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Nuclear DNA amounts in angiosperms: targets, trends and tomorrow
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527610921.ch15openalex-snapshot
Endopolyploidy in Plants and its Analysis by Flow Cytometry
inferredcites →https://doi.org/10.1002/9783527610921.ch18openalex-snapshot
FLOW ER : A Plant DNA Flow Cytometry Database
inferredcites →https://doi.org/10.1002/9783527610921.ch4openalex-snapshot
Nuclear DNA Content Measurement
inferredcites →https://doi.org/10.1002/9783527610921.ch7openalex-snapshot
Genome Size and its Uses: The Impact of Flow Cytometry
inferredcites →https://doi.org/10.1002/cyto.10030openalex-snapshot
Lack of correlation between AT frequency and genome size in higher plants and the effect of nonrandomness of base sequences on dye binding
inferredcites →https://doi.org/10.1002/cyto.990100606openalex-snapshot
Reference standards for flow cytometry and application in comparative studies of nuclear DNA content
inferredcites →https://doi.org/10.1002/cyto.a.20122openalex-snapshot
Are seeds suitable for flow cytometric estimation of plant genome size?
inferredcites →https://doi.org/10.1002/cyto.a.20760openalex-snapshot
Simultaneous flow cytometric quantification of plant nuclear DNA contents over the full range of described angiosperm 2C values
inferredcites →https://doi.org/10.1002/cyto.a.20907openalex-snapshot
The quest for suitable reference standards in genome size research
inferredcites →https://doi.org/10.1002/cyto.a.20915openalex-snapshot
Nuclear genome size: Are we getting closer?
inferredcites →https://doi.org/10.1002/j.1996-8175.1953.tb01457.xopenalex-snapshot
INTERNATIONAL CODE OF BOTANICAL NOMENCLATURE
inferredcites →https://doi.org/10.1002/jez.1401770108openalex-snapshot
DNA content, ribosomal gene multiplicity, and cell size in fish
inferredcites →https://doi.org/10.1002/pca.2800020402openalex-snapshot
Flow cytometric analysis of nuclear DNA content in higher plants
inferredcites →https://doi.org/10.1002/tax.581014openalex-snapshot
Coffea anthonyi , a new self‐compatible Central African coffee species, closely related to an ancestor of Coffea arabica
inferredcites →https://doi.org/10.1006/anbo.1997.0415openalex-snapshot
Nuclear DNA Amounts in Angiosperms—583 New Estimates
inferredcites →https://doi.org/10.1006/anbo.1998.0730openalex-snapshot
Plant Genome Size Estimation by Flow Cytometry: Inter-laboratory Comparison*1
inferredcites →https://doi.org/10.1006/anbo.1998.0785openalex-snapshot
DNA Amounts in Two Samples of Angiosperm Weeds
inferredcites →https://doi.org/10.1006/anbo.1999.0893openalex-snapshot
Confirmation of Ancient Polyploidy in Dahlia (Asteraceae) Species using Genomic In Situ Hybridization
inferredcites →https://doi.org/10.1006/anbo.2000.1187openalex-snapshot
Nucleus–Cytosol Interactions—A Source of Stoichiometric Error in Flow Cytometric Estimation of Nuclear DNA Content in Plants
inferredcites →https://doi.org/10.1006/anbo.2000.1200openalex-snapshot
Limited Genome Size Variation in Sesleria albicans
inferredcites →https://doi.org/10.1006/anbo.2000.1253openalex-snapshot
Nuclear DNA Amounts in Angiosperms and their Modern Uses—807 New Estimates
inferredcites →https://doi.org/10.1006/anbo.2000.1325openalex-snapshot
First Nuclear DNA C-values for 25 Angiosperm Families
inferredcites →https://doi.org/10.1006/anbo.2001.1528openalex-snapshot
First Nuclear DNA C-values for Another 25 Angiosperm Families
inferredcites →https://doi.org/10.1007/bf00220990openalex-snapshot
Nuclear DNA content of Vitis species, cultivars, and other genera of the Vitaceae
inferredcites →https://doi.org/10.1007/bf00222092openalex-snapshot
Molecular genetics of growth and development in Populus. I. Triploidy in hybrid poplars
inferredcites →https://doi.org/10.1007/bf00223656openalex-snapshot
Relationship between genome size and maturity group in soybean
inferredcites →https://doi.org/10.1007/bf00223672openalex-snapshot
Flow cytometric and Feulgen densitometric analysis of genome size variation in Pisum
inferredcites →https://doi.org/10.1007/bf02672069openalex-snapshot
Nuclear DNA content of some important plant species
inferredcites →https://doi.org/10.1007/bf02672073openalex-snapshot
Estimation of nuclear DNA content of plants by flow cytometry
inferredcites →https://doi.org/10.1007/bf02803047openalex-snapshot
Nuclear DNA content variation within the genusTaraxacum (Asteraceae)
inferredcites →https://doi.org/10.1007/bf02804286openalex-snapshot
Genome size discriminates between closely related taxaElytrigia repens andE. intermedia (Poaceae: Triticeae) and their hybrid
inferredcites →https://doi.org/10.1007/bf02920930openalex-snapshot
Flow cytometric estimation of nuclear DNA amount in diploid bananas (Musa acuminata andM. balbisiana)
inferredcites →https://doi.org/10.1007/bf02984203openalex-snapshot
The genetics and cytology of Dahlia species
inferredcites →https://doi.org/10.1007/s00122-004-1655-3openalex-snapshot
Analysis of the genetic stability of Eucalyptus globulus Labill. somatic embryos by flow cytometry
