𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The use of adenoviral vectors for gene therapy and gene transfer in vivo

✍ Scribed by Jonathan L Bramson; Frank L Graham; Jack Gauldie


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
584 KB
Volume
6
Category
Article
ISSN
0958-1669

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Successful gene therapy of the Gunn rat
✍ Marta Bellodi-Privato; Dominique Aubert; Virginie Pichard; Anne Myara; FranΓ§ois πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 250 KB

Crigler-Najjar type 1 disease (CN1) is a rare inherited metabolic disease characterized by complete absence of hepatic UDP-glucuronosyl transferase (UGT1), resulting in high levels of unconjugated bilirubin. CN1 is an attractive candidate disease for gene therapy. Here we show that in vivo neonatal

Encapsulated cells producing retroviral
✍ Robert M. Saller; Stefano Indraccolo; Vincenzo Coppola; Giovanni Esposito; Jan S πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 437 KB

## Abstract ## Background Because gene therapy of the future will primarily take an __in vivo__ approach, a number of problems associated with its current implementation exist. Currently, repeated delivery of a vector __in vivo__ is necessary to ensure adequate transfer of the therapeutic gene. Th