| Q35033398 | "The usual suspects"- analysis of transcriptome sequences reveals deviating B gene activity in C. vulgaris bud bloomers |
| Q35602955 | A de novo floral transcriptome reveals clues into Phalaenopsis orchid flower development |
| Q35050665 | A modified ABCDE model of flowering in orchids based on gene expression profiling studies of the moth orchid Phalaenopsis aphrodite |
| Q111629373 | A review of orchid pollination studies in China |
| Q33352365 | Agave tequilana MADS genes show novel expression patterns in meristems, developing bulbils and floral organs |
| Q28743271 | An overview of the Phalaenopsis orchid genome through BAC end sequence analysis |
| 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 |
| Q28757180 | Are petals sterile stamens or bracts? The origin and evolution of petals in the core eudicots |
| Q47717247 | B and E MADS-box genes determine the perianth formation in Cymbidium goeringii Rchb.f |
| Q42789685 | B-function expression in the flower center underlies the homeotic phenotype of Lacandonia schismatica (Triuridaceae). |
| Q37441507 | Chapter 4. New model systems for the study of developmental evolution in plants |
| Q46110829 | Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid |
| Q48077590 | Cloning and characterization of a novel PI-like MADS-box gene in Phalaenopsis orchid |
| Q21261983 | Comparison of transcripts in Phalaenopsis bellina and Phalaenopsis equestris (Orchidaceae) flowers to deduce monoterpene biosynthesis pathway |
| Q47311343 | Conserved differential expression of paralogous DEFICIENS- and GLOBOSA-like MADS-box genes in the flowers of Orchidaceae: refining the 'orchid code'. |
| Q33904080 | De novo transcriptome assembly from inflorescence of Orchis italica: analysis of coding and non-coding transcripts |
| Q37370184 | De novo transcriptome sequencing and comparative analysis to discover genes related to floral development in Cymbidium faberi Rolfe |
| Q35845124 | Digital Gene Expression Analysis Based on De Novo Transcriptome Assembly Reveals New Genes Associated with Floral Organ Differentiation of the Orchid Plant Cymbidium ensifolium |
| Q91708172 | Dissecting the Function of MADS-Box Transcription Factors in Orchid Reproductive Development |
| Q33343900 | Elaboration of B gene function to include the identity of novel floral organs in the lower eudicot Aquilegia |
| Q28751989 | Environmental control of sepalness and petalness in perianth organs of waterlilies: a new Mosaic theory for the evolutionary origin of a differentiated perianth |
| Q98465838 | Evolution and development of three highly specialized floral structures of bee-pollinated Phalaenopsis species |
| Q111629334 | Evolution and function of MADS-box genes involved in orchid floral development |
| Q39568590 | Evolution of bract development and B-class MADS box gene expression in petaloid bracts of Cornus s. l. (Cornaceae). |
| Q42138960 | Evolutionary and morphometric implications of morphological variation among flowers within an inflorescence: a case-study using European orchids. |
| Q111629361 | Evolutionary divergence of the PISTILLATA-like proteins in Hedyosmum orientale (Chloranthaceae) after gene duplication |
| Q28657888 | Expression of paralogous SEP-, FUL-, AG- and STK-like MADS-box genes in wild-type and peloric Phalaenopsis flowers |
| Q96640631 | Expression regulation of MALATE SYNTHASE involved in glyoxylate cycle during protocorm development in Phalaenopsis aphrodite (Orchidaceae) |
| Q28740986 | Flower development |
| Q33357934 | Flower development of Phalaenopsis orchid involves functionally divergent SEPALLATA-like genes |
| 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 |
| Q53208719 | Functional characterization of duplicated B-class MADS-box genes in Japanese gentian. |
| Q28742016 | Gene discovery using next-generation pyrosequencing to develop ESTs for Phalaenopsis orchids |
| Q37238220 | Genome-wide identification and characterization of TCP genes involved in ovule development of Phalaenopsis equestris |
| Q34680277 | Histone acetylation accompanied with promoter sequences displaying differential expression profiles of B-class MADS-box genes for phalaenopsis floral morphogenesis |
| Q46101540 | Interactions of B-class complex proteins involved in tepal development in Phalaenopsis orchid |
| Q28757186 | Molecular mechanisms underlying origin and diversification of the angiosperm flower |
| Q60844069 | Mutant flower morphologies in the wind orchid, a novel orchid model species |
| Q89948200 | New insight into the molecular mechanism of colour differentiation among floral segments in orchids |
| Q59693706 | Orchid diversity: an evolutionary consequence of deception? |
| Q34546830 | OrchidBase 2.0: comprehensive collection of Orchidaceae floral transcriptomes |
| Q33796199 | OrchidBase: a collection of sequences of the transcriptome derived from orchids |
| Q38103559 | Organ homologies in orchid flowers re-interpreted using the Musk Orchid as a model. |
| Q35984610 | Parallel evolution of TCP and B-class genes in Commelinaceae flower bilateral symmetry |
| Q89820712 | PeERF1, a SHINE-Like Transcription Factor, Is Involved in Nanoridge Development on Lip Epidermis of Phalaenopsis Flowers |
| Q48138056 | PeMADS6, a GLOBOSA/PISTILLATA-like gene in Phalaenopsis equestris involved in petaloid formation, and correlated with flower longevity and ovary development |
| Q37189880 | Perspectives on MADS-box expression during orchid flower evolution and development. |
| Q28754440 | Positive selection and ancient duplications in the evolution of class B floral homeotic genes of orchids and grasses |
| Q37906051 | Research on orchid biology and biotechnology |
| Q37858278 | Robustness and evolvability in the B-system of flower development |
| Q51041183 | SQUA-like genes in the orchid Phalaenopsis are expressed in both vegetative and reproductive tissues. |
| Q52341747 | Significance of whole-genome duplications on the emergence of evolutionary novelties. |
| Q82489522 | Spatiotemporal expression of duplicate AGAMOUS orthologues during floral development in Phalaenopsis |
| Q48082622 | Strategies for functional validation of genes involved in reproductive stages of orchids |
| Q42690185 | The Apostasia genome and the evolution of orchids |
| 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 |
| Q28742065 | The MADS and the Beauty: Genes Involved in the Development of Orchid Flowers |
| Q44168572 | The OitaAG and OitaSTK genes of the orchid Orchis italica: a comparative analysis with other C- and D-class MADS-box genes |
| Q39360252 | The Tarenaya hassleriana genome provides insight into reproductive trait and genome evolution of crucifers. |
| Q51860934 | The duplicated B-class MADS-box genes display dualistic characters in orchid floral organ identity and growth. |
| Q36905369 | The genome and transcriptome of Phalaenopsis yield insights into floral organ development and flowering regulation |
| Q34449281 | The genome sequence of the orchid Phalaenopsis equestris |
| Q39081321 | Three R2R3-MYB transcription factors regulate distinct floral pigmentation patterning in Phalaenopsis spp. |
| Q94565301 | Transcriptome Analysis Reveals Clues into leaf-like flower mutant in Chinese orchid Cymbidium ensifolium |
| Q33360576 | Transcriptome-wide analysis of the MADS-box gene family in the orchid Erycina pusilla |
| Q31033552 | Transference of function shapes organ identity in the dove tree inflorescence |
| Q37288709 | Why are orchid flowers so diverse? Reduction of evolutionary constraints by paralogues of class B floral homeotic genes. |