review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1000128333 |
P356 | DOI | 10.1186/1745-6150-6-19 |
P932 | PMC publication ID | 3072357 |
P698 | PubMed publication ID | 21414203 |
P5875 | ResearchGate publication ID | 50418993 |
P50 | author | Arnaud Le Rouzic | Q51650417 |
Thibaud S Boutin | Q56885255 | ||
Pierre Capy | Q87814617 | ||
P2093 | author name string | Jonathan Filée | |
Aurélie Hua-Van | |||
P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
RAG1 core and V(D)J recombination signal sequences were derived from Transib transposons | Q21092810 | ||
Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing | Q21144998 | ||
Recurrent insertion and duplication generate networks of transposable element sequences in the Drosophila melanogaster genome | Q21184150 | ||
Exaptation of an ancient Alu short interspersed element provides a highly conserved vitamin D-mediated innate immune response in humans and primates | Q21283760 | ||
Doubling genome size without polyploidization: dynamics of retrotransposition-driven genomic expansions in Oryza australiensis, a wild relative of rice | Q22065740 | ||
Massive Horizontal Gene Transfer in Bdelloid Rotifers | Q22065861 | ||
Transgenerational Epigenetic Inheritance: Prevalence, Mechanisms, and Implications for the Study of Heredity and Evolution | Q22066105 | ||
Heterochromatin protein 1 interacts with 5'UTR of transposable element ZAM in a sequence-specific fashion. | Q51581185 | ||
Genome-wide analysis of transposon insertion polymorphisms reveals intraspecific variation in cultivated rice. | Q51682948 | ||
Genome ecosystem and transposable elements species. | Q51716087 | ||
Wake up of transposable elements following Drosophila simulans worldwide colonization. | Q52573037 | ||
Accumulation of transposable elements in the genome of Drosophila melanogaster is associated with a decrease in fitness. | Q52649366 | ||
Recurrent recruitment of the THAP DNA-binding domain and molecular domestication of the P-transposable element. | Q52653717 | ||
Insertional polymorphism of a non-LTR mobile element (NLRCth1) in European populations of Chironomus riparius (Diptera, Chironomidae) as detected by transposon insertion display. | Q52654468 | ||
Abundant, diverse, and consequential P elements segregate in promoters of small heat-shock genes in Drosophila populations. | Q52682425 | ||
Gene regulation in evolution: a history. | Q53121570 | ||
A comparative study of retrotransposons in the centromeric regions of A and B chromosomes of maize. | Q53662232 | ||
Vertebrate DNA transposon as a natural mutator: the medaka fish Tol2 element contributes to genetic variation without recognizable traces. | Q54603948 | ||
Insights into the evolution of Yersinia pestis through whole-genome comparison with Yersinia pseudotuberculosis | Q22066387 | ||
Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans | Q22122205 | ||
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 | ||
The genome sequence of the filamentous fungus Neurospora crassa | Q22122516 | ||
Initial sequencing and comparative analysis of the mouse genome | Q22122521 | ||
Syncytin is a captive retroviral envelope protein involved in human placental morphogenesis | Q22253248 | ||
The SET domain protein Metnase mediates foreign DNA integration and links integration to nonhomologous end-joining repair | Q24298284 | ||
Selfish DNA: a sexually-transmitted nuclear parasite | Q24532152 | ||
The Saccharomyces retrotransposon Ty5 influences the organization of chromosome ends | Q24544047 | ||
Behavior of restriction-modification systems as selfish mobile elements and their impact on genome evolution | Q24555229 | ||
Evolution of hybrid dysgenesis determinants in Drosophila melanogaster | Q24601107 | ||
Origins and evolution of eukaryotic RNA interference | Q24647077 | ||
The evolution of RNAi as a defence against viruses and transposable elements | Q24651901 | ||
On the origin and functions of RNA-mediated silencing: from protists to man | Q24657546 | ||
sigmaB regulates IS256-mediated Staphylococcus aureus biofilm phenotypic variation | Q24680463 | ||
Distinct mechanisms determine transposon inheritance and methylation via small interfering RNA and histone modification | Q24800187 | ||
