ライフサイエンスコーパス: gas chromatography

1 ions were confirmed by mass spectrometry and gas chromatography.

2 hese compounds were applied using liquid and gas chromatography.

3 nd diet-related metabolites were measured by gas chromatography.

4 e quantified with closed static chambers and gas chromatography.

5 of blood lipid fractions were determined by gas chromatography.

6 Serum fatty acids were measured by gas chromatography.

7 We determined serum-PC fatty acids with gas chromatography.

8 tegrated with comprehensive two -dimensional gas chromatography.

9 e not available and had to be measured using gas chromatography.

10 in the practical domain of comprehensive 2D gas chromatography.

11 ed fires were achieved using two-dimensional gas chromatography.

12 using headspace solid-phase microextraction-gas chromatography.

13 A profiles of F&M samples were measured with gas chromatography.

14 aortic valves from 25 patients with AS using gas chromatography.

15 is developed for high-speed one-dimensional gas chromatography (1D-GC), comprehensive two-dimensiona

16 C(18:0)) fatty acids purified by preparative gas chromatography(5-8).

17 Spectroscopic and gas chromatography analyses are applied to evaluate the

18 n results were consistent with the data from gas chromatography analysis.

19 Gas chromatography and 3D-fluorescence enabled to differ

20 analyses using comprehensive two-dimensional gas chromatography and flame ionization detection, which

21 urine and fecal metabolites were analyzed by gas chromatography and liquid chromatography-mass spectr

22 During bulk electrolysis experiments, gas chromatography and mass spectrometry analysis of the

23 Here, we used gas chromatography and mass spectrometry to determine th

24 using headspace solid phase microextraction, gas chromatography and mass spectrometry, including 1-no

25 g derivatization followed by two-dimensional gas chromatography and time of flight mass spectrometry.

26 od cell fatty acid profiles were measured by gas chromatography and were used to estimate SCD-1 indic

27 The paper presents a parallel micro gas chromatography approach using three ionic liquid sem

28 thods for antibiotic detection, e.g., liquid/gas chromatography, are based on complicated instruments

29 Gas chromatography-atmospheric pressure chemical ionizat

30 ion and quantification of MeHg and InHg with gas chromatography-cold vapor atomic fluorescence spectr

31 capillary are widely used for combustion in gas chromatography combustion isotope ratio mass spectro

32 Gas chromatography-combustion-isotope ratio mass spectro

33 A gas chromatography-combustion-isotope ratio mass spectro

34 details the assessment of the suitability of gas chromatography-combustion-isotope ratio mass spectro

35 ne its delta(15)N value (delta(15)N(Arg)) by gas chromatography-combustion-isotope ratio mass spectro

36 romatography, and analyses were performed by gas chromatography/combustion/isotope ratio mass spectro

37 dem mass spectrometry) and fatty acid (using gas chromatography) concentrations were measured in huma

38 was established in the last decade employing gas chromatography connected to multiple-collector induc

39 id/acetate buffer, was applied together with gas chromatography coupled to a triple quadrupole mass s

40 in certain cases, degree of branching) using gas chromatography coupled to a unit-mass-resolution ele

41 hase microextraction (HS-SPME) technique and gas chromatography coupled to both mass spectrometry and

42 kaged from a batch of RM can be evaluated by gas chromatography coupled to flame ionization detection

43 ling of cereal lipids using high temperature gas chromatography coupled to high resolution mass spect

44 s-anethole) in different pepper varieties by gas chromatography coupled to high-resolution mass spect

45 enotypes using comprehensive two-dimensional gas chromatography coupled to high-resolution time-of-fl

46 Therefore, discovery-based multidimensional gas chromatography coupled to high-resolution time-of-fl

47 ith ethanol followed by quantification using gas chromatography coupled to mass spectrometry.

48 roducing compounds and were studied by using gas chromatography coupled to mass spectrometry.

