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Autor:
Katie Uhl, Shreya Paithankar, Dmitry Leshchiner, Tara E. Jager, Mohamed Abdelgied, Bhavna Dixit, Raya Marashdeh, Dewen Luo-Li, Kaylie Tripp, Angela M. Peraino, Maximiliano Tamae Kakazu, Cameron Lawson, Dave W. Chesla, Ningzhi Luo-Li, Edward T. Murphy, Jeremy Prokop, Bin Chen, Reda E. Girgis, Xiaopeng Li
Publikováno v:
Cells, Vol 12, Iss 20, p 2501 (2023)
Idiopathic pulmonary fibrosis (IPF) is a pathological condition wherein lung injury precipitates the deposition of scar tissue, ultimately leading to a decline in pulmonary function. Existing research indicates a notable exacerbation in the clinical
Externí odkaz:
https://doaj.org/article/28fa01fc1ab7447c8f380a819c22d5c8