| scholarly article | Q13442814 |
| P50 | author | Richard Lenski | Q713637 |
| Timothy F. Cooper | Q123559146 | ||
| P2093 | author name string | Dominique Schneider | |
| Duy M Dinh | |||
| Aisha I Khan | |||
| P2860 | cites work | The biochemical architecture of an ancient adaptive landscape | Q34461523 |
| Tests of parallel molecular evolution in a long-term experiment with Escherichia coli | Q34694847 | ||
| Epistasis correlates to genomic complexity | Q35080659 | ||
| Evidence for multiple adaptive peaks from populations of bacteria evolving in a structured habitat | Q35760235 | ||
| The dynamics of adaptation on correlated fitness landscapes | Q37399576 | ||
| Epistasis and the adaptability of an RNA virus | Q41907301 | ||
| Interactions between stressful environment and gene deletions alleviate the expected average loss of fitness in yeast. | Q42065537 | ||
| Epistatic buffering of fitness loss in yeast double deletion strains | Q42613014 | ||
| Exploring the effect of sex on empirical fitness landscapes | Q46501857 | ||
| The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
| LONG-TERM EXPERIMENTAL EVOLUTION IN ESCHERICHIA COLI. III. VARIATION AMONG REPLICATE POPULATIONS IN CORRELATED RESPONSES TO NOVEL ENVIRONMENTS. | Q54617461 | ||
| THE EVOLUTION OF POSTZYGOTIC ISOLATION: ACCUMULATING DOBZHANSKY-MULLER INCOMPATIBILITIES | Q56227508 | ||
| Sex and deleterious mutation | Q59036312 | ||
| Evolution of mutational robustness in an RNA virus | Q21563619 | ||
| Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations | Q22066139 | ||
| Historical contingency and the evolution of a key innovation in an experimental population of Escherichia coli | Q22066316 | ||
| Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 | ||
| Sex increases the efficacy of natural selection in experimental yeast populations | Q22122472 | ||
| Mutational robustness can facilitate adaptation | Q24624037 | ||
| Second-order selection for evolvability in a large Escherichia coli population | Q24635911 | ||
| Long-term experimental evolution in Escherichia coli. XI. Rejection of non-transitive interactions as cause of declining rate of adaptation | Q24794572 | ||
| Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations | Q28245607 | ||
| Selection for robustness in mutagenized RNA viruses | Q28469235 | ||
| Darwinian evolution can follow only very few mutational paths to fitter proteins | Q29616042 | ||
| The properties of adaptive walks in evolving populations of fungus | Q30947119 | ||
| Understanding the evolutionary fate of finite populations: the dynamics of mutational effects | Q33281050 | ||
| Fitness epistasis and constraints on adaptation in a human immunodeficiency virus type 1 protein region | Q33853183 | ||
| Evolvability of an RNA virus is determined by its mutational neighbourhood | Q33914492 | ||
| The population genetics of ecological specialization in evolving Escherichia coli populations | Q33922714 | ||
| Parallel changes in gene expression after 20,000 generations of evolution in Escherichiacoli | Q34171913 | ||
| Perspective: Sign epistasis and genetic constraint on evolutionary trajectories | Q34437784 | ||
| Test of synergistic interactions among deleterious mutations in bacteria | Q34448329 | ||
| P433 | issue | 6034 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | beneficial mutation | Q111187232 |
| P1104 | number of pages | 4 | |
| P304 | page(s) | 1193-1196 | |
| P577 | publication date | 2011-06-01 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Negative epistasis between beneficial mutations in an evolving bacterial population | |
| P478 | volume | 332 |
| Q41658937 | A Model for Designing Adaptive Laboratory Evolution Experiments |
| Q36182021 | A Mutational Hotspot and Strong Selection Contribute to the Order of Mutations Selected for during Escherichia coli Adaptation to the Gut |
| Q42551296 | A comprehensive biophysical description of pairwise epistasis throughout an entire protein domain |
| Q58827491 | A meta-analysis of the effects of plant traits and geographical scale on the magnitude of adaptive differentiation as measured by the difference between QST and FST |
| Q43110160 | A model of substitution trajectories in sequence space and long-term protein evolution. |
| Q51826213 | A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social trait. |
| Q35764270 | A tortoise-hare pattern seen in adapting structured and unstructured populations suggests a rugged fitness landscape in bacteria |
| Q37175865 | Adaptation in protein fitness landscapes is facilitated by indirect paths |
