| Literature DB >> 7579670 |
J L Bramson1, F L Graham, J Gauldie.
Abstract
Adenoviral vectors have proven to be excellent vehicles for gene delivery in vivo to a wide range of cell types. These vectors have been used to transfer genes such as CFTR to correct the defect in cystic fibrosis and, more recently, to supply serum blood factors and genetically modify tumors to enhance therapy.Entities:
Mesh:
Year: 1995 PMID: 7579670 DOI: 10.1016/0958-1669(95)80097-2
Source DB: PubMed Journal: Curr Opin Biotechnol ISSN: 0958-1669 Impact factor: 9.740