49 ne/polydimethylsiloxane (DVB/PDMS) fiber and gas chromatography coupled to mass spectrophotometry (GC

50 products using ultra performance liquid and gas chromatography coupled to tandem mass spectroscopy (

51 ese samples were analysed by high resolution gas chromatography coupled with accurate mass time-of-fl

52 d profile and cholesterol were determined by gas chromatography coupled with flame ionisation detecti

53 Samples were processed using Gas Chromatography coupled with Mass Spectrometry (GC-MS

54 coupled with mass spectrometry (HPLC-MS) and gas chromatography coupled with mass spectrometry (GC-MS

55 In this study, gas chromatography coupled with mass spectrometry (GC-MS

56 High-performance liquid chromatography or gas chromatography coupled with mass spectrometry was us

57 are a very promising approach alternative to gas chromatography coupled with mass spectrometry.

58 iquid extraction, solid-phase extraction and gas chromatography coupled with mass spectrometry.

59 The acrylamide level was quantified using gas chromatography coupled with the mass spectrometry (G

60 developed for comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spec

61 Coupled gas chromatography-electroantennography (GC-EAG) was use

62 ngle-drop microextraction method followed by gas chromatography-electron capture detection was develo

63 Gas chromatography/electron-ionization mass spectrometry

64 ase microextraction (HFLMP-SPME) followed by gas chromatography- flame ionization detection.

65 spectrometry, thin-layer chromatography, and gas chromatography-flame ionization detection analytical

66 tro models of oral mucosa, at equilibrium by Gas-Chromatography-Flame Ionization Detection (GC-FID) a

67 Single-crystal X-ray diffraction and gas chromatography further indicate that the metallocycl

68 ased systems (e.g. Time-of-Flight ToF-MS and gas chromatography GC combined with MS) and compact port

69 n column using comprehensive two-dimensional gas chromatography (GC x GC) for the separation of mixtu

70 ed into a comprehensive two-dimensional (2D) gas chromatography (GC x GC) system coupled with low- an

71 (1D-GC), comprehensive two-dimensional (2D) gas chromatography (GC x GC), and comprehensive three-di

72 spectrometry (FT-ICR MS) and two-dimensional gas chromatography (GC x GC), the results showed that th

73 C x GC), and comprehensive three-dimensional gas chromatography (GC(3)).

74 ion of the encapsulated EO was identified by gas chromatography (GC) and nuclear magnetic resonance (

75 hod where fluorinated compounds separated by gas chromatography (GC) are converted to Na(2)F(+) for n

76 A thermal desorber and a multicapillary gas chromatography (GC) column are coupled to a secondar

77 Head-space (HS) gas chromatography (GC) coupled to mass spectrometry (MS

78 cid, oxylipin and phenolic composition using gas chromatography (GC) coupled to mass spectrometry (MS

79 ed by thermal desorption in combination with gas chromatography (GC) coupled to single quadrupole mas

80 Nuclear magnetic resonance (NMR) and gas chromatography (GC) demonstrate that the hybrid elec

81 hemical ionization mass spectrometry (MS) or gas chromatography (GC) hyphenated with MS).

82 w rates (up to 4.0 mL/min) is delivered into gas chromatography (GC) open-tubular columns (OTC, 0.18

83 way of quantifying them is the use of online gas chromatography (GC), a method that is not compatible

84 red to PLS1-DA models using data obtained by gas chromatography (GC), or global composition through m

85 Ion Mobility Spectrometry (IMS) coupled to Gas Chromatography (GC), provides a rapid, sensitive, co

86 of flight mass spectrometry (MALDI-TOF MS), gas chromatography (GC), SDS-PAGE, Toll-like receptor 4

87 sidue analysis: the matrix effect related to gas chromatography (GC), which can adversely affect quan

88 ile organic compounds (VOCs), frequently use gas chromatography (GC), which typically requires high-p

89 nt ion is achieved when performing classical gas chromatography (GC)-EI-MS analysis.

