| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Margaret Kidwell | Q18356435 |
| P2093 | author name string | Lisch DR | |
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| Phenotypic diversity mediated by the maize transposable elements Ac and Spm. | Q39271760 | ||
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| Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era | Q28776504 | ||
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| Genomic and evolutionary analysis of Feilai, a diverse family of highly reiterated SINEs in the yellow fever mosquito, Aedes aegypti | Q30714853 | ||
| Presence of miniature inverted-repeat transposable elements (MITEs) in the genome of Arabidopsis thaliana: characterisation of the Emigrant family of elements | Q31978853 | ||
| Chromosome-specific molecular organization of maize (Zea mays L.) centromeric regions | Q31991592 | ||
| Structure of the chromosome VII centromere region in Neurospora crassa: degenerate transposons and simple repeats | Q32036956 | ||
| Undermethylation associated with retroelement activation and chromosome remodelling in an interspecific mammalian hybrid | Q32063623 | ||
| Position effects and epigenetic silencing of plant transgenes | Q33538759 | ||
| Revising the selfish DNA hypothesis: new evidence on accumulation of transposable elements in heterochromatin | Q33594313 | ||
| Intrachromosomal rearrangements mediated by hobo transposons in Drosophila melanogaster | Q33680665 | ||
| Extensive, nonrandom diversity of excision footprints generated by Ds-like transposon Ascot-1 suggests new parallels with V(D)J recombination | Q33775068 | ||
| Regulatory changes as a consequence of transposon insertion | Q33778110 | ||
| RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements | Q33778366 | ||
| Genetic variation: molecular mechanisms and impact on microbial evolution | Q33820587 | ||
| Invasion of a multitude of genetic niches by mobile endonuclease genes | Q33885297 | ||
| Transposable elements and host genome evolution | Q33890168 | ||
| Fission yeast homologs of human CENP-B have redundant functions affecting cell growth and chromosome segregation | Q33962852 | ||
| Molecular structure of a functional Drosophila centromere | Q34065770 | ||
| The evolution of virulence: a unifying link between parasitology and ecology | Q34288239 | ||
| Methylation and imprinting: from host defense to gene regulation? | Q34363070 | ||
| Transposable elements are stable structural components of Drosophila melanogaster heterochromatin | Q34380234 | ||
| LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis | Q34388506 | ||
| Molecular cloning of cDNA for CENP-B, the major human centromere autoantigen | Q34393316 | ||
| DNA sequence insertion and evolutionary variation in gene regulation | Q34395561 | ||
| Nested retrotransposons in the intergenic regions of the maize genome | Q34402279 | ||
| Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease | Q34463149 | ||
| The impact of L1 retrotransposons on the human genome | Q34468340 | ||
| Extended life-span and stress resistance in the Drosophila mutant methuselah | Q34477849 | ||
| Tightly regulated, developmentally specific expression of the first open reading frame from LINE-1 during mouse embryogenesis | Q34628234 | ||
| Matrix attachment regions and structural colinearity in the genomes of two grass species. | Q34655072 | ||
| Consensus inverted terminal repeat sequence of Paramecium IESs: resemblance to termini of Tc1-related and Euplotes Tec transposons. | Q34755067 | ||
| Gene number, noise reduction and biological complexity | Q40514856 | ||
| Epigenetic regulation of the maize Spm transposon | Q40520011 | ||
| Physiological stresses increase mouse short interspersed element (SINE) RNA expression in vivo | Q40630548 | ||
| Lateral transfer in natural populations of eukaryotes | Q40722162 | ||
| The strange phylogenies of transposable elements: are horizontal transfers the only explantation? | Q40735051 | ||
| Genomes were forged by massive bombardments with retroelements and retrosequences | Q40751648 | ||
| Retroelements in the human MHC class II region | Q40863445 | ||
| The first intron of the myelin proteolipid protein gene confers cell type-specific expression by a transcriptional repression mechanism in non-expressing cell types | Q40874690 | ||
| Retrohoming: cDNA-mediated mobility of group II introns requires a catalytic RNA. | Q40939387 | ||
| Cases of ancient mobile element DNA insertions that now affect gene regulation | Q41010165 | ||
| Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system | Q41011364 | ||
| LTR-retrotransposons and MITEs: important players in the evolution of plant genomes | Q41068242 | ||
| Turned on by stress. Plant retrotransposons | Q41110778 | ||
| The origins of V(D)J recombination | Q41329165 | ||
| Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome | Q41566242 | ||
| Molecular domestication of mobile elements | Q41688083 | ||
| Transposable element-host interactions: regulation of insertion and excision | Q41689480 | ||
| Mobile elements inserted in the distant past have taken on important functions | Q41699977 | ||
| Transposons in place of telomeric repeats at a Drosophila telomere | Q42610468 | ||
