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1 r a 1; hazelnut), and Dau c 1.0104 (Dau c 1; carrot).
2 ich in both types of carotenoids (atomic red carrots).
3 taining good results except for eggplant and carrot.
4 s of nitrogen decreased the quality of fresh carrot.
5 ocyanin bioaccessibility in masticated black carrot.
6 llowed the order: sanguinello>apricot>tomato>carrot.
7 on the same batches of broccoli, tomato and carrot.
8 arge proportion of the observed variation in carrots.
9 containing a frame-shift insertion in orange carrots.
10 ts, red carrots, red tomatoes and atomic red carrots.
11 r determinants of nutritional quality of the carrots.
12 a higher vitamin C content and stability in carrots.
13 respectively, after 4 days compared to whole carrots.
14 e slightly more retained in parsnips than in carrots.
15 alcium content in the edible portions of the carrots.
16 g of carrots was 41% +/- 2% higher in sCAX1 carrots.
17 carrots to obtain the calcium found in sCAX1 carrots.
18 ter, to remove difenoconazole and linuron in carrots.
19 re observed between conventional and organic carrots.
20 etween conventionally- and organically-grown carrots.
21 il, 200 g carrots + 19 g olive oil, or 200 g carrots.
23 ys: 200 g carrots + 6.53 g tributyrin, 200 g carrots + 13.15 g C8-dietary oil, 200 g carrots + 19 g o
25 following 4 meals on 4 different days: 200 g carrots + 6.53 g tributyrin, 200 g carrots + 13.15 g C8-
27 ese cellular insights confirm that the major carrot allergen has a special status among Bet v 1-relat
28 er Bet v 1-related food allergens, the major carrot allergen, Dau c 1, has been suggested to induce f
29 Serum IgE to carrot extract, recombinant carrot allergens (rDau c 1.0104; rDau c 1.0201; rDau c 4
30 ive of this study was to evaluate a panel of carrot allergens for diagnosis of carrot allergy in Spai
31 f sensitization to carrot components between carrot allergic and carrot-tolerant but pollen sensitize
34 ms were major allergens for Swiss and Danish carrot allergic patients, the profilin rDau c 4 for the
35 c IFR 2 were recognized by 6% and 20% of the carrot allergics, but did not contribute to a further in
37 PBMC of birch pollen-allergic patients with carrot allergy were analyzed for reactivity to Bet v 1,
40 ied apples, prunes, figs, raisins, apricots, carrot and sweet potato, stevia leaves and liquorice roo
41 or the extraction of carotenoids from orange carrot and the extraction parameters were optimized.
43 eters) in order to assess the quality of the carrots and address the question whether organic also me
47 al-stable isotope method with (42)Ca-labeled carrots and i.v. (46)Ca to determine the absorption of c
49 and 1,619 mug Trolox/mg phenolics for whole carrots and shreds, respectively, for Choctaw cultivar).
50 by treated wastewater-irrigated root crops (carrots and sweet potatoes) grown in lysimeters and to e
51 tion system on the metabolite composition of carrots and to build statistical models for prediction p
54 ited for prediction of carotenoids in orange carrots, and especially for ranking them according to th
56 etween conventionally- and organically-grown carrots, and no potential harm arising from heavy metal
57 th different anthocyanin extracts from black carrot (Anthocarrot), grape fruit skins (Enocolor), elde
60 in prolonging the color stability of purple carrot anthocyanins (0.025%) in model beverages (0.05% l
63 ther carotenoid accumulating systems, orange carrots are characterized by unusually high levels of al
65 tion of organically and conventionally grown carrots, as well as for the geographical origin differen
66 Conventionally-, organically- and self-grown carrots available across the Czech market were character
71 nd purple grape, purple sweet potato, purple carrot, black and purple bean, black lentil (BL), black
72 of vitamin C in the range 37.5-85%, whereas carrots blanched conventionally at 60 degrees C and by U
74 ility of phytoene and phytofluene in tomato, carrot, blood orange (sanguinello cultivar), and apricot
76 ces were most pronounced in aliquots from 83 carrot broth aliquots collected after 6 h (84.3%) compar
77 rly-aliquot carrot broth-enhanced PCR of 144 carrot broth aliquots collected after fewer than 6 h of
78 ds increased sensitivity compared to that of carrot broth culture alone for the detection of Streptoc
80 ced PCR) in instances of subsequent positive carrot broth culture or positive overnight clinical carr
