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1 ignificantly this content, compared to fresh broccoli.
2 o other Brassicaceae plants such as kale and broccoli.
3 l novel aptamers, including a 49-nt aptamer, Broccoli.
4 of glucoraphanin, the main glucosinolate in broccoli.
5 the isothiocyanate sulforaphane derived from broccoli.
6 ucoraphanin that specifically accumulates in broccoli.
7 ybrids have been commercialised as Beneforte broccoli.
8 n to sulforaphane (SF), the ITC derived from broccoli.
9 lly active phytochemical found abundantly in broccoli.
10 is most similar (66.1% identity) to that of broccoli.
11 , Se-methyl selenocysteine and myrosinase in broccoli.
12 s after digestion compared to longer-steamed broccoli.
13 a reduced level of off-flavour in processed broccoli.
14 eloped for the Brassica species pak choi and broccoli.
15 ntioxidant compounds in both cauliflower and broccoli.
16 nd in spinach, rocket, watercress, chard and broccoli.
17 ncluding tomato, carrot, grape, eggplant and broccoli.
18 designed to favor sulforaphane synthesis in broccoli.
19 ccoli (5:5 combination), 10% tomato plus 10% broccoli (10:10 combination) powders, or lycopene (23 or
21 ed diet was supplemented for 5 d with either broccoli (377 microg phylloquinone/d; broccoli diet) or
22 randomly assigned to consume 400 g standard broccoli, 400 g HG broccoli, or 400 g peas each week for
24 10% tomato, 10% broccoli, 5% tomato plus 5% broccoli (5:5 combination), 10% tomato plus 10% broccoli
25 6) were fed diets containing 10% tomato, 10% broccoli, 5% tomato plus 5% broccoli (5:5 combination),
28 t slowing tumor growth than either tomato or broccoli alone and supports the public health recommenda
30 mination of carbamate pesticides in cabbage, broccoli and apple samples without any spiking procedure
31 cosinolate precursor in certain varieties of broccoli and broccoli sprouts, is a potent bacteriostati
32 ne (SFN), a compound found at high levels in broccoli and broccoli sprouts, is a potent inducer of ph
33 s, endogenous mRNA molecules recruited Split-Broccoli and brought the two fragments into spatial prox
34 stantial levels in several food crops (e.g., broccoli and cabbage), forms DNA adducts in vitro and is
37 ere investigated in artichokes, green beans, broccoli and carrots cooked under different conditions.
38 and the different chemical species of Se in broccoli and carrots grown in soils amended with ground
39 s valuable as a soil amendment for enriching broccoli and carrots with healthful forms of organic-Se.
41 of cultivars of certain crucifers including broccoli and cauliflower contain 10-100 times higher lev
42 of flavonoids, carotenoids and vitamin A in broccoli and cauliflower inflorescences grown in an orga
43 family Cruciferae and genus Brassica (e.g., broccoli and cauliflower) contain substantial quantities
44 matrix samples such as garlic, onion, leek, broccoli and cauliflower, are the main advantages of IL-
45 nt increases from 34% to 100% of increase in broccoli and from 45% to 118% of increase in radish spro
46 d on the cells incubated with the mixture of broccoli and green tea than on cells exposed to control
47 nd increased glucosinolates concentration in broccoli and it decreased the formation of acrylamide in
49 ucOC values were lower (P = 0.001) after the broccoli and oil diets than after the mixed diet only.
