| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1999PNAS...96.7847Y |
| P356 | DOI | 10.1073/PNAS.96.14.7847 |
| P8608 | Fatcat ID | release_z5iv27rvw5f2xf4odcicjjh5ti |
| P932 | PMC publication ID | 22150 |
| P698 | PubMed publication ID | 10393910 |
| P5875 | ResearchGate publication ID | 12905152 |
| P50 | author | Thomas H Eickbush | Q125349370 |
| Harmit Singh Malik | Q30513673 | ||
| P2093 | author name string | Jin Yang | |
| P2860 | cites work | The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 |
| Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
| Evolutionary relationships among group II intron-encoded proteins and identification of a conserved domain that may be related to maturase function | Q24628951 | ||
| FokI dimerization is required for DNA cleavage | Q24657843 | ||
| The galvanization of biology: a growing appreciation for the roles of zinc | Q70995740 | ||
| Mobility of yeast mitochondrial group II introns: engineering a new site specificity and retrohoming via full reverse splicing | Q73266484 | ||
| Structure of FokI has implications for DNA cleavage | Q24657897 | ||
| Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices | Q27730748 | ||
| The crystal structure of EcoRV endonuclease and of its complexes with cognate and non-cognate DNA fragments | Q27732162 | ||
| Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 | ||
| 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 | ||
| Site-specific mutagenesis of AIDS virus reverse transcriptase | Q28338101 | ||
| Origin and evolution of retroelements based upon their reverse transcriptase sequences | Q29614742 | ||
| Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
| High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
| RNA-induced changes in the activity of the endonuclease encoded by the R2 retrotransposable element | Q33774211 | ||
| The age and evolution of non-LTR retrotransposable elements | Q33864837 | ||
| A new non-LTR retrotransposon porvides evidence for multiple distinct site-specific elements inCrithidia faciculataminiexon arrays | Q34764767 | ||
| R4, a non-LTR retrotransposon specific to the large subunit rRNA genes of nematodes | Q34780681 | ||
| Retroviral Reverse Transcription and Integration: Progress and Problems | Q35161317 | ||
| Transpositional recombination: mechanistic insights from studies of mu and other elements | Q35231355 | ||
| SLACS retrotransposon from Trypanosoma brucei gambiense is similar to mammalian LINEs | Q35828817 | ||
| Retrotransposon R1Bm endonuclease cleaves the target sequence. | Q35902897 | ||
| RNA template requirements for target DNA-primed reverse transcription by the R2 retrotransposable element | Q36552964 | ||
| Single amino acid substitutions uncouple the DNA binding and strand scission activities of Fok I endonuclease. | Q36601344 | ||
| A rapidly rearranging retrotransposon within the miniexon gene locus of Crithidia fasciculata | Q36717494 | ||
| Self-splicing group I and group II introns encode homologous (putative) DNA endonucleases of a new family | Q36722758 | ||
| Composite transposable elements in the Xenopus laevis genome | Q36769786 | ||
| The domain structure and retrotransposition mechanism of R2 elements are conserved throughout arthropods | Q38324626 | ||
| Dong, a non-long terminal repeat (non-LTR) retrotransposable element from Bombyx mori | Q40405885 | ||
| Antigenic variation in malaria | Q40442253 | ||
| A new member of a family of site-specific retrotransposons is present in the spliced leader RNA genes of Trypanosoma cruzi | Q40642442 | ||
| Functional expression of a sequence-specific endonuclease encoded by the retrotransposon R2Bm | Q42074188 | ||
| Zepp, a LINE-like retrotransposon accumulated in the Chlorella telomeric region | Q42622633 | ||
| 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 | ||
| Amino acid sequence motif of group I intron endonucleases is conserved in open reading frames of group II introns | Q42687817 | ||
| Are retrotransposons long-term hitchhikers? | Q48039375 | ||
| Quick-change pathogens gain an evolutionary edge | Q50136737 | ||
| Retrohoming of a bacterial group II intron: mobility via complete reverse splicing, independent of homologous DNA recombination | Q56902551 | ||
| Retrohoming of a Bacterial Group II Intron | Q59622194 | ||
| A site-directed mutagenesis study to identify amino acid residues involved in the catalytic function of the restriction endonuclease EcoRV | Q59648697 | ||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 7847-7852 | |
