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Volumn 85, Issue 2, 2002, Pages 187-197
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Approach to establishing a liver targeting gene therapeutic vector using naturally occurring defective hepatitis B viruses devoid of immunogenic T cell epitope
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Author keywords
Gene therapy; Hepatitis B virus; Liver; Vector development
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Indexed keywords
EPITOPE;
GREEN FLUORESCENT PROTEIN;
VIRUS VECTOR;
ARTICLE;
CONTROLLED STUDY;
DEFECTIVE VIRUS;
GENE DELETION;
GENE EXPRESSION;
GENE SEQUENCE;
GENE TARGETING;
GENE THERAPY;
GENETIC ANALYSIS;
HEPATITIS;
HEPATITIS B VIRUS;
HUMAN;
HUMAN CELL;
IMMUNOGENICITY;
LIVER;
LIVER CELL;
NONHUMAN;
PRIORITY JOURNAL;
STRUCTURAL GENE;
T LYMPHOCYTE;
VIRION;
VIRUS CULTURE;
VIRUS REPLICATION;
CELL LINE;
CELLS, CULTURED;
DEFECTIVE VIRUSES;
EPITOPES, T-LYMPHOCYTE;
GENE EXPRESSION;
GENE THERAPY;
GENE TRANSFER TECHNIQUES;
GENES, REPORTER;
GENETIC VECTORS;
GREEN FLUORESCENT PROTEINS;
HEPATITIS B VIRUS;
HEPATOCYTES;
HUMANS;
LIVER;
LUMINESCENT PROTEINS;
PEPTIDES;
VIRUS REPLICATION;
DNA VIRUSES;
HEPATITIS B VIRUS;
INSERTION SEQUENCES;
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EID: 0037053061
PISSN: 01681702
EISSN: None
Source Type: Journal
DOI: 10.1016/S0168-1702(02)00043-6 Document Type: Article |
Times cited : (8)
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References (46)
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