| Q37263496 | Adaptation of Enterococcus faecalis to daptomycin reveals an ordered progression to resistance |
| Q54253302 | Adaptation of Escherichia coli to glucose promotes evolvability in lactose. |
| Q35175854 | Adaptation of a cyanobacterium to a biochemically rich environment in experimental evolution as an initial step toward a chloroplast-like state |
| Q28647522 | Adaptation, Clonal Interference, and Frequency-Dependent Interactions in a Long-Term Evolution Experiment with Escherichia coli |
| Q34130237 | Adaptive evolution of the lactose utilization network in experimentally evolved populations of Escherichia coli. |
| Q34312048 | Adaptive evolution: evaluating empirical support for theoretical predictions |
| Q30419009 | Adaptive walks on the fitness landscape of music |
| Q59831979 | Adaptively evolved yeast mutants on galactose show trade-offs in carbon utilization on glucose |
| Q47587442 | Additive Phenotypes Underlie Epistasis of Fitness Effects |
| Q52758683 | Additive genetic architecture underlying a rapidly evolving sexual signaling phenotype in the Hawaiian cricket genus Laupala. |
| Q36306331 | An in vivo system for directed experimental evolution of rabbit haemorrhagic disease virus |
| Q48133871 | Analysis of bacterial genomes from an evolution experiment with horizontal gene transfer shows that recombination can sometimes overwhelm selection |
| Q28534615 | Bacterial adaptation through loss of function |
| Q38103942 | Bacterial genome evolution within a clonal population: from in vitro investigations to in vivo observations |
| Q37173084 | Benefit of transferred mutations is better predicted by the fitness of recipients than by their ecological or genetic relatedness |
| Q38254752 | Beyond genome sequencing: lineage tracking with barcodes to study the dynamics of evolution, infection, and cancer. |
| Q34443462 | Biased estimates of diminishing-returns epistasis? Empirical evidence revisited |
| Q35204371 | Biophysical fitness landscapes for transcription factor binding sites |
| Q90350496 | CRISPR/Cas9 recombineering-mediated deep mutational scanning of essential genes in Escherichia coli |
| Q34594904 | Can you sequence ecology? Metagenomics of adaptive diversification |
| Q28727500 | Cancer in light of experimental evolution |
| Q36485051 | Chromosomal duplication is a transient evolutionary solution to stress. |
| Q30300777 | Coevolution with bacteriophages drives genome-wide host evolution and constrains the acquisition of abiotic-beneficial mutations. |
| Q34497324 | Coevolutionary Landscape Inference and the Context-Dependence of Mutations in Beta-Lactamase TEM-1. |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q27938036 | Concerted evolution of life stage performances signals recent selection on yeast nitrogen use. |
| Q42906922 | Conservative sex and the benefits of transformation in Streptococcus pneumoniae |
| Q28647800 | Contingency and entrenchment in protein evolution under purifying selection |
| Q42204146 | Contribution of silent mutations to thermal adaptation of RNA bacteriophage Qβ |
| Q33608467 | Core Genes Evolve Rapidly in the Long-term Evolution Experiment with Escherichia coli |
| Q29011147 | Deleterious Passengers in Adapting Populations |
| Q29002206 | Detecting High-Order Epistasis in Nonlinear Genotype-Phenotype Maps |
| Q64929525 | Detecting adaptive convergent amino acid evolution. |
| Q42633184 | Detecting epistasis from an ensemble of adapting populations. |
| Q34992854 | Detecting rare structural variation in evolving microbial populations from new sequence junctions using breseq |
| Q34264500 | Differential epigenetic compatibility of qnr antibiotic resistance determinants with the chromosome of Escherichia coli. |
| Q36279809 | Differential paralog divergence modulates genome evolution across yeast species. |
| Q27683542 | Diminishing returns and tradeoffs constrain the laboratory optimization of an enzyme |
| Q53717083 | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus. |
| Q54219938 | Diminishing-returns epistasis decreases adaptability along an evolutionary trajectory. |
| Q28584571 | Disentangling genetic and epigenetic determinants of ultrafast adaptation |
| Q51300318 | Diverse phenotypic and genetic responses to short-term selection in evolving Escherichia coli populations. |
| Q90212325 | Diversification and Evolution of Vancomycin-Resistant Enterococcus faecium during Intestinal Domination |
| Q27693280 | Does your gene need a background check? How genetic background impacts the analysis of mutations, genes, and evolution |
| Q38187602 | Dynamics and constraints of enzyme evolution |
