| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1052307133 |
| P356 | DOI | 10.1038/NATURE03405 |
| P8608 | Fatcat ID | release_dmqk24yuyrfthgc5uko3p67fue |
| P3181 | OpenCitations bibliographic resource ID | 589181 |
| P698 | PubMed publication ID | 15800622 |
| P5875 | ResearchGate publication ID | 7934729 |
| P50 | author | Matthew Goddard | Q18911970 |
| Charles Godfray | Q5078068 | ||
| P2093 | author name string | Austin Burt | |
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| P433 | issue | 7033 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 636-640 | |
| P577 | publication date | 2005-03-31 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Sex increases the efficacy of natural selection in experimental yeast populations | |
| P478 | volume | 434 |
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| Q53819581 | Adaptation of S. cerevisiae to fermented food environments reveals remarkable genome plasticity and the footprints of domestication. |
| Q22252364 | Adaptive value of sex in microbial pathogens |
| Q33261436 | Allopatric origins of microbial species |
| Q39436153 | An antitumor cellular vaccine based on a mini-membrane IgE. |
| Q112737432 | Analysis of the pheromone signaling pathway by RT-qPCR in the budding yeast Saccharomyces cerevisiae |
| Q48456956 | Analytic approach to the evolutionary effects of genetic exchange |
| Q35002494 | Antitumor IgE adjuvanticity: key role of Fc epsilon RI. |
| Q90809817 | Assessing by Modeling the Consequences of Increased Recombination in Recurrent Selection of Oryza sativa and Brassica rapa |
| Q58034914 | Association between fertility and molecular sub-type of global isolates ofCryptococcus gattiimolecular type VGII |
| Q33299581 | Bacterial solutions to the problem of sex |
| Q28485185 | Biochemical diversification through foreign gene expression in bdelloid rotifers |
| Q36778128 | Both costs and benefits of sex correlate with relative frequency of asexual reproduction in cyclically parthenogenic Daphnia pulicaria populations |
| Q122964291 | CRYPTIC SPECIATION IN THE COSMOPOLITAN AND CLONAL HUMAN PATHOGENIC FUNGUS ASPERGILLUS FUMIGATUS |
| Q37159891 | Calpains are involved in asexual and sexual development, cell wall integrity and pathogenicity of the rice blast fungus. |
| Q56949434 | Characterization of the pheromone gene family of an Antarctic and Arctic protozoan ciliate, Euplotes nobilii |
| Q33852835 | Chemosensory and hyperoxia circuits in C. elegans males influence sperm navigational capacity. |
| Q41776099 | Clinical and environmental isolates of Cryptococcus gattii from Australia that retain sexual fecundity |
| Q42975316 | Clonality and recombination in genetically differentiated subgroups of Cryptococcus gattii |
| Q33839536 | Clonality and α-a recombination in the Australian Cryptococcus gattii VGII population--an emerging outbreak in Australia |
| Q41913350 | Coalescent Times and Patterns of Genetic Diversity in Species with Facultative Sex: Effects of Gene Conversion, Population Structure, and Heterogeneity |
| Q37076504 | Communities, populations and individuals of arbuscular mycorrhizal fungi |
| Q91355321 | Competition experiments between Brettanomyces bruxellensis strains reveal specific adaptation to sulfur dioxide and complex interactions at intraspecies level |
| Q97599890 | Conflict, Competition, and Cooperation Regulate Social Interactions in Filamentous Fungi |
| Q114075919 | Convergent consequences of parthenogenesis on stick insect genomes |
| Q46192416 | Cryptic speciation in the cosmopolitan and clonal human pathogenic fungus Aspergillus fumigatus |
| Q81301754 | Current awareness on yeast |
| Q38018134 | Current hypotheses for the evolution of sex and recombination |
| Q34815194 | Deleterious effects of recombination and possible nonrecombinatorial advantages of sex in a fungal model |
| Q34485612 | Digital genetics: unravelling the genetic basis of evolution |
| Q53092704 | Direct and indirect consequences of meiotic recombination: implications for genome evolution. |
| Q35641347 | Discovery of a phenotypic switch regulating sexual mating in the opportunistic fungal pathogen Candida tropicalis |
| Q34259568 | Disentangling the benefits of sex. |
| Q115469688 | Distribution and diversity of aquatic protists: an evolutionary and ecological perspective |
| Q33317645 | Divergent adaptation promotes reproductive isolation among experimental populations of the filamentous fungus Neurospora |
| Q34192808 | Does sex speed up evolutionary rate and increase biodiversity? |
