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Genomic Origin and Organization of the Allopolyploid Primula egaliksensis Investigated by in situ Hybridization
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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/bies.20374openalex-snapshot
Mechanisms of genomic rearrangements and gene expression changes in plant polyploids
inferredcites →https://doi.org/10.1007/bf00344156openalex-snapshot
Structure and chromosomal localization of DNA sequences related to ribosomal subrepeats in Vicia faba
inferredcites →https://doi.org/10.1007/bf02338802openalex-snapshot
Polymorphism and concerted evolution in a tandemly repeated gene family: 5S ribosomal DNA in diploid and allopolyploid cottons
inferredcites →https://doi.org/10.1007/bf02510039openalex-snapshot
Distribution of 5S and 18S-28S rDNA loci in a tetraploid cotton ( Gossypium hirsutum L.) and its putative diploid ancestors
inferredcites →https://doi.org/10.1007/s00299-006-0290-7openalex-snapshot
Unique chromosome behavior and genetic control in Brassica×Orychophragmus wide hybrids: a review
inferredcites →https://doi.org/10.1007/s004120050424openalex-snapshot
Gene conversion of ribosomal DNA in Nicotiana tabacum is associated with undermethylated, decondensed and probably active gene units
inferredcites →https://doi.org/10.1016/0022-2836(88)90434-2openalex-snapshot
Structure and evolution of the intergenic region in a ribosomal DNA repeat unit of wheat
inferredcites →https://doi.org/10.1016/j.pbi.2005.01.001openalex-snapshot
Polyploidy and genome evolution in plants
inferredcites →https://doi.org/10.1016/j.tplants.2006.04.002openalex-snapshot
History, protohistory and prehistory of the Arabidopsis thaliana chromosome complement
inferredcites →https://doi.org/10.1016/s0168-9525(00)02113-2openalex-snapshot
The epigenetics of nucleolar dominance
inferredcites →https://doi.org/10.1016/s1055-7903(03)00213-6openalex-snapshot
Epigenetic phenomena and the evolution of plant allopolyploids
inferredcites →https://doi.org/10.1023/a:1006392424384openalex-snapshot
Genome evolution in polyploids
inferredcites →https://doi.org/10.1038/88897openalex-snapshot
Mitotic recombination is suppressed by chromosomal divergence in hybrids of distantly related mouse strains
inferredcites →https://doi.org/10.1038/sj.hdy.6800001openalex-snapshot
Evolution and structure of 5S rDNA loci in allotetraploid Nicotiana tabacum and its putative parental species
inferredcites →https://doi.org/10.1038/sj.hdy.6800333openalex-snapshot
Ribosomal DNA evolution and gene conversion in Nicotiana rustica
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00948.xopenalex-snapshot
Advances in the study of polyploidy sincePlant speciation
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.92.1.280openalex-snapshot
Bidirectional interlocus concerted evolution following allopolyploid speciation in cotton (Gossypium).
inferredcites →https://doi.org/10.1073/pnas.92.17.7719openalex-snapshot
Rapid genome change in synthetic polyploids of Brassica and its implications for polyploid evolution.
inferredcites →https://doi.org/10.1080/07352689309701903openalex-snapshot
Molecular Data and the Dynamic Nature of Polyploidy
inferredcites →https://doi.org/10.1080/10635150490424402openalex-snapshot
Reticulate Evolution, Introgression, and Intertribal Gene Capture in an Allohexaploid Grass
inferredcites →https://doi.org/10.1080/106351598260879openalex-snapshot
Biogeography and Floral Evolution of Baobabs Adansonia, Bombacaceae as Inferred From Multiple Data Sets
inferredcites →https://doi.org/10.1083/jcb.101.5.2013openalex-snapshot
Mechanisms of nucleolar dominance in animals and plants.
