| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.GENE.2008.04.007 |
| P8608 | Fatcat ID | release_kuqwuvpkunbinaonnpfuyj3iba |
| P932 | PMC publication ID | 2491492 |
| P698 | PubMed publication ID | 18534786 |
| P5875 | ResearchGate publication ID | 5322388 |
| P50 | author | Prescott Deininger | Q42533877 |
| P2093 | author name string | Astrid M Roy-Engel | |
| Bradley J Wagstaff | |||
| Nicholas Wallace | |||
| 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 | ||
| Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution | Q22122484 | ||
| Identification and solution structure of a highly conserved C-terminal domain within ORF1p required for retrotransposition of long interspersed nuclear element-1 | Q27645863 | ||
| Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
| Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: A mechanism for non-LTR retrotransposition | Q28297748 | ||
| A novel active L1 retrotransposon subfamily in the mouse | Q28776432 | ||
| Mobile elements: drivers of genome evolution | Q29547669 | ||
| Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
| High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
| Alu repeats and human disease | Q29618262 | ||
| Human LINE retrotransposons generate processed pseudogenes | Q29618327 | ||
| Human L1 retrotransposition: cis preference versus trans complementation | Q29618363 | ||
| LINE-mediated retrotransposition of marked Alu sequences | Q29618440 | ||
| Cell type-specific expression of LINE-1 open reading frames 1 and 2 in fetal and adult human tissues | Q33200676 | ||
| The biological properties and evolutionary dynamics of mammalian LINE-1 retrotransposons | Q33851829 | ||
| SVA elements are nonautonomous retrotransposons that cause disease in humans | Q33905356 | ||
| DNA-directed DNA polymerase and strand displacement activity of the reverse transcriptase encoded by the R2 retrotransposon. | Q34007576 | ||
| Selective inhibition of Alu retrotransposition by APOBEC3G. | Q34048853 | ||
| The human LINE-1 retrotransposon creates DNA double-strand breaks. | Q34061457 | ||
| Human L1 element target-primed reverse transcription in vitro | Q34207225 | ||
| Mutation analysis in the BRCA2 gene in primary breast cancers | Q34381070 | ||
| The impact of L1 retrotransposons on the human genome | Q34468340 | ||
| LINE-1 RNA splicing and influences on mammalian gene expression | Q34483165 | ||
| Essential domains for ribonucleoprotein complex formation required for retrotransposition of telomere-specific non-long terminal repeat retrotransposon SART1 | Q34718262 | ||
| Distinct mechanisms for trans-mediated mobilization of cellular RNAs by the LINE-1 reverse transcriptase. | Q35757888 | ||
| Cytoplasmic ribonucleoprotein complexes containing human LINE-1 protein and RNA | Q35844482 | ||
| The LINE-1 DNA sequences in four mammalian orders predict proteins that conserve homologies to retrovirus proteins | Q36120853 | ||
| A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease | Q36177163 | ||
| Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
| Chicken repeat 1 elements contain a pol-like open reading frame and belong to the non-long terminal repeat class of retrotransposons | Q36516467 | ||
| Many human L1 elements are capable of retrotransposition | Q36859141 | ||
| Mobile DNA elements in primate and human evolution | Q37018755 | ||
| Evidence consistent with human L1 retrotransposition in maternal meiosis I. | Q37218145 | ||
| Deletion analysis defines distinct functional domains for protein-protein and nucleic acid interactions in the ORF1 protein of mouse LINE-1. | Q38306834 | ||
| Nucleic acid chaperone activity of the ORF1 protein from the mouse LINE-1 retrotransposon | Q39457323 | ||
| Upstream flanking sequences and transcription of SINEs | Q40858224 | ||
| The ORF1 protein encoded by LINE-1: structure and function during L1 retrotransposition | Q42373463 | ||
| An actively retrotransposing, novel subfamily of mouse L1 elements | Q42637048 | ||
| Comparative expression of the LINE-1 p40 protein in human breast carcinomas and normal breast tissues. | Q42642725 | ||
| Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence | Q42660978 | ||
| Adaptive evolution in LINE-1 retrotransposons | Q42664325 | ||
| Chicken repeat 1 (CR1) elements, which define an ancient family of vertebrate non-LTR retrotransposons, contain two closely spaced open reading frames | Q42665232 | ||
| Determination of the entire sequence of turtle CR1: the first open reading frame of the turtle CR1 element encodes a protein with a novel zinc finger motif | Q42669296 | ||
| Cis-preferential LINE-1 reverse transcriptase activity in ribonucleoprotein particles | Q42688858 | ||
| A highly active synthetic mammalian retrotransposon | Q42828794 | ||
| RNA truncation by premature polyadenylation attenuates human mobile element activity | Q42833909 | ||
| LINE-1 retrotransposition requires the nucleic acid chaperone activity of the ORF1 protein | Q46434712 | ||
| The evolution of modern lineages of mouse L1 elements | Q47802852 | ||
| SVA elements: a hominid-specific retroposon family. | Q51632064 | ||
| Targeting of human retrotransposon integration is directed by the specificity of the L1 endonuclease for regions of unusual DNA structure. | Q52533614 | ||
| Active LINE-1 retrotransposons in human testicular cancer | Q54067083 | ||
| L1-mediated retrotransposition of murine B1 and B2 SINEs recapitulated in cultured cells | Q81741443 | ||
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 1-2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1-6 | |
