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Volumn 82, Issue 4, 2002, Pages 953-960
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Feasibility of ex vivo gene therapy for neurological disorders using the new retroviral vector GCDNsap packaged in the vesicular stomatitis virus G protein
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Author keywords
Gene therapy; Neuronal progenitor cell; Pseudo typed retroviral vector; Transplantation
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Indexed keywords
ADENOVIRUS VECTOR;
EPIDERMAL GROWTH FACTOR;
GENE PRODUCT;
GREEN FLUORESCENT PROTEIN;
PROTEIN GCDNSAP;
UNCLASSIFIED DRUG;
VESICULAR STOMATITIS VIRUS G PROTEIN;
VIRUS PROTEIN;
ANIMAL CELL;
ANIMAL MODEL;
ARTICLE;
BRAIN REGION;
CELL DIFFERENTIATION;
CELL MATURATION;
CELL RENEWAL;
CONTROLLED STUDY;
DNA MODIFICATION;
FETAL CALF SERUM;
GENE TARGETING;
GENE THERAPY;
GENE TRANSFER;
GENETIC ENGINEERING;
GENETIC TRANSDUCTION;
MALE;
MOUSE;
NERVE CELL;
NEUROLOGIC DISEASE;
NONHUMAN;
PRIORITY JOURNAL;
REPORTER GENE;
STEM CELL;
ANIMALS;
CELLS, CULTURED;
CLONE CELLS;
CORPUS STRIATUM;
FEASIBILITY STUDIES;
GENE THERAPY;
GENES, REPORTER;
GENETIC VECTORS;
GRAFT SURVIVAL;
LUMINESCENT PROTEINS;
MALE;
MEMBRANE GLYCOPROTEINS;
MICE;
MICE, INBRED C57BL;
NERVOUS SYSTEM DISEASES;
RETROVIRIDAE;
STEM CELL TRANSPLANTATION;
STEM CELLS;
TRANSDUCTION, GENETIC;
VIRAL ENVELOPE PROTEINS;
ADENOVIRIDAE;
ANIMALIA;
UNIDENTIFIED RETROVIRUS;
VESICULAR STOMATITIS VIRUS;
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EID: 0036678957
PISSN: 00223042
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1471-4159.2002.01048.x Document Type: Article |
Times cited : (63)
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References (18)
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