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1 of the product by in situ ambient ionization mass spectrometry.
2 , can be combined with proteomic analysis by mass spectrometry.
3 rformance liquid chromatography ion mobility-mass spectrometry.
4 sotope dilution-multiple-reaction monitoring-mass spectrometry.
5 e oil matrix, followed by Gas Chromatography/Mass Spectrometry.
6 d and analyzed using drift time ion mobility mass spectrometry.
7 D) in-line with LC, IMS, and high resolution mass spectrometry.
8 by Fourier transform ion cyclotron resonance mass spectrometry.
9 nd liquid chromatography coupled with tandem mass spectrometry.
10 e can easily be studied using single droplet mass spectrometry.
11 le organic analysis by liquid chromatography/mass spectrometry.
12 omatography isotope-dilution high-resolution mass spectrometry.
13 ability of CM-101 in rats were measured with mass spectrometry.
14  using flow injection analysis with orbitrap mass spectrometry.
15               Stool samples were analyzed by mass spectrometry.
16 mutagenesis, and hydrogen/deuterium exchange-mass spectrometry.
17 alysis by using liquid chromatography-tandem mass spectrometry.
18  on reverse phase liquid chromatography with mass spectrometry.
19 easured based on (2) H labeling using tandem mass spectrometry.
20 phase microextraction and gas chromatography-mass spectrometry.
21 known as megalin, by immunoprecipitation and mass spectrometry.
22 rption/ionization time-of-flight (MALDI-TOF) mass spectrometry.
23 nofluorescence microscopy with validation by mass spectrometry.
24 he proteins that adsorbed were identified by mass spectrometry.
25 ic-enzymatic assay and liquid chromatography/mass spectrometry.
26  quantification of abrin and its isoforms by mass spectrometry.
27 uid chromatography-quadrupole time-of-flight mass spectrometry.
28 raphy high resolution mass or time-of-flight mass spectrometry.
29 onal gel electrophoresis were analyzed using mass spectrometry.
30  chromatography-multiple reaction monitoring/mass spectrometry.
31 em cells by affinity purification coupled to mass spectrometry.
32  and Ultra-Performance Liquid Chromatography Mass Spectrometry.
33 re of the catalyst, coupled with end-of-pipe mass spectrometry.
34 o results from NMR and liquid chromatography-mass spectrometry.
35 sing high-resolution spectro(micro)scopy and mass spectrometry.
36  identification of O-linked glycopeptides by mass spectrometry.
37 vely control the total ionization charges in mass spectrometry.
38 ment was detected at m/z 1088 by a MALDI-TOF mass spectrometry.
39 we identified interacting proteins by tandem mass spectrometry.
40 sing liquid chromatography coupled to tandem mass spectrometry.
41 gly precise data obtained via multicollector mass spectrometry.
42 rption/ionization time of flight (MALDI-TOF) mass spectrometry.
43  selection of GDBT were identified by tandem mass spectrometry.
44 nalyzed by gas chromatography time-of-flight mass spectrometry.
45 hy coupled with single- or triple-quadrupole mass spectrometry.
46  spectroscopy and single droplet paper spray mass spectrometry.
47 lid-phase microextraction/gas chromatography-mass spectrometry.
48 ysed by capillary electrophoresis coupled to mass spectrometry.
49  to restriction and by liquid chromatography-mass spectrometry.
50 was assessed with inductively coupled plasma mass spectrometry.
51 1T Fourier transform ion cyclotron resonance mass spectrometry (21T FT-ICR MS).
52 al Fourier transform ion cyclotron resonance mass spectrometry (2D FTICR MS or 2D MS) allows direct c
53 c tools, including vacuum UV photoionization mass spectrometry, absorption and action spectroscopy in
54          Here, we demonstrate that MALDI-TOF mass spectrometry accurately identified all of the test
55                                       Tandem mass spectrometry after digestion with three proteases a
56 mbination with high mass accuracy/resolution mass spectrometry after direct infusion (i.e., shotgun l
57 icrogram amounts of paCOS using quantitative mass spectrometry, allowing one to rapidly analyze the s
58                   The crystal structures and mass spectrometry also show that when these herbicides b
59 l complementary techniques including aerosol mass spectrometry (AMS), high-resolution nanospray desor
60 s for radiocarbon analysis using accelerator mass spectrometry (AMS).
