| scholarly article | Q13442814 |
| P50 | author | Daniel S. Fisher | Q1162465 |
| P2093 | author name string | Andrew W Murray | |
| Michael M Desai | |||
| P2860 | cites work | EVOLUTION OF SEXRESOLVING THE PARADOX OF SEX AND RECOMBINATION | Q22121995 |
| Sex releases the speed limit on evolution | Q22122522 | ||
| The evolutionary advantage of recombination | Q24533419 | ||
| The rate of adaptation in asexuals | Q24548116 | ||
| Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
| New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
| Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae | Q28131610 | ||
| A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
| Linkage and the limits to natural selection | Q28769449 | ||
| The evolution of recombination: removing the limits to natural selection. | Q33971025 | ||
| Selection for high mutation rates in chemostats | Q33989687 | ||
| Characteristic genome rearrangements in experimental evolution of Saccharomyces cerevisiae | Q34415662 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| The solitary wave of asexual evolution | Q34470274 | ||
| Spontaneous mutations in diploid Saccharomyces cerevisiae: more beneficial than expected | Q34569445 | ||
| Adaptation in sexuals vs. asexuals: clonal interference and the Fisher-Muller model | Q34589967 | ||
| Fitness evolution and the rise of mutator alleles in experimental Escherichia coli populations. | Q34616140 | ||
| Selective Sweeps in the Presence of Interference Among Partially Linked Loci | Q34617552 | ||
| The speed of adaptation in large asexual populations | Q34645731 | ||
| Limits to adaptation in asexual populations | Q36201707 | ||
| Mutators and sex in bacteria: conflict between adaptive strategies | Q37247776 | ||
| Diminishing returns of population size in the rate of RNA virus adaptation | Q39590442 | ||
| Clonal interference and the evolution of RNA viruses. | Q40929879 | ||
| Evolution of recombination due to random drift | Q42128822 | ||
| The effect of deleterious alleles on adaptation in asexual populations. | Q42534673 | ||
| High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
| The rhythm of microbial adaptation. | Q52054921 | ||
| The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
| Microevolution in an electronic microcosm. | Q54318570 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| The fixation probability of a beneficial allele in a population dividing by binary fission | Q57416620 | ||
| MUTATIONAL EFFECTS ON THE CLONAL INTERFERENCE PHENOMENON | Q60167644 | ||
| What use is sex? | Q71767825 | ||
| The effect of linkage on limits to artificial selection | Q72951099 | ||
| Selection for recombination in small populations | Q77401068 | ||
| The probability that beneficial mutations are lost in populations with periodic bottlenecks | Q77605341 | ||
| An evolutionary advantage of haploidy in large yeast populations | Q78835308 | ||
| Adaptive evolution of asexual populations under Muller's ratchet | Q80514758 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 385-394 | |
| P577 | publication date | 2007-03-01 | |
| P1433 | published in | Current Biology | Q1144851 |
| P1476 | title | The speed of evolution and maintenance of variation in asexual populations | |
| P478 | volume | 17 |
| Q41658937 | A Model for Designing Adaptive Laboratory Evolution Experiments |
| Q46880291 | A mean field model for competition: from neutral ecology to the Red Queen |
| Q36663520 | A synthetic Escherichia coli predator-prey ecosystem |
| Q51537286 | Accumulation of beneficial mutations in one dimension. |
| Q59446840 | Adaptive evolution of a key phytoplankton species to ocean acidification |
| Q41582528 | An ABC method for estimating the rate and distribution of effects of beneficial mutations |
| Q99578991 | Application of simultaneous selective pressures slows adaptation |
| Q35672470 | Backbones of evolutionary history test biodiversity theory for microbes |
| Q33299581 | Bacterial solutions to the problem of sex |
| Q24685465 | Beneficial mutation selection balance and the effect of linkage on positive selection |
