| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Philip Hastings | Q89772028 |
| P2093 | author name string | Susan M Rosenberg | |
| Raul Correa | |||
| Philip C Thornton | |||
| P2860 | cites work | Free radicals and antioxidants in normal physiological functions and human disease | Q21710698 |
| Mechanisms of change in gene copy number | Q22122003 | ||
| Spontaneous point mutations that occur more often when advantageous than when neutral | Q24532456 | ||
| 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 | ||
| Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms | Q24796250 | ||
| Free radicals in the physiological control of cell function | Q27860480 | ||
| Migrating bubble during break-induced replication drives conservative DNA synthesis | Q27932674 | ||
| A switch between DNA polymerases δ and λ promotes error-free bypass of 8-oxo-G lesions | Q28279783 | ||
| The beta clamp targets DNA polymerase IV to DNA and strongly increases its processivity | Q30641251 | ||
| On the mechanism of gene amplification induced under stress in Escherichia coli | Q33239373 | ||
| Relaxation of transcription-induced negative supercoiling is an essential function of Escherichia coli DNA topoisomerase I. | Q54094644 | ||
| A sliding-clamp toolbelt binds high- and low-fidelity DNA polymerases simultaneously. | Q54478815 | ||
| A switch from high-fidelity to error-prone DNA double-strand break repair underlies stress-induced mutation. | Q54478818 | ||
| Recombination in adaptive mutation. | Q54635736 | ||
| Interplay among replicative and specialized DNA polymerases determines failure or success of translesion synthesis pathways. | Q55044345 | ||
| Template switching during break-induced replication | Q56521356 | ||
| If it smells like a unicorn · · · | Q59010359 | ||
| A unicorn in the garden | Q59085860 | ||
| Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance | Q64389723 | ||
| The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
| Activation of the bgl operon by adaptive mutation | Q74275840 | ||
| Break-induced replication occurs by conservative DNA synthesis | Q37103994 | ||
| DinB upregulation is the sole role of the SOS response in stress-induced mutagenesis in Escherichia coli | Q37173424 | ||
| Alternative lengthening of human telomeres is a conservative DNA replication process with features of break-induced replication | Q37515442 | ||
| Pif1 helicase and Polδ promote recombination-coupled DNA synthesis via bubble migration. | Q37558760 | ||
| Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase | Q37574376 | ||
| Break-induced replication: functions and molecular mechanism | Q38116136 | ||
| Cellular mechanisms and physiological consequences of redox-dependent signalling | Q38214052 | ||
| Transcription-associated mutagenesis | Q38253934 | ||
| LC-MS/MS proteomic analysis of starved Bacillus subtilis cells overexpressing ribonucleotide reductase (nrdEF): implications in stress-associated mutagenesis | Q38669825 | ||
| Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli | Q38670044 | ||
| Beta-glucoside (bgl) operon of Escherichia coli K-12: nucleotide sequence, genetic organization, and possible evolutionary relationship to regulatory components of two Bacillus subtilis genes | Q39956885 | ||
| Collapse and repair of replication forks in Escherichia coli | Q40416038 | ||
| Environmental change drives accelerated adaptation through stimulated copy number variation | Q41028053 | ||
| Dps proteins prevent Fenton-mediated oxidative damage by trapping hydroxyl radicals within the protein shell | Q43247879 | ||
| A repair system for 8-oxo-7,8-dihydrodeoxyguanine | Q43687308 | ||
| Roles of chromosomal and episomal dinB genes encoding DNA pol IV in targeted and untargeted mutagenesis in Escherichia coli. | Q43781879 | ||
| Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site. | Q43937118 | ||
| Fidelity of Escherichia coli DNA polymerase IV. Preferential generation of small deletion mutations by dNTP-stabilized misalignment | Q44049947 | ||
| Increased transcription rates correlate with increased reversion rates in leuB and argH Escherichia coli auxotrophs | Q44888185 | ||
| Mitochondrial redox signaling enables repair of injured skeletal muscle cells | Q46311660 | ||
| The importance of an interaction network for proper DNA polymerase ζ heterotetramer activity. | Q47391938 | ||
| New aspects of RNA-based regulation by Hfq and its partner sRNAs | Q47416504 | ||
| Escherichia coli cytochrome c peroxidase is a respiratory oxidase that enables the use of hydrogen peroxide as a terminal electron acceptor | Q47837168 | ||
| Functional cooperation of MutT, MutM and MutY proteins in preventing mutations caused by spontaneous oxidation of guanine nucleotide in Escherichia coli | Q49201462 | ||
| Adaptive amplification: an inducible chromosomal instability mechanism | Q50117945 | ||
| Mutability and importance of a hypermutable cell subpopulation that produces stress-induced mutants in Escherichia coli | Q33373675 | ||
| A microhomology-mediated break-induced replication model for the origin of human copy number variation | Q33404060 | ||
| Polymerase exchange on single DNA molecules reveals processivity clamp control of translesion synthesis | Q33694470 | ||
| Break-induced replication is highly inaccurate | Q33828325 | ||
| Reactive oxygen and reactive nitrogen intermediates in innate and specific immunity | Q33840513 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| The SOS response regulates adaptive mutation | Q33903483 | ||
| 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 | ||
| Medicine. Combating evolution to fight disease | Q33980301 | ||
| The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli | Q34017416 | ||
| Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli | Q34049897 | ||
| Iron and hydrogen peroxide detoxification properties of DNA-binding protein from starved cells. A ferritin-like DNA-binding protein of Escherichia coli. | Q34128990 | ||
| E. coli Transcription repair coupling factor (Mfd protein) rescues arrested complexes by promoting forward translocation | Q34135671 | ||
| General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli | Q34643555 | ||
| The dinB operon and spontaneous mutation in Escherichia coli | Q35098519 | ||
| Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli | Q35170976 | ||
| Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo | Q35208627 | ||
| Reactive oxygen species prime Drosophila haematopoietic progenitors for differentiation | Q35234787 | ||
| Clustered mutations in yeast and in human cancers can arise from damaged long single-strand DNA regions. | Q35992079 | ||
| Escherichia coli DNA polymerase IV (Pol IV), but not Pol II, dynamically switches with a stalled Pol III* replicase | Q36086538 | ||
| Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli | Q36365259 | ||
| The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
| Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine | Q36496909 | ||
| Escherichia coli DNA polymerase III is responsible for the high level of spontaneous mutations in mutT strains | Q36566407 | ||
| Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription | Q36574251 | ||
| Transpososome dynamics and regulation in Tn10 transposition | Q36648422 | ||
| DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage. | Q36663129 | ||
| Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli | Q36713351 | ||
| R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli | Q37025967 | ||
| Real-time transposable element activity in individual live cells. | Q37065183 | ||
| Single-strand interruptions in replicating chromosomes cause double-strand breaks | Q37093293 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 4 | |
| P921 | main subject | stress | Q123414 |
| DNA repair | Q210538 | ||
| P304 | page(s) | 769-776 | |
| P577 | publication date | 2018-01-02 | |
| 2018-08-01 | |||
| P1433 | published in | Current Genetics | Q15765847 |
| P1476 | title | Oxygen and RNA in stress-induced mutation | |
| P478 | volume | 64 |
| Q92083775 | Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. | cites work | P2860 |
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