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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
27
|
| pubmed:dateCreated |
1993-3-25
|
| pubmed:abstractText |
Oligoribonucleotides consisted of modified nucleotides at 3'-turmini were chemically synthesized on the solid phase method. Moreover, these analogues were investigated the stability in a prokaryotic cell-free translation system and the resistance against a few kind of nucleases containing 3'-exonuclease activity.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0261-3166
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
195-6
|
| pubmed:dateRevised |
2000-12-18
|
| pubmed:meshHeading | |
| pubmed:year |
1992
|
| pubmed:articleTitle |
Inhibitory effect of oligoribonucleotide phosphorodithioates against the 3'-exonuclease activity.
|
| pubmed:affiliation |
Department of Industrial Chemistry, Chiba Institute of Technology, Japan.
|
| pubmed:publicationType |
Journal Article
|