In VivoTargeting of Tumor Endothelial Cells by Systemic Delivery of Lentiviral Vectors-Reference-Cited by-同舟云学术

In VivoTargeting of Tumor Endothelial Cells by Systemic Delivery of Lentiviral Vectors

Published:2003-08-10 Issue:12 Volume:14 Page:1193-1206
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

De Palma Michele¹,Venneri Mary Anna¹,Naldini Luigi²

Affiliation:

1. Laboratory for Gene Transfer and Therapy, IRCC, Institute for Cancer Research and Treatment, University of Turin Medical School, 10060 Candiolo (Turin), Italy

2. HSR-TIGET, San Raffaele Telethon Institute for Gene Therapy, 20132 Milan, Italy

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/104303403322168028

Reference42 articles.

1. Molecular Evidence of Lentiviral Vector-Mediated Gene Transfer into Human Self-Renewing, Multi-potent, Long-Term NOD/SCID Repopulating Hematopoietic Cells

2. Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model

3. The Bystander Effect of the Nitroreductase/CB 1954 Enzyme/Prodrug System Is Due to a Cell-Permeable Metabolite

4. Angiogenesis in cancer and other diseases

5. A monoclonal antibody to vascular endothelial–cadherin inhibits tumor angiogenesis without side effects on endothelial permeability

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