| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1046/J.1462-2920.2003.00488.X |
| P953 | full work available at URL | http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1462-2920.2003.00488.x/fullpdf |
| https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1462-2920.2003.00488.x | ||
| P698 | PubMed publication ID | 14510835 |
| P5875 | ResearchGate publication ID | 9079060 |
| P50 | author | Maia Kivisaar | Q20528388 |
| P2860 | cites work | Lateral gene transfer and the nature of bacterial innovation | Q22122396 |
| Selfish genes, the phenotype paradigm and genome evolution | Q22122418 | ||
| SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness | Q24530758 | ||
| Altered nucleotide misinsertion fidelity associated with poliota-dependent replication at the end of a DNA template. | Q24535441 | ||
| Variations in rRNA content of marine Vibrio spp. during starvation-survival and recovery | Q39891881 | ||
| Adaptive evolution of highly mutable loci in pathogenic bacteria | Q40629814 | ||
| An active DNA transposon family in rice | Q40678570 | ||
| AID is essential for immunoglobulin V gene conversion in a cultured B cell line | Q40746479 | ||
| Genetic barriers among bacteria. | Q41120565 | ||
| Genome organization, natural genetic engineering and adaptive mutation | Q41379575 | ||
| Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
| Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis | Q41734679 | ||
| Enrichment and elimination of mutY mutators in Escherichia coli populations | Q42031695 | ||
| An aerobic recA-, umuC-dependent pathway of spontaneous base-pair substitution mutagenesis in Escherichia coli | Q42498856 | ||
| UV light induces IS10 transposition in Escherichia coli. | Q42571999 | ||
| The length of a tetranucleotide repeat tract in Haemophilus influenzae determines the phase variation rate of a gene with homology to type III DNA methyltransferases. | Q42617085 | ||
| Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation | Q42674600 | ||
| Sequence analysis of mutations arising during prolonged starvation of Salmonella typhimurium | Q42861600 | ||
| Bacterial Community Structure in Relation to the Carbon Environments in Lettuce and Tomato Rhizospheres and in Bulk Soil | Q43982690 | ||
| Immunology: the roots of antibody diversity | Q44127132 | ||
| Immunoglobulin isotype switching is inhibited and somatic hypermutation perturbed in UNG-deficient mice | Q44194766 | ||
| Analysis of the stimulation of DNA polymerase V of Escherichia coli by processivity proteins | Q44228115 | ||
| Environmentally directed mutations in the dehalogenase system of Pseudomonas putida strain PP3. | Q45270028 | ||
| Mutators in Escherichia coli | Q46057951 | ||
| All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis | Q24597093 | ||
| Adaptive mutation: implications for evolution | Q24623723 | ||
| 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 | ||
| Managing DNA polymerases: coordinating DNA replication, DNA repair, and DNA recombination | Q24631110 | ||
| DNA polymerase eta is an A-T mutator in somatic hypermutation of immunoglobulin variable genes | Q28190856 | ||
| AID mutates E. coli suggesting a DNA deamination mechanism for antibody diversification | Q28208979 | ||
| DNA mismatch repair and mutation avoidance pathways | Q28211143 | ||
| Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
| MutT protein specifically hydrolyses a potent mutagenic substrate for DNA synthesis | Q28343030 | ||
| Characterization of the GO system of Pseudomonas aeruginosa | Q28492940 | ||
| The significance of responses of the genome to challenge | Q28913697 | ||
| Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG | Q29616532 | ||
| Insertion sequence-related genetic variation in resting Escherichia coli K-12. | Q30011213 | ||
| The beta clamp targets DNA polymerase IV to DNA and strongly increases its processivity | Q30641251 | ||
| New data on excisions of Mu from E. coli MCS2 cast doubt on directed mutation hypothesis | Q30670768 | ||
| Somatic hypermutation and the three R's: repair, replication and recombination | Q33545735 | ||
| Are adaptive mutations due to a decline in mismatch repair? The evidence is lacking | Q33545737 | ||
| Molecular cloning and functional analysis of the MutY homolog of Deinococcus radiodurans | Q33553542 | ||
