| scholarly article | Q13442814 |
| P2093 | author name string | Haig H Kazazian | |
| John L Goodier | |||
| Prabhat K Mandal | |||
| Dustin C Hancks | |||
| Ling E Cheung | |||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Characterization of LINE-1 ribonucleoprotein particles | Q21092434 | ||
| Active Alu retrotransposons in the human genome | Q22065778 | ||
| Hot L1s account for the bulk of retrotransposition in the human population | Q22066292 | ||
| LINE-1 ORF1 protein localizes in stress granules with other RNA-binding proteins, including components of RNA interference RNA-induced silencing complex | Q24309597 | ||
| Molecular mechanisms of autosomal recessive hypercholesterolemia | Q24315900 | ||
| Non-LTR retrotransposons encode noncanonical RRM domains in their first open reading frame | Q24316232 | ||
| An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy | Q24320265 | ||
| The impact of retrotransposons on human genome evolution | Q24594901 | ||
| The human genome browser at UCSC | Q24672361 | ||
| A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus | Q24675271 | ||
| Molecular archeology of L1 insertions in the human genome. | Q24794428 | ||
| WebLogo: A Sequence Logo Generator | Q27860646 | ||
| Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
| Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene dupli | Q28250748 | ||
| A de novo Alu insertion results in neurofibromatosis type 1 | Q28281046 | ||
| 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 | ||
| L1 recombination-associated deletions generate human genomic variation | Q28755851 | ||
| Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
| 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 | ||
| Natural mutagenesis of human genomes by endogenous retrotransposons | Q29619443 | ||
| Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons | Q30004188 | ||
| Cellular inhibitors of long interspersed element 1 and Alu retrotransposition. | Q30445599 | ||
| Epigenetic silencing of engineered L1 retrotransposition events in human embryonic carcinoma cells. | Q30498112 | ||
| A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes | Q30830058 | ||
| Mobile element scanning (ME-Scan) by targeted high-throughput sequencing | Q33622007 | ||
| SVA elements are nonautonomous retrotransposons that cause disease in humans | Q33905356 | ||
| Multiple fates of L1 retrotransposition intermediates in cultured human cells. | Q33925050 | ||
| SVA retrotransposons: Evolution and genetic instability | Q34156329 | ||
| Human L1 element target-primed reverse transcription in vitro | Q34207225 | ||
| A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis | Q34228966 | ||
| Unconventional translation of mammalian LINE-1 retrotransposons. | Q34324122 | ||
| L1 integration in a transgenic mouse model | Q34338865 | ||
| A human genome structural variation sequencing resource reveals insights into mutational mechanisms | Q34519304 | ||
| Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. | Q34553577 | ||
| L1 retrotransposition in nondividing and primary human somatic cells | Q34650044 | ||
| Mammalian non-LTR retrotransposons: for better or worse, in sickness and in health | Q34747080 | ||
| Tracking an embryonic L1 retrotransposition event | Q34762192 | ||
| Alu repeat discovery and characterization within human genomes | Q35020122 | ||
| Frequent human genomic DNA transduction driven by LINE-1 retrotransposition | Q35026231 | ||
| Active retrotransposition by a synthetic L1 element in mice | Q35214717 | ||
| Emergence of primate genes by retrotransposon-mediated sequence transduction | Q35214933 | ||
| Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism | Q35677795 | ||
| Distinct mechanisms for trans-mediated mobilization of cellular RNAs by the LINE-1 reverse transcriptase. | Q35757888 | ||
| Endonuclease-independent insertion provides an alternative pathway for L1 retrotransposition in the human genome | Q35893869 | ||
| An indicator gene for detection of germline retrotransposition in transgenic Drosophila demonstrates RNA-mediated transposition of the LINE I element. | Q35927262 | ||
| A novel human nonviral retroposon derived from an endogenous retrovirus | Q36294749 | ||
| Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
| LINE-1 ORF1 protein enhances Alu SINE retrotransposition. | Q36800521 | ||
| Many human L1 elements are capable of retrotransposition | Q36859141 | ||
| Structural analysis of the major immediate early gene of human cytomegalovirus | Q36911017 | ||
| Diverse cis factors controlling Alu retrotransposition: what causes Alu elements to die? | Q37150856 | ||
| An alternative pathway for Alu retrotransposition suggests a role in DNA double-strand break repair | Q37167429 | ||
| L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism | Q37240559 | ||
| The L1 retrotransposition assay: a retrospective and toolkit | Q37392305 | ||
| Exon-trapping mediated by the human retrotransposon SVA. | Q37417310 | ||
| 5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome | Q37417316 | ||
| Determination of L1 retrotransposition kinetics in cultured cells | Q39586006 | ||
| A Tetrahymena thermophila ribozyme-based indicator gene to detect transposition of marked retroelements in mammalian cells | Q39615704 | ||
| LINE-1 retrotransposition in human embryonic stem cells | Q40139315 | ||
| Endonuclease-independent LINE-1 retrotransposition at mammalian telomeres | Q40161913 | ||