Evidence for the adaptive significance of an LTR retrotransposon sequence in a Drosophila heterochromatic gene | Q24806427 | ||
Paucity of chimeric gene-transposable element transcripts in the Drosophila melanogaster genome | Q24815141 | ||
RNA regulation of epigenetic processes | Q28109351 | ||
The complex language of chromatin regulation during transcription | Q28131748 | ||
Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi | Q28218870 | ||
Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms | Q28246746 | ||
Alu-SINE exonization: en route to protein-coding function | Q28251519 | ||
Mobile DNA and evolution in the 21st century | Q28748605 | ||
New superfamilies of eukaryotic DNA transposons and their internal divisions | Q28751928 | ||
Multiple waves of recent DNA transposon activity in the bat, Myotis lucifugus | Q28754842 | ||
Convergent domestication of pogo-like transposases into centromere-binding proteins in fission yeast and mammals | Q28755338 | ||
Transposable elements and the evolution of regulatory networks | Q28756349 | ||
RNAi: a defensive RNA-silencing against viruses and transposable elements. | Q34478583 | ||
Mobile elements as a combination of functional modules. | Q34499476 | ||
Natural genetic variation caused by transposable elements in humans | Q34569749 | ||
The first steps of transposable elements invasion: parasitic strategy vs. genetic drift | Q34570688 | ||
Mavericks, a novel class of giant transposable elements widespread in eukaryotes and related to DNA viruses | Q34573336 | ||
The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster. | Q34586900 | ||
Centromere sequence and dynamics in Dictyostelium discoideum | Q34603834 | ||
Genomewide comparative analysis of the highly abundant transposable element DINE-1 suggests a recent transpositional burst in Drosophila yakuba | Q34611547 | ||
Population dynamics of an Ac-like transposable element in self- and cross-pollinating arabidopsis | Q34612987 | ||
Mu killer Causes the Heritable Inactivation of the Mutator Family of Transposable Elements in Zea mays | Q34618803 | ||
A bacterial genetic screen identifies functional coding sequences of the insect mariner transposable element Famar1 amplified from the genome of the earwig, Forficula auricularia | Q34643747 | ||
Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs) | Q34648743 | ||
Crosstalk among Histone Modifications | Q34657658 | ||
Helitrons on a roll: eukaryotic rolling-circle transposons | Q34686529 | ||
Transposable elements and the evolution of genome size in eukaryotes | Q34790131 | ||
Molecular domestication of transposable elements: from detrimental parasites to useful host genes. | Q34918319 | ||
Conjugative transposons: the tip of the iceberg. | Q34985996 | ||
The biogenesis and function of PIWI proteins and piRNAs: progress and prospect | Q34990505 | ||
Genomic organization of the Drosophila telomere retrotransposable elements | Q35056707 | ||
The fate of transposable elements in asexual populations | Q35082947 | ||
Epigenetic regulation of stress responses in plants | Q35114858 | ||
Organization of chromosome ends in the rice blast fungus, Magnaporthe oryzae | Q35128001 | ||
Dramatic amplification of a rice transposable element during recent domestication | Q35214942 | ||
The outs and ins of transposition: from mu to kangaroo | Q35610274 | ||
Insertion sequence diversity in archaea | Q35740880 | ||
Conservation and divergence of DNA methylation in eukaryotes: new insights from single base-resolution DNA methylomes | Q35754817 | ||
RIP: the evolutionary cost of genome defense | Q35864153 | ||
Evolutionary dynamics of transposable elements at the centromere | Q35937314 | ||
The ecology of the genome - mobile DNA elements and their hosts | Q36004587 | ||
Transposable elements as sources of variation in animals and plants | Q36010477 | ||
Arabidopsis epigenetics: when RNA meets chromatin. | Q36064248 | ||
LINE-1 elements and X chromosome inactivation: a function for "junk" DNA? | Q36102401 | ||
Drosophila telomeric retrotransposons derived from an ancestral element that was recruited to replace telomerase | Q36177426 | ||
LTR retrotransposons and flowering plant genome size: emergence of the increase/decrease model | Q36225278 | ||
Triton, a novel family of miniature inverted-repeat transposable elements (MITEs) in Trichosanthes kirilowii Maximowicz and its effect on gene regulation. | Q50858815 | ||
