scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Bridges BA | |
P2860 | cites work | [Metastable phenotype of bacteria] | Q74774685 |
The role of DNA damage in stationary phase ('adaptive') mutation | Q74808472 | ||
Radiation-induced germline instability at minisatellite loci | Q77768546 | ||
Is DNA replication a necessary condition for spontaneous mutation? | Q79007527 | ||
Spontaneous point mutations that occur more often when advantageous than when neutral | Q24532456 | ||
Rates of spontaneous mutation | Q24548000 | ||
Adaptive mutation: the uses of adversity | Q24596056 | ||
Mechanisms of accurate translesion synthesis by human DNA polymerase eta | Q24678700 | ||
The human DINB1 gene encodes the DNA polymerase Poltheta | Q24683573 | ||
Increased spontaneous mutation and alkylation sensitivity of Escherichia coli strains lacking the ogt O6-methylguanine DNA repair methyltransferase | Q28268090 | ||
A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
The origin of mutants | Q28288915 | ||
Hypermutation in derepressed operons of Escherichia coli K12 | Q28776505 | ||
The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication | Q31422789 | ||
Reversion of the tyrosine ochre strain Escherichia coli WU3610 under starvation conditions depends on a new gene tas. | Q32066417 | ||
Escherichia coli mutator genes | Q33539352 | ||
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 | ||
Singlet oxygen-induced mutations in M13 lacZ phage DNA | Q33929734 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
A search for a general phenomenon of adaptive mutability | Q33967644 | ||
Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. | Q34019746 | ||
Fidelity of replication of phage phi X174 DNA by DNA polymerase III holoenzyme: spontaneous mutation by misincorporation | Q34035189 | ||
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 | ||
Genetic analysis of transcription-associated mutation in Saccharomyces cerevisiae. | Q34608617 | ||
Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination | Q34609122 | ||
On the dependence of spontaneous mutation rates on the functional state of genes | Q34621585 | ||
Highly mutagenic replication by DNA polymerase V (UmuC) provides a mechanistic basis for SOS untargeted mutagenesis | Q34964296 | ||
Mismatch repair protein MutL becomes limiting during stationary-phase mutation | Q35190848 | ||
Recombination in adaptive mutation. | Q54635736 | ||
Spontaneous mutation in stationary-phase Escherichia coli WP2 carrying various DNA repair alleles | Q54655623 | ||
Mutagenic DNA repair in Escherichia coli. XIV. Influence of two DNA polymerase III mutator alleles on spontaneous and UV mutagenesis. | Q54763531 | ||
Genetic analysis of mutagenesis in aging Escherichia coli colonies | Q56944661 | ||
Transgenerational mutation by radiation | Q59068054 | ||
mutY 'directs' mutation? | Q59096554 | ||
Elements regulating somatic hypermutation of an immunoglobulin κ gene: Critical role for the intron enhancer/matrix attachment region | Q60370477 | ||
DNA replication errors produced by the replicative apparatus of Escherichia coli. | Q64994677 | ||
Mutagenesis by proximity to the recA gene of Escherichia coli | Q68932044 | ||
Biological function for 6-methyladenine residues in the DNA of Escherichia coli K12 | Q69351303 | ||
Induction of a germline mutation at a hypervariable mouse minisatellite locus by 252Cf radiation | Q71977365 | ||
Dose—response of a Radiation Induction of a Germline Mutation at a Hypervariable Mouse Minisatellite Locus | Q72018290 | ||
Association of increased spontaneous mutation rates with high levels of transcription in yeast | Q72304795 | ||
Mouse minisatellite mutations induced by ionizing radiation | Q72556660 | ||
Radiation induction of germline mutation at a hypervariable mouse minisatellite locus | Q72677377 | ||
Kinetic basis of spontaneous mutation. Misinsertion frequencies, proofreading specificities and cost of proofreading by DNA polymerases of Escherichia coli | Q72760046 | ||
Contribution of 3′ → 5′ exonuclease activity of DNA polymerase III holoenzyme from Escherichia coli to specificity | Q72785630 | ||