inferredcites →https://doi.org/10.1086/323444openalex-snapshot
Phylogenetic Relationships in Primula L. and Related Genera (Primulaceae) Based on Noncoding Chloroplast DNA
inferredcites →https://doi.org/10.1086/419073openalex-snapshot
Concerted Evolution of Repetitive DNA Sequences in Eukaryotes
inferredcites →https://doi.org/10.1093/aob/mch172openalex-snapshot
The Effect of Stress on Genome Regulation and Structure
inferredcites →https://doi.org/10.1093/genetics/153.1.415openalex-snapshot
Meiotic Drive of Chromosomal Knobs Reshaped the Maize Genome
inferredcites →https://doi.org/10.1093/genetics/162.3.1435openalex-snapshot
Highly Condensed Potato Pericentromeric Heterochromatin Contains rDNA-Related Tandem Repeats
inferredcites →https://doi.org/10.1093/genetics/166.4.1935openalex-snapshot
Dynamic Changes in the Distribution of a Satellite Homologous to Intergenic 26-18S rDNA Spacer in the Evolution of Nicotiana
inferredcites →https://doi.org/10.1093/genetics/34.5.524openalex-snapshot
NUMBERS AND DISTRIBUTION OF CHROMOSOME KNOBS IN UNITED STATES MAIZE
inferredcites →https://doi.org/10.1093/oso/9780195138597.001.0001openalex-snapshot
The Role of Chromosomal Change in Plant Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004182openalex-snapshot
Retrotransposons and Genomic Stability in Populations of the Young Allopolyploid Species Spartina anglica C.E. Hubbard (Poaceae)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025705openalex-snapshot
Persistent nuclear ribosomal DNA sequence polymorphism in the Amelanchier agamic complex (Rosaceae)
inferredcites →https://doi.org/10.1093/sysbio/43.2.250openalex-snapshot
Surveys of Gene Families Using Polymerase Chain Reaction: PCR Selection and PCR Drift
inferredcites →https://doi.org/10.1098/rstb.1990.0015openalex-snapshot
DNA methylation and epigenetic inheritance
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00334.xopenalex-snapshot
Spartina anglica C. E. Hubbard: a natural model system for analysing early evolutionary changes that affect allopolyploid genomes
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00344.xopenalex-snapshot
Genome evolution in allotetraploid Nicotiana
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00345.xopenalex-snapshot
Concerted evolution of 18-5.8-26S rDNA repeats in Nicotiana allotetraploids
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00346.xopenalex-snapshot
Genetic and epigenetic reprogramming of the wheat genome upon allopolyploidization
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00349.xopenalex-snapshot
Genome downsizing in polyploid plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01297.xopenalex-snapshot
Preferential elimination of repeated DNA sequences from the paternal, Nicotiana tomentosiformis genome donor of a synthetic, allotetraploid tobacco
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01379.xopenalex-snapshot
Ancient and recent polyploidy in angiosperms
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01480.xopenalex-snapshot
Long‐term genome diploidization in allopolyploidNicotianasectionRepandae(Solanaceae)
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01700.xopenalex-snapshot
Are any primroses (Primula) primitively monomorphic?
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01722.xopenalex-snapshot
Evolution of biogeographic patterns, ploidy levels, and breeding systems in a diploid–polyploid species complex of Primula
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02121.xopenalex-snapshot
Sequence of events leading to near‐complete genome turnover in allopolyploid Nicotiana within five million years
inferredcites →https://doi.org/10.1126/science.15739260openalex-snapshot
The Significance of Responses of the Genome to Challenge
inferredcites →https://doi.org/10.1139/g01-011openalex-snapshot
Polyploid formation in cotton is not accompanied by rapid genomic changes
inferredcites →https://doi.org/10.1146/annurev.bi.49.070180.003455openalex-snapshot
Repeated Genes in Eukaryotes
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/10.1146/annurev.genet.34.1.401openalex-snapshot
POLYPLOID INCIDENCE AND EVOLUTION
inferredcites →https://doi.org/10.1159/000082406openalex-snapshot
Genome evolution of allopolyploids: a process of cytological and genetic diploidization
inferredcites →https://doi.org/10.1186/gb-2000-1-1-reviews107openalex-snapshot
The many hues of plant heterochromatin.
