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Updated: Feb 16, 2026

07:49
CRISPR Epigenome Editing in Human Cells using Plasmid DNA Transfection and mRNA Nucleofection Delivery
Published on: May 30, 2025
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Turning up the Heat with Therapeutic Epigenome Editing
Alexandra Zezulin1, Kiran Musunuru1
1Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cell Stem Cell
|January 6, 2018
Abstract:
CRISPR-Cas9 has been touted for therapeutic genome editing, but limitations include inefficient correction of disease-causing mutations and off-target mutagenesis. In the latest issue of Cell, Liao et al. (2017) show that a modified version of CRISPR-Cas9 can target and activate key therapeutic genes in vivo without altering DNA sequence identity.
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