| Q47877246 | Effects of Beneficial Mutations in pykF Gene Vary over Time and across Replicate Populations in a Long-Term Experiment with Bacteria. |
| Q26783005 | Elucidating the molecular architecture of adaptation via evolve and resequence experiments |
| Q89723844 | Emerging Frontiers in the Study of Molecular Evolution |
| Q38218962 | Empirical fitness landscapes and the predictability of evolution |
| Q34313206 | Engineering ecosystems and synthetic ecologies |
| Q37412772 | Environment determines epistatic patterns for a ssDNA virus |
| Q55436455 | Environmental change exposes beneficial epistatic interactions in a catalytic RNA. |
| Q50716194 | Epistasis and maternal effects in experimental adaptation to chronic nutritional stress in Drosophila. |
| Q39162611 | Epistasis and the Evolution of Antimicrobial Resistance |
| Q40725548 | Epistasis and the Structure of Fitness Landscapes: Are Experimental Fitness Landscapes Compatible with Fisher's Geometric Model? |
| Q28653314 | Epistasis can accelerate adaptive diversification in haploid asexual populations |
| Q51332673 | Epistasis from functional dependence of fitness on underlying traits. |
| Q53156835 | Epistatic interactions between ancestral genotype and beneficial mutations shape evolvability in Pseudomonas aeruginosa. |
| Q54304014 | Epistatic interactions determine the mutational pathways and coexistence of lineages in clonal Escherichia coli populations. |
| Q33583647 | Epistatically interacting substitutions are enriched during adaptive protein evolution |
| Q34332944 | Evolution in response to climate change: in pursuit of the missing evidence |
| Q90743445 | Evolution in the light of fitness landscape theory |
| Q34596522 | Evolution of Escherichia coli rifampicin resistance in an antibiotic-free environment during thermal stress |
| Q42369791 | Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome |
| Q43101601 | Evolution of clonal populations approaching a fitness peak. |
| Q41227508 | Evolution of organismal stoichiometry in a long-term experiment with Escherichia coli |
| Q39675173 | Evolution of sex: Using experimental genomics to select among competing theories |
| Q92879130 | Evolutionary Dynamics in the RNA Bacteriophage Qβ Depends on the Pattern of Change in Selective Pressures |
| Q34005257 | Evolutionary accessibility of mutational pathways |
| Q36242283 | Evolutionary adaptation after crippling cell polarization follows reproducible trajectories |
| Q89545822 | Evolutionary constraints in fitness landscapes |
| Q51461404 | Evolutionary history and genetic parallelism affect correlated responses to evolution. |
| Q41132191 | Evolutionary implications of Liebig's law of the minimum: Selection under low concentrations of two nonsubstitutable nutrients |
| Q37983903 | Evolutionary insight from whole-genome sequencing of experimentally evolved microbes. |
| Q83227516 | Evolutionary pathways to antibiotic resistance are dependent upon environmental structure and bacterial lifestyle |
| Q35867457 | Evolvability of an Optimal Recombination Rate |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
| Q34289524 | Experimental evolution |
| Q38683209 | Experimental evolution and the dynamics of adaptation and genome evolution in microbial populations |
| Q28661568 | Experimental evolution of an alternating uni- and multicellular life cycle in Chlamydomonas reinhardtii. |
| Q34362047 | Experiments on the role of deleterious mutations as stepping stones in adaptive evolution |
| Q42695844 | Exploiting ecology in drug pulse sequences in favour of population reduction |
| Q38414823 | Fighting microbial drug resistance: a primer on the role of evolutionary biology in public health |
| Q36410897 | First-Step Mutations during Adaptation Restore the Expression of Hundreds of Genes |
| Q51313054 | Fisher's geometric model predicts the effects of random mutations when tested in the wild. |
| Q33575800 | Fisher's geometrical model emerges as a property of complex integrated phenotypic networks |
| Q41849560 | Fitness conferred by replaced amino acids declines with time |
| Q64101025 | Fluctuating environments select for short-term phenotypic variation leading to long-term exploration |
| Q58703918 | From Local Adaptation to Speciation: Specialization and Reinforcement |
| Q36586464 | Functional evolution of an anthocyanin pathway enzyme during a flower color transition |
| Q35004076 | Generation and study of the strains of streptomycetes - heterologous hosts for production of moenomycin |
| Q43184230 | Genetic background affects epistatic interactions between two beneficial mutations |
