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Molecular evidence of reticulate evolution in the subgenus Plantago (Plantaginaceae)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1991.tb11415.xopenalex-snapshot
HOMOPLOID RETICULATE EVOLUTION IN HELIANTHUS (ASTERACEAE): EVIDENCE FROM RIBOSOMAL GENES
inferredcites →https://doi.org/10.1007/s001220100741openalex-snapshot
PCR-mediated recombination in amplification products derived from polyploid cotton
inferredcites →https://doi.org/10.1007/s00606-006-0417-xopenalex-snapshot
Polyploidy, hybridization and reticulate evolution: lessons from the Brassicaceae
inferredcites →https://doi.org/10.1007/s10265-006-0286-yopenalex-snapshot
Evaluation of morphological and molecular variation in Plantago asiatica var. densiuscula, with special reference to the systematic treatment of Plantago asiatica var. yakusimensis
inferredcites →https://doi.org/10.1016/j.ympev.2006.01.027openalex-snapshot
Allopolyploid origin of Cardamine asarifolia (Brassicaceae): Incongruence between plastid and nuclear ribosomal DNA sequences solved by a single-copy nuclear gene
inferredcites →https://doi.org/10.1016/j.ympev.2007.01.011openalex-snapshot
Reticulate evolution and phylogeography in Asarum sect. Asiasarum (Aristolochiaceae) documented in internal transcribed spacer sequences (ITS) of nuclear ribosomal DNA
inferredcites →https://doi.org/10.1016/s0031-9422(00)00306-xopenalex-snapshot
Chemotaxonomy of Plantago. Iridoid glucosides and caffeoyl phenylethanoid glycosides
inferredcites →https://doi.org/10.1016/s1360-1385(98)01249-7openalex-snapshot
Genetic map-based studies of reticulate evolution in plants
inferredcites →https://doi.org/10.1016/s1389-1723(03)90130-7openalex-snapshot
Bias and Artifacts in Multitemplate Polymerase Chain Reactions(PCR)
inferredcites →https://doi.org/10.1038/hdy.1990.104openalex-snapshot
Evidence for autotetraploidy in Plantago media and comparisons between natural and artificial cytotypes concerning cell size and fertility
inferredcites →https://doi.org/10.1038/nature06151openalex-snapshot
Gene duplication and the adaptive evolution of a classic genetic switch
inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00070.xopenalex-snapshot
Phylogenetic relationships within Plantago (Plantaginaceae): evidence from nuclear ribosomal ITS and plastid trnL-F sequence data
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.09010093.xopenalex-snapshot
Expression of the PmSUC1 sucrose carrier gene from Plantago major L. is induced during seed development
inferredcites →https://doi.org/10.1055/s-2006-924659openalex-snapshot
Immunolocalization of the PmSUC1 Sucrose Transporter in Plantago major Flowers and Reporter‐Gene Analyses of the PmSUC1 Promoter Suggest a Role in Sucrose Release from the Inner Integument
inferredcites →https://doi.org/10.1073/pnas.0407258102openalex-snapshot
Chromosomal locus rearrangements are a rapid response to formation of the allotetraploid Arabidopsis suecica genome
inferredcites →https://doi.org/10.1073/pnas.0408302101openalex-snapshot
Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants
inferredcites →https://doi.org/10.1073/pnas.0711043105openalex-snapshot
Preferential protection of protein interaction network hubs in yeast: Evolved functionality of genetic redundancy
inferredcites →https://doi.org/10.1073/pnas.242415399openalex-snapshot
Allopolyploidization and evolution of species with reduced floral structures in Lepidium L. (Brassicaceae)
inferredcites →https://doi.org/10.1073/pnas.33.6.158openalex-snapshot
On the Evolution of the Genus Nicotiana
inferredcites →https://doi.org/10.1073/pnas.77.4.2158openalex-snapshot
Rapid duplication and loss of genes coding for the alpha chains of hemoglobin.
inferredcites →https://doi.org/10.1073/pnas.92.1.280openalex-snapshot
Bidirectional interlocus concerted evolution following allopolyploid speciation in cotton (Gossypium).
