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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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: John Wiley and Sons Inc. 2019
Assuntos:
Articles
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares