Published in BMC Evol Biol on April 21, 2009
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bZIP transcription factors in the oomycete phytophthora infestans with novel DNA-binding domains are involved in defense against oxidative stress. Eukaryot Cell (2013) 0.81
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Agave tequilana MADS genes show novel expression patterns in meristems, developing bulbils and floral organs. Sex Plant Reprod (2011) 0.80
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The Y-segment of novel cold dehydrin genes is conserved and codons in the PR-10 genes are under positive selection in Oxytropis (Fabaceae) from contrasting climates. Mol Genet Genomics (2011) 0.76
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Exploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system. BMC Evol Biol (2017) 0.75
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Analysis of the petunia MADS-box transcription factor family. Mol Genet Genomics (2003) 1.38
An expanded plastid DNA phylogeny of Orchidaceae and analysis of jackknife branch support strategy. Am J Bot (2004) 1.38
Variation and selection at the CAULIFLOWER floral homeotic gene accompanying the evolution of domesticated Brassica oleracea. Genetics (2000) 1.37
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Divergence of the Dof gene families in poplar, Arabidopsis, and rice suggests multiple modes of gene evolution after duplication. Plant Physiol (2006) 1.32
Four DEF-like MADS box genes displayed distinct floral morphogenetic roles in Phalaenopsis orchid. Plant Cell Physiol (2004) 1.31
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MADS about the evolution of orchid flowers. Trends Plant Sci (2008) 1.24
Role of positive selection in the retention of duplicate genes in mammalian genomes. Proc Natl Acad Sci U S A (2006) 1.24
Evolution of class B floral homeotic proteins: obligate heterodimerization originated from homodimerization. Mol Biol Evol (2002) 1.24
Floral organ identity genes in the orchid Dendrobium crumenatum. Plant J (2006) 1.20
To B or Not to B a flower: the role of DEFICIENS and GLOBOSA orthologs in the evolution of the angiosperms. J Hered (2005) 1.20
Why are orchid flowers so diverse? Reduction of evolutionary constraints by paralogues of class B floral homeotic genes. Ann Bot (2009) 1.18
Molecular evolution of the teosinte branched gene among maize and related grasses. Mol Biol Evol (2001) 1.15
In vivo imaging of MADS-box transcription factor interactions. J Exp Bot (2005) 1.14
Accelerated regulatory gene evolution in an adaptive radiation. Proc Natl Acad Sci U S A (2001) 1.13
A simplified explanation for the frameshift mutation that created a novel C-terminal motif in the APETALA3 gene lineage. BMC Evol Biol (2006) 1.13
Evolution of reproductive structures in grasses (Poaceae) inferred by sister-group comparison with their putative closest living relatives, Ecdeiocoleaceae. Am J Bot (2005) 1.11
Comparative study of SBP-box gene family in Arabidopsis and rice. Gene (2007) 1.09
MADS-box gene evolution-structure and transcription patterns. Mol Phylogenet Evol (2002) 1.08
Heterogeneous selection on LEGCYC paralogs in relation to flower morphology and the phylogeny of Lupinus (Leguminosae). Mol Biol Evol (2003) 1.08
PeMADS6, a GLOBOSA/PISTILLATA-like gene in Phalaenopsis equestris involved in petaloid formation, and correlated with flower longevity and ovary development. Plant Cell Physiol (2005) 1.08
Conservation of B class gene expression in the second whorl of a basal grass and outgroups links the origin of lodicules and petals. Proc Natl Acad Sci U S A (2007) 1.06
Functional diversification of B MADS-box homeotic regulators of flower development: Adaptive evolution in protein-protein interaction domains after major gene duplication events. Mol Biol Evol (2006) 1.04
An orchid (Oncidium Gower Ramsey) AP3-like MADS gene regulates floral formation and initiation. Plant Cell Physiol (2002) 1.04
On the origin of class B floral homeotic genes: functional substitution and dominant inhibition in Arabidopsis by expression of an orthologue from the gymnosperm Gnetum. Plant J (2002) 0.99
Function and diversification of MADS-box genes in rice. ScientificWorldJournal (2006) 0.99
Conserved C-terminal motifs of the Arabidopsis proteins APETALA3 and PISTILLATA are dispensable for floral organ identity function. Plant Physiol (2007) 0.97
Directed mutagenesis confirms the functional importance of positively selected sites in polygalacturonase inhibitor protein. Mol Biol Evol (2005) 0.96
Molecular population genetics of redundant floral-regulatory genes in Arabidopsis thaliana. Mol Biol Evol (2004) 0.96
Positive selection for single amino acid change promotes substrate discrimination of a plant volatile-producing enzyme. Mol Biol Evol (2007) 0.93