| LINE-1: a human transposable element | Q42611087 | ||
| Zepp, a LINE-like retrotransposon accumulated in the Chlorella telomeric region | Q42622633 | ||
| The evolution of MHC diversity by segmental duplication and transposition of retroelements. | Q42669974 | ||
| Structural, genomic, and phylogenetic analysis of Lian, a novel family of non-LTR retrotransposons in the yellow fever mosquito, Aedes aegypti | Q42680422 | ||
| A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion | Q42693461 | ||
| Genomic characterization of the region between HLA-B and TNF: implications for the evolution of multicopy gene families | Q44367449 | ||
| An ancient provirus has imposed androgen regulation on the adjacent mouse sex-limited protein gene | Q44863120 | ||
| Sequence and analysis of chromosome 2 of the plant Arabidopsis thaliana | Q44963941 | ||
| Modulation of immune responses to parasitoids by polydnaviruses | Q46050678 | ||
| Tissue-specific accumulation of MURB, a protein encoded by MuDR, the autonomous regulator of the Mutator transposable element family | Q46088617 | ||
| Repeated sequence target sites for maternal DNA-binding proteins in genes activated in early sea urchin development | Q46113260 | ||
| Evolution of a bacteria/plasmid association | Q46676230 | ||
| Strategies for the in vitro evolution of protein function: enzyme evolution by random recombination of improved sequences | Q46855416 | ||
| Structure of the segmentation gene paired and the Drosophila PRD gene set as part of a gene network | Q47069959 | ||
| The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene | Q47333248 | ||
| DNA transposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations | Q47750695 | ||
| Internal eliminated sequences interrupting the Oxytricha 81 locus: allelic divergence, conservation, conversions, and possible transposon origins | Q47815545 | ||
| Evolutionary dynamics of the SGM transposon family in the Drosophila obscura species group | Q47815964 | ||
| Evidence for the role of recombination in the regulatory evolution of Saccharomyces cerevisiae Ty elements | Q47843738 | ||
| A satellite DNA containing CENP-B box-like motifs is present in the antarctic scallop Adamussium colbecki | Q47867541 | ||
| A P element has induced intron formation in Drosophila | Q47913927 | ||
| Capture of a genomic HMG domain sequence by the En/Spm-related transposable element Tpn1 in the Japanese morning glory | Q47964834 | ||
| Nonmethylated transposable elements and methylated genes in a chordate genome | Q47987079 | ||
| Short inverted-repeat transposable elements in teleost fish and implications for a mechanism of their amplification | Q47997908 | ||
| Something from nothing: the evolution and utility of satellite repeats | Q48013054 | ||
| L1 repeat is a basic unit of heterochromatin satellites in cetaceans | Q48038251 | ||
| Centromeres, CENP-B and Tigger too. | Q48052113 | ||
| High intrinsic rate of DNA loss in Drosophila | Q48057637 | ||
| Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks | Q48058936 | ||
| Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice | Q48071134 | ||
| A novel group of families of short interspersed repetitive elements (SINEs) in Xenopus: evidence of a specific target site for DNA-mediated transposition of inverted-repeat SINEs | Q48073725 | ||
| Structure and expression of clustered P element homologues in Drosophila subobscura and Drosophila guanche | Q48074399 | ||
| Tourist: a large family of small inverted repeat elements frequently associated with maize genes | Q48156212 | ||
| A tissue-specific transcription enhancer element is located in the major intron of a rearranged immunoglobulin heavy chain gene | Q48397674 | ||
| Cleavage at a V(D)J recombination signal requires only RAG1 and RAG2 proteins and occurs in two steps | Q49167454 | ||
| Cytotype control of Drosophila P element transposition: the 66 kd protein is a repressor of transposase activity. | Q52449696 | ||
| The absence of detectable methylated bases in Drosophila melanogaster DNA. | Q52527850 | ||
| The Ty1-copia group retrotransposons of Allium cepa are distributed throughout the chromosomes but are enriched in the terminal heterochromatin. | Q52550896 | ||
| Intragenomic distribution and stability of transposable elements in euchromatin and heterochromatin of Drosophila melanogaster: non-LTR retrotransposon. | Q52553655 | ||
| Heterochromatin protein 1 binds transgene arrays. | Q52567649 | ||
| Recent, extensive, and preferential insertion of members of the miniature inverted-repeat transposable element family Heartbreaker into genic regions of maize | Q35009215 | ||
| Frequent human genomic DNA transduction driven by LINE-1 retrotransposition | Q35026231 | ||
| A hierarchical approach to protein molecular evolution | Q35056515 | ||
| Rodent BC1 RNA gene as a master gene for ID element amplification | Q35185755 | ||
| Mobile elements and chromosomal evolution in the virilis group of Drosophila | Q35280826 | ||
| The relationship between genetic and physical distances in the cloned a1-sh2 interval of the Zea mays L. genome. | Q35692044 | ||
| Retrotransposons in the flanking regions of normal plant genes: a role for copia-like elements in the evolution of gene structure and expression | Q35939137 | ||
