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1 alyzed by liquid chromatography electrospray ionization mass spectrometry.
2 ser source is coupled with nano-electrospray ionization mass spectrometry.
3 les analyzed by direct infusion electrospray ionization mass spectrometry.
4 a hyphenated acoustic levitation and ambient ionization mass spectrometry.
5 ectroscopy, and mega-electron volt-secondary ionization mass spectrometry.
6 y 1:10 by liquid chromatography-electrospray ionization mass spectrometry.
7 n spectroscopy, and time-of-flight secondary ionization mass spectrometry.
8 ography and matrix-assisted laser desorption/ionization mass spectrometry.
9 array and positive mode in-line electrospray ionization mass spectrometry.
10 ubjected to matrix-assisted laser desorption/ionization mass spectrometry.
11 ted in solution for analysis by electrospray ionization mass spectrometry.
12 entified by matrix-assisted laser desorption/ionization mass spectrometry.
13 C and also can be characterized by electron ionization mass spectrometry.
14 ing in situ NMR experiments and electrospray ionization mass spectrometry.
15 y identified by high-resolution electrospray ionization mass spectrometry.
16 on of the Pu isotopic composition by thermal ionization mass spectrometry.
17 h LSPR and surface-assisted laser desorption/ionization mass spectrometry.
18 canning the gel with the electrostatic spray ionization mass spectrometry.
19 detection of the product by in situ ambient ionization mass spectrometry.
20 nanotube (CNT)-assisted low-voltage ambient ionization mass spectrometry.
21 uid chromatography coupled with electrospray ionization mass spectrometry.
22 on reaction using time-resolved electrospray ionization mass spectrometry.
23 pectroscopy and high-resolution electrospray ionization mass spectrometry.
24 cluster size was determined via electrospray ionization mass spectrometry.
25 ased upon liquid chromatography-electrospray ionization mass spectrometry.
26 carried out followed by three stage thermal ionization mass spectrometry (3STIMS) measurements for p
28 iving polymerase chain reaction/electrospray ionization-mass spectrometry a sensitivity of 81%, speci
29 chromatography-photodiode array-electrospray ionization-mass spectrometry (AccQ*Tag-UPLC-PDA-ESI-MS)
31 f water purification membranes using ambient ionization mass spectrometry, an attempt has been made t
32 By using matrix-assisted laser desorption ionization mass spectrometry analysis, we here identify
33 timing of the key events (sample desorption/ionization, mass spectrometry analysis, and sample trans
35 coupled to matrix-assisted laser desorption/ionization mass spectrometry and CLIP-Seq sequencing, we
37 lambdamax = 433 nm), confirmed by cryo-spray ionization mass spectrometry and EPR spectroscopy, along
38 rized using matrix-assisted laser desorption/ionization mass spectrometry and gel permeation chromato
40 ce (NMR) spectroscopy, nanoflow electrospray ionization mass spectrometry and size-exclusion chromato
41 s of a complex of ICL1:2-VIC by electrospray ionization mass spectrometry and X-ray crystallography c
42 ation by (1)H NMR spectroscopy, electrospray ionization mass spectrometry, and isothermal titration c
43 veromyces lactis, with nanoflow electrospray ionization mass spectrometry, and mapped intermolecular
45 ow by (27) Al NMR spectroscopy, electrospray-ionization mass spectrometry, and small- and wide-angle
46 or conjugation was confirmed by electrospray ionization-mass spectrometry, and radiolabeling was moni
47 hy (HPLC) with atmospheric pressure chemical ionization mass spectrometry (APCI-MS) is performed.
48 irect infusion atmospheric pressure chemical ionization mass spectrometry (APCI-MS) was compared to f
52 In particular, atmospheric pressure chemical ionization mass spectrometry ((-)APCI-MS) provided measu
55 on, scanning Auger microscopy, and secondary ionization mass spectrometry are used to characterize th
56 when using matrix-assisted laser desorption/ionization mass spectrometry as the detection method.
57 when using matrix-assisted laser desorption/ionization mass spectrometry as the detection method.
