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[DOI] [PMC free article] [PubMed] [Google Scholar] (129).Barker CA, Allison SE, Zlitni S, Nguyen ND, Das R, Melacini G, Capretta AA, and Brown ED (2013) Degradation of MAC13243 and studies of the interaction of resulting thiourea compounds with the lipoprotein targeting chaperone LolA

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2 Overview of idiopathic pulmonary fibrosis 2.1 Characterization of idiopathic pulmonary fibrosis Histologically, IPF is characterized by UIP patterning, in which the lung interstitiuma band-like tissue supporting alveoliundergoes ECM deposition and architectural disorganization ( 2.2 Pathogenesis and therapeutic targets of idiopathic pulmonary fibrosis 2.2.1 Alveolar epithelial cell injury and abnormal repair The etiology and pathogenesis of PF, particularly IPF, are largely undetermined, but notable advancements and consensus have been achieved in the field

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