Tracking the connection between evolutionary and functional shifts using the fungal lipase/feruloyl esterase A family. BMC Evol Biol (2006) 0.92
The MIK region rather than the C-terminal domain of AP3-like class B floral homeotic proteins determines functional specificity in the development and evolution of petals. New Phytol (2008) 0.92
The C-terminal sequence of LMADS1 is essential for the formation of homodimers for B function proteins. J Biol Chem (2003) 0.91
Excess non-synonymous substitutions suggest that positive selection episodes occurred during the evolution of DNA-binding domains in the Arabidopsis R2R3-MYB gene family. Plant Mol Biol (2003) 0.91
Selection on coding regions determined Hox7 genes evolution. Mol Biol Evol (2003) 0.91
Adaptive evolution of Hox-gene homeodomains after cluster duplications. BMC Evol Biol (2006) 0.90
The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. orientalis (Agapanthaceae) flowers. Plant Mol Biol (2005) 0.90
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An antirrhinum ternary complex factor specifically interacts with C-function and SEPALLATA-like MADS-box factors. Plant Mol Biol (2003) 0.85
Molecular evolution of the OrcPI locus in natural populations of Mediterranean orchids. Gene (2007) 0.79
Chromosome triplication found across the tribe Brassiceae. Genome Res (2005) 3.92
The major clades of MADS-box genes and their role in the development and evolution of flowering plants. Mol Phylogenet Evol (2003) 3.47
The Selaginella genome identifies genetic changes associated with the evolution of vascular plants. Science (2011) 3.10
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Cabbage family affairs: the evolutionary history of Brassicaceae. Trends Plant Sci (2010) 1.89
Genetic consequences of Pleistocene range shifts: contrast between the Arctic, the Alps and the East African mountains. Mol Ecol (2007) 1.76
Toward a global phylogeny of the Brassicaceae. Mol Biol Evol (2006) 1.67
Worldwide phylogeny and biogeography of Cardamine flexuosa (Brassicaceae) and its relatives. Am J Bot (2006) 1.64
Poorly known relatives of Arabidopsis thaliana. Trends Plant Sci (2006) 1.62
Conservation and divergence in the AGAMOUS subfamily of MADS-box genes: evidence of independent sub- and neofunctionalization events. Evol Dev (2006) 1.57
Structural diversification and neo-functionalization during floral MADS-box gene evolution by C-terminal frameshift mutations. Nucleic Acids Res (2003) 1.54
Molecular phylogenetics, temporal diversification, and principles of evolution in the mustard family (Brassicaceae). Mol Biol Evol (2010) 1.47
Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana). Plant Mol Biol (2003) 1.36
And then there were many: MADS goes genomic. Trends Plant Sci (2003) 1.35
The dynamic ups and downs of genome size evolution in Brassicaceae. Mol Biol Evol (2008) 1.34
Two ancient classes of MIKC-type MADS-box genes are present in the moss Physcomitrella patens. Mol Biol Evol (2002) 1.29
Missing links: the genetic architecture of flowers [correction of flower] and floral diversification. Trends Plant Sci (2002) 1.29
MADS about the evolution of orchid flowers. Trends Plant Sci (2008) 1.24
Evolution of class B floral homeotic proteins: obligate heterodimerization originated from homodimerization. Mol Biol Evol (2002) 1.24
Phylogeography of a living fossil: pleistocene glaciations forced Ginkgo biloba L. (Ginkgoaceae) into two refuge areas in China with limited subsequent postglacial expansion. Mol Phylogenet Evol (2008) 1.23
The class E floral homeotic protein SEPALLATA3 is sufficient to loop DNA in 'floral quartet'-like complexes in vitro. Nucleic Acids Res (2008) 1.23
Sexual reproduction, hybridization, apomixis, and polyploidization in the genus Boechera (Brassicaceae). Am J Bot (2005) 1.20
Why are orchid flowers so diverse? Reduction of evolutionary constraints by paralogues of class B floral homeotic genes. Ann Bot (2009) 1.18
Genomewide structural annotation and evolutionary analysis of the type I MADS-box genes in plants. J Mol Evol (2003) 1.18
Reconstitution of 'floral quartets' in vitro involving class B and class E floral homeotic proteins. Nucleic Acids Res (2009) 1.17
Functional conservation and diversification of class E floral homeotic genes in rice (Oryza sativa). Plant J (2009) 1.15
Characterization of MADS-box genes in charophycean green algae and its implication for the evolution of MADS-box genes. Proc Natl Acad Sci U S A (2005) 1.13
The evolutionary history of the Arabidopsis lyrata complex: a hybrid in the amphi-Beringian area closes a large distribution gap and builds up a genetic barrier. BMC Evol Biol (2010) 1.12
