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Human Gene Therapy|April 29, 1998
Selective gene transfer into the liver of non-human primates with E1-deleted, E2A-defective, or E1-E4 deleted recombinant adenovirusesS E Raper, Z J Haskal, X Ye, et al.Human Gene Therapy|April 29, 1998
Recombinant E1-deleted adenovirus-mediated gene therapy for cancer: efficacy studies with p53 tumor suppressor gene and liver histology in tumor xenograft modelsL L Nielsen, M Gurnani, J Syed, et al.Human Gene Therapy|August 29, 2025
Biacore Analysis of Cross-Reactive Adeno-Associated Virus Antibodies in Monkeys Following Intravenous Administration of AAV5, AAV8, and AAV9 VectorsYanshan Dai, Glen Banks, Grace Wu, et al.Human Gene Therapy|August 2, 2016
Chimeric Antigen Receptor T Cell Therapy Targeting CD19-Positive Leukemia and Lymphoma in the Context of Stem Cell TransplantationMaria-Luisa Schubert, Angela Hückelhoven, Jean-Marc Hoffmann, et al.Human Gene Therapy|May 5, 2020
Volume and Infusion Rate Dynamics of Intraparenchymal Central Nervous System Infusion in a Large Animal ModelToloo Taghian, Erin Horn, Mohammed Salman Shazeeb, et al.Human Gene Therapy|June 11, 2015
A Genetically Modified Adenoviral Vector with a Phage Display-Derived Peptide Incorporated into Fiber Fibritin Chimera Prolongs Survival in Experimental GliomaJulius W Kim, J Robert Kane, Jacob S Young, et al.Human Gene Therapy|June 16, 2015
CRISPR/Cas9-Mediated Genome Editing of Epigenetic Factors for Cancer TherapyShaohua Yao, Zhiyao He, Chong ChenHuman Gene Therapy|June 17, 2015
Human α7 Integrin Gene (ITGA7) Delivered by Adeno-Associated Virus Extends Survival of Severely Affected Dystrophin/Utrophin-Deficient MiceKristin N Heller, Chrystal L Montgomery, Kimberly M Shontz, et al.Human Gene Therapy|July 16, 2016
Stem Cell Therapy for the Central Nervous System in Lysosomal Storage DiseasesFaez Siddiqi, John H WolfeHuman Gene Therapy|July 22, 2016
Highly Efficient Delivery of Adeno-Associated Viral Vectors to the Primate RetinaShannon E Boye, John J Alexander, C Douglas Witherspoon, et al.Pageof 414