scholarly article | Q13442814 |
P50 | author | Richard Lenski | Q713637 |
Jeffrey E Barrick | Q42531828 | ||
P2093 | author name string | Christopher C Strelioff | |
Mark R Kauth | |||
P2860 | cites work | EVOLUTION OF EVOLVABILITY IN A DEVELOPMENTAL MODEL | Q22065653 |
Historical contingency and the evolution of a key innovation in an experimental population of Escherichia coli | Q22066316 | ||
The scale independence of evolution | Q22121945 | ||
Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria | Q22122042 | ||
Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 | ||
Evolvability is a selectable trait | Q24564104 | ||
Evolvability | Q24595167 | ||
The distribution of fitness effects of beneficial mutations in Pseudomonas aeruginosa | Q28474903 | ||
Genome-wide mutational diversity in an evolving population of Escherichia coli | Q28751288 | ||
Compensatory mutations, antibiotic resistance and the population genetics of adaptive evolution in bacteria | Q28769089 | ||
Evolution by small steps and rugged landscapes in the RNA virus phi6 | Q33853501 | ||
Evolvability of an RNA virus is determined by its mutational neighbourhood | Q33914492 | ||
Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
Efficient step size selection for the tau-leaping simulation method | Q34491625 | ||
Compensatory evolution in rifampin-resistant Escherichia coli | Q34610970 | ||
Adaptive mutations in bacteria: high rate and small effects | Q34661718 | ||
Experimental evolution: experimental evolution and evolvability | Q34739570 | ||
Robustness promotes evolvability of thermotolerance in an RNA virus | Q36843864 | ||
Clonal interference, multiple mutations and adaptation in large asexual populations | Q37011413 | ||
The fixation probability of beneficial mutations | Q37229521 | ||
Mutational analysis of structure-function relationship of RNA polymerase in Escherichia coli | Q41100211 | ||
Gene replacement without selection: regulated suppression of amber mutations in Escherichia coli | Q44508201 | ||
EXPERIMENTAL STUDIES OF PLEIOTROPY AND EPISTASIS IN ESCHERICHIA COLI. II. COMPENSATION FOR MALADAPTIVE EFFECTS ASSOCIATED WITH RESISTANCE TO VIRUS T4. | Q45328632 | ||
Genome sequences of Escherichia coli B strains REL606 and BL21(DE3). | Q45331719 | ||
An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
PERSPECTIVE: COMPLEX ADAPTATIONS AND THE EVOLUTION OF EVOLVABILITY. | Q51606245 | ||
THE POPULATION GENETICS OF ADAPTATION: THE DISTRIBUTION OF FACTORS FIXED DURING ADAPTIVE EVOLUTION. | Q53762739 | ||
The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
Fitness effects of fixed beneficial mutations in microbial populations. | Q54541810 | ||
A multidimensional version of the Kolmogorov–Smirnov test | Q56050220 | ||
Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
Relative fitness can decrease in evolving asexual populations of S. cerevisiae | Q59051577 | ||
Pervasive compensatory adaptation in Escherichia coli | Q73593267 | ||
The probability that beneficial mutations are lost in populations with periodic bottlenecks | Q77605341 | ||
Evolvability | Q79207684 | ||
COMPETITION BETWEEN HIGH AND LOW MUTATING STRAINS OF ESCHERICHIA COLI | Q88206326 | ||
P433 | issue | 6 | |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 1338-1347 | |
P577 | publication date | 2010-01-27 | |
P1433 | published in | Molecular Biology and Evolution | Q1992656 |
P1476 | title | Escherichia coli rpoB mutants have increased evolvability in proportion to their fitness defects | |
P478 | volume | 27 |
Q41658937 | A Model for Designing Adaptive Laboratory Evolution Experiments |
Q35838433 | A method to infer positive selection from marker dynamics in an asexual population. |
Q54253302 | Adaptation of Escherichia coli to glucose promotes evolvability in lactose. |
Q46274966 | Adaptive Evolution under Extreme Genetic Drift in Oxidatively Stressed Caenorhabditis elegans |
Q35644230 | Alarmingly High Segregation Frequencies of Quinolone Resistance Alleles within Human and Animal Microbiomes Are Not Explained by Direct Clinical Antibiotic Exposure |
Q41582528 | An ABC method for estimating the rate and distribution of effects of beneficial mutations |
Q51544118 | Antibiotic resistance and stress in the light of Fisher's model. |
Q37173084 | Benefit of transferred mutations is better predicted by the fitness of recipients than by their ecological or genetic relatedness |
Q28082810 | Can the experimental evolution programme help us elucidate the genetic basis of adaptation in nature? |
Q64063950 | Changes in Intrinsic Antibiotic Susceptibility during a Long-Term Evolution Experiment with Escherichia coli |
