ライフサイエンスコーパス: pedicel

1 controls the separation of a grain from the pedicel.

2 d in the growing leaf and at the base of the pedicel.

3 ding increase in hydraulic resistance in the pedicel.

4 very floral primordium produces a flowerless pedicel.

5 verproduction of vascular tissues in central pedicels.

6 used by BOP1/2 gain of function in stems and pedicels.

7 organ development in young leaves, buds and pedicels; (2) at and near the junction between two organ

8 In placenta/pedicel, 79 genes were significantly affected by stress

9 stveraison, suggesting that across the grape pedicel, a xylem pathway of reduced kh remains functiona

10 ethylene evolution and ovary senescence and pedicel abscission in fruits that were not pollinated un

11 derivatives determined whether a functional pedicel abscission zone formed.

12 ylem results from disruption or occlusion of pedicel and berry xylem conduits (hydraulic isolation).

13 At 9 d after pollination (DAP), placenta/pedicel and endosperm differed considerably in their tra

14 ilking; dissected into cob, spikelet, and/or pedicel and kernel fractions; then analyzed for amino ac

15 ort style and in guard cells of the silique, pedicel and stem but not in mature leaves.

16 re, we show that mn1-1 basal kernel regions (pedicels and basal endosperm transfer layer) accumulate

17 ; or MKKs), MKK4/MKK5, resulted in shortened pedicels and clustered inflorescences.

18 h human-selected retention of rice grains on pedicels and for naturally selected differences in dehis

19 ntless mutation fail to develop AZs on their pedicels and so abscission of flowers or fruit does not

20 of epidermal and cortex cells in Arabidopsis pedicels and used computational modeling to analyze cell

21 ra line 38-G-81, where it was limited to the pedicels (and, in some cases, the sepals).

22 ens attach to the receptacle, at the base of pedicels, and at the base of petioles where leaves attac

23 , round, dark-green leaves, and short stems, pedicels, and petioles.

24 s in the development of the gynoecia, flower pedicels, and stamens.

25 by affecting elongation of the internode and pedicels, as well as the shape of lateral organs.

26 and BOP2, whose expression is restricted to pedicel axils.

27 SS accounts for the failure of activation of pedicel AZ development in jointless tomato plants.

28 Pedicel browning was inhibited by CaCl2 at 0.2% and 0.5%

29 more, we show that CLV1 expressed within the pedicel can partially replace the function of the ERECTA

30 tations partially suppressed clv2 floral and pedicel defects in a dominant fashion, and almost comple

31 t mutant and wild-type L3-derived tissues in pedicels developed autonomously, indicating little or no

32 onstrate that during the first two stages of pedicel development ERECTA is important for the rate of

33 pedicel were capable of orchestrating normal pedicel development in overlying tissues, revealing the

34 zones of the leaf petiole, flower and fruit pedicel, flower corolla, and fruit calyx.

35 four distinct morphological regions (scape, pedicel, funicle and club).

36 Throughout the first two stages pedicel growth is exponential, while during the final st

37 t of ERECTA, a gene with strong influence on pedicel growth.

38 velopmental stages were distinguished during pedicel growth: a proliferative stage, a stomata differe

39 sepals while stemlike organs (filaments and pedicels) had larger sectors.

40 udy on grape (Vitis vinifera), we determined pedicel hydraulic conductivity (kh) from pressure-flow r

41 However, it is unknown how pedicel hydraulics change developmentally in relation to

42 htly shorter than that in the wild type, the pedicel is slightly longer than that in the wild type, a

43 In flowers GUS activity was observed in the pedicel joints and ovaries, whereas in fruits it was str

44 at initiates the abscission zone in the seed-pedicel junction.

45 ages provided direct evidence that losses in pedicel kh were associated with blockages in vessel elem

46 , floral primordia occasionally give rise to pedicels lacking flowers at their ends.

47 tside of the meristem: POL and PLL1 regulate pedicel length in interaction with ERECTA, while PLL4 an

48 Pedicels offer multiple advantages for such a study, as

49 d biochemical processes related to fruit and pedicel quality was investigated on two major cultivars.

50 dient of signal(s) derived from the maternal pedicel region.

51 as well as decreased elongation of siliques, pedicels, roots, and the inflorescence.

52 are expressed at moderate levels in leaves, pedicels, sepals, pistils and petals, and at very low le

53 iders usually adopt positions on or near the pedicel; some species may enter the spider's book lungs.

54 cular bundles were identified in the pith of pedicels supporting the fruitlets with the lowest abscis

55 le eggs, yet emerged from galls with shorter pedicels than those of female wasps.

56 of tomato results in the formation of flower pedicels that lack an abscission zone and inflorescence

57 riptional profiles of endosperm and placenta/pedicel tissues in developing maize kernels under water

58 e-specifically regulated in the floral/fruit/pedicel tissues of pea.

59 S and PsACO in the ovaries, and PsACO in the pedicels was correlated with higher ethylene evolution a

60 ly the outermost L3-derived cells within the pedicel were capable of orchestrating normal pedicel dev

61 Abscission at the base of the pedicel, where AtEXP10 is endogenously expressed, was en

62 In leaf petiole and flower pedicel zones this activity was enhanced by ethylene and