| Q35895511 | Does the avoidance of sexual costs increase fitness in asexual invaders? |
| Q37246333 | Domestication and Divergence of Saccharomyces cerevisiae Beer Yeasts |
| Q48074667 | Dynamic analysis of genetic diversity of gag and env regions of HIV-1 CRF07_BC recombinant in intravenous drug users in Xinjiang Uvghur Autonomous Region, China |
| Q22065653 | EVOLUTION OF EVOLVABILITY IN A DEVELOPMENTAL MODEL |
| Q37031024 | Effect of manipulating recombination rates on response to selection in livestock breeding programs |
| Q34646355 | Elimination of altered karyotypes by sexual reproduction preserves species identity |
| Q26783005 | Elucidating the molecular architecture of adaptation via evolve and resequence experiments |
| Q58699034 | Engineering Kluyveromyces marxianus as a Robust Synthetic Biology Platform Host |
| Q90370673 | Estimating the number of sexual events per generation in a facultatively sexual haploid population |
| Q35575485 | Eukaryotic microbes, species recognition and the geographic limits of species: examples from the kingdom Fungi |
| Q35673582 | Evidence for genetic differentiation and variable recombination rates among Dutch populations of the opportunistic human pathogen Aspergillus fumigatus. |
| Q47778112 | Evidence for inefficient selection against deleterious mutations in cytochrome oxidase I of asexual bdelloid rotifers |
| Q38780287 | Evidence for microbial local adaptation in nature |
| Q46495792 | Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi. |
| Q36222765 | Evolution of Transcription Networks — Lessons from Yeasts |
| Q34308296 | Evolution of fungal sexual reproduction |
| Q39675173 | Evolution of sex: Using experimental genomics to select among competing theories |
| Q28261551 | Evolution of sex: why do organisms shuffle their genotypes? |
| Q38266677 | Evolutionary Perspectives on Human Fungal Pathogens |
| Q84927048 | Evolutionary biology: Why reproduction often takes two |
| Q38597929 | Evolutionary genetic consequences of facultative sex and outcrossing |
| Q43184349 | Evolutionary rescue of a green alga kept in the dark |
| Q85304924 | Evolutionary rescue of sexual and asexual populations in a deteriorating environment |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q33877473 | Experimental Evolution with Caenorhabditis Nematodes. |
| Q34289524 | Experimental evolution |
| Q55246206 | Experimental evolution of a microbial predator's ability to find prey. |
| Q35854631 | Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits |
| Q36552063 | Experimental evolution with yeast |
| Q34739570 | Experimental evolution: experimental evolution and evolvability |
| Q90571837 | Experimental manipulation of selfish genetic elements links genes to microbial community function |
| Q38260194 | Experimental microbial evolution: history and conceptual underpinnings |
| Q39922265 | Experiments with digital organisms on the origin and maintenance of sex in changing environments |
| Q43065670 | Extensive chromosomal reshuffling drives evolution of virulence in an asexual pathogen |
| Q22242225 | Extensive recombination among human immunodeficiency virus type 1 quasispecies makes an important contribution to viral diversity in individual patients |
| Q41508221 | Fitness Effects of Thermal Stress Differ Between Outcrossing and Selfing Populations in Caenorhabditis elegans. |
| Q59670416 | Fluctuating environments select for short-term phenotypic variation leading to long-term exploration |
| Q64101025 | Fluctuating environments select for short-term phenotypic variation leading to long-term exploration |
| Q112294230 | Forest Saccharomyces paradoxus are robust to seasonal biotic and abiotic changes |
| Q42285821 | Frequent coinfection reduces RNA virus population genetic diversity |
| Q34700529 | Functional divergence of former alleles in an ancient asexual invertebrate |
| Q107968578 | Fungal diversity from communities to genes |
| Q37672042 | Fungal sex and pathogenesis |
| Q59520532 | Gene drives do not always increase in frequency: from genetic models to risk assessment |
| Q56533409 | Gene-flow between niches facilitates local adaptation in sexual populations |
| Q41826271 | Genetic Causes of Phenotypic Adaptation to the Second Fermentation of Sparkling Wines in Saccharomyces cerevisiae. |
| Q38750053 | Genetic Dissection of Heritable Traits in Yeast Using Bulk Segregant Analysis. |
| Q58689527 | Genetic Structure of Sympatric Sexually and Parthenogenetically Reproducing Population of Chara canescens (Charophyta) |
| Q47557179 | Genetic constraints on adaptation: a theoretical primer for the genomics era. |
