review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Kuzminov A | |
P2860 | cites work | The double-strand-break repair model for recombination | Q28267259 |
DNA Sequence and Analysis of 136 Kilobases of the Escherichia coli Genome: Organizational Symmetry around the Origin of Replication | Q34306353 | ||
The recombination hotspot chi is a regulatory sequence that acts by attenuating the nuclease activity of the E. coli RecBCD enzyme | Q34355622 | ||
Conjugational recombination in E. coli: myths and mechanisms | Q37623662 | ||
Resolution of Holliday junctions by RuvC resolvase: cleavage specificity and DNA distortion. | Q38315860 | ||
Homologous pairing in vitro stimulated by the recombination Hotspot, Chi | Q38334215 | ||
Transduction versus "Conjuduction": Evidence for Multiple Roles for Exonuclease V in Genetic Recombination in Escherichia coli | Q39895818 | ||
Repair of DNA double-strand breaks in Escherichia coli, which requires recA function and the presence of a duplicate genome | Q40840136 | ||
Characterization of DNA adenine methylation mutants of Escherichia coli K12 | Q41039288 | ||
Molecular and functional analysis of the ruv region of Escherichia coli K-12 reveals three genes involved in DNA repair and recombination | Q41866318 | ||
Hyper-recombination in dam mutants of Escherichia coli K-12 | Q42007594 | ||
Substrate specificity of the DNA unwinding activity of the RecBC enzyme of Escherichia coli | Q44449043 | ||
Replication of bacteriophage lambda DNA dependent on the function of host and viral genes. I. Interaction of red, gam and rec. | Q45302058 | ||
Reverse branch migration of Holliday junctions by RecG protein: a new mechanism for resolution of intermediates in recombination and DNA repair. | Q54649605 | ||
Discontinuous DNA replication in a lig-7 strain of Escherichia coli is not the result of mismatch repair, nucleotide-excision repair, or the base-excision repair of DNA uracil. | Q54721276 | ||
Recombination of bacteriophage lambda in recD mutants of Escherichia coli. | Q54736666 | ||
Formation of a RuvAB-Holliday Junction Complex in Vitro | Q58028630 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 373-384 | |
P577 | publication date | 1995-05-01 | |
P1433 | published in | Molecular Microbiology | Q6895967 |
P1476 | title | Collapse and repair of replication forks in Escherichia coli | |
P478 | volume | 16 |
Q48031487 | A broadening view of recombinational DNA repair in bacteria |
Q43879381 | A dynamic RecA filament permits DNA polymerase-catalyzed extension of the invading strand in recombination intermediates |
Q53651010 | A homozygous recA mutant of Synechocystis PCC6803: construction strategy and characteristics eliciting a novel RecA independent UVC resistance in dark. |
Q64387298 | A new role for Escherichia coli Dam DNA methylase in prevention of aberrant chromosomal replication |
Q34585540 | A novel family of regulated helicases/nucleases from Gram-positive bacteria: insights into the initiation of DNA recombination. |
Q73316835 | A single nuclease active site of the Escherichia coli RecBCD enzyme catalyzes single-stranded DNA degradation in both directions |
Q27931070 | A yeast gene, MGS1, encoding a DNA-dependent AAA(+) ATPase is required to maintain genome stability. |
Q35169608 | AKT1/BRCA1 in the control of homologous recombination and genetic stability: the missing link between hereditary and sporadic breast cancers |
Q47848559 | Abortive recombination in Escherichia coli ruv mutants blocks chromosome partitioning |
Q34088211 | Adaptive mutation in Escherichia coli |
Q34603905 | Adaptive mutation: has the unicorn landed? |
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 |
Q34605521 | Alteration of N-terminal phosphoesterase signature motifs inactivates Saccharomyces cerevisiae Mre11. |
Q33961513 | An antitumor drug-induced topoisomerase cleavage complex blocks a bacteriophage T4 replication fork in vivo |
Q33602920 | Analysis of the SOS response in Salmonella enterica serovar typhimurium using RNA fingerprinting by arbitrarily primed PCR. |
Q33778360 | Asymmetric substitution patterns: a review of possible underlying mutational or selective mechanisms |
Q33527006 | BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice |
Q89965269 | Bacillus subtilis RarA Acts as a Positive RecA Accessory Protein |
Q57753310 | Bacillus subtilis RarA modulates replication restart |
Q55315209 | Bacterial RecA Protein Promotes Adenoviral Recombination during In Vitro Infection. |
Q60921634 | Biological consequences for bacteria of homologous recombination |
