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1 oils (olive oil, sunflower oil, soy oil and corn oil).
2 mice were fed control diet or diet with 20% corn oil.
3 0% fish and 20% borage oil, as compared with corn oil.
4 0% fish and 20% borage oil, as compared with corn oil.
5 oil and fish and borage oil as compared with corn oil.
6 0% fish and 20% borage oil, as compared with corn oil.
7 e, progesterone, a combination of the two or corn oil.
8 and borage oil as compared with fish oil and corn oil.
9 continued on the low-fat diet containing 5% corn oil.
10 mals were fed the low-fat diet containing 5% corn oil.
11 receive w-3 CA and 6539 (50%) randomized to corn oil.
12 carboxylic acid (CA) or an inert comparator, corn oil.
13 feeding C18:1 rich macadamia oil compared to corn oil.
14 lmitic, stearic, oleic and linoleic acids of corn oil.
15 ith volume fractions (0-100%) of rapeseed or corn oil.
16 corn oil produced a stronger gel than crude corn oil.
17 ethanol (or dextrose) and 25% of calories as corn oil.
18 monds, almond oil, or a mix of safflower and corn oils.
19 were used with gavage of heteroarotinoids in corn oil [0.1, 0.2, 0.4, or 0.8 mg/kg] and with 0.01 or
21 randomly assigned to either placebo (1 g/d, corn oil; 15 VF+, 11 VF-) or n-3 PUFA (1-4 g/d, docosahe
23 the total calories from fat with either 97% corn oil, 20% fish oil, 20% fish and 5% borage oil, or 2
24 the total calories from fat with either 97% corn oil, 20% fish oil, or 20% fish and 20% borage oil f
25 redosed with atRA (30 mg . kg-1 . d-1 PO) or corn oil 4 days before balloon withdrawal injury (BWI) o
27 after which they were given a daily dose of corn oil alone or 75 mg curcumin/kg in corn oil for 14 d
28 ic acid (ATRA)/kg body weight in corn oil or corn oil alone per os on days after inoculation (DAI) -1
29 d oil (obtained from Brassica napus) or with corn oil (also named maize oil, obtained from Zea mays,
31 erred to experimental diets containing 23.5% corn oil and 20.5% fish oil + 3% corn oil, whereas one g
32 The major result was that preloads of 25% corn oil and 25% mineral oil that produced equivalent in
33 tered equivolumetric gastric preloads of 25% corn oil and 25% mineral oil to pups on P9-12 and counte
34 il-in water emulsions were produced from 40% corn oil and 6% chickpea protein (w/w) with/without addi
36 nd ethanol showed only fatty liver, rats fed corn oil and ethanol showed fatty liver with moderate ne
37 y rats fed palm oil and ethanol and rats fed corn oil and ethanol, whereas rats fed MCTs and ethanol
39 nonparenchymal cell supernatant in rats fed corn oil and ethanol; plasma levels of TGF-beta 1 were n
40 nt intragastric infusions of maltodextrin or corn oil and for a flavor paired with delayed maltodextr
46 ute of Nutrition-76A diet containing low-fat corn oil and were given s.c. injections of AOM dissolved
47 semipurified AIN-76A diet containing low-fat corn oil and were s.c. injected azoxymethane (AOM) disso
48 fat as a source of lipids, diet B contained corn oil, and control diet C was a standard AIN-76A semi
49 reated them with RARgamma agonist or vehicle corn oil, and examined the effects of RARgamma agonist o
52 vitamin D3 decreased in the following order: corn oil approximately fish oil > orange oil > mineral o
53 ng order: medium chain triglycerides (MCT) > corn oil approximately fish oil > orange oil > mineral o
56 phytosterols were added back to sterol-free corn oil at a concentration of 150 mg/test meal, cholest
57 he microemulsion (CsA-ME; Neoral) versus the corn oil-based (CsA-GC; Sandimmune) gel capsule formulat
60 out in domestic felines to determine whether corn oil-based maternal diets are an adequate source of
62 different ratios of SO (soybean oil) and CO (corn oil) by nuclear magnetic resonance ((1)H NMR), comp
63 ent food grade vegetative oils (Coconut oil, Corn oil, Canola oil, Avocado oil, Sunflower oil, Olive
64 d 1 mg [(13)C(10)]retinyl acetate in a 0.5-g corn oil capsule and 300 g white maize porridge with 20
66 either fish oil (FO), flaxseed oil (FSO) or corn oil capsules (CO, served as a control group) and fo
69 rosomes prepared from male rats treated with corn oil (CO) or inducers of CYP2B (PB; phenobarbital) a
78 there was no difference between MCT and the corn oil control supplement in the intestinal messenger
