| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | John F Y Brookfield | |
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Hot L1s account for the bulk of retrotransposition in the human population | Q22066292 | ||
| Selfish DNA: the ultimate parasite | Q22122417 | ||
| Selfish genes, the phenotype paradigm and genome evolution | Q22122418 | ||
| Genome size and extinction risk in vertebrates | Q28765431 | ||
| Differential alu mobilization and polymorphism among the human and chimpanzee lineages | Q28775829 | ||
| Mobile elements: drivers of genome evolution | Q29547669 | ||
| Role of transposable elements in heterochromatin and epigenetic control | Q29616253 | ||
| Origin of a substantial fraction of human regulatory sequences from transposable elements | Q29617225 | ||
| Molecular reconstruction of Sleeping Beauty, a Tc1-like transposon from fish, and its transposition in human cells | Q29617246 | ||
| High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
| Cytosine methylation and the ecology of intragenomic parasites | Q29618264 | ||
| LINE-mediated retrotransposition of marked Alu sequences | Q29618440 | ||
| Exon shuffling by L1 retrotransposition | Q29622913 | ||
| Strong selective sweep associated with a transposon insertion in Drosophila simulans. | Q30336352 | ||
| Transposable elements and host genome evolution | Q33890168 | ||
| Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome | Q33897588 | ||
| Allelic Heterogeneity in LINE-1 Retrotransposition Activity | Q33905345 | ||
| An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications | Q33906041 | ||
| Mobile elements and the human genome | Q33938490 | ||
| Transposable elements in mammals promote regulatory variation and diversification of genes with specialized functions | Q34268983 | ||
| Mobile elements and mammalian genome evolution. | Q34279041 | ||
| The evolutionary life history of P transposons: from horizontal invaders to domesticated neogenes | Q34341621 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| Fruit flies and humans respond differently to retrotransposons | Q34528988 | ||
| Estimates of the genomic mutation rate for detrimental alleles in Drosophila melanogaster | Q34645040 | ||
| Molecular resurrection of an extinct ancestral promoter for mouse L1. | Q35058895 | ||
| Retrotransposons provide an evolutionarily robust non-telomerase mechanism to maintain telomeres | Q35582993 | ||
| L1 (LINE-1) retrotransposon diversity differs dramatically between mammals and fish. | Q35617763 | ||
| Active Alu element "A-tails": size does matter | Q35786538 | ||
| High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes | Q35814612 | ||
| RNAi protects the Caenorhabditis elegans germline against transposition | Q35818458 | ||
| RIP: the evolutionary cost of genome defense | Q35864153 | ||
| How did alternative splicing evolve? | Q35930718 | ||
| Transposable elements as sources of variation in animals and plants | Q36010477 | ||
| Duplication, coclustering, and selection of human Alu retrotransposons | Q36017653 | ||
| Genome-wide comparative analysis of the transposable elements in the related species Arabidopsis thaliana and Brassica oleracea | Q37682144 | ||
| The population genetics of Drosophila transposable elements | Q38321781 | ||
| Alu-containing exons are alternatively spliced | Q39860930 | ||
| The Frog Prince: a reconstructed transposon from Rana pipiens with high transpositional activity in vertebrate cells | Q40315373 | ||
| Analysis of the human Alu Ya-lineage | Q40525133 | ||
| Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes | Q40554054 | ||
| The birth of an alternatively spliced exon: 3' splice-site selection in Alu exons | Q40645427 | ||
| Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system | Q41011364 | ||
| Modern thoughts on an ancyent marinere: function, evolution, regulation | Q41689471 | ||
| Non-LTR retrotransposons in the African malaria mosquito, Anopheles gambiae: unprecedented diversity and evidence of recent activity | Q42602529 | ||
| Pack-MULE transposable elements mediate gene evolution in plants | Q42637232 | ||
| Teleost fish genomes contain a diverse array of L1 retrotransposon lineages that exhibit a low copy number and high rate of turnover. | Q42640984 | ||
| Phylogenetic analysis of a retrotransposon with implications for strong evolutionary constraints on reverse transcriptase | Q42648307 | ||
