review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Patricia L. Foster | Q41469351 |
P2860 | cites work | SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness | Q24530758 |
Spontaneous point mutations that occur more often when advantageous than when neutral | Q24532456 | ||
Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability | Q24542676 | ||
Adaptive mutation: the uses of adversity | Q24596056 | ||
Signal transduction and regulatory mechanisms involved in control of the sigma(S) (RpoS) subunit of RNA polymerase | Q28220384 | ||
The origin of mutants | Q28288915 | ||
Different characteristics distinguish early versus late arising adaptive mutations in Escherichia coli FC40. | Q31881646 | ||
cAMP-dependent SOS induction and mutagenesis in resting bacterial populations. | Q33719467 | ||
DNA polymerase II is encoded by the DNA damage-inducible dinA gene of Escherichia coli | Q33825068 | ||
Mutation and selection in bacterial populations: alternatives to the hypothesis of directed mutation | Q33850651 | ||
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 | ||
Mutants of Escherichia coli with increased fidelity of DNA replication | Q33961314 | ||
Population dynamics of a Lac- strain of Escherichia coli during selection for lactose utilization | Q33963607 | ||
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 | ||
Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification | Q34012598 | ||
Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. | Q34019746 | ||
Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli | Q34049897 | ||
Adaptive mutation in Escherichia coli | Q34088211 | ||
Error-prone repair DNA polymerases in prokaryotes and eukaryotes | Q34131455 | ||
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 | ||
Phage lambda red-mediated adaptive mutation. | Q34313875 | ||
Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
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 | ||
General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli | Q34643555 | ||
Genome stability and the processing of damaged replication forks by RecG. | Q34762160 | ||
Transposon stability and a role for conjugational transfer in adaptive mutability | Q35159404 | ||
Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
Recent horizontal transmission of plasmids between natural populations of Escherichia coli and Salmonella enterica | Q35620558 | ||
Negative regulation of mutS and mutH repair gene expression by the Hfq and RpoS global regulators of Escherichia coli K-12. | Q35633546 | ||
Directed mutation: between unicorns and goats | Q35917475 | ||
Involvement of Escherichia coli DNA polymerase II in response to oxidative damage and adaptive mutation | Q35979376 | ||
beta-Galactosidase chimeras: primary structure of a lac repressor-beta-galactosidase protein | Q35994224 | ||
The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
Adaptive mutation: General mutagenesis is not a programmed response to stress but results from rare coamplification of dinB with lac | Q36689838 | ||
An inhibitor of SOS induction, specified by a plasmid locus in Escherichia coli | Q37393311 | ||
Induction of a DNA nickase in the presence of its target site stimulates adaptive mutation in Escherichia coli. | Q39694895 | ||
Error-prone polymerase, DNA polymerase IV, is responsible for transient hypermutation during adaptive mutation in Escherichia coli. | Q39753960 | ||
Conjugation is not required for adaptive reversion of an episomal frameshift mutation in Escherichia coli | Q39839215 | ||
Genetic analysis of the recG locus of Escherichia coli K-12 and of its role in recombination and DNA repair | Q39938960 | ||
Mechanisms of directed mutation | Q41110210 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
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 | ||
Identification of additional genes belonging to the LexA regulon in Escherichia coli | Q42486422 | ||
Adaptive mutation of a lacZ amber allele. | Q42566683 | ||
Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence. | Q42960926 | ||
Mosaic structure of plasmids from natural populations of Escherichia coli. | Q42966739 | ||
Adaptive mutation and slow-growing revertants of an Escherichia coli lacZ amber mutant | Q42967224 | ||
Adaptive amplification: an inducible chromosomal instability mechanism | Q50117945 | ||
Evidence that gene amplification underlies adaptive mutability of the bacterial lac operon | Q50128814 | ||
Role of mutator alleles in adaptive evolution. | Q54564129 | ||
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 | ||
Control of the LexA regulon by pH: evidence for a reversible inactivation of the LexA repressor during the growth cycle of Escherichia coli. | Q54634670 | ||
Recombination in adaptive mutation. | Q54635736 | ||
Mechanism for induction of adaptive mutations in Escherichia coli. | Q54715058 | ||
Origin of bacterial variants. | Q55047163 | ||
F- phenocopies: characterization of expression of the F transfer region in stationary phase | Q58010899 | ||
Mutagenic specificity of ultraviolet light | Q69946985 | ||
Gene amplification in the lac region of E. coli | Q70212173 | ||
Genetic and sequence analysis of frameshift mutations induced by ICR-191 | Q70226477 | ||
COMPETITION BETWEEN HIGH AND LOW MUTATING STRAINS OF ESCHERICHIA COLI | Q88206326 | ||
P433 | issue | 15 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 4846-52 | |
P577 | publication date | 2004-08-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Adaptive mutation in Escherichia coli | |
P478 | volume | 186 |
Q24796250 | Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms |
Q21092806 | After 30 years of study, the bacterial SOS response still surprises us |
Q34599104 | Amplification of lac cannot account for adaptive mutation to Lac+ in Escherichia coli. |
Q33602374 | Ancient genes establish stress-induced mutation as a hallmark of cancer |
Q36178618 | Diversify or die: generation of diversity in response to stress. |
Q34195488 | Effect of growth under selection on appearance of chromosomal mutations in Salmonella enterica |
Q28659029 | Engineering Escherichia coli K12 MG1655 to use starch |
Q33411553 | Expansion of a chromosomal repeat in Escherichia coli: roles of replication, repair, and recombination functions |
Q22066338 | Extreme polyploidy in a large bacterium |
Q90534492 | Genetic Adaptation of a Mevalonate Pathway Deficient Mutant in Staphylococcus aureus |
Q28536837 | Genome-wide mutation avalanches induced in diploid yeast cells by a base analog or an APOBEC deaminase |
Q42552100 | Increased mutation frequency in redox-impaired Escherichia coli due to RelA- and RpoS-mediated repression of DNA repair |
Q35924951 | Mismatch repair-dependent mutagenesis in nondividing cells. |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q37194752 | Oxidative damage and mutagenesis in Saccharomyces cerevisiae: genetic studies of pathways affecting replication fidelity of 8-oxoguanine |
Q42125442 | Polyphosphate kinase regulates error-prone replication by DNA polymerase IV in Escherichia coli |
Q41763723 | Rebuttal: adaptive mutation in Escherichia coli (Foster) |
Q41073501 | Rebuttal: adaptive mutation in Escherichia coli (Foster). |
Q41073476 | Rebuttal: adaptive point mutation (Rosenberg and Hastings). |
Q42793640 | Rebuttal: adaptive point mutation (Rosenberg and Hastings). |
Q41073469 | Rebuttal: growth under selection stimulates Lac(+) reversion (Roth and Andersson). |
Q42793523 | Rebuttal: growth under selection stimulates Lac(+) reversion (Roth and Andersson). |
Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
Q35986593 | Stress responses and genetic variation in bacteria. |
Q40459862 | Stress-Induced Mutagenesis. |
Q36961683 | Stress-induced mutagenesis in bacteria. |
Q41996473 | The Escherichia coli histone-like protein HU has a role in stationary phase adaptive mutation |
Q34337115 | The SOS Regulatory Network |
Q36491712 | Too many mutants with multiple mutations |
Q35693750 | Urinary tract infection drives genome instability in uropathogenic Escherichia coli and necessitates translesion synthesis DNA polymerase IV for virulence |
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