inferredcites →https://doi.org/10.1385/1-59745-003-0:173openalex-snapshot
Cytogenetic Analyses of Arabidopsis
inferredcites →https://doi.org/10.1534/genetics.104.027896openalex-snapshot
Stochastic and Epigenetic Changes of Gene Expression in Arabidopsis Polyploids
inferredcites →https://doi.org/10.2307/1551324openalex-snapshot
The Genus Primula as a Model for Evolution in the Alaskan Flora
inferredcites →https://doi.org/10.2307/2656583openalex-snapshot
Physical mapping of ribosomal RNA genes in peonies (Paeonia, Paeoniaceae) by fluorescent in situ hybridization: implications for phylogeny and concerted evolution
inferredcites →https://doi.org/10.3732/ajb.90.7.988openalex-snapshot
Rapid evolution of parental rDNA in a synthetic tobacco allotetraploid line
inferredcites →https://doi.org/10.3732/ajb.93.6.875openalex-snapshot
A genetic appraisal of a new synthetic Nicotiana tabacum (Solanaceae) and the Kostoff synthetic tobacco
inferredcites →https://doi.org/10.5281/zenodo.16215362openalex-snapshot
Taxonomy of Primula sects. Aleuritia and Armerina in North America
inferredcites →https://doi.org/10.7302/9660openalex-snapshot
A Biosystematic Study Of Primula Mistassinica, Michx.
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.392.3.1zenodo-depositor-declared
Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
inferred← citeshttps://doi.org/10.1002/ece3.73024openalex-snapshot
Multiple Glacial Refugia and Complex Postglacial Dynamics of Primula sikkimensis (Primuaceae) in the Heterogeneous Qinghai‐Tibet Plateau
inferred← citeshttps://doi.org/10.1007/978-1-4939-7318-7_31openalex-snapshot
Technical Review: Microscopy and Image Processing Tools to Analyze Plant Chromatin: Practical Considerations
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.04.009openalex-snapshot
Molecular and cytogenetic evidence for an allotetraploid origin of Chenopodium quinoa and C. berlandieri (Amaranthaceae)
inferred← citeshttps://doi.org/10.1017/s1477200009003041openalex-snapshot
Allopolyploid origin of Mediterranean species inHelictotrichon(Poaceae) and its consequences for karyotype repatterning and homogenisation of rDNA repeat units
inferred← citeshttps://doi.org/10.1038/s41598-025-24871-2openalex-snapshot
Hybridization and embryological patterns underpinning reproductive barriers in Dactylorhiza (Orchidaceae)
inferred← citeshttps://doi.org/10.1080/11263504.2013.826745openalex-snapshot
Evidence of hybrid speciation in the North American primroses Primula suffrutescens P. parryi P. rusbyi and P. angustifolia (Primulaceae)
inferred← citeshttps://doi.org/10.1080/14772000.2015.1023867openalex-snapshot
Genome evolution in a Mediterranean species complex: phylogeny and cytogenetics ofHelictotrichon(Poaceae) allopolyploids based on nuclear DNA sequences (rDNA, topoisomerase gene) and FISH
inferred← citeshttps://doi.org/10.1080/17550870802331904openalex-snapshot
The Arctic – an evolutionary freezer?
