| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1008145739 |
| P356 | DOI | 10.1038/355467A0 |
| P953 | full work available at URL | http://www.nature.com/articles/355467a0 |
| http://www.nature.com/articles/355467a0.pdf | ||
| P698 | PubMed publication ID | 1734285 |
| P2093 | author name string | Schroeder C | |
| Krüger DH | |||
| Bickle TA | |||
| Meisel A | |||
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| P433 | issue | 6359 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 467-469 | |
| P577 | publication date | 1992-01-01 | |
| 1992-01-30 | |||
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Type III restriction enzymes need two inversely oriented recognition sites for DNA cleavage | |
| P478 | volume | 355 |
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| Q35259150 | DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion. |
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| Q39922663 | DNA supercoiling enables the type IIS restriction enzyme BspMI to recognise the relative orientation of two DNA sequences |
| Q37839479 | DNA translocation by type III restriction enzymes: a comparison of current models of their operation derived from ensemble and single-molecule measurements |
| Q35493879 | Digital gene expression for non-model organisms |
| Q42264175 | Dissociation from DNA of Type III Restriction-Modification enzymes during helicase-dependent motion and following endonuclease activity |
| Q38087543 | Diverse functions of restriction-modification systems in addition to cellular defense |
| Q37698622 | Diversity of DNA methyltransferases that recognize asymmetric target sequences |
| Q30437064 | EXPRSS: an Illumina based high-throughput expression-profiling method to reveal transcriptional dynamics. |
| Q37183920 | EcoR124I: from plasmid-encoded restriction-modification system to nanodevice |
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| Q32084623 | Endonuclease II of coliphage T4: a recombinase disguised as a restriction endonuclease? |
| Q42965698 | Functional analysis of MmeI from methanol utilizer Methylophilus methylotrophus, a subtype IIC restriction-modification enzyme related to type I enzymes |
| Q38336578 | Functional analysis of conserved motifs in type III restriction-modification enzymes |
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| Q33974590 | Gene expression analysis of plant host-pathogen interactions by SuperSAGE |
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| Q35315461 | Genome-wide DNA methylation analysis of Haloferax volcanii H26 and identification of DNA methyltransferase related PD-(D/E)XK nuclease family protein HVO_A0006. |
| Q40855229 | Genomic structure of the human DNA methyltransferase gene |
| Q38154090 | Highlights of the DNA cutters: a short history of the restriction enzymes |
| Q36318953 | Lineage-Specific Methyltransferases Define the Methylome of the Globally Disseminated Escherichia coli ST131 Clone. |
| Q34003605 | Linking promoters to functional transcripts in small samples with nanoCAGE and CAGEscan |
| Q37713815 | Maintaining a sense of direction during long-range communication on DNA. |
| Q52208938 | Mitochondrial DNA rearrangements: intracellular information system. |
| Q34598959 | MmeI: a minimal Type II restriction-modification system that only modifies one DNA strand for host protection |
| Q34041447 | Molecular bases and role of viruses in the human microbiome |
| Q34760153 | New restriction enzymes discovered from Escherichia coli clinical strains using a plasmid transformation method |
| Q24555228 | Nucleoside triphosphate-dependent restriction enzymes |
| Q34211653 | Origin of the diversity in DNA recognition domains in phasevarion associated modA genes of pathogenic Neisseria and Haemophilus influenzae |
| Q36917132 | Phase variable type III restriction-modification systems of host-adapted bacterial pathogens |
| Q33883325 | Reactions of type II restriction endonucleases with 8-base pair recognition sites |
| Q41078620 | Repercussions of DNA tracking by the type IC restriction endonuclease EcoR124I on linear, circular and catenated substrates. |
| Q41064710 | Restriction by EcoKI is enhanced by co-operative interactions between target sequences and is dependent on DEAD box motifs. |
| Q34037954 | Revenge of the phages: defeating bacterial defences |
| Q44608364 | S-Adenosyl Methionine Prevents Promiscuous DNA Cleavage by the EcoP1I type III Restriction Enzyme |
| Q42128175 | S-adenosyl homocysteine and DNA ends stimulate promiscuous nuclease activities in the Type III restriction endonuclease EcoPI |
| Q27316873 | SMRT sequencing of the Campylobacter coli BfR-CA-9557 genome sequence reveals unique methylation motifs. |
| Q36834032 | Short-range and long-range context effects on coliphage T4 endonuclease II-dependent restriction |
| Q64389526 | Single-site DNA cleavage by Type III restriction endonuclease requires a site-bound enzyme and a trans-acting enzyme that are ATPase-activated |
| Q35813483 | Structural basis of asymmetric DNA methylation and ATP-triggered long-range diffusion by EcoP15I |
| Q42790905 | Switching roles for a helicase |
| Q34316330 | The Type ISP Restriction-Modification enzymes LlaBIII and LlaGI use a translocation-collision mechanism to cleave non-specific DNA distant from their recognition sites. |
| Q89081042 | The crystal structure of the Helicobacter pylori LlaJI.R1 N-terminal domain provides a model for site-specific DNA binding |
| Q40462523 | The helicase-like domains of type III restriction enzymes trigger long-range diffusion along DNA |
| Q34097495 | The phasevarion: phase variation of type III DNA methyltransferases controls coordinated switching in multiple genes |
| Q42957729 | The single polypeptide restriction-modification enzyme LlaGI is a self-contained molecular motor that translocates DNA loops |
| Q34320449 | Transcriptional phase variation of a type III restriction-modification system in Helicobacter pylori |
| Q42131651 | Type III restriction endonuclease EcoP15I is a heterotrimeric complex containing one Res subunit with several DNA-binding regions and ATPase activity |
| Q39095250 | Type III restriction endonucleases are heterotrimeric: comprising one helicase-nuclease subunit and a dimeric methyltransferase that binds only one specific DNA. |
| Q37698719 | Type III restriction endonucleases translocate DNA in a reaction driven by recognition site-specific ATP hydrolysis |
| Q30494970 | Type III restriction enzymes cleave DNA by long-range interaction between sites in both head-to-head and tail-to-tail inverted repeat |
| Q37078204 | Type III restriction enzymes communicate in 1D without looping between their target sites |
| Q39360960 | Type III restriction is alleviated by bacteriophage (RecE) homologous recombination function but enhanced by bacterial (RecBCD) function |
| Q34358103 | Type III restriction-modification enzymes: a historical perspective |
| Q40404726 | Unidirectional translocation from recognition site and a necessary interaction with DNA end for cleavage by Type III restriction enzyme |
| Q28742836 | Unusual structures are present in DNA fragments containing super-long Huntingtin CAG repeats |
| Q53064050 | WITHDRAWN: Type III restriction-modification enzyme EcoP15I's base flipping mechanism and its mismatch cleavage on two head-to-head oriented recognition sites. |
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