scholarly article | Q13442814 |
P50 | author | Olin K. Silander | Q54188764 |
Olivier Tenaillon | Q89436407 | ||
P2093 | author name string | Lin Chao | |
P2860 | cites work | The distribution of fitness effects caused by single-nucleotide substitutions in an RNA virus | Q22066390 |
Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation | Q22122024 | ||
Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria | Q22122042 | ||
Distribution of fitness effects caused by random insertion mutations in Escherichia coli | Q22122455 | ||
Evidence for Positive Epistasis in HIV-1 | Q22242281 | ||
Estimate of the mutation rate per nucleotide in humans | Q24548130 | ||
Long-term experimental evolution in Escherichia coli. XI. Rejection of non-transitive interactions as cause of declining rate of adaptation | Q24794572 | ||
Evidence for widespread degradation of gene control regions in hominid genomes | Q24804367 | ||
Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations | Q28245607 | ||
The distribution of mutation effects on viability in Drosophila melanogaster | Q28769454 | ||
A Phylogenetic Method for Detecting Positive Epistasis in Gene Sequences and Its Application to RNA Virus Evolution | Q29014235 | ||
Evolution by small steps and rugged landscapes in the RNA virus phi6 | Q33853501 | ||
Weak selection revealed by the whole-genome comparison of the X chromosome and autosomes of human and chimpanzee | Q33932596 | ||
Comparative evolutionary genetics of spontaneous mutations affecting fitness in rhabditid nematodes | Q33936846 | ||
Muller's ratchet under epistatic selection | Q33962825 | ||
Estimation of deleterious-mutation parameters in natural populations | Q33968381 | ||
THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER. I. SPONTANEOUS MUTATION RATE OF POLYGENES CONTROLLING VIABILITY | Q33981138 | ||
Toward a realistic model of mutations affecting fitness | Q34191607 | ||
Bayesian analysis suggests that most amino acid replacements in Drosophila are driven by positive selection | Q34303973 | ||
Dobzhansky-Muller incompatibilities in protein evolution | Q34380180 | ||
High genomic deleterious mutation rates in hominids | Q34491535 | ||
The coupon collector and the suppressor mutation: estimating the number of compensatory mutations by maximum likelihood. | Q34576506 | ||
EMS-induced polygenic mutation rates for nine quantitative characters in Drosophila melanogaster | Q34602537 | ||
Mutators, population size, adaptive landscape and the adaptation of asexual populations of bacteria | Q34607018 | ||
Spontaneous mutational effects on reproductive traits of arabidopsis thaliana | Q34609437 | ||
Estimates of the rate and distribution of fitness effects of spontaneous mutation in Saccharomyces cerevisiae | Q34611665 | ||
Positive and negative selection on the human genome | Q34612936 | ||
Mutation accumulation in populations of varying size: the distribution of mutational effects for fitness correlates in Caenorhabditis elegans | Q34643894 | ||
Epistasis and its relationship to canalization in the RNA virus phi 6. | Q34645008 | ||
Spontaneous deleterious mutation in Arabidopsis thaliana | Q35649504 | ||
The contribution of epistasis to the architecture of fitness in an RNA virus | Q37593251 | ||
Mutations of intermediate effect are responsible for adaptation in evolving Pseudomonas fluorescens populations | Q38786690 | ||
PERSPECTIVE: SPONTANEOUS DELETERIOUS MUTATION. | Q39341914 | ||
Fitness of RNA virus decreased by Muller's ratchet | Q41211936 | ||
Influence of random genetic drift on human immunodeficiency virus type 1 env evolution during chronic infection | Q41828783 | ||
Inference of genome-wide mutation rates and distributions of mutation effects for fitness traits: a simulation study | Q42566369 | ||
Compensated deleterious mutations in insect genomes | Q44162643 | ||
Adaptive evolution of non-coding DNA in Drosophila | Q46601551 | ||
An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
Estimate of the genomic mutation rate deleterious to overall fitness in E. coli. | Q51030744 | ||
A comprehensive model of mutations affecting fitness and inferences for Arabidopsis thaliana. | Q52041272 | ||
Towards a theory of evolutionary adaptation. | Q52237130 | ||
The cost of inbreeding in Arabidopsis. | Q52595244 | ||
High mutation rate and predominance of insertions in the Caenorhabditis elegans nuclear genome. | Q52965913 | ||
Experimental tests of the roles of adaptation, chance, and history in evolution. | Q54619014 | ||
Big-benefit mutations in a bacteriophage inhibited with heat | Q56901737 | ||
Quantifying the Slightly Deleterious Mutation Model of Molecular Evolution | Q57675399 | ||
Mutagenic treatment of double- and single-stranded DNA phages T4 and S13 with hydroxylamine | Q72074448 | ||
The fitness effects of spontaneous mutations in Caenorhabditis elegans | Q73002426 | ||
Pervasive compensatory adaptation in Escherichia coli | Q73593267 | ||
Divergent evolution during an experimental adaptive radiation | Q73788732 | ||