Transposition of ampicillin resistance from RP4 to other replicons. | Q54643018 | ||
The genetic basis of a flower color polymorphism in the common morning glory (Ipomoea purpurea). | Q54736414 | ||
A universal classification of eukaryotic transposable elements implemented in Repbase. | Q55049714 | ||
Epigenome dynamics: a quantitative genetics perspective. | Q55050875 | ||
The functional role of pack-MULEs in rice inferred from purifying selection and expression profile | Q57067104 | ||
On the Origin of Species by Means of Natural Selection, or the Preservation of Favoured Races in the Struggle for Life | Q58704769 | ||
The evolutionary dynamics of repetitive DNA in eukaryotes | Q59090793 | ||
Selfish DNAs with self-restraint | Q59091956 | ||
A Single-Copy IS5-Like Transposon in the Genome of a Bdelloid Rotifer | Q60147001 | ||
Reactivation of Mutator transposable elements of maize by ultraviolet light | Q61236248 | ||
The wrinkled-seed character of pea described by Mendel is caused by a transposon-like insertion in a gene encoding starch-branching enzyme | Q68446914 | ||
On the role of unequal exchange in the containment of transposable element copy number | Q69851798 | ||
Recombination load associated with selection for increased recombination | Q71781379 | ||
Sequence rearrangement in the AT-rich minisatellite of the novel rice transposable element Basho | Q74186710 | ||
Is the evolution of transposable elements modular? | Q74203293 | ||
Transposable element number in mixed mating populations | Q74313724 | ||
Dynamics of transposable elements in metapopulations: a model of P element invasion in Drosophila | Q77228663 | ||
A novel mechanism of phase variation of virulence in Staphylococcus epidermidis: evidence for control of the polysaccharide intercellular adhesin synthesis by alternating insertion and excision of the insertion sequence element IS256 | Q77410702 | ||
I am what I eat and I eat what I am: acquisition of bacterial genes by giant viruses | Q79365031 | ||
Revisiting horizontal transfer of transposable elements in Drosophila | Q81138212 | ||
Models of the population genetics of transposable elements | Q81240283 | ||
Periodic extinctions of transposable elements in bacterial lineages: evidence from intragenomic variation in multiple genomes | Q82062766 | ||
Population frequencies of transposable elements in selfing and outcrossing Caenorhabditis nematodes | Q82230505 | ||
Too many ends: aberrant transposition | Q83773117 | ||
A blessing in disguise: Transposable elements are more than parasites | Q84199102 | ||
Revising the selfish DNA hypothesis: new evidence on accumulation of transposable elements in heterochromatin | Q33594313 | ||
Epigenetic histone modifications of human transposable elements: genome defense versus exaptation | Q33717279 | ||
Regulatory changes as a consequence of transposon insertion | Q33778110 | ||
Genome comparison and context analysis reveals putative mobile forms of restriction-modification systems and related rearrangements | Q33783220 | ||
Genomic imprinting-an epigenetic gene-regulatory model | Q33814499 | ||
Diverse DNA transposons in rotifers of the class Bdelloidea | Q33920253 | ||
Flower color variation: a model for the experimental study of evolution | Q33946994 | ||
Three retrotransposon families in the genome of Giardia lamblia: two telomeric, one dead | Q33951984 | ||
The silence of the genes | Q34026959 | ||
Stress and transposable elements: co-evolution or useful parasites? | Q34049943 | ||
Repetitive DNA elements, nucleosome binding and human gene expression | Q34065350 | ||
Evidence for maternally transmitted small interfering RNA in the repression of transposition in Drosophila virilis | Q34116149 | ||
Histone variants in metazoan development | Q34149623 | ||
Perspective: transposable elements, parasitic DNA, and genome evolution | Q34192362 | ||
Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica | Q34221221 | ||
The endogenous retroviral locus ERVWE1 is a bona fide gene involved in hominoid placental physiology | Q34294325 | ||
Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome | Q34315324 | ||
Shaping bacterial genomes with integrative and conjugative elements | Q34327965 | ||
