| Q47172267 | "Evolution of a dominant natural isolate of Escherichia coli in the human gut over a year suggests a neutral evolution with reduced effective population size". |
| Q34528722 | A Comprehensive, CRISPR-based Functional Analysis of Essential Genes in Bacteria |
| Q41658937 | A Model for Designing Adaptive Laboratory Evolution Experiments |
| Q34791987 | A case of adaptation through a mutation in a tandem duplication during experimental evolution in Escherichia coli |
| Q33595748 | A passive mutualistic interaction promotes the evolution of spatial structure within microbial populations |
| Q36810635 | A population-based experimental model for protein evolution: effects of mutation rate and selection stringency on evolutionary outcomes. |
| Q35261713 | A recurrent regulatory change underlying altered expression and Wnt response of the stickleback armor plates gene EDA. |
| Q51826213 | A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social trait. |
| Q57213572 | A simple genetic basis of adaptation to a novel thermal environment results in complex metabolic rewiring in Drosophila |
| Q57793787 | ALEdb 1.0: a database of mutations from adaptive laboratory evolution experimentation |
| Q41970825 | Accelerated gene evolution through replication-transcription conflicts |
| Q42371063 | Accumulation of Deleterious Mutations During Bacterial Range Expansions |
| Q45063009 | Acid Evolution of Escherichia coli K-12 Eliminates Amino Acid Decarboxylases and Reregulates Catabolism. |
| Q37263496 | Adaptation of Enterococcus faecalis to daptomycin reveals an ordered progression to resistance |
| Q37685579 | Adaptation of Escherichia coli to Long-Term Serial Passage in Complex Medium: Evidence of Parallel Evolution |
| Q35175854 | Adaptation of a cyanobacterium to a biochemically rich environment in experimental evolution as an initial step toward a chloroplast-like state |
| Q36596823 | Adaptation to Parasites and Costs of Parasite Resistance in Mutator and Nonmutator Bacteria |
| Q90296006 | Adaptation, chance, and history in experimental evolution reversals to unicellularity |
| Q33659055 | Adaptive Laboratory Evolution of Antibiotic Resistance Using Different Selection Regimes Lead to Similar Phenotypes and Genotypes |
| Q46093243 | Adaptive Mutations in RNA Polymerase and the Transcriptional Terminator Rho Have Similar Effects on Escherichia coli Gene Expression. |
| Q38118393 | Adaptive laboratory evolution -- principles and applications for biotechnology |
| Q64106194 | Adaptive laboratory evolution of a genome-reduced Escherichia coli |
| Q88182869 | Altered access to beneficial mutations slows adaptation and biases fixed mutations in diploids |
| Q38201031 | Analyzing the genomic variation of microbial cell factories in the era of "New Biotechnology". |
| Q37421974 | Ancestral population reconstitution from isofemale lines as a tool for experimental evolution |
| Q89874524 | Ancient balancing selection on heterocyst function in a cosmopolitan cyanobacterium |
| Q34280527 | Ancient homology underlies adaptive mimetic diversity across butterflies |
| Q89637612 | Antagonistic pleiotropy conceals molecular adaptations in changing environments |
| Q51544118 | Antibiotic resistance and stress in the light of Fisher's model. |
| Q52577417 | Assessing the benefits of horizontal gene transfer by laboratory evolution and genome sequencing. |
| Q30558527 | Bacteriophage vB_EcoM_FV3: a new member of "rV5-like viruses". |
| Q64112083 | Bayesian Detection of Convergent Rate Changes of Conserved Noncoding Elements on Phylogenetic Trees |
| Q50926101 | Biosensor-driven adaptive laboratory evolution of l-valine production in Corynebacterium glutamicum. |
| Q86832377 | Bypass of genetic constraints during mutator evolution to antibiotic resistance |
| Q28082810 | Can the experimental evolution programme help us elucidate the genetic basis of adaptation in nature? |
| Q26767415 | Cancer Evolution and the Limits of Predictability in Precision Cancer Medicine |
| Q28727500 | Cancer in light of experimental evolution |
| Q64064301 | Capacity for survival in global warming: Adaptation of mesophiles to the temperature upper limit |
| Q51122897 | Chaos and unpredictability in evolution. |
| Q36596557 | Characterization of acetic acid-detoxifying Escherichia coli evolved under phosphate starvation conditions |
