ライフサイエンスコーパス: gas chromatography-mass spectrometry

1 type of mass spectrum commonly generated by gas chromatography mass spectrometry).

2 ited testing laboratory with high-resolution gas chromatography mass spectrometry.

3 Sediment PAH levels were determined using gas chromatography mass spectrometry.

4 ssessed by solid-phase microextraction using gas chromatography mass spectrometry.

5 ns of head space solid phase microextraction gas chromatography mass-spectrometry.

6 s for 175 pesticides amenable to liquid- and gas chromatography-mass spectrometry.

7 analysed by solid-phase microextraction and gas chromatography-mass spectrometry.

8 dynamic headspace extraction and analyzed by gas chromatography-mass spectrometry.

9 volatile compounds was analysed by headspace gas chromatography-mass spectrometry.

10 eed with the fatty acid profiles gathered by gas chromatography-mass spectrometry.

11 han traditional methods (2.5 mug/L) based on gas chromatography-mass spectrometry.

12 asted chicken meat stored in plastic bags by gas chromatography-mass spectrometry.

13 Bs), and two organochlorine pesticides using gas chromatography-mass spectrometry.

14 dynamic headspace extraction and analysed by gas chromatography-mass spectrometry.

15 , and polychlorinated biphenyls (PCBs) using gas chromatography-mass spectrometry.

16 myces cerevisiae was evaluated by liquid and gas chromatography-mass spectrometry.

17 matography with tandem mass spectrometry and gas chromatography-mass spectrometry.

18 and 15 PCBs were measured by high resolution gas chromatography-mass spectrometry.

19 precursors were prepared and investigated by gas chromatography-mass spectrometry.

20 lysed by gas chromatography-olfactometry and gas chromatography-mass spectrometry.

21 postnatal day 7 and day 14) were measured by gas chromatography-mass spectrometry.

22 Dust was analyzed for 13 pesticides using gas chromatography-mass spectrometry.

23 vacuum cleaners, and measured 12 PAHs using gas chromatography-mass spectrometry.

24 were analysed by solid-phase microextraction/gas chromatography-mass spectrometry.

25 Region (Southern Italy), were analyzed using gas chromatography-mass spectrometry.

26 loids was obtained by pyrolysis coupled with gas chromatography-mass spectrometry.

27 ds determined by solid-phase microextraction gas chromatography-mass spectrometry.

28 0 and 2462 subjects from NHANES 2009-2010 by gas chromatography-mass spectrometry.

29 and 40 control subjects with diabetes using gas chromatography-mass spectrometry.

30 characterisation using whole-rock pyrolysis-gas chromatography-mass spectrometry.

31 transformation products using derivatization gas chromatography-mass spectrometry.

32 quency (MF) technique, and dynamic headspace gas chromatography-mass spectrometry.

33 The PCB contents were determined using gas chromatography-mass spectrometry.

34 flame retardants (BFRs), were measured using gas chromatography-mass spectrometry.

35 old transgenic sheep and matched controls by gas chromatography-mass spectrometry.

36 metabolites were determined using liquid and gas chromatography-mass spectrometry.

37 after post-harvest ripening, was explored by gas chromatography-mass spectrometry.

38 derivatization processes were determined by gas chromatography/mass spectrometry.

39 using headspace solid phase micro extraction gas chromatography/mass spectrometry.

40 lysed using Solid Phase Micro-Extraction and gas chromatography/mass spectrometry.

41 as measured using stable isotope tracers and gas chromatography/mass spectrometry.

42 rs of the best eb-SWPH were identified using gas chromatography/mass spectrometry.

43 ampled from the headspace, and determined by gas chromatography/mass spectrometry.

44 liquid chromatography/mass spectrometry and gas chromatography/mass spectrometry.

45 esis and glycosyl composition analysis using gas chromatography/mass spectrometry.

46 of PDMS/DVB into the oil matrix, followed by Gas Chromatography/Mass Spectrometry.

47 serum neuroactive steroids were measured by gas chromatography/mass spectrometry.

48 stocks were then analyzed for impurities by gas chromatography/mass spectrometry.