Conserved themes in small-RNA-mediated transposon control | Q34370338 | ||
SINEs and LINEs: symbionts of eukaryotic genomes with a common tail | Q34442069 | ||
Repeated horizontal transfer of a DNA transposon in mammals and other tetrapods | Q28756606 | ||
Evolutionary dynamics of transposable elements in the short-tailed opossum Monodelphis domestica | Q28757513 | ||
The significance of responses of the genome to challenge | Q28913697 | ||
Controlling elements and the gene | Q28913699 | ||
Gene duplication and exon shuffling by helitron-like transposons generate intraspecies diversity in maize | Q29300755 | ||
A diversity of uncharacterized reverse transcriptases in bacteria | Q29542735 | ||
The origins of genome complexity | Q29547507 | ||
Role of transposable elements in heterochromatin and epigenetic control | Q29616253 | ||
DNA methylation landscapes: provocative insights from epigenomics | Q29617144 | ||
DNA transposons and the evolution of eukaryotic genomes | Q29617153 | ||
A unified classification system for eukaryotic transposable elements | Q29617222 | ||
Transposable elements and the epigenetic regulation of the genome | Q29617224 | ||
Origin of a substantial fraction of human regulatory sequences from transposable elements | Q29617225 | ||
CRISPR interference: RNA-directed adaptive immunity in bacteria and archaea | Q29617488 | ||
Linking DNA methylation and histone modification: patterns and paradigms | Q29617801 | ||
Insertion sequence-related genetic variation in resting Escherichia coli K-12. | Q30011213 | ||
Strong selective sweep associated with a transposon insertion in Drosophila simulans. | Q30336352 | ||
Prokaryotic homologs of Argonaute proteins are predicted to function as key components of a novel system of defense against mobile genetic elements | Q30490196 | ||
Multiple lineages of the non-LTR retrotransposon Rex1 with varying success in invading fish genomes | Q30619568 | ||
Comparative genomics and evolutionary dynamics of Saccharomyces cerevisiae Ty elements | Q30908618 | ||
The transposon Galileo generates natural chromosomal inversions in Drosophila by ectopic recombination. | Q30913673 | ||
Horizontal escape of the novel Tc1-like lepidopteran transposon TCp3.2 into Cydia pomonella granulovirus. | Q32133100 | ||
Identification and mapping of expressed genes, simple sequence repeats and transposable elements in centromeric regions of rice chromosomes | Q33273734 | ||
Telomeric trans-silencing: an epigenetic repression combining RNA silencing and heterochromatin formation | Q33302942 | ||
Biased exonization of transposed elements in duplicated genes: A lesson from the TIF-IA gene | Q33307791 | ||
Repetitive element-mediated recombination as a mechanism for new gene origination in Drosophila | Q33315562 | ||
How Athila retrotransposons survive in the Arabidopsis genome | Q33334647 | ||
Regulation of transcription in plants: mechanisms controlling developmental switches | Q33350086 | ||
The evolving functions of DNA methylation | Q33367277 | ||
High rate of recent transposable element-induced adaptation in Drosophila melanogaster | Q33378679 | ||
The effect of transposable element insertions on gene expression evolution in rodents | Q33404584 | ||
Darwinian evolution in the light of genomics | Q33408694 | ||
Whole genome surveys of rice, maize and sorghum reveal multiple horizontal transfers of the LTR-retrotransposon Route66 in Poaceae. | Q33418756 | ||
Transposable elements and an epigenetic basis for punctuated equilibria | Q33453627 | ||
Dynamics of transposable elements: towards a community ecology of the genome | Q33470970 | ||
Helicobacter Pylori's plasticity zones are novel transposable elements | Q33499692 | ||
A novel mechanism of transposon-mediated gene activation | Q33510907 | ||
Jumping genes and epigenetics: Towards new species | Q33526699 | ||
Repetitive DNA is associated with centromeric domains in Trypanosoma brucei but not Trypanosoma cruzi. | Q39315224 | ||
Alu-containing exons are alternatively spliced | Q39860930 | ||
Epigenetics for ecologists | Q40153209 | ||
Molecular characterization of two natural hotspots in the Drosophila buzzatii genome induced by transposon insertions | Q40415138 | ||
Evolution and consequences of transposable elements | Q40719873 | ||
