| scholarly article | Q13442814 |
| P50 | author | Jacques Elion | Q59198601 |
| Rodney Rothstein | Q56908395 | ||
| P2093 | author name string | C Acquaviva | |
| F Taddei | |||
| O Tenaillon | |||
| E Denamur | |||
| G Lecointre | |||
| C Sayada | |||
| I Matic | |||
| M Radman | |||
| I Sunjevaric | |||
| P Darlu | |||
| P2860 | cites work | Barriers to genetic exchange between bacterial species: Streptococcus pneumoniae transformation | Q24548990 |
| Molecular keys to speciation: DNA polymorphism and the control of genetic exchange in enterobacteria | Q24643432 | ||
| Horizontal gene transfer among genomes: the complexity hypothesis | Q24651300 | ||
| Gene Trees in Species Trees | Q59699645 | ||
| The evolution of recombination in changing environments | Q63379855 | ||
| Effect of base pair mismatches on recombination via the RecBCD pathway | Q69356233 | ||
| Insertions, deletions and mismatches in heteroduplex DNA made by recA protein | Q70179308 | ||
| Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism | Q71751695 | ||
| Phylogenetic analysis of Escherichia coli strains causing neonatal meningitis suggests horizontal gene transfer from a predominant pool of highly virulent B2 group strains | Q74302625 | ||
| Testing Significance of Incongruence | Q92270877 | ||
| A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
| Escherichia coli molecular phylogeny using the incongruence length difference test | Q31946089 | ||
| Evidence for horizontal gene transfer in Escherichia coli speciation | Q33290386 | ||
| Escherichia coli mutator genes | Q33539352 | ||
| Chromosomal regions specific to pathogenic isolates of Escherichia coli have a phylogenetically clustered distribution. | Q33725483 | ||
| Evidence for the adaptive evolution of mutation rates | Q33967135 | ||
| Characterization of broadly pleiotropic phenotypes caused by an hfq insertion mutation in Escherichia coli K-12. | Q34327163 | ||
| Spectra of spontaneous mutations in Escherichia coli strains defective in mismatch correction: the nature of in vivo DNA replication errors. | Q34343418 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
| Recombinational basis of serovar diversity in Salmonella enterica | Q35122179 | ||
| Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs | Q35163740 | ||
| Proliferation of mutators in A cell population | Q35618973 | ||
| Structures of and allelic diversity and relationships among the major outer membrane protein (ompA) genes of the four chlamydial species | Q35966460 | ||
| Recombination in Escherichia coli and the definition of biological species | Q36166012 | ||
| Escherichia coli mutator mutants deficient in methylation-instructed DNA mismatch correction | Q36357026 | ||
| Identification and characterization of the mutL and mutS gene products of Salmonella typhimurium LT2. | Q36423731 | ||
| Barriers to recombination between closely related bacteria: MutS and RecBCD inhibit recombination between Salmonella typhimurium and Salmonella typhi. | Q36574936 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Evidence for inclusion of regions of nonhomology in heteroduplex products of bacteriophage lambda recombination | Q37577591 | ||
| Phylogenetic distribution of branched RNA-linked multicopy single-stranded DNA among natural isolates of Escherichia coli | Q37608280 | ||
| The frequency of mutators in populations of Escherichia coli | Q38304923 | ||
| MUST, a computer package of Management Utilities for Sequences and Trees | Q38567793 | ||
| Chi and the RecBC D enzyme of Escherichia coli | Q40614043 | ||
| Mismatch recognition in chromosomal interactions and speciation | Q40843091 | ||
| Genetic barriers among bacteria. | Q41120565 | ||
| Spontaneous mutators in bacteria: insights into pathways of mutagenesis and repair | Q46617407 | ||
| High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
| Clonal divergence in Escherichia coli as a result of recombination, not mutation | Q48077857 | ||
| Horizontal gene transfer of the Escherichia coli pap and prs pili operons as a mechanism for the development of tissue-specific adhesive properties | Q48164165 | ||
