scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.TIG.2010.10.003 |
P953 | full work available at URL | https://api.elsevier.com/content/article/PII:S016895251000209X?httpAccept=text/plain |
https://api.elsevier.com/content/article/PII:S016895251000209X?httpAccept=text/xml | ||
P698 | PubMed publication ID | 21074888 |
P5875 | ResearchGate publication ID | 47790319 |
P50 | author | Justin P. Blumenstiel | Q37830139 |
P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes | Q22065831 | ||
Selfish DNA: a sexually-transmitted nuclear parasite | Q24532152 | ||
The evolution of RNAi as a defence against viruses and transposable elements | Q24651901 | ||
Small silencing RNAs: an expanding universe | Q24653997 | ||
Unique germ-line organelle, nuage, functions to repress selfish genetic elements in Drosophila melanogaster | Q24683818 | ||
Positive selection drives the evolution of rhino, a member of the heterochromatin protein 1 family in Drosophila | Q24811626 | ||
The small RNA profile during Drosophila melanogaster development | Q28201894 | ||
RNA-mediated chromatin-based silencing in plants | Q28236381 | ||
gurken and the I factor retrotransposon RNAs share common localization signals and machinery | Q28259364 | ||
The molecular basis of P-M hybrid dysgenesis: the role of the P element, a P-strain-specific transposon family | Q28265035 | ||
RITS acts in cis to promote RNA interference-mediated transcriptional and post-transcriptional silencing | Q28287265 | ||
Discrete small RNA-generating loci as master regulators of transposon activity in Drosophila | Q28292093 | ||
Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality | Q28507386 | ||
A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice | Q28511242 | ||
Developmentally regulated piRNA clusters implicate MILI in transposon control | Q28593121 | ||
A stepwise pathway for biogenesis of 24-nt secondary siRNAs and spreading of DNA methylation | Q28755663 | ||
Transposable elements and the evolution of regulatory networks | Q28756349 | ||
Population bottlenecks as a potential major shaping force of human genome architecture | Q28757319 | ||
Collapse of Germline piRNAs in the Absence of Argonaute3 Reveals Somatic piRNAs in Flies | Q29028136 | ||
Mobile elements: drivers of genome evolution | Q29547669 | ||
The Piwi-piRNA pathway provides an adaptive defense in the transposon arms race | Q29614715 | ||
A distinct small RNA pathway silences selfish genetic elements in the germline | Q29614717 | ||
Small RNAs as guardians of the genome | Q29617221 | ||
Transposable elements and the epigenetic regulation of the genome | Q29617224 | ||
Alu repeats and human genomic diversity | Q29618341 | ||
The rde-1 gene, RNA interference, and transposon silencing in C. elegans | Q29618386 | ||
An epigenetic role for maternally inherited piRNAs in transposon silencing | Q33585189 | ||
Population dynamics of PIWI-interacting RNAs (piRNAs) and their targets in Drosophila | Q33618933 | ||
MicroRNA activity is suppressed in mouse oocytes | Q33667949 | ||
Transposable elements in natural populations of Drosophila melanogaster | Q33856655 | ||
MicroRNA function is globally suppressed in mouse oocytes and early embryos | Q33859934 | ||
Proviral amplification of the Gypsy endogenous retrovirus of Drosophila melanogaster involves env-independent invasion of the female germline | Q33890892 | ||
Specialized piRNA pathways act in germline and somatic tissues of the Drosophila ovary | Q33901565 | ||
RNAi and heterochromatin repress centromeric meiotic recombination | Q33928327 | ||
The maternally inherited regulation of P elements in Drosophila melanogaster can be elicited by two P copies at cytological site 1A on the X chromosome | Q33958564 | ||
Hybrid dysgenesis in Drosophila melanogaster: the biology of female and male sterility | Q33993352 | ||
Evidence for maternally transmitted small interfering RNA in the repression of transposition in Drosophila virilis | Q34116149 | ||
Eggs to die for: cell death during Drosophila oogenesis | Q34119271 | ||
Perspective: transposable elements, parasitic DNA, and genome evolution | Q34192362 | ||
The first steps of transposable elements invasion: parasitic strategy vs. genetic drift | Q34570688 | ||
Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila | Q34597710 | ||
Mu killer Causes the Heritable Inactivation of the Mutator Family of Transposable Elements in Zea mays | Q34618803 | ||
zucchini and squash encode two putative nucleases required for rasiRNA production in the Drosophila germline | Q34633591 | ||
Viral particles of the endogenous retrovirus ZAM from Drosophila melanogaster use a pre-existing endosome/exosome pathway for transfer to the oocyte. | Q34881282 | ||
The fate of transposable elements in asexual populations | Q35082947 | ||
Element 1360 and RNAi components contribute to HP1-dependent silencing of a pericentric reporter | Q35239502 | ||
The ecology of the genome - mobile DNA elements and their hosts | Q36004587 | ||
