Tartrate-resistant acid phosphatase 5 promotes pulmonary fibrosis by modulating β-catenin signaling

Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease with limited therapeutic options. Tartrate-resistant acid phosphatase 5 (ACP5) performs a variety of functions. However, its role in IPF remains unclear. Here, we demonstrate that the levels of ACP5 are increased in IPF patient...

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Detalles Bibliográficos
Autores principales: Hu, Yinan, Wang, Qi, Yu, Jun, Zhou, Qing, Deng, Yanhan, Liu, Juan, Zhang, Lei, Xu, Yongjian, Xiong, Weining, Wang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748833/
https://www.ncbi.nlm.nih.gov/pubmed/35013220
http://dx.doi.org/10.1038/s41467-021-27684-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748833/
https://www.ncbi.nlm.nih.gov/pubmed/35013220
http://dx.doi.org/10.1038/s41467-021-27684-9

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