Lentiviral vectors - The promise of gene therapy within reach?

Science

Volumn 285, Issue 5428, 1999, Pages 674-676

  Amado, Rafael G ^a   Chen, Irvin S Y ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENO ASSOCIATED VIRUS; CANCER RISK; EXPRESSION VECTOR; GENE TARGETING; GENE THERAPY; GENE TRANSFER; GENETIC DISORDER; HEMOPHILIA B; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; LENTIVIRINAE; NONHUMAN; PRIORITY JOURNAL; RECOMBINANT DNA TECHNOLOGY; RETINITIS PIGMENTOSA; SAFETY; SHORT SURVEY; STEM CELL; VIRUS GENOME; VIRUS RECOMBINANT;

ANIMALS; CELL LINE; GENE THERAPY; GENE TRANSFER TECHNIQUES; GENES, VIRAL; GENETIC VECTORS; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HEMATOPOIETIC STEM CELLS; HIV; HIV INFECTIONS; HUMANS; LENTIVIRUS; MUTAGENESIS, INSERTIONAL; PLASMIDS; RECOMBINATION, GENETIC; RETINITIS PIGMENTOSA; TRANSFECTION; VIRUS REPLICATION;

ADENO-ASSOCIATED VIRUS; HUMAN IMMUNODEFICIENCY VIRUS; LENTIVIRUS;

EID: 0033618547     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.285.5428.674     Document Type: Short Survey

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