inferredcites →https://doi.org/10.1007/s00299-002-0522-4openalex-snapshot
Cytometric determination of genome size in Colchicum species (Liliales, Colchicaceae) of the western Mediterranean area
inferredcites →https://doi.org/10.1007/s00299-003-0651-4openalex-snapshot
Flow cytometric analysis of the cell cycle in different coconut palm ( Cocos nucifera L.) tissues cultured in vitro
inferredcites →https://doi.org/10.1007/s00299-006-0162-1openalex-snapshot
Nuclear DNA content of Vitis vinifera cultivars and ploidy level analyses of somatic embryo-derived plants obtained from anther culture
inferredcites →https://doi.org/10.1007/s002990050339openalex-snapshot
Comparative flow cytometric estimation of nuclear DNA content in oil palm (Elaeis guineensis Jacq) tissue cultures and seed-derived plants
inferredcites →https://doi.org/10.1007/s00425-005-1492-xopenalex-snapshot
Assessment of ploidy stability of the somatic embryogenesis process in Quercus suber L. using flow cytometry
inferredcites →https://doi.org/10.1007/s00497-007-0053-9openalex-snapshot
Male gametophyte development and two different DNA classes of pollen grains in Rumex acetosa L., a plant with an XX/XY1Y2 sex chromosome system and a female-biased sex ratio
inferredcites →https://doi.org/10.1007/s00606-002-0240-yopenalex-snapshot
Chromosomal differentiation and genome size in three European mountain Lilium species
inferredcites →https://doi.org/10.1007/s00606-003-0016-zopenalex-snapshot
The systematic value of nuclear DNA content in Galanthus
inferredcites →https://doi.org/10.1007/s00606-003-0038-6openalex-snapshot
Taxonomic implications of genome size and pollen colour and vitality for species of Agapanthus L?H�ritier (Agapanthaceae)
inferredcites →https://doi.org/10.1007/s00606-003-0071-5openalex-snapshot
Variation in Lamium subg. Galeobdolon (Lamiaceae) ? insights from ploidy levels, morphology and isozymes
inferredcites →https://doi.org/10.1007/s00606-003-0075-0openalex-snapshot
Ploidy level and origin of the European invasive weed Senecio inaequidens (Asteraceae)
inferredcites →https://doi.org/10.1007/s00606-004-0244-xopenalex-snapshot
Taxonomic implications of genome size for all species of the genus Gasteria Duval (Aloaceae)
inferredcites →https://doi.org/10.1007/s00606-004-0280-6openalex-snapshot
Genome size variation in Macaronesian angiosperms: forty percent of the Canarian endemic flora completed
inferredcites →https://doi.org/10.1007/s00606-004-0282-4openalex-snapshot
Does Lilium bosniacum merit species rank? A classical and molecular-cytogenetic analysis
inferredcites →https://doi.org/10.1007/s00606-005-0359-8openalex-snapshot
Cryptopolyploidy revisited: the case of Vinca (Apocynaceae)
inferredcites →https://doi.org/10.1007/s00606-005-0364-yopenalex-snapshot
2C DNA variation and relationships among New World species of the genus Lupinus (Fabaceae)
inferredcites →https://doi.org/10.1007/s00606-005-0381-xopenalex-snapshot
Genome size for the species of Nerine Herb. (Amaryllidaceae) and its evident correlation with growth cycle, leaf width and other morphological characters
inferredcites →https://doi.org/10.1007/s00606-005-0384-7openalex-snapshot
Genome size in Bulgarian Centaurea s.l. (Asteraceae)
inferredcites →https://doi.org/10.1007/s00606-007-0552-zopenalex-snapshot
Flow cytometric analysis reveals different nuclear DNA contents in cultivated Fonio (Digitaria spp.) and some wild relatives from West-Africa
inferredcites →https://doi.org/10.1007/s00606-007-0564-8openalex-snapshot
Flow cytometric and cytogenetic analyses of Iberian Peninsula Festuca spp.
inferredcites →https://doi.org/10.1007/s00606-007-0613-3openalex-snapshot
Flow cytometric measurements do not reveal different ploidy levels in Minthostachys (Lamiaceae)
inferredcites →https://doi.org/10.1007/s00606-008-0015-1openalex-snapshot
The systematic value of nuclear DNA content for all species of Narcissus L. (Amaryllidaceae)
inferredcites →https://doi.org/10.1007/s00606-008-0075-2openalex-snapshot
Flow cytometric analysis in Lagenaria siceraria (Cucurbitaceae) indicates correlation of genome size with usage types and growing elevation
inferredcites →https://doi.org/10.1007/s006060170027openalex-snapshot
Ploidy level of the invasive weed Rubus alceifolius (Rosaceae) in its native range and in areas of introduction
inferredcites →https://doi.org/10.1007/s10265-005-0191-9openalex-snapshot
Nuclear DNA content in the genus Hepatica (Ranunculaceae)
inferredcites →https://doi.org/10.1007/s10493-008-9227-xopenalex-snapshot
The nuclear genome of the phytoseiid Metaseiulus occidentalis (Acari: Phytoseiidae) is among the smallest known in arthropods
inferredcites →https://doi.org/10.1007/s10535-005-0011-zopenalex-snapshot
Genome size variation in some representatives of the genus Tripleurospermum
inferredcites →https://doi.org/10.1007/s10577-006-1077-yopenalex-snapshot
Genome size, karyotype, meiosis and a novel extra chromosome in Torenia fournieri, T. baillonii and their hybrid
inferredcites →https://doi.org/10.1007/s10681-005-5341-6openalex-snapshot
Genome size and Giemsa C-banded karyotype of tetraploid Bromus ciliatus L.
