| scholarly article | Q13442814 |
| P50 | author | Sheila Lutz | Q28833250 |
| Tammy A Morrish | Q56507933 | ||
| P2093 | author name string | John V Moran | |
| Nicolas Gilbert | |||
| 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 | ||
| Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
| Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene | Q24555185 | ||
| Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination | Q24647405 | ||
| BLAT—The BLAST-Like Alignment Tool | Q24682492 | ||
| Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
| DNA deamination: not just a trigger for antibody diversification but also a mechanism for defense against retroviruses | Q28182624 | ||
| Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: A mechanism for non-LTR retrotransposition | Q28297748 | ||
| Capture of DNA sequences at double-strand breaks in mammalian chromosomes | Q28346450 | ||
| Recombination creates novel L1 (LINE-1) elements in Rattus norvegicus | Q28769427 | ||
| High efficiency transformation of Escherichia coli with plasmids | Q29616589 | ||
| Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
| High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
| Exon shuffling by L1 retrotransposition | Q29622913 | ||
| Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons | Q30004188 | ||
| A new family of chimeric retrotranscripts formed by a full copy of U6 small nuclear RNA fused to the 3' terminus of l1. | Q30738344 | ||
| Cell type-specific expression of LINE-1 open reading frames 1 and 2 in fetal and adult human tissues | Q33200676 | ||
| Multiple homing pathways used by yeast mitochondrial group II introns | Q33605483 | ||
| Sequence-specific single-strand RNA binding protein encoded by the human LINE-1 retrotransposon | Q33887614 | ||
| Allelic Heterogeneity in LINE-1 Retrotransposition Activity | Q33905345 | ||
| Defining the beginning and end of KpnI family segments | Q33939728 | ||
| Promiscuous patching of broken chromosomes in mammalian cells with extrachromosomal DNA. | Q33948430 | ||
| Expansions and contractions in a tandem repeat induced by double-strand break repair | Q33994800 | ||
| Human L1 element target-primed reverse transcription in vitro | Q34207225 | ||
| The unusual phylogenetic distribution of retrotransposons: a hypothesis | Q34227405 | ||
| The optimization of preparations of competent cells for transformation of E. coli. | Q34331706 | ||
| Efficient copying of nonhomologous sequences from ectopic sites via P-element-induced gap repair | Q34336201 | ||
| LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis | Q34388506 | ||
| Abortive transposition by a group II intron in yeast mitochondria | Q34567148 | ||
| Cytoplasmic ribonucleoprotein complexes containing human LINE-1 protein and RNA | Q35844482 | ||
| Homology-directed repair is a major double-strand break repair pathway in mammalian cells | Q36065571 | ||
| The LINE-1 DNA sequences in four mammalian orders predict proteins that conserve homologies to retrovirus proteins | Q36120853 | ||
| Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
| Mobile group II introns of yeast mitochondrial DNA are novel site-specific retroelements | Q36551136 | ||
| Gene conversion as a secondary mechanism of short interspersed element (SINE) evolution | Q36566264 | ||
| Unit-length line-1 transcripts in human teratocarcinoma cells | Q36785924 | ||
| Many human L1 elements are capable of retrotransposition | Q36859141 | ||
| A YY1-binding site is required for accurate human LINE-1 transcription initiation | Q37346150 | ||
| Studies on p40, the leucine zipper motif-containing protein encoded by the first open reading frame of an active human LINE-1 transposable element | Q38325406 | ||
| Nucleic acid chaperone activity of the ORF1 protein from the mouse LINE-1 retrotransposon | Q39457323 | ||
| Role of the nucleotide excision repair gene ERCC1 in formation of recombination-dependent rearrangements in mammalian cells | Q39584494 | ||
| Non-homologous DNA end joining in plant cells is associated with deletions and filler DNA insertions | Q39721716 | ||
| The human genome contains many types of chimeric retrogenes generated through in vivo RNA recombination | Q39808514 | ||
| Group II intron mobility using nascent strands at DNA replication forks to prime reverse transcription | Q39918422 | ||
| Twin priming: a proposed mechanism for the creation of inversions in L1 retrotransposition | Q40415833 | ||
| Species-specific double-strand break repair and genome evolution in plants | Q40430402 | ||