| Q33887661 | Characterizing the molecular basis of attenuation of Marek's disease virus via in vitro serial passage identifies de novo mutations in the helicase-primase subunit gene UL5 and other candidates associated with reduced virulence. |
| Q54251489 | Clonal interference can cause wavelet-like oscillations of multilocus linkage disequilibrium. |
| Q37272922 | Comparative analyses identify the contributions of exotic donors to disease resistance in a barley experimental population. |
| Q44030517 | Comparative genomics and transcriptomics analysis of experimentally evolved Escherichia coli MC1000 in complex environments |
| Q41857177 | Comparative genomics provides insight into maize adaptation in temperate regions. |
| Q38178893 | Constraint-based models predict metabolic and associated cellular functions. |
| Q42204146 | Contribution of silent mutations to thermal adaptation of RNA bacteriophage Qβ |
| Q39357322 | Convergence in organ size but not energy metabolism enzyme activities among wild Lake Whitefish (Coregonus clupeaformis) species pairs |
| Q28551346 | Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level |
| Q28296812 | Convergent evolution of hyperswarming leads to impaired biofilm formation in pathogenic bacteria |
| Q35549129 | Convergent evolution of the genomes of marine mammals |
| Q47397497 | Convergent selection pressures drive the evolution of rhodopsin kinetics at high altitudes via nonparallel mechanisms. |
| Q28082095 | Costs of antibiotic resistance - separating trait effects and selective effects |
| Q34992854 | Detecting rare structural variation in evolving microbial populations from new sequence junctions using breseq |
| Q57814102 | Determinants of selection in yeast evolved by genome shuffling |
| Q98895036 | Developing rapid growing Bacillus subtilis for improved biochemical and recombinant protein production |
| Q41507951 | Development of a Comprehensive Genotype-to-Fitness Map of Adaptation-Driving Mutations in Yeast |
| Q34082927 | Different tradeoffs result from alternate genetic adaptations to a common environment |
| Q90042482 | Diffusion-driven enhancement of the antibiotic resistance selection window |
| Q51300318 | Diverse phenotypic and genetic responses to short-term selection in evolving Escherichia coli populations. |
| Q60947411 | Does the Genomic Landscape of Species Divergence in Beans Coerce Parallel Signatures of Adaptation and Domestication? |
| Q38403177 | Dynamics and genetic diversification of Escherichia coli during experimental adaptation to an anaerobic environment |
| Q36574555 | Dynamics of Dark-Fly Genome Under Environmental Selections |
| Q30679608 | Ecological genomics of local adaptation |
| Q60503746 | Effective models and the search for quantitative principles in microbial evolution |
| Q26783005 | Elucidating the molecular architecture of adaptation via evolve and resequence experiments |
| Q38218962 | Empirical fitness landscapes and the predictability of evolution |
| Q34313206 | Engineering ecosystems and synthetic ecologies |
| Q51463292 | Epistasis and allele specificity in the emergence of a stable polymorphism in Escherichia coli. |
| Q39162611 | Epistasis and the Evolution of Antimicrobial Resistance |
| Q54304014 | Epistatic interactions determine the mutational pathways and coexistence of lineages in clonal Escherichia coli populations. |
| Q92215133 | Escherichia coli adaptation and response to exposure to heavy atmospheric pollution |
| Q54204592 | Escherichia coli as a host for metabolic engineering. |
| Q90064873 | Estimating the predictability of cancer evolution |
| Q46723730 | Evolution Is an Experiment: Assessing Parallelism in Crop Domestication and Experimental Evolution: (Nei Lecture, SMBE 2014, Puerto Rico). |
| Q46241227 | Evolution as an ecosystem process: insights from genomics. |
| Q41839414 | Evolution by flight and fight: diverse mechanisms of adaptation by actively motile microbes |
| Q28550649 | Evolution of E. coli on [U-13C]Glucose Reveals a Negligible Isotopic Influence on Metabolism and Physiology |
| Q34596522 | Evolution of Escherichia coli rifampicin resistance in an antibiotic-free environment during thermal stress |
| Q34201864 | Evolution of Escherichia coli to 42 °C and subsequent genetic engineering reveals adaptive mechanisms and novel mutations |
