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1 photo diode array and positive mode in-line electrospray ionization mass spectrometry.
2 and transported in solution for analysis by electrospray ionization mass spectrometry.
3 in detail using in situ NMR experiments and electrospray ionization mass spectrometry.
4 py and finally identified by high-resolution electrospray ionization mass spectrometry.
5 l of SelS was determined to be -234 mV using electrospray ionization mass spectrometry.
6 DOSY, and NOESY) NMR spectroscopy as well as electrospray ionization mass spectrometry.
7 when eluted with mobile phases preferred for electrospray ionization mass spectrometry.
8 A in amplified products was identified using electrospray ionization mass spectrometry.
9 s that were confirmed to be monodispersed by electrospray ionization mass spectrometry.
10 nt phospholipids using liquid chromatography/electrospray ionization mass spectrometry.
11 (11)NO(2))(n)Me] (n </= 3), as determined by electrospray ionization mass spectrometry.
12 es can then be detected and quantified using electrospray ionization mass spectrometry.
13 a well-observed and discussed phenomenon in electrospray ionization mass spectrometry.
14 ot be distinguished by identity testing with electrospray ionization mass spectrometry.
15 roposed lipid A structures were confirmed by electrospray ionization mass spectrometry.
16 by liquid chromatography-positive ion tandem electrospray ionization mass spectrometry.
17 terized by multinuclear NMR spectroscopy and electrospray ionization mass spectrometry.
18 s and has a M(r) of 9046.1 Da, determined by electrospray ionization mass spectrometry.
19 rformance liquid chromatography coupled with electrospray ionization mass spectrometry.
20 ster conversion reaction using time-resolved electrospray ionization mass spectrometry.
21 user effect spectroscopy and high-resolution electrospray ionization mass spectrometry.
22 One, the cluster size was determined via electrospray ionization mass spectrometry.
23 soft drinks based upon liquid chromatography-electrospray ionization mass spectrometry.
24 tides were analyzed by liquid chromatography electrospray ionization mass spectrometry.
25 a handheld laser source is coupled with nano-electrospray ionization mass spectrometry.
26 complex samples analyzed by direct infusion electrospray ionization mass spectrometry.
27 approximately 1:10 by liquid chromatography-electrospray ionization mass spectrometry.
28 o molecules of cardiolipin, as determined by electrospray ionization-mass spectrometry.
29 high-performance liquid chromatography, and electrospray ionization-mass spectrometry.
30 ycans was confirmed by liquid chromatography-electrospray ionization-mass spectrometry.
31 lism of mitoxantrone is studied by microchip electrospray ionization-mass spectrometry.
32 384 cases, giving polymerase chain reaction/electrospray ionization-mass spectrometry a sensitivity
33 mance liquid chromatography-photodiode array-electrospray ionization-mass spectrometry (AccQ*Tag-UPLC
35 ydroxy selenane intermediate was observed by electrospray ionization mass spectrometry and (77)Se NMR
36 veloped based upon targeted PCR, followed by electrospray ionization mass spectrometry and amplicon b
37 The reaction mechanism was investigated by electrospray ionization mass spectrometry and DFT calcul
39 e formation of complexes was evident in both electrospray ionization mass spectrometry and isothermal
40 ltransferase, MGMT) by liquid chromatography/electrospray ionization mass spectrometry and pyrosequen
41 netic resonance (NMR) spectroscopy, nanoflow electrospray ionization mass spectrometry and size-exclu