49 chromatography/tandem mass spectrometry and gas chromatography/mass spectrometry.

50 were chemically extracted and analysed using Gas Chromatography - Mass Spectrometry.

51 ion (dHS-SPME) combined with one-dimensional gas chromatography-mass spectrometry (1D-GC-qMS).

52 state NMR spectroscopy of the powders and by gas chromatography-mass spectrometry analyses of compoun

53 Gas chromatography-mass spectrometry analyses reveal tha

54 Gas chromatography-mass spectrometry analyses revealed a

55 sample and time consuming using traditional gas chromatography mass spectrometry analysis.

56 saccharides from a drop of whole blood using gas chromatography-mass spectrometry analysis (GC-MS) of

57 pace solid phase microextraction followed by gas chromatography-mass spectrometry analysis (HS-SPME-G

58 ompare it to conventional techniques such as gas chromatography-mass spectrometry analysis and TBARS

59 Combined gas chromatography-mass spectrometry analysis of acid hy

60 A Solid-Phase Microextraction method for the Gas Chromatography-Mass Spectrometry analysis of blackbe

61 eling of barley (Hordeum vulgare) plants and gas chromatography-mass spectrometry analysis of free am

62 of V CS and V PC fluxes using a combined NMR/gas chromatography-mass spectrometry analysis of plasma

63 Crude dissection of the seed followed by gas chromatography-mass spectrometry analysis of polar m

64 Gas chromatography-mass spectrometry analysis revealed t

65 Thin-layer chromatography and gas chromatography-mass spectrometry analysis suggested

66 Gas chromatography-mass spectrometry analysis was used f

67 y and total fatty acid content obtained from gas chromatography-mass spectrometry analysis.

68 acrylamide in various food samples prior to gas chromatography-mass spectrometry analysis.

69 IVOCs were quantified through gas chromatography/mass spectrometry analysis of adsorbe

70 d lignin chemistry on the basis of pyrolysis-gas chromatography/mass spectrometry analysis.

71 s an unresolved complex mixture (UCM) during gas-chromatography mass-spectrometry analysis.

72 were analysed by dynamic headspace sampling gas chromatography-mass spectrometry and descriptive ana

73 We also identified host-derived odorants by gas chromatography-mass spectrometry and found that many

74 or the FA composition (molar percentage) and gas chromatography-mass spectrometry and gas chromatogra

75 -AP by instrumental techniques, particularly gas chromatography-mass spectrometry and gas chromatogra

76 tween veraison and maturity, and analysed by gas chromatography-mass spectrometry and liquid chromato

77 nalis L. essential oil (REO) was analysed by gas chromatography-mass spectrometry and nuclear magneti

78 observational study of metabolomics by using gas chromatography-mass spectrometry and ultrahigh-perfo

79 e newer techniques with the more established gas chromatography/mass spectrometry and attenuated tota

80 etabolic profiling were performed by coupled gas chromatography/mass spectrometry and high-performanc

81 analyzed by thermal desorption combined with gas chromatography/mass spectrometry and HPLC/UV analysi

82 ing a stable isotope infusion of D3-leucine, gas chromatography/mass spectrometry, and multicompartme

83 c carbon (DOC), volatile organic analysis by gas chromatography/mass spectrometry, and nonvolatile or

84 In this work, we apply a recently developed gas chromatography mass spectrometry approach utilizing

85 liquid-liquid microextraction combined with gas chromatography-mass spectrometry as a new, fast and

86 le methodology Stir-Bar-Sorptive-Adsorption, Gas Chromatography-Mass Spectrometry based, permits the

87 d in the Portuguese coast was carried out by gas chromatography-mass spectrometry before and after al

88 nsive two-dimensional gas chromatography and gas chromatography/mass spectrometry by monitoring impor

89 In this study Curie-Point pyrolysis-gas chromatography-mass spectrometry combined with therm

90 intensive care unit validated via hyphenated gas chromatography-mass spectrometry confirm the viabili

91 e composition by Solid Phase Microextraction-Gas Chromatography/Mass Spectrometry confirmed that oxid

92 The extraction amount was quantified by gas chromatography-mass spectrometry coupled with a ther

93 ss analytical technology pipeline, combining gas chromatography-mass spectrometry data preprocessing

94 Based on gas chromatography-mass spectrometry data, approximately

95 Volatile compounds were analysed by gas chromatography-mass spectrometry detection after acc

96 factorial design matrix and desorbed into a gas chromatography-mass spectrometry detector.

