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1 also unveil roles in the development of rice gynoecium.
2 ors restrict sensitivity to cytokinin in the gynoecium.
3 shment during development of the Arabidopsis gynoecium.
4 that is elongating within the solid maternal gynoecium.
5  a seedpod that develops from the fertilized gynoecium.
6 l domains along the apical-basal axis of the gynoecium.
7  the three positional axes of the developing gynoecium.
8 h encompass these regions of the Arabidopsis gynoecium.
9 arpels leads to the formation of an enclosed gynoecium.
10 h a CRABS-CLAW mutant that maintains an open gynoecium.
11 tion of the transmitting tract in the female gynoecium.
12 transfer along the transmitting tract of the gynoecium.
13 , and apical-basal patterning defects in the gynoecium.
14  regional differentiation in stamens and the gynoecium.
15 y with Auxin Response Factor 4 (ARF4) in the gynoecium.
16 pping targets of ETT/ARF4 in the Arabidopsis gynoecium.
17  by their physical interaction in the apical gynoecium.
18 s of floral organs, as well as an apocarpous gynoecium.
19                                          The gynoecium, a highly specialized structure in flowering p
20 DI1 (KAN1) organize the Arabidopsis thaliana gynoecium along two distinct polarity axes.
21 n alters the expression of genes involved in gynoecium and embryo development, lipid metabolism, auxi
22 tterning of the root, the development of the gynoecium and female gametophyte, and organogenesis and
23 ich DELLA proteins contribute to GA-mediated gynoecium and fruit development remains to be clarified.
24 arge number of mutants that display abnormal gynoecium and fruit development.
25 vule patterning and thereby seed number with gynoecium and fruit growth through a set of shared recep
26 that the spacing of ovules in the developing gynoecium and fruits is controlled by two secreted pepti
27 e ovule and the septum, resulting in a split gynoecium and no observable embryo sac.
28 cally expressed in particular regions of the gynoecium and ovule, only during and after floral develo
29 ontrol the initiation and development of the gynoecium and resulting fruit.
30 in Response Factors, ARF6 and ARF8, regulate gynoecium and stamen development in immature flowers.
31 rms relies on the precise development of the gynoecium and the anther, because their primary function
32 contribute to cell division in the leaf, the gynoecium and the ovules in A. fimbriata.
33 hment and breaking of radial symmetry at the gynoecium apex (style) remain unknown.
34 sed the block in pollen release, but not the gynoecium arrest.
35 istem before morphological appearance of the gynoecium, consistent with the proposal that ETT is invo
36       The Arabidopsis (Arabidopsis thaliana) gynoecium consists of two congenitally fused carpels mad
37 served synergism between the two pathways in gynoecium development and suggest a role for ARF4 in the
38 owever, ETT/ARF4 targets with known roles in gynoecium development did not conform to models of A-B A
39  of auxin and cytokinin responses to control gynoecium development in Arabidopsis.
40                          Characterization of gynoecium development in receptor mutants revealed incre
41                          Here we showed that gynoecium development is affected in different multiple
42           Our analysis focuses on stamen and gynoecium development, where we find that NUB acts redun
43 process that finds a parallel in Arabidopsis gynoecium development.
44 motion of petal epidermal cell identity, and gynoecium development.
45 ing an apical-basal gradient of auxin during gynoecium development.
46 cytokinin regulates auxin homeostasis during gynoecium development.
47  direct targets of BPCs and thus involved in gynoecium development.
48 ETT)-mediated pathway in contexts outside of gynoecium development.
49 s, ensuring correct domain specification and gynoecium development.
50                  In Arabidopsis flowers, the gynoecium develops as an open, vase-like structure that
51 bilaterally symmetric stage ingrained in the gynoecium due to its evolutionary origin to a radially s
52 he fruit, which develops from the fertilised gynoecium formed in the innermost whorl of the flower, i
53                     The medial domain of the gynoecium gives rise to the ovules, and several other st
54 ich infect inflorescences either through the gynoecium (group 2) or systemically through the apical m
55 e region of the ovule facing the base of the gynoecium (gynobasal).
56 ture of the medial domain of the Arabidopsis gynoecium, highlighting the developmental stages that im
57 ishing the apical-basal polarity axis of the gynoecium, indicating that they function in differentiat
58 ation of the apical style in the Arabidopsis gynoecium involves a bilateral-to-radial symmetry transi
59 equires that anthers release pollen when the gynoecium is competent to support fertilization.
60 um of the Arabidopsis (Arabidopsis thaliana) gynoecium is composed of two congenitally fused, lateral
61                      In flowering plants the gynoecium is the female reproductive structure and the s
62 bidopsis thaliana female reproductive organ (gynoecium) is a crucial biological process linked to pla
63 ors, ARF6 and ARF8, regulate both stamen and gynoecium maturation.
64 ng in diverse developmental contexts such as gynoecium morphogenesis, lateral root emergence, ovule d
65 IG all affect floral organ number as well as gynoecium morphology.
66                                   The mature gynoecium of Arabidopsis is composed of an apical stigma
67                  This organization makes the gynoecium one of the most complex plant structures, and
68  cytokinin-auxin feedback model during early gynoecium patterning and hormone homeostasis.
69                                              Gynoecium patterning is dependent on the dynamic distrib
70                             NPA's effects on gynoecium patterning mimic the phenotype of mutations in
71 d to a premature SlTCP2/LA expression during gynoecium patterning, which results in modified cell div
72 PA), highlighting their role in mediolateral gynoecium patterning.
73  function in leaf polarity specification and gynoecium patterning.
74 obably involved in auxin-mediated control of gynoecium patterning.
75 interactions pivotal for patterning of early gynoecium primordia remain unknown.
76 atterning apical and basal boundaries in the gynoecium primordium.
77  delivered to the interior of the developing gynoecium prior to locule closure if efficient transform
78 e apex of the female reproductive organ, the gynoecium, remain poorly understood, despite its fundame
79                    Proper development of the gynoecium requires that the early gynoecial primordium b
80 polarity by promoting basal cell fate in the gynoecium, restricting the expression domain of the basi
81 involved in medial tissue development in the gynoecium such as HECATE, BELL1 and NGATHA1.
82 ially symmetrical flowers with a conspicuous gynoecium surrounded by prominent nectar reward, organiz
83 sion in tissues other than the androecium or gynoecium, termed secondary sexual characters, suggests
84 3000 species of Brassicaceae, develop from a gynoecium that consists of two fused carpels.
85       The Arabidopsis (Arabidopsis thaliana) gynoecium, the female floral reproductive structure, req
86 nerates ovules from the medial domain of the gynoecium, the female floral reproductive structure.
87 erning of the female reproductive organ, the gynoecium, the flow as well as the temporal and spatial
88      Considering the fundamental role of the gynoecium, which affects the reproductive success of the
89 a of the anthers and the carpel walls of the gynoecium, which enclose the ovules.
90 eproductive organ development, including the gynoecium, which is the female reproductive structure an