JCM | Free Full-Text | Emerging Immunogenicity and Genotoxicity Considerations of Adeno-Associated Virus Vector Gene Therapy for Hemophilia
Integration of adeno-associated virus (AAV) into the genomes of most Thai and Mongolian liver cancer patients does not induce oncogenesis | BMC Genomics | Full Text
Epigenetic Silencing of Recombinant Adeno-associated Virus Genomes by NP220 and the HUSH Complex
AAV integration into the human genome. Wild-type AAV vectors encoding... | Download Scientific Diagram
Emerging Issues in AAV-Mediated In Vivo Gene Therapy - ScienceDirect
AAV-Genome Population Sequencing of Vectors Packaging CRISPR Components Reveals Design-Influenced Heterogeneity - ScienceDirect
Frontiers | Answered and Unanswered Questions in Early-Stage Viral Vector Transduction Biology and Innate Primary Cell Toxicity for Ex-Vivo Gene Editing
Introduction to Adeno-Associated Viruses (AAV) – Vector Biolabs
Engineering adeno-associated virus vectors for gene therapy | Nature Reviews Genetics
High levels of AAV vector integration into CRISPR-induced DNA breaks | Nature Portfolio Bioengineering Community
Figure 3 from Adeno-associated virus (AAV) site-specific recombination does not require a Rep-dependent origin of replication within the AAV terminal repeat | Semantic Scholar
Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders | Science Advances
Site-specific integration of adeno-associated virus involves partial duplication of the target locus | PNAS
Viruses | Free Full-Text | The Interplay between Adeno-Associated Virus and Its Helper Viruses
AAV genome organization and integration capture sequencing schematic.... | Download Scientific Diagram
Frontiers | The Role of Recombinant AAV in Precise Genome Editing
Adeno-associated virus - Wikipedia
AAV and hepatocellular carcinoma. Genomic integration of wild-type (WT)... | Download Scientific Diagram
Frontiers | The Role of Recombinant AAV in Precise Genome Editing
Adeno-associated virus vector as a platform for gene therapy delivery | Nature Reviews Drug Discovery
Adeno Associated Virus (AAV) for Cell and Gene Therapy
Synthetic Biology: Emerging Concepts to Design and Advance Adeno‐Associated Viral Vectors for Gene Therapy - Wagner - 2021 - Advanced Science - Wiley Online Library
Adeno-Associated Virus-Based Gene Therapy for Lifelong Correction of Genetic Disease
