| scholarly article | Q13442814 |
| P2093 | author name string | Daniel Segrè | |
| Christopher J Marx | |||
| Hsin-Hung Chou | |||
| Hsuan-Chao Chiu | |||
| Nigel F Delaney | |||
| P2860 | cites work | Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems | Q22122008 |
| Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation | Q22122024 | ||
| Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 | ||
| Fast growth increases the selective advantage of a mutation arising recurrently during evolution under metal limitation | Q28476065 | ||
| Darwinian evolution can follow only very few mutational paths to fitter proteins | Q29616042 | ||
| Reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape | Q33892372 | ||
| Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans | Q34152058 | ||
| Formaldehyde-detoxifying role of the tetrahydromethanopterin-linked pathway in Methylobacterium extorquens AM1. | Q34231710 | ||
| Optimality and evolutionary tuning of the expression level of a protein | Q34437723 | ||
| The biochemical architecture of an ancient adaptive landscape | Q34461523 | ||
| Evolution of hormone-receptor complexity by molecular exploitation | Q34511638 | ||
| Bacterial growth inhibition by overproduction of protein | Q36823896 | ||
| The dynamics of adaptation on correlated fitness landscapes | Q37399576 | ||
| The contribution of epistasis to the architecture of fitness in an RNA virus | Q37593251 | ||
| Impact of individual mutations on increased fitness in adaptively evolved strains of Escherichia coli | Q39765598 | ||
| C1 transfer enzymes and coenzymes linking methylotrophic bacteria and methanogenic Archaea | Q48036772 | ||
| Modular epistasis in yeast metabolism. | Q51982575 | ||
| Distributions of epistasis in microbes fit predictions from a fitness landscape model. | Q54444950 | ||
| Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells | Q58862259 | ||
| P433 | issue | 6034 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | beneficial mutation | Q111187232 |
| P304 | page(s) | 1190-1192 | |
| P577 | publication date | 2011-06-01 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Diminishing returns epistasis among beneficial mutations decelerates adaptation | |
| P478 | volume | 332 |
| Q41658937 | A Model for Designing Adaptive Laboratory Evolution Experiments |
| Q36182021 | A Mutational Hotspot and Strong Selection Contribute to the Order of Mutations Selected for during Escherichia coli Adaptation to the Gut |
| Q34707855 | A novel pair of inducible expression vectors for use in Methylobacterium extorquens |
| Q51826213 | A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social trait. |
| Q35764270 | A tortoise-hare pattern seen in adapting structured and unstructured populations suggests a rugged fitness landscape in bacteria |
| Q57793787 | ALEdb 1.0: a database of mutations from adaptive laboratory evolution experimentation |
| Q43757497 | Accessible mutational trajectories for the evolution of pyrimethamine resistance in the malaria parasite Plasmodium vivax |
| Q37263496 | Adaptation of Enterococcus faecalis to daptomycin reveals an ordered progression to resistance |
| Q54253302 | Adaptation of Escherichia coli to glucose promotes evolvability in lactose. |
| Q34312048 | Adaptive evolution: evaluating empirical support for theoretical predictions |
| Q30419009 | Adaptive walks on the fitness landscape of music |
| Q47587442 | Additive Phenotypes Underlie Epistasis of Fitness Effects |
| Q52758683 | Additive genetic architecture underlying a rapidly evolving sexual signaling phenotype in the Hawaiian cricket genus Laupala. |
| Q36306331 | An in vivo system for directed experimental evolution of rabbit haemorrhagic disease virus |
| Q99578991 | Application of simultaneous selective pressures slows adaptation |
| Q46750014 | Association mapping in Populus reveals the interaction between Pto-miR530a and its target Pto-KNAT1. |
| Q38103942 | Bacterial genome evolution within a clonal population: from in vitro investigations to in vivo observations |
| Q37173084 | Benefit of transferred mutations is better predicted by the fitness of recipients than by their ecological or genetic relatedness |