58 first time, matrix-assisted laser desorption ionization-mass spectrometry as a fast, reproducible and
59 were observed by gas-phase and electrospray ionization mass spectrometry, as well as by Fourier tran
61 observed using high-resolution electrospray ionization mass spectrometry, but these products are ide
62 new high-precision chemical abrasion thermal ionization mass spectrometry (CA-TIMS) U-Pb zircon ages
65 lication of a catch-and-release electrospray ionization mass spectrometry (CaR-ESI-MS) assay to quant
66 say, based on catch-and-release electrospray ionization mass spectrometry (CaR-ESI-MS), capable of si
67 cation of the catch-and-release electrospray ionization-mass spectrometry (CaR-ESI-MS) assay, impleme
68 , and capillary electrophoresis electrospray ionization mass spectrometry (CE-ESI-MS) to enable direc
70 cts was also conducted using online chemical ionization mass spectrometry (CI-TOFMS) where formamide,
71 h BrO and Br2, were conducted using chemical ionization mass spectrometry (CIMS) during the Bromine,
72 we used a coated-wall flow tube and chemical ionization mass spectrometry (CIMS) to study the pH depe
73 NOD2 activity were analyzed by electrospray ionization mass spectrometry, confirming the presence of
74 ery, we performed time-resolved electrospray ionization mass spectrometry coupled to hydrogen-deuteri
76 laboratory study for desorption electrospray ionization mass spectrometry (DESI MS) measurements has
77 branes, we have used desorption electrospray ionization mass spectrometry (DESI MS), where ion format
80 The use of ambient desorption electrospray ionization mass spectrometry (DESI-MS) and liquid extrac
81 and identified using desorption electrospray ionization mass spectrometry (DESI-MS) and nanoDESI-MS.
83 c breast cancer with Desorption Electrospray Ionization Mass Spectrometry (DESI-MS) imaging validated
85 on was enabled using desorption electrospray ionization mass spectrometry (DESI-MS) in combination wi
86 position of the CEI, desorption electrospray ionization mass spectrometry (DESI-MS) is applied to stu
87 ry on performance in desorption electrospray ionization mass spectrometry (DESI-MS) is assessed, as t
88 own on agar media by desorption electrospray ionization mass spectrometry (DESI-MS) is quite challeng
90 metry (ToF-SIMS) and desorption electrospray ionization mass spectrometry (DESI-MS) was demonstrated.
92 illustrates reactive desorption electrospray ionization mass spectrometry (DESI-MS) with a stable dic
93 techniques, such as desorption electrospray ionization mass spectrometry (DESI-MS), but such techniq
96 n that liquid sample desorption electrospray ionization-mass spectrometry (DESI-MS) is able to measur
99 er technique and gas chromatography/electron ionization mass spectrometry, enabled a comprehensive ch
100 with online detection by native electrospray ionization mass spectrometry (ESI MS) allows characteriz
101 NP) folding via high-resolution electrospray ionization mass spectrometry (ESI MS) coupled with size
102 In this work we use native electrospray ionization mass spectrometry (ESI MS) in combination wit
103 with online detection by native electrospray ionization mass spectrometry (ESI MS) to characterize a
104 of the hydrolysis of ACh using electrospray ionization mass spectrometry (ESI MS) to find out the me
105 t removal is a prerequisite for electrospray ionization mass spectrometry (ESI-MS) analysis of biolog
106 tripping (AP-CS) method for the electrospray ionization mass spectrometry (ESI-MS) analysis of hetero
109 of the ADC was characterized by electrospray ionization mass spectrometry (ESI-MS) and capillary isoe
110 l processing were identified by electrospray ionization mass spectrometry (ESI-MS) and characterized
111 purpose of this study is to use electrospray ionization mass spectrometry (ESI-MS) and immunohistoche
112 haracterized by low-temperature electrospray ionization mass spectrometry (ESI-MS) and IR spectroscop
113 urther structure elucidation by electrospray ionization mass spectrometry (ESI-MS) and measurements o
114 owerful new assay that combines electrospray ionization mass spectrometry (ESI-MS) and picodiscs, whi
115 which combines the proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay and model me
120 udies utilizing high-resolution electrospray ionization mass spectrometry (ESI-MS) identified several
121 iline (CPA, 1) and styrene 2 by electrospray ionization mass spectrometry (ESI-MS) in combination wit
122 liquid chromatography (LC) with electrospray ionization mass spectrometry (ESI-MS) in native conditio
123 t was recently established that electrospray ionization mass spectrometry (ESI-MS) is capable of capt
124 uid chromatography coupled with electrospray ionization mass spectrometry (ESI-MS) is routinely used
125 al challenge by enabling inline electrospray ionization mass spectrometry (ESI-MS) of low molecular w
127 l X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the clust
128 herograms and interference-free electrospray ionization mass spectrometry (ESI-MS) spectra of selecte