61 ification membranes using ambient ionization mass spectrometry, an attempt has been made to understan
62  C, but not at 20 degrees C, by SDS-page and mass spectrometry analyses as well as electron microscop
63                     The EPR measurements and mass spectrometry analyses further reveal that nitric ox
64 cations to CP2 based on crystallographic and mass spectrometry analyses results in variants with grea
65                         Yet, high-resolution mass spectrometry analyses reveal a huge chemical divers
66 electrophoresis and major spots subjected to mass spectrometry analysis and identification.
67                                              Mass spectrometry analysis demonstrated that cytoplasmic
68                                 Furthermore, mass spectrometry analysis indicated Lys-72 as an acetyl
69 n of the seed followed by gas chromatography-mass spectrometry analysis of polar metabolites also rev
70                 Liquid chromatography-tandem mass spectrometry analysis revealed marked differences b
71              Immunoprecipitation followed by mass spectrometry analysis showed that several N-termina
72                                        Using mass spectrometry analysis, we found that VLVs contained
73  studies, mass analysis, and high-resolution mass spectrometry analysis.
74 bulin as was observed by electrophoresis and mass spectrometry analysis.
75 (AT) using high-resolution Fourier-transform mass spectrometry and a novel algorithm of quantitative
76 rd" of the interaction that is measured with mass spectrometry and because it is compatible with labo
77  samples were analyzed using high-resolution mass spectrometry and electron-capture detection to iden
78            Here the authors show that native mass spectrometry and high resolution electron microscop
79  of RNA demethylases, along with advances in mass spectrometry and high-throughput sequencing techniq
80 for haptenation by AX has been approached by mass spectrometry and immunoaffinity techniques.
81                   We applied high-resolution mass spectrometry and mass-defect filtering to four PAH-
82 mics, intact proteins are analyzed by tandem mass spectrometry and proteoforms, which are defined for
83 cterized using gas chromatography coupled to mass spectrometry and spectroscopic techniques such as i
84  and subjected to inductively coupled plasma mass spectrometry and transmission electron microscopy f
85 d manganese using inductively coupled plasma mass spectrometry, and assessed neurodevelopment using t
86 ray absorption (near-edge) spectroscopy, ESI mass spectrometry, and DFT methods.
87 orescence difference gel electrophoresis and mass spectrometry, and further verified by Western blott
88 mpA) using fluorescence spectroscopy, native mass spectrometry, and molecular dynamics simulations.
89 atile organic analysis by gas chromatography/mass spectrometry, and nonvolatile organic analysis by l
90 low cytometry or cytometry by time-of-flight mass spectrometry, and such tests could be performed aft
91 d by (1)H NMR spectroscopy, IR spectroscopy, mass spectrometry, and X-ray crystallography.
92 ource, followed by quadrupole time-of-flight mass spectrometry (APCI-qTOF-MS), operated in full scan
93                                        Using mass spectrometry approaches, we identified 16 VTPs of t
94                             Immunoassays and mass spectrometry are two main technologies for quantify
95                         Ultrahigh-resolution mass spectrometry, as well as optical measurements revea
96 y available liquid chromatography and tandem mass spectrometry assay; follicle-stimulating hormone le
97                                     Targeted mass spectrometry assays for protein quantitation monito
98 sed on epi-marks that cannot be detected via mass spectrometry based methods for quantifying the abun
99  study, we attempted to validate a MALDI-ToF mass spectrometry-based assay for the antifungal suscept
100                We demonstrate the utility of mass spectrometry-based global exposure metabolomics com
101                                              Mass spectrometry-based imaging indicated a differential
102 ing an alkylating resin-assisted capture and mass spectrometry-based label-free strategy for studying
103 es were analyzed using liquid chromatography-mass spectrometry-based metabolomics.
