Source:http://linkedlifedata.com/resource/pubmed/id/14592428
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2003-10-31
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pubmed:abstractText |
The major challenges for anti-hepatitis B Virus (HBV) therapy are the low efficacy of current drugs and the occurrence of drug resistant HBV mutations. A drug with new target sites or independent metabolic pathways may overcome these shortcomings. Small interfering RNA (siRNA) offers the possibility of developing a new anti-HBV therapy. Here we describe the almost complete inhibition of HBV replication by stably expressed 21-mer short hairpin RNAs (shRNA). Besides the conventional targets on HBV reverse-transcriptase, we also systemically targeted other sites of pregenomic RNA, including direct repeat (DR) elements, S, core, and X gene. Our results indicated that shRNAs can serve as efficient alternative anti-HBV agents. They can also be used in combination with chemotherapy, because they showed better effects on the inhibition of HBV replication due to different mechanisms of drug actions.
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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:month |
Nov
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pubmed:issn |
0006-291X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
14
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pubmed:volume |
311
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
398-404
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14592428-Carcinoma, Hepatocellular,
pubmed-meshheading:14592428-Cell Line, Tumor,
pubmed-meshheading:14592428-Gene Expression Regulation, Viral,
pubmed-meshheading:14592428-Gene Therapy,
pubmed-meshheading:14592428-Hepatitis B virus,
pubmed-meshheading:14592428-Humans,
pubmed-meshheading:14592428-Lamivudine,
pubmed-meshheading:14592428-RNA, Small Interfering,
pubmed-meshheading:14592428-Virus Replication
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pubmed:year |
2003
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pubmed:articleTitle |
Inhibition of hepatitis B virus replication by stably expressed shRNA.
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pubmed:affiliation |
The Institute of Molecular Biology and Open Laboratory of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Hong Kong, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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