79 ant Long-Evans rats were administered either corn oil (control) or 6 mg/kg/day of a commercial PCB mi
80 Mice were fed diets containing 5 g/100 g corn oil (control), 4 g/100 g fish oil (contains a mixtu
82 supplementation with 20 g MCT oil/d or 20 g corn oil/d on the kinetics of apolipoprotein (apo) B-48-
84 660 mg docosohexaenoic acid) versus placebo (corn oil) daily to standard of care in patients aged 70
87 s rich in omega-3 fatty acids, and a low-fat corn oil diet (LFCO) on the formation of chemically indu
89 by 142% (P < 0.001); supplementation of the corn oil diet increased plasma lutein by 50% (P < 0.05)
92 :5n-6 in the brains of animals in all of the corn oil-diet groups suggested that young felines have a
99 wo experimental groups (fish oil/ethanol and corn oil/ethanol) that had liver necrosis and inflammati
104 arts of BALB/c mice fed 3% and those fed 20% corn oil for 2 weeks and in liver (p < 0.05) from the sa
106 tients treated with the w-3 CA compared with corn oil for the top tertile of achieved EPA and DHA pla
108 the plasma TG excursions in db/db mice after corn-oil gavage (iAUC, 1,500 +/- 470 mg/dL.h for NT ASO
109 lease during reflow averaged 44 U/g/h in the corn oil group and 32 U/g/h in the fish oil group, but w
110 eached a maximum value of 62 nmol/g/h in the corn oil group, but only reached 43 nmol/g/h and 34 nmol
112 with omega-3 CA vs 795 (12.2%) treated with corn oil (hazard ratio, 0.99 [95% CI, 0.90-1.09]; P = .8
113 of zinc in various edible oils (canola oil, corn oil, hazelnut oil, olive oil, and sunflower oil) pr
114 nsferred to a high-fat diet containing 23.5% corn oil (HFCO) or 20.5% fish oil + 3% corn oil (HFFO).
115 ve experimental diets were provided high-fat corn oil (HFCO) or high-fat fish oil (HFFO) mixed in sem
116 76A diets containing high levels of high-fat corn oil (HFCO) rich in omega-6 fatty acids or high leve
118 isit May 14, 2020) comparing omega-3 CA with corn oil in statin-treated participants with high cardio
119 rograms/d on days 6 through 10 by fortifying corn oil in the diet with phylloquinone (supplemented di
121 nsfer of monosaccharides, amino acids, and a corn oil-in-water emulsion across a cellulose membrane w
122 oxides and headspace hexanal in the 5.0%(wt) corn oil-in-water emulsion from 4 to 9 and 14 days, resp
124 ion and beta-carotene bioaccessibility using corn oil-in-water emulsions with different initial dropl
125 the effect of polylysine on the digestion of corn oil-in-water emulsions, using a simulated gastroint
128 demonstrate that a high-fat diet containing corn oil increases colonic mucosal and tumor PLA2 and PI
129 independent ingestion (II), but preloads of corn oil inhibited intake significantly more than preloa
132 -dose and high-dose fish oil versus placebo (corn oil, linoleic acid) in 24 participants with drug re
133 s presented an equally complete digestion as corn oil LNPs and a high beta-carotene bioaccessibility,
136 oil and fish and borage oil as compared with corn oil may ameliorate endotoxin-induced acute lung inj
138 mparator (similar doses of maltodextrin plus corn oil; MD + CO) for 30 d, followed by a 60-d washout
141 reatments differing only in the type of fat (corn oil/n-6 PUFA, fish oil/n-3 PUFA, or olive oil/n-9 m
142 a-3 PUFA (flaxseed oil; N3) or omega-6 PUFA (corn oil, N6) on blood, muscle and follicular cell fatty
144 days and different diets were enriched with corn oil (omega-6), canola oil (omega-3 and omega-9), fi
145 nd esterified phytosterols were removed from corn oil on a kilogram scale by a new technique of compe
146 re gavaged with TBMEHP (200 or 500 mg/kg) or corn oil on gestational days 18 and 19, and dams and fet
147 mpared with an n-6 fatty acid-enriched diet (corn oil) on the following: a) lung microvascular protei
151 trans retinoic acid (ATRA)/kg body weight in corn oil or corn oil alone per os on days after inoculat
154 model studies demonstrated that high dietary corn oil or safflower oil rich in omega-6 fatty acids in
155 up) were fed ethanol or dextrose with either corn oil or saturated fat for 1-, 2-, and 4-week periods
156 given intraperitoneal injections of vehicle (corn oil) or 1alpha,25-dihydroxyvitamin D3 (1,25[OH]2D3;
157 egnancy and suckling, a control diet (4% w/w corn oil) or a fatty acid supplemented diet (24% w/w).
