par VandenDriessche, Thierry;Chuah Lay Khim, Marinee
Référence Blood, 122, 12, page (1993-1994)
Publication Publié, 2013-09
Article révisé par les pairs
Résumé : In this issue of Blood, Abel et al designed lentiviral vectors (LVs) enabling specific gene delivery into endothelial cells in vivo. This opens new perspectives for gene therapy of hereditary disorders, cardiovascular diseases, and cancer. 1 © 2013 by The American Society of Hematology.