scholarly article | Q13442814 |
P50 | author | Yoav Ram | Q63611078 |
Lilach Hadany | Q90025218 | ||
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IPython: A System for Interactive Scientific Computing | Q24492861 | ||
Rates of spontaneous mutation | Q24548000 | ||
Mutation Rate Inferred From Synonymous Substitutions in a Long-Term Evolution Experiment With Escherichia coli | Q24617859 | ||
Human cancers express a mutator phenotype | Q24673022 | ||
Evolution of mutation rates in bacteria | Q28238561 | ||
The hitch-hiking effect of a favourable gene | Q28241578 | ||
The yeast environmental stress response regulates mutagenesis induced by proteotoxic stress | Q28535023 | ||
Evolution of the cancer genome | Q28678232 | ||
Mutation rate dynamics in a bacterial population reflect tension between adaptation and genetic load | Q28710085 | ||
Optimization of DNA polymerase mutation rates during bacterial evolution | Q33667067 | ||
The optimal rate of chromosome loss for the inactivation of tumor suppressor genes in cancer | Q33782233 | ||
The evolution of mutation rates: separating causes from consequences | Q33925698 | ||
Is Wright's shifting balance process important in evolution? | Q33998946 | ||
The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli | Q34017416 | ||
The rate of fitness-valley crossing in sexual populations. | Q34141931 | ||
The evolution of stress-induced hypermutation in asexual populations | Q34285727 | ||
Implications of stress-induced genetic variation for minimizing multidrug resistance in bacteria | Q34378318 | ||
The rise and fall of mutator bacteria. | Q34392588 | ||
Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
Mutators, population size, adaptive landscape and the adaptation of asexual populations of bacteria | Q34607018 | ||
The consequences of growth of a mutator strain of Escherichia coli as measured by loss of function among multiple gene targets and loss of fitness | Q34609052 | ||
The fate of microbial mutators | Q34623647 | ||
Adaptive mutation in Saccharomyces cerevisiae | Q34661313 | ||
A switch from high-fidelity to error-prone DNA double-strand break repair underlies stress-induced mutation. | Q54478818 | ||
Role of mutator alleles in adaptive evolution. | Q54564129 | ||
Mild environmental stress elicits mutations affecting fitness in Chlamydomonas. | Q55691280 | ||
Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
The exquisite corpse: a shifting view of the shifting balance | Q58034980 | ||
Variance-Induced Peak Shifts | Q58035005 | ||
Nonequilibrium model for estimating parameters of deleterious mutations | Q60220520 | ||
Biological cost of hypermutation in Pseudomonas aeruginosa strains from patients with cystic fibrosis | Q61477562 | ||
The accumulation of deleterious genes in a population--Muller's Ratchet | Q67444775 | ||
The evolution of mutation rates | Q69536377 | ||
Modifiers of mutation rate: a general reduction principle | Q69602852 | ||
Biochemical genetics of a natural population of Escherichia coli: seasonal changes in alleles and haplotypes | Q72293767 | ||
Adaptation to the fitness costs of antibiotic resistance in Escherichia coli | Q73792447 | ||
The mutation rate and cancer | Q74481910 | ||
Evolutionarily stable mutation rates | Q77431507 | ||
Fitness-associated recombination on rugged adaptive landscapes | Q79321153 | ||
A paradigm for direct stress-induced mutation in prokaryotes | Q79401112 | ||
The constraints of finite size in asexual populations and the rate of the ratchet | Q82914578 | ||
FOUNDER EFFECTS AND PEAK SHIFTS WITHOUT GENETIC DRIFT: ADAPTIVE PEAK SHIFTS OCCUR EASILY WHEN ENVIRONMENTS FLUCTUATE SLIGHTLY | Q88201101 | ||
A SIMULATION OF WRIGHT'S SHIFTING-BALANCE PROCESS: MIGRATION AND THE THREE PHASES | Q88205915 | ||
Vibrio cholerae triggers SOS and mutagenesis in response to a wide range of antibiotics: a route towards multiresistance | Q34933315 | ||
Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli | Q35170976 | ||
Evolutionary significance of stress-induced mutagenesis in bacteria | Q35785631 | ||
Mutation as a stress response and the regulation of evolvability | Q35869358 | ||
Mismatch repair-dependent mutagenesis in nondividing cells. | Q35924951 | ||
Evidence for elevated mutation rates in low-quality genotypes | Q35925034 | ||
An analogy between the evolution of drug resistance in bacterial communities and malignant tissues | Q36369411 | ||
Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine | Q36496909 | ||
Bacterial stationary-state mutagenesis and Mammalian tumorigenesis as stress-induced cellular adaptations and the role of epigenetics | Q36499774 | ||
Hypermutable bacteria isolated from humans--a critical analysis | Q36583214 | ||
Regulation of DNA repair in hypoxic cancer cells | Q36784378 | ||
Selection intensity for codon bias and the effective population size of Escherichia coli | Q36824400 | ||
