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1                The sealing properties of the epicuticular and intracuticular layers were not correlat
2                   In these species, both the epicuticular and intracuticular waxes contributed equall
3                              Even though the epicuticular and intracuticular waxes of these species h
4  adaxial and abaxial petal sides and between epicuticular and intracuticular waxes.
5 onsistent with its role in the production of epicuticular and pollen coat lipids >28 carbons long.
6 ated that resistant mosquitoes had a thicker epicuticular layer and a significant increase in cuticul
7        Moreover, within the adaxial wax, the epicuticular layer contained more wax and a higher relat
8 a-diketone waxes are major components of the epicuticular layer leading to the bluish-white glaucous
9 hers are a common compound type found on the epicuticular layer of arthropods, e.g., spiders.
10                                The outermost epicuticular layer or waxy layer of the insect represent
11 d also accumulate on the surface, forming an epicuticular layer.
12 barley (Hordeum vulgare) mutant with reduced epicuticular leaf waxes on which spores of adapted and n
13 genetically based intraspecific variation in epicuticular lipids and have important implications for
14 changes in topography result from removal of epicuticular lipids and that the changes in leaf surface
15 dopted for the mass spectrometric imaging of epicuticular lipids on the surface of Arabidopsis thalia
16                                              Epicuticular lipids provide the primary barrier to water
17                                 Variation in epicuticular wax accumulation, composition, and nanoscal
18 glossy genes was confirmed to participate in epicuticular wax accumulation.
19 of epidermal cells, and barley's distinctive epicuticular wax blooms, as well as stomatal patterning
20 veal a petunia MYB regulator that interlinks epicuticular wax composition and volatile emission, thus
21 en the PAH concentration in cuticles and the epicuticular wax content was found.
22 s, trichome density, stomatal frequency, and epicuticular wax content were significant, with resistan
23 tants is due to complete loss of the abaxial epicuticular wax crystals and reduced surface hydrophobi
24  can decouple diffraction from cellulose and epicuticular wax crystals in cell walls.
25  seem likely to include effects from loss of epicuticular wax crystals, effects from preservation tec
26 provided new insights into the complexity of epicuticular wax deposition at the cellular-resolution s
27 still unclear, although its effect on normal epicuticular wax deposition was the characteristic that
28                                              Epicuticular wax forms a layer of hydrophobic material o
29 ate the significance of different classes of epicuticular wax in abiotic stress such as cuticular wat
30 icular wax metabolism and transport and that epicuticular wax influences spore differentiation of hos
31 conservation and the chemical composition of epicuticular wax layer are factors that determine fruit
32 ormed by the intracuticular wax but that the epicuticular wax layer may also contribute to it, depend
33 ace water barrier was found to reside in the epicuticular wax layer of the petal and only one-third i
34 emical composition of the intracuticular and epicuticular wax layers.
35 strate that PALM1 plays a role in regulating epicuticular wax metabolism and transport and that epicu
36 tudy investigates the influence of RH on the epicuticular wax metabolism during citrus fruit storage,
37 y loss (4 d 2 uL L(-1)), ethylene redirected epicuticular wax metabolism towards the synthesis of pri
38 ) was employed to directly profile and image epicuticular wax metabolites on a variety of different s
39 ron microscopy (SEM) revealed differences in epicuticular wax morphology, and gas chromatography-mass
40                                              Epicuticular wax on the outer surface of the cuticle mod
41                                              Epicuticular wax production was evaluated along the leng
42 of the genes involved in the accumulation of epicuticular wax, and provide two maize glossy genes and
43                                              Epicuticular waxes are elements of the future bioenginee
44                                              Epicuticular waxes are important natural compounds that
45  waxes revealed that intracuticular, but not epicuticular waxes are required to regulate cuticular tr
46 ime that P. fructicola can not only dissolve epicuticular waxes but also partially penetrate the cuti
47 imal cuticle, which is thicker and richer in epicuticular waxes compared with the cuticle in the smoo
48 e pe mutant are also cutin deficient and the epicuticular waxes contain a lower proportion of long-ch
49 er-za.227 and cer-ye.267, and the removal of epicuticular waxes indicate that the cuticular barrier f
50           Here, a model cuticle based on the epicuticular waxes of Petunia hybrida flower petals was
51  glossy loci exhibit altered accumulation of epicuticular waxes on juvenile leaves.
52                                              Epicuticular waxes provide a hydrophobic barrier that pr
53 aphy/gas chromatography-MS analyses of petal epicuticular waxes revealed substantial reductions in wa
54                                   Removal of epicuticular waxes revealed that intracuticular, but not
55 environment is provided for aerial organs by epicuticular waxes that have been extensively studied.
56 pecifically affected, while the reduction of epicuticular waxes was mainly observed in primary long c
57 ical analysis of plant cell wall components, epicuticular waxes, and the deposition of agrochemical f
58 ossy mutants that reduce the accumulation of epicuticular waxes, eight non-allelic glossy mutants wer
59                                These include epicuticular waxes, leaf hairs, and cell wall characteri
60 cid elongation and required for synthesis of epicuticular waxes.
61 olymer matrix (cutin) and intracuticular and epicuticular waxes.
62 g-chain fatty acids, which are precursors of epicuticular waxes.
63 tants of gl4 lack the normal accumulation of epicuticular waxes.
64 on of LTPs in the deposition of cuticular or epicuticular waxes.
65 iles by fine-tuning the composition of petal epicuticular waxes.