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1            Finally, we show that Arabidopsis cauline and senescing leaves accumulate apigenin, demons
2 e-dependent pattern, with high expression in cauline and senescing leaves.
3 s pin-like inflorescence, reduced numbers of cauline branches, reduced numbers of secondary rosette i
4 s enhancing and suppressing the outgrowth of cauline branches, respectively.
5 phenotypes, including curled stems and extra cauline branches.
6  DEFICIENT IN ABSCISSION (IDA) is induced in cauline leaf abscission zones when the leaves become wil
7                                              Cauline leaf development represents an intermediate phas
8 hereas euFUL genes control phase transition, cauline leaf growth and fruit development.
9 PL11, SPL13, and SPL15, redundantly regulate cauline leaf identity, affecting both cauline leaf shape
10 vers a SOC1/FUL-SPL-BRI1 module that governs cauline leaf identity, providing new insights into the r
11 oral induction pathways to the regulation of cauline leaf identity.
12 of their morphology and the establishment of cauline leaf identity.
13 tic and environmental factors that determine cauline leaf number, less attention has been given to th
14 gulate cauline leaf identity, affecting both cauline leaf shape and the number of leaves on secondary
15 hether the meristem develops on a rosette or cauline leaf, respectively.
16     FFO1 and FFO3 have specific functions in cauline leaf/stem separation and in first- and third-who
17 corporated into phenotypically normal stems, cauline leaves and flowers.
18 -cells outside phloem bundles in rosette and cauline leaves and in flower stalks were visualised usin
19 ted rosette leaves and systemically infected cauline leaves and inflorescence.
20 is co-expressed with miR156-targeted SPLs in cauline leaves and is a direct target of SPL9.
21 tion to the effect on fruit development, ful cauline leaves are broader than those of wild type and s
22 m identity genes, which affect the number of cauline leaves by promoting floral fate.
23 eins were detectable in cotyledons, while in cauline leaves the transcript encoding the chloroplastic
24  and the partial conversion of later-arising cauline leaves to petals.
25  Pc-G activity show a remarkable increase of cauline leaves under noninductive conditions and floral
26 he plants show upward curling of rosette and cauline leaves, in addition to early flowering.
27  tissues examined, including rosette leaves, cauline leaves, inflorescence stems, flowers, and siliqu
28 cumulation in mature plants was localized in cauline leaves, pollen, stigmata, and floral primordia,
29                    Subtilases in rosette and cauline leaves, stems, flowers, and siliques could be di
30 trichome reduction on the adaxial surface of cauline leaves, thereby illuminating the significance of
31 her levels of expression in roots, stems and cauline leaves.
32 es with extreme apical dominance and twisted cauline leaves.
33  was highest in senescing rosette leaves and cauline leaves.
34  and inflorescence stems than in rosette and cauline leaves.
35 ssion C24 conferred reduced branching in the cauline leaves.
36 on, van inflorescence stems have clusters of cauline leaves; typically three are produced at each nod
37 ed axillary buds in most of the axils of the cauline (stem) leaves, but formed such buds in almost al