| Q39322429 | Evolution of bacterial virulence |
| Q36293883 | Evolution of protein-protein interaction networks in yeast. |
| Q40502218 | Evolutionary Genomics. |
| Q28710050 | Evolutionary biology for the 21st century |
| Q48183271 | Evolutionary convergence in experimental Pseudomonas populations |
| Q61811295 | Evolutionary dynamics of bacteria in the gut microbiome within and across hosts |
| Q89703616 | Evolutionary genomics can improve prediction of species' responses to climate change |
| Q51461404 | Evolutionary history and genetic parallelism affect correlated responses to evolution. |
| Q92153252 | Experimental Challenges for Reduced Genomes: The Cell Model Escherichia coli |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
| Q38683209 | Experimental evolution and the dynamics of adaptation and genome evolution in microbial populations |
| Q52340379 | Experimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate. |
| Q99551370 | Experimental evolution reveals nitrate tolerance mechanisms in Desulfovibrio vulgaris |
| Q36895756 | Experimental interrogation of the path dependence and stochasticity of protein evolution using phage-assisted continuous evolution |
| Q38109292 | Exploring the costs of horizontal gene transfer. |
| Q35780684 | Extent of QTL Reuse During Repeated Phenotypic Divergence of Sympatric Threespine Stickleback |
| Q46126018 | Fast growth phenotype of E. coli K-12 from adaptive laboratory evolution does not require intracellular flux rewiring |
| Q34497933 | Fine-tuning citrate synthase flux potentiates and refines metabolic innovation in the Lenski evolution experiment. |
| Q36410897 | First-Step Mutations during Adaptation Restore the Expression of Hundreds of Genes |
| Q28607448 | Fitness Trade-Offs Determine the Role of the Molecular Chaperonin GroEL in Buffering Mutations |
| Q34302180 | Fitness landscape transformation through a single amino acid change in the rho terminator |
| Q26830798 | From systems to structure: bridging networks and mechanism |
| Q36586464 | Functional evolution of an anthocyanin pathway enzyme during a flower color transition |
| Q35544402 | Gene acquisition convergence between entomopoxviruses and baculoviruses |
| Q54202540 | Genetic Adaptation to Growth Under Laboratory Conditions in Escherichia coli and Salmonella enterica. |
| Q64243934 | Genetic redundancy fuels polygenic adaptation in Drosophila |
| Q28651650 | Genome dynamics during experimental evolution |
| Q47567388 | Genome-Wide Analysis of Starvation-Selected Drosophila melanogaster-A Genetic Model of Obesity |
| Q31037384 | Genome-environment association study suggests local adaptation to climate at the regional scale in Fagus sylvatica. |
| Q42738785 | Genome-wide analysis captures the determinants of the antibiotic cross-resistance interaction network. |
| Q34680352 | Genome-wide analysis of long-term evolutionary domestication in Drosophila melanogaster |
| Q90049157 | Genome-wide analysis reveals molecular convergence underlying domestication in 7 bird and mammals |
| Q36219845 | Genome-wide mapping of mutations at single-nucleotide resolution for protein, metabolic and genome engineering. |
| Q104581398 | Genomic Convergence in the Adaptation to Extreme Environments |
| Q90289542 | Genomic Insights into the Adaptive Convergent Evolution |
| Q31150861 | Genomic Trajectories to Desiccation Resistance: Convergence and Divergence Among Replicate Selected Drosophila Lines |
| Q41944661 | Genomic basis of evolutionary change: evolving immunity |
| Q64267970 | Genomic correlates of extraintestinal infection are linked with changes in cell morphology in Campylobacter jejuni |
| Q28082330 | Genomic investigations of evolutionary dynamics and epistasis in microbial evolution experiments |
| Q49679448 | Genomics of Adaptation Depends on the Rate of Environmental Change in Experimental Yeast Populations. |
| Q33590796 | Genomics of Parallel Experimental Evolution in Drosophila |
| Q33836661 | Genomics of rapid adaptation to antibiotics: convergent evolution and scalable sequence amplification |
| Q45003436 | Genotype-by-environment interactions due to antibiotic resistance and adaptation in Escherichia coli |
| Q36860964 | Global Rebalancing of Cellular Resources by Pleiotropic Point Mutations Illustrates a Multi-scale Mechanism of Adaptive Evolution |
| Q42518786 | Global relationships in fluctuation and response in adaptive evolution |
| Q36084626 | Growth phase-specific evolutionary benefits of natural transformation in Acinetobacter baylyi |
| Q100737041 | Heat-responsive and time-resolved transcriptome and metabolome analyses of Escherichia coli uncover thermo-tolerant mechanisms |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q36160359 | High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations. |
| Q102379151 | High-throughput laboratory evolution reveals evolutionary constraints in Escherichia coli |
| Q50080966 | Highly Expressed Genes Are Preferentially Co-Opted for C4 Photosynthesis |
| Q43163360 | History, chance and selection during phenotypic and genomic experimental evolution: replaying the tape of life at different levels |
| Q41292956 | Hitchhiking and epistasis give rise to cohort dynamics in adapting populations |
| Q58782393 | Hotspot mutations and ColE1 plasmids contribute to the fitness of Salmonella Heidelberg in poultry litter |
| Q60938695 | How adaptive evolution reshapes metabolism to improve fitness: recent advances and future outlook |
| Q34571328 | How and why cells grow as rods |
| Q26853716 | How does adaptation sweep through the genome? Insights from long-term selection experiments |
| Q88011723 | How to Build a Bacterial Cell: MreB as the Foreman of E. coli Construction |
| Q92283288 | IAMBEE: a web-service for the identification of adaptive pathways from parallel evolved clonal populations |
| Q90164326 | Identification of Loci Associated with Enhanced Virulence in Spodoptera litura Nucleopolyhedrovirus Isolates Using Deep Sequencing |
| Q58697126 | Identifying Drivers of Parallel Evolution: A Regression Model Approach |
| Q30872404 | Identifying structural variation in haploid microbial genomes from short-read resequencing data using breseq |
| Q38902848 | Implications of evolutionary engineering for growth and recombinant protein production in methanol-based growth media in the yeast Pichia pastoris. |
| Q57165484 | Increased biofilm formation due to high-temperature adaptation in marine Roseobacter |
| Q51002018 | Initial Molecular-Level Response to Artificial Selection for Increased Aerobic Metabolism Occurs Primarily through Changes in Gene Expression. |
| Q46753712 | Interactions between genotype and environment drive the metabolic phenotype within Escherichia coli isolates |
| Q58609065 | Isolation of A Novel Phage Representing A New Phage Lineage and Characterization of Its Endolysin |
| Q45345601 | Key Metabolites and Mechanistic Changes for Salt Tolerance in an Experimentally Evolved Sulfate-Reducing Bacterium, Desulfovibrio vulgaris. |
| Q33560343 | Laboratory selection quickly erases historical differentiation |
| Q36153069 | Local adaptation (mostly) remains local: reassessing environmental associations of climate-related candidate SNPs in Arabidopsis halleri. |
| Q43231261 | Long-term diversity and genome adaptation of Acinetobacter baylyi in a minimal-medium chemostat |
| Q40567914 | Love the one you're with: replicate viral adaptations converge on the same phenotypic change |
| Q35105723 | Mapping the fitness landscape of gene expression uncovers the cause of antagonism and sign epistasis between adaptive mutations. |
| Q92141659 | Microbial Experimental Evolution - a proving ground for evolutionary theory and a tool for discovery |
| Q34091835 | Microbial communities evolve faster in extreme environments |
| Q38055376 | Microbial evolution in vivo and in silico: methods and applications. |
| Q39169158 | Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity |
| Q38759067 | Microdiversity shapes the traits, niche space, and biogeography of microbial taxa. |
| Q33730850 | Millstone: software for multiplex microbial genome analysis and engineering |
| Q33590430 | Modeling Tumor Clonal Evolution for Drug Combinations Design |
| Q64232908 | Modular epistasis and the compensatory evolution of gene deletion mutants |
| Q93011563 | Modulation of Quorum Sensing as an Adaptation to Nodule Cell Infection during Experimental Evolution of Legume Symbionts |
| Q111629301 | Molecular bases for parallel evolution of translucent bracts in an alpine “glasshouse” plant Rheum alexandrae (Polygonaceae) |
| Q30882294 | Molecular proxies for climate maladaptation in a long-lived tree (Pinus pinaster Aiton, Pinaceae). |
