戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 1 promotes branching through local action in axillary buds.
2             Grasses possess basal and aerial axillary buds.
3 abidopsis is determined by the activation of axillary buds.
4 nins and strigolactones, which can move into axillary buds.
5 gan senescence, and permanent suppression of axillary buds.
6 were equally abundant in growing and dormant axillary buds.
7  late response to far-red light treatment in axillary buds.
8 mportant role in inhibiting the outgrowth of axillary buds, a phenomenon known as apical dominance.
9 on repeatedly forcing shoot development from axillary buds, a process that was guided by the size and
10                    We observed that isolated axillary buds activate in two genetically and physiologi
11 psis (Arabidopsis thaliana) both by delaying axillary bud activation and by attenuating the basipetal
12 whereby the shoot tip inhibits the growth of axillary buds along the stem.
13   The PsBRC1 gene is mostly expressed in the axillary bud and is transcriptionally up-regulated by di
14 etween specific changes in auxin efflux from axillary buds and bud outgrowth after shoot tip removal
15 ally in growing organs (root apices, growing axillary buds and elongating stems) compared with their
16 otein (RanBP) in Arabidopsis results in more axillary buds and reduced apical dominance compared to W
17 ot apex and the secondary meristem producing axillary buds and vascular tissues of young leaves and s
18 that SLs do not affect the delivery of CK to axillary buds and vice versa.
19 uch as the basic shoot units made of a leaf, axillary bud, and internode.
20    The expression of TRU1 and TB1 overlap in axillary buds, and TB1 binds to two locations in the tru
21  highly expressed in shoot apical meristems, axillary buds, and young leaves.
22              At early stages of development, axillary buds are inhibited by shoot apex-produced auxin
23 nts each bearing one leaf and its associated axillary bud - are a simplified system to understand the
24 en buds, using Arabidopsis explants with two axillary buds as a minimal system.
25 bidopsis thaliana) inhibits the outgrowth of axillary buds as part of the whole plant senescence prog
26 o) and phosphate availability, such that the axillary bud at node 7 varied from deeply dormant to rap
27 r, as an elongated branch, develops from the axillary bud (AXB) in the leaf axil and is crucial for t
28 osed based on AP2 transcript accumulation in axillary buds before and after budbreak.
29 the main stem and inhibits the growth of the axillary buds below it, contributing to apical dominance
30 owing shoot tip suppresses the growth of the axillary buds below.
31 lts imply that POTM1 mediates the control of axillary bud development by regulating cell growth in ve
32                                       During axillary bud development in a model petiole-leaf cutting
33 gene to characterize D14 function from early axillary bud development through to lateral shoot outgro
34 at axil and leaf boundary regions to control axillary bud differentiation as well as the development
35 ristem arrest by repressing genes related to axillary bud dormancy in the SAM and negative regulators
36    This occurs by regulating the activity of axillary buds established in each leaf axil.
37  fruit removal resembled changes observed in axillary buds following release from apical dominance.
38           EBE overexpression also stimulates axillary bud formation and outgrowth, while repressing i
39 y bud growth was not the result of increased axillary bud formation.
40 ipt is regulated by light quality, such that axillary buds growing in added far-red light have greatl
41 s and, in a model system, exhibited enhanced axillary bud growth instead of producing a tuber.
42                                This enhanced axillary bud growth was not the result of increased axil
43 scription factor that acts as a repressor of axillary bud growth.
44 ced tillering, deregulation of the number of axillary buds in an axil, and alterations in leaf proxim
45 ason, we have forced precocious sprouting of axillary buds in fruit-bearing shoots, and examined the
46 d number of plants were detected that lacked axillary buds in most of the axils of the cauline (stem)
47 he miR156 targets, directly regulated aerial axillary bud initiation.
48                             The outgrowth of axillary buds into branches is regulated systemically vi
49 ression of auxin transport/canalization from axillary buds into the main stem and is enhanced by a lo
50 ppressing auxin canalization and export from axillary buds into the main stem.