44 tion is investigated using NMR spectroscopy, electrospray ionization mass spectrometry, and deuterium
45 g NMR, UV-vis and fluorescence spectroscopy, electrospray ionization mass spectrometry, and electroch
46 Raman, and NMR spectroscopy, high resolution electrospray ionization mass spectrometry, and electroch
47 ther investigation by (1)H NMR spectroscopy, electrospray ionization mass spectrometry, and isotherma
48 Its composition was primarily determined by electrospray ionization mass spectrometry, and it was fu
49 he yeast Kluyveromyces lactis, with nanoflow electrospray ionization mass spectrometry, and mapped in
51 I)(4) and characterized by NMR spectroscopy, electrospray ionization mass spectrometry, and single-cr
53 action and show by (27) Al NMR spectroscopy, electrospray-ionization mass spectrometry, and small- an
55 intermediates were observed by gas-phase and electrospray ionization mass spectrometry, as well as by
58 ucts that are observed using high-resolution electrospray ionization mass spectrometry, but these pro
62 ation-free assay, based on catch-and-release electrospray ionization mass spectrometry (CaR-ESI-MS),
63 bes the application of the catch-and-release electrospray ionization-mass spectrometry (CaR-ESI-MS) a
64 te extraction, and capillary electrophoresis electrospray ionization mass spectrometry (CE-ESI-MS) to
65 able, a sheathless capillary electrophoresis-electrospray ionization-mass spectrometry (CE-ESI-MS) st
66 hat displayed NOD2 activity were analyzed by electrospray ionization mass spectrometry, confirming th
67 drive allostery, we performed time-resolved electrospray ionization mass spectrometry coupled to hyd
68 me-resolved small-angle X-ray scattering and electrospray ionization mass spectrometry demonstrated t
69 ndards) interlaboratory study for desorption electrospray ionization mass spectrometry (DESI MS) meas
70 ification membranes, we have used desorption electrospray ionization mass spectrometry (DESI MS), whe
72 ucosal metabolome profiling using desorption electrospray ionization mass spectrometry (DESI-MS) anal
73 d, detected, and identified using desorption electrospray ionization mass spectrometry (DESI-MS) and
75 croextraction (SPME) fibers using desorption electrospray ionization mass spectrometry (DESI-MS) for
78 rine xenografts were subjected to desorption electrospray ionization mass spectrometry (DESI-MS) imag
79 le of necrotic breast cancer with Desorption Electrospray Ionization Mass Spectrometry (DESI-MS) imag
80 The detection was enabled using desorption electrospray ionization mass spectrometry (DESI-MS) in c
81 tence and composition of the CEI, desorption electrospray ionization mass spectrometry (DESI-MS) is a
82 gn and geometry on performance in desorption electrospray ionization mass spectrometry (DESI-MS) is a
83 cocultures grown on agar media by desorption electrospray ionization mass spectrometry (DESI-MS) is q
86 ss spectrometry (LESA-MS/MS), and desorption electrospray ionization mass spectrometry (DESI-MS) was
87 mass spectrometry (ToF-SIMS) and desorption electrospray ionization mass spectrometry (DESI-MS) was
88 This work illustrates reactive desorption electrospray ionization mass spectrometry (DESI-MS) with
89 nt ionization techniques, such as desorption electrospray ionization mass spectrometry (DESI-MS), but
91 tion products from the surface by desorption electrospray ionization mass spectrometry (DESI-MS).
94 omas can be rapidly classified by desorption electrospray ionization-mass spectrometry (DESI-MS) imag
95 eviously shown that liquid sample desorption electrospray ionization-mass spectrometry (DESI-MS) is a
97 ition of organic aerosols, namely extractive electrospray ionization mass spectrometry (EESI-MS).
