scholarly article | Q13442814 |
P2093 | author name string | John B Moldovan | |
John V Moran | |||
Christine R Beck | |||
Jeffrey M Kidd | |||
Naveen Jasti | |||
Peter A Larson | |||
P2860 | cites work | The human L1 promoter: variable transcription initiation sites and a major impact of upstream flanking sequence on promoter activity | Q40299427 |
Twin priming: a proposed mechanism for the creation of inversions in L1 retrotransposition | Q40415833 | ||
Identification of an internal cis-element essential for the human Li transcription and a nuclear factor(s) binding to the element | Q40422731 | ||
Selective cloning and sequence analysis of the human L1 (LINE-1) sequences which transposed in the relatively recent past | Q40518428 | ||
Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes | Q40554054 | ||
Transduction of 3'-flanking sequences is common in L1 retrotransposition | Q40896511 | ||
The non-autonomous retrotransposon SVA is trans-mobilized by the human LINE-1 protein machinery | Q41577828 | ||
A 3' Poly(A) Tract Is Required for LINE-1 Retrotransposition | Q41836965 | ||
Synchronous expression of LINE-1 RNA and protein in mouse embryonal carcinoma cells | Q41851241 | ||
Engineered LINE-1 retrotransposition in nondividing human neurons | Q42317742 | ||
Isolation of an active human transposable element | Q42614185 | ||
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence | Q42660978 | ||
Characterization of a non-long terminal repeat retrotransposon cDNA (L1Tc) from Trypanosoma cruzi: homology of the first ORF with the ape family of DNA repair enzymes. | Q42675207 | ||
Cis-preferential LINE-1 reverse transcriptase activity in ribonucleoprotein particles | Q42688858 | ||
RNA truncation by premature polyadenylation attenuates human mobile element activity | Q42833909 | ||
Molecular evolution and tempo of amplification of human LINE-1 retrotransposons since the origin of primates. | Q43192302 | ||
Ancient repeat sequence derived from U6 snRNA in primate genomes. | Q45900098 | ||
LINE-1 retrotransposition requires the nucleic acid chaperone activity of the ORF1 protein | Q46434712 | ||
Ancestral, mammalian-wide subfamilies of LINE-1 repetitive sequences | Q47207133 | ||
Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells | Q47948394 | ||
The structure of the guanine-rich polypurine:polypyrimidine sequence at the right end of the rat L1 (LINE) element | Q48287136 | ||
DNA repair mediated by endonuclease-independent LINE-1 retrotransposition | Q48304886 | ||
Base sequence studies of 300 nucleotide renatured repeated human DNA clones | Q48408328 | ||
A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events. | Q53905712 | ||
L1 family of repetitive DNA sequences in primates may be derived from a sequence encoding a reverse transcriptase-related protein | Q56905068 | ||
A modified indicator gene for selection of retrotransposition events in mammalian cells | Q72769685 | ||
Apolipoprotein(a) gene enhancer resides within a LINE element | Q74016300 | ||
Genomic deletions created upon LINE-1 retrotransposition | Q74604693 | ||
Human l1 retrotransposition is associated with genetic instability in vivo | Q74604697 | ||
Selection against LINE-1 retrotransposons results principally from their ability to mediate ectopic recombination | Q79393368 | ||
[A key role of the internal region of the 5'-untranslated region in the human L1 retrotransposon transcription activity] | Q80763976 | ||
Initial sequencing and analysis of the human genome | Q21045365 | ||
Characterization of LINE-1 ribonucleoprotein particles | Q21092434 | ||
Gene copy-number polymorphism caused by retrotransposition in humans | Q21144898 | ||
Retrotransposition of gene transcripts leads to structural variation in mammalian genomes | Q21183991 | ||
Members of the SRY family regulate the human LINE retrotransposons | Q22010959 | ||
Hot L1s account for the bulk of retrotransposition in the human population | Q22066292 | ||
NIH Image to ImageJ: 25 years of image analysis | Q23319322 | ||
An evolutionary arms race between KRAB zinc-finger genes ZNF91/93 and SVA/L1 retrotransposons | Q24304980 | ||
Affinity proteomics reveals human host factors implicated in discrete stages of LINE-1 retrotransposition | Q24309049 | ||