158 ant Long-Evans female rats received vehicle (corn oil) or DEHP at 10, 100, or 750 mg/kg by oral gavag
160 ntains a mixture of n-3 PUFA) plus 1 g/100 g corn oil, or 4 g/100 g corn oil plus 1 g/100 g DHA ethyl
165 iration of feeding hydrogenated coconut oil, corn oil, or menhaden oil (MO) to diabetes-prone BHE/cdb
166 the evolution of the minor compounds in the corn oil oxidation process, through the information prov
170 PUFA) plus 1 g/100 g corn oil, or 4 g/100 g corn oil plus 1 g/100 g DHA ethyl ester for 14 days.
172 part of the cholesterol-lowering activity of corn oil previously attributed solely to unsaturated fat
174 -knockout (dKO) mice liquid diets containing corn oil resulted in a percentage fat-dependent increase
175 mice isocaloric, high-fat diets composed of corn oil (rich in n-6 polyunsaturated fatty acids [n-6 P
176 injected with estrogen (30 microg/100 microl corn oil, s.c.) at 1000 h and on the 9th day they were i
177 injected with progesterone (2 mg/100 microl corn oil, s.c.) at 1000 h and subjected to push-pull per
178 ere fed isocaloric diets modified to include corn oil, safflower oil, or DFO (doses ranging from 0.75
179 Phytosterols comprising < 1% of commercial corn oil substantially reduced cholesterol absorption an
181 higher after consumption of the sterol-free corn oil than after consumption of commercial corn oil w
184 ing tallow, used cooking oil, and distillers corn oil to biodiesel and RD could achieve higher GHG re
186 Rats were fed a high-fat AIN-76A diet (23.5% corn oil) to mimic the Western dietary composition.
187 k, the addition of omega-3 CA, compared with corn oil, to usual background therapies resulted in no s
189 from tolerant mice were similar compared to corn oil-treated controls, while subtle shifts in organe
191 pants (5175 w-3 CA patients [49.8%] and 5207 corn oil-treated patients [50.2%]; mean [SD] age, 62.5 [
197 ally, from day 2 to day 9 after hatching) or corn oil vehicle (VEH) with or without monocular form de
200 following ovariectomy (day 0), injected with corn oil (vehicle), estrogen, or estrogen plus progester
201 0.21, 0.70 or 2.2mum) and oil digestibility (corn oil versus mineral oil) on the bioavailability of a
202 It was possible to determine rapeseed or corn oil volume fractions added into the olive oil using
203 h in saturated fat diet (VHF) (20 % lard and corn oil w/w) from weaning until adulthood, and througho
204 pH stat model also confirmed that emulsified corn oil was digestible, whereas emulsified mineral oil
209 e for hepatic Delta-6 desaturase in mice fed corn oil were 70 and 50% lower than in mice fed triolein
210 ostaglandin F1alpha, and thromboxane B2 with corn oil were significantly increased with endotoxin as
213 s for deep-frying: Wendy's clearly used only corn oil, whereas McDonald's and Burger King favored oth
214 ining 23.5% corn oil and 20.5% fish oil + 3% corn oil, whereas one group continued on the low-fat die
215 al chain restaurants served fries containing corn oil, whereas this was true for only a minority (20%
216 3% (high-fat) or 16% (low-fat) calories from corn oil, which consists mostly of n-6 polyunsaturated f
217 t) or 43% or 46% (high fat) of calories from corn oil, which primarily contains the n - 6 polyunsatur
218 to receive 4 g/d of omega-3 CA (n = 6539) or corn oil, which was intended to serve as an inert compar
219 orn oil than after consumption of commercial corn oil with an identical fatty acid content (P = 0.005
220 Furthermore, DRA in vitamin E-containing corn oil, with or without the addition of 4.6 mmol all-r
221 e hypothesis that removing phytosterols from corn oil would increase cholesterol absorption when meas