| Q30000694 | Multi-locus analysis of genomic time series data from experimental evolution |
| Q35863603 | Multifactorial Competition and Resistance in a Two-Species Bacterial System |
| Q43245159 | Multiple Resistance at No Cost: Rifampicin and Streptomycin a Dangerous Liaison in the Spread of Antibiotic Resistance. |
| Q35210627 | Multiple phenotypic changes associated with large-scale horizontal gene transfer |
| Q36014236 | Mutation-Driven Divergence and Convergence Indicate Adaptive Evolution of the Intracellular Human-Restricted Pathogen, Bartonella bacilliformis |
| Q47613442 | Mutation-Driven Parallel Evolution during Viral Adaptation |
| Q53158429 | Mutational signatures indicative of environmental stress in bacteria. |
| Q34550797 | Mutational spectrum drives the rise of mutator bacteria |
| Q34679960 | Mutations in global regulators lead to metabolic selection during adaptation to complex environments |
| Q36676963 | Natural genome diversity of AI-2 quorum sensing in Escherichia coli: conserved signal production but labile signal reception |
| Q31039375 | Network-Based Analysis of eQTL Data to Prioritize Driver Mutations |
| 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 |
| Q58794260 | Non-cyp51A Azole-Resistant Aspergillus fumigatus Isolates with Mutation in HMG-CoA Reductase |
| Q54242442 | Parallel Evolution of High-Level Aminoglycoside Resistance in Escherichia coli Under Low and High Mutation Supply Rates. |
| Q36129774 | Parallel Mutations Result in a Wide Range of Cooperation and Community Consequences in a Two-Species Bacterial Consortium |
| Q28595783 | Parallel and Divergent Evolutionary Solutions for the Optimization of an Engineered Central Metabolism in Methylobacterium extorquens AM1 |
| Q33645881 | Parallel developmental genetic features underlie stickleback gill raker evolution |
| Q57135429 | Parallel genetic adaptation across environments differing in mode of growth or resource availability |
| Q36198245 | Parallel genetic changes and nonparallel gene-environment interactions characterize the evolution of drug resistance in yeast |
| Q90595302 | Parallel genomic architecture underlies repeated sexual signal divergence in Hawaiian Laupala crickets |
| Q55078002 | Parallels between experimental and natural evolution of legume symbionts. |
| Q28608029 | Past climate change on Sky Islands drives novelty in a core developmental gene network and its phenotype |
| Q92568694 | Patterns and Mechanisms of Diminishing Returns from Beneficial Mutations |
| Q46797589 | Patterns of variation during adaptation in functionally linked loci |
| Q34358875 | Pervasive genetic hitchhiking and clonal interference in forty evolving yeast populations |
| Q64251970 | Phage Reduce Stability for Regaining Infectivity during Antagonistic Coevolution with Host Bacterium |
| Q40898690 | Phenotypic and genotypic convergences are influenced by historical contingency and environment in yeast |
| Q35762881 | Phenotypic convergence in bacterial adaptive evolution to ethanol stress |
| Q98225901 | Phenotypic responses to temperature in the ciliate Tetrahymena thermophila |
| Q54226446 | Population size changes and selection drive patterns of parallel evolution in a host-virus system. |
| Q38798070 | Predictability and parallelism of multi-trait adaptation |
| Q33680845 | Predictable phenotypic, but not karyotypic, evolution of populations with contrasting initial history |
| Q54295384 | Predicting evolution. |
| Q60916118 | Predicting mutational routes to new adaptive phenotypes |
| Q51249955 | Predicting the basis of convergent evolution. |
| Q34596567 | Predicting the evolution of antibiotic resistance |
| Q42630520 | Prediction of Cross-resistance and Collateral Sensitivity by Gene Expression profiles and Genomic Mutations |
| Q34454311 | Prediction of antibiotic resistance by gene expression profiles. |
| Q35079781 | Properties of selected mutations and genotypic landscapes under Fisher's geometric model. |
| Q58599703 | Proteome evolution under non-substitutable resource limitation |
| Q47898799 | Quantifying Selection with Pool-Seq Time Series Data |
| Q30373007 | RNA chaperones buffer deleterious mutations in E. coli. |
| Q39436445 | ROS mediated selection for increased NADPH availability in Escherichia coli |
| Q101216896 | Rampant loss of social traits during domestication of a Bacillus subtilis natural isolate |