97 perimentally determined retention times from gas chromatography-mass spectrometry facilitated the ide

98 ase microextraction, and then analysed using gas chromatography-mass spectrometry/flame ionisation de

99 liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry for metabolite iden

100 asa', 'Williams' and 'Zelig') was studied by gas chromatography-mass spectrometry for the first time.

101 safe (QuEChERS) method and determination by gas chromatography mass spectrometry (GC-EI-MS).

102 ison with authentic standards analysed using gas chromatography mass spectrometry (GC-MS) and High Re

103 t detection (UV) and mass spectrometry (MS), gas chromatography mass spectrometry (GC-MS) and nuclear

104 ese aroma compounds was then evaluated using gas chromatography mass spectrometry (GC-MS) with headsp

105 Using gas chromatography mass spectrometry (GC-MS), we identif

106 .1 +/- 0.8% (n = 3, 1sigma) as measured with gas chromatography mass spectrometry (GC-MS).

107 orrelate with TCA cycle flux, as measured by gas chromatography mass spectrometry (GC-MS); and electr

108 Here, non-targeted metabolomics utilizing gas chromatography mass spectrometry (GC-MS/MS) and liqu

109 hromatography, and ionization, especially in gas chromatography mass spectrometry (GC/MS).

110 ns using headspace and direct immersion SPME gas chromatography mass spectrometry (GC/MS).

111 n of esters of the acids by multidimensional gas chromatography-mass spectrometry (GC x GC-MS), but r

112 and the volatiles released--by comprehensive gas chromatography-mass spectrometry (GC x GC-ToF-MS).

113 safe (QuEChERS) method and determination by gas chromatography-mass spectrometry (GC-EI-MS).

114 eatinine interconversion during LC-MS/MS and gas chromatography-mass spectrometry (GC-MS) analyses an

115 The gas chromatography-mass spectrometry (GC-MS) analyses re

116 Gas chromatography-mass spectrometry (GC-MS) analysis in

117 In addition we performed gas chromatography-mass spectrometry (GC-MS) analysis of

118 s-2-decenoic acid production, as revealed by gas chromatography-mass spectrometry (GC-MS) analysis of

119 Gas chromatography-mass spectrometry (GC-MS) analysis re

120 Gas chromatography-mass spectrometry (GC-MS) analysis re

121 e A and type B) from baby foods, followed by gas chromatography-mass spectrometry (GC-MS) analysis.

122 ted by solid phase extraction of samples and gas chromatography-mass spectrometry (GC-MS) analysis.

123 raction (DHE), solid-phase extraction (SPE), gas chromatography-mass spectrometry (GC-MS) and gas chr

124 extraction (SPE), respectively, followed by gas chromatography-mass spectrometry (GC-MS) and gas chr

125 European raw ham using a headspace (HS)-Trap gas chromatography-mass spectrometry (GC-MS) and GC-flam

126 Gas chromatography-mass spectrometry (GC-MS) and liquid

127 lipophilic leaf extracts were analyzed with gas chromatography-mass spectrometry (GC-MS) and preproc

128 truffles by using Electronic nose (E-nose), gas chromatography-mass spectrometry (GC-MS) and sensory

129 ction yield or contamination contrary to the gas chromatography-mass spectrometry (GC-MS) approach wh

130 Conventional analyses based on gas chromatography-mass spectrometry (GC-MS) are limited

131 Using gas chromatography-mass spectrometry (GC-MS) as a system

132 gnetic resonance spectroscopy ((1)H NMR) and gas chromatography-mass spectrometry (GC-MS) based metab

133 nvolves a concerted approach by applying the gas chromatography-mass spectrometry (GC-MS) fingerprint

