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1 al role of Phe in supplying nutrients to the young seedling.
2 that seed weight affects many root traits of young seedlings.
3 rs are only induced at high stress levels in young seedlings.
4 3, while the other AMTs were not detected in young seedlings.
5 g has focused on lateral root development in young seedlings.
6  the primary root tip is limited severely in young seedlings.
7 nted in the context of pigment production in young seedlings.
8  the dark-to-light transition in Arabidopsis young seedlings.
9 le stress signals and abscisic acid (ABA) in young seedlings.
10 ltered thylakoid organization, especially in young seedlings.
11 pestris)-infected plants, callus, roots, and young seedlings.
12 ination is a widely used method to phenotype young seedlings.
13 expressed, with highest levels registered in young seedlings.
14 oter activity is found primarily in roots of young seedlings.
15 trogenous nutrients to support the growth of young seedlings.
16 t the plasma membrane after establishment of young seedlings.
17  lysine 9 acetylation (H3K9ac) enrichment in young seedling and husk tissue.
18  was carried out for total leaf proteomes of young seedlings and for chloroplast proteomes of fully d
19  is required for efficient photosynthesis in young seedlings and for survival under iron-limiting con
20 further localized on the surface of roots in young seedlings and in pollen.
21                  PGX2 is widely expressed in young seedlings and in roots, stems, leaves, flowers, an
22 avonoid accumulation pattern was examined in young seedlings and mature tissues of wild-type Arabidop
23 seed development ensures the survival of the young seedling, and also provides nutrition to humans an
24 of polysaccharide release along root axes of young seedlings, and their presence at root hair surface
25 aves, hypocotyl hooks, developing seeds, and young seedlings, and they decreased in mature tissues su
26 ght and ABA signal integration that may help young seedlings better adapt to environmental stresses.
27                                           In young seedlings, both IBA and IAA were transported only
28 Only four genes were abundantly expressed in young seedlings, both in roots and shoots.
29  regulator of phyA-mediated de-etiolation of young seedlings, but its roles in adult plants have not
30 nduced by ABA and/or dehydrating stresses in young seedlings, but the developmental timing of their i
31 tric analyses of preparations generated from young seedlings confirmed that the 2.5-MDa CP-regulatory
32 experiments using purified mitochondria from young seedlings demonstrated accumulation of ORF239 only
33  CRY1 is a soluble protein expressed in both young seedlings grown either in the dark or under light,
34                                           In young seedlings GUS reporter activity was observed mainl
35 is not efficiently recycled back into TAG in young seedlings, instead partitioning into the membrane
36  conversion of eoplasts into chloroplasts in young seedlings is critical for the seedlings to start c
37                       After germination, the young seedling must rapidly establish its root system an
38 sinolates, which are only found in seeds and young seedlings of A. thaliana.
39 caspase9 (MC9; AT5G04200) were identified in young seedlings of Arabidopsis thaliana on the proteome-
40  resulted in higher root and shoot growth of young seedlings of both tested species.
41 ic ethephon solutions applied to one side of young seedlings of cocklebur, tomato, sunflower (Heliant
42 ench is that it can be used for VIGS in very young seedlings, something not possible by the leaf infi
43 on global auxin-regulated gene expression in young seedlings, suggesting that ARF2 does not participa
44 nt, including the hypocotyl-root boundary in young seedlings, the anther-filament junction in mature
45 sized GFP reporters reveals that embryos and young seedlings traffic proteins at least 54 kDa in size
46                                              Young seedlings transitioning from dark to light undergo
47 nscriptome and methylome from germination to young seedlings under aerobic and anaerobic conditions r
48  in roots of adult plants; its expression in young seedlings was up-regulated by abscisic acid.
49 ormal in mature prf1-1 plants, the levels in young seedlings were only one-half those observed in wil
50 seeds sown in seed trays containing peat and young seedlings were transplanted in 2L pots containing
51        This is in contrast to root growth in young seedlings where transformed plants performed equiv
52               AAAs inhibited DHS activity in young seedlings, where AthDHS2 is highly expressed, but
53  the root elongation zone after treatment of young seedlings with 10(-7) M IAA.
54   The second method involves infiltration of young seedlings with Agrobacterium.
55                           Treating seeds and young seedlings with fungicides significantly reduced th