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1 EDS (despite high levels of eDNA loss during desorption).
2 rom photo-oxidation because of rapid thermal desorption.
3 DFT and confirmed by temperature-programmed desorption.
4 stribution in the particle plume after laser desorption.
5 uous-time random walks and simple adsorption-desorption.
6 a rigid porous form that is irreversible via desorption.
7 ion of adsorbed intermediate COOH* to be CO* desorption.
8 formation of the citrate-binding mode during desorption.
9 e pai-adsorption, but also enhanced ethylene desorption.
10 stability of vesicles after polymeric blend desorption.
11 fraction, (29)Si NMR and nitrogen adsorption-desorption.
12 50 mug of magnetic HLB particles, and 5 s of desorption.
15 e SMS unit was tested with automated thermal desorption after SMS to collect samples for GC-mass spec
16 ce, and, in particular, emphasizes roles for desorption and colloid formation in its mobilization.
17 um laser fluency of 27 W/mm(2) for efficient desorption and detection, providing the possibility for
24 copper/nanodiamond interface, suppressing CO desorption and promoting C(2) production by lowering the
27 died how pH changes the role of reduced S in desorption and retention of presorbed As in model peat.
30 contractile stress upon water absorption and desorption, and the rapid exchange of water drives locom
31 y atomic force microscopy, by inducing ssDNA desorption, and with molecular dynamics simulations.
32 n, As(V) electro-sorption, and As(V) electro-desorption are affected by aqueous pH with high oxidatio
33 ristics, capability, and origin of shale gas desorption are significant for understanding the shale g
34 mounted on the tip of the pen, magnifies the desorption area and enables a simple positioning of the
36 ite per mass of sorbent and was resilient to desorption at high ionic strength and in the presence of
38 t into the molecular composition and thermal desorption behavior of SOA that both clarifies and expan
41 hibits a positive correlation with shale gas desorption capability due to its large pores but low spe
45 investigated to validate its adsorption and desorption capacities for the zinc subgroup ions Zn(II),
46 Further, we proposed a two-stage adsorption/desorption chromatography comprising macroporous resin a
47 dic conditions but significantly enhanced As desorption compared to controls at neutral to alkaline p
49 or the understanding of Auger-stimulated ion desorption, Coulombic decay, photodynamic cancer therapi
50 tube mass spectrometry (SIFT-MS) and thermal desorption coupled to gas chromatography-mass spectromet
57 s with extraordinary stability to adsorption-desorption cycling with simulated humid flue gas and ena
58 ed, and the results reveal that sorption and desorption depend on the crystallinity, elasticity, and
60 tible chemical imaging of small molecules by desorption electrospray ionization (DESI) - MS of a comp
61 hard to overstate the tremendous utility of desorption electrospray ionization (DESI) and its variou
62 ssisted laser desorption ionization (MALDI), desorption electrospray ionization (DESI) and secondary
63 emonstrate the use of a HT platform based on desorption electrospray ionization (DESI) MS for the lab
64 ent implementation of this method for online desorption electrospray ionization (DESI) MS imaging of
65 powerful new chemical imaging capability in desorption electrospray ionization (DESI) MSI, which ena
69 this study, infrared, matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mass spe
71 of add-on components that adapt a commercial Desorption Electrospray Ionization Mass Spectrometry (DE
73 escribe a method using metabolic analysis by desorption electrospray ionization mass spectrometry (DE
74 strate the use of accelerated reactions with desorption electrospray ionization mass spectrometry (DE
75 od for the identification of CF by combining desorption electrospray ionization mass spectrometry and
80 her corroborated by a temperature-programmed desorption experiment, revealing the desorption of Ge-TP
84 l cores were removed from the field, used in desorption experiments, and characterized using wet chem
87 have been evaluated in an ambient air laser-desorption flexible microtube plasma ionization (LD-FmuT
88 oft ionization techniques such as soft laser desorption, for applications in areas like high-throughp
89 idation, As mobilization occurs via arsenate desorption from Fe-(hydr)oxides, primarily associated wi
95 of volatile GeO(x) formation and consequent desorption from the SiGe with ozone insertion during the
96 ificantly enhances discrimination of thermal desorption gas chromatography time-of-flight mass spectr
98 ation, and performance validation of a laser desorption imaging interface composed of add-on componen
99 simultaneous solvent regeneration and CO(2) desorption in a continuous system using a H(2)-recycling
100 PCS due to the vapor molecule adsorption and desorption induced changes in both polymer thickness and
101 te, whereas the dissociated methyl disfavors desorption into gas phase under the reactive conditions.
