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1 tio would determine the final probability to abscise.
2  53 kD in flower abscission zones induced to abscise.
3 c levels in the fruitlet and its tendency to abscise.
4                In Arabidopsis, floral organs abscise after pollination, and this cell separation even
5 nic acid (Ethephon, in the following ETH) as abscising agent on cv. Crimson Seedless table grape was
6                  The effectiveness of ETH as abscising agent was ascertained with ETH concentration r
7 , we uncover a form of cell subdivision that abscises apical cell membrane and mediates neuron detach
8                   The branches were probably abscised as frond-like modules.
9 declined rapidly until all viable leaves had abscised by 18 days.
10 orescent protein-tagged cells, released from abscising floral organs, and used to generate a compleme
11                            In both naturally abscising flowers and flower explants induced to abscise
12 e expression were then analyzed in naturally abscising flowers and flower explants.
13 ruit cortex, which were shown to increase in abscising fruitlets with respect to nonabscising ones.
14 on the volatile organic compounds emitted by abscising fruitlets, allowing for identification of isop
15 ising flowers and flower explants induced to abscise in air or ethylene, both new cellulase mRNAs wer
16 degrees C were stunted and had chlorotic and abscised leaves and essentially no tuber formation.
17 ows produce strain-rate rotational avulsion, abscising the optic nerve with minimal internal globe di
18 es with the formation of a midbody, which is abscised to form individual daughter cells.
19                     In other species, petals abscise while still turgid.

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