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1 and 71.4-67.1% (dough incorporated with 15% wheat bran).
2 d storage of systems with native and toasted wheat bran.
3 ectively, by subcritical water extraction of wheat bran.
4 cation of arabinoxylan oligosaccharides from wheat bran.
5 to medium and fine treatments from the same wheat bran.
6 llium (0.3 +/- 0.3 s P = 0.009), a fall with wheat bran (-0.2 +/- 0.2 s; P = 0.02), but no change wit
7 The total phenolic acid (TPA) quantity in wheat bran (2711-2913mug/g) was significantly higher tha
8 1.8/100g dry weight basis, dwb), followed by wheat bran (57.2/100 g dwb) and oat sample 2 (53.0/100 g
9 lium (mean +/- SD: 14 +/- 5 h) compared with wheat bran (6 +/- 2 h, P = 0.003) and was associated wit
10 esults of this work prove that albumins from wheat bran, a byproduct obtained from the milling indust
11 the activity of a commercial endoxylanase on wheat bran; a steady release of xylose monosaccharide wa
13 noxylan (AX) is an abundant hemicellulose in wheat bran and an important functional component in bake
14 nt substrates, including the plant extracts, wheat bran and commercially available carbohydrates.
16 03].Breath hydrogen rose significantly after wheat bran and nopal but not after psyllium (P < 0.0001)
17 physicochemical properties of potato fibre, wheat bran and oat samples were investigated, along with
19 n coarse, ground, and pericarp-enriched (PE) wheat bran and refined flour was investigated using time
23 ds in the colon derived from dietary pectin, wheat bran, and oat bran are protective against the deve
24 this study, ARs (C17-C25) were isolated from wheat bran, and their antioxidant activity was tested in
27 New insights in the hydration properties of wheat bran as function of particle size were gained base
28 y analysis that providing amylase-pretreated wheat bran as the sole added energy source to human inte
30 all fibers; nopal stimulated more water than wheat bran [AUC mean (95% CI) difference: 7.1 (0.6, 13.8
31 in extracting health promoting compounds in wheat bran because the extraction of antioxidant and phe
32 stigated the colonization and degradation of wheat bran by the A. niger reference strain CBS 137562 a
34 peaks after addition of resistant starch and wheat bran, coinciding with an increase in crumb hardnes
40 hindgut OMD values ranging from 55% to 79% (Wheat Bran Diet and Pectin Diet, respectively) using an
43 al probiotic) was immobilized on delignified wheat bran (DWB) and was used to produce a functional po
45 ethanol formation and metabolite profile of wheat bran fermented in either aerated or anaerobic cond
46 yses were based on 1287 men and women in the wheat bran fiber (WBF) study, a randomized, double-blind
47 on daily stool output, even though > 90% of wheat bran fiber but only 50-60% of oat bran fiber is in
49 of 2 large clinical intervention trials: the Wheat Bran Fiber Trial and the Polyp Prevention Trial.
50 hose in the intervention group of either the Wheat Bran Fiber Trial or the Polyp Prevention Trial was
52 used in this study, a dietary supplement of wheat-bran fiber does not protect against recurrent colo
53 termine whether dietary supplementation with wheat-bran fiber reduces the rate of recurrence of color
57 ant difference was found between the OBC and wheat-bran groups in any of the postprandial variables m
61 rched, protein depleted and xylanase treated wheat bran has been subjected to hydrothermal pretreatme
62 or the first time that the lipid fraction of wheat bran has strong colon tumor inhibitor properties.
67 deflectus AUMC 15761 was demonstrated to use wheat bran in solid state fermentation (SSF) at optimum
69 c acid (FA), a phytochemical concentrated in wheat bran, influences structural characteristics of ara
70 ossibilities for the cascade valorization of wheat bran into enriched protein and non-starch polysacc
72 proteins and feruloylated arabinoxylan from wheat bran is proposed, involving a protein isolation st
74 vel adsorbents, wheat bran (WB) and modified wheat bran (M-WB) with tartaric acid were developed and
75 ally, it hydrolyzed beta-glucan from oat and wheat brans mainly to tri- and tetraoligosaccharides.
76 sed in this study, microfluidisation reduced wheat bran median particle size to 14.8 mum and disinteg
79 ixtures that mimic the digestion products of wheat bran, oat bran, pectin, and cellulose (as control)
83 al particle size) on important properties of wheat bran (particle size, microstructure, chemical comp
84 ruggled to survive on the smooth side of the wheat bran particles after 20 and 40 h post inoculation.
85 physical entrapment of oil within the large wheat bran particles protects RP from the action of wate
89 lation in alpha-cyclodextrins (alpha-CDs) of wheat bran, pumpkin and tomato oleoresins, extracted by
91 was fortified with modified dietary fibers (wheat bran, resistant starch and inulin) and their effec
92 e recovery of phenolic acids from the spiked wheat bran sample was higher than from either the whole
93 ectin-rich sugar beet pulp and to xylan-rich wheat bran showed high pectinolytic and high xylanolytic
96 eric tannins (both in situ and when added to wheat brans) strongly inhibited volatile and non-volatil
101 line extraction reduced the recalcitrance of wheat bran, thus improving the total yields of the subse
102 tially purified (E2) arabinoxylans (AX) from wheat bran to partially replace flour during baking, wer
103 y to induce physicochemical modifications in wheat bran using microfluidisation was investigated.
104 digestibility of neutral sugars provided by wheat bran was 56%; the apparent digestibility of those
106 olonization ability of the smooth surface of wheat bran was linked to reduced potential of DeltaxlnR
107 basidium pullulans NRRL Y-2311-1 produced on wheat bran was purified by a single-step chromatographic
108 strated ferulic acid release from destarched wheat bran was strongly potentiated by co-incubation wit
115 ation on the analysis of phenolic acids from wheat bran, whole-wheat, and refined flour samples was i
116 Mixolab studies revealed that replacing wheat bran with barley bran increased dough water absorp