scholarly article | Q13442814 |
P819 | ADS bibcode | 1993PNAS...90.6513D |
P356 | DOI | 10.1073/PNAS.90.14.6513 |
P932 | PMC publication ID | 46962 |
P698 | PubMed publication ID | 8393568 |
P5875 | ResearchGate publication ID | 14804875 |
P2093 | author name string | Kazazian HH Jr | |
Dombroski BA | |||
Scott AF | |||
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Identification of an internal cis-element essential for the human Li transcription and a nuclear factor(s) binding to the element | Q40422731 | ||
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Characterization of a nondeleterious L1 insertion in an intron of the human factor VIII gene and further evidence of open reading frames in functional L1 elements | Q42640219 | ||
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Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene | Q45872014 | ||
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P433 | issue | 14 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | retrotransposon | Q413988 |
P304 | page(s) | 6513-6517 | |
P577 | publication date | 1993-07-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | |
P478 | volume | 90 |
Q36365928 | A cell type-specific enhancer in the human B7.1 gene regulated by NF-kappaB |
Q36959154 | A hot L1 retrotransposon evades somatic repression and initiates human colorectal cancer |
Q42693461 | A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion |
Q36177163 | A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease |
Q37730711 | APOBEC3A deaminates transiently exposed single-strand DNA during LINE-1 retrotransposition |
Q33905045 | ATLAS: a system to selectively identify human-specific L1 insertions. |
Q33905345 | Allelic Heterogeneity in LINE-1 Retrotransposition Activity |
Q42844670 | Analysis of 5' junctions of human LINE-1 and Alu retrotransposons suggests an alternative model for 5'-end attachment requiring microhomology-mediated end-joining |
Q36626051 | Analysis of integrated ground squirrel hepatitis virus and flanking host DNA in two hepatocellular carcinomas. |
Q42648703 | Analysis of orthologous retrovirus-like elements in the white-footed mouse, Peromyscus leucopus |
Q38767206 | Analysis of the human immunodeficiency virus-1 RNA packageome |
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Q21092434 | Characterization of LINE-1 ribonucleoprotein particles |
Q42688858 | Cis-preferential LINE-1 reverse transcriptase activity in ribonucleoprotein particles |
Q45881268 | Condensin II and GAIT complexes cooperate to restrict LINE-1 retrotransposition in epithelial cells. |
Q28757270 | CpG dinucleotides and the mutation rate of non-CpG DNA |
Q36620357 | DNA methylation and expression of LINE-1 and HERV-K provirus sequences in urothelial and renal cell carcinomas |
Q35757888 | Distinct mechanisms for trans-mediated mobilization of cellular RNAs by the LINE-1 reverse transcriptase. |
Q64076955 | Dynamic Methylation of an L1 Transduction Family during Reprogramming and Neurodifferentiation |
Q37408919 | Evidence for L1-associated DNA rearrangements and negligible L1 retrotransposition in glioblastoma multiforme. |
Q41128916 | Evolution and biological significance of human retroelements |
Q33900194 | Evolutionary conservation of the functional modularity of primate and murine LINE-1 elements |
Q25255521 | Gamma radiation increases endonuclease-dependent L1 retrotransposition in a cultured cell assay |
Q28776429 | Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion |
Q24813998 | Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages |
Q41199624 | Heritable L1 retrotransposition in the mouse primordial germline and early embryo |
Q22066292 | Hot L1s account for the bulk of retrotransposition in the human population |
Q52643023 | Human LINE-1 retrotransposition requires a metastable coiled coil and a positively charged N-terminus in L1ORF1p. |
Q34658368 | Human genomic deletions mediated by recombination between Alu elements. |
Q42608529 | Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences |
Q71890837 | IR hybrid dysgenesis increases the frequency of recombination in Drosophila melanogaster |
Q21045365 | Initial sequencing and analysis of the human genome |
Q55692166 | L1 retrotransposition in the soma: a field jumping ahead. |
Q36800521 | LINE-1 ORF1 protein enhances Alu SINE retrotransposition. |
Q38605923 | LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo |
Q28743798 | LINE-1 retrotransposition activity in human genomes |
Q48053235 | LINE-I element insertion at the t(11;22) translocation breakpoint of a desmoplastic small round cell tumor |
Q36859141 | Many human L1 elements are capable of retrotransposition |
Q24794428 | Molecular archeology of L1 insertions in the human genome. |
Q36475386 | Molecular reconstruction of extinct LINE-1 elements and their interaction with nonautonomous elements |
Q40695421 | More active human L1 retrotransposons produce longer insertions |
Q33925050 | Multiple fates of L1 retrotransposition intermediates in cultured human cells. |
Q28769442 | Mus spretus LINE-1s in the Mus musculus domesticus inbred strain C57BL/6J are from two different Mus spretus LINE-1 subfamilies |
Q35378502 | Phosphorylation of ORF1p is required for L1 retrotransposition |
Q34249538 | Potential for genomic instability associated with retrotranspositionally-incompetent L1 loci |
Q28660459 | RNase L restricts the mobility of engineered retrotransposons in cultured human cells |
Q28776447 | Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition |
Q28769427 | Recombination creates novel L1 (LINE-1) elements in Rattus norvegicus |
Q35155981 | Retrotransposition of marked SVA elements by human L1s in cultured cells |
Q24336732 | Ribonucleoprotein particle formation is necessary but not sufficient for LINE-1 retrotransposition |
Q34048853 | Selective inhibition of Alu retrotransposition by APOBEC3G. |
Q52673975 | Spliced integrated retrotransposed element (SpIRE) formation in the human genome. |
Q26851352 | The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes |
Q37392305 | The L1 retrotransposition assay: a retrospective and toolkit |
Q37175149 | The MOV10 helicase inhibits LINE-1 mobility. |
Q28661506 | The Microprocessor controls the activity of mammalian retrotransposons |
Q38601704 | The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology |
Q33434436 | The RNA polymerase dictates ORF1 requirement and timing of LINE and SINE 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 |
Q36289181 | The genomic sequences bound to special AT-rich sequence-binding protein 1 (SATB1) in vivo in Jurkat T cells are tightly associated with the nuclear matrix at the bases of the chromatin loops |
Q40396339 | The mammalian genome shaping activity of reverse transcriptase |
Q39272696 | The minimal active human SVA retrotransposon requires only the 5'-hexamer and Alu-like domains |
Q37433509 | Transduction-specific ATLAS reveals a cohort of highly active L1 retrotransposons in human populations |
Q35438613 | Ubiquitous L1 mosaicism in hippocampal neurons |
Q36106578 | Vaccination with cancer- and HIV infection-associated endogenous retrotransposable elements is safe and immunogenic |
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