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doi:10.1016/j.explore.2021.09.006 Pakowska-Godzik E, Lachowicz K, Rosoowska-Huszcz D

Exosomes and Exosome-Inspired vesicles for targeted drug delivery

Idiopathic pulmonary fibrosis Idiopathic pulmonary fibrosis ( IPF ), formerly known as cryptogenic fibrosing alveolitis , [5] is a rare, progressive illness of the respiratory system, characterized by the thickening and stiffening of lung tissue, that surrounds the air sacs, and is associated with the formation of scar tissue

AmAc-UA mice has lower gastrocnemius muscle mass compared to PBS-VWR (p=0.004) or PBS-UA (p=0.003)

Aquaporin-4 gene variant independently associated with oedema after intracerebral haemorrhage