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D B Kohn

Showing results (101-110 of 111) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986
Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transferP W Kantoff, D B Kohn, H Mitsuya, et al.
Blood|December 15, 1993
Transduction of human melanoma cell lines with the human interleukin-7 gene using retroviral-mediated gene transfer: comparison of immunologic properties with interleukin-2A R Miller, W H McBride, S M Dubinett, et al.
Nature Medicine|October 1, 1995
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiencyD B Kohn, K I Weinberg, J A Nolta, et al.
Ciba Foundation Symposium|January 1, 1987
Gene therapy: efforts at developing large animal models for autologous bone marrow transplant and gene transfer with retroviral vectorsM A Eglitis, P W Kantoff, J R McLachlin, et al.
The Journal of Experimental Medicine|July 1, 1987
Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transferP W Kantoff, A P Gillio, J R McLachlin, et al.
Gene Therapy|May 21, 2010
Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vectorP S Becker, J A Taylor, G D Trobridge, et al.
The Journal of Biological Chemistry|June 6, 1997
Inhibition of HIV-1 replication using a mutated tRNALys-3 primerY Lu, V Planelles, X Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectorsS S Case, M A Price, C T Jordan, et al.
Human Gene Therapy|December 16, 1998
Retroviral transfer of the glucocerebrosidase gene into CD34+ cells from patients with Gaucher disease: in vivo detection of transduced cells without myeloablationC E Dunbar, D B Kohn, R Schiffmann, et al.
Blood|June 25, 1999
A clinical trial of retroviral-mediated transfer of a rev-responsive element decoy gene into CD34(+) cells from the bone marrow of human immunodeficiency virus-1-infected childrenD B Kohn, G Bauer, C R Rice, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986
Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transferP W Kantoff, D B Kohn, H Mitsuya, et al.
Blood|December 15, 1993
Transduction of human melanoma cell lines with the human interleukin-7 gene using retroviral-mediated gene transfer: comparison of immunologic properties with interleukin-2A R Miller, W H McBride, S M Dubinett, et al.
Nature Medicine|October 1, 1995
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiencyD B Kohn, K I Weinberg, J A Nolta, et al.
Ciba Foundation Symposium|January 1, 1987
Gene therapy: efforts at developing large animal models for autologous bone marrow transplant and gene transfer with retroviral vectorsM A Eglitis, P W Kantoff, J R McLachlin, et al.
The Journal of Experimental Medicine|July 1, 1987
Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transferP W Kantoff, A P Gillio, J R McLachlin, et al.
Gene Therapy|May 21, 2010
Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vectorP S Becker, J A Taylor, G D Trobridge, et al.
The Journal of Biological Chemistry|June 6, 1997
Inhibition of HIV-1 replication using a mutated tRNALys-3 primerY Lu, V Planelles, X Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectorsS S Case, M A Price, C T Jordan, et al.
Human Gene Therapy|December 16, 1998
Retroviral transfer of the glucocerebrosidase gene into CD34+ cells from patients with Gaucher disease: in vivo detection of transduced cells without myeloablationC E Dunbar, D B Kohn, R Schiffmann, et al.
Blood|June 25, 1999
A clinical trial of retroviral-mediated transfer of a rev-responsive element decoy gene into CD34(+) cells from the bone marrow of human immunodeficiency virus-1-infected childrenD B Kohn, G Bauer, C R Rice, et al.
Pageof 12