| Characterization of double-strand break-induced recombination: homology requirements and single-stranded DNA formation | Q40653881 | ||
| More active human L1 retrotransposons produce longer insertions | Q40695421 | ||
| Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity | Q40790401 | ||
| The origin of interspersed repeats in the human genome | Q41312150 | ||
| Cin4, an insert altering the structure of the A1 gene in Zea mays, exhibits properties of nonviral retrotransposons | Q41358296 | ||
| Isolation of an active human transposable element | Q42614185 | ||
| Subfamilies of CR1 non-LTR retrotransposons have different 5'UTR sequences but are otherwise conserved | Q42645272 | ||
| Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence | Q42660978 | ||
| A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion | Q42693461 | ||
| A potential role for the nucleolus in L1 retrotransposition | Q44804000 | ||
| Recombination between subtypes creates a mosaic lineage of LINE-1 that is expressed and actively retrotransposing in the mouse genome | Q47754730 | ||
| Genomic rearrangements of the APC tumor-suppressor gene in familial adenomatous polyposis. | Q47830163 | ||
| Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells | Q47948394 | ||
| The structures of mouse and human L1 elements reflect their insertion mechanism. | Q48125977 | ||
| DNA repair mediated by endonuclease-independent LINE-1 retrotransposition | Q48304886 | ||
| Recently integrated Alu elements and human genomic diversity. | Q51639129 | ||
| The disabled 1 gene is disrupted by a replacement with L1 fragment in yotari mice. | Q52171405 | ||
| Targeting of human retrotransposon integration is directed by the specificity of the L1 endonuclease for regions of unusual DNA structure. | Q52533614 | ||
| A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events. | Q53905712 | ||
| Dispersal process associated with the L1 family of interspersed repetitive DNA sequences | Q70652228 | ||
| A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion | Q73704837 | ||
| L1 (LINE-1) retrotransposon evolution and amplification in recent human history | Q73837883 | ||
| High processivity of the reverse transcriptase from a non-long terminal repeat retrotransposon | Q74420441 | ||
| Genomic deletions created upon LINE-1 retrotransposition | Q74604693 | ||
| Human l1 retrotransposition is associated with genetic instability in vivo | Q74604697 | ||
| The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin | Q77599411 | ||
| Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genes | Q77986277 | ||
| How plants make ends meet: DNA double-strand break repair | Q78004553 | ||
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 7780-7795 | |
| P577 | publication date | 2005-09-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Multiple fates of L1 retrotransposition intermediates in cultured human cells | |
| P478 | volume | 25 |
| Q28657858 | 2013 Curt Stern Award Address |
| Q33872587 | A LINE-1 component to human aging: do LINE elements exact a longevity cost for evolutionary advantage? |
| Q52346741 | A Role for Retrotransposons in Chromothripsis. |
| Q36959154 | A hot L1 retrotransposon evades somatic repression and initiates human colorectal cancer |
| Q34519304 | A human genome structural variation sequencing resource reveals insights into mutational mechanisms |
| Q64949170 | A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element. |
| Q34077410 | A mobile threat to genome stability: The impact of non-LTR retrotransposons upon the human genome |
| Q61454317 | A study of meiomitosis and novel pathways of genomic instability in cutaneous T-cell lymphomas (CTCL) |
| Q33293405 | A yeast model for target-primed (non-LTR) retrotransposition |
| Q37730711 | APOBEC3A deaminates transiently exposed single-strand DNA during LINE-1 retrotransposition |
| Q29617668 | Active human retrotransposons: variation and disease |
| Q35214717 | Active retrotransposition by a synthetic L1 element in mice |
| Q37167429 | An alternative pathway for Alu retrotransposition suggests a role in DNA double-strand break repair |
| Q35650901 | Ataxia telangiectasia mutated (ATM) modulates long interspersed element-1 (L1) retrotransposition in human neural stem cells |
| Q89637760 | BRCA1 and S phase DNA repair pathways restrict LINE-1 retrotransposition in human cells |
| Q48323081 | Behavior genetics and postgenomics |
