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Fine-tuning the ubiquitin-proteasome system to treat pulmonary fibrosis

Idiopathic pulmonary fibrosis is an extremely aggressive lung disease that develops almost exclusively in older individuals, carries a very poor prognosis, and lacks any truly effective therapies. The current conceptual model is that IPF develops because of an age-related decline in the ability of t...

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Dettagli Bibliografici
Pubblicato in:Connect Tissue Res
Autori principali: Roque, Willy, Summer, Ross, Romero, Freddy
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6373466/
https://ncbi.nlm.nih.gov/pubmed/30343604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/03008207.2018.1529174
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