| The mutY gene: a mutator locus in Escherichia coli that generates G.C----T.A transversions | Q33567384 | ||
| The extreme mutator effect of Escherichia coli mutD5 results from saturation of mismatch repair by excessive DNA replication errors | Q33586319 | ||
| Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
| cAMP-dependent SOS induction and mutagenesis in resting bacterial populations. | Q33719467 | ||
| Molecular switches--the ON and OFF of bacterial phase variation. | Q33727880 | ||
| Adaptation to the environment: Streptococcus pneumoniae, a paradigm for recombination-mediated genetic plasticity? | Q33826507 | ||
| Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
| Homeologous recombination and mismatch repair during transformation in Streptococcus pneumoniae: saturation of the Hex mismatch repair system | Q33883002 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| Mutation frequencies and antibiotic resistance | Q33945503 | ||
| Evolution-driving genes | Q33949870 | ||
| SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification | Q33953638 | ||
| Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
| 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 | ||
| Evidence for the adaptive evolution of mutation rates | Q33967135 | ||
| High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
| Evolutionary implications of the frequent horizontal transfer of mismatch repair genes | Q50117948 | ||
| Changes in viability and macromolecular content of long-term batch cultures of Salmonella typhimurium measured by flow cytometry | Q50119830 | ||
| Evidence that gene amplification underlies adaptive mutability of the bacterial lac operon | Q50128814 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| Damage-repair error-prone polymerases of eubacteria: association with mobile genome elements. | Q54541302 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| Microbial genetics. Hypermutation under stress. | Q54564293 | ||
| Effect of mutY and mutM/fpg-1 mutations on starvation-associated mutation in Escherichia coli: implications for the role of 7,8-dihydro-8-oxoguanine. | Q54587020 | ||
| Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
| IncN plasmids mediate UV resistance and error-prone repair in Pseudomonas aeruginosa PAO. | Q54644118 | ||
| Isolation and characterization of the Escherichia coli mutL gene product. | Q54734906 | ||
| Adaptive radiation in a heterogeneous environment | Q56038387 | ||
| Enzymes of evolutionary change | Q56902070 | ||
| Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli | Q56944671 | ||
| Bacterial activity along a young barley root measured by the thymidine and leucine incorporation techniques | Q57265117 | ||
| Growth Rates of Bacterial Communities in Soils at Varying pH: A Comparison of the Thymidine and Leucine Incorporation Techniques | Q57265118 | ||
| Decreased Frequency of Somatic Hypermutation and Impaired Affinity Maturation but Intact Germinal Center Formation in Mice Expressing Antisense RNA to DNA Polymerase | Q58424602 | ||
| Origin of Antibody Variation | Q59057486 | ||
| Transposable elements as mutator genes in evolution | Q59084250 | ||
| A UmuD,C-dependent pathway for spontaneous G:C to C:G transversions in stationary phase Escherichia coli mut Y | Q73094277 | ||
| Adaptive mutagenesis: a process that generates almost exclusively beneficial mutations | Q77161202 | ||
| Starvation-induced Mucts62-mediated coding sequence fusion: a role for ClpXP, Lon, RpoS and Crp | Q77410696 | ||
| The viable-but-nonculturable state induced by abiotic stress in the biocontrol agent Pseudomonas fluorescens CHA0 does not promote strain persistence in soil | Q33986994 | ||
| Role of the DmpR-mediated regulatory circuit in bacterial biodegradation properties in methylphenol-amended soils. | Q33988525 | ||
| Escherichia coli DNA polymerase IV mutator activity: genetic requirements and mutational specificity | Q33994529 | ||
| Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification | Q34012598 | ||
| Mutator clones of Neisseria meningitidis in epidemic serogroup A disease | Q34028018 | ||
| DNA mismatch repair and genetic instability | Q34090778 | ||
| Correlation of somatic hypermutation specificity and A-T base pair substitution errors by DNA polymerase eta during copying of a mouse immunoglobulin kappa light chain transgene. | Q34098247 | ||
| Error-prone repair DNA polymerases in prokaryotes and eukaryotes | Q34131455 | ||
