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1 ized in branched tendrils, but not in simple tendrils.
2 ignoniaceae, leaf parts can be modified into tendrils.
3  as rings within swarms toward the extending tendrils.
4  overproduced HAA exhibited slender swarming tendrils.
5 patterns characterized by irregularly shaped tendrils.
6 otransposon-induced insertion mutant lacking tendrils.
7 cture, such as leaf-like stipules, spines or tendrils.
8 ils have a smoother surface than high-energy tendrils.
9 are finer ( 22 nm diameter) than high-energy tendrils ( 176 nm diameter), and low-energy tendrils hav
10                                              Tendril and distal branches were spatially segregated an
11 pea including roots, stems, leaves, flowers, tendrils and developing seeds, as determined by northern
12  crops, are climbers and have characteristic tendrils and pepo fruits.
13             Distinctly identifiable primary, tendril, and distal branches could be operationally diff
14 ox1 transgenic plants had longer internodes, tendrils, and fruits, larger stipules, and displayed del
15                                   Low energy tendrils are finer ( 22 nm diameter) than high-energy te
16                               In Bignonieae, tendrils are modified leaflets that, as a result of prem
17               Cucumber (Cucumis sativus, Cs) tendrils are slender vegetative organs that typically re
18 n's widely accepted interpretation of coiled tendrils as soft springs, their mechanical behavior rema
19 t motions, where a variety of organs such as tendrils, bracts, leaves and flowers respond to environm
20 ociated with regions from which leaflets and tendril branches originate.
21 ession was found to be polarized in branched tendrils, but not in simple tendrils.
22 iments on cucumber tendrils demonstrate that tendril coiling occurs via asymmetric contraction of an
23 ctively, our study illuminates the origin of tendril coiling, quantifies Darwin's original proposal,
24                              The high-energy tendrils consisted of very large (>100 nm) grains compar
25  in various plant organs and tissues such as tendrils, contractile roots, and tension wood.
26 cucumber genes regulating tendril formation, Tendril (CsTEN) and Unusual Floral Organs (CsUFO), was s
27                  Our experiments on cucumber tendrils demonstrate that tendril coiling occurs via asy
28       Moreover, PHAN is probably involved in tendril diversification in Bignonieae, as it has distinc
29                                       Dodder tendrils excised from hosts can grow in vitro for weeks
30                               After in vitro tendrils excised from LL hosts reparasitized new CN and
31 ension, both extracted fiber ribbons and old tendrils exhibit twistless overwinding rather than unwin
32 corrole particle size of 32 nm, with protein tendrils extending from the core (conjugate size is ~100
33 sm of wave propagation as well as a branched tendril formation at the edge of the population that dep
34  possesses a divergent function in promoting tendril formation but also that CsREV retains its conser
35                  Knocking out CsTL repressed tendril formation but did not affect branch initiation,
36 gacS increased sliding motility and restored tendril formation to spreading colonies, while transposo
37  expression of two cucumber genes regulating tendril formation, Tendril (CsTEN) and Unusual Floral Or
38 ndaries tended to be high angle; high energy tendril grain boundaries were not observed.
39 pping the distal end of in vivo and in vitro tendrils, growing on or excised from LibertyLink (LL; PA
40                Electron diffraction measured tendril growth axes and grain boundary angle/axis pairs;
41                 The helical coiling of plant tendrils has fascinated scientists for centuries, yet th
42  tendrils ( 176 nm diameter), and low-energy tendrils have a smoother surface than high-energy tendri
43          We found that the cucurbit-specific tendril identity gene TEN originated from a paleo-polypl
44 igh-angle grain boundaries in the low-energy tendrils implies that as the tendrils twist or bend, str
45 sTL resulted in the formation of two or more tendrils in one leaf axil.
46 eplacement of leaflets by a branched mass of tendrils in the compound leaves of pea - Pisum sativum L
47 inhibited branch formation without affecting tendril initiation.
48 h function regeneration inspired by cucumber tendril is developed using shape memory polymer poly(gly
49 pping and molecular studies demonstrate that tendrils is allelic to rhea, which encodes Drosophila ta
50 y, no data are available on genic control of tendrilled leaf development outside Fabaceae.
51 ioides, bearing multifid, trifid, and simple-tendrilled leaves, respectively.
52                 Here, we identified cucumber tendril-less (tl), a Tnt1 retrotransposon-induced insert
53 lation, we report utilizing angle-programmed tendril-like grasping trajectories for an ultragentle ye
54  extracellular factors capable of modulating tendril movement, and genetic analysis revealed that mod
55 ia migrate as defined groups, referred to as tendrils, moving in a coordinated manner capable of sens
56 heroid beta-integrin protein is disrupted in tendrils mutant terminal cells.
57                 Here, we describe Drosophila tendrils mutations that compromise maintenance of trache
58  roots to appendages modified into hooks and tendrils on the leaves [3].
59 n-stem-twiners, which attach to supports via tendrils or adventitious roots.
60 n wind around solid objects similar to plant tendrils or lift suspended objects with a positive corre
61 ginosa often, but not always, forms branched tendril patterns during swarming; this phenomena occurs
62  chain, and thus the chains exhibit periodic tendril perversion.
63  and inflated alpha-integrins, also show the tendrils phenotype, and localization of myospheroid beta
64  helical structure, such as a climbing plant tendril, refers to a kink that connects two helices with
65                                              Tendrils share some anatomical similarities with leaflet
66  very large (>100 nm) grains compared to the tendril size, so the nature of the high energy irradiati
67 n dynamic helical systems as seen in coiling tendrils, spasmoneme springs, and the opening of chiral
68                                              Tendril STS lead with a CPS Locator 3D catheter and Sele
69                        Oxygen was present at tendril surfaces, but tendrils were all BCC tungsten met
70                                   Homozygous tendrils terminal cell clones have fewer terminal branch
71 of their petioles, petiolules, leaflets, and tendrils through histological analyses.
72 in liquid film and by propagating toward the tendril tips.
73 nsion (SEFEX) of IL-17RA acts as a molecular tendril to help anchor the ACT1 protomers.
74 nical movements, such as those used by plant tendrils to help the plant access sunlight.
75 ith light, in a manner that mimics how plant tendrils twist and turn under the effect of differential
76  the low-energy tendrils implies that as the tendrils twist or bend, strain must accumulate until nuc
77  level of PAT in in vivo and in vitro dodder tendrils was quantified by enzyme-linked immunosorbent a
78  Oxygen was present at tendril surfaces, but tendrils were all BCC tungsten metal.
79  expansion rate as well as cell alignment in tendrils were confirmed experimentally.
80 gafactin production exhibited broad swarming tendrils, while a syringafactin-producing strain that ov