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Human Gene Therapy|February 19, 2026
A Tripartite AAV System with Engineered Lox Sites Enables Efficient Delivery of the EYS Gene for Retinal Gene TherapyKun-Do Rhee, Poppy Datta, Clairissa Baccam, et al.Human Gene Therapy|March 17, 2026
Quantification of Lentiviral Vectors with Nucleic Acid DyesJian Xu, Nancy Zhao, Morgane Chiesa, et al.Human Gene Therapy|March 11, 2026
Morphological and Molecular Detection of AAV Vector Genome and Transgene mRNA in the Oocytes of Female Cynomolgus Monkey Following Systemic Intravenous AdministrationBasel T Assaf, Joshua G DeKeyserHuman Gene Therapy|February 22, 2024
Combination Immunotherapy of Oncolytic Flu-Vectored Virus and Programmed Cell Death 1 Blockade Enhances Antitumor Activity in Hepatocellular CarcinomaHongyu Yu, Fang Sun, Yan Xu, et al.Human Gene Therapy|February 22, 2024
Current Status and Prospects of Viral Vector-Based Gene Therapy to Treat Kidney DiseasesLouise Medaer, Koenraad Veys, Rik GijsbersHuman Gene Therapy|March 27, 2024
Development of AAV-Mediated Gene Therapy Approaches to Treat Skeletal DiseasesChujiao Lin, Matthew B Greenblatt, Guangping Gao, et al.Human Gene Therapy|May 8, 2024
CRISPR-Cas Genome Editing in Ex Vivo Human Lungs to Rewire the Translational Path of Genome-Targeting TherapeuticsKumi Mesaki, Haruchika Yamamoto, Stephen Juvet, et al.Human Gene Therapy|April 25, 2024
Advances in Bone-Targeting Drug Delivery: Emerging Strategies Using Adeno-Associated VirusTadatoshi Sato, Sachin Chaugule, Matthew B Greenblatt, et al.Human Gene Therapy|September 6, 2023
Hemophilia Gene Therapy: The End of the Beginning?Dries De Wolf, Kshitiz Singh, Marinee K Chuah, et al.Human Gene Therapy|September 6, 2023
Gene Therapy for Immunoglobulin E, Complement-Mediated, and Eosinophilic DisordersOdelya E Pagovich, Ronald G CrystalPageof 414