Discovery to Impact: The Medicine by Design Project Showcase in pictures
Full day event celebrates eight years of success and explores future directions
Full day event celebrates eight years of success and explores future directions
Pitches focused on treating a difficult form of cancer and enhancing gene therapy treatments take the top spots
$25K and $10K will be awarded to the top regenerative or precision medicine innovations
Event hosted by Medicine by Design’s Healthy and Inclusive Labs committee and Working Towards Inclusivity in Chemistry Toronto
Medicine by Design-funded researchers are leading the way in ground-breaking liver research
Stem cell pioneer Gordon Keller, director of the University Health Network's McEwen Stem Cell Institute, leads a team of eight labs focused on harnessing the liver’s power to regenerate. Read more.
The University of Toronto's Gary Bader, along with University Health Network researchers Sonya MacParland, and Ian McGilvray, have collaborated on a world first: generating a “map” of all cells of the human liver. Read more.
The University of Toronto's Axel Guenther’s lab has developed collagen tubes that hold potential to be developed into lab-grown bile ducts, with the aim of being able to replace this part of the organ in a patient. Read more.
Christine Bear's lab at The Hospital for Sick Children (SickKids), along with other labs, is working on treating cystic fibrosis-linked liver disease with regenerative medicine approaches. Read more.
Shinichiro Ogawa, a scientist at the McEwen Stem Cell Institute, University Health Network, is focused on the early-stage translation of the liver cells from experiment to clinical application. Read more.
For Canadians to benefit from biomedical innovations, we must build a thriving ecosystem
Innovative study unveils rare liver disease secrets
The symposium — themed “Intentional Innovation” — attracted more than 750 registrants
This alliance is set to unlock Toronto's potential as a globally-leading ecosystem for regenerative medicine
New research could transform cell therapies for incurable diseases