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Archives of pathology & laboratory medicine, 1990 Some of the next articles are maybe not open access.
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Restriction Enzyme Computation
2003In this paper implementation of an inner hair cell model, including macromechanics and mechanical to neural transduction process is presented and discussed. The well-known Meddis model will be use as the reference system, and a high level synthesis will provide a parametrizable implementation and a reusability code, which allows future refinements on ...
Olgierd Unold, Maciej Troc
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Restriction enzymes in cells, not eppendorfs
Trends in Microbiology, 1994Restriction enzymes are essential reagents to molecular biologists, but their relevance to bacterial populations is less obvious. Most bacteria encode restriction and modification systems and these are commonly considered to be a barrier to phage infection. Current evidence also supports a more general role for them in genetic recombination.
G, King, N E, Murray
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Recognition Sequence of a Restriction Enzyme
Nature New Biology, 1973Restriction endonuclease EcoRII makes about twenty double-stranded breaks per molecule of λh80 DNA. The 5′-terminal sequences are pC-C-A-G-G and pC-C-T-G-G. These are complementary and rotationally symmetrical, showing how the enzyme may produce DNA fragments with short cohesive ends.
C H, Bigger, K, Murray, N E, Murray
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ATP-dependent restriction enzymes
2000The phenomenon of restriction and modification (R-M) was first observed in the course of studies on bacteriophages in the early 1950s. It was only in the 1960s that work of Arber and colleagues provided a molecular explanation for the host specificity.
Rao, Desirazu N +2 more
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Class-IIS restriction enzymes — a review
Gene, 1991Class-IIS restriction enzymes (ENases-IIS) interact with two discrete sites on double-stranded DNA: the recognition site, which is 4-7 bp long, and the cleavage site, usually 1-20 bp away from the recognition site. The recognition sequences of ENases-IIS are totally (or partially) asymmetric and all of the characterized ENases-IIS are monomeric.
Szybalski, W +3 more
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Restriction enzymes are bacterial enzymes that cleave DNA at specific recognition sequences, usually consisting of four to eight base pairs. These enzymes have become invaluable tools in molecular biology, enabling scientists to manipulate and analyze DNA in various ways. Restriction enzymes are used in various applications, including gene cloning, DNA
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Model for wandering restriction enzymes
Nature, 1974I WISH to propose a model for those DNA restriction enzymes which, although requiring specific recognition sites, make a limited number of cuts at apparently random sites, far from the recognition sites.
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High Throughput Cloning with Restriction Enzymes
2008The systematic structural analysis of many target proteins involves generating expression clones in high throughput. This requires robust laboratory procedures and benefits from laboratory automation and data management systems. This chapter gives an overview of the Protein Structure Factory, a structural genomics project focusing on human proteins ...
Sievert, V., Ergin, A., Büssow, K.
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