| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Yves Van de Peer | Q28468994 |
| Steven Maere | Q40464536 | ||
| P2093 | author name string | Kevin Vanneste | |
| P2860 | cites work | Reconstruction of ancestral metabolic enzymes reveals molecular mechanisms underlying evolutionary innovation through gene duplication | Q21145729 |
| Relaxed phylogenetics and dating with confidence | Q21146068 | ||
| Nothing in Biology Makes Sense except in the Light of Evolution | Q22064567 | ||
| Polyploid Incidence and Evolution | Q22065392 | ||
| PATHWAYS, MECHANISMS, AND RATES OF POLYPLOID FORMATION IN FLOWERING PLANTS | Q22065403 | ||
| Ploidy influences rarity and invasiveness in plants | Q22065697 | ||
| ‘Why polyploidy is rarer in animals than in plants’: myths and mechanisms | Q22065707 | ||
| The Impact of Fossils and Taxon Sampling on Ancient Molecular Dating Analyses | Q22066011 | ||
| The role of extinction in evolution | Q22066197 | ||
| Independent sorting-out of thousands of duplicated gene pairs in two yeast species descended from a whole-genome duplication | Q22066319 | ||
| The advantages and disadvantages of being polyploid | Q22122019 | ||
| The tomato genome sequence provides insights into fleshy fruit evolution | Q22122151 | ||
| The Medicago genome provides insight into the evolution of rhizobial symbioses | Q22122164 | ||
| The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla | Q22122214 | ||
| Cycles in fossil diversity | Q22122474 | ||
| Bayesian phylogenetics with BEAUti and the BEAST 1.7 | Q24286945 | ||
| Preservation of duplicate genes by complementary, degenerative mutations | Q24548042 | ||
| Widespread genome duplications throughout the history of flowering plants | Q24548315 | ||
| Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms | Q24564444 | ||
| Efficient storage of high throughput DNA sequencing data using reference-based compression | Q24607081 | ||
| Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids | Q24679271 | ||
| Genomic and epigenetic insights into the molecular bases of heterosis | Q26809972 | ||
| Fractionation mutagenesis and similar consequences of mechanisms removing dispensable or less-expressed DNA in plants | Q26809985 | ||
| A unifying theory for general multigenic heterosis: energy efficiency, protein metabolism, and implications for molecular breeding | Q26809996 | ||
| Sexual polyploidization in plants--cytological mechanisms and molecular regulation | Q26827323 | ||
| State-of the art methodologies dictate new standards for phylogenetic analysis | Q27023650 | ||
| The evolutionary fate and consequences of duplicate genes | Q27861065 | ||
| The spandrels of San Marco and the Panglossian paradigm: a critique of the adaptationist programme | Q28237797 | ||
| Time scales of critical events around the Cretaceous-Paleogene boundary | Q28285178 | ||
| Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the Cretaceous-Paleogene boundary | Q28654997 | ||
| A well-constrained estimate for the timing of the salmonid whole genome duplication reveals major decoupling from species diversification | Q28659717 | ||
| A unified model of autopolyploid establishment and evolution | Q28680711 | ||
| Aberrant Classopollis pollen reveals evidence for unreduced (2n) pollen in the conifer family Cheirolepidiaceae during the Triassic-Jurassic transition | Q28681350 | ||
| Polyploidy and its effect on evolutionary success: old questions revisited with new tools | Q28709534 | ||
| Increased phenotypic plasticity to climate may have boosted the invasion success of polyploid Centaurea stoebe | Q28710579 | ||
| A genome triplication associated with early diversification of the core eudicots | Q28730462 | ||
| Genome-wide analysis of syntenic gene deletion in the grasses | Q28730772 | ||
| The more the better? The role of polyploidy in facilitating plant invasions | Q28741287 | ||
| Polyploidy did not predate the evolution of nodulation in all legumes | Q28750317 | ||
| Calibrating the Tree of Life: fossils, molecules and evolutionary timescales | Q28751368 | ||
| The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution | Q28752488 | ||
| An uncorrelated relaxed-clock analysis suggests an earlier origin for flowering plants | Q28752634 | ||
| Plants with double genomes might have had a better chance to survive the Cretaceous-Tertiary extinction event | Q28754782 | ||
