| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | T. Ryan Gregory | Q7668648 |
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Polyploid Incidence and Evolution | Q22065392 | ||
| A revised six-kingdom system of life | Q22065662 | ||
| The Genome Sequence of the Malaria Mosquito Anopheles gambiae | Q22065828 | ||
| Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes | Q22065831 | ||
| Evolution of DNA amounts across land plants (embryophyta) | Q22066091 | ||
| Analysis of the genome sequence of the flowering plant Arabidopsis thaliana | Q22122387 | ||
| Selfish DNA: the ultimate parasite | Q22122417 | ||
| Selfish genes, the phenotype paradigm and genome evolution | Q22122418 | ||
| Genome evolution in polyploids | Q22122457 | ||
| Initial sequencing and comparative analysis of the mouse genome | Q22122521 | ||
| The constancy of desoxyribose nucleic acid in plant nuclei | Q24519271 | ||
| Somatic polyploidization and cellular proliferation drive body size evolution in nematodes | Q24658321 | ||
| B-chromosome evolution | Q24676371 | ||
| Extensive genomic duplication during early chordate evolution | Q27104011 | ||
| Genome sequence of the nematode C. elegans: a platform for investigating biology | Q27860527 | ||
| The genome sequence of Drosophila melanogaster | Q27860796 | ||
| Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma | Q28185889 | ||
| A bird's-eye view of the C-value enigma: genome size, cell size, and metabolic rate in the class aves | Q28210020 | ||
| From pixels to picograms: a beginners' guide to genome quantification by Feulgen image analysis densitometry | Q28218299 | ||
| The large genome constraint hypothesis: evolution, ecology and phenotype | Q28651140 | ||
| Nuclear DNA content estimates in multicellular green, red and brown algae: phylogenetic considerations | Q28651144 | ||
| The desoxyribonucleic acid content of animal cells and its evolutionary significance | Q28756221 | ||
| Discovery of tetraploidy in a mammal | Q29013058 | ||
| Stomatal size in fossil plants: evidence for polyploidy in majority of angiosperms | Q29547784 | ||
| Genome size and the accumulation of simple sequence repeats: implications of new data from genome sequencing projects | Q30715117 | ||
| Intron size and genome size in plants | Q47175193 | ||
| Genome size and developmental parameters in the homeothermic vertebrates | Q47175681 | ||
| Slow but Steady: Reduction of Genome Size through Biased Mutation | Q47177532 | ||
| Evolution of genome size: new approaches to an old problem | Q47220744 | ||
| Nucleotypic effects without nuclei: genome size and erythrocyte size in mammals | Q47225383 | ||
| Evolutionary implications of the relationship between genome size and body size in flatworms and copepods | Q47241976 | ||
| Genome size of man and animals relative to the plant Allium cepa | Q47247029 | ||
| Intron-genome size relationship on a large evolutionary scale | Q47258179 | ||
| Genome size and intron size in Drosophila | Q47288037 | ||
| Size differences between human X and Y spermatozoa and prefertilization diagnosis | Q47317314 | ||
| Genome size and karyotype length in some interstitial polychaete species of the genus Ophryotrocha (Dorvilleidae). | Q47389579 | ||
| Intra- and interspecific genome-size variation in the Salmonidae | Q47419361 | ||
| Nonadditive changes in genome size during allopolyploidization in the wheat (aegilops-triticum) group | Q47450196 | ||
| The correlation between rDNA copy number and genome size in eukaryotes | Q48000583 | ||
| Mechanisms and rates of genome expansion and contraction in flowering plants. | Q52115877 | ||
| Do Plants Have a One-Way Ticket to Genomic Obesity? | Q58045061 | ||
| Reply | Q58045074 | ||
| Genetic stock assessment of spawning arctic cisco (Coregonus autumnalis) populations by flow cytometric determination of DNA content | Q70162588 | ||
| Unusual features of the urodele genome: do they have a role in evolution and development? | Q71698514 | ||
