‘Advanced’ generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo-Reference-Cited by-同舟云学术

‘Advanced’ generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo

Published:2003-04 Issue:8 Volume:10 Page:630-636
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Bonci D,Cittadini A,Latronico M V G,Borello U,Aycock J K,Drusco A,Innocenzi A,Follenzi A,Lavitrano M,Monti M G,Ross J,Naldini L,Peschle C,Cossu G,Condorelli G

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3301936.pdf

Reference14 articles.

1. Hajjar RJ, del Monte F, Matsui T, Rosenzweig A . Prospects for gene therapy for heart failure. Circ Res 2000; 86: 616–621.

2. Svensson EC et al. Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors. Circulation 1999; 99: 201–205.

3. Kay MA, Glorioso JC, Naldini L . Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics. Nat Med 2001; 7: 33–40.

4. Zennou V et al. HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 2000; 101: 173–185.

5. Follenzi A et al. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat Genet 2000; 25: 217–222.

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