| Q38639465 | Genetic variation in adaptability and pleiotropy in budding yeast |
| Q28651650 | Genome dynamics during experimental evolution |
| Q21560957 | Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment |
| Q22122302 | Genome-scale engineering for systems and synthetic biology |
| Q28082330 | Genomic investigations of evolutionary dynamics and epistasis in microbial evolution experiments |
| Q34708295 | Genotype to phenotype mapping and the fitness landscape of the E. coli lac promoter |
| Q34489656 | Hidden epistastic interactions can favour the evolution of sex and recombination |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q36372082 | High-order epistasis shapes evolutionary trajectories |
| Q41292956 | Hitchhiking and epistasis give rise to cohort dynamics in adapting populations |
| Q35943086 | Horizontal DNA Transfer Mechanisms of Bacteria as Weapons of Intragenomic Conflict. |
| Q37184676 | How Good Are Statistical Models at Approximating Complex Fitness Landscapes? |
| Q48142732 | How Many Biochemistries Are Available To Build a Cell? |
| Q92283288 | IAMBEE: a web-service for the identification of adaptive pathways from parallel evolved clonal populations |
| Q36368892 | Identification of the potentiating mutations and synergistic epistasis that enabled the evolution of inter-species cooperation |
| Q99207734 | Idiosyncratic epistasis creates universals in mutational effects and evolutionary trajectories |
| Q30380900 | In vitro selection of miltefosine resistance in promastigotes of Leishmania donovani from Nepal: genomic and metabolomic characterization. |
| Q92471939 | Increasing growth rate slows adaptation when genotypes compete for diffusing resources |
| Q33730568 | Inferring fitness landscapes by regression produces biased estimates of epistasis. |
| Q47102776 | Inferring genetic interactions from comparative fitness data. |
| Q52591835 | Innovation in an E. coli evolution experiment is contingent on maintaining adaptive potential until competition subsides. |
| Q30560970 | Interaction-based feature selection and classification for high-dimensional biological data |
| Q35616623 | Investigating the Role of Gene-Gene Interactions in TB Susceptibility |
| Q45345601 | Key Metabolites and Mechanistic Changes for Salt Tolerance in an Experimentally Evolved Sulfate-Reducing Bacterium, Desulfovibrio vulgaris. |
| Q51438302 | Less is more: selective advantages can explain the prevalent loss of biosynthetic genes in bacteria. |
| Q43231261 | Long-term diversity and genome adaptation of Acinetobacter baylyi in a minimal-medium chemostat |
| Q45261637 | Long-term dynamics of adaptation in asexual populations |
| Q40567914 | Love the one you're with: replicate viral adaptations converge on the same phenotypic change |
| Q37311367 | Low selection pressure aids the evolution of cooperative ribozyme mutations in cells |
| Q34241242 | Many pathways in laboratory evolution can lead to improved enzymes: how to escape from local minima. |
| Q35105723 | Mapping the fitness landscape of gene expression uncovers the cause of antagonism and sign epistasis between adaptive mutations. |
| Q35764471 | Measuring ruggedness in fitness landscapes. |
| Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
| Q34405876 | Metabolic erosion primarily through mutation accumulation, and not tradeoffs, drives limited evolution of substrate specificity in Escherichia coli |
| Q36330218 | Metabolic specialization and the assembly of microbial communities |
| Q39169158 | Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity |
| Q42771933 | Microbiology. Antibiotic resistance, not shaken or stirred |
| Q59789922 | Modeling genome-wide enzyme evolution predicts strong epistasis underlying catalytic turnover rates |
| Q64232908 | Modular epistasis and the compensatory evolution of gene deletion mutants |
| Q58709856 | Modulation of ACD6 dependent hyperimmunity by natural alleles of an Arabidopsis thaliana NLR resistance gene |
| Q28647014 | Molecular Clock of Neutral Mutations in a Fitness-Increasing Evolutionary Process |
| Q40134218 | Multi-hierarchical profiling: an emerging and quantitative approach to characterizing diverse biological networks |
| Q43245159 | Multiple Resistance at No Cost: Rifampicin and Streptomycin a Dangerous Liaison in the Spread of Antibiotic Resistance. |
| Q57118367 | Multiplexed deactivated CRISPR-Cas9 gene expression perturbations deter bacterial adaptation by inducing negative epistasis |
| Q35583838 | Multiplexed tracking of combinatorial genomic mutations in engineered cell populations |
