| Systematic survey of plant LTR-retrotransposons elucidates phylogenetic relationships of their polyprotein domains and provides a reference for element classification |
36 |
| L1 retrotransposition in the soma: a field jumping ahead |
17 |
| Diseases of the nERVous system: retrotransposon activity in neurodegenerative disease |
15 |
| Mouse germ line mutations due to retrotransposon insertions |
14 |
| Variation in proviral content among human genomes mediated by LTR recombination |
11 |
| Sex and the TEs: transposable elements in sexual development and function in animals |
11 |
| The case for not masking away repetitive DNA |
11 |
| Transcriptionally promiscuous blurry promoters in Tc1/mariner transposons allow transcription in distantly related genomes |
8 |
| The Transposon Registry |
8 |
| The landscape of transposable elements and satellite DNAs in the genome of a dioecious plant spinach (Spinacia oleracea L.) |
8 |
| Genetic exchange in eukaryotes through horizontal transfer: connected by the mobilome |
7 |
| Carbapenemases on the move: it's good to be on ICEs |
7 |
| LTR_FINDER_parallel: parallelization of LTR_FINDER enabling rapid identification of long terminal repeat retrotransposons |
6 |
| Properties of LINE-1 proteins and repeat element expression in the context of amyotrophic lateral sclerosis |
6 |
| Transposon insertion profiling by sequencing (TIPseq) for mapping LINE-1 insertions in the human genome |
6 |
| The SAMHD1-mediated block of LINE-1 retroelements is regulated by phosphorylation |
6 |
| A benchmark of transposon insertion detection tools using real data |
6 |
| LINE-1 ORF2p expression is nearly imperceptible in human cancers |
6 |
| The impact of transposable element activity on therapeutically relevant human stem cells |
6 |
| Tools and best practices for retrotransposon analysis using high-throughput sequencing data |
5 |
| Phylogeographic diversity and mosaicism of the Helicobacter pylori tfs integrative and conjugative elements |
5 |
| Insertion of a chimeric retrotransposon sequence in mouse Axin1 locus causes metastable kinky tail phenotype |
4 |
| Deletion of the sex-determining gene SXI1 alpha enhances the spread of mitochondrial introns in Cryptococcus neoformans |
4 |
| Impact of non-LTR retrotransposons in the differentiation and evolution of anatomically modern humans |
4 |
| A computational reconstruction of Papio phylogeny using Alu insertion polymorphisms |
4 |
| Transposable elements and gene expression during the evolution of amniotes |
4 |
| Incomer, a DD36E family of Tc1/mariner transposons newly discovered in animals |
4 |
| Extensive exchange of transposable elements in the Drosophila pseudoobscura group |
4 |
| Length variations within the Merle retrotransposon of canine PMEL: correlating genotype with phenotype |
4 |
| Human transposable elements in Repbase: genomic footprints from fish to humans |
4 |
| Differential retention of transposable element-derived sequences in outcrossing Arabidopsis genomes |
3 |
| Human transposons are an abundant supply of transcription factor binding sites and promoter activities in breast cancer cell lines |
3 |
| Long interspersed nuclear element-1 expression and retrotransposition in prostate cancer cells |
3 |
| High-performance gene expression and knockout tools using sleeping beauty transposon system |
3 |
| The dynamic intein landscape of eukaryotes |
3 |
| Paired-end mappability of transposable elements in the human genome |
3 |
| Identification of charged amino acids required for nuclear localization of human L1 ORF1 protein |
3 |
| Retrotransposons evolution and impact on lncRNA and protein coding genes in pigs |
3 |
| sRNAPipe: a Galaxy-based pipeline for bioinformatic in-depth exploration of small RNAseq data |
3 |
| Alu insertion polymorphisms shared by Papio baboons and Theropithecus gelada reveal an intertwined common ancestry |
3 |
| Characterization of a relaxase belonging to the MOBT family, a widespread family in Firmicutes mediating the transfer of ICEs |
3 |
| The toxic guardians multiple toxin-antitoxin systems provide stability, avoid deletions and maintain virulence genes of Pseudomonas syringae virulence plasmids |
3 |
| Nucleotide composition of transposable elements likely contributes to AT/GC compositional homogeneity of teleost fish genomes |
3 |
| AluMine: alignment-free method for the discovery of polymorphic Alu element insertions |
3 |
| A mobile restriction modification system consisting of methylases on the IncA/C plasmid |
3 |
| Drosophila parasitoid wasps bears a distinct DNA transposon profile |
2 |
| Subtype classification and functional annotation of L1Md retrotransposon promoters |
2 |
| Evolution of Mutator transposable elements across eukaryotic diversity |
2 |
| Analysis of lineage-specific Alu subfamilies in the genome of the olive baboon, Papio anubis |
2 |
| flam piRNA precursors channel from the nucleus to the cytoplasm in a temporally regulated manner along Drosophila oogenesis |
2 |
