review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1038/SJ.HDY.6800791 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/sj.hdy.6800791 |
P698 | PubMed publication ID | 16449982 |
P5875 | ResearchGate publication ID | 7323998 |
P50 | author | Douda Bensasson | Q57267884 |
P2093 | author name string | Belshaw R | |
P2860 | cites work | Mitochondrial evolution | Q22065556 |
Length distribution of long interspersed nucleotide elements (LINEs) and processed pseudogenes of human endogenous retroviruses: implications for retrotransposition and pseudogene detection | Q22330802 | ||
Retroposed new genes out of the X in Drosophila | Q35806781 | ||
Distribution and characterization of regulatory elements in the human genome | Q35807015 | ||
New Drosophila introns originate by duplication | Q35880119 | ||
Mobile group II introns | Q35965810 | ||
Toward a resolution of the introns early/late debate: only phase zero introns are correlated with the structure of ancient proteins | Q36064406 | ||
The recent origins of introns | Q37068347 | ||
Functional constraints and frequency of deleterious mutations in noncoding DNA of rodents | Q37089364 | ||
Origins of recently gained introns in Caenorhabditis | Q37388384 | ||
The signature of selection mediated by expression on human genes | Q40830000 | ||
Implications of RNA⋅RNA Splicing in Evolution of Eukaryotic Cells | Q40972436 | ||
Conservation, regulation, synteny, and introns in a large-scale C. briggsae-C. elegans genomic alignment | Q41757662 | ||
A handful of intron-containing genes produces the lion's share of yeast mRNA. | Q43206498 | ||
Determinants of plant U12-dependent intron splicing efficiency | Q44853494 | ||
Can codon usage bias explain intron phase distributions and exon symmetry? | Q47293682 | ||
The evolutionary gain of spliceosomal introns: sequence and phase preferences | Q47350883 | ||
Intron length and codon usage. | Q52927377 | ||
Retrotransposition of the Ll.LtrB group II intron proceeds predominantly via reverse splicing into DNA targets. | Q52946056 | ||
Group II self-splicing introns in bacteria. | Q54045224 | ||
Erratum: Retrotransposition of a bacterial group II intron | Q59066149 | ||
Erratum: correction: Retrotransposition of a bacterial group II intron | Q59091836 | ||
Genes in pieces: were they ever together? | Q59092219 | ||
Pseudogenes in yeast? | Q68942578 | ||
The exon theory of genes | Q69034342 | ||
Imprinted genes have few and small introns | Q70972792 | ||
Introns resolve the conflict between base order-dependent stem-loop potential and the encoding of RNA or protein: further evidence from overlapping genes | Q74014223 | ||
Footprints of primordial introns on the eukaryotic genome: still no clear traces | Q77228579 | ||
Intron evolution as a population-genetic process | Q24534216 | ||
Patterns of intron gain and loss in fungi | Q24798152 | ||
Patterns of intron sequence evolution in Drosophila are dependent upon length and GC content | Q24811259 | ||
Gametophytic selection in Arabidopsis thaliana supports the selective model of intron length reduction | Q24813367 | ||
Correlation of DNA exonic regions with protein structural units in haemoglobin | Q28280219 | ||
Pre-mRNA splicing: awash in a sea of proteins | Q29547272 | ||
An extensive network of coupling among gene expression machines | Q29547273 | ||
Why genes in pieces? | Q29618207 | ||
Multigene analyses of bilaterian animals corroborate the monophyly of Ecdysozoa, Lophotrochozoa, and Protostomia | Q29618582 | ||
Testing the exon theory of genes: the evidence from protein structure | Q30420431 | ||
Retroids in archaea: phylogeny and lateral origins | Q30940021 | ||
Remarkable interkingdom conservation of intron positions and massive, lineage-specific intron loss and gain in eukaryotic evolution | Q30980287 | ||
Compilation and analysis of group II intron insertions in bacterial genomes: evidence for retroelement behavior | Q33583987 | ||
Evolution of evolvability. | Q33692297 | ||
The pattern of intron loss | Q33756723 | ||
Evolution of organellar genomes | Q33801588 | ||
