| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Philip Gerrish | Q42842789 |
| P2093 | author name string | Paul D Sniegowski | |
| P2860 | cites work | Molecular Evolution Over the Mutational Landscape | Q22064602 |
| Fitness effects of advantageous mutations in evolving Escherichia coli populations | Q22066182 | ||
| Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria | Q22122042 | ||
| Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 | ||
| Sex releases the speed limit on evolution | Q22122522 | ||
| The evolutionary advantage of recombination | Q24533419 | ||
| Clonal interference and the periodic selection of new beneficial mutations in Escherichia coli | Q24545892 | ||
| Rates of spontaneous mutation | Q24548000 | ||
| Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
| Direct estimate of the mutation rate and the distribution of fitness effects in the yeast Saccharomyces cerevisiae | Q28362113 | ||
| Genome-wide mutational diversity in an evolving population of Escherichia coli | Q28751288 | ||
| Genomewide patterns of substitution in adaptively evolving populations of the RNA bacteriophage MS2 | Q28754815 | ||
| Linkage and the limits to natural selection | Q28769449 | ||
| Experimental evolution and genome sequencing reveal variation in levels of clonal interference in large populations of bacteriophage phiX174. | Q33325656 | ||
| The generation of multiple co-existing mal-regulatory mutations through polygenic evolution in glucose-limited populations of Escherichia coli | Q44935797 | ||
| Comparative genome sequencing of Escherichia coli allows observation of bacterial evolution on a laboratory timescale | Q46069507 | ||
| An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
| The rhythm of microbial adaptation. | Q52054921 | ||
| The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
| Fitness effects of fixed beneficial mutations in microbial populations. | Q54541810 | ||
| Experimental evolution yields hundreds of mutations in a functional viral genome | Q56900292 | ||
| Adaptive mgl-regulatory mutations and genetic diversity evolving in glucose-limited Escherichia coli populations | Q56902325 | ||
| Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
| Frequency of fixation of adaptive mutations is higher in evolving diploid than haploid yeast populations | Q59092867 | ||
| The accumulation of deleterious genes in a population--Muller's Ratchet | Q67444775 | ||
| A simple stochastic gene substitution model | Q71016135 | ||
| The effect of linkage on limits to artificial selection | Q72951099 | ||
| RNA virus evolution via a fitness-space model | Q74568198 | ||
| Selective mechanisms in bacteria | Q76199621 | ||
| Clonal interference is alleviated by high mutation rates in large populations | Q80018606 | ||
| The repertoire and dynamics of evolutionary adaptations to controlled nutrient-limited environments in yeast | Q33392677 | ||
| Avoiding dangerous missense: thermophiles display especially low mutation rates | Q33471395 | ||
| Experiments with the Chemostat on spontaneous mutations of bacteria | Q33711073 | ||
| Periodic selection in Escherichia coli | Q33711273 | ||
| The population genetics of beneficial mutations | Q33856621 | ||
| Modeling and optimization of populations subject to time-dependent mutation | Q33958359 | ||
| The pertinence of the periodic selection phenomenon to prokaryote evolution | Q33989659 | ||
| The speed of evolution and maintenance of variation in asexual populations | Q34330675 | ||
| The solitary wave of asexual evolution | Q34470274 | ||
| Different trajectories of parallel evolution during viral adaptation | Q34504264 | ||
| Evolution of an obligate social cheater to a superior cooperator | Q34528080 | ||
| Spontaneous mutations in diploid Saccharomyces cerevisiae: more beneficial than expected | Q34569445 | ||
| Adaptation in sexuals vs. asexuals: clonal interference and the Fisher-Muller model | Q34589967 | ||
| Experimental analysis of molecular events during mutational periodic selections in bacterial evolution. | Q34611032 | ||
| Profiles of adaptation in two similar viruses | Q34613893 | ||
| Fitness evolution and the rise of mutator alleles in experimental Escherichia coli populations. | Q34616140 | ||
| The speed of adaptation in large asexual populations | Q34645731 | ||
| Adaptive mutations in bacteria: high rate and small effects | Q34661718 | ||
| Complete genetic linkage can subvert natural selection | Q35748721 | ||
| Testing the extreme value domain of attraction for distributions of beneficial fitness effects | Q35945772 | ||
| Clonal interference in large populations | Q36156834 | ||
| Limits to adaptation in asexual populations | Q36201707 | ||
| Genomic evolution during a 10,000-generation experiment with bacteria | Q36451882 | ||