Repeat-associated siRNAs cause chromatin silencing of retrotransposons in the Drosophila melanogaster germline | Q36059543 | ||
Control of female gamete formation by a small RNA pathway in Arabidopsis | Q36185453 | ||
piRNA-mediated nuclear accumulation of retrotransposon transcripts in the Drosophila female germline | Q36937109 | ||
The Argonaute protein family | Q37096233 | ||
A bioinformatics search pipeline, RNA2DSearch, identifies RNA localization elements in Drosophila retrotransposons. | Q37111421 | ||
Epigenetic reprogramming and small RNA silencing of transposable elements in pollen | Q37142129 | ||
Roles of RNA polymerase IV in gene silencing | Q37178200 | ||
Epigenetic silencing of transposable elements: a trade-off between reduced transposition and deleterious effects on neighboring gene expression | Q37287376 | ||
Epigenetic regulation of transposable elements in plants | Q37324789 | ||
Symmetry breaking during Drosophila oogenesis | Q37342310 | ||
The Drosophila HP1 homolog Rhino is required for transposon silencing and piRNA production by dual-strand clusters. | Q37406170 | ||
Evolution of the Caenorhabditis elegans genome | Q37415864 | ||
Transposable elements in the mammalian germline: a comfortable niche or a deadly trap? | Q37742436 | ||
The population genetics of Drosophila transposable elements | Q38321781 | ||
Mut-7 of C. elegans, required for transposon silencing and RNA interference, is a homolog of Werner syndrome helicase and RNaseD. | Q39749476 | ||
Transposon dynamics and the breeding system | Q40751654 | ||
Sure facts, speculations, and open questions about the evolution of transposable element copy number | Q41756995 | ||
Transposable elements in inbreeding and outbreeding populations | Q42965601 | ||
Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage | Q44285291 | ||
Heritable transposon silencing initiated by a naturally occurring transposon inverted duplication | Q46098533 | ||
Gypsy/Ty3-like elements in the genome of the terrestrial Salamander hydromantes (Amphibia, Urodela). | Q48057183 | ||
Different regulatory mechanisms underlie similar transposable element profiles in pufferfish and fruitflies | Q48175103 | ||
Measuring the rates of transcriptional elongation in the female Drosophila melanogaster germ line by nuclear run-on. | Q51759762 | ||
Conserved ribonuclease, Eri1, negatively regulates heterochromatin assembly in fission yeast. | Q52014102 | ||
hobo is responsible for the induction of hybrid dysgenesis by strains of Drosophila melanogaster bearing the male recombination factor 23.5MRF. | Q52457922 | ||
The genomic rate of transposable element movement in Drosophila melanogaster. | Q52540829 | ||
Positive association between copia transposition rate and copy number in Drosophila melanogaster. | Q52549518 | ||
Size matters: non-LTR retrotransposable elements and ectopic recombination in Drosophila. | Q52605438 | ||
Tethering RITS to a nascent transcript initiates RNAi- and heterochromatin-dependent gene silencing. | Q53619809 | ||
Uniparental expression of PolIV-dependent siRNAs in developing endosperm of Arabidopsis | Q56926914 | ||
Selfish genetic elements and speciation | Q57212768 | ||
The population dynamics of transposable elements | Q59508972 | ||
On the role of unequal exchange in the containment of transposable element copy number | Q69851798 | ||
The molecular basis of I-R hybrid dysgenesis in Drosophila melanogaster: identification, cloning, and properties of the I factor | Q72388917 | ||
Transposable element number in mixed mating populations | Q74313724 | ||
Parent-dependent loss of gene silencing during interspecies hybridization | Q79849968 | ||
Fixation of transposable elements in the Drosophila melanogaster genome | Q81240290 | ||
Population frequencies of transposable elements in selfing and outcrossing Caenorhabditis nematodes | Q82230505 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | transposable element | Q121438 |
molecular evolution | Q856529 | ||
evolutionary dynamics | Q5418700 | ||
P304 | page(s) | 23-31 | |
P577 | publication date | 2010-11-11 | |
P1433 | published in | Trends in Genetics | Q2451468 |
P1476 | title | Evolutionary dynamics of transposable elements in a small RNA world | |
P478 | volume | 27 |
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Q56992563 | An introduction to the vast world of transposable elements – what about the diatoms? |
Q37003089 | Analysis of piRNA-mediated silencing of active TEs in Drosophila melanogaster suggests limits on the evolution of host genome defense |
Q33642563 | Billions of basepairs of recently expanded, repetitive sequences are eliminated from the somatic genome during copepod development. |
Q46681274 | Bioinformatics and genomic analysis of transposable elements in eukaryotic genomes |
Q33575809 | Birth, death, and diversification of mobile promoters in prokaryotes |
Q38039110 | Can silencing of transposons contribute to variation in effector gene expression in Phytophthora infestans? |
