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Human Gene Therapy|April 22, 2025
Deciphering Key Adenoviral Elements in the Production of Recombinant Adeno-Associated Virus VectorsSofia Fernandes, Júlia Guerra, Mariana V Ferreira, et al.Human Gene Therapy|June 6, 2023
Screening an Effective Dual-Adeno-Associated Virus Split-Cytosine Base Editor System for C-to-T ConversionQianyi Liu, Yuxi Chen, Sihui Hu, et al.Human Gene Therapy|June 5, 2023
Improvement of Precision in Recombinant Adeno-Associated Virus Infectious Titer Assay with Droplet Digital PCR as an Endpoint MeasurementTam Duong, James McAllister, Khalid Eldahan, et al.Human Gene Therapy|June 2, 2023
Characteristics, Recombination Methods, and Applications Progresses of Split-Cas9 SystemZhixi Liu, Lu Huang, Han Deng, et al.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.Pageof 413