| The distribution of beneficial and fixed mutation fitness effects close to an optimum | Q36724374 | ||
| Beneficial fitness effects are not exponential for two viruses. | Q37009661 | ||
| Clonal interference, multiple mutations and adaptation in large asexual populations | Q37011413 | ||
| Convergent and divergent sequence evolution in the surface envelope glycoprotein of human immunodeficiency virus type 1 within a single infected patient | Q37031589 | ||
| The genetics of adaptation for eight microvirid bacteriophages | Q37353497 | ||
| Punctuated evolution caused by selection of rare beneficial mutations. | Q38563665 | ||
| Diminishing returns of population size in the rate of RNA virus adaptation | Q39590442 | ||
| Periodic selection, infectious gene exchange and the genetic structure of E. coli populations. | Q40329946 | ||
| Clonal interference and the evolution of RNA viruses. | Q40929879 | ||
| The distribution of beneficial mutant effects under strong selection. | Q41081632 | ||
| Molecular characterization of clonal interference during adaptive evolution in asexual populations of Saccharomyces cerevisiae | Q41182739 | ||
| The traveling-wave approach to asexual evolution: Muller's ratchet and speed of adaptation | Q41853709 | ||
| The population genetics of mutations: good, bad and indifferent | Q42778842 | ||
| P433 | issue | 1544 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | beneficial mutation | Q111187232 |
| P304 | page(s) | 1255-1263 | |
| P577 | publication date | 2010-04-01 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | Beneficial mutations and the dynamics of adaptation in asexual populations | |
| P478 | volume | 365 |
| Q51537286 | Accumulation of beneficial mutations in one dimension. |
| Q35091312 | Accurate reconstruction of the temporal order of mutations in neoplastic progression |
| Q41986173 | Adaptation in tunably rugged fitness landscapes: the rough Mount Fuji model |
| Q50532537 | Adaptation of Drosophila melanogaster to increased NaCl concentration due to dominant beneficial mutations. |
| Q33806975 | Adaptation to fluctuating temperatures in an RNA virus is driven by the most stringent selective pressure |
| Q37990734 | Advances and developments in strategies to improve strains of Saccharomyces cerevisiae and processes to obtain the lignocellulosic ethanol--a review. |
| Q99578991 | Application of simultaneous selective pressures slows adaptation |
| Q47106674 | Beneficial mutation-selection dynamics in finite asexual populations: a free boundary approach. |
| Q26767415 | Cancer Evolution and the Limits of Predictability in Precision Cancer Medicine |
| Q47313036 | Cancer Progression Models and Fitness Landscapes: a Many-to-Many Relationship |
| Q28727500 | Cancer in light of experimental evolution |
| Q50134382 | Circuit-Host Coupling Induces Multifaceted Behavioral Modulations of a Gene Switch |
| Q42113492 | Cost of antibiotic resistance and the geometry of adaptation. |
| Q29011147 | Deleterious Passengers in Adapting Populations |
| Q37366710 | Depletion of Key Meiotic Genes and Transcriptome-Wide Abiotic Stress Reprogramming Mark Early Preparatory Events Ahead of Apomeiotic Transition |
| Q28584571 | Disentangling genetic and epigenetic determinants of ultrafast adaptation |
| Q35542057 | Distinguishing driver and passenger mutations in an evolutionary history categorized by interference |
| Q35882382 | Distribution of fixed beneficial mutations and the rate of adaptation in asexual populations |
| Q28654404 | Drake's rule as a consequence of approaching channel capacity |
| Q53566921 | Dynamics and Fate of Beneficial Mutations Under Lineage Contamination by Linked Deleterious Mutations. |
| Q37194798 | Empirical complexities in the genetic foundations of lethal mutagenesis |
| Q40771994 | Epigenetic mutations can both help and hinder adaptive evolution. |
| Q52654022 | Essential is not irreplaceable: fitness dynamics of experimental E. coli RNase P RNA heterologous replacement. |
| Q92367961 | Every which way? On predicting tumor evolution using cancer progression models |
| Q34549616 | Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus. |
| Q37248273 | Evolution of Ecological Diversity in Biofilms of Pseudomonas aeruginosa by Altered Cyclic Diguanylate Signaling |
| Q43101601 | Evolution of clonal populations approaching a fitness peak. |
| Q33743097 | Evolved osmotolerant Escherichia coli mutants frequently exhibit defective N-acetylglucosamine catabolism and point mutations in cell shape-regulating protein MreB. |
| Q26865383 | Experimental evolution and the dynamics of genomic mutation rate modifiers |
| Q26768691 | Experimental evolution in biofilm populations. |
| Q46131539 | Experimental evolution of ultraviolet radiation resistance in Escherichia coli |
| Q90070163 | Fail-safe genetic codes designed to intrinsically contain engineered organisms |