90 and most of them can be detected using both gas chromatography (GC)-MS and liquid chromatography (LC

91 rized and quantified by EPR spectroscopy and gas chromatography (GC).

92 dour using electroantennography coupled with gas chromatography (GC-EAG), with 16 peaks triggering re

93 high-performance, stainless-steel microchip gas-chromatography (GC) column that is capable of analyz

94 e early 1990s, comprehensive two-dimensional gas chromatography (GCxGC) has evolved from a separation

95 Comprehensive two-dimensional gas chromatography (GCxGC) is a powerful analytical tool

96 resentation in comprehensive two-dimensional gas chromatography (GCxGC) is described.

97 d PACs, we use comprehensive two-dimensional gas chromatography-high resolution mass spectrometry (GC

98 g of diesel oil spills using two-dimensional gas chromatography-high resolution mass spectrometry (GC

99 assays and were in this study analyzed using gas chromatography-high resolution mass spectrometry for

100 ce solid-phase microextraction combined with gas chromatography (HS-SPME/GC), fluorescence and circul

101 to overcome the main obstacle for the use of gas chromatography in metabolomics, namely, the derivati

102 Gas chromatography-ion mobility spectrometry enables non

103 st in vivo study that shows the potential of gas chromatography-ion mobility spectrometry for early d

104 Gas chromatography-ion mobility spectrometry gas analysi

105 The dual separation in gas chromatography-ion mobility spectrometry generates c

106 ilator-associated pneumonia we determined if gas chromatography-ion mobility spectrometry is able to

107 o IR spectra measured both in the gas phase (gas chromatography IR) and in solution.

108 ss spectrometry (LC-IRMS) and derivatization gas chromatography-IRMS (GC-IRMS), respectively.

109 A nano-gravimetric detector (NGD) for gas chromatography is based on a nanoelectromechanical a

110 nced photoacoustic spectroscopy coupled with gas chromatography is used to quantitatively analyze a m

111 (+0.05 per mille) by complementary methods (gas chromatography-isotope ratio mass spectrometry, GC-I

112 chromatography-mass spectrometry (GC-MS) and gas chromatography-isotope ratio mass spectromety (GC-IR

113 each of the current monitoring technologies (gas chromatography, lead acetate tape, electrochemical,

114 d very low-density lipoprotein palmitate via gas chromatography mass spectometry.

115 rsion-solid-phase microextraction coupled to gas chromatography mass spectrometry (DI-SPME-GC-MS) was

116 ed organochlorine pesticides and hormones by gas chromatography mass spectrometry (GC-MS).

117 sed by headspace solid-phase microextraction gas chromatography mass spectrometry (HS-SPME-GC-MS), id

118 pace solid-phase microextraction followed by gas chromatography mass spectrometry (HS-SPME/GC-MS).

119 combination of flash pyrolysis coupled with gas chromatography mass spectrometry (Py-GC-MS) together

120 used in SOPs identification, like pyrolysis gas chromatography mass spectrometry (Py-GC/MS), direct-

121 then employ metabolomics workflows utilizing gas chromatography mass spectrometry and liquid chromato

122 Often pyrolysis gas chromatography mass spectrometry has been used as pa

123 quantitative analysis method using pyrolysis gas chromatography mass spectrometry to improve the dete

124 ouble-shot microfurnace pyrolysis coupled to gas chromatography mass spectrometry.

125 ign approach and samples were analysed using gas chromatography mass spectrometry.

126 specimens, next-generation metagenomics, and gas chromatography mass spectrometry.

127 Headspace solid-phase microextraction gas-chromatography mass-spectrometry was chosen to quant

128 silicone rod extraction, thermal desorption gas chromatography - mass spectrometry (GC-MS) to addres

129 on and identification by Electron-Ionization Gas Chromatography-Mass Spectrometry (EI-GC-MS) is prese

130 ight mass spectrometry (PTR-ToF-MS) and fast gas chromatography-mass spectrometry (fast-GC-MS).

