CRISPR – Gene Editing – Waisman Center – UW–Madison

Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins

Accounting for diversity in the design of CRISPR-based therapeutic genome editing

Production and characterization of virus-free, CRISPR-CAR T cells capable of inducing solid tumor regression

CRISPR Generated SIX6 and POU4F2 Reporters Allow Identification of Brain and Optic Transcriptional Differences in Human PSC-Derived Organoids

Fluorescent tagging of endogenous proteins with CRISPR/Cas9 in primary mouse neural stem cells

One-Step Generation of Seamless Luciferase Gene Knockin Using CRISPR/Cas9 Genome Editing in Human Pluripotent Stem Cells

High content analysis platform for optimization of lipid mediated CRISPR-Cas9 delivery strategies in human cells