Non-targeted mutagenesis of unirradiated lambda phage in Escherichia coli host cells irradiated with ultraviolet light | Q72808157 | ||
The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
A UmuD,C-dependent pathway for spontaneous G:C to C:G transversions in stationary phase Escherichia coli mut Y | Q73094277 | ||
[Mutation of bacteriophage induced by irradiation of bacterial host alone before infection] | Q73460861 | ||
Preferential mutagenesis of lacZ integrated at unique sites in the Escherichia coli chromosome | Q73689702 | ||
DNA polymerase accuracy and spontaneous mutation rates: frequencies of purine.purine, purine.pyrimidine, and pyrimidine.pyrimidine mismatches during DNA replication | Q35399078 | ||
UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
Role of RecA protein in untargeted UV mutagenesis of bacteriophage lambda: evidence for the requirement for the dinB gene | Q35608675 | ||
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 | ||
The fidelity of base selection by the polymerase subunit of DNA polymerase III holoenzyme | Q36058122 | ||
recA mutations that reduce the constitutive coprotease activity of the RecA1202(Prtc) protein: possible involvement of interfilament association in proteolytic and recombination activities | Q36123041 | ||
Biochemical basis of SOS-induced mutagenesis in Escherichia coli: reconstitution of in vitro lesion bypass dependent on the UmuD'2C mutagenic complex and RecA protein. | Q36275662 | ||
Plaque color method for rapid isolation of novel recA mutants of Escherichia coli K-12: new classes of protease-constitutive recA mutants | Q36364061 | ||
A hypermutable insert in an immunoglobulin transgene contains hotspots of somatic mutation and sequences predicting highly stable structures in the RNA transcript | Q36404086 | ||
Stage specificity, dose response, and doubling dose for mouse minisatellite germ-line mutation induced by acute radiation | Q37393920 | ||
Mutator tRNAs are encoded by the Escherichia coli mutator genes mutA and mutC: a novel pathway for mutagenesis | Q37637992 | ||
Mutagenic repair in Escherichia coli: products of the recA gene and of the umuD and umuC genes act at different steps in UV-induced mutagenesis | Q37692184 | ||
Genetic mechanisms of bacterial antigenic variation | Q39470842 | ||
Mutation drift and repertoire shift in the maturation of the immune response | Q39658890 | ||
Timing, genetic requirements and functional consequences of somatic hypermutation during B-cell development. | Q39658899 | ||
Escherichia coli MutY protein has a guanine-DNA glycosylase that acts on 7,8-dihydro-8-oxoguanine:guanine mispair to prevent spontaneous G:C-->C:G transversions | Q39725401 | ||
Adaptive mutations produce resistance to ciprofloxacin. | Q39784978 | ||
Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | Q39841075 | ||
Elevated mutation rate in mutT bacteria during starvation: evidence for DNA turnover? | Q39841278 | ||
Generation of an endogenous DNA-methylating agent by nitrosation in Escherichia coli | Q39842494 | ||
Somatic hypermutation: how many mechanisms diversify V region sequences? | Q40410605 | ||
DNA polymerase mu (Pol mu), homologous to TdT, could act as a DNA mutator in eukaryotic cells | Q40410915 | ||
Adaptive evolution of highly mutable loci in pathogenic bacteria | Q40629814 | ||
Persistently elevated frequency of spontaneous mutations in progeny of CHO clones surviving X-irradiation: association with delayed reproductive death phenotype | Q41094230 | ||
Stress response induced by DNA damage leads to specific, delayed and untargeted mutations | Q41109122 | ||
Experimental evidence for an alternative to directed mutation in the bgl operon | Q41115000 | ||
Concomitant induction of signal transduction pathways and genetic instability by the tumor promoter 12-O-tetradecanoylphorbol-13-acetate | Q41180905 | ||
Does selective gene activation direct evolution? | Q41334517 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