Transposon dynamics and the breeding system | Q40751654 | ||
Cases of ancient mobile element DNA insertions that now affect gene regulation | Q41010165 | ||
LTR-retrotransposons and MITEs: important players in the evolution of plant genomes | Q41068242 | ||
Extensive demethylation of repetitive elements during seed development underlies gene imprinting | Q41107458 | ||
Reverse transcriptase: mediator of genomic plasticity | Q41128928 | ||
Sure facts, speculations, and open questions about the evolution of transposable element copy number | Q41756995 | ||
Evolution of the mammalian transcription factor binding repertoire via transposable elements | Q41955907 | ||
UV light induces IS10 transposition in Escherichia coli. | Q42571999 | ||
Toothed whale monophyly reassessed by SINE insertion analysis: the absence of lineage sorting effects suggests a small population of a common ancestral species | Q42607222 | ||
Active site sharing and subterminal hairpin recognition in a new class of DNA transposases | Q42670024 | ||
Transposable elements in inbreeding and outbreeding populations | Q42965601 | ||
Transposable element distributions in Drosophila | Q42968252 | ||
Transposable element distribution in Drosophila. | Q42968255 | ||
Genetic interactions underlying flower color patterns in Antirrhinum majus | Q44538635 | ||
Cryptons: a group of tyrosine-recombinase-encoding DNA transposons from pathogenic fungi | Q44643960 | ||
A retrotransposon-mediated gene duplication underlies morphological variation of tomato fruit | Q44685385 | ||
The mariner transposable element in natural populations of Drosophila simulans | Q44707755 | ||
The few virus-like genes of Cotesia congregata bracovirus. | Q45419697 | ||
A genome-wide view of miniature inverted-repeat transposable elements (MITEs) in rice, Oryza sativa ssp. japonica | Q45897464 | ||
Horizontal transfer and selection in the evolution of P elements. | Q45994077 | ||
Heritable transposon silencing initiated by a naturally occurring transposon inverted duplication | Q46098533 | ||
A transcriptionally active copia-like retroelement in Citrus limon. | Q46179916 | ||
Genome structure of bdelloid rotifers: shaped by asexuality or desiccation? | Q47391017 | ||
The paleontology of intergene retrotransposons of maize | Q47750190 | ||
Centromeres, CENP-B and Tigger too. | Q48052113 | ||
Causes of insertion sequences abundance in prokaryotic genomes | Q48082049 | ||
Mobile genetic elements and sexual reproduction | Q36225341 | ||
Long-term evolution of transposable elements | Q36288596 | ||
Turning junk into gold: domestication of transposable elements and the creation of new genes in eukaryotes | Q36579703 | ||
Transposable elements and the plant pan-genomes | Q36735901 | ||
Quelling: post-transcriptional gene silencing guided by small RNAs in Neurospora crassa. | Q36774878 | ||
The plant genome's methylation status and response to stress: implications for plant improvement | Q36806055 | ||
The role of IS6110 in the evolution of Mycobacterium tuberculosis | Q36879772 | ||
Demography and weak selection drive patterns of transposable element diversity in natural populations of Arabidopsis lyrata | Q36893624 | ||
Sustained retrotransposition is mediated by nucleotide deletions and interelement recombinations. | Q36926862 | ||
piRNA-mediated nuclear accumulation of retrotransposon transcripts in the Drosophila female germline | Q36937109 | ||
The Whole-genome sequencing of the obligate intracellular bacterium Orientia tsutsugamushi revealed massive gene amplification during reductive genome evolution | Q36955974 | ||
Give-and-take: interactions between DNA transposons and their host plant genomes | Q36962591 | ||
Induction of the mobile genetic element Dm-412 transpositions in the Drosophila genome by heat shock treatment | Q37070442 | ||
Population epigenetics | Q37109033 | ||
Epigenetic interactions between transposons and genes: lessons from plants | Q37109738 | ||
Alternative Ac/Ds transposition induces major chromosomal rearrangements in maize | Q37141803 | ||
Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes. | Q37173703 | ||
Epigenetic, transposon and small RNA determinants of hybrid dysfunctions | Q37188499 | ||
Large-scale analysis of exonized mammalian-wide interspersed repeats in primate genomes | Q37201010 | ||
