ライフサイエンスコーパス: etiolation

1 stresses (cold, wounding, drought, mannitol, etiolation).

2 ur during plant development (e.g., during de-etiolation).

3 to prevent photo-oxidative damage during de-etiolation.

4 rocess to control hypocotyl growth during de-etiolation.

5 es, including photomorphogenesis and root de-etiolation.

6 ed role during long-term dark adaptation and etiolation.

7 light-induced nor clock-regulated during de-etiolation.

8 fully functional during initial seedling de-etiolation.

9 ses of photoreceptors to mediate seedling de-etiolation.

10 n-specific fashion in regulating seedling de-etiolation.

11 chlorophyll accumulation during seedling de-etiolation.

12 , accelerated flowering time, and reduced de-etiolation.

13 tion of the Arabidopsis HEMA1 gene during de-etiolation.

14 lant fast growth is required, such as during etiolation.

15 absorbing cryptochromes regulate seedling de-etiolation and flowering responses.

16 c plant developmental processes including de-etiolation and hypocotyl elongation.

17 ays a primary role in initiating seedling de-etiolation and is the only plant photoreceptor known to

18 iptional regulation patterns that lead to de-etiolation and photoacclimation.

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

20 and far-red radiation effects on seedling de-etiolation and yet act in a complementary manner to regu

21 ed by developmental processes (etiolation/de-etiolation) and by wounding.

22 esponses during the life cycle, including de-etiolation, and is also involved in regulating flowering

23 xtreme dwarfism, altered leaf morphology, de-etiolation, and reduced fertility, all strikingly simila

24 s highly induced by light during seedling de-etiolation as well as seed germination.

25 es not only seed germination and seedling de-etiolation but also circadian rhythms and flowering time

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

27 ression involved in promotion of seedling de-etiolation, circadian clock function, and photoperiod pe

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

29 ene is regulated by developmental processes (etiolation/de-etiolation) and by wounding.

30 The de-etiolation defect could not be rescued by the hormones t

31 In plants they mediate de-etiolation, developmental and stress responses resulting

32 isrupts thylakoid development and reduces de-etiolation efficiency in seedlings, suggesting that FtsH

33 This phytochrome mediates seedling de-etiolation for the developmental transition from heterot

34 ressed primarily early in development-during etiolation, germination and greening.

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

36 nesis in the light and skotomorphogenesis or etiolation in darkness.

37 GATED HYPOCOTYL3 (FHY3) promotes seedling de-etiolation in far-red light, which is perceived by phyto

38 enotypic behavior of seedlings undergoing de-etiolation in response to continuous red light (Rc), pre

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

40 undergo photomorphogenesis in the light and etiolation in the dark.

41 mediately turn off ethylene signaling for de-etiolation initiation.

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

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

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

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

46 ronment: photomorphogenesis in the light and etiolation or skotomorphogenesis in darkness.

47 olletotrichum infection, skotomorphogenesis (etiolation), ovary, immature panicle, and embryo.

48 erin around twisted vascular bundles, the de-etiolation phenotype, and continuation of shoot developm

49 ontrol, we are investigating the seedling de-etiolation phenotypes of mutants carrying T-DNA insertio

50 genic plants also displayed hyposensitive de-etiolation phenotypes, and the expression of these pheno

51 involved in other important facets of the de-etiolation process in the apical region, such as cotyled

52 ome (cry) 1 (hy4-2.23n) were examined for de-etiolation responses in high-fluence red, far-red, blue,

53 dramatic developmental transition termed de-etiolation that requires immediate termination of ethyle

54 During de-etiolation, the co-ordinated synthesis of chlorophyll an

55 Our data show that during de-etiolation, the increased expression of nucleolin mRNA i

56 ng the photomorphogenic response known as de-etiolation, the transformation of a dark-grown seedling

57 ght (Rc) during the induction of seedling de-etiolation, we have performed time-course, microarray-ba

58 The mutants also show reduced etiolation when grown in darkness.