scholarly article | Q13442814 |
P50 | author | Nicholas W Jeffery | Q56333613 |
P2093 | author name string | France Dufresne | |
P2860 | cites work | C value and cell volume: their significance in the evolution and development of amphibians | Q71071100 |
Interspecific variability of DNA content in Amphibia | Q71417645 | ||
Retrotransposon BARE-1 and Its Role in Genome Evolution in the Genus Hordeum | Q72994180 | ||
Larger genomes for molluskan land pioneers | Q73507172 | ||
Patterns and rates of indel evolution in processed pseudogenes from humans and murids | Q74166748 | ||
Testing genome complexity | Q79934669 | ||
Amphipod genome sizes: first estimates for Arctic species reveal genomic giants | Q80422856 | ||
Evidence for DNA Loss as a Determinant of Genome Size | Q21038813 | ||
Initial sequencing and analysis of the human genome | Q21045365 | ||
Two rounds of whole genome duplication in the ancestral vertebrate | Q21090230 | ||
Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis | Q21092720 | ||
Polyploid Incidence and Evolution | Q22065392 | ||
Genome sequence of Aedes aegypti, a major arbovirus vector | Q22065874 | ||
The C-value enigma in plants and animals: a review of parallels and an appeal for partnership | Q22066092 | ||
Draft genome of the globally widespread and invasive Argentine ant (Linepithema humile) | Q22066296 | ||
Synergy between sequence and size in Large-scale genomics | Q22122020 | ||
The sequence and de novo assembly of the giant panda genome | Q22122211 | ||
Genome analysis of the platypus reveals unique signatures of evolution | Q22122225 | ||
DNA loss and evolution of genome size in Drosophila | Q22122458 | ||
DNA repeat arrays in chicken and human genomes and the adaptive evolution of avian genome size | Q24804338 | ||
What can you do with 0.1× genome coverage? A case study based on a genome survey of the scuttle fly Megaselia scalaris (Phoridae) | Q27489427 | ||
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 | ||
Happy together: the life and times of Ty retrotransposons and their hosts | Q28266629 | ||
The impact of next-generation sequencing technology on genetics | Q28268088 | ||
The large genome constraint hypothesis: evolution, ecology and phenotype | Q28651140 | ||
Bursts and horizontal evolution of DNA transposons in the speciation of pseudotetraploid salmonids | Q28755949 | ||
The desoxyribonucleic acid content of animal cells and its evolutionary significance | Q28756221 | ||
Evolutionary dynamics of transposable elements in the short-tailed opossum Monodelphis domestica | Q28757513 | ||
A transposon-based strategy for sequencing repetitive DNA in eukaryotic genomes | Q28776464 | ||
A BIRD'S-EYE VIEW OF THE C-VALUE ENIGMA: GENOME SIZE, CELL SIZE, AND METABOLIC RATE IN THE CLASS AVES | Q29394267 | ||
Molecular evidence for an ancient duplication of the entire yeast genome | Q29547472 | ||
The origins of genome complexity | Q29547507 | ||
A whole-genome assembly of Drosophila | Q29616863 | ||
Small RNAs as guardians of the genome | Q29617221 | ||
Evolutionary inventions and continuity of CORE-SINEs in mammals | Q42624526 | ||
Teleost fish genomes contain a diverse array of L1 retrotransposon lineages that exhibit a low copy number and high rate of turnover. | Q42640984 | ||
Evolution of the genome and cell sizes in salamanders | Q43647808 | ||
Survey of genome size in 28 hydrothermal vent species covering 10 families | Q44004598 | ||
DNA content, ribosomal gene multiplicity, and cell size in fish | Q44305446 | ||
Cellular DNA content of the Mollusca | Q44925565 | ||
Large genomes among caridean shrimp | Q44975828 | ||
Tiny genomes and endoreduplication in Strepsiptera | Q45154132 | ||
Intron size and genome size in plants | Q47175193 | ||
Evolution of genome size: new approaches to an old problem | Q47220744 | ||
Nucleotypic effects without nuclei: genome size and erythrocyte size in mammals | Q47225383 | ||
