| Q35729697 | A Genetic Incompatibility Accelerates Adaptation in Yeast |
| Q37630251 | A Mobile Element in mutS Drives Hypermutation in a Marine Vibrio |
| Q33917768 | A biochemical mechanism for nonrandom mutations and evolution |
| Q93064899 | A proofreading-impaired herpesvirus generates populations with quasispecies-like structure |
| Q36344782 | A single nucleotide change in mutY increases the emergence of antibiotic-resistant Campylobacter jejuni mutants |
| Q51489925 | A trade-off between oxidative stress resistance and DNA repair plays a role in the evolution of elevated mutation rates in bacteria. |
| Q59335721 | Access to high-impact mutations constrains the evolution of antibiotic resistance in soft agar |
| Q51064794 | Active causation and the origin of meaning. |
| Q64933411 | Adaptive dynamics of unstable cancer populations: The canonical equation. |
| Q59757712 | Adaptive mutation in Escherichia coli |
| Q24623723 | Adaptive mutation: implications for evolution |
| Q36369411 | An analogy between the evolution of drug resistance in bacterial communities and malignant tissues |
| Q28393123 | An evolutionary paradigm for carcinogenesis? |
| Q39448750 | An experimental evaluation of drug-induced mutational meltdown as an antiviral treatment strategy |
| Q52007778 | Analysis of convergence of an evolutionary algorithm with self-adaptation using a stochastic Lyapunov function. |
| Q44282478 | Analysis of the Pseudomonas aeruginosa oprD gene from clinical and environmental isolates. |
| Q34047307 | Animal Mitochondrial DNA as We Do Not Know It: mt-Genome Organization and Evolution in Nonbilaterian Lineages. |
| Q41937031 | Antibiotic resistance in Pseudomonas aeruginosa strains with increased mutation frequency due to inactivation of the DNA oxidative repair system. |
| Q36933558 | Association between hypermutator phenotype, clinical variables, mucoid phenotype, and antimicrobial resistance in Pseudomonas aeruginosa |
| Q33992054 | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level. |
| Q33946964 | Bacteria are different: observations, interpretations, speculations, and opinions about the mechanisms of adaptive evolution in prokaryotes |
| Q38103942 | Bacterial genome evolution within a clonal population: from in vitro investigations to in vivo observations |
| Q37794342 | Bacterial hypermutation in cystic fibrosis, not only for antibiotic resistance |
| Q90129566 | Baker's Yeast Clinical Isolates Provide a Model for How Pathogenic Yeasts Adapt to Stress |
| Q34606746 | Beneficial mutations, hitchhiking and the evolution of mutation rates in sexual populations |
| Q28748265 | Biological species is the only possible form of existence for higher organisms: the evolutionary meaning of sexual reproduction |
| Q52245251 | Biomathematics. Merging lines and emerging levels. |
| Q28727500 | Cancer in light of experimental evolution |
| Q33692244 | Chance favors the prepared genome |
| Q28247346 | Chaperonin overexpression promotes genetic variation and enzyme evolution |
| Q39494379 | Chromosomal changes during experimental evolution in laboratory populations of Escherichia coli |
| Q34491552 | Clinical significance of microbial infection and adaptation in cystic fibrosis |
| Q24545892 | Clonal interference and the periodic selection of new beneficial mutations in Escherichia coli |
| Q33943859 | Clusters of mutations from transient hypermutability |
| Q34722064 | Coevolution with viruses drives the evolution of bacterial mutation rates. |
| Q35350270 | Coexistence and within-host evolution of diversified lineages of hypermutable Pseudomonas aeruginosa in long-term cystic fibrosis infections. |
| Q36914997 | Combating bacteria and drug resistance by inhibiting mechanisms of persistence and adaptation. |
| Q35032768 | Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation |
| Q51069725 | Comparative transcriptomes reveal novel evolutionary strategies adopted by Saccharomyces cerevisiae with improved xylose utilization capability. |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q42736352 | Competition between high- and higher-mutating strains of Escherichia coli |
| Q33692357 | Contingency loci, mutator alleles, and their interactions. Synergistic strategies for microbial evolution and adaptation in pathogenesis |
| Q36076137 | Contrasting dynamics of a mutator allele in asexual populations of differing size. |
