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 Genome Editing 

Genome editing technology is advancing at a breathtaking rate. In particular, programmable nucleases based on the CRISPR/Cas9 system are enabling basic and translational research that holds promise for the development of new therapeutics.

 What We Do 

MCCB researchers are applying this new technology across a number of different platforms to model and treat human diseases, including cancer. In particular, these new tools provide the possibility for gene correction in cases of congenital human disease. Indeed, collaborative efforts between MCCB researchers and other groups on campus are focused on correction of monogenic disorders, such as Huntington’s Disease and Chronic Granulomatous Disease, as well as the eradication of HIV from latent cellular reservoirs. In these cases, nuclease technology is being coupled with viral delivery systems through collaborations with the UMass Horae Gene Therapy Center and RNA Therapeutics Institute to create gene correction therapies or autologous cell-replacement therapies.

Click below to see more about how MCCB researchers apply or develop genome editing in their studies:

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Lawson Lab

Wolfe Lab