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1 apical meristem activity, and inflorescence phyllotaxy.
2 significantly reduced rate and with altered phyllotaxy.
3 ion between auxin and cytokinin signaling in phyllotaxy.
4 ic arrangement of leaves and flowers, called phyllotaxy.
5 lating trichome morphology and inflorescence phyllotaxy.
6 meristem in a stereotypical pattern known as phyllotaxy.
7 aneously supporting establishment of correct phyllotaxy.
8 pposite pairs, in a pattern termed decussate phyllotaxy.
9 th, i.e. they arise sequentially in a spiral phyllotaxy.
10 modified leaves, short internodes and spiral phyllotaxy.
11 f lateral branches, internode elongation and phyllotaxy.
12 auxin and cytokinin signaling for control of phyllotaxy.
13 s, this resulted in fasciated stems, altered phyllotaxy, a cessation of primordia differentiation, or
14 premature inflorescence development, altered phyllotaxy along the stem, reduced petal size, abnormal
15 ermination of the shoot and an alteration of phyllotaxy along the stem, suggesting that ESD4 has a br
16 tive development, including defective floral phyllotaxy and increased floral organ merosity, especial
18 tropically affects meristem identity, floral phyllotaxy and organ initiation and is conserved among a
21 (rad23a, rad23c, and rad23d) or induce mild phyllotaxy and sterility defects (rad23b), higher-order
22 ies, including early flowering time, altered phyllotaxy, and abnormal numbers and shapes of flower or
25 m, which initiate floral organs in a defined phyllotaxy before being consumed in the production of an
26 aphy, I show how shifts in leaf arrangement (phyllotaxy) can developmentally reshape the organization
29 cally, transitions from spiral to non-spiral phyllotaxy directly lead to shifts from radial to dorsiv
30 ly across capitula to generate iconic spiral phyllotaxy, during anthesis floret development occurs in
32 e control of greening, hypocotyl elongation, phyllotaxy, floral organ initiation, accessory meristem
33 The third pathway controls the switch in phyllotaxy from decussate to spiral and is activated ind
34 tree height and altered leaf morphology and phyllotaxy, implicating PP2C phosphatases as growth regu
35 olling quantitative aspects of inflorescence phyllotaxy in maize, consistent with their candidacy for
37 s, selection seems to have acted directly on phyllotaxy, not on novel vascular variants, in the evolu
38 in contrast to the alternating or distichous phyllotaxy observed in wild-type maize and other grasses
39 ernode elongation, shortened roots, aberrant phyllotaxy of flowers, aberrant sepal development, flora
40 ypes retain the typical alternate-distichous phyllotaxy of maize, their leaves grow parallel to those
44 on, and its transport has been implicated in phyllotaxy regulation in Arabidopsis (Arabidopsis thalia
46 ffect hormone levels, ultimately controlling phyllotaxy, the transition to flowering and general grow