Pulmonary Arterial Hypertension Due to NPR-C Mutation: A Novel Paradigm for Normal and Pathologic Remodeling?

Idiopathic Pulmonary Arterial Hypertension (IPAH) is a deadly and disabling disease characterized by severe vascular remodeling of small pulmonary vessels by fibroblasts, myofibroblasts and vascular smooth muscle cell proliferation. Recent studies suggest that the Natriuretic Peptide Clearance Recep...

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Detalles Bibliográficos
Autor principal: Egom, Emmanuel Eroume-A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628360/
https://www.ncbi.nlm.nih.gov/pubmed/31234560
http://dx.doi.org/10.3390/ijms20123063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628360/
https://www.ncbi.nlm.nih.gov/pubmed/31234560
http://dx.doi.org/10.3390/ijms20123063

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