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1 ure population-scale genome-wide analyses of blueberry.
2 ults highly comparable to that of commercial blueberry.
3 ntation of genome-based breeding methods for blueberry.
4 indering genetic research and improvement in blueberry.
5 genetic factors influencing these traits in blueberry.
6 for the application of genomic prediction in blueberry.
7 and syringic acid (147.14%) was observed in blueberry.
8 creasing order of blackberry>black raspberry>blueberry.
9 tent of the three groups of phenolics in the blueberries.
10 From these, 10 were previously reported in blueberries.
11 a-rhamnoside was found for the first time in blueberries.
12 content of individual phytochemicals in ripe blueberries.
13 anthocyanin levels found in blackberries and blueberries.
14 a-rhamnoside was found for the first time in blueberries.
15 soft-skinned fruits such as strawberries and blueberries.
16 collection representing cultivated highbush blueberries.
17 uents and antioxidant capacity of dehydrated blueberries.
18 were unaffected after postprandial and 6-mo blueberries.
19 mnetin were also found for the first time in blueberries.
20 s extracted and characterized from high-bush blueberries.
21 xidant capacity and texture of frozen/thawed blueberries.
22 f drying, on the rehydration kinetics of dry blueberries.
23 Catechin had the highest bioaccessibility in blueberry (270.71%), blackberry (137.51%), and jabuticab
24 polyphenols present in one serving of fresh blueberries (73g) were delivered in just 1.4 g of bluebe
28 Herein, a food-to-food fortification with blueberries and black tea was performed for people suffe
30 n-3-glucoside (M3G), an anthocyanin found in blueberries and grapes, shows promise as a natural anti-
32 perm with the order Ericales (which includes blueberries and persimmons), was obtained with these dat
34 s antioxidant-rich berry diets, specifically blueberries and strawberries, countered the deleterious
35 Combined intake of 2 anthocyanin-rich foods, blueberries and strawberries, tended to be associated wi
38 ove the antioxidant properties of cranberry, blueberry and apple juices was evaluated for the formula
39 ps on diets with high complexation ratios of blueberry and cranberry aggregates showed significant re
40 on was reduced in a dose-dependent manner in blueberry and cranberry complexed peanut protein supplem
41 easured by FRAP assay of concentrated apple, blueberry and cranberry juice was increased by 40%, 34%,
42 LDL oxidation inhibition by concentrated blueberry and cranberry juice was increased up to 41% an
43 oybean flour (DSF) can sorb polyphenols from blueberry and cranberry juices while separating them fro
46 polyphenols (anthocyanins) from blackberry, blueberry and grumixama residues using combined ultrason
47 cles, created by complexing polyphenols from blueberry and muscadine grape pomaces with a rice-pea pr
48 present post-digestion) was 69% and 62% from blueberry and muscadine grape protein-polyphenol particl
50 d during the first 50min in presence of both blueberry and pomegranate juices, then a constant decrea
51 after Elliott blueberry relative to Olympia blueberry and protein bar (21% and 29%, respectively).