| Mutations in AtPS1 (Arabidopsis thaliana parallel spindle 1) lead to the production of diploid pollen grains | Q28756577 | ||
| Increased glycolytic flux as an outcome of whole-genome duplication in yeast | Q28757241 | ||
| Evolution of pigment synthesis pathways by gene and genome duplication in fish | Q28757593 | ||
| Environmental mutagenesis during the end-Permian ecological crisis | Q28770128 | ||
| Biosystematics and Evolutionary Noise | Q28953117 | ||
| Minority Cytotype Exclusion in Local Plant Populations | Q28954054 | ||
| Host sanctions and the legume–rhizobium mutualism | Q29012560 | ||
| Evolutionary consequences of autopolyploidy | Q29394621 | ||
| Estimating absolute rates of molecular evolution and divergence times: a penalized likelihood approach | Q29547754 | ||
| Bayesian estimation of species divergence times under a molecular clock using multiple fossil calibrations with soft bounds | Q29547833 | ||
| Accounting for calibration uncertainty in phylogenetic estimation of evolutionary divergence times | Q29547849 | ||
| Reading the entrails of chickens: molecular timescales of evolution and the illusion of precision | Q29616173 | ||
| Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics | Q29616221 | ||
| The evolutionary significance of ancient genome duplications | Q29617105 | ||
| Ancestral polyploidy in seed plants and angiosperms | Q29617362 | ||
| Polyploidy and angiosperm diversification | Q29617868 | ||
| The probability of duplicate gene preservation by subfunctionalization | Q29618530 | ||
| Major ecological transitions in wild sunflowers facilitated by hybridization | Q30004700 | ||
| Old gene duplication facilitates origin and diversification of an innovative communication system--twice | Q30497745 | ||
| Estimating divergence dates and evaluating dating methods using phylogenomic and mitochondrial data in squamate reptiles | Q30566044 | ||
| Ecological differentiation and diploid superiority across a moving ploidy contact zone. | Q51186954 | ||
| Polyploidization mechanisms: temperature environment can induce diploid gamete formation in Rosa sp. | Q51886732 | ||
| Polyploidy-associated genomic instability in Arabidopsis thaliana. | Q53343041 | ||
| Ploidy frequencies in plants with ploidy heterogeneity: fitting a general gametic model to empirical population data. | Q54969562 | ||
| K-Pg extinction: Reevaluation of the heat-fire hypothesis | Q55872493 | ||
| Ecology of seed dispersal | Q55921319 | ||
| The global invasion success of Central European plants is related to distribution characteristics in their native range and species traits | Q56770533 | ||
| Polyploidy in arctic plants | Q57061530 | ||
| Phylogeny of Nymphaea (Nymphaeaceae): Evidence from Substitutions and Microstructural Changes in the Chloroplast trnT‐trnF Region | Q57095322 | ||
| Reciprocal gene loss between Tetraodon and zebrafish after whole genome duplication in their ancestor | Q57252794 | ||
| Kernel density estimation via diffusion | Q57308724 | ||
| Significance and Biological Consequences of Polyploidization in Land Plant Evolution | Q58198682 | ||
| Rewiring of the Yeast Transcriptional Network Through the Evolution of Motif Usage | Q58485110 | ||
| SOS and Mayday: multiple inducible mutagenic pathways in Escherichia coli | Q78167610 | ||
| Transcriptome shock after interspecific hybridization in senecio is ameliorated by genome duplication | Q80141703 | ||
| The evolutionary dynamics of polyploid plants: origins, establishment and persistence | Q83208053 | ||
| Gene-balanced duplications, like tetraploidy, provide predictable drive to increase morphological complexity | Q36526608 | ||
| Evolution of duplicate gene expression in polyploid and hybrid plants | Q36701858 | ||
| Surviving the K-T mass extinction: new perspectives of polyploidization in angiosperms | Q37153819 | ||
| An examination of phylogenetic models of substitution rate variation among lineages | Q37186295 | ||
| The flowering world: a tale of duplications | Q37612237 | ||
| Redundancy and rewiring of genetic networks following genome-wide duplication events | Q37981369 | ||
| Rarely successful polyploids and their legacy in plant genomes | Q38000342 | ||
| Comparative genomics suggests that an ancestral polyploidy event leads to enhanced root nodule symbiosis in the Papilionoideae. | Q38486098 | ||
| Polyploids exhibit higher potassium uptake and salinity tolerance in Arabidopsis | Q39527908 | ||