| Q41255353 | Contribution of increased mutagenesis to the evolution of pollutants-degrading indigenous bacteria |
| Q30869765 | DNA polymerase active site is highly mutable: evolutionary consequences |
| Q37109944 | DNA polymerases in adaptive immunity |
| Q36071909 | DNA replication: one strand may be more equal. |
| 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. |
| Q34725734 | Decay of unused characters by selection and drift |
| Q50130080 | Detection of mutator subpopulations in Salmonella typhimurium LT2 by reversion of his alleles |
| Q42111438 | Developing controllable hypermutable Clostridium cells through manipulating its methyl-directed mismatch repair system |
| Q39683024 | Digital evolution in time-dependent fitness landscapes |
| Q33991388 | Direct selection for mutators in Escherichia coli. |
| Q50056870 | Distribution of mutation frequencies among Salmonella enterica isolates from animal and human sources and genetic characterization of a Salmonella Heidelberg hypermutator |
| Q36178618 | Diversify or die: generation of diversity in response to stress. |
| Q90148668 | Dynamic Emergence of Mismatch Repair Deficiency Facilitates Rapid Evolution of Ceftazidime-Avibactam Resistance in Pseudomonas aeruginosa Acute Infection |
| Q28247846 | Dynamics of cancer progression |
| Q31029779 | Dynamics of mutator and antibiotic-resistant populations in a pharmacokinetic/pharmacodynamic model of Pseudomonas aeruginosa biofilm treatment. |
| Q92650977 | Eco-evolutionary community turnover following environmental change |
| Q39632553 | Efflux-pump-derived multiple drug resistance to ethambutol monotherapy in Mycobacterium tuberculosis and the pharmacokinetics and pharmacodynamics of ethambutol |
| Q92266072 | Elucidating the functional role of Mycobacterium smegmatis recX in stress response |
| Q36643853 | Emergence of DNA polymerase ε antimutators that escape error-induced extinction in yeast |
| Q37100886 | Emergence of species in evolutionary "simulated annealing". |
| Q52881848 | Environmental fluctuations do not select for increased variation or population-based resistance in Escherichia coli. |
| Q35058954 | Environmental regulation of mutation rates at specific sites. |
| Q50123026 | Environmentally constrained mutation and adaptive evolution in Salmonella |
| Q56902070 | Enzymes of evolutionary change |
| Q54517598 | Equilibrium Distribution of Mutators in the Single Fitness Peak Model |
| Q76399123 | Error and repair catastrophes: A two-dimensional phase diagram in the quasispecies model |
| Q34049897 | Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli |
| Q35599902 | Escherichia coli populations in unpredictably fluctuating environments evolve to face novel stresses through enhanced efflux activity |
| Q86095467 | Evaluating evolutionary models of stress-induced mutagenesis in bacteria |
| Q64104894 | Evolthon: A community endeavor to evolve lab evolution |
| Q34082906 | Evolution and adaptation in Pseudomonas aeruginosa biofilms driven by mismatch repair system-deficient mutators. |
| Q42741265 | Evolution of Mutation Rates in Rapidly Adapting Asexual Populations. |
| Q40877493 | Evolution of antibiotic resistance |
| Q28207333 | Evolution of digital organisms at high mutation rates leads to survival of the flattest |
| Q33692297 | Evolution of evolvability. |
| Q34429727 | Evolution of high mutation rates in experimental populations of E. coli |
| Q52568580 | Evolution of high-level resistance during low-level antibiotic exposure. |
| Q36456226 | Evolution of microbial diversity during prolonged starvation |
| Q28238561 | Evolution of mutation rates in bacteria |
| Q24642537 | Evolution of mutation rates: phylogenomic analysis of the photolyase/cryptochrome family |
| Q27312240 | Evolution of mutational robustness in the yeast genome: a link to essential genes and meiotic recombination hotspots |
| Q33762702 | Evolution of the linear chromosomal DNA in Streptomyces: is genomic variability developmentally modulated? |
| Q30243898 | Evolution, genomics and epidemiology of Pseudomonas syringae: Challenges in Bacterial Molecular Plant Pathology. |
| Q33949870 | Evolution-driving genes |
| Q73592523 | Evolution: setting the mutation rate |
| Q34169739 | Evolution: the evolvability enigma |
| Q34094904 | Evolutionary changes in mutation rates and spectra and their influence on the adaptation of pathogens |
