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1 type of mass spectrum commonly generated by gas chromatography mass spectrometry).
2 ouble-shot microfurnace pyrolysis coupled to gas chromatography mass spectrometry.
3 ign approach and samples were analysed using gas chromatography mass spectrometry.
4 ssessed by solid-phase microextraction using gas chromatography mass spectrometry.
5 ited testing laboratory with high-resolution gas chromatography mass spectrometry.
6 specimens, next-generation metagenomics, and gas chromatography mass spectrometry.
7 chromatography-tandem mass spectrometry and gas chromatography-mass spectrometry.
8 rofiling of cholesterols was performed using gas chromatography-mass spectrometry.
9 phenotyping platform, enzymatic assays, and gas chromatography-mass spectrometry.
10 alysis using solid-phase microextraction and gas chromatography-mass spectrometry.
11 easured END and ENL in 24-h urine samples by gas chromatography-mass spectrometry.
12 were analysed by solid-phase microextraction/gas chromatography-mass spectrometry.
13 analysed by solid-phase microextraction and gas chromatography-mass spectrometry.
14 Region (Southern Italy), were analyzed using gas chromatography-mass spectrometry.
15 Nicotine yield was quantified using gas chromatography-mass spectrometry.
16 loids was obtained by pyrolysis coupled with gas chromatography-mass spectrometry.
17 ds determined by solid-phase microextraction gas chromatography-mass spectrometry.
18 lar fractions, and composition determined by gas chromatography-mass spectrometry.
19 0 and 2462 subjects from NHANES 2009-2010 by gas chromatography-mass spectrometry.
20 nalyzed for a suite of PFAS using liquid and gas chromatography-mass spectrometry.
21 and 40 control subjects with diabetes using gas chromatography-mass spectrometry.
22 characterisation using whole-rock pyrolysis-gas chromatography-mass spectrometry.
23 transformation products using derivatization gas chromatography-mass spectrometry.
24 quency (MF) technique, and dynamic headspace gas chromatography-mass spectrometry.
25 The PCB contents were determined using gas chromatography-mass spectrometry.
26 flame retardants (BFRs), were measured using gas chromatography-mass spectrometry.
27 old transgenic sheep and matched controls by gas chromatography-mass spectrometry.
28 metabolites were determined using liquid and gas chromatography-mass spectrometry.
29 after post-harvest ripening, was explored by gas chromatography-mass spectrometry.
30 s for 175 pesticides amenable to liquid- and gas chromatography-mass spectrometry.
31 dynamic headspace extraction and analyzed by gas chromatography-mass spectrometry.
32 berries, blueberries, and raspberries) using gas chromatography-mass spectrometry.
33 volatile compounds was analysed by headspace gas chromatography-mass spectrometry.
34 eed with the fatty acid profiles gathered by gas chromatography-mass spectrometry.
35 han traditional methods (2.5 mug/L) based on gas chromatography-mass spectrometry.
36 asted chicken meat stored in plastic bags by gas chromatography-mass spectrometry.
37 Bs), and two organochlorine pesticides using gas chromatography-mass spectrometry.
38 olid-phase microextraction and quantified by gas chromatography-mass spectrometry.
39 e photometric detection, and confirmed using gas chromatography-mass spectrometry.
40 uran performed by isotope dilution headspace gas chromatography-mass spectrometry.
41 al and umbilical vein plasma was measured by gas chromatography-mass spectrometry.
42 lysis, transmission electron microscopy, and gas chromatography-mass spectrometry.
43 chemicals were identified and quantified by gas chromatography-mass spectrometry.
44 78 cats (>=7 y) in New York and Oregon using gas chromatography-mass spectrometry.
45 ied in Fucus algae, 14 could be confirmed by gas chromatography-mass spectrometry.
46 agnetic resonance experiments in addition to gas chromatography-mass spectrometry.
47 g gas chromatography-olfactometry as well as gas chromatography-mass spectrometry.
48 of PDMS/DVB into the oil matrix, followed by Gas Chromatography/Mass Spectrometry.
49 as measured using stable isotope tracers and gas chromatography/mass spectrometry.
50 serum neuroactive steroids were measured by gas chromatography/mass spectrometry.
51 stocks were then analyzed for impurities by gas chromatography/mass spectrometry.
52 chromatography/tandem mass spectrometry and gas chromatography/mass spectrometry.
53 derivatization processes were determined by gas chromatography/mass spectrometry.
54 using headspace solid phase micro extraction gas chromatography/mass spectrometry.
55 ing the carbon module labeling technique and gas chromatography/mass spectrometry.
56 d by nontargeted metabolomics analysis using gas chromatography/mass spectrometry.
