| P50 | author | Laryssa L Barnett | Q51576300 |
| | Jacob B. Landis | Q51576307 |
| | Lena Hileman | Q42824950 |
| P2860 | cites work | Virus induced gene silencing of a DEFICIENS ortholog in Nicotiana benthamiana | Q43934856 |
| | The K domain mediates heterodimerization of the Arabidopsis floral organ identity proteins, APETALA3 and PISTILLATA. | Q44565187 |
| | Convergence, constraint and the role of gene expression during adaptive radiation: floral anthocyanins in Aquilegia | Q44838412 |
| | Molecular evolution of PISTILLATA-like genes in the dogwood genus Cornus (Cornaceae). | Q44873130 |
| | Function and regulation of the Arabidopsis floral homeotic gene PISTILLATA. | Q45932115 |
| | The homeotic gene APETALA3 of Arabidopsis thaliana encodes a MADS box and is expressed in petals and stamens | Q46435786 |
| | Conservation of B-class floral homeotic gene function between maize and Arabidopsis | Q46493450 |
| | 'Living stones' reveal alternative petal identity programs within the core eudicots | Q46544476 |
| | Petal-specific subfunctionalization of an APETALA3 paralog in the Ranunculales and its implications for petal evolution | Q47299329 |
| | Two GLOBOSA-like genes are expressed in second and third whorls of homochlamydeous flowers in Asparagus officinalis L. | Q47870106 |
| | Molecular evolution of the petal and stamen identity genes, APETALA3 and PISTILLATA, after petal loss in the Piperales | Q48078747 |
| | Flower colour intensity depends on specialized cell shape controlled by a Myb-related transcription factor | Q48081666 |
| | Analysis of the Petunia TM6 MADS box gene reveals functional divergence within the DEF/AP3 lineage. | Q48086026 |
| | Functional analyses of two tomato APETALA3 genes demonstrate diversification in their roles in regulating floral development | Q48086027 |
| | Expression of AODEF, a B-functional MADS-box gene, in stamens and inner tepals of the dioecious species Asparagus officinalis L. | Q48244340 |
| | Conical epidermal cells allow bees to grip flowers and increase foraging efficiency. | Q51934560 |
| | Functional analyses of genetic pathways controlling petal specification in poppy. | Q51974227 |
| | Molecular and phylogenetic analyses of the MADS-box gene family in tomato. | Q52009229 |
| | Development of three different cell types is associated with the activity of a specific MYB transcription factor in the ventral petal of Antirrhinum majus flowers. | Q52062335 |
| | Functional analysis of the rice AP3 homologue OsMADS16 by RNA interference | Q52099116 |
| | Identification of class B and class C floral organ identity genes from rice plants. | Q52228677 |
| | Molecular evidence for naturalness of genera in the tribe Antirrhineae (Scrophulariaceae) and three independent evolutionary lineages from the New World and the Old | Q54561014 |
| | Genetic Control of Flower Development by Homeotic Genes in Antirrhinum majus. | Q55044428 |
| | GENEALOGICAL EVIDENCE OF HOMOPLOID HYBRID SPECIATION IN AN ADAPTIVE RADIATION OF SCAEVOLA (GOODENIACEAE) IN THE HAWAIIAN ISLANDS | Q56113858 |
| | A MADS box gene from lily (Lilium Longiflorum) is sufficient to generate dominant negative mutation by interacting with PISTILLATA (PI) in Arabidopsis thaliana | Q74844983 |
| | APETALA3 and PISTILLATA homologs exhibit novel expression patterns in the unique perianth of Aristolochia (Aristolochiaceae) | Q80917931 |
| | Deficiens, a homeotic gene involved in the control of flower morphogenesis in Antirrhinum majus: the protein shows homology to transcription factors | Q24556559 |
| | MUSCLE: multiple sequence alignment with high accuracy and high throughput | Q24613456 |
| | The duplicated B-class heterodimer model: whorl-specific effects and complex genetic interactions in Petunia hybrida flower development | Q24631669 |
| | Genes directing flower development in Arabidopsis | Q24677252 |
| | MrBayes 3: Bayesian phylogenetic inference under mixed models | Q26778438 |
| | MRBAYES: Bayesian inference of phylogenetic trees | Q27860538 |
| | Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana) | Q28185210 |
| | The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. orientalis (Agapanthaceae) flowers | Q28261866 |
| | Bird-pollinated flowers in an evolutionary and molecular context | Q28271924 |
| | The Arabidopsis homeotic genes APETALA3 and PISTILLATA are sufficient to provide the B class organ identity function | Q28273540 |
| | Are petals sterile stamens or bracts? The origin and evolution of petals in the core eudicots | Q28757180 |
| | The war of the whorls: genetic interactions controlling flower development | Q29616801 |
| | Phylogeny of the Caryophyllales Sensu Lato: Revisiting Hypotheses on Pollination Biology and Perianth Differentiation in the Core Caryophyllales | Q30051846 |
| | Ectopic expression of rice OsMADS1 reveals a role in specifying the lemma and palea, grass floral organs analogous to sepals | Q33335769 |
| | GLOBOSA: a homeotic gene which interacts with DEFICIENS in the control of Antirrhinum floral organogenesis. | Q33338909 |
| | Elaboration of B gene function to include the identity of novel floral organs in the lower eudicot Aquilegia | Q33343900 |
| | Conservation and divergence of APETALA1/FRUITFULL-like gene function in grasses: evidence from gene expression analyses | Q33344315 |
| | Floral homeotic mutations produced by transposon-mutagenesis in Antirrhinum majus | Q33347940 |
| | An ortholog of MIXTA-like2 controls epidermal cell shape in flowers of Thalictrum | Q33491222 |
| | 'Who's who' in two different flower types of Calluna vulgaris (Ericaceae): morphological and molecular analyses of flower organ identity. | Q33517997 |
| | More is better: the uses of developmental genetic data to reconstruct perianth evolution | Q33917723 |
| | Floral variation and floral genetics in basal angiosperms | Q33917729 |
| | One size fits all? Molecular evidence for a commonly inherited petal identity program in Ranunculales | Q34188587 |
| | Genealogical evidence of homoploid hybrid speciation in an adaptive radiation of Scaevola (goodeniaceae) in the Hawaiian Islands | Q34447680 |
| | Genetic interactions among floral homeotic genes of Arabidopsis | Q34549006 |
| | Double-stranded RNA interference of a rice PI/GLO paralog, OsMADS2, uncovers its second-whorl-specific function in floral organ patterning | Q34619225 |
| | Evolution of petal identity | Q37483097 |
| | The ABC model and the diversification of floral organ identity | Q37641465 |
| | Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots | Q41745278 |
| | Functional characterization of B class MADS-box transcription factors in Gerbera hybrida. | Q41853570 |
| | Petaloidy and petal identity MADS-box genes in the balsaminoid genera Impatiens and Marcgravia | Q42692173 |
| P433 | issue | 1 | |
| P304 | page(s) | 19-28 | |
| P577 | publication date | 2011-12-24 | |
| P1433 | published in | Development Genes and Evolution | Q2935926 |
| P1476 | title | Evolution of petaloid sepals independent of shifts in B-class MADS box gene expression. | |
| P478 | volume | 222 | |