| Q37976151 | Fitness effects of mutations in bacteria. |
| Q34005325 | Frequent beneficial mutations during single-colony serial transfer of Streptococcus pneumoniae. |
| Q36596516 | Genetic diversity and the structure of genealogies in rapidly adapting populations |
| Q33704988 | Genomic mutation rates that neutralize adaptive evolution and natural selection |
| Q92824265 | Genomic, metabolic and phenotypic variability shapes ecological differentiation and intraspecies interactions of Alteromonas macleodii |
| Q27320149 | Group Selection and Contribution of Minority Variants during Virus Adaptation Determines Virus Fitness and Phenotype |
| Q56895118 | Harnessing recombination to speed adaptive evolution in Escherichia coli |
| Q21145699 | Host-Pathogen Coevolution: The Selective Advantage of Bacillus thuringiensis Virulence and Its Cry Toxin Genes |
| Q33895065 | How to infer relative fitness from a sample of genomic sequences |
| Q37922538 | Hypermutation and stress adaptation in bacteria |
| Q89766030 | Hypermutator Pseudomonas aeruginosa exploits multiple genetic pathways to develop multidrug resistance during long-term infections in the airways of cystic fibrosis patients |
| Q38803776 | In-host adaptation and acquired triazole resistance in Aspergillus fumigatus: a dilemma for clinical management |
| Q88622233 | Increase in viability due to the accumulation of X chromosome mutations in Drosophila melanogaster males |
| Q39028906 | Interfering waves of adaptation promote spatial mixing. |
| Q90590262 | Larger bacterial populations evolve heavier fitness trade-offs and undergo greater ecological specialization |
| Q45261637 | Long-term dynamics of adaptation in asexual populations |
| Q37208314 | Macrophage adaptation leads to parallel evolution of genetically diverse Escherichia coli small-colony variants with increased fitness in vivo and antibiotic collateral sensitivity |
| Q55415773 | Molecular evolution between chemistry and biology : The interplay of competition, cooperation, and mutation. |
| Q37793329 | Next-generation sequencing as a tool to study microbial evolution. |
| Q44603862 | On the occurrence of intracolonial genotypic variability in highly clonal populations of the hydrocoral Millepora platyphylla at Moorea (French Polynesia). |
| Q35061276 | Population dynamics of metastable growth-rate phenotypes |
| Q38966881 | Potential for adaptation overrides cost of resistance. |
| Q35920941 | Practical Approaches for Detecting Selection in Microbial Genomes |
| Q34082630 | Quantifying selection acting on a complex trait using allele frequency time series data. |
| Q21563371 | Quantifying the adaptive potential of an antibiotic resistance enzyme |
| Q100465126 | Rapid evolution destabilizes species interactions in a fluctuating environment |
| Q30555815 | Rate of adaptation in sexuals and asexuals: a solvable model of the Fisher-Muller effect |
| Q28728760 | Real time forecasting of near-future evolution |
| Q28540044 | Recombination accelerates adaptation on a large-scale empirical fitness landscape in HIV-1 |
| Q24635911 | Second-order selection for evolvability in a large Escherichia coli population |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q47254650 | Sexual recombination and increased mutation rate expedite evolution of Escherichia coli in varied fitness landscapes |
| Q33786307 | Single-mutation fitness landscapes for an enzyme on multiple substrates reveal specificity is globally encoded |
| Q33455287 | Tangled bank of experimentally evolved Burkholderia biofilms reflects selection during chronic infections |
| Q47136281 | The Nonstationary Dynamics of Fitness Distributions: Asexual Model with Epistasis and Standing Variation |
| Q34468851 | The effect of bacterial recombination on adaptation on fitness landscapes with limited peak accessibility |
| Q36177833 | The effects of a deleterious mutation load on patterns of influenza A/H3N2's antigenic evolution in humans |
| Q92544990 | The emergence of adaptive laboratory evolution as an efficient tool for biological discovery and industrial biotechnology |
| Q37696346 | The fates of mutant lineages and the distribution of fitness effects of beneficial mutations in laboratory budding yeast populations |
| Q28235419 | The first steps of adaptation of Escherichia coli to the gut are dominated by soft sweeps |
| Q35069183 | The genetic basis of Escherichia coli pathoadaptation to macrophages. |
| Q55510467 | The genomics of adaptation. |
| Q42778842 | The population genetics of mutations: good, bad and indifferent |
| Q34220937 | The rate of beneficial mutations surfing on the wave of a range expansion |
| Q49957624 | Variation in Mutational Robustness between Different Proteins and the Predictability of Fitness Effects. |
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