review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | John R Roth | |
Sophie Maisnier-Patin | |||
P2860 | cites work | Spontaneous point mutations that occur more often when advantageous than when neutral | Q24532456 |
Mutations of Bacteria from Virus Sensitivity to Virus Resistance | Q24533278 | ||
Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability | Q24542676 | ||
Adaptive mutation: the uses of adversity | Q24596056 | ||
The tandem inversion duplication in Salmonella enterica: selection drives unstable precursors to final mutation types | Q24616733 | ||
Ohno's dilemma: evolution of new genes under continuous selection | Q24675391 | ||
Replica plating and indirect selection of bacterial mutants | Q24676225 | ||
Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms | Q24796250 | ||
The origin of mutants | Q28288915 | ||
Poxviruses deploy genomic accordions to adapt rapidly against host antiviral defenses | Q28712008 | ||
On the mechanism of gene amplification induced under stress in Escherichia coli | Q33239373 | ||
Duplication frequency in a population of Salmonella enterica rapidly approaches steady state with or without recombination | Q33834935 | ||
Short palindromic repetitive DNA elements in enterobacteria: a survey | Q33836563 | ||
Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
Amplification of the gene for isoleucyl-tRNA synthetase facilitates adaptation to the fitness cost of mupirocin resistance in Salmonella enterica | Q33853188 | ||
Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification | Q33953638 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
An examination of adaptive reversion in Saccharomyces cerevisiae | Q33959891 | ||
Population dynamics of a Lac- strain of Escherichia coli during selection for lactose utilization | Q33963607 | ||
Two enzymes, both of which process recombination intermediates, have opposite effects on adaptive mutation in Escherichia coli. | Q33966542 | ||
Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation | Q33966750 | ||
Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification | Q34012598 | ||
Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli | Q34049897 | ||
Adaptive mutation in Escherichia coli | Q34088211 | ||
Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation | Q34229499 | ||
Evolving responsively: adaptive mutation | Q34297067 | ||
Real-time evolution of new genes by innovation, amplification, and divergence | Q34307457 | ||
Adaptive mutation in Escherichia coli: a role for conjugation. | Q34308488 | ||
Amplification-mutagenesis--how growth under selection contributes to the origin of genetic diversity and explains the phenomenon of adaptive mutation | Q34327959 | ||
Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis | Q34436201 | ||
Roles of E. coli double-strand-break-repair proteins in stress-induced mutation | Q34470485 | ||
Plasmid copy number underlies adaptive mutability in bacteria | Q34471714 | ||
Gene amplification in cancer | Q34540289 | ||
Reducing the fitness cost of antibiotic resistance by amplification of initiator tRNA genes | Q34598420 | ||
Y-family DNA polymerases in Escherichia coli | Q34598779 | ||
Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination | Q34609122 | ||
Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. | Q34617476 | ||
General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli | Q34643555 | ||
Multiple pathways of selected gene amplification during adaptive mutation. | Q35125285 | ||
Transposon stability and a role for conjugational transfer in adaptive mutability | Q35159404 | ||
Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli | Q35170976 | ||
Unicorns revisited | Q35574042 | ||
Redundant homosexual F transfer facilitates selection-induced reversion of plasmid mutations | Q35607773 | ||
Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
Adaptive mutation and amplification in Escherichia coli: two pathways of genome adaptation under stress | Q35811218 | ||
Mutation as a stress response and the regulation of evolvability | Q35869358 | ||
Stress responses and genetic variation in bacteria. | Q35986593 | ||
Multiple pathways of duplication formation with and without recombination (RecA) in Salmonella enterica. | Q36268081 | ||
Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. | Q36339832 | ||
The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
Environmental stress and lesion-bypass DNA polymerases | Q36486062 | ||
Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine | Q36496909 | ||
Origin of mutations under selection: the adaptive mutation controversy. | Q36500577 | ||
Adaptive mutation: General mutagenesis is not a programmed response to stress but results from rare coamplification of dinB with lac | Q36689838 | ||
Stress-induced mutagenesis in bacteria. | Q36961683 | ||
DinB upregulation is the sole role of the SOS response in stress-induced mutagenesis in Escherichia coli | Q37173424 | ||
Bacterial gene amplification: implications for the evolution of antibiotic resistance | Q37553896 | ||
The roles of starvation and selective substrates in the emergence of araB-lacZ fusion clones. | Q37638181 | ||
Escherichia coli Y family DNA polymerases | Q37881670 | ||
Formation of an F' plasmid by recombination between imperfectly repeated chromosomal Rep sequences: a closer look at an old friend (F'(128) pro lac). | Q39714248 | ||
Conjugation is not required for adaptive reversion of an episomal frameshift mutation in Escherichia coli | Q39839215 | ||
Mechanisms of directed mutation | Q41110210 | ||
Methods for determining spontaneous mutation rates | Q42620101 | ||
Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence. | Q42960926 | ||
Contribution of gene amplification to evolution of increased antibiotic resistance in Salmonella typhimurium | Q43067316 | ||
Roles of chromosomal and episomal dinB genes encoding DNA pol IV in targeted and untargeted mutagenesis in Escherichia coli. | Q43781879 | ||
Escape from growth restriction in small colony variants of Salmonella typhimurium by gene amplification and mutation | Q50044240 | ||
A switch from high-fidelity to error-prone DNA double-strand break repair underlies stress-induced mutation. | Q54478818 | ||
Evidence that F plasmid transfer replication underlies apparent adaptive mutation. | Q54613748 | ||
Recombination in adaptive mutation. | Q54635736 | ||
Origin of bacterial variants. | Q55047163 | ||
A unicorn in the garden | Q59085860 | ||
The Origin of Mutants under Selection: Interactions of Mutation, Growth, and Selection | Q60921362 | ||
Evidence that DNA helicase I and oriT site-specific nicking are both functions of the F TraI protein | Q69847405 | ||
Stimulation of precise excision and recombination by conjugal proficient F'plasmids | Q69882483 | ||
Observations on the formation of clones containing araB-lacZ cistron fusions | Q72815889 | ||
P433 | issue | 7 | |
P304 | page(s) | a018176 | |
P577 | publication date | 2015-07-01 | |
P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
P1476 | title | The Origin of Mutants Under Selection: How Natural Selection Mimics Mutagenesis (Adaptive Mutation) | |
P478 | volume | 7 |
Q42357050 | Classic Spotlight: Look, Max-No Math Required! |
Q50428952 | Evolutionary biology today and the call for an extended synthesis |
Q42267578 | Generation of mutation hotspots in ageing bacterial colonies |
Q36308276 | Hierarchical mutational events compensate for glutamate auxotrophy of a Bacillus subtilis gltC mutant. |
Q40987278 | Hopping into a hot seat: Role of DNA structural features on IS5-mediated gene activation and inactivation under stress |
Q53061267 | Inducing stable reversion to achieve cancer control. |
Q40559189 | Natural selection underlies apparent stress-induced mutagenesis in a bacteriophage infection model. |
Q38820376 | Phenotypic heterogeneity in a bacteriophage population only appears as stress-induced mutagenesis. |
Q49388555 | Recombination Is Responsible for the Increased Recovery of Drug-Resistant Mutants with Hypermutated Genomes in Resting Yeast Diploids Expressing APOBEC Deaminases. |
Q36709418 | Reinterpreting Long-Term Evolution Experiments: Is Delayed Adaptation an Example of Historical Contingency or a Consequence of Intermittent Selection? |
Q50186955 | Selection-Enhanced Mutagenesis of lac Genes Is Due to Their Co-amplification with dinB Encoding an Error-Prone DNA Polymerase |
Q90021671 | The Role of Mutation Bias in Adaptive Evolution |
Q53254709 | The sources of adaptive variation. |
Q90433877 | Transposable element insertions in fission yeast drive adaptation to environmental stress |
Q42795926 | Transposon-mediated activation of the Escherichia coli glpFK operon is inhibited by specific DNA-binding proteins: Implications for stress-induced transposition events |
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