| Q38254752 | Beyond genome sequencing: lineage tracking with barcodes to study the dynamics of evolution, infection, and cancer. |
| Q34443462 | Biased estimates of diminishing-returns epistasis? Empirical evidence revisited |
| Q35204371 | Biophysical fitness landscapes for transcription factor binding sites |
| Q34594904 | Can you sequence ecology? Metagenomics of adaptive diversification |
| Q28727500 | Cancer in light of experimental evolution |
| Q38413449 | Clarity: an open-source manager for laboratory automation. |
| Q30300777 | Coevolution with bacteriophages drives genome-wide host evolution and constrains the acquisition of abiotic-beneficial mutations. |
| Q34497324 | Coevolutionary Landscape Inference and the Context-Dependence of Mutations in Beta-Lactamase TEM-1. |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q36152829 | Complete genome sequences of six strains of the genus Methylobacterium |
| Q92126113 | Computational Complexity as an Ultimate Constraint on Evolution |
| Q27938036 | Concerted evolution of life stage performances signals recent selection on yeast nitrogen use. |
| Q47894409 | Construction and Optimization of a Heterologous Pathway for Protocatechuate Catabolism in Escherichia coli Enables Bioconversion of Model Aromatic Compounds. |
| Q28647800 | Contingency and entrenchment in protein evolution under purifying selection |
| Q34864126 | Contrasting modes and tempos of venom expression evolution in two snake species |
| Q42204146 | Contribution of silent mutations to thermal adaptation of RNA bacteriophage Qβ |
| Q28296812 | Convergent evolution of hyperswarming leads to impaired biofilm formation in pathogenic bacteria |
| Q29011147 | Deleterious Passengers in Adapting Populations |
| Q29002206 | Detecting High-Order Epistasis in Nonlinear Genotype-Phenotype Maps |
| Q42633184 | Detecting epistasis from an ensemble of adapting populations. |
| Q34706940 | Development of an optimized medium, strain and high-throughput culturing methods for Methylobacterium extorquens |
| Q36082359 | Difference in C3-C4 metabolism underlies tradeoff between growth rate and biomass yield in Methylobacterium extorquens AM1. |
| Q27683542 | Diminishing returns and tradeoffs constrain the laboratory optimization of an enzyme |
| Q53717083 | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus. |
| Q54219938 | Diminishing-returns epistasis decreases adaptability along an evolutionary trajectory. |
| Q89972110 | Direct coupling analysis of epistasis in allosteric materials |
| Q35525132 | Directed evolution of cell size in Escherichia coli |
| Q28584571 | Disentangling genetic and epigenetic determinants of ultrafast adaptation |
| Q41819484 | Dissection of allelic interactions among Pto-miR257 and its targets and their effects on growth and wood properties in Populus |
| Q51300318 | Diverse phenotypic and genetic responses to short-term selection in evolving Escherichia coli populations. |
| Q90212325 | Diversification and Evolution of Vancomycin-Resistant Enterococcus faecium during Intestinal Domination |
| Q38187602 | Dynamics and constraints of enzyme evolution |
| Q34737585 | Effective use of a horizontally-transferred pathway for dichloromethane catabolism requires post-transfer refinement |
| Q47877246 | Effects of Beneficial Mutations in pykF Gene Vary over Time and across Replicate Populations in a Long-Term Experiment with Bacteria. |
| Q26783005 | Elucidating the molecular architecture of adaptation via evolve and resequence experiments |
| Q38218962 | Empirical fitness landscapes and the predictability of evolution |
| Q34313206 | Engineering ecosystems and synthetic ecologies |
| Q37412772 | Environment determines epistatic patterns for a ssDNA virus |
| Q55436455 | Environmental change exposes beneficial epistatic interactions in a catalytic RNA. |
| Q28272911 | Environmental changes bridge evolutionary valleys |
| Q50716194 | Epistasis and maternal effects in experimental adaptation to chronic nutritional stress in Drosophila. |
| Q39162611 | Epistasis and the Evolution of Antimicrobial Resistance |
