ライフサイエンスコーパス: spectrometry

1 uished from their (14)N counterparts by mass spectrometry.

2 on, absorbance spectroscopy, and tandem mass spectrometry.

3 tivity of electrospray ionization (ESI) mass spectrometry.

4 me and phosphoproteome were analyzed by mass spectrometry.

5 thromycin, detected in stool samples by mass spectrometry.

6 asured using inductively coupled plasma mass spectrometry.

7 led with electrospray ionization tandem mass spectrometry.

8 and 3TC-TP using liquid chromatography-mass spectrometry.

9 hromatography and liquid chromatography-mass spectrometry.

10 radical intermediates when coupled with mass spectrometry.

11 by reverse-phase liquid chromatography-mass spectrometry.

12 g targeted liquid chromatography-tandem mass spectrometry.

13 ntified from virally infected cells via mass spectrometry.

14 model sulfoxonium ylide was observed by mass spectrometry.

15 ssure freezing protocol compatible with mass spectrometry.

16 rs in sinonasal tissue were measured by mass spectrometry.

17 phase liquid chromatography with tandem mass spectrometry.

18 rometry (IMS) quadrupole time-of-flight mass spectrometry.

19 ser-ablation inductively-coupled plasma mass spectrometry.

20 confirmation was carried out by tandem mass spectrometry.

21 analysis by nanoelectrospray ionization mass spectrometry.

22 ear Magnetic Resonance spectroscopy and mass spectrometry.

23 tation in Mycobacterium smegmatis using mass spectrometry.

24 pyrolysis coupled to gas chromatography mass spectrometry.

25 of reagents that are incompatible with mass spectrometry.

26 on metagenomics, and gas chromatography mass spectrometry.

27 ectrospray ionization-Fourier transform-mass spectrometry.

28 ured using liquid chromatography-tandem mass spectrometry (21 phosphatidylcholines (PCs), 7 lysophosp

29 ultraviolet fragmentation spectroscopy-mass spectrometry (2D UV-MS) of cold ions.

30 imensional liquid chromatography-tandem mass spectrometry (2D-LC-MS/MS) method which combines commerc

31 We present an acoustic ejection mass spectrometry (AEMS) setup for contactless electrospray i

32 try and Hg by cold vapor atomic fluorescence spectrometry after ultrasound-assisted emulsification an

33 Mass spectrometry analyses reveal that HIPK2 is at least O-Gl

34 ed in the H1N1 antigenic variants using mass spectrometry analyses.

35 aeological pottery based on accelerator mass spectrometry analysis of (14)C in absorbed food residues

36 Mass spectrometry analysis of fibrinogen proteolytic reaction

37 nocarcinoma (PDAC), we performed tandem mass spectrometry analysis of HLA class I-bound peptides from

38 romatography coupled to high resolution mass spectrometry analysis of the 105 samples did not show tr

39 Moreover, using O-GlcNAc-specific mass spectrometry analysis of the aging hippocampus, together

40 Mass spectrometry analysis showed that H2A.Z.1 and H2A.Z.2 ha

41 We reveal by coimmunoprecipitation and mass spectrometry analysis that alpha-tubulin interacts with

42 We performed immunoprecipitation-mass spectrometry analysis to detect in vivo interactors of A

43 f gammaTuRC, combined with crosslinking mass spectrometry analysis, reveals an asymmetric conformatio

44 interacting partner for IAV HA through mass spectrometry analysis.

45 ing and click chemistry with subsequent mass spectrometry analysis.

46 ular furnace and subsequent ICP-MS (ICP Mass Spectrometry) analysis of the obtained residues allowed

47 n ionization/time-of-flight (MALDI/ToF) mass spectrometry and (1)H NMR were used for the structural i

48 Based on untargeted mass spectrometry and 16S rRNA gene sequencing, both stress a

49 in agreement with those furnished by UV-vis spectrometry and endorsed by statistical tests.

50 acting proteins in Arabidopsis roots by mass spectrometry and established an interactome of IRT1.

51 Here, we combined quantitative mass spectrometry and genetic studies to analyze the componen

52 es by hydride generation atomic fluorescence spectrometry and Hg by cold vapor atomic fluorescence sp

53 pairs, we performed gas chromatography-mass spectrometry and identified 134 metabolites in maternal

54 elevant small amyloid-beta oligomers by mass spectrometry and ion mobility spectrometry, revealing fu

55 nded well to inductively-coupled plasma-mass spectrometry and laser-ablation inductively-coupled plas

56 Hydrogen/deuterium exchange mass spectrometry and mutagenesis studies reveal that the eng

57 Mass spectrometry and nuclear magnetic resonance are the most

58 ed by untargeted high resolution tandem mass spectrometry and the resulting fragmentation spectra wer

59 -bodily, correlating the results with UV-vis spectrometry and/or ion chromatography.