| Q42227289 | Rapid Genetic Adaptation during the First Four Months of Survival under Resource Exhaustion |
| Q39587390 | Rapid divergence and convergence of life-history in experimentally evolved Drosophila melanogaster |
| Q100465126 | Rapid evolution destabilizes species interactions in a fluctuating environment |
| Q59336057 | Recombination-independent rapid convergent evolution of the gastric pathogen Helicobacter pylori |
| Q47142889 | Refactoring the Genetic Code for Increased Evolvability |
| Q26774050 | Replaying the tape of life in the twenty-first century |
| Q34504896 | Replaying the tape of life: quantification of the predictability of evolution |
| Q37545723 | Revealing the genetic basis of natural bacterial phenotypic divergence. |
| Q92982207 | Scalable, Continuous Evolution of Genes at Mutation Rates above Genomic Error Thresholds |
| Q36269559 | Seeking Goldilocks During Evolution of Drug Resistance |
| Q28602407 | Selection on different genes with equivalent functions: the convergence story told by Hox genes along the evolution of aquatic mammalian lineages |
| Q89637630 | Sex alters molecular evolution in diploid experimental populations of S. cerevisiae |
| Q34154596 | Short-term differential adaptation to anaerobic stress via genomic mutations by Escherichia coli strains K-12 and B lacking alcohol dehydrogenase |
| Q44208060 | Sign epistasis limits evolutionary trade-offs at the confluence of single- and multi-carbon metabolism in Methylobacterium extorquens AM1. |
| Q52897789 | Signatures of local adaptation in lowland and highland teosintes from whole-genome sequencing of pooled samples. |
| Q36504175 | Small changes in enzyme function can lead to surprisingly large fitness effects during adaptive evolution of antibiotic resistance |
| Q37695988 | Specificity of genome evolution in experimental populations of Escherichia coli evolved at different temperatures |
| Q39137548 | Standing genetic variation drives repeatable experimental evolution in outcrossing populations of Saccharomyces cerevisiae |
| Q52605047 | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry. |
| Q38156504 | Strategies for the multiplex mapping of genes to traits |
| Q41023000 | Stress-response balance drives the evolution of a network module and its host genome |
| Q37184562 | Structural systems biology evaluation of metabolic thermotolerance in Escherichia coli |
| Q35907808 | Synonymous and nonsynonymous distances help untangle convergent evolution and recombination |
| Q99731167 | Synthetic reconstruction of extreme high hydrostatic pressure resistance in Escherichia coli |
| Q35692242 | Tandem Duplications and the Limits of Natural Selection in Drosophila yakuba and Drosophila simulans |
| Q34535938 | Tempo and mode of genome evolution in a 50,000-generation experiment |
| Q52609532 | The Antarctic sea ice alga Chlamydomonas sp. ICE-L provides insights into adaptive patterns of chloroplast evolution. |
| Q90729739 | The Genomic Basis for Short-Term Evolution of Environmental Adaptation in Maize |
| Q36009835 | The Genomic Basis of Evolutionary Innovation in Pseudomonas aeruginosa. |
| Q36291382 | The Genomic Impacts of Drift and Selection for Hybrid Performance in Maize |
| Q51531906 | The Loci of repeated evolution: a catalog of genetic hotspots of phenotypic variation. |
| Q35675296 | The Molecular and Genetic Basis of Repeatable Coevolution between Escherichia coli and Bacteriophage T3 in a Laboratory Microcosm |
| Q41773166 | The Rho Termination Factor of Clostridium botulinum Contains a Prion-Like Domain with a Highly Amyloidogenic Core. |
| Q38689208 | The Utility of Fisher's Geometric Model in Evolutionary Genetics |
| Q38630215 | The adaptive landscape of wildtype and glycosylation-deficient populations of the industrial yeast Pichia pastoris. |
| Q39450951 | The competition between simple and complex evolutionary trajectories in asexual populations. |
| Q34277589 | The conserved nhaAR operon is drastically divergent between B2 and non-B2 Escherichia coli and is involved in extra-intestinal virulence |
| Q34342693 | The convergent evolution of blue iris pigmentation in primates took distinct molecular paths. |
| Q34893085 | The cost of antibiotic resistance depends on evolutionary history in Escherichia coli. |
| Q30235995 | The coupon collector urn model with unequal probabilities in ecology and evolution |
