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1 n oil enrichments compared with mono- and di-glycerides.
2 ain the endogenous cannabinoid 2-arachidonyl glyceride (2-AG), as identified by reverse phase high-pe
3 egio- and stereochemistry of the unsaturated glycerides, a sample pretreatment consisting of olefin c
8 sphates, sterol lipids, acyl carnitines, and glycerides) being detected in rat liver and bovine lens
10 y lipid wax, cholesterol ester terpenoid and glyceride composition, saturation, oxidation, and CH(2)
11 a good pPAF-AH substrate is the portion of a glyceride derivative that includes an sn-2 ester and a r
12 rometry (MS/MS) to quantify oxidized lipids (glycerides, fatty acids, phospholipids, lysophospholipid
14 is of glucose in the liver and kidney and of glyceride-glycerol in white adipose tissue and the small
19 e prolipoprotein signal peptidase requires a glyceride modified cysteine residue at the cleavage site
20 cture of triacylglycerols (TAGs) and partial glycerides of crude palm oil obtained from interspecific
23 s including potato dextrose agar, olive oil, glyceride trioleate, oleic acid and the alkane, C16 .
24 mple assay, we successfully discriminated 20 glycerides via principal component analysis and linear d
29 is of conjugated linoleic acid (CLA) partial glycerides, which presented nutraceutical properties.
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