Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.

Bullboard - Stock Discussion Forum Satellos Bioscience Inc T.MSCL

Alternate Symbol(s):  MSCLF

Satellos Bioscience Inc. is a Canada-based a drug discovery and development company with a focus on muscle regeneration. The Company is focused on developing medicines to treat degenerative muscle conditions. Its MyoReGenX platform is specifically designed to recreate the specialized muscle stem cell niche in vitro. MyoReGenX platform enables to map pathways which modulate muscle repair and... see more

TSX:MSCL - Post Discussion

Satellos Bioscience Inc > Defeat Duchenne Canada
View:
Post by db2067 on Jul 04, 2022 10:02am

Defeat Duchenne Canada

https://musculardystrophynews.com/2022/06/16/defeat-duchenne-canada-grants-1m-dmd-treatment-research/ Defeat Duchenne Canada grant recipients for this year include Michael Rudnicki, PhD, director of the Regenerative Medicine Program at the Ottawa Hospital Research Institute, Ottawa, Ontario. He’s discovered a protein called Wnt7a that could become a DMD treatment candidate due to its ability to repair muscle damage. Rudnicki will work to deliver the protein via circulation to all bodily muscles. In particular, his team is investigating exosomes, small vesicles found naturally in human bodies and which carry information between cells. Through the project, titled “Systemic Delivery of Wnt7a for Treating Duchenne Muscular Dystrophy,” Rudnicki and his lab will engineer new versions of exosomes carrying Wnt7a for delivery to muscle cells. The hope is that the prospective therapy will stimulate the muscles’ own capacity for regeneration and growth, independent of the underlying mutation.
Be the first to comment on this post
The Market Update
{{currentVideo.title}} {{currentVideo.relativeTime}}
< Previous bulletin
Next bulletin >

At the Bell logo
A daily snapshot of everything
from market open to close.

{{currentVideo.companyName}}
{{currentVideo.intervieweeName}}{{currentVideo.intervieweeTitle}}
< Previous
Next >
Dealroom for high-potential pre-IPO opportunities