Why are orchid flowers so diverse? Reduction of evolutionary constraints by paralogues of class B floral homeotic genes.
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Evolution of Gene Duplication in PlantsExpression of paralogous SEP-, FUL-, AG- and STK-like MADS-box genes in wild-type and peloric Phalaenopsis flowersAnalysis of the APETALA3- and PISTILLATA-like genes in Hedyosmum orientale (Chloranthaceae) provides insight into the evolution of the floral homeotic B-function in angiospermsPhylogenetics of tribe Orchideae (Orchidaceae: Orchidoideae) based on combined DNA matrices: inferences regarding timing of diversification and evolution of pollination syndromesEvolution and biogeography of the slipper orchids: Eocene vicariance of the conduplicate genera in the Old and New World TropicsThe MADS and the Beauty: Genes Involved in the Development of Orchid FlowersPositive selection and ancient duplications in the evolution of class B floral homeotic genes of orchids and grassesTranscriptome and proteome data reveal candidate genes for pollinator attraction in sexually deceptive orchidsExploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system.Transcriptome-wide analysis of the MADS-box gene family in the orchid Erycina pusilla.Molecular basis of floral petaloidy: insights from androecia of Canna indica.The analysis of the inflorescence miRNome of the orchid Orchis italica reveals a DEF-like MADS-box gene as a new miRNA targetIntegrated mRNA and microRNA transcriptome variations in the multi-tepal mutant provide insights into the floral patterning of the orchid Cymbidium goeringiiDe novo transcriptome assembly from inflorescence of Orchis italica: analysis of coding and non-coding transcripts.Eugenol synthase genes in floral scent variation in Gymnadenia species.Histone acetylation accompanied with promoter sequences displaying differential expression profiles of B-class MADS-box genes for phalaenopsis floral morphogenesisMolecular phylogenetics and morphological reappraisal of the Platanthera clade (Orchidaceae: Orchidinae) prompts expansion of the generic limits of Galearis and PlatantheraDeep sequencing-based analysis of the Cymbidium ensifolium floral transcriptome.Functional analysis reveals the possible role of the C-terminal sequences and PI motif in the function of lily (Lilium longiflorum) PISTILLATA (PI) orthologues.Development and evolution of extreme synorganization in angiosperm flowers and diversity: a comparison of Apocynaceae and Orchidaceae.Perspectives on MADS-box expression during orchid flower evolution and development.Orchid biology: from Linnaeus via Darwin to the 21st century. PrefaceDe novo transcriptome sequencing and comparative analysis to discover genes related to floral development in Cymbidium faberi RolfeEvolution and Expression Patterns of TCP Genes in Asparagales.Orchid pollination by sexual deception: pollinator perspectives.Organ homologies in orchid flowers re-interpreted using the Musk Orchid as a model.Role of transcriptional regulation in the evolution of plant phenotype: A dynamic systems approach.Genomic diversity guides conservation strategies among rare terrestrial orchid species when taxonomy remains uncertain.Evaluation of internal control for gene expression in Phalaenopsis by quantitative real-time PCR.The Tarenaya hassleriana genome provides insight into reproductive trait and genome evolution of crucifers.Evolution of bract development and B-class MADS box gene expression in petaloid bracts of Cornus s. l. (Cornaceae).Recent advances in understanding the roles of whole genome duplications in evolution.The Apostasia genome and the evolution of orchids.B-function expression in the flower center underlies the homeotic phenotype of Lacandonia schismatica (Triuridaceae).Change of Fate and Staminodial Laminarity as Potential Agents of Floral Diversification in the Zingiberales.Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid.Approaches to Macroevolution: 1. General Concepts and Origin of Variation.Conserved differential expression of paralogous DEFICIENS- and GLOBOSA-like MADS-box genes in the flowers of Orchidaceae: refining the 'orchid code'.Aquilegia B gene homologs promote petaloidy of the sepals and maintenance of the C domain boundary.B and E MADS-box genes determine the perianth formation in Cymbidium goeringii Rchb.f.
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Why are orchid flowers so diverse? Reduction of evolutionary constraints by paralogues of class B floral homeotic genes.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 13 January 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Why are orchid flowers so dive ...... class B floral homeotic genes.
@en
Why are orchid flowers so dive ...... class B floral homeotic genes.
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type
label
Why are orchid flowers so dive ...... class B floral homeotic genes.
@en
Why are orchid flowers so dive ...... class B floral homeotic genes.
@nl
prefLabel
Why are orchid flowers so dive ...... class B floral homeotic genes.
@en
Why are orchid flowers so dive ...... class B floral homeotic genes.
@nl
P2860
P356
P1433
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Why are orchid flowers so dive ...... class B floral homeotic genes
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P2093
Günter Theissen
P2860
P304
P356
10.1093/AOB/MCN258
P407
P577
2009-01-13T00:00:00Z