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Methods (San Diego, Calif.)|May 4, 2004
Utilization of adenovirus vectors for multiple gene transfer applicationsAndrea AmalfitanoCurrent Opinion in Molecular Therapeutics|September 30, 2003
Use of multiply deleted adenovirus vectors to probe adenovirus vector performance and toxicitiesAndrea AmalfitanoHuman Immunology|March 1, 2019
The role of ERAP1 in autoinflammation and autoimmunityYuliya Pepelyayeva, Andrea AmalfitanoCurrent Pharmaceutical Design|July 22, 2011
Gene therapy for lysosomal storage diseases: progress, challenges and future prospectsSergey S Seregin, Andrea AmalfitanoViruses|October 14, 2011
Improving adenovirus based gene transfer: strategies to accomplish immune evasionSergey S Seregin, Andrea AmalfitanoCurrent Gene Therapy|July 12, 2002
Separating fact from fiction: assessing the potential of modified adenovirus vectors for use in human gene therapyAndrea Amalfitano, Robin J ParksMolecular Therapy : the Journal of the American Society of Gene Therapy|June 7, 2007
Toll-like receptors impact on safety and efficacy of gene transfer vectorsScott E Hensley, Andrea AmalfitanoVaccine|June 12, 2012
Malaria vaccines: focus on adenovirus based vectorsNathaniel J Schuldt, Andrea AmalfitanoThe Application of Clinical Genetics|July 15, 2015
Recent advances in gene therapy for lysosomal storage disordersDavid Pw Rastall, Andrea AmalfitanoExpert Opinion on Biological Therapy|September 29, 2009
Overcoming pre-existing adenovirus immunity by genetic engineering of adenovirus-based vectorsSergey S Seregin, Andrea AmalfitanoPageof 10