Association Of Avian Veterinarians (Aav) company information, Employees & Contact Information

Enhancing AAV-microdystrophin gene therapy after repeat dosing by blocking phagocytosis Frontiers

Biophysical and structural insights into AAV genome ejection ASM Journals

The 9th of Av - Tisha B'Av 2025 Chabad

An AAV capsid reprogrammed to bind human transferrin receptor mediates brain-wide gene delivery Science | AAAS

AAV gene therapy for Duchenne muscular dystrophy: the EMBARK phase 3 randomized trial Nature

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AAV-Mediated Delivery of Plakophilin-2a Arrests Progression of Arrhythmogenic Right Ventricular Cardiomyopathy in Murine Hearts: Preclinical Evidence Supporting Gene Therapy in Humans | Circulation: Genomic and Precision Medicine American Heart Association Journals

Thrombotic microangiopathy following systemic AAV administration is dependent on anti-capsid antibodies JCI.org

Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species ScienceDirect.com

Analysis of Host Cell Proteins in AAV Products with ProteoMiner Protein Enrichment Technology ACS Publications

AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient Nature

Human Immune Responses to Adeno-Associated Virus (AAV) Vectors Frontiers

PCDH15 dual-AAV gene therapy for deafness and blindness in Usher syndrome type 1F models JCI.org

In Vivo Silencing of Regulatory Elements Using a Single AAV-CRISPRi Vector | Circulation Research American Heart Association Journals

Adeno-associated virus as a delivery vector for gene therapy of human diseases Nature

Gene Therapy Advances: A Meta-Analysis of AAV Usage in Clinical Settings Frontiers

Transcriptional linkage analysis with in vivo AAV-Perturb-seq Nature

Deep Parallel Characterization of AAV Tropism and AAV-Mediated Transcriptional Changes via Single-Cell RNA Sequencing Frontiers

An engineered AAV targeting integrin alpha V beta 6 presents improved myotropism across species Nature

Integrated vector genomes may contribute to long-term expression in primate liver after AAV administration Nature

Comparative analysis of AAV serotypes for transduction of olfactory sensory neurons Frontiers

Quantitative analysis of preferential utilization of AAV ITR as the packaging terminal signal Frontiers

Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing Nature

Therapeutic efficacy of AAV-mediated restoration of PKP2 in arrhythmogenic cardiomyopathy Nature

Assessment of systemic AAV-microdystrophin gene therapy in the GRMD model of Duchenne muscular dystrophy Science | AAAS

Disrupting the LINC complex by AAV mediated gene transduction prevents progression of Lamin induced cardiomyopathy Nature

Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo Nature

Mitigating the Immunogenicity of AAV-Mediated Gene Therapy with an Immunosuppressive Phosphoserine-Containing Zwitterionic Peptide ACS Publications

The Role of Recombinant AAV in Precise Genome Editing Frontiers

Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models Nature

Analytical characterization of full, intermediate, and empty AAV capsids Nature

Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders Science | AAAS

Identification of a myotropic AAV by massively parallel in vivo evaluation of barcoded capsid variants Nature

The AAV capsid can influence the epigenetic marking of rAAV delivered episomal genomes in a species dependent manner Nature

AAV process intensification by perfusion bioreaction and integrated clarification Frontiers

AAV‐mediated delivery of an anti‐BACE1 VHH alleviates pathology in an Alzheimer's disease model EMBO Press

Suppression of heterotopic ossification in fibrodysplasia ossificans progressiva using AAV gene delivery Nature

Hardwiring tissue-specific AAV transduction in mice through engineered receptor expression Nature

Low-dose AAV-CRISPR-mediated liver-specific knock-in restored hemostasis in neonatal hemophilia B mice with subtle antibody response Nature

Improving adeno-associated viral (AAV) vector-mediated transgene expression in retinal ganglion cells: comparison of five promoters | Gene Therapy Nature

Immunogenicity and toxicity of AAV gene therapy Frontiers

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model PNAS

AAV‐Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness Wiley

Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness | EMBO Molecular Medicine EMBO Press

AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model EMBO Press

Synaptic Specificity and Application of Anterograde Transsynaptic AAV for Probing Neural Circuitry Journal of Neuroscience

In Vivo AAV-CRISPR/Cas9–Mediated Gene Editing Ameliorates Atherosclerosis in Familial Hypercholesterolemia American Heart Association Journals

Standard screening methods underreport AAV-mediated transduction and gene editing Nature

High levels of AAV vector integration into CRISPR-induced DNA breaks Nature

Positron emission tomography imaging of novel AAV capsids maps rapid brain accumulation Nature

Targeting oxidized phospholipids by AAV-based gene therapy in mice with established hepatic steatosis prevents progression to fibrosis Science | AAAS

Ca2+ activity maps of astrocytes tagged by axoastrocytic AAV transfer Science | AAAS

CNS Transduction Benefits of AAV-PHP.eB over AAV9 Are Dependent on Administration Route and Mouse Strain ScienceDirect.com

AAV-delivered eCD4-Ig protects rhesus macaques from high-dose SIVmac239 challenges Science | AAAS

The atomic structure of adeno-associated virus (AAV-2), a vector for human gene therapy PNAS

AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome American Heart Association Journals

AAV-ie enables safe and efficient gene transfer to inner ear cells Nature

Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice Nature

Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system Science | AAAS

AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells Nature

Adeno-associated Virus (AAV) Serotypes Have Distinctive Interactions with Domains of the Cellular AAV Receptor ASM Journals

Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting Frontiers

Production of adeno-associated virus vectors for in vitro and in vivo applications | Scientific Reports Nature

AAV-mediated in vivo functional selection of tissue-protective factors against ischaemia Nature