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4 nge-peeled fruits represent a rich source of provitamin A (ca. 124 mug retinol-activity-equivalents/1
5 n of fruit development and ripening; neither provitamin A (carotenoids) nor vitamin E contents were m
6 Treatment for STH significantly increases provitamin A (e.g., beta-carotene) levels but is associa
8 a unique ability to promote and/or stabilize provitamin A accumulation during plant growth and post-h
9 sociation between intake of carotenoids with provitamin A activity and carotid artery plaques in 12,7
12 the activities of dietary beta-carotene as a provitamin A and as a modulator of risk for cardiovascul
13 gress on biofortification of micronutrients (provitamin A and folates) and an essential amino acid (l
14 respectively, and the total daily supply of provitamin A and vitamin A from diet and supplements was
15 r RA production in adipocytes and implicates provitamin A as a dietary regulator of body fat reserves
17 bal health burden, can be alleviated through provitamin A carotenoid biofortification of major crop s
18 Conventionally bred maize hybrids with high provitamin A carotenoid concentrations may have the pote
20 15'-monooxygenase 1 (BCMO1), a key enzyme in provitamin A carotenoid metabolism, as a surrogate for c
25 [odds ratio (OR): 0.31; 95% CI: 0.04, 2.44], provitamin A carotenoids (OR: 0.31; 95% CI: 0.03, 2.84),
29 take of vitamin A in the form of retinol and provitamin A carotenoids and the prevalence of bronchial
30 cesses through which beta-carotene and other provitamin A carotenoids are converted to vitamin A, the
33 ur results show that BCO1 favors full-length provitamin A carotenoids as substrates, with the notable
34 e (BCO1) catalyzes the oxidative cleavage of provitamin A carotenoids at the central 15-15' double bo
35 BCO2 catalyzes the oxidative cleavage of the provitamin A carotenoids beta-carotene, alpha-carotene,
36 imating the metabolic vitamin A potential of provitamin A carotenoids by using [2H4]retinyl acetate (
37 ess the bioavailability and bioconversion of provitamin A carotenoids have advanced significantly in
38 for stabilizing and increasing the level of provitamin A carotenoids in seeds of major food crops.
41 in A value of individual plant foods rich in provitamin A carotenoids may vary significantly and need
44 mucosa plays a key role in the metabolism of provitamin A carotenoids such as beta-carotene, thus gre
45 ltimately they must derive them from dietary provitamin A carotenoids through a process known as caro
46 xcentric cleavage of both provitamin and non-provitamin A carotenoids to form apo-10'-carotenoids, in
47 catalyzes the oxidative cleavage of dietary provitamin A carotenoids to retinal (vitamin A aldehyde)
48 measurement of the bioconversion of dietary provitamin A carotenoids to vitamin A is reviewed in thi
49 s of the food matrix on the bioconversion of provitamin A carotenoids to vitamin A, dietary fat effec
52 cleavage of 9-cis-beta-carotene and the non-provitamin A carotenoids zeaxanthin and lutein, and is i
55 of lutein/zeaxanthin, lycopene, sum of the 3 provitamin A carotenoids, beta-carotene, and beta-crypto
56 e human and other species clearly absorb non-provitamin A carotenoids, little is known of the extent
57 ed to estimate dietary intake of retinol and provitamin A carotenoids, tobacco exposure, and asbestos
64 les and 2) retinyl palmitate formed from the provitamin A carotenoids.Women (n = 12) each consumed 5
76 cy of red palm oil in increasing retinol and provitamin A status in pregnant and lactating women.
77 aize meal can provide significant amounts of provitamin A to diets of Zambians even after 4months of
78 rovided the greatest amount of bioaccessible provitamin A with 1850 mug/100g dry matter (DM) versus 7
80 nventional white cassava roots are devoid of provitamin A, biofortified yellow varieties are naturall
81 These carotenoid-derived products include provitamin A, hormones, and flavor and fragrance molecul
82 entation with red palm oil, which is rich in provitamin A, increased alpha- and beta-carotene concent
83 Development of a rice variety enriched in provitamin A, the accumulation of polyhydroxybutyrate po
84 feature to measure electronic properties of provitamin A, vitamin E, and vitamin K1 in the gas phase
89 can catalyze the excentric cleavage of both provitamin and non-provitamin A carotenoids to form apo-
90 ts competition between BCO1 and BCO2 for the provitamin and the production of noncanonical beta-carot
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