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Human Gene Therapy|September 6, 2023
Prevention of Portal-Tract Fibrosis in Zfyve19 Mouse Model with Adeno-Associated Virus Vector Delivering ZFYVE19Yanan Zhang, Dingyue Tang, Li Wang, et al.Human Gene Therapy|September 7, 2023
Gene Therapy for HemoglobinopathiesMaria Rosa Lidonnici, Samantha Scaramuzza, Giuliana FerrariHuman Gene Therapy|August 29, 2023
The Opportunities and Challenges of Gene Therapy for Treatment of Inherited Forms of Vision and Hearing LossEmmanuel J Simons, Ivana TrapaniHuman Gene Therapy|September 2, 2023
Limitations of Dual-Single Guide RNA CRISPR Strategies for the Treatment of Central Nervous System Genetic DisordersFábio Duarte, Gabriel Vachey, Nicholas S Caron, et al.Human Gene Therapy|April 10, 2026
SG33, a Vaccine Strain of Myxoma Virus with Oncolytic Potential, Exploits Macropinocytosis and Clathrin-Mediated Endocytosis for Entry into Pancreatic Cancer CellsNikolaos Kontopoulos, Noémie Delenclos, Laetitia Ligat, et al.Human Gene Therapy|March 26, 2026
Lipid Nanoparticle-Delivered mRNA Therapy Corrects Neonatal Murine MPS I-HJiamei Fu, Mei Luo, Xiu Jin, et al.Human Gene Therapy|April 3, 2026
Retroviral Transduction of Human CD4+ T Cells with Membrane-Attached IL-10 Generates Type 1-Like Regulatory T CellsDayana Blokon-Kogan, Shaul Davidson, Maya Levi-Mann, et al.Human Gene Therapy|April 24, 2026
Strategies and Advances in Site-Specific Integration of Exogenous Large GenesZhencheng Wu, Jia Chen, Manqi Huang, et al.Human Gene Therapy|April 17, 2026
Harvest Process and Affinity Resin Selection Impacts on Adeno-Associated Virus Residual Host Cell Protein RetentionThomas M Leibiger, Lie Min, Kelvin H LeeHuman Gene Therapy|June 16, 2026
In Vivo Genome Editing Approach to Disrupt Hydroxyacid Oxidase 1 for the Treatment of Primary Hyperoxaluria Type 1Jenny A Greig, Camilo Breton, Melanie K Smith, et al.Pageof 414