Hardwiring tissue-specific AAV transduction in mice through engineered receptor expression | Nature Methods
New Gene Therapy Approach Improves Metabolic Function and Behavior in Mouse Model of PWS
Gaia Trincucci on X: "🐭New AAV-hACE2 mouse model of #SARSCoV2 infection from @VirusesImmunity, @benisraelow, @ericsongg & colleagues @YaleIBIO @YaleMed. Interesting insights on the role of Type I IFNs & lung pathology! https://t.co/W6EYxnq6rg #
Frontiers | AAV Delivery of shRNA Against TRPC6 in Mouse Hippocampus Impairs Cognitive Function
Analyzing efficacy, stability, and safety of AAV-mediated optogenetic hearing restoration in mice | Life Science Alliance
Biomedicines | Free Full-Text | Adeno-Associated Viruses for Modeling Neurological Diseases in Animals: Achievements and Prospects
Low incidence of hepatocellular carcinoma in mice and cats treated with systemic adeno-associated viral vectors: Molecular Therapy - Methods & Clinical Development
Selection of an Efficient AAV Vector for Robust CNS Transgene Expression - ScienceDirect
AAV‐mediated delivery of an anti‐BACE1 VHH alleviates pathology in an Alzheimer's disease model | EMBO Molecular Medicine
Controlling AAV receptor expression to improve testing and validation of AAV gene therapy products | Explore Technologies
Adeno‐associated virus‐based Alzheimer's disease mouse models and potential new therapeutic avenues - Ittner - 2019 - British Journal of Pharmacology - Wiley Online Library
A Single Intravenous Injection of AAV-PHP.B-hNDUFS4 Ameliorates the Phenotype of Ndufs4−/− Mice - ScienceDirect
AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model | EMBO Molecular Medicine
Standard screening methods underreport AAV-mediated transduction and gene editing | Nature Communications
Characterization of a flexible AAV-DTR/DT mouse model of acute epithelial lung injury | American Journal of Physiology-Lung Cellular and Molecular Physiology
Split AAV-Mediated Gene Therapy Restores Ureagenesis in a Murine Model of Carbamoyl Phosphate Synthetase 1 Deficiency: Molecular Therapy
AAV-PHP.B-Mediated Global-Scale Expression in the Mouse Nervous System Enables GBA1 Gene Therapy for Wide Protection from Synucleinopathy - ScienceDirect
Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders | Science Advances
AAV-Mediated Astrocyte-Specific Gene Expression under Human <i>ALDH1L1</i> Promoter in Mouse Thalamus
Biomolecules | Free Full-Text | Optimized AAV Vectors for TMC1 Gene Therapy in a Humanized Mouse Model of DFNB7/11
Rapid generation of mouse model for emerging infectious disease with the case of severe COVID-19 | PLOS Pathogens
Cockroach allergen–induced mouse model with AAV–miR-511-3p–infected... | Download Scientific Diagram
Experimental Variables that Affect Human Hepatocyte AAV Transduction in Liver Chimeric Mice - ScienceDirect
AAV vector-mediated expression of foreign gene in mouse brain. a The... | Download Scientific Diagram
Adeno‐associated virus‐based Alzheimer's disease mouse models and potential new therapeutic avenues - Ittner - 2019 - British Journal of Pharmacology - Wiley Online Library
Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness | EMBO Molecular Medicine
AAV-Mediated Progranulin Delivery to a Mouse Model of Progranulin Deficiency Causes T Cell-Mediated Toxicity: Molecular Therapy
Large1 gene transfer in older myd mice with severe muscular dystrophy restores muscle function and greatly improves survival | Science Advances