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Phylogeographic structure of the chloroplast DNA gene pool in North American Boechera--a genus and continental-wide perspective. Mol Phylogenet Evol (2009) 1.06
Interspecific and interploidal gene flow in Central European Arabidopsis (Brassicaceae). BMC Evol Biol (2011) 1.05
Conserved differential expression of paralogous DEFICIENS- and GLOBOSA-like MADS-box genes in the flowers of Orchidaceae: refining the 'orchid code'. Plant J (2011) 1.02
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Petaloidy and petal identity MADS-box genes in the balsaminoid genera Impatiens and Marcgravia. Plant J (2006) 1.00
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Lepidium as a model system for studying the evolution of fruit development in Brassicaceae. J Exp Bot (2008) 0.95
Evolutionary game theory: cells as players. Mol Biosyst (2014) 0.93
A world-wide perspective on crucifer speciation and evolution: phylogenetics, biogeography and trait evolution in tribe Arabideae. Ann Bot (2013) 0.92
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The MIK region rather than the C-terminal domain of AP3-like class B floral homeotic proteins determines functional specificity in the development and evolution of petals. New Phytol (2008) 0.92
GORDITA (AGL63) is a young paralog of the Arabidopsis thaliana B(sister) MADS box gene ABS (TT16) that has undergone neofunctionalization. Plant J (2010) 0.91
Molecular phylogeny and systematics of the genus Draba (Brassicaceae) and identification of its most closely related genera. Mol Phylogenet Evol (2010) 0.91
The evolutionary history of the Arabidopsis arenosa complex: diverse tetraploids mask the Western Carpathian center of species and genetic diversity. PLoS One (2012) 0.91
Systematics and evolution of Arctic-Alpine Arabis alpina (Brassicaceae) and its closest relatives in the eastern Mediterranean. Am J Bot (2012) 0.90
A continental-wide perspective: the genepool of nuclear encoded ribosomal DNA and single-copy gene sequences in North American Boechera (Brassicaceae). PLoS One (2012) 0.90
The naked and the dead: the ABCs of gymnosperm reproduction and the origin of the angiosperm flower. Semin Cell Dev Biol (2009) 0.90
Ancestry and diversity of BEL1-like homeobox genes revealed by gymnosperm ( Gnetum gnemon) homologs. Dev Genes Evol (2002) 0.88
Molecular phylogeny of the genus Vitis (Vitaceae) based on plastid markers. Am J Bot (2010) 0.88
Developmental robustness by obligate interaction of class B floral homeotic genes and proteins. PLoS Comput Biol (2009) 0.87
Cooperation and cheating in microbial exoenzyme production--theoretical analysis for biotechnological applications. Biotechnol J (2010) 0.87
Molecular interactions of orthologues of floral homeotic proteins from the gymnosperm Gnetum gnemon provide a clue to the evolutionary origin of 'floral quartets'. Plant J (2010) 0.86
Biogeographic variation in genetic variability, apomixis expression and ploidy of St. John's wort (Hypericum perforatum) across its native and introduced range. Ann Bot (2013) 0.86
Catching a 'hopeful monster': shepherd's purse (Capsella bursa-pastoris) as a model system to study the evolution of flower development. J Exp Bot (2006) 0.85
The importance of Anatolian mountains as the cradle of global diversity in Arabis alpina, a key arctic-alpine species. Ann Bot (2011) 0.84
Characterization of candidate class A, B and E floral homeotic genes from the perianthless basal angiosperm Chloranthus spicatus (Chloranthaceae). Dev Genes Evol (2005) 0.82
Understanding the formation of Mediterranean-African-Asian disjunctions: evidence for Miocene climate-driven vicariance and recent long-distance dispersal in the Tertiary relict Smilax aspera (Smilacaceae). New Phytol (2014) 0.82
A double-flowered variety of lesser periwinkle (Vinca minor fl. pl.) that has persisted in the wild for more than 160 years. Ann Bot (2011) 0.81
Distinct MADS-box gene expression patterns in the reproductive cones of the gymnosperm Gnetum gnemon. Dev Genes Evol (2003) 0.80
Evolutionary game theory: molecules as players. Mol Biosyst (2014) 0.79
A simple method for predicting the functional differentiation of duplicate genes and its application to MIKC-type MADS-box genes. Nucleic Acids Res (2005) 0.79
SplamiR--prediction of spliced miRNAs in plants. Bioinformatics (2011) 0.78
MADS and more: transcription factors that shape the plant. Methods Mol Biol (2011) 0.78
To be or not to be the odd one out--allele-specific transcription in pentaploid dogroses (Rosa L. sect. Caninae (DC.) Ser). BMC Plant Biol (2011) 0.78
Hotspots of diversity in a clonal world--the Mediterranean moss Pleurochaete squarrosa in Central Europe. Mol Ecol (2008) 0.77
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