| Q33641954 | Evolutionary genetics: The economics of mutation |
| Q79750953 | Evolutionary genetics: sexually selected mutation rates |
| Q50117948 | Evolutionary implications of the frequent horizontal transfer of mismatch repair genes |
| Q35960653 | Evolutionary origins of invasive populations |
| Q59090104 | Evolving evolvability |
| Q33837103 | Evolving mutation rate advances the invasion speed of a sexual species |
| Q46352624 | Excess of non-conservative amino acid changes in marine bacterioplankton lineages with reduced genomes. |
| Q34611032 | Experimental analysis of molecular events during mutational periodic selections in bacterial evolution. |
| Q26865383 | Experimental evolution and the dynamics of genomic mutation rate modifiers |
| Q64124033 | Extensive loss of cell-cycle and DNA repair genes in an ancient lineage of bipolar budding yeasts |
| Q24633927 | Extreme-longevity mutations orchestrate silencing of multiple signaling pathways |
| Q38616021 | Fidelity Variants and RNA Quasispecies. |
| Q38414823 | Fighting microbial drug resistance: a primer on the role of evolutionary biology in public health |
| Q34616140 | Fitness evolution and the rise of mutator alleles in experimental Escherichia coli populations. |
| Q34575830 | Fitness landscapes and evolvability |
| Q41778880 | Fixation probability of rare nonmutator and evolution of mutation rates |
| Q95840911 | Genes and Proteomes Associated With Increased Mutation Frequency and Multidrug Resistance of Naturally Occurring Mismatch Repair-Deficient Salmonella Hypermutators |
| Q41366386 | Genetic adaptation of Pseudomonas aeruginosa to the airways of cystic fibrosis patients is catalyzed by hypermutation |
| Q33963695 | Genetic analysis of Pseudomonas aeruginosa isolates from the sputa of Australian adult cystic fibrosis patients |
| Q33804007 | Genetic instability and darwinian selection in tumours |
| Q56687584 | Genetic instability and darwinian selection in tumours |
| Q40106664 | Genetic recombinational events in prokaryotes and their viruses: insight into the study of evolution and biodiversity |
| Q37376525 | Genome replication engineering assisted continuous evolution (GREACE) to improve microbial tolerance for biofuels production |
| Q34719336 | Genomewide screen for modulators of evolvability under toxic antibiotic exposure. |
| Q64963172 | Genomic clustering of fitness-affecting mutations favors the evolution of chromosomal instability. |
| Q55041884 | Genomic confirmation of nutrient-dependent mutability of mutators in Escherichia coli. |
| Q40423782 | Genomic evolution of bacterial populations under coselection by antibiotics and phage |
| Q33836661 | Genomics of rapid adaptation to antibiotics: convergent evolution and scalable sequence amplification |
| Q52136186 | Hereditary stability and variation in evolution and development. |
| Q54271627 | High Recombinant Frequency in Extraintestinal Pathogenic Escherichia coli Strains. |
| Q39694657 | High frequency of mutator strains among human uropathogenic Escherichia coli isolates. |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q51711564 | High relatedness selects against hypermutability in bacterial metapopulations. |
| Q34617567 | Horizontal acquisition of divergent chromosomal DNA in bacteria: effects of mutator phenotypes |
| Q34220245 | Horizontal gene transfer: a critical view |
| Q34603856 | Hypermutability in carcinogenesis |
| Q44350722 | Hypermutable Staphylococcus aureus strains present at high frequency in subclinical bovine mastitis isolates are associated with the development of antibiotic resistance |
| Q37922538 | Hypermutation and stress adaptation in bacteria |
| Q37598703 | Hypermutation and the preexistence of antibiotic-resistant Pseudomonas aeruginosa mutants: implications for susceptibility testing and treatment of chronic infections |
| Q79162727 | Hypermutation as a Factor Contributing to the Acquisition of Antimicrobial Resistance |
| Q41974061 | Hypermutation is a key factor in development of multiple-antimicrobial resistance in Pseudomonas aeruginosa strains causing chronic lung infections |
| Q89766030 | Hypermutator Pseudomonas aeruginosa exploits multiple genetic pathways to develop multidrug resistance during long-term infections in the airways of cystic fibrosis patients |