57 tyrosine, serine and GABA were quantified by gas-chromatography-mass spectrometry.
58 " aromatic compounds were also quantified by gas-chromatography/mass-spectrometry.
59 were chemically extracted and analysed using Gas Chromatography - Mass Spectrometry.
65 saccharides from a drop of whole blood using gas chromatography-mass spectrometry analysis (GC-MS) of
67 of V CS and V PC fluxes using a combined NMR/gas chromatography-mass spectrometry analysis of plasma
68 Crude dissection of the seed followed by gas chromatography-mass spectrometry analysis of polar m
75 then employ metabolomics workflows utilizing gas chromatography mass spectrometry and liquid chromato
76 were identified as silylated derivatives by gas chromatography-mass spectrometry and by detecting th
77 t we identified via its methyl ester through gas chromatography-mass spectrometry and comparison with
78 were analysed by dynamic headspace sampling gas chromatography-mass spectrometry and descriptive ana
79 -AP by instrumental techniques, particularly gas chromatography-mass spectrometry and gas chromatogra
80 or the FA composition (molar percentage) and gas chromatography-mass spectrometry and gas chromatogra
81 In 940 mother-offspring pairs, we performed gas chromatography-mass spectrometry and identified 134
82 tween veraison and maturity, and analysed by gas chromatography-mass spectrometry and liquid chromato
83 nalis L. essential oil (REO) was analysed by gas chromatography-mass spectrometry and nuclear magneti
84 eostasis using comprehensive two-dimensional gas chromatography-mass spectrometry and real-time PCR (
85 min C and vitamin E content was performed by gas chromatography-mass spectrometry and the zinc and co
86 observational study of metabolomics by using gas chromatography-mass spectrometry and ultrahigh-perfo
87 etabolic profiling were performed by coupled gas chromatography/mass spectrometry and high-performanc
88 ill fluids were identified and quantified by gas chromatography-mass spectrometry, and two commonly u
89 ing a stable isotope infusion of D3-leucine, gas chromatography/mass spectrometry, and multicompartme
90 c carbon (DOC), volatile organic analysis by gas chromatography/mass spectrometry, and nonvolatile or
91 cinal plant extracts were investigated using gas chromatography-mass spectrometry, antiviral tests, a
92 liquid-liquid microextraction combined with gas chromatography-mass spectrometry as a new, fast and
94 le methodology Stir-Bar-Sorptive-Adsorption, Gas Chromatography-Mass Spectrometry based, permits the
96 dation, and photo-oxidation was untangled by gas chromatography-mass spectrometry-based oil fingerpri
97 d in the Portuguese coast was carried out by gas chromatography-mass spectrometry before and after al
98 nsive two-dimensional gas chromatography and gas chromatography/mass spectrometry by monitoring impor
100 e composition by Solid Phase Microextraction-Gas Chromatography/Mass Spectrometry confirmed that oxid
101 ualitative and semi-quantitative analysis by gas chromatography-mass spectrometry coupled to thermal
103 rsion-solid-phase microextraction coupled to gas chromatography mass spectrometry (DI-SPME-GC-MS) was
104 n-microextraction in solid phase followed by gas chromatography/mass spectrometry (DI-SPME-GC/MS).
105 on and identification by Electron-Ionization Gas Chromatography-Mass Spectrometry (EI-GC-MS) is prese
106 like high-performance liquid chromatography, gas chromatography-mass spectrometry, enzyme-linked immu
107 perimentally determined retention times from gas chromatography-mass spectrometry facilitated the ide
109 by stable isotope tracer analysis coupled to gas chromatography-mass spectrometry following treatment
110 liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry for metabolite iden
111 combined with comprehensive two-dimensional gas chromatography-mass spectrometry from a set of repre
112 silicone rod extraction, thermal desorption gas chromatography - mass spectrometry (GC-MS) to addres
115 ison with authentic standards analysed using gas chromatography mass spectrometry (GC-MS) and High Re
116 t detection (UV) and mass spectrometry (MS), gas chromatography mass spectrometry (GC-MS) and nuclear
117 ese aroma compounds was then evaluated using gas chromatography mass spectrometry (GC-MS) with headsp
121 Here, non-targeted metabolomics utilizing gas chromatography mass spectrometry (GC-MS/MS) and liqu
123 n of esters of the acids by multidimensional gas chromatography-mass spectrometry (GC x GC-MS), but r
124 and the volatiles released--by comprehensive gas chromatography-mass spectrometry (GC x GC-ToF-MS).