| Transposition of the LINE-like retrotransposon TART to Drosophila chromosome termini | Q35988239 | ||
| Transposable elements as sources of variation in animals and plants | Q36010477 | ||
| The role of robustness and changeability on the origin and evolution of genetic codes | Q36064324 | ||
| Directed evolution of a fucosidase from a galactosidase by DNA shuffling and screening | Q36137488 | ||
| A unique sequence related to the ecotropic murine leukemia virus is associated with the Fv-4 resistance gene | Q36254251 | ||
| Neocentromere-mediated chromosome movement in maize | Q36274334 | ||
| High genetic instability of heterochromatin after transposition of the LINE-like I factor in Drosophila melanogaster | Q36300860 | ||
| Cloning of inversion breakpoints in the Anopheles gambiae complex traces a transposable element at the inversion junction | Q36525010 | ||
| Purification and characterization of a CENP-B homologue protein that binds to the centromeric K-type repeat DNA of Schizosaccharomyces pombe | Q36541953 | ||
| Germ line-specific expression of intracisternal A-particle retrotransposons in transgenic mice | Q36561660 | ||
| Three novel families of miniature inverted-repeat transposable elements are associated with genes of the yellow fever mosquito, Aedes aegypti | Q36658748 | ||
| The pvB370 BamHI satellite DNA family of the Drosophila virilis group and its evolutionary relation to mobile dispersed genetic pDv elements | Q36671534 | ||
| Explosive invasion of plant mitochondria by a group I intron | Q36732891 | ||
| Stowaway: a new family of inverted repeat elements associated with the genes of both monocotyledonous and dicotyledonous plants | Q36737301 | ||
| Positional cloning of the mouse retrovirus restriction gene Fv1. | Q36812909 | ||
| RAG3 gene and transcriptional regulation of the pyruvate decarboxylase gene in Kluyveromyces lactis | Q36818140 | ||
| A new family of site-specific retrotransposons, SART1, is inserted into telomeric repeats of the silkworm, Bombyx mori | Q36852682 | ||
| Escape from evolutionary stasis by transposon-mediated deleterious mutations | Q36880049 | ||
| Elements in microbial evolution | Q37354164 | ||
| Reduced DNA methylation in Arabidopsis thaliana results in abnormal plant development | Q37405920 | ||
| Induction of centromeric activity in maize by suppressor of meiotic drive 1. | Q37408565 | ||
| P-element homologous sequences are tandemly repeated in the genome of Drosophila guanche | Q37599742 | ||
| Eukaryotic transposable elements and genome evolution | Q38272219 | ||
| Presence and abundance of CENP-B box sequences in great ape subsets of primate-specific alpha-satellite DNA. | Q38290990 | ||
| Polymorphisms and genomic organization of repetitive DNA from centromeric regions of Arabidopsis chromosomes | Q38329719 | ||
| Organization of the 1.9-kb repeat unit RCE1 in the centromeric region of rice chromosomes | Q38501422 | ||
| Drosophila telomeres: new views on chromosome evolution. | Q38561575 | ||
| P433 | issue | 1 | |
| P1104 | number of pages | 24 | |
| P304 | page(s) | 1-24 | |
| P577 | publication date | 2001-01-01 | |
| P1433 | published in | Evolution | Q4038411 |
| P1476 | title | Perspective: transposable elements, parasitic DNA, and genome evolution | |
| P478 | volume | 55 |
| Q43494494 | 'Junk' DNA and phenotypic evolution in Silene section Siphonomorpha |
| Q42924129 | 'Satellite DNA transcripts have diverse biological roles in Drosophila'. |
| Q37173147 | 3'UTR-located ALU elements: donors of potential miRNA target sites and mediators of network miRNA-based regulatory interactions |
| Q28608107 | A Novel Terminal-Repeat Retrotransposon in Miniature (TRIM) Is Massively Expressed in Echinococcus multilocularis Stem Cells |
| Q41405238 | A functional role for transposases in a large eukaryotic genome |
| Q39639675 | A novel class of miniature inverted repeat transposable elements (MITEs) that contain hitchhiking (GTCY)n microsatellites |
| Q45356927 | A rapid decrease in number of the complete ninja element and concomitant increase of the defective element in a strain of Drosophila simulans |
| Q37324379 | A recent adaptive transposable element insertion near highly conserved developmental loci in Drosophila melanogaster |
| Q38387036 | A survey of transposable element classification systems--a call for a fundamental update to meet the challenge of their diversity and complexity. |
| Q46179916 | A transcriptionally active copia-like retroelement in Citrus limon. |
| Q37619228 | Accommodating the load: The transposable element content of very large genomes |
| Q28603245 | Accurate Transposable Element Annotation Is Vital When Analyzing New Genome Assemblies |
| Q44835568 | Activation of a rice endogenous retrotransposon Tos17 in tissue culture is accompanied by cytosine demethylation and causes heritable alteration in methylation pattern of flanking genomic regions |
| Q33245406 | Alu elements contain many binding sites for transcription factors and may play a role in regulation of developmental processes |
| Q33262669 | An analysis of mobile genetic elements in three Plasmodium species and their potential impact on the nucleotide composition of the P. falciparum genome |