| Q40731504 | Impact of mutS inactivation on foreign DNA acquisition by natural transformation in Pseudomonas stutzeri |
| Q38241740 | Implications of new research and technologies for malolactic fermentation in wine. |
| Q58758641 | In search of the Goldilocks zone for hybrid speciation |
| Q35879421 | In vivo-selected mutations in methyl-directed mismatch repair suppress the virulence attenuation of Salmonella dam mutant strains following intraperitoneal, but not oral, infection of naïve mice |
| Q93047512 | Inactivation of a Mismatch-Repair System Diversifies Genotypic Landscape of Escherichia coli During Adaptive Laboratory Evolution |
| Q42560500 | Inactivation of the mismatch repair system in Pseudomonas aeruginosa attenuates virulence but favors persistence of oropharyngeal colonization in cystic fibrosis mice. |
| 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 |
| Q39551661 | Independence of evolutionary and mutational rates after transmission of avian influenza viruses to swine. |
| Q43181792 | Induction and inhibition of ciprofloxacin resistance-conferring mutations in hypermutator bacteria |
| Q42574139 | Inherited and environmentally induced differences in mutation frequencies between wild strains of Sordaria fimicola from "Evolution Canyon". |
| Q24807229 | Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori |
| Q34102811 | Interactions among strategies associated with bacterial infection: pathogenicity, epidemicity, and antibiotic resistance |
| Q42705384 | Intermediate mutation frequencies favor evolution of multidrug resistance in Escherichia coli |
| Q33543179 | Interplay between pleiotropy and secondary selection determines rise and fall of mutators in stress response |
| Q89782907 | Intratumor Heterogeneity and Therapy Resistance: Contributions of Dormancy, Apoptosis Reversal (Anastasis) and Cell Fusion to Disease Recurrence |
| Q41830947 | Kick-starting the ratchet: the fate of mutators in an asexual population |
| Q52682692 | Known mutator alleles do not markedly increase mutation rate in clinical Saccharomyces cerevisiae strains. |
| Q39955018 | Lack of association between hypermutation and antibiotic resistance development in Pseudomonas aeruginosa isolates from intensive care unit patients |
| Q34420742 | Lateral and oblique gene transfer |
| Q28756839 | Lethal mutagenesis of bacteria |
| Q37596302 | Long-term effect of mutagenic DNA repair on accumulation of mutations in Pseudomonas syringae B86-17. |
| Q37052306 | Long-term effects of inducible mutagenic DNA repair on relative fitness and phenotypic diversification in Pseudomonas cichorii 302959. |
| Q90186558 | Low mutational load and high mutation rate variation in gut commensal bacteria |
| Q46324175 | Mechanisms and consequences of diversity-generating immune strategies. |
| Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
| Q34011353 | Mechanisms causing rapid and parallel losses of ribose catabolism in evolving populations of Escherichia coli B. |
| Q33847662 | Mechanisms of stationary phase mutation: a decade of adaptive mutation |
| Q30754550 | Microbial astronauts: assembling microbial communities for advanced life support systems |
| Q34232235 | Microbial domestication signatures of Lactococcus lactis can be reproduced by experimental evolution. |
| Q52262067 | Microbial genetics. The tinkerer's evolving tool-box. |
| Q22122024 | Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation |
| Q55691280 | Mild environmental stress elicits mutations affecting fitness in Chlamydomonas. |
| Q48244295 | Mismatch Repair Incompatibilities in Diverse Yeast Populations |
| Q43212807 | Modelling the evolution of genetic instability during tumour progression |
| Q28647014 | Molecular Clock of Neutral Mutations in a Fitness-Increasing Evolutionary Process |
| Q26823667 | Molecular epidemiology and genomics of group A Streptococcus |
| Q34117477 | Mucoidy, quorum sensing, mismatch repair and antibiotic resistance in Pseudomonas aeruginosa from cystic fibrosis chronic airways infections |
| Q33690962 | Multiple genetic switches spontaneously modulating bacterial mutability |
| Q46296390 | Mutation Rate Evolution in Partially Selfing and Partially Asexual Organisms |
| Q36590556 | Mutation accumulation and fitness in mutator subpopulations of Escherichia coli |
| Q46334331 | Mutation accumulation under UV radiation in Escherichia coli |
