[Inhibition of hepatitis C virus by antisense oligodeoxynucleotide in vitro].
Identifieur interne : 002B39 ( Ncbi/Curation ); précédent : 002B38; suivant : 002B40[Inhibition of hepatitis C virus by antisense oligodeoxynucleotide in vitro].
Auteurs : Y. Liu [République populaire de Chine] ; Z. Chen ; N. HeSource :
- Zhonghua yi xue za zhi [ 0376-2491 ] ; 1997.
Descripteurs français
- KwdFr :
- MESH :
- biosynthèse : ARN messager, Antigènes de l'hépatite C.
- cytologie : Lymphocytes T CD4+.
- génétique : Hepacivirus.
- pharmacologie : Oligonucléotides antisens.
- Cellules cultivées, Hepacivirus, Humains, Réplication virale.
English descriptors
- KwdEn :
- MESH :
- chemical , biosynthesis : Hepatitis C Antigens, RNA, Messenger.
- cytology : CD4-Positive T-Lymphocytes.
- drug effects : Hepacivirus, Virus Replication.
- genetics : Hepacivirus.
- chemical , pharmacology : Oligonucleotides, Antisense.
- Cells, Cultured, Humans.
Abstract
To study inhibitory effect of antisense oligodeoxynucleotide (asODN) on HCV in vitro.
PubMed: 9772458
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pubmed:9772458Le document en format XML
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<affiliation wicri:level="3"><nlm:affiliation>Institute of Infectious Disease, Zhejiang Medical University, Hangzhou.</nlm:affiliation>
<country>République populaire de Chine</country>
<placeName><settlement type="city">Hangzhou</settlement>
<region type="province">Zhejiang</region>
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<wicri:orgArea>Institute of Infectious Disease, Zhejiang Medical University</wicri:orgArea>
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<author><name sortKey="Chen, Z" sort="Chen, Z" uniqKey="Chen Z" first="Z" last="Chen">Z. Chen</name>
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<series><title level="j">Zhonghua yi xue za zhi</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>CD4-Positive T-Lymphocytes (cytology)</term>
<term>Cells, Cultured</term>
<term>Hepacivirus (drug effects)</term>
<term>Hepacivirus (genetics)</term>
<term>Hepatitis C Antigens (biosynthesis)</term>
<term>Humans</term>
<term>Oligonucleotides, Antisense (pharmacology)</term>
<term>RNA, Messenger (biosynthesis)</term>
<term>Virus Replication (drug effects)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager (biosynthèse)</term>
<term>Antigènes de l'hépatite C (biosynthèse)</term>
<term>Cellules cultivées</term>
<term>Hepacivirus ()</term>
<term>Hepacivirus (génétique)</term>
<term>Humains</term>
<term>Lymphocytes T CD4+ (cytologie)</term>
<term>Oligonucléotides antisens (pharmacologie)</term>
<term>Réplication virale ()</term>
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<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Hepatitis C Antigens</term>
<term>RNA, Messenger</term>
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<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>ARN messager</term>
<term>Antigènes de l'hépatite C</term>
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<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Lymphocytes T CD4+</term>
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<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>CD4-Positive T-Lymphocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Hepacivirus</term>
<term>Virus Replication</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hepacivirus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Hepacivirus</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Oligonucléotides antisens</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Oligonucleotides, Antisense</term>
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<term>Humans</term>
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<front><div type="abstract" xml:lang="en">To study inhibitory effect of antisense oligodeoxynucleotide (asODN) on HCV in vitro.</div>
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