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1 als but is a key step in the biosynthesis of plant sterols.
2 hereditary phytosterolemia and were rich in plant sterols.
3 erol absorption because it is independent of plant sterols.
4 ABCG5/G8 knockout mice a diet enriched with plant sterols.
5 absorption and promote excretion of dietary plant sterols.
7 supplementation with orange juice containing plant sterols (2 g/d) significantly reduced LDL choleste
8 -binding cassette transporters G5/8 regulate plant sterol absorption and also the secretion into bile
9 The aim of this study was to examine whether plant sterols affect CRP concentrations and the lipoprot
11 Eskimo woman had consumed a diet very low in plant sterols and moderate to low in cholesterol content
12 ol absorption is a selective process in that plant sterols and other non-cholesterol sterols are abso
13 by very high levels of sitosterol and other plant sterols and premature atherothrombotic vascular di
14 itro and ex vivo studies have suggested that plant sterols and stanols can shift the T helper (Th) 1/
17 e these new data support the conclusion that plant sterols are excluded from the body because they ar
23 timibe inhibits the intestinal absorption of plant sterols as well as cholesterol, leading to reducti
24 omplex (G5G8) that opposes the absorption of plant sterols but is also expressed in liver where it pr
25 d hepatobiliary secretion of cholesterol and plant sterols by 1.5-2-fold, increased the amount of int
27 altered substrate specificity: transport of plant sterols by the heterodimer was preserved, whereas
28 Respectively, cholestanol/cholesterol and plant sterols campesterol/cholesterol and sitosterol/cho
31 ificant and progressive reductions in plasma plant sterol concentrations in patients with sitosterole
32 effective in milligram doses, lowers plasma plant sterol concentrations in sitosterolemic subjects,
35 complexity of grapevine, we investigated the plant sterol content of berry and seed tissues at pre-ve
36 phenolics, carotenoids, coumarins, saponins, plant sterols, curcumins, and phthalides have been ident
37 mo ligands previously identified include the plant sterol cyclopamine (and its therapeutically useful
39 n Abcg5- and Abcg8-deficient mice fed a high plant sterol diet resulted in accumulation of free stero
40 These data indicate that selected dietary plant sterols disrupt cholesterol homeostasis by affecti
43 ied the degradation of cholesterol and three plant sterols during a 360 min heating treatment (180 de
44 e demonstrate that both stereoisomers of the plant sterol, (E)- and (Z)-GS, bind to the steroid recep
48 f stearidonic acid (SDA) and 0.65 g/100mL of plant sterol esters (PSE) were prepared without or with
52 p promoting active efflux of cholesterol and plant sterols from enterocytes back into the intestinal
57 ults for the first time demonstrate that the plant sterol guggulsterone suppresses ocular inflammatio
58 either VLDL or LDL there was no increase in plant sterols in bile, but with perfusion of HDL, the se
59 and G8 are known to cause an accumulation of plant sterols in blood and tissues (sitosterolemia).
61 ped a phenotype that included high levels of plant sterols in many tissues, liver abnormalities, and
66 in which patients accumulate cholesterol and plant sterols in the circulation and develop premature C
67 s with this disease have very high levels of plant sterols in the plasma and develop tendon and tuber
68 s with this disease have very high levels of plant sterols in the plasma, and develop tendon and tube
71 ced-calorie orange juice beverage containing plant sterols is effective in reducing CRP and LDL chole
72 hich serve numerous biochemical functions in plants: sterols (isoprenoids with a C30 backbone) are es
73 nd ABO have been associated with circulating plant sterol levels and CVD, thereby suggesting atheroge
74 from this disease have very elevated plasma plant sterol levels and develop tendon and tuberous xant
75 er genes besides ABCG5ABCG8 influence plasma plant sterol levels and now become candidates to explain
78 inhibitor of cholesterol absorption, reduces plant sterol levels in patients with sitosterolemia.
79 cross between F(1)s was performed and plasma plant sterol levels measured in 102 male and 99 female F
80 take yields a 2-fold increase in circulating plant sterol levels that equally represent markers of ch
82 analysis of these mutants has revealed that plant sterols may be key signaling molecules influencing
83 evated cholesterol absorption rather than by plant sterols may therefore mediate the relationships of
84 no acid identity to recently isolated higher-plant sterol methyltransferases from soybean and Arabido
85 anges, we examined the effects of individual plant sterols on cholesterol metabolism in cultured adre
87 study evaluated the influence of esterified plant sterols on serum lipid concentrations in adults wi
99 letate and linolenate) on a mixture of three plant sterols (PS: campesterol, stigmasterol and beta-si
103 porter cause accumulation of cholesterol and plant sterols, resulting in premature coronary atheroscl
107 CAT) 2 to differentiate cholesterol from the plant sterol, sitosterol, was compared with that of the
108 surrogate markers of cholesterol absorption (plant sterols: sitosterol, campesterol) and synthesis (c
109 l-related molecules (cholesterol precursors, plant sterols, some oxysterols, cholesterol sulfate, cho
111 ools of cholesterol and very elevated plasma plant-sterol species and frequently develop tendon and t
114 lemented by exogenous stigmasterol, the main plant sterol, suggesting that sterols are required for T
121 but with perfusion of HDL, the secretion of plant sterols was increased two- to threefold (P = 0.000
124 ma plant sterols were highest, while hepatic plant sterols were lower compared with Abcg5 ko (P < 0.0
125 lating perfusions, hepatic concentrations of plant sterols were not different after different lipopro
126 ease in the fractional absorption of dietary plant sterols, which was associated with an approximatel
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