| Q33856627 | Beneficial mutations and the dynamics of adaptation in asexual populations. |
| Q38254752 | Beyond genome sequencing: lineage tracking with barcodes to study the dynamics of evolution, infection, and cancer. |
| Q35202364 | CRISPR-induced distributed immunity in microbial populations. |
| Q95310233 | Can gene-inactivating mutations lead to evolutionary novelty? |
| Q34594904 | Can you sequence ecology? Metagenomics of adaptive diversification |
| Q28727500 | Cancer in light of experimental evolution |
| Q54251489 | Clonal interference can cause wavelet-like oscillations of multilocus linkage disequilibrium. |
| Q36156834 | Clonal interference in large populations |
| Q37011413 | Clonal interference, multiple mutations and adaptation in large asexual populations |
| Q38940477 | Collective Fluctuations in the Dynamics of Adaptation and Other Traveling Waves |
| Q27480938 | Collective properties of evolving molecular quasispecies |
| Q56378897 | Competition along trajectories governs adaptation rates towards antimicrobial resistance |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q57143902 | Construction of arbitrarily strong amplifiers of natural selection using evolutionary graph theory |
| Q36076137 | Contrasting dynamics of a mutator allele in asexual populations of differing size. |
| Q26823351 | Cutting through the complexity of cell collectives |
| 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 |
| Q90596125 | Directional Selection Rather Than Functional Constraints Can Shape the G Matrix in Rapidly Adapting Asexuals |
| Q35882382 | Distribution of fixed beneficial mutations and the rate of adaptation in asexual populations |
| Q36154438 | Dynamic mutation-selection balance as an evolutionary attractor |
| Q53566921 | Dynamics and Fate of Beneficial Mutations Under Lineage Contamination by Linked Deleterious Mutations. |
| Q64065847 | Ecological and Evolutionary Processes Shaping Viral Genetic Diversity |
| Q46974837 | Effect of Population Size and Mutation Rate on the Evolution of RNA Sequences on an Adaptive Landscape Determined by RNA Folding |
| Q59353300 | Effects of Transmission Bottlenecks on the Diversity of Influenza A Virus |
| Q36643853 | Emergence of DNA polymerase ε antimutators that escape error-induced extinction in yeast |
| Q35620493 | Emergent neutrality in adaptive asexual evolution |
| Q55436455 | Environmental change exposes beneficial epistatic interactions in a catalytic RNA. |
| Q92440432 | Epistasis detectably alters correlations between genomic sites in a narrow parameter window |
| Q34549616 | Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus. |
| Q42741265 | Evolution of Mutation Rates in Rapidly Adapting Asexual Populations. |
| Q47143320 | Evolution with a seed bank: The population genetic consequences of microbial dormancy |
| Q64274021 | Evolutionary Changes after Translational Challenges Imposed by Horizontal Gene Transfer |
| Q116206084 | Evolutionary Dynamics and Consequences of Parthenogenesis in Vertebrates |
| Q90186568 | Evolutionary repair: Changes in multiple functional modules allow meiotic cohesin to support mitosis |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q59359098 | Experimental Evolution in Yeast |
| Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
| Q33325656 | Experimental evolution and genome sequencing reveal variation in levels of clonal interference in large populations of bacteriophage phiX174. |
| Q46131539 | Experimental evolution of ultraviolet radiation resistance in Escherichia coli |
| Q34464683 | FREQ-Seq: a rapid, cost-effective, sequencing-based method to determine allele frequencies directly from mixed populations |
| Q90070163 | Fail-safe genetic codes designed to intrinsically contain engineered organisms |
| Q35916749 | Fast stochastic algorithm for simulating evolutionary population dynamics |
| Q37976151 | Fitness effects of mutations in bacteria. |
| Q33732926 | Fitness flux and ubiquity of adaptive evolution |
| Q88017658 | Frequent ploidy changes in growing yeast cultures |
| Q44946361 | Functional heterogeneity and heritability in CHO cell populations |