| Q35869358 | Mutation as a stress response and the regulation of evolvability |
| Q41703503 | Mutation for survival |
| Q33945503 | Mutation frequencies and antibiotic resistance |
| Q33952076 | Mutation frequency and biological cost of antibiotic resistance in Helicobacter pylori |
| Q36128650 | Mutation hot spots in yeast caused by long-range clustering of homopolymeric sequences |
| Q52010693 | Mutation landscapes. |
| Q36048167 | Mutation rate and evolution of fluoroquinolone resistance in Escherichia coli isolates from patients with urinary tract infections. |
| 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 |
| Q51327741 | Mutation rate evolution in replicator dynamics. |
| Q92752649 | Mutation rate variability as a driving force in adaptive evolution |
| Q36885382 | Mutation rate variation in multicellular eukaryotes: causes and consequences |
| Q36395099 | Mutation, recombination, and incipient speciation of bacteria in the laboratory |
| Q38578737 | Mutation--The Engine of Evolution: Studying Mutation and Its Role in the Evolution of Bacteria |
| Q36014236 | Mutation-Driven Divergence and Convergence Indicate Adaptive Evolution of the Intracellular Human-Restricted Pathogen, Bartonella bacilliformis |
| Q34550797 | Mutational spectrum drives the rise of mutator bacteria |
| Q39646894 | Mutations in polI but not mutSLH destabilize Haemophilus influenzae tetranucleotide repeats |
| Q34502921 | Mutations in putative mutator genes of Mycobacterium tuberculosis strains of the W-Beijing family |
| Q34113782 | Mutator bacteria as a risk factor in treatment of infectious diseases |
| Q52043835 | Mutator dynamics in fluctuating environments. |
| Q37678002 | Mutators and hypermutability in bacteria: the Escherichia coli paradigm |
| Q37247776 | Mutators and sex in bacteria: conflict between adaptive strategies |
| Q40507706 | Mutators in space: the dynamics of high-mutability clones in a two-patch model |
| Q34607018 | Mutators, population size, adaptive landscape and the adaptation of asexual populations of bacteria |
| 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. |
| Q37997288 | New insights into bacterial adaptation through in vivo and in silico experimental evolution |
| Q33194639 | Nitrogen-Regulated Hypermutator Strain of Synechococcus sp. for Use in In Vivo Artificial Evolution |
| Q34232085 | Nonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model. |
| Q46063964 | Nutrient co-limited Trichodesmium as nitrogen source or sink in a future ocean |
| Q53395950 | Nutrient-dependent growth defects and mutability of mutators in Escherichia coli. |
| Q24794536 | Occurrence of leu+ revertants under starvation cultures in Escherichia coli is growth-dependent |
| Q42240703 | Occurrence of weak mutators among avian pathogenic Escherichia coli (APEC) isolates causing salpingitis and peritonitis in broiler breeders |
| Q60939386 | Old Trade, New Tricks: Insights into the Spontaneous Mutation Process from the Partnering of Classical Mutation Accumulation Experiments with High-Throughput Genomic Approaches |
| Q33667067 | Optimization of DNA polymerase mutation rates during bacterial evolution |
| Q54242442 | Parallel Evolution of High-Level Aminoglycoside Resistance in Escherichia coli Under Low and High Mutation Supply Rates. |
| Q34351963 | Parasitic plants have increased rates of molecular evolution across all three genomes |
| Q36139867 | Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis |
| Q56431644 | Phenotypic and Genomic Evolution during a 20,000-Generation Experiment with the Bacterium Escherichia coli |
| Q36367007 | Phenotypic heterogeneity promotes adaptive evolution. |
| Q33307180 | Phenotypic mutation rates and the abundance of abnormal proteins in yeast |
| Q28215261 | Platelet-activating factor receptor and ADAM10 mediate responses to Staphylococcus aureus in epithelial cells |
| Q35121892 | Polarisation of prokaryotic chromosomes |
| Q39005916 | Population Heterogeneity in Mutation Rate Increases the Frequency of Higher-Order Mutants and Reduces Long-Term Mutational Load. |
| Q28256131 | Prokaryotic DNA mismatch repair |
| Q40166144 | Rapid and Consistent Evolution of Colistin Resistance in Extensively Drug-Resistant Pseudomonas aeruginosa during Morbidostat Culture |
| Q51206475 | Rapid evolution as an ecological process. |
| Q39492100 | Rapid evolution of novel traits in microorganisms |