| LINEs mobilize SINEs in the eel through a shared 3' sequence. | Q42687400 | ||
| A highly active synthetic mammalian retrotransposon | Q42828794 | ||
| RNA truncation by premature polyadenylation attenuates human mobile element activity | Q42833909 | ||
| A simple method for genome-wide screening for advantageous insertions of mobile DNAs in Escherichia coli | Q43996519 | ||
| Human Alu element retrotransposition induced by genotoxic stress | Q44632338 | ||
| Expression of the telomeric retrotransposon HeT-A in Drosophila melanogaster is correlated with cell proliferation | Q46044021 | ||
| Efficient induction and preparation of fusion proteins from recombinant phage lambda gt11 clones | Q46735744 | ||
| Evolution of genome size in Drosophila. is the invader's genome being invaded by transposable elements? | Q47183075 | ||
| A co-opted gypsy-type LTR-retrotransposon is conserved in the genomes of humans, sheep, mice, and rats | Q47378704 | ||
| Genomic analysis of Drosophila melanogaster telomeres: full-length copies of HeT-A and TART elements at telomeres | Q47427652 | ||
| Gene regulation: selfish elements make a mark | Q47580987 | ||
| S-element insertions are associated with the evolution of the Hsp70 genes in Drosophila melanogaster | Q48280058 | ||
| Taming of transposable elements by homology-dependent gene silencing. | Q50532962 | ||
| Mutator dynamics in fluctuating environments. | Q52043835 | ||
| Complex evolution of gypsy in Drosophilid species. | Q52648566 | ||
| Accumulation of transposable elements in the genome of Drosophila melanogaster is associated with a decrease in fitness. | Q52649366 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| The evolution of mutation rates: separating causes from consequences | Q55878709 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| Mutation accumulation and the effect of copia insertions in Drosophila melanogaster | Q57933469 | ||
| Transiently Beneficial Insertions Could Maintain Mobile DNA Sequences in Variable Environments | Q58416317 | ||
| The evolutionary dynamics of repetitive DNA in eukaryotes | Q59090793 | ||
| CpG Islands in Human X-Inactivation | Q62644519 | ||
| A novel approach for identifying candidate imprinted genes through sequence analysis of imprinted and control genes | Q62644545 | ||
| The distinguishing sequence characteristics of mouse imprinted genes | Q62644573 | ||
| On the role of unequal exchange in the containment of transposable element copy number | Q69851798 | ||
| Population dynamics of the copia, mdg1, mdg3, gypsy, and P transposable elements in a natural population of Drosophila melanogaster | Q72180669 | ||
| Alu: a parasite's parasite? | Q73882088 | ||
| Population genetics models of transposable elements | Q74081159 | ||
| Selfish DNA is maladaptive: evidence from the plant Red List | Q79224478 | ||
| P433 | issue | 2 | |
| P6104 | maintained by WikiProject | WikiProject Ecology | Q10818384 |
| P304 | page(s) | 128-136 | |
| P577 | publication date | 2005-02-01 | |
| P1433 | published in | Nature Reviews Genetics | Q1071824 |
| P1476 | title | The ecology of the genome - mobile DNA elements and their hosts | |
| P478 | volume | 6 |
| Q34386811 | A brief history of the status of transposable elements: from junk DNA to major players in evolution |
| Q91584454 | A genomic survey of transposable elements in the choanoflagellate Salpingoeca rosetta reveals selection on codon usage |
| Q43754238 | A novel application of ecological analyses to assess transposable element distributions in the genome of the domestic cow, Bos taurus. |
| Q42090483 | A synthetic biology approach allows inducible retrotransposition in whole plants |
| Q84906717 | A systematic search and classification of T2 family miniature inverted-repeat transposable elements (MITEs) in Xenopus tropicalis suggests the existence of recently active MITE subfamilies |
| Q52682425 | Abundant, diverse, and consequential P elements segregate in promoters of small heat-shock genes in Drosophila populations. |
| Q34044711 | Acytota - associated kingdom of neglected life |
| Q40097182 | Adaptive evolution of rhizobial symbiotic compatibility mediated by co-evolved insertion sequences. |
| Q35616849 | Applying ecological models to communities of genetic elements: the case of neutral theory |
| Q33575809 | Birth, death, and diversification of mobile promoters in prokaryotes |
| Q37677327 | Chromosomal replication dynamics and interaction with the β sliding clamp determine orientation of bacterial transposable elements. |