| Q36596516 | Genetic diversity and the structure of genealogies in rapidly adapting populations |
| Q35222738 | Genetic variation and the fate of beneficial mutations in asexual populations |
| Q45179007 | Genome architecture is a selectable trait that can be maintained by antagonistic pleiotropy |
| Q51610625 | Genome structure and the benefit of sex |
| Q33834503 | Genomes by design |
| Q28754815 | Genomewide patterns of substitution in adaptively evolving populations of the RNA bacteriophage MS2 |
| Q28082330 | Genomic investigations of evolutionary dynamics and epistasis in microbial evolution experiments |
| Q33772117 | Haploids adapt faster than diploids across a range of environments |
| Q49913057 | Heterogeneity and mutation in KRAS and associated oncogenes: evaluating the potential for the evolution of resistance to targeting of KRAS G12C. |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q91272592 | High-resolution lineage tracking reveals travelling wave of adaptation in laboratory yeast |
| Q26853716 | How does adaptation sweep through the genome? Insights from long-term selection experiments |
| 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 |
| Q47554536 | Immune loss as a driver of coexistence during host-phage coevolution |
| Q59867557 | Impact of epistasis and pleiotropy on evolutionary adaptation |
| Q33709997 | Impacts of mutation effects and population size on mutation rate in asexual populations: a simulation study |
| Q28709417 | Improved use of a public good selects for the evolution of undifferentiated multicellularity |
| Q39028906 | Interfering waves of adaptation promote spatial mixing. |
| Q29620149 | Intra-tumour heterogeneity: a looking glass for cancer? |
| Q48304487 | Intrinsic adaptive value and early fate of gene duplication revealed by a bottom-up approach |
| Q48062443 | Lack of Evidence for Sign Epistasis Between Beneficial Mutations in an RNA Bacteriophage |
| Q90590262 | Larger bacterial populations evolve heavier fitness trade-offs and undergo greater ecological specialization |
| Q34582984 | Leading the dog of selection by its mutational nose |
| Q92729806 | Limits on amplifiers of natural selection under death-Birth updating |
| Q43231261 | Long-term diversity and genome adaptation of Acinetobacter baylyi in a minimal-medium chemostat |
| Q45261637 | Long-term dynamics of adaptation in asexual populations |
| Q28596367 | Long-term dynamics of adaptive evolution in a globally important phytoplankton species to ocean acidification |
| Q40567914 | Love the one you're with: replicate viral adaptations converge on the same phenotypic change |
| Q52651882 | Modeling evolution of crosstalk in noisy signal transduction networks. |
| Q41182739 | Molecular characterization of clonal interference during adaptive evolution in asexual populations of Saccharomyces cerevisiae |
| Q34477455 | Mutational effects and population dynamics during viral adaptation challenge current models |
| Q46274173 | Mutator genomes decay, despite sustained fitness gains, in a long-term experiment with bacteria |
| Q34055320 | Mutator suppression and escape from replication error-induced extinction in yeast |
| Q37229440 | Myelodysplasia and acute leukemia as late complications of marrow failure: future prospects for leukemia prevention. |
| Q46812108 | Negative Epistasis in Experimental RNA Fitness Landscapes. |
| Q37793329 | Next-generation sequencing as a tool to study microbial evolution. |
| Q28659275 | Noise in biology |
| Q55502548 | Noise-induced stabilization and fixation in fluctuating environment. |
| Q42254765 | Optimization of gene expression through divergent mutational paths. |
| Q34358875 | Pervasive genetic hitchhiking and clonal interference in forty evolving yeast populations |
| Q38650449 | Ploidy Variation in Fungi: Polyploidy, Aneuploidy, and Genome Evolution |
| Q35835073 | Polyploidy can drive rapid adaptation in yeast |
| Q39005916 | Population Heterogeneity in Mutation Rate Increases the Frequency of Higher-Order Mutants and Reduces Long-Term Mutational Load. |
| Q35061276 | Population dynamics of metastable growth-rate phenotypes |