85 We investigated the prospect of reducing the carrot broth incubation time prior to PCR performance.
92 In the context of the result on day 1, both carrot broth- and LIM broth-enhanced PCRs generated more
93 ed sensitivity and specificity comparable to carrot broth- and LIM broth-enhanced real-time PCRs.
94 The predictive values for both protocols of carrot broth- or LIM broth-enhanced PCR were >/=95.4%.
95 . agalactiae detection rate by early-aliquot carrot broth-enhanced PCR (66.1%) exceeded that observed
96 liquots from 227 specimens were subjected to carrot broth-enhanced PCR (early-aliquot carrot broth-en
99 In vitro experimentation demonstrated that carrot broth-enhanced PCR nominally detected 10 CFU S. a
100 e samples (51.8%; P<0.0002) or early-aliquot carrot broth-enhanced PCR of 144 carrot broth aliquots c
102 to carrot broth-enhanced PCR (early-aliquot carrot broth-enhanced PCR) in instances of subsequent po
103 h culture using the BD GeneOhm StrepB assay (carrot broth-enhanced PCR) yields increased sensitivity
107 to enhance the antioxidant capacity (AC) of carrots by increasing the synthesis of phenolic compound
111 e commercial fresh-cut carrot products (baby carrots, carrot stixx, shredded carrots, crinkle cut coi
113 ffect was attributed to strengthening of the carrot cell walls under high pressure, thereby hindering
122 ns and in the prevalence of sensitization to carrot components between carrot allergic and carrot-tol
123 e portion size of the first course increased carrot consumption by 47%, or 12 +/- 2 g (P < 0.0001).
125 of 2-furoylmethyl-amino acids were found in carrots conventionally blanched with water at 95 degrees
127 oducts (baby carrots, carrot stixx, shredded carrots, crinkle cut coins, and oblong chips) were evalu
129 the estimated activation energy of the three carrot cultivars situated between 114.33 and 191.45 kJ/m
132 osynthesis of phenolic antioxidants in three carrots cultivars (Navajo, Legend and Choctaw) were stud
134 ike proteins rDau c IFR 1, rDau c IFR 2; the carrot cyclophilin rDau c Cyc) were analyzed by ImmunoCA
135 hromosome-scale assembly and analysis of the carrot (Daucus carota) genome, the first sequenced genom
136 were performed on mycorrhizas of transformed carrot (Daucus carota) roots and Glomus intraradices gro
137 plant-specific insoluble nuclear protein in carrot (Daucus carota), called Nuclear Matrix Constituen
138 roccoli (Brassica oleracea L. var. italica), carrot (Daucus carota), corn (Zea mays), and tomato (Sol
140 ascorbic acid oxidase (AAO) on vitamin C in carrots (Daucus carota subsp. sativus), namely Nantes, E
141 use using 660 seeds originating from 33 wild carrots (Daucus carota) collected near the Chernobyl nuc
142 oid accumulation in cultivated orange-rooted carrots (Daucus carota) is determined by a high protein
143 HPHT) processing on the volatile fraction of carrots, differently coloured cultivars exhibiting orang
144 d several fractures on both raw and blanched carrots due to ice crystals formation and re-crystallisa
145 cids as indicators of the damage suffered by carrots during their blanching and subsequent drying.
