Related Experiment Video
Updated: Jan 26, 2026

CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation
Published on: June 20, 2019
Measure Twice, Cut Once: Therapeutic Editing of HSPCs Requires Precise Planning
Rachel E Rau1, Margaret A Goodell1
1Department of Pediatrics, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine and Texas Children's Hospital, One Baylor Plaza, Houston, TX 77030, USA.
Abstract:
Hematologic diseases may be among the first clinical targets for therapeutic gene editing. In this issue of Cell Stem Cell, Schiroli et al. (2019) report a thorough, unbiased investigation of the impact of gene editing on hematopoietic stem and progenitor function and offer a clear path forward for editing in multiple tissues and conditions.
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