Genome-wide analyses of alternative splicing in plants: opportunities and challenges. | Q37231296 | ||
Retrotransposable elements and human disease | Q37250896 | ||
Epigenetic silencing of transposable elements: a trade-off between reduced transposition and deleterious effects on neighboring gene expression | Q37287376 | ||
A recent adaptive transposable element insertion near highly conserved developmental loci in Drosophila melanogaster | Q37324379 | ||
Epigenetic regulation of transposable elements in plants | Q37324789 | ||
Genetic and molecular analysis of the gypsy chromatin insulator of Drosophila | Q37350050 | ||
The evolution of plant genomes: scaling up from a population perspective | Q37364908 | ||
The Drosophila HP1 homolog Rhino is required for transposon silencing and piRNA production by dual-strand clusters. | Q37406170 | ||
Distribution, diversity, evolution, and survival of Helitrons in the maize genome | Q37446470 | ||
Transposable elements: powerful facilitators of evolution | Q37470360 | ||
CRISPR-based adaptive and heritable immunity in prokaryotes | Q37568446 | ||
P-element homologous sequences are tandemly repeated in the genome of Drosophila guanche | Q37599742 | ||
Epigenetic transitions in germ cell development and meiosis | Q37809239 | ||
Structural domains and matrix attachment regions along colinear chromosomal segments of maize and sorghum. | Q38500156 | ||
P275 | copyright license | Creative Commons Attribution 2.0 Generic | Q19125117 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | DNA | Q7430 |
P304 | page(s) | 19 | |
P577 | publication date | 2011-03-17 | |
P1433 | published in | Biology Direct | Q1954915 |
P1476 | title | The struggle for life of the genome's selfish architects | |
P478 | volume | 6 |
Q38755420 | A Perspective on CRN Proteins in the Genomics Age: Evolution, Classification, Delivery and Function Revisited |
Q34411888 | A gene family derived from transposable elements during early angiosperm evolution has reproductive fitness benefits in Arabidopsis thaliana |
Q64274260 | A re-annotation of the Anopheles darlingi mobilome |
Q36302696 | A repetitive elements perspective in Polycomb epigenetics |
Q37619228 | Accommodating the load: The transposable element content of very large genomes |
Q34234396 | Analysis of plant LTR-retrotransposons at the fine-scale family level reveals individual molecular patterns |
Q35595309 | Ancient horizontal gene transfer and the last common ancestors |
Q45883685 | Asexual evolution: do intragenomic parasites maintain sex? |
Q83228043 | Asexual reproduction reduces transposable element load in experimental yeast populations |
Q28743132 | Assessing the role of tandem repeats in shaping the genomic architecture of great apes |
Q37616629 | BuT2 is a member of the third major group of hAT transposons and is involved in horizontal transfer events in the genus Drosophila. |
Q33713113 | Casposons: a new superfamily of self-synthesizing DNA transposons at the origin of prokaryotic CRISPR-Cas immunity |
Q35196860 | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus. |
Q64099173 | Characterization of repeated DNA sequences in genomes of blue-flowered flax |
Q89701667 | Complex Evolutionary History of Mboumar, a Mariner Element Widely Represented in Ant Genomes |
Q35861667 | Copy number variation of ribosomal DNA and Pokey transposons in natural populations of Daphnia. |
Q35006300 | DIRS and Ngaro Retrotransposons in Fungi |
Q91627561 | DNA sequences homologous to hepatitis C virus (HCV) in the extrachromosomal circular DNA in peripheral blood mononuclear cells of HCV-negative subjects |
Q28648065 | Detecting endogenous retrovirus-driven tissue-specific gene transcription |
Q111347555 | Determination of host adaptation for wild highland population of Microgastrinae (Hymenoptera: Braconidae) using viral Histone H4 |
Q92187281 | Differential retention of transposable element-derived sequences in outcrossing Arabidopsis genomes |
Q30426258 | Distinguishing ecological from evolutionary approaches to transposable elements. |
Q48293223 | Diversity, distribution and dynamics of full-length Copia and Gypsy LTR retroelements in Solanum lycopersicum. |
Q55180020 | Drosophila relics hobo and hobo-MITEs transposons as raw material for new regulatory networks. |