THE RATE AND EFFECTS DISTRIBUTION OF VIABILITY MUTATION IN DROSOPHILA: MINIMUM DISTANCE ESTIMATION | Q88201063 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e94 | |
P577 | publication date | 2007-04-01 | |
P1433 | published in | PLOS Biology | Q1771695 |
P1476 | title | Understanding the evolutionary fate of finite populations: the dynamics of mutational effects | |
P478 | volume | 5 |
Q28754894 | A framework for evolutionary systems biology |
Q92620768 | A little bit of sex prevents mutation accumulation even in apomictic polyploid plants |
Q36677347 | Accelerating Mutational Load Is Not Due to Synergistic Epistasis or Mutator Alleles in Mutation Accumulation Lines of Yeast |
Q50532537 | Adaptation of Drosophila melanogaster to increased NaCl concentration due to dominant beneficial mutations. |
Q38059441 | Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective |
Q46274966 | Adaptive Evolution under Extreme Genetic Drift in Oxidatively Stressed Caenorhabditis elegans |
Q64241424 | Adaptive Landscapes in the Age of Synthetic Biology |
Q36976911 | An Evolving Genetic Architecture Interacts with Hill-Robertson Interference to Determine the Benefit of Sex. |
Q34290505 | Bacteriophage PhiX174's ecological niche and the flexibility of its Escherichia coli lipopolysaccharide receptor |
Q37088726 | Capturing the mutational landscape of the beta-lactamase TEM-1. |
Q33296520 | Clinal variation in MHC diversity with temperature: evidence for the role of host-pathogen interaction on local adaptation in Atlantic salmon |
Q29464175 | Collective Infectious Units in Viruses |
Q36052336 | Complex genetic changes in strains of Saccharomyces cerevisiae derived by selection in the laboratory |
Q37428442 | Contribution of selection for protein folding stability in shaping the patterns of polymorphisms in coding regions |
Q29011147 | Deleterious Passengers in Adapting Populations |
Q91949265 | Dissection of the mutation accumulation process during bacterial range expansions |
Q22065129 | Distribution of fitness effects caused by single-nucleotide substitutions in bacteriophage f1 |
Q38760797 | Distributions of Mutational Effects and the Estimation of Directional Selection in Divergent Lineages of Arabidopsis thaliana |
Q36154438 | Dynamic mutation-selection balance as an evolutionary attractor |
Q53566921 | Dynamics and Fate of Beneficial Mutations Under Lineage Contamination by Linked Deleterious Mutations. |
Q37443408 | Effective population size and the rate and pattern of nucleotide substitutions |
Q28748858 | Elastic, not plastic species: frozen plasticity theory and the origin of adaptive evolution in sexually reproducing organisms |
Q35620493 | Emergent neutrality in adaptive asexual evolution |
Q37764210 | Environmental duress and epistasis: how does stress affect the strength of selection on new mutations? |
Q52881848 | Environmental fluctuations do not select for increased variation or population-based resistance in Escherichia coli. |
Q35583653 | Evolution of bow-tie architectures in biology |
Q42380178 | Evolution of drift robustness in small populations |
Q46839587 | Evolution of pleiotropic costs in experimental populations |
Q40873790 | Evolutionary dynamics of viral escape under antibodies stress: A biophysical model. |
Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
Q47238297 | Experimental determination and prediction of the fitness effects of random point mutations in the biosynthetic enzyme HisA. |
Q33523627 | Experimental evolution with E. coli in diverse resource environments. I. Fluctuating environments promote divergence of replicate populations |
Q33320201 | Expression profiles reveal parallel evolution of epistatic interactions involving the CRP regulon in Escherichia coli |
Q46804320 | Field measurements of genotype by environment interaction for fitness caused by spontaneous mutations in Arabidopsis thaliana. |
Q51313054 | Fisher's geometric model predicts the effects of random mutations when tested in the wild. |
Q22122004 | Fitness and its role in evolutionary genetics |
Q52627115 | Fitness of Arabidopsis thaliana mutation accumulation lines whose spontaneous mutations are known. |
Q28477614 | Fitness ranking of individual mutants drives patterns of epistatic interactions in HIV-1 |
Q34203627 | Fitness recovery and compensatory evolution in natural mutant lines of C. elegans |
Q34005325 | Frequent beneficial mutations during single-colony serial transfer of Streptococcus pneumoniae. |
Q34376116 | Genetic changes during a laboratory adaptive evolution process that allowed fast growth in glucose to an Escherichia coli strain lacking the major glucose transport system |
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 |
Q33704988 | Genomic mutation rates that neutralize adaptive evolution and natural selection |
Q33322521 | Heterogeneous adaptive trajectories of small populations on complex fitness landscapes |
Q99207734 | Idiosyncratic epistasis creates universals in mutational effects and evolutionary trajectories |
