| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2001PNAS...98.8334B |
| P356 | DOI | 10.1073/PNAS.151009798 |
| P932 | PMC publication ID | 37440 |
| P698 | PubMed publication ID | 11459972 |
| P5875 | ResearchGate publication ID | 11881986 |
| P2093 | author name string | M J Lombardo | |
| S M Rosenberg | |||
| H J Bull | |||
| 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 | ||
| Multiple pathways for SOS-induced mutagenesis in Escherichia coli: an overexpression of dinB/dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA | Q24628966 | ||
| Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli | Q24631035 | ||
| One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
| Break-induced replication: a review and an example in budding yeast | Q27933666 | ||
| The origin of mutants | Q28288915 | ||
| The distribution of the numbers of mutants in bacterial populations | Q29620123 | ||
| Somatic hypermutation and the three R's: repair, replication and recombination | Q33545735 | ||
| Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
| Mechanisms of genome-wide hypermutation in stationary phase | Q33692333 | ||
| cAMP-dependent SOS induction and mutagenesis in resting bacterial populations. | Q33719467 | ||
| Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| The SOS response regulates adaptive mutation | Q33903483 | ||
| Mutation frequencies and antibiotic resistance | Q33945503 | ||
| SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification | Q33953638 | ||
| Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
| DNA synthesis errors associated with double-strand-break repair | Q33965497 | ||
| 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 | ||
| Chromosome brekage accompanying genetic recombination in bacteriophage | Q33970377 | ||
| A role for REV3 in mutagenesis during double-strand break repair in Saccharomyces cerevisiae | Q33971118 | ||
| Rec-mediated recombinational hot spot activity in bacteriophage lambda. I. Hot spot activity associated with spi-deletions and bio substitutions. | Q33989752 | ||
| Escherichia coli DNA polymerase IV mutator activity: genetic requirements and mutational specificity | Q33994529 | ||
| radC102 of Escherichia coli is an allele of recG | Q33994900 | ||
| Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. | Q34019746 | ||
| Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation | Q34229499 | ||
| Adaptive mutation in Escherichia coli: a role for conjugation. | Q34308488 | ||
| Recombination and recombination-dependent DNA replication in bacteriophage T4. | Q34490524 | ||
| Transient and heritable mutators in adaptive evolution in the lab and in nature | Q34603730 | ||
| The chromosome bias of misincorporations during double-strand break repair is not altered in mismatch repair-defective strains of Saccharomyces cerevisiae. | Q34604064 | ||
| Some features of the mutability of bacteria during nonlethal selection | Q34608581 | ||
| Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination | Q34609122 | ||
| Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo | Q35208627 | ||
| Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
| Recent horizontal transmission of plasmids between natural populations of Escherichia coli and Salmonella enterica | Q35620558 | ||
| The many faces of DNA polymerases: strategies for mutagenesis and for mutational avoidance | Q36099918 | ||
| Selection for loss of tetracycline resistance by Escherichia coli. | Q36322268 | ||
| The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
| DNA-damaging agents stimulate gene expression at specific loci in Escherichia coli | Q36389606 | ||
| 7 Uses of transposons with emphasis on Tn10 | Q36439570 | ||
| Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections. | Q36574313 | ||
| The origin of point mutations in human tumor cells | Q36729577 | ||
| Two recombination-dependent DNA replication pathways of bacteriophage T4, and their roles in mutagenesis and horizontal gene transfer | Q37095668 | ||
| Accuracy of lesion bypass by yeast and human DNA polymerase eta. | Q37097247 | ||
| The roles of starvation and selective substrates in the emergence of araB-lacZ fusion clones. | Q37638181 | ||
| Conjugation is not required for adaptive reversion of an episomal frameshift mutation in Escherichia coli | Q39839215 | ||
| Resolution of Holliday intermediates in recombination and DNA repair: indirect suppression of ruvA, ruvB, and ruvC mutations. | Q39929442 | ||
| Genetic analysis of the recG locus of Escherichia coli K-12 and of its role in recombination and DNA repair | Q39938960 | ||
| Somatic hypermutation: how many mechanisms diversify V region sequences? | Q40410605 | ||
| Adaptive evolution of highly mutable loci in pathogenic bacteria | Q40629814 | ||
| Chapter 1 Measuring Spontaneous Mutation Rates in Yeast | Q40936432 | ||
| Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
| Mutation for survival | Q41703503 | ||
| The contribution of bacterial hypermutators to mutation in stationary phase | Q42551098 | ||
| Recombination-dependent mutation in Escherichia coli occurs in stationary phase | Q42573518 | ||
| Mosaic structure of plasmids from natural populations of Escherichia coli. | Q42966739 | ||
| A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. | Q54567733 | ||
| Evidence that F plasmid transfer replication underlies apparent adaptive mutation. | Q54613748 | ||
| Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
| Recombination in adaptive mutation. | Q54635736 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| Genetic analysis of mutagenesis in aging Escherichia coli colonies | Q56944661 | ||
| Maturation and recombination of bacteriophage lambda DNA molecules in the absence of DNA duplication | Q69194016 | ||
| Role of Escherichia coli RecBC enzyme in SOS induction | Q69926365 | ||
| Characterization of a New Radiation-Sensitive Mutant, Escherichia coli K-12 radC102 | Q70358438 | ||
| Genetics of selection-induced mutations: I. uvrA, uvrB, uvrC, and uvrD are selection-induced specific mutator loci | Q72151726 | ||
| The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