| Detection of mutator subpopulations in Salmonella typhimurium LT2 by reversion of his alleles | Q50130080 | ||
| Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species. | Q50144938 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| Incidence of mutator strains in Escherichia coli and coliforms in nature. | Q54538245 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| Recombination and clonality in natural populations of Escherichia coli. | Q54572405 | ||
| Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli | Q56944671 | ||
| Localized sex in bacteria | Q59062612 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 711-721 | |
| P577 | publication date | 2000-11-01 | |
| P1433 | published in | Cell | Q655814 |
| P1476 | title | Evolutionary implications of the frequent horizontal transfer of mismatch repair genes | |
| P478 | volume | 103 |
| Q30884662 | 2-aminopurine allows interspecies recombination by a reversible inactivation of the Escherichia coli mismatch repair system |
| Q35729697 | A Genetic Incompatibility Accelerates Adaptation in Yeast |
| Q33576726 | A MATE-family efflux pump rescues the Escherichia coli 8-oxoguanine-repair-deficient mutator phenotype and protects against H(2)O(2) killing |
| Q37630251 | A Mobile Element in mutS Drives Hypermutation in a Marine Vibrio |
| Q33284831 | A non-sense mutation in the putative anti-mutator gene ada/alkA of Mycobacterium tuberculosis and M. bovis isolates suggests convergent evolution |
| Q38718356 | A null model for microbial diversification. |
| Q33996324 | Amplification of mutator cells in a population as a result of horizontal transfer |
| Q58192777 | An Efficient Algorithm for the Detection and Classification of Horizontal Gene Transfer Events and Identification of Mosaic Genes |
| Q34396299 | Analysis of a comprehensive dataset of diversity generating retroelements generated by the program DiGReF. |
| Q33410818 | Are protein domains modules of lateral genetic transfer? |
| Q53939141 | Bacterial multicellularity as a possible source of antibiotic resistance. |
| Q90129566 | Baker's Yeast Clinical Isolates Provide a Model for How Pathogenic Yeasts Adapt to Stress |
| Q24633740 | Biased distribution of DNA uptake sequences towards genome maintenance genes |
| Q60921634 | Biological consequences for bacteria of homologous recombination |
| Q24805023 | Bootstrap, Bayesian probability and maximum likelihood mapping: exploring new tools for comparative genome analyses |
| Q42944112 | Ciliates rapidly enhance the frequency of conjugation between Escherichia coli strains through bacterial accumulation in vesicles |
| Q51931024 | Codon usage and selection on proteins. |
| Q42286301 | Coevolution with phages does not influence the evolution of bacterial mutation rates in soil |
| Q34722064 | Coevolution with viruses drives the evolution of bacterial mutation rates. |
| Q21092503 | Comparative and evolutionary analysis of the bacterial homologous recombination systems |
| Q34671940 | Comparative genomics of Wolbachia and the bacterial species concept |
| Q35071154 | Complex minisatellite rearrangements generated in the total or partial absence of Rad27/hFEN1 activity occur in a single generation and are Rad51 and Rad52 dependent. |
| Q46323402 | Constraint and Contingency Pervade the Emergence of Novel Phenotypes in Complex Metabolic Systems |
| Q41255353 | Contribution of increased mutagenesis to the evolution of pollutants-degrading indigenous bacteria |
| Q30596244 | Correlation between the genomic o454-nlpD region polymorphisms, virulence gene equipment and phylogenetic group of extraintestinal Escherichia coli (ExPEC) enables pathotyping irrespective of host, disease and source of isolation |
| Q26825267 | Culture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transition |
| Q41440067 | DNA Repair Is Associated with Information Content in Bacteria, Archaea, and DNA Viruses. |
| Q37292860 | Dealing with incongruence in phylogenomic analyses |
