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1 ignaling control cell differentiation at the shoot apex.
2 otic stress with cell differentiation at the shoot apex.
3 flowers at the periphery of the reproductive shoot apex.
4 ains patterned at a fixed distance below the shoot apex.
5 ported to axillary mersitems rather than the shoot apex.
6 monal effects with KNOX gene function at the shoot apex.
7 ctive signals transmitted from leaves to the shoot apex.
8 ion phloem and traffic cell to cell into the shoot apex.
9 genesis driven by lateral inhibitions at the shoot apex.
10 ein in sections through the maize (Zea mays) shoot apex.
11 w of symplastic tracers from the leaf to the shoot apex.
12 , and develop a mass of callus tissue at the shoot apex.
13 have no detectable AtZFP1 expression in the shoot apex.
14 ranscripts from the body of the plant to the shoot apex.
15 tive to reproductive phase transition of the shoot apex.
16 ds to cell division plane orientation at the shoot apex.
17 ends on a group of meristematic cells in the shoot apex.
18 key regulator of stem cell activation at the shoot apex.
19 insects and diseases that attack the growing shoot apex.
20 and leaf tissue, rather than leaves, at the shoot apex.
21 xamined, with the highest levels seen in the shoot apex.
22 ne the development of organ primordia at the shoot apex.
23 7 reversibly arrests leaf development at the shoot apex.
26 e for the severe alterations observed in the shoot apex and reproductive organs under salinity condit
27 ids inhibit auxin transport primarily at the shoot apex and root tip and appear to modulate vesicular
29 hat promoter activity is associated with the shoot apex and the base of leaf petioles throughout the
31 e in the rapidly growing regions such as the shoot apex and the secondary meristem producing axillary
33 th gene expression and cell mechanics at the shoot apex and, by extension, in the epidermis of any th
34 tage, dramatically increases the size of the shoot apex and, like xtc1 and xtc2, produces enlarged le
36 ue to deficiencies in auxin transport in the shoot apex, as judged by altered expression of PIN1, the
37 Expression of LEAFY and AGAMOUS-LIKE8 in the shoot apex at the time of floral determination is also c
38 do not clearly alter node distance, from the shoot apex, at which axillary shoot meristems initiate b
41 red for high levels of FLC expression in the shoot apex, but it is not required for FLC expression in
42 incipient and emergent leaf primordia at the shoot apex, but not in the vegetative meristem or stem.
47 s for two family members were highest in the shoot apex, dry seeds (hmg1), and bark (hmg3) which are
50 nt regeneration procedure was developed from shoot apex explants and used to downregulate expression
51 a threshold level of dlf1 is required in the shoot apex for proper timing of the floral transition.
52 in maize by the isolation and culture of the shoot apex from an adult phase plant: an 'adult' meriste
53 r bud outgrowth during the transition of the shoot apex from the vegetative to the reproductive stage
54 ts is a consequence of the transition of the shoot apex from vegetative to reproductive growth in res
56 PGP1 and PGP19 colocalized with PIN1 in the shoot apex in Arabidopsis thaliana and with PIN1 and PIN
57 ocious germination, primordia develop at the shoot apex in the mode characteristic of postgerminative
58 meristem identity genes at the centre of the shoot apex in two ways; first by delaying their upregula
59 AGL15 protein accumulates transiently in the shoot apex in young Arabidopsis and Brassica seedlings a
60 otein 1), is expressed at high levels in the shoot apex, including the apical meristem, developing le
61 d spatial pattern of IAA localization in the shoot apex indicates a change in IAA source during leaf
62 chastic model of primordia initiation at the shoot apex, integrating locality and stochasticity in th
65 ristem, a small dome-shaped structure at the shoot apex, is responsible for the initiation of all pos
66 vealed that Fv SOC1 activates Fv TFL1 in the shoot apex, leading to the repression of flowering in st
67 f the Blec4 promoter in the epidermis of the shoot apex makes it particularly suitable for geneticall
68 a finely resolved time course, comparing the shoot apex (meristem and leaf primordia) and the cotyled
69 al hypoxia induces Adh/GUS expression in the shoot apex, no apex staining was observed in the spacefl
71 development, axillary buds are inhibited by shoot apex-produced auxin, a mechanism known as apical d
74 velopmental decision to flower occurs in the shoot apex, requiring the transmission of flowering info
76 as root tips, lateral root primordia and the shoot apex, supporting a role for FTase in the control o
77 rophilic molecules are likely to move to the shoot apex symplastically via the phloem and/or via cell
79 Because flowers form at a distant site, the shoot apex, these data suggest that FT primarily control
82 ressed unique transcripts were identified in shoot apex tissue between fast- and slow-developing RILs
83 nd the ld mutation converts the reproductive shoot apex to a more vegetative state, a phenotype that
84 globular-to-heart transition but permit the shoot apex to develop to an unusually advanced stage lat
87 y transported from sites of synthesis in the shoot apex to their sites of action in the basal regions
89 rceived in the leaves and transmitted to the shoot apex, where the vegetative shoot apical meristem i
90 id-chloroplast transition takes place at the shoot apex, which consists of the shoot apical meristem
91 o the divisions occurring in the Arabidopsis shoot apex, which contains domains with anisotropic curv
92 2 is expressed in the endosperm, embryo, and shoot apex, which explains the pleiotropic nature of the
94 assess the status of individual cells in the shoot apex with regard to the transition between embryon
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