ライフサイエンスコーパス: tendril

1 ized in branched tendrils, but not in simple tendrils.

2 ignoniaceae, leaf parts can be modified into tendrils.

3 ils have a smoother surface than high-energy tendrils.

4 as rings within swarms toward the extending tendrils.

5 overproduced HAA exhibited slender swarming tendrils.

6 patterns characterized by irregularly shaped tendrils.

7 are finer ( 22 nm diameter) than high-energy tendrils ( 176 nm diameter), and low-energy tendrils hav

8 Tendril and distal branches were spatially segregated an

9 pea including roots, stems, leaves, flowers, tendrils and developing seeds, as determined by northern

10 Distinctly identifiable primary, tendril, and distal branches could be operationally diff

11 ox1 transgenic plants had longer internodes, tendrils, and fruits, larger stipules, and displayed del

12 Low energy tendrils are finer ( 22 nm diameter) than high-energy te

13 In Bignonieae, tendrils are modified leaflets that, as a result of prem

14 n's widely accepted interpretation of coiled tendrils as soft springs, their mechanical behavior rema

15 t motions, where a variety of organs such as tendrils, bracts, leaves and flowers respond to environm

16 ociated with regions from which leaflets and tendril branches originate.

17 ession was found to be polarized in branched tendrils, but not in simple tendrils.

18 iments on cucumber tendrils demonstrate that tendril coiling occurs via asymmetric contraction of an

19 ctively, our study illuminates the origin of tendril coiling, quantifies Darwin's original proposal,

20 The high-energy tendrils consisted of very large (>100 nm) grains compar

21 in various plant organs and tissues such as tendrils, contractile roots, and tension wood.

22 Our experiments on cucumber tendrils demonstrate that tendril coiling occurs via asy

23 Moreover, PHAN is probably involved in tendril diversification in Bignonieae, as it has distinc

24 Dodder tendrils excised from hosts can grow in vitro for weeks

25 After in vitro tendrils excised from LL hosts reparasitized new CN and

26 ension, both extracted fiber ribbons and old tendrils exhibit twistless overwinding rather than unwin

27 sm of wave propagation as well as a branched tendril formation at the edge of the population that dep

28 gacS increased sliding motility and restored tendril formation to spreading colonies, while transposo

29 ndaries tended to be high angle; high energy tendril grain boundaries were not observed.

30 pping the distal end of in vivo and in vitro tendrils, growing on or excised from LibertyLink (LL; PA

31 Electron diffraction measured tendril growth axes and grain boundary angle/axis pairs;

32 The helical coiling of plant tendrils has fascinated scientists for centuries, yet th

33 tendrils ( 176 nm diameter), and low-energy tendrils have a smoother surface than high-energy tendri

34 igh-angle grain boundaries in the low-energy tendrils implies that as the tendrils twist or bend, str

35 pping and molecular studies demonstrate that tendrils is allelic to rhea, which encodes Drosophila ta

36 y, no data are available on genic control of tendrilled leaf development outside Fabaceae.

37 ioides, bearing multifid, trifid, and simple-tendrilled leaves, respectively.

38 extracellular factors capable of modulating tendril movement, and genetic analysis revealed that mod

39 ia migrate as defined groups, referred to as tendrils, moving in a coordinated manner capable of sens

40 heroid beta-integrin protein is disrupted in tendrils mutant terminal cells.

41 Here, we describe Drosophila tendrils mutations that compromise maintenance of trache

42 ginosa often, but not always, forms branched tendril patterns during swarming; this phenomena occurs

43 and inflated alpha-integrins, also show the tendrils phenotype, and localization of myospheroid beta

44 helical structure, such as a climbing plant tendril, refers to a kink that connects two helices with

45 Tendrils share some anatomical similarities with leaflet

46 very large (>100 nm) grains compared to the tendril size, so the nature of the high energy irradiati

47 n dynamic helical systems as seen in coiling tendrils, spasmoneme springs, and the opening of chiral

48 Oxygen was present at tendril surfaces, but tendrils were all BCC tungsten met

49 Homozygous tendrils terminal cell clones have fewer terminal branch

50 of their petioles, petiolules, leaflets, and tendrils through histological analyses.

51 in liquid film and by propagating toward the tendril tips.

52 nical movements, such as those used by plant tendrils to help the plant access sunlight.

53 ith light, in a manner that mimics how plant tendrils twist and turn under the effect of differential

54 the low-energy tendrils implies that as the tendrils twist or bend, strain must accumulate until nuc

55 level of PAT in in vivo and in vitro dodder tendrils was quantified by enzyme-linked immunosorbent a

56 Oxygen was present at tendril surfaces, but tendrils were all BCC tungsten metal.

57 expansion rate as well as cell alignment in tendrils were confirmed experimentally.

58 gafactin production exhibited broad swarming tendrils, while a syringafactin-producing strain that ov