| Q33490644 | Deciphering Evolutionary Mechanisms Between Mutualistic and Pathogenic Symbioses |
| Q54509542 | Decreasing the effects of horizontal gene transfer on bacterial phylogeny: the Escherichia coli case study. |
| Q34420747 | Detection of lateral gene transfer among microbial genomes. |
| Q50108488 | Detection of recombination among Salmonella enterica strains using the incongruence length difference test |
| Q35806050 | Development of a stress-induced mutagenesis module for autonomous adaptive evolution of Escherichia coli to improve its stress tolerance |
| Q36178618 | Diversify or die: generation of diversity in response to stress. |
| Q38202864 | Ecological and temporal constraints in the evolution of bacterial genomes. |
| Q38396383 | Ecologically driven competence for exogenous DNA uptake in yeast |
| Q51778469 | Engineering stress tolerance of Escherichia coli by stress-induced mutagenesis (SIM)-based adaptive evolution. |
| Q33901410 | Evolution in an oncogenic bacterial species with extreme genome plasticity: Helicobacter pylori East Asian genomes |
| Q28238561 | Evolution of mutation rates in bacteria |
| Q24642537 | Evolution of mutation rates: phylogenomic analysis of the photolyase/cryptochrome family |
| Q34131691 | Evolutionary dynamics of complete Campylobacter pan-genomes and the bacterial species concept |
| Q34297067 | Evolving responsively: adaptive mutation |
| Q26865383 | Experimental evolution and the dynamics of genomic mutation rate modifiers |
| Q33700686 | Frail hypotheses in evolutionary biology |
| Q40929065 | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
| Q33997106 | Functions of the mismatch repair gene mutS from Acinetobacter sp. strain ADP1. |
| Q77486982 | Gene patents: are they socially acceptable monopolies, essential for drug discovery? -- reply |
| Q28651650 | Genome dynamics during experimental evolution |
| Q64229648 | Genomic Characteristics of Tokyo 01 Implying Horizontal Gene Transfer Among Phylogenetically Dispersed Filamentous Gliding Bacteria |
| Q39600720 | Genomic repeats, genome plasticity and the dynamics of Mycoplasma evolution |
| Q41469199 | Genomic variability among enteric pathogens: the case of the mutS-rpoS intergenic region |
| Q35046890 | HIV mutagenesis and the evolution of antiretroviral drug resistance |
| Q39694657 | High frequency of mutator strains among human uropathogenic Escherichia coli isolates. |
| Q34617567 | Horizontal acquisition of divergent chromosomal DNA in bacteria: effects of mutator phenotypes |
| Q52604616 | Horizontal gene transfer of Chlamydia: Novel insights from tree reconciliation. |
| Q33303661 | Horizontal gene transfer regulation in bacteria as a "spandrel" of DNA repair mechanisms |
| Q35069306 | How big is the iceberg of which organellar genes in nuclear genomes are but the tip? |
| Q51821002 | Hyper-recombination, diversity, and antibiotic resistance in pneumococcus. |
| Q40731504 | Impact of mutS inactivation on foreign DNA acquisition by natural transformation in Pseudomonas stutzeri |
| Q37745973 | Impact of recombination on bacterial evolution |
| Q57802932 | Incompatibilities in Mismatch Repair Genes Contribute to a Wide Range of Mutation Rates in Human Isolates of Baker's Yeast |
| Q33345237 | Incompatibilities involving yeast mismatch repair genes: a role for genetic modifiers and implications for disease penetrance and variation in genomic mutation rates |
| Q24807229 | Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori |
| Q34889744 | Interactions in the microbiome: communities of organisms and communities of genes |
| Q33543179 | Interplay between pleiotropy and secondary selection determines rise and fall of mutators in stress response |
| Q34420742 | Lateral and oblique gene transfer |
| Q37827559 | Lateral genetic transfer and the construction of genetic exchange communities |
| Q37538149 | Lateral genetic transfer: open issues |
| Q33633619 | Lateral transfer of genes and gene fragments in prokaryotes |
| Q34790534 | Limited boundaries for extensive horizontal gene transfer among Salmonella pathogens |
