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1 ur during plant development (e.g., during de-etiolation).
2 stresses (cold, wounding, drought, mannitol, etiolation).
3  the intricacy of miRNA biogenesis during de-etiolation.
4 lant fast growth is required, such as during etiolation.
5 rocess to control hypocotyl growth during de-etiolation.
6 ed role during long-term dark adaptation and etiolation.
7  light-induced nor clock-regulated during de-etiolation.
8  also undergoes regulatory changes during de-etiolation.
9  fully functional during initial seedling de-etiolation.
10 ses of photoreceptors to mediate seedling de-etiolation.
11 n-specific fashion in regulating seedling de-etiolation.
12  chlorophyll accumulation during seedling de-etiolation.
13 , accelerated flowering time, and reduced de-etiolation.
14 tion of the Arabidopsis HEMA1 gene during de-etiolation.
15  to prevent photo-oxidative damage during de-etiolation.
16 microgreens could be enhanced by 5-7 days of etiolation.
17 es, including photomorphogenesis and root de-etiolation.
18 ized thylakoid membrane maturation during de-etiolation.
19 absorbing cryptochromes regulate seedling de-etiolation and flowering responses.
20  expressions for the given number of days of etiolation and growth.
21 c plant developmental processes including de-etiolation and hypocotyl elongation.
22 ays a primary role in initiating seedling de-etiolation and is the only plant photoreceptor known to
23 G-protein complex in Arabidopsis and affects etiolation and leaf morphology.
24 thylakoid plasticity, also participate in de-etiolation and modulate PLB geometry and density.
25 iptional regulation patterns that lead to de-etiolation and photoacclimation.
26 only functional phyA displayed R-mediated de-etiolation and survived to flowering.
27 and far-red radiation effects on seedling de-etiolation and yet act in a complementary manner to regu
28 ed by developmental processes (etiolation/de-etiolation) and by wounding.
29 esponses during the life cycle, including de-etiolation, and is also involved in regulating flowering
30 xtreme dwarfism, altered leaf morphology, de-etiolation, and reduced fertility, all strikingly simila
31  maintenance and their disassembly during de-etiolation are poorly understood.
32 s highly induced by light during seedling de-etiolation as well as seed germination.
33 etail thylakoid membrane expansion during de-etiolation at the seedling level and the relative contri
34 , and HYPONASTIC LEAVES 1, whereas during de-etiolation both pri-miRNAs and the processing components
35 es not only seed germination and seedling de-etiolation but also circadian rhythms and flowering time
36  plant nucleolin mRNA is regulated during de-etiolation by phytochrome.
37 ression involved in promotion of seedling de-etiolation, circadian clock function, and photoperiod pe
38  defects in seed germination and seedling de-etiolation compared to wild-type.
39 ene is regulated by developmental processes (etiolation/de-etiolation) and by wounding.
40                                       The de-etiolation defect could not be rescued by the hormones t
41                    In plants they mediate de-etiolation, developmental and stress responses resulting
42 isrupts thylakoid development and reduces de-etiolation efficiency in seedlings, suggesting that FtsH
43        This phytochrome mediates seedling de-etiolation for the developmental transition from heterot
44 ressed primarily early in development-during etiolation, germination and greening.
45                In this report, we use the de-etiolation ("greening") of maize (Zea mays) chloroplasts
46 nesis in the light and skotomorphogenesis or etiolation in darkness.
47 GATED HYPOCOTYL3 (FHY3) promotes seedling de-etiolation in far-red light, which is perceived by phyto
48 enotypic behavior of seedlings undergoing de-etiolation in response to continuous red light (Rc), pre
49  phyA and phyB will substantially promote de-etiolation in sparse vegetation.
50                       Here we report that DE-ETIOLATION IN THE DARK AND YELLOWING IN THE LIGHT (DAY),
51  undergo photomorphogenesis in the light and etiolation in the dark.
52            Plants that lack both PGR5 and DE-ETIOLATION-INDUCED PROTEIN1 (DEIP1)/NEW TINY ALBINO1 (NT
53 mediately turn off ethylene signaling for de-etiolation initiation.
54 act in a complementary manner to regulate de-etiolation, irrespective of spectral composition.
55                                   We used de-etiolation of C(4) Gynandropsis gynandra and C(3) Arabid
56  sterility; reduced apical dominance; and de-etiolation of dark-grown seedlings.
57  and GA 3beta-hy mRNA accumulation during de-etiolation of pea seedlings.
58  as a negative regulator of phyA-mediated de-etiolation of young seedlings, but its roles in adult pl
59 ronment: photomorphogenesis in the light and etiolation or skotomorphogenesis in darkness.
60 olletotrichum infection, skotomorphogenesis (etiolation), ovary, immature panicle, and embryo.
61 erin around twisted vascular bundles, the de-etiolation phenotype, and continuation of shoot developm
62 ontrol, we are investigating the seedling de-etiolation phenotypes of mutants carrying T-DNA insertio
63 genic plants also displayed hyposensitive de-etiolation phenotypes, and the expression of these pheno
64 bidopsis thaliana), cryptochromes mediate de-etiolation, photoperiodic control of flowering, entrainm
65 involved in other important facets of the de-etiolation process in the apical region, such as cotyled
66                           However, prolonged etiolation reduced overall antioxidant capacities of mic
67                                 The term "de-etiolation" refers to the light-dependent differentiatio
68 ome (cry) 1 (hy4-2.23n) were examined for de-etiolation responses in high-fluence red, far-red, blue,
69 ich is non-DNA-binding, was identified in de-etiolation studies and proposed to interact with LONG HY
70  dramatic developmental transition termed de-etiolation that requires immediate termination of ethyle
71                                    During de-etiolation, the co-ordinated synthesis of chlorophyll an
72                 Our data show that during de-etiolation, the increased expression of nucleolin mRNA i
73 ng the photomorphogenic response known as de-etiolation, the transformation of a dark-grown seedling
74 ght (Rc) during the induction of seedling de-etiolation, we have performed time-course, microarray-ba
75                The mutants also show reduced etiolation when grown in darkness.