| Twin priming: a proposed mechanism for the creation of inversions in L1 retrotransposition | Q40415833 | ||
| Transduction of 3'-flanking sequences is common in L1 retrotransposition | Q40896511 | ||
| The ORF1 protein encoded by LINE-1: structure and function during L1 retrotransposition | Q42373463 | ||
| Mobile interspersed repeats are major structural variants in the human genome | Q42423737 | ||
| Novel family of human transposable elements formed due to fusion of the first exon of gene MAST2 with retrotransposon SVA. | Q43229749 | ||
| Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene | Q43863876 | ||
| Phylogenetic analysis of a retroposon family in african great apes | Q46529605 | ||
| Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells | Q47948394 | ||
| DNA repair mediated by endonuclease-independent LINE-1 retrotransposition | Q48304886 | ||
| Mobile DNA in Old World monkeys: a glimpse through the rhesus macaque genome. | Q51626987 | ||
| SVA elements: a hominid-specific retroposon family. | Q51632064 | ||
| Unusual mutations in Btk: an insertion, a duplication, an inversion, and four large deletions. | Q52533352 | ||
| A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events. | Q53905712 | ||
| A Genome-Wide Screen for Normally Methylated Human CpG Islands That Can Identify Novel Imprinted Genes | Q56783008 | ||
| A modified indicator gene for selection of retrotransposition events in mammalian cells | Q72769685 | ||
| Molecular characterization of germline NF2 gene rearrangements | Q73704297 | ||
| Genomic deletions created upon LINE-1 retrotransposition | Q74604693 | ||
| Human l1 retrotransposition is associated with genetic instability in vivo | Q74604697 | ||
| A mouse model of human L1 retrotransposition | Q78471092 | ||
| Deletion of entire HLA-A gene accompanied by an insertion of a retrotransposon | Q80566336 | ||
| P433 | issue | 17 | |
| P304 | page(s) | 3386-3400 | |
| P577 | publication date | 2011-06-02 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Retrotransposition of marked SVA elements by human L1s in cultured cells | |
| P478 | volume | 20 |
| Q41836965 | A 3' Poly(A) Tract Is Required for LINE-1 Retrotransposition |
| Q33558345 | A comprehensive approach to expression of L1 loci |
| Q36393956 | A conserved role for the ESCRT membrane budding complex in LINE retrotransposition |
| Q36618572 | A tale of an A-tail: The lifeline of a SINE. |
| Q92861893 | Aberrantly High Levels of Somatic LINE-1 Expression and Retrotransposition in Human Neurological Disorders |
| Q29617668 | Active human retrotransposons: variation and disease |
| Q36729306 | Active transposition in genomes |
| Q56765662 | Activity of Retrotransposons in Stem Cells and Differentiated Cells |
| Q27015853 | Alu elements: an intrinsic source of human genome instability |
| Q34732755 | Characterisation of the potential function of SVA retrotransposons to modulate gene expression patterns |
| Q87013508 | Copy number variation of transposable elements in Triticum-Aegilops genus suggests evolutionary and revolutionary dynamics following allopolyploidization |
| Q58116185 | DNA repair protein Rad18 restricts LINE-1 mobility |
| Q47132084 | Detection of the LINE-1 retrotransposon RNA-binding protein ORF1p in different anatomical regions of the human brain |
| Q28650052 | Dispersal of an ancient retroposon in the TP53 promoter of Bovidae: phylogeny, novel mechanisms, and potential implications for cow milk persistency |
| Q46534463 | Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker |
| Q35040960 | Diversity through duplication: whole-genome sequencing reveals novel gene retrocopies in the human population |
| 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 |
| Q37111967 | Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles |
| Q36446178 | Extensive somatic L1 retrotransposition in colorectal tumors |
| Q28680646 | Functional impact of the human mobilome |
| Q39957898 | Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination |
| Q26742086 | Guardian of the Human Genome: Host Defense Mechanisms against LINE-1 Retrotransposition |
| 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. |
| Q42095539 | How do mammalian transposons induce genetic variation? A conceptual framework: the age, structure, allele frequency, and genome context of transposable elements may define their wide-ranging biological impacts |
| Q47160381 | Human transposable elements in Repbase: genomic footprints from fish to humans |
| Q89784447 | Human transposon insertion profiling by sequencing (TIPseq) to map LINE-1 insertions in single cells |
| Q42035265 | Human transposon insertion profiling: Analysis, visualization and identification of somatic LINE-1 insertions in ovarian cancer |
| Q27010001 | Human transposon tectonics |
| Q92102903 | Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology |
| Q36091437 | Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA) |
| Q37200472 | Impact of retrotransposons in pluripotent stem cells |
| Q64068782 | Insertion of a chimeric retrotransposon sequence in mouse locus causes metastable kinky tail phenotype |
| Q83771726 | Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of Lynch syndrome |
| Q49109205 | Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event |
| Q42136407 | Is somatic retrotransposition a parasitic or symbiotic phenomenon? |
| Q55692166 | L1 retrotransposition in the soma: a field jumping ahead. |