| Q34679960 | Mutations in global regulators lead to metabolic selection during adaptation to complex environments |
| Q31039375 | Network-Based Analysis of eQTL Data to Prioritize Driver Mutations |
| Q37997288 | New insights into bacterial adaptation through in vivo and in silico experimental evolution |
| Q92216184 | Noise-precision tradeoff in predicting combinations of mutations and drugs |
| Q37493368 | On the (un)predictability of a large intragenic fitness landscape |
| Q46337805 | On the challenge of exploring the evolutionary trajectory from phosphotriesterase to arylesterase using computer simulations |
| Q41987306 | Optimizing complex phenotypes through model-guided multiplex genome engineering |
| Q28595783 | Parallel and Divergent Evolutionary Solutions for the Optimization of an Engineered Central Metabolism in Methylobacterium extorquens AM1 |
| Q45994253 | Parallel emergence of negative epistasis across experimental lineages. |
| Q92568694 | Patterns and Mechanisms of Diminishing Returns from Beneficial Mutations |
| Q41864870 | Patterns of Epistasis between beneficial mutations in an antibiotic resistance gene |
| Q50914574 | Phase transition in random adaptive walks on correlated fitness landscapes. |
| Q51367880 | Plasticity and epistasis strongly affect bacterial fitness after losing multiple metabolic genes. |
| Q38966881 | Potential for adaptation overrides cost of resistance. |
| Q58760610 | Power law fitness landscapes and their ability to predict fitness |
| Q35079781 | Properties of selected mutations and genotypic landscapes under Fisher's geometric model. |
| Q92601578 | Pseudomonas aeruginosa Interstrain Dynamics and Selection of Hyperbiofilm Mutants during a Chronic Infection |
| Q55208702 | Quantifying natural seasonal variation in mutation parameters with mutation accumulation lines. |
| Q41911214 | Rates of fitness decline and rebound suggest pervasive epistasis |
| Q38254854 | Recent advances in the evolutionary engineering of industrial biocatalysts |
| Q90244482 | Recent insights into the genotype-phenotype relationship from massively parallel genetic assays |
| Q28540044 | Recombination accelerates adaptation on a large-scale empirical fitness landscape in HIV-1 |
| Q41592999 | Recovery of phenotypes obtained by adaptive evolution through inverse metabolic engineering |
| Q46298833 | Recurrent Reverse Evolution Maintains Polymorphism after Strong Bottlenecks in Commensal Gut Bacteria. |
| Q41987123 | Regulatory revolution: evolving the "anti-LacI" repressor |
| Q41905788 | Repeatability of evolution on epistatic landscapes |
| Q28607370 | Reverse evolution leads to genotypic incompatibility despite functional and active site convergence |
| Q41758914 | Rewiring of genetic networks in response to modification of genetic background |
| Q45071448 | Seasonally fluctuating selection can maintain polymorphism at many loci via segregation lift. |
| Q36269559 | Seeking Goldilocks During Evolution of Drug Resistance |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q42324334 | Selection Limits to Adaptive Walks on Correlated Landscapes |
| Q44581995 | Selection biases the prevalence and type of epistasis along adaptive trajectories |
| Q34325560 | Selection-driven gene loss in bacteria |
| Q35761876 | Selective Sweeps and Parallel Pathoadaptation Drive Pseudomonas aeruginosa Evolution in the Cystic Fibrosis Lung |
| Q60960612 | Sex-specific dominance reversal of genetic variation for fitness |
| Q35035921 | Should evolutionary geneticists worry about higher-order epistasis? |
| Q28597478 | Should tissue structure suppress or amplify selection to minimize cancer risk? |
| Q93013409 | Simulations reveal challenges to artificial community selection and possible strategies for success |
| Q36504175 | Small changes in enzyme function can lead to surprisingly large fitness effects during adaptive evolution of antibiotic resistance |
| Q28547894 | Steering Evolution with Sequential Therapy to Prevent the Emergence of Bacterial Antibiotic Resistance |
| Q35748281 | Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution |
| Q92488321 | Stochastic tunneling across fitness valleys can give rise to a logarithmic long-term fitness trajectory |
| Q28551065 | Strong Selection Significantly Increases Epistatic Interactions in the Long-Term Evolution of a Protein |
| Q37346935 | Substrate ambiguous enzymes within the Escherichia coli proteome offer different evolutionary solutions to the same problem |
| Q53247059 | Sustained fitness gains and variability in fitness trajectories in the long-term evolution experiment with Escherichia coli. |
| Q38017457 | Synthetic approaches to understanding biological constraints |