| Q33773663 | Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2. |
| Q35641945 | Cell divisions are required for L1 retrotransposition |
| Q64084268 | Centromere Repeats: Hidden Gems of the Genome |
| Q40074657 | Characterisation of cytoplasmic DNA complementary to non-retroviral RNA viruses in human cells |
| Q35748445 | Characterization of pre-insertion loci of de novo L1 insertions |
| Q36846293 | Chimeric retrogenes suggest a role for the nucleolus in LINE amplification |
| Q36435097 | Circular retrotransposition products generated by a LINE retrotransposon |
| Q42688858 | Cis-preferential LINE-1 reverse transcriptase activity in ribonucleoprotein particles |
| Q60935156 | Common Chromosomal Fragile Sites-Conserved Failure Stories |
| Q45881268 | Condensin II and GAIT complexes cooperate to restrict LINE-1 retrotransposition in epithelial cells. |
| Q90662874 | Contribution of retrotransposition to developmental disorders |
| Q28654545 | Control of mammalian retrotransposons by cellular RNA processing activities |
| Q26770538 | Crossing the LINE Toward Genomic Instability: LINE-1 Retrotransposition in Cancer |
| Q35016894 | DNA damage and L1 retrotransposition |
| Q28762973 | Different evolutionary fates of recently integrated human and chimpanzee LINE-1 retrotransposons |
| Q42093576 | Different integration site structures between L1 protein-mediated retrotransposition in cis and retrotransposition in trans |
| Q36337667 | Discovery and characterization of Alu repeat sequences via precise local read assembly |
| Q28602929 | Discovery of a new repeat family in the Callithrix jacchus genome |
| Q35757888 | Distinct mechanisms for trans-mediated mobilization of cellular RNAs by the LINE-1 reverse transcriptase. |
| Q37150856 | Diverse cis factors controlling Alu retrotransposition: what causes Alu elements to die? |
| Q35894840 | Double strand break repair by capture of retrotransposon sequences and reverse-transcribed spliced mRNA sequences in mouse zygotes |
| Q64076955 | Dynamic Methylation of an L1 Transduction Family during Reprogramming and Neurodifferentiation |
| Q35333511 | Dynamic interactions between transposable elements and their hosts |
| Q33654825 | Dynamic silencing of somatic L1 retrotransposon insertions reflects the developmental and cellular contexts of their genomic integration |
| Q34768580 | ERCC1/XPF limits L1 retrotransposition |
| Q40161913 | Endonuclease-independent LINE-1 retrotransposition at mammalian telomeres |
| Q35893869 | Endonuclease-independent insertion provides an alternative pathway for L1 retrotransposition in the human genome |
| Q37111967 | Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles |
| Q43104160 | Estimating the age of retrotransposon subfamilies using maximum likelihood |
| Q37408919 | Evidence for L1-associated DNA rearrangements and negligible L1 retrotransposition in glioblastoma multiforme. |
| Q33491932 | Evolution of serum albumin intron-1 is shaped by a 5' truncated non-long terminal repeat retrotransposon in western Palearctic water frogs (Neobatrachia). |
| Q34597888 | Extensive individual variation in L1 retrotransposition capability contributes to human genetic diversity |
| Q36446178 | Extensive somatic L1 retrotransposition in colorectal tumors |
| Q36700166 | Extensive variation between inbred mouse strains due to endogenous L1 retrotransposition |
| Q25255521 | Gamma radiation increases endonuclease-dependent L1 retrotransposition in a cultured cell assay |
| Q36523920 | Generation of neuronal variability and complexity |
| Q28475291 | Genetic evidence that the non-homologous end-joining repair pathway is involved in LINE retrotransposition |
| Q42872535 | Genetically tagged TRE5-A retrotransposons reveal high amplification rates and authentic target site preference in the Dictyostelium discoideum genome |
| Q92905141 | Genome-wide de novo L1 Retrotransposition Connects Endonuclease Activity with Replication |
| Q24813998 | Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages |
| Q39957898 | Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination |
| Q28748535 | Heads or tails: L1 insertion-associated 5' homopolymeric sequences |
| 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. |
| Q30439401 | High G+C Content of Herpes Simplex Virus DNA: Proposed Role in Protection Against Retrotransposon Insertion |
| Q24625056 | Human LINE-1 restriction by APOBEC3C is deaminase independent and mediated by an ORF1p interaction that affects LINE reverse transcriptase activity |