| Algae: Amounts of DNA and Organic Carbon in Single Cells | Q72494402 | ||
| Difference in volume of X- and Y-chromosome-bearing bovine sperm heads matches difference in DNA content | Q73163411 | ||
| Mammalian sperm morphometry | Q74218610 | ||
| Feast and famine in plant genomes | Q74630698 | ||
| The desoxyribose nucleic acid content of animal nuclei | Q80763959 | ||
| ??? | Q28262074 | ||
| Insertion-deletion biases and the evolution of genome size | Q30827086 | ||
| Is small indel bias a determinant of genome size? | Q30980345 | ||
| Horsetails and ferns are a monophyletic group and the closest living relatives to seed plants. | Q30981847 | ||
| C-value estimates for 31 species of ladybird beetles (Coleoptera: Coccinellidae). | Q33200851 | ||
| The modulation of DNA content: proximate causes and ultimate consequences | Q33595936 | ||
| Plant retrotransposons | Q33847714 | ||
| The bigger the C-value, the larger the cell: genome size and red blood cell size in vertebrates | Q34108746 | ||
| Comparisons with Caenorhabditis (approximately 100 Mb) and Drosophila (approximately 175 Mb) using flow cytometry show genome size in Arabidopsis to be approximately 157 Mb and thus approximately 25% larger than the Arabidopsis genome initiative est | Q34184796 | ||
| Molecular melodies in high and low C. | Q34186655 | ||
| Perspective: transposable elements, parasitic DNA, and genome evolution | Q34192362 | ||
| Are all fishes ancient polyploids? | Q34210327 | ||
| Mechanisms of recent genome size variation in flowering plants | Q34582833 | ||
| Genome reduction in a hemiclonal frog Rana esculenta from radioactively contaminated areas. | Q34606477 | ||
| The DNA content of sperm of Drosophila melanogaster | Q34704536 | ||
| Mutational equilibrium model of genome size evolution | Q34776798 | ||
| Genome size and developmental complexity | Q34790119 | ||
| Transposable elements and the evolution of genome size in eukaryotes | Q34790131 | ||
| Is "junk" DNA mostly intron DNA? | Q35030102 | ||
| Genome evolution of wild barley (Hordeum spontaneum) by BARE-1 retrotransposon dynamics in response to sharp microclimatic divergence. | Q35789298 | ||
| Intraspecific variation in genome size in angiosperms: identifying its existence | Q35982449 | ||
| Retrotransposon-mediated genome evolution on a local ecological scale | Q36102660 | ||
| The genetic organization of chromosomes | Q36227854 | ||
| Influence of light on DNA content of Helianthus annuus Linnaeus | Q37319090 | ||
| Nuclear DNA amounts in angiosperms | Q39100593 | ||
| Cell size and the concept of wasteful and frugal evolutionary strategies | Q39502814 | ||
| Genome size reduction through illegitimate recombination counteracts genome expansion in Arabidopsis | Q39860924 | ||
| Nuclear DNA content and minimum generation time in herbaceous plants | Q39907465 | ||
| A survey of DNA content per cell and per chromosome of prokaryotic and eukaryotic organisms: some evolutionary considerations | Q39917042 | ||
| The Structure and Function of Chromatin | Q39928800 | ||
| Skeletal DNA and the evolution of genome size | Q40335452 | ||
| Genome sizes of spiders | Q40568291 | ||
| Nonspecific resistance and the DNA content in the genome of amphibians | Q40766897 | ||
| Evolution of Genome Size by DNA Doublings | Q41077149 | ||
| NUCLEOTYPIC EFFECT IN HOMEOTHERMS: BODY-MASS-CORRECTED BASAL METABOLIC RATE OF MAMMALS IS RELATED TO GENOME SIZE. | Q42510503 | ||
| Intraspecific variation in nuclear DNA content among world populations of a mosquito, Aedes albopictus (Skuse). | Q42997677 | ||
| Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide | Q43008592 | ||
| PHENOTYPIC CORRELATES OF GENOME SIZE VARIATION IN AEDES ALBOPICTUS. | Q43039135 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 133-46 | |
| P577 | publication date | 2005-01-01 | |
| P1433 | published in | Annals of Botany | Q1821243 |
| P1476 | title | The C-value enigma in plants and animals: a review of parallels and an appeal for partnership | |