Controlling mutation: intervening in evolution as a therapeutic strategy | Q36961674 | ||
Stress-induced mutagenesis in bacteria. | Q36961683 | ||
Selective pressures for and against genetic instability in cancer: a time-dependent problem | Q37020378 | ||
Hypoxia and metabolism. Hypoxia, DNA repair and genetic instability. | Q37084096 | ||
The fixation probability of beneficial mutations | Q37229521 | ||
Mutators and sex in bacteria: conflict between adaptive strategies | Q37247776 | ||
Role of hypoxia in the hallmarks of human cancer | Q37500308 | ||
Mechanisms of stationary-phase mutagenesis in bacteria: mutational processes in pseudomonads | Q37767248 | ||
Fitness effects of mutations in bacteria. | Q37976151 | ||
Varying migration and deme size and the feasibility of the shifting balance | Q39345696 | ||
The mutational meltdown in asexual populations | Q41067565 | ||
The rate at which asexual populations cross fitness valleys | Q41491337 | ||
Elevated mutagenesis does not explain the increased frequency of antibiotic resistant mutants in starved aging colonies | Q41855236 | ||
Temperature, stress and spontaneous mutation in Caenorhabditis briggsae and Caenorhabditis elegans | Q42138275 | ||
Mismatch Repair Modulation of MutY Activity Drives Bacillus subtilis Stationary-Phase Mutagenesis | Q42166009 | ||
The effect of deleterious alleles on adaptation in asexual populations. | Q42534673 | ||
Competition between high- and higher-mutating strains of Escherichia coli | Q42736352 | ||
Identity and function of a large gene network underlying mutagenic repair of DNA breaks | Q42969505 | ||
Stress-induced mutagenesis in bacteria | Q44459277 | ||
ON PHASE THREE OF THE SHIFTING-BALANCE THEORY. | Q45995423 | ||
Fitness-dependent mutation rates in finite populations | Q46328071 | ||
Wright's shifting balance theory: an experimental study | Q46776856 | ||
Effect of subinhibitory concentrations of antibiotics on mutation frequency in Streptococcus pneumoniae | Q46986600 | ||
On the survival probability of a slightly advantageous mutant gene with a general distribution of progeny size?A branching process model | Q47286535 | ||
Estimate of the genomic mutation rate deleterious to overall fitness in E. coli. | Q51030744 | ||
A trade-off between oxidative stress resistance and DNA repair plays a role in the evolution of elevated mutation rates in bacteria. | Q51489925 | ||
Adaptive peak shifts in a heterogenous environment. | Q52027057 | ||
Maturation of the humoral immune response as an optimization problem | Q52443852 | ||
PHASE THREE OF WRIGHT'S SHIFTING-BALANCE THEORY. | Q52491553 | ||
Rapid evolutionary escape by large populations from local fitness peaks is likely in nature. | Q52565464 | ||
P433 | issue | 1792 | |
P577 | publication date | 2014-10-01 | |
P1433 | published in | Proceedings of the Royal Society B | Q2625424 |
P1476 | title | Stress-induced mutagenesis and complex adaptation | |
P478 | volume | 281 |
Q36395746 | A shifting mutational landscape in 6 nutritional states: Stress-induced mutagenesis as a series of distinct stress input-mutation output relationships. |
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Q47652171 | Antibiotic resistance mutations induced in growing cells of Bacillus-related thermophiles. |
Q28547150 | Atypical Role for PhoU in Mutagenic Break Repair under Stress in Escherichia coli |
Q90505681 | Bacterial phenotypic heterogeneity in DNA repair and mutagenesis |
Q27025256 | Coping with stress and the emergence of multidrug resistance in fungi |
Q47098951 | Errors in mutagenesis and the benefit of cell-to-cell signalling in the evolution of stress-induced mutagenesis |
Q38980350 | Genetic drift, selection and the evolution of the mutation rate |
Q92752649 | Mutation rate variability as a driving force in adaptive evolution |
Q90389384 | On the feasibility of saltational evolution |
Q38670044 | Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli |
Q39005916 | Population Heterogeneity in Mutation Rate Increases the Frequency of Higher-Order Mutants and Reduces Long-Term Mutational Load. |
Q36365259 | Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli |
Q33676605 | Simplification, Innateness, and the Absorption of Meaning from Context: How Novelty Arises from Gradual Network Evolution |
Q92827050 | Somatic maintenance impacts the evolution of mutation rate |
Q64389723 | Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance |
Q39326888 | The Small RNA GcvB Promotes Mutagenic Break Repair by Opposing the Membrane Stress Response |
Q64096919 | What is mutation? A chapter in the series: How microbes "jeopardize" the modern synthesis |
Q36407945 | With a little help from my friends: cooperation can accelerate the rate of adaptive valley crossing |
Q39362711 | Zinc-Induced Transposition of Insertion Sequence Elements Contributes to Increased Adaptability of Cupriavidus metallidurans |
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