Consequences of BMPR2 Deficiency in the Pulmonary Vasculature and Beyond: Contributions to Pulmonary Arterial Hypertension

Since its association with familial pulmonary arterial hypertension (PAH) in 2000, Bone Morphogenetic Protein Receptor II (BMPR2) and its related signaling pathway have become recognized as a key regulator of pulmonary vascular homeostasis. Herein, we define BMPR2 deficiency as either an inactivatio...

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Detalles Bibliográficos
Autores principales: Andruska, Adam, Spiekerkoetter, Edda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165502/
https://www.ncbi.nlm.nih.gov/pubmed/30149506
http://dx.doi.org/10.3390/ijms19092499

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165502/
https://www.ncbi.nlm.nih.gov/pubmed/30149506
http://dx.doi.org/10.3390/ijms19092499

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