102 ptimisation and utilisation of ambient laser desorption ionisation (ALDI) for improved speciation acc
103 n a previously devised Matrix Assisted Laser Desorption Ionisation Mass Spectrometry (MALDI MS)-prote
105 urce platforms such as matrix-assisted laser desorption ionization (MALDI) and electrospray ionizatio
106 advantages compared to matrix-assisted laser desorption ionization (MALDI) and other IMS methods thro
108 spectrometry imaging: Matrix Assisted Laser Desorption Ionization (MALDI) Imaging and Laser Ablation
109 he landmark feature of matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry
110 ere investigated using matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry
113 ging methods including matrix-assisted laser desorption ionization (MALDI), desorption electrospray i
114 ection analysis (FIA), matrix assisted laser desorption ionization (MALDI), including MALDI-MS imagin
115 endogenous matrix in a matrix-assisted laser desorption ionization (MALDI)-like scenario, leading to
116 oring (MRM) and immuno-matrix-assisted laser desorption ionization (MALDI)] enables the development o
117 sing ORIGIN, a compact and lightweight laser desorption ionization - mass spectrometer designed and d
118 gs were followed up by matrix-assisted laser desorption ionization imaging, clinical chemistry, immun
119 resolved mass spectrometry (DTMS), and laser desorption ionization mass spectrometry (LDIMS), can be
120 ions by use of refined matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI M
122 ge tryptic peptides by matrix-assisted laser desorption ionization mass spectrometry of decalcified,
125 oupled to quantitative matrix-assisted laser desorption ionization time of flight mass spectrometry (
126 transform ion-cyclotron resonance and laser desorption ionization time-of-flight mass spectrometry,
127 and spatially resolved by low-fluence laser desorption ionization, coupled with high-resolution mass
128 and capsid dynamics by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analyse
129 rial identification by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass sp
130 atory methods included matrix-assisted laser desorption ionization-time of flight mass spectrometry (
131 probes (PNA-FISH) and matrix-assisted laser desorption ionization-time of flight mass spectrometry (
133 ing ARESdb compared to matrix-assisted laser desorption ionization-time of flight mass spectrometry (
135 colistin resistance by matrix-assisted laser desorption ionization-time of flight mass spectrometry (
136 NTM were identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry (
137 c biochemical testing, matrix-assisted laser desorption ionization-time of flight mass spectrometry (
138 phylococcus aureus One matrix-assisted laser desorption ionization-time of flight mass spectrometry (
139 ence typing (MLST) and Matrix-assisted laser desorption ionization-time of flight mass spectrometry (
140 's SOC, which included matrix-assisted laser desorption ionization-time of flight mass spectrometry (
141 ns confirmed as GAS by matrix-assisted laser desorption ionization-time of flight mass spectrometry p
145 ic analysis, especially exploited by ambient desorption/ionization (ADI) methods, provides numerous m
146 d atmospheric pressure matrix-assisted laser desorption/ionization (AP-MALDI) setup for high-throughp
147 For atmospheric pressure matrix assisted desorption/ionization (AP-MALDI), several ion sources, o
149 e Mycetocola proteome, matrix-assisted laser desorption/ionization (MALDI) analyses, and heterologous
150 One example of this is matrix-assisted laser desorption/ionization (MALDI) combined with in-source de
152 thodology that enables matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry
153 nd phospholipids using matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry
155 biological surfaces by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging
156 tify a multifunctional matrix-assisted laser desorption/ionization (MALDI) matrix for spatially resol
158 m rat brain tissue via matrix-assisted laser desorption/ionization (MALDI) with 1,4-phenylenedipropio
159 of these techniques is matrix-assisted laser desorption/ionization (MALDI), combined with in-source d
161 s were profiled using surface-enhanced laser desorption/ionization (SELDI) with time-of flight (TOF)
