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1                   We propose that LEUNIG and AINTEGUMENTA act together to control the expression of c
2 s between two related transcription factors: AINTEGUMENTA and AINTEGUMENTA-LIKE6.
3 ion of polar auxin transport and the loss of aintegumenta and revoluta activity.
4                                              Aintegumenta and revoluta are likely to function in para
5 nhance the medial domain defects observed in aintegumenta and revoluta mutant genotypes.
6  subtending leaf, the expression patterns of AINTEGUMENTA and SHOOT MERISTEMLESS RNAs during flower d
7 resent in the Arabidopsis proteins APETALA2, AINTEGUMENTA, and TINY; the tobacco ethylene response el
8 /PLT) transcription factor family, including AINTEGUMENTA (ANT) and AIL6/PLT3, are important regulato
9 psis thaliana, floral organogenesis requires AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE 6 (AIL6)/PLETHO
10                                              AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6 (AIL6) are two
11                                              AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6 (AIL6) encode
12 ng to the AINTEGUMENTA-LIKE/PLETHORA family, AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6/PLETHORA3 (AIL
13 osely related to the floral development gene AINTEGUMENTA (ANT) and show that all AINTEGUMENTA-like (
14                              The Arabidopsis AINTEGUMENTA (ANT) gene has been shown previously to be
15                 The INNER NO OUTER (INO) and AINTEGUMENTA (ANT) genes are essential for ovule integum
16              We show that PLETHORA (PLT) and AINTEGUMENTA (ANT) genes, which encode stem cell-promoti
17                      The Arabidopsis protein AINTEGUMENTA (ANT) is a member of a plant-specific famil
18                      The Arabidopsis protein AINTEGUMENTA (ANT) is an important regulator of organ gr
19                             Mutations in the AINTEGUMENTA (ANT) locus of Arabidopsis have a profound
20 ince it is well reported in Arabidopsis that AINTEGUMENTA (ANT) regulates cell proliferation and orga
21 ential downstream targets of SEUSS (SEU) and AINTEGUMENTA (ANT) regulation.
22 e have investigated the relationship between AINTEGUMENTA (ANT), a gene that promotes initiation and
23 ncode related AIL/PLT transcription factors: AINTEGUMENTA (ANT), AINTEGUMENTA-LIKE6 (AIL6)/PLETHORA3
24                                  Arabidopsis AINTEGUMENTA (ANT), an AP2 transcription factor, is know
25 code the transcriptional regulators IAA9 and AINTEGUMENTA (ANT), respectively, to control thermosensi
26 evelopment of this pattern, we have examined AINTEGUMENTA (ANT), UNUSUAL FLORAL ORGANS (UFO) and CLAV
27 ate is the AP2/ERF-type transcription factor AINTEGUMENTA (ANT), which has been proposed to act downs
28 omoters of CUP-SHAPED COTYLEDON 3 (CUC3) and AINTEGUMENTA (ANT).
29 tant combinations such as leunig apetala2 or aintegumenta apetala2.
30       In this study, we show that LEUNIG and AINTEGUMENTA are two critical regulators of marginal tis
31 ne homologues known in angiosperms: WUSCHEL, AINTEGUMENTA, BELL1, KANADI, UNICORN, and C3HDZip.
32  of INO, including INO, SUPERMAN, BELL1, and AINTEGUMENTA, did not detectably interact with POS9 in y
33        This effect is specific to the leunig aintegumenta double mutant and is not found in other dou
34 at the absence of marginal tissues in leunig aintegumenta double mutants is not mediated by ectopic A
35                     Double mutants of leunig aintegumenta fail to develop placentas, ovules, septa, s
36 the expression of the SHOOT MERISTEMLESS and AINTEGUMENTA genes.
37 rupted early in the development of the seuss aintegumenta gynoecia and we identify PHABULOSA (PHB), R
38 nt gene AINTEGUMENTA (ANT) and show that all AINTEGUMENTA-like (AIL) genes are transcribed in multipl
39  promote the expression of CAMBIUM-EXPRESSED AINTEGUMENTA-LIKE (CAIL) transcription factors to define
40 nscriptional regulators RINGLET 2 (RLT2) and AINTEGUMENTA-LIKE 5 (AIL5) as being essential for phas t
41 rganogenesis requires AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE 6 (AIL6)/PLETHORA 3 (PLT3), two member
42 formed the characterization of the grapevine AINTEGUMENTA-LIKE family, since it is well reported in A
43 transcriptome was constructed from which one AINTEGUMENTA-LIKE unigene, CrANT, was identified.
44  (SCR), SHORT ROOT (SHR), and members of the AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) and WUSCHEL-related
45 ORA 3 (PLT3), two members of the Arabidopsis AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) transcription facto
46                       Several members of the AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) transcription facto
47 t two transcription factors belonging to the AINTEGUMENTA-LIKE/PLETHORA family, AINTEGUMENTA (ANT) an
48  (LFY), which specifies floral fate, and two AINTEGUMENTA-LIKE/PLETHORA transcription factors, key re
49  a highly specific temporal induction of the AINTEGUMENTA LIKE1 (PtAIL1) transcription factor of the
50                       AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6 (AIL6) are two related transcription
51                       AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6 (AIL6) encode related transcription f
52 T transcription factors: AINTEGUMENTA (ANT), AINTEGUMENTA-LIKE6 (AIL6)/PLETHORA3 (PLT3) and AINTEGUME
53               Here, I show that the related, AINTEGUMENTA-LIKE6 (AIL6)/PLETHORA3 gene acts redundantl
54                        Ectopic expression of AINTEGUMENTA-LIKE6 at high levels alters floral organ in
55 ated transcription factors: AINTEGUMENTA and AINTEGUMENTA-LIKE6.
56 LIKE/PLETHORA family, AINTEGUMENTA (ANT) and AINTEGUMENTA-LIKE6/PLETHORA3 (AIL6/PLT3), act in paralle
57 NTEGUMENTA-LIKE6 (AIL6)/PLETHORA3 (PLT3) and AINTEGUMENTA-LIKE7 (AIL7)/PLETHORA7 (PLT7).
58 gistic genetic interaction between seuss and aintegumenta mutants resulting in a complete loss of ovu
59 o cell wall remodeling and regulation of the AINTEGUMENTA, PLETHORA, and BABY BOOM2 (APB2) and APB3 t
60  of the embryo, and they fail to express the AINTEGUMENTA transcript normally found in cotyledons.
61 he Arabidopsis regulatory genes APETALA2 and AINTEGUMENTA, which act primarily to regulate floral org