inferredcites →https://doi.org/10.1093/aob/mcm331openalex-snapshot
Allopolyploidization-accommodated Genomic Sequence Changes in Triticale
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/nar/19.14.4008openalex-snapshot
‘Touchdown’ PCR to circumvent spurious priming during gene amplification
inferredcites →https://doi.org/10.1093/nar/23.11.2049openalex-snapshot
Template-switching during DNA synthesis byThermus aquaticusDNA polymerase I
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/nar/26.7.1819openalex-snapshot
Stimulation and suppression of PCR-mediated recombination
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025797openalex-snapshot
Recombinant DNA sequences generated by PCR amplification
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025811openalex-snapshot
Bayesian phylogenetic inference using DNA sequences: a Markov Chain Monte Carlo Method
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1093/sysbio/18.1.1openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.1093/sysbio/40.3.315openalex-snapshot
The Discovery and Importance of Multiple Islands of Most-Parsimonious Trees
inferredcites →https://doi.org/10.1105/tpc.107.054346openalex-snapshot
Genomic Changes in Resynthesized Brassica napus and Their Effect on Gene Expression and Phenotype
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01135.xopenalex-snapshot
REPRODUCTIVE ISOLATION BETWEEN TWO CLOSELY RELATED HUMMINGBIRD POLLINATED NEOTROPICAL GINGERS
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01892.xopenalex-snapshot
RAPID DIVERSIFICATION, INCOMPLETE ISOLATION, AND THE "SPECIATION CLOCK" IN NORTH AMERICAN SALAMANDERS (GENUS PLETHODON): TESTING THE HYBRID SWARM HYPOTHESIS OF RAPID RADIATION
inferredcites →https://doi.org/10.1111/j.0908-8857.2004.03297.xopenalex-snapshot
Glacial history and colonization of Europe by the blue tit Parus caeruleus
inferredcites →https://doi.org/10.1111/j.1095-8312.1992.tb00867.xopenalex-snapshot
Single cytotype areas in autopolyploid Plantago media L.*
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00368.xopenalex-snapshot
Molecular and morphological data reveal cryptic taxonomic diversity in the terrestrial slug complex Arion subfuscus/fuscus (Mollusca, Pulmonata, Arionidae) in continental north-west Europe
inferredcites →https://doi.org/10.1111/j.1095-8339.1996.tb00484.xopenalex-snapshot
A phylogenetic study of the Plantaginaceae
inferredcites →https://doi.org/10.1111/j.1096-0031.1989.tb00573.xopenalex-snapshot
THE RETENTION INDEX AND THE RESCALED CONSISTENCY INDEX
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1756-1051.1984.tb01986.xopenalex-snapshot
Plantago sect. Oliganthos in southern South America, a taxonomic revision
inferredcites →https://doi.org/10.1111/j.1756-1051.1985.tb02083.xopenalex-snapshot
Plantago sect. Carpophorae, a taxonomic study
inferredcites →https://doi.org/10.1146/annurev.ecolsys.29.1.467openalex-snapshot
PATHWAYS, MECHANISMS, AND RATES OF POLYPLOID FORMATION IN FLOWERING PLANTS
inferredcites →https://doi.org/10.1159/000082407openalex-snapshot
Allopolyploidy – a shaping force in the evolution of wheat genomes
inferredcites →https://doi.org/10.1534/genetics.104.032839openalex-snapshot
Rapid Concerted Evolution of Nuclear Ribosomal DNA in Two Tragopogon Allopolyploids of Recent and Recurrent OriginSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession nos. AY458586, AY458588, AY458589, and AY458587
inferredcites →https://doi.org/10.2307/2412407openalex-snapshot
Quantitative Phyletics and the Evolution of Anurans
inferredcites →https://doi.org/10.2307/2992325openalex-snapshot
The Discovery and Importance of Multiple Islands of Most-Parsimonious Trees
inferredcites →https://doi.org/10.3732/ajb.0800132openalex-snapshot
Molecular phylogeny and adaptive radiation of the endemic Hawaiian Plantago species (Plantaginaceae)
inferredcites →https://doi.org/10.3732/ajb.90.3.429openalex-snapshot
Molecular systematics and biogeography of the amphibious genus Littorella (Plantaginaceae)
inferredcites →https://doi.org/10.3732/ajb.94.11.1837openalex-snapshot
High‐resolution phylogeny for Helianthus (Asteraceae) using the 18S‐26S ribosomal DNA external transcribed spacer
inferredcites →https://doi.org/10.3732/ajb.95.2.241openalex-snapshot
Phylogenetics and reticulate evolution in Pistacia (Anacardiaceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.221.3.2zenodo-depositor-declared
