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Human Gene Therapy|September 10, 1996
Construction of human factor IX expression vectors in retroviral vector frames optimized for muscle cellsJ M Wang, H Zheng, Y Sugahara, et al.Human Gene Therapy|May 1, 1996
Retrovirus-mediated suicide gene transduction in the vitreous cavity of the eye: feasibility in prevention of proliferative vitreoretinopathyH Kimura, T Sakamoto, J A Cardillo, et al.Human Gene Therapy|May 1, 1996
Gene therapy for amyotrophic lateral sclerosis (ALS) using a polymer encapsulated xenogenic cell line engineered to secrete hCNTFP Aebischer, N A Pochon, B Heyd, et al.Human Gene Therapy|January 5, 1999
Enhanced in vivo airway gene transfer via transient modification of host barrier properties with a surface-active agentD W Parsons, B R Grubb, L G Johnson, et al.Human Gene Therapy|January 5, 1999
Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody: immunogene approachJ Chen, S Gamou, A Takayanagi, et al.Human Gene Therapy|January 5, 1999
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicityN Morral, R J Parks, H Zhou, et al.Human Gene Therapy|January 5, 1999
Lentivirus-mediated transduction of islet grafts with interleukin 4 results in sustained gene expression and protection from insulitisW S Gallichan, T Kafri, T Krahl, et al.Human Gene Therapy|June 13, 1998
Toxin gene-mediated growth inhibition of lung adenocarcinoma in an animal model of pleural malignancyD K Hoganson, H Matsui, R K Batra, et al.Human Gene Therapy|June 13, 1998
Biosafety monitoring of patients receiving intracerebral injections of murine retroviral vector producer cellsZ Long, L P Li, T Grooms, et al.Human Gene Therapy|June 13, 1998
Selective and rapid uptake of adeno-associated virus type 2 in brainJ S Bartlett, R J Samulski, T J McCownPageof 413