| pubmed-article:2838807 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0028630 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0012906 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0028621 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0041917 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:2838807 | lifeskim:mentions | umls-concept:C0332256 | lld:lifeskim |
| pubmed-article:2838807 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:2838807 | pubmed:dateCreated | 1988-8-5 | lld:pubmed |
| pubmed-article:2838807 | pubmed:abstractText | Decadeoxyribonucleotides containing uracil, 5-bromouracil, 5-cyanouracil and 5-ethyluracil in recognition sequences of restriction endonucleases Bgl II, Sau 3AI, Mbo I were synthesized. Decanucleotides containing 5-bromouracil in place of thymine had essentially the same susceptibility to all the restriction endonucleases. Uracil-containing decanucleotides were however very resistant to attack. Decanucleotides containing 5-cyanouracil in the recognition sequence were strongly resistant to hydrolysis by Sau 3AI, but were hydrolysed by Bgl II and Mbo I as well as the parent decanucleotide. Decanucleotides containing 5-ethyluracil were strongly resistant to hydrolysis by Sau 3AI, but were partially resistant to hydrolysis by Bgl II and Mbo I. | lld:pubmed |
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| pubmed-article:2838807 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2838807 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2838807 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2838807 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2838807 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:2838807 | pubmed:issn | 0305-1048 | lld:pubmed |
| pubmed-article:2838807 | pubmed:author | pubmed-author:HayakawaTT | lld:pubmed |
| pubmed-article:2838807 | pubmed:author | pubmed-author:UedaTT | lld:pubmed |
| pubmed-article:2838807 | pubmed:author | pubmed-author:OnoAA | lld:pubmed |
| pubmed-article:2838807 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2838807 | pubmed:day | 10 | lld:pubmed |
| pubmed-article:2838807 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:2838807 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2838807 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2838807 | pubmed:pagination | 4761-76 | lld:pubmed |
| pubmed-article:2838807 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:2838807 | pubmed:meshHeading | pubmed-meshheading:2838807-... | lld:pubmed |
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| pubmed-article:2838807 | pubmed:meshHeading | pubmed-meshheading:2838807-... | lld:pubmed |
| pubmed-article:2838807 | pubmed:year | 1988 | lld:pubmed |
| pubmed-article:2838807 | pubmed:articleTitle | Synthesis of decadeoxyribonucleotides containing 5-modified uracils and their interactions with restriction endonucleases Bgl II, Sau 3AI and Mbo I (nucleosides and nucleotides 82). | lld:pubmed |
| pubmed-article:2838807 | pubmed:affiliation | Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan. | lld:pubmed |
| pubmed-article:2838807 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2838807 | pubmed:publicationType | Comparative Study | lld:pubmed |
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