| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1050549639 |
| P356 | DOI | 10.1038/384346A0 |
| P8608 | Fatcat ID | release_qilsjnarhjhwdklopvxke6xcsy |
| P698 | PubMed publication ID | 8934517 |
| P50 | author | Dmitri A. Petrov | Q23718985 |
| P2093 | author name string | Hartl DL | |
| Lozovskaya ER | |||
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| P433 | issue | 6607 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 346-349 | |
| P577 | publication date | 1996-11-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | High intrinsic rate of DNA loss in Drosophila | |
| P478 | volume | 384 |
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| Q35214955 | Analysis of retrotransposon structural diversity uncovers properties and propensities in angiosperm genome evolution |
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| Q36726482 | Ancestral whole-genome duplication in the marine chelicerate horseshoe crabs |
| Q24803725 | Assessing the impact of comparative genomic sequence data on the functional annotation of the Drosophila genome |
| Q28754671 | Automated paleontology of repetitive DNA with REANNOTATE |
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| Q52696216 | Cloning and sequencing of the breakpoint regions of inversion 5g fixed in Drosophila buzzatii. |
| Q29614229 | Comparative genome and proteome analysis of Anopheles gambiae and Drosophila melanogaster |
| Q22065751 | Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution |
| Q33971721 | Comparative sequence analysis of plant nuclear genomes:m microcolinearity and its many exceptions |
| Q30834511 | Comparative validation of the D. melanogaster modENCODE transcriptome annotation. |
| Q33891354 | Comprehensive analysis of amino acid and nucleotide composition in eukaryotic genomes, comparing genes and pseudogenes |
| Q42027396 | Conservation of regulatory sequences and gene expression patterns in the disintegrating Drosophila Hox gene complex |
| Q33834930 | Convergently recruited nuclear transport retrogenes are male biased in expression and evolving under positive selection in Drosophila |
| Q35839562 | Correlated expression of retrocopies and parental genes in zebrafish. |
| Q90520485 | Death of new microRNA genes in Drosophila via gradual loss of fitness advantages |
| Q46411441 | Deletion-bias in DNA double-strand break repair differentially contributes to plant genome shrinkage. |
| Q33633504 | Deletional bias across the three domains of life. |
| Q33253683 | Detecting the limits of regulatory element conservation and divergence estimation using pairwise and multiple alignments |
| Q47369552 | Differences in genome size between closely related species: the Drosophila melanogaster species subgroup |
| Q64387585 | Differences in the processing of DNA ends in Arabidopsis thaliana and tobacco: possible implications for genome evolution |
| Q44205396 | Digging deep for ancient relics: a survey of protein motifs in the intergenic sequences of four eukaryotic genomes |
| Q38668496 | Digging for dead genes: an analysis of the characteristics of the pseudogene population in the Caenorhabditis elegans genome |
| Q40670980 | Distinct molecular evolutionary mechanisms underlie the functional diversification of the Wnt and TGFbeta signaling pathways |
| Q58045061 | Do Plants Have a One-Way Ticket to Genomic Obesity? |
| Q22065740 | Doubling genome size without polyploidization: dynamics of retrotransposition-driven genomic expansions in Oryza australiensis, a wild relative of rice |
| Q28776436 | Drosophila euchromatic LTR retrotransposons are much younger than the host species in which they reside |
| Q33392690 | Duplication and gene conversion in the Drosophila melanogaster genome |
| Q34613042 | Dynamics of R1 and R2 elements in the rDNA locus of Drosophila simulans |
| Q37682315 | Dynamics of genome size evolution in birds and mammals |
| Q41445767 | Dynamics of genomic innovation in the unicellular ancestry of animals |
| Q33334443 | EST analysis of Ostreococcus lucimarinus, the most compact eukaryotic genome, shows an excess of introns in highly expressed genes |
| Q37412780 | Estimation of the spontaneous mutation rate per nucleotide site in a Drosophila melanogaster full-sib family. |
| Q24628063 | Evolution of a distinct genomic domain in Drosophila: comparative analysis of the dot chromosome in Drosophila melanogaster and Drosophila virilis |
| Q47220744 | Evolution of genome size: new approaches to an old problem |
| Q41876083 | Evolution of multigene families by gene duplication. A haploid model |
| Q33398518 | Evolution of regulatory sequences in 12 Drosophila species |
