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Human Gene Therapy|January 10, 2002
Lethal toxicity, severe endothelial injury, and a threshold effect with high doses of an adenoviral vector in baboonsNúria Morral, Wanda K O'Neal, Karen Rice, et al.
Human Gene Therapy|July 31, 2012
Targeted delivery of self-complementary adeno-associated virus serotype 9 to the brain, using magnetic resonance imaging-guided focused ultrasoundEmmanuel Thévenot, Jessica F Jordão, Meaghan A O'Reilly, et al.
Human Gene Therapy|January 20, 1996
A neural cell-type-specific expression system using recombinant adenovirus vectorsM Hashimoto, J Aruga, Y Hosoya, et al.
Human Gene Therapy|July 10, 2026
CAR-T Cell Therapy: Manufacturing Platforms and Clinical ConsequencesDuc-Hiep Bach, Thanh Liem Nguyen
Human Gene Therapy|July 7, 2026
The German National Strategy for Gene- and Cell-Based Therapies: Generating Impact by Employing a Novel Multi-Stakeholder ApproachChristian Gallus, Francis Ayuk, Philipp Beckhove, et al.
Human Gene Therapy|February 9, 2016
FusX: A Rapid One-Step Transcription Activator-Like Effector Assembly System for Genome ScienceAlvin C Ma, Melissa S McNulty, Tanya L Poshusta, et al.
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.
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