inferredcites →https://doi.org/10.1007/s10722-006-9115-3openalex-snapshot
Nuclear DNA content estimations in wild olive (Olea europaea L. ssp. europaea var. sylvestris Brot.) and Portuguese cultivars of O. europaea using flow cytometry
inferredcites →https://doi.org/10.1007/s10722-007-9268-8openalex-snapshot
Genetic characterisation of olive trees from Madeira Archipelago using flow cytometry and microsatellite markers
inferredcites →https://doi.org/10.1007/s10722-008-9390-2openalex-snapshot
Use and variation of Pandanus tectorius Parkinson (P. fascicularis Lam.) along the coastline of Orissa, India
inferredcites →https://doi.org/10.1007/s11240-005-9023-9openalex-snapshot
Agrobacterium-mediated transformation and inbred line development in the model grass Brachypodium distachyon
inferredcites →https://doi.org/10.1007/s11240-007-9264-xopenalex-snapshot
Variable DNA content of Cyclamen persicum regenerated via somatic embryogenesis: rethinking the concept of long-term callus and suspension cultures
inferredcites →https://doi.org/10.1007/s12284-009-9025-zopenalex-snapshot
De Novo Next Generation Sequencing of Plant Genomes
inferredcites →https://doi.org/10.1016/0014-4827(65)90006-6openalex-snapshot
Relationships between mitotic cycle duration, S period duration and the average rate of DNA synthesis in the root meristem cells of several plants
inferredcites →https://doi.org/10.1016/0248-4900(93)90113-sopenalex-snapshot
A cytometric exercise in plant DNA histograms, with 2C values for 70 species
inferredcites →https://doi.org/10.1016/b978-012301463-4/50003-6openalex-snapshot
Genome Size Evolution in Animals
inferredcites →https://doi.org/10.1016/b978-012301463-4/50004-8openalex-snapshot
Genome Size Evolution in Plants
inferredcites →https://doi.org/10.1016/j.aquabot.2008.04.009openalex-snapshot
Amounts of nuclear DNA in marine halophytes
inferredcites →https://doi.org/10.1016/j.biolcel.2003.11.005openalex-snapshot
Genome size in Echinops L. and related genera (Asteraceae, Cardueae): karyological, ecological and phylogenetic implications
inferredcites →https://doi.org/10.1016/j.bse.2007.02.005openalex-snapshot
Effect of the environmental conditions on essential oil profile in two Dinaric Salvia species: S. brachyodon Vandas and S. officinalis L.
inferredcites →https://doi.org/10.1016/j.envexpbot.2004.11.005openalex-snapshot
Genome size in Bituminaria bituminosa (L.) C.H. Stirton (Fabaceae) populations: separation of “true” differences from environmental effects on DNA determination
inferredcites →https://doi.org/10.1016/j.fgb.2009.03.009openalex-snapshot
Karyotype analysis, genome organization, and stable genetic transformation of the root colonizing fungus Piriformospora indica
inferredcites →https://doi.org/10.1016/j.plantsci.2005.12.007openalex-snapshot
Genetic characterization of selected Trifolium species as revealed by nuclear DNA content and ITS rDNA region analysis
inferredcites →https://doi.org/10.1016/j.plantsci.2007.03.002openalex-snapshot
Evaluation of polysomaty and estimation of genome size in Polygala vayredae and P. calcarea using flow cytometry
inferredcites →https://doi.org/10.1016/j.plantsci.2008.03.010openalex-snapshot
Genome size, base composition and karyotype of Jatropha curcas L., an important biofuel plant
inferredcites →https://doi.org/10.1016/j.tplants.2009.09.005openalex-snapshot
The science and economics of ex situ plant conservation
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.2006.06.016openalex-snapshot
Circumpolar phylogeography of Juncus biglumis (Juncaceae) inferred from AFLP fingerprints, cpDNA sequences, nuclear DNA content and chromosome numbers
inferredcites →https://doi.org/10.1016/s0168-9452(02)00344-8openalex-snapshot
Flow cytometric analysis of nuclear DNA content in cloudberry (Rubus chamaemorus L.) in vitro cultures
inferredcites →https://doi.org/10.1016/s0168-9452(03)00256-5openalex-snapshot
Genome size analysis in the genus Cucurbita and its use for determination of interspecific hybrids obtained using the embryo-rescue technique
inferredcites →https://doi.org/10.1016/s0304-3770(03)00072-xopenalex-snapshot
Genome size of Adriatic seagrasses
inferredcites →https://doi.org/10.1023/a:1020610129424openalex-snapshot
Variation in chromosome numbers and nuclear DNA contents in genetic resources of Lactuca L. species (Asteraceae)
inferredcites →https://doi.org/10.1038/163666a0openalex-snapshot
Variable and Constant Components of Chromosomes
inferredcites →https://doi.org/10.1038/171737a0openalex-snapshot
Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid
inferredcites →https://doi.org/10.1038/211828a0openalex-snapshot
Nuclear Variation between Diploid Angiosperms
inferredcites →https://doi.org/10.1038/233350a0openalex-snapshot
Mitotic Cycles in Dicotyledons and Monocotyledons
inferredcites →https://doi.org/10.1038/35048692openalex-snapshot
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/425890aopenalex-snapshot
Biodiversity schemes take root in China
inferredcites →https://doi.org/10.1038/hdy.1965.9openalex-snapshot
Nuclear DNA and the evolution of wheat
inferredcites →https://doi.org/10.1038/hdy.1993.139openalex-snapshot
Heterosis and nuclear DNA content in maize
inferredcites →https://doi.org/10.1038/hdy.1993.42openalex-snapshot
Nuclear DNA content in F1 hybrids of maize
inferredcites →https://doi.org/10.1038/hdy.1997.170openalex-snapshot
The ten cytological races of the Scilla autumnalis species complex
inferredcites →https://doi.org/10.1038/hdy.1997.85openalex-snapshot
Genome size and maturity group in Glycine max (soybean)
inferredcites →https://doi.org/10.1038/nature06856openalex-snapshot
The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus)
inferredcites →https://doi.org/10.1038/nature07723openalex-snapshot
The Sorghum bicolor genome and the diversification of grasses
inferredcites →https://doi.org/10.1038/nature08747openalex-snapshot
Genome sequencing and analysis of the model grass Brachypodium distachyon
inferredcites →https://doi.org/10.1038/nbt0510-426openalex-snapshot
Third-generation sequencing fireworks at Marco Island
inferredcites →https://doi.org/10.1038/ng.475openalex-snapshot
The genome of the cucumber, Cucumis sativus L.