| Q33891788 | Computational methods for the analysis of primate mobile elements |
| Q60534777 | Conserved gene order belies rapid genome turnover: The dynamic interplay between genomic DNA and the outside world |
| Q33815667 | Considering transposable element diversification in de novo annotation approaches |
| Q48647191 | Convergent adaptive evolution in marginal environments: unloading transposable elements as a common strategy among mangrove genomes |
| Q100713252 | Copia retrotransposons of two disjunctive Panax species: P. ginseng and P. quinquefolius |
| Q33619213 | Copy number variation and transposable elements feature in recent, ongoing adaptation at the Cyp6g1 locus |
| Q33281083 | De novo identification of LTR retrotransposons in eukaryotic genomes |
| Q47434809 | Discovery of novel genes derived from transposable elements using integrative genomic analysis |
| Q30426258 | Distinguishing ecological from evolutionary approaches to transposable elements. |
| Q37575853 | Diversity, distribution, and significance of transposable elements in the genome of the only selfing hermaphroditic vertebrate Kryptolebias marmoratus |
| Q28727984 | Drosophila errantiviruses |
| Q35874389 | Dynamics of bacterial insertion sequences: can transposition bursts help the elements persist? |
| Q33470970 | Dynamics of transposable elements: towards a community ecology of the genome |
| Q36281102 | Ecological networks to unravel the routes to horizontal transposon transfers |
| Q28601408 | Enrichment analysis of Alu elements with different spatial chromatin proximity in the human genome |
| Q35982916 | Env-less endogenous retroviruses are genomic superspreaders |
| Q34618183 | Epigenomic plasticity within populations: its evolutionary significance and potential. |
| Q33290219 | Evolution of hydra, a recently evolved testis-expressed gene with nine alternative first exons in Drosophila melanogaster |
| Q34833252 | Evolutionary dynamics of retrotransposable elements Rex1, Rex3 and Rex6 in neotropical cichlid genomes. |
| Q33924878 | Evolutionary dynamics of retrotransposons assessed by high-throughput sequencing in wild relatives of wheat |
| Q41139114 | Evolutionary dynamics of retrotransposons following autopolyploidy in the Buckler Mustard species complex |
| Q37809269 | Evolutionary dynamics of transposable elements in a small RNA world |
| Q35750879 | Evolutionary transitions in the Asteraceae coincide with marked shifts in transposable element abundance. |
| Q36820014 | Exogenous gypsy insulator sequences modulate transgene expression in the malaria vector mosquito, Anopheles stephensi. |
| Q34137519 | Gene properties and chromatin state influence the accumulation of transposable elements in genes |
| Q38622812 | Genome size in arthropods; different roles of phylogeny, habitat and life history in insects and crustaceans |
| Q64064856 | Genome streamlining via complete loss of introns has occurred multiple times in lichenized fungal mitochondria |
| Q21266642 | Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus |
| Q34692463 | Genomic repeat abundances contain phylogenetic signal. |
| Q35622072 | HTT-DB: horizontally transferred transposable elements database |
| Q26747716 | Horizontal transfer - imperative mission of acellular life forms,Acytota |
| Q33334647 | How Athila retrotransposons survive in the Arabidopsis genome |
| Q42235273 | How does selfing affect the dynamics of selfish transposable elements? |
| Q38068090 | How important are transposons for plant evolution? |
| Q38668427 | In search of lost trajectories: Recovering the diversification of transposable elements |
| Q42705482 | Insertional polymorphism and antiquity of PDR1 retrotransposon insertions in pisum species. |
| Q92796876 | Insights into TLCΦ lysogeny: A twist in the mechanism of IMEX integration |
| Q37135161 | Integration target site selection by a resurrected human endogenous retrovirus |
| Q35195382 | Large-scale genomic analysis suggests a neutral punctuated dynamics of transposable elements in bacterial genomes. |
| Q36288596 | Long-term evolution of transposable elements |
| Q36000665 | Male germline control of transposable elements |
| Q36830873 | Microbial variome database: point mutations, adaptive or not, in bacterial core genomes |
| Q52613189 | Modeling Interactions between Transposable Elements and the Plant Epigenetic Response: A Surprising Reliance on Element Retention. |
