Jason K. W. Cheng

In vivo gene editing in dystrophic mouse muscle and muscle stem cells

George M. Church, Ru Xiao, Le Cong, 2016, Science.

CRISPR-Cas12a System With Synergistic Phage Recombination Proteins for Multiplex Precision Editing in Human Cells

Le Cong, Nicholas W. Hughes, Jason K. W. Cheng, 2022, Frontiers in Cell and Developmental Biology.

A multifunctional AAV–CRISPR–Cas9 and its host response

Prashant Mali, George M Church, G. Church, 2016, Nature Methods.

Therapeutic Gene Editing in Muscles and Muscle Stem Cells

A. Wagers, Mohammadsharif Tabebordbar, Jason K. W. Cheng, 2017 .

Microbial single-strand annealing proteins enable CRISPR gene-editing tools with improved knock-in efficiencies and reduced off-target effects

Le Cong, M. Winslow, Nicholas W. Hughes, 2021, Nucleic acids research.

dCas9-based gene editing for cleavage-free genomic knock-in of long sequences

Nicholas W. Hughes, Jason K. W. Cheng, Le Cong, 2022, Nature Cell Biology.

dCas9-based gene editing for cleavage-free genomic knock-in of long sequences

Le Cong, Nicholas W. Hughes, Jason K. W. Cheng, 2022, Nature cell biology.

In Situ Modification of Tissue Stem and Progenitor Cell Genomes

A. Wagers, Mohammadsharif Tabebordbar, K. Zhu, 2019, Cell reports.