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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.
6                                              Ion mobility spectrometry allows for the measurement of
7                                              Ion mobility spectrometry allows one to determine ion co
8 zed and differentiated by thermal desorption ion mobility spectrometry and chemometric modeling.
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
11  diketopiperazines by liquid chromatography, ion mobility spectrometry, and mass spectrometry.
12              Atmospheric pressure drift tube ion mobility spectrometry (AP-DTIMS) was coupled with Fo
13                  Here, mass spectrometry and ion mobility spectrometry are used to investigate a mixt
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
16                A corona discharge ionization-ion mobility spectrometry (CD-IMS) with a novel sample i
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
19                                              Ion mobility spectrometry combined with multicapillary c
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
22                                   Drift tube ion mobility spectrometry coupled with mass spectrometry
23                          For the first time, ion mobility spectrometry coupled with rapid gas chromat
24 sed as an ionization source for differential ion mobility spectrometry (DMS) for the first time.
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
29  an electrospray ionization high-performance ion mobility spectrometry (ESI-HPIMS).
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
32 predict separation efficiency for drift tube ion mobility spectrometry experiments.
33 lso were observed selectively in iAbeta42 in ion mobility spectrometry experiments.
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
37                                 Differential ion mobility spectrometry (FAIMS) can baseline-resolve m
38          Full scan field asymmetric waveform ion mobility spectrometry (FAIMS) combined with liquid c
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
45                    Field asymmetric waveform ion mobility spectrometry (FAIMS) has emerged as a power
46                    Field asymmetric waveform ion mobility spectrometry (FAIMS) has emerged as an anal
47                    Field asymmetric waveform ion mobility spectrometry (FAIMS) has significant potent
48 he utility of high-field asymmetric waveform ion mobility spectrometry (FAIMS) in quantitative bioana
49                                 Differential ion mobility spectrometry (FAIMS) integrated with mass s
50               High-field asymmetric waveform ion mobility spectrometry (FAIMS) is an atmospheric pres
51                    Field asymmetric waveform ion mobility spectrometry (FAIMS) is emerging as a major
52 turized ultra high field asymmetric waveform ion mobility spectrometry (FAIMS) is used for the select
53             A high-field asymmetric waveform ion mobility spectrometry (FAIMS) system that is physica
54          The resolving power of differential ion mobility spectrometry (FAIMS) was dramatically incre
55           Using high-definition differential ion mobility spectrometry (FAIMS) with electron transfer
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
63                                 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
66                              High-resolution ion mobility spectrometry has been combined with time-of
67 gases to alter separation factors (alpha) in ion mobility spectrometry has been demonstrated.
68  with subsequent separation and detection by ion mobility spectrometry has been studied.
69 findings allow for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strat
70                                              Ion mobility spectrometry (IMS) affords miniaturized han
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
73                          In combination with ion mobility spectrometry (IMS) and formaldehyde labelin
74 cedure, based on the combined application of Ion Mobility Spectrometry (IMS) and Infrared Spectroscop
75                      A growing number of new ion mobility spectrometry (IMS) and ITMS applications ar
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
78 dustrial polymers may be moderated by use of ion mobility spectrometry (IMS) and MS in series.
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
83                                              Ion mobility spectrometry (IMS) can separate and charact
84 s (QSPRs) have been developed to predict the ion mobility spectrometry (IMS) collision cross sections
85                                              Ion mobility spectrometry (IMS) coupled to orthogonal ti
86 elationship between the output signal of the ion mobility spectrometry (IMS) detector and the concent
87      Due to the inherently low duty cycle of ion mobility spectrometry (IMS) experiments that sample
88 mplexity in the absence of any solvent using ion mobility spectrometry (IMS) followed by MS detection
89                               The utility of ion mobility spectrometry (IMS) for separation of mixtur
90                                   The use of ion mobility spectrometry (IMS) for the determination of
91                                              Ion mobility spectrometry (IMS) has been explored for de
92 ar gas chromatography (GC) column coupled to ion mobility spectrometry (IMS) has been explored to cla
93                                              Ion mobility spectrometry (IMS) has been increasingly em
94                                              Ion mobility spectrometry (IMS) has been shown to be a v
95                                    Recently, ion mobility spectrometry (IMS) has been shown to effect
96                                    Recently, ion mobility spectrometry (IMS) has been used to support
97                                              Ion mobility spectrometry (IMS) has gained significant t
98                                              Ion mobility spectrometry (IMS) has proven to be useful
99                                     Although ion mobility spectrometry (IMS) has shown great promise
100                                              Ion mobility spectrometry (IMS) in conjunction with mass
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
104                                              Ion mobility spectrometry (IMS) is a fast and sensitive
105                                              Ion mobility spectrometry (IMS) is a gas phase separatio
106                                              Ion mobility spectrometry (IMS) is a rapid, gas-phase se
107                                              Ion mobility spectrometry (IMS) is a technique attractiv
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
110                                              Ion mobility spectrometry (IMS) is capable of providing
111                           Miniaturization of ion mobility spectrometry (IMS) is expected to have many
112 etection of black powder (BP) by stand-alone ion mobility spectrometry (IMS) is full of challenges.
