| scholarly article | Q13442814 |
| P50 | author | M.Alejandra Jaramillo | Q26713969 |
| P2093 | author name string | Elena M Kramer | |
| Billie Gould | |||
| Dimitriy Setnikov | |||
| Lynn Holappa | |||
| Philip M Santiago | |||
| P2860 | cites work | Molecular evolution of genes controlling petal and stamen development: duplication and divergence within the APETALA3 and PISTILLATA MADS-box gene lineages | Q24548012 |
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| Dimerization specificity of Arabidopsis MADS domain homeotic proteins APETALA1, APETALA3, PISTILLATA, and AGAMOUS | Q24601528 | ||
| 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 | ||
| Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana) | Q28185210 | ||
| Prediction of plant microRNA targets | Q28219387 | ||
| The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. orientalis (Agapanthaceae) flowers | Q28261866 | ||
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| Control of organ asymmetry in flowers of Antirrhinum | Q33334122 | ||
| The Arabidopsis floral homeotic gene PISTILLATA is regulated by discrete cis-elements responsive to induction and maintenance signals. | Q33334541 | ||
| GLOBOSA: a homeotic gene which interacts with DEFICIENS in the control of Antirrhinum floral organogenesis. | Q33338909 | ||
| Floral homeotic mutations produced by transposon-mutagenesis in Antirrhinum majus | Q33347940 | ||
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| The mechanics of cell fate determination in petals | Q34701677 | ||
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| The major clades of MADS-box genes and their role in the development and evolution of flowering plants. | Q35582655 | ||
| Applications and advantages of virus-induced gene silencing for gene function studies in plants. | Q35865214 | ||
| To B or Not to B a flower: the role of DEFICIENS and GLOBOSA orthologs in the evolution of the angiosperms. | Q36032674 | ||
| Genetic basis for innovations in floral organ identity | Q36120079 | ||
| Alteration of floral organ identity in rice through ectopic expression of OsMADS16. | Q38519793 | ||
| Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots | Q41745278 | ||
| Virus-induced gene silencing is an effective tool for assaying gene function in the basal eudicot species Papaver somniferum (opium poppy). | Q42485022 | ||
| Phylogeny and diversification of B-function MADS-box genes in angiosperms: evolutionary and functional implications of a 260-million-year-old duplication | Q42604019 | ||
| Petaloidy and petal identity MADS-box genes in the balsaminoid genera Impatiens and Marcgravia | Q42692173 | ||
| Evolution of class B floral homeotic proteins: obligate heterodimerization originated from homodimerization. | Q43694111 | ||
| Virus induced gene silencing of a DEFICIENS ortholog in Nicotiana benthamiana | Q43934856 | ||
| Arabidopsis homeotic gene APETALA3 ectopic expression: transcriptional and posttranscriptional regulation determine floral organ identity | Q44194928 | ||
| Chalcone synthase as a reporter in virus-induced gene silencing studies of flower senescence | Q45190606 | ||
| Technical Advance. Tobacco rattle virus as a vector for analysis of gene function by silencing | Q45224043 | ||
| Duplication of floral regulatory genes in the Lamiales | Q45325029 | ||
| Function and regulation of the Arabidopsis floral homeotic gene PISTILLATA. | Q45932115 | ||
| Role of SUPERMAN in maintaining Arabidopsis floral whorl boundaries. | Q45965383 | ||
| 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 | ||
| Recruitment of CRABS CLAW to promote nectary development within the eudicot clade | Q46670400 | ||
| Phylogeny and divergence of basal angiosperms inferred from APETALA3- and PISTILLATA-like MADS-box genes | Q47616623 | ||
| Two GLOBOSA-like genes are expressed in second and third whorls of homochlamydeous flowers in Asparagus officinalis L. | Q47870106 | ||
| Discrete spatial and temporal cis-acting elements regulate transcription of the Arabidopsis floral homeotic gene APETALA3. | Q48037547 | ||
| 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 | ||
| Four DEF-like MADS box genes displayed distinct floral morphogenetic roles in Phalaenopsis orchid | Q48178748 | ||
