Multigene lentiviral vectors based on differential splicing and translational control

Molecular Therapy

Volumn 4, Issue 4, 2001, Pages 375-382

  Zhu, Yonghong ^a   Feuer, Gerold ^b   Day, Shannon L ^a   Wrzesinski, Stephen ^b   Planelles, Vicente ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b State University of New York Upstate Medical University: College of Medicine   (United States)

Author keywords

B7.1; Dicistronic; Gene therapy; GFP; IRES; Lentiviral vector; Multigene; rev; Splicing; tat

Indexed keywords

CIS ACTING ELEMENT; MESSENGER RNA; MUTANT PROTEIN; REV PROTEIN; TRANSACTIVATOR PROTEIN; VIRUS RNA; VIRUS VECTOR;

APOPTOSIS; ARTICLE; CELL DIVISION; CONTROLLED STUDY; ENCEPHALOMYOCARDITIS VIRUS; GENE CONSTRUCT; GENE EXPRESSION REGULATION; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; LENTIVIRINAE; MARKER GENE; MULTIGENE FAMILY; PROTEIN DOMAIN; REPORTER GENE; RIBOSOME; RNA SPLICING; RNA TRANSCRIPTION; SIGNAL TRANSDUCTION; VIRUS INFECTION; VIRUS TITRATION; VIRUS TRANSCRIPTION;

ENCEPHALOMYOCARDITIS VIRUS; HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; LENTIVIRUS; RNA VIRUSES;

EID: 0034763057     PISSN: 15250016     EISSN: None     Source Type: Journal    
DOI: 10.1006/mthe.2001.0469     Document Type: Article

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