Histological hallmarks and role of Slug/PIP axis in pulmonary hypertension secondary to pulmonary fibrosis

Pulmonary hypertension secondary to pulmonary fibrosis (PF‐PH) is one of the most common causes of PH, and there is no approved therapy. The molecular signature of PF‐PH and underlying mechanism of why pulmonary hypertension (PH) develops in PF patients remains understudied and poorly understood. We...

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Pubblicato in:EMBO Mol Med
Autori principali: Ruffenach, Gregoire, Umar, Soban, Vaillancourt, Mylene, Hong, Jason, Cao, Nancy, Sarji, Shervin, Moazeni, Shayan, Cunningham, Christine M, Ardehali, Abbas, Reddy, Srinivasa T, Saggar, Rajan, Fishbein, Gregory, Eghbali, Mansoureh
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2019
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Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6728601/
https://ncbi.nlm.nih.gov/pubmed/31468711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201810061
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