| Evolution of the APETALA3 and PISTILLATA lineages of MADS-box-containing genes in the basal angiosperms | Q48213704 | ||
| Expression of AODEF, a B-functional MADS-box gene, in stamens and inner tepals of the dioecious species Asparagus officinalis L. | Q48244340 | ||
| Expression of floral MADS-box genes in basal angiosperms: implications for the evolution of floral regulators. | Q52041244 | ||
| The Arabidopsis floral homeotic gene APETALA3 differentially regulates intercellular signaling required for petal and stamen development. | Q52144391 | ||
| Nuclear localization of the Arabidopsis APETALA3 and PISTILLATA homeotic gene products depends on their simultaneous expression. | Q52200603 | ||
| Methods for studying the evolution of plant reproductive structures: comparative gene expression techniques. | Q54665642 | ||
| Functional analysis of the Antirrhinum floral homeotic DEFICIENS gene in vivo and in vitro by using a temperature-sensitive mutant | Q71733915 | ||
| A MADS box gene from lily (Lilium Longiflorum) is sufficient to generate dominant negative mutation by interacting with PISTILLATA (PI) in Arabidopsis thaliana | Q74844983 | ||
| SUPERWOMAN1 and DROOPING LEAF genes control floral organ identity in rice | Q78728638 | ||
| APETALA3 and PISTILLATA homologs exhibit novel expression patterns in the unique perianth of Aristolochia (Aristolochiaceae) | Q80917931 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 750-766 | |
| P577 | publication date | 2007-03-30 | |
| P1433 | published in | The Plant Cell | Q3988745 |
| P1476 | title | Elaboration of B gene function to include the identity of novel floral organs in the lower eudicot Aquilegia | |
| P478 | volume | 19 |
| Q35033398 | "The usual suspects"- analysis of transcriptome sequences reveals deviating B gene activity in C. vulgaris bud bloomers |
| Q46544476 | 'Living stones' reveal alternative petal identity programs within the core eudicots |
| Q26829373 | Adaptation in flower form: a comparative evodevo approach |
| Q33356192 | An APETALA3 homolog controls both petal identity and floral meristem patterning in Nigella damascena L. (Ranunculaceae). |
| Q51977211 | Analyses of the floral organ morphogenesis and the differentially expressed genes of an apetalous flower mutant in Brassica napus. |
| Q28662199 | Analysis of the APETALA3- and PISTILLATA-like genes in Hedyosmum orientale (Chloranthaceae) provides insight into the evolution of the floral homeotic B-function in angiosperms |
| Q47361832 | Aquilegia B gene homologs promote petaloidy of the sepals and maintenance of the C domain boundary |
| Q33521802 | Aquilegia as a model system for the evolution and ecology of petals |
| Q37441507 | Chapter 4. New model systems for the study of developmental evolution in plants |
| Q36247661 | Characterization and Functional Analysis of Five MADS-Box B Class Genes Related to Floral Organ Identification in Tagetes erecta |
| Q33351865 | Characterization of Linaria KNOX genes suggests a role in petal-spur development |
| Q46110829 | Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid |
| Q34353241 | Cladodes, leaf-like organs in Asparagus, show the significance of co-option of pre-existing genetic regulatory circuit for morphological diversity of plants |
| Q46857802 | Co-modification of class B genes TfDEF and TfGLO in Torenia fournieri Lind. alters both flower morphology and inflorescence architecture |
| Q92786337 | Comparative transcriptomics of early petal development across four diverse species of Aquilegia reveal few genes consistently associated with nectar spur development |
| Q35047563 | Conserved roles for Polycomb Repressive Complex 2 in the regulation of lateral organ development in Aquilegia x coerulea 'Origami'. |
| Q33680692 | CsPI from the perianthless early-diverging Chloranthus spicatus show function on petal development in Arabidopsis thaliana |
| Q35182443 | DEF- and GLO-like proteins may have lost most of their interaction partners during angiosperm evolution |
| Q90224728 | Developmental and Molecular Changes Underlying the Vernalization-Induced Transition to Flowering in Aquilegia coerulea (James) |
| Q89756576 | Developmental and molecular characterization of novel staminodes in Aquilegia |
