| P50 | author | Steve Petrovski | Q48060637 |
| P2093 | author name string | Vilma A Stanisich | |
| P2860 | cites work | Studies on transformation of Escherichia coli with plasmids | Q27860598 |
| | Mechanisms of, and barriers to, horizontal gene transfer between bacteria | Q28270244 |
| | Construction and characterization of new cloning vehicle. II. A multipurpose cloning system | Q28298407 |
| | Mobile gene cassettes and integrons: capture and spread of genes by site-specific recombination | Q28303444 |
| | Arrayed transposase-binding sequences on the ends of transposon Tn5090/Tn402 | Q30978563 |
| | Beginning a Genetic Analysis of Conjugational Transfer Determined by the F Factor inEscherichia coliby Isolation and Characterization of Transfer-Deficient Mutants | Q33775853 |
| | Family of class 1 integrons related to In4 from Tn1696. | Q33983281 |
| | Characterization and movement of the class 1 integron known as Tn2521 and Tn1405. | Q34107574 |
| | Bacterial mercury resistance from atoms to ecosystems | Q34209269 |
| | Tn7: smarter than we thought | Q34443592 |
| | The integrons In0, In2, and In5 are defective transposon derivatives | Q35610259 |
| | Region-specific insertion of transposons in combination with selection for high plasmid transferability and stability accounts for the structural similarity of IncP-1 plasmids | Q35759677 |
| | Integrons found in different locations have identical 5' ends but variable 3' ends | Q35979487 |
| | Inversions and deletions generated by a mini-gamma delta (Tn1000) transposon | Q36105620 |
| | Nosocomial bacterial infections in Intensive Care Units. I: Organisms and mechanisms of antibiotic resistance | Q36237707 |
| | Mobile genetic elements: the agents of open source evolution | Q36247081 |
| | The IS 1111 Family Members IS 4321 and IS 5075 Have Subterminal Inverted Repeats and Target the Terminal Inverted Repeats of Tn 21 Family Transposons | Q36371031 |
| | A chromosomally located transposon in Pseudomonas aeruginosa | Q36387358 |
| | Characterization of a translocation unit encoding resistance to mercuric ions that occurs on a nonconjugative plasmid in Pseudomonas aeruginosa | Q36598223 |
| | Tn402: a new transposable element determining trimethoprim resistance that inserts in bacteriophage lambda | Q36599148 |
| | Four genes, two ends, and a res region are involved in transposition of Tn5053: a paradigm for a novel family of transposons carrying either a mer operon or an integron | Q36794970 |
| | Genomics of IncP-1 antibiotic resistance plasmids isolated from wastewater treatment plants provides evidence for a widely accessible drug resistance gene pool | Q36841958 |
| | Structure of Haloacetate-Catabolic IncP-1β Plasmid pUO1 and Genetic Mobility of Its Residing Haloacetate-Catabolic Transposon | Q37052103 |
| | Simple and efficient generation in vitro of nested deletions and inversions: Tn5 intramolecular transposition | Q39723566 |
| | Transposon Tn5090 of plasmid R751, which carries an integron, is related to Tn7, Mu, and the retroelements | Q39932101 |
| | Characterization of In0 of Pseudomonas aeruginosa plasmid pVS1, an ancestor of integrons of multiresistance plasmids and transposons of gram-negative bacteria | Q39935989 |
| | Genetic and molecular characterization of Tn21, a multiple resistance transposon from R100.1 | Q39984238 |
| | Transposition of TnA does not generate deletions | Q40802245 |
| | Complete nucleotide sequence of Birmingham IncP alpha plasmids. Compilation and comparative analysis | Q42597254 |
| | Analysis of the multimer resolution system encoded by the parCBA operon of broad-host-range plasmid RP4. | Q42599469 |
| | Transposon targeting determined by resolvase | Q42624850 |
| | Sequence of the 68,869 bp IncP-1alpha plasmid pTB11 from a waste-water treatment plant reveals a highly conserved backbone, a Tn402-like integron and other transposable elements | Q43320985 |
| | Isolation and characterisation of deletion mutants involving the transfer genes of P-group plasmids in Pseudomonas aeruginosa | Q43684931 |
| | Characterization of Pseudomonas mercury-resistance transposon Tn502, which has a preferred insertion site in RP1. | Q43770966 |
| | R Factors from Proteus morganii | Q44749700 |
| | Present-day mercury resistance transposons are common in bacteria preserved in permafrost grounds since the Upper Pleistocene. | Q47257926 |
| | Tn5053 family transposons are res site hunters sensing plasmidal res sites occupied by cognate resolvases | Q47931334 |
| | Complete sequence of the IncPbeta plasmid R751: implications for evolution and organisation of the IncP backbone | Q48019720 |
| | Sequence of plasmid pBS228 and reconstruction of the IncP-1alpha phylogeny | Q48081324 |
| | tnpM: a novel regulatory gene that enhances Tn21 transposition and suppresses cointegrate resolution | Q48375870 |
| | The properties and host range of male-specific bacteriophages of Pseudomonas aeruginosa. | Q54634171 |
| | Cloning and genetic analysis of tra cistrons of the Tra 2/Tra 3 region of plasmid RP1 | Q64450930 |
| | Spontaneous deletions of the chromosome-mobilizing plasmid R68.45 in Pseudomonas aeruginosa PAO | Q67280928 |
| | Characterization of a Tra 2 function of RP1 that affects growth of Pseudomonas aeruginosa PAO and surface exclusion in Escherichia coli K12 | Q67490736 |
| | Genetic and molecular characterization of the Pseudomonas plasmid pVS1 | Q72387480 |
| | The location of sequences of TnA required for the establishment of transposition immunity | Q72923957 |
| | [Incorporation of Tn5053 and Tn402 into various plasmids] | Q73198970 |
| | High copy number plasmids compatible with commonly used cloning vectors | Q73562808 |
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1865-1874 | |
| P577 | publication date | 2010-01-29 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | Tn502 and Tn512 are res site hunters that provide evidence of resolvase-independent transposition to random sites | |
| P478 | volume | 192 | |