AAV Gene Transfer to the Heart | SpringerLink
Frontiers | Adeno-Associated Viruses (AAV) and Host Immunity – A Race Between the Hare and the Hedgehog | Immunology
Antigen suppression effect of the core protein allosteric modulator RO7049389 in AAV-HBV mice is accompanied by transient upregulation of immune-cell gene signatures in the liver
Plateforme Technologique Bertarelli de thérapie génique ‐ EPFL
Gene Therapy Engine | Our Science | Sarepta Therapeutics
Plan a Vacation to Switzerland – AAV Travel & Romance
Triple Vectors Expand AAV Transfer Capacity in the Retina: Molecular Therapy
Ex Vivo/In vivo Gene Editing in Hepatocytes Using “All-in-One” CRISPR-Adeno-Associated Virus Vectors with a Self-Linearizing Repair Template - ScienceDirect
Adeno-associated virus-binding antibodies detected in cats living in the Northeastern United States lack neutralizing activity | Scientific Reports
Synthetic Biology: Emerging Concepts to Design and Advance Adeno‐Associated Viral Vectors for Gene Therapy - Wagner - 2021 - Advanced Science - Wiley Online Library
Martina Hruzova – ETH Zürich – Zürich, Schweiz | LinkedIn
Structural characterization of a novel human adeno-associated virus capsid with neurotropic properties | Nature Communications
PLOS ONE: Pre-existing antibodies to candidate gene therapy vectors (adeno-associated vector serotypes) in domestic cats
Quantification of AAV Capsid Loading Fractions - Beckman Coulter
A Multifaceted Strategy For Viral Safety In AAV Processes
AAV | L'entreprise centenaire spécialiste en construction métallique
Cross-Packaging and Capsid Mosaic Formation in Multiplexed AAV Libraries: Molecular Therapy - Methods & Clinical Development
High levels of AAV vector integration into CRISPR-induced DNA breaks | Nature Communications
AAV Contractors SA - Home | Facebook
Synthetic Biology: Emerging Concepts to Design and Advance Adeno‐Associated Viral Vectors for Gene Therapy - Wagner - 2021 - Advanced Science - Wiley Online Library
PDF) Scalable Production of AAV Vectors in Orbitally Shaken HEK293 Cells | Daniel Blessing, Catherine Pythoud, Bernard Schneider, and Nicole Déglon - Academia.edu
IJMS | Free Full-Text | AAV-Mediated Gene Delivery to 3D Retinal Organoids Derived from Human Induced Pluripotent Stem Cells | HTML
Synthetic Biology: Emerging Concepts to Design and Advance Adeno‐Associated Viral Vectors for Gene Therapy - Wagner - 2021 - Advanced Science - Wiley Online Library
