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1 al role of Phe in supplying nutrients to the young seedling.
2 the primary root tip is limited severely in young seedlings.
3 nted in the context of pigment production in young seedlings.
4 le stress signals and abscisic acid (ABA) in young seedlings.
5 ltered thylakoid organization, especially in young seedlings.
6 pestris)-infected plants, callus, roots, and young seedlings.
7 expressed, with highest levels registered in young seedlings.
8 oter activity is found primarily in roots of young seedlings.
9 trogenous nutrients to support the growth of young seedlings.
10 rs are only induced at high stress levels in young seedlings.
11 3, while the other AMTs were not detected in young seedlings.
12 g has focused on lateral root development in young seedlings.
14 was carried out for total leaf proteomes of young seedlings and for chloroplast proteomes of fully d
15 is required for efficient photosynthesis in young seedlings and for survival under iron-limiting con
18 avonoid accumulation pattern was examined in young seedlings and mature tissues of wild-type Arabidop
19 seed development ensures the survival of the young seedling, and also provides nutrition to humans an
20 aves, hypocotyl hooks, developing seeds, and young seedlings, and they decreased in mature tissues su
21 ght and ABA signal integration that may help young seedlings better adapt to environmental stresses.
24 regulator of phyA-mediated de-etiolation of young seedlings, but its roles in adult plants have not
25 nduced by ABA and/or dehydrating stresses in young seedlings, but the developmental timing of their i
26 tric analyses of preparations generated from young seedlings confirmed that the 2.5-MDa CP-regulatory
27 experiments using purified mitochondria from young seedlings demonstrated accumulation of ORF239 only
28 CRY1 is a soluble protein expressed in both young seedlings grown either in the dark or under light,
30 is not efficiently recycled back into TAG in young seedlings, instead partitioning into the membrane
31 conversion of eoplasts into chloroplasts in young seedlings is critical for the seedlings to start c
34 caspase9 (MC9; AT5G04200) were identified in young seedlings of Arabidopsis thaliana on the proteome-
35 ic ethephon solutions applied to one side of young seedlings of cocklebur, tomato, sunflower (Heliant
36 ench is that it can be used for VIGS in very young seedlings, something not possible by the leaf infi
37 on global auxin-regulated gene expression in young seedlings, suggesting that ARF2 does not participa
38 nt, including the hypocotyl-root boundary in young seedlings, the anther-filament junction in mature
39 sized GFP reporters reveals that embryos and young seedlings traffic proteins at least 54 kDa in size
40 nscriptome and methylome from germination to young seedlings under aerobic and anaerobic conditions r
42 ormal in mature prf1-1 plants, the levels in young seedlings were only one-half those observed in wil
43 seeds sown in seed trays containing peat and young seedlings were transplanted in 2L pots containing
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