| Q41722793 | Rapid in vivo evolution of a beta-lactamase using phagemids |
| Q37716243 | Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli |
| Q24548000 | Rates of spontaneous mutation |
| Q46838890 | Reductive genome evolution at both ends of the bacterial population size spectrum. |
| Q34617476 | Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. |
| Q34434306 | Regulation of mutY and nature of mutator mutations in Escherichia coli populations under nutrient limitation |
| Q55067610 | Retroviruses, ascorbate, and mutations, in the evolution of Homo sapiens. |
| Q36843864 | Robustness promotes evolvability of thermotolerance in an RNA virus |
| Q42012937 | Role of DNA base excision repair in the mutability and virulence of Streptococcus mutans |
| Q44034811 | Role of a short tandem leucine/arginine repeat in strong mutator phenotype acquisition in a clinical isolate of Salmonella Typhimurium |
| Q33975727 | Role of genomic typing in taxonomy, evolutionary genetics, and microbial epidemiology |
| Q42754912 | Role of mutS and mutL genes in hypermutability and recombination in Staphylococcus aureus |
| Q21144990 | SOS response induces persistence to fluoroquinolones in Escherichia coli |
| Q37197670 | Saccharomyces cerevisiae: a sexy yeast with a prion problem |
| Q45950358 | Second-order cooperation: Cooperative offspring as a living public good arising from second-order selection on non-cooperative individuals. |
| Q34203956 | Second-order selection in bacterial evolution: selection acting on mutation and recombination rates in the course of adaptation |
| Q55003119 | Selection and Neutral Mutations Drive Pervasive Mutability Losses in Long-Lived Anti-HIV B-Cell Lineages. |
| Q38201509 | Selection of antibiotic resistance at very low antibiotic concentrations |
| Q37028295 | Self-structuring in spatial evolutionary ecology |
| Q73423086 | Sequence variation in Helicobacter pylori |
| Q36660289 | Sexual selection and the evolution of evolvability. |
| Q24799773 | Sexual selection, germline mutation rate and sperm competition |
| Q37406333 | Side effects of antibiotics on genetic variability. |
| Q51148036 | Sign of selection on mutation rate modifiers depends on population size. |
| Q33846180 | Significance of multiple mutations in cancer |
| Q36474342 | Spontaneously Arising mutL Mutators in Evolving Escherichia coli Populations Are the Result of Changes in Repeat Length |
| Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
| Q35986593 | Stress responses and genetic variation in bacteria. |
| Q34504117 | Stress-induced evolution and the biosafety of genetically modified microorganisms released into the environment |
| Q51052567 | Stress-induced mutagenesis and complex adaptation. |
| Q36961683 | Stress-induced mutagenesis in bacteria. |
| Q41200966 | Stress-induced mutagenesis: Stress diversity facilitates the persistence of mutator genes |
| Q30327563 | Superbugs: How They Evolve and Minimize the Cost of Resistance. |
| Q37571299 | Supra-operonic clusters of functionally related genes (SOCs) are a source of horizontal gene co-transfers |
| Q51168768 | Temperature effects on life-history trade-offs, germline maintenance and mutation rate under simulated climate warming. |
| Q22122206 | The Beagle in a bottle |
| Q40615967 | The CRISPR case, « ready-made » mutations and Lamarckian evolution of an adaptive immunity system |
| Q29301497 | The Evolution of Mutation Rate in Finite Asexual Populations |
| Q92857979 | The Mutator Phenotype: Adapting Microbial Evolution to Cancer Biology |
| Q47100798 | The Red Queen and King in finite populations |
| Q90038371 | The SNAP hypothesis: Chromosomal rearrangements could emerge from positive Selection during Niche Adaptation |
| Q35077947 | The advantage of arriving first: characteristic times in finite size populations of error-prone replicators |
| Q73373285 | The approach to mutation-selection balance in an infinite asexual population, and the evolution of mutation rates |
| Q38517985 | The balance between mutators and nonmutators in asexual populations |
| Q54222557 | The complexities of viral mutation rates. |
| Q34609052 | The consequences of growth of a mutator strain of Escherichia coli as measured by loss of function among multiple gene targets and loss of fitness |
| Q43560044 | The conserved active site motif A of Escherichia coli DNA polymerase I is highly mutable |
