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Updated: Aug 18, 2025

A Standard Methodology to Examine On-site Mutagenicity As a Function of Point Mutation Repair Catalyzed by CRISPR/Cas9 and SsODN in Human Cells
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Prime Editing for the Installation and Correction of Mutations Causing Inherited Retinal Disease: A Brief Methodology

Yi-Ting Tsai1, Bruna Lopes da Costa1,2,3, Nicholas D Nolan1,2,3

  • 1Columbia University, Department of Biomedical Engineering, New York, NY, USA.

Methods in Molecular Biology (Clifton, N.J.)
|December 9, 2022
PubMed

Keywords:
CRISPR/Cas9 systemsGene editingInherited retinal diseases (IRDs)OphthalmologyPde6bPrime editingRd10Retinal degenerationRetinitis pigmentosa (RP)

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