134 For this, gas chromatography-mass spectrometry (GC-MS) has been la

135 phase microextraction (HS-SPME) coupled with gas chromatography-mass spectrometry (GC-MS) is commonly

136 ols: BinVestigate, which queries the BinBase gas chromatography-mass spectrometry (GC-MS) metabolome

137 A simple, fast, sensitive, and robust gas chromatography-mass spectrometry (GC-MS) method for

138 A reproducible gas chromatography-mass spectrometry (GC-MS) method usin

139 A gas chromatography-mass spectrometry (GC-MS) method was

140 able to a well-optimized but more cumbersome gas chromatography-mass spectrometry (GC-MS) method.

141 (LSC), the compounds can be quantified using gas chromatography-mass spectrometry (GC-MS) or liquid c

142 Unbiased gas chromatography-mass spectrometry (GC-MS) profiling r

143 Chemical characterisation of mentha oil by gas chromatography-mass spectrometry (GC-MS) revealed th

144 30 different glycan nodes are detectable per gas chromatography-mass spectrometry (GC-MS) run.

145 the saffron were separated and determined by gas chromatography-mass spectrometry (GC-MS) technique.

146 The analyses were carried out by gas chromatography-mass spectrometry (GC-MS) using micro

147 Gas chromatography-mass spectrometry (GC-MS) was used to

148 n-Alkane profiles established by gas chromatography-mass spectrometry (GC-MS) were used t

149 dynamic headspace sampling (DHS) coupled to gas chromatography-mass spectrometry (GC-MS), 79 volatil

150 petroleum have relied almost exclusively on gas chromatography-mass spectrometry (GC-MS), although m

151 solvent-assisted flavour evaporation (SAFE), gas chromatography-mass spectrometry (GC-MS), gas chroma

152 s of solid-phase microextraction followed by gas chromatography-mass spectrometry (GC-MS), GC-olfacto

153 btained by hydrodistillation and analyzed by gas chromatography-mass spectrometry (GC-MS), giving car

154 gae of the Portuguese coast were analysed by gas chromatography-mass spectrometry (GC-MS), leading to

155 ed using well-established techniques such as gas chromatography-mass spectrometry (GC-MS), liquid chr

156 id chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), nuclear ma

157 space solid-phase microextraction (SPME) and gas chromatography-mass spectrometry (GC-MS), using the

158 on-mass spectrometry (APCI-MS), coupled with gas chromatography-mass spectrometry (GC-MS), was used t

159 horus detection was used in conjunction with gas chromatography-mass spectrometry (GC-MS), which dete

160 IR) analysis, X-ray diffractometry (XRD) and gas chromatography-mass spectrometry (GC-MS).

161 been tentatively identified with the aid of gas chromatography-mass spectrometry (GC-MS).

162 The laser plume was analyzed by gas chromatography-mass spectrometry (GC-MS).

163 s performed in methanol and then analyzed by gas chromatography-mass spectrometry (GC-MS).

164 d phase extraction (SPE), and analysed using gas chromatography-mass spectrometry (GC-MS).

165 dmium (Cd) stresses has been performed using gas chromatography-mass spectrometry (GC-MS).

166 Aroma composition of papaya was analysed by gas chromatography-mass spectrometry (GC-MS).

167 g fruit ripening in mango (cv. Chausa) using gas chromatography-mass spectrometry (GC-MS).

168 action (HS-SPME) and separation/detection by gas chromatography-mass spectrometry (GC-MS).

169 occo were analysed by gas chromatography and gas chromatography-mass spectrometry (GC-MS).

170 PUF/XAD-4/PUF adsorbents and measured using gas chromatography-mass spectrometry (GC-MS).

171 isation Detection (GC-FID) and identified by Gas Chromatography-Mass Spectrometry (GC-MS).

172 romatography-mass spectrometry (HPLC-MS) and gas chromatography-mass spectrometry (GC-MS).

173 with a PDMS/Carboxen/DVB fibre, coupled with gas chromatography-mass spectrometry (GC-MS).