131 Gas chromatography-mass spectrometry (GC-MS) analyses of

132 ferences in epicuticular wax morphology, and gas chromatography-mass spectrometry (GC-MS) analysis co

133 On the basis of gas chromatography-mass spectrometry (GC-MS) analysis, t

134 enty serum fatty acids were quantified using gas chromatography-mass spectrometry (GC-MS) analysis.

135 ork presents a metabolomics study of cork by gas chromatography-mass spectrometry (GC-MS) and (1)H nu

136 igration to food simulants was determined by gas chromatography-mass spectrometry (GC-MS) and atmosph

137 We performed gas chromatography-mass spectrometry (GC-MS) and gas chr

138 tion or tandem mass spectrometry (MS/MS) and gas chromatography-mass spectrometry (GC-MS) are limited

139 Gas chromatography-mass spectrometry (GC-MS) combined wi

140 oach, MSHub, to enable auto-deconvolution of gas chromatography-mass spectrometry (GC-MS) data.

141 s study, targeted and untargeted analysis by gas chromatography-mass spectrometry (GC-MS) is proposed

142 h (13)C-labeled glucose tracers, followed by gas chromatography-mass spectrometry (GC-MS) measurement

143 id-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS) to identify

144 In this study, gas chromatography-mass spectrometry (GC-MS) was employe

145 Gas chromatography-mass spectrometry (GC-MS) was used fo

146 used include ion mobility mass spectrometry, gas chromatography-mass spectrometry (GC-MS), and liquid

147 fying these compounds on-site using portable gas chromatography-mass spectrometry (GC-MS), samples we

148 ride and glycosyl-linkage compositions using gas chromatography-mass spectrometry (GC-MS).

149 croextraction (SPME) and were analyzed using gas chromatography-mass spectrometry (GC-MS).

150 d from grave exhumations were analysed using gas chromatography-mass spectrometry (GC-MS).

151 hase microextraction (HS-SPME) combined with gas chromatography-mass spectrometry (GC-MS).

152 high throughput metabolomics analysis using gas chromatography-mass spectrometry (GC-MS).

153 etic resonance spectrometry ((13)C-NMR), and gas chromatography-mass spectrometry (GC-MS).

154 (AEDA) but remained difficult to quantify by gas chromatography-mass spectrometry (GC-MS).

155 , gas chromatography-olfactometry (GC-O) and gas chromatography-mass spectrometry (GC-MS).

156 rgy dispersive x-ray spectroscopy (EDX), and Gas chromatography-mass spectrometry (GC/MS) were perfor

157 using head space-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) in

158 elop a headspace solid-phase microextraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) met

159 ace solid-phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME-GC-MS) was

160 zed by Headspace Solid Phase Microextraction-Gas Chromatography-Mass Spectrometry (HS-SPME-GC-MS).

161 via a static headspace sampler, followed by gas chromatography-mass spectrometry (SHS-GC/MS/MS).

162 (SIFT-MS) and thermal desorption coupled to gas chromatography-mass spectrometry (TD-GC-MS).

163 The results of gas chromatography-mass spectrometry analyses and bioass

164 ormed by Magnetic Resonance Spectroscopy and Gas Chromatography-Mass Spectrometry analyses.

165 Gas chromatography-mass spectrometry analysis further in

166 ns of free and bound VOCs were determined by gas chromatography-mass spectrometry analysis.

