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Human Gene Therapy|August 3, 2026
Novel VSV-G Variants with Enhanced Blinding for Targeted Delivery of Lentiviral VectorsFelix L Warnecke, Moritz Ertelt, Anjali Shrivastava, et al.Human Gene Therapy|August 17, 2026
Durational Study of Persistent Transduction of Rhesus Macaque Lung and Other Organs Following Single Dosing with AAV1-CFTRPrajita Paul, Tanvi Sharma, Masoud Afshani, et al.Human Gene Therapy|August 24, 2026
Engineering Human Hematopoietic Stem and Progenitor Cells for Antigen Expression in Antigen-Presenting CellsClara Heider, Meg Louise Donovan, Carina Walpole, et al.Human Gene Therapy|September 16, 2026
Development of an AAV-Encoded Adenine Base Editor for Duchenne Muscular DystrophyIna Luksch, Christine M Poch, Aylin Mayer, et al.Human Gene Therapy|October 16, 2026
Ocular Gene Therapy in China: Technological Framework, Clinical Translation, and Future PerspectivesDi Zhang, Ziyan He, Fang Lu, et al.Human Gene Therapy|October 20, 2026
Novel Technologies and Clinical Breakthroughs: The Evolving Landscape of Gene Therapy in ChinaJunshu Li, Yuntian Deng, Jinhu Ma, et al.Human Gene Therapy|July 19, 2003
Construction of a cytomegalovirus-based amplicon: a vector with a unique transfer capacityEva Maria Borst, Martin MesserleHuman Gene Therapy|July 19, 2003
Genetic correction of DNA repair-deficient/cancer-prone xeroderma pigmentosum group C keratinocytesCatherine Arnaudeau-Bégard, Florence Brellier, Odile Chevallier-Lagente, et al.Human Gene Therapy|July 30, 2003
Antiangiogenic cancer therapy with microencapsulated cellsPasquale Cirone, Jacqueline M Bourgeois, Patricia L ChangHuman Gene Therapy|June 14, 2003
Adenovirus serotype 5 fiber shaft influences in vivo gene transfer in miceTheodore A G Smith, Neeraja Idamakanti, Michele L Rollence, et al.Pageof 414