Human gene therapy - JoVE Visualize

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Human Gene Therapy|February 9, 2026

Preferential Encapsulation of DNA Impurities Derived from pAAV Plasmid Backbone into Recombinant Adeno-Associated Virus CapsidsYuzhe Yuan, Kiyoko Higashiyama, Emi Ito-Kudo, et al.

Human Gene Therapy|February 4, 2026

Less Invasive Light Irradiation Methods for Inner Ear Gene Therapy Based on Photoswitch Technology: Toward Clinical TranslationMasao Noda, Takahiro Otabe, Ryota Koshu, et al.

Human Gene Therapy|January 27, 2026

Advances in Precision Editing Therapies for Alpha-1 Antitrypsin DeficiencyJenny Gao, Erik Sontheimer, Terence R Flotte, et al.

Human Gene Therapy|February 27, 1999

DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscleH H Chen, L M Mack, S Y Choi, et al.

Human Gene Therapy|February 27, 1999

A novel tetracycline-inducible viral replication switchF Yao, E Eriksson

Human Gene Therapy|February 18, 1999

Delivery of recombinant gene products to the central nervous system with nonautologous cells in alginate microcapsulesC J Ross, M Ralph, P L Chang

Human Gene Therapy|April 21, 1999

Early cell loss after angioplasty results in a disproportionate decrease in percutaneous gene transfer to the vessel wallA Rivard, Z Luo, H Perlman, et al.

Human Gene Therapy|April 21, 1999

Successful culture and sustainability in vivo of gene-modified human oral mucosal epitheliumH Mizuno, N Emi, A Abe, et al.

Human Gene Therapy|December 13, 2003

Liver toxicities typically induced by first-generation adenoviral vectors can be reduced by use of E1, E2b-deleted adenoviral vectorsR S Everett, B L Hodges, E Y Ding, et al.

Human Gene Therapy|December 13, 2003

Comparison of murine leukemia virus, human immunodeficiency virus, and adeno-associated virus vectors for gene transfer in multiple myeloma: lentiviral vectors demonstrate a striking capacity to transduce low-proliferating primary tumor cellsJohn De Vos, Claude Bagnis, Lydie Bonnafoux, et al.

Pageof 414

Showing results (1201-1210 of 4,138) with videos related to

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Pageof 414

Human Gene Therapy|February 9, 2026

Preferential Encapsulation of DNA Impurities Derived from pAAV Plasmid Backbone into Recombinant Adeno-Associated Virus CapsidsYuzhe Yuan, Kiyoko Higashiyama, Emi Ito-Kudo, et al.

Human Gene Therapy|February 4, 2026

Less Invasive Light Irradiation Methods for Inner Ear Gene Therapy Based on Photoswitch Technology: Toward Clinical TranslationMasao Noda, Takahiro Otabe, Ryota Koshu, et al.

Human Gene Therapy|January 27, 2026

Advances in Precision Editing Therapies for Alpha-1 Antitrypsin DeficiencyJenny Gao, Erik Sontheimer, Terence R Flotte, et al.

Human Gene Therapy|February 27, 1999

DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscleH H Chen, L M Mack, S Y Choi, et al.

Human Gene Therapy|February 27, 1999

A novel tetracycline-inducible viral replication switchF Yao, E Eriksson

Human Gene Therapy|February 18, 1999

Delivery of recombinant gene products to the central nervous system with nonautologous cells in alginate microcapsulesC J Ross, M Ralph, P L Chang

Human Gene Therapy|April 21, 1999

Early cell loss after angioplasty results in a disproportionate decrease in percutaneous gene transfer to the vessel wallA Rivard, Z Luo, H Perlman, et al.

Human Gene Therapy|April 21, 1999

Successful culture and sustainability in vivo of gene-modified human oral mucosal epitheliumH Mizuno, N Emi, A Abe, et al.

Human Gene Therapy|December 13, 2003

Liver toxicities typically induced by first-generation adenoviral vectors can be reduced by use of E1, E2b-deleted adenoviral vectorsR S Everett, B L Hodges, E Y Ding, et al.

Human Gene Therapy|December 13, 2003

Comparison of murine leukemia virus, human immunodeficiency virus, and adeno-associated virus vectors for gene transfer in multiple myeloma: lentiviral vectors demonstrate a striking capacity to transduce low-proliferating primary tumor cellsJohn De Vos, Claude Bagnis, Lydie Bonnafoux, et al.

Pageof 414