pubmed-article:8785472 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0600436 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C1979882 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0683598 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0178499 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0205430 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0205171 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0871161 | lld:lifeskim |
pubmed-article:8785472 | lifeskim:mentions | umls-concept:C0597094 | lld:lifeskim |
pubmed-article:8785472 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:8785472 | pubmed:dateCreated | 1996-9-26 | lld:pubmed |
pubmed-article:8785472 | pubmed:abstractText | 4'-Thio-beta-D-oligoribonucleotides (12 mer and 16 mer) containing a mixed base sequence were synthesized via the phosphoramidite solid support approach. These RNA analogs showed very good nuclease resistance as compared with wild-type RNA. Furthermore, 4'-thio-beta-D-oligoribonucleotides were shown to hybridize with a complementary DNA or RNA strand to form a duplex or with a DNA hairpin to form a triple helix. 4'-Thio-RNA binds more tightly to its complementary RNA strand than to its complementary DNA strand. A 4'-thio-RNA:RNA duplex is as stable as a 2'-O-methyl-RNA:RNA duplex. 4'-Thio-RNA, however, forms a 4'-thio-RNA:DNA:DNA triplex with a stability similar to the corresponding triplex with all wild-type DNA. | lld:pubmed |
pubmed-article:8785472 | pubmed:language | eng | lld:pubmed |
pubmed-article:8785472 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8785472 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8785472 | pubmed:issn | 1050-5261 | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:ImbachJ LJL | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:RaynesAA | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:MorvanFF | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:BarascutJ LJL | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:BelloyCC | lld:pubmed |
pubmed-article:8785472 | pubmed:author | pubmed-author:LeydierCC | lld:pubmed |
pubmed-article:8785472 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8785472 | pubmed:volume | 5 | lld:pubmed |
pubmed-article:8785472 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8785472 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8785472 | pubmed:pagination | 167-74 | lld:pubmed |
pubmed-article:8785472 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:8785472 | pubmed:meshHeading | pubmed-meshheading:8785472-... | lld:pubmed |
pubmed-article:8785472 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:8785472 | pubmed:articleTitle | 4'-Thio-RNA: synthesis of mixed base 4'-thio-oligoribonucleotides, nuclease resistance, and base pairing properties with complementary single and double strand. | lld:pubmed |
pubmed-article:8785472 | pubmed:affiliation | Laboratoire de Chimie Bio-Organique, URA 488, CNRS, Université de Montpellier II, France. | lld:pubmed |
pubmed-article:8785472 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8785472 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:8785472 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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