Q36215513 | Dynamics of Rex3 in the genomes of endangered Iberian Leuciscinae (Teleostei, Cyprinidae) and their natural hybrids |
Q35874389 | Dynamics of bacterial insertion sequences: can transposition bursts help the elements persist? |
Q36281102 | Ecological networks to unravel the routes to horizontal transposon transfers |
Q35669157 | Effects of heat and UV radiation on the mobilization of transposon mariner-Mos1. |
Q39252070 | Emerging roles of macrosatellite repeats in genome organization and disease development. |
Q40975327 | Evidence of ectopic recombination and a repeat-induced point (RIP) mutation in the genome of Sclerotinia sclerotiorum, the agent responsible for white mold |
Q52745073 | Evolution and dynamics of small RNA response to a retroelement invasion in Drosophila. |
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 |
Q26752905 | Evolutionary interaction between W/Y chromosome and transposable elements |
Q37534111 | Experimental evolution reveals hyperparasitic interactions among transposable elements. |
Q21203760 | Families of transposable elements, population structure and the origin of species |
Q42613447 | First insights on the retroelement Rex1 in the cytogenetics of frogs |
Q42239689 | Genetic Drift, Not Life History or RNAi, Determine Long-Term Evolution of Transposable Elements |
Q49183514 | Genetic exchange in eukaryotes through horizontal transfer: connected by the mobilome |
Q61806050 | Genome Size Reversely Correlates With Host Plant Range in Species |
Q34587213 | Genome differentiation in a species pair of coregonine fishes: an extremely rapid speciation driven by stress-activated retrotransposons mediating extensive ribosomal DNA multiplications. |
Q34273327 | Genome evolution in filamentous plant pathogens: why bigger can be better |
Q33801920 | Genomic landscape of human, bat, and ex vivo DNA transposon integrations |
Q35622072 | HTT-DB: horizontally transferred transposable elements database |
Q51149629 | Horizontal acquisition of transposable elements and viral sequences: patterns and consequences. |
Q38026538 | Horizontal transposon transfer in eukarya: detection, bias, and perspectives |
Q42235273 | How does selfing affect the dynamics of selfish transposable elements? |
Q58754303 | Human Endogenous Retroviruses Are Ancient Acquired Elements Still Shaping Innate Immune Responses |
Q43826028 | Human repetitive sequence densities are mostly negatively correlated with R/Y-based nucleosome-positioning motifs and positively correlated with W/S-based motifs |
Q35595059 | Identification and characterization of expressed retrotransposons in the genome of the Paracoccidioides species complex |
Q46264964 | Impact of Lateral Transfers on the Genomes of Lepidoptera |
Q46842707 | Insights on genome size evolution from a miniature inverted repeat transposon driving a satellite DNA. |
Q42292495 | LoRTE: Detecting transposon-induced genomic variants using low coverage PacBio long read sequences |
Q28727809 | Losing identity: structural diversity of transposable elements belonging to different classes in the genome of Anopheles gambiae |
Q64083450 | Low coverage sequencing for repetitive DNA analysis in Passiflora edulis Sims: citogenomic characterization of transposable elements and satellite DNA |
Q35868318 | Mariner transposons are sailing in the genome of the blood-sucking bug Rhodnius prolixus |
Q35565375 | Microbial Consortium Associated with the Antarctic Marine Ciliate Euplotes focardii: An Investigation from Genomic Sequences |
Q40328444 | Microsatellite evolutionary rate and pattern in Schistocerca gregaria inferred from direct observation of germline mutations. |
Q28604038 | No Accumulation of Transposable Elements in Asexual Arthropods |
Q57773764 | Novel Transposable Elements in Solanaceae: Evolutionary Relationships among Tnt1-related Sequences in Wild Petunia Species |
Q46473437 | Profiling Transposable Elements and Their Epigenetic Effects in Non-model Species. |
Q28831298 | Profuse evolutionary diversification and speciation on volcanic islands: transposon instability and amplification bursts explain the genetic paradox |
Q89146094 | RNA Degradation in Neurodegenerative Disease |
Q53656938 | Rare horizontal transmission does not hide long-term inheritance of SINE highly conserved domains in the metazoan evolution. |
