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W F Anderson

Showing results (391-400 of 417) with videos related to

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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.
Annals of the New York Academy of Sciences|May 31, 1994
Gene marking and autologous bone marrow transplantationM K Brenner, D R Rill, R C Moen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cellsS F Yu, T von Rüden, P W Kantoff, et al.
Journal of Cellular Physiology|April 1, 1975
Activation and inactivation of genes determining hemoglobin types.20sW F Anderson, J E Barker, N A Elson, et al.
Human Gene Therapy|January 1, 1990
In vivo expression and survival of gene-modified T lymphocytes in rhesus monkeysK W Culver, R A Morgan, W R Osborne, et al.
Transactions of the Association of American Physicians|January 1, 1990
A genetic therapy for familial hypercholesterolemiaD A Dichek, G L Bratthauer, Z H Beg, et al.
Pageof 42

Showing results (391-400 of 417) with videos related to

Sort By:
Pageof 42
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.
Annals of the New York Academy of Sciences|May 31, 1994
Gene marking and autologous bone marrow transplantationM K Brenner, D R Rill, R C Moen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cellsS F Yu, T von Rüden, P W Kantoff, et al.
Journal of Cellular Physiology|April 1, 1975
Activation and inactivation of genes determining hemoglobin types.20sW F Anderson, J E Barker, N A Elson, et al.
Human Gene Therapy|January 1, 1990
In vivo expression and survival of gene-modified T lymphocytes in rhesus monkeysK W Culver, R A Morgan, W R Osborne, et al.
Transactions of the Association of American Physicians|January 1, 1990
A genetic therapy for familial hypercholesterolemiaD A Dichek, G L Bratthauer, Z H Beg, et al.
Pageof 42