| Q39869214 | 25 years on and no end in sight: a perspective on the role of RecG protein |
| Q39547900 | A RecG-independent nonconservative branch migration mechanism in Escherichia coli recombination |
| Q48031487 | A broadening view of recombinational DNA repair in bacteria |
| Q46566186 | A genetic screen identifies genes and sites involved in pilin antigenic variation in Neisseria gonorrhoeae |
| Q38311217 | A mutation in helicase motif III of E. coli RecG protein abolishes branch migration of Holliday junctions |
| Q48292116 | A novel DNA repair enzyme containing RNA recognition, G-patch and specific splicing factor 45-like motifs in the protozoan parasite Toxoplasma gondii |
| Q46704758 | A role for topoisomerase III in a recombination pathway alternative to RuvABC. |
| Q24532894 | A sister-strand exchange mechanism for recA-independent deletion of repeated DNA sequences in Escherichia coli |
| Q33885962 | ATP-dependent resolution of R-loops at the ColE1 replication origin by Escherichia coli RecG protein, a Holliday junction-specific helicase |
| Q47848559 | Abortive recombination in Escherichia coli ruv mutants blocks chromosome partitioning |
| Q74499929 | Action of RuvAB at replication fork structures |
| Q40519763 | An E. coli RuvC mutant defective in cleavage of synthetic Holliday junctions. |
| Q33887041 | Bacteriophage T4 UvsW protein is a helicase involved in recombination, repair and the regulation of DNA replication origins |
| Q24634614 | Biochemistry of homologous recombination in Escherichia coli |
| Q28731284 | Bleomycin sensitivity in Escherichia coli is medium-dependent |
| Q71977426 | Blocked RecA Protein-mediated DNA Strand Exchange Reactions Are Reversed by the RuvA and RuvB Proteins |
| Q40788775 | Branch migration of three-strand recombination intermediates by RecG, a possible pathway for securing exchanges initiated by 3′-tailed duplex DNA |
| Q35221144 | Branch migration prevents DNA loss during double-strand break repair |
| Q39769826 | Cellular location and activity of Escherichia coli RecG proteins shed light on the function of its structurally unresolved C-terminus |
| Q38311085 | Characterisation of the catalytically active form of RecG helicase |
| Q33960250 | Chi enhances heteroduplex DNA levels during recombination |
| Q41852842 | Chi-dependent intramolecular recombination in Escherichia coli. |
| Q36016450 | Chromosome demise in the wake of ligase-deficient replication |
| Q35606793 | Cloning, sequencing, and expression of ruvB and characterization of RuvB proteins from two distantly related thermophilic eubacteria |
| Q42154440 | Conjugational recombination in Escherichia coli: genetic analysis of recombinant formation in Hfr x F- crosses |
| Q33266305 | Conjugative transfer can be inhibited by blocking relaxase activity within recipient cells with intrabodies. |
| Q40458920 | DNA Helicases. |
| Q39721275 | DNA binding and helicase domains of the Escherichia coli recombination protein RecG. |
| Q54491835 | DNA binding by the substrate specificity (wedge) domain of RecG helicase suggests a role in processivity. |
| Q52116526 | DNA binding of PriA protein requires cooperation of the N-terminal D-loop/arrested-fork binding and C-terminal helicase domains. |
| Q54549876 | Direct rescue of stalled DNA replication forks via the combined action of PriA and RecG helicase activities. |
| Q35821550 | Dissociation of RecA filaments from duplex DNA by the RuvA and RuvB DNA repair proteins |
| Q40871651 | Dissociation of synthetic Holliday junctions by E. coli RecG protein. |
| Q28210616 | Do bacteria have sex? |
| Q35208627 | Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo |
| Q37091823 | Effects of mutations involving cell division, recombination, and chromosome dimer resolution on a priA2::kan mutant |
| Q54660900 | Escherichia coli RuvA and RuvB proteins involved in recombination repair: physical properties and interactions with DNA. |
| Q39566865 | Escherichia coli strains lacking protein HU are UV sensitive due to a role for HU in homologous recombination |
| Q46085410 | Evidence for the role of Mycobacterium tuberculosis RecG helicase in DNA repair and recombination |
| Q45273557 | Evolution of a phage RuvC endonuclease for resolution of both Holliday and branched DNA junctions |
| Q33411553 | Expansion of a chromosomal repeat in Escherichia coli: roles of replication, repair, and recombination functions |
| Q34619495 | Fission yeast Mus81.Eme1 Holliday junction resolvase is required for meiotic crossing over but not for gene conversion |
| Q38331746 | Formation and resolution of recombination intermediates by E. coli RecA and RuvC proteins. |
