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Development of a Gene Edited Next-Generation Hematopoietic Cell Transplant to Enable Acute Myeloid Leukemia Treatment by Solving Off-Tumor Toxicity

Molecular Therapy - Methods &amp Clinical Development(2023)

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acute myeloid leukemia,immunotherapy,CRISPR-Cas9,hematopoietic stem cell,CD33,genome engineering,IND-enabled,pharmacology/toxicology
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