129 s, we have developed the use of electrospray ionization mass spectrometry (ESI-MS) to measure femtomo
131 ed polypeptide ions produced in electrospray ionization mass spectrometry (ESI-MS) with a beam of hig
132 We addressed here, by means of electrospray ionization mass spectrometry (ESI-MS) with ultrahigh res
133 Here, we used high-resolution electron-spray ionization mass spectrometry (ESI-MS), Carr-Purcell-Meib
142 e energy have been subjected to electrospray ionization mass spectrometry (ESI/MS) as well as to atte
144 d by swabbing and extracted for electrospray ionization-mass spectrometry (ESI-MS) analysis via a sim
145 strate narrow dynamic ranges in electrospray ionization-mass spectrometry (ESI-MS) and sought to esta
146 d rhG-CSF or pegfilgrastim), by electrospray ionization-mass spectrometry (ESI-MS) constitutes a chal
147 (EME) probe directly coupled to electrospray ionization-mass spectrometry (ESI-MS) for rapid extracti
148 H) and analyze all compounds by electrospray ionization-mass spectrometry (ESI-MS) in positive ion mo
150 id chromatography (UHPSFC) with electrospray ionization-mass spectrometry (ESI-MS) is presented in th
151 o not provide strong signals by electrospray ionization-mass spectrometry (ESI-MS) owing especially t
155 cal platforms, e.g., based upon electrospray ionization-mass spectrometry (ESI-MS), and software tool
156 change and it was confirmed by electrospray ionization-mass spectrometry (ESI-MS), proton nuclear ma
158 spectrometry (APCI-MS) was compared to field ionization mass spectrometry (FI-MS) for the determinati
159 injection analysis coupled with electrospray ionization mass spectrometry (FIA-ESI-MS).We used series
161 pability of matrix-assisted laser desorption ionization mass spectrometry for characterization of pep
162 phy coupled to atmospheric pressure chemical ionization mass spectrometry (GC-APCI-MS), a state of th
163 a complementary gas chromatography-electron ionization mass spectrometry (GC-EIMS) screen that utili
164 are derived from gas chromatography/electron ionization mass spectrometry (GC/EI-MS) measurements.
165 d directly by ambient-pressure helium-plasma ionization-mass spectrometry (HePI-MS), without the need
167 mance thin-layer chromatography-electrospray ionization mass spectrometry (HPTLC-ESI-MS) via the elut
169 ples, polymerase chain reaction/electrospray ionization-mass spectrometry identified a pathogen in 22
170 microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging (AP-SMALDI MSI) has
171 cer tissue that uses desorption electrospray ionization mass spectrometry imaging (DESI MSI), both as
172 feasibility of using desorption electrospray ionization mass spectrometry imaging (DESI-MSI) for iden
174 n approach combining desorption electrospray ionization mass spectrometry imaging (DESI-MSI) with the
176 rk, we used matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) to exam
177 n this work matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI MSI) was use
178 , including matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI MSI), liquid
179 resolution matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) and com
180 analysis by matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) and LES
182 e digestion matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) can be
183 tissue for matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) general
184 nd employed matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) in orde
185 We employed matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI), which
188 In situ nanospray desorption electrospray ionization mass spectrometry imaging (nano-DESI MSI) was
190 compounds, matrix-assisted laser desorption/ionization mass spectrometry imaging was utilized to vis
191 Utilizing matrix-assisted laser desorption ionization mass spectrometry imaging, we identified a nu
192 mineral surfaces by desorption electrospray ionization-mass spectrometry imaging (DESI-MSI) gives a
197 ization and matrix-assisted laser desorption ionization mass spectrometry in conjunction with thermog
198 zation of O isotope fractionation by thermal ionization mass spectrometry in variable loading and run
199 pled plasma-mass spectrometry]-[electrospray ionization-mass spectrometry]) in whole-plant extracts a
204 -cell capillary electrophoresis-electrospray ionization mass spectrometry is able to test whether dif
210 thod with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) for estimating
211 roach for liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS), where the elue
212 amples by liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) is often diffic
213 iquid chromatography coupled to electrospray ionization mass spectrometry (LC/MS) and the data proces
214 iquid chromatography coupled to electrospray ionization-mass spectrometry (LC-ESI-MS) is a versatile
215 aser desorption dielectric barrier discharge ionization mass spectrometry (LD-DBDI-MS)) is presented
