CRISPR – Gene Editing – Waisman Center – UW–Madison

Genome-Wide CRISPR Screening Identifies Cellular Factors Controlling Nonviral Genome Editing Efficiency

Evaluation of subretinally delivered Cas9 ribonucleoproteins in murine and porcine animal models highlights key considerations for therapeutic translation of genetic medicines

CRISPR-based genetic screens in human pluripotent stem cells derived neurons and brain organoids

Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport

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