| Q34575163 | Developmental genetics of the perianthless flowers and bracts of a paleoherb species, Saururus chinensis |
| Q36729622 | Disruption of the petal identity gene APETALA3-3 is highly correlated with loss of petals within the buttercup family (Ranunculaceae). |
| Q34446966 | Distinct double flower varieties in Camellia japonica exhibit both expansion and contraction of C-class gene expression |
| Q42183321 | Distinct subfunctionalization and neofunctionalization of the B-class MADS-box genes in Physalis floridana |
| Q38927099 | Diversity, expansion, and evolutionary novelty of plant DNA-binding transcription factor families |
| Q59790351 | Dosage imbalance of B- and C-class genes causes petaloid-stamen relating to F hybrid variation |
| Q45365073 | Empowering plant evo-devo: virus induced gene silencing validates new and emerging model systems |
| Q33350644 | Environmental and molecular analysis of the floral transition in the lower eudicot Aquilegia formosa |
| Q28751989 | Environmental control of sepalness and petalness in perianth organs of waterlilies: a new Mosaic theory for the evolutionary origin of a differentiated perianth |
| Q41874877 | Establishment of zygomorphy on an ontogenic spiral and evolution of perianth in the tribe Delphinieae (Ranunculaceae). |
| Q64100554 | Evidence of a largely staminal origin for the (Solanaceae) floral corona |
| Q111629450 | Evolution and developmental genetics of floral display—A review of progress |
| Q26747070 | Evolution of Gene Duplication in Plants |
| Q36228952 | Evolution of floral diversity: genomics, genes and gamma |
| Q37483097 | Evolution of petal identity |
| Q51576245 | Evolution of petaloid sepals independent of shifts in B-class MADS box gene expression. |
| Q33362881 | Evolution of the APETALA2 Gene Lineage in Seed Plants |
| Q42292749 | Evolutionary Analysis of Snf1-Related Protein Kinase2 (SnRK2) and Calcium Sensor (SCS) Gene Lineages, and Dimerization of Rice Homologs, Suggest Deep Biochemical Conservation across Angiosperms |
| Q36904228 | Evolutionary Dynamics of Floral Homeotic Transcription Factor Protein-Protein Interactions |
| Q111629361 | Evolutionary divergence of the PISTILLATA-like proteins in Hedyosmum orientale (Chloranthaceae) after gene duplication |
| Q35981852 | Evolving Ideas on the Origin and Evolution of Flowers: New Perspectives in the Genomic Era. |
| Q30842859 | Exploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system |
| Q36070298 | Expression of B-class MADS-box genes in response to variations in photoperiod is associated with chasmogamous and cleistogamous flower development in Viola philippica |
| Q36050750 | Expression of floral MADS-box genes in Sinofranchetia chinensis (Lardizabalaceae): implications for the nature of the nectar leaves |
| Q33363267 | Flexibility in the structure of spiral flowers and its underlying mechanisms |
| Q36363487 | Flower Development and Perianth Identity Candidate Genes in the Basal Angiosperm Aristolochia fimbriata (Piperales: Aristolochiaceae) |
| Q33348748 | Functional analysis of B and C class floral organ genes in spinach demonstrates their role in sexual dimorphism |
| Q35663136 | Functional analysis reveals the possible role of the C-terminal sequences and PI motif in the function of lily (Lilium longiflorum) PISTILLATA (PI) orthologues |
| Q37346937 | Functional recapitulation of transitions in sexual systems by homeosis during the evolution of dioecy in Thalictrum. |
| Q42660080 | Gamma paleohexaploidy in the stem lineage of core eudicots: significance for MADS-box gene and species diversification |
| Q52599669 | Gene Duplication and Transference of Function in the paleoAP3 Lineage of Floral Organ Identity Genes. |
| Q34988981 | Gene duplication and evolutionary novelty in plants |
| Q111629516 | Genetic diversity and evolutionary history of four closely related Aquilegia species revealed by 10 nuclear gene fragments |
| Q38774896 | Genetics of flower development in Ranunculales - a new, basal eudicot model order for studying flower evolution |
| Q46040957 | Geometric morphometrics reveals shifts in flower shape symmetry and size following gene knockdown of CYCLOIDEA and ANTHOCYANIDIN SYNTHASE. |
| Q41090700 | High rates of virus-induced gene silencing by tobacco rattle virus in Populus |