51 reby the impact of any SL signal reaching an axillary bud is modulated by the responsiveness of these
52            In this theory, auxin flow out of axillary buds is a prerequisite for bud outgrowth, and b
53 thaliana gene BRANCHED1 (BRC1), expressed in axillary buds, is required for branch suppression in res
54 nt mutant was used in a SL bioassay based on axillary bud length after direct SL application on the b
55 e application and decapitation by increasing axillary bud length, implicating a PsBRC1-independent co
56 rs are vegetative branches that develop from axillary buds located in the leaf axils at the base of m
57 ism underlying NtBRC2A-mediated outgrowth of axillary buds needs to be further addressed.
58  accelerated spikelet initiation and reduced axillary bud number in a photoperiod-independent manner
59                          Cytokinin levels in axillary buds of a transgenic suppression line increased
60 PCIB), effectively blocked auxin efflux from axillary buds of intact and decapitated plants without a
61 tokinins were significantly increased in the axillary buds of the fvemyb117a mutant.
62 e TEOSINTE BRANCHED1 gene were quantified in axillary buds only 6 h after application of SLs.
63                      Loss of both apical and axillary buds or inhibition of polar auxin transport did
64            Consequently, SLs can repress (in axillary buds) or promote (in the stem) cell division in
65 ision during branch development: whether the axillary bud, or branch primordium, grows out to give a
66  shows that MAX2 acts locally, either in the axillary bud, or in adjacent stem or petiole tissue.
67 r that affects cell proliferation as well as axillary bud outgrowth and shoot branching in Arabidopsi
68 t that a flavonoid-based mechanism regulates axillary bud outgrowth and that this mechanism is under
69 hoot tip's strong demand for sugars inhibits axillary bud outgrowth by limiting the amount of sugar t
70 hat MAX1, a specific repressor of vegetative axillary bud outgrowth in Arabidopsis, acts a positive r
71                                              Axillary bud outgrowth in general is negatively regulate
72 ation of decapitation- and cytokinin-induced axillary bud outgrowth is independent of auxin canalizat
73        Inhibitory effects of PCIB and NPA on axillary bud outgrowth only became apparent from 48 h af
74                       The fhy3 phenotypes of axillary bud outgrowth suppression and of stress-induced
75         We speculate that MAX1 could repress axillary bud outgrowth via regulating flavonoid-dependen
76 polar auxin transport stream (PATS) inhibits axillary bud outgrowth, its role in regulating the phyB
77 mental signals involved in the regulation of axillary bud outgrowth.
78 asome and abrogate its activity in promoting axillary bud outgrowth.
79  is reduced branching through suppression of axillary bud outgrowth.
80 2-1 backgrounds, resulted from inhibition of axillary bud outgrowth.
81  the group of hormones that are required for axillary bud outgrowth.
82                      Colchicine treatment of axillary buds resulted in a set of autotetraploid S. vim
83 in young, but not old leaves, revealing that axillary buds retain a silenced version of the floral re
84 d on the Agrobacterium T-DNA injected at the axillary bud site, resulting in the excision of the targ
85 ture is largely determined by the pattern of axillary buds that grow into lateral branches, the regul
86  seq, hormone and sugar measurements on 1 mm axillary bud tissue, we identify the genetic pathways pu
87 ght and nutrition, are integrated within the axillary bud to promote or suppress the growth of the bu
88 short branches (crowns) develop from dormant axillary buds to form inflorescences and flowers.
89 el, Fv SOC1 regulates the differentiation of axillary buds to runners or axillary leaf rosettes, prob
90 e levels of POTM1-1 transcripts were high in axillary buds, underground stolen tips, and newly formed
91                                              Axillary buds were also activated in aerial tissues of m
92  in the development of increasing numbers of axillary buds with time in storage, suggesting the need
93 le, and biosynthesis and transport genes, in axillary buds within 3 h after application.
94 buted over large distances and accumulate in axillary buds within a timeframe that correlates with bu