scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | P L Foster | |
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 | ||
Adaptive mutation: the uses of adversity | Q24596056 | ||
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 | ||
Initiation of genetic recombination and recombination-dependent replication | Q28141289 | ||
The origin of mutants | Q28288915 | ||
The importance of repairing stalled replication forks | Q29614220 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda | Q29619755 | ||
Are adaptive mutations due to a decline in mismatch repair? The evidence is lacking | Q33545737 | ||
Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
Coping with replication 'train wrecks' in Escherichia coli using Pol V, Pol II and RecA proteins | Q33885426 | ||
Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
The SOS response regulates adaptive mutation | Q33903483 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
Antimutator mutations in the alpha subunit of Escherichia coli DNA polymerase III: identification of the responsible mutations and alignment with other DNA polymerases | Q33961328 | ||
Population dynamics of a Lac- strain of Escherichia coli during selection for lactose utilization | Q33963607 | ||
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 | ||
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 | ||
Reverse branch migration of Holliday junctions by RecG protein: a new mechanism for resolution of intermediates in recombination and DNA repair. | Q54649605 | ||
Mechanism for induction of adaptive mutations in Escherichia coli. | Q54715058 | ||
Enzymes of evolutionary change | Q56902070 | ||
F- phenocopies: characterization of expression of the F transfer region in stationary phase | Q58010899 | ||
A unicorn in the garden | Q59085860 | ||
The role of oriT in tra-dependent enhanced recombination between mini-F-lac-oriT and lambda plac5 | Q64389911 | ||
Role of Escherichia coli RecBC enzyme in SOS induction | Q69926365 | ||
Mutagenic specificity of ultraviolet light | Q69946985 | ||
Genetic and sequence analysis of frameshift mutations induced by ICR-191 | Q70226477 | ||
Observations on the formation of clones containing araB-lacZ cistron fusions | Q72815889 | ||
The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
Modulation of RNA polymerase by (p)ppGpp reveals a RecG-dependent mechanism for replication fork progression | Q73707166 | ||
RuvAB acts at arrested replication forks | Q77550034 | ||
Is DNA replication a necessary condition for spontaneous mutation? | Q79007527 | ||
Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation | Q33966750 | ||
Differential suppression of priA2::kan phenotypes in Escherichia coli K-12 by mutations in priA, lexA, and dnaC | Q33967442 | ||
A role for REV3 in mutagenesis during double-strand break repair in Saccharomyces cerevisiae | Q33971118 | ||
Spontaneous Mutation in Non-Dividing Bacteria. | Q33976223 | ||
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 | ||
Adaptive mutation: has the unicorn landed? | Q34603905 | ||
Increased episomal replication accounts for the high rate of adaptive mutation in recD mutants of Escherichia coli | Q34606847 | ||
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 end repair via the RecBC pathway in Escherichia coli primes DNA replication | Q35188037 | ||
UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
A phenotype for enigmatic DNA polymerase II: a pivotal role for pol II in replication restart in UV-irradiated Escherichia coli | Q35600177 | ||
The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair | Q35603171 | ||
Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
Involvement of Escherichia coli DNA polymerase II in response to oxidative damage and adaptive mutation | Q35979376 | ||
Is RecF a DNA replication protein? | Q36152798 | ||
Spontaneous and UV-induced mutations in Escherichia coli K-12 strains with altered or absent DNA polymerase I. | Q36176656 | ||
The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription | Q36574251 | ||
Enhanced recombination between lambda plac5 and F42lac: identification of cis- and trans-acting factors | Q37579071 | ||
Lac repressor can be fused to β-galactosidase | Q38361160 | ||
Conjugation is not required for adaptive reversion of an episomal frameshift mutation in Escherichia coli | Q39839215 | ||
Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | Q39841075 | ||
Resolution of Holliday intermediates in recombination and DNA repair: indirect suppression of ruvA, ruvB, and ruvC mutations. | Q39929442 | ||
Evidence that recBC-dependent degradation of duplex DNA in Escherichia coli recD mutants involves DNA unwinding | Q39935833 | ||
Genetic analysis of the recG locus of Escherichia coli K-12 and of its role in recombination and DNA repair | Q39938960 | ||
traY and traI are required for oriT-dependent enhanced recombination between lac-containing plasmids and lambda plac5 | Q39938974 | ||
Collapse and repair of replication forks in Escherichia coli | Q40416038 | ||
Branch migration of three-strand recombination intermediates by RecG, a possible pathway for securing exchanges initiated by 3′-tailed duplex DNA | Q40788775 | ||
Mechanisms of directed mutation | Q41110210 | ||
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 | ||
Mutation and cancer: the antecedents to our studies of adaptive mutation. | Q41749616 | ||
Transient mutators: a semiquantitative analysis of the influence of translation and transcription errors on mutation rates | Q41999710 | ||
A genetic strategy to demonstrate the occurrence of spontaneous mutations in nondividing cells within colonies of Escherichia coli | Q42968100 | ||
