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1 no effect is observed with the corresponding fatty alcohol.
2 acyl-CoAs enabled the efficient synthesis of fatty alcohols.
3 ing strategy to enable sustainable supply of fatty alcohols.
4 ta consistent with cationic trimethylarsenio fatty alcohols.
5 of fatty acid derivatives, including primary fatty alcohols.
6 l-acyl carrier protein substrates to primary fatty alcohols.
7 ly affected by the number of carbon chain of fatty alcohols.
8 encoded isozymes that reduced fatty acids to fatty alcohols.
9 ose cells and results in the accumulation of fatty alcohols.
10 il bodies) were enzymatically converted into fatty alcohols across a broad chain-length range (C(8)-C
11 os have an endogenous fatty acyl-coenzyme A: fatty alcohol acyl-transferase activity that could accou
12 x synthase (WS, fatty acyl-coenzyme A [coA]: fatty alcohol acyltransferase) catalyzes the final step
15 Nevertheless, the 75% reduction in total fatty alcohol and diol loads in the seed coat resulted i
16 FADH proteins are active on very-long-chain fatty alcohol and fatty aldehyde substrates, respectivel
19 hyl-delta(22)-coprostenol, several secondary fatty alcohols and dicarboxylic acids were identified fo
24 t level during seed desiccation, whereas the fatty alcohols and saturated omega-hydroxy fatty acids c
25 ingle-chain amphiphiles such as fatty acids, fatty alcohols, and fatty-acid glycerol esters are extre
27 ucturally tailored fatty esters (biodiesel), fatty alcohols, and waxes directly from simple sugars.
29 refore, our results indicate that esterified fatty alcohols, both soluble and polymerized forms, repr
30 , the catalytic conversion of fatty acids to fatty alcohols (C(8)-C(16)) or fatty alkanes (C(7)-C(15)
32 maceuticals and cosmetics while medium chain fatty alcohols (C6-C12) could be used as diesel-like bio
33 in root waxes of NaCl-treated wild-type and fatty alcohol:caffeoyl-CoA caffeoyl transferase plants.
35 hain length and specific for fatty acids and fatty alcohols containing very long saturated acyl chain
37 eport, for the first time, that medium chain fatty alcohols could be produced in yeast via targeted e
38 l-coenzyme A to omega-hydroxyfatty acids and fatty alcohols, demonstrating that the gene encodes a fe
39 raction has led to the isolation of five new fatty alcohol derivatives, avocadenols A-D (1-4) and avo
40 t altered, indicating that reduced levels of fatty alcohols did not influence the suberin polymerizat
41 for 9d, suggesting that the straight-chained fatty alcohol esters were more therapeutically selective
42 carbons - HCs, free fatty acids - FFAs, free fatty alcohols - FALs and wax esters - WEs) of natural w
43 FAR1 reduces fatty acids to their respective fatty alcohols for the plasmalogen-biosynthesis pathway.
44 R4, and FAR5, which collectively produce the fatty alcohols found in suberin, reduced their levels by
50 named this enzyme P. trichocarpa hydroxyacid/fatty alcohol hydroxycinnamoyltransferase 1 (PtFHT1).
51 d esters between selected phenolic acids and fatty alcohols in a binary solvent system, composed of h
52 is of the distribution of the C18:0 to C22:0 fatty alcohols in Arabidopsis (Arabidopsis thaliana) roo
54 ine, CHO-K1, that is deficient in long-chain fatty alcohol:NAD+ oxidoreductase (FAO; EC 1.1.1.192).
55 ass spectrometry techniques that most of the fatty alcohols not covalently linked to the suberin poly
56 ulsion systems, caffeic acid esterified with fatty alcohols of different chain lengths (C1-C20) were
57 examine the effect of carbon chain length of fatty alcohols on the reaction rate, the esterifications
59 to fatty acids by the sequential action of a fatty alcohol oxidase (FAO) and a fatty aldehyde dehydro
60 on analyses suggested that the deficiency in fatty alcohol oxidation in the FAA.K1A cells and the SLS
62 FAO and FADH constitute the very-long-chain fatty alcohol oxidation pathway that is likely to be nec
63 eate, arachidonate, and docosahexanoate), or fatty alcohols (palmityl, petrosenlinyl, and ricinolenyl
64 , only the LPA(2) receptor-selective agonist fatty alcohol phosphate-12 mimics the IL-4-dependent eff
65 esis and pharmacological characterization of fatty alcohol phosphates (FAP) containing saturated hydr
71 sis root waxes and that FAR1/4/5 provide the fatty alcohols required for alkyl hydroxycinnamate synth
72 eductase 1 (Far1) is essential for supplying fatty alcohols required for ether bond formation in ethe
73 data showed esterified and free fatty acids, fatty alcohol, sterols, alkanes and aromatic acid deriva
75 y for the production of alcohols, especially fatty alcohols that find broad applications in consumer
78 the reduction of fatty acid methyl esters to fatty alcohols to facilitate high-quality chromatographi
79 compound belonging to tocopherol long-chain fatty alcohols, to promote oligodendrocyte regeneration
80 squalene, sterols, triterpene acids/esters, fatty alcohols, wax esters and phenols (lignans, tyrosol
81 ion using glucose as the sole carbon source, fatty alcohols were produced at 1.3 g/L, including 6.9%
82 FAR-like domain produced both 16:0 and 18:0 fatty alcohols, whereas the C-terminal acyltransferase-l
83 alyzed reduction of fatty acyl-coenzyme A to fatty alcohols, which are possible precursors of platele
84 lipids and wax esters requires as precursors fatty alcohols, which are synthesized by fatty acyl redu
85 tion, WE hydrolysis releases very-long-chain fatty alcohols, which must be oxidized to fatty acids by
86 the esterifications of C4-C18 straight-chain fatty alcohol with dihydrocaffeic acid (DHCA), as a mode
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