Human gene therapy - JoVE Visualize

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Human Gene Therapy|December 31, 1997

Efficient transduction of mammalian cells by a recombinant baculovirus having the vesicular stomatitis virus G glycoproteinJ Barsoum, R Brown, M McKee, et al.

Human Gene Therapy|December 31, 1997

Overexpression of adenovirus-encoded transgenes from the cytomegalovirus immediate early promoter in irradiated tumor cellsD C Tang, R S Jennelle, Z Shi, et al.

Human Gene Therapy|December 31, 1997

Retrovirus-mediated gene transfer of ornithine-delta-aminotransferase into keratinocytes from gyrate atrophy patientsT G Jensen, D M Sullivan, R A Morgan, et al.

Human Gene Therapy|May 8, 2015

Development of Recombinant Adeno-Associated Virus Serotype 2/8 Carrying Kringle Domains of Human Plasminogen for Sustained Expression and Cancer TherapyCheng-Hsiang Kuo, Bi-Ing Chang, Fang-Tzu Lee, et al.

Human Gene Therapy|May 15, 1998

Double suicide gene (cytosine deaminase and herpes simplex virus thymidine kinase) but not single gene transfer allows reliable elimination of tumor cells in vivoW Uckert, T Kammertöns, K Haack, et al.

Human Gene Therapy|April 29, 1998

Inhibition of human immunodeficiency virus type 1 replication by nuclear chimeric anti-HIV ribozymes in a human T lymphoblastoid cell lineA Michienzi, L Conti, B Varano, et al.

Human Gene Therapy|April 29, 1998

Selective gene transfer into the liver of non-human primates with E1-deleted, E2A-defective, or E1-E4 deleted recombinant adenovirusesS E Raper, Z J Haskal, X Ye, et al.

Human Gene Therapy|April 29, 1998

Recombinant E1-deleted adenovirus-mediated gene therapy for cancer: efficacy studies with p53 tumor suppressor gene and liver histology in tumor xenograft modelsL L Nielsen, M Gurnani, J Syed, et al.

Human Gene Therapy|August 29, 2025

Biacore Analysis of Cross-Reactive Adeno-Associated Virus Antibodies in Monkeys Following Intravenous Administration of AAV5, AAV8, and AAV9 VectorsYanshan Dai, Glen Banks, Grace Wu, et al.

Human Gene Therapy|August 2, 2016

Chimeric Antigen Receptor T Cell Therapy Targeting CD19-Positive Leukemia and Lymphoma in the Context of Stem Cell TransplantationMaria-Luisa Schubert, Angela Hückelhoven, Jean-Marc Hoffmann, et al.

Pageof 413

Showing results (1521-1530 of 4,124) with videos related to

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Pageof 413

Human Gene Therapy|December 31, 1997

Efficient transduction of mammalian cells by a recombinant baculovirus having the vesicular stomatitis virus G glycoproteinJ Barsoum, R Brown, M McKee, et al.

Human Gene Therapy|December 31, 1997

Overexpression of adenovirus-encoded transgenes from the cytomegalovirus immediate early promoter in irradiated tumor cellsD C Tang, R S Jennelle, Z Shi, et al.

Human Gene Therapy|December 31, 1997

Retrovirus-mediated gene transfer of ornithine-delta-aminotransferase into keratinocytes from gyrate atrophy patientsT G Jensen, D M Sullivan, R A Morgan, et al.

Human Gene Therapy|May 8, 2015

Development of Recombinant Adeno-Associated Virus Serotype 2/8 Carrying Kringle Domains of Human Plasminogen for Sustained Expression and Cancer TherapyCheng-Hsiang Kuo, Bi-Ing Chang, Fang-Tzu Lee, et al.

Human Gene Therapy|May 15, 1998

Double suicide gene (cytosine deaminase and herpes simplex virus thymidine kinase) but not single gene transfer allows reliable elimination of tumor cells in vivoW Uckert, T Kammertöns, K Haack, et al.

Human Gene Therapy|April 29, 1998

Inhibition of human immunodeficiency virus type 1 replication by nuclear chimeric anti-HIV ribozymes in a human T lymphoblastoid cell lineA Michienzi, L Conti, B Varano, et al.

Human Gene Therapy|April 29, 1998

Selective gene transfer into the liver of non-human primates with E1-deleted, E2A-defective, or E1-E4 deleted recombinant adenovirusesS E Raper, Z J Haskal, X Ye, et al.

Human Gene Therapy|April 29, 1998

Recombinant E1-deleted adenovirus-mediated gene therapy for cancer: efficacy studies with p53 tumor suppressor gene and liver histology in tumor xenograft modelsL L Nielsen, M Gurnani, J Syed, et al.

Human Gene Therapy|August 29, 2025

Biacore Analysis of Cross-Reactive Adeno-Associated Virus Antibodies in Monkeys Following Intravenous Administration of AAV5, AAV8, and AAV9 VectorsYanshan Dai, Glen Banks, Grace Wu, et al.

Human Gene Therapy|August 2, 2016

Chimeric Antigen Receptor T Cell Therapy Targeting CD19-Positive Leukemia and Lymphoma in the Context of Stem Cell TransplantationMaria-Luisa Schubert, Angela Hückelhoven, Jean-Marc Hoffmann, et al.

Pageof 413