Non-LTR retrotransposons encode noncanonical RRM domains in their first open reading frame | Q24316232 | ||
Ribonucleoprotein particle formation is necessary but not sufficient for LINE-1 retrotransposition | Q24336732 | ||
Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes | Q24550997 | ||
Human branch point consensus sequence is yUnAy | Q24646378 | ||
An important role for RUNX3 in human L1 transcription and retrotransposition | Q24670621 | ||
NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins | Q24676525 | ||
BLAT—The BLAST-Like Alignment Tool | Q24682492 | ||
Molecular archeology of L1 insertions in the human genome. | Q24794428 | ||
Role of the Bombyx mori R2 element N-terminal domain in the target-primed reverse transcription (TPRT) reaction | Q24817137 | ||
A global reference for human genetic variation | Q25909434 | ||
Roles for retrotransposon insertions in human disease | Q26751314 | ||
The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes | Q26851352 | ||
Identification and solution structure of a highly conserved C-terminal domain within ORF1p required for retrotransposition of long interspersed nuclear element-1 | Q27645863 | ||
Trimeric structure and flexibility of the L1ORF1 protein in human L1 retrotransposition | Q27671601 | ||
Retrotransposition and Crystal Structure of an Alu RNP in the Ribosome-Stalling Conformation | Q27702648 | ||
CAP3: A DNA sequence assembly program | Q27860964 | ||
Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
Binding of the ubiquitous nuclear transcription factor YY1 to a cis regulatory sequence in the human LINE-1 transposable element | Q28257706 | ||
Point mutations close to the AUG initiator codon affect the efficiency of translation of rat preproinsulin in vivo | Q28272278 | ||
Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: A mechanism for non-LTR retrotransposition | Q28297748 | ||
Mammalian small nucleolar RNAs are mobile genetic elements | Q28469078 | ||
The Zinc-Finger Antiviral Protein ZAP Inhibits LINE and Alu Retrotransposition | Q28547090 | ||
Activation of individual L1 retrotransposon instances is restricted to cell-type dependent permissive loci | Q28602786 | ||
U6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in Mammals | Q28648093 | ||
LINE-1 elements in structural variation and disease | Q28654758 | ||
Analysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell division | Q28661361 | ||
Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition | Q28681448 | ||
LINE-1 retrotransposition activity in human genomes | Q28743798 | ||
Multiple sequence alignment using ClustalW and ClustalX | Q29547698 | ||
Interspersed repeats and other mementos of transposable elements in mammalian genomes | Q29615764 | ||
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 | ||
Human LINE retrotransposons generate processed pseudogenes | Q29618327 | ||
Processed pseudogenes: characteristics and evolution | Q29618329 | ||
Human L1 retrotransposition: cis preference versus trans complementation | Q29618363 | ||
LINE-mediated retrotransposition of marked Alu sequences | Q29618440 | ||
The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences | Q29619441 | ||
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 | ||
Cell type-specific expression of LINE-1 open reading frames 1 and 2 in fetal and adult human tissues | Q33200676 | ||
A comprehensive approach to expression of L1 loci | Q33558345 | ||
Trimeric structure for an essential protein in L1 retrotransposition | Q33713168 | ||
Translation of LINE-1 DNA elements in vitro and in human cells | Q33785234 | ||
Sequence-specific single-strand RNA binding protein encoded by the human LINE-1 retrotransposon | Q33887614 | ||
SVA elements are nonautonomous retrotransposons that cause disease in humans | Q33905356 | ||
Multiple fates of L1 retrotransposition intermediates in cultured human cells. | Q33925050 | ||
Defining the beginning and end of KpnI family segments | Q33939728 | ||
Pre-mRNA splicing in the new millennium | Q33946020 | ||
Somatic expression of LINE-1 elements in human tissues. | Q33959421 | ||
The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertion | Q34085626 | ||