167 were identified as silylated derivatives by gas chromatography-mass spectrometry and by detecting th

168 t we identified via its methyl ester through gas chromatography-mass spectrometry and comparison with

169 In 940 mother-offspring pairs, we performed gas chromatography-mass spectrometry and identified 134

170 eostasis using comprehensive two-dimensional gas chromatography-mass spectrometry and real-time PCR (

171 min C and vitamin E content was performed by gas chromatography-mass spectrometry and the zinc and co

172 Gas chromatography-mass spectrometry based untargeted me

173 ualitative and semi-quantitative analysis by gas chromatography-mass spectrometry coupled to thermal

174 by stable isotope tracer analysis coupled to gas chromatography-mass spectrometry following treatment

175 combined with comprehensive two-dimensional gas chromatography-mass spectrometry from a set of repre

176 ven potential biomarkers were highlighted by gas chromatography-mass spectrometry in a training cohor

177 ore and after PEA treatment were measured by gas chromatography-mass spectrometry in relevant brain r

178 mpound identification and peak annotation in gas chromatography-mass spectrometry is usually made usi

179 Gas chromatography-mass spectrometry measurements of the

180 6 subjects) was carried out using liquid and gas chromatography-mass spectrometry metabolomics and st

181 ectral deconvolution workflow for untargeted gas chromatography-mass spectrometry metabolomics.

182 Gas chromatography-mass spectrometry profiling is the mo

183 microextraction and results were analyzed by gas chromatography-mass spectrometry quadrupole time-of-

184 The total bacteria count and gas chromatography-mass spectrometry results revealed th

185 thylsilyltrifluoroacetamide using a targeted gas chromatography-mass spectrometry running in selectiv

186 Headspace solid-phase microextraction with gas chromatography-mass spectrometry showed that as suga

187 -MCPD and 1,3-DCP contents using a validated gas chromatography-mass spectrometry technique.

188 We conducted two case-control studies using gas chromatography-mass spectrometry to analyse maternal

189 ry and used untargeted liquid chromatography-gas chromatography-mass spectrometry to measure the milk

190 Further targeted metabolomics by gas chromatography-mass spectrometry uncovered the ident

191 on solid phase microextraction coupled with gas chromatography-mass spectrometry was optimized by te

192 mated solid-phase microextraction coupled to gas chromatography-mass spectrometry was used to measure

193 Gas chromatography-mass spectrometry was used.

194 ill fluids were identified and quantified by gas chromatography-mass spectrometry, and two commonly u

195 cinal plant extracts were investigated using gas chromatography-mass spectrometry, antiviral tests, a

196 like high-performance liquid chromatography, gas chromatography-mass spectrometry, enzyme-linked immu

197 The find was analyzed using pyrolysis-gas chromatography-mass spectrometry, X-ray micro-comput

198 A highly sensitive, gas chromatography-mass spectrometry-based method was de

199 dation, and photo-oxidation was untangled by gas chromatography-mass spectrometry-based oil fingerpri

200 described and compared for the first time by gas chromatography-mass spectrometry-olfactometry (GC-MS

201 on-stir bar sorptive extraction coupled with gas chromatography-mass spectrometry-olfactometry and ar

202 uran performed by isotope dilution headspace gas chromatography-mass spectrometry.

203 al and umbilical vein plasma was measured by gas chromatography-mass spectrometry.

204 lysis, transmission electron microscopy, and gas chromatography-mass spectrometry.

205 chemicals were identified and quantified by gas chromatography-mass spectrometry.

206 78 cats (>=7 y) in New York and Oregon using gas chromatography-mass spectrometry.

207 ied in Fucus algae, 14 could be confirmed by gas chromatography-mass spectrometry.

208 agnetic resonance experiments in addition to gas chromatography-mass spectrometry.

209 g gas chromatography-olfactometry as well as gas chromatography-mass spectrometry.

210 chromatography-tandem mass spectrometry and gas chromatography-mass spectrometry.

211 rofiling of cholesterols was performed using gas chromatography-mass spectrometry.

212 phenotyping platform, enzymatic assays, and gas chromatography-mass spectrometry.

213 alysis using solid-phase microextraction and gas chromatography-mass spectrometry.

214 easured END and ENL in 24-h urine samples by gas chromatography-mass spectrometry.

215 Nicotine yield was quantified using gas chromatography-mass spectrometry.

216 lar fractions, and composition determined by gas chromatography-mass spectrometry.

