Targeting mechanosensitive protein could treat pulmonary fibrosis, study suggests

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Targeting mechanosensitive protein could treat pulmonary fibrosis, study suggests

Researchers at the University of Alabama at Birmingham have identified a new molecular target that could potentially treat the deadly, aging-related lung disease idiopathic pulmonary fibrosis (IPF). The study, which will be published March 10 in the Journal of Experimental Medicine (JEM), suggests that targeting a protein called MDM4 could prevent respiratory failure by initiating a genetic program that removes scar tissue from the lungs.

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