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1 eristem dome and primordia and in developing stolons.
2 sues and induced by short days in leaves and stolons.
3 ole of PP2A in the tuberization induction in stolons.
4 sport from the leaf to the stem and into the stolons.
5 sect predation on leaves, and photoperiod in stolons.
6 o a short-day photoperiod in both leaves and stolons.
7 d high in the apical 1 to 2 mm of tuberizing stolons.
8 being detected in leaves and the highest in stolons.
9 ld increase in fruit yield at the expense of stolons.
10 sues and induced by short-days in leaves and stolons.
11 into a branch crown (a flowering shoot) or a stolon (a horizontal stem that produces daughter plants)
15 ed miR156 accumulation accompanied by aerial stolons and tubers from axillary nodes, similar to miR15
17 ofiled ~200,000 Hydractinia cells, including stolons and two polyp types, identifying major cell type
18 scripts was restricted to developing tubers, stolons, and roots and that mRNA accumulation correlated
24 3'-untranslated region, are not expressed in stolons but display a gradual increase in expression lev
26 nvertase in the subapical region of swelling stolons, consistent with the switch from apoplastic to s
29 tuberosum), tubers develop from underground stolons, diageotropic stems which originate from basal s
33 abolished GA20ox4 expression and eliminated stolon formation, a phenotype rescued by exogenous gibbe
34 d main branches than control plants, reduced stolon formation, together with a dwarfing phenotype and
38 The expression profile of StBEL5 induced in stolons from plants grown under long-day conditions reve
40 ly propagated by daughter-plants produced by stolons, fruit yield is further dependent on the trade-o
41 strategy of large colonies, we suggest that stolons function to limit space occupied by small coloni
42 ectly antagonising the function of StSP6A in stolons, identifying StCEN as a breeding marker to impro
43 at is transcribed in leaves, moves down into stolons in response to short days, and induces tuber for
44 ion during the developmental transition from stolons into tubers, in which there is an increased dema
47 a complex life history of multigenerational, stolon-like asexual reproduction, interspersed with disp
51 al programme by which cells in the subapical stolon region divide and radially expand to further diff
53 s and (14)C sugar partitioning in tuberizing stolons revealed a distinct difference between the apica
54 ase activity in nontuberizing and tuberizing stolons revealed a marked decline in soluble invertase i
57 ) gene was obtained while screening a potato stolon tip cDNA expression library with 35S-labeled calm
62 t but insensitive to photoperiod, whereas in stolon tips growing in the dark, promoter activity is en
66 ecific promoter, the movement of BEL5 RNA to stolon tips was facilitated by a short-day photoperiod,
70 reased by almost 80% during development from stolons to mature tubers but it increased about seven-fo
72 n gene expression during the transition from stolons to tubers coincides with an increase of histone
73 in abundance of miR156 has been observed in stolons under tuber-inductive (short-day) conditions, in
75 lants, StMSI1 and miR156 levels increased in stolon, whereas StBMI1-1 decreased under SD conditions.
76 port of their mRNAs from leaves to roots and stolons, whereas suppression lines of these two RNAs exh
78 ion rates in vitro, as compared to wild type stolons, with no differences in the number of tubers obt