Article
CRISPR/Cas9-Mediated Introduction of Specific Heterozygous Mutations in Human Induced Pluripotent Stem Cells.
Methods in molecular biology (Clifton, N.J.) - 1 Jan 2022
Brandão Karina O, Grandela Catarina, Yiangou Loukia, Mummery Christine L, Davis Richard P
Abstract excerpt
Advances in genome editing and our ability to derive and differentiate human induced pluripotent stem cells (hiPSCs) into a wide variety of cell types present in the body is revolutionizing how we model human diseases in vitro. Central to this has been the development of the CRISPR/Cas9 system as an inexpensive and highly efficient tool for introducing or correcting disease-associated mutations. However, the ease...
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