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1 enables the separation of isotopologues with ion mobility spectrometry.
2 sequently analyzed by means of tandem MS and ion mobility spectrometry.
3 ime scales, and can readily be combined with ion mobility spectrometry.
4 e investigated using electrospray ionization ion mobility spectrometry.
5 e high-performance liquid chromatography and ion mobility spectrometry.
9 imination of oligosaccharide isomers by both ion mobility spectrometry and tandem mass spectrometry.
10 ng or steering beams of charged particles in ion mobility spectrometry and time-of-flight mass spectr
14 This work demonstrates the first example of ion mobility spectrometry at pressures above ambient.
15 chains of insulin, were characterized using ion mobility spectrometry-based mass spectrometry and at
17 ation of OzID in a high-pressure region, the ion-mobility spectrometry cell, of a contemporary quadru
18 his article introduces the concept of chiral ion mobility spectrometry (CIMS) and presents examples d
20 eparation and analysis of the products using ion mobility spectrometry coupled to conventional mass s
21 rk explores the capabilities of differential ion mobility spectrometry coupled to tandem mass spectro
25 s tissue extraction followed by differential ion mobility spectrometry (DMS) mass spectrometry for an
26 estion (PD) is demonstrated using drift tube ion mobility spectrometry (DTIMS) coupled with linear io
27 ) can be directly calculated from drift tube ion mobility spectrometry (DTIMS) data, measurements mad
28 rtcomings of atmospheric pressure drift tube ion mobility spectrometry (DTIMS) is its intrinsically l
30 the high-resolution electrospray ionization ion mobility spectrometry (ESI-IMS) technique as an anal
31 ic macromolecules by electrospray ionization/ion mobility spectrometry (ESI/IMS) at atmospheric press
34 d intensity (E) in field asymmetric waveform ion mobility spectrometry (FAIMS) analyses was doubled t
35 Microchip-based field asymmetric waveform ion mobility spectrometry (FAIMS) analyzers featuring a
36 miniaturized high-field asymmetric waveform ion mobility spectrometry (FAIMS) and mass spectrometry
39 lication of a high-field asymmetric waveform ion mobility spectrometry (FAIMS) device as an interface
40 a chip-based high-field asymmetric waveform ion mobility spectrometry (FAIMS) device to image metabo
41 We show that high-resolution differential ion mobility spectrometry (FAIMS) employing helium-rich
42 e benefits of high-field asymmetric waveform ion mobility spectrometry (FAIMS) for proteomics have be
43 coupled with high field asymmetric waveform ion mobility spectrometry (FAIMS) for top-down protein a
44 key application of field asymmetric waveform ion mobility spectrometry (FAIMS) has been in selectivel
48 he utility of high-field asymmetric waveform ion mobility spectrometry (FAIMS) in quantitative bioana
52 turized ultra high field asymmetric waveform ion mobility spectrometry (FAIMS) is used for the select
56 ombination of high-field asymmetric waveform ion mobility spectrometry (FAIMS) with Fourier transform
57 lity spectrometry (field asymmetric waveform ion mobility spectrometry (FAIMS)) is emerging as a broa
58 demonstrate that high field asymmetric wave ion mobility spectrometry (FAIMS), also known as differe
59 t coupling of high field asymmetric waveform ion mobility spectrometry (FAIMS), also known as differe
60 eferred to as high-field asymmetric waveform ion mobility spectrometry (FAIMS), is a rapidly advancin
61 lity spectrometry (field asymmetric waveform ion mobility spectrometry, FAIMS) employing H2/N2 gas mi
62 e states by the new approach of differential ion mobility spectrometry (field asymmetric waveform ion
64 the continued development and application of ion mobility spectrometry for the distinction and resolu
65 to study the potential of gas chromatography-ion mobility spectrometry (GC-IMS) to differentiate lact
69 findings allow for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strat
71 cisely localize d-amino acids in peptides by ion mobility spectrometry (IMS) analysis of mass spectro