| Q90741087 | Genetic variability and transgenerational regulation of investment in sex in the monogonont rotifer Brachionus plicatilis |
| Q38639465 | Genetic variation in adaptability and pleiotropy in budding yeast |
| Q30823989 | Genetics of dioecy and causal sex chromosomes in plants |
| Q89173981 | Genome-specific histories of divergence and introgression between an allopolyploid unisexual salamander lineage and two ancestral sexual species |
| Q100307503 | Genomic Features of Parthenogenetic Animals |
| Q63976749 | Genomic features of asexual animals |
| Q35864089 | Genomics and the making of yeast biodiversity |
| Q37620315 | Global Population Genetic Analysis of Aspergillus fumigatus |
| Q58431968 | Global analysis of mutations driving microevolution of a heterozygous diploid fungal pathogen |
| Q37456378 | Habitat heterogeneity favors asexual reproduction in natural populations of grassthrips |
| Q24617585 | Heterothallism in Saccharomyces cerevisiae isolates from nature: effect of HO locus on the mode of reproduction |
| Q33323317 | High genetic variance in life-history strategies within invasive populations by way of multiple introductions |
| Q52811545 | High-resolution mapping of the recombination landscape of the phytopathogen Fusarium graminearum suggests two-speed genome evolution. |
| Q37598990 | Higher rates of sex evolve during adaptation to more complex environments |
| Q43922104 | Higher rates of sex evolve in spatially heterogeneous environments |
| Q112782185 | How Do Species Interactions Affect Evolutionary Dynamics Across Whole Communities? |
| Q91616861 | How Evolution Modifies the Variability of Range Expansion |
| Q40083686 | In search of new tractable diatoms for experimental biology |
| Q52676527 | Increased outbreeding in yeast in response to dispersal by an insect vector. |
| Q33419818 | Independent S-locus mutations caused self-fertility in Arabidopsis thaliana |
| Q35167621 | Induction of sexual reproduction and genetic diversity in the cheese fungus Penicillium roqueforti |
| Q34271733 | Inferring outcrossing in the homothallic fungus Sclerotinia sclerotiorum using linkage disequilibrium decay |
| Q35641863 | Influences of dominance and evolution of sex in finite diploid populations |
| Q38206761 | Insights into molecular evolution from yeast genomics |
| Q34126347 | Interspecific sex in grass smuts and the genetic diversity of their pheromone-receptor system |
| Q45238736 | Investigating the production of sexual resting structures in a plant pathogen reveals unexpected self-fertility and genotype-by-environment effects |
| Q42236265 | Just like the rest of evolution in Mother Nature, the evolution of cancers may be driven by natural selection, and not by haphazard mutations |
| Q28607893 | Large-scale assessment of olfactory preferences and learning in Drosophila melanogaster: behavioral and genetic components |
| Q34493389 | Last hope for the doomed? Thoughts on the importance of a parasexual cycle for the yeast Candida albicans |
| Q87407141 | Learn from the fungi: adaptive evolution without sex in fungal pathogens (comment on DOI 10.1002/bies.201300155) |
| Q21144916 | Limits to the rate of adaptive substitution in sexual populations |
| Q45108087 | Long-distance dispersal and recombination in environmental populations of Cryptococcus neoformans var. grubii from India |
| Q36476716 | Looking for sex in the fungal pathogens Cryptococcus neoformans and Cryptococcus gattii |
| Q34157632 | Loss of dispensable genes is not adaptive in yeast |
| Q24816315 | Low effective dispersal of asexual genotypes in heterogeneous landscapes by the endemic pathogen Penicillium marneffei |
| Q34482596 | Maintenance of sex-related genes and the co-occurrence of both mating types in Verticillium dahliae |
| Q36394128 | Marine Biodiversity, Biogeography, Deep-Sea Gradients, and Conservation |
| Q36236229 | Maternal source of variability in the embryo development of an annual killifish. |
| Q37841850 | Mechanisms of unisexual mating in Cryptococcus neoformans. |
| Q92141659 | Microbial Experimental Evolution - a proving ground for evolutionary theory and a tool for discovery |
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| Q36336523 | Molecular features and functional constraints in the evolution of the mammalian X chromosome. |
| Q34588507 | Multilocus sequence typing reveals three genetic subpopulations of Cryptococcus neoformans var. grubii (serotype A), including a unique population in Botswana |
| Q21283912 | Multiple losses of sex within a single genus of Microsporidia |