| Q40725548 | Epistasis and the Structure of Fitness Landscapes: Are Experimental Fitness Landscapes Compatible with Fisher's Geometric Model? |
| Q28653314 | Epistasis can accelerate adaptive diversification in haploid asexual populations |
| Q51332673 | Epistasis from functional dependence of fitness on underlying traits. |
| Q53156835 | Epistatic interactions between ancestral genotype and beneficial mutations shape evolvability in Pseudomonas aeruginosa. |
| Q54304014 | Epistatic interactions determine the mutational pathways and coexistence of lineages in clonal Escherichia coli populations. |
| Q33583647 | Epistatically interacting substitutions are enriched during adaptive protein evolution |
| Q42909565 | Et tu, Brute? Not Even Intracellular Mutualistic Symbionts Escape Horizontal Gene Transfer. |
| Q34671996 | Evolution after introduction of a novel metabolic pathway consistently leads to restoration of wild-type physiology |
| Q41839414 | Evolution by flight and fight: diverse mechanisms of adaptation by actively motile microbes |
| Q90743445 | Evolution in the light of fitness landscape theory |
| Q34596522 | Evolution of Escherichia coli rifampicin resistance in an antibiotic-free environment during thermal stress |
| Q43101601 | Evolution of clonal populations approaching a fitness peak. |
| Q39675173 | Evolution of sex: Using experimental genomics to select among competing theories |
| Q92879130 | Evolutionary Dynamics in the RNA Bacteriophage Qβ Depends on the Pattern of Change in Selective Pressures |
| Q34005257 | Evolutionary accessibility of mutational pathways |
| Q89545822 | Evolutionary constraints in fitness landscapes |
| Q41132191 | Evolutionary implications of Liebig's law of the minimum: Selection under low concentrations of two nonsubstitutable nutrients |
| Q37983903 | Evolutionary insight from whole-genome sequencing of experimentally evolved microbes. |
| Q90414037 | Evolving generalists in switching rugged landscapes |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q37255898 | Experimental Horizontal Gene Transfer of Methylamine Dehydrogenase Mimics Prevalent Exchange in Nature and Overcomes the Methylamine Growth Constraints Posed by the Sub-Optimal N-Methylglutamate Pathway |
| Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
| Q34289524 | Experimental evolution |
| Q52340379 | Experimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate. |
| Q34362047 | Experiments on the role of deleterious mutations as stepping stones in adaptive evolution |
| Q42695844 | Exploiting ecology in drug pulse sequences in favour of population reduction |
| Q38109292 | Exploring the costs of horizontal gene transfer. |
| Q34464683 | FREQ-Seq: a rapid, cost-effective, sequencing-based method to determine allele frequencies directly from mixed populations |
| Q35916749 | Fast stochastic algorithm for simulating evolutionary population dynamics |
| Q38414823 | Fighting microbial drug resistance: a primer on the role of evolutionary biology in public health |
| Q36410897 | First-Step Mutations during Adaptation Restore the Expression of Hundreds of Genes |
| Q33575800 | Fisher's geometrical model emerges as a property of complex integrated phenotypic networks |
| Q41849560 | Fitness conferred by replaced amino acids declines with time |
| Q58703918 | From Local Adaptation to Speciation: Specialization and Reinforcement |
| Q36586464 | Functional evolution of an anthocyanin pathway enzyme during a flower color transition |
| Q35004076 | Generation and study of the strains of streptomycetes - heterologous hosts for production of moenomycin |
| Q43184230 | Genetic background affects epistatic interactions between two beneficial mutations |
| Q38639465 | Genetic variation in adaptability and pleiotropy in budding yeast |
| Q28651650 | Genome dynamics during experimental evolution |
| Q21560957 | Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment |
| Q22122302 | Genome-scale engineering for systems and synthetic biology |
| Q28082330 | Genomic investigations of evolutionary dynamics and epistasis in microbial evolution experiments |
