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Targeted Cell Entry of Lentiviral Vectors

Published:2008-08 Issue:8 Volume:16 Page:1427-1436
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Funke Sabrina,Maisner Andrea,Mühlebach Michael D,Koehl Ulrike,Grez Manuel,Cattaneo Roberto,Cichutek Klaus,Buchholz Christian J

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference50 articles.

1. Gene delivery by lentivirus vectors;Cockrell;Mol Biotechnol,2007

2. Gene transfer in humans using a conditionally replicating lentiviral vector;Levine;Proc Natl Acad Sci USA,2006

3. Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer;Brown;Nat Med,2006

4. Pseudotyping of murine leukemia virus with the envelope glycoproteins of HIV generates a retroviral vector with specificity of infection for CD4-expressing cells;Schnierle;Proc Natl Acad Sci USA,1997

5. Selective transduction of malignant glioma by lentiviral vectors pseudotyped with lymphocytic choriomeningitis virus glycoproteins;Miletic;Hum Gene Ther,2004

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