Showing results (271-280 of 300) with videos related to
Sort By:
Pageof 30
Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1989
Establishment and characterization of adenosine deaminase-deficient human T cell linesD B Kohn, H Mitsuya, M Ballow, et al.The New England Journal of Medicine|August 25, 1977
Continuous subcutaneous administration of deferoxamine in patients with iron overloadR D Propper, B Cooper, R R Rufo, et al.Human Gene Therapy|January 1, 1994
Improved methods of retroviral vector transduction and production for gene therapyH Kotani, P B Newton, S Zhang, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Human gene transfer: characterization of human tumor-infiltrating lymphocytes as vehicles for retroviral-mediated gene transfer in manA Kasid, S Morecki, P Aebersold, et al.International Journal of Molecular Medicine|September 20, 2001
Retroviral vectors bearing IgG-binding motifs for antibody-mediated targeting of vascular endothelial growth factor receptorsR Masood, E M Gordon, M D Whitley, et al.Proceedings of the National Academy of Sciences of the United States of America|April 15, 1991
Lymphocytes as cellular vehicles for gene therapy in mouse and manK Culver, K Cornetta, R Morgan, et al.Advances in Experimental Medicine and Biology|January 1, 1988
Retroviral-mediated gene transfer into hemopoietic cellsM A Eglitis, P W Kantoff, D B Kohn, et al.Blood|May 15, 1994
Genetic marking shows that Ph+ cells present in autologous transplants of chronic myelogenous leukemia (CML) contribute to relapse after autologous bone marrow in CMLA B Deisseroth, Z Zu, D Claxton, et al.Human Gene Therapy|August 7, 1998
In utero gene therapy: transfer and long-term expression of the bacterial neo(r) gene in sheep after direct injection of retroviral vectors into preimmune fetusesC D Porada, N Tran, M Eglitis, et al.Human Gene Therapy|August 1, 1993
Treatment of severe combined immunodeficiency disease (SCID) due to adenosine deaminase deficiency with CD34+ selected autologous peripheral blood cells transduced with a human ADA gene. Amendment to clinical research project, Project 90-C-195, January 10, 1992R M Blaese, K W Culver, L Chang, et al.Pageof 30