## Abstract ## Background A large‐volume intravenous (i.v.) injection of DNA, i.e. a hydrodynamics‐based transfection procedure, is known to be an efficient and liver‐specific method of __in vivo__ gene delivery. However, little is available on an applicable particle size in the procedure. ## Met
A novel adenovirus-based system for facilitating retroviral hepatic gene transfer in vivo
✍ Scribed by M Ott; S G Gupta
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 158 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0270-9139
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✦ Synopsis
A NOVEL ADENOVIRUS-BASED SYSTEM FOR limits the number of cells that may be transduced. Retroviral gene transfer also requires proviral integration
FACILITATING RETROVIRAL HEPATIC GENE TRANSFER IN VIVO
into the genome, which is greatly facilitated by DNA synthesis; however, hepatocytes are proliferatively qui-Lieber A, Vrancken Peeters M-JTFD, Meuse L, Fausto escent (only 0.005% of unperturbed hepatocytes may N, Perkins J, Kay MA. Adenovirus-mediated urokinase be in S-phase). For in vivo hepatic gene therapy, DNA gene transfer induces liver regeneration and allows for synthesis is induced at present by partial hepatectomy, efficient retrovirus transduction of hepatocytes in vivo. which is cumbersome and potentially risky. Also, liver
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