| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/0092-8674(78)90316-1 |
| P953 | full work available at URL | https://api.elsevier.com/content/article/PII:0092867478903161?httpAccept=text/plain |
| https://api.elsevier.com/content/article/PII:0092867478903161?httpAccept=text/xml | ||
| P698 | PubMed publication ID | 350412 |
| P2093 | author name string | N. D. Grindley | |
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| Restriction endonucleases | Q34325231 | ||
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| Translocatable elements in procaryotes | Q40779727 | ||
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| A simple method for the preparation of 32P-labelled adenosine triphosphate of high specific activity | Q42958965 | ||
| Two sequence-specific endonucleases from Moraxella bovis | Q43964746 | ||
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| Multiple copies of the insertion-DNA sequences IS1 and IS2 in the chromosome of E. coli K-12 | Q53877266 | ||
| A specific endonuclease from Haemophilus haemolyticus | Q56256626 | ||
| Bacteriophage mu as a transposition element | Q67501100 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 419-426 | |
| P577 | publication date | 1978-03-01 | |
| P1433 | published in | Cell | Q655814 |
| P1476 | title | IS1 insertion generates duplication of a nine base pair sequence at its target site | |
| P478 | volume | 13 |
| Q24644871 | A gene between polA and glnA retards growth of Escherichia coli when present in multiple copies: physiological effects of the gene for spot 42 RNA |
| Q35424135 | A mechanism of DNA transposition |
| Q72925979 | A symmetrical six-base-pair target site sequence determines Tn10 insertion specificity |
| Q33929247 | Base substitutions in transposable element IS1 cause DNA duplication of variable length at the target site for plasmid co-integration. |
| Q54798497 | Both inverted repeat sequences located at the ends of IS1 provide promoter functions |
| Q41052555 | Characterisation of Tn1721, a new transposon containing tetracycline resistance genes capable of amplification |
| Q36162829 | Characterization of the defect in the Escherichia coli mutT1 mutator gene |
| Q34277232 | Characterization of translational initiation sites in E. coli |
| Q41079515 | Cloning and endonuclease restriction analysis of argF and of the control region of the argECBH bipolar operon in Escherichia coli |
| Q40996511 | Close vicinity of IS1 integration sites in the leader sequence of the gal operon of E. coli |
| Q40952793 | Complex Evolution of 7E Olfactory Receptor Genes in Segmental Duplications |
| Q38071427 | DNA Intermediates of Avian RNA Tumor Viruses |
| Q41062661 | DNA sequence analysis of Tn10 insertions: Origin and role of 9 bp flanking repetitions during Tn10 translocation |
| Q34051124 | DNA sequence analysis of the transposon Tn3: Three genes and three sites involved in transposition of Tn3 |
| Q40897843 | DNA sequence at the integration sites of the insertion element IS1 |
| Q41038873 | DNA sequence of the transposable element IS1 |
| Q50217918 | DNA sequences at the sites of three insertions of the transposable element Tn5 in the histidine operon of Salmonella |
| Q40501735 | DNA sequences of the integration sites and “inverted repeated structure of transposon Tn3 |
| Q72856814 | Deletions and an inversion induced by a resident IS1 of the lactose transposon Tn951 |
| Q36312072 | Deoxyribonucleic Acid Sequence Homologies Among Bacterial Insertion Sequence Elements and Genomes of Various Organisms |
| Q72856825 | Does the insertion element IS1 transpose preferentially into A+T-rich DNA segments? |
| Q41099754 | E. coli galactose-1-phosphate uridyl transferase: N-terminal and C-terminal sequences |
| Q48414425 | Effect of DNA sequences adjacent to the termini of Tn3 on sequential translocation |
| Q34364110 | Efficient Tn10 transposition into a DNA insertion hot spot in vivo requires the 5-methyl groups of symmetrically disposed thymines within the hot-spot consensus sequence |
| Q42069697 | Escherichia coli O-Antigen Gene Clusters of Serogroups O62, O68, O131, O140, O142, and O163: DNA Sequences and Similarity between O62 and O68, and PCR-Based Serogrouping. |
| Q40280306 | Excision sequences in the mitochondrial genome of yeast. |
| Q36276043 | Factors determining frequency of plasmid cointegration mediated by insertion sequence IS 1 |
| Q36387445 | Fate of donor insertion sequence IS1 during transposition |
| Q36332999 | Five mutations in the promoter region of the araBAD operon of Escherichia coli B/r |
| Q44542121 | Four types of IS1 with differences in nucleotide sequence reside in the Escherichia coli K-12 chromosome |
| Q33924006 | Frequent site-specific deletion of coliphage lambda murine sarcoma virus recombinants and its use in the identification of a retrovirus integration site |
| Q72887848 | Genetic analysis of transpositions in the lac region of Escherichia coli |
| Q40789850 | IS1-mediated intramolecular rearrangements: formation of excised transposon circles and replicative deletions |
| Q41148080 | IS4 is found between eleven or twelve base pair duplications |
| Q41037024 | Identification of the translocatable element IS1 in a molecular chimera constructed with plasmid pBR322 DNA into which a bacteriophage MS2 DNA copy was inserted by the poly(dA)·Poly(dT) linker method |
| Q36783201 | Insertion and excision of Caenorhabditis elegans transposable element Tc1. |
| Q29617579 | Insertion sequences |
| Q70214787 | Insertions of transposable elements in the promoter proximal region of the gene cluster for Escherichia coli H+-ATPase: 8 base pair repeat generated by insertion of IS1 |
| Q36400832 | Integration in vivo into simian virus 40 DNA of a sequence that resembles a certain family of genomic interspersed repeated sequences |
