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…
-
General18 hours agoCoroner to examine treatment of woman who died three days after surgery performed by former Queensland premier’s partner
-
Business17 hours agoWhy Antipa, Cettire, Magnetic Resources, and Steadfast shares are pushing higher
-
General19 hours agoToo skewed, too gentlemanly | The Spectator Australia
-
General20 hours agoAlbanese beats drum on economy as trade clouds gather