60 ns of eight phthalate metabolites using mass spectrometry, and biomarkers of thyroid function [thyroi

61 ron microscopy (cryo-EM), cross-linking mass spectrometry, and homology modeling.

62 m was confirmed by exhaustive dialysis, mass spectrometry, and in vitro evaluation against the C165S

63 coupled liquid chromatography, ion mobility spectrometry, and mass spectrometry (LC-IMS-MS) to rapid

64 n liquid chromatography-high resolution mass spectrometry, and the data evidenced a strong correlatio

65 ve-ionization mode with high-resolution mass spectrometry appeared promising to improve the sensibili

66 also likely to be impactful for tandem mass spectrometry applications in other areas.

67 y, using a non-targeted high-resolution mass spectrometry approach, a selection of chemical markers r

68 a problem-solving toolbox that enables mass spectrometry as a valuable tool for HOS elucidation.

69 characterized by means of (1)H and (13)C NMR spectrometry as well as single-crystal X-ray diffraction

70 Mass spectrometry-based analysis identified the chelating sid

71 A novel mass spectrometry-based approach allows investigation of the

72 rmation needed for the design of tandem mass spectrometry-based CAD sequencing strategies for mixture

73 After purification and mass spectrometry-based characterization, its oral bioavailab

74 e fruit metabolome was determined using mass spectrometry-based metabolomics targeting nutrients and

75 To overcome this issue, we developed a mass spectrometry-based method that quantitatively evaluates

76 Based on the accurate and reproducible mass spectrometry-based method, a pulse labeling approach usi

77 We used mass spectrometry-based proteomic and phenotypic assays to de

78 The integration of mass spectrometry-based proteomics with next-generation DNA a

79 resource for reproducible quantitative mass spectrometry-based proteomics, which is compatible with

80 identification is a central problem in mass spectrometry-based proteomics.

81 or issue in quantitative data-dependent mass spectrometry-based proteomics.

82 cal inhibitors of SOX10, we performed a mass spectrometry-based screen in human melanoma cells.

83 Metabolomics using nontargeted tandem mass spectrometry can detect thousands of molecules in a biol

84 ae We combined whole-cell cross-linking mass spectrometry, cellular cryo-electron tomography, and int

85 zed F-TD inlet with chemical ionization mass spectrometry (CIMS) and ultraperformance liquid chromato

86 urier transform ion cyclotron resonance mass spectrometry considering six replicates in three differe

87 FT ICR mass spectrometry continues to be the leader in the resolving

88 erformance liquid chromatography-tandem mass spectrometry coupling (HPLC-MS/MS) is classically used t

89 nner using direct analysis in real-time mass spectrometry (DART-MS).

90 roteomics, which is compatible with all mass spectrometry data acquisition types and computational an

91 enated components using high-resolution mass spectrometry data files generated by an atmospheric pres

92 ized processing of ultrahigh-resolution mass spectrometry data of complex molecular mixtures.

93 spectrum_utils is a Python package for mass spectrometry data processing and visualization.

94 selected based on ultrahigh-resolution mass spectrometry data revealed that, while DOM does indeed f

95 ication of endogenous USP13 followed by mass spectrometry demonstrated that cohesin is its primary in

96 onization (+)-quadrupole time-of-flight mass spectrometry detection.

97 nd structurally characterized by tandem mass spectrometry, deuterium labeling, and UV/Vis action spec

98 ifferences as observed by secondary-ion mass spectrometry, differential scanning calorimetry (DSC), g

99 eaction cell inductively coupled plasma mass spectrometry (DRC-ICP-MS).

100 ser ablation-inductively coupled plasma-mass spectrometry elemental mapping.

101 udy, quantitative affinity purification-mass spectrometry enabled the delineation of the CD22 interac

102 We utilized mass spectrometry enhanced by affinity hydrogel particles (an

103 (CE) coupled to electrospray ionization mass spectrometry (ESI-MS) is implemented to analyze complex

104 for contactless electrospray ionization mass spectrometry (ESI-MS)-based sample injection at a sampli

105 detection using electrospray ionization mass spectrometry (ESI-MS).