| Q108126714 | Multiple mechanisms drive genomic adaptation to extreme O levels in Drosophila melanogaster |
| Q34279988 | Mutation load and rapid adaptation favour outcrossing over self-fertilization. |
| Q43412322 | Natural transformation increases the rate of adaptation in the human pathogen Helicobacter pylori. |
| Q104497956 | Nature Abhors a Vacuum: Highly Diverse Mechanisms Enable Spoilage Fungi to Disperse, Survive, and Propagate in Commercially Processed and Preserved Foods |
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| Q45892629 | On Variation of Polyandry in a Bush-Cricket, Metrioptera roeselii, in Northern Europe. |
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| Q40045106 | Parasex Generates Phenotypic Diversity de Novo and Impacts Drug Resistance and Virulence in Candida albicans |
| Q37469557 | Parasexuality and ploidy change in Candida tropicalis. |
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| Q44130339 | Rapid adaptation to a novel host in a seed beetle (Callosobruchus maculatus): the role of sexual selection. |
| Q42267948 | Rapid adaptive amplification of preexisting variation in an RNA virus |
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| Q33688865 | Rate of adaptation in large sexual populations |
| Q48521753 | Recombination Alters the Dynamics of Adaptation on Standing Variation in Laboratory Yeast Populations. |
| Q28540044 | Recombination accelerates adaptation on a large-scale empirical fitness landscape in HIV-1 |
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| Q46553041 | Reduction in the sex ability of worldwide clonal populations of Puccinia striiformis f.sp. tritici. |
| Q37324343 | Relative effects of segregation and recombination on the evolution of sex in finite diploid populations |
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| Q37197670 | Saccharomyces cerevisiae: a sexy yeast with a prion problem |
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| Q34587456 | Selection for recombination in structured populations |
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| Q100526704 | Selective Interference and the Evolution of Sex |
| Q59096223 | Sex accelerates adaptation |
| Q89637630 | Sex alters molecular evolution in diploid experimental populations of S. cerevisiae |
| Q28714252 | Sex and speciation: the paradox that non-recombining DNA promotes recombination |
| Q34577438 | Sex and virulence of human pathogenic fungi |
| Q46625832 | Sex at the origin: an Asian population of the rice blast fungus Magnaporthe oryzae reproduces sexually |
| Q51768817 | Sex chromosomes in flowering plants. |
| Q51723842 | Sex drives intracellular conflict in yeast. |
| Q34214176 | Sex enhances adaptation by unlinking beneficial from detrimental mutations in experimental yeast populations |
| Q38952339 | Sex in a test tube: testing the benefits of in vitro recombination |
| Q21133888 | Sex in cheese: evidence for sexuality in the fungus Penicillium roqueforti |
| Q88337985 | Sex in the wild: How and why field-based studies contribute to solving the problem of sex |
| Q60173382 | Sex in the wild: how and why field-based studies contribute to solving the problem of sex |
| Q92727755 | Sex increases the probability of evolutionary rescue in the presence of a competitor |
| Q33479136 | Sex is always well worth its two-fold cost |
| Q40947611 | Sex speeds adaptation by altering the dynamics of molecular evolution. |
| Q51432660 | Sex uncovered: the evolutionary biology of reproductive systems. |
| Q38003708 | Sex, outcrossing and mating types: unsolved questions in fungi and beyond |
| Q112736050 | Sexual morph specialisation in a trioecious nematode balances opposing selective forces |
| Q115468351 | Sexual recombination and temporal gene flow maintain host resistance and genetic diversity |
| Q37394392 | Sexual reproduction and dimorphism in the pathogenic basidiomycetes |
| Q34562954 | Sexual reproduction and the evolution of microbial pathogens |
| Q37765495 | Sexual reproduction in the Candida clade: cryptic cycles, diverse mechanisms, and alternative functions |
| Q34619503 | Sexual selection hinders adaptation in experimental populations of yeast |
| Q52719872 | Short-term consequences of reproductive mode variation on the genetic architecture of energy metabolism and life-history traits in the pea aphid. |
| Q41932337 | Sources of Fungal Genetic Variation and Associating It with Phenotypic Diversity |
| Q80589171 | Spontaneous emergence of modularity in a model of evolving individuals |
| Q47948410 | Spontaneous emergence of modularity in a model of evolving individuals and in real networks |
