scholarly article | Q13442814 |
P356 | DOI | 10.1126/SCIENCE.8023163 |
P698 | PubMed publication ID | 8023163 |
P2093 | author name string | Rosenberg SM | |
Harris RS | |||
Gee P | |||
Longerich S | |||
P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
P433 | issue | 5170 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 405-407 | |
P577 | publication date | 1994-07-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Adaptive mutation by deletions in small mononucleotide repeats. | |
P478 | volume | 265 |
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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 |
Q41073516 | Adaptive point mutation and adaptive amplification pathways in the Escherichia coli Lac system: stress responses producing genetic change |
Q41572901 | Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs |
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Q28478172 | An active site aromatic triad in Escherichia coli DNA Pol IV coordinates cell survival and mutagenesis in different DNA damaging agents |
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. |
Q37952382 | Biological pathways to adaptability--interactions between genome, epigenome, nervous system and environment for adaptive behavior |
Q33594339 | Competition of Escherichia coli DNA polymerases I, II and III with DNA Pol IV in stressed cells |
Q38446575 | Competitive growth advantage of nontoxigenic mutants in the stationary phase in archival cultures of pathogenic Vibrio cholerae strains |
Q22122370 | Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18 |
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Q35002361 | Damage-induced localized hypermutability. |
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. |
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Q33886793 | Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation |
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 |
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 |
Q33736829 | Is homologous recombination really an error-free process? |
Q35841424 | Mapping and analysis of simple sequence repeats in the Arabidopsis thaliana genome |
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 |
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 |
Q34465215 | Mutation frequency and spectrum of mutations vary at different chromosomal positions of Pseudomonas putida |
Q37655530 | Mutational dynamics of microsatellites |
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. |
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Q33239373 | On the mechanism of gene amplification induced under stress in Escherichia coli |
Q46325763 | Origins of cancer symposium 2016: exploring tumor complexity |
Q38670044 | Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli |
Q40744317 | Phylogeny and strain typing of Escherichia coli, inferred from variation at mononucleotide repeat loci |
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 |
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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. |
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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 |
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Q34738348 | Simple sequence repeats as a source of quantitative genetic variation |
Q40412255 | Simple sequence repeats in Escherichia coli: abundance, distribution, composition, and polymorphism |
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 |
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Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
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Q40459862 | Stress-Induced Mutagenesis. |
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Q36961683 | Stress-induced mutagenesis in bacteria. |
Q36496909 | Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine |
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Q33903483 | The SOS response regulates adaptive mutation |
Q41999656 | The effect of adaptive mutagenesis on genetic variation at a linked, neutral locus. |
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 |
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Q33966542 | Two enzymes, both of which process recombination intermediates, have opposite effects on adaptive mutation in Escherichia coli. |
Q36713351 | Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli |
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Q37976150 | What limits the efficiency of double-strand break-dependent stress-induced mutation in Escherichia coli? |
Q33719467 | cAMP-dependent SOS induction and mutagenesis in resting bacterial populations. |
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