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1 ly disjoint: Flux Balance Analysis and (13)C Metabolic Flux Analysis.
2 lux analysis and isotopically non-stationary metabolic flux analysis.
3 nce precludes the use of standard stationary metabolic flux analysis.
4 itrogen supply were further explored through metabolic flux analysis.
5 C-labeled metabolites is a powerful tool for metabolic flux analysis.
6 atography/tandem mass spectrometry for (13)C-metabolic flux analysis.
12 luding flux balance analysis (FBA) and (13)C-metabolic flux analysis ((13)C-MFA), offer direct insigh
13 ethod are similar to those found through 13C Metabolic Flux Analysis (13C MFA) for central carbon met
14 ethod of measuring intracellular fluxes, 13C Metabolic Flux Analysis (13C MFA), uses the labeling pat
18 in PPP/glycolysis ratios were determined via metabolic flux analysis after spiking (13)C1,2,3-glucose
19 levant metabolic pathways revealed by recent metabolic flux analysis and discuss the consequences of
20 otrophic, and heterotrophic conditions using metabolic flux analysis and isotopic tracers such as (2)
21 e package that can perform both steady-state metabolic flux analysis and isotopically non-stationary
22 Isotope-based methods are commonly used for metabolic flux analysis and metabolite quantification in
23 fore, there is a need to develop a "unified" metabolic flux analysis approach that could be similarly
26 rovides valuable information for later (13)C metabolic flux analysis as indicated by a labeling exper
29 re this technology is key is in the field of metabolic flux analysis because the resolution of these
33 g transients in cellular metabolism, dynamic metabolic flux analysis (DMFA), and dynamic flux balance
35 sotopomer analysis has extended the reach of metabolic flux analysis from steady-state to highly dyna
40 opose ITOCSY as a practical NMR strategy for metabolic flux analysis, isotope dilution experiments, a
41 approach involving stable isotopes (such as metabolic flux analysis) may be better suited to provide
48 ondrial pyruvate transport, we applied (13)C metabolic flux analysis (MFA) to cells after transcripti
49 ngs, novel genome-scale models (GSMs), (13)C-metabolic flux analysis (MFA), and machine-learning appr
51 y correlated with results from prior (1)(3)C metabolic flux analysis of B. napus developing embryos.
52 eling in cell wall precursors makes possible metabolic flux analysis of cell wall biosynthesis based
53 racterized mutants were now studied by (13)C metabolic flux analysis of cultured developing embryos b
65 n the past, as they are a central element of metabolic flux analysis, the distribution of kinetic con
66 lize one such approach, thermodynamics-based metabolic flux analysis (TMFA), to make genome-scale, qu
69 elopment and application of a computer-aided metabolic flux analysis tool that enables the concurrent
72 pathways involved in hepatic lipoapoptosis, metabolic flux analysis using [U-(13)C(5)]glutamine as a
76 To probe metabolic state of hepatocytes, metabolic flux analysis was used to obtain the metabolic
78 -genome sequencing and high-resolution (13)C-metabolic flux analysis were performed on 10 adaptively
79 table isotope labeling and computer-assisted metabolic flux analysis were used to investigate the met
80 vides a powerful new toolbox for (13)C-based metabolic flux analysis, which is an emerging strategy i
81 sure liquid chromatography-mass spectrometry metabolic flux analysis with redox and switch-tag proteo
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