174 drop microextraction (MD-HS-SDME) coupled to gas chromatography-mass spectrometry (GC-MS).

175 phase microextraction (HS-SPME) coupled with gas chromatography-mass spectrometry (GC-MS).

176 e were identified and quantified by means of gas chromatography-mass spectrometry (GC-MS).

177 ne fatty acids were isolated and analyzed by gas chromatography-mass spectrometry (GC-MS).

178 solid-phase microextraction (MA-HS-SPME) and gas chromatography-mass spectrometry (GC-MS).

179 lora L. by hydrodistillation and analysed by gas chromatography-mass spectrometry (GC-MS).

180 handling system to enable their detection by gas chromatography-mass spectrometry (GC-MS).

181 dispersive liquid-liquid microextraction and gas chromatography-mass spectrometry (GC-MS).

182 ce solid phase microextraction (HS-SPME) and gas chromatography-mass spectrometry (GC-qMS) analysis,

183 microextraction (automated DLLME) coupled to gas chromatography-mass spectrometry (GC/MS) analysis, h

184 magnetic resonance ((1)H NMR) spectroscopy, gas chromatography-mass spectrometry (GC/MS) fingerprint

185 Eight F-acids were identified by gas chromatography-mass spectrometry (GC/MS) in male gon

186 Currently, there is radioimmunoassay, gas chromatography-mass spectrometry (GC/MS), and liquid

187 extraction (SPE) to later be analysed using gas chromatography-mass spectrometry (GC/MS).

188 ed by solid phase microextraction (SPME) and gas chromatography-mass-spectrometry (GC/MS), showed mor

189 module (fast-GC module) for direct-sampling gas chromatography/mass spectrometry (GC-MS).

190 lidated by species-specific isotope dilution gas chromatography/mass spectrometry (GC/MS) analysis of

191 jected to Solid Phase Microextraction (SPME) Gas Chromatography/Mass Spectrometry (GC/MS) analysis.

192 ombines denuder sampling of gaseous I(2) and gas chromatography/mass spectrometry (GC/MS) analysis.

193 interpreted using analytical methods such as gas chromatography/mass spectrometry (GC/MS) and gas chr

194 es combined with mass spectrometric methods (gas chromatography/mass spectrometry (GC/MS) and liquid

195 romatography-mass spectrometry (HPLC-MS) and gas chromatography/mass spectrometry (GC/MS) data object

196 urately classified by pattern recognition of gas chromatography/mass spectrometry (GC/MS) data.

197 the difficulties to extract from the NMR or gas chromatography/mass spectrometry (GC/MS) experimenta

198 Gas chromatography/mass spectrometry (GC/MS) has long be

199 Gas chromatography/mass spectrometry (GC/MS) is a primar

200 To quantify these compounds gas chromatography/mass spectrometry (GC/MS) is used.

201 Head-space gas chromatography/mass spectrometry (GC/MS) of urinary

202 irmed their expected behavior based on prior gas chromatography/mass spectrometry (GC/MS) studies.

203 he instrumentation and can be adapted to any gas chromatography/mass spectrometry (GC/MS) system, as

204 be confidently identified using traditional gas chromatography/mass spectrometry (GC/MS) techniques.

205 l detected solvent-extractable components by gas chromatography/mass spectrometry (GC/MS), also corre

206 id chromatography-mass spectrometry (LC-MS), gas chromatography/mass spectrometry (GC/MS), capillary

207 a painting, in conjunction with analyses by gas chromatography/mass spectrometry (GC/MS), provided i

208 Identification of unknown peaks in gas chromatography/mass spectrometry (GC/MS)-based disco

209 determination of derivatized amino acids by gas chromatography/mass spectrometry (GC/MS).

210 ne for electron ionization (EI) spectra from gas chromatography/mass spectrometry (GC/MS).

211 major components of microbial biomass using gas chromatography/mass spectrometry (GC/MS).

212 precursor: lathosterol) were carried out by gas chromatography/mass spectrometry (GC/MS).

213 rmination of their ethyl esters by headspace gas chromatography/mass spectrometry (GC/MS).