104                                        Using mass spectrometry-based phosphoproteomics, we have ident
105                                              Mass spectrometry-based protein analysis has become an i
106 racy of an OFFGEL electrophoresis and tandem mass spectrometry-based proteomic approach with a DNA-ba
107                                              Mass spectrometry-based proteomic profiling was performe
108 ate that single time point pulse-chase SILAC mass spectrometry-based proteomics (pSILAC MS) is a sens
109  in lung metastasis, we applied quantitative mass spectrometry-based proteomics and identified 392 br
110                                              Mass spectrometry-based targeted proteomics (e.g., selec
111 this Perspective, we discuss developments in mass-spectrometry-based proteomic technology over the pa
112 tion of inorganic clusters relies heavily on mass spectrometry because of, in most cases, their poor
113                      Carbon fiber ionization mass spectrometry (CFI-MS), which uses a carbon fiber bu
114 Using hydrogen-deuterium exchange coupled to mass spectrometry, combined with in vitro and in vivo mu
115             Direct phosphorylation assay and mass spectrometry confirm that PKM2 phosphorylates SNAP-
116 hyscomitrella patens Immunoblot analysis and mass spectrometry confirmed enrichment of PpCesA5.
117 electron microscopy, as well as ion mobility-mass spectrometry coupled to infrared (IR) spectroscopy
118                                   The use of mass spectrometry coupled with chemical cross-linking of
119               Based on cross-linking-coupled mass spectrometry, crystal structure of the CPSF160-WDR3
120 s worldwide, we demonstrate that using SWATH-mass spectrometry data acquisition we can consistently d
121           The algorithm uses high-resolution mass spectrometry data for a series of samples with comm
122 dy, a data-dependent, high-resolution tandem mass spectrometry (ddHRMS/MS) method capable of detectin
123 e labeling with multiple reaction monitoring-mass spectrometry demonstrated that hypoxia and rapamyci
124 is very well suited for online coupling with mass spectrometry due to the relatively high volatility
125 k (ULF) and infant formula (IF) using tandem mass spectrometry (electron transfer dissociation).
126                  Recent advances in top-down mass spectrometry enabled identification of intact prote
127 on Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICRMS) and discovers additional
128 nes the proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay and model membranes of
129 matography (LC) with electrospray ionization mass spectrometry (ESI-MS) in native conditions to study
130  negative-ion electrospray ionization tandem mass spectrometry (ESI-MS/MS) method has been developed
131 lecular beam vacuum-UV (VUV) photoionization mass spectrometry experiments were performed to understa
132                                        Also, mass spectrometry, flow cytometry, and electron microsco
133 mics approach based on liquid chromatography-mass spectrometry for revealing subtle biogeographical t
134 monstration is provided of the use of native mass spectrometry for screening fragments against a prot
135  a one-pot two-nanoprobe approach coupled to mass spectrometry for simultaneous quantification and po
136 ance liquid chromatography coupled to tandem mass spectrometry for the detection of blood-derived pro
137 hAP-MS (chromatin affinity purification with mass spectrometry), for the affinity purification of a s
138 ng Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS) and quantify DOM photochem
139 by Fourier Transform-Ion Cyclotron Resonance-Mass Spectrometry (FT-ICR-MS), which delivered the molec
140 D) Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS).
141 as chromatography-inductively coupled plasma mass spectrometry (GC-ICPMS) measurement conditions are
142                           Gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-tand
143 st, sensitive, and robust gas chromatography-mass spectrometry (GC-MS) method for the simultaneous de
144                     Using gas chromatography mass spectrometry (GC-MS), we identified compounds typic
145 anol and then analyzed by gas chromatography-mass spectrometry (GC-MS).
146 ned olive oil: (i) gas chromatography-tandem mass spectrometry (GC-MS/MS) for GC-amenable pesticides;
147           Gas cluster ion beam-secondary ion mass spectrometry (GCIB-SIMS) has shown the full potenti
148             Herein, using Gas Chromatography Mass Spectrometry (GCMS), we demonstrate that the major
149                                              Mass spectrometry has become a primary tool for glycan a
150                                              Mass spectrometry has become an enabling technology for
151 ation of high-resolution techniques, such as mass spectrometry-has led to enhancements of our knowled
152 tion provided by hydrogen/deuterium exchange mass spectrometry (HDX-MS) in the protein therapeutic fi
153 ere, we show how hydrogen/deuterium-exchange mass spectrometry (HDX-MS) provides detailed insight int
154  mutagenesis and hydrogen deuterium exchange mass spectrometry (HDX-MS) to identify critical residues
155 ry approaches of hydrogen/deuterium exchange mass spectrometry (HDX-MS), fast photochemical oxidation
156 cit water, complemented by hydrogen exchange mass spectrometry (HDX/MS).