147 ols and phenolic acids) in tomato, broccoli, carrot, eggplant and grape has been carried out by ultra
148 beta-carotene isomerisation in an olive oil/carrot emulsion and pure olive oil phase enriched with c
151 y, pectin in tissue particles of LTB and HTB carrots exhibited low degree of methylesterification (DM
152 ong pollen allergic controls, 34% had IgE to carrot extract, 18% to each of rDau c 1.0104, rDau c 1.0
159 g of exposure affected the acceptance of the carrot flavor that did not generalize to the novel brocc
160 7.9 mo of age, infants' acceptance of plain, carrot-flavor (exposed flavor), and broccoli-flavor (non
161 e, which resulted in a faster rate of eating carrot-flavored cereal than that in infants who were exp
162 ronomic rules for iodine biofortification of carrot for: (a) consumption and/or processing directly a
163 In order to speed up the breeding of orange carrots for high carotenoid content it is imperative to
164 ents, both occurring after the divergence of carrot from members of the Asterales order, clarifying t
165 different matrices such as tomato, broccoli, carrot, grape and eggplant, observing that chlorogenic a
168 erent chemical species of Se in broccoli and carrots grown in soils amended with ground shoots of the
174 vitamin A in humans after consumption of raw carrots.Healthy adults (n = 12) consumed a meal containi
185 so), associated with vegetative disorders in carrots, is transmitted by the carrot psyllid Bactericer
186 oxidant capacity and phenolic acids in black carrot jams and marmalades after processing, storage and
187 conclusion, current study highlighted black carrot jams and marmalades as good sources of polyphenol
189 (P = 0.004) but not of the control solutions carrot juice (P = 0.26), NaCl (P = 0.68), caffeine (P =
190 re employed in the formulation of functional carrot juice and functional juices were treated using th
191 ch focuses on the study of polyacetylenes in carrot juice and their response to pH, storage and therm
192 (FaDOAc) and falcarinol (FaOH) were in fresh carrot juice at concentrations of 73 and 233 mug/L, resp
193 ing technology for preserving the quality of carrot juice by minimising the physicochemical changes d
195 ween phenolic acids (PA) derived from purple carrot juice concentrate (PCJC) and PCW components.
198 ication of the method to a BoNT-contaminated carrot juice sample resulted in the identification of 98
200 vels was applied for the optimization of the carrot juice with peel (CJPL) and pulp (CJPP) extracts.
201 digestion of carotenoids and retinoids from carrot juice, raw and cooked spinach, micronutrient-fort
204 g mothers drank vegetable, beet, celery, and carrot juices for 1 mo beginning at 0.5, 1.5, or 2.5 mo
206 (BA) of carotenoids from edible portions of carrot, mango, papaya, and tomato was compared using an
209 of the agricultural system of the harvested carrots on the basis of features determined by liquid ch
210 gy and associated food allergy to hazelnuts, carrots, or both were analyzed for IgE cross-reactivity,
211 Oil-in-water emulsions were prepared with carrot- or tomato-enriched olive oil (5%w/v) and stabili
216 ene) from yellow and green leafy vegetables [carrots, pechay (bok choy), squash, and kangkong (swamp
218 res were also detected in extracts of intact carrot plants cultivated on triclosan contaminated soils
219 e different anthocyanin compounds from black carrot pomace with cyanidin-3-xyloside-galactoside-gluco
223 Association mapping analysis using a large carrot population revealed a significant association of
227 properties have been evaluated in air-dried carrots previously subjected to different ultrasound (US
229 nica (dicot, Apiaceae), also known as deadly carrot, produces the highly toxic compound thapsigargin.