inferredcites →https://doi.org/10.1038/nmeth0409-244aopenalex-snapshot
Cheap third-generation sequencing
inferredcites →https://doi.org/10.1038/nprot.2007.310openalex-snapshot
Estimation of nuclear DNA content in plants using flow cytometry
inferredcites →https://doi.org/10.1038/sj.hdy.6800643openalex-snapshot
A secondary hybrid zone between diploid Dactylorhiza incarnata ssp. cruenta and allotetraploid D. lapponica (Orchidaceae)
inferredcites →https://doi.org/10.1043/0363-6445-26.4.722openalex-snapshot
The Origin of the Low Chromosome Number in Cryptanthus (Bromeliaceae)
inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00096.xopenalex-snapshot
DNA C-values in seven families fill phylogenetic gaps in the basal angiosperms
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.00988.xopenalex-snapshot
Endopolyploidy in seed plants is differently correlated to systematics, organ, life strategy and genome size
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01681.xopenalex-snapshot
Methylation of histone H3 in euchromatin of plant chromosomes depends on basic nuclear DNA content
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00822.xopenalex-snapshot
Identifying model metal hyperaccumulating plants: germplasm analysis of 20 Brassicaceae accessions from a wide geographical area
inferredcites →https://doi.org/10.1055/s-2004-821235openalex-snapshot
Nuclear DNA Amounts in 112 Species of Tropical Hardwoods ‐ New Estimates
inferredcites →https://doi.org/10.1055/s-2005-865693openalex-snapshot
Nuclear DNA Content and Chromosome Number in Some Diploid and Tetraploid Centaurea (Asteraceae: Cardueae) from the Dalmatia Region
inferredcites →https://doi.org/10.1055/s-2005-865878openalex-snapshot
Climate and Growth Form: The Consequences for Genome Size in Plants
inferredcites →https://doi.org/10.1055/s-2006-924101openalex-snapshot
Smallest Angiosperm Genomes Found in Lentibulariaceae, with Chromosomes of Bacterial Size
inferredcites →https://doi.org/10.1055/s-2007-965165openalex-snapshot
Genome Size Estimations On Ulmus minor Mill., Ulmus glabra Huds., and Celtis australis L. Using Flow Cytometry
inferredcites →https://doi.org/10.1073/pnas.36.11.643openalex-snapshot
The Constancy of Desoxyribose Nucleic Acid in Plant Nuclei
inferredcites →https://doi.org/10.1073/pnas.95.5.2011openalex-snapshot
Plant genome values: How much do we know?
inferredcites →https://doi.org/10.1080/00087114.1986.10797792openalex-snapshot
NuclearDNAAmounts in Some Tropical Hardwoods
inferredcites →https://doi.org/10.1080/00087114.1998.10589127openalex-snapshot
Estimation of nuclear DNA content inSesleria(Poaceae)
inferredcites →https://doi.org/10.1080/00087114.2005.10589457openalex-snapshot
Characterisation of the low-chromosome number grass Colpodium versicolor (Stev.) Schmalh. (2n = 4) by molecular cytogenetics
inferredcites →https://doi.org/10.1080/0028825x.2003.9512832openalex-snapshot
Variation in DNA C‐value and haploid genome size in New Zealand native grasses
inferredcites →https://doi.org/10.1080/11263500701872143openalex-snapshot
Nuclear DNA content variation in Halimium and Xolantha (Cistaceae)
inferredcites →https://doi.org/10.1093/aob/mcf167openalex-snapshot
Nuclear DNA C-values in 30 Species Double the Familial Representation in Pteridophytes
inferredcites →https://doi.org/10.1093/aob/mcg005openalex-snapshot
First Nuclear DNA C-values for 28 Angiosperm Genera
inferredcites →https://doi.org/10.1093/aob/mcg057openalex-snapshot
Comparisons with Caenorhabditis (100 Mb) and Drosophila (175 Mb) Using Flow Cytometry Show Genome Size in Arabidopsis to be 157 Mb and thus 25 % Larger than the Arabidopsis Genome Initiative Estimate of 125 Mb
inferredcites →https://doi.org/10.1093/aob/mcg104openalex-snapshot
Nuclear DNA Amounts in Macaronesian Angiosperms
inferredcites →https://doi.org/10.1093/aob/mcg105openalex-snapshot
Analysis of Nuclear DNA Content in Capsicum (Solanaceae) by Flow Cytometry and Feulgen Densitometry
inferredcites →https://doi.org/10.1093/aob/mcg145openalex-snapshot
Nuclear DNA Content Variation and Species Relationships in the Genus Lupinus (Fabaceae)
inferredcites →https://doi.org/10.1093/aob/mcg183openalex-snapshot
Genome Size Variations in Diploid African Coffea Species
inferredcites →https://doi.org/10.1093/aob/mch037openalex-snapshot
Genome Size Variation among Accessions of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/aob/mch151openalex-snapshot
Genome Size Variation in Central European Species of Cirsium (Compositae) and their Natural Hybrids
inferredcites →https://doi.org/10.1093/aob/mch219openalex-snapshot
Genome Size Variation and Evolution in Veronica
inferredcites →https://doi.org/10.1093/aob/mci001openalex-snapshot
Plant Genome Size Research: A Field In Focus
inferredcites →https://doi.org/10.1093/aob/mci003openalex-snapshot
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects
inferredcites →https://doi.org/10.1093/aob/mci004openalex-snapshot
Intraspecific Variation in Genome Size in Angiosperms: Identifying its Existence
inferredcites →https://doi.org/10.1093/aob/mci005openalex-snapshot
Plant DNA Flow Cytometry and Estimation of Nuclear Genome Size
inferredcites →https://doi.org/10.1093/aob/mci012openalex-snapshot
Life History Evolution and Genome Size in Subtribe Oncidiinae (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mci014openalex-snapshot
Evolution of DNA Amounts Across Land Plants (Embryophyta)
inferredcites →https://doi.org/10.1093/aob/mci015openalex-snapshot
Genome Evolution in the Genus Sorghum (Poaceae)
inferredcites →https://doi.org/10.1093/aob/mci016openalex-snapshot
Evolution of Genome Size in Brassicaceae
inferredcites →https://doi.org/10.1093/aob/mci019openalex-snapshot
The Origin, Evolution and Proposed Stabilization of the Terms 'Genome Size' and 'C-Value' to Describe Nuclear DNA Contents
inferredcites →https://doi.org/10.1093/aob/mci078openalex-snapshot
Estimation of the Nuclear DNA Content of Gossypium Species
inferredcites →https://doi.org/10.1093/aob/mci170openalex-snapshot
First Nuclear DNA Amounts in more than 300 Angiosperms
inferredcites →https://doi.org/10.1093/aob/mci281openalex-snapshot