106 by positive-ion electrospray ionization-mass spectrometry (ESI-MS).

107 high-field asymmetric waveform ion mobility spectrometry (FAIMS) interface to evaluate the potential

108 High-field Asymmetric Waveform Ion Mobility Spectrometry (FAIMS) is used to improve quantitative acc

109 formulas, were found by high-resolution mass spectrometry, following bench-scale chlor(am)ination.

110 lind using liquid chromatography-tandem mass spectrometry for ART.

111 aphy (UPLC) coupled with intact protein mass spectrometry for profiling of mispairing and other produ

112 R stimulation and affinity-purification mass spectrometry for the LTbetaR signaling protein TNFR-asso

113 urier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) enables extensive compositional

114 urier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) offers the highest mass spectra

115 and mass accuracy of Fourier transform mass spectrometry (FT-MS) has made it an increasingly popular

116 urier transform ion cyclotron resonance mass spectrometry (FTICR MS) provides a unique opportunity fo

117 omatography coupled with time-of-flight mass spectrometry (GC x GC-TOFMS).

118 were analyzed using gas chromatography-mass spectrometry (GC-MS).

119 e analyzed by gas chromatography-tandem mass spectrometry (GC-MS/MS) with sum of concentrations (gas

120 (DSC), and hydrogen-deuterium exchange mass spectrometry (H/D exchange MS), to characterize the glob

121 Shotgun tandem mass spectrometry has been demonstrated to be a powerful tool

122 Analysis of intact proteins by native mass spectrometry has emerged as a powerful tool for obtainin

123 el-free high-throughput screening using mass spectrometry has the potential to provide rapid large-sc

124 The field of high-resolution mass spectrometry has undergone a rapid progress in the last

125 n/Deuterium Exchange (HDX) coupled with Mass Spectrometry (HDX-MS) is a sensitive and robust method t

126 drogen-deuterium exchange combined with mass spectrometry (HDX-MS) is a widely applied biophysical te

127 Hydrogen-Deuterium eXchange coupled to Mass Spectrometry (HDX-MS) is now common practice in structur

128 Hydrogen/deuterium exchange mass spectrometry (HDX-MS) of complexes I and II on membranes

129 we employed hydrogen-deuterium exchange-mass spectrometry (HDX-MS) to investigate how FIXa responds t

130 the use of hydrogen-deuterium exchange mass spectrometry (HDX-MS).

131 nteraction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS).

132 -inductively coupled plasma-optical emission spectrometry (HPLC-ICP-OES) in addition to determination

133 in embedded kidney biopsy tissue, using mass spectrometry (HPLC-MS/MS) (n = 27) and immunohistochemis

134 liquid chromatograph triple quadrupole mass spectrometry (HPLC-MS/MS) were used to characterize raw

135 coupled with quadrupole time of flight mass spectrometry (HPLC-QTOF-MS) was used to analyze residues

136 titative strategies for high-resolution mass spectrometry (HRMS) combined with profiling qualitative

137 s were characterized by high-resolution mass spectrometry (HRMS), NMR, and X-ray crystallography.

138 and 2D NMR) and high-resolution tandem mass spectrometry (HRMS/MS) analysis.

139 hase microextraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) method for the quantificati

140 (LTMS) and hydrogen-deuterium exchange mass spectrometry (HXMS) are applied to wild-type and VWD var

141 This individual ion mass spectrometry (I(2)MS) method for charge detection enable

142 ysis by bulk inductively coupled plasma mass spectrometry (ICP-MS) and single-particle ICP-MS.

143 rmined using inductively coupled plasma mass spectrometry (ICP-MS) following e-liquid extraction.

144 ly sensitive inductively coupled plasma mass spectrometry (ICP-MS) operated in single particle (SP) m

145 Inductively coupled plasma mass spectrometry (ICP-MS) showed titanium presence in all gr

146 n granola by inductively coupled plasma mass spectrometry (ICP-MS) was proposed.

147 matography - inductively coupled plasma mass spectrometry (ICPMS), and hydrophilic interaction liquid

148 analysis by inductively-coupled plasma mass spectrometry (ICPMS).

