Jarron Roy

  • Graduate Student

Targeted delivery of biologics

Dawid Maciorowski

Dawid Maciorowski headshot

MD-PhD Candidate

  • Graduate Student

Novel CRISPR-based gene editing strategies to investigate treatments for pediatric cancer

Jacobus (Jack) Burger

Jack Burger headshot

  • Graduate Student

Developing biomedical nanomaterials for drug delivery applications

UW Researchers Partner with US Department of Defense to Develop Stem Cell Therapy for Combat-Related Eye Injuries

Using an ingenious microscopic retinal patch, eye researchers at UW‒Madison will develop and test a new way to treat United States military personnel blinded in combat. WID’s Sarah Gong is a collaborator on the project.

Randolph Ashton and Collaborators Win WARF Innovation Award

WID’s Randolph Ashton, Gavin Knight, Benjamin Knudsen, and Nisha Iyer take top honors from the Wisconsin Alumni Research Foundation’s Innovation Awards. Their work, Superior Neural Tissue Models for Disease Modeling, Drug Development and More, was selected from more than 400 innovation disclosures.

Dan Cappabianca

  • Graduate Student

Novel CAR T Cell therapy development in translational and bench top settings

Brady Lundin

  • Graduate Student

Creating and utilizing neural tissue engineering platforms for the study of clinical disease.

Human Nature Screening

The the MS Biotechnology program at UW and the Wisconsin Institute for Discovery are partnering to screen the documentary film “Human Nature”, an exploration of gene editing and its implications both biological and ethical.

Huaguang Yang

  • Postdoctoral Associate

Polymer Processing, Polymer Foaming, Composites, Injection molding and innovative plastics manufacturing processes

Xiuxiu Wang

  • Postdoctoral Associate

Research interests focus on design of multi-functional nanocarriers for targeted drug delivery

Tiny Capsules Packed with Gene-Editing Tools Offer Alternative to Viral Delivery of Gene Therapy

An interdisciplinary pair of WID researchers has developed a new nanocapsule delivery method for delivering the CRISPR-Cas9 gene editing tool. The new system could be used for many types of gene therapies.

Shivani Saxena

  • Graduate Student

Engineering cells and organism via genome editing and studying the delivery method for CRISPR/Cas9

Min Zhu

MIn Zhu

  • Graduate Student

Nanoparticles for delivery of therapeutic agents and with gene-editing