98 graphy (IXC) with online detection by native electrospray ionization mass spectrometry (ESI MS) allow
99 oparticle (SCNP) folding via high-resolution electrospray ionization mass spectrometry (ESI MS) coupl
100 d charging, or supercharging, of analytes in electrospray ionization mass spectrometry (ESI MS) facil
104 combination with online detection by native electrospray ionization mass spectrometry (ESI MS) to ch
105 me monitoring of the hydrolysis of ACh using electrospray ionization mass spectrometry (ESI MS) to fi
106 use size exclusion chromatography (SEC) and electrospray ionization mass spectrometry (ESI MS) to mo
109 sure charge stripping (AP-CS) method for the electrospray ionization mass spectrometry (ESI-MS) analy
111 bum samples were detected by direct infusion electrospray ionization mass spectrometry (ESI-MS) analy
112 itrap-MS and compared to those obtained with electrospray ionization mass spectrometry (ESI-MS) and a
113 tion profile of the ADC was characterized by electrospray ionization mass spectrometry (ESI-MS) and c
114 during thermal processing were identified by electrospray ionization mass spectrometry (ESI-MS) and c
115 OA that cannot be detected using traditional electrospray ionization mass spectrometry (ESI-MS) and f
117 , which was characterized by low-temperature electrospray ionization mass spectrometry (ESI-MS) and I
120 describe a powerful new assay that combines electrospray ionization mass spectrometry (ESI-MS) and p
121 ty measurements carried out using the direct electrospray ionization mass spectrometry (ESI-MS) assay
122 al approach, which combines the proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay
126 graphy (LC) coupled to diode array (DAD) and electrospray ionization mass spectrometry (ESI-MS) detec
128 act ionization mass spectrometry (EI-MS) and electrospray ionization mass spectrometry (ESI-MS) for s
130 echanistic studies utilizing high-resolution electrospray ionization mass spectrometry (ESI-MS) ident
131 cyclopropylaniline (CPA, 1) and styrene 2 by electrospray ionization mass spectrometry (ESI-MS) in co
132 cRn affinity liquid chromatography (LC) with electrospray ionization mass spectrometry (ESI-MS) in na
133 luster, Au(25)(SG)(18), we present optimized electrospray ionization mass spectrometry (ESI-MS) instr
137 this analytical challenge by enabling inline electrospray ionization mass spectrometry (ESI-MS) of lo
140 Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revea
141 cterized by (1)H, (13)C NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS) spect
142 4)D) electropherograms and interference-free electrospray ionization mass spectrometry (ESI-MS) spect
143 ochemical scanner has also been coupled with electrospray ionization mass spectrometry (ESI-MS) to as
144 ut in droplets, we have developed the use of electrospray ionization mass spectrometry (ESI-MS) to me
146 sis sampling was coupled with segmented flow electrospray ionization mass spectrometry (ESI-MS) to pe
148 Single crystal X-ray crystallography and electrospray ionization mass spectrometry (ESI-MS) unequ
149 omatography (HILIC) followed by positive-ion electrospray ionization mass spectrometry (ESI-MS) using
153 erformance liquid chromatography (UPLC) with electrospray ionization mass spectrometry (ESI-MS) we de
154 iply protonated polypeptide ions produced in electrospray ionization mass spectrometry (ESI-MS) with
156 roscopy, pulse radiolysis, stopped flow, and electrospray ionization mass spectrometry (ESI-MS) with
157 luding FT-IR spectroscopy, NMR spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and
158 e basis of nuclear magnetic resonance (NMR), electrospray ionization mass spectrometry (ESI-MS), and
159 etabolome and metabolite identification from electrospray ionization mass spectrometry (ESI-MS)-based
160 en its widespread use in protein analysis by electrospray ionization mass spectrometry (ESI-MS).
161 e course of the reaction was also studied by electrospray ionization mass spectrometry (ESI-MS).
162 LC coupled to diode array detector (DAD) and electrospray ionization mass spectrometry (ESI-MS).
163 condary ion mass spectrometry (ToF-SIMS) and electrospray ionization mass spectrometry (ESI-MS).
164 tional properties of membrane proteins using electrospray ionization mass spectrometry (ESI-MS).
165 ent of hGal-9 (hGal-9N), were measured using electrospray ionization mass spectrometry (ESI-MS).
166 gical analytes, have a deleterious effect on electrospray ionization mass spectrometry (ESI-MS).
167 B capsules in the gas phase was confirmed by electrospray ionization mass spectrometry (ESI-MS).
168 ee-flow electrophoresis (FFE) and sheathless electrospray ionization mass spectrometry (ESI-MS).
170 roscopies, elemental (C H N S) analysis, and electrospray ionization mass spectrometry (ESI-MS).
171 h-tBu)52, was verified using high resolution electrospray ionization mass spectrometry (ESI-MS).