| Starvation-induced Mucts62-mediated coding sequence fusion: a role for ClpXP, Lon, RpoS and Crp | Q77410696 | ||
| EXO1 of Saccharomyces cerevisiae functions in mutagenesis during double-strand break repair | Q78026677 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 8334-8341 | |
| P577 | publication date | 2001-07-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence | |
| P478 | volume | 98 |
| Q42274110 | A ΔdinB mutation that sensitizes Escherichia coli to the lethal effects of UV- and X-radiation |
| Q24796250 | Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms |
| Q35893213 | Adaptive mutation: how growth under selection stimulates Lac(+) reversion by increasing target copy number |
| Q41073516 | Adaptive point mutation and adaptive amplification pathways in the Escherichia coli Lac system: stress responses producing genetic change |
| Q34599104 | Amplification of lac cannot account for adaptive mutation to Lac+ in Escherichia coli. |
| Q34012598 | Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification |
| Q35760045 | Catastrophe and what to do about it if you are a bacterium: the importance of frameshift mutants |
| Q36742888 | Conserved rates and patterns of transcription errors across bacterial growth states and lifestyles |
| Q36961674 | Controlling mutation: intervening in evolution as a therapeutic strategy |
| Q26825267 | Culture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transition |
| Q43264411 | Degradation of nitroaromatic compounds: a model to study evolution of metabolic pathways |
| Q39680847 | Different spectra of stationary-phase mutations in early-arising versus late-arising mutants of Pseudomonas putida: involvement of the DNA repair enzyme MutY and the stationary-phase sigma factor RpoS. |
| Q36178618 | Diversify or die: generation of diversity in response to stress. |
| Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
| Q30989309 | Evidence that mutation is universally biased towards AT in bacteria |
| Q24542676 | Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability |
| Q34297067 | Evolving responsively: adaptive mutation |
| Q39714248 | Formation of an F' plasmid by recombination between imperfectly repeated chromosomal Rep sequences: a closer look at an old friend (F'(128) pro lac). |
| Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
| Q35170976 | Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli |
| Q35037445 | In pursuit of a molecular mechanism for adaptive gene amplification |
| Q38339816 | Increased dNTP binding affinity reveals a nonprocessive role for Escherichia coli beta clamp with DNA polymerase IV. |
| Q21146100 | Inhibition of mutation and combating the evolution of antibiotic resistance |
| Q40763644 | Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida |
| Q24651873 | Is evolution Darwinian or/and Lamarckian? |
| Q35028138 | Minisatellite alterations in ZRT1 mutants occur via RAD52-dependent and RAD52-independent mechanisms in quiescent stationary phase yeast cells |
| Q54692751 | Modulation of base-specific mutation and recombination rates enables functional adaptation within the context of the genetic code. |
| Q33373675 | Mutability and importance of a hypermutable cell subpopulation that produces stress-induced mutants in Escherichia coli |
| Q92256237 | Mutation and Recombination Rates Vary Across Bacterial Chromosome |
| Q35869358 | Mutation as a stress response and the regulation of evolvability |
| Q44455145 | Mutations arise independently of transcription in non-dividing bacteria |
| Q42203307 | Near-zero growth kinetics of Pseudomonas putida deduced from proteomic analysis |
| Q42412527 | Oxidative DNA damage defense systems in avoidance of stationary-phase mutagenesis in Pseudomonas putida |
| Q38670044 | Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli |
| Q27308031 | Phenotypic variation in the plant pathogenic bacterium Acidovorax citrulli |
| Q41090654 | Processing closely spaced lesions during Nucleotide Excision Repair triggers mutagenesis in E. coli. |
| Q33282780 | Protecting exons from deleterious R-loops: a potential advantage of having introns |
| Q37672417 | RNA Primer Extension Hinders DNA Synthesis by Escherichia coli Mutagenic DNA Polymerase IV. |
| Q34617476 | Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. |
| Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
| Q36365259 | Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli |
| Q34119281 | Separate DNA Pol II- and Pol IV-dependent pathways of stress-induced mutation during double-strand-break repair in Escherichia coli are controlled by RpoS. |
| Q34514283 | Single-strand-specific exonucleases prevent frameshift mutagenesis by suppressing SOS induction and the action of DinB/DNA polymerase IV in growing cells |
| Q36961669 | Stationary phase mutagenesis in B. subtilis: a paradigm to study genetic diversity programs in cells under stress |
| Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
| Q37274991 | Steric gate variants of UmuC confer UV hypersensitivity on Escherichia coli. |
| Q37355812 | Stress-induced beta-lactam antibiotic resistance mutation and sequences of stationary-phase mutations in the Escherichia coli chromosome. |
| Q36496909 | Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine |
| Q35037449 | The "A" rule revisited: polymerases as determinants of mutational specificity |
| Q36588940 | The DNA polymerase III holoenzyme contains γ and is not a trimeric polymerase |
| Q34570766 | The amplification model for adaptive mutation: simulations and analysis. |
| Q42676720 | The mutational specificity of the Dbh lesion bypass polymerase and its implications |
| Q35013053 | The nonmutagenic repair of broken replication forks via recombination |
| Q41862731 | The optimal burst of mutation to create a phenotype |
| Q34509062 | Translesion DNA Synthesis |
| Q34356338 | Translesion DNA polymerases |
| Q36713351 | Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli |
| Q37976150 | What limits the efficiency of double-strand break-dependent stress-induced mutation in Escherichia coli? |
| Q36416305 | Zinc regulates the stability of repetitive minisatellite DNA tracts during stationary phase |
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