| Q37059813 | Functions of the gene products of Escherichia coli. |
| Q35568725 | Genetic analysis of recombination in prokaryotes |
| Q40000545 | Genetic recombination in Bacillus subtilis 168: contribution of Holliday junction processing functions in chromosome segregation |
| Q34762160 | Genome stability and the processing of damaged replication forks by RecG. |
| Q24554445 | Helicobacter pylori mutants defective in RuvC Holliday junction resolvase display reduced macrophage survival and spontaneous clearance from the murine gastric mucosa |
| Q24631768 | Historical overview: searching for replication help in all of the rec places |
| Q33731119 | Holliday junction processing in bacteria: insights from the evolutionary conservation of RuvABC, RecG, and RusA |
| Q34308000 | Homologous Recombination-Experimental Systems, Analysis, and Significance |
| Q33367250 | Homologous genetic recombination: the pieces begin to fall into place |
| Q34588314 | Homologous recombination prevents methylation-induced toxicity in Escherichia coli |
| Q34057928 | Homologous recombination-dependent initiation of DNA replication from DNA damage-inducible origins in Escherichia coli |
| Q40733607 | Hotspots of homologous recombination |
| Q26999878 | I came to a fork in the DNA and there was RecG |
| Q40445651 | Identification of Salmonella functions critical for bacterial cell division within eukaryotic cells |
| Q40733589 | In vitro reconstitution of homologous recombination reactions |
| Q36074341 | Inefficient replication reduces RecA-mediated repair of UV-damaged plasmids introduced into competent Escherichia coli |
| Q37060462 | Interaction of Escherichia coli RuvA and RuvB proteins with synthetic Holliday junctions |
| Q41020200 | Interaction of branch migration translocases with the Holliday junction-resolving enzyme and their implications in Holliday junction resolution |
| Q36868446 | Interactions between branched DNAs and peptide inhibitors of DNA repair |
| Q24555268 | Inverted repeats as genetic elements for promoting DNA inverted duplication: implications in gene amplification |
| Q44582419 | Loss of lambda prophage recombinogenicity in UV-irradiated Escherichia coli: the role of host genes ruvA, ruvB, ruvC, and recG. |
| Q47430442 | Mitochondrial helicase Irc3 translocates along double-stranded DNA. |
| Q41885642 | Modulation of DNA damage tolerance in Escherichia coli recG and ruv strains by mutations affecting PriB, the ribosome and RNA polymerase |
| Q37425044 | Modulation of DNA repair and recombination by the bacteriophage lambda Orf function in Escherichia coli K-12. |
| Q73707166 | Modulation of RNA polymerase by (p)ppGpp reveals a RecG-dependent mechanism for replication fork progression |
| Q39843576 | Modulation of recombination and DNA repair by the RecG and PriA helicases of Escherichia coli K-12. |
| Q36164197 | Molecular organization and nucleotide sequence of the recG locus of Escherichia coli K-12. |
| Q57296948 | Movement of the RecG Motor Domain upon DNA Binding Is Required for Efficient Fork Reversal |
| Q42671634 | Mutation of D. radiodurans in a gene homologous to ruvB of E. coli |
| Q39930943 | Mutation of recF, recJ, recO, recQ, or recR improves Hfr recombination in resolvase-deficient ruv recG strains of Escherichia coli |
| Q38297065 | Mycobacterium tuberculosis RecG protein but not RuvAB or RecA protein is efficient at remodeling the stalled replication forks: implications for multiple mechanisms of replication restart in mycobacteria |
| Q33966750 | Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation |
| Q41859747 | Pathological replication in cells lacking RecG DNA translocase |
| Q21562309 | Physical analyses of E. coli heteroduplex recombination products in vivo: on the prevalence of 5' and 3' patches |
| Q54530429 | PriA supports two distinct pathways for replication restart in UV-irradiated Escherichia coli cells. |
| Q40733598 | Processing of Holliday junctions by the Escherichia coli RuvA, RuvB, RuvC and RecG proteins |
| Q40794340 | Processing of intermediates in recombination and DNA repair: identification of a new endonuclease that specifically cleaves Holliday junctions |
| Q40406462 | Processing of recombination intermediates by the RecG and RuvAB proteins of Escherichia coli |
| Q40587137 | Promoting and avoiding recombination: contrasting activities of the Escherichia coli RuvABC Holliday junction resolvase and RecG DNA translocase |
| Q44131194 | Purification and properties of the RuvA and RuvB proteins of Escherichia coli |
| Q24561435 | RecBCD enzyme is altered upon cutting DNA at a chi recombination hotspot |
| Q35922661 | RecG Directs DNA Synthesis during Double-Strand Break Repair. |
