1977
DOI: 10.1016/0014-5793(77)80875-2
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Human erythrocyte metabolism studies by 1H spin echo NMR

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Cited by 285 publications
(129 citation statements)
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“…An increasing number of publications have described metabonomics using analytical techniques including 1 H NMR, gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (UPLC-MS) [6]. 1 H NMR, which is as one of the first methods used for metabonomics, represents a rapid, non-destructive and highly robust technology that provide highly informative structural information [7]. 1 H NMR is often used without any pre-separation process and unlike chromatography it does not require development.…”
Section: Metabonomic Analytical Technologiesmentioning
confidence: 99%
“…An increasing number of publications have described metabonomics using analytical techniques including 1 H NMR, gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (UPLC-MS) [6]. 1 H NMR, which is as one of the first methods used for metabonomics, represents a rapid, non-destructive and highly robust technology that provide highly informative structural information [7]. 1 H NMR is often used without any pre-separation process and unlike chromatography it does not require development.…”
Section: Metabonomic Analytical Technologiesmentioning
confidence: 99%
“…NMR offers several potential advantages: continuous non-destructive monitoring of pH in vivo; spatial resolution and simultaneous determination of pH in several compartments [4,5]. NMR has been used to monitor titratable groups of endogenous metabolites on the basis of chemical shift with respect to changing pH; in particular 3'P NMR of inorganic phosphate (Pi) [5,6] or phosphomonoesters [7] or 'H NMR of carnosine [8] or histidine [9]. pH measurement using endogenous metabolites is not always successful owing to crowded spectra, broad lines or low metabolite concentration.…”
Section: Introductionmentioning
confidence: 99%
“…Although the concentration of glutathione (y-Lglutamyl-L-cysteinyl-glycine, GSH) in human erythrocytes is generally found to be -2 mM [ 1,2], it is in a dynamic state, continually being degraded to and resynthesized from its constituent amino acids. The details of the degradation and synthesis reactions are the subject of considerable research [3,4], as is the mechanism by which the GSH level is regulated [l].…”
Section: Introductionmentioning
confidence: 99%