| P577 | publication date | 1999-07-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Identification of the endonuclease domain encoded by R2 and other site-specific, non-long terminal repeat retrotransposable elements | |
| P478 | volume | 96 |
| Q31044230 | A non-long terminal repeat retrotransposon family is restricted to the germ line micronucleus of the ciliated protozoan Tetrahymena thermophila |
| Q24791795 | A search for reverse transcriptase-coding sequences reveals new non-LTR retrotransposons in the genome of Drosophila melanogaster |
| Q38387036 | A survey of transposable element classification systems--a call for a fundamental update to meet the challenge of their diversity and complexity. |
| Q36225311 | APE-type non-LTR retrotransposons: determinants involved in target site recognition |
| Q34297022 | An Entamoeba histolytica LINE/SINE pair inserts at common target sites cleaved by the restriction enzyme-like LINE-encoded endonuclease |
| Q28775890 | An active non-LTR retrotransposon with tandem structure in the compact genome of the pufferfish Tetraodon nigroviridis |
| Q42004177 | An extraordinary retrotransposon family encoding dual endonucleases |
| Q42674553 | Ancient lineages of non-LTR retrotransposons in the primitive eukaryote, Giardia lamblia |
| Q38360036 | Characterization of the C-terminal DNA-binding/DNA endonuclease region of a group II intron-encoded protein |
| Q35010566 | Characterization of the restriction enzyme-like endonuclease encoded by the Entamoeba histolytica non-long terminal repeat retrotransposon EhLINE1. |
| Q34366495 | Chimeric RNA transposition intermediates of the I factor produce precise retrotransposed copies |
| Q33737255 | Chimeric restriction enzymes: what is next? |
| Q92492918 | Completion of LINE integration involves an open '4-way' branched DNA intermediate |
| Q28742951 | Crypton transposons: identification of new diverse families and ancient domestication events |
| Q38339071 | Crystal structure of the endonuclease domain encoded by the telomere-specific long interspersed nuclear element, TRAS1. |
| Q95815638 | Current awareness on yeast |
| Q34007576 | DNA-directed DNA polymerase and strand displacement activity of the reverse transcriptase encoded by the R2 retrotransposon. |
| Q57272811 | Dual recognition–incision enzymes might be involved in mismatch repair and meiosis |
| Q35333511 | Dynamic interactions between transposable elements and their hosts |
| Q38362416 | EcoRII: a restriction enzyme evolving recombination functions? |
| Q36817979 | Endonuclease domain of non-LTR retrotransposons: loss-of-function mutants and modeling of the R2Bm endonuclease |
| Q40118342 | Endonuclease domain of the Drosophila melanogaster R2 non-LTR retrotransposon and related retroelements: a new model for transposition |
| Q35641477 | Finely orchestrated movements: evolution of the ribosomal RNA genes |
| Q24791608 | Functional roles of 3'-terminal structures of template RNA during in vivo retrotransposition of non-LTR retrotransposon, R1Bm |
| Q28776429 | Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion |
| Q74420441 | High processivity of the reverse transcriptase from a non-long terminal repeat retrotransposon |
| Q34207225 | Human L1 element target-primed reverse transcription in vitro |
| Q33983519 | Identification of RNA binding motifs in the R2 retrotransposon-encoded reverse transcriptase |
| Q43582678 | Identification of a PD-(D/E)XK-like domain with a novel configuration of the endonuclease active site in the methyl-directed restriction enzyme Mrr and its homologs |
| Q24811792 | Identification of novel restriction endonuclease-like fold families among hypothetical proteins |
| Q42226271 | In and out of the rRNA genes: characterization of Pokey elements in the sequenced Daphnia genome |
| Q38667938 | Independently derived targeting of 28S rDNA by A- and D-clade R2 retrotransposons: Plasticity of integration mechanism |
| Q36969573 | Insulator and Ovo proteins determine the frequency and specificity of insertion of the gypsy retrotransposon in Drosophila melanogaster |
| Q33961271 | Integration of Bombyx mori R2 sequences into the 28S ribosomal RNA genes of Drosophila melanogaster |
| Q37518614 | Integration of the 5' end of the retrotransposon, R2Bm, can be complemented by homologous recombination |
| Q38912198 | Integration site selection by retroviruses and transposable elements in eukaryotes |
| Q26851814 | Integration, Regulation, and Long-Term Stability of R2 Retrotransposons |