52 wing Elliott blueberry compared with Olympia blueberry and protein bar (26.63 and 25.32 ng/mL higher,
54 rosehip, chokeberry, hawthorn, blackcurrant, blueberry and rowanberry via different methods (ORAC, TR
55 ality control and authentication analyses of blueberry and strawberry fruits and their commercial foo
56 creases in intakes of tea, red wine, apples, blueberries, and oranges tended to be associated with lo
57 tardants in red fruit samples (strawberries, blueberries, and raspberries) using gas chromatography-m
59 nkle plants with virescence, and blackberry, blueberry, and raspberry plants displaying yellowing and
60 sed to quantify anthocyanins in red cabbage, blueberry, and strawberry samples with improved analytic
62 ion and juice dilution, the concentration of blueberry anthocyanins and total polyphenols sorbed to D
63 re intestinal absorption/bioaccessibility of blueberry anthocyanins under different digestive conditi
65 Although the flavonoid constituents of ripe blueberries are known, the molecular genetics underlying
71 at such supplements (strawberry, spinach, or blueberry at 14.8, 9.1, or 18.6 gm of dried aqueous extr
72 d at each farm are not registered for use on blueberry at any time (55.2% of AIs detected), including
73 ing a one-time exposure to the novel odor of blueberry bars or cornnuts, in contrast to presentation
74 w) or high (40%; w/w) complexation ratios of blueberry (BB-Low and BB-High) and cranberry (CB-Low and
75 nce and pairing demonstrated that tetraploid blueberry behaves as an autotetraploid with tetrasomic i
76 and quantified with HPLC-MS(n) in fruits of blueberry, bilberry, cranberry, lingonberry, eastern sha
77 rent soft fruits (strawberries, raspberries, blueberries, blackberries and currants) produced in a no
78 ar) and on 1500 samples of northern highbush blueberry (Bluecrop, Jersey, and Liberty) for hyperspect
79 new cultivars released from the New Zealand blueberry breeding programme and selected for the longes
83 In conclusion, ABA delayed the ripening of blueberries, but did not affect total phenolic content,
84 re-treatment reduced the moisture content of blueberries by 56 % in 6 min, reducing the complete dehy
85 onducted on 300 samples of southern highbush blueberry (Camellia, Rebel, and Star) and on 1500 sample
86 ised in powdered berry extracts of bilberry, blueberry, chokeberry, acai berry and cranberry by HPTLC
90 )propanoic acid was higher following Elliott blueberry compared with Olympia blueberry and protein ba
91 fied using frozen blueberry (n = 4 studies), blueberry concentrate (n = 2), beverage (n = 3), capsule
92 ne and 1, 2, 4, and 6 h after consumption of blueberry containing 766, 1278, and 1791 mg total bluebe
93 of papanridins is prevalent in cacao, grape, blueberry, corn, rice, Arabidopsis, and other species in
97 xenal were key compounds that differentiated blueberry cultivars via Principal Component Analysis (PC
98 and anthocyanin metabolism in two rabbiteye blueberry cultivars, Premier and Powderblue, during frui
104 and for pomegranate and 1.7 per thousand for blueberry, demonstrating the potential hypoglycemic effe
106 the best manufacturing procedure to prepare blueberry-derived products, well accepted by the consume
110 ost studies identify only a few flavonols in blueberries due to separation and identification issues.
111 ed in their pollen are registered for use on blueberry during bloom (56.9% of AIs detected), though f
112 ty of genomic prediction has been proven for blueberry, enabling a reduction in the breeding cycle ti
114 he performance of the radiated animals given blueberry extract did not differ from the radiated anima
115 investigated the chemopreventive activity of blueberry extract in triple-negative breast cancer cell
117 ity via ORAC, TRAP and HORAC assays, whereas blueberry extract was the most potent inhibitor of lipid
118 cterization of the antioxidant capacity of a blueberry extract while demonstrating that it had no per
121 present study, the chemoprotective action of blueberry extracts against cadmium toxicity was investig
124 f encapsulation on the release properties of blueberry extracts during simulated gastrointestinal dig
126 Immunohistochemical analysis of tumors from blueberry-fed mice showed decreased activation of AKT an
127 Degradation of boscalid was studied in a blueberry field located in Concordia, Argentina, with fr
129 actices to both increase the productivity of blueberry fields and the wellbeing of honey bees within
134 e very limited data regarding the effects of blueberry flavonoid intake on vascular function in healt
136 on, respectively) than those observed in the blueberry (FRAP: 10 +/- 2 and 19 +/- 3 muM FeSO4/gFW; TE
137 re, the higher total phenolic content in the blueberry fruit and jam justified their greater antioxid
139 laid on, and 65% fewer adults emerged from, blueberry fruit treated with either the 'fruit' or 'colo
140 pressed sequence tag libraries from ripening blueberry fruit were constructed as a resource for gene
142 applied to detect potential changes on fresh blueberry fruits in commercial storage temperature.