| Q30545725 | RecG and UvsW catalyse robust DNA rewinding critical for stalled DNA replication fork rescue |
| Q39117161 | RecG controls DNA amplification at double-strand breaks and arrested replication forks |
| Q47864494 | RecG helicase promotes DNA double-strand break repair |
| Q42410405 | RecG protein and single-strand DNA exonucleases avoid cell lethality associated with PriA helicase activity in Escherichia coli |
| Q33759205 | RecQ-dependent death-by-recombination in cells lacking RecG and UvrD |
| Q37412734 | Recombination and annealing pathways compete for substrates in making rrn duplications in Salmonella enterica |
| Q40672412 | Recombination genes and proteins |
| Q39498597 | Recombination is essential for viability of an Escherichia coli dam (DNA adenine methyltransferase) mutant |
| 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 |
| Q41831376 | Rep and PriA helicase activities prevent RecA from provoking unnecessary recombination during replication fork repair |
| Q39758873 | Repair and antirepair DNA helicases in Helicobacter pylori |
| Q36102308 | Repair of heteroduplex DNA molecules with multibase loops in Escherichia coli |
| Q42696576 | Replication fork collisions cause pathological chromosomal amplification in cells lacking RecG DNA translocase |
| Q47814162 | Requirement for RecFOR-mediated recombination in priA mutant |
| Q39493365 | Requirement of DNA repair mechanisms for survival of Burkholderia cepacia G4 upon degradation of trichloroethylene |
| Q34311622 | Rescue of arrested replication forks by homologous recombination |
| Q39929442 | Resolution of Holliday intermediates in recombination and DNA repair: indirect suppression of ruvA, ruvB, and ruvC mutations. |
| Q39958180 | Resolution of Holliday junctions in Escherichia coli: identification of the ruvC gene product as a 19-kilodalton protein |
| Q38134624 | Resolving branched DNA intermediates with structure-specific nucleases during replication in eukaryotes. |
| Q24539558 | Role for radA/sms in recombination intermediate processing in Escherichia coli |
| Q33992862 | Roles of RuvC and RecG in phage lambda red-mediated recombination |
| Q36101351 | RuvA and RuvB proteins of Escherichia coli exhibit DNA helicase activity in vitro |
| Q77550034 | RuvAB acts at arrested replication forks |
| Q79661973 | SSB as an organizer/mobilizer of genome maintenance complexes |
| Q36535282 | SSB binds to the RecG and PriA helicases in vivo in the absence of DNA. |
| Q38346395 | Situational repair of replication forks: roles of RecG and RecA proteins |
| Q27635329 | Structural analysis of DNA replication fork reversal by RecG |
| Q37178493 | Superfamily 2 helicases |
| Q39533792 | The Balance between Recombination Enzymes and Accessory Replicative Helicases in Facilitating Genome Duplication |
| Q48120447 | The RECG1 DNA Translocase Is a Key Factor in Recombination Surveillance, Repair, and Segregation of the Mitochondrial DNA in Arabidopsis. |
| Q42123307 | The RuvAB branch migration translocase and RecU Holliday junction resolvase are required for double-stranded DNA break repair in Bacillus subtilis |
| Q39840417 | The RuvABC proteins and Holliday junction processing in Escherichia coli |
| Q27937940 | The Saccharomyces cerevisiae RuvB-like protein, Tih2p, is required for cell cycle progression and RNA polymerase II-directed transcription |
| Q40388120 | The acidic pin of RuvA modulates Holliday junction binding and processing by the RuvABC resolvasome. |
| Q58388571 | The core stimulon of Corynebacterium pseudotuberculosis strain 1002 identified using ab initio methodologies |
| Q40605233 | The nucleotide excision repair system of Borrelia burgdorferi is the sole pathway involved in repair of DNA damage by UV light |
| Q35980025 | The phage lambda orf gene encodes a trans-acting factor that suppresses Escherichia coli recO, recR, and recF mutations for recombination of lambda but not of E. coli |
| Q34243612 | Therefore, what are recombination proteins there for? |
| Q40406287 | Two cDNAs from the plant Arabidopsis thaliana that partially restore recombination proficiency and DNA-damage resistance to E. coli mutants lacking recombination-intermediate-resolution activities |
| Q33356622 | Unveiling novel RecO distant orthologues involved in homologous recombination |
| Q33994900 | radC102 of Escherichia coli is an allele of recG |
| Q33325899 | ruvA Mutants that resolve Holliday junctions but do not reverse replication forks |
| Q43196483 | ruvA and ruvB mutants specifically impaired for replication fork reversal |
| Q53912911 | xni-deficient Escherichia coli are proficient for recombination and multiple pathways of repair |