| scholarly article | Q13442814 |
| P2093 | author name string | Lin Chao | |
| Edward C Cox | |||
| P433 | issue | 1 | |
| P921 | main subject | Escherichia coli | Q25419 |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 125-134 | |
| P577 | publication date | 1983-01-01 | |
| P1433 | published in | Evolution | Q4038411 |
| P1476 | title | COMPETITION BETWEEN HIGH AND LOW MUTATING STRAINS OF ESCHERICHIA COLI | |
| P478 | volume | 37 |
| 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 |
| Q36662285 | A novel enrichment strategy reveals unprecedented number of novel transcription start sites at single base resolution in a model prokaryote and the gut microbiome |
| Q51489925 | A trade-off between oxidative stress resistance and DNA repair plays a role in the evolution of elevated mutation rates in bacteria. |
| Q59757712 | Adaptive mutation in Escherichia coli |
| Q27024636 | Antimutator variants of DNA polymerases |
| Q90129566 | Baker's Yeast Clinical Isolates Provide a Model for How Pathogenic Yeasts Adapt to Stress |
| Q46348708 | Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair |
| Q24545892 | Clonal interference and the periodic selection of new beneficial mutations in Escherichia coli |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q42736352 | Competition between high- and higher-mutating strains of Escherichia coli |
| Q70409687 | Competition between isogenic mutS and mut+ populations of Escherichia coli K12 in continuously growing cultures |
| Q36878608 | Competitive fitness during feast and famine: how SOS DNA polymerases influence physiology and evolution in Escherichia coli |
| Q36076137 | Contrasting dynamics of a mutator allele in asexual populations of differing size. |
| Q28305177 | DNA replication error-induced extinction of diploid yeast |
| Q37627287 | Darwinism for the Genomic Age: Connecting Mutation to Diversification |
| Q55162233 | Death and population dynamics affect mutation rate estimates and evolvability under stress in bacteria. |
| Q50130080 | Detection of mutator subpopulations in Salmonella typhimurium LT2 by reversion of his alleles |
| Q33991388 | Direct selection for mutators in Escherichia coli. |
| Q52223545 | Directional mutation pressure, mutator mutations, and dynamics of molecular evolution. |
| Q90148668 | Dynamic Emergence of Mismatch Repair Deficiency Facilitates Rapid Evolution of Ceftazidime-Avibactam Resistance in Pseudomonas aeruginosa Acute Infection |
| Q53566921 | Dynamics and Fate of Beneficial Mutations Under Lineage Contamination by Linked Deleterious Mutations. |
| Q35874389 | Dynamics of bacterial insertion sequences: can transposition bursts help the elements persist? |
| Q36643853 | Emergence of DNA polymerase ε antimutators that escape error-induced extinction in yeast |
| Q35058954 | Environmental regulation of mutation rates at specific sites. |
| Q33860371 | Escherichia coli rpoB mutants have increased evolvability in proportion to their fitness defects |
| Q42741265 | Evolution of Mutation Rates in Rapidly Adapting Asexual Populations. |
| Q52568580 | Evolution of high-level resistance during low-level antibiotic exposure. |
| Q73592523 | Evolution: setting the mutation rate |
| Q34094904 | Evolutionary changes in mutation rates and spectra and their influence on the adaptation of pathogens |
| Q28359832 | Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model |
| Q33641954 | Evolutionary genetics: The economics of mutation |
| Q26865383 | Experimental evolution and the dynamics of genomic mutation rate modifiers |
| Q28611338 | Extinction events can accelerate evolution |
| Q54541810 | Fitness effects of fixed beneficial mutations in microbial populations. |
| Q33700686 | Frail hypotheses in evolutionary biology |
| Q58599727 | Gene inversion potentiates bacterial evolvability and virulence |
| Q41620371 | Genetic variability and adaptation to stress. |
| Q37513651 | Genomic changes arising in long-term stab cultures of Escherichia coli |
| Q64963172 | Genomic clustering of fitness-affecting mutations favors the evolution of chromosomal instability. |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q37922538 | Hypermutation and stress adaptation in bacteria |
| Q93047512 | Inactivation of a Mismatch-Repair System Diversifies Genotypic Landscape of Escherichia coli During Adaptive Laboratory Evolution |
| Q57802932 | Incompatibilities in Mismatch Repair Genes Contribute to a Wide Range of Mutation Rates in Human Isolates of Baker's Yeast |
| Q24807229 | Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori |
| Q41888126 | Interrelationship between HIV-1 fitness and mutation rate. |
| Q38165448 | Intra-tumor heterogeneity: lessons from microbial evolution and clinical implications |
| Q52682692 | Known mutator alleles do not markedly increase mutation rate in clinical Saccharomyces cerevisiae strains. |