| P478 | volume | 95 |
| Q37951390 | A guided tour of large genome size in animals: what we know and where we are heading. |
| Q33924790 | Association of intron loss with high mutation rate in Arabidopsis: implications for genome size evolution |
| Q36560882 | Can resource costs of polyploidy provide an advantage to sex? |
| Q35026956 | Cell size and cancer: a new solution to Peto's paradox? |
| Q35781250 | Chromosomal distribution and evolution of abundant retrotransposons in plants: gypsy elements in diploid and polyploid Brachiaria forage grasses |
| Q55653163 | Comparative cytogenetics and derived phylogenic relationship among Sitophilus grain weevils (Coleoptera, Curculionidae, Dryophthorinae). |
| Q33436057 | DIRS1-like retrotransposons are widely distributed among Decapoda and are particularly present in hydrothermal vent organisms |
| Q46892823 | DNA content in South American endemic species of Lathyrus |
| Q37500266 | DNA content variation and its significance in the evolution of the genus Micrasterias (Desmidiales, Streptophyta). |
| Q47369552 | Differences in genome size between closely related species: the Drosophila melanogaster species subgroup |
| Q52314285 | Divergent genome evolution caused by regional variation in DNA gain and loss between human and mouse. |
| Q33862468 | Does variation in genome sizes reflect adaptive or neutral processes? New clues from Passiflora |
| Q42912789 | Drosophila Females Undergo Genome Expansion after Interspecific Hybridization |
| Q33334443 | EST analysis of Ostreococcus lucimarinus, the most compact eukaryotic genome, shows an excess of introns in highly expressed genes |
| Q36539208 | Effects of polyploidy and reproductive mode on life history trait expression |
| Q47374034 | Endopolyploidy, genome size, and flow cytometry. |
| Q28651821 | Environmental adaptation in stomatal size independent of the effects of genome size |
| Q36830697 | Epigenetic inheritance in plants. |
| Q24631846 | Estimates of nuclear DNA content in 98 species of brown algae (Phaeophyta) |
| Q35828311 | Estimates of nuclear DNA content in red algal lineages |
| Q60305442 | Evaluation and Recommendations for Routine Genotyping Using Skim Whole Genome Re-sequencing in Canola |
| Q22066091 | Evolution of DNA amounts across land plants (embryophyta) |
| Q50547618 | Evolutionary Growth of Genome Representations on Artificial Cellular Organisms with Indirect Encodings |
| Q46933463 | Evolutionary comparisons of miRNA regulation system in six model organisms |
| Q28654471 | Evolutionary constraints or opportunities? |
| Q37948969 | Genetic variation and DNA replication timing, or why is there late replicating DNA? |
| Q38562840 | Genome Biology and the Evolution of Cell-Size Diversity |
| Q37433823 | Genome Sizes of Nine Insect Species Determined by Flow Cytometry and k-mer Analysis |
| Q50986417 | Genome size correlates with reproductive fitness in seed beetles |
| Q28749369 | Genome size evolution in relation to leaf strategy and metabolic rates revisited |
| Q47172937 | Genome size of 14 species of fireflies (Insecta, Coleoptera, Lampyridae). |
| Q47363102 | Genome size of two cebus species (primates: platyrrhini) with a fertile hybrid and their quantitative genomic differences |
| Q111629525 | Genome size variation and evolution in the grape family Vitaceae |
| Q38067391 | Genome size variation and incidence of polyploidy in Scrophulariaceae sensu lato from the Iberian Peninsula |
| Q41496400 | Genome size variation in diploid and tetraploid wild wheats |
| Q41905354 | Genome size variation in the genus Carthamus (Asteraceae, Cardueae): systematic implications and additive changes during allopolyploidization. |
| Q31161088 | Genome size, cytogenetic data and transferability of EST-SSRs markers in wild and cultivated species of the genus Theobroma L. (Byttnerioideae, Malvaceae). |
| Q38283784 | Genomic characterization of Neoparamoeba pemaquidensis (Amoebozoa) and its kinetoplastid endosymbiont. |