| Q38399916 | The dynamics of diverse segmental amplifications in populations of Saccharomyces cerevisiae adapting to strong selection |
| Q39030319 | The effect of selection environment on the probability of parallel evolution. |
| Q92544990 | The emergence of adaptive laboratory evolution as an efficient tool for biological discovery and industrial biotechnology |
| Q35544067 | The enduring utility of continuous culturing in experimental evolution |
| Q35579831 | The evolutionarily stable distribution of fitness effects |
| Q53734019 | The fitness costs and benefits of antibiotic resistance in drug-free microenvironments encountered in the human body. |
| Q38150710 | The genetic causes of convergent evolution |
| Q53743078 | The genomic basis of adaptation to the fitness cost of rifampicin resistance in Pseudomonas aeruginosa. |
| Q35231934 | The genomic landscape of compensatory evolution |
| Q88785739 | The genomic landscape of evolutionary convergence in mammals, birds and reptiles |
| Q55510467 | The genomics of adaptation. |
| Q94599629 | The hidden chemolithoautotrophic metabolism of Geobacter sulfurreducens uncovered by adaptation to formate |
| Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
| Q36245287 | The multiplicity of divergence mechanisms in a single evolving population |
| Q35761704 | The phenotypic signature of adaptation to thermal stress in Escherichia coli |
| Q98623946 | The population genetics of pathogenic Escherichia coli |
| Q37671984 | The power to detect quantitative trait loci using resequenced, experimentally evolved populations of diploid, sexual organisms |
| Q37612743 | The predictability of molecular evolution during functional innovation. |
| Q53107952 | The probability of genetic parallelism and convergence in natural populations. |
| Q38726566 | The role of recombination in evolutionary adaptation of Escherichia coli to a novel nutrient |
| Q26864257 | The spectrum of adaptive mutations in experimental evolution |
| Q53007409 | The topology of evolutionary novelty and innovation in macroevolution. |
| Q28652451 | Thermal and solvent stress cross-tolerance conferred to Corynebacterium glutamicum by adaptive laboratory evolution |
| Q46138830 | Thermosensitivity of growth is determined by chaperone-mediated proteome reallocation |
| Q46298824 | Thinking big: the tunability of bacterial cell size |
| Q57825311 | To mutate or not to mutate: Genetic and epigenetic heterogeneity contribute to bacterial adaptation (comment on DOI 10.1002/bies.201400153) |
| Q35050923 | Too much of a good thing: the unique and repeated paths toward copper adaptation |
| Q42272002 | Tracking recent adaptive evolution in microbial species using TimeZone |
| Q48378861 | Transcription termination factor Rho and microbial phenotypic heterogeneity. |
| Q42321297 | Transcriptome-Level Signatures in Gene Expression and Gene Expression Variability during Bacterial Adaptive Evolution |
| Q34082875 | Transient Darwinian selection in Salmonella enterica serovar Paratyphi A during 450 years of global spread of enteric fever |
| Q35787623 | Unique evolutionary trajectories in repeated adaptation to hydrogen sulphide-toxic habitats of a neotropical fish (Poecilia mexicana). |
| Q34747829 | Use of adaptive laboratory evolution to discover key mutations enabling rapid growth of Escherichia coli K-12 MG1655 on glucose minimal medium |
| Q47165136 | Using long-term experimental evolution to uncover the patterns and determinants of molecular evolution of an Escherichia coli natural isolate in the streptomycin-treated mouse gut. |
| Q40446556 | What drives parallel evolution?: How population size and mutational variation contribute to repeated evolution. |
| Q89346241 | What genomic data can reveal about eco-evolutionary dynamics |
| Q44740449 | What paths do advantageous alleles take during short-term evolutionary change? |
| Q36575453 | Whole Genome Shotgun Sequencing Shows Selection on Leptospira Regulatory Proteins During in vitro Culture Attenuation |
| Q34387997 | Whole genome, whole population sequencing reveals that loss of signaling networks is the major adaptive strategy in a constant environment |
| Q34288700 | Widespread signals of convergent adaptation to high altitude in Asia and america |
| Q54332246 | [Genetic adaptation of bacteria]. |