Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum.
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Petunia Ap2-like genes and their role in flower and seed developmentMultiple AGAMOUS homologs from cucumber and petunia differ in their ability to induce reproductive organ fateThe transcription factor FLC confers a flowering response to vernalization by repressing meristem competence and systemic signaling in ArabidopsisPreservation of duplicate genes by complementary, degenerative mutationsSeparation of genetic functions controlling organ identity in flowersThe petunia MADS box gene FBP11 determines ovule identityNuclear import of the transcription factor SHOOT MERISTEMLESS depends on heterodimerization with BLH proteins expressed in discrete sub-domains of the shoot apical meristem of Arabidopsis thalianaRole of the FUL-SHP network in the evolution of fruit morphology and functionMolecular and genetic mechanisms of floral controlMolecular mechanisms underlying origin and diversification of the angiosperm flowerMolecular evolution of flower development: diversification of the plant MADS-box regulatory gene familyFlower development and evolution: new answers and new questionsGeneration of shape complexity through tissue conflict resolution.Transference of function shapes organ identity in the dove tree inflorescence.Conservation of Arabidopsis flowering genes in model legumes.A pectate lyase from Zinnia elegans is auxin inducible.Characterization of MdMADS2, a member of the SQUAMOSA subfamily of genes, in apple.The expression of D-cyclin genes defines distinct developmental zones in snapdragon apical meristems and is locally regulated by the Cycloidea gene.Expression patterns of genes encoding HD-ZipIV homeo domain proteins define specific domains in maize embryos and meristems.The MADS-box gene DEFH28 from Antirrhinum is involved in the regulation of floral meristem identity and fruit development.The cycloidea gene can respond to a common dorsoventral prepattern in Antirrhinum.Role of petunia pMADS3 in determination of floral organ and meristem identity, as revealed by its loss of function.The DORNROSCHEN/ENHANCER OF SHOOT REGENERATION1 gene of Arabidopsis acts in the control of meristem ccll fate and lateral organ development.Ectopic expression of an orchid (Oncidium Gower Ramsey) AGL6-like gene promotes flowering by activating flowering time genes in Arabidopsis thaliana.Patterns of gene duplication and functional evolution during the diversification of the AGAMOUS subfamily of MADS box genes in angiospermsFunctional diversification of the two C-class MADS box genes OSMADS3 and OSMADS58 in Oryza sativa.Conservation and divergence in the AGAMOUS subfamily of MADS-box genes: evidence of independent sub- and neofunctionalization events.delayed flowering1 Encodes a basic leucine zipper protein that mediates floral inductive signals at the shoot apex in maize.Involvement of the MADS-box gene ZMM4 in floral induction and inflorescence development in maize.Time to stop: flower meristem termination.Floral homeotic C function genes repress specific B function genes in the carpel whorl of the basal eudicot California poppy (Eschscholzia californica)Alternate transcripts of a floral developmental regulator have both distinct and redundant functions in opium poppy.Genetic interaction of OsMADS3, DROOPING LEAF, and OsMADS13 in specifying rice floral organ identities and meristem determinacy.Identification and characterization of flowering genes in kiwifruit: sequence conservation and role in kiwifruit flower development.Specific expression of LATERAL SUPPRESSOR is controlled by an evolutionarily conserved 3' enhancer.The invention of WUS-like stem cell-promoting functions in plants predates leptosporangiate ferns.Analysis of the Arabidopsis shoot meristem transcriptome during floral transition identifies distinct regulatory patterns and a leucine-rich repeat protein that promotes flowering.Rice APC/C(TE) controls tillering by mediating the degradation of MONOCULM 1Functional analyses of AGAMOUS family members in Nicotiana benthamiana clarify the evolution of early and late roles of C-function genes in eudicots.Loss of deeply conserved C-class floral homeotic gene function and C- and E-class protein interaction in a double-flowered ranunculid mutant
P2860
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P2860
Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@en
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@nl
type
label
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@en
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@nl
prefLabel
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@en
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@nl
P2093
P1433
P1476
Complementary floral homeotic ...... he plena locus of Antirrhinum.
@en
P2093
P356
10.1016/0092-8674(93)90052-R
P407
P577
1993-01-01T00:00:00Z