Nuclear magnetic resonance spectroscopy.
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Mrs O'Neill returned home four years ago when her husband's health deteriorated.
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Mrs Spelman said: We need to make the new CAP fundamentally different.
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Mrs Carr said the result was not a win for animal activists.
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Yes, yes, of course she is.' Mrs Castaway stirs the glue-pot pensively.
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Mrs Turei said the situation was now collapsing in on the government.
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Metabolites were quantified by nuclear magnetic resonance spectroscopy from fasting serum samples.
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Brain metabolite concentrations were determined in vivo by proton magnetic resonance spectroscopy.
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Structural determinations were carried out by chemical analysis and nuclear magnetic resonance spectroscopy.
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Tumor energy metabolism was investigated in vivo by 31P nuclear magnetic resonance spectroscopy.
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Frequent regional node involvement facilitates surface coil investigation with phosphorus-31 magnetic resonance spectroscopy.
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H-1 MR spectroscopy revealed normal metabolite levels, except for increased PHE levels.
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To the authors' knowledge, MR spectroscopy has never been used to investigate NMO.
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Proton MR spectroscopy in one child showed elevated white matter myo-inositol.
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Interest has been focused mainly on information provided by MR imaging and MR spectroscopy.
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All patients underwent proton MR spectroscopy at short echo times.
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Metabolites were quantified by nuclear magnetic resonance spectroscopy from fasting serum samples.
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Structural determinations were carried out by chemical analysis and nuclear magnetic resonance spectroscopy.
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Tumor energy metabolism was investigated in vivo by 31P nuclear magnetic resonance spectroscopy.
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Body composition of mice was analysed via nuclear magnetic resonance spectroscopy and microcomputed tomography.
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Hepatic glycogen concentrations were determined noninvasively using in vivo 13C nuclear magnetic resonance spectroscopy.
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The structure of the compounds was assigned by IR and NMR spectroscopy.
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We have determined the structure of the free PBX homeodomain using NMR spectroscopy.
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Here we report the three-dimensional structure of human CXCR1 determined by NMR spectroscopy.
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We describe structural studies of the C-peptide using 2D NMR spectroscopy.
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Using NMR spectroscopy, we identified the biosynthetic product as MEL-A with altered sugar conformation.
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Here we present a three-dimensional structure of this protein as determined by NMR spectroscopy.
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NMR spectroscopy confirmed the cross-linker synthesis and the preservation of the active maleimide function.
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The compounds were characterised by NMR spectroscopy and X-ray crystallography.
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The induced asymmetry is consistent with the complex's solution properties as determined using NMR spectroscopy.
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Their structures were determined by MS and NMR spectroscopies.
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The structures of synthesized compounds were fully characterized by multinuclear NMR spectroscopy and X-ray crystallography.
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For some toxins, the three-dimensional structure has been solved by X-ray diffraction and NMR spectroscopy.
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Structural compositions of the conjugates were verified by 1H NMR spectroscopy and CHN elemental analyses.
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The structures of the esters were elucidated by means of spectral data, including 2D NMR spectroscopy.
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NMR spectroscopy provides evidence of intramolecular hydrogen bonding under physiological conditions in two of the inhibitors.
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Our NMR spectroscopy data indicated that the presence of D137L introduced long range rearrangements in TM structure.