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1  an approximately 30-fold increase in plasma sitosterol.
2 d 0.92 (0.85, 1.00; P-trend = 0.09) for beta-sitosterol.
3 ene, while increasing that of its derivative sitosterol.
4 ontaining 25 % or 32 % oil with lecithin and sitosterol.
5 erved in all samples with enhanced levels of sitosterol.
6 er selectively for cholesterol compared with sitosterol.
7 trong preference for cholesterol rather than sitosterol.
8 tact cells loaded with either cholesterol or sitosterol.
9 to efficiently esterify both cholesterol and sitosterol.
10 sterol by LCAT was only 15% greater than for sitosterol.
11 heptadecanyl n-octadec-9-enoate (1) and beta-sitosterol (2) on the basis of chromatographic and spect
12 proportions of Delta5 sterols including beta-sitosterol, 24-methylenecholesterol and isofucosterol, w
13 droxyphenethyl alcohol, ocotillone, and beta-sitosterol 3-O-beta-D-glucopyranoside, were also isolate
14  acid, alpha-tocopherol, threonic acid, beta-sitosterol, 4-hydroxybutyric acid, ferulic acid, and tot
15  Bioactive composition were as follows; beta-sitosterol ~40 %, campesterol ~33 %, brassicasterol ~22
16 ne-third nonesterified and consisted of beta-sitosterol (48%), campesterol (27%), and stigmasterol (2
17       The most abundant phytosterol was beta-sitosterol (974-1494 mg/kg) followed by campesterol then
18                                 We show that sitosterol, a common sterol of plants, is the most abund
19 , both ACAT1 and ACAT2 were able to esterify sitosterol albeit with lower efficiencies than cholester
20 )-avenasterol, 24-methylene-cholesterol/beta-sitosterol and 24-methylene-cholesterol.
21                             The content of B-sitosterol and a-tocopherol was 359.5-514.5 and 65.38-11
22 r concentrations of lutein, chlorophyll a, B-sitosterol and a-tocopherol.
23                                       Plasma sitosterol and campesterol concentrations significantly
24 cholestyramine therapy, the patient's plasma sitosterol and campesterol levels decreased by approxima
25 uence of markedly elevated plasma and tissue sitosterol and campesterol levels, premature atheroscler
26 re analysed, as well as the contents of beta-sitosterol and campesterol oxidation products.
27                            A mixture of beta-sitosterol and campesterol was incorporated into triacyl
28 -keto-, 7-hydroxy- and triol-PS derived from sitosterol and campesterol were 40.0, 34.4, 21.5 and 4.0
29 l (PS) oxidation products (POP) derived from sitosterol and campesterol were measured in 15 foods coo
30 evated plasma plant sterol levels (mean beta-Sitosterol and campesterol, respectively, 160.3+/-107.1
31 idin-3-O-glucoside, gallic acid, germanicol, sitosterol and erythrodiol correlated negatively to the
32 have been: avenasterol, linolenic acid, beta-sitosterol and gadoleico.
33 ), rice bran waxes (RW) or a mixture of beta-sitosterol and gamma-oryzanol (PS).
34 se inhibitor NB-598 prevented growth in beta-sitosterol and greatly reduced growth in campesterol.
35                     24-methylenecholesterol, sitosterol and isofucosterol were the most common and ab
36  Consistent bioactive compounds such as Beta-Sitosterol and Isorhamnetin underscore the known health
37             Growth of cells cultured in beta-sitosterol and NB-598 was restored by adding small amoun
38 disease characterized by very high levels of sitosterol and other plant sterols and premature atherot
39 bulus terrestris; saw palmetto berries; beta-sitosterol and other related sterols; and wild yams (dio
40 abolites including emodin, aloe-emodin, beta-sitosterol and rutin.
41 metabolites including emodin, aloe-emodin, B-sitosterol and rutin.
42 sterol exhibits a stronger ability than beta-sitosterol and stigmasterol to order model membranes.
43 alpha-methyl-sterols, with reduced levels of sitosterol and stigmasterol-indicating a defect in stero
44 effective for determination of analytes beta-sitosterol and stigmasterol.
45 e most representative phytosterols were beta-sitosterol and stigmasterol.
46 um plant sterols (stigmasterol, avenasterol, sitosterol, and campesterol), cholestanol, and cholester
47 s of the side chain (e.g., campesterol, beta-sitosterol, and desmosterol) supported long-term growth
48 l, campesterol, cholest-4-ene-3-one and beta-sitosterol] and flavonoids (2-3 folds) during blanching
49              All citrus by-products showed B-sitosterol as the major phytosterol, followed by B-campe
50                  The antioxidative effect of sitosterol at 1, 2 and 5% levels, in triolein, refined c
51  responsible for the antioxidative effect of sitosterol at frying temperatures.
