scholarly article | Q13442814 |
P2093 | author name string | P J Hastings | |
Susan M Rosenberg | |||
S M Rosenberg | |||
H J Bull | |||
G J McKenzie | |||
Gregory J McKenzie | |||
Harold J Bull | |||
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 | ||
recD: the gene for an essential third subunit of exonuclease V | Q24630457 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
The origin of mutants | Q28288915 | ||
Hypermutation in derepressed operons of Escherichia coli K12 | Q28776505 | ||
Somatic hypermutation and the three R's: repair, replication and recombination | Q33545735 | ||
Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
Mechanisms of genome-wide hypermutation in stationary phase | Q33692333 | ||
DNA double-strand breaks caused by replication arrest | Q33886030 | ||
Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
Microbial genetics. Hypermutation under stress. | Q54564293 | ||
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 | ||
Evolutionary biology. A boost for "adaptive" mutation. | Q54630370 | ||
Reverse branch migration of Holliday junctions by RecG protein: a new mechanism for resolution of intermediates in recombination and DNA repair. | Q54649605 | ||
Biochemical and physical characterization of exonuclease V from Escherichia coli. Comparison of the catalytic activities of the RecBC and RecBCD enzymes. | Q54716964 | ||
Recombination of bacteriophage lambda in recD mutants of Escherichia coli. | Q54736666 | ||
‘Selfers’ and High Mutation Rate during Meiosis in Ascobolus immersus | Q59090212 | ||
PsiB, an anti‐SOS protein, is transiently expressed by the F sex factor during its transmission to an Escherichia coli K‐12 recipient | Q67489740 | ||
Genetics of selection-induced mutations: I. uvrA, uvrB, uvrC, and uvrD are selection-induced specific mutator loci | Q72151726 | ||
The evolution of genetic intelligence | Q72336913 | ||
How the genome readies itself for evolution | Q77292572 | ||
RuvAB acts at arrested replication forks | Q77550034 | ||
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 | ||
Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation | Q33966750 | ||
A search for a general phenomenon of adaptive mutability | Q33967644 | ||
A role for REV3 in mutagenesis during double-strand break repair in Saccharomyces cerevisiae | Q33971118 | ||
Different Rates of Spontaneous Mutation during Mitosis and Meiosis in Yeast | Q33979691 | ||
SELFER MUTANTS OF SALMONELLA TYPHIMURIUM | Q33980009 | ||
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 | ||
The recombination hot spot chi is a regulatory element that switches the polarity of DNA degradation by the RecBCD enzyme | Q34423136 | ||
Transient and heritable mutators in adaptive evolution in the lab and in nature | Q34603730 | ||
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 | ||
Mismatch repair protein MutL becomes limiting during stationary-phase mutation | Q35190848 | ||
Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo | Q35208627 | ||
Redundant homosexual F transfer facilitates selection-induced reversion of plasmid mutations | Q35607773 | ||
Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli | Q36104718 | ||
Identification and characterization of recD, a gene affecting plasmid maintenance and recombination in Escherichia coli | Q36249724 | ||
The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
"SELFERS"-ATTRIBUTED TO UNEQUAL CROSSOVERS IN SALMONELLA. | Q36396536 | ||
Replication fork assembly at recombination intermediates is required for bacterial growth | Q36443290 | ||
Spontaneous mutation | Q37041840 | ||
The split-end model for homologous recombination at double-strand breaks and at Chi. | Q37361171 | ||
A new class of Escherichia coli recBC mutants: implications for the role of RecBC enzyme in homologous recombination | Q37580459 | ||
The roles of starvation and selective substrates in the emergence of araB-lacZ fusion clones. | Q37638181 | ||
Modulation of recombination and DNA repair by the RecG and PriA helicases of Escherichia coli K-12. | Q39843576 | ||
Somatic hypermutation: how many mechanisms diversify V region sequences? | Q40410605 | ||
Collapse and repair of replication forks in Escherichia coli | Q40416038 | ||
Editing DNA replication and recombination by mismatch repair: from bacterial genetics to mechanisms of predisposition to cancer in humans | Q40522942 | ||
Programmed cell death in bacterial populations | Q40586191 | ||
Chi and the RecBC D enzyme of Escherichia coli | Q40614043 | ||
Analysis of the sequence and gene products of the transfer region of the F sex factor | Q40625554 | ||
Adaptive mutation: a general phenomenon or special case? | Q41329242 | ||
Genome organization, natural genetic engineering and adaptive mutation | Q41379575 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
Mutation for survival | Q41703503 | ||
Transient mutators: a semiquantitative analysis of the influence of translation and transcription errors on mutation rates | Q41999710 | ||
Diploid yeast cells yield homozygous spontaneous mutations. | Q46053570 | ||
Francis Ryan and the origins of directed mutagenesis | Q48958607 | ||
The DNA replication protein PriA and the recombination protein RecG bind D-loops. | Q54562206 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P1104 | number of pages | 11 | |
P304 | page(s) | 1427-1437 | |
P577 | publication date | 2000-04-01 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination | |
Evidence That Stationary-Phase Hypermutation in the Escherichia coli Chromosome Is Promoted by Recombination | |||
P478 | volume | 154 |
Q34088211 | 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 |
Q34436201 | Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis |
Q34012598 | Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification |
Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
Q33770256 | Hypermutation in bacteria and other cellular systems |
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 |
Q35130221 | Novel role of mfd: effects on stationary-phase mutagenesis in Bacillus subtilis |
Q39684752 | Phylogenetic and functional analysis of the bacteriophage P1 single-stranded DNA-binding protein |
Q89636195 | Role of Mfd and GreA in Bacillus subtilis Base Excision Repair-Dependent Stationary-Phase-Mutagenesis |
Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
Q43067321 | Sexual isolation in Acinetobacter baylyi is locus-specific and varies 10,000-fold over the genome |
Q37096423 | Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence |
Q40459862 | Stress-Induced Mutagenesis. |
Q64389723 | Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance |
Q34504117 | Stress-induced evolution and the biosafety of genetically modified microorganisms released into the environment |
Q36961683 | Stress-induced mutagenesis in bacteria. |
Q38541782 | The Origin of Mutants Under Selection: How Natural Selection Mimics Mutagenesis (Adaptive Mutation) |
Q33903483 | The SOS response regulates adaptive mutation |
Q34616322 | The roles of REV3 and RAD57 in double-strand-break-repair-induced mutagenesis of Saccharomyces cerevisiae |
Q36491712 | Too many mutants with multiple mutations |
Q36713351 | Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli |
Q64096919 | What is mutation? A chapter in the series: How microbes "jeopardize" the modern synthesis |
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