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1 The pH 4.5 induced higher decrease in (-)-epigallocatechin gallate (71% and 79%) and quercetin-3-g
4 hemolysis while (-)-epicatechin gallate, (-)-epigallocatechin gallate and (-)-epigallocatechin protec
5 also show that addition of the antioxidants epigallocatechin gallate and alpha-lipoic acid reduces p
7 control model beverages were incubated with epigallocatechin gallate and green tea extract at 62 or
9 lly relevant Abeta oligomers is inhibited by epigallocatechin gallate and increased by the A2V mutati
10 ment Abeta(25-35) by two amyloid inhibitors (epigallocatechin gallate and scyllo-inositol) that are c
12 (125-1,000 ppm), including (+)-catechin, (-)-epigallocatechin gallate, and green tea extract were add
13 that the astringent- and bitter-tasting (-)-epigallocatechin gallate, bitter-tasting caffeine, and t
14 The experiments reveal that polyphenols (epigallocatechin gallate, bromophenol blue, and resverat
15 , with (+)-catechin, (-)-epicatechin, or (-)-epigallocatechin gallate (EGCG) added as chain breakers.
17 that two of the polyphenols from green tea (epigallocatechin gallate (EGCG) and epicatechin gallate
19 us green tea constituents, in particular (-)-epigallocatechin gallate (EGCG) and other polyphenols wi
22 special, hitherto-unexplored property of (-)-epigallocatechin gallate (EGCG) as a chiral solvating ag
24 etermine whether an ingredient of green tea, epigallocatechin gallate (EGCG) could attenuate oxidativ
26 y-Arg-Pro-Pro-Gln-Gly and the polyphenol (-)-epigallocatechin gallate (EGCG) has been determined usin
28 The encapsulation of green tea catechin and epigallocatechin gallate (EGCG) in soy lecithin liposome
29 ons of the tea catechins epicatechin (EC) or epigallocatechin gallate (EGCG) inhibited formation of h
32 microscopy (AFM), that the commonly used (-)-epigallocatechin gallate (EGCG) is a much less efficient
34 ory have demonstrated that the GT polyphenol epigallocatechin gallate (EGCG) is capable of antagonizi
39 en tea extract (GTE) supplementation high in epigallocatechin gallate (EGCG) on blood lipids in healt
40 luence of the polyphenolic amyloid inhibitor epigallocatechin gallate (EGCG) on the aggregation pathw
41 pared to standard green tea shoot (GL) while epigallocatechin gallate (EGCG) recorded higher levels i
42 t higher levels of the catechins, especially epigallocatechin gallate (EGCG) were found in green teas
44 study was to examine whether the antioxidant epigallocatechin gallate (EGCG), a catechin-base flavono
45 aim of this study was to provide support for epigallocatechin gallate (EGCG), a component of green te
46 antly, we also identified in this study that epigallocatechin gallate (EGCG), a green tea-derived cat
48 cently demonstrated that the antioxidant (-)-epigallocatechin gallate (EGCG), a major component in gr
51 nhibitory effects of curcumin, caffeine, (-)-epigallocatechin gallate (EGCG), and tea in animal model
52 acid, caffeic acid, caffeine, curcumin, (-)-epigallocatechin gallate (EGCG), gallic acid, propyl gal
53 omponent of green tea extracts, catechin (-)-Epigallocatechin gallate (EGCg), has been reported to be
54 Indian medicine and the green tea flavonoid, epigallocatechin gallate (EGCG), is reported to have glu
58 this hypothesis, we evaluated the effect of epigallocatechin gallate (EGCG), the main antioxidant de
64 opically with caffeine (6.2 micromol) or (-)-epigallocatechin gallate (EGCG; 6.5 micromol) once a day
65 We hypothesized that prostate tumor specific epigallocatechin-gallate (EGCg) functionalized radioacti
66 nt with Dyrk1A inhibitor, green tea flavonol epigallocatechin-gallate (EGCG), from gestation to adult
68 rahydrofolate (l-5-MTHF) in combination with epigallocatechin-gallate-enriched extract (EGCGe) and ep
69 sed, and when treated with 20 micromol/L (-)-epigallocatechin gallate (green tea) was restored back t
70 quillaja saponin and polyphenols (vanillin, epigallocatechin gallate, green tea extract, and protoca
73 ertain tea polyphenols, such as catechin and epigallocatechin gallate, have been used to augment the
74 0.3 muM, which was smaller than that of (-)-epigallocatechin gallate in Phase III clinical trials an
75 asured, confirming the major contribution of epigallocatechin gallate in the peroxyl radical scavengi
76 ls tested, TF-2 and, to a lesser degree, (-)-epigallocatechin gallate inhibited cyclooxygenase (Cox)-
77 ine levels that were dose dependent, whereas epigallocatechin gallate levels did not accumulate nor a
79 nhibition of Bcl-2 by the green tea compound epigallocatechin gallate results in an increase in [Ca(2
80 and lactate and the thermosensitive compound epigallocatechin gallate were recovered without signific
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