166 alysis, the utility of matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) is li
167 screening (HiTES) with matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for t
169 spectrometry (CE-MS), matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS), and
170 sembled monolayers for matrix-assisted laser desorption/ionization mass spectrometry (SAMDI-MS) analy
171 sembled monolayers for matrix-assisted laser desorption/ionization mass spectrometry (SAMDI-MS) to an
173 Recent advancements in matrix-assisted laser desorption/ionization mass spectrometry have enabled the
176 In this article, a matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI M
177 ultures (spheroids) by matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI M
178 om serum that combines matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI M
179 g acid hydrolysis with matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-M
180 y, we demonstrate that matrix assisted laser desorption/ionization mass spectrometry imaging (MALDI-M
181 pecific localizations, matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-M
182 urs, three-dimensional matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-M
184 eagent P) coupled with matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-M
186 abolites were obtained with ultraviolet (UV) desorption/ionization mass spectrometry imaging (UV-LDI-
187 roof-of-concept study, matrix-assisted laser desorption/ionization mass spectrometry imaging combined
189 the optimized ferric particle-assisted laser desorption/ionization mass spectrometry within 1 s using
191 zation (MALDI)-like scenario, leading to the desorption/ionization of biomolecules (lipids, metabolit
192 c protein oxidation by matrix-assisted laser desorption/ionization time of flight mass spectrometry (
193 ed and synthesized for matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass sp
194 ion platforms based on matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) MS anal
195 manual examination of matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) spectra
196 ophoresis coupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometer a
197 e separated conidia by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
198 s fingerprint (PMF) by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
199 short analysis times, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
200 ace of stainless-steel matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
201 cally characterized by Matrix Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (
202 or bacteria, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
203 AC) were determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
204 In this work, the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (
205 izing living chains by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry,
207 n shown to be effective substrates for laser desorption/ionization-mass spectrometry (LDI-MS) and hav
208 A), and is examined by matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS).
209 g application areas of matrix-assisted laser desorption/ionization-mass spectrometry imaging (MALDI-M
211 abolite profiling with matrix-assisted laser desorption/ionization-mass spectrometry imaging to inves
212 gh spectral resolution matrix-assisted laser desorption/ionization-mass spectrometry imaging was perf
213 trate the potential of matrix-assisted laser desorption/ionization-mass spectrometry imaging with PBC
214 ptide of histone H4 by matrix-assisted laser desorption/ionization-Q-MSI (MALDI-Q-MSI), using a mixtu
215 horesis (SDS-PAGE) and matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass sp
216 ria were identified by matrix-assisted laser desorption/ionization-time of flight mass spectrometry,
217 f infectious diseases, matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (
220 were characterized using nitrogen adsorption/desorption isotherms, scanning electron microscopy, Four
221 is approach for the quantification of soil P desorption kinetic parameters found a wide range of equa
222 e phosphorus labile pool (P(labile)) and its desorption kinetics were simultaneously evaluated in 10
223 ery restricted, which affects their sorption/desorption kinetics when used as sorbent materials.
