Targeting lentiviral vectors to specific cell types in vivo

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 31, 2006, Pages 11479-11484

  Yang, Lili ^a   Bailey, Leslie ^b   Baltimore, David ^a   Wang, Pin ^b  

^a CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

^b University of Southern California ^*  (United States)

Author keywords

Antibody; Gene therapy; Lentivirus; Retrovirus; Targeted gene delivery

Indexed keywords

ANTIBODY; BINDING PROTEIN; CD20 ANTIGEN; HYBRID PROTEIN; LENTIVIRUS VECTOR; VIRUS ENVELOPE PROTEIN;

ANIMAL EXPERIMENT; ANTIGEN ANTIBODY COMPLEX; ARTICLE; B LYMPHOCYTE; CELL SURFACE; CELL TYPE; CONTROLLED STUDY; CYTOSOL; ENDOCYTOSIS; ENDOSOME; GENE TARGETING; GENETIC TRANSDUCTION; HUMAN; HUMAN CELL; IN VIVO STUDY; MEMBRANE FUSION; MOLECULAR RECOGNITION; MOUSE; NONHUMAN; PH; PRIORITY JOURNAL; RECEPTOR BINDING; VIRAL GENE THERAPY;

ANIMALS; ANTIBODIES; ANTIGENS, CD20; B-LYMPHOCYTES; CELL LINE; FEMALE; GENETIC VECTORS; HUMANS; HYDROGEN-ION CONCENTRATION; LENTIVIRUS; MEMBRANE FUSION; MICE; MICE, KNOCKOUT; RECOMBINANT FUSION PROTEINS; TRANSDUCTION, GENETIC; VIRAL ENVELOPE PROTEINS;

ANIMALIA; LENTIVIRUS;

EID: 33746833330     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0604993103     Document Type: Article

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