| scholarly article | Q13442814 |
| P2093 | author name string | Daniel M Weinreich | |
| Christopher J Graves | |||
| P2860 | cites work | COMPETITION BETWEEN HIGH AND LOW MUTATING STRAINS OF ESCHERICHIA COLI | Q88206326 |
| THE MAINTENANCE OF SEX BY GROUP SELECTION | Q88207306 | ||
| The loss of adaptive plasticity during long periods of environmental stasis | Q22066109 | ||
| Sexual reproduction as an adaptation to resist parasites (a review) | Q22066201 | ||
| The frailty of adaptive hypotheses for the origins of organismal complexity | Q22066346 | ||
| Fitness and its role in evolutionary genetics | Q22122004 | ||
| Group Selection and Kin Selection | Q22122436 | ||
| Sex increases the efficacy of natural selection in experimental yeast populations | Q22122472 | ||
| Sex releases the speed limit on evolution | Q22122522 | ||
| Generalized population models and the nature of genetic drift | Q22162499 | ||
| On the probability of fixation of mutant genes in a population | Q24533316 | ||
| Running with the Red Queen: host-parasite coevolution selects for biparental sex | Q24630269 | ||
| The evolution of bet-hedging adaptations to rare scenarios | Q24678043 | ||
| Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
| Bet hedging in yeast by heterogeneous, age-correlated expression of a stress protectant | Q27319462 | ||
| Developmental cheating in the social bacterium Myxococcus xanthus | Q28141858 | ||
| The major evolutionary transitions | Q28235986 | ||
| Evolution of mutation rates in bacteria | Q28238561 | ||
| The genetical evolution of social behaviour. I | Q28256872 | ||
| Coevolution of hosts and parasites | Q28273046 | ||
| Aggressive chemotherapy and the selection of drug resistant pathogens | Q28533328 | ||
| Does High-Dose Antimicrobial Chemotherapy Prevent the Evolution of Resistance? | Q28552950 | ||
| Improved use of a public good selects for the evolution of undifferentiated multicellularity | Q28709417 | ||
| Linkage and the limits to natural selection | Q28769449 | ||
| The Evolution of Mutation Rate in Finite Asexual Populations | Q29301497 | ||
| Bacterial persistence as a phenotypic switch | Q29618111 | ||
| Daniel Bernoulli (1738): evolution and economics under risk | Q33181208 | ||
| Recombination speeds adaptation by reducing competition between beneficial mutations in populations of Escherichia coli | Q33294903 | ||
| Virulence evolution and the trade-off hypothesis: history, current state of affairs and the future | Q40004898 | ||
| Quantitative evolutionary dynamics using high-resolution lineage tracking | Q40499709 | ||
| Strategies of microbial cheater control | Q40523188 | ||
| Adaptive evolution of highly mutable loci in pathogenic bacteria | Q40629814 | ||
| Short-sighted evolution and the virulence of pathogenic microorganisms | Q40739465 | ||
| Sex speeds adaptation by altering the dynamics of molecular evolution. | Q40947611 | ||
| Snowdrift game dynamics and facultative cheating in yeast | Q41200215 | ||
| A unifying framework reveals key properties of multilevel selection | Q42264666 | ||
| Evolution of Mutation Rates in Rapidly Adapting Asexual Populations. | Q42741265 | ||
| Natural selection promotes antigenic evolvability. | Q42906925 | ||
| Nautural selection for within-generation variance in offspring number | Q42973492 | ||
| Infection biology: Cheats never prosper | Q43581710 | ||
| Bet hedging in desert winter annual plants: optimal germination strategies in a variable environment | Q43988636 | ||
| Microbial evolution: regulatory design prevents cancer-like overgrowths | Q44058093 | ||
| Evolution of virulence: interdependence, constraints, and selection using nested models | Q44755803 | ||
| Prisoner's dilemma in an RNA virus | Q45750074 | ||
| Invasion fitness, inclusive fitness, and reproductive numbers in heterogeneous populations | Q46535034 | ||
| Expected relative fitness and the adaptive topography of fluctuating selection | Q46536579 | ||
| High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
| Stabilization of cooperative virulence by the expression of an avirulent phenotype. | Q50018280 | ||
| Emergence of cooperation and evolutionary stability in finite populations. | Q51003681 | ||
| Evolutionary bet-hedging in the real world: empirical evidence and challenges revealed by plants. | Q51147284 | ||
| Towards a general theory of group selection. | Q51208887 | ||
| PERSPECTIVE: COMPLEX ADAPTATIONS AND THE EVOLUTION OF EVOLVABILITY. | Q51606245 | ||
| Is evolvability evolvable? | Q51697895 | ||
| Evaluating the importance of within- and between-host selection pressures on the evolution of chronic pathogens. | Q51905100 | ||
