| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1029996655 |
| P356 | DOI | 10.1186/1745-6150-2-11 |
| P932 | PMC publication ID | 1863416 |
| P698 | PubMed publication ID | 17459149 |
| P5875 | ResearchGate publication ID | 6370337 |
| P50 | author | Deng-Ke Niu | Q50637620 |
| P2860 | cites work | Please hold--the next available exon will be right with you | Q83887943 |
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| Evaluating hypotheses for the origin of eukaryotes | Q28280467 | ||
| The origin of mutants | Q28288915 | ||
| Exon tethering in transcription by RNA polymerase II | Q28302498 | ||
| The natural history of group I introns | Q28303356 | ||
| A unified theory of gene expression | Q29615022 | ||
| Introns and the origin of nucleus-cytosol compartmentalization | Q29618633 | ||
| In exponentially growing Saccharomyces cerevisiae cells, rRNA synthesis is determined by the summed RNA polymerase I loading rate rather than by the number of active genes | Q30310526 | ||
| mRNA-mediated intron losses: evidence from extraordinarily large exons | Q31155910 | ||
| A high density of ancient spliceosomal introns in oxymonad excavates | Q33241069 | ||
| The origin of introns and their role in eukaryogenesis: a compromise solution to the introns-early versus introns-late debate? | Q33253857 | ||
| Complex early genes | Q33836616 | ||
| Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| Mechanism of non-spliceosomal mRNA splicing in the unfolded protein response pathway | Q33891036 | ||
| Spliceosomal introns in the deep-branching eukaryote Trichomonas vaginalis | Q33930440 | ||
| Selective forces for the origin of the eukaryotic nucleus | Q33995072 | ||
| A spliceosomal intron in Giardia lamblia | Q34019814 | ||
| Selection for short introns in highly expressed genes | Q34140547 | ||
| Cotranscriptionally Formed DNA:RNA Hybrids Mediate Transcription Elongation Impairment and Transcription-Associated Recombination | Q34267573 | ||
| Crystal structure of a self-splicing group I intron with both exons | Q34324406 | ||
| Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability | Q34442378 | ||
| The biology of intron gain and loss. | Q34467973 | ||
| The evolution of spliceosomal introns: patterns, puzzles and progress | Q34495531 | ||
| Origins and evolution of spliceosomal introns | Q34580514 | ||
| Selective and mutational patterns associated with gene expression in humans: influences on synonymous composition and intron presence | Q34645301 | ||
| The tiny enslaved genome of a rhizarian alga | Q34686911 | ||
| Messenger RNA surveillance and the evolutionary proliferation of introns | Q35091311 | ||
| Introns in gene evolution | Q35179945 | ||
| Keeping RNA and DNA Apart during Transcription | Q35550748 | ||
| Minimal introns are not "junk". | Q35786108 | ||
| Why is transcription coupled to translation in bacteria? | Q35921500 | ||
| Mobile group II introns | Q35965810 | ||
| Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA. | Q36021428 | ||
| Analysis of evolution of exon-intron structure of eukaryotic genes | Q36173290 | ||
| Growth inhibition mediated by excess negative supercoiling: the interplay between transcription elongation, R-loop formation and DNA topology | Q36371631 | ||
| The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
| Cotranscriptional processes and their influence on genome stability. | Q36538957 | ||
| Intron-rich ancestors | Q36542186 | ||
| Duplication-targeted DNA methylation and mutagenesis in the evolution of eukaryotic chromosomes | Q36819409 | ||
| Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence | Q37096423 | ||
| Intron phylogeny: a new hypothesis | Q37778081 | ||
| Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae. | Q39528577 | ||
| The signature of selection mediated by expression on human genes | Q40830000 | ||
| Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA | Q41023029 | ||
| Did group II intron proliferation in an endosymbiont-bearing archaeon create eukaryotes? | Q41978462 | ||
| A stem-loop "kissing" model for the initiation of recombination and the origin of introns | Q43629561 | ||
| Eukaryotic evolution: early origin of canonical introns. | Q44143060 | ||
| Introns: mighty elements from the RNA world | Q47293905 | ||
| Hypervariable and highly divergent intron-exon organizations in the chordate Oikopleura dioica | Q47299262 | ||
| Why do genes have introns? Recombination might add a new piece to the puzzle. | Q52587080 | ||
| Molecular biology: RNA lost in translation. | Q53631052 | ||
| A switch from high-fidelity to error-prone DNA double-strand break repair underlies stress-induced mutation. | Q54478818 | ||
| Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processing | Q58866839 | ||
| Human antisense genes have unusually short introns: evidence for selection for rapid transcription | Q59303885 | ||
| High Deleterious Genomic Mutation Rate in Stationary Phase of Escherichia coli | Q60057535 | ||
| mRNA processing and genomic instability | Q63383462 | ||
| Are introns in-series error-detecting sequences? | Q71107670 | ||
| Factors affecting ectopic gene conversion in mice | Q74450777 | ||
| Starvation in yeast increases non-adaptive mutation | Q74609074 | ||
| Transcription and translation are coupled in Archaea | Q79609849 | ||
| RNA displacement and resolution of the transcription bubble during transcription by T7 RNA polymerase | Q80531683 | ||
| P304 | page(s) | 11 | |
| P577 | publication date | 2007-04-25 | |
| P1433 | published in | Biology Direct | Q1954915 |
| P1476 | title | Protecting exons from deleterious R-loops: a potential advantage of having introns | |
| P478 | volume | 2 |
| Q35004875 | An overview of the introns-first theory |
| Q33924790 | Association of intron loss with high mutation rate in Arabidopsis: implications for genome size evolution |
| Q33857851 | Conservation in first introns is positively associated with the number of exons within genes and the presence of regulatory epigenetic signals |
| Q33350157 | DNA double-strand break repair and the evolution of intron density |
| Q33700757 | Evaluation of models of the mechanisms underlying intron loss and gain in Aspergillus fungi. |
| Q28757923 | Evidence against the energetic cost hypothesis for the short introns in highly expressed genes |
| Q30485377 | Exon definition as a potential negative force against intron losses in evolution |
| Q36387310 | Gene expression levels are correlated with synonymous codon usage, amino acid composition, and gene architecture in the red flour beetle, Tribolium castaneum |
| Q33829781 | Genome-wide functional analysis of human 5' untranslated region introns |
| Q33526480 | Molecular diversity of antimicrobial effectors in the oyster Crassostrea gigas |
| Q37043759 | Reverse transcriptase and intron number evolution |
| Q41728634 | Survey of group I and group II introns in 29 sequenced genomes of the Bacillus cereus group: insights into their spread and evolution |
| Q33904719 | Why eukaryotic cells use introns to enhance gene expression: splicing reduces transcription-associated mutagenesis by inhibiting topoisomerase I cutting activity. |
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