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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

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