217 nalyzed for a suite of PFAS using liquid and gas chromatography-mass spectrometry.

218 berries, blueberries, and raspberries) using gas chromatography-mass spectrometry.

219 olid-phase microextraction and quantified by gas chromatography-mass spectrometry.

220 e photometric detection, and confirmed using gas chromatography-mass spectrometry.

221 y (PTR-ToF-MS), Solid Phase Micro Extraction-Gas Chromatography-Mass Spectroscopy (SPME-GC-MS), High-

222 and the intermediate products identified by gas chromatography-mass spectrum, we found that at 20 GP

223 tyrosine, serine and GABA were quantified by gas-chromatography-mass spectrometry.

224 ons using thermal desorption two-dimensional gas-chromatography-mass-spectrometry with electron impac

225 n-microextraction in solid phase followed by gas chromatography/mass spectrometry (DI-SPME-GC/MS).

226 ring of thousands of features extracted from gas chromatography/mass spectrometry (GC/MS) data from h

227 ted online dynamic in-tube extraction (ITEX)-gas chromatography/mass spectrometry (GC/MS) method for

228 itol acetate derivatives was confirmed using gas chromatography/mass spectrometry (GC/MS).

229 sis, pyrolysis-comprehensive two-dimensional gas chromatography/mass spectrometry (Py-GC x GC-MS), at

230 d microspectroscopy (mu-FTIR), and pyrolysis-gas chromatography/mass spectrometry (pyr-GC/MS).

231 hermally assisted hydrolysis and methylation gas chromatography/mass spectrometry (THM-GC/MS) to supp

232 rmally assisted hydrolysis and methylation - gas chromatography/mass spectrometry (THM-GC/MS), optica

233 ana using passive organic vapor monitors and gas chromatography/mass spectrometry to determine if sel

234 hemical composition, measured with pyrolysis-gas chromatography/mass spectrometry, this being most im

235 The furan content was quantified using gas chromatography/mass spectrometry, while the correspo

236 ing the carbon module labeling technique and gas chromatography/mass spectrometry.

237 d by nontargeted metabolomics analysis using gas chromatography/mass spectrometry.

238 The aroma profiles were characterized using Gas Chromatography/Mass Spectrometry/Olfactometry (GC/MS

239 " aromatic compounds were also quantified by gas-chromatography/mass-spectrometry.

240 er of complex samples using multidimensional gas chromatography (MDGC), the selectivity of the employ

241 orption spectroscopy (Cu L-edge), and online gas chromatography measurements.

242 otic cells, we find good agreement with bulk gas chromatography measurements.

243 monstrated the unique abilities of the first gas chromatography-molecular rotational resonance spectr

244 ope ratio mass spectrometry, GC-IRMS, versus gas chromatography-multicollector inductively coupled pl

245 ombination of photoacoustic spectroscopy and gas chromatography offers a viable solution for compact

246 Gas chromatography offers high sample capacity, separati

247 ates were characterized by sensory analysis, gas chromatography-olfactometry (GC-O) and gas chromatog

248 inegars from Modena (PGI) were determined by gas chromatography-olfactometry (GC-O) using frequency o

249 ushroom species with trained assessors using gas chromatography-olfactometry as well as gas chromatog

250 titation in non-fragrant varieties; however, gas chromatography-olfactometry of samples indicated the

251 Gas chromatography-olfactometry was used to assess odori

252 c bags, tetrabrik and box, were evaluated by gas chromatography-olfactometry-mass spectrometry (GC-O-

253 out extract analyzed by atmospheric pressure gas chromatography-quadrupole time-of-flight (APGC-QToF)

254 a files generated by an atmospheric pressure gas chromatography-quadrupole time-of-flight mass spectr

255 pectrometry (GC-MS) and atmospheric pressure gas chromatography-quadrupole-time of flight mass spectr

256 Here we used Gas chromatography-Recomposition-Olfactometry (GC-R) to

257 A gas chromatography-single quadrupole mass spectrometry m

258 exploitation of Solid-Phase Micro Extraction Gas Chromatography (SPME-GC-MS) technique and associated

259 s by semivolatile thermal desorption aerosol gas chromatography (SV-TAG) were used to investigate how

260 extract II was analyzed simultaneously using gas chromatography tandem mass spectrometry (GC-MS/MS).

