Synthetically Engineered Adeno-Associated Virus for Efficient, Safe, and Versatile Gene Therapy Applications | ACS Nano
Relevance of Assembly-Activating Protein for Adeno-associated Virus Vector Production and Capsid Protein Stability in Mammalian and Insect Cells | Journal of Virology
The AAV vector toolkit: poised at the clinical crossroads. - Abstract - Europe PMC
Adeno-associated virus vectors for human gene therapy
PDF) Efficient intracerebral delivery of AAV5 vector encoding human ARSA in non-human primate
Adeno-associated virus vectors for human gene therapy
Median raphe controls acquisition of negative experience in the mouse | Science
Acute Knockdown of Importin a5 in the Ventral Hippocampus of Adult Mice... | Download Scientific Diagram
Restoring brain cholesterol turnover improves autophagy and has therapeutic potential in mouse models of spinocerebellar ataxia
Terminal N-Linked Galactose Is the Primary Receptor for Adeno-associated Virus 9* - Journal of Biological Chemistry
A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency
Adeno-associated virus vectors for human gene therapy
Generation of Cell Lines Capable of Producing High-titer Viral Stocks for Use in Vaccine Manufacture and Gene Therapy | ATCC
Molecular and neural basis of pleasant touch sensation | Science
Translation of MicroRNA-Based Huntingtin-Lowering Therapies from Preclinical Studies to the Clinic: Molecular Therapy
Best of most possible worlds: Hybrid gene therapy vectors based on parvoviruses and heterologous viruses - ScienceDirect
Upstream Manufacturing of Gene Therapy Viral Vectors
Cross-Packaging of a Single Adeno-Associated Virus (AAV) Type 2 Vector Genome into Multiple AAV Serotypes Enables Transduction w
Best of most possible worlds: Hybrid gene therapy vectors based on parvoviruses and heterologous viruses: Molecular Therapy
HI loop comparison of various AAV serotypes and autonomous... | Download Scientific Diagram
Cross-Packaging of a Single Adeno-Associated Virus (AAV) Type 2 Vector Genome into Multiple AAV Serotypes Enables Transduction w
Generation of Cell Lines Capable of Producing High-titer Viral Stocks for Use in Vaccine Manufacture and Gene Therapy | ATCC
