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Molecular Therapy. Methods & Clinical Development|August 11, 2020
The Art and Science of Selecting a CD123-Specific Chimeric Antigen Receptor for Clinical TestingJanice M Riberdy, Sheng Zhou, Fei Zheng, et al.
Molecular Therapy. Methods & Clinical Development|January 1, 2020
Production of Lentiviral Vectors Using Suspension Cells Grown in Serum-free MediaMatthew Bauler, Jessica K Roberts, Chang-Chih Wu, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Alternative organelle targeting of OPA1 mediates fatty acid release from lipid dropletsXiao Li, Dennis Voronin, Rikshita Bhattacharyya, et al.
Vaccines|November 19, 2020
Antibody Responses to SARS-CoV-2 Antigens in Humans and AnimalsHyunsuh Kim, Patrick Seiler, Jeremy C Jones, et al.
Molecular Therapy. Advances|May 15, 2026
Rational engineering of the P5 TRS-mimic site and REP78/68 start codon yields promoter variants that improve rAAV purity while maintaining high titersStephen M Winston, Mark A Brimble, Kristin B Wiggins, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
A fluorogenic complementation tool kit for interrogating lipid droplet-organelle interactionXiao Li, Rico Gamuyao, Ming-Lun Wu, et al.
The Journal of Cell Biology|July 1, 2024
A fluorogenic complementation tool kit for interrogating lipid droplet-organelle interactionXiao Li, Rico Gamuyao, Ming-Lun Wu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2024
Preclinical development of lentiviral vector gene therapy for Diamond-Blackfan anemia syndromeSenthil Velan Bhoopalan, Thiyagaraj Mayuranathan, Nana Liu, et al.
Science Translational Medicine|April 29, 2021
Sustained fetal hemoglobin induction in vivo is achieved by BCL11A interference and coexpressed truncated erythropoietin receptorNaoya Uchida, Francesca Ferrara, Claire M Drysdale, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Reprogramming CAR T-Cells with designed bioPROTACsVivek S Peche, Sebastian Kenny, Tae Gun Kang, et al.
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