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Human Gene Therapy|September 13, 2018
Application of Ultrasound-Targeted Microbubble Destruction-Mediated Exogenous Gene Transfer in Treating Various Renal DiseasesShuaishuai Huang, Yu Ren, Xue Wang, et al.
Human Gene Therapy|August 31, 2018
Preclinical Development of a Hematopoietic Stem and Progenitor Cell Bioengineered Factor VIII Lentiviral Vector Gene Therapy for Hemophilia AChristopher B Doering, Gabriela Denning, Jordan E Shields, et al.
Human Gene Therapy|September 29, 2018
Immunoengineering of the Vascular Endothelium to Silence MHC Expression During Normothermic Ex Vivo Lung PerfusionConstanca Figueiredo, Marco Carvalho Oliveira, Chen Chen-Wacker, et al.
Human Gene Therapy|September 30, 2018
Efficient Reconstitution of Hepatic Microvasculature by Endothelin Receptor Antagonism in Liver Sinusoidal Endothelial CellsNeelam Yadav, Fadi Luc Jaber, Yogeshwar Sharma, et al.
Human Gene Therapy|May 1, 2019
Assessing the Impact of Cyclosporin A on Lentiviral Transduction and Preservation of Human Hematopoietic Stem Cells in Clinically Relevant Ex Vivo Gene Therapy SettingsCarolina Petrillo, Andrea Calabria, Francesco Piras, et al.
Human Gene Therapy|May 7, 2019
Multiplex Epigenome Editing of Dorsal Root Ganglion Neuron Receptors Abolishes Redundant Interleukin 6, Tumor Necrosis Factor Alpha, and Interleukin 1β Signaling by the Degenerative Intervertebral DiscJoshua D Stover, Niloofar Farhang, Brandon Lawrence, et al.
Human Gene Therapy|April 4, 2022
Preclinical Safety and Biodistribution in Mice Following Single-Dose Intramuscular Inoculation of Tumor DNA Vaccine by ElectroporationLing Dong, Mengfan Feng, Yaru Qiao, et al.
Human Gene Therapy|March 17, 2022
Development of a Beta Cell-Specific Expression Control Element for Recombinant Adeno-Associated VirusSunghee Chai, Youngjin Kim, Feorillo Galivo, et al.
Human Gene Therapy|March 17, 2022
AAV-p40 Bioengineering Platform for Variant Selection Based on Transgene ExpressionAdrian Westhaus, Marti Cabanes-Creus, Timo Jonker, et al.
Human Gene Therapy|March 16, 2022
Conversion of the Liver into a Biofactory for DNaseI Using Adeno-Associated Virus Vector Gene Transfer Reduces Neutrophil Extracellular Traps in a Model of Systemic Lupus ErythematosusAmina Ahmad, Mawj Mandwie, Kim M O'Sullivan, et al.
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