review article | Q7318358 |
scholarly article | Q13442814 |
P819 | ADS bibcode | 2000PNAS...97.6981L |
P356 | DOI | 10.1073/PNAS.97.13.6981 |
P932 | PMC publication ID | 34373 |
P698 | PubMed publication ID | 10860960 |
P5875 | ResearchGate publication ID | 12457679 |
P50 | author | Carl Bergstrom | Q5039895 |
P2093 | author name string | B R Levin | |
P2860 | cites work | Clone-Selection and Optimal Rates of Mutation | Q22064580 |
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Common themes in microbial pathogenicity revisited | Q24643808 | ||
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Compensatory mutations, antibiotic resistance and the population genetics of adaptive evolution in bacteria | Q28769089 | ||
How clonal are bacteria? | Q29618572 | ||
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DNA repair and the evolution of transformation in Haemophilus influenzae | Q33960256 | ||
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Horizontal transfer of penicillin-binding protein genes in penicillin-resistant clinical isolates of Streptococcus pneumoniae | Q34319265 | ||
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Virulence of antibiotic-resistant Salmonella typhimurium | Q36013861 | ||
Recombination in Escherichia coli and the definition of biological species | Q36166012 | ||
Coexistence of two competitors on one resource and one inhibitor: a chemostat model based on bacteria and antibiotics | Q39800210 | ||
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The accessory genetic elements of bacteria: existence conditions and (co)evolution | Q40719863 | ||
Pathogenicity islands and the evolution of bacterial pathogens | Q41098213 | ||
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Functional gene transfer from intracellular bacteria to mammalian cells | Q41484997 | ||
Mobile gene cassettes and integrons: moving antibiotic resistance genes in gram-negative bacteria | Q41504182 | ||
The population biology of bacterial viruses: why be temperate | Q41577540 | ||
How Salmonella became a pathogen | Q41592946 | ||
The population biology of bacterial plasmids: a priori conditions for the existence of mobilizable nonconjugative factors | Q41874294 | ||
Adapt globally, act locally: the effect of selective sweeps on bacterial sequence diversity | Q42561668 | ||
The Population Biology of Bacterial Plasmids: A PRIORI Conditions for the Existence of Conjugationally Transmitted Factors. | Q42974347 | ||
Evolution of a bacteria/plasmid association | Q46676230 | ||
A global gene pool in the neisseriae | Q48060395 | ||
The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
Role of mutator alleles in adaptive evolution. | Q54564129 | ||
Reducing antibiotic resistance. | Q54588726 | ||
COEVOLUTION IN BACTERIAL-PLASMID POPULATIONS. | Q54622642 | ||
Santa Rosalia revisited: why are there so many species of bacteria? | Q56069219 | ||
Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
Genes for breakfast: the have-your-cake-and-eat-it-too of bacterial transformation | Q70503890 | ||
Gene transfer from bacteria to mammalian cells | Q71360369 | ||
Adaptation to the fitness costs of antibiotic resistance in Escherichia coli | Q73792447 | ||
P433 | issue | 13 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | prokaryotes | Q19081 |
adaptive evolution | Q113049937 | ||
bacterial evolution | Q115395667 | ||
P304 | page(s) | 6981-6985 | |
P577 | publication date | 2000-06-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Bacteria are different: observations, interpretations, speculations, and opinions about the mechanisms of adaptive evolution in prokaryotes | |
P478 | volume | 97 |
Q37556879 | A mechanistic explanation linking adaptive mutation, niche change, and fitness advantage for the wrinkly spreader |
Q34314618 | Activation of prophage eib genes for immunoglobulin-binding proteins by genes from the IbrAB genetic island of Escherichia coli ECOR-9. |
Q52932913 | Analysis of the codon usage pattern in the Vibrio cholerae genome. |
Q48456956 | Analytic approach to the evolutionary effects of genetic exchange |
Q34272285 | Antibiotic and insecticide resistance modeling--is it time to start talking? |
Q39175007 | Are CDI Systems Multicolored, Facultative, Helping Greenbeards? |
Q34212856 | Asexual reproduction induces a rapid and permanent loss of sexual reproduction capacity in the rice fungal pathogen Magnaporthe oryzae: results of in vitro experimental evolution assays |
Q33477667 | Association of virulence plasmid and antibiotic resistance determinants with chromosomal multilocus genotypes in Mexican Salmonella enterica serovar Typhimurium strains |
Q28657639 | Bacterial genome instability |
Q74424395 | Can smart bullets penetrate magic bullet-proof vests? |
Q33990330 | Characterization by 16S rRNA sequence analysis of pseudomonads causing blotch disease of cultivated Agaricus bisporus |
Q47590326 | Clonal population structure of Pseudomonas avellanae strains of different origin based on multilocus enzyme electrophoresis |
Q36297131 | Competition between conjugation and M13 phage infection in Escherichia coli in the absence of selection pressure: a kinetic study |
Q33720153 | Conjugal TOL transfer from Pseudomonas putida to Pseudomonas aeruginosa: effects of restriction proficiency, toxicant exposure, cell density ratios, and conjugation detection method on observed transfer efficiencies |
Q37538155 | Conjugative plasmids: vessels of the communal gene pool |
Q91776942 | Connecting iron acquisition and biofilm formation in the ESKAPE pathogens as a strategy for combatting antibiotic resistance |
Q28210616 | Do bacteria have sex? |
Q57016766 | Dynamic fitness landscapes: expansions for small mutation rates |
Q33250075 | E. coli microcosms indicate a tight link between predictability of ecosystem dynamics and diversity |