Taxonomic novelties in Plantago section Virginica (Plantaginaceae) and an updated identification key
inferred← citeshttps://doi.org/10.11646/phytotaxa.296.3.4zenodo-depositor-declared
Reestablishment of Plantago bradei (Plantaginaceae), an overlooked narrowly endemic species from Serra do Caparaó, eastern Brazil, and range extension of P. guilleminiana
inferred← citeshttps://doi.org/10.11646/phytotaxa.306.1.6zenodo-depositor-declared
The intricate nomenclatural questions around Plantago holosteum (Plantaginaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.316.1.1zenodo-depositor-declared
Contributions to the knowledge of the genus Plantago (Plantaginaceae) in the Central-West region of Brazil
inferred← citeshttps://doi.org/10.1002/ece3.71144openalex-snapshot
Allotetraploid Origin and Putative Ancient Introgression in Plantago hakusanensis (Plantaginaceae)
inferred← citeshttps://doi.org/10.1002/tax.12035openalex-snapshot
Phylogenetic and morphometric analysis of Plantago section Coronopus (Plantaginaceae)
inferred← citeshttps://doi.org/10.1002/tax.70230openalex-snapshot
All pieces together now? A phylogenomic analysis and tribe‐level classification of the heterogeneous family Plantaginaceae
inferred← citeshttps://doi.org/10.1007/978-3-319-62229-3_9openalex-snapshot
How Far Advanced is the DNA-Based Identification of the BELFRIT-List?
inferred← citeshttps://doi.org/10.1007/s10265-011-0467-1openalex-snapshot
A hypothesis on the origin of genetic heterozygosity in diploids and triploids in Japanese Cayratia japonica species complex (Vitaceae)
inferred← citeshttps://doi.org/10.1016/j.flora.2012.06.018openalex-snapshot
Genetic diversity and relationships among species of the genus Thymus L. (section Serpyllum)
inferred← citeshttps://doi.org/10.1016/j.flora.2017.06.009openalex-snapshot
Cytomorphological variations and new reports of B-chromosomes in the genus Plantago (Plantaginaceae) from the Northwest Himalaya
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.124485openalex-snapshot
A haplotype-resolved chromosome-level genome of the hexaploid medicinal plant Plantago asiatica reveals subgenome asymmetry in bioactive compound biosynthesis
inferred← citeshttps://doi.org/10.1016/j.sajb.2013.06.018openalex-snapshot
Phylogenetic utility of 19 low copy nuclear genes in closely related genera and species of caesalpinioid legumes
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.02.023openalex-snapshot
Complex evolution in Arundinarieae (Poaceae: Bambusoideae): Incongruence between plastid and nuclear GBSSI gene phylogenies
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.01.027openalex-snapshot
Lineage diversification and hybridization in the Cayratia japonica–Cayratia tenuifolia species complex
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.013openalex-snapshot
The application of high-throughput sequencing for taxonomy: The case of Plantago subg. Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107217openalex-snapshot
Plastomes from tribe Plantagineae (Plantaginaceae) reveal infrageneric structural synapormorphies and localized hypermutation for Plantago and functional loss of ndh genes from Littorella
inferred← citeshttps://doi.org/10.1071/sb09040openalex-snapshot
DNA sequences from three genomes reveal multiple long-distance dispersals and non-monophyly of sections in Australasian Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1071/sb09040_eropenalex-snapshot
Erratum to : DNA sequences from three genomes reveal multiple long-distance dispersals and non-monophyly of sections in Australasian Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/00087114.2015.1032605openalex-snapshot
A karyological study on taxa ofCoronopusD.C. section ofPlantagoL. genus (Plantaginaceae) in Turkey
inferred← citeshttps://doi.org/10.1080/00173134.2020.1736147openalex-snapshot
A palynological study of the genus Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/0028825x.2010.515598openalex-snapshot
New chromosome counts in New Zealand species of Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/0028825x.2010.518318openalex-snapshot
Testing species limits of New Zealand Plantago (Plantaginaceae) using internal transcribed spacer (ITS) DNA sequences
inferred← citeshttps://doi.org/10.1080/0028825x.2012.671179openalex-snapshot