Starvation-associated mutation in Escherichia coli: a spontaneous lesion hypothesis for "directed" mutation | Q41661611 | ||
Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis | Q41734679 | ||
Transient mutators: a semiquantitative analysis of the influence of translation and transcription errors on mutation rates | Q41999710 | ||
Replication errors: cha(lle)nging the genome | Q42660015 | ||
Adaptive mutation and slow-growing revertants of an Escherichia coli lacZ amber mutant | Q42967224 | ||
Starvation-associated mutation in E. coli strains with and without reverse transcriptase | Q44212063 | ||
Fidelity of Escherichia coli DNA polymerase III holoenzyme. The effects of beta, gamma complex processivity proteins and epsilon proofreading exonuclease on nucleotide misincorporation efficiencies | Q46320742 | ||
Low fidelity DNA synthesis by human DNA polymerase-eta | Q50335566 | ||
Indirect mutagenesis in phage lambda by ultraviolet preirradiation of host bacteria | Q52869067 | ||
Fidelity of replication of bacteriophage X174 DNA in vitro and in Vivo | Q52873405 | ||
Delayed mutation in Chinese hamster cells. | Q54415538 | ||
A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. | Q54567733 | ||
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 | ||
Targeting of non-Ig sequences in place of the V segment by somatic hypermutation. | Q54608320 | ||
Evidence that F plasmid transfer replication underlies apparent adaptive mutation. | Q54613748 | ||
The formation of one-G deletions as a consequence of single-oxygen-induced DNA damage. | Q54630024 | ||
Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
P433 | issue | 1405 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 29-39 | |
P577 | publication date | 2001-01-01 | |
P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
P1476 | title | Hypermutation in bacteria and other cellular systems | |
P478 | volume | 356 |
Q44282478 | Analysis of the Pseudomonas aeruginosa oprD gene from clinical and environmental isolates. |
Q53939141 | Bacterial multicellularity as a possible source of antibiotic resistance. |
Q52282006 | Bacterial resistance: origins, epidemiology, and impact. |
Q35013064 | Cell-selfish modes of evolution and mutations directed after transcriptional bypass |
Q42426869 | Distinct signatures for mutator sensitivity of lacZ reversions and for the spectrum of lacI/lacO forward mutations on the chromosome of nondividing Escherichia coli |
Q90148668 | Dynamic Emergence of Mismatch Repair Deficiency Facilitates Rapid Evolution of Ceftazidime-Avibactam Resistance in Pseudomonas aeruginosa Acute Infection |
Q44428651 | Eliminating tyrosine sequence variants in CHO cell lines producing recombinant monoclonal antibodies |
Q35058954 | Environmental regulation of mutation rates at specific sites. |
Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
Q33935770 | Escherichia coli K1 polysialic acid O-acetyltransferase gene, neuO, and the mechanism of capsule form variation involving a mobile contingency locus |
Q34700410 | Ig gene hypermutation: a mechanism is due. |
Q44179101 | Lack of dependance of transcription-induced cytosine deaminations on protein synthesis |
Q36369839 | Long-term survival during stationary phase: evolution and the GASP phenotype |
Q38055376 | Microbial evolution in vivo and in silico: methods and applications. |
Q41643081 | Molecular polygamy: The promiscuity of l-phenylalanyl-tRNA-synthetase triggers misincorporation of meta- and ortho-tyrosine in monoclonal antibodies expressed by Chinese hamster ovary cells |
Q44455145 | Mutations arise independently of transcription in non-dividing bacteria |
Q40829913 | Sixty alleles of the ALS7 open reading frame in Candida albicans: ALS7 is a hypermutable contingency locus |
Q34504117 | Stress-induced evolution and the biosafety of genetically modified microorganisms released into the environment |
Q35177659 | The role of mutators in the emergence of antibiotic-resistant bacteria |
Q36380747 | Zinc blocks SOS-induced antibiotic resistance via inhibition of RecA in Escherichia coli |
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