| Q24817207 | Modeling the amplification dynamics of human Alu retrotransposons |
| Q55334623 | Multiple massive domestication and recent amplification of Kolobok superfamily transposons in the clawed frog Xenopus. |
| Q92219573 | Nested plant LTR retrotransposons target specific regions of other elements, while all LTR retrotransposons often target palindromes and nucleosome-occupied regions: in silico study |
| Q60146999 | Neutral Theory, Transposable Elements, and Eukaryotic Genome Evolution. |
| Q34782633 | Neutral theory predicts the relative abundance and diversity of genetic elements in a broad array of eukaryotic genomes |
| Q64079956 | Novel Insights into Plant Genome Evolution and Adaptation as Revealed through Transposable Elements and Non-Coding RNAs in Conifers |
| Q57163834 | POPULATION DYNAMICS OF TRANSPOSABLE ELEMENTS: COPY NUMBER REGULATION AND SPECIES INVASION REQUIREMENTS |
| Q28744450 | PiggyBac-ing on a primate genome: novel elements, recent activity and horizontal transfer |
| Q33618933 | Population dynamics of PIWI-interacting RNAs (piRNAs) and their targets in Drosophila |
| Q35083007 | Population genetics models of competition between transposable element subfamilies |
| Q39875107 | Preferential epigenetic suppression of the autonomous MusD over the nonautonomous ETn mouse retrotransposons |
| Q28652686 | RNA sociology: group behavioral motifs of RNA consortia |
| Q57288715 | Rapid expansion of a highly germline-expressed mariner element acquired by horizontal transfer in the fire ant genome |
| Q51180823 | Rapid structural and epigenetic reorganization near transposable elements in hybrid and allopolyploid genomes in Spartina. |
| Q83204283 | Recent transposition activity of Xenopus T2 family miniature inverted-repeat transposable elements |
| Q38937848 | Resolving fine-grained dynamics of retrotransposons: comparative analysis of inferential methods and genomic resources. |
| Q35611983 | Restless genomes humans as a model organism for understanding host-retrotransposable element dynamics |
| Q52680372 | Retrotransposon gtwin in the Drosophila melanogaster laboratory strain G-32: an increased number of copies of this element in the genome caused chromosomal aberration. |
| Q25255710 | Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line |
| Q26827477 | Retroviruses and the placenta |
| Q50214187 | Stochastic Predator-Prey Dynamics of Transposons in the Human Genome |
| Q34207726 | Structural and sequence diversity of the transposon Galileo in the Drosophila willistoni genome |
| Q35930322 | Survey sequencing reveals elevated DNA transposon activity, novel elements, and variation in repetitive landscapes among vesper bats. |
| Q22122020 | Synergy between sequence and size in Large-scale genomics |
| Q34335133 | Teaching an old dog new tricks: SINEs of canine genomic diversity |
| Q93221880 | Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell |
| Q38555824 | The DNA Habitat and its RNA Inhabitants: At the Dawn of RNA Sociology |
| Q52692382 | The hobo-related elements in the melanogaster species group. |
| Q28658097 | The holozoan Capsaspora owczarzaki possesses a diverse complement of active transposable element families |
| Q37412262 | The role of repetitive DNA in structure and evolution of sex chromosomes in plants. |
| Q34770063 | The struggle for life of the genome's selfish architects |
| Q30492223 | The tempo and mode of evolution of transposable elements as revealed by molecular phylogenies reconstructed from mosquito genomes |
| Q28756349 | Transposable elements and the evolution of regulatory networks |
| Q35996731 | Transposase interaction with the β sliding clamp: effects on insertion sequence proliferation and transposition rate |
| Q37982079 | Tropical Africa as a cradle for horizontal transfers of transposable elements between species of the genera Drosophila and Zaprionus |
| Q91841209 | Variation in base composition underlies functional and evolutionary divergence in non-LTR retrotransposons |
| Q42642146 | Virus-like particle formation and translational start site choice of the plant retrotransposon Tto1. |
| Q37207183 | Widespread evidence for horizontal transfer of transposable elements across Drosophila genomes |
| Q52701237 | hAT transposable elements and their derivatives: an analysis in the 12 Drosophila genomes. |
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