216 esorption atmospheric pressure photochemical ionization mass spectrometry (LD/APPCI MS) for rapid thr
219 le profiling and imaging by laser-desorption ionization mass spectrometry (LDI-MS), but so far there
220 -MCEM) coupled with laser-induced desorption/ionization mass spectrometry (LDI-MS)-for the detection
222 The ionization of LS samples in desorption ionization mass spectrometry (LS DESI MS), supplied cont
224 analyzed by matrix assisted laser desorption/ionization mass spectrometry (MALDI MS) and liquid chrom
225 we applied matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) for the analysis
226 handling in matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) peptide and prot
228 grated with matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) analysis offers
229 lication of matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for the analysis
230 imaging by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a well-establ
231 ompounds by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is an important
232 formance of matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) is frequently co
233 lication of matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) profiling and im
234 e (SPR) and matrix assisted laser desorption ionization mass spectrometry (MALDI-MS) were used in com
240 od based on matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF MS) that allows
241 analyzed by matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS) except the phosp
242 orted using matrix assisted laser desorption/ionization-mass spectrometry (MALDI-MS), a common techni
244 Here, we present multicollector thermal ionization mass spectrometry (MC-TIMS) and multicollecto
248 ominated by strategies based on electrospray ionization, mass spectrometry (MS) methods using matrix-
250 resolution nanospray desorption electrospray ionization mass spectrometry (nano-DESI/HRMS), and ultra
252 nanoflow liquid chromatography-electrospray ionization-mass spectrometry (nanoLC-ESI-MS) detection.
253 e and polymerase chain reaction/electrospray ionization-mass spectrometry negative in 13 cases, and b
254 However, WO3(-) analysis by negative thermal ionization mass spectrometry normally results in a resid
255 nd subsequent offline secondary electrospray ionization mass spectrometry of exhaled breath and UHPLC
258 introduced plasma-assisted reaction chemical ionization mass spectrometry (PARCI-MS) for elemental an
259 PCR amplification coupled with electrospray ionization mass spectrometry (PCR-ESI-MS) plus blood cul
262 MD platforms, PCR combined with electrospray ionization mass spectrometry (PCR/ESI-MS) and molecular
263 describe the application of PCR-electrospray ionization mass spectrometry (PCR/ESI-MS) using a sample
272 This work shows the ability of resonance ionization mass spectrometry (RIMS) to determine (99g)Tc
274 -coupled plasma mass spectrometry or thermal-ionization mass spectrometry, secondary ion mass spectro
275 ystal X-ray crystallography and electrospray ionization mass spectrometry show that the cluster assem
279 that polymerase chain reaction/electrospray ionization-mass spectrometry technology could potentiall
280 ndent polymerase chain reaction/electrospray ionization-mass spectrometry technology with those obtai
281 ) under combustion-like conditions by photo-ionization mass spectrometry, the very first direct expe
283 tudies made largely possible by electrospray ionization mass spectrometry to determine the role of in
285 tion surface sampling probe for electrospray ionization-mass spectrometry to extract and ionize metab
286 ial resolution, and time-of-flight secondary ionization mass spectrometry (ToF-SIMS), a 2D chemical i
287 rformance liquid chromatography-electrospray ionization-mass spectrometry (UHPLC-ESI-MS), and partial
288 ce liquid chromatography-tandem electrospray ionization mass spectrometry (UPLC-MS/MS), vasculature-m
289 phy (GC) coupled to high-resolution electron ionization mass spectrometry, using both headspace and l
290 ements, using bulk sampling and electrospray ionization mass spectrometry, various low-molecular-weig
293 laser desorption/ionization and electrospray ionization mass spectrometry, we probe the nature of the
294 Using liquid chromatography-electrospray ionization-mass spectrometry, we identified 69 serum GPC
295 rmined with matrix-assisted laser desorption/ionization-mass spectrometry, whereas species with two 1
296 can be directly probed by means of chemical ionization mass spectrometry with a detection limit of a
297 lity of capillary microsampling electrospray ionization mass spectrometry with ion mobility separatio
298 C-ESI-MS (liquid chromatography-electrospray ionization-mass spectrometry) with the right chromatogra
299 ation, electron microscopy, and electrospray ionization mass spectrometry, with a molecular weight of
300 T and Au38Q, as evidenced using electrospray ionization mass spectrometry, X-ray photoelectron spectr
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