149 Ion mobility-mass spectrometry (IM-MS) has become a powerful tool for glyc

150 cross sections (CCSs) from ion mobility mass spectrometry (IM-MS) measurements are routinely compared

151 Cancer phospholipidomes quantified with mass spectrometry imaging (MSI) can support objective diagnos

152 Mass spectrometry imaging (MSI) is an established analytical

153 Mass spectrometry imaging is a powerful tool of increasing ut

154 Behavioral, histological, mass spectrometry imaging, and biosensor-mediated measures of

155 onization, coupled with high-resolution mass spectrometry imaging.

156 isualization techniques in the field of mass spectrometry imaging: t-distributed stochastic neighborh

157 Imaging mass spectrometry (imaging MS) is a prominent technique for c

158 MALDI-FTICR mass spectrometry, immunohistochemistry, 3D confocal microsco

159 Aerosol mass spectrometry improves the time resolution of experimenta

160 ) technique in combination with ion mobility spectrometry (IMS) and mass spectrometry (MS) measuremen

161 r desorption ionization (MALDI) imaging mass spectrometry (IMS) combined with time-of-flight secondar

162 microglial cells by drift-tube ion mobility spectrometry (IMS) quadrupole time-of-flight mass spectr

163 a few microseconds or less for ion mobility spectrometry (IMS)-based separations on the order of 100

164 studies using ion-mobility spectrometry mass spectrometry (IMS-MS) could be performed.

165 using in operando liquid secondary ion mass spectrometry in combination with molecular dynamics simu

166 ivity, and these pools were analysed by mass spectrometry in order to identify the peptides responsib

167 established modifications observable by mass spectrometry in strains with the most conserved genes of

168 ethods have revolutionized biomolecular mass spectrometry, in particular native and top-down protein

169 ic analysis, inductively coupled plasma mass spectrometry, infrared spectroscopy, and X-ray absorptio

170 Using isotopic ratio mass spectrometry (IRMS) measurements, this study analyzed sa

171 Fourier transform-ion mobility spectrometry is implemented by coupling a 3D-printed dri

172 Ultrahigh-resolution mass spectrometry is one of the most powerful tools in this c

173 Mass spectrometry is the premier tool for identifying and qua

174 h as liquid chromatography-fluorescence-mass spectrometry (LC-FLR-MS) workflows have been limited wit

175 ography, ion mobility spectrometry, and mass spectrometry (LC-IMS-MS) to rapidly characterize both kn

176 tible with direct liquid chromatography-mass spectrometry (LC-MS) analysis.

177 X in the brain by liquid chromatography-mass spectrometry (LC-MS) at PND 22 or at 7 weeks of age.

178 ntegration in raw liquid chromatography-mass spectrometry (LC-MS) data.

179 were validated by liquid chromatography-mass spectrometry (LC-MS), exhibiting a high agreement betwee

180 dies rely on liquid chromatography with mass spectrometry (LC-MS), which could miss detection or beco

181 Liquid chromatography-tandem mass spectrometry (LC-MS/MS) assays were developed to measure

182 hich makes liquid chromatography tandem mass spectrometry (LC-MS/MS) highly useful in MFA due to its

183 esolved by liquid chromatography-tandem mass spectrometry (LC-MS/MS) providing information on the lev

184 thod using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

185 quantified using liquid chromatography-mass spectrometry (LC-MS/MS).

186 matography/electrospray/high-resolution mass spectrometry (LC/ESI/HRMS) are gaining importance as the

187 in the RPE using liquid chromatography/mass spectrometry (LC/MS) showing that compensated FAF intens

188 most commonly by liquid chromatography/mass spectrometry (LC/MS).

189 Limited trypsinolysis mass spectrometry (LTMS) and hydrogen-deuterium exchange mass

190 tion cooperativity, confirmed by native mass spectrometry, makes the gates largely insensitive to sto

191 ix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is an important tool for high-th

192 er desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) plates, termed fast lipid an

193 er desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) with only 1 muL of sample in

194 er desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS).

195 lected structural studies using ion-mobility spectrometry mass spectrometry (IMS-MS) could be perform

196 A novel magnetic blade spray-tandem mass spectrometry (MBS-MS/MS) assay was developed and optimiz

197 ctrochemistry-capillary electrophoresis-mass spectrometry measurements revealed that two isobaric iso

198 e is a Windows application for targeted mass spectrometry method creation and quantitative data analy

199 ose, a new liquid chromatography tandem mass spectrometry method for the quantification of fifteen ca

200 dapted the multiple reaction monitoring mass spectrometry method for use in glycan biomarker research

201 ime-resolved inductively coupled plasma-mass spectrometry methodology.

