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Science 23 November 2001:
Vol. 294. no. 5547, pp. 1638 - 1642
DOI: 10.1126/science.294.5547.1638

News Focus

GENE THERAPY:
Safer and Virus-Free?

Dan Ferber

Most nonviral vectors for gene therapy fly under the radar of the immune system, and they're cheaper and easier to manufacture than viral vectors. But most of them have not been as efficient as viruses in shuttling genes into cells, and the genes that were delivered didn't remain active for long. In the past few years, though, that has begun to change.

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
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Computational and Analytical Modeling of Cationic Lipid-DNA Complexes.
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Adenovirus Fiber Shaft Contains a Trimerization Element That Supports Peptide Fusion for Targeted Gene Delivery.
J. Li, S. Lad, G. Yang, Y. Luo, M. Iacobelli-Martinez, F. J. Primus, R. A. Reisfeld, and E. Li (2006)
J. Virol. 80, 12324-12331
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Direct Evidence of Multicompartment Aggregates in Polyelectrolyte-Charged Liposome Complexes.
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Effect of Cell Electroporation on the Conductivity of a Cell Suspension.
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Pulsed High-Intensity Focused Ultrasound Enhances Systemic Administration of Naked DNA in Squamous Cell Carcinoma Model: Initial Experience.
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Ribozymes: Applications to Functional Analysis and Gene Discovery.
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Three-Dimensional Imaging of Lipid Gene-Carriers: Membrane Charge Density Controls Universal Transfection Behavior in Lamellar Cationic Liposome-DNA Complexes.
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Antibody-Mediated Targeting of an Adenovirus Vector Modified To Contain a Synthetic Immunoglobulin G-Binding Domain in the Capsid.
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Retrovirus-Mediated Modification of Male Germline Stem Cells in Rats.
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Defining Gene Transfer Before Expecting Gene Therapy: Putting the Horse Before the Cart.
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Science. ISSN 0036-8075 (print), 1095-9203 (online)