Q36845153 | Borrelia burgdorferi vlsE antigenic variation is not mediated by RecA |
Q34037586 | Break-induced DNA replication |
Q27933666 | Break-induced replication: a review and an example in budding yeast |
Q38116136 | Break-induced replication: functions and molecular mechanism |
Q52664387 | Broken replication forks trigger heritable DNA breaks in the terminus of a circular chromosome. |
Q35150239 | Bypass of a nick by the replisome of bacteriophage T7 |
Q52190263 | Cell division is required for resolution of dimer chromosomes at the dif locus of Escherichia coli. |
Q39939404 | Cell-cycle coordination between DNA replication and recombination revealed by a vertebrate N-end rule degron-Rad51. |
Q60529742 | Characteristics of Chi distribution on different bacterial genomes |
Q28343741 | Characterization of homologous recombination induced by replication inhibition in mammalian cells |
Q28205315 | Chromosomal stability and the DNA double-stranded break connection |
Q36016450 | Chromosome demise in the wake of ligase-deficient replication |
Q34311628 | Circles: the replication-recombination-chromosome segregation connection |
Q33525506 | Co-orientation of replication and transcription preserves genome integrity |
Q54453203 | Concerted action of plasmid maintenance functions: partition complexes create a requirement for dimer resolution. |
Q64388320 | Control of crossing over |
Q34723611 | Cooperation of RAD51 and RAD54 in regression of a model replication fork |
Q53054701 | DNA Methylation. |
Q34509028 | DNA Mismatch Repair |
Q24643546 | DNA gyrase, topoisomerase IV, and the 4-quinolones |
Q37821754 | DNA motifs that sculpt the bacterial chromosome. |
Q28278869 | DNA polymerase II (epsilon) of Saccharomyces cerevisiae dissociates from the DNA template by sensing single-stranded DNA |
Q24630816 | DNA replication meets genetic exchange: chromosomal damage and its repair by homologous recombination |
Q35037441 | Defending genome integrity during S-phase: putative roles for RecQ helicases and topoisomerase III. |
Q33886806 | Deletions at stalled replication forks occur by two different pathways |
Q47238083 | Direct observation of end resection by RecBCD during double-stranded DNA break repair in vivo |
Q28210616 | Do bacteria have sex? |
Q35188037 | Double-strand end repair via the RecBC pathway in Escherichia coli primes DNA replication |
Q35208627 | Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo |
Q92266072 | Elucidating the functional role of Mycobacterium smegmatis recX in stress response |
Q42967681 | Enhanced deletion formation by aberrant DNA replication in Escherichia coli |
Q37585041 | Enlightenment of yeast mitochondrial homoplasmy: diversified roles of gene conversion |
Q34609122 | Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination |
Q34297067 | Evolving responsively: adaptive mutation |
Q34604021 | Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiae |
Q37093000 | Formation of Holliday junctions by regression of nascent DNA in intermediates containing stalled replication forks: RecG stimulates regression even when the DNA is negatively supercoiled |
Q33700686 | Frail hypotheses in evolutionary biology |
Q47968713 | Functional uncoupling of twin polymerases: mechanism of polymerase dissociation from a lagging-strand block. |
Q41713848 | Genetic instability of the Streptomyces chromosome |
Q33967556 | Genetic requirements for RAD51- and RAD54-independent break-induced replication repair of a chromosomal double-strand break |
Q24563143 | Genome of bacteriophage P1 |
Q33886793 | Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation |
Q53940315 | Genomics, Chi sites and codons: 'islands of preferred DNA pairing' are oceans of ORFs. |
Q34435844 | Group I intron homing in Bacillus phages SPO1 and SP82: a gene conversion event initiated by a nicking homing endonuclease |
Q60919860 | Guidelines for DNA recombination and repair studies: Cellular assays of DNA repair pathways |
Q24631768 | Historical overview: searching for replication help in all of the rec places |
Q37574376 | Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase |
Q27929886 | Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism |
Q34308000 | Homologous Recombination-Experimental Systems, Analysis, and Significance |
Q64389088 | How Acts of Infidelity Promote DNA Break Repair: Collision and Collusion Between DNA Repair and Transcription |
Q33635502 | Human MUS81-EME2 can cleave a variety of DNA structures including intact Holliday junction and nicked duplex |
Q33302939 | Identification of DNA motifs implicated in maintenance of bacterial core genomes by predictive modeling |
Q35740518 | Identification of the lactococcal exonuclease/recombinase and its modulation by the putative Chi sequence. |
Q33993117 | Imbalanced base excision repair increases spontaneous mutation and alkylation sensitivity in Escherichia coli |
Q34933382 | Impact of ciprofloxacin exposure on Staphylococcus aureus genomic alterations linked with emergence of rifampin resistance |
Q34271071 | Impairment of lagging strand synthesis triggers the formation of a RuvABC substrate at replication forks |
Q33714636 | In vivo evidence for a recA-independent recombination process in Escherichia coli that permits completion of replication of DNA containing UV damage in both strands |
Q43993843 | Inactivation of Mre11 does not affect VSG gene duplication mediated by homologous recombination in Trypanosoma brucei. |
Q48300492 | Inactivation of genes involved in base excision repair of Corynebacterium glutamicum and survival of the mutants in presence of various mutagens |
Q53052801 | Increased ultraviolet radiation sensitivity of Escherichia coli grown at low temperature. |
Q39694895 | Induction of a DNA nickase in the presence of its target site stimulates adaptive mutation in Escherichia coli. |
Q39845234 | Influence of disruption of the recA gene on genetic instability and genome rearrangement in Streptomyces lividans |
Q28141289 | Initiation of genetic recombination and recombination-dependent replication |
Q24548334 | Interaction of human rad51 recombination protein with single-stranded DNA binding protein, RPA |
Q35738776 | Interplay between DNA replication, recombination and repair based on the structure of RecG helicase |
Q39729394 | Isolation and characterization of the C-terminal nuclease domain from the RecB protein of Escherichia coli |
Q38257014 | Linking RNA polymerase backtracking to genome instability in E. coli |
Q30412742 | Mechanisms for Structural Variation in the Human Genome |
Q22065788 | Mechanisms of gene duplication and amplification |
Q37586957 | Mechanisms of mutagenesis: DNA replication in the presence of DNA damage |
Q33692291 | Mechanisms of mutation in nondividing cells. Insights from the study of adaptive mutation in Escherichia coli |
Q59198308 | Mechanisms of regulation of eukaryotic homologous DNA recombination |
Q33847662 | Mechanisms of stationary phase mutation: a decade of adaptive mutation |
Q92083775 | Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. |
Q42110225 | Meiotic deletion at the BUF1 locus of the fungus Magnaporthe grisea is controlled by interaction with the homologous chromosome |
Q27932674 | Migrating bubble during break-induced replication drives conservative DNA synthesis |
Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
Q39843576 | Modulation of recombination and DNA repair by the RecG and PriA helicases of Escherichia coli K-12. |
Q36268081 | Multiple pathways of duplication formation with and without recombination (RecA) in Salmonella enterica. |
Q35870700 | Multiple pathways process stalled replication forks |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q42524559 | Mutations in the yeast SRB2 general transcription factor suppress hpr1-induced recombination and show defects in DNA repair |
Q36254839 | New insights into the kinetic resistance to anticancer agents |
Q28610023 | Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage |
Q33966750 | Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation |
Q30499016 | Oxidative stress resistance in Deinococcus radiodurans |
Q47558874 | Oxygen and RNA in stress-induced mutation. |
Q42557010 | Palindromes as substrates for multiple pathways of recombination in Escherichia coli |
Q39958831 | Partial suppression of the fission yeast rqh1(-) phenotype by expression of a bacterial Holliday junction resolvase |
Q42283278 | Pathways for Homologous Recombination Between Chromosomal Direct Repeats in Salmonella typhimurium |
Q46724332 | Patterns of chromosomal fragmentation due to uracil-DNA incorporation reveal a novel mechanism of replication-dependent double-stranded breaks |
Q47673536 | Phenotypes of dnaXE145A Mutant Cells Indicate that the Escherichia coli Clamp Loader Has a Role in the Restart of Stalled Replication Forks. |
Q39432621 | Precarious maintenance of simple DNA repeats in eukaryotes |
Q33938191 | PriA and phage T4 gp59: factors that promote DNA replication on forked DNA substrates microreview |
Q64387578 | PriA mediates DNA replication pathway choice at recombination intermediates |
Q73329368 | Progressive loss of lambda prophage recombinogenicity in UV-irradiated Escherichia coli: the role of RecBCD enzyme |