Q38202864 | Ecological and temporal constraints in the evolution of bacterial genomes. |
Q35694144 | Environmental genomics, the big picture? |
Q37152731 | Episodic selection and the maintenance of competence and natural transformation in Bacillus subtilis |
Q42909565 | Et tu, Brute? Not Even Intracellular Mutualistic Symbionts Escape Horizontal Gene Transfer. |
Q57896385 | Evolution of DNA Uptake Signal Sequences |
Q36161987 | Evolution of antifungal-drug resistance: mechanisms and pathogen fitness |
Q35556394 | Evolution of the soluble diiron monooxygenases |
Q34240776 | Evolution of variation in presence and absence of genes in bacterial pathways |
Q24564104 | Evolvability is a selectable trait |
Q34464918 | Exploration of sequence space for protein engineering. |
Q35967505 | Frequent recombination shapes the epidemic population structure of Planktothrix (Cyanoprokaryota) in Italian subalpine lakes |
Q39678808 | Gene transfer between Salmonella enterica serovar Typhimurium inside epithelial cells |
Q42617215 | Genetic diversity at alkB locus in Brucella abortus. |
Q34002507 | Genetic information transfer promotes cooperation in bacteria |
Q30408281 | Genomic heterogeneity and ecological speciation within one subspecies of Bacillus subtilis |
Q42961961 | Genomics and the bacterial species problem |
Q36084626 | Growth phase-specific evolutionary benefits of natural transformation in Acinetobacter baylyi |
Q30480620 | Influence of antibiotic selection on genetic composition of Escherichia coli populations from conventional and organic dairy farms |
Q36618578 | Integrons: Vehicles and pathways for horizontal dissemination in bacteria. |
Q34102811 | Interactions among strategies associated with bacterial infection: pathogenicity, epidemicity, and antibiotic resistance |
Q37124884 | Large linear plasmids of Borrelia species that cause relapsing fever |
Q39541574 | Large-scale intersubspecific recombination in the plant-pathogenic bacterium Xylella fastidiosa is associated with the host shift to mulberry. |
Q24795078 | Lateral gene transfer (LGT) between Archaea and Escherichia coli is a contributor to the emergence of novel infectious disease |
Q36994408 | Loss of a biofilm-inhibiting glycosyl hydrolase during the emergence of Yersinia pestis |
Q50762751 | Lost in the map. |
Q22122024 | Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation |
Q37784107 | Mobility of plasmids. |
Q33283537 | Molecular approaches: advantages and artifacts in assessing bacterial diversity |
Q40673000 | Molecular evidence for the evolution of metal homeostasis genes by lateral gene transfer in bacteria from the deep terrestrial subsurface |
Q34610282 | Natural selection, infectious transfer and the existence conditions for bacterial plasmids |
Q39803117 | New findings on evolution of metal homeostasis genes: evidence from comparative genome analysis of bacteria and archaea |
Q34998550 | Normal mutation rate variants arise in a Mutator (Mut S) Escherichia coli population. |
Q33335917 | Optimal control and analysis of two-color genomotyping experiments using bacterial multistrain arrays |
Q37895335 | Origins of bacterial diversity through horizontal genetic transfer and adaptation to new ecological niches |
Q36671962 | Patterns of antigenic diversity and the mechanisms that maintain them |
Q29617350 | Prokaryotic evolution in light of gene transfer |
Q35911596 | Recombination Does Not Hinder Formation or Detection of Ecological Species of Synechococcus Inhabiting a Hot Spring Cyanobacterial Mat. |
Q35301668 | Recombination drives genome evolution in outbreak-related Legionella pneumophila isolates. |
Q35280072 | Ribosomal frameshifting and dual-target antiactivation restrict quorum-sensing-activated transfer of a mobile genetic element |
Q30995707 | Salmonella Typhimurium ST213 is associated with two types of IncA/C plasmids carrying multiple resistance determinants |
Q46445165 | Search and analysis of genes involved in antibiotic resistance in Chilean strains of Piscirickettsia salmonis |
Q53895187 | Shooting the messenger of antibiotic resistance: plasmid elimination as a potential counter-evolutionary tactic. |
Q38498367 | Silencing quorum sensing and ICE mobility through antiactivation and ribosomal frameshifting |
Q57922176 | Size doesn’t matter: towards a more inclusive philosophy of biology |
Q34567837 | Speedy speciation in a bacterial microcosm: new species can arise as frequently as adaptations within a species |
Q49588422 | The Experimental Study of Bacterial Evolution and Its Implications for the Modern Synthesis of Evolutionary Biology |
Q42032715 | The MG1363 and IL1403 laboratory strains of Lactococcus lactis and several dairy strains are diploid |
Q27680786 | The Multidrug Resistance IncA/C Transferable Plasmid Encodes a Novel Domain-swapped Dimeric Protein-disulfide Isomerase |
Q48221507 | The Plasmid Genome Database |
Q38072072 | The impact of transposable elements in environmental adaptation. |
Q41081153 | The maintenance of sex in bacteria is ensured by its potential to reload genes. |
Q37279482 | The population and evolutionary dynamics of homologous gene recombination in bacterial populations |
Q48264479 | Transmission as a basic process in microbial biology. Lwoff Award Prize Lecture. |
Q41130310 | Tuning fresh: radiation through rewiring of central metabolism in streamlined bacteria |
Q30852941 | Use of genetically modified bacteria for drug delivery in humans: Revisiting the safety aspect |
Q28776172 | Variation and evolution in plants and microorganisms: toward a new synthesis 50 years after Stebbins |
Q51702438 | Variation in gene content among geographically diverse Sulfolobus isolates. |
Q50058827 | Weak Epistasis May Drive Adaptation in Recombining Bacteria |
Q41952522 | Why bacteriophage encode exotoxins and other virulence factors |
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