113                                              Ion mobility spectrometry (IMS) is increasingly used to
114                        One major drawback of ion mobility spectrometry (IMS) is the dependence of the
115   Detection by mass spectrometry (MS) and/or ion mobility spectrometry (IMS) is traditionally difficu
116                                              Ion mobility spectrometry (IMS) may be used to show sepa
117                                          The ion mobility spectrometry (IMS) methods are grouped into
118  matrix-assisted laser desorption/ionization ion mobility spectrometry (IMS) MS instrument.
119  and solvent-free gas-phase separation using ion mobility spectrometry (IMS) MS.
120 nt effects upon performance are expected for ion mobility spectrometry (IMS) of larger ions.
121  produced can be dispersed again in a second ion mobility spectrometry (IMS) region prior to addition
122  acquired from two samples and two different ion mobility spectrometry (IMS) sensors.
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
125 lly been served well by atmospheric pressure ion mobility spectrometry (IMS) systems.
126                        Conversely, gas phase ion mobility spectrometry (IMS) techniques can be used t
127 xamined employing mass spectrometry (MS) and ion mobility spectrometry (IMS) techniques in combinatio
128                            The potential for ion mobility spectrometry (IMS) to provide rapid at-line
129                           The application of ion mobility spectrometry (IMS) was explored, but succes
130             Separation of d/l-peptides using ion mobility spectrometry (IMS) was impeded by small col
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
134                           The integration of ion mobility spectrometry (IMS) with mass spectrometry (
135  two-dimensional gas chromatography (GCxGC), ion mobility spectrometry (IMS), and capillary electroph
136                                              Ion mobility spectrometry (IMS), and particularly differ
137 on with mass spectrometry (MS), conventional ion mobility spectrometry (IMS), or both.
138 ns, including isotopomers and isobars, using ion mobility spectrometry (IMS), specifically, the field
139                              The progress of ion mobility spectrometry (IMS), together with its assoc
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
142                         MAIV-MS coupled with ion mobility spectrometry (IMS)-MS and tandem mass spect
143 ion allows for comparison of two-dimensional ion mobility spectrometry (IMS)-MS data sets in a pixel-
144  has been successfully used for electrospray ion mobility spectrometry (IMS)-MS experiments.
145 d in the gas phase using ESI-MS coupled with ion mobility spectrometry (IMS).
146 -sampled trace explosives detectors based on ion mobility spectrometry (IMS).
147 tities, affecting ion mobilities measured in ion mobility spectrometry (IMS).
148  a table-top field explosives detector based ion mobility spectrometry (IMS).
149 oroformate as the derivatization reagent and ion mobility spectrometry (IMS).
150 ed as a nonradioactive ionization source for ion mobility spectrometry (IMS).
151 d in baby formula samples and detected using ion mobility spectrometry (IMS).
152 e for direct liquid sampling and analysis by ion mobility spectrometry (IMS).
153 yses by chromatography, electrophoresis, and ion mobility spectrometry (IMS).
154 orm ion cyclotron resonance (FT-ICR) MS, and ion mobility spectrometry (IMS).
155                             Multidimensional ion mobility spectrometry (IMS-IMS and IMS-IMS-IMS) tech
156                              Two-dimensional ion mobility spectrometry (IMS-IMS) coupled with mass sp
157 ncreasing the efficiency of multidimensional ion mobility spectrometry (IMS-IMS) measurements (as def
158 y can be accurately calibrated against other ion-mobility spectrometry (IMS) techniques.