157 drogen-deuterium exchange (HDX) coupled with mass spectrometry (HDXMS) is a rapid and effective metho
158 lic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) for polar pesticides, an
159 chromatography-diode array detection- tandem mass spectrometry (HPLC-DAD-MS/MS) identified 29 phenoli
160 igh-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method with multiple reac
161 y, we have developed a novel high-resolution mass spectrometry (HRMS) based approach for analyzing la
162 w analytical methods such as high-resolution mass spectrometry (HRMS) can help to characterize chemic
163 ve electron spray ionization high resolution mass spectrometry (hydrophilic fraction) and fluorescenc
164 ples were measured using inductively coupled mass spectrometry (ICP-MS) and high-resolution ICP-MS, r
165 ectroscopy (EDX), inductively coupled plasma mass spectrometry (ICP-MS), amino acid analysis, and spe
166 ere quantified by Inductively Coupled Plasma Mass Spectrometry (ICP-MS), single-particle-ICP-MS (sp-I
167 was determined by inductively coupled plasma mass spectrometry (ICPMS).
168                          Immunoprecipitation-mass spectrometry identified ribosome-binding protein 1
169     Analysis by liquid chromatography tandem mass spectrometry identified this compound as prostaglan
170 CS) measurements resulting from ion mobility-mass spectrometry (IM-MS) experiments provide a promisin
171 DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM-MS), AFM, and TEM.
172 frozen, and cryosectioned in preparation for mass spectrometry imaging (MSI).
173 try, liquid chromatography-fluorescence, and mass spectrometry imaging approaches to profile and visu
174                                              Mass spectrometry imaging was applied to compare NIMS se
175  matrix-assisted laser desorption ionization mass spectrometry imaging, we identified a number of lip
176                           Direct analysis by mass spectrometry (imaging) has become increasingly depl
177 ere measured using gas chromatography-tandem mass spectrometry in 80 children aged 15-71 months.
178 sis followed by liquid chromatography-tandem mass spectrometry, in order to detect biomarkers useful
179 and hydrogen/deuterium exchange monitored by mass spectrometry indicated that a loss of 4-5 kJ/mol/pr
180 dvances in analytical separation techniques, mass spectrometry instrumentation, and data processing p
181       Using various low- and high-resolution mass spectrometry instruments with several collision ene
182 Remicade and Remsima were examined by native mass spectrometry, ion mobility, and quantitative peptid
183  for these measurements, i.e., isotope ratio mass spectrometry (IRMS), with very encouraging results.
184                      Electrospray ionization mass spectrometry is used extensively to measure the equ
185                                      Aerosol mass spectrometry is used to investigate how the ozone (
186 op-down ultraviolet photodissociation (UVPD) mass spectrometry is used to track snapshots of conforma
187 ia laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS).
188 spray ionization ion mobility time-of-flight mass spectrometry (LAESI-IMS-TOF-MS) was used for the an
189 IMS) combined with liquid chromatography and mass spectrometry (LC-FAIMS-MS) is shown to enhance peak
190 liquid chromatography high resolution tandem mass spectrometry (LC-HRMS/MS).
191 isotopic patterns from liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-MS (GC-
192 on (MISPE) followed by liquid chromatography-mass spectrometry (LC-MS) for biomarker determination us
193 d the development of a liquid chromatography-mass spectrometry (LC-MS) method to separate and quantif
194        In spite of the liquid chromatography-mass spectrometry (LC-MS)-based detection of BPDE-N(2)-d
195             Untargeted liquid-chromatography-mass spectrometry (LC-MS)-based metabolomics analysis of
196                 Liquid chromatography tandem mass spectrometry (LC-MS/MS) has proven to be a powerful
197       Sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) screening for 23 classes of
198 n (TF-SPME) and liquid chromatography tandem mass spectrometry (LC-MS/MS) was used for collection, id
199 try (GC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were used to quantify volat
200 e identified by liquid chromatography-tandem mass spectrometry (LC-MS/MS) within the hydrolysates.
201 metabolites via liquid chromatography-tandem mass spectrometry (LC-MS/MS), (13)C6-metabolites were ra
202 d analyzed with liquid chromatography-tandem mass spectrometry (LC-MS/MS).
203 phy coupled with radioactivity detection and mass spectrometry (LC-RAD/MS).
