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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 CrystalHuman 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.Pageof 413