New therapeutic strategies for sickle cell disease using CRISPR/Cas9 to produce he...
Genomic editing with CRISPR/Cas9 for production of hereditary persistance of fetal...
Investigation of transcription factors involved in HBG1 gene expression regulation...
Multiplex CRISPR/Cas9 genome editing using ribonucleoprotein complexes for the gen...
Pathophysiological mechanisms and treatment of red blood cell abnormalities
Multi-user equipment approved in grant 19/18886-1: PeriCam PSI NR
Development of CRISPR/Cas9-based genome editing for the generation of allogeneic C...