| Applying population-genetic models in theoretical evolutionary epidemiology. | Q51906282 | ||
| Phenotypic diversity, population growth, and information in fluctuating environments. | Q51965535 | ||
| Bet-Hedging Diapause Strategies in Stochastic Environments. | Q52578946 | ||
| Evolution of cooperation and conflict in experimental bacterial populations. | Q53651280 | ||
| Lineage selection and the evolution of multistage carcinogenesis. | Q55032938 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli | Q56944671 | ||
| A general model for the evolution of recombination | Q71859154 | ||
| Evolvability | Q79207684 | ||
| Hedging one's evolutionary bets, revisited | Q83177410 | ||
| Adaptive phenotypic plasticity: consensus and controversy | Q83210482 | ||
| Targeting virulence: can we make evolution-proof drugs? | Q87435859 | ||
| Mutual policing and repression of competition in the evolution of cooperative groups | Q33366828 | ||
| Dormancy contributes to the maintenance of microbial diversity | Q33540950 | ||
| The effect of population bottlenecks on mutation rate evolution in asexual populations | Q33763823 | ||
| The evolution of mutation rates: separating causes from consequences | Q33925698 | ||
| Adaptive virulence evolution: the good old fitness-based approach | Q34043639 | ||
| Deleterious mutations and the evolution of sexual reproduction | Q34164458 | ||
| On the evolutionary effect of recombination | Q34235292 | ||
| Maintenance of genetic heterogeneity | Q34241342 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| There is no fitness but fitness, and the lineage is its bearer | Q34507378 | ||
| Adaptation of HIV-1 to human leukocyte antigen class I | Q34604811 | ||
| The language of gene interaction | Q34604883 | ||
| A chance at survival: gene expression noise and phenotypic diversification strategies | Q34946251 | ||
| Evolution of cooperation by multilevel selection | Q34984209 | ||
| Should evolutionary geneticists worry about higher-order epistasis? | Q35035921 | ||
| The evolution of drug resistance and the curious orthodoxy of aggressive chemotherapy | Q35092451 | ||
| Theory and empiricism in virulence evolution | Q35362151 | ||
| Risk-spreading and bet-hedging in insect population biology | Q35687342 | ||
| Fate of a mutation in a fluctuating environment. | Q36056919 | ||
| On population growth in a randomly varying environment | Q36449855 | ||
| Common strategies for antigenic variation by bacterial, fungal and protozoan pathogens | Q36913862 | ||
| Within-host and between-host evolutionary rates across the HIV-1 genome | Q36937390 | ||
| The fixation probability of rare mutators in finite asexual populations. | Q37152739 | ||
| Competition between recombination and epistasis can cause a transition from allele to genotype selection | Q37167732 | ||
| Evolutionary selection between alternative modes of gene regulation | Q37211321 | ||
| Linking within- and between-host dynamics in the evolutionary epidemiology of infectious diseases | Q37227830 | ||
| Effect of temporal fluctuation of selection coefficient on gene frequency in a population | Q37460915 | ||
| Multiple infections and the evolution of virulence. | Q38076466 | ||
| Beyond genome sequencing: lineage tracking with barcodes to study the dynamics of evolution, infection, and cancer. | Q38254752 | ||
| On the fixation process of a beneficial mutation in a variable environment | Q38517810 | ||
| How Can Evolution Learn? | Q38679827 | ||
| Seed Germination in Desert Annuals: An Empirical Test of Adaptive Bet Hedging | Q38948360 | ||
| Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity | Q39169158 | ||
| A global genetic interaction network maps a wiring diagram of cellular function | Q39318959 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 399-417 | |
| P577 | publication date | 2017-08-28 | |
| P1433 | published in | Annual Review of Ecology, Evolution, and Systematics | Q4034066 |
| P1476 | title | Variability in fitness effects can preclude selection of the fittest | |
| P478 | volume | 48 |
| Q92573678 | Individuals' expected genetic contributions to future generations, reproductive value, and short-term metrics of fitness in free-living song sparrows (Melospiza melodia) |
| Q96822207 | Prior evolution in stochastic versus constant temperatures affects RNA virus evolvability at a thermal extreme |
| Q58570246 | The causes of evolvability and their evolution |
| Q92967633 | The effects of individual nonheritable variation on fitness estimation and coexistence |
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