| P50 | author | Tadeusz Kaczorowski | Q76375400 |
| P2093 | author name string | Olesia Werbowy | |
| P2860 | cites work | Unique type of plasmid maintenance function: postsegregational killing of plasmid-free cells | Q24630262 |
| | Bacterial gene transfer by natural genetic transformation in the environment | Q24634610 |
| | To be or not to be: regulation of restriction-modification systems and other toxin-antitoxin systems | Q26865951 |
| | Horizontal gene transfer and the evolution of bacterial and archaeal population structure | Q27006506 |
| | The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers | Q28131744 |
| | Genetic exchange between bacteria in the environment | Q28144472 |
| | Construction and characterization of new cloning vehicle. II. A multipurpose cloning system | Q28298407 |
| | Plasmids of psychrophilic and psychrotolerant bacteria and their role in adaptation to cold environments | Q28652561 |
| | Natural DNA uptake by Escherichia coli | Q28730500 |
| | Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid | Q29614535 |
| | Genetic Stabilization of the Drug-Resistant PMEN1 Pneumococcus Lineage by Its Distinctive DpnIII Restriction-Modification System | Q30375739 |
| | Gene expression analysis indicates extensive genotype-specific crosstalk between the conjugative F-plasmid and the E. coli chromosome | Q30823734 |
| | Cellular responses to postsegregational killing by restriction-modification genes | Q33789255 |
| | Differential distribution of novel restriction-modification systems in clonal lineages of Neisseria meningitidis | Q33889686 |
| | Transduction, restriction and recombination patterns in Escherichia coli | Q33964276 |
| | A type III-like restriction endonuclease functions as a major barrier to horizontal gene transfer in clinical Staphylococcus aureus strains | Q33977856 |
| | The virulence plasmid of Salmonella typhimurium is self-transmissible | Q33991319 |
| | Stability of EcoRI restriction-modification enzymes in vivo differentiates the EcoRI restriction-modification system from other postsegregational cell killing systems. | Q34077198 |
| | Natural genetic transformation of clinical isolates of Escherichia coli in urine and water | Q34097581 |
| | Competence for natural transformation in Neisseria gonorrhoeae: components of DNA binding and uptake linked to type IV pilus expression | Q34157267 |
| | Neisseria meningitidis is structured in clades associated with restriction modification systems that modulate homologous recombination | Q34168120 |
| | Plasmids foster diversification and adaptation of bacterial populations in soil | Q34186192 |
| | Predicting plasmid promiscuity based on genomic signature | Q34291217 |
| | Bacterial transformation: distribution, shared mechanisms and divergent control | Q34403233 |
| | Horizontal gene transfer contributes to the wide distribution and evolution of type II restriction-modification systems | Q34407489 |
| | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts | Q34433472 |
| | A rapid and simple method for detection of type II restriction endonucleases in cells of bacteria with high activity of nonspecific nucleases | Q85371217 |
| | Escherichia coli is naturally transformable in a novel transformation system. | Q51112311 |
| | Transformation of colonial Escherichia coli on solid media. | Q51658326 |
| | Characterization of the stable maintenance of the Shigella flexneri plasmid pHS-2. | Q53979815 |
| | New plasmids carrying antibiotic-resistance cassettes. | Q54157574 |
| | Multimerization of high copy number plasmids causes instability: Cole 1 encodes a determinant essential for plasmid monomerization and stability | Q54477200 |
| | Trans-complementable copy-number mutants of plasmid ColE1. | Q54559090 |
| | Two related recombinases are required for site-specific recombination at dif and cer in E. coli K12. | Q54649603 |
| | Activity of DNA modification and restriction enzymes in KGB, a potassium glutamate buffer | Q64140384 |
| | Three new Escherichia coli O antigens O154, O155 and O156, and one new K antigen, K94 | Q67255364 |
| | Release of transforming plasmid and chromosomal DNA from two cultured soil bacteria | Q67862693 |
| | Multicopy plasmid stability in Escherichia coli requires host-encoded functions that lead to plasmid site-specific recombination | Q70248003 |
| | Transfer and maintenance of small, mobilizable plasmids with ColE1 replication origins in Legionella pneumophila | Q70258735 |
| | An improvement in electrophoretic transfer of DNA from a gel to DEAE-cellulose membrane | Q72837920 |
| | Interactions between the F conjugal transfer system and CloDF13::TnA plasmids | Q72873216 |
| | Post-segregational killing by restriction modification gene complexes: observations of individual cell deaths | Q73205987 |
