Health
Treating cystic fibrosis with mRNA therapy or CRISPR – EurekAlert
The potential for treating cystic fibrosis (CF) using mRNA therapies or CRISPR gene editing is possible regardless of the causative mutation. CF clinical trials…
IMAGE: Field and provides all-inclusive access to the critical pillars of human gene therapy: research, methods, and clinical applications.
view more
Credit: Mary Ann Liebert, Inc., publishers
New Rochelle, NY, October 8, 2020–The potential for treating cystic fibrosis (CF) using mRNA therapies or CRISPR gene editing is possible regardless of the causative mutation. CF clinical trials showing that a genotype-agnostic gene therapy for CF is possible are reviewed in the peer-reviewed journal…
-
Business23 hours agoWhat Warren Buffett’s farewell letter means for Berkshire Hathaway investors
-
General23 hours agoEnvironment Bill passes Senate as Greens cut deal with Labor
-
General7 hours agoQantas terminal at Melbourne Airport evacuated and flights delayed due to fire
-
General22 hours agoCalls for states to change alcohol laws ahead of women’s ministers meeting