Q42049424 | Impact of increased mutagenesis on adaptation to high temperature in bacteriophage Qβ. |
Q33709997 | Impacts of mutation effects and population size on mutation rate in asexual populations: a simulation study |
Q41986317 | Interactions between evolutionary processes at high mutation rates |
Q42065537 | Interactions between stressful environment and gene deletions alleviate the expected average loss of fitness in yeast. |
Q40471201 | Lethal mutagenesis in a structured environment. |
Q42393627 | Loss of least-loaded class in asexual populations due to drift and epistasis |
Q46527713 | Major histocompatibility complex diversity is positively associated with stream water temperatures in proximate populations of sockeye salmon |
Q26861515 | Merging molecular mechanism and evolution: theory and computation at the interface of biophysics and evolutionary population genetics |
Q33784387 | Molecular hyperdiversity and evolution in very large populations |
Q33321332 | Muller's Ratchet and compensatory mutation in Caenorhabditis briggsae mitochondrial genome evolution |
Q27310283 | Mutation rules and the evolution of sparseness and modularity in biological systems |
Q34477455 | Mutational effects and population dynamics during viral adaptation challenge current models |
Q44010374 | Negative epistasis between beneficial mutations in an evolving bacterial population |
Q37793329 | Next-generation sequencing as a tool to study microbial evolution. |
Q42326356 | Nucleoside analogue mutagenesis of a single-stranded DNA virus: evolution and resistance. |
Q28754380 | On the potential for extinction by Muller's ratchet in Caenorhabditis elegans |
Q93101105 | Parallel evolution of HIV-1 in a long-term experiment |
Q92568694 | Patterns and Mechanisms of Diminishing Returns from Beneficial Mutations |
Q28476356 | Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations |
Q33531914 | Phenotypic effect of mutations in evolving populations of RNA molecules |
Q33504539 | Predicting the evolution of sex on complex fitness landscapes |
Q33789108 | Purging deleterious mutations under self fertilization: paradoxical recovery in fitness with increasing mutation rate in Caenorhabditis elegans |
Q30829788 | Quantifying organismal complexity using a population genetic approach |
Q28755128 | Quantifying the threat of extinction from Muller's ratchet in the diploid Amazon molly (Poecilia formosa) |
Q46686223 | Rapid increase in viability due to new beneficial mutations in Drosophila melanogaster |
Q37716243 | Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli |
Q41911214 | Rates of fitness decline and rebound suggest pervasive epistasis |
Q37215211 | Selection for chaperone-like mediated genetic robustness at low mutation rate: impact of drift, epistasis and complexity |
Q33394067 | Similar rates of protein adaptation in Drosophila miranda and D. melanogaster, two species with different current effective population sizes |
Q33521759 | Standing variation and new mutations both contribute to a fast response to selection for flowering time in maize inbreds. |
Q35748281 | Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution |
Q37380183 | Stochasticity in evolution. |
Q36954344 | Synonymous genes explore different evolutionary landscapes. |
Q42237691 | Systemic properties of metabolic networks lead to an epistasis-based model for heterosis |
Q42694955 | The Fitness Effects of Spontaneous Mutations Nearly Unseen by Selection in a Bacterium with Multiple Chromosomes |
Q38689208 | The Utility of Fisher's Geometric Model in Evolutionary Genetics |
Q22122013 | The distribution of fitness effects of new mutations |
Q50021304 | The distribution of mutational fitness effects of phage φX174 on different hosts |
Q37399576 | The dynamics of adaptation on correlated fitness landscapes |
Q31040305 | The emergence of complexity and restricted pleiotropy in adapting networks |
Q43138629 | The evolution of epistasis and its links with genetic robustness, complexity and drift in a phenotypic model of adaptation |
Q35579831 | The evolutionarily stable distribution of fitness effects |
Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
Q46185374 | The molecular diversity of adaptive convergence. |
Q42123470 | The nearly neutral and selection theories of molecular evolution under the fisher geometrical framework: substitution rate, population size, and complexity. |
Q30947119 | The properties of adaptive walks in evolving populations of fungus |
Q39024576 | The rule of declining adaptability in microbial evolution experiments. |
Q55213258 | Uniparental Inheritance Promotes Adaptive Evolution in Cytoplasmic Genomes. |
Q33612170 | Variable mutation rates as an adaptive strategy in replicator populations |
Q51302402 | Viral mutation rates: modelling the roles of within-host viral dynamics and the trade-off between replication fidelity and speed. |
Q52682134 | When the going gets tough, beneficial mutations get going. |
Search more.