ライフサイエンスコーパス: gynoecium

1 ors restrict sensitivity to cytokinin in the gynoecium.

2 shment during development of the Arabidopsis gynoecium.

3 that is elongating within the solid maternal gynoecium.

4 a seedpod that develops from the fertilized gynoecium.

5 l domains along the apical-basal axis of the gynoecium.

6 the three positional axes of the developing gynoecium.

7 h encompass these regions of the Arabidopsis gynoecium.

8 arpels leads to the formation of an enclosed gynoecium.

9 h a CRABS-CLAW mutant that maintains an open gynoecium.

10 transfer along the transmitting tract of the gynoecium.

11 , and apical-basal patterning defects in the gynoecium.

12 regional differentiation in stamens and the gynoecium.

13 DI1 (KAN1) organize the Arabidopsis thaliana gynoecium along two distinct polarity axes.

14 n alters the expression of genes involved in gynoecium and embryo development, lipid metabolism, auxi

15 tterning of the root, the development of the gynoecium and female gametophyte, and organogenesis and

16 ich DELLA proteins contribute to GA-mediated gynoecium and fruit development remains to be clarified.

17 arge number of mutants that display abnormal gynoecium and fruit development.

18 e ovule and the septum, resulting in a split gynoecium and no observable embryo sac.

19 cally expressed in particular regions of the gynoecium and ovule, only during and after floral develo

20 ontrol the initiation and development of the gynoecium and resulting fruit.

21 in Response Factors, ARF6 and ARF8, regulate gynoecium and stamen development in immature flowers.

22 rms relies on the precise development of the gynoecium and the anther, because their primary function

23 sed the block in pollen release, but not the gynoecium arrest.

24 istem before morphological appearance of the gynoecium, consistent with the proposal that ETT is invo

25 The Arabidopsis (Arabidopsis thaliana) gynoecium consists of two congenitally fused carpels mad

26 of auxin and cytokinin responses to control gynoecium development in Arabidopsis.

27 Characterization of gynoecium development in receptor mutants revealed incre

28 Our analysis focuses on stamen and gynoecium development, where we find that NUB acts redun

29 cytokinin regulates auxin homeostasis during gynoecium development.

30 s, ensuring correct domain specification and gynoecium development.

31 motion of petal epidermal cell identity, and gynoecium development.

32 ing an apical-basal gradient of auxin during gynoecium development.

33 In Arabidopsis flowers, the gynoecium develops as an open, vase-like structure that

34 bilaterally symmetric stage ingrained in the gynoecium due to its evolutionary origin to a radially s

35 he fruit, which develops from the fertilised gynoecium formed in the innermost whorl of the flower, i

36 The medial domain of the gynoecium gives rise to the ovules, and several other st

37 ich infect inflorescences either through the gynoecium (group 2) or systemically through the apical m

38 e region of the ovule facing the base of the gynoecium (gynobasal).

39 ture of the medial domain of the Arabidopsis gynoecium, highlighting the developmental stages that im

40 ishing the apical-basal polarity axis of the gynoecium, indicating that they function in differentiat

41 equires that anthers release pollen when the gynoecium is competent to support fertilization.

42 um of the Arabidopsis (Arabidopsis thaliana) gynoecium is composed of two congenitally fused, lateral

43 In flowering plants the gynoecium is the female reproductive structure and the s

44 ors, ARF6 and ARF8, regulate both stamen and gynoecium maturation.

45 ng in diverse developmental contexts such as gynoecium morphogenesis, lateral root emergence, ovule d

46 IG all affect floral organ number as well as gynoecium morphology.

47 The mature gynoecium of Arabidopsis is composed of an apical stigma

48 This organization makes the gynoecium one of the most complex plant structures, and

49 cytokinin-auxin feedback model during early gynoecium patterning and hormone homeostasis.

50 NPA's effects on gynoecium patterning mimic the phenotype of mutations in

51 function in leaf polarity specification and gynoecium patterning.

52 PA), highlighting their role in mediolateral gynoecium patterning.

53 obably involved in auxin-mediated control of gynoecium patterning.

54 interactions pivotal for patterning of early gynoecium primordia remain unknown.

55 atterning apical and basal boundaries in the gynoecium primordium.

56 delivered to the interior of the developing gynoecium prior to locule closure if efficient transform

57 Proper development of the gynoecium requires that the early gynoecial primordium b

58 polarity by promoting basal cell fate in the gynoecium, restricting the expression domain of the basi

59 involved in medial tissue development in the gynoecium such as HECATE, BELL1 and NGATHA1.

60 ially symmetrical flowers with a conspicuous gynoecium surrounded by prominent nectar reward, organiz

61 3000 species of Brassicaceae, develop from a gynoecium that consists of two fused carpels.

62 The Arabidopsis (Arabidopsis thaliana) gynoecium, the female floral reproductive structure, req

63 nerates ovules from the medial domain of the gynoecium, the female floral reproductive structure.

64 erning of the female reproductive organ, the gynoecium, the flow as well as the temporal and spatial

65 a of the anthers and the carpel walls of the gynoecium, which enclose the ovules.

66 eproductive organ development, including the gynoecium, which is the female reproductive structure an