143 red raspberry, strawberry, sweet cherry and blueberry fruits produced in the subtropical areas of Br
146 lavonols, phenolic acids, and resveratrol in blueberry genotypes with fruit color ranging from deep p
147 berry, raspberry, blackberry, black currant, blueberry, gooseberry, chokeberry, cape gooseberry, and
148 a multiresidue panel of pesticides in apple, blueberry, grape, and strawberry through direct-coupling
149 The Principal Component Analysis showed that blueberry groups can be distinguished based on their phe
150 ccinii is now spreading rapidly across major blueberry-growing regions, including China, Morocco, Mex
151 he highest LP activity was found for Chilean blueberries (>95%) followed by calafate fruits (91.27%)
157 s (compound had the highest concentration in blueberry honey), and interval ratio-markers (the ratio
158 ingle-markers (compound was only detected in blueberry honey), threshold single-markers (compound had
164 f pterostilbene (PS), a natural component of blueberries, in preventing ocular surface inflammation u
167 r tested as sanitizing washes on lettuce and blueberries inoculated with food-borne bacterial biofilm
170 RCT to date, we examined the effect of 6-mo blueberry intake on insulin resistance and cardiometabol
172 conducted, which fed 2 dietarily achievable blueberry intakes [equivalent to 1/2 and 1 cup/d (75/150
176 verage nucleotide identity (ANI) between the blueberry isolate and type strains of Agrobacterium spec
178 the extracted filtrates and mycelium from 15 blueberry isolates of this endophyte revealed difference
181 ere determined in acai, cupuacu, blackberry, blueberry, jabuticaba, raspberry, caja and soursop froze
184 (McIlvaine buffer, pH=3.6, the typical pH of blueberry juice) during thermal (40-80 degrees C) and co
185 ) in Mcllvaine buffer (pH=3.6, typical pH of blueberry juice) was subjected to processing at isotherm
187 owders of raspberry (R), blackberry (B), and blueberry (L) were used to replace 2 % of the starch in
188 this study, we investigated whether highbush blueberry leaves (BL) can serve as a source of bioactive
191 amples, including mixed flavonoid standards, blueberry, mizuna, purple mustard, red cabbage, and red
192 eleven articles were identified using frozen blueberry (n = 4 studies), blueberry concentrate (n = 2)
194 emented with either spinach, strawberries or blueberries, nutritional sources of antioxidants, revers
195 n of anthocyanin monomeric isomers from wild blueberries of Lake Saint-Jean region (Quebec, Canada) w
196 exin (4), were isolated from the neotropical blueberry of Anthopterus wardii, a so-called "superfruit
198 vegetable extracts high in antioxidants (eg, blueberry or spinach extracts) might decrease the enhanc
199 ioxidant-rich berry diets, specifically a 2% blueberry or strawberry diet, fed for 8 weeks prior to r
200 ous research has shown that diets containing blueberry or strawberry extract can ameliorate the defic
201 Rats were placed on diets containing 2% blueberry or strawberry extract for 2 months prior to ex
203 lmness significantly improved after 1 cup of blueberries (P = 0.01; q = 0.04; with an 11.6% improveme
204 l score averaging all 6 cognitive tests, for blueberries: p-trend = 0.014 and mean difference = 0.04,
206 t of bound anthocyanins that interacted with blueberry pectin increased as the number of hydroxyl gro
208 d the stability and inactivation kinetics of blueberry peroxidase in model systems (McIlvaine buffer,
209 ese data illustrate the inhibitory effect of blueberry phytochemicals on the growth and metastatic po
211 plete BRRV genome from roots of asymptomatic blueberry plants and in Florida through in silico analys
212 ranscriptomes from eight clonally propagated blueberry plants of cultivar 'Emerald' (interspecific hy
213 alysis revealed multiple origins of highbush blueberry plastomes, likely due to the hybridization eve
216 oss of 68 g per d for colonies in commercial blueberry pollination, although weight data indicated gr
217 ncreased dose dependently to </=766 mg total blueberry polyphenol intake, after which FMD plateaued.