Copepod development rates in relation to genome size and 18S rDNA copy number | Q47225392 | ||
Genome size diversity in the family Drosophilidae | Q47231071 | ||
Evolutionary implications of the relationship between genome size and body size in flatworms and copepods | Q47241976 | ||
Intron-genome size relationship on a large evolutionary scale | Q47258179 | ||
Genome size and intron size in Drosophila | Q47288037 | ||
The size differences among mammalian introns are due to the accumulation of small deletions | Q47328011 | ||
The nucleotypic effects of cellular DNA content in cartilaginous and ray-finned fishes | Q47382908 | ||
Genome size and chromatin condensation in vertebrates | Q47395442 | ||
The evolutionary dynamics of autonomous non-LTR retrotransposons in the lizard Anolis carolinensis shows more similarity to fish than mammals. | Q50594942 | ||
Mechanisms and rates of genome expansion and contraction in flowering plants. | Q52115877 | ||
High mutation rate and predominance of insertions in the Caenorhabditis elegans nuclear genome. | Q52965913 | ||
Nuclear DNA amounts in crustacea | Q54767479 | ||
Genome-size evolution in fishes | Q56983664 | ||
Genome size estimates for some oligochaete annelids | Q56983722 | ||
Genome size variation in aphids | Q56984005 | ||
Genome downsizing in polyploid plants | Q57067661 | ||
DNA endoreduplication and polyteny understood as evolutionary strategies | Q59085679 | ||
Changes in the Amount of DNA in Cell Nuclei during Vertebrate Evolution | Q59085694 | ||
Small genomes for better flyers | Q59096723 | ||
Differences in the processing of DNA ends in Arabidopsis thaliana and tobacco: possible implications for genome evolution | Q64387585 | ||
Nuclear DNA amounts in pacific Crustacea | Q69599603 | ||
Relationships between DNA content and cell morphometric parameters in reptiles | Q70364865 | ||
Estimation of synteny conservation and genome compaction between pufferfish (Fugu) and human | Q30649558 | ||
Insertion-deletion biases and the evolution of genome size | Q30827086 | ||
C-value estimates for 31 species of ladybird beetles (Coleoptera: Coccinellidae). | Q33200851 | ||
The time and duration of meiosis | Q33341816 | ||
Sequencing the genome of the Atlantic salmon (Salmo salar). | Q33708187 | ||
Paleogenomic data suggest mammal-like genome size in the ancestral amniote and derived large genome size in amphibians. | Q33751716 | ||
Transposable elements and the evolution of eukaryotic genomes | Q34000882 | ||
The role of transposable elements in the evolution of non-mammalian vertebrates and invertebrates | Q34024461 | ||
Deletions in processed pseudogenes accumulate faster in rodents than in humans | Q34427987 | ||
Genome size and developmental complexity | Q34790119 | ||
Transposable elements and the evolution of genome size in eukaryotes | Q34790131 | ||
Genomic insight into the common carp (Cyprinus carpio) genome by sequencing analysis of BAC-end sequences | Q34871477 | ||
A Sanger/pyrosequencing hybrid approach for the generation of high-quality draft assemblies of marine microbial genomes | Q34983920 | ||
Genome Size Evolution in Pufferfish: A Comparative Analysis of Diodontid and Tetraodontid Pufferfish Genomes | Q35021831 | ||
AVID: A global alignment program | Q35023871 | ||
A contiguous 66-kb barley DNA sequence provides evidence for reversible genome expansion. | Q35028669 | ||
L1 (LINE-1) retrotransposon diversity differs dramatically between mammals and fish. | Q35617763 | ||
The mode and tempo of genome size evolution in eukaryotes. | Q35757863 | ||
Transposable elements in sexual and ancient asexual taxa | Q35845955 | ||
Hox clusters as models for vertebrate genome evolution | Q36168876 | ||
Stress activation and genomic impact of Tnt1 retrotransposons in Solanaceae | Q36225302 | ||
Transposable elements, gene creation and genome rearrangement in flowering plants | Q36283968 | ||
Analysis of Drosophila species genome size and satellite DNA content reveals significant differences among strains as well as between species | Q36287893 | ||
