| pubmed-article:2838824 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0000263 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0011516 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0028948 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0243126 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0332256 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
| pubmed-article:2838824 | lifeskim:mentions | umls-concept:C1527240 | lld:lifeskim |
| pubmed-article:2838824 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:2838824 | pubmed:dateCreated | 1988-8-11 | lld:pubmed |
| pubmed-article:2838824 | pubmed:abstractText | A protected 2-aminopurine nucleoside suitable for incorporation into oligodeoxynucleotides using phosphite triester chemical synthesis procedures has been prepared via oxidation of a purine hydrazino derivative with silver (I) oxide. Five oligodeoxynucleotides containing Eco RI and Bam HI recognition sites have been prepared such that, in the double stranded form, the 2-aminopurine base has either a complementary thymine or cytosine nucleobase. The helix character and thermodynamic parameters for helix formation have been examined. | lld:pubmed |
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| pubmed-article:2838824 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:2838824 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2838824 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2838824 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:2838824 | pubmed:issn | 0305-1048 | lld:pubmed |
| pubmed-article:2838824 | pubmed:author | pubmed-author:McLaughlinL... | lld:pubmed |
| pubmed-article:2838824 | pubmed:author | pubmed-author:LeoniJJ | lld:pubmed |
| pubmed-article:2838824 | pubmed:author | pubmed-author:BenselerFF | lld:pubmed |
| pubmed-article:2838824 | pubmed:author | pubmed-author:PielNN | lld:pubmed |
| pubmed-article:2838824 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2838824 | pubmed:day | 24 | lld:pubmed |
| pubmed-article:2838824 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:2838824 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2838824 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2838824 | pubmed:pagination | 5631-44 | lld:pubmed |
| pubmed-article:2838824 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:2838824 | pubmed:year | 1988 | lld:pubmed |
| pubmed-article:2838824 | pubmed:articleTitle | A new approach to the synthesis of a protected 2-aminopurine derivative and its incorporation into oligodeoxynucleotides containing the Eco RI and Bam HI recognition sites. | lld:pubmed |
| pubmed-article:2838824 | pubmed:affiliation | Department of Chemistry, Boston College, Chestnut Hill, MA 02167. | lld:pubmed |
| pubmed-article:2838824 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2838824 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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