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1 one by electron energy loss spectroscopy and secondary ion mass spectrometry.
2 ion, desorption electrospray ionization, and secondary ion mass spectrometry.
3 terial, analogous to the sputtering yield in secondary ion mass spectrometry.
4 have been studied as primary ions for use in secondary ion mass spectrometry.
5 hotoelectron spectroscopy and time-of-flight secondary ion mass spectrometry.
6 ction products as NGLs by in situ TLC/liquid secondary ion mass spectrometry.
7 cent neoglycolipids, and sequenced by liquid secondary-ion mass spectrometry.
8 T and stable isotope labelling by nano-scale secondary ion mass spectrometry ((15)NH(3) assimilation)
9 An extraterrestrial origin is inferred from secondary ion mass spectrometry (18)O/(16)O and (17)O/(1
11 mbined fluorescent in situ hybridization and secondary ion mass spectrometry analyses, to identify an
14 as performed using 15 keV Ga+ time-of-flight secondary ion mass spectrometry and grazing incidence in
15 ntal imaging platform combining coregistered secondary ion mass spectrometry and high resolution seco
16 fficacy of ILs as matrices in time-of-flight secondary ion mass spectrometry and in mass spectrometri
18 alysis of organic surfaces in time-of-flight secondary ion mass spectrometry and opened up new capabi
20 ical analysis, scanning electron microscopy, secondary ion mass spectrometry and SDS-PAGE indicate th
21 sured by isotope-ratio mass spectrometry and secondary ion mass spectrometry) and redox-sensitive det
22 sing high-pressure freezing, high-resolution secondary ion mass spectrometry, and transmission electr
23 secondary ion mass spectrometry, high-energy secondary ion mass spectrometry, and X-ray photoelectron
24 n spectroscopy, Auger electron spectroscopy, secondary ion mass spectrometry, and X-ray photoelectron
25 elucidated by disaccharide analysis, liquid secondary-ion mass spectrometry, and 1H/13C NMR spectros
29 ance over random sampling is demonstrated on secondary ion mass spectrometry data, making it an inter
32 id-phase drug, was studied by time-of-flight secondary ion mass spectrometry employing 15-keV Ga+ and
34 try or thermal-ionization mass spectrometry, secondary ion mass spectrometry enables one to determine
35 ition method is effective for time-of-flight secondary ion mass spectrometry examination of polymers.
37 e in situ hybridization coupled to nanoscale secondary ion mass spectrometry (FISH-NanoSIMS), we dire
39 , imaging technique based on nanometer-scale secondary ion mass spectrometry for mapping the 3D eleme
40 boratories participated using time-of-flight secondary-ion mass spectrometry for analysis, three of t
44 ssisted laser desorption, and time-of-flight secondary ion mass spectrometry have been explored as po
47 chemical images created from time of flight-secondary ion mass spectrometry images from a patterned
51 e in situ hybridization with high-resolution secondary ion mass spectrometry imaging to characterize
52 This is particularly true of time-of-flight secondary ion mass spectrometry imaging where recent adv
54 ic force microscopy) and chemical (nanoscale secondary ion mass spectrometry) imaging on the same sam
55 ll as fluoride and chloride) was analyzed by secondary ion mass spectrometry in apatite [Ca(5)(PO(4))
56 species within intact mammalian cells using secondary ion mass spectrometry, including the simultane
58 methodologies with the latest generation of secondary ion mass spectrometry instrumentation, we show
62 secondary ion clusters using time-of-flight secondary ion mass spectrometry is reported for the firs
65 the target peptides were analyzed by liquid secondary ion mass spectrometry (LSIMS) and subjected to
66 e nearly simultaneous capabilities of liquid secondary ion mass spectrometry (LSIMS), matrix-assisted
67 lyzed by fast-atom bombardment (FAB), liquid secondary ion mass spectrometry (LSIMS), or electrospray
69 ethod has been developed for matrix-enhanced-secondary ion mass spectrometry (ME-SIMS) to investigate
70 ironmental temperature, further supported by secondary ion mass spectrometry measurements of in situ
74 table isotope probing coupled with nanoscale secondary ion mass spectrometry (nanoSIMS) and fluoresce
75 ter at the submicrometer scale, such as Nano Secondary Ion Mass Spectrometry (NanoSIMS) and Scanning
82 the nominal spatial resolution of nanoscale secondary ion mass spectrometry (NanoSIMS, 50-100 nm).
