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AAV genome modification for efficient AAV production

Syngeneic AAV Pseudo-particles Potentiate Gene Transduction of AAV Vectors

T Cell-Mediated Immune Responses to AAV and AAV Vectors

Anti-AAV Antibodies in AAV Gene Therapy: Current Challenges and Possible Solutions

Chem-AAV: Chemically Modified AAV for Gene Therapy

Chem-AAV: Chemically Modified AAV for Targeting Gene Delivery

An Alternate Route for Adeno-associated Virus (AAV) Entry Independent of AAV Receptor

Successful Transduction with AAV Vectors after Selective Depletion of Anti-AAV Antibodies by Immunoadsorption

Intrathymic AAV gene delivery

AAV-8 and AAV-9 Vectors Cooperate with Serum Proteins Differently Than MV-1 and AAV-6

Novel AAV ITR Sequencing and AAV Plasmid Preparation Protocols to Advance Research and Therapies UsingAAV Vectors

AAV Capsid ELISA Automation for High-Throughput AAV Titer Determination

AAV development program: towards next generation of livertropic AAV variants

AAV Vector Mobilization is a Concern for AAV Gene Therapy

From AAV virus to AAV vector: characterization of a collection of AAV capsid variants isolated from human

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