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1 ction efficiencies measured by earthworm for coconut AC and corn stover biochar were generally less t
3 responding to an odorant zone reminiscent of coconut and dried figs as 5,6-dihydro-6-pentyl-2H-pyran-
4 was obtained in contrast to the samples with coconut and palm oil, where the substantial overlapping
6 anola, soybean, sunflower, maize, peanut and coconut) and showed high sensitivity in a broad linear d
8 um, barley, sugarcane, pineapple, banana and coconut are the major sources of agro-based biofibers.
9 ide residues in the food products containing coconut are within the maximum residue limits (MRLs), en
11 ide probe synthesised based on complementary Coconut Cadang-Cadang Viroid (CCCVd) RNA sequence, was c
16 to determine the biochemical constituents in coconut (Cocos nucifera L.) haustorium, a spongy tissue
18 t is a waste stream from food crops, such as coconut (Cocos nucifera) shell, which is nonedible, not
20 ruits (Artocarpus heterophyllus), and mature coconuts (Cocos nucifera) from different Brazilian regio
21 leata], carnauba [Copernicia prunifera], and coconut [Cocos nucifera]) endocarps contain lignin polym
26 profiles and antimicrobial activity of crude coconut fat hydrolysates obtained in solid-state cultiva
27 this, we pyrolysed curcumin with and without coconut fat or olive oil, and analysed the products by h
28 e, were co-immobilized onto a novel chitosan/coconut fibre/zinc oxide nanoparticles (CS/CF/nZnO) hybr
29 d by complexing wheat flour, chickpea flour, coconut flour and soy protein isolate with aqueous wild
32 ng nutritionally balanced formulations using coconut haustorium, which will be useful for lactose int
35 hese results show that chemical treatment of coconut kernel by-products can enhance the performance o
38 quence tag was identified by homology with a coconut LPAAT and used to isolate a full-length human cD
39 kernel residues obtained after extraction of coconut milk (MR) and virgin coconut oil (VOR) were anal
40 nt and precipitate protein powders from both coconut milk and oil cakes were compared based on their
43 ones may contribute individually to mint and coconut odors, sensory studies suggested for the first t
47 r extraction of coconut milk (MR) and virgin coconut oil (VOR) were analysed for their potential as d
48 ried out in a solvent-free system of lipase, coconut oil and ethanol or fusel alcohols to ascertain t
49 cream and its analogues with sunflower oil, coconut oil and palm oil in different milk fat/vegetable
51 stem is also effective for the conversion of coconut oil derived fatty acid methyl esters to detergen
52 ing suspensions of tri-iodothyronine (T3) in coconut oil into the midbrain ventricle or into the eye,
57 lenic acid from canola oil, lauric acid from coconut oil, and palmitic and stearic acids from cocoa b
58 l than from a mixture of 60% soy oil and 40% coconut oil, and that absorption of calcium is less from
59 after safflower oil; 14 h after cocoa utter, coconut oil, canola oil, and menhaden oil (eicosapentaen
60 hondrial respiration of feeding hydrogenated coconut oil, corn oil, or menhaden oil (MO) to diabetes-
62 fatty acid-generating lipase, natural oils (coconut oil, palm oil, and algal oil bodies) were enzyma
65 r diets contained only corn and hydrogenated coconut oils as their source of fat in ratios of 1:9, 3:
68 the proliferation of the commonly introduced coconut palm, Cocos nucifera, interrupts the flow of all
77 m different precursor materials (coal, peat, coconut shell, hardwood, and phenolic resin) were electr
80 , macadamia nut, pistachio nut, chestnut and coconut; to determine the presence of trace levels of pe
83 Six processing treatments were applied to coconut water and analyzed: two control (with and withou
88 operties and enzyme inactivation kinetics of coconut water were compared between immature (IMC), matu
89 hibitor used: palm approximately corn>canola>coconut which also depended on their ability to transfer
90 antly suppress strawberry/lactic/red fruity, coconut/wood/vanilla and humidity/TCA notes, but not the
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