83 isted laser desorption/ionization and liquid secondary ion mass spectrometry of the first of two majo
84 sis required to obtain high depth resolution secondary ion mass spectrometry profiles from multiple G
85 nd infrared spectroscopy, and time-of-flight secondary ion mass spectrometry provided evidence for th
90 on of fluorescence in situ hybridization and secondary ion mass spectrometry shows that cells belongi
93 ased ion gun has been widely utilized in the secondary ion mass spectrometry (SIMS) analysis of organ
96 two powerful characterization tools, in situ secondary ion mass spectrometry (SIMS) and ex situ surfa
97 to prepare polymer bevel cross sections for secondary ion mass spectrometry (SIMS) applications was
99 acquisition during sputtering (e.g., dynamic secondary ion mass spectrometry (SIMS) depth profiling).
100 irradiation was used to greatly enhance the secondary ion mass spectrometry (SIMS) detection of Cs(+
101 etic cluster ion beams is a unique aspect of secondary ion mass spectrometry (SIMS) experiments.
103 e then used to direct subsequent microscopic secondary ion mass spectrometry (SIMS) imaging and tande
107 layer on glycine were examined with cluster secondary ion mass spectrometry (SIMS) in the event-by-e
112 doses much larger than the so-called static secondary ion mass spectrometry (SIMS) limit and demonst
113 m interference device (SQUID) microscopy and secondary ion mass spectrometry (SIMS) of sulfur isotope
114 drug and show, for the first time, that the secondary ion mass spectrometry (SIMS) positive ionizati
117 roduced during the Trinity nuclear test by a secondary ion mass spectrometry (SIMS) scanning ion imag
118 eeded to reach the peak of the corresponding secondary ion mass spectrometry (SIMS) signal response i
121 , X-ray photoelectron spectrometry (XPS) and secondary ion mass spectrometry (SIMS) were used to exam
122 er-resolution chemical images obtained using secondary ion mass spectrometry (SIMS) with the high-res
123 om positron annihilation spectroscopy (PAS), secondary ion mass spectrometry (SIMS), and deep level t
124 it is demonstrated that, when combined with secondary ion mass spectrometry (SIMS), it can provide c
126 e regarded as a specialized form of scanning secondary ion mass spectrometry (SIMS), referred to here
128 amples were also analyzed by 25 keV Bi(3)(+) secondary ion mass spectrometry (SIMS), with the negativ
135 It combines the high spatial resolution of secondary ion mass spectrometry (SIMS; under 200 nm for
136 C60+ results in high quality time-of-flight secondary ion mass spectrometry spectra, even during ion
139 synchrotron infrared spectroscopy, and nano-secondary ion mass spectrometry studies of these diamond
143 (C(60)) primary ion beam with time-of-flight secondary ion mass spectrometry to create molecule-speci
145 In this work, we have used high-resolution secondary ion mass spectrometry to directly map the dist
148 ted this hypothesis by using high-resolution secondary ion mass spectrometry to image the distributio
149 Here we make use of considerable advances in secondary ion mass spectrometry to obtain improved limit
151 , atomic force microscopy and time-of-flight secondary ion mass spectrometry to provide structural in
153 surements of worn surfaces by time-of-flight-secondary ion mass spectrometry (TOF-SIMS) accompanied f
155 Three-spatial-dimension (3D) time-of-flight-secondary ion mass spectrometry (TOF-SIMS) analysis can
156 nables in situ reactivity and time-of-flight secondary ion mass spectrometry (TOF-SIMS) analysis of s
158 ere performed primarily using time-of-flight secondary ion mass spectrometry (ToF-SIMS) and atomic fo
159 urface of a fingerprint using time-of-flight secondary ion mass spectrometry (ToF-SIMS) and desorptio
160 ptake batch experiments using time of flight-secondary ion mass spectrometry (ToF-SIMS) and detailed
161 th traditional MS techniques: time-of-flight secondary ion mass spectrometry (ToF-SIMS) and electrosp
164 analytical techniques such as time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray pho