| Q56992563 | An introduction to the vast world of transposable elements – what about the diatoms? |
| Q35139009 | Analysis of insertion sequences in thermophilic cyanobacteria: exploring the mechanisms of establishing, maintaining, and withstanding high insertion sequence abundance |
| Q30818151 | Analysis of similarity within 142 pairs of orthologous intergenic regions of Caenorhabditis elegans and Caenorhabditis briggsae |
| Q33877367 | Ancestral repeats have shaped epigenome and genome composition for millions of years in Arabidopsis thaliana |
| Q36498920 | Applying mobile genetic elements for genome analysis and evolution |
| Q34996975 | Assessment and reconstruction of novel HSP90 genes: duplications, gains and losses in fungal and animal lineages |
| Q31016080 | BEL/Pao retrotransposons in metazoan genomes |
| Q28657639 | Bacterial genome instability |
| Q24545998 | Birth of a chimeric primate gene by capture of the transposase gene from a mobile element |
| Q64965393 | Birth, School, Work, Death, and Resurrection: The Life Stages and Dynamics of Transposable Element Proliferation. |
| Q37616629 | BuT2 is a member of the third major group of hAT transposons and is involved in horizontal transfer events in the genus Drosophila. |
| Q48082049 | Causes of insertion sequences abundance in prokaryotic genomes |
| Q33715125 | Cell size as a link between noncoding DNA and metabolic rate scaling |
| Q21198753 | Characterization and potential functional significance of human-chimpanzee large INDEL variation |
| Q52852291 | Characterization of irritans mariner-like elements in the olive fruit fly Bactrocera oleae (Diptera: Tephritidae): evolutionary implications. |
| Q42648306 | Characterization of new hAT transposable elements in 12 Drosophila genomes |
| Q52621574 | Characterization of transcriptional activation and inserted-into-gene preference of various transposable elements in the Brassica species. |
| Q43502291 | Characterizing the composition and evolution of homoeologous genomes in hexaploid wheat through BAC-end sequencing on chromosome 3B. |
| Q37202290 | Chromodomains and LTR retrotransposons in plants |
| Q33979735 | Coexistence of trichome variation in a natural plant population: a combined study using ecological and candidate gene approaches. |
| Q46421915 | Collinearity between potato (Solanum tuberosum L.) and wild relatives assessed by comparative cytogenetic mapping |
| Q24813273 | Combined evidence annotation of transposable elements in genome sequences |
| Q36377751 | Combining Mass Spectrometric Metabolic Profiling with Genomic Analysis: A Powerful Approach for Discovering Natural Products from Cyanobacteria |
| Q57800851 | Comparative analysis of repetitive sequences among species from the potato and the tomato clades |
| Q89701667 | Complex Evolutionary History of Mboumar, a Mariner Element Widely Represented in Ant Genomes |
| Q42644440 | Conserved motifs and dynamic aspects of the terminal inverted repeat organization within Bari-like transposons |
| Q92915469 | DNA transposon invasion and microsatellite accumulation guide W chromosome differentiation in a Neotropical fish genome |
| Q29617153 | DNA transposons and the evolution of eukaryotic genomes |
| Q28751993 | DNA transposons: nature and applications in genomics |
| Q39229220 | Degeneration of a homing endonuclease and its target sequence in a wild yeast strain |
| Q28648065 | Detecting endogenous retrovirus-driven tissue-specific gene transcription |
| Q52699869 | Detection of P element transcripts in embryos of Drosophila melanogaster and D. willistoni. |
| Q31155225 | Discovery and assembly of repeat family pseudomolecules from sparse genomic sequence data using the Assisted Automated Assembler of Repeat Families (AAARF) algorithm |
| Q47434809 | Discovery of novel genes derived from transposable elements using integrative genomic analysis |
| Q30426258 | Distinguishing ecological from evolutionary approaches to transposable elements. |
| Q42630683 | Distribution dynamics of the Tnt1 retrotransposon in tobacco |
| Q33850911 | Diversity and evolution of mariner-like elements in aphid genomes |
| Q48795964 | Domesticated P elements in the Drosophila montium species subgroup have a new function related to a DNA binding property |
| Q51743629 | Duplicate gene evolution toward multiple fates at the Drosophila melanogaster HIP/HIP-Replacement locus. |
| Q42117447 | Duplication count distributions in DNA sequences |
| 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 |
| Q29619890 | Endogenous viruses: insights into viral evolution and impact on host biology |
| Q28601408 | Enrichment analysis of Alu elements with different spatial chromatin proximity in the human genome |
| Q24564861 | Epigenetics and its implications for plant biology 2. The 'epigenetic epiphany': epigenetics, evolution and beyond |
| Q36389323 | Evaluating the protein coding potential of exonized transposable element sequences |
| Q24805200 | Evolution and distribution of RNA polymerase II regulatory sites from RNA polymerase III dependant mobile Alu elements |
| Q90975451 | Evolution and diversity of transposable elements in fish genomes |
