Quantification of Lung Fibrosis in IPF-Like Mouse Model and Pharmacological Response to Treatment by Micro-Computed Tomography

Idiopathic pulmonary fibrosis (IPF) is a chronic progressive degenerative lung disease leading to respiratory failure and death. Although anti-fibrotic drugs are now available for treating IPF, their clinical efficacy is limited and lung transplantation remains the only modality to prolong survival...

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Vydáno v:Front Pharmacol
Hlavní autoři: Ruscitti, Francesca, Ravanetti, Francesca, Bertani, Valeria, Ragionieri, Luisa, Mecozzi, Laura, Sverzellati, Nicola, Silva, Mario, Ruffini, Livia, Menozzi, Valentina, Civelli, Maurizio, Villetti, Gino, Stellari, Franco Fabio
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2020
Témata:
Pharmacology
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7385278/
https://ncbi.nlm.nih.gov/pubmed/32792953
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2020.01117
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