| Altering the pathway of immunoglobulin hypermutation by inhibiting uracil-DNA glycosylase. | Q34147986 | ||
| Induction of somatic hypermutation in immunoglobulin genes is dependent on DNA polymerase iota. | Q34157224 | ||
| The simple sequence contingency loci of Haemophilus influenzae and Neisseria meningitidis | Q34187179 | ||
| Second-order selection in bacterial evolution: selection acting on mutation and recombination rates in the course of adaptation | Q34203956 | ||
| Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation | Q34229499 | ||
| Adaptive mutations in Escherichia coli as a model for the multiple mutational origins of tumors | Q34247386 | ||
| Evolving responsively: adaptive mutation | Q34297067 | ||
| Microbial Competition: Escherichia coli Mutants That Take Over Stationary Phase Cultures | Q34305902 | ||
| Adaptive mutation in Escherichia coli: a role for conjugation. | Q34308488 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| Regulation of mutY and nature of mutator mutations in Escherichia coli populations under nutrient limitation | Q34434306 | ||
| Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis | Q34436201 | ||
| High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
| Emerging links between hypermutation of antibody genes and DNA polymerases | Q34572184 | ||
| Mechanism and control of interspecies recombination in Escherichia coli. I. Mismatch repair, methylation, recombination and replication functions. | Q34605476 | ||
| 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 | ||
| Saturation of DNA mismatch repair and error catastrophe by a base analogue in Escherichia coli. | Q34615754 | ||
| Somatic hypermutation of immunoglobulin genes: merging mechanisms for genetic diversity | Q34619789 | ||
| Specialized DNA polymerases, cellular survival, and the genesis of mutations | Q34662609 | ||
| In pursuit of a molecular mechanism for adaptive gene amplification | Q35037445 | ||
| Environmental regulation of mutation rates at specific sites. | Q35058954 | ||
| Mismatch repair protein MutL becomes limiting during stationary-phase mutation | Q35190848 | ||
| Mutagenesis induced by bacterial UmuDC proteins and their plasmid homologues | Q35401590 | ||
| Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
| Promoter-creating mutations in Pseudomonas putida: a model system for the study of mutation in starving bacteria | Q36079713 | ||
| Differential activity of a transposable element in Escherichia coli colonies | Q36184008 | ||
| Expression of error-prone polymerases in BL2 cells activated for Ig somatic hypermutation | Q36533627 | ||
| Fate and activity of microorganisms introduced into soil | Q36574230 | ||
| Clusters of point mutations are found exclusively around rearranged antibody variable genes | Q36593569 | ||
| Resistance to ultraviolet light in Pseudomonas syringae: sequence and functional analysis of the plasmid-encoded rulAB genes | Q36832867 | ||
| Spontaneous mutation | Q37041840 | ||
| Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence | Q37096423 | ||
| Evidence that MutY and MutM combine to prevent mutations by an oxidatively damaged form of guanine in DNA | Q37132610 | ||
| H-NS and RpoS regulate emergence of Lac Ara+ mutants of Escherichia coli MCS2. | Q38344584 | ||
| Bacterial activity in the rhizosphere analyzed at the single-cell level by monitoring ribosome contents and synthesis rates | Q39485135 | ||
| Rapid method of determining factors limiting bacterial growth in soil. | Q39490546 | ||
| Carbon limitation induces sigma(S)-dependent gene expression in Pseudomonas fluorescens in soil | Q39491890 | ||
| Survival response and rearrangement of plasmid DNA of Lactococcus lactis during long-term starvation | Q39492823 | ||
| Analysis of the role of recA in phenotypic switching of Pseudomonas tolaasii. | Q39501425 | ||
| Initiation of biofilm formation by Pseudomonas aeruginosa 57RP correlates with emergence of hyperpiliated and highly adherent phenotypic variants deficient in swimming, swarming, and twitching motilities | Q39502437 | ||
| Phylogenetic evidence for horizontal transfer of mutS alleles among naturally occurring Escherichia coli strains | Q39502754 | ||
| Involvement of sigma(S) in starvation-induced transposition of Pseudomonas putida transposon Tn4652. | Q39504849 | ||
