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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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