| Contrasting patterns of evolution following whole genome versus tandem duplication events in Populus | Q39996455 | ||
| Gamma paleohexaploidy in the stem lineage of core eudicots: significance for MADS-box gene and species diversification | Q42660080 | ||
| The type II Arabidopsis formin14 interacts with microtubules and microfilaments to regulate cell division | Q42937231 | ||
| All duplicates are not equal: the difference between small-scale and genome duplication | Q43049884 | ||
| Dosage and parent-of-origin effects shaping aneuploid swarms in A. thaliana | Q44482846 | ||
| Proceedings of the SMBE Tri-National Young Investigators' Workshop 2005. What is the role of genome duplication in the evolution of complexity and diversity? | Q45382084 | ||
| Mitotic instability in resynthesized and natural polyploids of the genus Arabidopsis (Brassicaceae). | Q45772076 | ||
| Two-phase resolution of polyploidy in the Arabidopsis metabolic network gives rise to relative and absolute dosage constraints | Q47301236 | ||
| Land plant evolutionary timeline: gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates | Q47781411 | ||
| An ERF transcription factor in Medicago truncatula that is essential for Nod factor signal transduction | Q48080023 | ||
| The Arabidopsis mutant jason produces unreduced first division restitution male gametes through a parallel/fused spindle mechanism in meiosis II. | Q49074626 | ||
| Production of diploid male gametes in Arabidopsis by cold-induced destabilization of postmeiotic radial microtubule arrays | Q49149793 | ||
| Genomic changes in synthetic Arabidopsis polyploids | Q30979821 | ||
| Subfunction partitioning, the teleost radiation and the annotation of the human genome. | Q33206755 | ||
| Genome evolution and biodiversity in teleost fish | Q33211247 | ||
| Evidence of interaction network evolution by whole-genome duplications: a case study in MADS-box proteins | Q33266895 | ||
| Evolutionary persistence of functional compensation by duplicate genes in Arabidopsis | Q33633613 | ||
| Genetic variation: molecular mechanisms and impact on microbial evolution | Q33820587 | ||
| Altered gene expression and ecological divergence in sibling allopolyploids of Dactylorhiza (Orchidaceae) | Q33882312 | ||
| Production of viable male unreduced gametes in Brassica interspecific hybrids is genotype specific and stimulated by cold temperatures. | Q33929728 | ||
| Modeling gene and genome duplications in eukaryotes | Q33936694 | ||
| Evolution-driving genes | Q33949870 | ||
| Recently formed polyploid plants diversify at lower rates | Q33996502 | ||
| Testing the impact of calibration on molecular divergence times using a fossil-rich group: the case of Nothofagus (Fagales). | Q34112527 | ||
| The impact of the representation of fossil calibrations on Bayesian estimation of species divergence times | Q34119190 | ||
| LysM-type mycorrhizal receptor recruited for rhizobium symbiosis in nonlegume Parasponia | Q34157448 | ||
| Understanding mechanisms of novel gene expression in polyploids | Q34180932 | ||
| Ancient whole genome duplications, novelty and diversification: the WGD Radiation Lag-Time Model | Q34223112 | ||
| Polyploid organisms | Q34273385 | ||
| Nonrandom Survival of Gene Conversions among Yeast Ribosomal Proteins Duplicated through Genome Doubling | Q34334466 | ||
| Duplication and divergence: the evolution of new genes and old ideas | Q34371877 | ||
| Genome duplication, extinction and vertebrate evolution | Q34526190 | ||
| Genomewide nonadditive gene regulation in Arabidopsis allotetraploids | Q34587400 | ||
| Coordinating nodule morphogenesis with rhizobial infection in legumes. | Q34774796 | ||
| The impact of environmental stress on male reproductive development in plants: biological processes and molecular mechanisms | Q34795263 | ||
| Distinguishing among evolutionary models for the maintenance of gene duplicates | Q34992045 | ||
| Precision of molecular time estimates | Q35756628 | ||
| Comparative genomics of rhizobia nodulating soybean suggests extensive recruitment of lineage-specific genes in adaptations | Q36001229 | ||
| Anthropogenic disturbance as a driver of microspatial and microhabitat segregation of cytotypes of Centaurea stoebe and cytotype interactions in secondary contact zones. | Q36104632 | ||