| Q64096634 | Population structure determines the tradeoff between fixation probability and fixation time |
| Q38071593 | Pre-tumour clones, periodic selection and clonal interference in the origin and progression of gastrointestinal cancer: potential for biomarker development. |
| Q41686698 | Predicting metabolic adaptation from networks of mutational paths |
| Q35077513 | Quantifying the similarity of monotonic trajectories in rough and smooth fitness landscapes |
| Q40499709 | Quantitative evolutionary dynamics using high-resolution lineage tracking |
| Q42267948 | Rapid adaptive amplification of preexisting variation in an RNA virus |
| Q28540044 | Recombination accelerates adaptation on a large-scale empirical fitness landscape in HIV-1 |
| Q41905788 | Repeatability of evolution on epistatic landscapes |
| Q92982207 | Scalable, Continuous Evolution of Genes at Mutation Rates above Genomic Error Thresholds |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q42324334 | Selection Limits to Adaptive Walks on Correlated Landscapes |
| Q36969662 | Selective sweep at a quantitative trait locus in the presence of background genetic variation |
| Q42202619 | Spatial structure increases the waiting time for cancer. |
| Q35748281 | Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution |
| Q28651496 | Sulfur isotope fractionation during the evolutionary adaptation of a sulfate-reducing bacterium |
| Q36643918 | Synchronous waves of failed soft sweeps in the laboratory: remarkably rampant clonal interference of alleles at a single locus |
| Q55024258 | The Critical Role of Inflammation in the Pathogenesis and Progression of Myeloid Malignancies. |
| Q47136281 | The Nonstationary Dynamics of Fitness Distributions: Asexual Model with Epistasis and Standing Variation |
| Q37134524 | The cost of gene expression underlies a fitness trade-off in yeast |
| Q28752372 | The dynamic genetic repertoire of microbial communities |
| Q42145476 | The dynamics of adapting, unregulated populations and a modified fundamental theorem |
| Q38399916 | The dynamics of diverse segmental amplifications in populations of Saccharomyces cerevisiae adapting to strong selection |
| Q38844301 | The effect of spatial structure on adaptation in Escherichia coli |
| Q28751643 | The evolution of sex: a perspective from the fungal kingdom |
| 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 |
| Q41365692 | The fitness effects of a point mutation in Escherichia coli change with founding population density |
| Q37229521 | The fixation probability of beneficial mutations |
| Q37152739 | The fixation probability of rare mutators in finite asexual populations. |
| Q33504886 | The impact of population size on the evolution of asexual microbes on smooth versus rugged fitness landscapes |
| Q35095531 | The impact of spatial structure on viral genomic diversity generated during adaptation to thermal stress |
| Q34081814 | The influence of deleterious mutations on adaptation in asexual populations |
| Q36245287 | The multiplicity of divergence mechanisms in a single evolving population |
| Q34549815 | The noisy edge of traveling waves |
| Q34398123 | The rate of adaptation in large sexual populations with linear chromosomes |
| Q33392677 | The repertoire and dynamics of evolutionary adaptations to controlled nutrient-limited environments in yeast |
| Q36665927 | The stochastic edge in adaptive evolution |
| Q35247990 | The time scale of evolutionary innovation |
| Q33699718 | The timetable of evolution |
| Q46904792 | Turning ecology and evolution against cancer |
| Q92267080 | Uncovering the rules of microbial community invasions |
| Q28649451 | Unifying ecology and macroevolution with individual-based theory |
| Q49957624 | Variation in Mutational Robustness between Different Proteins and the Predictability of Fitness Effects. |
| Q41901107 | Visualizing evolution in real-time method for strain engineering. |
| Q34387997 | Whole genome, whole population sequencing reveals that loss of signaling networks is the major adaptive strategy in a constant environment |
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