| Q38953067 | The conserved phylogeny of blood microbiome |
| Q55430533 | The cost of replication fidelity in human immunodeficiency virus type 1. |
| Q33692274 | The distribution of rates of spontaneous mutation over viruses, prokaryotes, and eukaryotes |
| Q35115441 | The dynamics of repeated elements: applications to the epidemiology of tuberculosis. |
| Q36004587 | The ecology of the genome - mobile DNA elements and their hosts |
| Q64056369 | The effect of bacterial mutation rate on the evolution of CRISPR-Cas adaptive immunity |
| Q33763823 | The effect of population bottlenecks on mutation rate evolution in asexual populations |
| Q22065663 | The emergence of antibiotic resistance by mutation |
| Q54652456 | The evolution of bacterial mutation rates under simultaneous selection by interspecific and social parasitism. |
| Q34617981 | The evolution of mutator genes in bacterial populations: the roles of environmental change and timing. |
| Q34285727 | The evolution of stress-induced hypermutation in asexual populations |
| Q37152739 | The fixation probability of rare mutators in finite asexual populations. |
| Q38304923 | The frequency of mutators in populations of Escherichia coli |
| Q44935797 | The generation of multiple co-existing mal-regulatory mutations through polygenic evolution in glucose-limited populations of Escherichia coli |
| Q54525605 | The influence of cellular physiology on the initiation of mutational pathways inEscherichia colipopulations |
| Q34611553 | The influence of hitchhiking and deleterious mutation upon asexual mutation rates |
| Q35362334 | The lower bound to the evolution of mutation rates |
| Q28492576 | The mismatch repair system (mutS, mutL and uvrD genes) in Pseudomonas aeruginosa: molecular characterization of naturally occurring mutants |
| Q42758515 | The mutL mutation in Pseudomonas aeruginosa isolates reveals multidrug-resistant traits and possible evolutionary trends |
| Q74481910 | The mutation rate and cancer |
| Q41862731 | The optimal burst of mutation to create a phenotype |
| Q35885995 | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
| Q24619467 | The rate of establishment of complex adaptations |
| Q37323963 | The rich phase structure of a mutator model. |
| Q36098286 | The rise and spread of a new pathogen: seroresistant Moraxella catarrhalis |
| Q41613054 | The role of genomics in studying genetic susceptibility to infectious disease |
| Q35177659 | The role of mutators in the emergence of antibiotic-resistant bacteria |
| Q27011463 | The role of robustness in phenotypic adaptation and innovation |
| Q34330675 | The speed of evolution and maintenance of variation in asexual populations |
| Q37120152 | Thioridazine as Chemotherapy for Mycobacterium avium Complex Diseases |
| Q42248684 | Time-Resolved Tracking of Mutations Reveals Diverse Allele Dynamics during Escherichia coli Antimicrobial Adaptive Evolution to Single Drugs and Drug Pairs. |
| Q50132690 | To be a mutator, or how pathogenic and commensal bacteria can evolve rapidly |
| Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
| Q53428207 | Transient appearance of the mutator phenotype during carcinogenesis as a possible explanation for the lack of mini/microsatellite instability in many late stage tumors. |
| Q34220343 | Transition from positive to neutral in mutation fixation along with continuing rising fitness in thermal adaptive evolution. |
| Q34974987 | Tuberculosis chemotherapy: the influence of bacillary stress and damage response pathways on drug efficacy |
| Q40711295 | Ultra Deep Sequencing of a Baculovirus Population Reveals Widespread Genomic Variations |
| Q60535165 | Urbanization erodes ectomycorrhizal fungal diversity and may cause microbial communities to converge. |
| Q51302402 | Viral mutation rates: modelling the roles of within-host viral dynamics and the trade-off between replication fidelity and speed. |
| Q43514301 | Virus mutators and antimutators: roles in evolution, pathogenesis and emergence |
| Q38665569 | Weak mutators can drive the evolution of fluoroquinolone resistance in Escherichia coli |
| Q28536445 | Whole genome sequencing reveals complex evolution patterns of multidrug-resistant Mycobacterium tuberculosis Beijing strains in patients |
| Q28072013 | Within-host evolution of bacterial pathogens |