A new mouse model mimicking the liver symptoms of myotonic dystrophy type 1 — the most prevalent form of adult-onset muscular dystrophy — provides insight into why patients develop fatty liver disease and display hypersensitivity to medications, making treatment difficult. The new model opens avenues for screening new medications for liver toxicity prior to patient trials.
Categories
Recent Posts
- REGENXBIO completes dosing in Duchenne gene therapy confirmation study; planning BLA submission to FDA in Q3 2026
- Life with Lily: My Favorite Accessible Fashion & Beauty Tips
- CITGO Lake Charles golf classic raises record $756K to support MDA
- Five Things You’ll Find at MDA Engage
- At PPMD, I get to be part of a fraternity that none of us signed up for
Archive
- June 2026
- May 2026
- April 2026
- March 2026
- February 2026
- January 2026
- December 2025
- November 2025
- October 2025
- September 2025
- August 2025
- July 2025
- June 2025
- May 2025
- April 2025
- March 2025
- February 2025
- January 2025
- December 2024
- November 2024
- October 2024
- September 2024
- August 2024
- July 2024
- June 2024
- May 2024
- April 2024
- March 2024
- February 2024
- January 2024
