ライフサイエンスコーパス: de-etiolation

1 occur during plant development (e.g., during de-etiolation).

2 nes to prevent photo-oxidative damage during de-etiolation.

3 t process to control hypocotyl growth during de-etiolation.

4 esses, including photomorphogenesis and root de-etiolation.

5 her light-induced nor clock-regulated during de-etiolation.

6 not fully functional during initial seedling de-etiolation.

7 lasses of photoreceptors to mediate seedling 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 ht-absorbing cryptochromes regulate seedling de-etiolation and flowering responses.

13 asic plant developmental processes including de-etiolation and hypocotyl elongation.

14 plays a primary role in initiating seedling de-etiolation and is the only plant photoreceptor known

15 scriptional regulation patterns that lead to de-etiolation and photoacclimation.

16 ng only functional phyA displayed R-mediated de-etiolation and survived to flowering.

17 ed and far-red radiation effects on seedling de-etiolation and yet act in a complementary manner to r

18 lated by developmental processes (etiolation/de-etiolation) and by wounding.

19 t responses during the life cycle, including de-etiolation, and is also involved in regulating flower

20 s extreme dwarfism, altered leaf morphology, de-etiolation, and reduced fertility, all strikingly sim

21 3 is highly induced by light during seedling de-etiolation as well as seed germination.

22 lates not only seed germination and seedling de-etiolation but also circadian rhythms and flowering t

23 of plant nucleolin mRNA is regulated during de-etiolation by phytochrome.

24 expression involved in promotion of seedling de-etiolation, circadian clock function, and photoperiod

25 any defects in seed germination and seedling de-etiolation compared to wild-type.

26 The de-etiolation defect could not be rescued by the hormone

27 In plants they mediate de-etiolation, developmental and stress responses result

28 t disrupts thylakoid development and reduces de-etiolation efficiency in seedlings, suggesting that F

29 This phytochrome mediates seedling de-etiolation for the developmental transition from hete

30 In this report, we use the de-etiolation ("greening") of maize (Zea mays) chloropla

31 LONGATED HYPOCOTYL3 (FHY3) promotes seedling de-etiolation in far-red light, which is perceived by ph

32 phenotypic behavior of seedlings undergoing de-etiolation in response to continuous red light (Rc),

33 by phyA and phyB will substantially promote de-etiolation in sparse vegetation.

34 immediately turn off ethylene signaling for de-etiolation initiation.

35 et act in a complementary manner to regulate de-etiolation, irrespective of spectral composition.

36 les sterility; reduced apical dominance; and de-etiolation of dark-grown seedlings.

37 -ox and GA 3beta-hy mRNA accumulation during de-etiolation of pea seedlings.

38 cts as a negative regulator of phyA-mediated de-etiolation of young seedlings, but its roles in adult

39 suberin around twisted vascular bundles, the de-etiolation phenotype, and continuation of shoot devel

40 ) control, we are investigating the seedling de-etiolation phenotypes of mutants carrying T-DNA inser

41 ansgenic plants also displayed hyposensitive de-etiolation phenotypes, and the expression of these ph

42 et involved in other important facets of the de-etiolation process in the apical region, such as coty

43 chrome (cry) 1 (hy4-2.23n) were examined for de-etiolation responses in high-fluence red, far-red, bl

44 s a dramatic developmental transition termed de-etiolation that requires immediate termination of eth

45 During de-etiolation, the co-ordinated synthesis of chlorophyll

46 Our data show that during de-etiolation, the increased expression of nucleolin mRN

47 uring the photomorphogenic response known as de-etiolation, the transformation of a dark-grown seedli

48 light (Rc) during the induction of seedling de-etiolation, we have performed time-course, microarray