scholarly article | Q13442814 |
P2093 | author name string | Tim F Cooper | |
P2860 | cites work | Parasites and mutational load: an experimental test of a pluralistic theory for the evolution of sex. | Q54491549 |
Fitness effects of fixed beneficial mutations in microbial populations. | Q54541810 | ||
Mutational analysis of the Escherichia coli spoT gene identifies distinct but overlapping regions involved in ppGpp synthesis and degradation. | Q54592691 | ||
Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
Classification of hypotheses on the advantage of amphimixis | Q70503887 | ||
The effect of linkage on limits to artificial selection | Q72951099 | ||
Fitness effects of advantageous mutations in evolving Escherichia coli populations | Q22066182 | ||
EVOLUTION OF SEXRESOLVING THE PARADOX OF SEX AND RECOMBINATION | Q22121995 | ||
Interference among deleterious mutations favours sex and recombination in finite populations | Q22122238 | ||
Distribution of fitness effects caused by random insertion mutations in Escherichia coli | Q22122455 | ||
Sex increases the efficacy of natural selection in experimental yeast populations | Q22122472 | ||
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 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Sex and virulence in Escherichia coli: an evolutionary perspective | Q28768050 | ||
Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients | Q29615301 | ||
Evolutionary traction: the cost of adaptation and the evolution of sex. | Q33340891 | ||
Periodic selection in Escherichia coli | Q33711273 | ||
Evolution by small steps and rugged landscapes in the RNA virus phi6 | Q33853501 | ||
Multidimensional epistasis and the disadvantage of sex. | Q33947009 | ||
A ruby in the rubbish: beneficial mutations, deleterious mutations and the evolution of sex | Q33963090 | ||
Doing the conjugative two-step: evidence of recipient autonomy in retrotransfer. | Q33968038 | ||
Parallel changes in gene expression after 20,000 generations of evolution in Escherichiacoli | Q34171913 | ||
Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation | Q34229499 | ||
Test of synergistic interactions among deleterious mutations in bacteria | Q34448329 | ||
High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
Adaptation in sexuals vs. asexuals: clonal interference and the Fisher-Muller model | Q34589967 | ||
Natural selection, infectious transfer and the existence conditions for bacterial plasmids | Q34610282 | ||
Fitness evolution and the rise of mutator alleles in experimental Escherichia coli populations. | Q34616140 | ||
Drift increases the advantage of sex in RNA bacteriophage Phi6. | Q34643339 | ||
The speed of adaptation in large asexual populations | Q34645731 | ||
Recent horizontal transmission of plasmids between natural populations of Escherichia coli and Salmonella enterica | Q35620558 | ||
Limits to adaptation in asexual populations | Q36201707 | ||
Conjugational recombination in E. coli: myths and mechanisms | Q37623662 | ||
Clonal interference and the evolution of RNA viruses. | Q40929879 | ||
The evolution of epistasis and the advantage of recombination in populations of bacteriophage T4 | Q41055566 | ||
The effect of deleterious alleles on adaptation in asexual populations. | Q42534673 | ||
The evolutionary advantage of recombination. II. Individual selection for recombination | Q42974108 | ||
Mutator mutations in Escherichia coli induced by the insertion of phage mu and the transposable resistance elements Tn5 and Tn10. | Q43524969 | ||
Rates of DNA sequence evolution in experimental populations of Escherichia coli during 20,000 generations | Q44381822 | ||
Sexual recombination and the power of natural selection | Q44880753 | ||
The effects of sex and mutation rate on adaptation in test tubes and to mouse hosts by Saccharomyces cerevisiae | Q48944495 | ||
An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
The advantage of sex in evolving yeast populations. | Q50943803 | ||
The ecology and genetics of fitness in Chlamydomonas. XII. Repeated sexual episodes increase rates of adaptation to novel environments. | Q51198876 | ||
The ecology and genetics of fitness in Chlamydomonas. VIII. The dynamics of adaptation to novel environments after a single episode of sex. | Q51200540 | ||
The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
beneficial mutation | Q111187232 | ||
P304 | page(s) | e225 | |
P577 | publication date | 2007-09-01 | |
P1433 | published in | PLOS Biology | Q1771695 |
P1476 | title | Recombination speeds adaptation by reducing competition between beneficial mutations in populations of Escherichia coli | |
P478 | volume | 5 |
Q34080514 | A genome-wide identification of genes undergoing recombination and positive selection in Neisseria |
Q48133871 | Analysis of bacterial genomes from an evolution experiment with horizontal gene transfer shows that recombination can sometimes overwhelm selection |
Q56439466 | Asexual plants change just as often and just as fast as do sexual plants when introduced to a new range |
Q53399821 | Bacterial recombination promotes the evolution of multi-drug-resistance in functionally diverse populations. |
Q33299581 | Bacterial solutions to the problem of sex |
Q37173084 | Benefit of transferred mutations is better predicted by the fitness of recipients than by their ecological or genetic relatedness |
Q39404926 | Benefits of a Recombination-Proficient Escherichia coli System for Adaptive Laboratory Evolution |
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Q51461404 | Evolutionary history and genetic parallelism affect correlated responses to evolution. |
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Q34289524 | Experimental evolution |
Q38683209 | Experimental evolution and the dynamics of adaptation and genome evolution in microbial populations |
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Q54271627 | High Recombinant Frequency in Extraintestinal Pathogenic Escherichia coli Strains. |
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Q39028906 | Interfering waves of adaptation promote spatial mixing. |
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Q41813010 | Introgression in the genus Campylobacter: generation and spread of mosaic alleles |
Q35132965 | Introgressive hybridization and latitudinal admixture clines in North Atlantic eels. |
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Q36939050 | Isolates of Cryptococcus neoformans from infected animals reveal genetic exchange in unisexual, alpha mating type populations |
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Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
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Q41932622 | No effect of natural transformation on the evolution of resistance to bacteriophages in the Acinetobacter baylyi model system. |
Q33691470 | Optimal strategy for competence differentiation in bacteria. |
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