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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
8 a-diketone waxes are major components of the epicuticular layer leading to the bluish-white glaucous
11 barley (Hordeum vulgare) mutant with reduced epicuticular leaf waxes on which spores of adapted and n
12 genetically based intraspecific variation in epicuticular lipids and have important implications for
13 changes in topography result from removal of epicuticular lipids and that the changes in leaf surface
14 dopted for the mass spectrometric imaging of epicuticular lipids on the surface of Arabidopsis thalia
17 tants is due to complete loss of the abaxial epicuticular wax crystals and reduced surface hydrophobi
18 provided new insights into the complexity of epicuticular wax deposition at the cellular-resolution s
19 still unclear, although its effect on normal epicuticular wax deposition was the characteristic that
21 icular wax metabolism and transport and that epicuticular wax influences spore differentiation of hos
22 ormed by the intracuticular wax but that the epicuticular wax layer may also contribute to it, depend
23 ace water barrier was found to reside in the epicuticular wax layer of the petal and only one-third i
25 strate that PALM1 plays a role in regulating epicuticular wax metabolism and transport and that epicu
26 ) was employed to directly profile and image epicuticular wax metabolites on a variety of different s
28 ime that P. fructicola can not only dissolve epicuticular waxes but also partially penetrate the cuti
29 e pe mutant are also cutin deficient and the epicuticular waxes contain a lower proportion of long-ch
31 environment is provided for aerial organs by epicuticular waxes that have been extensively studied.
32 ical analysis of plant cell wall components, epicuticular waxes, and the deposition of agrochemical f
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