202 leader in the resolving power among all mass spectrometry methods.

203 developed multiple reaction monitoring mass spectrometry (MRM-MS) assays that detected M. tuberculos

204 cross-linked peptides using multistage mass spectrometry (MS(n)).

205 re readily derived from high-resolution mass spectrometry (MS) and tandem-MS (MS(n)), the localizatio

206 Recently, mass spectrometry (MS) based proteomics analysis has emerged

207 e characterization of these polymers by mass spectrometry (MS) continues to be very challenging due t

208 Leveraging glycoproteomic analysis via mass spectrometry (MS) could provide the insight into the alt

209 Elemental mass spectrometry (MS) coupled to chromatography offers a fac

210 and by analyzing ribosome-profiling and mass spectrometry (MS) data.

211 multiangle light scattering and native mass spectrometry (MS) for the biophysical characterization o

212 logical processes and lipid analysis by mass spectrometry (MS) has significantly advanced lipidomic s

213 Although recent advances in mass spectrometry (MS) have enabled meaningful glycoproteomic

214 sorption electrospray ionization (DESI)-mass spectrometry (MS) imaging was applied to study the metab

215 ds for absolute protein quantitation by mass spectrometry (MS) involve the digestion of target protei

216 Native mass spectrometry (MS) is a powerful means for studying macro

217 ith ion mobility spectrometry (IMS) and mass spectrometry (MS) measurements.

218 Native mass spectrometry (MS) provides the capacity to monitor membr

219 Native mass spectrometry (MS) reveals that the modular OGD architect

220 When coupled online with mass spectrometry (MS), widely applied water-in-oil droplet-b

221 the "functional" proteome has empowered mass spectrometry (MS)-based methods to delve more deeply and

222 Combining this technology with mass spectrometry (MS)-based proteomics allows us to obtain s

223 he rapid development and application of mass spectrometry (MS)-based technologies have markedly impro

224 gnetic resonance (NMR) spectroscopy and mass spectrometry (MS).

225 egies to facilitate their detection via mass spectrometry (MS).

226 lipids fingerprint by routine MALDI-TOF mass spectrometry (MS).

227 romatography coupled to high-resolution mass spectrometry (MS).

228 After DMS separation, tandem mass spectrometry (MS/MS) analyses of the separated isomers a

229 ractionation and high-resolution tandem mass spectrometry (MS/MS) for peptide quantification and then

230 rotein groups were identified by tandem mass spectrometry (MS/MS) from single HeLa cells, and 874 pro

231 ghput analyses of sphingolipids, tandem mass spectrometry (MS/MS) is the method of choice, offering s

232 Tandem mass spectrometry (MS/MS) strategies, including a variety of

233 ion in the MS scan, followed by tandem mass spectrometry (MS2) fragmentation by CID in the ion trap.

234 erformance liquid chromatography tandem mass spectrometry multi-method based on an ACN-precipitation

235 llets by nanoscale secondary ionization mass spectrometry (NanoSIMS), which reveals a comparable U is

236 no-electrospray ionisation ion mobility-mass spectrometry (nESI-IM-MS), we characterize the heterogen

237 on experiments, electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy, a

238 gnetic resonance (NMR) spectroscopy and mass spectrometry of active fractions led to the identificati

239 ser ablation inductively coupled plasma mass spectrometry of polished flat ore surfaces revealed that

240 Chemical cross-linking coupled with mass spectrometry offers an alternative that has seen increas

241 per-loaded direct analysis in real time mass spectrometry (pDART-MS).

242 Gas chromatography-mass spectrometry profiling is the most established method fo

243 Recent advances in mass spectrometry proteomics have made it possible to deciphe

244 Using mass spectrometry proteomics, changes in hepatocyte protein e

245 Mass spectrometry provided site-specific compositions of dens

246 spectroscopy and paper spray ionization mass spectrometry (PSI-MS) on a single instrumental platform.

247 IA) mode with quadrupole time-of-flight mass spectrometry (QTOF-MS).

248 than weak acid or weak base and boosts mass spectrometry responses (signal-to-noise ratio) of peptid

249 gomers by mass spectrometry and ion mobility spectrometry, revealing functionally relevant structural

250 H combined with electrospray-ionization mass spectrometry (SEC-ESI-MS) is a useful tool to study prot

251 particles) were characterized through UV-VIS spectrometry, SEM, optical microscopy, and light exposur

252 t on the use of high-resolution ion mobility spectrometry separations in structures for lossless ion

253 re, we develop a "Shotgun" Ion Mobility Mass Spectrometry Sequencing (SIMMS(2)) method in which intac

254 sing supercritical fluid chromatography-mass spectrometry (SFC-MS).