125 eatinine interconversion during LC-MS/MS and gas chromatography-mass spectrometry (GC-MS) analyses an
128 ferences in epicuticular wax morphology, and gas chromatography-mass spectrometry (GC-MS) analysis co
132 e A and type B) from baby foods, followed by gas chromatography-mass spectrometry (GC-MS) analysis.
133 enty serum fatty acids were quantified using gas chromatography-mass spectrometry (GC-MS) analysis.
134 ork presents a metabolomics study of cork by gas chromatography-mass spectrometry (GC-MS) and (1)H nu
135 igration to food simulants was determined by gas chromatography-mass spectrometry (GC-MS) and atmosph
137 European raw ham using a headspace (HS)-Trap gas chromatography-mass spectrometry (GC-MS) and GC-flam
140 tion or tandem mass spectrometry (MS/MS) and gas chromatography-mass spectrometry (GC-MS) are limited
141 gnetic resonance spectroscopy ((1)H NMR) and gas chromatography-mass spectrometry (GC-MS) based metab
144 phase microextraction (HS-SPME) coupled with gas chromatography-mass spectrometry (GC-MS) is commonly
145 s study, targeted and untargeted analysis by gas chromatography-mass spectrometry (GC-MS) is proposed
146 h (13)C-labeled glucose tracers, followed by gas chromatography-mass spectrometry (GC-MS) measurement
147 ols: BinVestigate, which queries the BinBase gas chromatography-mass spectrometry (GC-MS) metabolome
151 able to a well-optimized but more cumbersome gas chromatography-mass spectrometry (GC-MS) method.
152 (LSC), the compounds can be quantified using gas chromatography-mass spectrometry (GC-MS) or liquid c
154 id-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS) to identify
159 dynamic headspace sampling (DHS) coupled to gas chromatography-mass spectrometry (GC-MS), 79 volatil
160 used include ion mobility mass spectrometry, gas chromatography-mass spectrometry (GC-MS), and liquid
161 solvent-assisted flavour evaporation (SAFE), gas chromatography-mass spectrometry (GC-MS), gas chroma
162 s of solid-phase microextraction followed by gas chromatography-mass spectrometry (GC-MS), GC-olfacto
163 id chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), nuclear ma
164 fying these compounds on-site using portable gas chromatography-mass spectrometry (GC-MS), samples we
165 on-mass spectrometry (APCI-MS), coupled with gas chromatography-mass spectrometry (GC-MS), was used t
184 rgy dispersive x-ray spectroscopy (EDX), and Gas chromatography-mass spectrometry (GC/MS) were perfor
187 jected to Solid Phase Microextraction (SPME) Gas Chromatography/Mass Spectrometry (GC/MS) analysis.
188 es combined with mass spectrometric methods (gas chromatography/mass spectrometry (GC/MS) and liquid
189 transform mid infrared spectroscopy (FTIR), gas chromatography/mass spectrometry (GC/MS) and thermoc
190 ring of thousands of features extracted from gas chromatography/mass spectrometry (GC/MS) data from h
191 the difficulties to extract from the NMR or gas chromatography/mass spectrometry (GC/MS) experimenta
193 ted online dynamic in-tube extraction (ITEX)-gas chromatography/mass spectrometry (GC/MS) method for
195 irmed their expected behavior based on prior gas chromatography/mass spectrometry (GC/MS) studies.
196 he instrumentation and can be adapted to any gas chromatography/mass spectrometry (GC/MS) system, as
197 l detected solvent-extractable components by gas chromatography/mass spectrometry (GC/MS), also corre
198 a painting, in conjunction with analyses by gas chromatography/mass spectrometry (GC/MS), provided i
204 f fractions by comprehensive two-dimensional gas-chromatography mass-spectrometry (GC x GC/MS) and/or
205 Polar metabolite profiles were studied by gas-chromatography mass-spectrometry (GC-MS) and results
207 f subjects and therefore sample batching for gas-chromatography/mass spectrometry (GC/MS) non-targete
211 More than 50 compounds were identified in a gas chromatography-mass spectrometry headspace analysis
212 15 NAFLD-Ob) and 20 CTs without obesity, by gas chromatography-mass spectrometry, homeostasis model
213 sed by headspace solid-phase microextraction gas chromatography mass spectrometry (HS-SPME-GC-MS), id
214 tified by using solid phase micro-extraction gas chromatography mass spectrometry (HS-SPME-GC/MS).
215 pace solid-phase microextraction followed by gas chromatography mass spectrometry (HS-SPME/GC-MS).