Q28603871 | Contrasting effects of historical contingency on phenotypic and genomic trajectories during a two-step evolution experiment with bacteria |
Q42113492 | Cost of antibiotic resistance and the geometry of adaptation. |
Q34082927 | Different tradeoffs result from alternate genetic adaptations to a common environment |
Q54219938 | Diminishing-returns epistasis decreases adaptability along an evolutionary trajectory. |
Q51748076 | Directed combinatorial mutagenesis of Escherichia coli for complex phenotype engineering. |
Q35542057 | Distinguishing driver and passenger mutations in an evolutionary history categorized by interference |
Q36154438 | Dynamic mutation-selection balance as an evolutionary attractor |
Q58997135 | Environmental pleiotropy and demographic history direct adaptation under antibiotic selection |
Q53156835 | Epistatic interactions between ancestral genotype and beneficial mutations shape evolvability in Pseudomonas aeruginosa. |
Q52654022 | Essential is not irreplaceable: fitness dynamics of experimental E. coli RNase P RNA heterologous replacement. |
Q34596522 | Evolution of Escherichia coli rifampicin resistance in an antibiotic-free environment during thermal stress |
Q41584086 | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli. |
Q59350377 | Existing host range mutations constrain further emergence of RNA viruses |
Q50644075 | Expanded Genetic Codes Create New Mutational Routes to Rifampicin Resistance in Escherichia coli. |
Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
Q90345321 | Experimental Studies of Evolutionary Dynamics in Microbes |
Q37976151 | Fitness effects of mutations in bacteria. |
Q36187249 | General and inducible hypermutation facilitate parallel adaptation in Pseudomonas aeruginosa despite divergent mutation spectra. |
Q38639465 | Genetic variation in adaptability and pleiotropy in budding yeast |
Q28606509 | Genome sequences of two closely related strains of Escherichia coli K-12 GM4792 |
Q28082330 | Genomic investigations of evolutionary dynamics and epistasis in microbial evolution experiments |
Q45003436 | Genotype-by-environment interactions due to antibiotic resistance and adaptation in Escherichia coli |
Q28703571 | Genotypic but not phenotypic historical contingency revealed by viral experimental evolution |
Q36860964 | Global Rebalancing of Cellular Resources by Pleiotropic Point Mutations Illustrates a Multi-scale Mechanism of Adaptive Evolution |
Q41347133 | Inference for one-step beneficial mutations using next generation sequencing |
Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
Q39169158 | Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity |
Q36349644 | Multidrug-resistant bacteria compensate for the epistasis between resistances. |
Q35835073 | Polyploidy can drive rapid adaptation in yeast |
Q38966881 | Potential for adaptation overrides cost of resistance. |
Q58769267 | Predicting the evolution of Escherichia coli by a data-driven approach |
Q46298833 | Recurrent Reverse Evolution Maintains Polymorphism after Strong Bottlenecks in Commensal Gut Bacteria. |
Q24635911 | Second-order selection for evolvability in a large Escherichia coli population |
Q34567837 | Speedy speciation in a bacterial microcosm: new species can arise as frequently as adaptations within a species |
Q41904371 | Spontaneous mutation accumulation in multiple strains of the green alga, Chlamydomonas reinhardtii |
Q53247059 | Sustained fitness gains and variability in fitness trajectories in the long-term evolution experiment with Escherichia coli. |
Q30393531 | Tackling Drug Resistant Infection Outbreaks of Global Pandemic Escherichia coli ST131 Using Evolutionary and Epidemiological Genomics |
Q38689208 | The Utility of Fisher's Geometric Model in Evolutionary Genetics |
Q37696346 | The fates of mutant lineages and the distribution of fitness effects of beneficial mutations in laboratory budding yeast populations |
Q28235419 | The first steps of adaptation of Escherichia coli to the gut are dominated by soft sweeps |
Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
Q35761704 | The phenotypic signature of adaptation to thermal stress in Escherichia coli |
Q39024576 | The rule of declining adaptability in microbial evolution experiments. |
Q26864257 | The spectrum of adaptive mutations in experimental evolution |
Q35890750 | Trade-Offs of Escherichia coli Adaptation to an Intracellular Lifestyle in Macrophages |
Q37119684 | Transcriptome analysis of Pseudomonas aeruginosa PAO1 grown at both body and elevated temperatures |
Search more.