| Q51947595 | Evolution in biological and nonbiological systems under different mechanisms of generation and inheritance. |
| Q42658397 | Evolution of full-length and deleted forms of the mariner-like element, Botmar1, in the Genome of the bumble bee, Bombus terrestris (Hymenoptera: Apidae). |
| Q30670491 | Evolution of genome-phenome diversity under environmental stress |
| Q28650495 | Evolutionary dynamics of hAT DNA transposon families in Saccharomycetaceae |
| Q37596083 | Evolutionary dynamics of insertion sequences in Helicobacter pylori. |
| Q34833252 | Evolutionary dynamics of retrotransposable elements Rex1, Rex3 and Rex6 in neotropical cichlid genomes. |
| Q33808851 | Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae |
| Q37809269 | Evolutionary dynamics of transposable elements in a small RNA world |
| Q28757513 | Evolutionary dynamics of transposable elements in the short-tailed opossum Monodelphis domestica |
| Q38621273 | Evolutionary history of the mariner element galluhop in avian genomes |
| Q45918618 | Evolutionary implications of multiple SINE insertions in an intronic region from diverse mammals. |
| Q33335382 | Evolutionary rates and patterns for human transcription factor binding sites derived from repetitive DNA |
| Q34649872 | Evolutionary tinkering with transposable elements |
| Q38164153 | Evolutionary transitions in individuality: insights from transposable elements |
| Q33295352 | Exonization of the LTR transposable elements in human genome |
| Q28655926 | Explaining bathymetric diversity patterns in marine benthic invertebrates and demersal fishes: physiological contributions to adaptation of life at depth |
| Q27490892 | Exploring Repetitive DNA Landscapes Using REPCLASS, a Tool That Automates the Classification of Transposable Elements in Eukaryotic Genomes |
| Q56992558 | Expression of the retrotransposonsSurcoufandBlackbeardin the marine diatomPhaeodactylum tricornutumunder thermal stress |
| Q47830904 | FB elements can promote exon shuffling: a promoter-less white allele can be reactivated by FB mediated transposition in Drosophila melanogaster. |
| Q21203760 | Families of transposable elements, population structure and the origin of species |
| Q34648165 | First comparative transcriptomic analysis of wild adult male and female Lutzomyia longipalpis, vector of visceral leishmaniasis |
| Q21267189 | Fosmid library end sequencing reveals a rarely known genome structure of marine shrimp Penaeus monodon |
| Q36193675 | From the margins of the genome: mobile elements shape primate evolution |
| Q42489598 | Function of the genetic element 'Mona' associated with fungicide resistance in Monilinia fructicola |
| Q52745440 | General survey of hAT transposon superfamily with highlight on hobo element in Drosophila. |
| Q28682334 | Genesis and regulatory wiring of retroelement-derived domesticated genes: a phylogenomic perspective |
| Q42239689 | Genetic Drift, Not Life History or RNAi, Determine Long-Term Evolution of Transposable Elements |
| Q35137510 | Genetics of cryptic speciation within an Arctic mustard, Draba nivalis |
| Q22122336 | Genetics: Junk DNA as an evolutionary force |
| Q50986417 | Genome size correlates with reproductive fitness in seed beetles. |
| Q38622812 | Genome size in arthropods; different roles of phylogeny, habitat and life history in insects and crustaceans |
| Q35088732 | Genome-Wide Identification and Classification of MicroRNAs Derived from Repetitive Elements |
| Q92565403 | Genome-Wide Identification of Microsatellites and Transposable Elements in the Dromedary Camel Genome Using Whole-Genome Sequencing Data |
| Q28510627 | Genome-wide B1 retrotransposon binds the transcription factors dioxin receptor and Slug and regulates gene expression in vivo |
| Q35198293 | Genome-wide analysis of mobile genetic element insertion sites |
| Q36282101 | Genome-wide analysis of transposable elements in the coffee berry borer Hypothenemus hampei (Coleoptera: Curculionidae): description of novel families. |
| Q39172561 | Genome-wide identification and expression profiling of DNA methyltransferase gene family in maize |
| Q45487545 | Genomic amplification of the Gret1 retroelement in white-fruited accessions of wild vitis and interspecific hybrids |
| Q28817262 | Genomic characterization of Ensifer aridi, a proposed new species of nitrogen-fixing rhizobium recovered from Asian, African and American deserts. |
| Q34185737 | Genomic diversity in two related plant species with and without sex chromosomes--Silene latifolia and S. vulgaris |
| Q51644456 | Genomics in the light of evolutionary transitions. |
| Q49767833 | Glassy dynamics in the adaptive immune response prevents autoimmune disease |
| Q34511101 | HERV-K(HML-2), a seemingly silent subtenant - but still waters run deep |
| Q40082961 | Hawaiian Drosophila genomes: size variation and evolutionary expansions |
| Q33259824 | Heat-shock promoters: targets for evolution by P transposable elements in Drosophila |
| Q57177754 | Hemochorial placentation: development, function, and adaptations |
| Q28686989 | Hidden magicians of genome evolution |
| Q33378679 | High rate of recent transposable element-induced adaptation in Drosophila melanogaster |