50 successful and feasible treatment to produce broccoli and radish sprouts with enhanced levels of heal
52 Among specific foods high in carotenoids, broccoli and spinach were most consistently associated w
55 sprouts of two Brassica oleracea varieties, broccoli and Tuscan black kale, and two Raphanus sativus
56 nent of Brassica vegetables such as cabbage, broccoli, and Brussels sprouts, has been shown to reduce
58 and then were served a main course of pasta, broccoli, applesauce, and milk, which was also consumed
59 sponses to diet in individuals within the HG broccoli arm, differentiated by single nucleotide polymo
63 c cauliflower) and B. oleracea ssp. italica (broccoli), both of which show evolutionary modifications
65 that resolves all major carotenoids found in broccoli (Brassica oleracea L. var. italica), carrot (Da
66 ively, in vegetative tissues of Arabidopsis, broccoli (Brassica oleracea L.), and mustard (Brassica n
67 involved in Se volatilization from plants, a broccoli (Brassica oleracea var italica) cDNA encoding C
74 to quantify 10 individual glucosinolates in broccoli, broccoli sprouts, Brussels sprouts, and caulif
75 avity (MHG) technology was used to dehydrate broccoli by-products and simultaneously recover the wate
76 ential of MHG technology for valorisation of broccoli by-products by its simultaneous stabilization b
77 imed to characterize and quantify industrial broccoli by-products for their glucosinolate and polyphe
80 rial with 12% moisture in 43min when 550g of broccoli by-products were used, preserving polysaccharid
82 ng component of Brassica vegetables, such as broccoli, cabbage, and Brussels sprouts, induces a G(1)
83 etary intake of Brassica vegetables, such as broccoli, cabbage, and Brussels sprouts, protects agains
86 Antioxidant activity of six Brassica crops-broccoli, cabbage, cauliflower, kale, nabicol and tronch
88 complexes, including Spinach, Spinach2, and Broccoli, can be used to tag RNAs and to image their loc
89 ts glucosinolate precursor which is found in broccoli, can prevent cartilage destruction in cells, in
90 es, flavonols and phenolic acids) in tomato, broccoli, carrot, eggplant and grape has been carried ou
91 pplied to different matrices such as tomato, broccoli, carrot, grape and eggplant, observing that chl
92 luding (orange, mango, apple, kiwi, lettuce, broccoli, carrot, squash, eggplant, radish, mushroom, cu
93 t in plants of the Brassica genus, including broccoli, cauliflower, and Brussels sprouts, exhibits pr
94 st extensively consumed Brassica vegetables (broccoli, cauliflower, green cabbage, Chinese cabbage, k
95 sticide residues at trace levels in cabbage, broccoli, cauliflower, lettuce, celery, spinach, and mus
97 between organic and conventional vegetables (broccoli, collard greens, carrots and beets), both raw a
99 e pesticides by 30-70% on tomato, rice, tea, broccoli, cucumber, strawberry, and other plants when tr
101 bined procedures were applied to a sample of broccoli (cultivar SAGA), in order to resolve and identi
105 content of ascorbic acid and glutathione in broccoli degraded during storage at 23 degrees C, for at
106 foraphane (SFN), a synthetic analogue of the broccoli-derived l-isomer, is a highly promising cancer
108 The metabolic changes observed with the HG broccoli diet are consistent with a rebalancing of anapl
109 either broccoli (377 microg phylloquinone/d; broccoli diet) or phylloquinone-fortified oil (417 micro
112 any edible cruciferous vegetables, including broccoli, effectively suppresses proliferation of cancer
114 f pyrethroid-resistant aphids that fed on Bt broccoli expressing Cry1Ab or Cry1C, or on non-Bt brocco
115 he effects of enzymatic-digested Se-enriched broccoli extracts (SeB) and selenocompounds on growth an
117 f plain, carrot-flavor (exposed flavor), and broccoli-flavor (nonexposed flavor) cereals was assessed
118 of ascorbic acid and glutathione content in broccoli florets (Brassica oleracea L. italica cv. Bells
119 nt of total ascorbic acid and glutathione in broccoli florets averaged at 5.18 +/- 0.23 and 0.70 +/-
120 nt of total ascorbic acid and glutathione in broccoli florets before and after mechanical processing
123 edge structure (XANES) analysis performed on broccoli florets, carrot roots and shoots, dried ground
124 hotoperiods influence the sensory quality of broccoli florets, while contents of different bioactive
125 The acidic alpha-glucosidase activity from broccoli flower buds was purified using concanavalin A a
129 the incorporation of red cabbage, radish and broccoli germinated seeds into the diet to promote poten
131 hree industrially relevant green vegetables: broccoli, green pepper and spinach treated with thermal
133 l, physicochemical and functional changes of broccoli head samples stored at 1-2 degrees C and 85-90%
140 f optimal fertilization strategies to enrich broccoli in Se with minimal impairment of antioxidants p
143 protein (GFP)-mimicking turn-on RNA aptamer, Broccoli, into two split fragments that could tandemly b
149 es and glycosidases, including myrosinase in broccoli, is key to the final metabolite composition and
150 bitterness intensity of PROP (P = 0.007) and broccoli juice (P = 0.004) but not of the control soluti
151 ry and concentration of phytotherapeutics in broccoli juice was investigated to develop a natural pro