214 able-isotope labeling in algal biomass using gas chromatography/mass spectrometry (GC/MS).

215 In this study, we used a targeted gas-chromatography mass spectrometry (GC-MS) approach to

216 were the primary chemicals identified using gas-chromatography mass spectrometry (GC-MS).

217 f fractions by comprehensive two-dimensional gas-chromatography mass-spectrometry (GC x GC/MS) and/or

218 Polar metabolite profiles were studied by gas-chromatography mass-spectrometry (GC-MS) and results

219 Gas-chromatography-mass spectrometry (GC-MS) and gas-chr

220 f subjects and therefore sample batching for gas-chromatography/mass spectrometry (GC/MS) non-targete

221 Herein, using Gas Chromatography Mass Spectrometry (GCMS), we demonstr

222 s from the same patients was investigated by gas chromatography-mass spectrometry (GCMS)-based metabo

223 id-phase microextraction (SPME) coupled with gas-chromatography mass spectrometry (GCMS).

224 Comprehensive gas chromatography-mass spectrometry (GCxGC-ToF-MS) was

225 More than 50 compounds were identified in a gas chromatography-mass spectrometry headspace analysis

226 15 NAFLD-Ob) and 20 CTs without obesity, by gas chromatography-mass spectrometry, homeostasis model

227 phase micro-extraction (SPME), coupled with gas chromatography-mass spectrometry (HRGC-MS).

228 bed and applied to the analysis of headspace gas chromatography mass spectrometry (HS-GC/MS) data of

229 Headspace solid-phase microextraction gas chromatography mass spectrometry (HS-SPME-GC-MS) exp

230 tified by using solid phase micro-extraction gas chromatography mass spectrometry (HS-SPME-GC/MS).

231 phase micro-extraction technique coupled to gas chromatography-mass spectrometry (HS-SPME-GC-MS) was

232 ng headspace solid-phase microextraction and gas chromatography-mass spectrometry (HS-SPME-GC/MS).

233 A nontargeted metabolomic approach, using gas chromatography-mass spectrometry, identifies fumarat

234 lpha was measured primarily by ELISA, and by gas chromatography-mass spectrometry in a subset, expres

235 ylalanine enrichments were assessed by using gas chromatography-mass spectrometry in duodenal protein

236 ification of the analytes was carried out by gas chromatography-mass spectrometry in negative chemica

237 olid phase microextraction and chirospecific gas chromatography-mass spectrometry in selected ion mon

238 d from cupressaceous trees, as determined by gas chromatography-mass spectrometry, infrared spectrosc

239 ring to attention that the protocol used for gas chromatography/mass spectrometry involved hydrolysis

240 ilanol in air, as well as a preconcentration gas chromatography/mass spectrometry laboratory method f

241 In this study, we utilize a combination of gas chromatography-mass spectrometry, liquid chromatogra

242 (e.g., attenuated total reflection infrared, gas chromatography-mass spectrometry, liquid-state nucle

243 Gas chromatography-mass spectrometry metabolomics analys

244 ackages that preprocess untargeted liquid or gas chromatography-mass spectrometry metabolomics data b

245 We performed targeted and nontargeted gas chromatography/mass spectrometry metabolomics on mat

246 A sensitive, selective, efficient gas chromatography-mass spectrometry method for the simu

247 With the aim to develop a new gas chromatography-mass spectrometry method to analyze 2

248 We established a gas chromatography-mass spectrometry method, which allow

249 alysis patients and healthy controls using a gas chromatography-mass spectrometry method.

250 ork, we established and validated liquid and gas chromatography-mass spectrometry methods to determin

251 tions to OMCOARSE, which in combination with gas chromatography mass spectrometry molecular markers q

252 ing three hyphenated metabolomics platforms: gas chromatography-mass spectrometry (MS); liquid chroma

253 Gas chromatography mass spectrometry-olfactometry and fl

254 to (Lycopersicum esculentum) was analyzed by gas chromatography-mass spectrometry-olfactometry (GC-MS

255 saffron (Crocus sativus L.) were analyzed by gas chromatography-mass spectrometry-olfactometry.

