scholarly article | Q13442814 |
P2093 | author name string | P L Foster | |
J M Trimarchi | |||
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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
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Frameshift mutation: determinants of specificity | Q37794682 | ||
Lac repressor can be fused to β-galactosidase | Q38361160 | ||
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Sequence analysis of mutations arising during prolonged starvation of Salmonella typhimurium | Q42861600 | ||
Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
Recombination in adaptive mutation. | Q54635736 | ||
Spectrum of mutations that occur under selective and non-selective conditions in E. coli | Q54704156 | ||
Mechanism for induction of adaptive mutations in Escherichia coli. | Q54715058 | ||
Slippery DNA and diseases | Q59070212 | ||
Genetic and sequence analysis of frameshift mutations induced by ICR-191 | Q70226477 | ||
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P433 | issue | 5170 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 407-409 | |
P577 | publication date | 1994-07-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | |
P478 | volume | 265 |
Q54567733 | A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. |
Q56903124 | A quantum-theoretical approach to the phenomenon of directed mutations in bacteria (hypothesis) |
Q35878792 | Abundant microsatellite polymorphism in Saccharomyces cerevisiae, and the different distributions of microsatellites in eight prokaryotes and S. cerevisiae, result from strong mutation pressures and a variety of selective forces |
Q95719585 | Activation of silent gal genes in the lac-gal regulon of Streptococcus thermophilus |
Q50117945 | Adaptive amplification: an inducible chromosomal instability mechanism |
Q42967224 | Adaptive mutation and slow-growing revertants of an Escherichia coli lacZ amber mutant |
Q59757712 | Adaptive mutation in Escherichia coli |
Q34088211 | Adaptive mutation in Escherichia coli |
Q34661313 | Adaptive mutation in Saccharomyces cerevisiae |
Q33640315 | Adaptive mutation sequences reproduced by mismatch repair deficiency |
Q36689838 | Adaptive mutation: General mutagenesis is not a programmed response to stress but results from rare coamplification of dinB with lac |
Q34603905 | Adaptive mutation: has the unicorn landed? |
Q39784978 | Adaptive mutations produce resistance to ciprofloxacin. |
Q41073516 | Adaptive point mutation and adaptive amplification pathways in the Escherichia coli Lac system: stress responses producing genetic change |
Q34229499 | Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation |
Q31881456 | Adaptive reversions of a frameshift mutation in arrested Saccharomyces cerevisiae cells by simple deletions in mononucleotide repeats |
Q34436201 | Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis |
Q33545737 | Are adaptive mutations due to a decline in mismatch repair? The evidence is lacking |
Q28547150 | Atypical Role for PhoU in Mutagenic Break Repair under Stress in Escherichia coli |
Q53939141 | Bacterial multicellularity as a possible source of antibiotic resistance. |
Q33594339 | Competition of Escherichia coli DNA polymerases I, II and III with DNA Pol IV in stressed cells |
Q37513635 | Contribution of the mismatch DNA repair system to the generation of stationary-phase-induced mutants of Bacillus subtilis |
Q39841075 | Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells |
Q31881646 | Different characteristics distinguish early versus late arising adaptive mutations in Escherichia coli FC40. |
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 |
Q28346858 | Effect of endogenous carotenoids on "adaptive" mutation in Escherichia coli FC40 |
Q24674122 | Emergence of nylon oligomer degradation enzymes in Pseudomonas aeruginosa PAO through experimental evolution |
Q51778469 | Engineering stress tolerance of Escherichia coli by stress-induced mutagenesis (SIM)-based adaptive evolution. |
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 |
Q34609122 | Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination |
Q40521401 | Evolutionary genetics. Directed mutations slip-sliding away? |
Q56080686 | Evolutionary tuning knobs |
Q34297067 | Evolving responsively: adaptive mutation |
Q33411553 | Expansion of a chromosomal repeat in Escherichia coli: roles of replication, repair, and recombination functions |
Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
Q40442293 | Genetic instability as a consequence of inappropriate entry into and progression through S-phase. |
Q72151726 | Genetics of selection-induced mutations: I. uvrA, uvrB, uvrC, and uvrD are selection-induced specific mutator loci |
Q28606509 | Genome sequences of two closely related strains of Escherichia coli K-12 GM4792 |
Q37271649 | Genome-wide In Silico Analysis, Characterization and Identification of Microsatellites in Spodoptera littoralis Multiple nucleopolyhedrovirus (SpliMNPV). |
Q42325513 | Gross chromosomal rearrangement mediated by DNA replication in stressed cells: evidence from Escherichia coli |
Q33770256 | Hypermutation in bacteria and other cellular systems |
Q42969505 | Identity and function of a large gene network underlying mutagenic repair of DNA breaks |
