Biblio
CRISPR/Cas9n-mediated ELANE promoter editing for gene therapy of severe congenital neutropenia. Mol Ther. 2024.
Design of novel granulopoietic proteins by topological rescaffolding. PLoS Biol. 2020;18(12):e3000919.
Gene Knockout in Hematopoietic Stem and Progenitor Cells Followed by Granulocytic Differentiation. Methods Mol Biol. 2020;2115:455-469.
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