| Diversify or die: generation of diversity in response to stress. | Q36178618 | ||
| From 2R to 3R: evidence for a fish-specific genome duplication (FSGD). | Q36233924 | ||
| The evolutionary dynamics of the Saccharomyces cerevisiae protein interaction network after duplication | Q36458856 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1648 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | eukaryote | Q19088 |
| genetic variation | Q349856 | ||
| environment | Q2249676 | ||
| Cretaceous | Q44626 | ||
| whole genome duplication | Q63285481 | ||
| biomedical investigative technique | Q66648976 | ||
| P304 | page(s) | 20130353 | |
| P577 | publication date | 2014-08-05 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | Tangled up in two: a burst of genome duplications at the end of the Cretaceous and the consequences for plant evolution | |
| P478 | volume | 369 |
| Q28604047 | A Time-Calibrated Road Map of Brassicaceae Species Radiation and Evolutionary History |
| Q48183706 | A Transcriptomic Approach to Evolutionary Genetics of Giant Horsetail |
| Q104486503 | A chromosome-scale reference genome of Lobularia maritima, an ornamental plant with high stress tolerance |
| Q86423750 | A genome to unveil the mysteries of orchids |
| Q39979480 | Analyses of transcriptome sequences reveal multiple ancient large-scale duplication events in the ancestor of Sphagnopsida (Bryophyta). |
| Q34480598 | Basic principles of yeast genomics, a personal recollection |
| Q46279820 | Comparative transcriptome analysis reveals whole-genome duplications and gene selection patterns in cultivated and wild Chrysanthemum species. |
| Q42710106 | Contemporary and future studies in plant speciation, morphological/floral evolution and polyploidy: honouring the scientific contributions of Leslie D. Gottlieb to plant evolutionary biology |
| Q47630787 | Coordinated Functional Divergence of Genes after Genome Duplication in Arabidopsis thaliana |
| Q36837933 | Developmental mechanisms underlying variable, invariant and plastic phenotypes. |
| Q64055379 | Diversification of cytokinin phosphotransfer signaling genes in Medicago truncatula and other legume genomes |
| Q64083611 | Early consequences of allopolyploidy alter floral evolution in Nicotiana (Solanaceae) |
| Q36539208 | Effects of polyploidy and reproductive mode on life history trait expression |
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| Q41490694 | Evidence for an ancient whole genome duplication in the cycad lineage |
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| Q26747070 | Evolution of Gene Duplication in Plants |
| Q36064208 | Evolution of RLSB, a nuclear-encoded S1 domain RNA binding protein associated with post-transcriptional regulation of plastid-encoded rbcL mRNA in vascular plants |
| Q36228952 | Evolution of floral diversity: genomics, genes and gamma |
| Q33603957 | Evolution of the 3R-MYB Gene Family in Plants |
| Q92358527 | Functional and morphological evolution in gymnosperms: A portrait of implicated gene families |
| Q46613613 | Gene Duplicability of Core Genes Is Highly Consistent across All Angiosperms. |
| Q56689607 | Genetic and Biochemical Consequences of Polyploidy in Tragopogon |
| Q31154693 | Genome Sequencing Reveals the Origin of the Allotetraploid Arabidopsis suecica |
| Q33578807 | Genome expression balance in a triploid trihybrid vertebrate |
| Q35219067 | Genome-wide identification of evolutionarily conserved alternative splicing events in flowering plants |
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| Q28647254 | Horsetails Are Ancient Polyploids: Evidence from Equisetum giganteum |
| Q89813152 | Impact of whole genome triplication on the evolutionary history and the functional dynamics of regulatory genes involved in Brassica self-incompatibility signalling pathway |
| Q46301401 | Improved transcriptome sampling pinpoints 26 ancient and more recent polyploidy events in Caryophyllales, including two allopolyploidy events |
| Q31059382 | Improvement of the banana "Musa acuminata" reference sequence using NGS data and semi-automated bioinformatics methods |
| Q55446915 | Inferring duplication episodes from unrooted gene trees. |
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| Q33363444 | Knockdown of strigolactone biosynthesis genes in Populus affects BRANCHED1 expression and shoot architecture |
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