Cystic Fibrosis: Engineered Proteins Can 'Bypass' Genetic Defect

Courtesy ScienceDaily  Fri, 08/29/2008 - 00:15

By manipulating the machinery used by our cells for quality control, researchers have found a way to restore the function of cystic fibrosis (CF) airway cells.

This could significantly reduce the sticky mucus that plugs the lungs of CF patients, which leads to antibiotic-resistant infections and untimely death.


 

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