ライフサイエンスコーパス: leaf blade

1 veloping zones to one another and the mature leaf blade.

2 t is critical to their ability to generate a leaf blade.

3 ntly reduces or eliminates macrohairs in the leaf blade.

4 cessary for lateral growth of the developing leaf blade.

5 that specify macrohair initiation within the leaf blade.

6 tes macrohair initiation specifically in the leaf blade.

7 ne and sometimes glutamine compared to older leaf blades.

8 hesis genes was higher in younger than older leaf blades.

9 ed the amino acid levels in center and outer leaf blades.

10 ntally regulated auxin gradient in expanding leaf blades.

11 lateral organs results in upward curling of leaf blades.

12 ntly downregulated in affected areas of sxd1 leaf blades.

13 een tissues, with highest levels in maturing leaf blades.

14 The adaxialized leaves fail to develop leaf blades.

15 was increased up to 32.5-fold in 8-week-old leaf blades.

16 In growing maize (Zea mays) leaf blades, a defined developmental gradient facilitate

17 treatment caused cell death in B. distachyon leaf blades, an effect that was reversed by the addition

18 does, and can substitute for STF function in leaf blade and flower development if expressed under the

19 ddish-brown vascular tissue in the stem, the leaf blade and sheath.

20 odulate cell proliferation in the developing leaf blade and specific floral tissues; a role that was

21 ally dissimilar to native SAPs, having wider leaf blades and greater leaf area, dense and evenly dist

22 ler rosettes because of shorter petioles and leaf blades and often acquired a twisted leaf morphology

23 developmental trajectories in Kranz (foliar leaf blade) and non-Kranz (husk leaf sheath) leaves of t

24 tly overrepresented among 25 E- > E+ DEGs in leaf blade, and a number of other DEGs were associated w

25 xial cells is important for formation of the leaf blade, and the MYB transcription factor gene PHANTA

26 plants had slightly longer petioles, larger leaf blades, and larger cells than controls.

27 observed in sepal and petal development, but leaf blades are apparently normal.

28 tem; however, add3 prevents the expansion of leaf blades at high temperature.

29 Liguleless3-O (Lg3-O) transforms the leaf blade, auricle and ligule into sheath around the mi

30 related with a similar reduction in expanded leaf blade chlorophyll levels.

31 equency of polyploid cells in basal zones of leaf blades, consistent with the disruption of cytokines

32 roxy-beta-diketones in the peduncle and flag leaf blade cuticles.

33 tant bladekiller1-R (blk1-R) is defective in leaf blade development and meristem maintenance and exhi

34 To help understand regulation of maize leaf blade development, including sink-source transition

35 rice, WOX3 homologs are major regulators of leaf blade development.

36 control points in gene expression along the leaf blade developmental gradient.

37 s diversity is achieved by the modulation of leaf blade dissection to form lobes or leaflets.

38 queous auxin application inhibited long-term leaf blade elongation.

39 ptoms, including shoestring leaves that lack leaf blade expansion.

40 apical hook maintenance, and abaxial/adaxial leaf-blade expansion.

41 n biosynthesis and auxin biosynthesis in the leaf blade followed by auxin long-distance transport to

42 Comparisons included leaf blades from apple, grape, corn, and tomato and leaf

43 pecific stages along the developmental maize leaf blade gradient.

44 normal adaxial/abaxial polarity and generate leaf blades in the normal position, but the adaxial meso

45 plants can be described as simple, where the leaf blade is entire, or dissected, where the blade is d

46 Initiation and growth of leaf blades is oriented by an adaxial/abaxial axis align

47 ablished along the developmental axis of the leaf blade, leading from an undifferentiated leaf base j

48 transcriptionally repress its targets during leaf blade morphogenesis.

49 types differed at two major loci controlling leaf blade Na(+) accumulation.

50 rate genetic traits that interact to control leaf blade Na(+).

51 Younger leaf blades of aposymbiotic plants (no endophyte present

52 ent was 2-fold elevated in BdWRI1-expressing leaf blades of B. distachyon.

53 hondrial transcripts in stage 2 semi-emerged leaf blades of one month-old maize plants.

54 hanges in the cell wall composition of csld1 leaf blades or epidermal peels, yet a greater abundance

55 a, and Nicotiana sylvestris are required for leaf blade outgrowth and floral organ development as dem

56 gene, STENOFOLIA (STF), plays a key role in leaf blade outgrowth by promoting cell proliferation at

57 development, but LFL has no obvious role in leaf blade outgrowth in M. truncatula on its own or in c

58 a WOX gene, STENOFOLIA (STF), in controlling leaf blade outgrowth.

59 ades from apple, grape, corn, and tomato and leaf blade, petiole, stem, and pod tissues from soybean

60 biotic (E+) vs endophyte-free (E-) clones in leaf blades, pseudostems, crowns and roots.

61 oduct, which is involved in establishing the leaf blade-sheath boundary.

62 tions in young (center) versus older (outer) leaf blades, so LOL gene expression was compared in thes

63 ted developmental time, and is restricted to leaf blade tissue.

64 acceptable results for cyclitol analysis in leaf blade tissue.

65 1A6, which occurred predominantly within the leaf blade tissues.

66 by changing gene expression from the distal leaf blade to its base.

67 The auricles act as a hinge, allowing the leaf blade to project at an angle from the stem, while t

68 in dorsoventrality and lateral growth of the leaf blade was investigated in the 'bladeless' lam1 muta

69 cell division and expansion at the bases of leaf blades, where cytokinesis and cross-wall formation

70 expression was similar in younger and older leaf blades, whereas expression of N. uncinatum LOL gene

71 A lam1-lam1-glauca chimera generated a leaf blade with lam1 cells in the L1-derived epidermis a