256 mical-sensory analyses with multidimensional gas-chromatography-mass spectrometry-olfactometry improv

257 racterized and compared using purge and trap gas chromatography-mass spectrometry (PT-GC-MS).

258 Pyrolysis gas chromatography/mass spectrometry (Py-GC-MS) is used

259 ionisation detection (Py-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and scan

260 Pyrolysis coupled to gas chromatography/mass spectrometry (Py-GC/MS) was used

261 TAG accumulation was verified using gas chromatography-mass spectrometry quantification of t

262 Gas chromatography-mass spectrometry revealed higher fae

263 Gas chromatography-mass spectrometry selected ion monito

264 Gas chromatography-mass spectrometry showed that the pre

265 using headspace solid phase microextraction gas chromatography mass spectrometry (SPME-GC-MS), and q

266 e analyzed using solid-phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS) and tw

267 ette smoke using solid-phase microextraction gas chromatography-mass spectrometry (SPME-GC-MS).

268 e ((1)H NMR) and Solid Phase Microextraction-Gas Chromatography/Mass Spectrometry (SPME-GC/MS).

269 e in order to improve the sensitivity of the gas chromatography-mass spectrometry system.

270 -free thermal modulator for thermal analysis-gas chromatography-mass spectrometry (TA-GC-MS).

271 in this work by thermal analysis coupled to gas chromatography-mass spectrometry (TA-GC-MS).

272 D5 in end-exhaled air by thermal desorption gas chromatography mass spectrometry (TD-GC-MS), to dete

273 and processed offline by thermal-desorption gas chromatography-mass spectrometry (TD-GC-MS).

274 g in a thermodenuder, and thermal desorption/gas chromatography/mass spectrometry (TD-GC-MS) analysis

275 er (TD) measurements, and thermal-desorption gas-chromatography mass-spectrometry (TD-GC-MS).

276 ions were determined with thermal extraction-gas chromatography-mass spectrometry (TE-GC-MS) and ther

277 chromatography-tandem mass spectrometry and gas chromatography-mass spectrometry techniques that mos

278 Here we used gas-chromatography/mass-spectrometry techniques to decon

279 l ether analyses were performed by headspace-gas chromatography-mass spectrometry/thermal conductivit

280 ization of these extracts was carried out by gas chromatography-mass spectrometry: three iminosugars

281 We employed gas chromatography-mass spectrometry to identify the deg

282 determined by using a lipidomic analysis and gas chromatography-mass spectrometry to provide objectiv

283 This study used gas chromatography-mass spectrometry to quantify 94 urin

284 We used solid-phase microextraction and gas chromatography/mass spectrometry to identify volatil

285 ve metabolomic profiling was performed using gas-chromatography/mass-spectrometry to compare urine sp

286 fraction released by HyPy was determined by gas chromatography-mass spectrometry, together with the

287 with solid phase micro extraction coupled to gas chromatography mass spectrometry was also performed.

288 Liquid and gas chromatography mass spectrometry was used to profile

289 oextraction (UDSA-DLLME) method coupled with gas chromatography-mass spectrometry was developed for t

290 Gas chromatography-mass spectrometry was used to assess

291 lid-phase micro-extraction method coupled to gas chromatography-mass spectrometry was used to determi

292 demulsification (AAD)-DLLME integrated with gas chromatography/mass spectrometry was developed for t

293 Using gas chromatography-mass spectrometry, we first identifie

294 Using thermal desorption-gas chromatography/mass spectrometry, we characterized t

295 p and the residues were finally estimated by gas chromatography mass spectrometry with selected react

296 A reliable gas chromatography-mass spectrometry with a QuEChERS pro

297 Samples were analyzed using pyrolysis-gas chromatography-mass spectrometry with in situ hexame

298 n heated purge-and-trap preconcentration and gas chromatography/mass spectrometry with selected-ion s

299 etection is a fundamental step for liquid or gas chromatography mass spectrometry (XC-MS) data analys

300 employing pressurized liquid extraction and gas chromatography-mass spectrometry yielded efficient r