216 using head space-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) in
217 ents a headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) met
218 elop a headspace solid-phase microextraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) met
219 phase micro-extraction technique coupled to gas chromatography-mass spectrometry (HS-SPME-GC-MS) was
220 ace solid-phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME-GC-MS) was
221 zed by Headspace Solid Phase Microextraction-Gas Chromatography-Mass Spectrometry (HS-SPME-GC-MS).
222 A nontargeted metabolomic approach, using gas chromatography-mass spectrometry, identifies fumarat
223 ven potential biomarkers were highlighted by gas chromatography-mass spectrometry in a training cohor
224 ore and after PEA treatment were measured by gas chromatography-mass spectrometry in relevant brain r
225 olid phase microextraction and chirospecific gas chromatography-mass spectrometry in selected ion mon
226 mpound identification and peak annotation in gas chromatography-mass spectrometry is usually made usi
227 In this study, we utilize a combination of gas chromatography-mass spectrometry, liquid chromatogra
228 (e.g., attenuated total reflection infrared, gas chromatography-mass spectrometry, liquid-state nucle
231 6 subjects) was carried out using liquid and gas chromatography-mass spectrometry metabolomics and st
232 ackages that preprocess untargeted liquid or gas chromatography-mass spectrometry metabolomics data b
239 tions to OMCOARSE, which in combination with gas chromatography mass spectrometry molecular markers q
240 ing three hyphenated metabolomics platforms: gas chromatography-mass spectrometry (MS); liquid chroma
242 described and compared for the first time by gas chromatography-mass spectrometry-olfactometry (GC-MS
243 on-stir bar sorptive extraction coupled with gas chromatography-mass spectrometry-olfactometry and ar
245 mical-sensory analyses with multidimensional gas-chromatography-mass spectrometry-olfactometry improv
246 The aroma profiles were characterized using Gas Chromatography/Mass Spectrometry/Olfactometry (GC/MS
249 combination of flash pyrolysis coupled with gas chromatography mass spectrometry (Py-GC-MS) together
250 used in SOPs identification, like pyrolysis gas chromatography mass spectrometry (Py-GC/MS), direct-
251 sis, pyrolysis-comprehensive two-dimensional gas chromatography/mass spectrometry (Py-GC x GC-MS), at
253 ionisation detection (Py-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and scan
255 microextraction and results were analyzed by gas chromatography-mass spectrometry quadrupole time-of-
259 thylsilyltrifluoroacetamide using a targeted gas chromatography-mass spectrometry running in selectiv
260 Headspace solid-phase microextraction with gas chromatography-mass spectrometry showed that as suga
261 via a static headspace sampler, followed by gas chromatography-mass spectrometry (SHS-GC/MS/MS).
262 e analyzed using solid-phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS) and tw
271 chromatography-tandem mass spectrometry and gas chromatography-mass spectrometry techniques that mos
272 hemical composition, measured with pyrolysis-gas chromatography/mass spectrometry, this being most im
273 hermally assisted hydrolysis and methylation gas chromatography/mass spectrometry (THM-GC/MS) to supp
274 rmally assisted hydrolysis and methylation - gas chromatography/mass spectrometry (THM-GC/MS), optica
275 ization of these extracts was carried out by gas chromatography-mass spectrometry: three iminosugars
276 quantitative analysis method using pyrolysis gas chromatography mass spectrometry to improve the dete
277 We conducted two case-control studies using gas chromatography-mass spectrometry to analyse maternal
279 ry and used untargeted liquid chromatography-gas chromatography-mass spectrometry to measure the milk
280 ana using passive organic vapor monitors and gas chromatography/mass spectrometry to determine if sel
281 We used solid-phase microextraction and gas chromatography/mass spectrometry to identify volatil
282 ve metabolomic profiling was performed using gas-chromatography/mass-spectrometry to compare urine sp
283 fraction released by HyPy was determined by gas chromatography-mass spectrometry, together with the
285 with solid phase micro extraction coupled to gas chromatography mass spectrometry was also performed.
287 oextraction (UDSA-DLLME) method coupled with gas chromatography-mass spectrometry was developed for t
288 on solid phase microextraction coupled with gas chromatography-mass spectrometry was optimized by te
289 lid-phase micro-extraction method coupled to gas chromatography-mass spectrometry was used to determi
290 mated solid-phase microextraction coupled to gas chromatography-mass spectrometry was used to measure
292 demulsification (AAD)-DLLME integrated with gas chromatography/mass spectrometry was developed for t
297 p and the residues were finally estimated by gas chromatography mass spectrometry with selected react
298 n heated purge-and-trap preconcentration and gas chromatography/mass spectrometry with selected-ion s
299 ons using thermal desorption two-dimensional gas-chromatography-mass-spectrometry with electron impac