| Q81712034 | Evolutionary aspects of functional and pseudogene members of the phytochrome gene family in Scots pine |
| Q52567247 | Evolutionary biology. A plastic genome. |
| Q51833620 | Evolutionary characterization of Ty3/gypsy-like LTR retrotransposons in the parasitic cestode Echinococcus granulosus. |
| Q37280065 | Evolutionary course of CsRn1 long-terminal-repeat retrotransposon and its heterogeneous integrations into the genome of the liver fluke, Clonorchis sinensis |
| Q35038009 | Evolutionary history of Cer elements and their impact on the C. elegans genome |
| Q24684628 | Evolutionary rate analyses of orthologs and paralogs from 12 Drosophila genomes |
| Q35904937 | Expression of the Retrotransposon Helena Reveals a Complex Pattern of TE Deregulation in Drosophila Hybrids |
| Q36238572 | Extremely Rare Polymorphisms in Saccharomyces cerevisiae Allow Inference of the Mutational Spectrum |
| Q26809985 | Fractionation mutagenesis and similar consequences of mechanisms removing dispensable or less-expressed DNA in plants |
| Q34148263 | Gene alterations at Drosophila inversion breakpoints provide prima facie evidence for natural selection as an explanation for rapid chromosomal evolution |
| Q37176337 | General gene movement off the X chromosome in the Drosophila genus |
| Q35021831 | Genome Size Evolution in Pufferfish: A Comparative Analysis of Diodontid and Tetraodontid Pufferfish Genomes |
| Q41979481 | Genome size variation and evolution in Veronica. |
| Q28749630 | Genome-wide analysis of major intrinsic proteins in the tree plant Populus trichocarpa: characterization of XIP subfamily of aquaporins from evolutionary perspective |
| Q53147973 | Genome-wide identification and characterization of aquaporin genes (AQPs) in Chinese cabbage (Brassica rapa ssp. pekinensis). |
| Q46601420 | Genome-wide identification, classification, and analysis of NADP-ME family members from 12 crucifer species |
| Q36099668 | Genome-wide variation in recombination rate in Eucalyptus |
| Q47643960 | Genomic gigantism: DNA loss is slow in mountain grasshoppers |
| Q34570725 | Genomic heterogeneity of background substitutional patterns in Drosophila melanogaster |
| Q47312431 | Genomic paleontology provides evidence for two distinct origins of Asian rice (Oryza sativa L.). |
| Q47681271 | Genomics: protein fossils live on as RNA. |
| Q30837285 | Global patterns of sequence evolution in Drosophila |
| Q52940179 | Growth and decline of introns. |
| Q28654895 | Hellbender genome sequences shed light on genomic expansion at the base of crown salamanders |
| Q52965913 | High mutation rate and predominance of insertions in the Caenorhabditis elegans nuclear genome. |
| Q48086162 | High rate of chimeric gene origination by retroposition in plant genomes |
| Q36525030 | Highlight--making it big: salamanders keep DNA near and dear |
| Q34616282 | How intron splicing affects the deletion and insertion profile in Drosophila melanogaster |
| Q24550371 | Identification of pseudogenes in the Drosophila melanogaster genome |
| Q28079314 | Independent evolution of genomic characters during major metazoan transitions |
| Q21045365 | Initial sequencing and analysis of the human genome |
| Q33801561 | Insights into the evolutionary process of genome degradation |
| Q35023564 | Intra-genomic variation in the ribosomal repeats of nematodes |
| Q47255836 | Intron size and natural selection |
| Q34644075 | Intron size correlates positively with recombination rate in Caenorhabditis elegans |
| Q42058893 | Intron splice sites of Papilio glaucus PglRh3 corroborate insect opsin phylogeny |
| Q34504653 | Intron-exon structures of eukaryotic model organisms |
| Q30980345 | Is small indel bias a determinant of genome size? |
| Q36878104 | Isolation and properties of Drosophila melanogaster ferritin--molecular cloning of a cDNA that encodes one subunit, and localization of the gene on the third chromosome |
| Q36225278 | LTR retrotransposons and flowering plant genome size: emergence of the increase/decrease model |
| Q33290247 | LTR retrotransposons in rice (Oryza sativa, L.): recent burst amplifications followed by rapid DNA loss |
| Q33801891 | Landscape of standing variation for tandem duplications in Drosophila yakuba and Drosophila simulans |
| Q33511369 | Large introns in relation to alternative splicing and gene evolution: a case study of Drosophila bruno-3 |
| Q36672362 | Large-scale analysis of transcriptional cis-regulatory modules reveals both common features and distinct subclasses |
| Q34330528 | Long deletion hot spots inside retrotransposon 297. |
| Q28727809 | Losing identity: structural diversity of transposable elements belonging to different classes in the genome of Anopheles gambiae |