72 This strategy was developed by combining ion mobility spectrometry (IMS) and collision-induced di
74 cedure, based on the combined application of Ion Mobility Spectrometry (IMS) and Infrared Spectroscop
76 e analytical separation techniques including ion mobility spectrometry (IMS) and liquid chromatograph
77 y, and their conformations were probed using ion mobility spectrometry (IMS) and Monte Carlo minimiza
79 ncreasingly involve gas-phase separations by ion mobility spectrometry (IMS) and particularly differe
80 aceutical drug formulations using hyphenated ion mobility spectrometry (IMS) and time-of-flight mass
81 qualitative and quantitative capabilities of ion mobility spectrometry (IMS) as a comprehensive and p
82 rrival time distributions (ATDs) recorded by ion mobility spectrometry (IMS) can often be interpreted
84 s (QSPRs) have been developed to predict the ion mobility spectrometry (IMS) collision cross sections
86 elationship between the output signal of the ion mobility spectrometry (IMS) detector and the concent
88 mplexity in the absence of any solvent using ion mobility spectrometry (IMS) followed by MS detection
92 ar gas chromatography (GC) column coupled to ion mobility spectrometry (IMS) has been explored to cla
101 developed for detecting heavy metals via the ion mobility spectrometry (IMS) in the negative mode.
102 owever, both tandem spectrometry (MS(2)) and ion mobility spectrometry (IMS) indicated structural dif
103 o substrates suitable for calibration of the ion mobility spectrometry (IMS) instruments currently de
108 ry within trace detection techniques such as ion mobility spectrometry (IMS) is an area of intense in
109 Traditionally, the spectrum acquired using ion mobility spectrometry (IMS) is an average of multipl
112 etection of black powder (BP) by stand-alone ion mobility spectrometry (IMS) is full of challenges.
115 Detection by mass spectrometry (MS) and/or ion mobility spectrometry (IMS) is traditionally difficu
121 produced can be dispersed again in a second ion mobility spectrometry (IMS) region prior to addition
123 ributions are extensively compared to recent ion mobility spectrometry (IMS) studies reported in the
124 ect of space charge on the performance of an Ion Mobility Spectrometry (IMS) system becomes more impo
127 xamined employing mass spectrometry (MS) and ion mobility spectrometry (IMS) techniques in combinatio
131 es (extra virgin, virgin and lampante) using Ion Mobility Spectrometry (IMS) was improved by replacin
132 id-phase microextraction (SPME) coupled with ion mobility spectrometry (IMS) was used for the detecti
133 rich gases has recently enabled differential ion mobility spectrometry (IMS) with a resolving power u
135 two-dimensional gas chromatography (GCxGC), ion mobility spectrometry (IMS), and capillary electroph
138 ns, including isotopomers and isobars, using ion mobility spectrometry (IMS), specifically, the field
140 e, store, and eject ions in conjunction with ion mobility spectrometry (IMS), which elevated the char
141 itional gas-phase separation dimension using ion mobility spectrometry (IMS), which is a method in wh
143 ion allows for comparison of two-dimensional ion mobility spectrometry (IMS)-MS data sets in a pixel-
157 ncreasing the efficiency of multidimensional ion mobility spectrometry (IMS-IMS) measurements (as def
160 oices include liquid chromatography (LC) and ion-mobility spectrometry (IMS), in which separation tak
167 ay ionization-high field asymmetric waveform ion mobility spectrometry-mass spectrometry (ESI-FAIMS-M
168 for interrogation by electrospray ionization-ion mobility spectrometry-mass spectrometry (ESI-IMS-MS)
170 ated as a shift reagent for multidimensional ion mobility spectrometry-mass spectrometry (IMS-IMS-MS)
173 trospray ionization and analyzed by combined ion mobility spectrometry-mass spectrometry (IMS-MS) tec
174 we report a high-throughput method based on ion mobility spectrometry-mass spectrometry (IMS-MS) tha
176 inum coordination, have been investigated by ion mobility spectrometry-mass spectrometry (IMS-MS).