| Q34708295 | Genotype to phenotype mapping and the fitness landscape of the E. coli lac promoter |
| Q100737041 | Heat-responsive and time-resolved transcriptome and metabolome analyses of Escherichia coli uncover thermo-tolerant mechanisms |
| Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
| Q96609310 | Highly parallel lab evolution reveals that epistasis can curb the evolution of antibiotic resistance |
| Q35943086 | Horizontal DNA Transfer Mechanisms of Bacteria as Weapons of Intragenomic Conflict. |
| Q37184676 | How Good Are Statistical Models at Approximating Complex Fitness Landscapes? |
| Q35956363 | Identification of cis-suppression of human disease mutations by comparative genomics |
| Q36368892 | Identification of the potentiating mutations and synergistic epistasis that enabled the evolution of inter-species cooperation |
| Q99207734 | Idiosyncratic epistasis creates universals in mutational effects and evolutionary trajectories |
| Q92471939 | Increasing growth rate slows adaptation when genotypes compete for diffusing resources |
| Q33730568 | Inferring fitness landscapes by regression produces biased estimates of epistasis. |
| Q35616623 | Investigating the Role of Gene-Gene Interactions in TB Susceptibility |
| Q45345601 | Key Metabolites and Mechanistic Changes for Salt Tolerance in an Experimentally Evolved Sulfate-Reducing Bacterium, Desulfovibrio vulgaris. |
| Q35079613 | Laboratory divergence of Methylobacterium extorquens AM1 through unintended domestication and past selection for antibiotic resistance |
| Q43231261 | Long-term diversity and genome adaptation of Acinetobacter baylyi in a minimal-medium chemostat |
| Q45261637 | Long-term dynamics of adaptation in asexual populations |
| Q40567914 | Love the one you're with: replicate viral adaptations converge on the same phenotypic change |
| Q37311367 | Low selection pressure aids the evolution of cooperative ribozyme mutations in cells |
| Q35105723 | Mapping the fitness landscape of gene expression uncovers the cause of antagonism and sign epistasis between adaptive mutations. |
| Q52431249 | Mapping the in vivo fitness landscape of lung adenocarcinoma tumor suppression in mice. |
| Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
| Q38515559 | Metabolism at evolutionary optimal States. |
| Q39169158 | Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity |
| Q42771933 | Microbiology. Antibiotic resistance, not shaken or stirred |
| Q59789922 | Modeling genome-wide enzyme evolution predicts strong epistasis underlying catalytic turnover rates |
| Q64232908 | Modular epistasis and the compensatory evolution of gene deletion mutants |
| Q36349644 | Multidrug-resistant bacteria compensate for the epistasis between resistances. |
| Q35210627 | Multiple phenotypic changes associated with large-scale horizontal gene transfer |
| Q57118367 | Multiplexed deactivated CRISPR-Cas9 gene expression perturbations deter bacterial adaptation by inducing negative epistasis |
| Q34679960 | Mutations in global regulators lead to metabolic selection during adaptation to complex environments |
| Q31039375 | Network-Based Analysis of eQTL Data to Prioritize Driver Mutations |
| Q42419706 | OASIS: an automated program for global investigation of bacterial and archaeal insertion sequences |
| Q46337805 | On the challenge of exploring the evolutionary trajectory from phosphotriesterase to arylesterase using computer simulations |
| Q42254765 | Optimization of gene expression through divergent mutational paths. |
| Q41987306 | Optimizing complex phenotypes through model-guided multiplex genome engineering |
| Q36270529 | Overcoming an optimization plateau in the directed evolution of highly efficient nerve agent bioscavengers |
| Q28595783 | Parallel and Divergent Evolutionary Solutions for the Optimization of an Engineered Central Metabolism in Methylobacterium extorquens AM1 |
| Q45994253 | Parallel emergence of negative epistasis across experimental lineages. |
| Q92568694 | Patterns and Mechanisms of Diminishing Returns from Beneficial Mutations |
| Q41864870 | Patterns of Epistasis between beneficial mutations in an antibiotic resistance gene |