| Q37136141 | Mechanisms of ectopic gene conversion |
| Q36343551 | Meningococcal genome dynamics. |
| Q34091835 | Microbial communities evolve faster in extreme environments |
| Q48244295 | Mismatch Repair Incompatibilities in Diverse Yeast Populations |
| Q48248666 | Molecular analysis of mutS expression and mutation in natural isolates of pathogenic Escherichia coli |
| Q36150392 | Molecular applications for identifying microbial pathogens in the post-9/11 era. |
| Q42112596 | Molecular evolution perspectives on intraspecific lateral DNA transfer of topoisomerase and gyrase loci in Streptococcus pneumoniae, with implications for fluoroquinolone resistance development and spread |
| Q33381851 | Multiple genome alignment for identifying the core structure among moderately related microbial genomes |
| Q46777863 | Mutability in Pseudomonas viridiflava as a programmed balance between antibiotic resistance and pathogenicity. |
| Q35869358 | Mutation as a stress response and the regulation of evolvability |
| Q91902524 | Mutation bias and GC content shape antimutator invasions |
| Q80114206 | Mutation rate and genome reduction in endosymbiotic and free-living bacteria |
| Q28710085 | Mutation rate dynamics in a bacterial population reflect tension between adaptation and genetic load |
| Q36048384 | Mutations in the DNA mismatch repair proteins MutS and MutL of oxazolidinone-resistant or -susceptible Enterococcus faecium |
| Q46274173 | Mutator genomes decay, despite sustained fitness gains, in a long-term experiment with bacteria |
| Q37678002 | Mutators and hypermutability in bacteria: the Escherichia coli paradigm |
| Q41671780 | Natural mismatch repair mutations mediate phenotypic diversity and drug resistance in Cryptococcus deuterogattii |
| Q34480201 | Negative epistasis between natural variants of the Saccharomyces cerevisiae MLH1 and PMS1 genes results in a defect in mismatch repair |
| Q57071583 | New Biological Insights Into How Deforestation in Amazonia Affects Soil Microbial Communities Using Metagenomics and Metagenome-Assembled Genomes |
| Q34998550 | Normal mutation rate variants arise in a Mutator (Mut S) Escherichia coli population. |
| Q21090212 | Organised genome dynamics in the Escherichia coli species results in highly diverse adaptive paths |
| Q39600777 | Over-representation of repeats in stress response genes: a strategy to increase versatility under stressful conditions? |
| Q36139867 | Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis |
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| Q36933187 | Phage-associated mutator phenotype in group A streptococcus |
| Q39606842 | Polymorphic mutation frequencies of clinical and environmental Stenotrophomonas maltophilia populations. |
| Q37521859 | Population structure of the Bacillus cereus group as determined by sequence analysis of six housekeeping genes and the plcR Gene |
| Q51624923 | Problems in monitoring horizontal gene transfer in field trials of transgenic plants. |
| Q33952890 | Recombination and mutation during long-term gastric colonization by Helicobacter pylori: estimates of clock rates, recombination size, and minimal age. |
| Q46838890 | Reductive genome evolution at both ends of the bacterial population size spectrum. |
| Q33953638 | SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification |
| Q33780703 | Selection-driven transcriptome polymorphism in Escherichia coli/Shigella species |
| Q28768050 | Sex and virulence in Escherichia coli: an evolutionary perspective |
| Q39983675 | Similar compositional biases are caused by very different mutational effects. |
| Q42932042 | Single-nucleotide polymorphism phylotyping of Escherichia coli |
| Q42067390 | Single-nucleotide polymorphisms of the Trypanosoma cruzi MSH2 gene support the existence of three phylogenetic lineages presenting differences in mismatch-repair efficiency |
| Q33909592 | Small variable segments constitute a major type of diversity of bacterial genomes at the species level |
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