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1 gulated carotenoid formation, such as during deetiolation.
2 sport facilitators during the first hours of deetiolation.
3 n photosynthesis and stress signaling during deetiolation.
4 ion start sites, were detected within 1 h of deetiolation.
5 rome A (phyA) plays a major role in seedling deetiolation.
6 negative regulator of phyB-mediated seedling deetiolation.
7 egradation in maize (Zea mays) leaves during deetiolation.
8 regulating plastidial metabolic flux during deetiolation.
9 hat mediates phytochrome control of seedling deetiolation.
10 gulator of phyB signaling mediating seedling deetiolation.
11 that cr88 is defective in red light-mediated deetiolation.
12 alleles induce chloroplast biogenesis during deetiolation.
13 onstrate that SUS protein degradation during deetiolation: (1) is selective; (2) can be triggered by
14 two organs, suggesting disruption of normal deetiolation; 13 (41%) lines displayed significant defec
15 educed rates of chlorophyll synthesis during deetiolation and enhanced rates of chlorophyll loss in l
16 ene expression responsible for both seedling deetiolation and phasing of the circadian clock in respo
17 ch the phytochromes pleiotropically regulate deetiolation and that at least some of the rapidly light
18 hrome A (phyA) is the major photoreceptor of deetiolation, and phyA expression is reversibly represse
20 ent in the parental phyA-105 mutant, such as deetiolation, anthocyanin accumulation, and a far-red li
22 transition, not only during initial seedling deetiolation, but daily at dawn under diurnal light-dark
23 A, a predominant photoreceptor for seedling deetiolation, colocalizes in nuclear bodies with CONSTIT
26 sis-related genes in seven of these enhanced deetiolation (end) mutants and found that photosynthesis
28 helix-loop-helix family, PIF5, during early deetiolation, immediately following initial exposure of
29 s constitutively phosphorylated, it promotes deetiolation in both dark and light, and it activates fl
31 e signaling constrains leaf expansion during deetiolation in pea and provide further evidence that do
32 eracting bHLH factors in modulating seedling deetiolation in prolonged red light may not be as phy-ac
33 in Arabidopsis thaliana seed germination and deetiolation in response to environmental light signals.
37 ATED HYPOCOTYL5 (HY5), a master regulator of deetiolation, in the wild type and not in phytochrome A
39 seedling development, far-red-light-induced deetiolation is mediated primarily by phytochrome A (phy
40 tochrome A (phyA), whereas red-light-induced deetiolation is mediated primarily by phytochrome B (phy
41 27 is correlated with gene activation during deetiolation of Arabidopsis thaliana seedlings, but less
46 (phy) photosensory system initiates both the deetiolation process in dark-germinated seedlings upon f
47 om FHY1 phosphorylation ensures the seedling deetiolation process in response to a R-enriched light c
49 ed in a critical facet of the early seedling deetiolation process, the generation of a functional pho
53 hotoreceptors contributed to most blue light deetiolation responses, either redundantly or additively
54 ents or phytochromes (phy) regulate seedling deetiolation responses, photoperiodic flowering, and cir
57 nificant overlap between shade avoidance and deetiolation transcript profiles in Arabidopsis (Arabido
58 ied a mutant that displayed reduced seedling deetiolation under continuous red light, but little if a
60 don growth as diagnostic criteria for normal deetiolation, we identified three major mutant response
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