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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.
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
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
59 l complementary techniques including aerosol mass spectrometry (AMS), high-resolution nanospray desor
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
64 cations to CP2 based on crystallographic and mass spectrometry analyses results in variants with grea
69 n of the seed followed by gas chromatography-mass spectrometry analysis of polar metabolites also rev
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
79 of RNA demethylases, along with advances in mass spectrometry and high-throughput sequencing techniq
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
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
92 ource, followed by quadrupole time-of-flight mass spectrometry (APCI-qTOF-MS), operated in full scan
96 y available liquid chromatography and tandem mass spectrometry assay; follicle-stimulating hormone le
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
102 ing an alkylating resin-assisted capture and mass spectrometry-based label-free strategy for studying
106 racy of an OFFGEL electrophoresis and tandem mass spectrometry-based proteomic approach with a DNA-ba
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
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
114 Using hydrogen-deuterium exchange coupled to mass spectrometry, combined with in vitro and in vivo mu
117 electron microscopy, as well as ion mobility-mass spectrometry coupled to infrared (IR) spectroscopy
120 s worldwide, we demonstrate that using SWATH-mass spectrometry data acquisition we can consistently d
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).
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
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
141 as chromatography-inductively coupled plasma mass spectrometry (GC-ICPMS) measurement conditions are
143 st, sensitive, and robust gas chromatography-mass spectrometry (GC-MS) method for the simultaneous de
146 ned olive oil: (i) gas chromatography-tandem mass spectrometry (GC-MS/MS) for GC-amenable pesticides;
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
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
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
173 try, liquid chromatography-fluorescence, and mass spectrometry imaging approaches to profile and visu
175 matrix-assisted laser desorption ionization mass spectrometry imaging, we identified a number of lip
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
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.
186 op-down ultraviolet photodissociation (UVPD) mass spectrometry is used to track snapshots of conforma
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
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
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
204 w- and high-resolution liquid chromatography-mass spectrometry (LC/MS) techniques to investigate the
206 utilize a combination of gas chromatography-mass spectrometry, liquid chromatography-fluorescence, a
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
212 ithout amyloid deposition by a novel precise mass spectrometry method at the Washington University Sc
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
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,
229 wo types of amino acids, here we used modern mass spectrometry (MS)-based techniques to separate and
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
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
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
249 dy complexes and hydrogen-deuterium exchange mass spectrometry revealed molecular insights about mole
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
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
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
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
283 n conjunction with capillary electrophoresis mass spectrometry was applied to 13 Buyid silk specimens
285 id chromatography-high resolution (Orbitrap) mass spectrometry we identified 33 AMI metabolites (both
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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