Human L1 element target-primed reverse transcription in vitro | Q34207225 | ||
Unconventional translation of mammalian LINE-1 retrotransposons. | Q34324122 | ||
The impact of L1 retrotransposons on the human genome | Q34468340 | ||
LINE-1 RNA splicing and influences on mammalian gene expression | Q34483165 | ||
Primate-specific ORF0 contributes to retrotransposon-mediated diversity | Q34499238 | ||
Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. | Q34553577 | ||
Identification, characterization, and cell specificity of a human LINE-1 promoter | Q34570051 | ||
L1 retrotransposition in nondividing and primary human somatic cells | Q34650044 | ||
Fitness cost of LINE-1 (L1) activity in humans | Q34687090 | ||
The specificity and flexibility of l1 reverse transcription priming at imperfect T-tracts | Q34722563 | ||
Human Splicing Finder: an online bioinformatics tool to predict splicing signals | Q34973311 | ||
Frequent human genomic DNA transduction driven by LINE-1 retrotransposition | Q35026231 | ||
Retrotransposition of marked SVA elements by human L1s in cultured cells | Q35155981 | ||
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 | ||
Influence of RNA secondary structure on the pre-mRNA splicing process | Q35968217 | ||
The LINE-1 DNA sequences in four mammalian orders predict proteins that conserve homologies to retrovirus proteins | Q36120853 | ||
Discovery and characterization of Alu repeat sequences via precise local read assembly | Q36337667 | ||
Poly(A) binding protein C1 is essential for efficient L1 retrotransposition and affects L1 RNP formation | Q36362853 | ||
Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
L1 retrotransposition requires rapid ORF1p oligomerization, a novel coiled coil-dependent property conserved despite extensive remodeling | Q36443314 | ||
The impact of multiple splice sites in human L1 elements | Q36515503 | ||
Developmental and cell type specificity of LINE-1 expression in mouse testis: implications for transposition | Q36650559 | ||
Translation of the human LINE-1 element, L1Hs | Q36712171 | ||
Ribonucleoprotein particles with LINE-1 RNA in mouse embryonal carcinoma cells | Q36733242 | ||
Many human L1 elements are capable of retrotransposition | Q36859141 | ||
A hot L1 retrotransposon evades somatic repression and initiates human colorectal cancer | Q36959154 | ||
A YY1-binding site is required for accurate human LINE-1 transcription initiation | Q37346150 | ||
Transduction-specific ATLAS reveals a cohort of highly active L1 retrotransposons in human populations | Q37433509 | ||
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 | ||
The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology | Q38601704 | ||
LINE-1 Cultured Cell Retrotransposition Assay | Q38792667 | ||
Nucleic acid chaperone activity of the ORF1 protein from the mouse LINE-1 retrotransposon | Q39457323 | ||
Determination of L1 retrotransposition kinetics in cultured cells | Q39586006 | ||
Discrete subcellular partitioning of human retrotransposon RNAs despite a common mechanism of genome insertion | Q39741192 | ||
Efficient translation initiation directed by the 900-nucleotide-long and GC-rich 5' untranslated region of the human retrotransposon LINE-1 mRNA is strictly cap dependent rather than internal ribosome entry site mediated | Q40139032 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e2003067 | |
P577 | publication date | 2018-03-05 | |
P1433 | published in | PLOS Biology | Q1771695 |
P1476 | title | Spliced integrated retrotransposed element (SpIRE) formation in the human genome. | |
P478 | volume | 16 |
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Q55692166 | L1 retrotransposition in the soma: a field jumping ahead. |
Q96640370 | Measuring and interpreting transposable element expression |
Q52673987 | Reading the tea leaves: Dead transposon copies reveal novel host and transposon biology. |
Q91712521 | The UCSC repeat browser allows discovery and visualization of evolutionary conflict across repeat families |
Q64112074 | The impact of transposable element activity on therapeutically relevant human stem cells |
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