Nuclear DNA Variation, Chromosome Numbers and Polyploidy in the Endemic and Indigenous Grass Flora of New Zealand
inferredcites →https://doi.org/10.1093/aob/mci283openalex-snapshot
First Nuclear DNA C-values for 18 Eudicot Families
inferredcites →https://doi.org/10.1093/aob/mci284openalex-snapshot
The Relationship Between Nuclear DNA Content and Leaf Strategy in Seed Plants
inferredcites →https://doi.org/10.1093/aob/mcj050openalex-snapshot
Genome Size Variation in the Genus Carthamus (Asteraceae, Cardueae): Systematic Implications and Additive Changes During Allopolyploidization
inferredcites →https://doi.org/10.1093/aob/mcl077openalex-snapshot
Nuclear DNA Content Variation among Central European Koeleria Taxa
inferredcites →https://doi.org/10.1093/aob/mcl140openalex-snapshot
Flow Cytometric and Microscopic Analysis of the Effect of Tannic Acid on Plant Nuclei and Estimation of DNA Content
inferredcites →https://doi.org/10.1093/aob/mcl141openalex-snapshot
Comparison of Four Nuclear Isolation Buffers for Plant DNA Flow Cytometry
inferredcites →https://doi.org/10.1093/aob/mcl271openalex-snapshot
Genome Size Evolution in Relation to Leaf Strategy and Metabolic Rates Revisited
inferredcites →https://doi.org/10.1093/aob/mcl273openalex-snapshot
Distribution of Flower Morphs, Ploidy Level and Sexual Reproduction of the Invasive Weed Oxalis pes-caprae in the Western Area of the Mediterranean Region
inferredcites →https://doi.org/10.1093/aob/mcm144openalex-snapshot
Chromosome Numbers and Genome Size Variation in Indian Species of Curcuma (Zingiberaceae)
inferredcites →https://doi.org/10.1093/aob/mcm152openalex-snapshot
Two New Nuclear Isolation Buffers for Plant DNA Flow Cytometry: A Test with 37 Species
inferredcites →https://doi.org/10.1093/aob/mcm218openalex-snapshot
Genome Size Variation and Species Relationships in Hieracium Sub-genus Pilosella (Asteraceae) as Inferred by Flow Cytometry
inferredcites →https://doi.org/10.1093/aob/mcm303openalex-snapshot
Anthocyanin Inhibits Propidium Iodide DNA Fluorescence in Euphorbia pulcherrima: Implications for Genome Size Variation and Flow Cytometry
inferredcites →https://doi.org/10.1093/aob/mcm307openalex-snapshot
Genome Size and GC Content Evolution of Festuca: Ancestral Expansion and Subsequent Reduction
inferredcites →https://doi.org/10.1093/aob/mcm326openalex-snapshot
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inferredcites →https://doi.org/10.1093/aob/mcq011openalex-snapshot
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inferredcites →https://doi.org/10.1093/genetics/164.2.685openalex-snapshot
Characterization of High-Copy-Number Retrotransposons From the Large Genomes of the Louisiana Iris Species and Their Use as Molecular Markers
inferredcites →https://doi.org/10.1093/jhered/esg053openalex-snapshot
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inferredcites →https://doi.org/10.1093/molbev/msh092openalex-snapshot
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inferredcites →https://doi.org/10.1093/molbev/msn223openalex-snapshot
The Dynamic Ups and Downs of Genome Size Evolution in Brassicaceae
inferredcites →https://doi.org/10.1093/nar/gng056openalex-snapshot
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inferredcites →https://doi.org/10.1098/rspb.1972.0042openalex-snapshot
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inferredcites →https://doi.org/10.1098/rstb.1976.0044openalex-snapshot
Nuclear DNA amounts in angiosperms
inferredcites →https://doi.org/10.1101/gr.3766306openalex-snapshot
The Oryza bacterial artificial chromosome library resource: Construction and analysis of 12 deep-coverage large-insert BAC libraries that represent the 10 genome types of the genus Oryza
inferredcites →https://doi.org/10.1104/pp.107.104380openalex-snapshot
Ancestral Chromosomal Blocks Are Triplicated in Brassiceae Species with Varying Chromosome Number and Genome Size
inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
inferredcites →https://doi.org/10.1111/j.0014-3820.2005.tb01035.xopenalex-snapshot
PHYLETIC HOT SPOTS FOR B CHROMOSOMES IN ANGIOSPERMS
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00524.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1095-8339.2004.00379.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1095-8339.2005.00377.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1095-8339.2006.00500.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1095-8339.2010.01072.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1365-2583.2006.00690.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1399-3054.1992.tb04764.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1420-9101.2004.00801.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1420-9101.2006.01275.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01416.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1438-8677.1997.tb00614.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1469-8137.1987.tb04689.xopenalex-snapshot
VARIATION IN GENOMIC FORM IN PLANTS AND ITS ECOLOGICAL IMPLICATIONS
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01433.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01820.xopenalex-snapshot
Assessment of plants from the Brassicaceae family as genetic models for the study of nickel and zinc hyperaccumulation
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01919.xopenalex-snapshot
Correlated evolution of genome size and seed mass
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02093.xopenalex-snapshot
Sexing pollen reveals female bias in a dioecious plant
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02528.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1529-8817.2008.00476.xopenalex-snapshot
INTER‐ AND INTRASPECIFIC RELATIONSHIPS BETWEEN NUCLEAR DNA CONTENT AND CELL SIZE IN SELECTED MEMBERS OF THE CENTRIC DIATOM GENUS THALASSIOSIRA (BACILLARIOPHYCEAE)1
inferredcites →https://doi.org/10.1111/j.1601-5223.2004.01739.xopenalex-snapshot
Flow cytometric analysis of genome size variation in some Passiflora species
inferredcites →https://doi.org/10.1111/j.1744-7348.2006.00079.xopenalex-snapshot
Genome size variation in pumpkin (Cucurbita sp.)