Q40587137 | Promoting and avoiding recombination: contrasting activities of the Escherichia coli RuvABC Holliday junction resolvase and RecG DNA translocase |
Q36853184 | Prompt repair of hydrogen peroxide-induced DNA lesions prevents catastrophic chromosomal fragmentation |
Q44837014 | Purification and characterization of DnaC810, a primosomal protein capable of bypassing PriA function |
Q37025967 | R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli |
Q35583008 | RecA-Dependent Recovery of Arrested DNA Replication Forks |
Q37621630 | RecA-dependent mutants in Escherichia coli reveal strategies to avoid chromosomal fragmentation. |
Q41982811 | RecA-dependent replication in the nrdA101(Ts) mutant of Escherichia coli under restrictive conditions |
Q39527474 | RecA-mediated rescue of Escherichia coli strains with replication forks arrested at the terminus |
Q24650931 | RecBCD enzyme and the repair of double-stranded DNA breaks |
Q35908909 | RecBCD is required to complete chromosomal replication: Implications for double-strand break frequencies and repair mechanisms |
Q39728517 | RecG helicase activity at three- and four-strand DNA structures. |
Q42410405 | RecG protein and single-strand DNA exonucleases avoid cell lethality associated with PriA helicase activity in Escherichia coli |
Q34108141 | Recombination at double-strand breaks and DNA ends: conserved mechanisms from phage to humans. |
Q42046114 | Recombination enhancement by replication (RER) in Rhizobium etli. |
Q39498597 | Recombination is essential for viability of an Escherichia coli dam (DNA adenine methyltransferase) mutant |
Q33858878 | Recombination phenotypes of Escherichia coli greA mutants |
Q41984467 | Recombination-dependent growth in exonuclease-depleted recBC sbcBC strains of Escherichia coli K-12. |
Q64387300 | Recombinational DNA repair in a cellular context: a search for the homology search |
Q33962242 | Recombinational repair and restart of damaged replication forks. |
Q29619755 | Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda |
Q43725800 | Recombinational repair of chromosomal DNA double-strand breaks generated by a restriction endonuclease |
Q46145277 | Reconstitution of an SOS response pathway: derepression of transcription in response to DNA breaks |
Q37214505 | Reduced lipopolysaccharide phosphorylation in Escherichia coli lowers the elevated ori/ter ratio in seqA mutants |
Q39758873 | Repair and antirepair DNA helicases in Helicobacter pylori |
Q57753866 | Replication Fork Breakage and Restart in Escherichia coli |
Q43910861 | Replication arrests during a single round of replication of the Escherichia coli chromosome in the absence of DnaC activity |
Q33885416 | Replication fork arrest and DNA recombination |
Q34089698 | Replication fork collapse at replication terminator sequences |
Q33835816 | Replication fork inhibition in seqA mutants of Escherichia coli triggers replication fork breakage |
Q35839032 | Replication forks stalled at ultraviolet lesions are rescued via RecA and RuvABC protein-catalyzed disintegration in Escherichia coli |
Q34311622 | Rescue of arrested replication forks by homologous recombination |
Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
Q42094982 | Roles of ExoI and SbcCD nucleases in "reckless" DNA degradation in recA mutants of Escherichia coli |
Q77550034 | RuvAB acts at arrested replication forks |
Q30008790 | SSB and the RecG DNA helicase: an intimate association to rescue a stalled replication fork |
Q33326797 | SSB antagonizes RecX-RecA interaction |
Q74297494 | Saccharomyces cerevisiae lacking Snm1, Rev3 or Rad51 have a normal S-phase but arrest permanently in G2 after cisplatin treatment |
Q53627728 | Selection for chromosome architecture in bacteria. |
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. |
Q37093293 | Single-strand interruptions in replicating chromosomes cause double-strand breaks |
Q33743436 | Sister chromatid exchange frequencies in Escherichia coli analyzed by recombination at the dif resolvase site. |
Q61799278 | Spatial and temporal organization of RecA in the DNA-damage response |
Q39494346 | Specific effects of a recB mutation on the HfrH strain of Escherichia coli. |
Q37352792 | Specificity in suppression of SOS expression by recA4162 and uvrD303. |
Q39844324 | Stability of linear DNA in recA mutant Escherichia coli cells reflects ongoing chromosomal DNA degradation |
Q36574251 | Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription |
Q40459862 | Stress-Induced Mutagenesis. |
Q27635329 | Structural analysis of DNA replication fork reversal by RecG |
