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1 occur during plant development (e.g., during de-etiolation).
2 for the intricacy of miRNA biogenesis during de-etiolation.
3 t process to control hypocotyl growth during de-etiolation.
4 her light-induced nor clock-regulated during de-etiolation.
5 not fully functional during initial seedling de-etiolation.
6 lasses of photoreceptors to mediate seedling de-etiolation.
7 sis also undergoes regulatory changes during de-etiolation.
8 rgan-specific fashion in regulating seedling de-etiolation.
9 and chlorophyll accumulation during seedling de-etiolation.
10 ate, accelerated flowering time, and reduced de-etiolation.
11 ulation of the Arabidopsis HEMA1 gene during de-etiolation.
12 ganized thylakoid membrane maturation during de-etiolation.
13 nes to prevent photo-oxidative damage during de-etiolation.
14 esses, including photomorphogenesis and root de-etiolation.
15 ht-absorbing cryptochromes regulate seedling de-etiolation and flowering responses.
16 asic plant developmental processes including de-etiolation and hypocotyl elongation.
17  plays a primary role in initiating seedling de-etiolation and is the only plant photoreceptor known
18 nd thylakoid plasticity, also participate in de-etiolation and modulate PLB geometry and density.
19 scriptional regulation patterns that lead to de-etiolation and photoacclimation.
20 ng only functional phyA displayed R-mediated de-etiolation and survived to flowering.
21 ed and far-red radiation effects on seedling de-etiolation and yet act in a complementary manner to r
22 lated by developmental processes (etiolation/de-etiolation) and by wounding.
23 t responses during the life cycle, including de-etiolation, and is also involved in regulating flower
24 s extreme dwarfism, altered leaf morphology, de-etiolation, and reduced fertility, all strikingly sim
25 PLB maintenance and their disassembly during de-etiolation are poorly understood.
26 3 is highly induced by light during seedling de-etiolation as well as seed germination.
27 a detail thylakoid membrane expansion during de-etiolation at the seedling level and the relative con
28 ATE, and HYPONASTIC LEAVES 1, whereas during de-etiolation both pri-miRNAs and the processing compone
29 lates not only seed germination and seedling de-etiolation but also circadian rhythms and flowering t
30  of plant nucleolin mRNA is regulated during de-etiolation by phytochrome.
31 expression involved in promotion of seedling de-etiolation, circadian clock function, and photoperiod
32 any defects in seed germination and seedling de-etiolation compared to wild-type.
33                                          The de-etiolation defect could not be rescued by the hormone
34                       In plants they mediate de-etiolation, developmental and stress responses result
35 t disrupts thylakoid development and reduces de-etiolation efficiency in seedlings, suggesting that F
36           This phytochrome mediates seedling de-etiolation for the developmental transition from hete
37                   In this report, we use the de-etiolation ("greening") of maize (Zea mays) chloropla
38 LONGATED HYPOCOTYL3 (FHY3) promotes seedling de-etiolation in far-red light, which is perceived by ph
39  phenotypic behavior of seedlings undergoing de-etiolation in response to continuous red light (Rc),
40  by phyA and phyB will substantially promote de-etiolation in sparse vegetation.
41                          Here we report that DE-ETIOLATION IN THE DARK AND YELLOWING IN THE LIGHT (DA
42               Plants that lack both PGR5 and DE-ETIOLATION-INDUCED PROTEIN1 (DEIP1)/NEW TINY ALBINO1
43  immediately turn off ethylene signaling for de-etiolation initiation.
44 et act in a complementary manner to regulate de-etiolation, irrespective of spectral composition.
45                                      We used de-etiolation of C(4) Gynandropsis gynandra and C(3) Ara
46 les sterility; reduced apical dominance; and de-etiolation of dark-grown seedlings.
47 -ox and GA 3beta-hy mRNA accumulation during de-etiolation of pea seedlings.
48 cts as a negative regulator of phyA-mediated de-etiolation of young seedlings, but its roles in adult
49 suberin around twisted vascular bundles, the de-etiolation phenotype, and continuation of shoot devel
50 ) control, we are investigating the seedling de-etiolation phenotypes of mutants carrying T-DNA inser
51 ansgenic plants also displayed hyposensitive de-etiolation phenotypes, and the expression of these ph
52 Arabidopsis thaliana), cryptochromes mediate de-etiolation, photoperiodic control of flowering, entra
53 et involved in other important facets of the de-etiolation process in the apical region, such as coty
54                                    The term "de-etiolation" refers to the light-dependent differentia
55 chrome (cry) 1 (hy4-2.23n) were examined for de-etiolation responses in high-fluence red, far-red, bl
56  which is non-DNA-binding, was identified in de-etiolation studies and proposed to interact with LONG
57 s a dramatic developmental transition termed de-etiolation that requires immediate termination of eth
58                                       During de-etiolation, the co-ordinated synthesis of chlorophyll
59                    Our data show that during de-etiolation, the increased expression of nucleolin mRN
60 uring the photomorphogenic response known as de-etiolation, the transformation of a dark-grown seedli
61  light (Rc) during the induction of seedling de-etiolation, we have performed time-course, microarray