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A Draft Sequence of the Rice Genome ( Oryza sativa L. ssp. indica )
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The Genome of the Diatom Thalassiosira Pseudonana : Ecology, Evolution, and Metabolism
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The Genome of Black Cottonwood, Populus trichocarpa (Torr. & Gray)
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inferredcites →https://doi.org/10.1126/science.282.5396.2012openalex-snapshot
Genome Sequence of the Nematode C. elegans : A Platform for Investigating Biology
showing the first 200 of 241 · page through all 241
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The C- and G-value paradox with polyploidy, repeatomes, introns, phenomes and cell economy
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Genome size variation among and within Ophiopogoneae species by flow cytometric analysis
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Visualization of smaller chromosomes from unicellular microalgae
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Characterization and expression analysis of bHLH transcription factors reveal their putative regulatory effects on nectar spur development in Aquilegia species
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Floral pigmentation pattern in Oriental hybrid lily (Lilium spp.) cultivar ‘Dizzy’ is caused by transcriptional regulation of anthocyanin biosynthesis genes
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A new index for the quantification of chromosome number variation: An application to selected animal and plant groups
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Genome size variation among 3 selected genera of Zingiberoideae
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Evaluation of ploidy level and endoreduplication in carnation (Dianthus spp.)
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Evolutionary expansion, functional diversification, and transcript profiling of plant Glutathione Peroxidases
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The effects of fresh and rapid desiccated tissue on estimates of Ophiopogoneae genome size
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inferred← citeshttps://doi.org/10.1016/j.scienta.2015.06.018openalex-snapshot
Karyotype diversity analysis and nuclear genome size estimation for Pennisetum Rich. (Poaceae) ornamental grasses reveal genetic relationship and chromosomal evolution
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109532openalex-snapshot
Karyotype and nuclear DNA content variation in Passiflora L
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109570openalex-snapshot
MYB19LONG is involved in brushmark pattern development in Asiatic hybrid lily (Lilium spp.) flowers
inferred← citeshttps://doi.org/10.1016/j.tplants.2014.01.014openalex-snapshot
DNA methylation as a system of plant genomic immunity
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.05.007openalex-snapshot
Angiosperm Plant Desiccation Tolerance: Hints from Transcriptomics and Genome Sequencing
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.100832openalex-snapshot
High-quality genomes of Bombax ceiba and Ceiba pentandra provide insights into the evolution of Malvaceae species and differences in their natural fiber development
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.026openalex-snapshot
Phylogeny, rate variation, and genome size evolution of Pelargonium (Geraniaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.04.010openalex-snapshot
Insights into evolution in Andean Polystichum (Dryopteridaceae) from expanded understanding of the cytosolic phosphoglucose isomerase gene
inferred← citeshttps://doi.org/10.1038/nature22011openalex-snapshot
Genomic innovation for crop improvement
inferred← citeshttps://doi.org/10.1038/s41467-024-53157-wopenalex-snapshot
Chromosome-level baobab genome illuminates its evolutionary trajectory and environmental adaptation
inferred← citeshttps://doi.org/10.1038/s41598-018-31079-0openalex-snapshot
Expression of key genes affecting artemisinin content in five Artemisia species
inferred← citeshttps://doi.org/10.1038/s41598-019-48806-wopenalex-snapshot
Comparative transcriptome and metabolite profiling of four tissues from Alisma orientale (Sam.) Juzep reveals its inflorescence developmental and medicinal characteristics
inferred← citeshttps://doi.org/10.1038/s41598-024-79474-0openalex-snapshot
Molecular characteristics and expression pattern of the FAR1 gene during spike sprouting in quinoa
inferred← citeshttps://doi.org/10.1038/srep11636openalex-snapshot
Nitrogen limitation as a driver of genome size evolution in a group of karst plants
inferred← citeshttps://doi.org/10.1071/bt14287openalex-snapshot
Cytological study of Polystichum (Dryopteridaceae) species from southern South America
inferred← citeshttps://doi.org/10.1071/bt25093openalex-snapshot
Polyploidy arises independently of hybrid status in clonal narrow-range endemic Callistemon from East Gippsland, Victoria
inferred← citeshttps://doi.org/10.1071/sb16019openalex-snapshot
Effective application of next-generation sequencing (NGS) approaches in systematics and population genetics: case studies in Eucalyptus and Acacia
inferred← citeshttps://doi.org/10.1079/9781789242492.0020aopenalex-snapshot
Fig Genetics, Genomics, and Transcriptomics
inferred← citeshttps://doi.org/10.1080/00087114.2013.859443openalex-snapshot
New reports of nuclear DNA content for 66 traditional Chinese medicinal plant taxa in China
inferred← citeshttps://doi.org/10.1080/00087114.2015.1032575openalex-snapshot
Nuclear genome size and cytotype analysis inAgave parvifloraTorr. subsp.flexifloraGentry (Asparagales, Asparagaceae)
inferred← citeshttps://doi.org/10.1080/00087114.2015.1109940openalex-snapshot
Cytological studies of sporophytic and gametophytic generation of two bulbaceous species Ledebouria revoluta and Drimiopsis botryoides (Asparagaceae)
inferred← citeshttps://doi.org/10.1080/00087114.2017.1279931openalex-snapshot
Nuclear genome size and karyotype analysis ofAgave angustifoliaHaw. “Cimarron” and “Lineño” (Asparagales, Asparagaceae)
inferred← citeshttps://doi.org/10.1080/00087114.2017.1403762openalex-snapshot
Determination of the chromosome number and genome size ofGarcinia mangostanaL. via cytogenetics, flow cytometry and k-mer analyses
inferred← citeshttps://doi.org/10.1080/00087114.2018.1440826openalex-snapshot
Nuclear genome size and chromosome number in the Mexican genusPittocaulon(Asteraceae)
inferred← citeshttps://doi.org/10.1080/00087114.2018.1460057openalex-snapshot
Genome size in some taxa ofCrepisL. (Asteraceae) from Turkey