Q46200700 | Suppression of spontaneous chromosomal rearrangements by S phase checkpoint functions in Saccharomyces cerevisiae |
Q58732442 | The ATPase activity of E. coli RecA prevents accumulation of toxic complexes formed by erroneous binding to undamaged double stranded DNA |
Q46027925 | The AddAB helicase/nuclease forms a stable complex with its cognate chi sequence during translocation. |
Q33960277 | The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae |
Q35193453 | The RecBC enzyme loads RecA protein onto ssDNA asymmetrically and independently of chi, resulting in constitutive recombination activation |
Q39679859 | The RuvABC resolvase is indispensable for recombinational repair in sbcB15 mutants of Escherichia coli |
Q44267647 | The S. cerevisiae Mag1 3-methyladenine DNA glycosylase modulates susceptibility to homologous recombination. |
Q34491677 | The SMC-like protein complex SbcCD enhances DNA polymerase IV-dependent spontaneous mutation in Escherichia coli |
Q33903483 | The SOS response regulates adaptive mutation |
Q27935475 | The Saccharomyces cerevisiae RAD9, RAD17, RAD24 and MEC3 genes are required for tolerating irreparable, ultraviolet-induced DNA damage |
Q34748884 | The SbcCD nuclease of Escherichia coli is a structural maintenance of chromosomes (SMC) family protein that cleaves hairpin DNA |
Q24630851 | The architecture of the human Rad54-DNA complex provides evidence for protein translocation along DNA |
Q33867563 | The breast cancer susceptibility gene, BRCA2: at the crossroads between DNA replication and recombination? |
Q26859022 | The chromosome cycle of prokaryotes |
Q27860542 | The complete genome sequence of Escherichia coli K-12 |
Q29614220 | The importance of repairing stalled replication forks |
Q31497967 | The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders |
Q42637285 | The mutT defect does not elevate chromosomal fragmentation in Escherichia coli because of the surprisingly low levels of MutM/MutY-recognized DNA modifications |
Q41728146 | The nuclease activity of the yeast DNA2 protein, which is related to the RecB-like nucleases, is essential in vivo |
Q52927782 | The orientation bias of Chi sequences is a general tendency of G-rich oligomers. |
Q33347783 | The role of the Fanconi anemia network in the response to DNA replication stress |
Q34017416 | The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli |
Q42550654 | The transcription factor DksA prevents conflicts between DNA replication and transcription machinery |
Q41924740 | The transcription fidelity factor GreA impedes DNA break repair |
Q34433258 | The translocating RecBCD enzyme stimulates recombination by directing RecA protein onto ssDNA in a chi-regulated manner |
Q47955222 | Thermostable flap endonuclease from the archaeon, Pyrococcus horikoshii, cleaves the replication fork-like structure endo/exonucleolytically |
Q40423760 | Tn7 recognizes transposition target structures associated with DNA replication using the DNA-binding protein TnsE. |
Q64388355 | Tn7 transposes proximal to DNA double-strand breaks and into regions where chromosomal DNA replication terminates |
Q64387291 | Tools To Live By: Bacterial DNA Structures Illuminate Cancer |
Q42430219 | Top1- and Top2-mediated topological transitions at replication forks ensure fork progression and stability and prevent DNA damage checkpoint activation |
Q39500237 | Transcriptional and mutational analyses of the Streptomyces lividans recX gene and its interference with RecA activity |
Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
Q37398739 | Trapping and breaking of in vivo nicked DNA during pulsed field gel electrophoresis |
Q36186742 | Travel, sex, and food: what's speciation got to do with it? |
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 |
Q34612124 | Two types of recombination hotspots in bacteriophage T4: one requires DNA damage and a replication origin and the other does not. |
Q33984271 | Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae |
Q33995863 | Viability of rep recA mutants depends on their capacity to cope with spontaneous oxidative damage and on the DnaK chaperone protein |
Q33993510 | Visualization of repair of double-strand breaks in the bacteriophage T7 genome without normal DNA replication |
Q37976150 | What limits the efficiency of double-strand break-dependent stress-induced mutation in Escherichia coli? |
Q41352428 | When checkpoints fail |
Q74825051 | Yeast ARMs (DNA at-risk motifs) can reveal sources of genome instability |
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