172 l of resonance energy have been subjected to electrospray ionization mass spectrometry (ESI/MS) as we
174 o be recovered by swabbing and extracted for electrospray ionization-mass spectrometry (ESI-MS) analy
176 lecules demonstrate narrow dynamic ranges in electrospray ionization-mass spectrometry (ESI-MS) and s
177 tor (PEGylated rhG-CSF or pegfilgrastim), by electrospray ionization-mass spectrometry (ESI-MS) const
178 e extraction (EME) probe directly coupled to electrospray ionization-mass spectrometry (ESI-MS) for r
179 hydrazide (CHH) and analyze all compounds by electrospray ionization-mass spectrometry (ESI-MS) in po
180 henation of miniaturized sampling devices to electrospray ionization-mass spectrometry (ESI-MS) is at
182 rcritical fluid chromatography (UHPSFC) with electrospray ionization-mass spectrometry (ESI-MS) is pr
183 ng ion-pair chromatography (IPC) online with electrospray ionization-mass spectrometry (ESI-MS) is th
184 developed and applied a rapid and sensitive electrospray ionization-mass spectrometry (ESI-MS) metho
185 t typically do not provide strong signals by electrospray ionization-mass spectrometry (ESI-MS) owing
187 aring MALDI results to those of our previous electrospray ionization-mass spectrometry (ESI-MS) studi
189 lable analytical platforms, e.g., based upon electrospray ionization-mass spectrometry (ESI-MS), and
190 fluorescence change and it was confirmed by electrospray ionization-mass spectrometry (ESI-MS), prot
191 er electrospray mass spectrometry (LEMS) and electrospray ionization-mass spectrometry (ESI-MS).
192 lls using capillary electrophoresis (CE) and electrospray ionization-mass spectrometry (ESI-MS).
194 mass spectrometry analysis of amplicons (PCR/electrospray ionization-mass spectrometry [ESI-MS]) to d
195 ilizing flow injection analysis coupled with electrospray ionization mass spectrometry (FIA-ESI-MS).W
197 n adversely affect the performance of native electrospray ionization mass spectrometry for the analys
198 nline high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS)
199 y high-performance thin-layer chromatography-electrospray ionization mass spectrometry (HPTLC-ESI-MS)
201 e organic aerosol (OA) using high-resolution electrospray ionization mass spectrometry (HR-ESI-MS).
202 infection samples, polymerase chain reaction/electrospray ionization-mass spectrometry identified a p
203 in breast cancer tissue that uses desorption electrospray ionization mass spectrometry imaging (DESI
205 etermine the feasibility of using desorption electrospray ionization mass spectrometry imaging (DESI-
208 We applied an approach combining desorption electrospray ionization mass spectrometry imaging (DESI-
211 n of reactive mineral surfaces by desorption electrospray ionization-mass spectrometry imaging (DESI-
212 ma was objectively detected using desorption electrospray ionization-mass spectrometry imaging (DESI-
213 roof-of-principal analysis shows that native electrospray ionization mass spectrometry in combination
214 chlorinated lipid species of these acids by electrospray ionization mass spectrometry in the negativ
216 ductively coupled plasma-mass spectrometry]-[electrospray ionization-mass spectrometry]) in whole-pla
218 (1)H NMR, cyclic voltammetry, and desorption electrospray ionization mass spectrometry indicate that
219 by high pH anion exchange chromatography and electrospray ionization mass spectrometry indicated the
221 l as in comparison to a conventional nano-LC-electrospray ionization-mass spectrometry interface.
223 e that single-cell capillary electrophoresis-electrospray ionization mass spectrometry is able to tes
224 products, as online monitored by desorption electrospray ionization mass spectrometry is highly info
225 ion kinetics of intermediates in solution by electrospray ionization mass spectrometry is presented.