52 r phytosterols: brassicasterol, campesterol, sitosterol, avenasterol and two phytostanols: sitostanol
53 were isolated from n-hexane while betulin, B-sitosterol, B-amyrin, oleanolic acid (3-6) were isolated
54 ase initiates glucan polymerization by using sitosterol-beta-glucoside (SG) as primer.
55 of pure DPPC, pure DOPC, and mixed DOPC-beta-sitosterol bilayers solvated in a vitrification solution
56 a is a bona fide sterol-binding protein with sitosterol-binding properties.
57 ing the levels of sterols, particularly beta-sitosterol, both in grapes and in microvinificates.
58 ]cholesterol and a trace amount of [beta-14C]sitosterol by gavage.
59 elta-tocopherol, beta-carotene, lutein, beta-sitosterol, campesterol and brassicasterol.
60 rs of cholesterol absorption (plant sterols: sitosterol, campesterol) and synthesis (cholesterol prec
61 gosterol), allochthonous (stigmasterol, beta-sitosterol, campesterol, and stigmastanol) and anthropog
62 s of cholesterol intestinal absorption (beta-sitosterol, campesterol, cholestanol), and synthesis (de
63            Cotton fiber membranes synthesize sitosterol-cellodextrins (SCDs) from SG and uridine 5'-d
64 nd plant sterols campesterol/cholesterol and sitosterol/cholesterol (cholesterol absorption markers)
65 was ruled out by documenting a normal plasma sitosterol:cholesterol ratio.
66 e measured in rats treated with cholesterol, sitosterol, cholic acid, deoxycholic acid, ursodeoxychol
67                                              Sitosterol concentrations decreased by 21% (P<0.001) in
68 we show here that macrophages incubated with sitosterol-containing lipoproteins accumulate free stero
69 ssays, we show that these animals synthesize sitosterol de novo using a noncanonical C-24 sterol meth
70 ls, including metabolites of cholesterol and sitosterol degradation or 25-OH-vitamin D(3).
71                            Campesterol, beta-sitosterol, Delta(7)-campesterol/Delta(5,24)-stigmastadi
72 isation of pecan nut oils revealed that beta-sitosterol, Delta5-avenasterol, and campesterol were the
73 ely occurring campesta-5,24(25)-dienol, beta-sitosterol, Delta5-avenasterol, campesterol, and cycloar
74 eased activity 84% (P < .05) and intravenous sitosterol did not change activity.
75 rafficking to the endoplasmic reticulum, and sitosterol-enriched endoplasmic reticulum membranes show
76      The mass ratios of cholesterol ester to sitosterol ester formed by ACAT1 and ACAT2 were 1.6 and
77 a few free fatty acids, hydroxyceramides and sitosterol esters were also observed.
78 ur detected in AF/ESI, respectively), and 12 sitosterol esters, not yet reported in mammalian cell cu
79 anol ferulate, campesterol ferulate and beta-sitosterol ferulate.
80 rol ferulate, cycloartenol ferulate and beta-sitosterol ferulate.
81 es, the most representative phytosterol is B-sitosterol, followed by campesterol or stigmasterol and
82  the most representative phytosterol is beta-sitosterol, followed by campesterol or stigmasterol and
83                The main phytosterol was beta-sitosterol, followed by stigmasterol and campesterol.
84 fferent molar ratios of cholesterol and beta-sitosterol for their impact on the physicochemical prope
85 ethyl to 24-ethyl sterol in the direction of sitosterol formation.
86 eric and cerotic acids, docosanol, a-amyrin, sitosterol, friedelin and friedelanone contents.
87  and cerotic acids, docosanol, alpha-amyrin, sitosterol, friedelin and friedelanone contents.
88                             The reduction in sitosterol from baseline was progressive, with further d
89 imulate the transfer of cholesterol and beta-sitosterol from liposomes to heat-treated mitochondria i
90    The recovery of alpha-tocopherol and beta-sitosterol from the deodorizer distillate of sunflower o
91 ), sunflower wax (SW), and a mixture of beta-sitosterol/gamma-oryzanol (PS).
92 ixture of stigmasterol glucoside (STG) and B-sitosterol glucoside (BSG) in the fruits of Momordica ch
93 ure of stigmasterol glucoside (STG) and beta-sitosterol glucoside (BSG) in the fruits of Momordica ch
94 easing order: campesterol approximately beta-sitosterol&gt;/=stigmasterol>cholesterol.
95            The major plant sterol species is sitosterol; hence the name of the disorder.
96  supplements of zinc, saw palmetto, and beta-sitosterol in relieving BPH symptoms have had mixed resu
97 accumulation of cholestanol, campesterol and sitosterol in serum and stones suggesting their particip
98 olestanone in intestine and muscle, and beta-sitosterol in spleen.