261 ations, we have developed a simple and rapid gas chromatography tandem mass spectrometry (GC/MS/MS) m

262 fruit, pineapple and grapes) prior to their gas chromatography tandem mass spectrometry analysis.

263 oid hormones and SHBG were quantitated using gas chromatography-tandem mass spectrometry (GC-MS/MS) a

264 Seven UV compounds were analyzed by gas chromatography-tandem mass spectrometry (GC-MS/MS) w

265 Asians Living in America pilot study using a gas chromatography-tandem mass spectrometry analytical m

266 describe the development and validation of a gas chromatography-tandem mass spectrometry method to an

267 Histochemical staining and gas chromatography-tandem mass spectrometry quantificati

268 olid-phase microextraction (SPME) coupled to gas chromatography-tandem mass spectrometry to detect an

269 turing process for green and black tea using gas chromatography-tandem mass spectrometry.

270 Gas chromatography/tandem mass spectrometry (GC-MS/MS) w

271 oid hormones and SHBG were quantitated using gas chromatography/tandem mass spectrometry and competit

272 Conventionally, gas chromatography techniques are used to detect key lip

273 en and Mg(2+) in solution were detected by a gas chromatography-thermal conductivity detector and ion

274 of primary metabolite and phospholipid using gas chromatography time-of-flight mass spectrometry (GC-

275 metabolic and lipidomic signatures based on gas chromatography time-of-flight mass spectrometry (GC-

276 se microextraction (HS-SPME) two-dimensional gas chromatography time-of-flight mass spectrometry (GCx

277 nhances discrimination of thermal desorption gas chromatography time-of-flight mass spectrometry (TD-

278 analysed using an untargeted two-dimensional gas chromatography time-of-flight mass spectrometry meta

279 analyzed using comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry, and

280 ing coupled to comprehensive two-dimensional gas chromatography - time-of-flight mass spectrometry (G

281 d for use with comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry (GC

282 combined with comprehensive two-dimensional gas-chromatography/time-of-flight mass-spectrometry (GC

283 ction and used comprehensive two-dimensional gas chromatography to quantify and characterize direct a

284 establish the analytical method of titration gas chromatography to quantify the contribution of unrea

285 lecular hydrogen, which was analyzed through gas chromatography to validate the reaction mechanism.

286 As determined by gas chromatography-triple quadruple mass spectrometry, t

287 glycolate, and glyoxylate were measured on a gas chromatography-triple quadrupole mass spectrometry s

288 d-phase microextraction (HS-SPME) coupled to gas chromatography-triple quadrupole/mass spectrometry d

289 We applied headspace gas chromatography using a dual column/dual flame ioniza

290 Firstly, gas chromatography was employed to analyze fatty acid pr

291 iquid-liquid extraction methods, followed by gas chromatography with electron capture detection, to m

292 rganophosphorus residues in curry leaf using gas chromatography with flame photometric detection, and

293 e Sorptive Extraction methodology coupled to Gas Chromatography with Mass Spectrometry Detection (MHS

294 An efficient single quadrupole gas chromatography with mass spectrometry method was dev

295 aman/surface-enhanced Raman spectroscopy and gas chromatography with mass spectroscopy, respectively.

296 and tissue PCB profiles were assessed using gas chromatography with tandem mass spectrometry (GC-MS/

297 The samples were analyzed by two-dimensional gas chromatography with time-of-flight mass spectral det

298 Comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry

299 ree analytical methods using two-dimensional gas chromatography with time-of-flight mass spectrometry

300 nalyses were performed using two-dimensional gas chromatography with time-of-flight mass spectrometry