152 All the bioactive compounds identified in broccoli juice was well preserved during subsequent 6-fo
154 of this study was to evaluate the effect of broccoli leaf powder (BLP) on the content of biologicall
156 Finally, glucosinolates were analyzed in broccoli leaf samples from six different cultivars (Ramo
157 E; neoglucobrassicin, NEO; sinigrin, SIN) in broccoli leaves using liquid chromatography (LC) coupled
159 cancer and in control subjects were spinach, broccoli, lettuce, tomatoes, oranges and orange juice, c
166 to consume 400 g standard broccoli, 400 g HG broccoli, or 400 g peas each week for 12 wk, with no oth
169 que model system consisting of Bt transgenic broccoli plants and the diamondback moth, Plutella xylos
170 esis using a unique model system composed of broccoli plants transformed to express different Cry tox
171 oli expressing Cry1Ab or Cry1C, or on non-Bt broccoli plants treated or not treated with the pyrethro
172 Surely the panellists ate more than just the broccoli portion - please clarify vitro experiments; fur
173 per, chemical and sensory data obtained from broccoli, potatoes, salmon and cocoa cakes cooked using
174 rged inflorescence (curd) of cauliflower and broccoli provide not only a popular vegetable for human
175 he volatile profile of differently processed broccoli puree, and to investigate if any relationship p
176 fingerprinting of the differently processed broccoli purees revealed that an adequate combination of
177 ost suitable postharvest treatment to extend broccoli quality during storage and shelf life, in terms
179 isothiocyanates derived from watercress and broccoli, respectively) and correlate structural feature
180 p to 10 times higher in raw and 1min steamed broccoli samples after digestion compared to longer-stea
181 w antiproliferative activity, the extract of broccoli seedlings biofortified with selenium stood out,
183 ile sulphoraphane, the dominant bioactive in broccoli seedlings, inhibited NF-kappaB activity with an
188 powdered mustard seeds to the heat processed broccoli significantly increased the formation of sulfor
190 , an Nrf2 activator) and its natural source, broccoli sprout extract (BSE) by gavage every other day
191 chemical sulforaphane (n = 29)--derived from broccoli sprout extracts--or indistinguishable placebo (
193 polyphenols (GTPs) and sulforaphane (SFN) in broccoli sprouts (BSp) on neutralizing epigenetic aberra
197 half-serving (30 g) or one serving (60 g) of broccoli sprouts on the urinary concentrations of biomar
199 n of sulforaphane-rich extracts of 3-day-old broccoli sprouts up-regulated phase 2 enzymes in the mou
200 fy 10 individual glucosinolates in broccoli, broccoli sprouts, Brussels sprouts, and cauliflower.
201 ecursor in certain varieties of broccoli and broccoli sprouts, is a potent bacteriostatic agent again
202 ompound found at high levels in broccoli and broccoli sprouts, is a potent inducer of phase 2 detoxif
207 predominantly located in the outer cortex of broccoli stems and in vascular tissue, especially in lea
209 many edible cruciferous vegetables including broccoli, suppresses growth of prostate cancer cells in
210 Sulforaphane (SFN) is an isothiocyanate from broccoli that induces phase 2 detoxification enzymes.
211 dible seeds, showing red cabbage, radish and broccoli the highest contents (21.6, 20.4 and 16.4 mg GA
212 owerful Phase 2 enzyme inducer isolated from broccoli), the toxicities of the oxidants were markedly
213 n glucosinolate genetics from Arabidopsis to broccoli, the use of wild Brassica species to develop cu
214 re not affected when fed aphids reared on Bt broccoli, thus demonstrating the safety of these Bt plan
215 ng at 90 degrees C determines the pattern of broccoli tissue disruption, resulting into different mic
216 ilarity of the Brassica homolog IPMS-Bo from broccoli to its Arabidopsis counterpart IPMS-At was on t
217 ves, cucumbers, carrots, red pepper, and raw broccoli) to consume in a free-choice intake test and to
218 te images of objects (e.g., a baseball and a broccoli) to each eye using a mirror stereoscope and ask
219 steps on global phytochemical composition of broccoli, tomato and carrot purees were investigated by
221 For some raw vegetables, such as spinach or broccoli, underestimation of vitamin E in nutrient datab
222 onsible for SeMSC formation, was cloned from broccoli using a homocysteine S-methyltransferase gene p
225 esilient isoform of myrosinase, to processed broccoli was investigated with a view to intensify the f
228 coraphanin (less than 12%) was observed when broccoli was placed in vacuum sealed bag (sous vide) and
229 ost to flavonoid intake in this cohort, only broccoli was strongly associated with reduced risk of CH
230 om chestnut, red and white grapes, olive and broccoli wastes, the relative antioxidative abilities of
231 en successfully applied to determine ITCs in broccoli, white cabbage, garden cress, radish, horseradi
233 ditions of drying processes to produce dried broccoli with optimal MYR retention for human health.
234 ate found in cruciferous vegetables, such as broccoli, with potent chemoprotective effects in several
235 ry intervention with high-glucoraphanin (HG) broccoli would modify biomarkers of CVD risk and plasma
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