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3.2.3 Treatment of pulmonary diseases Idiopathic pulmonary fibrosis is a chronic and progressive interstitial lung disease characterized by excessive fibrosis of the lung tissue and is associated with high morbidity and mortality rates (Blackwell et al., 2014)

Fisher M, VandenBranden M, Findlay K, Burchell B, Thummel K, Hall S, Wrighton SA: Tissue distribution and interindividual variation in human UDP-glucuronosyltransferase activity: relationship between UGT1A1 promoter genotype and variability in a liver bank

The tissue sections from all experimental groups were dewaxed and hydrated (Alomar et al., 2021)

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Nevertheless, expansion is constrained by low mechanization, inconsistent quality standards, and limited integration into value chains