230 (PAL) activity of five commercial fresh-cut carrot products (baby carrots, carrot stixx, shredded ca
235 n = 12) consumed a meal containing 300 g raw carrot (providing 27.3 mg beta-carotene and 18.7 mg alph
237 tion describing the elemental composition of carrots published previously, recommended daily intakes,
238 omanian agro-industrial wastes (apple peels, carrot pulp, white- and red-grape peels and red-beet pee
239 of endogenous ascorbic acid oxidase (AAO) in carrot puree (Daucus carota cv. Nantes) after being trea
240 the same order of magnitude as the untreated carrot puree after being exposed to pulsed electrical en
241 rrot puree could be related to the resulting carrot puree composition, alteration in intracellular en
242 nzyme kinetics and thermostability of AAO in carrot puree could be related to the resulting carrot pu
243 f k value (Ea value) for AAO inactivation in carrot puree decreased, indicating that the changes in k
244 processing on the bioprotective capacity of carrot puree for White Belgian, Yellow Solar, Nantes, Nu
245 apolation of data for these model systems to carrot puree suggests that nutritionally-significant amo
248 pressure high temperature (HPHT) sterilised carrot purees using a 'fingerprinting kinetics' approach
249 chemical composition of broccoli, tomato and carrot purees were investigated by using a range of comp
250 s (with I and N application) with respect to carrot quality when compared to results obtained after t
253 In fact, overexpression of CYP97A3 in orange carrots restored leaf carotenoid patterns almost to thos
255 three orders of magnitude, while the dynamic carrot root (DCR) portion overpredicted by a single orde
256 analysis (PCA) revealed metabolic variety of carrot root composition depending on root color and bota
259 NES) analysis performed on broccoli florets, carrot roots and shoots, dried ground S. pinnata, and th
260 s, anthocyanins and carotenoids was noted in carrot roots directly after the harvest as well as at th
261 he best markers that could differentiate the carrot samples grown in Transylvania, Romania, from thos
262 dentified for the first time in freeze-dried carrot samples that were collected over 25 years ago as
263 able to differentiate the organically grown carrots samples in a percent of 83.3% (initial classific
268 in beta-carotene, such as natural (spinach, carrots, spirulina), hybrid (high-beta-carotene yellow m
269 ange, mango, apple, kiwi, lettuce, broccoli, carrot, squash, eggplant, radish, mushroom, cucumber, an
271 ial fresh-cut carrot products (baby carrots, carrot stixx, shredded carrots, crinkle cut coins, and o
273 at conditions carotenoid accumulation (Y) in carrot taproot and is coexpressed with several isoprenoi
276 e required twice the serving size of control carrots to obtain the calcium found in sCAX1 carrots.
278 ot allergic patients, 71 pollen allergic but carrot-tolerant patients and 63 nonatopic controls were
279 28 teeth had significantly lower intakes of carrots, tossed salads, and dietary fiber than did fully
280 that when people were fed sCAX1 and control carrots, total calcium absorption per 100 g of carrots w
282 alose was able to limit the hardness loss of carrots undergone to B, C and D blanching pre-treatments
283 Regarding sensorial analysis of rehydrated carrots, US-pretreated samples presented acceptable qual
284 In 3 of the meals, a first course of raw carrots varied in portion size (30, 60, or 90 g), and no
287 on of total arsenic in potatoes, swedes, and carrots was lower in peeled produce compared to unpeeled
288 age of absorption of alpha-carotene from raw carrots was not significantly different from beta-carote
290 y related cyanidin-3-O-glycosides from black carrot were investigated in aqueous solutions (pH 3.6 an
293 of phytochemicals was higher when fresh-cut carrots were stored at 4 degrees C regardless of the pre
295 among samples A and B water-blanched and raw carrot while a thermo-protective effect due to the sugar
297 activation was found in 80 degrees C-treated carrots with high vitamin C retention predominantly in l
298 randomized trials, we labeled these modified carrots with isotopic calcium and fed them to mice and h
299 treatments at high temperature gave rise to carrots with retention of vitamin C in the range 37.5-85
300 vels of total phenolic acids compared to the carrots with the supplement of B (e.g. -Ca treatment and
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