| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/EMBOJ/16.11.3303 |
| P953 | full work available at URL | http://emboj.embopress.org/content/16/11/3303.full.pdf |
| https://europepmc.org/articles/PMC1169946 | ||
| https://europepmc.org/articles/PMC1169946?pdf=render | ||
| https://doi.org/10.1093/emboj/16.11.3303 | ||
| https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1093%2Femboj%2F16.11.3303 | ||
| https://onlinelibrary.wiley.com/doi/full/10.1093/emboj/16.11.3303 | ||
| P932 | PMC publication ID | 1169946 |
| P698 | PubMed publication ID | 9214645 |
| P5875 | ResearchGate publication ID | 14004147 |
| P50 | author | Susan M Rosenberg | Q89466623 |
| P2093 | author name string | R. S. Harris | |
| C. Thulin | |||
| J. Nagendran | |||
| J. Torkelson | |||
| M. J. Lombardo | |||
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| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | evolution | Q1063 |
| mutagenesis | Q149299 | ||
| genetic recombination | Q211675 | ||
| bacterial genome | Q4839988 | ||
| P304 | page(s) | 3303-3311 | |
| P577 | publication date | 1997-06-01 | |
| 1997-06-02 | |||
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | |
| P478 | volume | 16 |
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| Q34603905 | Adaptive mutation: has the unicorn landed? |
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| Q24623723 | Adaptive mutation: implications for evolution |
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| Q31881456 | Adaptive reversions of a frameshift mutation in arrested Saccharomyces cerevisiae cells by simple deletions in mononucleotide repeats |
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| 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 |
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| Q36499774 | Bacterial stationary-state mutagenesis and Mammalian tumorigenesis as stress-induced cellular adaptations and the role of epigenetics |
| Q39847729 | Carbon starvation of Salmonella typhimurium does not cause a general increase of mutation rates |
| Q35760045 | Catastrophe and what to do about it if you are a bacterium: the importance of frameshift mutants |
| Q35013064 | Cell-selfish modes of evolution and mutations directed after transcriptional bypass |
| Q73197734 | Characterization of an OprF-deficient mutant suggests that OprF is an essential protein for Pseudomonas fluorescens strain MF0 |
| Q33943859 | Clusters of mutations from transient hypermutability |
| Q33594339 | Competition of Escherichia coli DNA polymerases I, II and III with DNA Pol IV in stressed cells |
| Q38446575 | Competitive growth advantage of nontoxigenic mutants in the stationary phase in archival cultures of pathogenic Vibrio cholerae strains |
| Q28658067 | Constraint and opportunity in genome innovation |
| Q33692357 | Contingency loci, mutator alleles, and their interactions. Synergistic strategies for microbial evolution and adaptation in pathogenesis |
| Q55162233 | Death and population dynamics affect mutation rate estimates and evolvability under stress in bacteria. |
| Q50130080 | Detection of mutator subpopulations in Salmonella typhimurium LT2 by reversion of his alleles |
| 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. |
| Q37173424 | DinB upregulation is the sole role of the SOS response in stress-induced mutagenesis in Escherichia coli |
| Q39477342 | Effect of drug concentration on emergence of macrolide resistance in Mycobacterium avium |
| Q28346858 | Effect of endogenous carotenoids on "adaptive" mutation in Escherichia coli FC40 |
| Q34195488 | Effect of growth under selection on appearance of chromosomal mutations in Salmonella enterica |
| Q42719517 | Effect of translesion DNA polymerases, endonucleases and RpoS on mutation rates in Salmonella typhimurium |
| Q36788747 | Empirical laws of survival and evolution: their universality and implications |
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| Q35037445 | In pursuit of a molecular mechanism for adaptive gene amplification |
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| Q39694895 | Induction of a DNA nickase in the presence of its target site stimulates adaptive mutation in Escherichia coli. |
| Q34102811 | Interactions among strategies associated with bacterial infection: pathogenicity, epidemicity, and antibiotic resistance |
| Q89782907 | Intratumor Heterogeneity and Therapy Resistance: Contributions of Dormancy, Apoptosis Reversal (Anastasis) and Cell Fusion to Disease Recurrence |