223 ient and cost-effective technique to produce blueberry-polyphenol food ingredients with preserved phy
227 erry containing 766, 1278, and 1791 mg total blueberry polyphenols or a macronutrient- and micronutri
235 ur and soy protein isolate with aqueous wild blueberry pomace extracts, then spray drying, freeze dry
236 ore efficiently captured and stabilized wild blueberry pomace phytochemicals than other protein sourc
237 tion of anthocyanin-rich foods, particularly blueberries (pooled HR: 0.77 from a comparison of >/=2 s
239 cated greater foraging effort by colonies in blueberries, possibly due to the proximity and abundance
241 the primary effect of consuming freeze-dried blueberry powder, compared against an isocaloric placebo
244 bene), a phytoalexin found in red grapes and blueberries, protects the cerebellar granule neurons aga
245 30 commercial dehydrated fruits (strawberry, blueberry, raspberry, cranberry, cherry, apple, grapefru
246 including 105 SHB, 17 NHB, and 10 rabbiteye blueberry (RE) (Vaccinium virgatum Aiton), from the acce
248 ect bioavailability following consumption of blueberries relative to a blueberry-rich protein bar, su
249 higher total urinary recovery after Elliott blueberry relative to Olympia blueberry and protein bar
252 ing consumption of blueberries relative to a blueberry-rich protein bar, suggesting (poly)phenol-dens
256 predictive of 12-15% reductions in CVD risk, blueberries should be included in dietary strategies to
258 , with seven "reported" hosts (blackberries, blueberries, sweet cherries, table grapes, peaches, rasp
262 eration (Ki-67 expression) were decreased in blueberry-treated mice, where apoptosis (caspase-3 expre
264 obs roll, pitch and yaw; but green chillies, blueberries, tropical berries, red grapes, oblong grapes
266 ultivars of Highbush and Rabbiteye Brazilian blueberries (Vaccinium corymbosum L. and Vacciniumashei
268 from bilberries (Vaccinium myrtillusL.) and blueberries (Vaccinium corymbosumL.); the bilberry extra
271 of phenolic compounds and anthocyanins from blueberry (Vaccinium ashei) wine pomace", Food Chemistry
272 An electrochemical study of lyophilized blueberry (Vaccinium corymbosum L.) and raspberry (Rubus
273 highlight the potential of this strategy for blueberry (Vaccinium corymbosum L.), a crop heavily reli
274 first phytochemical examination of highbush blueberry (Vaccinium corymbosum) flowers, which yielded
276 properties of juices of newly bred and known blueberry (Vaccinium corymbosum) genotypes and wild bog
280 Vaccinium corymbosum) genotypes and wild bog blueberry (Vaccinium uliginosum) were evaluated by ABTS(
282 bolites was similar following consumption of blueberry varieties of differing (poly)phenol compositio
286 metastatic potential of MDA-MB-231 cells by blueberry was shown through inhibition of cell motility
287 d total flavonols content increased when the blueberries were grown under open-field conditions.
288 ic compounds and the antioxidant capacity of blueberries were not negatively affected by water restri
293 and polyphenol extracts from pomegranate and blueberries were used individually and in combination to
294 und forms of blackberry, black raspberry and blueberry were identified and quantified using high-perf
295 nt fruit wines, chokeberry, blackcurrant and blueberry, were spray-dried using hydroxypropyl-beta-cyc
296 o non-meaningful combinations, such as "fast blueberry," when compared to the effects observed during
301 intake of >/=2 servings of anthocyanin-rich blueberries/wk was associated with slower decline in FEV