Human gene therapy - JoVE Visualize

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Human Gene Therapy|November 24, 1999

Novel human gene transfer vectors: evaluation of wild-type and recombinant animal adenoviruses in human-derived cellsU B Rasmussen, M Benchaibi, V Meyer, et al.

Human Gene Therapy|November 24, 1999

Subcellular trafficking of the cytoplasmic expression systemM Brisson, W C Tseng, C Almonte, et al.

Human Gene Therapy|November 24, 1999

RNA melanoma vaccine: induction of antitumor immunity by human glycoprotein 100 mRNA immunizationW Z Zhou, D S Hoon, S K Huang, et al.

Human Gene Therapy|July 13, 2000

Percutaneous gene therapy using recombinant adenoviruses encoding human herpes simplex virus thymidine kinase, human PAI-1, and human NOS3 in balloon-injured porcine coronary arteriesO Varenne, P Sinnaeve, H Gillijns, et al.

Human Gene Therapy|June 2, 2000

Optimization of adenoviral vector-mediated gene transfer to pulmonary arteries in newborn swineS Badran, S K Schachtner, H S Baldwin, et al.

Human Gene Therapy|June 2, 2000

Reversal of pathology in the entire brain of mucopolysaccharidosis type VII mice after lentivirus-mediated gene transferA Bosch, E Perret, N Desmaris, et al.

Human Gene Therapy|June 2, 2000

Retrovirus-mediated gene transfer in primary T lymphocytes: influence of the transduction/selection process and of ex vivo expansion on the T cell receptor beta chain hypervariable region repertoireC Ferrand, E Robinet, E Contassot, et al.

Human Gene Therapy|June 2, 2000

Restoration of cognitive and motor functions by ciliary neurotrophic factor in a primate model of Huntington's diseaseV Mittoux, J M Joseph, F Conde, et al.

Human Gene Therapy|April 11, 2000

Immune response to adenovirus-delivered antigens upregulates utrophin and results in mitigation of muscle pathology in mdx miceK Yamamoto, K Yuasa, Y Miyagoe, et al.

Human Gene Therapy|April 11, 2000

Long-term persistence of human bone marrow stromal cells transduced with factor VIII-retroviral vectors and transient production of therapeutic levels of human factor VIII in nonmyeloablated immunodeficient miceM K Chuah, A Van Damme, H Zwinnen, et al.

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Showing results (2031-2040 of 4,124) with videos related to

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Pageof 413

Human Gene Therapy|November 24, 1999

Novel human gene transfer vectors: evaluation of wild-type and recombinant animal adenoviruses in human-derived cellsU B Rasmussen, M Benchaibi, V Meyer, et al.

Human Gene Therapy|November 24, 1999

Subcellular trafficking of the cytoplasmic expression systemM Brisson, W C Tseng, C Almonte, et al.

Human Gene Therapy|November 24, 1999

RNA melanoma vaccine: induction of antitumor immunity by human glycoprotein 100 mRNA immunizationW Z Zhou, D S Hoon, S K Huang, et al.

Human Gene Therapy|July 13, 2000

Percutaneous gene therapy using recombinant adenoviruses encoding human herpes simplex virus thymidine kinase, human PAI-1, and human NOS3 in balloon-injured porcine coronary arteriesO Varenne, P Sinnaeve, H Gillijns, et al.

Human Gene Therapy|June 2, 2000

Optimization of adenoviral vector-mediated gene transfer to pulmonary arteries in newborn swineS Badran, S K Schachtner, H S Baldwin, et al.

Human Gene Therapy|June 2, 2000

Reversal of pathology in the entire brain of mucopolysaccharidosis type VII mice after lentivirus-mediated gene transferA Bosch, E Perret, N Desmaris, et al.

Human Gene Therapy|June 2, 2000

Retrovirus-mediated gene transfer in primary T lymphocytes: influence of the transduction/selection process and of ex vivo expansion on the T cell receptor beta chain hypervariable region repertoireC Ferrand, E Robinet, E Contassot, et al.

Human Gene Therapy|June 2, 2000

Restoration of cognitive and motor functions by ciliary neurotrophic factor in a primate model of Huntington's diseaseV Mittoux, J M Joseph, F Conde, et al.

Human Gene Therapy|April 11, 2000

Immune response to adenovirus-delivered antigens upregulates utrophin and results in mitigation of muscle pathology in mdx miceK Yamamoto, K Yuasa, Y Miyagoe, et al.

Human Gene Therapy|April 11, 2000

Long-term persistence of human bone marrow stromal cells transduced with factor VIII-retroviral vectors and transient production of therapeutic levels of human factor VIII in nonmyeloablated immunodeficient miceM K Chuah, A Van Damme, H Zwinnen, et al.

Pageof 413