| scholarly article | Q13442814 |
| P2093 | author name string | John V Moran | |
| Raheleh Rahbari | |||
| Richard M Badge | |||
| Christine R Beck | |||
| Catriona M Macfarlane | |||
| John F Wagstaff | |||
| Pamela Collier | |||
| Samantha Igoe | |||
| 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 | ||
| Positional cloning of the gene for X-linked retinitis pigmentosa 2 | Q24322014 | ||
| Mapping copy number variation by population-scale genome sequencing | Q24615307 | ||
| A map of human genome variation from population-scale sequencing | Q24617794 | ||
| BLAT—The BLAST-Like Alignment Tool | Q24682492 | ||
| Basic local alignment search tool | Q25938991 | ||
| Structural constraints on RNA virus evolution | Q27469715 | ||
| Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
| Mammalian small nucleolar RNAs are mobile genetic elements | Q28469078 | ||
| LINE-1 elements in structural variation and disease | Q28654758 | ||
| LINE-1 retrotransposition activity in human genomes | Q28743798 | ||
| Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans | Q28744043 | ||
| High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes | Q28749562 | ||
| Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion | Q28776429 | ||
| Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition | Q28776447 | ||
| A greedy algorithm for aligning DNA sequences | Q29547622 | ||
| High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
| Human LINE retrotransposons generate processed pseudogenes | Q29618327 | ||
| Human L1 retrotransposition: cis preference versus trans complementation | Q29618363 | ||
| LINE-mediated retrotransposition of marked Alu sequences | Q29618440 | ||
| Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition | Q29618826 | ||
| A new exon created by intronic insertion of a rearranged LINE-1 element as the cause of chronic granulomatous disease | Q74297952 | ||
| High polymorphism level of genomic sequences flanking insertion sites of human endogenous retroviral long terminal repeats | Q74456195 | ||
| L1 retrotransposition in human neural progenitor cells | Q29619265 | ||
| Natural mutagenesis of human genomes by endogenous retrotransposons | Q29619443 | ||
| Somatic retrotransposition alters the genetic landscape of the human brain | Q29622895 | ||
| Exon shuffling by L1 retrotransposition | Q29622913 | ||
| A new family of chimeric retrotranscripts formed by a full copy of U6 small nuclear RNA fused to the 3' terminus of l1. | Q30738344 | ||
| ATLAS: a system to selectively identify human-specific L1 insertions. | Q33905045 | ||
| SVA elements are nonautonomous retrotransposons that cause disease in humans | Q33905356 | ||
| Multiple fates of L1 retrotransposition intermediates in cultured human cells. | Q33925050 | ||
| Disruption of the APC gene by a retrotransposal insertion of L1 sequence in a colon cancer | Q34233218 | ||
| Rescuing Alu: recovery of new inserts shows LINE-1 preserves Alu activity through A-tail expansion | Q34388491 | ||
| A human genome structural variation sequencing resource reveals insights into mutational mechanisms | Q34519304 | ||
| Natural genetic variation caused by transposable elements in humans | Q34569749 | ||
| Identification, characterization, and cell specificity of a human LINE-1 promoter | Q34570051 | ||
| Multiplex allele-specific target amplification based on PCR suppression | Q34590290 | ||
| Extensive individual variation in L1 retrotransposition capability contributes to human genetic diversity | Q34597888 | ||
| L1 retrotransposition in neurons is modulated by MeCP2 | Q34686579 | ||
| Frequent human genomic DNA transduction driven by LINE-1 retrotransposition | Q35026231 | ||
| Retrotransposition of marked SVA elements by human L1s in cultured cells | Q35155981 | ||
| Similarities between long interspersed element-1 (LINE-1) reverse transcriptase and telomerase. | Q35650833 | ||
| Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon | Q35672729 | ||
| Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
| Many human L1 elements are capable of retrotransposition | Q36859141 | ||
| A comprehensive analysis of recently integrated human Ta L1 elements | Q37218123 | ||
| Evidence consistent with human L1 retrotransposition in maternal meiosis I. | Q37218145 | ||
| L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism | Q37240559 | ||
| LINE-1 retrotransposition in human embryonic stem cells | Q40139315 | ||
| More active human L1 retrotransposons produce longer insertions | Q40695421 | ||
| Transduction of 3'-flanking sequences is common in L1 retrotransposition | Q40896511 | ||
| Mobile interspersed repeats are major structural variants in the human genome | Q42423737 | ||
| IAP display: a simple method to identify mouse strain specific IAP insertions | Q42587636 | ||
| Isolation of an active human transposable element | Q42614185 | ||
| Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence | Q42660978 | ||
| Cis-preferential LINE-1 reverse transcriptase activity in ribonucleoprotein particles | Q42688858 | ||
| A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion | Q42693461 | ||
| Estimating the age of retrotransposon subfamilies using maximum likelihood | Q43104160 | ||
| Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells | Q47948394 | ||
| L1 retrotransposition can occur early in human embryonic development. | Q51986818 | ||
| A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events. | Q53905712 | ||
| Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon | Q59409782 | ||
| L1 (LINE-1) retrotransposon evolution and amplification in recent human history | Q73837883 | ||
| Selection against deleterious LINE-1-containing loci in the human lineage | Q73923911 | ||
| P433 | issue | 7 | |
| P921 | main subject | retrotransposon | Q413988 |
| P304 | page(s) | 974-985 | |
| P577 | publication date | 2013-04-23 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | Transduction-specific ATLAS reveals a cohort of highly active L1 retrotransposons in human populations | |
| P478 | volume | 34 |
| Q33558345 | A comprehensive approach to expression of L1 loci |
| Q28602786 | Activation of individual L1 retrotransposon instances is restricted to cell-type dependent permissive loci |
| Q47163077 | Detection of subclonal L1 transductions in colorectal cancer by long-distance inverse-PCR and Nanopore sequencing |
| Q64076955 | Dynamic Methylation of an L1 Transduction Family during Reprogramming and Neurodifferentiation |
| Q35575837 | Genome-wide amplification of proviral sequences reveals new polymorphic HERV-K(HML-2) proviruses in humans and chimpanzees that are absent from genome assemblies |
| Q64913254 | Heritable L1 Retrotransposition Events During Development: Understanding Their Origins: Examination of heritable, endogenous L1 retrotransposition in mice opens up exciting new questions and research directions. |
| Q41199624 | Heritable L1 retrotransposition in the mouse primordial germline and early embryo |
| Q52593254 | L1 retrotransposition is a common feature of mammalian hepatocarcinogenesis. |
| Q35234637 | Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes |
| Q35687336 | Mobile element insertions are frequent in oesophageal adenocarcinomas and can mislead paired-end sequencing analysis |
| Q36012836 | Next-generation sequencing-based detection of germline L1-mediated transductions |
| Q52673975 | Spliced integrated retrotransposed element (SpIRE) formation in the human genome. |
| Q39130945 | The Human Long Interspersed Element-1 Retrotransposon: An Emerging Biomarker of Neoplasia. |
| Q26851352 | The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes |
| Q38601704 | The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology |
| Q32183705 | The Role of Somatic L1 Retrotransposition in Human Cancers |
| Q39392722 | Transposable elements in cancer |
| Q28648093 | U6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in Mammals |
| Q35438613 | Ubiquitous L1 mosaicism in hippocampal neurons |
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