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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 interstitium—a band-like tissue supporting alveoli—undergoes 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
Dr. Esther Kbeauty
Amount:10 Grams
Julia Oyet represented the Fund at the 31st ICPAU Annual Seminar, that was held under the theme “Sustaining Institutions and Lives for Sustainable Growth.” DPF was mong the sponsors for the event
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