| Q41172106 | Integration of IS3 into IS2 generates a short sequence duplication |
| Q54543527 | Integration specificity of an artificial kanamycin transposon constructed by the in vitro insertion of an internal Tn5 fragment into IS2 |
| Q40081391 | Is elements and transposons |
| Q54564298 | Isolation and characterization of IS1 circles |
| Q33916109 | Isolation and characterization of recombinant DNA clones of avian retroviruses: size heterogeneity and instability of the direct repeat |
| Q39905138 | Lambda transducing phages derived from a finO- R100::λ cointegrate plasmid: Proteins encoded by the R100 replication/incompatibility region and the antibiotic resistance determinant |
| Q42682463 | Letting Escherichia coli teach me about genome engineering |
| Q45935768 | Mechanism for DNA transposons to generate introns on genomic scales. |
| Q35281190 | Mobile Minos elements from Drosophila hydei encode a two-exon transposase with similarity to the paired DNA-binding domain |
| Q48413668 | Molecular consequences of deletion formation mediated by the transposon TN9 |
| Q24597239 | Molecular model for the transposition and replication of bacteriophage Mu and other transposable elements |
| Q41004020 | Mu insertion duplicates a 5 base pair sequence at the host inserted site |
| Q48408583 | Multiple copies of iso-insertion sequences of IS1 in Shigella dysenteriae chromosome |
| Q36325178 | New class of mutations in Escherichia coli (uup) that affect precise excision of insertion elements and bacteriophage Mu growth |
| Q48416026 | Nucleotide sequence at the insertion sites of a kanamycin transposon |
| Q35687823 | Nucleotide sequence of IS26, a new prokaryotic mobile genetic etement |
| Q40481773 | Nucleotide sequence of the gene ompA coding the outer membrane protein II*of Escherichia coli K-12 |
| Q41083829 | Nucleotide sequence of the trpC-trpB intercistronic region from Salmonella typhimurium |
| Q48416484 | Nucleotide sequences at the ends of bacteriophage Mu DNA |
| Q36396830 | Nucleotide sequences of integrated Moloney sarcoma provirus long terminal repeats and their host and viral junctions |
| Q41053189 | Nucleotide sequences of the attachment sites of bacteriophage Mu DNA |
| Q40418917 | Nucleotide sequences of the gal E gene and the gal T gene of E. coli |
| Q37330006 | Organization of a hybrid between phage f1 and plasmid pSC101. |
| Q72899329 | Organization of chimeras between filamentous bacteriophage f1 and plasmid pSC101 |
| Q35994567 | Ovalbumin gene: evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries |
| Q54484978 | Plasmid R46 provides a function that promotes recA-independent deletion, fusion and resolution of replicon. |
| Q36354982 | Plasmids containing insertion elements are potential transposons |
| Q34842642 | Presence of a characteristic D-D-E motif in IS1 transposase |
| Q40196894 | Proviruses of avian sarcoma virus are terminally redundant, co-extensive with unintegrated linear DNA and integrated at many sites |
| Q40174433 | Recognition of messenger RNA during translational initiation in Escherichia coli |
| Q35235332 | Regulatory and coding potential of the mouse mammary tumor virus long terminal redundancy |
| Q54485830 | Replicon fusion mediated by a single-ended derivative of transposon Tn1721 |
| Q72887851 | Sequence analysis of Tn9 insertions in the lacZ gene |
| Q41548912 | Sequence of retrovirus provirus resembles that of bacterial transposable elements |
| Q39673181 | Sequences at the somatic recombination sites of immunoglobulin light-chain genes |
| Q39638807 | Sequences of mouse immunoglobulin light chain genes before and after somatic changes |
| Q72405852 | Specificity of Tn5 insertions into a 36-bp DNA sequence repeated in tandem seven times |
| Q39791956 | Split Genes and RNA Splicing |
| Q36179025 | Stimulation of IS1 excision by bacteriophage P1 ref function |
| Q41062598 | Structural features of λ site-specific recombination at a secondary att site in galT |
| Q40418448 | Structure of the DNA distal to the gene for ribosomal protein S20 in Escherichia coli K12: presence of a strong terminator and an IS1 element |
| Q42078020 | The dna sequence of bombyx mori fibroin gene including the 5′ flanking, mRNA coding, entire intervening and fibroin protein coding regions |
| Q41823889 | The evolution and consequences of snaR family transposition in primates |
| Q34142686 | The evolution and expression of the snaR family of small non-coding RNAs |
| Q48408759 | The nucleotide sequence of IS5 from Escherichia coli |
| Q34713767 | The nucleotide sequence of the gal T gene of Escherichia coli |
| Q72903676 | The requirement for both DNA polymerase and 5' to 3' exonuclease activities of DNA polymerase I during Tn5 transposition |
| Q38356749 | The ribosome binding sites recognized by E. coli ribosomes have regions with signal character in both the leader and protein coding segments. |
| Q35837514 | The transposable element Uhu from Hawaiian Drosophila--member of the widely dispersed class of Tc1-like transposons |
| Q40976480 | The transposon Tn9 generates a 9 bp repeated sequence during integration |
| Q48412952 | The yeast transposon Ty1 generates duplications of target DNA on insertion |
| Q37676993 | Transposable element IS1 intrinsically generates target duplications of variable length |
| Q41038958 | Transposition of DNA inserted into deletions of the Tn5 kanamycin resistance element |
| Q44283654 | Transposition of IS1-λBIO-IS1 from a bacteriophage λ derivative carrying the IS1-cat-IS1 transposon (Tn9) |
| Q34034537 | Transposition of the Escherichia coli insertion element gamma generates a five-base-pair repeat |
| Q72915933 | Variant insertion element IS1 generates 8-base pair duplications of the target sequence |
| Q42818905 | Virus genome integration as a function of the host cell genome replicative cycle |
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