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Rational Design of AAV-rh74, AAV3B, and AAV8 with Limited Liver Targeting

AAV Immunotoxicity: Implications in Anti-HBV Gene Therapy

Inhibition of HBV Expression in HBV Transgenic Mice Using AAV-Delivered CRISPR-SaCas9

Prevalence of pre-existing immunity to AAV8 and other AAV serotypes in healthy individuals

Detection of the hepatitis B virus (HBV) covalently-closed-circular DNA (cccDNA) in mice transduced witha recombinant AAV-HBV vector

AAV-HBV mouse model replicates immune exhaustion patterns of chronic HBV patients at single-cell level

AAV-8 and AAV-9 Vectors Cooperate with Serum Proteins Differently Than MV-1 and AAV-6

Novel human liver-tropic AAV variants define transferable domains that markedly enhance the human tropismof AAV7 and AAV8

Analysis of Adeno-Associated Virus Serotype 8 (AAV8)-antibody complexes using epitope mapping by molecularimprinting leads to the identification of Fab peptides that potentially evade AAV8 neutralisation

APPARENT VIROLOGICAL CURE OF HBV INFECTION BY THE NOVEL CAPSID/ CGAS BIFUNCTIONAL MOLECULE LW231 IN AAV- HBV MICE

TIMING OF ADMINISTRATION OF ANTI-PD-1 IS IMPORTANT TO INCREASE HBV-SPECIFIC IMMUNE RESPONSES IN AAV-HBV

SHORTENING HBV TREATMENT AND PREVENTING HBV RELAPSE BY ADDING AN ANTI-HBS EXPRESSING AAV-VECTOR TO ENTECAVIRTHERAPY IN HBV INFECTED uPA/SCID CHIMERIC MICE

Liver-directed Pdx1 expression using recombinant AAV-2 and AAV-DJ/8 vectors in diabetic mouse model

Human carbonic anhydrase-8 AAV8 gene therapy inhibits nerve growth factor signaling producing prolonged

Development of AAV Transduction and Potency Assays to Evaluate Quality Attributes of ASC618, a SecondGeneration AAV8-Based Hemophilia A Gene Therapy

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