| | Molecular evolution of the Escherichia coli chromosome. V. Recombination patterns among strains of diverse origin. | Q34607902 |
| | The EcoKI type I restriction-modification system in Escherichia coli affects but is not an absolute barrier for conjugation | Q34746929 |
| | Genetic Organization and Molecular Analysis of the Eco VIII Restriction-Modification System of Escherichia coli E1585-68 and Its Comparison with Isospecific Homologs | Q34987193 |
| | Genetic transformation in freshwater: Escherichia coli is able to develop natural competence | Q35193810 |
| | Replication initiator protein RepE of mini-F plasmid: functional differentiation between monomers (initiator) and dimers (autogenous repressor). | Q35200597 |
| | The biology of restriction and anti-restriction | Q36175695 |
| | Mobile genetic elements: the agents of open source evolution | Q36247081 |
| | Distribution and function of plasmids in Salmonella enterica | Q36319720 |
| | Regulation of plasmid replication | Q37060891 |
| | Homologous recombination drives both sequence diversity and gene content variation in Neisseria meningitidis. | Q37208928 |
| | DNA-uptake machinery of naturally competent Vibrio cholerae | Q37276485 |
| | The ecology of transfer of mobile genetic elements | Q37587421 |
| | Natural competence and the evolution of DNA uptake specificity | Q37713204 |
| | Mobility of plasmids. | Q37784107 |
| | Origins of bacterial diversity through horizontal genetic transfer and adaptation to new ecological niches | Q37895335 |
| | Diverse functions of restriction-modification systems in addition to cellular defense | Q38087543 |
| | The roles of extracellular DNA in the structural integrity of extracellular polymeric substance and bacterial biofilm development | Q38163928 |
| | Role of Restriction-Modification Systems in Prokaryotic Evolution and Ecology | Q38633219 |
| | Replication of plasmids in gram-negative bacteria | Q38733478 |
| | Functional analysis of putative restriction-modification system genes in the Helicobacter pylori J99 genome | Q39584191 |
| | Mutational analysis of the R64 oriT region: requirement for precise location of the NikA-binding sequence | Q39848060 |
| | Recombination at ColE1 cer requires the Escherichia coli xerC gene product, a member of the lambda integrase family of site-specific recombinases | Q39952069 |
| | Analysis of the sequence and gene products of the transfer region of the F sex factor | Q40625554 |
| | xerB, an Escherichia coli gene required for plasmid ColE1 site-specific recombination, is identical to pepA, encoding aminopeptidase A, a protein with substantial similarity to bovine lens leucine aminopeptidase | Q40817978 |
| | Bacterial Autoimmunity Due to a Restriction-Modification System | Q40820300 |
| | The arginine repressor is essential for plasmid-stabilizing site-specific recombination at the ColE1 cer locus | Q41096438 |
| | Phylogeny of the Enterobacteriaceae based on genes encoding elongation factor Tu and F-ATPase beta-subunit | Q41456831 |
| | Genetic analysis of maintenance of pEC156, a naturally occurring Escherichia coli plasmid that carries genes of the EcoVIII restriction-modification system | Q41699338 |
| | Inactivation of the SauI type I restriction-modification system is not sufficient to generate Staphylococcus aureus strains capable of efficiently accepting foreign DNA. | Q42172191 |
| | Characterization of pEC156, a ColE1-type plasmid from Escherichia coli E1585-68 that carries genes of the EcoVIII restriction-modification system | Q42660968 |
| | Characterization of pECL18 and pKPN2: a proposed pathway for the evolution of two plasmids that carry identical genes for a Type II restriction-modification system | Q44230072 |
| | Maintenance of species identity and controlling speciation of bacteria: a new function for restriction/modification systems? | Q44625634 |
| | Characterization of the LlaCI methyltransferase from Lactococcus lactis subsp. cremoris W15 provides new insights into the biology of type II restriction–modification systems | Q44643993 |
| | Plasmid host-range: restrictions to F replication in Pseudomonas | Q46567220 |
| | Transformation of Shewanella baltica with ColE1-like and P1 plasmids and their maintenance during bacterial growth in cultures | Q46701338 |
| | Molecular characterization of functional modules of plasmid pWKS1 of Paracoccus pantotrophus DSM 11072. | Q48284340 |
| | Characterization of the ColE1 mobilization region and its protein products | Q48295354 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Escherichia coli | Q25419 |
| P304 | page(s) | e0148355 | |
| P577 | publication date | 2016-01-01 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Plasmid pEC156, a Naturally Occurring Escherichia coli Genetic Element That Carries Genes of the EcoVIII Restriction-Modification System, Is Mobilizable among Enterobacteria | |
| P478 | volume | 11 | |