| Q34658368 | Human genomic deletions mediated by recombination between Alu elements. |
| Q34579710 | Integrated mechanism for the generation of the 5' junctions of LINE inserts |
| Q38912198 | Integration site selection by retroviruses and transposable elements in eukaryotes |
| Q37442539 | Internal priming: an opportunistic pathway for L1 and Alu retrotransposition in hominins |
| Q39268078 | Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network |
| Q50514705 | Involvement of retrotransposition of long interspersed nucleotide element-1 in skin tumorigenesis induced by 7,12-dimethylbenz[a]anthracene and 12-O-tetradecanoylphorbol-13-acetate. |
| Q34338865 | L1 integration in a transgenic mouse model |
| Q29619265 | L1 retrotransposition in human neural progenitor cells |
| Q34650044 | L1 retrotransposition in nondividing and primary human somatic cells |
| Q55692166 | L1 retrotransposition in the soma: a field jumping ahead. |
| Q52593254 | L1 retrotransposition is a common feature of mammalian hepatocarcinogenesis. |
| Q41507104 | LEAP: L1 Element Amplification Protocol |
| Q90798404 | LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV |
| Q38792667 | LINE-1 Cultured Cell Retrotransposition Assay |
| Q24309597 | LINE-1 ORF1 protein localizes in stress granules with other RNA-binding proteins, including components of RNA interference RNA-induced silencing complex |
| Q42908408 | LINE-1 activation and epigenetic silencing of suppressor genes in cancer: Causally related events? |
| Q28654758 | LINE-1 elements in structural variation and disease |
| Q38579541 | LINE-1 in cancer: multifaceted functions and potential clinical implications |
| Q28743798 | LINE-1 retrotransposition activity in human genomes |
| Q40139315 | LINE-1 retrotransposition in human embryonic stem cells |
| Q37052335 | LINE-like retrotransposition in Saccharomyces cerevisiae |
| Q33891862 | Laboratory methods for the analysis of primate mobile elements |
| Q51506637 | Large-scale DNA editing of retrotransposons accelerates mammalian genome evolution. |
| Q34795214 | Links between repeated sequences |
| Q90123824 | Long INterspersed element-1 mobility as a sensor of environmental stresses |
| Q37226797 | Long interspersed element-1 is differentially regulated by food-borne carcinogens via the aryl hydrocarbon receptor |
| Q28469078 | Mammalian small nucleolar RNAs are mobile genetic elements |
| Q36513588 | Mechanism of Alu integration into the human genome |
| Q38227447 | Mobile DNA elements in the generation of diversity and complexity in the brain |
| Q45870074 | Mobile DNA in Health and Disease |
| Q37363166 | Mobile elements create structural variation: analysis of a complete human genome. |
| Q45912497 | Mobility pathways for vertebrate L1, L2, CR1, and RTE clade retrotransposons. |
| Q35999488 | Modes of retrotransposition of long interspersed element-1 by environmental factors |
| Q30409886 | Mosaic copy number variation in human neurons |
| Q64117464 | Mouse germ line mutations due to retrotransposon insertions |
| Q34315696 | Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations. |
| Q42229646 | Novel retrotransposon analysis reveals multiple mobility pathways dictated by hosts |
| Q28749650 | Origin and evolution of LINE-1 derived "half-L1" retrotransposons (HAL1) |
| Q89556828 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition |
| Q37392213 | Plug and play modular strategies for synthetic retrotransposons. |
| Q51401747 | Positive selection of the TRIM family regulatory region in primate genomes. |
| Q41789519 | Processed pseudogene insertions in somatic cells |
| Q36739673 | Progress in understanding the biology of the human mutagen LINE-1. |
| Q36150521 | R2 and R2/R1 hybrid non-autonomous retrotransposons derived by internal deletions of full-length elements |
| Q90240488 | RNA ligation precedes the retrotransposition of U6/LINE-1 chimeric RNA |
| Q41642419 | Recessive inheritance of population-specific intronic LINE-1 insertion causes a rotor syndrome phenotype |
| Q35214947 | Recurrent duplication-driven transposition of DNA during hominoid evolution |
| Q35762302 | Repetitive sequence environment distinguishes housekeeping genes |
| Q35605212 | Reprogramming somatic cells into iPS cells activates LINE-1 retroelement mobility |
| Q36511186 | Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells |
| Q34388491 | Rescuing Alu: recovery of new inserts shows LINE-1 preserves Alu activity through A-tail expansion |
