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Updated: Jan 28, 2026

CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications
Published on: August 9, 2022
Gene Editing of Mouse Embryonic and Epiblast Stem Cells
Tennille Sibbritt1,2, Pierre Osteil1,2, Xiaochen Fan1
1The University of Sydney, Children's Medical Research Institute, Westmead, NSW, Australia.
Abstract:
Efficient and reliable methods for gene editing are critical for the generation of loss-of-gene function stem cells and genetically modified mice. Here, we outline the application of CRISPR-Cas9 technology for gene editing in mouse embryonic stem cells (mESCs) to generate knockout ESC chimeras for the fast-tracked analysis of gene function. Furthermore, we describe the application of gene editing directly to mouse epiblast stem cells (mEpiSCs) for modelling germ layer differentiation in vitro.
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