inferred← citeshttps://doi.org/10.1080/0144235x.2014.974358openalex-snapshot
Online resources for chromosome number databases
inferred← citeshttps://doi.org/10.1080/07352689.2014.898462openalex-snapshot
Achievements and Challenges in Improving Temperate Perennial Forage Legumes
inferred← citeshttps://doi.org/10.1080/07352689.2023.2210922openalex-snapshot
An Integrative Review of Drivers and Responses of Grassland Phenology under Global Change
inferred← citeshttps://doi.org/10.1080/11263504.2012.717973openalex-snapshot
Cytotaxonomy: The end of childhood
inferred← citeshttps://doi.org/10.1080/11263504.2013.861530openalex-snapshot
Nuclear DNA C-values for biodiversity screening: Case of the Lebanese flora
inferred← citeshttps://doi.org/10.1080/11263504.2013.863811openalex-snapshot
New data on genome size in 128 Asteraceae species and subspecies, with first assessments for 40 genera, 3 tribes and 2 subfamilies
inferred← citeshttps://doi.org/10.1080/11263504.2014.941036openalex-snapshot
Relationship between ploidy level and genome size in strawberries
inferred← citeshttps://doi.org/10.1080/11263504.2016.1218967openalex-snapshot
Karyomorphology of Turkish species in Centaurea sections Centaurea and Phalolepis (Asteraceae) and implications for taxonomy
inferred← citeshttps://doi.org/10.1080/12538078.2015.1132008openalex-snapshot
First genome size assessment, heterochromatin and rDNA chromosome mapping in the genus Sclerocarya (Anacardiaceae): insight into the new basic chromosome number
inferred← citeshttps://doi.org/10.1080/17550874.2016.1267274openalex-snapshot
Genome size variation and evolution in Dipterocarpaceae
inferred← citeshttps://doi.org/10.1080/23818107.2023.2244179openalex-snapshot
Karyotype analysis and genome size estimation of Sapindus mukorossi Gaertn. an economical important tree species in China
inferred← citeshttps://doi.org/10.1086/688873openalex-snapshot
Ionizing Radiation from Chernobyl and the Fraction of Viable Pollen
inferred← citeshttps://doi.org/10.1086/692763openalex-snapshot
Radiation Levels Affect Pollen Viability and Germination among Sites and Species at Chernobyl
inferred← citeshttps://doi.org/10.1089/omi.2011.0133openalex-snapshot
Clarifying Omics Concepts, Challenges, and Opportunities for Prunus Breeding in the Postgenomic Era
inferred← citeshttps://doi.org/10.1093/aob/mcaa133openalex-snapshot
Substantial intraspecific genome size variation in golden-brown algae and its phenotypic consequences
inferred← citeshttps://doi.org/10.1093/aob/mcs222openalex-snapshot
New reports of nuclear DNA content for 407 vascular plant taxa from the United States
inferred← citeshttps://doi.org/10.1093/aob/mcs297openalex-snapshot
Role of adaptive and non-adaptive mechanisms forming complex patterns of genome size variation in six cytotypes of polyploid Allium oleraceum (Amaryllidaceae) on a continental scale
inferred← citeshttps://doi.org/10.1093/aob/mcu189openalex-snapshot
Evolution of genome size and chromosome number in the carnivorous plant genus Genlisea (Lentibulariaceae), with a new estimate of the minimum genome size in angiosperms
inferred← citeshttps://doi.org/10.1093/aob/mcx079openalex-snapshot
Polyploidy and interspecific hybridization: partners for adaptation, speciation and evolution in plants
inferred← citeshttps://doi.org/10.1093/aob/mcy028openalex-snapshot
A reassessment of the genome size–invasiveness relationship in reed canarygrass (Phalaris arundinacea)
inferred← citeshttps://doi.org/10.1093/aob/mcy066openalex-snapshot
Analysis of retrotransposon abundance, diversity and distribution in holocentric Eleocharis (Cyperaceae) genomes
inferred← citeshttps://doi.org/10.1093/bfgp/elu005openalex-snapshot
Plant genome size variation: bloating and purging DNA
inferred← citeshttps://doi.org/10.1093/botlinnean/box052openalex-snapshot
Recent autopolyploidization in a naturalized population of Mimulus guttatus (Phrymaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/box101openalex-snapshot
Reconstruction of ancestral genome size in Pitcairnioideae (Bromeliaceae): what can genome size tell us about the evolutionary history of its five genera?
inferred← citeshttps://doi.org/10.1093/database/baz098openalex-snapshot
Progress in the study of genome size evolution in Asteraceae: analysis of the last update
inferred← citeshttps://doi.org/10.1093/nar/gkt1195openalex-snapshot
Recent updates and developments to plant genome size databases
inferred← citeshttps://doi.org/10.1093/plphys/kiaf203openalex-snapshot
Three transcription factors form an activation–inhibition module to regulate anthocyanin accumulation in Asiatic hybrid lilies
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaa135openalex-snapshot
The tight genome size of ants: diversity and evolution under ancestral state reconstruction and base composition
inferred← citeshttps://doi.org/10.1098/rsif.2013.1043openalex-snapshot
The energy components of stacked chromatin layers explain the morphology, dimensions and mechanical properties of metaphase chromosomes
inferred← citeshttps://doi.org/10.1101/2022.04.20.488976openalex-snapshot
Genome-wide identification and expression analysis of bHLH transcription factors reveal their putative regulatory effects on petal nectar spur development in Aquilegia
inferred← citeshttps://doi.org/10.1101/2024.04.14.589434openalex-snapshot
Chromosome-level baobab ( Adansonia digitata ) genome illuminates its evolutionary insights
inferred← citeshttps://doi.org/10.1101/2025.04.07.647530openalex-snapshot
Eukaryotes evade information storage-replication rate trade-off with endosymbiont assistance leading to larger genomes
inferred← citeshttps://doi.org/10.1101/351429openalex-snapshot
The genome and metabolome of the tobacco tree, Nicotiana glauca : a potential renewable feedstock for the bioeconomy
inferred← citeshttps://doi.org/10.1105/tpc.18.00606openalex-snapshot
Breaking Free: The Genomics of Allopolyploidy-Facilitated Niche Expansion in White Clover
inferred← citeshttps://doi.org/10.1111/1755-0998.12506openalex-snapshot
Optimization of AFLP for extremely large genomes over 70 Gb
inferred← citeshttps://doi.org/10.1111/boj.12027openalex-snapshot
Genome size variation in Orchidaceae subfamily Apostasioideae: filling the phylogenetic gap
inferred← citeshttps://doi.org/10.1111/boj.12226openalex-snapshot
Divergent genome sizes reflect the infrafamilial subdivision of the neotropical woody Marcgraviaceae
inferred← citeshttps://doi.org/10.1111/boj.12232openalex-snapshot
Evolutionary trends in Iridaceae: new cytogenetic findings from the New World
inferred← citeshttps://doi.org/10.1111/boj.12276openalex-snapshot
Is genome downsizing associated with diversification in polyploid lineages ofVeronica?