| Q52703732 | Hosimary: a new hAT transposon group involved in horizontal transfer. |
| Q93085933 | Host-transposon interactions: conflict, cooperation, and cooption |
| Q41089812 | Hsp90 and Physiological Stress Are Linked to Autonomous Transposon Mobility and Heritable Genetic Change in Nematodes |
| Q36109600 | Human endogenous retroviruses and their possible impact on dermatology. |
| Q47978465 | IHF is the limiting host factor in transposition of Pseudomonas putida transposon Tn4652 in stationary phase |
| Q28601586 | Identification and characterization of abundant repetitive sequences in Eragrostis tef cv. Enatite genome |
| Q41638647 | Identification and chromosome mapping of repetitive elements in the Astyanax scabripinnis (Teleostei: Characidae) species complex |
| Q51554989 | Identification of Transcription Factor Binding Sites Derived from Transposable Element Sequences Using ChIP-seq |
| Q47988068 | Identification of Ty1-copia retrotransposons in three ectomycorrhizal basidiomycetes: evolutionary relationships and use as molecular markers |
| Q33235037 | Identifying repeat domains in large genomes |
| Q37638210 | Identifying repeats and transposable elements in sequenced genomes: how to find your way through the dense forest of programs. |
| Q34134111 | Illumina TruSeq synthetic long-reads empower de novo assembly and resolve complex, highly-repetitive transposable elements |
| Q34254216 | Impact of foreign DNA integration on tumor biology and on evolution via epigenetic alterations |
| Q34442055 | Impact of transposable elements on the evolution of mammalian gene regulation |
| Q35852303 | In Depth Characterization of Repetitive DNA in 23 Plant Genomes Reveals Sources of Genome Size Variation in the Legume Tribe Fabeae. |
| Q24809485 | Insertion bias and purifying selection of retrotransposons in the Arabidopsis thaliana genome |
| Q37548915 | Insertion sequence distribution bias in Archaea |
| Q34168666 | Insights into the transposable mobilome of Paracoccus spp. (Alphaproteobacteria) |
| Q34477499 | Intrinsic characteristics of neighboring DNA modulate transposable element activity in Drosophila melanogaster |
| Q30980345 | Is small indel bias a determinant of genome size? |
| Q47788081 | Jittery, a Mutator distant relative with a paradoxical mobile behavior: excision without reinsertion |
| Q52596119 | Large Diversity of Nonstandard Genes and Dynamic Evolution of Chloroplast Genomes in Siphonous Green Algae (Bryopsidales, Chlorophyta). |
| Q36439815 | Long-term and short-term evolutionary impacts of transposable elements on Drosophila |
| Q28727809 | Losing identity: structural diversity of transposable elements belonging to different classes in the genome of Anopheles gambiae |
| Q38347641 | MAX, a novel retrotransposon of the BEL-Pao family, is nested within the Bari1 cluster at the heterochromatic h39 region of chromosome 2 in Drosophila melanogaster. |
| Q36000665 | Male germline control of transposable elements |
| Q41786794 | Mar, a MITE family of hAT transposons in Drosophila |
| Q35629302 | Massive amplification of rolling-circle transposons in the lineage of the bat Myotis lucifugus |
| Q62964509 | Meiotic silencing by unpaired DNA |
| Q31138327 | Metagenomic analysis of size-fractionated picoplankton in a marine oxygen minimum zone |
| Q64059832 | Microsatellite Borders and Micro-sequence Conservation in Juglans |
| Q21198751 | Mobile DNA and the TE-Thrust hypothesis: supporting evidence from the primates |
| Q30428528 | Mobilomics in Saccharomyces cerevisiae strains |
| Q37197116 | Molecular Evolution of Drosophila Germline Stem Cell and Neural Stem Cell Regulating Genes |
| Q33292644 | Molecular analysis of a novel tandemly organized repetitive DNA sequence in Citrus limon (L.) Burm. |
| Q42666672 | Molecular characterization of mariner-like elements in emerald ash borer, Agrilus planipennis (Coleoptera, Polyphaga). |
| Q35163088 | Molecular characterization of the genomic region linked with apomixis in Pennisetum/Cenchrus |
| Q37255094 | Molecular evolution and phylogeny of the RPB2 gene in the genus Hordeum |
| Q35143591 | Molecular paleontology of transposable elements in the Drosophila melanogaster genome |
| Q59337341 | Mollusc genomes reveal variability in patterns of LTR-retrotransposons dynamics |
| Q38417739 | Nanger, Eudorcas, Gazella, and Antilope form a well-supported chromosomal clade within Antilopini (Bovidae, Cetartiodactyla). |
| Q35038542 | Natural history of transposition in the green alga Chlamydomonas reinhardtii: use of the AMT4 locus as an experimental system |
| Q41971208 | Natural selection on gene function drives the evolution of LTR retrotransposon families in the rice genome |
| Q51750516 | Nested Ty3-gypsy retrotransposons of a single Beta procumbens centromere contain a putative chromodomain. |
| Q60146999 | Neutral Theory, Transposable Elements, and Eukaryotic Genome Evolution. |
| Q35821676 | Nonadaptive explanations for signatures of partial selective sweeps in Drosophila |
| Q44944883 | Noncoding RNAs: persistent viral agents as modular tools for cellular needs |
| Q54243559 | Nonneutral GC3 and retroelement codon mimicry in Phytophthora. |
