scholarly article | Q13442814 |
P2093 | author name string | N Kleckner | |
R M Chalmers | |||
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Aberrant Transpositions of Maize Double Ds-Like Elements Usually Involve Ds Ends on Sister Chromatids | Q28202801 | ||
IS10 transposition is regulated by DNA adenine methylation | Q28286919 | ||
Genetic evidence that Tn10 transposes by a nonreplicative mechanism | Q28287295 | ||
Mutational analysis of IS10's outside end. | Q33570250 | ||
Transposase-induced excision and circularization of the bacterial insertion sequence IS911 | Q33969288 | ||
The two single-strand cleavages at each end of Tn10 occur in a specific order during transposition | Q34009809 | ||
Genetic engineering in vivo using translocatable drug-resistance elements. New methods in bacterial genetics | Q34177240 | ||
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Polynucleotidyl transfer reactions in transpositional DNA recombination | Q35339797 | ||
One-ended insertion of IS911. | Q36105445 | ||
Excision of Tn10 from the donor site during transposition occurs by flush double-strand cleavages at the transposon termini | Q37021318 | ||
Structural requirement for IS50-mediated gene transposition | Q37603099 | ||
Intramolecular transposition by a synthetic IS50 (Tn5) derivative | Q37608517 | ||
Identification and characterization of a pre-cleavage synaptic complex that is an early intermediate in Tn10 transposition | Q37622400 | ||
Tn 10 transposition in vivo: temporal separation of cleavages at the two transposon ends and roles of terminal basepairs subsequent to interaction of ends | Q37634736 | ||
Communication between segments of DNA during site-specific recombination | Q39506967 | ||
Implications of Tn5-associated adjacent deletions | Q39885182 | ||
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The maize transposable element activator (Ac). | Q40942852 | ||
Inversions and deletions of the Salmonella chromosome generated by the translocatable tetracycline resistance element Tn10 | Q41008331 | ||
Dissection of the transposition process: A transposon-encoded site-specific recombination system | Q41148030 | ||
Physical structures of Tn10-promoted deletions and inversions: role of 1400 bp inverted repetitions | Q41674392 | ||
Intermolecular transposition of IS10 causes coupled homologous recombination at the transposition site | Q42180580 | ||
Mechanism of IS1 transposition in E. coli: choice between simple insertion and cointegration | Q42958659 | ||
Replicative and conservative transpositional recombination of insertion sequences | Q44654526 | ||
Does Tn10 transpose via the cointegrate molecule? | Q54484797 | ||
Tn10/IS10 transposase purification, activation, and in vitro reaction. | Q54637566 | ||
Kinetic and structural analysis of a cleaved donor intermediate and a strand transfer intermediate in Tn10 transposition. | Q54701850 | ||
Tn10 transposition and circle formation in vitro. | Q54760105 | ||
A specific class of IS10 transposase mutants are blocked for target site interactions and promote formation of an excised transposon fragment | Q64390107 | ||
Efficient Mu transposition requires interaction of transposase with a DNA sequence at the Mu operator: implications for regulation | Q69353019 | ||
Intramolecular transposition by Tn10 | Q69358286 | ||
Cointegrate formation by IS50 requires multiple donor molecules | Q69822491 | ||
A genetic analysis of DNA sequence requirements for Dissociation state I activity in tobacco | Q70461776 | ||
The three chemical steps of Tn10/IS10 transposition involve repeated utilization of a single active site | Q70908577 | ||
Induction of the SOS response by IS1 transposase | Q72732383 | ||
A symmetrical six-base-pair target site sequence determines Tn10 insertion specificity | Q72925979 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 5112-5122 | |
P577 | publication date | 1996-09-01 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | IS10/Tn10 transposition efficiently accommodates diverse transposon end configurations | |
P478 | volume | 15 |
Q34485070 | A simple topological filter in a eukaryotic transposon as a mechanism to suppress genome instability |
Q39647805 | A target specificity switch in IS911 transposition: the role of the OrfA protein |
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Q34040145 | Crosstalk between transposase subunits during cleavage of the mariner transposon |
Q24791637 | Cyclic changes in the affinity of protein-DNA interactions drive the progression and regulate the outcome of the Tn10 transposition reaction |
Q39720223 | Deletion endpoint allele-specificity in the developmentally regulated elimination of an internal sequence (IES) in Paramecium |
Q35188701 | Drosophila P-element transposase is a novel site-specific endonuclease |
Q39961248 | Early intermediates of mariner transposition: catalysis without synapsis of the transposon ends suggests a novel architecture of the synaptic complex |
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Q33387425 | Factors acting on Mos1 transposition efficiency |
Q42095907 | Factors responsible for target site selection in Tn10 transposition: a role for the DDE motif in target DNA capture. |
Q37569830 | Gene therapy vectors: the prospects and potentials of the cut-and-paste transposons |
Q29617579 | Insertion sequences |
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Q35892099 | Nucleotide sequence and evolution of the five-plasmid complement of the phytopathogen Pseudomonas syringae pv. maculicola ES4326. |
Q39645547 | Protein-DNA contacts and conformational changes in the Tn10 transpososome during assembly and activation for cleavage |
Q42267002 | Temperature triggers immune evasion by Neisseria meningitidis |
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Q24674060 | The human SETMAR protein preserves most of the activities of the ancestral Hsmar1 transposase |
Q58764059 | Transposase subunit architecture and its relationship to genome size and the rate of transposition in prokaryotes and eukaryotes |
Q42238684 | Transposition of Mboumar-9: identification of a new naturally active mariner-family transposon |
Q42944896 | Transposition of the human Hsmar1 transposon: rate-limiting steps and the importance of the flanking TA dinucleotide in second strand cleavage. |