Anthocyanin inhibits propidium iodide DNA fluorescence in Euphorbia pulcherrima: implications for genome size variation and flow cytometry | Q37260715 | ||
Genome size reduction in the chicken has involved massive loss of ancestral protein-coding genes | Q37291092 | ||
Evolutionary dynamics of transposable elements in a small RNA world | Q37809269 | ||
The population genetics of Drosophila transposable elements | Q38321781 | ||
High rate of DNA loss in the Drosophila melanogaster and Drosophila virilis species groups | Q38553095 | ||
NUCLEOTYPIC EFFECT IN HOMEOTHERMS: BODY-MASS INDEPENDENT RESTING METABOLIC RATE OF PASSERINE BIRDS IS RELATED TO GENOME SIZE. | Q38751750 | ||
Cell size and the concept of wasteful and frugal evolutionary strategies | Q39502814 | ||
Nuclear DNA content and minimum generation time in herbaceous plants | Q39907465 | ||
Specific gene amplification in oocytes. Oocyte nuclei contain extrachromosomal replicas of the genes for ribosomal RNA. | Q39969348 | ||
Nucleotype and cell size in vertebrates: a review | Q40165474 | ||
On the evolution of genome size of birds | Q41170154 | ||
NUCLEOTYPIC EFFECT IN HOMEOTHERMS: BODY-MASS-CORRECTED BASAL METABOLIC RATE OF MAMMALS IS RELATED TO GENOME SIZE. | Q42510503 | ||
Sequence organization and conservation in sh2/a1-homologous regions of sorghum and rice. | Q42580747 | ||
P433 | issue | 7 | |
P304 | page(s) | 925-938 | |
P577 | publication date | 2011-10-01 | |
P1433 | published in | Chromosome Research | Q15765850 |
P1476 | title | A guided tour of large genome size in animals: what we know and where we are heading | |
P478 | volume | 19 |
Q34064879 | A generalized mechanistic codon model |
Q35665304 | A population genomic scan in Chorthippus grasshoppers unveils previously unknown phenotypic divergence |
Q33924790 | Association of intron loss with high mutation rate in Arabidopsis: implications for genome size evolution |
Q28652789 | Comparative analysis of transposable elements highlights mobilome diversity and evolution in vertebrates |
Q35011169 | Development, validation and high-throughput analysis of sequence markers in nonmodel species. |
Q64108996 | Draft genomes expand our view of ant genome size variation across climate gradients |
Q90145590 | Ecological constraints associated with genome size across salamander lineages |
Q51833620 | Evolutionary characterization of Ty3/gypsy-like LTR retrotransposons in the parasitic cestode Echinococcus granulosus. |
Q39487869 | Genome size and chromosome number in velvet worms (Onychophora). |
Q44999841 | Genome size estimates for crustaceans using Feulgen image analysis densitometry of ethanol-preserved tissues. |
Q90215770 | Genome size estimation of brackishwater fishes and penaeid shrimps by flow cytometry |
Q45800365 | Genome size evolution: patterns, mechanisms, and methodological advances |
Q38012958 | Genome size evolution: sizing mammalian genomes |
Q38622812 | Genome size in arthropods; different roles of phylogeny, habitat and life history in insects and crustaceans |
Q42281825 | Genome size variation in deep-sea amphipods. |
Q40097004 | Information in the Biosphere: Biological and Digital Worlds. |
Q28727429 | Large-scale transcriptome analysis of retroelements in the migratory locust, Locusta migratoria |
Q46421120 | Nuclear DNA content correlates with depth, body size, and diversification rate in amphipod crustaceans from ancient Lake Baikal, Russia. |
Q28591470 | Para-allopatry in hybridizing fire-bellied toads (Bombina bombina and B. variegata): Inference from transcriptome-wide coalescence analyses |
Q38358515 | The Genome 10K Project: a way forward |
Q89972258 | Triploidy in zebrafish larvae: Effects on gene expression, cell size and cell number, growth, development and swimming performance |
Q36064318 | What's in a genome? The C-value enigma and the evolution of eukaryotic genome content |
Search more.