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

1 cid methyl ester analysis was carried out by gas liquid chromatography.

2 of cholesterol precursors were measured with gas-liquid chromatography.

3 ored and short chain fatty acids analysed by gas-liquid chromatography.

4 Serum fatty acids were analyzed by capillary gas-liquid chromatography.

5 in situ hybridization and for SCFAs by using gas-liquid chromatography.

6 s were measured by high-resolution capillary gas-liquid chromatography.

7 FAs in diets and blood were determined by gas-liquid chromatography.

8 lectrospray ionization mass spectrometry and gas-liquid chromatography.

9 er analyzed by thin-layer chromatography and gas-liquid chromatography.

10 base hydrolysis, methylated, and analyzed by gas-liquid chromatography.

11 ood cells, liver, and ROS were determined by gas-liquid chromatography.

12 methyl esters were prepared and analyzed by gas-liquid chromatography.

13 trimethylsilyl derivatives were analyzed by gas-liquid chromatography.

14 atography, were elucidated and quantified by gas-liquid chromatography.

15 ations of SCFAs in feces were measured using gas-liquid chromatography.

16 ve % of total fatty acids) was determined by gas-liquid chromatography.

17 dney and gonad and the tissue FA measured by gas-liquid chromatography.

18 ell (RBC) fatty acids were measured by using gas-liquid chromatography.

19 and C24:0) in plasma and erythrocytes using gas-liquid chromatography among 794 incident coronary he

20 authors measured serum fatty acid levels by gas-liquid chromatography and analyzed their association

21 ic compounds of cell walls were performed by gas-liquid chromatography and HPLC, respectively.

22 and examined their chemical structures with gas-liquid chromatography and mass spectrometry.

23 biochemical tests, probes (Gen-Probe, Inc.), gas-liquid chromatography, and, when necessary, PCR-rest

24 iliary bile acid composition was analyzed by gas-liquid chromatography before and after 4 months of t

25 entration (isotherm) effects on retention in gas-liquid chromatography, configurational-bias Monte Ca

26 y high-performance liquid chromatography and gas-liquid chromatography demonstrated the presence of t

27 f previously collected blood was analyzed by gas-liquid chromatography for 94 men in whom sudden deat

28 The CDC group IIc strains were analyzed by gas-liquid chromatography for their cellular fatty acid

29 PUFAs were quantified by gas-liquid chromatography from plasma and adipose tissue

30 e an R package called "mzrtsim"' to simulate gas/liquid chromatography full scan raw data in the mzML

31 ed partition coefficient values derived from gas-liquid chromatography (GLC) are found to be consiste

32 lyzed by means of high-temperature capillary gas-liquid chromatography (GLC) in combination with low

33 gh pressure liquid chromatography (HPLC) and gas-liquid chromatography (GLC) in combination with mass

34 ), supercritical fluid chromatography (SFC), gas-liquid chromatography (GLC), and micellar electrokin

35 be especially useful as stationary phases in gas-liquid chromatography (GLC).

36 ic data, along with UV-vis spectroscopic and gas-liquid-chromatography (GLC) data, are consistent wit

37 at the gas-liquid interface on retention in gas-liquid chromatography has been controversial since t

38 anding coverage of chemical space, including gas/liquid chromatography-HRMS (GC-HRMS and LC-HRMS), an

39 ttock fatty acid composition was analyzed by gas-liquid chromatography in 1992 to 1993 and 2008.

40 and erythrocytes were measured by capillary gas-liquid chromatography in 306 US women aged 43-69 y.

41 Fatty acids were assessed by gas-liquid chromatography in adipose tissue samples coll

42 Analysis of cellular fatty acids by gas-liquid chromatography indicated a close clustering o

43 When used as stationary phases in gas-liquid chromatography, ionic liquids exhibit dual na

44 of the dithioacetal followed by chiral-phase gas-liquid chromatography is also described.

45 A unique type of gas-liquid chromatography is described in which both mob

46 d to detailed structural analyses, combining gas-liquid chromatography, mass spectrometry, and nuclea

47 Gas-liquid chromatography-mass spectrometry analysis of

48 Gas-liquid chromatography-mass spectrometry and nuclear

49 Gas-liquid chromatography-mass spectrometry and reverse

50 and the free fatty acid pool was measured by gas-liquid chromatography/mass spectrometry of the respe

51 , high-performance liquid chromatography, or gas-liquid chromatography) methods for identification of

52 The structures were corroborated by gas-liquid chromatography MS, matrix-assisted laser deso

53 omposition in serum, analyzed at baseline by gas-liquid chromatography (n = 1981), and single nucleot

54 pray ionization-tandem mass spectrometry and gas-liquid chromatography of the product generated in vi

55 cantly to the retentive behavior observed in gas-liquid chromatography on nonpolar capillary columns

56 ar magnetic resonance (NMR) spectroscopy and gas-liquid chromatography revealed two types of branched

57 Gas liquid chromatography shows that the fatty acid comp

58 The three-phase model may be applied to any gas-liquid chromatography stationary phase involving a p

59 the "three-phase" model in enantioselective gas-liquid chromatography utilizing a methylated cyclode

60 Using gas-liquid chromatography, we identified both cis ALA (m

61 ompositions of these strains, as analyzed by gas-liquid chromatography, were unique, characterized by

62 issue fatty acid composition was assessed by gas-liquid chromatography while 16S rRNA pyrosequencing

63 trospray ionization); and fatty acids (using gas-liquid chromatography with flame ionization detectio

64 -phase organic compounds was conducted using gas/liquid chromatography with traditional and high-reso