| P577 | publication date | 2008-04-24 | |
| P1433 | published in | Gene | Q5531065 |
| P1476 | title | LINE-1 ORF1 protein enhances Alu SINE retrotransposition | |
| P478 | volume | 419 |
| Q62619819 | ALUminating the Path of Atherosclerosis Progression: Chaos Theory Suggests a Role for Repeats in the Development of Atherosclerotic Vascular Disease |
| Q37404667 | APOBEC3G oligomerization is associated with the inhibition of both Alu and LINE-1 retrotransposition |
| Q34143181 | All y'all need to know 'bout retroelements in cancer. |
| Q27015853 | Alu elements: an intrinsic source of human genome instability |
| Q35907659 | Alu elements: know the SINEs |
| Q35569085 | Ancient traces of tailless retropseudogenes in therian genomes |
| Q36693449 | Association between blood pressure and DNA methylation of retrotransposons and pro-inflammatory genes |
| Q28396772 | Biomarkers of lead exposure and DNA methylation within retrotransposons |
| Q35064070 | Characterization of L1 ORF1p self-interaction and cellular localization using a mammalian two-hybrid system |
| Q37493074 | Clarifying assent in pediatric research |
| Q41552071 | Development of a monoclonal antibody specific to the endonuclease domain of the human LINE-1 ORF2 protein |
| Q42093576 | Different integration site structures between L1 protein-mediated retrotransposition in cis and retrotransposition in trans |
| Q39741192 | Discrete subcellular partitioning of human retrotransposon RNAs despite a common mechanism of genome insertion |
| Q47225302 | Dissection of affinity captured LINE-1 macromolecular complexes. |
| Q37150856 | Diverse cis factors controlling Alu retrotransposition: what causes Alu elements to die? |
| Q21135358 | ECAT11/L1td1 is enriched in ESCs and rapidly activated during iPSC generation, but it is dispensable for the maintenance and induction of pluripotency |
| Q37111967 | Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles |
| Q33900194 | Evolutionary conservation of the functional modularity of primate and murine LINE-1 elements |
| Q27026309 | Expressing genes do not forget their LINEs: transposable elements and gene expression |
| Q38273264 | Feedback inhibition of L1 and alu retrotransposition through altered double strand break repair kinetics. |
| Q40914883 | Genomic vulnerability to LINE-1 hypomethylation is a potential determinant of the clinicogenetic features of multiple myeloma. |
| Q28395565 | Global methylation, oxidative stress, and relative telomere length in biliary atresia patients |
| Q36959087 | Identification of L1 ORF2p sequence important to retrotransposition using Bipartile Alu retrotransposition (BAR). |
| Q64065729 | Identification of charged amino acids required for nuclear localization of human L1 ORF1 protein |
| Q37200472 | Impact of retrotransposons in pluripotent stem cells |
| Q34276908 | Induction of long interspersed nucleotide element-1 (L1) retrotransposition by 6-formylindolo[3,2- b ]carbazole (FICZ), a tryptophan photoproduct |
| Q26771437 | Insertion of Retrotransposons at Chromosome Ends: Adaptive Response to Chromosome Maintenance |
| Q39013867 | Involvement of Conserved Amino Acids in the C-Terminal Region of LINE-1 ORF2p in Retrotransposition |
| Q37442902 | LINE dancing in the human genome: transposable elements and disease |
| Q34469970 | LINE-1 retroelements complexed and inhibited by activation induced cytidine deaminase |
| Q28654440 | LINEs and SINEs of primate evolution |
| Q28729045 | LINEs, SINEs and other retroelements: do birds of a feather flock together? |
| Q37226797 | Long interspersed element-1 is differentially regulated by food-borne carcinogens via the aryl hydrocarbon receptor |
| Q41876220 | Lost in translation: The biogenesis of non-LTR retrotransposon proteins |
| Q34205284 | Managing incidental findings and research results in genomic research involving biobanks and archived data sets |
| Q35999488 | Modes of retrotransposition of long interspersed element-1 by environmental factors |
| Q36475386 | Molecular reconstruction of extinct LINE-1 elements and their interaction with nonautonomous elements |
| Q64117464 | Mouse germ line mutations due to retrotransposon insertions |
| Q28749650 | Origin and evolution of LINE-1 derived "half-L1" retrotransposons (HAL1) |
| Q100385894 | RNA-cDNA hybrids mediate transposition via different mechanisms |
| Q34388491 | Rescuing Alu: recovery of new inserts shows LINE-1 preserves Alu activity through A-tail expansion |
| Q35611983 | Restless genomes humans as a model organism for understanding host-retrotransposable element dynamics |
| Q35155981 | Retrotransposition of marked SVA elements by human L1s in cultured cells |
| Q61421735 | Reviving a 60 million year old LINE-1 element |
| Q26751314 | Roles for retrotransposon insertions in human disease |
| Q26851352 | The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes |
| Q37392305 | The L1 retrotransposition assay: a retrospective and toolkit |
| Q33434436 | The RNA polymerase dictates ORF1 requirement and timing of LINE and SINE retrotransposition |
| Q24594901 | The impact of retrotransposons on human genome evolution |
| Q64275381 | Tracing the history of LINE and SINE extinction in sigmodontine rodents |
| Q41693943 | Truncated ORF1 proteins can suppress LINE-1 retrotransposition in trans |
| Q28648093 | U6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in Mammals |
| Q89490386 | Unveiling ncRNA regulatory axes in atherosclerosis progression |
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