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