Q36655543 | Recent Mobility of Casposons, Self-Synthesizing Transposons at the Origin of the CRISPR-Cas Immunity |
Q46572109 | Reconstructing the evolutionary history of gypsy retrotransposons in the Périgord black truffle (Tuber melanosporum Vittad.). |
Q28703889 | Reconstructing the evolutionary history of transposable elements |
Q35853168 | Repetitive DNA and Plant Domestication: Variation in Copy Number and Proximity to Genes of LTR-Retrotransposons among Wild and Cultivated Sunflower (Helianthus annuus) Genotypes |
Q22122001 | Repetitive DNA and next-generation sequencing: computational challenges and solutions |
Q28595512 | Reverse transcriptase genes are highly abundant and transcriptionally active in marine plankton assemblages |
Q28710323 | Selection-driven extinction dynamics for group II introns in Enterobacteriales |
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Q35755350 | Suppression of different classes of somatic mutations in Arabidopsis by vir gene-expressing Agrobacterium strains |
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Q39550085 | The cost of copy number in a selfish genetic element: the 2-μm plasmid of Saccharomyces cerevisiae. |
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Q86728322 | The genomic proliferation of transposable elements in colonizing populations: Schistosoma mansoni in the new world |
Q38072072 | The impact of transposable elements in environmental adaptation. |
Q58800718 | The interplay between the Argonaute proteins Piwi and Aub within Drosophila germarium is critical for oogenesis, piRNA biogenesis and TE silencing |
Q33556663 | The peculiar landscape of repetitive sequences in the olive (Olea europaea L.) genome |
Q52736667 | The role of vertical and horizontal transfer in the evolution of Paris-like elements in drosophilid species. |
Q53100967 | The sunflower (Helianthus annuus L.) genome reflects a recent history of biased accumulation of transposable elements. |
Q26825108 | The telomeric sync model of speciation: species-wide telomere erosion triggers cycles of transposon-mediated genomic rearrangements, which underlie the saltatory appearance of nonadaptive characters |
Q92150302 | Transposable Elements Adaptive Role in Genome Plasticity, Pathogenicity and Evolution in Fungal Phytopathogens |
Q90248311 | Transposable element discovery and characterization of LTR-retrotransposon evolutionary lineages in the tropical fruit species Passiflora edulis |
Q34007229 | Transposable element dynamics among asymbiotic and ectomycorrhizal Amanita fungi. |
Q34833364 | Transposable element islands facilitate adaptation to novel environments in an invasive species |
Q28710587 | Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE-Thrust hypothesis |
Q31157768 | Transposable elements as stress adaptive capacitors induce genomic instability in fungal pathogen Magnaporthe oryzae |
Q89784449 | Transposable elements contribute to the genomic response to insecticides in Drosophila melanogaster |
Q34408012 | Transposable elements in TDP-43-mediated neurodegenerative disorders |
Q28727822 | Transposable elements in phytopathogenic Verticillium spp.: insights into genome evolution and inter- and intra-specific diversification |
Q28660225 | Transposable elements: from DNA parasites to architects of metazoan evolution |
Q28661923 | Transposable elements: powerful contributors to angiosperm evolution and diversity |
Q28727065 | Transposon-derived and satellite-derived repetitive sequences play distinct functional roles in Mammalian intron size expansion |
Q39503795 | Ultra Large Gene Families: A Matter of Adaptation or Genomic Parasites? |
Q39487484 | Unraveling the evolutionary scenario of the hobo element in populations of Drosophila melanogaster and D. simulans in South America using the TPE repeats as markers |
Q38753540 | VHICA, a New Method to Discriminate between Vertical and Horizontal Transposon Transfer: Application to the Mariner Family within Drosophila. |
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Q53436919 | [ENCODE apophenia or a panglossian analysis of the human genome]. |
Q45820870 | hobo-brothers elements and their time and place for horizontal transfer |
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