inferred← citeshttps://doi.org/10.1086/593041openalex-snapshot
Phylogeny and Biogeography of Primula sect. Parryi (Primulaceae)
inferred← citeshttps://doi.org/10.1086/664710openalex-snapshot
Origin of Highly Polyploid Species: Different Pathways of Auto- and Allopolyploidy in 12–18x Species ofAvenula(Poaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcs128openalex-snapshot
Evolution of the tetraploid Anemone multifida (2n = 32) and hexaploid A. baldensis (2n = 48) (Ranunculaceae) was accompanied by rDNA loci loss and intergenomic translocation: evidence for their common genome origin
inferred← citeshttps://doi.org/10.1093/aob/mcu115openalex-snapshot
Incomplete sequence homogenization in 45S rDNA multigene families: intermixed IGS heterogeneity within the single NOR locus of the polyploid species Medicago arborea (Fabaceae)
inferred← citeshttps://doi.org/10.1093/biolinnean/blac041openalex-snapshot
Engines of innovation: biological origins of genome evolution
inferred← citeshttps://doi.org/10.1093/gbe/evae208openalex-snapshot
Unveiling the Genome-Wide Consequences of Range Expansion and Mating System Transitions in Primula vulgaris
inferred← citeshttps://doi.org/10.1093/molbev/msaf162openalex-snapshot
Genomic Patterns of Loss of Distyly and Polyploidization in Primroses
inferred← citeshttps://doi.org/10.1093/sysbio/syp010openalex-snapshot
Disentangling Reticulate Evolution in an Arctic–Alpine Polyploid Complex
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2010.02428.xopenalex-snapshot
Genome composition and origin of the polyploid Aegean grass Avenula agropyroides (Poaceae)
inferred← citeshttps://doi.org/10.1111/njb.01778openalex-snapshot
Recurrent hybridisation events between Primula vulgaris , P . veris and P . elatior (Primulaceae, Ericales) challenge the species boundaries: using molecular markers to re‐evaluate morphological identifications
inferred← citeshttps://doi.org/10.1111/nph.12567openalex-snapshot
The widespread crucifer species C ardamine flexuosa is an allotetraploid with a conserved subgenomic structure
inferred← citeshttps://doi.org/10.1111/nph.16849openalex-snapshot
Asymmetries of reproductive isolation are reflected in directionalities of hybridization: integrative evidence on the complexity of species boundaries
inferred← citeshttps://doi.org/10.1155/2017/7561909openalex-snapshot
Application of Genomic In Situ Hybridization in Horticultural Science
inferred← citeshttps://doi.org/10.1159/000361002openalex-snapshot
Polyploidy and Hybridization as Main Factors of Speciation: Complex Reticulate Evolution within the Grass Genus Helictochloa
inferred← citeshttps://doi.org/10.1186/1471-2148-10-98openalex-snapshot
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
inferred← citeshttps://doi.org/10.1186/1471-2148-12-56openalex-snapshot
Polyploid evolution and Pleistocene glacial cycles: A case study from the alpine primrose Primula marginata (Primulaceae)
inferred← citeshttps://doi.org/10.1186/1471-2156-14-75openalex-snapshot
Cytogenetic analysis of Phyllomedusa distincta Lutz, 1950 (2n = 2x = 26), P. tetraploidea Pombal and Haddad, 1992 (2n = 4x = 52), and their natural triploid hybrids (2n = 3x = 39) (Anura, Hylidae, Phyllomedusinae)
inferred← citeshttps://doi.org/10.1186/1471-2164-11-97openalex-snapshot
Homeolog loss and expression changes in natural populations of the recently and repeatedly formed allotetraploid Tragopogon mirus (Asteraceae)
inferred← citeshttps://doi.org/10.1186/s12862-015-0445-7openalex-snapshot
Phylogeny and biogeography of Primula sect. Armerina: implications for plant evolution under climate change and the uplift of the Qinghai-Tibet Plateau
inferred← citeshttps://doi.org/10.1186/s12870-024-05658-5openalex-snapshot
Does time matter? Intraspecific diversity of ribosomal RNA genes in lineages of the allopolyploid model grass Brachypodium hybridum with different evolutionary ages
inferred← citeshttps://doi.org/10.3119/0035-4902-113.955.280openalex-snapshot
Fruit and Seed Characters Help Distinguish Southern Illinois Dodecatheon (Primulaceae) Species and Highlight Unusual Intergrading Populations
inferred← citeshttps://doi.org/10.3390/genes1020166openalex-snapshot
Review of the Application of Modern Cytogenetic Methods (FISH/GISH) to the Study of Reticulation (Polyploidy/Hybridisation)
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