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01293.xopenalex-snapshot
Molecular phylogenetics of Paphiopedilum (Cypripedioideae; Orchidaceae) based on nuclear ribosomal ITS and plastid sequences
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04544.xopenalex-snapshot
Organisation of the plant genome in chromosomes
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03942.xopenalex-snapshot
Measurements of genomic GC content in plant genomes with flow cytometry: a test for reliability
inferred← citeshttps://doi.org/10.1111/jse.12310openalex-snapshot
Genome size variation and evolution in the grape family Vitaceae
inferred← citeshttps://doi.org/10.1111/njb.02337openalex-snapshot
Karyotype and genome size variation in Ajuga L. (Ajugoideae–Lamiaceae)
inferred← citeshttps://doi.org/10.1111/nph.12523openalex-snapshot
Reconstructing relative genome size of vascular plants through geological time
inferred← citeshttps://doi.org/10.1111/nph.12726openalex-snapshot
Adaptive and nonadaptive genome size evolution in Karst endemic flora of China
inferred← citeshttps://doi.org/10.1111/nph.12799openalex-snapshot
The contrasting effects of genome size, chromosome number and ploidy level on plant invasiveness: a global analysis
inferred← citeshttps://doi.org/10.1111/nph.13107openalex-snapshot
The hidden side of plant invasions: the role of genome size
inferred← citeshttps://doi.org/10.1111/nph.13191openalex-snapshot
The Chromosome Counts Database ( CCDB ) – a community resource of plant chromosome numbers
inferred← citeshttps://doi.org/10.1111/nph.13769openalex-snapshot
Testing the large genome constraint hypothesis: plant traits, habitat and climate seasonality in L iliaceae
inferred← citeshttps://doi.org/10.1111/nph.15996openalex-snapshot
Diversity in genome size and GC content shows adaptive potential in orchids and is closely linked to partial endoreplication, plant life‐history traits and climatic conditions
inferred← citeshttps://doi.org/10.1111/nph.70948openalex-snapshot
Warming‐induced miniaturization of plant community genome size in temperate grasslands over the last four decades
inferred← citeshttps://doi.org/10.1111/tpj.12048openalex-snapshot
Comparative analysis of genome composition in Triticeae reveals strong variation in transposable element dynamics and nucleotide diversity
inferred← citeshttps://doi.org/10.1111/tpj.15969openalex-snapshot
Mega‐sized pericentromeric blocks of simple telomeric repeats and their variants reveal patterns of chromosome evolution in ancient Cycadales genomes
inferred← citeshttps://doi.org/10.1111/tpj.16559openalex-snapshot
Testing the large genome constraint hypothesis in tropical rhizomatous herbs: life strategies, plant traits and habitat preferences in gingers
inferred← citeshttps://doi.org/10.11110/kjpt.2019.49.4.334openalex-snapshot
Genome size estimation of 43 Korean Carex
inferred← citeshttps://doi.org/10.1126/science.338.6108.758openalex-snapshot
Transposable Elements, Epigenetics, and Genome Evolution
inferred← citeshttps://doi.org/10.1134/s1062360420060041openalex-snapshot
Relationship of the Holoploid DNA Content with the Life Form and Duration of Plants’ Life Cycle
inferred← citeshttps://doi.org/10.1134/s2079059715030168openalex-snapshot
Repetitive DNA sequences in plant genomes
inferred← citeshttps://doi.org/10.1139/gen-2013-0041openalex-snapshot
Genome size increases in recently diverged hornwort clades
inferred← citeshttps://doi.org/10.1139/gen-2016-0011openalex-snapshot
Ribosomal DNA locus variation and REMAP analysis of the diploid and triploid complexes of Lilium lancifolium
inferred← citeshttps://doi.org/10.1139/gen-2019-0069openalex-snapshot
Relative genome size variation in the African agroforestry tree Parkia biglobosa (Fabaceae: Caesalpinioideae) and its relation to geography, population genetics, and morphology
inferred← citeshttps://doi.org/10.1139/gen-2021-0045openalex-snapshot
An 82 bp tandem repeat family typical of 3′ non-coding end of Gypsy/TAT LTR retrotransposons is conserved in Coffea spp. pericentromeres
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042916-041049openalex-snapshot
Novel Insights into Tree Biology and Genome Evolution as Revealed Through Genomics
inferred← citeshttps://doi.org/10.1155/2011/458684openalex-snapshot
Does Large Genome Size Limit Speciation in Endemic Island Floras?
inferred← citeshttps://doi.org/10.1155/2011/646198openalex-snapshot
The Genomes of All Angiosperms: A Call for a Coordinated Global Census
inferred← citeshttps://doi.org/10.1155/2018/9464592openalex-snapshot
Perspectives on Structural, Physiological, Cellular, and Molecular Responses to Desiccation in Resurrection Plants
inferred← citeshttps://doi.org/10.1186/1471-2164-14-356openalex-snapshot
Genomic analysis of the native European Solanum species, S. dulcamara
inferred← citeshttps://doi.org/10.1186/1471-2164-14-388openalex-snapshot
An integrated genetic linkage map for white clover (Trifolium repens L.) with alignment to Medicago
inferred← citeshttps://doi.org/10.1186/1471-2164-14-476openalex-snapshot
The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences
inferred← citeshttps://doi.org/10.1186/1471-2164-15-239openalex-snapshot
Characterization of the caleosin gene family in the Triticeae
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