There is detectable variation in the lipidomic profile between stable and progressive patients with idiopathic pulmonary fibrosis (IPF)

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterized by fibrosis and progressive loss of lung function. The pathophysiological pathways involved in IPF are not well understood. Abnormal lipid metabolism has been described in various other chronic lung...

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Detalles Bibliográficos
Autores principales: Nambiar, Shabarinath, Clynick, Britt, How, Bong S., King, Adam, Walters, E. Haydn, Goh, Nicole S., Corte, Tamera J., Trengove, Robert, Tan, Dino, Moodley, Yuben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033725/
https://www.ncbi.nlm.nih.gov/pubmed/33836757
http://dx.doi.org/10.1186/s12931-021-01682-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033725/
https://www.ncbi.nlm.nih.gov/pubmed/33836757
http://dx.doi.org/10.1186/s12931-021-01682-3

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