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1 ference was that adrenic acid (22:4 n-6) and docosapentaenoic acid (22:5 n-6), both metabolites of ar
2 d with 1-14C- or 3-14C-labeled 7,10,13,16,19-docosapentaenoic acid (22:5(n-3)), [1-14C]22:6(n-3), [3-
5 ons of eicosapentaenoic acid (20:5n-3; EPA), docosapentaenoic acid (22:5n-3; DPA), and docosahexaenoi
6 f DHA and significantly higher levels of n-6 docosapentaenoic acid (22:5n-6) in their ROS than defici
8 ecursors, results in replacement of DHA with docosapentaenoic acid (22:5n6, DPA), an omega-6 fatty ac
9 cosapentaenoic acid + docosahexaenoic acid + docosapentaenoic acid + alpha-linolenic acid) was associ
11 e predominantly eicosapentaenoic acid (EPA), docosapentaenoic acid, and docosahexaenoic acid (DHA).
13 hospholipid levels of eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid were mea
14 individual n-3 PUFAs eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid were obs
15 specifically those of eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid, were as
16 n-3 [VLC n-3; sum of eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid] and alp
17 nsaturated fatty acids eicosapentanoic acid, docosapentaenoic acid, and docosahexaenoic acid] was 1.1
18 were associated with eicosapentaenoic acid, docosapentaenoic acid, arachidonic acid, CLA:9c11t and g
19 o the structural elucidation of hydroxylated docosapentaenoic acid-containing diacyl-phosphatidylchol
20 as sufficient to elevate erythrocyte EPA and docosapentaenoic acid content, which shows the effective
21 le of total n-3 PUFAs (eicosapentaenoic acid+docosapentaenoic acid+docosahexaenoic acid) levels was 0
22 g eicosapentaenoic acid (EPA) (20:5omega-3), docosapentaenoic acid (DPA) (22:5omega-3), and docosahex
23 were not associated with HF, whereas plasma docosapentaenoic acid (DPA) showed a nonlinear inverse r
25 onance (NMR), alpha-linolenic acid (ALA) and docosapentaenoic acid (DPA) were rapidly cleaved by PPL
26 , 0.40 (0.20, 0.82; P for trend = 0.004) for docosapentaenoic acid (DPA), and 0.46 (0.18, 1.16; P for
27 oic acid (DHA), eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and arachidonic acid (AA) i
28 acids, the EGCG molecule was esterified with docosapentaenoic acid (DPA), upon which a mixture of est
29 O increased (P < 0.001) plasma ALA, EPA, and docosapentaenoic acid (DPA), with no change in DHA compa
33 % docosahexaenoic acid (DHA) and 11% omega-6 docosapentaenoic acid (DPA-n6) after partial hydrolysis
34 n-6 fatty acids, either arachidonic acid or docosapentaenoic acid (DPAn-6), diminished the efficacy
36 log10(Bayes Factor) = 6.16) and of PPT2 with docosapentaenoic acid (log10(Bayes Factor) = 6.24) were
37 D1(n-3 DPA)), 7,14-dihydroxy-8,10,12,16Z,19Z-docosapentaenoic acid (MaR1(n-3 DPA)) and related bioact
38 dihomo-GLA, docosatetraenoic acid (DTA), and docosapentaenoic acid (n6-DPA), with HRs between 1.13 to
39 increases over time in breast-milk 22:5n-3 (docosapentaenoic acid, or DPA) (P < 0.02), plasma DPA (P
40 es include 7,8,17-trihydroxy-9,11,13,15E,19Z-docosapentaenoic acid (RvD1(n-3 DPA)), 7,14-dihydroxy-8,
42 trations in healthy women and that increased docosapentaenoic acid was associated with a lower risk o
43 cenic, alpha-linolenic, eicosapentaenoic and docosapentaenoic acids were higher in cows with a low pr
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