| Q50914574 | Phase transition in random adaptive walks on correlated fitness landscapes. |
| Q33570193 | Phylogeny poorly predicts the utility of a challenging horizontally transferred gene in Methylobacterium strains |
| Q47156261 | Plasmid-Mediated Bioaugmentation for the Bioremediation of Contaminated Soils |
| Q51367880 | Plasticity and epistasis strongly affect bacterial fitness after losing multiple metabolic genes. |
| Q95315605 | Predictable properties of fitness landscapes induced by adaptational tradeoffs |
| Q58769267 | Predicting the evolution of Escherichia coli by a data-driven approach |
| Q41847189 | Production of 2-Hydroxyisobutyric Acid from Methanol by Methylobacterium extorquens AM1 Expressing (R)-3-Hydroxybutyryl Coenzyme A-Isomerizing Enzymes |
| Q35079781 | Properties of selected mutations and genotypic landscapes under Fisher's geometric model. |
| Q35090009 | Protein folding and binding can emerge as evolutionary spandrels through structural coupling. |
| Q64079419 | Quantifying local malignant adaptation in tissue‐specific evolutionary trajectories by harnessing cancer’s repeatability at the genetic level |
| Q92624051 | Rank orders and signed interactions in evolutionary biology |
| Q41911214 | Rates of fitness decline and rebound suggest pervasive epistasis |
| Q61817320 | Rationally designing antisense therapy to keep up with evolving bacterial resistance |
| Q90244482 | Recent insights into the genotype-phenotype relationship from massively parallel genetic assays |
| 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 |
| Q90404363 | Recombination drives the evolution of mutational robustness |
| Q34326811 | Recovering from a bad start: rapid adaptation and tradeoffs to growth below a threshold density |
| Q41592999 | Recovery of phenotypes obtained by adaptive evolution through inverse metabolic engineering |
| Q46298833 | Recurrent Reverse Evolution Maintains Polymorphism after Strong Bottlenecks in Commensal Gut Bacteria. |
| Q41987123 | Regulatory revolution: evolving the "anti-LacI" repressor |
| Q34270480 | Repeated, selection-driven genome reduction of accessory genes in experimental populations |
| Q28607370 | Reverse evolution leads to genotypic incompatibility despite functional and active site convergence |
| Q41758914 | Rewiring of genetic networks in response to modification of genetic background |
| Q45071448 | Seasonally fluctuating selection can maintain polymorphism at many loci via segregation lift. |
| Q36269559 | Seeking Goldilocks During Evolution of Drug Resistance |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q44581995 | Selection biases the prevalence and type of epistasis along adaptive trajectories |
| Q35761876 | Selective Sweeps and Parallel Pathoadaptation Drive Pseudomonas aeruginosa Evolution in the Cystic Fibrosis Lung |
| Q89637630 | Sex alters molecular evolution in diploid experimental populations of S. cerevisiae |
| Q35035921 | Should evolutionary geneticists worry about higher-order epistasis? |
| Q52321813 | Sign epistasis caused by hierarchy within signalling cascades. |
| Q44208060 | Sign epistasis limits evolutionary trade-offs at the confluence of single- and multi-carbon metabolism in Methylobacterium extorquens AM1. |
| Q93013409 | Simulations reveal challenges to artificial community selection and possible strategies for success |
| Q36504175 | Small changes in enzyme function can lead to surprisingly large fitness effects during adaptive evolution of antibiotic resistance |
| Q35748281 | Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution |
| Q92488321 | Stochastic tunneling across fitness valleys can give rise to a logarithmic long-term fitness trajectory |
| Q28551065 | Strong Selection Significantly Increases Epistatic Interactions in the Long-Term Evolution of a Protein |
| Q37346935 | Substrate ambiguous enzymes within the Escherichia coli proteome offer different evolutionary solutions to the same problem |
| Q28651496 | Sulfur isotope fractionation during the evolutionary adaptation of a sulfate-reducing bacterium |