| Q36098967 | Nonsense-mediated RNA decay: a molecular system micromanaging individual gene activities and suppressing genomic noise |
| Q35846296 | Origin and evolution of human microRNAs from transposable elements. |
| Q46356906 | Origin of a rapidly evolving homeostatic control system programming testis function |
| Q29617225 | Origin of a substantial fraction of human regulatory sequences from transposable elements |
| Q26824449 | Paleovirology of 'syncytins', retroviral env genes exapted for a role in placentation |
| Q47400161 | Parasitism, the diversity of life, and paleoparasitology |
| Q35867687 | Patterns of repeat-induced point mutation in transposable elements of basidiomycete fungi |
| Q43480410 | Phylogenomic analysis of chromoviruses |
| Q54398285 | Physical properties of DNA components affecting the transposition efficiency of the mariner Mos1 element. |
| Q80773252 | Plant cytosine-5 DNA methyltransferases: structure, function, and molecular evolution |
| Q38110530 | Polyploidy is genetic hence may cause non-adaptive radiations, whereas pseudopolyploidy is genomic hence may cause adaptive non-radiations |
| Q82230505 | Population frequencies of transposable elements in selfing and outcrossing Caenorhabditis nematodes |
| Q35083007 | Population genetics models of competition between transposable element subfamilies |
| Q34823735 | Population genomics of transposable elements in Drosophila melanogaster. |
| Q39109579 | Positive selection on transposase genes of insertion sequences in the Crocosphaera watsonii genome |
| Q34075724 | Prediction of transposable element derived enhancers using chromatin modification profiles |
| Q48062220 | Profile of the mosaic element BTMR1 in the genome of the bumble bee Bombus terrestris (Hymenoptera: Apidae). |
| Q28831298 | Profuse evolutionary diversification and speciation on volcanic islands: transposon instability and amplification bursts explain the genetic paradox |
| Q33227185 | REM1, a new type of long terminal repeat retrotransposon in Chlamydomonas reinhardtii. |
| Q57019817 | RNA Networks as Digital Control Circuits of Nuclear Functions |
| Q57288715 | Rapid expansion of a highly germline-expressed mariner element acquired by horizontal transfer in the fire ant genome |
| Q44139655 | Reciprocal sequence exchange between non-retro viruses and hosts leading to the appearance of new host phenotypes |
| Q46572109 | Reconstructing the evolutionary history of gypsy retrotransposons in the Périgord black truffle (Tuber melanosporum Vittad.). |
| Q39142974 | Reliability of the nanopheres-DNA immunization technology to produce polyclonal antibodies directed against human neogenic proteins |
| Q34065350 | Repetitive DNA elements, nucleosome binding and human gene expression |
| Q33315562 | Repetitive element-mediated recombination as a mechanism for new gene origination in Drosophila |
| Q38937848 | Resolving fine-grained dynamics of retrotransposons: comparative analysis of inferential methods and genomic resources. |
| Q35805976 | Retroelement distributions in the human genome: variations associated with age and proximity to genes |
| Q82880698 | Retrotransposon sequence variation in four asexual plant species |
| Q25255710 | Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line |
| Q50787017 | Role of DNA methylation in growth and differentiation in Physcomitrella patens and characterization of cytosine DNA methyltransferases. |
| Q48280058 | S-element insertions are associated with the evolution of the Hsp70 genes in Drosophila melanogaster |
| Q36689328 | SINEs of progress: Mobile element applications to molecular ecology |
| Q34998054 | Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation |
| Q34574805 | Self-synthesizing DNA transposons in eukaryotes |
| Q50335072 | Selfish genetic elements and the gene’s-eye view of evolution |
| Q51877826 | Selfish genetic elements favor the evolution of a distinction between soma and germline. |
| Q28742794 | Selfish genetic elements, genetic conflict, and evolutionary innovation |
| Q38822875 | Senescence Meets Dedifferentiation |
| Q46237996 | Sequence diversity of a domesticated transposase gene, MUG1, in Oryza species |
| Q37596279 | Sequence organization and insertion specificity of the novel chimeric ISHp609 transposable element of Helicobacter pylori. |
| Q42685576 | Species sympatry and horizontal transfers of Mariner transposons in marine crustacean genomes. |
| Q34104183 | Structural characterization of helitrons and their stepwise capturing of gene fragments in the maize genome |
| Q40481970 | Structural features of conopeptide genes inferred from partial sequences of the Conus tribblei genome. |
| Q33375773 | Survey of repetitive sequences in Silene latifolia with respect to their distribution on sex chromosomes. |
| Q22122020 | Synergy between sequence and size in Large-scale genomics |
| Q28741643 | T-lex: a program for fast and accurate assessment of transposable element presence using next-generation sequencing data |
| Q45854044 | TEtools facilitates big data expression analysis of transposable elements and reveals an antagonism between their activity and that of piRNA genes |
| Q47826784 | Tana1, a new putatively active Tc1-like transposable element in the genome of sturgeons. |