A taxonomic revision of native New Zealand Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/0028825x.2014.898664openalex-snapshot
In situ hybridization with genomic and rDNA probes reveals complex origins for polyploid New Zealand species of Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/00837792.2017.1349066openalex-snapshot
Nomenclatural and taxonomic notes on Mediterranean narrow-leaved plantains (Plantago section Maritima, Plantaginaceae)
inferred← citeshttps://doi.org/10.1080/03036758.2019.1676797openalex-snapshot
The importance and prevalence of allopolyploidy in Aotearoa New Zealand
inferred← citeshttps://doi.org/10.1080/23802359.2018.1553530openalex-snapshot
The complete chloroplast genome sequence of traditional medical herb, Plantago depressa Willd. (Plantaginaceae)
inferred← citeshttps://doi.org/10.1086/657657openalex-snapshot
Amplified Fragment Length Polymorphism Data Reveal a History of Auto- and Allopolyploidy in New Zealand Endemic Species of Plantago (Plantaginaceae): New Perspectives on a Taxonomically Challenging Group
inferred← citeshttps://doi.org/10.1086/714589openalex-snapshot
Plantago spp. as Models for Studying the Ecology and Evolution of Species Interactions across Environmental Gradients
inferred← citeshttps://doi.org/10.1093/dnares/dsad013openalex-snapshot
Genome assembly of the pioneer speciesPlantago majorL. (Plantaginaceae) provides insight into its global distribution and adaptation to metal-contaminated soil
inferred← citeshttps://doi.org/10.1093/jhered/ess049openalex-snapshot
Variable Changes in Genome Size Associated with Different Polyploid Events in Plantago (Plantaginaceae)
inferred← citeshttps://doi.org/10.1101/2020.07.31.230813openalex-snapshot
How to map a plantain: phylogeny of the diverse Plantagineae (Lamiales)
inferred← citeshttps://doi.org/10.1111/nph.14111openalex-snapshot
Next‐generation polyploid phylogenetics: rapid resolution of hybrid polyploid complexes using PacBio single‐molecule sequencing
inferred← citeshttps://doi.org/10.12705/635.32openalex-snapshot
Low‐copy nuclear data confirm rampant allopolyploidy in the Cystopteridaceae (Polypodiales)
inferred← citeshttps://doi.org/10.12705/663.14openalex-snapshot
Typification of the Linnaean names Plantago serraria and P. subulata ( Plantago subgenus Coronopus , Plantaginaceae)
inferred← citeshttps://doi.org/10.15560/11.2.1569openalex-snapshot
Clarifying the occurrence and conservation status of Plantago dielsiana Pilg. and P. australis Lam. subsp. pretoana Rahn (Plantaginaceae) in Brazil
inferred← citeshttps://doi.org/10.15560/15.1.13openalex-snapshot
First record of Plantago heterophylla Nutt. (Plantaginaceae) for the Brazilian flora
inferred← citeshttps://doi.org/10.3159/torrey-d-14-00029.1openalex-snapshot
Plantago corvensis(Plantaginaceae): a new narrowly endemic species from rocky cliffs in southern Brazil1
inferred← citeshttps://doi.org/10.3159/torrey-d-14-00070openalex-snapshot
The use of potential distribution models in the study of the distribution and conservation status of plants: The case of Plantago L. (Plantaginaceae) in Brazil1
inferred← citeshttps://doi.org/10.3390/plants10112299openalex-snapshot
Molecular and Morphological Data Improve the Classification of Plantagineae (Lamiales)
inferred← citeshttps://doi.org/10.3390/plants13192691openalex-snapshot
Comparative Plastomics of Plantains (Plantago, Plantaginaceae) as a Tool for the Development of Species-Specific DNA Barcodes
inferred← citeshttps://doi.org/10.3732/ajb.1400344openalex-snapshot
Chenopodium polyploidy inferences from Salt Overly Sensitive 1 (SOS1) data
inferred← citeshttps://doi.org/10.3732/ajb.1600303openalex-snapshot
Molecular bases for phyllomorph development in a one‐leaf plant, Monophyllaea glabra
inferred← citeshttps://doi.org/10.5007/2175-7925.2014v27n2p57openalex-snapshot
Descrição da espécie nova Plantago aparadensis (Plantaginaceae), endêmica dos Aparados da Serra Geral, sul do Brasil
inferred← citeshttps://doi.org/10.5897/ajb10.1893openalex-snapshot
Advances on research epigenetic change of hybrid and polyploidy in plants
inferred← citeshttps://doi.org/10.7717/peerj.2050openalex-snapshot
Yet another new species from one of the best-studied neotropical areas: Plantago humboldtiana (Plantaginaceae), an extremely narrow endemic new species from a waterfall in southern Brazil
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