| Q53247059 | Sustained fitness gains and variability in fitness trajectories in the long-term evolution experiment with Escherichia coli. |
| Q36643918 | Synchronous waves of failed soft sweeps in the laboratory: remarkably rampant clonal interference of alleles at a single locus |
| Q38017457 | Synthetic approaches to understanding biological constraints |
| Q91411182 | Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection |
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| Q55002438 | The Influence of Higher-Order Epistasis on Biological Fitness Landscape Topography. |
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| Q36490860 | The basis of antagonistic pleiotropy in hfq mutations that have opposite effects on fitness at slow and fast growth rates |
| Q54347187 | The battle of the SNPs. |
| Q26860873 | The causes of epistasis |
| Q58570246 | The causes of evolvability and their evolution |
| Q35172659 | The changing geometry of a fitness landscape along an adaptive walk |
| Q34399491 | The consistency of beneficial fitness effects of mutations across diverse genetic backgrounds |
| Q34893085 | The cost of antibiotic resistance depends on evolutionary history in Escherichia coli. |
| Q28681370 | The cost of efficiency in energy metabolism |
| Q42145476 | The dynamics of adapting, unregulated populations and a modified fundamental theorem |
| Q34468851 | The effect of bacterial recombination on adaptation on fitness landscapes with limited peak accessibility |
| Q51137906 | The effect of epistasis on sexually antagonistic genetic variation. |
| Q45120597 | The effects of stabilizing and directional selection on phenotypic and genotypic variation in a population of RNA enzymes |
| Q34671988 | The environment affects epistatic interactions to alter the topology of an empirical fitness landscape |
| Q40519553 | The evolution of antimicrobial peptide resistance in Pseudomonas aeruginosa is shaped by strong epistatic interactions |
| Q35579831 | The evolutionarily stable distribution of fitness effects |
| Q45344370 | The evolutionary epidemiology of multilocus drug resistance |
| Q28649903 | The functional basis of adaptive evolution in chemostats |
| Q34636314 | The genetic basis of natural variation in seed size and seed number and their trade-off using Arabidopsis thaliana MAGIC lines |
| Q88599476 | The geometry of partial fitness orders and an efficient method for detecting genetic interactions |
| Q41012991 | The impact of high-order epistasis in the within-host fitness of a positive-sense plant RNA virus |
| Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
| Q52732247 | The length scale of selection in protein evolution. |
| Q46185374 | The molecular diversity of adaptive convergence. |
| Q28732355 | The mystery of missing heritability: Genetic interactions create phantom heritability |
| Q39024576 | The rule of declining adaptability in microbial evolution experiments. |
| Q26864257 | The spectrum of adaptive mutations in experimental evolution |
| Q40587253 | The strength of genetic interactions scales weakly with mutational effects |
| Q38690951 | Thoughts Toward a Theory of Natural Selection: The Importance of Microbial Experimental Evolution |
| Q35050923 | Too much of a good thing: the unique and repeated paths toward copper adaptation |
| Q27003480 | Towards the identification of the loci of adaptive evolution |
| Q30828198 | Trade-offs drive resource specialization and the gradual establishment of ecotypes |
| Q28543649 | Transhydrogenase promotes the robustness and evolvability of E. coli deficient in NADPH production |
| Q51544809 | Understanding specialism when the Jack of all trades can be the master of all. |
| Q42389367 | Variance in epistasis links gene regulation and evolutionary rate in the yeast genetic interaction network |
| Q26830367 | What can we learn from fitness landscapes? |
| Q28818537 | Widespread Genetic Incompatibilities between First-Step Mutations during Parallel Adaptation of Saccharomyces cerevisiae to a Common Environment |
| Q54332246 | [Genetic adaptation of bacteria]. |
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