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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Shranjeno v:
Bibliografske podrobnosti
izdano v:EMBO Mol Med
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Articles
Online dostop: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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