255 Global profiling by mass spectrometry showed that placental EVs were enriched for

256 e analysis of KSO using high-resolution mass spectrometry showed that trilinoleate (C54:6) was the do

257 method known as selected ion flow tube-mass spectrometry (SIFT-MS).

258 r lossless ion manipulations coupled to mass spectrometry (SLIM IMS-MS) for the rapid and simultaneou

259 te reading by comparing with a gold-standard spectrometry technique.

260 Here, we characterized by mass spectrometry the protein composition of CAV1 immunopreci

261 of information that can be measured by mass spectrometry: the (absolute or relative) concentration o

262 Using mass spectrometry, theoretical simulations, dynamic nuclear p

263 pes), using HPLC high-resolution tandem mass spectrometry, thin-layer chromatography, and gas chromat

264 ed to an established thermal ionization mass spectrometry (TIMS) double-spike method and produce unbi

265 erienced by ions during trapped ion mobility spectrometry (TIMS) experiments.

266 Trapped ion mobility spectrometry (TIMS) is presented as a new and rapid meth

267 We used quantitative mass spectrometry to analyze the extracellular matrix (ECM),

268 n, live cell imaging, and cross-linking mass spectrometry to build integrative structural models of p

269 ontarget screening with high-resolution mass spectrometry to characterize the occurrence of contamina

270 Here, we used gas chromatography and mass spectrometry to determine that the majority (>85%) of no

271 face analysis and liquid chromatography-mass spectrometry to locate sterols in tissue slices (10 um)

272 AL fluid, we performed isotope dilution mass spectrometry to measure several priority toxicants: vita

273 tirred reactor (JSR) and time-of-flight mass spectrometry to probe intermediates formed.

274 massively parallel reporter assays with mass spectrometry to produce a base pair resolution dissectio

275 Time-of-flight secondary ion mass spectrometry (TOF-SIMS) detectors have been intensively

276 bined with time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging.

277 ble and predicts classes lacking tandem mass spectrometry training data.

278 e liquid chromatography high-resolution mass spectrometry (UHPLC-HRMS) method for salivary metabolic

279 e liquid chromatography high-resolution mass spectrometry (UHPLC-HRMS) supported by 1 and 2D NMR spec

280 e liquid chromatography-high-resolution mass spectrometry (UHPLC-HRMS) was used for detection of 14 u

281 tra high pressure liquid chromatography-mass spectrometry (UHPLC-MS), we show results on the rate of

282 chromatography/electrospray ionization mass spectrometry (UPLC/ESI-MS).

283 Hydrogen-deuterium exchange mass spectrometry was used to map their mutual interactions.

284 resonance energy transfer-based fluorescent spectrometry, was complemented with density ultracentrif

285 By mass spectrometry we confirm expression of newly-discovered p

286 Using mass spectrometry, we found that ACTN4 is phosphorylated at s

287 Using mass spectrometry, we found that the urine of pristane-inject

288 d chromatography-high resolution tandem mass spectrometry, we have discovered that mature frataxin in

289 tion, spectroscopy, chromatography, and mass spectrometry, we identify two novel eggshell pigments: y

290 Using mass spectrometry, we quantify nearly 1,000 protein succinyla

291 By using co-fractionation mass spectrometry, we recovered known complexes, confirmed co

292 graphy-quadrupole time-of-flight tandem mass spectrometry, we sought to identify candidate chemicals

293 ified from these lncRNA loci via tandem mass spectrometry, which paved the way for investigating thei

294 from the native spikes were analyzed by mass spectrometry, which revealed overall processing states o

295 d reaction environments compatible with mass spectrometry, which were decoupled from cell growth and

296 tion using liquid chromatography-tandem mass spectrometry with de novo-generated standards and an iso

297 el strategy that couples shotgun tandem mass spectrometry with gas-phase ion chemistry to achieve bot

298 st systematic study using secondary ion mass spectrometry with MeV ions (MeV-SIMS) for analysis of sy

299 Therefore, native mass spectrometry would greatly benefit from higher resolutio

300 nderstand how large-scale cross-linking mass spectrometry (XL-MS) can confirm and extend this interac