228 d (PCI-IS) method with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) fo
229 phy (IPC) approach for liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS), w
230 biological samples by liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) is
231 analyzed by liquid chromatography coupled to electrospray ionization mass spectrometry (LC/MS) and th
234 matrix and the formation of metal adducts in electrospray ionization mass spectrometry (MS) analysis
235 irmed by means of NMR and IR spectroscopies, electrospray ionization mass spectrometry (MS), and sing
237 is field is dominated by strategies based on electrospray ionization, mass spectrometry (MS) methods
238 (AMS), high-resolution nanospray desorption electrospray ionization mass spectrometry (nano-DESI/HRM
240 ) with online nanoflow liquid chromatography-electrospray ionization-mass spectrometry (nanoLC-ESI-MS
241 e was positive and polymerase chain reaction/electrospray ionization-mass spectrometry negative in 13
242 species over a length scale of 0.1-100 nm by electrospray ionization mass spectrometry, nuclear magne
243 sing online and subsequent offline secondary electrospray ionization mass spectrometry of exhaled bre
246 ryotic protein we use high-resolution native electrospray ionization mass spectrometry on a modified
247 romatography (UPLC) and monitored by ESI-MS (electrospray ionization-mass spectrometry) operating in
254 We describe here the use of PCR followed by electrospray ionization mass spectrometry (PCR/ESI-MS) i
257 A novel multiplex method, PCR coupled to electrospray ionization mass spectrometry (PCR/ESI-MS),
258 n the pathogen, we employed PCR coupled with electrospray ionization mass spectrometry (PCR/ESI-MS).
259 wed by desolvation and direct analysis using electrospray ionization mass spectrometry (PCR/ESI-MS).
260 curve analysis (PCR/HRMA) and PCR coupled to electrospray ionization-mass spectrometry (PCR/ESI-MS) t
261 consisting of charged droplets is common to electrospray ionization mass spectrometry, printing and
263 hods, including NMR and UV-vis spectroscopy, electrospray ionization mass spectrometry, pulsed field
264 We propose a novel application of secondary electrospray ionization-mass spectrometry (SESI-MS) as a
265 ects was analyzed during 9 days by secondary electrospray ionization-mass spectrometry (SESI-MS).
267 Single crystal X-ray crystallography and electrospray ionization mass spectrometry show that the
271 tates is achieved through thermal desorption electrospray ionization mass spectrometry (TD-ESI/MS).
272 ing a high-performance liquid chromatography/electrospray ionization mass spectrometry technique.
273 lts suggested that polymerase chain reaction/electrospray ionization-mass spectrometry technology cou
274 ulture-independent polymerase chain reaction/electrospray ionization-mass spectrometry technology wit
275 ased on capillary electrophoresis coupled to electrospray ionization mass spectrometry termed MINISEP
276 pe labeling studies made largely possible by electrospray ionization mass spectrometry to determine t
277 developed a rapid and sensitive method using electrospray ionization mass spectrometry to measure Cu,
279 Plaines, IL) incorporates multilocus PCR and electrospray ionization-mass spectrometry to detect and
280 uid microjunction surface sampling probe for electrospray ionization-mass spectrometry to extract and
281 echnology that couples PCR amplification and electrospray ionization-mass spectrometry to identify pa
282 ve employed liquid chromatography coupled to electrospray ionization mass spectrometry together with
283 In this work, we introduce time-resolved electrospray ionization mass spectrometry (TRESI-MS) as
284 ultrahigh-performance liquid chromatography-electrospray ionization-mass spectrometry (UHPLC-ESI-MS)
285 ltraperformance liquid chromatography-tandem electrospray ionization mass spectrometry (UPLC-MS/MS),
286 hiometries of the reaction were confirmed by electrospray ionization mass spectrometry, using an emul
287 Additional experimental characterization by electrospray ionization mass spectrometry, UV-vis spectr
288 erence measurements, using bulk sampling and electrospray ionization mass spectrometry, various low-m
293 rix-assisted laser desorption/ionization and electrospray ionization mass spectrometry, we probe the
294 e using nuclear magnetic resonance (NMR) and electrospray ionization-mass spectrometry, we evidence h
296 pectroscopy, thermogravimetric analysis, and electrospray ionization mass spectrometry, which remarka
297 trate the utility of capillary microsampling electrospray ionization mass spectrometry with ion mobil
299 ltracentrifugation, electron microscopy, and electrospray ionization mass spectrometry, with a molecu
300 isomers, Au38T and Au38Q, as evidenced using electrospray ionization mass spectrometry, X-ray photoel
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