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Human Gene Therapy|April 12, 2011
Optimizing promoters for recombinant adeno-associated virus-mediated gene expression in the peripheral and central nervous system using self-complementary vectorsSteven J Gray, Stacey B Foti, Joel W Schwartz, et al.Human Gene Therapy|August 5, 2026
Suppression of AAV-Delivered Transgene Expression Using Artificial MicroRNAs Delivered by an Alternative AAV SerotypeMiguel de Mulder Rougvie, Mara R Kebret, Youjun Wu, et al.Human Gene Therapy|July 16, 2026
Dichotomies in Ex Vivo and In Vivo Performance of Receptor-Binding Mutants of Adeno-Associated Virus VectorsOlaniyi Olarewaju, Martin Bentler, Jacqueline Breuer, et al.Human Gene Therapy|August 5, 2026
Safety, Tolerability, and Efficacy of a Prophylactic Sirolimus Protocol for Patients Receiving Delandistrogene Moxeparvovec-Rokl Gene TherapyZahraa Siddiqui, Serena Neumann, Daniel Guillen, et al.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|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.Pageof 413