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1 or both of these thioesterases for growth on conjugated linoleic acid.
2 s such as linoleic acid, linolenic acid, and conjugated linoleic acid.
3 that lipopolysaccharide and trans-10,cis-12-conjugated linoleic acid (10,12-CLA) activate the inflam
6 Fatty acid analysis showed incorporation of conjugated linoleic acid and there was a significant red
7 hidonic acid, linolenic acid, linoleic acid, conjugated linoleic acid, and eicosatetraynoic acid had
8 fect milk fat synthesis was trans-10, cis-12 conjugated linoleic acid, and its effects have been well
10 (C22:6n-3), alpha-linolenic acid (C18:3n-3), conjugated linoleic acid (C18:2n-7), and oleic acid (C18
11 uch as vaccenic acid (VA) and cis-9,trans-11 conjugated linoleic acid (c9,t11-CLA), are less clear.
14 We compared the effects of 2 dietary oils, conjugated linoleic acid (CLA) and safflower oil (SAF),
16 Previous research showed that treatment with conjugated linoleic acid (CLA) during the period of acti
21 significant health concern for the elderly; conjugated linoleic acid (CLA) has been shown to improve
23 how dietary calcium modulates the effects of conjugated linoleic acid (CLA) in preventing bone loss,
32 , fatty acid composition (GC-FID), including conjugated linoleic acid (CLA) isomeric profile (Ag(+)-H
33 A novel method for the identification of conjugated linoleic acid (CLA) isomers has been develope
35 ecular targets for the protective actions of conjugated linoleic acid (CLA) on experimental inflammat
36 selectivity were studied in the synthesis of conjugated linoleic acid (CLA) partial glycerides, which
37 reviously demonstrated that trans-10, cis-12 conjugated linoleic acid (CLA) reduced the triglyceride
39 ial strategy to reduce obesity is to consume conjugated linoleic acid (CLA) supplements containing is
40 une cells and animal models demonstrate that conjugated linoleic acid (CLA), a lipid, modulates immun
41 , odd chain-FA (OCFA), unsaturated FA (UFA), conjugated linoleic acid (CLA), n-3 FA, and C18:1cis9 to
42 et supplemented with fish oil, trans10,cis12 conjugated linoleic acid (CLA), or elaidic acid on lipid
43 C12:0 and C14:0, trans-fatty acids including conjugated linoleic acid (CLA), polyunsaturated fatty ac
47 cid (FA) profile, containing more n-3 FA and conjugated linoleic acids (CLA) than conventionally prod
49 ociation products of cis/trans and trans/cis conjugated linoleic acids (CLAs), as methyl esters, and
52 nding of n-3 fatty acids, linoleic acid, and conjugated linoleic acid in relation to possible effects
53 s premature to assign any beneficial role to conjugated linoleic acid in terms of its ability to impa
57 and coworkers also reported that growth on a conjugated linoleic acid isomer yields much higher level
58 lemented with the trans-10, cis-12 isomer of conjugated linoleic acid lead to ovary-independent allom
59 iry foods such as amino acid composition and conjugated linoleic acid may be instrumental in the bene
62 c acid, n-3 polyunsaturated fatty acids, and conjugated linoleic acid on mammary carcinogenesis in an
63 edium revealed the partial beta-oxidation of conjugated linoleic acid to 3,5-dodecadienoyl-CoA, which
64 erase function in the partial degradation of conjugated linoleic acid via the thioesterase-dependent
65 th induced by the trans-10, cis-12 isomer of conjugated linoleic acid was confirmed by its reversal u
67 ential conversion of nitro-linoleic to nitro-conjugated linoleic acids was explored via a facile base
68 were incubated with nanoemulsions containing conjugated linoleic acid, which suggested that this hydr
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