| Q38792667 | LINE-1 Cultured Cell Retrotransposition Assay |
| Q28654758 | LINE-1 elements in structural variation and disease |
| Q36586455 | LINE-1-derived poly(A) microsatellites undergo rapid shortening and create somatic and germline mosaicism in mice |
| Q35646781 | Library Construction for High-Throughput Mobile Element Identification and Genotyping |
| Q35608618 | Lineage specific evolution of the VNTR composite retrotransposon central domain and its role in retrotransposition of gibbon LAVA elements. |
| Q34456088 | MOV10 RNA helicase is a potent inhibitor of retrotransposition in cells |
| Q34249705 | Mechanism by which a LINE protein recognizes its 3' tail RNA. |
| Q38227447 | Mobile DNA elements in the generation of diversity and complexity in the brain |
| Q45870074 | Mobile DNA in Health and Disease |
| Q37609516 | Mobile element biology: new possibilities with high-throughput sequencing |
| Q35687336 | Mobile element insertions are frequent in oesophageal adenocarcinomas and can mislead paired-end sequencing analysis |
| Q34256832 | Mobile elements in the human genome: implications for disease |
| Q34310806 | Origin of a novel protein-coding gene family with similar signal sequence in Schistosoma japonicum |
| Q36141218 | Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy |
| Q35672729 | Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon |
| Q58735100 | Phylogenomic analysis reveals splicing as a mechanism of parallel evolution of non-canonical SVAs in hominine primates |
| Q36362853 | Poly(A) binding protein C1 is essential for efficient L1 retrotransposition and affects L1 RNP formation |
| Q41789519 | Processed pseudogene insertions in somatic cells |
| Q99240820 | Promoter methylation, transcription, and retrotransposition of LINE-1 in colorectal adenomas and adenocarcinomas |
| Q33613535 | Protein-Coding Genes' Retrocopies and Their Functions. |
| Q90240488 | RNA ligation precedes the retrotransposition of U6/LINE-1 chimeric RNA |
| Q28660459 | RNase L restricts the mobility of engineered retrotransposons in cultured human cells |
| Q41642419 | Recessive inheritance of population-specific intronic LINE-1 insertion causes a rotor syndrome phenotype |
| Q34276636 | Recombinant SINEs are formed at high frequency during induced retrotransposition in vivo |
| Q28241693 | Regulation of L1 expression and retrotransposition by melatonin and its receptor: implications for cancer risk associated with light exposure at night |
| Q26741496 | Restricting retrotransposons: a review |
| Q21183991 | Retrotransposition of gene transcripts leads to structural variation in mammalian genomes |
| Q93161855 | Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival |
| Q90321264 | Retrotransposon-induced mosaicism in the neural genome |
| Q26751314 | Roles for retrotransposon insertions in human disease |
| Q34501235 | SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints. |
| Q28066419 | SVA retrotransposons as potential modulators of neuropeptide gene expression |
| Q33888758 | Selective elimination of long INterspersed element-1 expressing tumour cells by targeted expression of the HSV-TK suicide gene |
| Q52673975 | Spliced integrated retrotransposed element (SpIRE) formation in the human genome. |
| Q44275871 | Structural variants caused by Alu insertions are associated with risks for many human diseases |
| Q37223545 | Structure and Expression Analyses of SVA Elements in Relation to Functional Genes |
| Q37521827 | The Flow of the Gibbon LAVA Element Is Facilitated by the LINE-1 Retrotransposition Machinery |
| 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 |
| Q28661506 | The Microprocessor controls the activity of mammalian retrotransposons |
| Q38601704 | The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology |
| Q32183705 | The Role of Somatic L1 Retrotransposition in Human Cancers |
| Q28547090 | The Zinc-Finger Antiviral Protein ZAP Inhibits LINE and Alu Retrotransposition |
| Q28087454 | The aging clock and circadian control of metabolism and genome stability |
| Q28828237 | The cancer-associated CTCFL/BORIS protein targets multiple classes of genomic repeats, with a distinct binding and functional preference for humanoid-specific SVA transposable elements |
| Q37261517 | The epigenetic regulator PLZF represses L1 retrotransposition in germ and progenitor cells |
| Q64112074 | The impact of transposable element activity on therapeutically relevant human stem cells |
| Q39016663 | The impact of transposable elements on mammalian development |
| 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 |
| Q101573956 | The tumor suppressor microRNA let-7 inhibits human LINE-1 retrotransposition |
| Q37433509 | Transduction-specific ATLAS reveals a cohort of highly active L1 retrotransposons in human populations |
| Q39392722 | Transposable elements in cancer |
| Q90084192 | Transposable elements in human genetic disease |
| Q26751043 | Transposable elements in the mammalian embryo: pioneers surviving through stealth and service |
| Q64116714 | Transposon insertion profiling by sequencing (TIPseq) for mapping LINE-1 insertions in the human genome |
| Q35438613 | Ubiquitous L1 mosaicism in hippocampal neurons |
| Q89784451 | sRNA/L1 retrotransposition: using siRNAs and miRNAs to expand the applications of the cell culture-based LINE-1 retrotransposition assay |
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