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Engineering resistance to CD33-targeted immunotherapy in normal hematopoiesis by CRISPR/Cas9-deletion of CD33 exon 2.

Olivier HumbertGeorge S LaszloSophie SichelChristina IronsideKevin G HaworthOlivia M BatesMary E BeddoeRay R CarrilloHans-Peter KiemRoland Bruno Walter
Published in: Leukemia (2018)
Keyphrases
  • crispr cas
  • genome editing
  • nk cells
  • cancer therapy
  • drug delivery