| Q28391909 | Systems biology of cancer: entropy, disorder, and selection-driven evolution to independence, invasion and "swarm intelligence" |
| Q37909892 | Systems-biology approaches for predicting genomic evolution |
| Q34535938 | Tempo and mode of genome evolution in a 50,000-generation experiment |
| Q41846993 | Testing the role of genetic background in parallel evolution using the comparative experimental evolution of antibiotic resistance. |
| Q55002438 | The Influence of Higher-Order Epistasis on Biological Fitness Landscape Topography. |
| Q47136281 | The Nonstationary Dynamics of Fitness Distributions: Asexual Model with Epistasis and Standing Variation |
| Q38689208 | The Utility of Fisher's Geometric Model in Evolutionary Genetics |
| Q28646039 | The Valley-of-Death: reciprocal sign epistasis constrains adaptive trajectories in a constant, nutrient limiting environment |
| Q36490860 | The basis of antagonistic pleiotropy in hfq mutations that have opposite effects on fitness at slow and fast growth rates |
| Q54347187 | The battle of the SNPs. |
| Q26860873 | The causes of epistasis |
| Q58570246 | The causes of evolvability and their evolution |
| Q35172659 | The changing geometry of a fitness landscape along an adaptive walk |
| Q34917226 | The conditional nature of genetic interactions: the consequences of wild-type backgrounds on mutational interactions in a genome-wide modifier screen |
| Q34399491 | The consistency of beneficial fitness effects of mutations across diverse genetic backgrounds |
| Q34893085 | The cost of antibiotic resistance depends on evolutionary history in Escherichia coli. |
| Q42145476 | The dynamics of adapting, unregulated populations and a modified fundamental theorem |
| Q34468851 | The effect of bacterial recombination on adaptation on fitness landscapes with limited peak accessibility |
| Q51137906 | The effect of epistasis on sexually antagonistic genetic variation. |
| Q45120597 | The effects of stabilizing and directional selection on phenotypic and genotypic variation in a population of RNA enzymes |
| Q34671988 | The environment affects epistatic interactions to alter the topology of an empirical fitness landscape |
| Q40519553 | The evolution of antimicrobial peptide resistance in Pseudomonas aeruginosa is shaped by strong epistatic interactions |
| Q35579831 | The evolutionarily stable distribution of fitness effects |
| Q45344370 | The evolutionary epidemiology of multilocus drug resistance |
| Q28706318 | The evolutionary time machine: using dormant propagules to forecast how populations can adapt to changing environments |
| Q28649903 | The functional basis of adaptive evolution in chemostats |
| Q55510467 | The genomics of adaptation. |
| Q41012991 | The impact of high-order epistasis in the within-host fitness of a positive-sense plant RNA virus |
| Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
| Q46185374 | The molecular diversity of adaptive convergence. |
| Q28732355 | The mystery of missing heritability: Genetic interactions create phantom heritability |
| Q35099403 | The origins of specialization: insights from bacteria held 25 years in captivity. |
| Q39024576 | The rule of declining adaptability in microbial evolution experiments. |
| Q26864257 | The spectrum of adaptive mutations in experimental evolution |
| Q40587253 | The strength of genetic interactions scales weakly with mutational effects |
| Q59353073 | The utility of fitness landscapes and big data for predicting evolution |
| Q41463308 | There and back again: consequences of biofilm specialization under selection for dispersal. |
| Q38690951 | Thoughts Toward a Theory of Natural Selection: The Importance of Microbial Experimental Evolution |
| Q27003480 | Towards the identification of the loci of adaptive evolution |
| Q51544809 | Understanding specialism when the Jack of all trades can be the master of all. |
| Q42389367 | Variance in epistasis links gene regulation and evolutionary rate in the yeast genetic interaction network |
| Q37651181 | Variant profiling of evolving prokaryotic populations |
| Q35224374 | Variation in the fitness effects of mutations with population density and size in Escherichia coli |
| Q26830367 | What can we learn from fitness landscapes? |
| Q36351996 | What is adaptation by natural selection? Perspectives of an experimental microbiologist |
| Q28818537 | Widespread Genetic Incompatibilities between First-Step Mutations during Parallel Adaptation of Saccharomyces cerevisiae to a Common Environment |
| Q54332246 | [Genetic adaptation of bacteria]. |
Search more.