ライフサイエンスコーパス: venation

1 twings retain noticeably more wild-type wing venation.

2 iterature on a wide range of aspects of leaf venation.

3 evolutionary dynamics of succulence and leaf venation.

4 aped, or fused cotyledons), and altered leaf venation.

5 L2 in multiple downstream pathways affecting venation.

6 commonness of reticulate, hierarchical leaf venation.

7 al information about leaf shape and existing venation.

8 ial resistance-32% and 49%- was in the minor venation, 18% and 21% in the major venation, and 14% and

9 parl1 mutants display parallel leaf venation, aberrant localization of the provascular marke

10 Venation and apposition of the wing surfaces are process

11 Three C(3) species have both increased venation and enlarged bundle sheath cells, and there is

12 cribe the development and plasticity of leaf venation and its adaptation across environments globally

13 ance, leaf hyponasty, and inhibition of leaf venation and lateral root development.

14 dicots, most monocot leaves display parallel venation and sheathing bases wherein the margins overlap

15 ith maximum photosynthetic rate through leaf venation and substantiate the theory that an increase in

16 mplications for the molecular development of venation and tissue differentiation, as well as the evol

17 the minor venation, 18% and 21% in the major venation, and 14% and 4% in the petiole.

18 traits relating to lamina and xylem anatomy, venation, and composition, but gs was not plastic with g

19 e findings point to a new functional role of venation architecture and small leaf size in drought tol

20 Additionally, venation architecture determines the sensitivity of K(le

21 Variation in Kleaf arose from differences in venation architecture that influenced xylem and especial

22 d leaves of woody angiosperms of contrasting venation architecture to severing treatments in vivo, an

23 aves vary enormously in their size and their venation architecture, of which one major function is to

24 ever been demonstrated for contrasting major venation architectures, including the most basic dichoto

25 The design and function of leaf venation are important to plant performance, with key im

26 ning of veins 3 and 4 and to prevent ectopic venation between them.

27 The large proportion of resistance in the venation can explain why stomata respond to leaf xylem d

28 he leaf resulted in the pathways outside the venation comprising only 36% and 26% of R(leaf).

29 , originally identified by its aberrant leaf venation, corresponds to the Arabidopsis nucleolin gene.

30 The repeated evolution of 3D venation decouples leaf water storage from hydraulic pat

31 nalysis we identified five genes that showed venation defects.

32 Leaf shape is associated with venation features that affect desiccation resistance.

33 leaves from fragments by calculating a "leaf venation fingerprint" from topology and geometry.

34 icted to provascular and procambial cells as venation forms.

35 assessed are C(3) plants but have increased venation in leaves.

36 he auxin efflux carrier PIN1, highly reduced venation, initiation of multiple cotyledons, and gradual

37 ange of plant biologists to incorporate leaf venation into their research.

38 esults reveal how the size structure of leaf venation is a critical determinant of the spread of embo

39 Leaf venation is a showcase of plant diversity, ranging from

40 This benefit for palmate venation is consistent with its repeated evolution and i

41 A principal function of the venation is to deliver water; however, a hydraulic signi

42 This apparent overinvestment in leaf venation may be explained from the selective pressure of

43 ndamental rule was that within an individual venation network, susceptibility to embolism always incr

44 We find that a leaf venation network, which possesses key characteristics of

45 ics and information on the structure of leaf venation networks and areoles.

46 leaves of angiosperms contain highly complex venation networks consisting of recursively nested, hier

47 Leaf venation networks mediate many plant resource fluxes and

48 Leaf venation networks provide an integrative linkage between

49 imaging can be successfully applied to leaf venation networks, facilitating research in multiple fie

50 The avb1 mutation did not affect leaf venation pattern and root vascular organization.

51 that causes leaf hyponasty and reduces leaf venation pattern complexity and auxin responsiveness.

52 The formation of the venation pattern in leaves is ideal for examining signal

53 uire an understanding of how the distinctive venation pattern in the leaves of C(4) plants is determi

54 n suggested by our results could explain the venation pattern, and the vascular hypertrophy caused by

55 wever, had a distinct three-dimensional (3D) venation pattern, which evolved 11-12 times within this

56 n was less prominent, resulting in a palmate venation pattern.

57 To gain insight into venation patterning mechanisms, we have characterized th

58 ts are defective in embryogenesis, cotyledon venation patterning, root growth, and root cap developme

59 Procrustes analysis quantitatively describes venation patterning.

60 atterns of blade outgrowth, hirsuteness, and venation patterning.

61 c alleles of these genes also display simple venation patterns, and their double mutant combinations

62 of the full-red pigmentation, red spots, and venation patterns, respectively.

63 t green bodies and delicate wings with dense venation patterns.

64 n the number of sensory bristles and on wing venation phenotypes induced by modified epidermal growth

65 thus constitutes a new dimension in the leaf venation phenotypic space.

66 ination, larval blood cell development, wing venation, planar polarity in the eye, and formation of o

67 A new study shows independent origins of 3D venation reflect hydraulic advantages for tissue succule

68 3D venation "resets" internal leaf distances, maintaining m

69 Leaf size and venation show remarkable diversity across dicotyledons,

70 aring LVD and other quantitative measures of venation structure across leaves.

71 ed directly from a chemically extracted leaf venation system.

72 e we present global scaling relationships of venation traits with leaf size.

73 ew taxon is characterized by unique forewing venation with the presence of forewing SC, 1-RS almost a