| Q41848190 | Lethal mutagenesis failure may augment viral adaptation |
| Q37596302 | Long-term effect of mutagenic DNA repair on accumulation of mutations in Pseudomonas syringae B86-17. |
| Q90186558 | Low mutational load and high mutation rate variation in gut commensal bacteria |
| Q34405876 | Metabolic erosion primarily through mutation accumulation, and not tradeoffs, drives limited evolution of substrate specificity in Escherichia coli |
| Q30754550 | Microbial astronauts: assembling microbial communities for advanced life support systems |
| Q58718678 | Minicells as a Damage Disposal Mechanism in Escherichia coli |
| Q48244295 | Mismatch Repair Incompatibilities in Diverse Yeast Populations |
| Q28710085 | Mutation rate dynamics in a bacterial population reflect tension between adaptation and genetic load |
| Q92752649 | Mutation rate variability as a driving force in adaptive evolution |
| Q36395099 | Mutation, recombination, and incipient speciation of bacteria in the laboratory |
| Q31016944 | Mutator dynamics in sexual and asexual experimental populations of yeast |
| Q34055320 | Mutator suppression and escape from replication error-induced extinction in yeast |
| Q37247776 | Mutators and sex in bacteria: conflict between adaptive strategies |
| Q46057951 | Mutators in Escherichia coli |
| Q21145371 | Natural selection fails to optimize mutation rates for long-term adaptation on rugged fitness landscapes |
| Q46527792 | Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations. |
| Q33572538 | Normally lethal amino acid substitutions suppress an ultramutator DNA Polymerase δ variant |
| Q33667067 | Optimization of DNA polymerase mutation rates during bacterial evolution |
| Q37007127 | Polymorphic mutation frequencies in Escherichia coli: emergence of weak mutators in clinical isolates |
| Q39492100 | Rapid evolution of novel traits in microorganisms |
| Q34434306 | Regulation of mutY and nature of mutator mutations in Escherichia coli populations under nutrient limitation |
| Q33975727 | Role of genomic typing in taxonomy, evolutionary genetics, and microbial epidemiology |
| Q37197670 | Saccharomyces cerevisiae: a sexy yeast with a prion problem |
| Q24635911 | Second-order selection for evolvability in a large Escherichia coli population |
| Q34203956 | Second-order selection in bacterial evolution: selection acting on mutation and recombination rates in the course of adaptation |
| Q41568929 | Selection against hypermutability in Escherichia coli during long term evolution |
| Q42022379 | Selection maintains signaling function of a highly diverged intrinsically disordered region |
| Q83227342 | Selection on mutators is not frequency-dependent |
| Q69905919 | Selective advantage of polA1 mutator over polA+ strains of Escherichia coli in a chemostat |
| Q47254650 | Sexual recombination and increased mutation rate expedite evolution of Escherichia coli in varied fitness landscapes |
| Q36474342 | Spontaneously Arising mutL Mutators in Evolving Escherichia coli Populations Are the Result of Changes in Repeat Length |
| Q35986593 | Stress responses and genetic variation in bacteria. |
| Q37571299 | Supra-operonic clusters of functionally related genes (SOCs) are a source of horizontal gene co-transfers |
| Q53786053 | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic. |
| Q38517985 | The balance between mutators and nonmutators in asexual populations |
| Q33763823 | The effect of population bottlenecks on mutation rate evolution in asexual populations |
| Q22065663 | The emergence of antibiotic resistance by mutation |
| Q35544067 | The enduring utility of continuous culturing in experimental evolution |
| Q73933148 | The evolutionary design of error-rates, and the fast fixation enigma |
| Q90084152 | The fitness cost of mismatch repair mutators in Saccharomyces cerevisiae: partitioning the mutational load |
| Q37152739 | The fixation probability of rare mutators in finite asexual populations. |
| Q38304923 | The frequency of mutators in populations of Escherichia coli |
| Q28649903 | The functional basis of adaptive evolution in chemostats |
| Q34611553 | The influence of hitchhiking and deleterious mutation upon asexual mutation rates |
| Q28212788 | The modern molecular clock |
| Q37323963 | The rich phase structure of a mutator model. |
| Q50132690 | To be a mutator, or how pathogenic and commensal bacteria can evolve rapidly |
| Q54487159 | Transposable element IS50 improves growth rate of E. coli cells without transposition |
| Q90399281 | Variability in fitness effects can preclude selection of the fittest |
| Q35616117 | dNTP pool levels modulate mutator phenotypes of error-prone DNA polymerase ε variants |
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