159                                              Ion-mobility spectrometry (IMS) was used to preliminaril
160 oices include liquid chromatography (LC) and ion-mobility spectrometry (IMS), in which separation tak
161                                      A novel ion mobility spectrometry instrument incorporating a cyc
162                                              Ion mobility spectrometry is a powerful and low-cost tec
163                                              Ion mobility spectrometry is a rapid scanning measuremen
164         The fundamental transport theory for ion mobility spectrometry is modified to include effects
165                                 Liquid phase ion mobility spectrometry (LPIMS) has the potential to b
166                               However, using ion mobility spectrometry mass spectrometry (IMS-MS), we
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)
169                Here, 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)
171                                      We used ion mobility spectrometry-mass spectrometry (IMS-MS) in
172                                     A recent ion mobility spectrometry-mass spectrometry (IMS-MS) stu
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
175                                     Previous ion mobility spectrometry-mass spectrometry (IMS-MS) wor
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)
178                In the present paper, trapped ion mobility spectrometry-mass spectrometry (TIMS-MS) ha
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
182        Central to our success was the use of ion mobility spectrometry-mass spectrometry and microsca
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
189                          Membrane-extraction ion mobility spectrometry (ME-IMS) has been developed fo
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
193 eptides and proteins using periodic focusing ion mobility spectrometry (PF IMS) is presented.
194                                              Ion mobility spectrometry provides ion separation in the
195                                              Ion mobility spectrometry provides the means to resolve
196                                              Ion-mobility spectrometry provides an accurate measure o
197               A pyrolysis-gas chromatography-ion mobility spectrometry (Py-GC-IMS) briefcase system h
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
201               Multiple charging enhances the ion mobility spectrometry separation of ions derived fro
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-
204                             Multidimensional ion mobility spectrometry techniques (IMS-IMS and IMS-IM
205 lity to separate isotopes by high-resolution ion mobility spectrometry techniques is considered as a
206                                     By using ion mobility spectrometry, the dopamine isomer, which ha
207 the peptide-crown complexes are separated by ion mobility spectrometry, the ions can be collisionally
208                                              Ion mobility spectrometry-time-of-flight mass spectromet
209                In the present paper, trapped ion mobility spectrometry (TIMS) and theoretical calcula
210  the Traveling Wave (TWIMS), and the Trapped Ion Mobility Spectrometry (TIMS) coupled to mass spectro
211       In the present work, we employ trapped ion mobility spectrometry (TIMS) for conformational anal
212                  For the first time, trapped ion mobility spectrometry (TIMS) in tandem with Fourier
213            The recent development of trapped ion mobility spectrometry (TIMS) provides a promising ne
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
217                              The addition of ion mobility spectrometry to liquid chromatography-mass
218         While the coupling of traveling wave ion mobility spectrometry (TWIMS) and mass spectrometry
219                   Integrating traveling wave ion mobility spectrometry (TWIMS) enables in-line gas ph
220  we describe how to integrate traveling-wave ion mobility spectrometry (TWIMS) into traditional LC-MS
221                               Traveling wave ion mobility spectrometry (TWIMS) isomer separation was
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
226 ass spectrometry coupled with traveling wave ion mobility spectrometry (TWIMS).
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
229                     A combination of CID and ion mobility spectrometry was applied for the first time
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
232                                  Here, using ion-mobility spectrometry, we investigated the impact of
233 isomers separated by both chromatography and ion mobility spectrometry were studied.
234                  Here, mass spectrometry and ion mobility spectrometry were used to investigate the e
235                 Native mass spectrometry and ion mobility spectrometry were used to investigate the g
236               CIMS is similar to traditional ion mobility spectrometry, where gas-phase ions, when su
237  of electrospray ionization ambient pressure ion mobility spectrometry with an orthogonal reflector t
238                                   We combine ion mobility spectrometry with cryogenic, messenger-tagg
239 The combination of field asymmetric waveform ion mobility spectrometry with liquid chromatography-mas
240  alpha-pinene are investigated using coupled ion mobility spectrometry with mass spectrometry.
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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