High levels of AAV vector integration into CRISPR-induced DNA breaks | Nature Portfolio Bioengineering Community
Adeno-associated virus vector as a platform for gene therapy delivery | Nature Reviews Drug Discovery
AAV integration into the human genome. Wild-type AAV vectors encoding... | Download Scientific Diagram
AAV and hepatocellular carcinoma. Genomic integration of wild-type (WT)... | Download Scientific Diagram
Adeno-Associated Virus-Based Gene Therapy for Lifelong Correction of Genetic Disease
AAV Vectors for the Nucleolus: Molecular Therapy
AAV vector system, AAV production, transduction and AAV gene therapy | GeneMedi
AAV
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
Adeno Associated Virus (AAV) for Cell and Gene Therapy
Addgene: Adeno-associated virus (AAV) Guide
Epigenetic Silencing of Recombinant Adeno-associated Virus Genomes by NP220 and the HUSH Complex
JCM | Free Full-Text | Emerging Immunogenicity and Genotoxicity Considerations of Adeno-Associated Virus Vector Gene Therapy for Hemophilia
Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders | Science Advances
Adeno-Associated Viral-Mediated Gene Transfer
Adeno-Associated Virus-Based Gene Therapy for Lifelong Correction of Genetic Disease | Human Gene Therapy
AAV Episomal Persistence Evaluation Service - Creative Biolabs
Frontiers | Answered and Unanswered Questions in Early-Stage Viral Vector Transduction Biology and Innate Primary Cell Toxicity for Ex-Vivo Gene Editing
AAV-Genome Population Sequencing of Vectors Packaging CRISPR Components Reveals Design-Influenced Heterogeneity - ScienceDirect
Synthetic Biology: Emerging Concepts to Design and Advance Adeno‐Associated Viral Vectors for Gene Therapy - Wagner - 2021 - Advanced Science - Wiley Online Library
Evaluating the state of the science for adeno-associated virus integration: An integrated perspective: Molecular Therapy
Adeno-Associated Virus Site-Specific Integration and AAVS1 Disruption | Journal of Virology
Adeno-associated virus (AAV) site-specific recombination does not require a Rep-dependent origin of replication within the AAV terminal repeat | PNAS
High levels of AAV vector integration into CRISPR-induced DNA breaks | Nature Communications
ITR-Seq, a next-generation sequencing assay, identifies genome-wide DNA editing sites in vivo following adeno-associated viral vector-mediated genome editing | BMC Genomics | Full Text
Frontiers | The Role of Recombinant AAV in Precise Genome Editing
Introduction of AAV : SignaGen Laboratories, A Gene Delivery Company Providing Custom AAV Adenovirus Lentivirus Production Services & Manufacturing DNA/siRNA Transfection Reagents..., SignaGen Laboratories, A Gene Delivery Company Providing Custom AAV ...
Integration Preferences of Wildtype AAV-2 for Consensus Rep-Binding Sites at Numerous Loci in the Human Genome | PLOS Pathogens
