Epigenetic Regulation of Pulmonary Arterial Hypertension-Induced Vascular and Right Ventricular Remodeling: New Opportunities?

Pulmonary artery hypertension (PAH) is a rare chronic disease with high impact on patients’ quality of life and currently no available cure. PAH is characterized by constant remodeling of the pulmonary artery by increased proliferation and migration of pulmonary arterial smooth muscle cells (PASMCs)...

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Detalles Bibliográficos
Autores principales: Kocken, Jordy M. M., da Costa Martins, Paula A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727715/
https://www.ncbi.nlm.nih.gov/pubmed/33255338
http://dx.doi.org/10.3390/ijms21238901

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727715/
https://www.ncbi.nlm.nih.gov/pubmed/33255338
http://dx.doi.org/10.3390/ijms21238901

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