Source:http://linkedlifedata.com/resource/pubmed/id/10474253
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0028953,
umls-concept:C0086418,
umls-concept:C0178499,
umls-concept:C0205369,
umls-concept:C0441655,
umls-concept:C0524637,
umls-concept:C0599219,
umls-concept:C0949374,
umls-concept:C1280500,
umls-concept:C1444754,
umls-concept:C1511636,
umls-concept:C1555721,
umls-concept:C1706204
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pubmed:issue |
6-7
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pubmed:dateCreated |
1999-9-30
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pubmed:abstractText |
We have identified phosphodiester oligonucleotides composed of G and T bases, named GTn, which are able to inhibit the cellular growth of human cancer cell lines by recognising specific nuclear proteins. We demonstrated that GTn oligonucleotides require a length of at least 20 nucleotides in order to exert a significant cytotoxic effect and to retain the specific protein binding ability. In addition, we found that GTn cytotoxicity was lost when A or C bases were introduced at either 3' and 5' end or within the GTn sequences.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0732-8311
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1711-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading | |
pubmed:articleTitle |
Effect of oligomer length and base substitutions on the cytotoxic activity and specific nuclear protein recognition of GTn oligonucleotides in the human leukemic CCRF-CEM cell line.
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pubmed:affiliation |
Department of Biomedical Sciences and Technologies, University of Udine, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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