| Q35970436 | Low Genetic Quality Alters Key Dimensions of the Mutational Spectrum |
| Q36995341 | Many or most genes in Arabidopsis transposed after the origin of the order Brassicales |
| Q35629302 | Massive amplification of rolling-circle transposons in the lineage of the bat Myotis lucifugus |
| Q52579535 | Master copy is not responsible for the high rate of copia transposition in Drosophila. |
| Q34582833 | Mechanisms of recent genome size variation in flowering plants |
| Q28775887 | Millions of years of evolution preserved: a comprehensive catalog of the processed pseudogenes in the human genome |
| Q33260766 | Minor shift in background substitutional patterns in the Drosophila saltans and willistoni lineages is insufficient to explain GC content of coding sequences |
| Q34193247 | Mitochondrial pseudogenes in the nuclear genomes of Drosophila |
| Q36287824 | Molecular evolution of glutathione S-transferases in the genus Drosophila. |
| Q42570550 | Molecular evolution of the Cecropin multigene family in Drosophila. functional genes vs. pseudogenes. |
| Q30665441 | Molecular evolution of the ocnus and janus genes in the Drosophila melanogaster species subgroup. |
| Q42672260 | Molecular evolution of the second ancient human mariner transposon, Hsmar2, illustrates patterns of neutral evolution in the human genome lineage |
| Q34186655 | Molecular melodies in high and low C. |
| Q34612043 | Molecular nature of 11 spontaneous de novo mutations in Drosophila melanogaster |
| Q38594040 | Multigene Family Evolution: Perspectives from Insect Chemoreceptors |
| Q51686575 | Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster. |
| Q39657313 | Neutral evolution of ten types of mariner transposons in the genomes of Caenorhabditis elegans and Caenorhabditis briggsae |
| Q34637058 | Newly evolved genes: moving from comparative genomics to functional studies in model systems. How important is genetic novelty for species adaptation and diversification? |
| Q33567253 | Non-random genomic integration - an intrinsic property of retrogenes in Drosophila? |
| Q36090359 | Novel genes from formation to function |
| Q22066328 | Nucleomorph genome of Hemiselmis andersenii reveals complete intron loss and compaction as a driver of protein structure and function |
| Q24655674 | On the origin of new genes in Drosophila |
| Q54981835 | On the possibility of death of new genes - evidence from the deletion of de novo microRNAs. |
| Q47861102 | Organization and structural evolution of four multigene families in Arabidopsis thaliana: AtLCAD, AtLGT, AtMYST and AtHD-GL2. |
| Q36010302 | Origin of genes |
| Q74166748 | Patterns and rates of indel evolution in processed pseudogenes from humans and murids |
| Q40497920 | Patterns of evolutionary constraints in intronic and intergenic DNA of Drosophila. |
| Q47194852 | Patterns of genome size evolution in tetraodontiform fishes |
| Q34994200 | Patterns of nucleotide substitution in Drosophila and mammalian genomes |
| Q36225396 | Penelope-like elements--a new class of retroelements: distribution, function and possible evolutionary significance. |
| Q34192362 | Perspective: transposable elements, parasitic DNA, and genome evolution |
| Q33970622 | Polymorphism and divergence at a Drosophila pseudogene locus. |
| Q52570701 | Polymorphism in structure of the retrotransposable element 412 in Drosophila simulans and D. melanogaster populations. |
| Q36778170 | Polytene chromosomal maps of 11 Drosophila species: the order of genomic scaffolds inferred from genetic and physical maps. |
| Q36023324 | Population Genomics of Infectious and Integrated Wolbachia pipientis Genomes in Drosophila ananassae |
| Q34823735 | Population genomics of transposable elements in Drosophila melanogaster. |
| Q34129172 | Population, evolutionary and genomic consequences of interference selection |
| Q24814659 | Positive selection of Iris, a retroviral envelope-derived host gene in Drosophila melanogaster |
| Q45302116 | Post-genomics and the neutral theory: variation and conservation in the tumor necrosis factor-alpha promoter |
| Q21563564 | Principles of genome evolution in the Drosophila melanogaster species group |
| Q42648137 | Pseudogenes, junk DNA, and the dynamics of Rickettsia genomes |
| Q34605437 | Quantitative genetic analysis of copia retrotransposon activity in inbred Drosophila melanogaster lines |
| Q28681186 | RNA-based gene duplication: mechanistic and evolutionary insights |
| Q37063145 | Rates and genomic consequences of spontaneous mutational events in Drosophila melanogaster |
