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Similar content being viewed by others Introduction Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease of unknown etiology 1 , demonstrating the high incidence and mortality 2

It is essential to cycle GHK-Cu to maintain receptor sensitivity and avoid copper dysregulation

Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular EhlersDanlos syndrome