| Q30002364 | Spore number control and breeding inSaccharomyces cerevisiae |
| Q46639463 | Sporulation in soil as an overwinter survival strategy in Saccharomyces cerevisiae |
| Q39137548 | Standing genetic variation drives repeatable experimental evolution in outcrossing populations of Saccharomyces cerevisiae |
| Q56341013 | THE ECOLOGY AND GENETICS OF FITNESS IN CHLAMYDOMONAS. XIII. FITNESS OF LONG-TERM SEXUAL AND ASEXUAL POPULATIONS IN BENIGN ENVIRONMENTS |
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| Q36990499 | Temporal dynamics of outcrossing and host mortality rates in host-pathogen experimental coevolution |
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| Q49885573 | The advantage of recombination when selection is acting at many genetic Loci |
| Q33691482 | The baker's yeast diploid genome is remarkably stable in vegetative growth and meiosis |
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| Q33831372 | The ecology of sexual reproduction |
| Q36274907 | The effect of sex on the repeatability of evolution in different environments |
| Q47209733 | The effects of transcription and recombination on mutational dynamics of short tandem repeats |
| Q39703923 | The evolution of mating type switching. |
| Q51150992 | The evolution of recombination rates in finite populations during ecological speciation. |
| Q31061059 | The evolution of sex is favoured during adaptation to new environments |
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| Q47234720 | The first glance into the Glomus genome: an ancient asexual scandal with meiosis? |
| Q43218024 | The genetic architecture of biofilm formation in a clinical isolate of Saccharomyces cerevisiae |
| Q51368206 | The impact of interspecific competition on lineage evolution and a rapid peak shift by interdemic genetic mixing in experimental bacterial populations. |
| Q104135815 | The intrinsic ability of double-stranded DNA to carry out D-loop and R-loop formation |
| Q37948449 | The many costs of sex. |
| Q33587478 | The mating type locus (MAT) and sexual reproduction of Cryptococcus heveanensis: insights into the evolution of sex and sex-determining chromosomal regions in fungi |
| Q38164183 | The mating type-like loci of Candida glabrata. |
| Q51685791 | The origin of the non-recombining region of sex chromosomes in Carica and Vasconcellea. |
| Q34368040 | The oxidative damage initiation hypothesis for meiosis |
| Q33332302 | The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains |
| Q86588078 | The phenotypic effects of spontaneous mutations in different environments |
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| Q38726566 | The role of recombination in evolutionary adaptation of Escherichia coli to a novel nutrient |
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| Q37959338 | The sex-specific region of sex chromosomes in animals and plants |
| Q28652321 | The spectrum of fungi that infects humans |
| Q51592663 | Thermal genetic adaptation in the water flea Daphnia and its impact: an evolving metacommunity approach. |
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| Q37203938 | Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation |
| Q39710445 | Two parthenogenetic populations of Chara canescens differ in their capacity to acclimate to irradiance and salinity. |
| Q111647155 | Understanding the drivers of dispersal evolution in range expansions and their ecological consequences |
| Q55213258 | Uniparental Inheritance Promotes Adaptive Evolution in Cytoplasmic Genomes. |
| Q37163188 | Using a meiosis detection toolkit to investigate ancient asexual "scandals" and the evolution of sex. |
| Q90399281 | Variability in fitness effects can preclude selection of the fittest |
| Q38866641 | Variation in Recombination Rate: Adaptive or Not? |
| Q114099850 | Vegetative cell enlargement in selected centric diatom species – an alternative way to propagate an individual genotype |
| Q38952350 | What do isogamous organisms teach us about sex and the two sexes? |
| Q90260179 | What's genetic variation got to do with it? Starvation-induced self-fertilization enhances survival in Paramecium |
| Q37193328 | Why are sex and recombination so common? |
| Q59094407 | Why sex is good |
| Q56654688 | Young species of cupuladriid bryozoans occupied new Caribbean habitats faster than old species |
| Q40012430 | cloncase: Estimation of sex frequency and effective population size by clonemate resampling in partially clonal organisms |
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