| Q34616178 | Rates of R1 and R2 retrotransposition and elimination from the rDNA locus of Drosophila melanogaster |
| Q36090183 | Recent LTR retrotransposon insertion contrasts with waves of non-LTR insertion since speciation in Drosophila melanogaster |
| Q34263156 | Recombination drives vertebrate genome contraction |
| Q33698604 | Recurrent Gene Duplication Leads to Diverse Repertoires of Centromeric Histones in Drosophila Species. |
| Q30860364 | Remarkable compartmentalization of transposable elements and pseudogenes in the heterochromatin of the Tetraodon nigroviridis genome |
| Q33315562 | Repetitive element-mediated recombination as a mechanism for new gene origination in Drosophila |
| Q58045074 | Reply |
| Q34570559 | Ribosomal DNA in the grasshopper Podisma pedestris: escape from concerted evolution |
| Q34140547 | Selection for short introns in highly expressed genes |
| Q42017329 | Selective constraints on intron evolution in Drosophila |
| Q47070815 | Selective sweep of a newly evolved sperm-specific gene in Drosophila |
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| Q34145763 | Sequencing of pooled DNA samples (Pool-Seq) uncovers complex dynamics of transposable element insertions in Drosophila melanogaster |
| Q44358075 | Short indels are subject to insertion-biased gene conversion |
| Q36525004 | Slow DNA loss in the gigantic genomes of salamanders |
| Q47177532 | Slow but Steady: Reduction of Genome Size through Biased Mutation |
| Q37063149 | Stabilizing selection, purifying selection, and mutational bias in finite populations |
| Q39740957 | Strong mutational bias toward deletions in the Drosophila melanogaster genome is compensated by selection |
| Q39735181 | Structural divergence of chromosomal segments that arose from successive duplication events in the Arabidopsis genome |
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| Q48042951 | Structure, organization and putative function of the genes identified within a 23.9-kb fragment from Arabidopsis thaliana chromosome IV. |
| Q33959836 | Studying genomes through the aeons: protein families, pseudogenes and proteome evolution |
| Q35598517 | Testing chromosomal phylogenies and inversion breakpoint reuse in Drosophila |
| Q30450703 | Testing for selection on synonymous sites in plant mitochondrial DNA: the role of codon bias and RNA editing |
| Q22122056 | The Arabidopsis lyrata genome sequence and the basis of rapid genome size change |
| Q37442744 | The adaptive role of transposable elements in the Drosophila genome |
| Q47836921 | The analysis of genomic structures in the L1 family of cell adhesion molecules provides no evidence for exon shuffling events after the separation of arthropod and chordate lineages |
| Q52551550 | The changing sizes of genes. |
| Q47830779 | The chicken genome contains no HMG1 retropseudogenes but a functional HMG1 gene with long introns. |
| Q33924285 | The correlation between intron length and recombination in drosophila. Dynamic equilibrium between mutational and selective forces. |
| Q52577664 | The evolution of an alpha-esterase pseudogene inactivated in the Drosophila melanogaster lineage. |
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| Q34382762 | The evolution of tRNA genes in Drosophila |
| Q33485535 | The evolutionary dynamics of the Helena retrotransposon revealed by sequenced Drosophila genomes |
| Q36810538 | The fate of Arabidopsis thaliana homeologous CNSs and their motifs in the Paleohexaploid Brassica rapa |
| Q35528859 | The landscape of transposable elements in the finished genome of the fungal wheat pathogen Mycosphaerella graminicola |
| Q28651140 | The large genome constraint hypothesis: evolution, ecology and phenotype |
| Q48104187 | The mariner transposons belonging to the irritans subfamily were maintained in chordate genomes by vertical transmission |
| Q22122023 | The origin of new genes: glimpses from the young and old |
| Q52692358 | The recent origin of the Sdic gene cluster in the melanogaster subgroup. |
| Q52836827 | The role of mRNA-based duplication in the evolution of the primate genome. |
| Q28646755 | The serine/threonine kinase 33 is present and expressed in palaeognath birds but has become a unitary pseudogene in neognaths about 100 million years ago |
| Q24803634 | The transposable elements of the Drosophila melanogaster euchromatin: a genomics perspective |
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| Q34467653 | Two large families of chemoreceptor genes in the nematodes Caenorhabditis elegans and Caenorhabditis briggsae reveal extensive gene duplication, diversification, movement, and intron loss |
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