177 es in multidimensional liquid chromatography-ion mobility spectrometry-mass spectrometry (LC-IMS-MS)
179 en/deuterium back exchange (HDX) and trapped ion mobility spectrometry-mass spectrometry (TIMS-MS).
180 shown here experimentally by traveling wave ion mobility spectrometry-mass spectrometry (TWIMS-MS) o
181 amyloid intermediates using a combination of ion mobility spectrometry-mass spectrometry and gas-phas
183 hormone as a model protein, the potential of ion mobility spectrometry-mass spectrometry as a tool to
184 thermore, we demonstrate the ease with which ion mobility spectrometry-mass spectrometry can guide th
185 loride ions using a novel technique coupling ion mobility spectrometry-mass spectrometry with infrare
186 es of molecular species using traveling wave ion-mobility spectrometry-mass spectrometry (TWIMS-MS) i
187 formulations directly by DESI combined with ion mobility spectrometry/mass spectrometry in approxima
188 taneously using a prototype multidimensional ion mobility spectrometry/mass spectrometry spectrometry
190 termined by a novel, portable, field-capable ion mobility spectrometry method described herein and en
191 s challenge, we developed a drift tube-based ion mobility spectrometry-Orbitrap mass spectrometer (IM
192 Oversampling Selective Accumulation Trapped Ion Mobility Spectrometry (OSA-TIMS) when coupled to ult
198 e use of a traditional ionization source for ion mobility spectrometry (radioactive nickel ((63)Ni) b
199 ycle, the Hadamard transform (HT) applied to ion mobility spectrometry represents a fresh alternative
200 present work, selected accumulation trapped ion mobility spectrometry (SA-TIMS) is coupled to Fourie
202 powder were also analyzed by two stand-alone ion mobility spectrometry systems, yielding an average r
203 n using electrospray ionization-differential ion mobility spectrometry-tandem mass spectrometry (ESI-
205 lity to separate isotopes by high-resolution ion mobility spectrometry techniques is considered as a
207 the peptide-crown complexes are separated by ion mobility spectrometry, the ions can be collisionally
210 the Traveling Wave (TWIMS), and the Trapped Ion Mobility Spectrometry (TIMS) coupled to mass spectro
214 which we have termed Transversal Modulation Ion Mobility Spectrometry (TM-IMS), utilizes only electr
215 The potential of a Transversal Modulation Ion Mobility Spectrometry (TMIMS) instrument for protein
216 troduced based on the transversal modulation ion mobility spectrometry (TMIMS) technique, which provi
220 we describe how to integrate traveling-wave ion mobility spectrometry (TWIMS) into traditional LC-MS
222 rift time determination using traveling wave ion mobility spectrometry (TWIMS) of poorly resolved or
223 the more recently introduced traveling wave ion mobility spectrometry (TWIMS) technique are usually
224 Although the hyphenation of traveling-wave ion mobility spectrometry (TWIMS) with high-resolution q
225 (UPLC-IM-TOFMS), integrating traveling wave ion mobility spectrometry (TWIMS) with negative electros
227 llisions in PF IMS compared to uniform field ion mobility spectrometry (UF IMS) for equivalent operat
228 s were determined by electrospray ionization ion mobility spectrometry using three different drift ga
230 ((63)Ni) beta emission ionization source for ion mobility spectrometry was employed with an atmospher
231 Here, using mass spectrometry coupled with ion mobility spectrometry, we demonstrate the conformati
237 of electrospray ionization ambient pressure ion mobility spectrometry with an orthogonal reflector t
239 The combination of field asymmetric waveform ion mobility spectrometry with liquid chromatography-mas
241 onstrate the application of corona discharge ion mobility spectrometry with orthogonal acceleration t
242 rformance is compared to conventional linear ion mobility spectrometry, with and without a radioactiv
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