapping method utilizing mass spectrometry to detect and quantify specific peptides of

271 We used EM and crosslinking mass spectrometry to dissect five conformational substates of

272 coupled to tandem liquid chromatography-mass spectrometry to identify and quantify proteins synthesiz

273 , we used liquid chromatographic tandem mass spectrometry to map phosphorylation sites to the otherwi

274 ion-exchange preconcentration and HPLC/mass spectrometry to measure arsenobetaine in seawater, and a

275 ser ablation inductively coupled plasma mass spectrometry) to artifacts previously studied separately

276 n impact (EI) ionization time-of-flight mass spectrometry (TOF-MS) allows the detection of thousands

277 ng cluster Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) as a label-free approach to chem

278 Time-of-flight secondary ion mass spectrometry (ToF-SIMS) has received attention for these

279 Combining mass spectrometry tools and NMR analyses, a total of 29 compo

280 alyzed by nanoUPLC and Ultra Definition Mass Spectrometry (UDMS(E)) label-free quantitative approach.

281 rsed-phase liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) for low to medium polarity pe

282 rospray ionization-ultrahigh resolution mass spectrometry (uHRMS) and based on the calculation of ele

283 iode detector-quadrupole/time of flight-mass spectrometry (UPLC-PDA-Q/TOF-MS) method.

284 hromatography-quadrupole-time-of-flight-mass spectrometry (UPLC-QToF-MS).

285 junction with capillary electrophoresis mass spectrometry was applied to 13 Buyid silk specimens from

286 Here, unbiased mass spectrometry was used to identify the microtubule affini

287 romatography-high resolution (Orbitrap) mass spectrometry we identified 33 AMI metabolites (both Phas

288 Through quantitative mass spectrometry, we find that the matricellular protein CCN

289 Using gas chromatography-mass spectrometry, we first identified the volatile compounds

290 Using mass spectrometry, we found that the intracellular region of

291 Using RNA-affinity chromatography and mass spectrometry, we further uncovered binding of the RNA-bi

292 Using label-free ToF-SIMS imaging mass spectrometry, we generated a map of small molecules diff

293 Using gas chromatography coupled to mass spectrometry, we identified statistically significant di

294 nesis, kinetic assays, and quantitative mass spectrometry, we precisely mapped key residues involved

295 , using in situ (18)O isotope labelling mass spectrometry, we provide direct experimental evidence th

296 ed by amide hydrogen-deuterium exchange mass spectrometry, we show progressive disruption of individu

297 y, and limited proteolysis coupled with mass spectrometry, we show that phosphorylated Pdc and 14-3-3

298 mbining cell biology, biochemistry, and mass spectrometry, we show that sphingosine, the cytotoxic me

299 try, real-time quantitative RT-PCR, and mass spectrometry were used to characterize EV morphology and

300 dependent acquisition is a challenge in mass spectrometry which is solved by two-dimensional (2D) Fou

301 was acquired by high-resolution native mass spectrometry, which revealed the co-occurrence of approx