Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I

Author:

Overturf Ken,Al-Dhalimy Muhsen,Tanguay Robert,Brantly Mark,Ou Ching-Nan,Finegold Milton,Grompe Markus

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference51 articles.

1. Arias, I.M. The Liver — Biology and Pathobiology (Raven Press, New York, 1994).

2. Scriver, C.R., Beaudet, A.L., Sly, W. & Valle, D. The Metabolic Basis of Inherited Disease (MacGraw-Hill, NewYork 1994).

3. Norwich, A.L. Inherited hepatic enzyme defects as candidates for liver-directed gene therapy. Curr. Topics Microbiol. Immun. 168, 185–200 (1991).

4. Grossman, M. & Wilson, J.M. Retroviruses: delivery vehicle to the liver. Curr. Opin. Genet Dev. 3, 110–114 (1993).

5. Li, Q., Kay, M.A., Finegold, M., Stratford-Perricaudet, L.D. & Woo, S.L. Assessment of recombinant adenoviral vectors for hepatic gene therapy. Hum. Gene Ther. 4, 403–409 (1993).

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