| Q28076462 | Targeted Cancer Therapy: Vital Oncogenes and a New Molecular Genetic Paradigm for Cancer Initiation Progression and Treatment |
| Q42640984 | Teleost fish genomes contain a diverse array of L1 retrotransposon lineages that exhibit a low copy number and high rate of turnover. |
| Q34478652 | The 4D nucleome: Evidence for a dynamic nuclear landscape based on co-aligned active and inactive nuclear compartments |
| Q59888641 | The Association Between Breeding System and Transposable Element Dynamics in Daphnia Pulex |
| Q22066092 | The C-value enigma in plants and animals: a review of parallels and an appeal for partnership |
| Q42642679 | The GC-rich transposon Bytmar1 from the deep-sea hydrothermal crab, Bythograea thermydron, may encode three transposase isoforms from a single ORF. |
| Q35849014 | The Importance of Fossils in Understanding the Evolution of Parasites and Their Vectors |
| Q33290342 | The Juan non-LTR retrotransposon in mosquitoes: genomic impact, vertical transmission and indications of recent and widespread activity |
| Q90188013 | The Telomere Paradox: Stable Genome Preservation with Rapidly Evolving Proteins |
| Q46924603 | The Tvv1 retrotransposon family is conserved between plant genomes separated by over 100 million years |
| Q37442744 | The adaptive role of transposable elements in the Drosophila genome |
| Q22065246 | The case for junk DNA |
| Q36052156 | The dynamics of the roo transposable element in mutation-accumulation lines and segregating populations of Drosophila melanogaster. |
| Q34569974 | The dynamics of transposable elements in structured populations |
| Q35082947 | The fate of transposable elements in asexual populations |
| Q38216621 | The genome as a developmental organ. |
| Q28754467 | The genome sizes of megabats (Chiroptera: Pteropodidae) are remarkably constrained |
| Q52692382 | The hobo-related elements in the melanogaster species group. |
| Q59693328 | The impact of genome defense on mobile elements in Microbotryum |
| Q45050393 | The non-LTR retrotransposon R2 in termites (Insecta, Isoptera): characterization and dynamics |
| Q34376988 | The origin and evolution of six miniature inverted-repeat transposable elements in Bombyx mori and Rhodnius prolixus. |
| Q26851498 | The other face of restriction: modification-dependent enzymes |
| Q37412262 | The role of repetitive DNA in structure and evolution of sex chromosomes in plants. |
| Q22122375 | The role of selfish genetic elements in eukaryotic evolution |
| 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 |
| Q34023612 | Tm1: a mutator/foldback transposable element family in root-knot nematodes |
| Q35074855 | Tracing floral adaptations from ecology to molecules |
| Q30653831 | Transposable Element Insertions in Long Intergenic Non-Coding RNA Genes |
| Q34972935 | Transposable element derived DNaseI-hypersensitive sites in the human genome. |
| Q34007229 | Transposable element dynamics among asymbiotic and ectomycorrhizal Amanita fungi. |
| Q52662835 | Transposable element orientation bias in the Drosophila melanogaster genome. |
| Q33453627 | Transposable elements and an epigenetic basis for punctuated equilibria |
| Q33881233 | Transposable elements and factors influencing their success in eukaryotes |
| Q38116552 | Transposable elements and microevolutionary changes in natural populations |
| Q28756349 | Transposable elements and the evolution of regulatory networks |
| Q28710587 | Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE-Thrust hypothesis |
| Q33279847 | Transposable elements are enriched within or in close proximity to xenobiotic-metabolizing cytochrome P450 genes |
| Q28660225 | Transposable elements: from DNA parasites to architects of metazoan evolution |
| Q37470360 | Transposable elements: powerful facilitators of evolution |
| Q34917208 | Transposon domestication versus mutualism in ciliate genome rearrangements |
| Q34347048 | Transposon insertion sequencing: a new tool for systems-level analysis of microorganisms. |
| Q33935404 | Transposons, environmental changes, and heritable induced phenotypic variability. |
| Q30961710 | Tropism switching in Bordetella bacteriophage defines a family of diversity-generating retroelements |
| Q36370833 | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
| Q92914698 | Unusual genome expansion and transcription suppression in ectomycorrhizal Tricholoma matsutake by insertions of transposable elements |
| Q38753540 | VHICA, a New Method to Discriminate between Vertical and Horizontal Transposon Transfer: Application to the Mariner Family within Drosophila. |
| Q36014539 | What Can Domesticated Genes Tell Us about the Intron Gain in Mammals? |
| Q27489427 | What can you do with 0.1× genome coverage? A case study based on a genome survey of the scuttle fly Megaselia scalaris (Phoridae) |
| Q28959214 | Why Do We Name Organisms? Some Reminders from the past |
| Q52701237 | hAT transposable elements and their derivatives: an analysis in the 12 Drosophila genomes. |
| Q36512094 | p53 cooperates with DNA methylation and a suicidal interferon response to maintain epigenetic silencing of repeats and noncoding RNAs |
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