Center-Authored Papers
Filters: Author is Chamberlain, Jeffrey S [Clear All Filters]
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2012.
Immunity and AAV-Mediated Gene Therapy for Muscular Dystrophies in Large Animal Models and Human Trials.. Frontiers in microbiology. 2:201. Abstract
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2011.
Gene therapy in large animal models of muscular dystrophy.. ILAR journal / National Research Council, Institute of Laboratory Animal Resources. 50(2):187-98. Abstract
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2009.
Immune responses to AAV in canine muscle monitored by cellular assays and noninvasive imaging.. Molecular therapy : the journal of the American Society of Gene Therapy. 18(3):617-24. Abstract
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2010.
Multi-Parametric MRI at 14T for Muscular Dystrophy Mice Treated with AAV Vector-Mediated Gene Therapy.. PloS one. 10(4):e0124914. Abstract
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2015.
Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy.. Human molecular genetics. 17(16):2507-17. Abstract
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2008.
Efficient transduction of skeletal muscle using vectors based on adeno-associated virus serotype 6.. Molecular therapy : the journal of the American Society of Gene Therapy. 10(4):671-8. Abstract
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2004.
Immune Responses to rAAV6: The Influence of Canine Parvovirus Vaccination and Neonatal Administration of Viral Vector.. Frontiers in microbiology. 2:220. Abstract
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2011. Doing Business with Arnold Library
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