204 w- and high-resolution liquid chromatography-mass spectrometry (LC/MS) techniques to investigate the
205 evealed through liquid chromatography/tandem mass spectrometry (LC/MS-MS).
206  utilize a combination of gas chromatography-mass spectrometry, liquid chromatography-fluorescence, a
207 igh-performance liquid chromatography tandem mass spectrometry (MAE-SPE-UHPLC-MS/MS).
208 d laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) after enzymatic digesti
209  matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF MS) that allows quantificat
210 rformed using a unique liquid chromatography-mass spectrometry/mass spectroscopy method quantifying c
211             Metabolite sampling, followed by mass spectrometry measurements, enabled the preservation
212 ithout amyloid deposition by a novel precise mass spectrometry method at the Washington University Sc
213 ility compared to data-dependent acquisition mass spectrometry methods.
214  glycosidic bond fragmentation during tandem mass spectrometry (MS(2)).
215  in vivo sampling and easily interfaced with mass spectrometry (MS) analyzers.
216                                Paired use of mass spectrometry (MS) for bacterial identification and
217 d to hybrid quadrupole time-of-flight (QTOF) mass spectrometry (MS) for determination of volatile com
218 l methods such as liquid chromatography (LC)-mass spectrometry (MS) for the determination of their ph
219                  Analytical methods based on mass spectrometry (MS) have been successfully applied in
220                                              Mass spectrometry (MS) indicated that OM-MOSP interacts
221                                              Mass spectrometry (MS) is an essential part of the cell
222 ities (Ga-10:1 NOTA-somatropin); (ii) native mass spectrometry (MS) offered in-depth information, a s
223 e protein quantification are based on either mass spectrometry (MS) or on immunochemical techniques,
224            Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) reports on backbone H-bond fluctu
225 e co-occurrence of approximately 50 distinct mass spectrometry (MS) signals.
226 R) immuno-biosensing with ambient ionization mass spectrometry (MS) was developed.
227                      Despite the ubiquity of mass spectrometry (MS), data processing tools can be sur
228                              Here, we used a mass spectrometry (MS)-based approach to map the complet
229 wo types of amino acids, here we used modern mass spectrometry (MS)-based techniques to separate and
230 ar Magnetic Resonance (NMR) spectroscopy and mass spectrometry (MS).
231 age-related macular degeneration (AMD) using mass spectrometry (MS).
232 ation of metabolites relies mainly on tandem mass spectrometry (MS/MS) analysis.
233 nanospray desorption electrospray ionization mass spectrometry (nano-DESI/HRMS), and ultrahigh resolu
234 probing coupled with nanoscale secondary ion mass spectrometry (nanoSIMS) and fluorescence-based bior
235 newly developed sensitive nanoflow-nanospray mass spectrometry nontargeted profiling technique to ide
236                                     Targeted mass spectrometry of a surrogate peptide panel is a powe
237                                       Tandem mass spectrometry of proteins in immunoprecipitates of m
238                                              Mass spectrometry of stool samples identified novel cand
239 ses with multidimensional gas-chromatography-mass spectrometry-olfactometry improved separating, isol
240  ultrahigh-performance liquid chromatography-mass spectrometry over a period of 2 y.Infants (n = 106)
241 olesterol measured by this paper-loaded DART mass spectrometry (pDART-MS) is statistically comparable
242 The analysis of nonplanar samples in ambient mass spectrometry poses a formidable challenge.
243                 Data-independent acquisition mass spectrometry promises higher performance in terms o
244 iology, nanodisc-technology and non-covalent mass spectrometry provides excellent synergies for the a
245 on (Py-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and scanning electron micro
246 onization (ESI(-))/quadrupole time-of-flight mass spectrometry (qTOF) was developed for the detection
247 lation was verified using gas chromatography-mass spectrometry quantification of total fatty acids, a
248       Diagnostic assessments were blinded to mass spectrometry results.
249 dy complexes and hydrogen-deuterium exchange mass spectrometry revealed molecular insights about mole
250                   Inductively coupled plasma mass spectrometry revealed significant tumor targeting a
251                          Affinity enrichment mass spectrometry revealed that the primary ciliogenesis
252                                 In solution, mass spectrometry shows dimers of G.
253 re, we combine X-ray crystallography, native mass spectrometry, single-channel electrical recording,
254 d laser desorption ionization time-of-flight mass spectrometry, size-exclusion chromatography, circul
255 o single particle inductively coupled plasma mass-spectrometry (SP-ICP-MS) was used for the first tim
256        New ultrahigh precision, double-spike mass spectrometry stable Pb isotope data allow clearer d
257                         While previous SWATH-mass spectrometry studies have shown high intra-lab repr
258                                              Mass spectrometry studies of payload release suggested t
259                             Ion mobility and mass spectrometry techniques are coupled with a temperat
260 ternative to state-of-the-art isotopic ratio mass spectrometry techniques.