Q35170976 | Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli |
Q35037445 | In pursuit of a molecular mechanism for adaptive gene amplification |
Q39572388 | In vitro expansion of mammalian telomere repeats by DNA polymerase alpha-primase |
Q34606847 | Increased episomal replication accounts for the high rate of adaptive mutation in recD mutants of Escherichia coli |
Q39694895 | Induction of a DNA nickase in the presence of its target site stimulates adaptive mutation in Escherichia coli. |
Q35979376 | Involvement of Escherichia coli DNA polymerase II in response to oxidative damage and adaptive mutation |
Q34617495 | Mathematical issues arising from the directed mutation controversy |
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 |
Q26771472 | Microsatellites in Pursuit of Microbial Genome Evolution |
Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
Q39829461 | Molecular variation in the major outer membrane protein P5 gene of nonencapsulated Haemophilus influenzae during chronic infections |
Q33965447 | Multiple trait analysis of genetic mapping for quantitative trait loci |
Q33373675 | Mutability and importance of a hypermutable cell subpopulation that produces stress-induced mutants in Escherichia coli |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q37056244 | Mutation at a distance caused by homopolymeric guanine repeats in Saccharomyces cerevisiae |
Q41703503 | Mutation for survival |
Q33945503 | Mutation frequencies and antibiotic resistance |
Q34465215 | Mutation frequency and spectrum of mutations vary at different chromosomal positions of Pseudomonas putida |
Q35620439 | Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli |
Q33816436 | Numerous length polymorphisms at short tandem repeats in human cytomegalovirus. |
Q33239373 | On the mechanism of gene amplification induced under stress in Escherichia coli |
Q33966750 | Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation |
Q34471714 | Plasmid copy number underlies adaptive mutability in bacteria |
Q42125442 | Polyphosphate kinase regulates error-prone replication by DNA polymerase IV in Escherichia coli |
Q33963607 | Population dynamics of a Lac- strain of Escherichia coli during selection for lactose utilization |
Q36079713 | Promoter-creating mutations in Pseudomonas putida: a model system for the study of mutation in starving bacteria |
Q34019746 | Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. |
Q39835578 | Redundant transfer of F' plasmids occurs between Escherichia coli cells during nonlethal selections |
Q34617476 | Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. |
Q33975727 | Role of genomic typing in taxonomy, evolutionary genetics, and microbial epidemiology |
Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
Q33953638 | SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification |
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. |
Q40927142 | Sexual potency and adaptive mutation in bacteria |
Q24548611 | Short-sequence DNA repeats in prokaryotic genomes |
Q30974317 | Simple sequence repeats and mucoid conversion: biased mucA mutagenesis in mismatch repair-deficient Pseudomonas aeruginosa. |
Q34738348 | Simple sequence repeats as a source of quantitative genetic variation |
Q24561717 | Simple tandem DNA repeats and human genetic disease |
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 |
Q39494235 | Spectra of spontaneous growth-dependent and adaptive mutations at ebgR. |
Q35610606 | Spontaneous and induced mutations in a single open reading frame alter both virulence and avirulence in Xanthomonas campestris pv. vesicatoria avrBs2. |
Q41147504 | Spontaneous mutations in bacteria: chance or necessity? |
Q36574251 | Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription |
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 |
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 |
Q35986593 | Stress responses and genetic variation in bacteria. |
Q40459862 | Stress-Induced Mutagenesis. |
Q64389723 | Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance |
Q37355812 | Stress-induced beta-lactam antibiotic resistance mutation and sequences of stationary-phase mutations in the Escherichia coli chromosome. |
Q36961683 | Stress-induced mutagenesis in bacteria. |
Q41996473 | The Escherichia coli histone-like protein HU has a role in stationary phase adaptive mutation |
Q33903483 | The SOS response regulates adaptive mutation |
Q41999656 | The effect of adaptive mutagenesis on genetic variation at a linked, neutral locus. |
Q71081544 | The effect of amino acid substitutions in the conserved aromatic region of subunit II of cytochrome c oxidase in Saccharomyces cerevisiae |
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 |
Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
Q33966542 | Two enzymes, both of which process recombination intermediates, have opposite effects on adaptive mutation in Escherichia coli. |
Q64096919 | What is mutation? A chapter in the series: How microbes "jeopardize" the modern synthesis |
Q33719467 | cAMP-dependent SOS induction and mutagenesis in resting bacterial populations. |
Q33994900 | radC102 of Escherichia coli is an allele of recG |
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