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

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.

journal_name

Curr Opin Biotechnol

authors

Bramson JL,Graham FL,Gauldie J

doi

10.1016/0958-1669(95)80097-2

subject

Has Abstract

pub_date

1995-10-01 00:00:00

pages

590-5

issue

5

eissn

0958-1669

issn

1879-0429

pii

0958-1669(95)80097-2

journal_volume

6

pub_type

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