| Q35990867 | Ionizing radiation and restriction enzymes induce microhomology-mediated illegitimate recombination in Saccharomyces cerevisiae |
| Q24651873 | Is evolution Darwinian or/and Lamarckian? |
| Q33783262 | Isolation, propagation and characterisation of Cryptosporidium. |
| Q34569161 | Isothermal amplification and molecular typing of the obligate intracellular pathogen Mycobacterium leprae isolated from tissues of unknown origins |
| Q33728224 | Levels of the Vsr endonuclease do not regulate stationary-phase reversion of a Lac- frameshift allele in Escherichia coli. |
| Q36369839 | Long-term survival during stationary phase: evolution and the GASP phenotype |
| Q33692333 | Mechanisms of genome-wide hypermutation in stationary phase |
| Q33692291 | Mechanisms of mutation in nondividing cells. Insights from the study of adaptive mutation in Escherichia coli |
| Q33847662 | Mechanisms of stationary phase mutation: a decade of adaptive mutation |
| Q42771933 | Microbiology. Antibiotic resistance, not shaken or stirred |
| Q35028138 | Minisatellite alterations in ZRT1 mutants occur via RAD52-dependent and RAD52-independent mechanisms in quiescent stationary phase yeast cells |
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| Q34471714 | Plasmid copy number underlies adaptive mutability in bacteria |
| Q73255932 | Prokaryote and eukaryote evolvability |
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| Q33953638 | SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification |
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| 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 |
| Q33545735 | Somatic hypermutation and the three R's: repair, replication and recombination |
| Q34608581 | Some features of the mutability of bacteria during nonlethal selection |
| Q42575524 | Some recollections and reflections on mutation rates. |
| Q85091258 | Spontaneous Mutation: Real-Time in Living Cells |
| Q61552520 | Starvation-associated mutagenesis in yeast Saccharomyces cerevisiae is affected by Ras2/cAMP signaling pathway |
| Q43686092 | Stationary phase deletions in Escherichia coli. I--Evidence for a new deletion pathway |
| 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 |
| Q37096423 | Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence |
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| Q35986593 | Stress responses and genetic variation in bacteria. |
| Q40459862 | Stress-Induced Mutagenesis. |
| Q64389723 | Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance |
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| Q37976153 | Stress-induced modulators of repeat instability and genome evolution |
| Q36961683 | Stress-induced mutagenesis in bacteria. |
| Q38541782 | The Origin of Mutants Under Selection: How Natural Selection Mimics Mutagenesis (Adaptive Mutation) |
| Q33903483 | The SOS response regulates adaptive mutation |
| Q39326888 | The Small RNA GcvB Promotes Mutagenic Break Repair by Opposing the Membrane Stress Response |
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| Q34570766 | The amplification model for adaptive mutation: simulations and analysis. |
| Q43993329 | The effect of genomic position on reversion of a lac frameshift mutation (lacIZ33) during non-lethal selection (adaptive mutation). |
| Q34347123 | The interface between molecular biology and cancer research |
| Q74808472 | The role of DNA damage in stationary phase ('adaptive') mutation |
| Q36384221 | The role of transient hypermutators in adaptive mutation in Escherichia coli |
| Q34616322 | The roles of REV3 and RAD57 in double-strand-break-repair-induced mutagenesis of Saccharomyces cerevisiae |
| Q34017416 | The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli |
| Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
| Q35159404 | Transposon stability and a role for conjugational transfer in adaptive mutability |
| Q27006818 | Transposon-mediated adaptive and directed mutations and their potential evolutionary benefits |
| Q36713351 | Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli |
| Q64096919 | What is mutation? A chapter in the series: How microbes "jeopardize" the modern synthesis |
| Q37976150 | What limits the efficiency of double-strand break-dependent stress-induced mutation in Escherichia coli? |
| Q33994900 | radC102 of Escherichia coli is an allele of recG |
| Q38464383 | rpoS mutants in archival cultures of Salmonella enterica serovar typhimurium |
| Q53912911 | xni-deficient Escherichia coli are proficient for recombination and multiple pathways of repair |
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