Q34223777 | Changes in DNA methylation and transgenerational mobilization of a transposable element (mPing) by the topoisomerase II inhibitor, etoposide, in rice |
Q37919383 | Co-evolution between transposable elements and their hosts: a major factor in genome size evolution? |
Q48647191 | Convergent adaptive evolution in marginal environments: unloading transposable elements as a common strategy among mangrove genomes |
Q46622606 | Differential introgression and reorganization of retrotransposons in hybrid zones between wild wheats |
Q91826280 | Diversification of Transposable Elements in Arthropods and Its Impact on Genome Evolution |
Q64993159 | Dynamics of Transposable Element Invasions with piRNA Clusters. |
Q38661616 | Ectopic application of the repressive histone modification H3K9me2 establishes post-zygotic reproductive isolation in Arabidopsis thaliana |
Q93025337 | Enforcement is central to the evolution of cooperation |
Q33674398 | Enhanced evolution by stochastically variable modification of epigenetic marks in the early embryo. |
Q36698269 | Evaluating risks of insertional mutagenesis by DNA transposons in gene therapy |
Q52745073 | Evolution and dynamics of small RNA response to a retroelement invasion in Drosophila. |
Q50068308 | Evolutionary Epigenomics of Retrotransposon-Mediated Methylation Spreading in Rice |
Q35810622 | Evolutionary Implications of Mechanistic Models of TE-Mediated Hybrid Incompatibility |
Q51833620 | Evolutionary characterization of Ty3/gypsy-like LTR retrotransposons in the parasitic cestode Echinococcus granulosus. |
Q42203493 | Evolutionary history of the Tip100 transposon in the genus Ipomoea. |
Q26752905 | Evolutionary interaction between W/Y chromosome and transposable elements |
Q38164153 | Evolutionary transitions in individuality: insights from transposable elements |
Q55481764 | Extensive exchange of transposable elements in the Drosophila pseudoobscura group. |
Q37948969 | Genetic variation and DNA replication timing, or why is there late replicating DNA? |
Q38562840 | Genome Biology and the Evolution of Cell-Size Diversity |
Q84206006 | Genome comparison of barley and maize smut fungi reveals targeted loss of RNA silencing components and species-specific presence of transposable elements |
Q34581766 | Genome sequencing of Sporisorium scitamineum provides insights into the pathogenic mechanisms of sugarcane smut |
Q36268123 | Genomic variation in natural populations of Drosophila melanogaster |
Q28727429 | Large-scale transcriptome analysis of retroelements in the migratory locust, Locusta migratoria |
Q36439815 | Long-term and short-term evolutionary impacts of transposable elements on Drosophila |
Q36000665 | Male germline control of transposable elements |
Q52613189 | Modeling Interactions between Transposable Elements and the Plant Epigenetic Response: A Surprising Reliance on Element Retention. |
Q34514478 | No detectable effect of the DNA methyltransferase DNMT2 on Drosophila meiotic recombination |
Q40984243 | Pervasive epigenetic effects of Drosophila euchromatic transposable elements impact their evolution. |
Q37568285 | Phenotypic diversification by gene silencing in Phytophthora plant pathogens |
Q58098393 | QTL mapping of natural variation reveals that the developmental regulator bruno reduces tolerance to P-element transposition in the Drosophila female germline |
Q38925580 | Reexamining the P-Element Invasion of Drosophila melanogaster Through the Lens of piRNA Silencing |
Q38883001 | Retroviruses and retroelements in diseases and in gene therapy: 15 years later |
Q28742794 | Selfish genetic elements, genetic conflict, and evolutionary innovation |
Q46090732 | Small RNA biology: from fundamental studies to applications |
Q46471181 | Small RNAs from a Big Genome: The piRNA Pathway and Transposable Elements in the Salamander Species Desmognathus fuscus |
Q91719698 | The Evolution of Small-RNA-Mediated Silencing of an Invading Transposable Element |
Q35126313 | The Hmr and Lhr hybrid incompatibility genes suppress a broad range of heterochromatic repeats |
Q86728322 | The genomic proliferation of transposable elements in colonizing populations: Schistosoma mansoni in the new world |
Q38270618 | The peculiarities of piRNA expression upon heat shock exposure in Drosophila melanogaster. |
Q57472098 | The somatic piRNA pathway controls germline transposition over generations |
Q47353087 | Unusual augmentation of germline genome size in Cyclops kolensis (Crustacea, Copepoda): further evidence in support of a revised model of chromatin diminution |
Q92219708 | Updates on Aptamer Research |
Q36926720 | What happens when Penelope comes?: An unusual retroelement invades a host species genome exploring different strategies |
Q35900544 | What makes transposable elements move in the Drosophila genome? |
Q90701901 | piRNA clusters need a minimum threshold size to control transposable element invasions |
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