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…
-
Noosa News17 hours agoQueensland weather forecast sees sunny weather for last week of winter
-
General20 hours agoFirst home buyers score early access to deposit scheme
-
Noosa News18 hours agoForum responds to urgent homelessness issues in Nambour
-
General17 hours agoEnergy provider ENGIE to ‘correct’ electricity bills for thousands of South Australian customers