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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

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H&E and Safranin-O/Fast green staining demonstrated that the mice in OA group showed disrupted articular cartilage, erosion, extensive proteoglycan loss, and cell reduction, while the ones in sham group maintained regular cartilage morphology (Fig