99 in efficient protein expression, albeit beta-sitosterol incorporation appeared to be associated with
100                                DOPE and beta-sitosterol incorporation in LNPs resulted in efficient p
101  whereas PS concentrations (campesterol+beta-sitosterol) increased (P = 0.03) in both groups after PS
102 on of the unfolded protein response and JNK, sitosterol-induced death is caspase-independent and invo
103                                      Second, sitosterol-induced macrophage death does not require ACA
104                          As with FC loading, sitosterol-induced macrophage death requires sterol traf
105            Addition of stigmasterol, but not sitosterol, inhibited SREBP-2 processing and reduced cho
106                         Despite similar beta-sitosterol intakes between the MS and MSF groups, plasma
107               HDL-cholesterol, triglyceride, sitosterol, lathosterol, campesterol, and proprotein con
108 C57BL6J had almost twice the campesterol and sitosterol levels compared with parental CASARk mice, an
109 Ibalpha were strongly correlated with plasma sitosterol levels in samples from human sitosterolemic p
110  significantly more ACAT activity than their sitosterol-loaded counterparts.
111                                           In sitosterol-loaded microsomes, both ACAT1 and ACAT2 were
112 le/surfactant, "Nok" (i.e., SPGS-550-M; beta-sitosterol methoxypolyethyleneglycol succinate), soon to
113 cture of non-polar dimers formed during beta-sitosterol oxidation at 180 degrees C in the presence of
114 edominant non-polar dimer formed during beta-sitosterol oxidative degradation has a configuration of
115                                     The beta-sitosterol oxides (7alpha/7beta-hydroxy, beta/alpha-epox
116 s diminished by about 21% based on low serum sitosterol (P = 0.0269) and campesterol (P = 0.0231) to
117 s, tocopherols, vitamin D, campesterol, beta-sitosterol, phosphatidylinositol and phosphatic acid, li
118 MG), rice wax (RW), gamma-oryzanol, and beta-sitosterol (PS), or ethylcellulose (EC).
119 ides, (MG), rice wax (RW), y-oryzanol, and B-sitosterol (PS), or ethylcellulose (EC).
120 rhetinic acid, lupeol, ursolic acid and beta-sitosterol showed a strong Th2-inclination and anti-infl
121 H, linoleic acid, saturated fatty acids beta-sitosterol, sn-1 and 3 diglyceride values.
122 g detection (ELSD) was used to quantify beta-sitosterol, stigmasterol, campesterol, and alpha-, delta
123                 This enzyme is essential for sitosterol synthesis in plants, but not known from most
124 CAT1-expressing cells esterified 4-fold more sitosterol than the ACAT2 cells.
125 or total phytosterols, campesterol, and beta-sitosterol: the risk reduction plateaued at intakes abov
126 rs differing in polarity, formed during beta-sitosterol thermo-oxidation.
127 des C22-sterol desaturase that converts beta-sitosterol to stigmasterol, was dramatically induced upo
128 s using an abundant plant feedstock and beta-sitosterol, together with succinic anhydride and PEG-550
129 , diosgenin, betulinic acid, escin, and beta-sitosterol treatments significantly inhibited both IL-2
130 high recoveries of alpha-tocopherol and beta-sitosterol, up to 99.20% and 97.32%, respectively, were
131 e of ripening were Delta(7)-campesterol/beta-sitosterol, uvaol/stigmasterol, clerosterol/Delta(5)-ave
132 1.29%) and lower oxidation susceptibility of sitosterol vs. campesterol.
133           The presence of enhanced levels of sitosterol was found to significantly decrease TG polyme
134 selectively esterified cholesterol even when sitosterol was loaded into the microsomes.
135                                         beta-Sitosterol was the dominant phytosterol (80-83%).
136                                            B-Sitosterol was the dominant phytosterol (80-83%).
137 en 62.0% and 75.7% of total sterols and beta-sitosterol was the first sterol in the two samples.
138                     Concerning sterols, beta-sitosterol was the main component in seed oils extracted
139                                         beta-Sitosterol was the most abundant component in berry tiss
140                                         beta-Sitosterol was the most important and representative phy
141                  Radiolabeled cholesterol or sitosterol was transferred from donor liposomes to G5- a
142 rols (PS: campesterol, stigmasterol and beta-sitosterol) was evaluated at 180 degrees C for up to 180
143 erentiate cholesterol from the plant sterol, sitosterol, was compared with that of the sterol esterif
144 ermination were 0.25g; 2.5mL; 300s; and beta-sitosterol were 0.25g; 5.4mL; 300s.
145 ta-tocopherol, campesterol, stigmasterol and sitosterol were quantified via GC-MS.
146 ,452-145,348 ng per beetle); cholesterol and sitosterol were the dominant sterols in both field-colle
147 lites, sinigrin, quercetin, campesterol, and sitosterol, were confirmed to regulate stomatal closure
148 reduced intestinal uptake of cholesterol and sitosterol, with dramatically reduced plasma phytosterol

 
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