| Distribution of bacterial growth activity in flow-chamber biofilms | Q39527850 | ||
| Over-representation of repeats in stress response genes: a strategy to increase versatility under stressful conditions? | Q39600777 | ||
| 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. | Q39680847 | ||
| 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 | ||
| Characterization of the sediment bacterial community in groundwater discharge zones of an alkaline fen: a seasonal study | Q39802722 | ||
| Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | Q39841075 | ||
| Carbon starvation of Salmonella typhimurium does not cause a general increase of mutation rates | Q39847729 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mutagenesis | Q149299 |
| microbiology | Q7193 | ||
| biological adaptation | Q67504163 | ||
| environmental stress | Q107365219 | ||
| P304 | page(s) | 814-827 | |
| P577 | publication date | 2003-10-01 | |
| P1433 | published in | Environmental Microbiology | Q15752447 |
| P1476 | title | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress | |
| P478 | volume | 5 |
| Q36686589 | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
| Q41255353 | Contribution of increased mutagenesis to the evolution of pollutants-degrading indigenous bacteria |
| Q43264411 | Degradation of nitroaromatic compounds: a model to study evolution of metabolic pathways |
| Q25257029 | Dispersal and regulation of an adaptive mutagenesis cassette in the bacteria domain |
| Q36178618 | Diversify or die: generation of diversity in response to stress. |
| Q36888586 | Haemophilus ducreyi Seeks Alternative Carbon Sources and Adapts to Nutrient Stress and Anaerobiosis during Experimental Infection of Human Volunteers |
| Q27679167 | How Hibernation Factors RMF, HPF, and YfiA Turn Off Protein Synthesis |
| Q47933499 | Impact of a mutator phenotype on motility and cell adherence in Salmonella Heidelberg |
| Q40763644 | Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida |
| Q36369839 | Long-term survival during stationary phase: evolution and the GASP phenotype |
| Q40875540 | Molecular nature of spontaneous modifications in gacS which cause colony phase variation in Pseudomonas sp. strain PCL1171 |
| Q35844390 | Multiple environmental stress tests show no common phenotypes shared among contemporary epidemic strains of Salmonella enterica |
| Q34465215 | Mutation frequency and spectrum of mutations vary at different chromosomal positions of Pseudomonas putida |
| Q21145371 | Natural selection fails to optimize mutation rates for long-term adaptation on rugged fitness landscapes |
| Q34531199 | Nucleoid-associated proteins affect mutation dynamics in E. coli in a growth phase-specific manner |
| Q33788362 | Persistence of Streptococcus pyogenes in stationary-phase cultures |
| Q27308031 | Phenotypic variation in the plant pathogenic bacterium Acidovorax citrulli |
| Q30230558 | Plant pathogen forensics: capabilities, needs, and recommendations |
| Q42711973 | Role of Base Excision Repair (BER) in Transcription-associated Mutagenesis of Nutritionally Stressed Nongrowing Bacillus subtilis Cell Subpopulations |
| Q89636195 | Role of Mfd and GreA in Bacillus subtilis Base Excision Repair-Dependent Stationary-Phase-Mutagenesis |
| Q64923883 | Small RNA AvrA Regulates IscR to Increase the Stress Tolerances in SmpB Deficiency of Aeromonas veronii. |
| Q46500880 | Starvation/stationary-phase survival of Rhodococcus erythropolis SQ1: a physiological and genetic analysis |
| Q36961669 | Stationary phase mutagenesis in B. subtilis: a paradigm to study genetic diversity programs in cells under stress |
| Q42524666 | The prince and the pauper: which one is real? The problem of secondary mutation during mutagenesis in Streptococcus pyogenes |
| Q40546569 | The risk of low concentrations of antibiotics in agriculture for resistance in human health care |
| Q36289571 | The role of phenotypic variation in rhizosphere Pseudomonas bacteria |
| Q37586990 | The sagA/pel locus does not regulate the expression of the M protein of the M1T1 lineage of group A Streptococcus |
| Q31120058 | Transcriptional and physiological responses of Bradyrhizobium japonicum to desiccation-induced stress |
| Q54493154 | Various effects on transposition activity and survival of Escherichia coli cells due to different ELF-MF signals. |
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