166 lopment of 3D imaging cluster Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) as a label-fr
167 on the future exploitation of time of flight-secondary ion mass spectrometry (TOF-SIMS) as a surface
168 k), characterized directly by Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) at liquid nit
171 crospots were correlated with time-of-flight secondary ion mass spectrometry (TOF-SIMS) chemical stat
172 that multivariate analysis of time-of-flight secondary ion mass spectrometry (TOF-SIMS) data can be u
173 atterns were analyzed using a time-of-flight secondary ion mass spectrometry (ToF-SIMS) equipped with
174 he performance of traditional time-of-flight secondary ion mass spectrometry (TOF-SIMS) experiments f
175 1, 2) primary ions in static time-of-flight secondary ion mass spectrometry (TOF-SIMS) experiments w
176 artilage environment, we used time-of-flight secondary ion mass spectrometry (TOF-SIMS) for label-fre
183 display of three-dimensional time-of-flight secondary ion mass spectrometry (ToF-SIMS) imaging data
184 as cluster ion beams (GCIBs), time-of-flight secondary ion mass spectrometry (ToF-SIMS) imaging is no
186 elution time was obtained by time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging using
188 ric materials, if analyzed by time-of-flight secondary ion mass spectrometry (ToF-SIMS) in dual beam
199 ectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (TOF-SIMS) now permit mo
200 e reports a detailed study of time-of-flight-secondary ion mass spectrometry (TOF-SIMS) positive ion
202 id mixtures from single-pixel time-of-flight secondary ion mass spectrometry (TOF-SIMS) spectra in mo
203 d for interpreting the static time-of-flight secondary ion mass spectrometry (TOF-SIMS) spectra of ad
206 ssibility, as corroborated by time-of-flight secondary ion mass spectrometry (TOF-SIMS) sputter depth
208 ectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (TOF-SIMS) to analyze th
210 tes the first reported use of time-of-flight secondary ion mass spectrometry (ToF-SIMS) to assess phy
211 d samples were analyzed using time-of-flight secondary ion mass spectrometry (ToF-SIMS) to characteri
212 lls were depth profiled using time-of-flight secondary ion mass spectrometry (ToF-SIMS) to examine ch
214 n this work, we have employed time-of-flight secondary ion mass spectrometry (ToF-SIMS) to image chem
215 hotoelectron spectroscopy and time-of-flight secondary ion mass spectrometry (TOF-SIMS) to investigat
217 n films was investigated with time-of-flight secondary ion mass spectrometry (TOF-SIMS) using 10 keV
222 electron microscopy (SEM) and time-of-flight secondary ion mass spectrometry (TOF-SIMS) were used to
223 an be difficult to achieve in time-of-flight secondary ion mass spectrometry (TOF-SIMS) when the anal
225 ucture spectroscopy (NEXAFS), time-of-flight secondary ion mass spectrometry (TOF-SIMS), and surface
226 infrared spectroscopy (FTIR), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and transmis
227 maged without labels by using time-of-flight secondary ion mass spectrometry (TOF-SIMS), quantifying
228 nsgenic AD mouse brains using time-of-flight secondary ion mass spectrometry (ToF-SIMS), simultaneous
229 y introducing GCIB sputter to time-of-flight secondary ion mass spectrometry (TOF-SIMS), we analyzed
245 Argon cluster ion sources for sputtering and secondary ion mass spectrometry use projectiles consisti
246 lselenophene), P3HS, was measured by dynamic secondary ion mass spectrometry using a model bilayer st
248 techniques (electron microprobe analysis and secondary ion mass spectrometry), we show that some heav
250 instrumental neutron activation analysis and secondary ion mass spectrometry, we have observed system
251 imaging the same regions with time-of-flight secondary-ion-mass spectrometry, we correlate this photo
252 was performed in situ by combining 2-keV Cs+ secondary ion mass spectrometry with FT-ICR detection of
253 1] surfaces was studied using time-of-flight secondary-ion mass spectrometry, X-ray photoelectron spe
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