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Suppression of heterotopic ossification in fibrodysplasia ossificans progressiva using AAV gene delivery.Academic Article Why?
AAV-mediated gene delivery attenuates neuroinflammation in feline Sandhoff disease.Academic Article Why?
Cellular and Tissue Selectivity of AAV Serotypes for Gene Delivery to Chondrocytes and Cartilage.Academic Article Why?
Intravenous Infusion of AAV for Widespread Gene Delivery to the Nervous System.Academic Article Why?
AAV-mediated gene delivery in a feline model of Sandhoff disease corrects lysosomal storage in the central nervous system.Academic Article Why?
AAV-mediated gene delivery in adult GM1-gangliosidosis mice corrects lysosomal storage in CNS and improves survival.Academic Article Why?
Microvesicle-associated AAV vector as a novel gene delivery system.Academic Article Why?
Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector.Academic Article Why?
Intrathecal Delivery of AAV Vectors in Cynomolgus Macaques for CNS Gene Therapy and Gene Expression Analysis in Microdissected Motor Neurons.Academic Article Why?
AAV9 delivering a modified human Mullerian inhibiting substance as a gene therapy in patient-derived xenografts of ovarian cancer.Academic Article Why?
Targeted gene delivery to the enteric nervous system using AAV: a comparison across serotypes and capsid mutants.Academic Article Why?
Adeno-associated virus (AAV) as a vehicle for therapeutic gene delivery: improvements in vector design and viral production enhance potential to prolong graft survival in pancreatic islet cell transplantation for the reversal of type 1 diabetes.Academic Article Why?
Subretinal delivery of recombinant AAV serotype 8 vector in dogs results in gene transfer to neurons in the brain.Academic Article Why?
Shim, Jae-HyuckPerson Why?
Flotte, TerencePerson Why?
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