In recent decades, treatment options for people with cystic fibrosis have improved dramatically. The newest drugs, known as potentiators, target a protein called cystic fibrosis transmembrane conductance regulator, which is mutated in people with the disease. Yet, while these medications can help some people with CF, they are far from perfect. Moreover, researchers haven’t been able to figure out how the drugs actually work—until now.
from http://besthealthnews.com/2019/07/hinge-like-protein-may-open-new-doors-in-cystic-fibrosis-treatment/
from
https://healthnews010.tumblr.com/post/186181031093
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