261                         However, single-cell mass spectrometry technologies have not yet been made co
262 pled to high-resolution accurate mass tandem mass spectrometry, the resulting degradation products of
263 using highly sensitive chromatography-tandem mass spectrometry.The mean +/- SD 25(OH)D3 concentration
264 ded PLIMSTEX (protein-ligand interactions by mass spectrometry, titration, and H/D exchange) to the r
265 ach that uses advanced approaches of NMR and mass spectrometry to analyze the fate of individual atom
266 we used chemical cross-linking combined with mass spectrometry to capture the transient interaction o
267    MAM is a peptide mapping method utilizing mass spectrometry to detect and quantify specific peptid
268                  We used EM and crosslinking mass spectrometry to dissect five conformational substat
269 n be coupled to tandem liquid chromatography-mass spectrometry to identify and quantify proteins synt
270      We have used co-immunoprecipitation and mass spectrometry to identify proteins that interact wit
271  Here, we used liquid chromatographic tandem mass spectrometry to map phosphorylation sites to the ot
272 ed on ion-exchange preconcentration and HPLC/mass spectrometry to measure arsenobetaine in seawater,
273 s, laser ablation inductively coupled plasma mass spectrometry) to artifacts previously studied separ
274 ectron impact (EI) ionization time-of-flight mass spectrometry (TOF-MS) allows the detection of thous
275 imaging cluster Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) as a label-free approach to
276                 Time-of-flight secondary ion mass spectrometry (ToF-SIMS) has received attention for
277                                    Combining mass spectrometry tools and NMR analyses, a total of 29
278 re analyzed by nanoUPLC and Ultra Definition Mass Spectrometry (UDMS(E)) label-free quantitative appr
279  reversed-phase liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) for low to medium polari
280 electrospray ionization-ultrahigh resolution mass spectrometry (uHRMS) and based on the calculation o
281 hotodiode detector-quadrupole/time of flight-mass spectrometry (UPLC-PDA-Q/TOF-MS) method.
282 uid chromatography-quadrupole-time-of-flight-mass spectrometry (UPLC-QToF-MS).
283 n conjunction with capillary electrophoresis mass spectrometry was applied to 13 Buyid silk specimens
284                               Here, unbiased mass spectrometry was used to identify the microtubule a
285 id chromatography-high resolution (Orbitrap) mass spectrometry we identified 33 AMI metabolites (both
286                         Through quantitative mass spectrometry, we find that the matricellular protei
287                     Using gas chromatography-mass spectrometry, we first identified the volatile comp
288                                        Using mass spectrometry, we found that the intracellular regio
289        Using RNA-affinity chromatography and mass spectrometry, we further uncovered binding of the R
290            Using label-free ToF-SIMS imaging mass spectrometry, we generated a map of small molecules
291          Using gas chromatography coupled to mass spectrometry, we identified statistically significa
292 utagenesis, kinetic assays, and quantitative mass spectrometry, we precisely mapped key residues invo
293  Here, using in situ (18)O isotope labelling mass spectrometry, we provide direct experimental eviden
294 nitored by amide hydrogen-deuterium exchange mass spectrometry, we show progressive disruption of ind
295 oscopy, and limited proteolysis coupled with mass spectrometry, we show that phosphorylated Pdc and 1
296 ch combining cell biology, biochemistry, and mass spectrometry, we show that sphingosine, the cytotox
297 ytometry, real-time quantitative RT-PCR, and mass spectrometry were used to characterize EV morpholog
298 ta-independent acquisition is a challenge in mass spectrometry which is solved by two-dimensional (2D
299 of C9 was acquired by high-resolution native mass spectrometry, which revealed the co-occurrence of a
300 ectly probed by means of chemical ionization mass spectrometry with a detection limit of about 10(4)-

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