| Q36723382 | Resolving rates of mutation in the brain using single-neuron genomics |
| Q35611983 | Restless genomes humans as a model organism for understanding host-retrotransposable element dynamics |
| Q37569864 | Retroelements and their impact on genome evolution and functioning |
| Q35737495 | Retrohoming of a Mobile Group II Intron in Human Cells Suggests How Eukaryotes Limit Group II Intron Proliferation |
| Q35155981 | Retrotransposition of marked SVA elements by human L1s in cultured cells |
| Q90321264 | Retrotransposon-induced mosaicism in the neural genome |
| Q24336732 | Ribonucleoprotein particle formation is necessary but not sufficient for LINE-1 retrotransposition |
| Q39126884 | Role of RNA polymerase III transcription factors in the selection of integration sites by the dictyostelium non-long terminal repeat retrotransposon TRE5-A. |
| Q26751314 | Roles for retrotransposon insertions in human disease |
| Q34048853 | Selective inhibition of Alu retrotransposition by APOBEC3G. |
| Q34472380 | Sequencing, identification and mapping of primed L1 elements (SIMPLE) reveals significant variation in full length L1 elements between individuals |
| Q41685071 | Similar Evolutionary Trajectories for Retrotransposon Accumulation in Mammals. |
| Q35650833 | Similarities between long interspersed element-1 (LINE-1) reverse transcriptase and telomerase. |
| Q64056736 | Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals |
| Q52673975 | Spliced integrated retrotransposed element (SpIRE) formation in the human genome. |
| Q36345993 | TRE5-A retrotransposition profiling reveals putative RNA polymerase III transcription complex binding sites on the Dictyostelium extrachromosomal rDNA element. |
| Q47841428 | Targeted deletion of a 170 kb cluster of LINE1 repeats: implications for regional control |
| Q37521827 | The Flow of the Gibbon LAVA Element Is Facilitated by the LINE-1 Retrotransposition Machinery |
| Q26851352 | The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes |
| Q37392305 | The L1 retrotransposition assay: a retrospective and toolkit |
| Q38601704 | The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology |
| Q34085626 | The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertion |
| Q36239040 | The Nucleotide Excision Repair Pathway Limits L1 Retrotransposition |
| Q28547090 | The Zinc-Finger Antiviral Protein ZAP Inhibits LINE and Alu Retrotransposition |
| Q36815466 | The endonuclease domain of the LINE-1 ORF2 protein can tolerate multiple mutations |
| Q24594901 | The impact of retrotransposons on human genome evolution |
| Q64112074 | The impact of transposable element activity on therapeutically relevant human stem cells |
| Q39272696 | The minimal active human SVA retrotransposon requires only the 5'-hexamer and Alu-like domains |
| Q41577828 | The non-autonomous retrotransposon SVA is trans-mobilized by the human LINE-1 protein machinery |
| Q28480874 | The retrohoming of linear group II intron RNAs in Drosophila melanogaster occurs by both DNA ligase 4-dependent and -independent mechanisms |
| Q34708776 | The reverse transcriptase encoded by the non-LTR retrotransposon R2 is as error-prone as that encoded by HIV-1 |
| Q34722563 | The specificity and flexibility of l1 reverse transcription priming at imperfect T-tracts |
| Q34804306 | The take and give between retrotransposable elements and their hosts |
| Q52609119 | Thrombopoietin protects hematopoietic stem cells from retrotransposon-mediated damage by promoting an antiviral response. |
| Q47148868 | Transcription coupled repair and biased insertion of human retrotransposon L1 in transcribed genes |
| Q37433509 | Transduction-specific ATLAS reveals a cohort of highly active L1 retrotransposons in human populations |
| Q39392722 | Transposable elements in cancer |
| Q48248558 | Transposable elements: genome innovation, chromosome diversity, and centromere conflict. |
| Q33301955 | Tripartite chimeric pseudogene from the genome of rice blast fungus Magnaporthe grisea suggests double template jumps during long interspersed nuclear element (LINE) reverse transcription |
| Q35451036 | Type I interferon controls propagation of long interspersed element-1. |
| Q28648093 | U6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in Mammals |
| Q35438613 | Ubiquitous L1 mosaicism in hippocampal neurons |
| Q37114645 | Viral protein R of human immunodeficiency virus type-1 induces retrotransposition of long interspersed element-1. |
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