| Q59061636 | Introns gain ground |
| Q39013867 | Involvement of Conserved Amino Acids in the C-Terminal Region of LINE-1 ORF2p in Retrotransposition |
| Q36141425 | L1 hybridization enrichment: a method for directly accessing de novo L1 insertions in the human germline. |
| Q42685877 | LINEs and SINE-like elements of the protist Entamoeba histolytica |
| Q34442041 | LINEs, SINEs and processed pseudogenes: parasitic strategies for genome modeling |
| Q33938490 | Mobile elements and the human genome |
| Q36225341 | Mobile genetic elements and sexual reproduction |
| Q31113756 | New Trypanosoma cruzi repeated element that shows site specificity for insertion. |
| Q33898508 | Non-long terminal repeat (non-LTR) retrotransposons: mechanisms, recent developments, and unanswered questions |
| Q90029453 | Novel ribozymes: discovery, catalytic mechanisms, and the quest to understand biological function |
| Q34467155 | Origins and evolution of viruses of eukaryotes: The ultimate modularity |
| Q53352662 | PPP1R13L variant associated with prognosis for patients with rectal cancer. |
| Q35121885 | Preferential occupancy of R2 retroelements on the B chromosomes of the grasshopper Eyprepocnemis plorans. |
| Q35842102 | Processing and translation initiation of non-long terminal repeat retrotransposons by hepatitis delta virus (HDV)-like self-cleaving ribozymes |
| Q39693170 | R2 retrotransposition on assembled nucleosomes depends on the translational position of the target site. |
| Q33925242 | R2 target-primed reverse transcription: ordered cleavage and polymerization steps by protein subunits asymmetrically bound to the target DNA. |
| Q24674917 | RNA from the 5' end of the R2 retrotransposon controls R2 protein binding to and cleavage of its DNA target site |
| Q34276636 | Recombinant SINEs are formed at high frequency during induced retrotransposition in vivo |
| Q24817137 | Role of the Bombyx mori R2 element N-terminal domain in the target-primed reverse transcription (TPRT) reaction |
| Q34688425 | SINEs and LINEs: the art of biting the hand that feeds you. |
| Q38354666 | Secondary structures for 5' regions of R2 retrotransposon RNAs reveal a novel conserved pseudoknot and regions that evolve under different constraints |
| Q39468357 | Sequence-specific recognition and cleavage of telomeric repeat (TTAGG)(n) by endonuclease of non-long terminal repeat retrotransposon TRAS1. |
| Q92756562 | Sequence-specific retrotransposition of 28S rDNA-specific LINE R2Ol in human cells |
| Q30665455 | Structural and phylogenetic analysis of TRAS, telomeric repeat-specific non-LTR retrotransposon families in Lepidopteran insects |
| Q52594699 | Tandem UAA repeats at the 3'-end of the transcript are essential for the precise initiation of reverse transcription of the I factor in Drosophila melanogaster. |
| Q38316095 | Target specificity of the endonuclease from the Xenopus laevis non-long terminal repeat retrotransposon, Tx1L |
| Q42108562 | Targeting novel sites: The N-terminal DNA binding domain of non-LTR retrotransposons is an adaptable module that is implicated in changing site specificities |
| Q42640984 | Teleost fish genomes contain a diverse array of L1 retrotransposon lineages that exhibit a low copy number and high rate of turnover. |
| Q34207786 | Telomere-targeted retrotransposons in the rice blast fungus Magnaporthe oryzae: agents of telomere instability |
| Q27660450 | The Crystal Structure of D212 from Sulfolobus Spindle-Shaped Virus Ragged Hills Reveals a New Member of the PD-(D/E)XK Nuclease Superfamily |
| Q38333658 | The R2 retrotransposon RNA families |
| Q34588175 | The diversity of retrotransposons and the properties of their reverse transcriptases |
| Q47620228 | The diversity of retrotransposons in the yeast Cryptococcus neoformans |
| Q44584038 | The herpesvirus alkaline exonuclease belongs to the restriction endonuclease PD-(D/E)XK superfamily: insight from molecular modeling and phylogenetic analysis |
| Q45050393 | The non-LTR retrotransposon R2 in termites (Insecta, Isoptera): characterization and dynamics |
| Q35610274 | The outs and ins of transposition: from mu to kangaroo |
| Q33951984 | Three retrotransposon families in the genome of Giardia lamblia: two telomeric, one dead |
| Q45959989 | Ticks have R2 retrotransposons but not the consensus transposon target site of other arthropods. |
| Q35002460 | Transcription of Endogenous and Exogenous R2 Elements in the rRNA Gene Locus of Drosophila melanogaster |
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