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Cell Stem Cell|November 12, 2024
Regulated GATA1 expression as a universal gene therapy for Diamond-Blackfan anemiaRichard A Voit, Xiaotian Liao, Alexis Caulier, et al.
The Journal of Clinical Investigation|September 8, 2020
BCL11A enhancer-edited hematopoietic stem cells persist in rhesus monkeys without toxicitySelami Demirci, Jing Zeng, Yuxuan Wu, et al.
The New England Journal of Medicine|October 15, 2025
Long-Term Safety and Efficacy of Gene Therapy for Adenosine Deaminase DeficiencyClaire Booth, Katelyn Masiuk, Konstantinos Vazouras, et al.
Biorxiv : the Preprint Server for Biology|June 9, 2023
Gene editing without <i>ex vivo</i> culture evades genotoxicity in human hematopoietic stem cellsJing Zeng, My Anh Nguyen, Pengpeng Liu, et al.
Cell Stem Cell|December 13, 2024
Gene editing without ex vivo culture evades genotoxicity in human hematopoietic stem cellsJing Zeng, My Anh Nguyen, Pengpeng Liu, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndromeAlessandro Aiuti, Luca Biasco, Samantha Scaramuzza, et al.
Blood|July 21, 2023
Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndromeRoxane Labrosse, Julia I Chu, Myriam A Armant, et al.
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