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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Articles
Acesso em linha: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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