Rates of intron loss and gain: implications for early eukaryotic evolution | Q33936911 | ||
Intron presence-absence polymorphism in Drosophila driven by positive Darwinian selection | Q34031425 | ||
Analysis of conserved noncoding DNA in Drosophila reveals similar constraints in intergenic and intronic sequences. | Q34085680 | ||
Endogenous retroviruses and the human germline | Q34087817 | ||
Eukaryotic intron loss | Q34201357 | ||
The unusual phylogenetic distribution of retrotransposons: a hypothesis | Q34227405 | ||
The spliceosome: the most complex macromolecular machine in the cell? | Q34278742 | ||
Root of the universal tree of life based on ancient aminoacyl-tRNA synthetase gene duplications | Q34308020 | ||
The Opisthokonta and the Ecdysozoa may not be clades: stronger support for the grouping of plant and animal than for animal and fungi and stronger support for the Coelomata than Ecdysozoa | Q34392765 | ||
Trans-activation of group II intron splicing by nuclear U5 snRNA. | Q34423493 | ||
Intron-exon structures of eukaryotic model organisms | Q34504653 | ||
Spliceosomal snRNAs: Mg(2+)-dependent chemistry at the catalytic core? | Q34635318 | ||
The evolution of spliceosomal introns | Q34998373 | ||
Messenger RNA surveillance and the evolutionary proliferation of introns | Q35091311 | ||
Database for mobile group II introns | Q35158532 | ||
Introns in gene evolution | Q35179945 | ||
Relationship between "proto-splice sites" and intron phases: evidence from dicodon analysis | Q35672875 | ||
Molecular evolution: introns fall into place | Q35761465 | ||
Minimal introns are not "junk". | Q35786108 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 208-213 | |
P577 | publication date | 2006-03-01 | |
P1433 | published in | Heredity | Q2261546 |
P1476 | title | The rise and falls of introns | |
P478 | volume | 96 |
Q33855773 | Both size and GC-content of minimal introns are selected in human populations |
Q34366688 | Characterization of newly gained introns in Daphnia populations. |
Q37197242 | Choosing and using introns in molecular phylogenetics. |
Q39523373 | Convergent Evolution of Fern-Specific Mitochondrial Group II Intron atp1i361g2 and Its Ancient Source Paralogue rps3i249g2 and Independent Losses of Intron and RNA Editing among Pteridaceae |
Q24604817 | Endogenous mechanisms for the origins of spliceosomal introns |
Q33533635 | Evolution of spliceosomal introns following endosymbiotic gene transfer |
Q36125393 | Evolution of the Exon-Intron Structure in Ciliate Genomes. |
Q42014026 | Evolutionary genomics of Colias Phosphoglucose Isomerase (PGI) introns |
Q41809804 | Extensive, recent intron gains in Daphnia populations |
Q33252919 | Genetic structure and evolution of the Vps25 family, a yeast ESCRT-II component |
Q48049590 | Loss of two introns from the Magnolia tripetala mitochondrial cox2 gene implicates horizontal gene transfer and gene conversion as a novel mechanism of intron loss |
Q38610998 | Mechanisms of intron gain and loss in Cryptococcus |
Q34684856 | Mechanisms of intron loss and gain in the fission yeast Schizosaccharomyces. |
Q62496245 | Modeling one thousand intron length distributions with fitild |
Q45762257 | Molecular phylogenetics of the lizard genus Microlophus (squamata:tropiduridae): aligning and retrieving indel signal from nuclear introns |
Q35025516 | Phyletic distribution of fatty acid-binding protein genes |
Q27342688 | Phylogenetic distribution of intron positions in alpha-amylase genes of bilateria suggests numerous gains and losses |
Q33730648 | Population genomics of intron splicing in 38 Saccharomyces cerevisiae genome sequences |
Q33268447 | Relationship between mRNA stability and intron presence |
Q35084731 | Structural genomics: correlation blocks, population structure, and genome architecture |
Q30894453 | The peculiarities of large intron splicing in animals |
Q28727065 | Transposon-derived and satellite-derived repetitive sequences play distinct functional roles in Mammalian intron size expansion |
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