| Q46306588 | Genotyping-by-sequencing through transcriptomics: implementation in a range of crop species with varying reproductive habits and ploidy levels. |
| Q83730385 | Giant yeast cells with nonrecyclable ribonucleotide reductase |
| Q41870357 | Global DNA cytosine methylation as an evolving trait: phylogenetic signal and correlated evolution with genome size in angiosperms |
| Q58652478 | Heavy Metal Pollution, Selection, and Genome Size: The Species of the Žerjav Study Revisited with Flow Cytometry |
| Q42186756 | Large-scale structure of genomic methylation patterns |
| Q28727429 | Large-scale transcriptome analysis of retroelements in the migratory locust, Locusta migratoria |
| Q34460544 | Mediterranean species of Caulerpa are polyploid with smaller genomes in the invasive ones |
| Q93529408 | NEW CHROMOSOME COUNTS IN OLD WORLD GESNERIACEAE: NUMBERS FOR SPECIES HITHERTO REGARDED ASCHIRITA, AND THEIR SYSTEMATIC AND EVOLUTIONARY SIGNIFICANCE |
| Q46424958 | Nuclear DNA content and chromosome number in some diploid and tetraploid Centaurea (Asteraceae: Cardueae) from the Dalmatia region |
| Q24649889 | Nuclear DNA content estimates in green algal lineages: chlorophyta and streptophyta |
| Q37306901 | Nuclear DNA content in Miscanthus sp. and the geographical variation pattern in Miscanthus lutarioriparius |
| Q83116340 | Nuclear DNA content variation associated with muscle fiber hypertrophic growth in fishes |
| Q41848220 | Nuclear DNA content variation in life history phases of the Bonnemasoniaceae (Rhodophyta). |
| Q34584128 | Nuclear DNA variation, chromosome numbers and polyploidy in the endemic and indigenous grass flora of New Zealand |
| Q42083247 | Nutrient reserves may allow for genome size increase: evidence from comparison of geophytes and their sister non-geophytic relatives |
| Q28069974 | Odonata (dragonflies and damselflies) as a bridge between ecology and evolutionary genomics |
| Q53585239 | Peculiar behavior of distinct chromosomal DNA elements during and after development in the dicyemid mesozoan Dicyema japonicum. |
| Q35982441 | Plant genome size research: a field in focus |
| Q38821202 | Put your 3D glasses on: plant chromatin is on show. |
| Q58652463 | Recent Insights into Mechanisms of Genome Size Change in Plants |
| Q44957192 | Reliable DNA ploidy determination in dehydrated tissues of vascular plants by DAPI flow cytometry--new prospects for plant research |
| Q33268637 | Retrotransposons and tandem repeat sequences in the nuclear genomes of cryptomonad algae |
| Q43242118 | 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 |
| Q47173451 | Selective significance of genome size in a plant community with heavy metal pollution |
| Q47557398 | Single-Cell Genomic Analysis in Plants. |
| Q64889554 | Small, but surprisingly repetitive genomes: transposon expansion and not polyploidy has driven a doubling in genome size in a metazoan species complex. |
| Q56225768 | Somatic meiosis in the life history ofBonnemaisonia asparagoidesandBonnemaisonia clavata(Bonnemaisoniales, Rhodophyta) from the Iberian peninsula |
| Q111629573 | Substrate switches, phenotypic innovations and allopatric speciation formed taxonomic diversity within the lichen genus Blastenia |
| Q44004598 | Survey of genome size in 28 hydrothermal vent species covering 10 families |
| Q22122020 | Synergy between sequence and size in Large-scale genomics |
| Q38358515 | The Genome 10K Project: a way forward |
| Q36752676 | The choice of model organisms in evo-devo |
| Q35757863 | The mode and tempo of genome size evolution in eukaryotes. |
| Q36299551 | The mode and tempo of genome size evolution in the subgenus Sophophora |
| Q91028357 | Variations in genome size between wild and domesticated lineages of fowls belonging to the Gallus gallus species |
| Q33565173 | Why assembling plant genome sequences is so challenging |
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