| Q47562576 | Identification of the Sex-Biased Gene Expression and Putative Sex-Associated Genes in Eucommia ulmoides Oliver Using Comparative Transcriptome Analyses |
| Q35841526 | In situ hybridization for the precise localization of transcripts in plants |
| Q46059074 | Insights into the Prunus-Specific S-RNase-Based Self-Incompatibility System from a Genome-Wide Analysis of the Evolutionary Radiation of S Locus-Related F-box Genes |
| Q38121084 | Modification and co-option of leaf developmental programs for the acquisition of flat structures in monocots: unifacial leaves in Juncus and cladodes in Asparagus. |
| Q51061595 | Molecular basis for three-dimensional elaboration of the Aquilegia petal spur. |
| Q33347096 | Old dogs, new tricks: regulatory evolution in conserved genetic modules leads to novel morphologies in plants |
| Q60936070 | PISTILLATA paralogs in Tarenaya hassleriana have diverged in interaction specificity |
| Q47299329 | Petal-specific subfunctionalization of an APETALA3 paralog in the Ranunculales and its implications for petal evolution |
| Q47449109 | Pistillata--duplications as a mode for floral diversification in (Basal) asterids |
| Q33352916 | Poppy APETALA1/FRUITFULL orthologs control flowering time, branching, perianth identity, and fruit development |
| Q30354501 | Protein change in plant evolution: tracing one thread connecting molecular and phenotypic diversity |
| Q50197555 | Quantitative Trait Transcripts Mapping Coupled with Expression Quantitative Trait Loci Mapping Reveal the Molecular Network Regulating the Apetalous Characteristic in Brassica napus L. |
| Q37858278 | Robustness and evolvability in the B-system of flower development |
| Q52341747 | Significance of whole-genome duplications on the emergence of evolutionary novelties. |
| Q34573661 | Spatiotemporal reconstruction of the Aquilegia rapid radiation through next-generation sequencing of rapidly evolving cpDNA regions. |
| Q44824961 | Sub- and neo-functionalization of APETALA3 paralogs have contributed to the evolution of novel floral organ identity in Aquilegia (columbine, Ranunculaceae). |
| Q33354982 | The Aquilegia FRUITFULL-like genes play key roles in leaf morphogenesis and inflorescence development |
| Q35794349 | The C-Terminal Sequence and PI motif of the Orchid (Oncidium Gower Ramsey) PISTILLATA (PI) Ortholog Determine its Ability to Bind AP3 Orthologs and Enter the Nucleus to Regulate Downstream Genes Controlling Petal and Stamen Formation |
| Q46430980 | The Origin of Floral Organ Identity Quartets. |
| Q39360252 | The Tarenaya hassleriana genome provides insight into reproductive trait and genome evolution of crucifers. |
| Q43407902 | The corona of the daffodil Narcissus bulbocodium shares stamen-like identity and is distinct from the orthodox floral whorls. |
| Q42383708 | The developmental and genetic bases of apetaly in Bocconia frutescens (Chelidonieae: Papaveraceae). |
| Q46671280 | The role of ABC genes in shaping perianth phenotype in the basal angiosperm Magnolia. |
| Q42434856 | The seirena B class floral homeotic mutant of California Poppy (Eschscholzia californica) reveals a function of the enigmatic PI motif in the formation of specific multimeric MADS domain protein complexes |
| Q33362991 | Tinkering with transcription factor networks for developmental robustness of Ranunculales flowers |
| Q102053967 | Transcriptome profiling and weighted gene co-expression network analysis of early floral development in Aquilegia coerulea |
| Q60570171 | Virus-induced gene silencing (VIGS) in Lilium leichtlinii using the Cucumber mosaic virus vector |
| Q37993478 | Virus-induced gene silencing and its application in plant functional genomics |
| Q33656460 | Virus-induced gene silencing as a tool for comparative functional studies in Thalictrum |
| Q40223865 | Virus-induced gene silencing as a tool for functional analyses in the emerging model plant Aquilegia (columbine, Ranunculaceae). |
| Q45356165 | Virus-induced gene silencing for Asteraceae--a reverse genetics approach for functional genomics in Gerbera hybrida. |
| Q33547463 | Within and between whorls: comparative transcriptional profiling of Aquilegia and Arabidopsis |
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