Gene Transfer into Hepatocytes Mediated by Helper Virus-Free HSV/AAV Hybrid Vectors-Reference-Cited by-同舟云学术

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Gene Transfer into Hepatocytes Mediated by Helper Virus-Free HSV/AAV Hybrid Vectors

Published:1997-12 Issue:12 Volume:3 Page:813-825
ISSN:1076-1551
Container-title:Molecular Medicine
language:en
Short-container-title:Mol Med

Author:

Fraefel Cornel,Jacoby David R.,Lage Christopher,Hilderbrand Harold,Chou Janice Y.,Alt Fred W.,Breakefield Xandra O.,Majzoub Joseph A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03401718.pdf

Reference45 articles.

1. Strauss M. (1994) Liver-directed gene therapy: prospects and problems. Gene Ther. 1: 156–164.

2. Mulligan RC. (1993) The basic science of gene therapy. Science 260: 926–932.

3. Ferry N, Duplessis O, Houssin D, Danos O, Heard JM. (1991) Retroviral-mediated gene transfer into hepatocytes in vivo. Proc. Natl. Acad. Sci. U.S.A. 88: 8377–8381.

4. Rettinger SD, Kennedy SC, Wu X, et al. (1994) Liver-directed gene therapy: Quantitative evaluation of promoter elements by using in vivo retroviral transduction. Proc. Natl. Acad. Sci. U.S.A. 91: 1460–1464.

5. Jaffe H, Danel C, Longenecker G, et al. (1992) Adenovirus-mediated in vivo gene transfer and expression in normal rat liver. Nat. Genet. 1: 372–378.

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