224 1) at 1 bar and 298 K), rapid adsorption and desorption kinetics, and promising CO(2)/CH(4) separatio
225 se brain and in human colon samples with the desorption laser spot size 15 mum, emphasizing the poten
227 ction (PXRD) studies and nitrogen adsorption-desorption measurements demonstrate the formation of pro
229 bited first-order growth kinetics, while the desorption mediated decay of the citrate signal followed
230 mation with m/z values identifiable with one desorption method sufficient to reveal cancer regions be
232 ermediate adsorption, electron transfer, and desorption occurring at the electrolyte-electrode interf
235 The measurement of the potential dependent desorption of a monolayer of a pyridine derivative (4-di
236 simply heating the sample in water, but the desorption of Br(-) ions will expose the underneath Pd a
240 Zn and Cu diel cycles as a combination of a desorption of exopolymeric substance-metal complexes and
242 ll allowed us to accomplish the simultaneous desorption of high-purity CO(2) stream and regeneration
244 e-programmed desorption of NH(3), adsorption/desorption of N(2) at -196 degrees C, and thermogravimet
245 y, X-ray diffraction, temperature-programmed desorption of NH(3), adsorption/desorption of N(2) at -1
247 ain homolog of PIP2, we showed that the fast desorption of PIP2 is facilitated by presence of an arac
248 at terraces and steps, leading to the abrupt desorption of poisoning CO from all crystal facets at th
249 mer film stability suggests that the partial desorption of polymers in the presence of the ions does
252 energies were used to determine the heat of desorption of the [EMIM][MeSO(3)]/water system, and the
253 at occurs on the surface species followed by desorption of the oxidized surface species from the gold
254 is attributed to competition between thermal desorption of the primary photoproduct and secondary pho
255 e waterborne exposure ceased, reflecting the desorption of weakly bound U from the insect's integumen
256 projected influence of rate-limited sorption/desorption on PFOS transport at the field scale was inve
257 we quantified the effect of this asymmetric desorption on the spontaneous membrane curvature. Furthe
258 mited, hysteretic, and irreversible sorption/desorption on transport was investigated through experim
259 tion and characteristics, and the adsorption-desorption operational parameters on the long-term stabi
260 of controlling both CO(2) adsorption and CO desorption over supported metal catalysts by employing a
261 of phthalate esters including adsorption and desorption parameters were investigated and optimized us
263 , and powder bed thickness on the adsorption-desorption process are explored for achieving optimal op
265 Ni and P atoms nearby Pv, and facilitate H* desorption process, contributing to outstanding HER acti
267 es, it is possible to control the adsorption/desorption processes as well as the organization and dyn
269 of micro- and nanoplastics based on thermal desorption-proton transfer reaction-mass spectrometry.
272 suggest mobilization to proceed via arsenite desorption, reaction with dissolved or surface-bound red
275 ion and preconcentration of antimony such as desorption solvent type, concentration and volume, desor
276 timulated desorption experiments and thermal desorption spectrometry further reveals that thermal rea
279 s spectrometry (GC-MS) combined with thermal desorption (TD-GC-MS) was used to identify and quantify
281 tion solvent type, concentration and volume, desorption temperature and time, sample pH, amount of so
284 s for promoted hydride coupling and hydrogen desorption, the catalysts produce hydrogen at a current
285 tion solvent type and volume, sample volume, desorption time, and ionic strength were studied and at
287 voltammetry (CV), and temperature-programmed desorption (TPD) measurements, this approach allows us (
288 ile organic compound emissions using thermal desorption two-dimensional gas-chromatography-mass-spect
289 perates under the concept of a flow-isolated desorption volume, which generates a stagnant droplet op
291 minutes after dilution, suggesting that the desorption was asymmetric and also generated membrane cu
294 O(3)]/water system, and the obtained heat of desorption was in good agreement with that calculated fr
295 ition of water was found to promote methanol desorption, water does not change the methanol steady st
298 tent U, increased with pH, likely reflecting desorption, while higher Cr and V levels were measured i
299 p chemistry dictated the kinetics of citrate desorption, while the guest ligand concentration played
300 conditions, we experimentally achieved CO(2) desorption with an energy consumption of 374 kJ.mol(-1)