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One or more keywords matched the following items that are connected to Keeler-Klunk, Allison
Item TypeName
Academic Article Modulation of exaggerated-IgE allergic responses by gene transfer-mediated antagonism of IL-13 and IL-17e.
Academic Article Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy.
Academic Article Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndrome.
Concept Genetic Therapy
Academic Article Systemic AAV9 gene transfer in adult GM1 gangliosidosis mice reduces lysosomal storage in CNS and extends lifespan.
Academic Article Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector.
Academic Article Gene Therapy 2017: Progress and Future Directions.
Academic Article Systemic Delivery of AAVB1-GAA Clears Glycogen and Prolongs Survival in a Mouse Model of Pompe Disease.
Academic Article AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency.
Academic Article Recombinant Adeno-Associated Virus Gene Therapy in Light of Luxturna (and Zolgensma and Glybera): Where Are We, and How Did We Get Here?
Academic Article Intralingual and Intrapleural AAV Gene Therapy Prolongs Survival in a SOD1 ALS Mouse Model.
Academic Article Novel Combinatorial MicroRNA-Binding Sites in AAV Vectors Synergistically Diminish Antigen Presentation and Transgene Immunity for Efficient and Stable Transduction.
Academic Article AAV gene therapy for Tay-Sachs disease.
Academic Article Rational Use of Immunosuppressive Corticosteroids in Liver-Directed Adeno-Associated Virus Gene Therapy Studies.
Academic Article Evaluating Readministration of Adeno-Associated Virus for Gene Therapy.
Academic Article Redosing Adeno-Associated Virus Gene Therapy to the Central Nervous System.
Academic Article Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer.
Academic Article Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy.
Academic Article Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy. Reply.
Academic Article Limb Perfusion Delivery of a rAAV1 Alpha-1 Antitrypsin Vector in Non-Human Primates Is Safe but Insufficient for Therapy.
Academic Article Immune responses to central nervous system directed adeno-associated virus gene therapy: Does direct CNS delivery make a difference?
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  • Gene therapy