Evidence that gene amplification underlies adaptive mutability of the bacterial lac operon | Q50128814 | ||
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 21-29 | |
P577 | publication date | 2000-01-01 | |
P1433 | published in | Cold Spring Harbor Symposia on Quantitative Biology | Q15758412 |
P1476 | title | Adaptive mutation in Escherichia coli. | |
P478 | volume | 65 |
Q36966953 | A novel mutator of Escherichia coli carrying a defect in the dgt gene, encoding a dGTP triphosphohydrolase. |
Q35971761 | Adaptation prevents the extinction of Chlamydomonas reinhardtii under toxic beryllium. |
Q59757712 | Adaptive mutation in Escherichia coli |
Q24623723 | Adaptive mutation: implications for evolution |
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. |
Q35760045 | Catastrophe and what to do about it if you are a bacterium: the importance of frameshift mutants |
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 |
Q36878608 | Competitive fitness during feast and famine: how SOS DNA polymerases influence physiology and evolution in Escherichia coli |
Q37358566 | DNA damage tolerance and a web of connections with DNA repair at Yale |
Q36268415 | Determinants of spontaneous mutation in the bacterium Escherichia coli as revealed by whole-genome sequencing |
Q35806050 | Development of a stress-induced mutagenesis module for autonomous adaptive evolution of Escherichia coli to improve its stress tolerance |
Q35746786 | Double-Strand Break Repair and Holliday Junction Processing Are Required for Chromosome Processing in Stationary-Phase Escherichia coli Cells |
Q43816434 | Efficiency and accuracy of SOS-induced DNA polymerases replicating benzo[a]pyrene-7,8-diol 9,10-epoxide A and G adducts |
Q33700107 | Error-prone DNA polymerase IV is regulated by the heat shock chaperone GroE in Escherichia coli |
Q39753960 | Error-prone polymerase, DNA polymerase IV, is responsible for transient hypermutation during adaptive mutation in Escherichia coli. |
Q34049897 | Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli |
Q34907780 | Escherichia coli Rep DNA helicase and error-prone DNA polymerase IV interact physically and functionally |
Q44049947 | Fidelity of Escherichia coli DNA polymerase IV. Preferential generation of small deletion mutations by dNTP-stabilized misalignment |
Q34568150 | How nucleotide excision repair protects against cancer |
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. |
Q39694895 | Induction of a DNA nickase in the presence of its target site stimulates adaptive mutation in Escherichia coli. |
Q35913829 | Interactions and Localization of Escherichia coli Error-Prone DNA Polymerase IV after DNA Damage |
Q42126464 | Involvement of Escherichia coli DNA polymerase IV in tolerance of cytotoxic alkylating DNA lesions in vivo. |
Q34697729 | Involvement of Y-family DNA polymerases in mutagenesis caused by oxidized nucleotides in Escherichia coli |
Q40763644 | Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida |
Q46014624 | Lessons from 50 years of SOS DNA-damage-induced mutagenesis. |
Q43937118 | Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site. |
Q92256237 | Mutation and Recombination Rates Vary Across Bacterial Chromosome |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q34077193 | Mutator phenotype resulting from DNA polymerase IV overproduction in Escherichia coli: preferential mutagenesis on the lagging strand |
Q42125442 | Polyphosphate kinase regulates error-prone replication by DNA polymerase IV in Escherichia coli |
Q43944895 | Replication restart in UV-irradiated Escherichia coli involving pols II, III, V, PriA, RecA and RecFOR proteins |
Q77322177 | Resolving a fidelity paradox: why Escherichia coli DNA polymerase II makes more base substitution errors in AT- compared with GC-rich DNA |
Q35130259 | Role of DNA polymerase IV in Escherichia coli SOS mutator activity |
Q33639091 | Role of Escherichia coli DNA polymerase I in chromosomal DNA replication fidelity |
Q35271644 | Role of Escherichia coli DNA polymerase IV in in vivo replication fidelity |
Q36483171 | Role of accessory DNA polymerases in DNA replication in Escherichia coli: analysis of the dnaX36 mutator mutant |
Q24631035 | Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli |
Q42738196 | RpoS, the stress response sigma factor, plays a dual role in the regulation of Escherichia coli's error-prone DNA polymerase IV. |
Q24530758 | SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness |
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 |
Q35986593 | Stress responses and genetic variation in bacteria. |
Q40459862 | Stress-Induced Mutagenesis. |
Q36961683 | Stress-induced mutagenesis in bacteria. |
Q35037449 | The "A" rule revisited: polymerases as determinants of mutational specificity |
Q41996473 | The Escherichia coli histone-like protein HU has a role in stationary phase adaptive mutation |
Q38541782 | The Origin of Mutants Under Selection: How Natural Selection Mimics Mutagenesis (Adaptive Mutation) |
Q34491677 | The SMC-like protein complex SbcCD enhances DNA polymerase IV-dependent spontaneous mutation in Escherichia coli |
Q35098519 | The dinB operon and spontaneous mutation in Escherichia coli |
Q34017416 | The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli |
Q42916075 | The transcription elongation factor NusA is required for stress-induced mutagenesis in Escherichia coli |
Q46375749 | To slip or skip, visualizing frameshift mutation dynamics for error-prone DNA polymerases |
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